Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.7669589_7676614delCA2499224945TP53c.-19_*21del
c.-21-1377_*21del
c.-19_*310del
c.-19_*222del
c.-253_*21del
c.-136_*222del
c.-136_*21del
c.-136_*310del
c.-136_983+1021del
 ClinVar
17g.7669609_7676594delCA2581463470TP53c.1_1182del
c.-21-1358_786del
c.1_903del
c.1_1161del
c.1_994-3365del
c.1_782+4572del
c.1_*289del
c.1_*201del
c.-234_1065del
c.-117_*201del
c.1_1149del
c.-117_1065del
c.-117_*289del
c.-117_983+1000del
17g.7673473_7673539dupCA2535386204TP53c.991_993+64dup
c.595_597+64dup
c.712_714+64dup
c.970_972+64dup
c.782+644_782+710dup (n.782+644_782+710dup)
c.51_53+64dup
c.874_876+64dup
c.514_516+64dup
c.958_960+64dup
 gnomAD v4
17g.7673473_7673475delinsACGCA2245947188TP53c.993+60_993+62delinsCGT (n.993+60_993+62delinsCGT)
c.597+60_597+62delinsCGT (n.597+60_597+62delinsCGT)
c.714+60_714+62delinsCGT (n.714+60_714+62delinsCGT)
c.972+60_972+62delinsCGT (n.972+60_972+62delinsCGT)
c.782+706_782+708delinsCGT (n.782+706_782+708delinsCGT)
c.53+60_53+62delinsCGT
c.876+60_876+62delinsCGT (n.876+60_876+62delinsCGT)
c.516+60_516+62delinsCGT (n.516+60_516+62delinsCGT)
c.960+60_960+62delinsCGT (n.960+60_960+62delinsCGT)
17g.7673474_7673475delCA914148883TP53c.993+60_993+61del (n.993+60_993+61del)
c.597+60_597+61del (n.597+60_597+61del)
c.714+60_714+61del (n.714+60_714+61del)
c.972+60_972+61del (n.972+60_972+61del)
c.782+706_782+707del (n.782+706_782+707del)
c.53+60_53+61del
c.876+60_876+61del (n.876+60_876+61del)
c.516+60_516+61del (n.516+60_516+61del)
c.960+60_960+61del (n.960+60_960+61del)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.7673475G>ACA287486479TP53c.993+60C>T (n.993+60C>T)
c.597+60C>T (n.597+60C>T)
c.714+60C>T (n.714+60C>T)
c.972+60C>T (n.972+60C>T)
c.782+706C>T (n.782+706C>T)
c.53+60C>T
c.876+60C>T (n.876+60C>T)
c.516+60C>T (n.516+60C>T)
c.960+60C>T (n.960+60C>T)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.7673475G>CCA2635873956TP53c.993+60C>G (n.993+60C>G)
c.597+60C>G (n.597+60C>G)
c.714+60C>G (n.714+60C>G)
c.972+60C>G (n.972+60C>G)
c.782+706C>G (n.782+706C>G)
c.53+60C>G
c.876+60C>G (n.876+60C>G)
c.516+60C>G (n.516+60C>G)
c.960+60C>G (n.960+60C>G)
 dbSNP gnomAD v4
17g.7673475G=CA2245947198TP53c.993+60C= (n.993+60C=)
c.597+60C= (n.597+60C=)
c.714+60C= (n.714+60C=)
c.972+60C= (n.972+60C=)
c.782+706C= (n.782+706C=)
c.53+60C=
c.876+60C= (n.876+60C=)
c.516+60C= (n.516+60C=)
c.960+60C= (n.960+60C=)
17g.7673475G>TCA2732940019TP53c.993+60C>A (n.993+60C>A)
c.597+60C>A (n.597+60C>A)
c.714+60C>A (n.714+60C>A)
c.972+60C>A (n.972+60C>A)
c.782+706C>A (n.782+706C>A)
c.53+60C>A
c.876+60C>A (n.876+60C>A)
c.516+60C>A (n.516+60C>A)
c.960+60C>A (n.960+60C>A)
 dbSNP
17g.7673475_7673476insTCTACA2245947206TP53c.993+59_993+60insTAGA (n.993+59_993+60insTAGA)
c.597+59_597+60insTAGA (n.597+59_597+60insTAGA)
c.714+59_714+60insTAGA (n.714+59_714+60insTAGA)
c.972+59_972+60insTAGA (n.972+59_972+60insTAGA)
c.782+705_782+706insTAGA (n.782+705_782+706insTAGA)
c.53+59_53+60insTAGA
c.876+59_876+60insTAGA (n.876+59_876+60insTAGA)
c.516+59_516+60insTAGA (n.516+59_516+60insTAGA)
c.960+59_960+60insTAGA (n.960+59_960+60insTAGA)
 dbSNP
17g.7673476G>ACA624865095TP53c.993+59C>T (n.993+59C>T)
c.597+59C>T (n.597+59C>T)
c.714+59C>T (n.714+59C>T)
c.972+59C>T (n.972+59C>T)
c.782+705C>T (n.782+705C>T)
c.53+59C>T
c.876+59C>T (n.876+59C>T)
c.516+59C>T (n.516+59C>T)
c.960+59C>T (n.960+59C>T)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.7673476G>CCA2732947530TP53c.993+59C>G (n.993+59C>G)
c.597+59C>G (n.597+59C>G)
c.714+59C>G (n.714+59C>G)
c.972+59C>G (n.972+59C>G)
c.782+705C>G (n.782+705C>G)
c.53+59C>G
c.876+59C>G (n.876+59C>G)
c.516+59C>G (n.516+59C>G)
c.960+59C>G (n.960+59C>G)
 dbSNP
17g.7673476G=CA2245947205TP53c.993+59C= (n.993+59C=)
c.597+59C= (n.597+59C=)
c.714+59C= (n.714+59C=)
c.972+59C= (n.972+59C=)
c.782+705C= (n.782+705C=)
c.53+59C=
c.876+59C= (n.876+59C=)
c.516+59C= (n.516+59C=)
c.960+59C= (n.960+59C=)
17g.7673476G>TCA2635873959TP53c.993+59C>A (n.993+59C>A)
c.597+59C>A (n.597+59C>A)
c.714+59C>A (n.714+59C>A)
c.972+59C>A (n.972+59C>A)
c.782+705C>A (n.782+705C>A)
c.53+59C>A
c.876+59C>A (n.876+59C>A)
c.516+59C>A (n.516+59C>A)
c.960+59C>A (n.960+59C>A)
 dbSNP gnomAD v4
17g.7673476_7673477insTCTAACA914148884TP53c.993+58_993+59insTTAGA (n.993+58_993+59insTTAGA)
c.597+58_597+59insTTAGA (n.597+58_597+59insTTAGA)
c.714+58_714+59insTTAGA (n.714+58_714+59insTTAGA)
c.972+58_972+59insTTAGA (n.972+58_972+59insTTAGA)
c.782+704_782+705insTTAGA (n.782+704_782+705insTTAGA)
c.53+58_53+59insTTAGA
c.876+58_876+59insTTAGA (n.876+58_876+59insTTAGA)
c.516+58_516+59insTTAGA (n.516+58_516+59insTTAGA)
c.960+58_960+59insTTAGA (n.960+58_960+59insTTAGA)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.7673477C>ACA2732962862TP53c.993+58G>T (n.993+58G>T)
c.597+58G>T (n.597+58G>T)
c.714+58G>T (n.714+58G>T)
c.972+58G>T (n.972+58G>T)
c.782+704G>T (n.782+704G>T)
c.53+58G>T
c.876+58G>T (n.876+58G>T)
c.516+58G>T (n.516+58G>T)
c.960+58G>T (n.960+58G>T)
 dbSNP
17g.7673477C=CA2245947213TP53c.993+58G= (n.993+58G=)
c.597+58G= (n.597+58G=)
c.714+58G= (n.714+58G=)
c.972+58G= (n.972+58G=)
c.782+704G= (n.782+704G=)
c.53+58G=
c.876+58G= (n.876+58G=)
c.516+58G= (n.516+58G=)
c.960+58G= (n.960+58G=)
17g.7673477C>GCA2732962863TP53c.993+58G>C (n.993+58G>C)
c.597+58G>C (n.597+58G>C)
c.714+58G>C (n.714+58G>C)
c.972+58G>C (n.972+58G>C)
c.782+704G>C (n.782+704G>C)
c.53+58G>C
c.876+58G>C (n.876+58G>C)
c.516+58G>C (n.516+58G>C)
c.960+58G>C (n.960+58G>C)
 dbSNP
17g.7673477C>TCA775168423TP53c.993+58G>A (n.993+58G>A)
c.597+58G>A (n.597+58G>A)
c.714+58G>A (n.714+58G>A)
c.972+58G>A (n.972+58G>A)
c.782+704G>A (n.782+704G>A)
c.53+58G>A
c.876+58G>A (n.876+58G>A)
c.516+58G>A (n.516+58G>A)
c.960+58G>A (n.960+58G>A)
 dbSNP gnomAD v3 gnomAD v4
17g.7673478A=CA2245947218TP53c.993+57T= (n.993+57T=)
c.597+57T= (n.597+57T=)
c.714+57T= (n.714+57T=)
c.972+57T= (n.972+57T=)
c.782+703T= (n.782+703T=)
c.53+57T=
c.876+57T= (n.876+57T=)
c.516+57T= (n.516+57T=)
c.960+57T= (n.960+57T=)
17g.7673478A>GCA287486480TP53c.993+57T>C (n.993+57T>C)
c.597+57T>C (n.597+57T>C)
c.714+57T>C (n.714+57T>C)
c.972+57T>C (n.972+57T>C)
c.782+703T>C (n.782+703T>C)
c.53+57T>C
c.876+57T>C (n.876+57T>C)
c.516+57T>C (n.516+57T>C)
c.960+57T>C (n.960+57T>C)
 dbSNP gnomAD v4
17g.7673479T>ACA2733123895TP53c.993+56A>T (n.993+56A>T)
c.597+56A>T (n.597+56A>T)
c.714+56A>T (n.714+56A>T)
c.972+56A>T (n.972+56A>T)
c.782+702A>T (n.782+702A>T)
c.53+56A>T
c.876+56A>T (n.876+56A>T)
c.516+56A>T (n.516+56A>T)
c.960+56A>T (n.960+56A>T)
 dbSNP
17g.7673479T>CCA2733123863TP53c.993+56A>G (n.993+56A>G)
c.597+56A>G (n.597+56A>G)
c.714+56A>G (n.714+56A>G)
c.972+56A>G (n.972+56A>G)
c.782+702A>G (n.782+702A>G)
c.53+56A>G
c.876+56A>G (n.876+56A>G)
c.516+56A>G (n.516+56A>G)
c.960+56A>G (n.960+56A>G)
 dbSNP
17g.7673479T>GCA2733123888TP53c.993+56A>C (n.993+56A>C)
c.597+56A>C (n.597+56A>C)
c.714+56A>C (n.714+56A>C)
c.972+56A>C (n.972+56A>C)
c.782+702A>C (n.782+702A>C)
c.53+56A>C
c.876+56A>C (n.876+56A>C)
c.516+56A>C (n.516+56A>C)
c.960+56A>C (n.960+56A>C)
 dbSNP
17g.7673480T>ACA2733123907TP53c.993+55A>T (n.993+55A>T)
c.597+55A>T (n.597+55A>T)
c.714+55A>T (n.714+55A>T)
c.972+55A>T (n.972+55A>T)
c.782+701A>T (n.782+701A>T)
c.53+55A>T
c.876+55A>T (n.876+55A>T)
c.516+55A>T (n.516+55A>T)
c.960+55A>T (n.960+55A>T)
 dbSNP
17g.7673480T>CCA2733123897TP53c.993+55A>G (n.993+55A>G)
c.597+55A>G (n.597+55A>G)
c.714+55A>G (n.714+55A>G)
c.972+55A>G (n.972+55A>G)
c.782+701A>G (n.782+701A>G)
c.53+55A>G
c.876+55A>G (n.876+55A>G)
c.516+55A>G (n.516+55A>G)
c.960+55A>G (n.960+55A>G)
 dbSNP
17g.7673480T>GCA2733123910TP53c.993+55A>C (n.993+55A>C)
c.597+55A>C (n.597+55A>C)
c.714+55A>C (n.714+55A>C)
c.972+55A>C (n.972+55A>C)
c.782+701A>C (n.782+701A>C)
c.53+55A>C
c.876+55A>C (n.876+55A>C)
c.516+55A>C (n.516+55A>C)
c.960+55A>C (n.960+55A>C)
 dbSNP
17g.7673481T>CCA2576230606TP53c.993+54A>G (n.993+54A>G)
c.597+54A>G (n.597+54A>G)
c.714+54A>G (n.714+54A>G)
c.972+54A>G (n.972+54A>G)
c.782+700A>G (n.782+700A>G)
c.53+54A>G
c.876+54A>G (n.876+54A>G)
c.516+54A>G (n.516+54A>G)
c.960+54A>G (n.960+54A>G)
17g.7673482T>ACA656753435TP53c.993+53A>T (n.993+53A>T)
c.597+53A>T (n.597+53A>T)
c.714+53A>T (n.714+53A>T)
c.972+53A>T (n.972+53A>T)
c.782+699A>T (n.782+699A>T)
c.53+53A>T
c.876+53A>T (n.876+53A>T)
c.516+53A>T (n.516+53A>T)
c.960+53A>T (n.960+53A>T)
 dbSNP COSMIC
17g.7673482T>CCA2733124081TP53c.993+53A>G (n.993+53A>G)
c.597+53A>G (n.597+53A>G)
c.714+53A>G (n.714+53A>G)
c.972+53A>G (n.972+53A>G)
c.782+699A>G (n.782+699A>G)
c.53+53A>G
c.876+53A>G (n.876+53A>G)
c.516+53A>G (n.516+53A>G)
c.960+53A>G (n.960+53A>G)
 dbSNP
17g.7673482T>GCA2635873977TP53c.993+53A>C (n.993+53A>C)
c.597+53A>C (n.597+53A>C)
c.714+53A>C (n.714+53A>C)
c.972+53A>C (n.972+53A>C)
c.782+699A>C (n.782+699A>C)
c.53+53A>C
c.876+53A>C (n.876+53A>C)
c.516+53A>C (n.516+53A>C)
c.960+53A>C (n.960+53A>C)
 gnomAD v4
17g.7673483G>ACA2733124123TP53c.993+52C>T (n.993+52C>T)
c.597+52C>T (n.597+52C>T)
c.714+52C>T (n.714+52C>T)
c.972+52C>T (n.972+52C>T)
c.782+698C>T (n.782+698C>T)
c.53+52C>T
c.876+52C>T (n.876+52C>T)
c.516+52C>T (n.516+52C>T)
c.960+52C>T (n.960+52C>T)
 dbSNP
17g.7673483G>CCA2733124122TP53c.993+52C>G (n.993+52C>G)
c.597+52C>G (n.597+52C>G)
c.714+52C>G (n.714+52C>G)
c.972+52C>G (n.972+52C>G)
c.782+698C>G (n.782+698C>G)
c.53+52C>G
c.876+52C>G (n.876+52C>G)
c.516+52C>G (n.516+52C>G)
c.960+52C>G (n.960+52C>G)
 dbSNP
17g.7673483G>TCA2733124121TP53c.993+52C>A (n.993+52C>A)
c.597+52C>A (n.597+52C>A)
c.714+52C>A (n.714+52C>A)
c.972+52C>A (n.972+52C>A)
c.782+698C>A (n.782+698C>A)
c.53+52C>A
c.876+52C>A (n.876+52C>A)
c.516+52C>A (n.516+52C>A)
c.960+52C>A (n.960+52C>A)
 dbSNP
17g.7673484A=CA2245947222TP53c.993+51T= (n.993+51T=)
c.597+51T= (n.597+51T=)
c.714+51T= (n.714+51T=)
c.972+51T= (n.972+51T=)
c.782+697T= (n.782+697T=)
c.53+51T=
c.876+51T= (n.876+51T=)
c.516+51T= (n.516+51T=)
c.960+51T= (n.960+51T=)
17g.7673484A>GCA001140TP53c.993+51T>C (n.993+51T>C)
c.597+51T>C (n.597+51T>C)
c.714+51T>C (n.714+51T>C)
c.972+51T>C (n.972+51T>C)
c.782+697T>C (n.782+697T>C)
c.53+51T>C
c.876+51T>C (n.876+51T>C)
c.516+51T>C (n.516+51T>C)
c.960+51T>C (n.960+51T>C)
 dbSNP ExAC gnomAD v2 gnomAD v4
17g.7673484A>TCA2732929147TP53c.993+51T>A (n.993+51T>A)
c.597+51T>A (n.597+51T>A)
c.714+51T>A (n.714+51T>A)
c.972+51T>A (n.972+51T>A)
c.782+697T>A (n.782+697T>A)
c.53+51T>A
c.876+51T>A (n.876+51T>A)
c.516+51T>A (n.516+51T>A)
c.960+51T>A (n.960+51T>A)
 dbSNP
17g.7673485G>ACA2733124131TP53c.993+50C>T (n.993+50C>T)
c.597+50C>T (n.597+50C>T)
c.714+50C>T (n.714+50C>T)
c.972+50C>T (n.972+50C>T)
c.782+696C>T (n.782+696C>T)
c.53+50C>T
c.876+50C>T (n.876+50C>T)
c.516+50C>T (n.516+50C>T)
c.960+50C>T (n.960+50C>T)
 dbSNP
17g.7673485G>CCA2733124134TP53c.993+50C>G (n.993+50C>G)
c.597+50C>G (n.597+50C>G)
c.714+50C>G (n.714+50C>G)
c.972+50C>G (n.972+50C>G)
c.782+696C>G (n.782+696C>G)
c.53+50C>G
c.876+50C>G (n.876+50C>G)
c.516+50C>G (n.516+50C>G)
c.960+50C>G (n.960+50C>G)
 dbSNP
17g.7673486T>ACA2732943607TP53c.993+49A>T (n.993+49A>T)
c.597+49A>T (n.597+49A>T)
c.714+49A>T (n.714+49A>T)
c.972+49A>T (n.972+49A>T)
c.782+695A>T (n.782+695A>T)
c.53+49A>T
c.876+49A>T (n.876+49A>T)
c.516+49A>T (n.516+49A>T)
c.960+49A>T (n.960+49A>T)
 dbSNP
17g.7673486T>CCA981209193TP53c.993+49A>G (n.993+49A>G)
c.597+49A>G (n.597+49A>G)
c.714+49A>G (n.714+49A>G)
c.972+49A>G (n.972+49A>G)
c.782+695A>G (n.782+695A>G)
c.53+49A>G
c.876+49A>G (n.876+49A>G)
c.516+49A>G (n.516+49A>G)
c.960+49A>G (n.960+49A>G)
 dbSNP gnomAD v3 gnomAD v4
17g.7673486T>GCA624865096TP53c.993+49A>C (n.993+49A>C)
c.597+49A>C (n.597+49A>C)
c.714+49A>C (n.714+49A>C)
c.972+49A>C (n.972+49A>C)
c.782+695A>C (n.782+695A>C)
c.53+49A>C
c.876+49A>C (n.876+49A>C)
c.516+49A>C (n.516+49A>C)
c.960+49A>C (n.960+49A>C)
 dbSNP gnomAD v2 gnomAD v4
17g.7673486T=CA2245947224TP53c.993+49A= (n.993+49A=)
c.597+49A= (n.597+49A=)
c.714+49A= (n.714+49A=)
c.972+49A= (n.972+49A=)
c.782+695A= (n.782+695A=)
c.53+49A=
c.876+49A= (n.876+49A=)
c.516+49A= (n.516+49A=)
c.960+49A= (n.960+49A=)
17g.7673487G>ACA2732960139TP53c.993+48C>T (n.993+48C>T)
c.597+48C>T (n.597+48C>T)
c.714+48C>T (n.714+48C>T)
c.972+48C>T (n.972+48C>T)
c.782+694C>T (n.782+694C>T)
c.53+48C>T
c.876+48C>T (n.876+48C>T)
c.516+48C>T (n.516+48C>T)
c.960+48C>T (n.960+48C>T)
 dbSNP
17g.7673487G>CCA624865097TP53c.993+48C>G (n.993+48C>G)
c.597+48C>G (n.597+48C>G)
c.714+48C>G (n.714+48C>G)
c.972+48C>G (n.972+48C>G)
c.782+694C>G (n.782+694C>G)
c.53+48C>G
c.876+48C>G (n.876+48C>G)
c.516+48C>G (n.516+48C>G)
c.960+48C>G (n.960+48C>G)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.7673487G=CA2245947227TP53c.993+48C= (n.993+48C=)
c.597+48C= (n.597+48C=)
c.714+48C= (n.714+48C=)
c.972+48C= (n.972+48C=)
c.782+694C= (n.782+694C=)
c.53+48C=
c.876+48C= (n.876+48C=)
c.516+48C= (n.516+48C=)
c.960+48C= (n.960+48C=)
17g.7673487G>TCA2635873988TP53c.993+48C>A (n.993+48C>A)
c.597+48C>A (n.597+48C>A)
c.714+48C>A (n.714+48C>A)
c.972+48C>A (n.972+48C>A)
c.782+694C>A (n.782+694C>A)
c.53+48C>A
c.876+48C>A (n.876+48C>A)
c.516+48C>A (n.516+48C>A)
c.960+48C>A (n.960+48C>A)
 gnomAD v4
17g.7673488T>ACA2733124151TP53c.993+47A>T (n.993+47A>T)
c.597+47A>T (n.597+47A>T)
c.714+47A>T (n.714+47A>T)
c.972+47A>T (n.972+47A>T)
c.782+693A>T (n.782+693A>T)
c.53+47A>T
c.876+47A>T (n.876+47A>T)
c.516+47A>T (n.516+47A>T)
c.960+47A>T (n.960+47A>T)
 dbSNP
17g.7673488T>CCA2733124145TP53c.993+47A>G (n.993+47A>G)
c.597+47A>G (n.597+47A>G)
c.714+47A>G (n.714+47A>G)
c.972+47A>G (n.972+47A>G)
c.782+693A>G (n.782+693A>G)
c.53+47A>G
c.876+47A>G (n.876+47A>G)
c.516+47A>G (n.516+47A>G)
c.960+47A>G (n.960+47A>G)
 dbSNP
17g.7673488T>GCA2733124152TP53c.993+47A>C (n.993+47A>C)
c.597+47A>C (n.597+47A>C)
c.714+47A>C (n.714+47A>C)
c.972+47A>C (n.972+47A>C)
c.782+693A>C (n.782+693A>C)
c.53+47A>C
c.876+47A>C (n.876+47A>C)
c.516+47A>C (n.516+47A>C)
c.960+47A>C (n.960+47A>C)
 dbSNP
17g.7673489T>ACA2733124561TP53c.993+46A>T (n.993+46A>T)
c.597+46A>T (n.597+46A>T)
c.714+46A>T (n.714+46A>T)
c.972+46A>T (n.972+46A>T)
c.782+692A>T (n.782+692A>T)
c.53+46A>T
c.876+46A>T (n.876+46A>T)
c.516+46A>T (n.516+46A>T)
c.960+46A>T (n.960+46A>T)
 dbSNP
17g.7673489T>CCA2635873991TP53c.993+46A>G (n.993+46A>G)
c.597+46A>G (n.597+46A>G)
c.714+46A>G (n.714+46A>G)
c.972+46A>G (n.972+46A>G)
c.782+692A>G (n.782+692A>G)
c.53+46A>G
c.876+46A>G (n.876+46A>G)
c.516+46A>G (n.516+46A>G)
c.960+46A>G (n.960+46A>G)
 dbSNP gnomAD v4
17g.7673489T>GCA2733124153TP53c.993+46A>C (n.993+46A>C)
c.597+46A>C (n.597+46A>C)
c.714+46A>C (n.714+46A>C)
c.972+46A>C (n.972+46A>C)
c.782+692A>C (n.782+692A>C)
c.53+46A>C
c.876+46A>C (n.876+46A>C)
c.516+46A>C (n.516+46A>C)
c.960+46A>C (n.960+46A>C)
 dbSNP
17g.7673490A>GCA2733124649TP53c.993+45T>C (n.993+45T>C)
c.597+45T>C (n.597+45T>C)
c.714+45T>C (n.714+45T>C)
c.972+45T>C (n.972+45T>C)
c.782+691T>C (n.782+691T>C)
c.53+45T>C
c.876+45T>C (n.876+45T>C)
c.516+45T>C (n.516+45T>C)
c.960+45T>C (n.960+45T>C)
 dbSNP
17g.7673490A>TCA2733124651TP53c.993+45T>A (n.993+45T>A)
c.597+45T>A (n.597+45T>A)
c.714+45T>A (n.714+45T>A)
c.972+45T>A (n.972+45T>A)
c.782+691T>A (n.782+691T>A)
c.53+45T>A
c.876+45T>A (n.876+45T>A)
c.516+45T>A (n.516+45T>A)
c.960+45T>A (n.960+45T>A)
 dbSNP
17g.7673490dupCA2635873992TP53c.993+45dup (n.993+45dup)
c.597+45dup (n.597+45dup)
c.714+45dup (n.714+45dup)
c.972+45dup (n.972+45dup)
c.782+691dup (n.782+691dup)
c.53+45dup
c.876+45dup (n.876+45dup)
c.516+45dup (n.516+45dup)
c.960+45dup (n.960+45dup)
 gnomAD v4
17g.7673491G>ACA2733124653TP53c.993+44C>T (n.993+44C>T)
c.597+44C>T (n.597+44C>T)
c.714+44C>T (n.714+44C>T)
c.972+44C>T (n.972+44C>T)
c.782+690C>T (n.782+690C>T)
c.53+44C>T
c.876+44C>T (n.876+44C>T)
c.516+44C>T (n.516+44C>T)
c.960+44C>T (n.960+44C>T)
 dbSNP
17g.7673491G>CCA2733124679TP53c.993+44C>G (n.993+44C>G)
c.597+44C>G (n.597+44C>G)
c.714+44C>G (n.714+44C>G)
c.972+44C>G (n.972+44C>G)
c.782+690C>G (n.782+690C>G)
c.53+44C>G
c.876+44C>G (n.876+44C>G)
c.516+44C>G (n.516+44C>G)
c.960+44C>G (n.960+44C>G)
 dbSNP
17g.7673491G>TCA2580612863TP53c.993+44C>A (n.993+44C>A)
c.597+44C>A (n.597+44C>A)
c.714+44C>A (n.714+44C>A)
c.972+44C>A (n.972+44C>A)
c.782+690C>A (n.782+690C>A)
c.53+44C>A
c.876+44C>A (n.876+44C>A)
c.516+44C>A (n.516+44C>A)
c.960+44C>A (n.960+44C>A)
 ClinVar dbSNP gnomAD v4
17g.7673492A>GCA2635873997TP53c.993+43T>C (n.993+43T>C)
c.597+43T>C (n.597+43T>C)
c.714+43T>C (n.714+43T>C)
c.972+43T>C (n.972+43T>C)
c.782+689T>C (n.782+689T>C)
c.53+43T>C
c.876+43T>C (n.876+43T>C)
c.516+43T>C (n.516+43T>C)
c.960+43T>C (n.960+43T>C)
 dbSNP gnomAD v4
17g.7673492A>TCA2733124801TP53c.993+43T>A (n.993+43T>A)
c.597+43T>A (n.597+43T>A)
c.714+43T>A (n.714+43T>A)
c.972+43T>A (n.972+43T>A)
c.782+689T>A (n.782+689T>A)
c.53+43T>A
c.876+43T>A (n.876+43T>A)
c.516+43T>A (n.516+43T>A)
c.960+43T>A (n.960+43T>A)
 dbSNP
17g.7673493C>ACA2733124807TP53c.993+42G>T (n.993+42G>T)
c.597+42G>T (n.597+42G>T)
c.714+42G>T (n.714+42G>T)
c.972+42G>T (n.972+42G>T)
c.782+688G>T (n.782+688G>T)
c.53+42G>T
c.876+42G>T (n.876+42G>T)
c.516+42G>T (n.516+42G>T)
c.960+42G>T (n.960+42G>T)
 dbSNP
17g.7673493C>GCA2733125050TP53c.993+42G>C (n.993+42G>C)
c.597+42G>C (n.597+42G>C)
c.714+42G>C (n.714+42G>C)
c.972+42G>C (n.972+42G>C)
c.782+688G>C (n.782+688G>C)
c.53+42G>C
c.876+42G>C (n.876+42G>C)
c.516+42G>C (n.516+42G>C)
c.960+42G>C (n.960+42G>C)
 dbSNP
17g.7673493C>TCA2733125003TP53c.993+42G>A (n.993+42G>A)
c.597+42G>A (n.597+42G>A)
c.714+42G>A (n.714+42G>A)
c.972+42G>A (n.972+42G>A)
c.782+688G>A (n.782+688G>A)
c.53+42G>A
c.876+42G>A (n.876+42G>A)
c.516+42G>A (n.516+42G>A)
c.960+42G>A (n.960+42G>A)
 dbSNP
17g.7673494T>ACA001147TP53c.993+41A>T (n.993+41A>T)
c.597+41A>T (n.597+41A>T)
c.714+41A>T (n.714+41A>T)
c.972+41A>T (n.972+41A>T)
c.782+687A>T (n.782+687A>T)
c.53+41A>T
c.876+41A>T (n.876+41A>T)
c.516+41A>T (n.516+41A>T)
c.960+41A>T (n.960+41A>T)
 dbSNP ExAC gnomAD v2 gnomAD v4
17g.7673494T>CCA624865098TP53c.993+41A>G (n.993+41A>G)
c.597+41A>G (n.597+41A>G)
c.714+41A>G (n.714+41A>G)
c.972+41A>G (n.972+41A>G)
c.782+687A>G (n.782+687A>G)
c.53+41A>G
c.876+41A>G (n.876+41A>G)
c.516+41A>G (n.516+41A>G)
c.960+41A>G (n.960+41A>G)
 dbSNP gnomAD v2
17g.7673494T=CA2245947232TP53c.993+41A= (n.993+41A=)
c.597+41A= (n.597+41A=)
c.714+41A= (n.714+41A=)
c.972+41A= (n.972+41A=)
c.782+687A= (n.782+687A=)
c.53+41A=
c.876+41A= (n.876+41A=)
c.516+41A= (n.516+41A=)
c.960+41A= (n.960+41A=)
17g.7673496G>ACA2733125096TP53c.993+39C>T (n.993+39C>T)
c.597+39C>T (n.597+39C>T)
c.714+39C>T (n.714+39C>T)
c.972+39C>T (n.972+39C>T)
c.782+685C>T (n.782+685C>T)
c.53+39C>T
c.876+39C>T (n.876+39C>T)
c.516+39C>T (n.516+39C>T)
c.960+39C>T (n.960+39C>T)
 dbSNP
17g.7673496G>TCA2733125060TP53c.993+39C>A (n.993+39C>A)
c.597+39C>A (n.597+39C>A)
c.714+39C>A (n.714+39C>A)
c.972+39C>A (n.972+39C>A)
c.782+685C>A (n.782+685C>A)
c.53+39C>A
c.876+39C>A (n.876+39C>A)
c.516+39C>A (n.516+39C>A)
c.960+39C>A (n.960+39C>A)
 dbSNP
17g.7673497A>CCA2733125155TP53c.993+38T>G (n.993+38T>G)
c.597+38T>G (n.597+38T>G)
c.714+38T>G (n.714+38T>G)
c.972+38T>G (n.972+38T>G)
c.782+684T>G (n.782+684T>G)
c.53+38T>G
c.876+38T>G (n.876+38T>G)
c.516+38T>G (n.516+38T>G)
c.960+38T>G (n.960+38T>G)
 dbSNP
17g.7673497A>GCA2733125186TP53c.993+38T>C (n.993+38T>C)
c.597+38T>C (n.597+38T>C)
c.714+38T>C (n.714+38T>C)
c.972+38T>C (n.972+38T>C)
c.782+684T>C (n.782+684T>C)
c.53+38T>C
c.876+38T>C (n.876+38T>C)
c.516+38T>C (n.516+38T>C)
c.960+38T>C (n.960+38T>C)
 dbSNP
17g.7673497A>TCA2733125133TP53c.993+38T>A (n.993+38T>A)
c.597+38T>A (n.597+38T>A)
c.714+38T>A (n.714+38T>A)
c.972+38T>A (n.972+38T>A)
c.782+684T>A (n.782+684T>A)
c.53+38T>A
c.876+38T>A (n.876+38T>A)
c.516+38T>A (n.516+38T>A)
c.960+38T>A (n.960+38T>A)
 dbSNP
17g.7673498A>GCA2635874014TP53c.993+37T>C (n.993+37T>C)
c.597+37T>C (n.597+37T>C)
c.714+37T>C (n.714+37T>C)
c.972+37T>C (n.972+37T>C)
c.782+683T>C (n.782+683T>C)
c.53+37T>C
c.876+37T>C (n.876+37T>C)
c.516+37T>C (n.516+37T>C)
c.960+37T>C (n.960+37T>C)
 dbSNP gnomAD v4
17g.7673498A>TCA2733125270TP53c.993+37T>A (n.993+37T>A)
c.597+37T>A (n.597+37T>A)
c.714+37T>A (n.714+37T>A)
c.972+37T>A (n.972+37T>A)
c.782+683T>A (n.782+683T>A)
c.53+37T>A
c.876+37T>A (n.876+37T>A)
c.516+37T>A (n.516+37T>A)
c.960+37T>A (n.960+37T>A)
 dbSNP
17g.7673499A=CA2245947234TP53c.993+36T= (n.993+36T=)
c.597+36T= (n.597+36T=)
c.714+36T= (n.714+36T=)
c.972+36T= (n.972+36T=)
c.782+682T= (n.782+682T=)
c.53+36T=
c.876+36T= (n.876+36T=)
c.516+36T= (n.516+36T=)
c.960+36T= (n.960+36T=)
17g.7673499A>CCA624865099TP53c.993+36T>G (n.993+36T>G)
c.597+36T>G (n.597+36T>G)
c.714+36T>G (n.714+36T>G)
c.972+36T>G (n.972+36T>G)
c.782+682T>G (n.782+682T>G)
c.53+36T>G
c.876+36T>G (n.876+36T>G)
c.516+36T>G (n.516+36T>G)
c.960+36T>G (n.960+36T>G)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.7673499A>GCA656753436TP53c.993+36T>C (n.993+36T>C)
c.597+36T>C (n.597+36T>C)
c.714+36T>C (n.714+36T>C)
c.972+36T>C (n.972+36T>C)
c.782+682T>C (n.782+682T>C)
c.53+36T>C
c.876+36T>C (n.876+36T>C)
c.516+36T>C (n.516+36T>C)
c.960+36T>C (n.960+36T>C)
 dbSNP COSMIC
17g.7673499A>TCA2732945373TP53c.993+36T>A (n.993+36T>A)
c.597+36T>A (n.597+36T>A)
c.714+36T>A (n.714+36T>A)
c.972+36T>A (n.972+36T>A)
c.782+682T>A (n.782+682T>A)
c.53+36T>A
c.876+36T>A (n.876+36T>A)
c.516+36T>A (n.516+36T>A)
c.960+36T>A (n.960+36T>A)
 dbSNP
17g.7673500C>ACA2732925028TP53c.993+35G>T (n.993+35G>T)
c.597+35G>T (n.597+35G>T)
c.714+35G>T (n.714+35G>T)
c.972+35G>T (n.972+35G>T)
c.782+681G>T (n.782+681G>T)
c.53+35G>T
c.876+35G>T (n.876+35G>T)
c.516+35G>T (n.516+35G>T)
c.960+35G>T (n.960+35G>T)
 dbSNP
17g.7673500C=CA2245947238TP53c.993+35G= (n.993+35G=)
c.597+35G= (n.597+35G=)
c.714+35G= (n.714+35G=)
c.972+35G= (n.972+35G=)
c.782+681G= (n.782+681G=)
c.53+35G=
c.876+35G= (n.876+35G=)
c.516+35G= (n.516+35G=)
c.960+35G= (n.960+35G=)
17g.7673500C>GCA001155TP53c.993+35G>C (n.993+35G>C)
c.597+35G>C (n.597+35G>C)
c.714+35G>C (n.714+35G>C)
c.972+35G>C (n.972+35G>C)
c.782+681G>C (n.782+681G>C)
c.53+35G>C
c.876+35G>C (n.876+35G>C)
c.516+35G>C (n.516+35G>C)
c.960+35G>C (n.960+35G>C)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.7673500C>TCA001153TP53c.993+35G>A (n.993+35G>A)
c.597+35G>A (n.597+35G>A)
c.714+35G>A (n.714+35G>A)
c.972+35G>A (n.972+35G>A)
c.782+681G>A (n.782+681G>A)
c.53+35G>A
c.876+35G>A (n.876+35G>A)
c.516+35G>A (n.516+35G>A)
c.960+35G>A (n.960+35G>A)
 dbSNP ExAC gnomAD v2 gnomAD v4
17g.7673501T>ACA2733125382TP53c.993+34A>T (n.993+34A>T)
c.597+34A>T (n.597+34A>T)
c.714+34A>T (n.714+34A>T)
c.972+34A>T (n.972+34A>T)
c.782+680A>T (n.782+680A>T)
c.53+34A>T
c.876+34A>T (n.876+34A>T)
c.516+34A>T (n.516+34A>T)
c.960+34A>T (n.960+34A>T)
 dbSNP
17g.7673501T>CCA2733125417TP53c.993+34A>G (n.993+34A>G)
c.597+34A>G (n.597+34A>G)
c.714+34A>G (n.714+34A>G)
c.972+34A>G (n.972+34A>G)
c.782+680A>G (n.782+680A>G)
c.53+34A>G
c.876+34A>G (n.876+34A>G)
c.516+34A>G (n.516+34A>G)
c.960+34A>G (n.960+34A>G)
 dbSNP
17g.7673502T>ACA2733125446TP53c.993+33A>T (n.993+33A>T)
c.597+33A>T (n.597+33A>T)
c.714+33A>T (n.714+33A>T)
c.972+33A>T (n.972+33A>T)
c.782+679A>T (n.782+679A>T)
c.53+33A>T
c.876+33A>T (n.876+33A>T)
c.516+33A>T (n.516+33A>T)
c.960+33A>T (n.960+33A>T)
 dbSNP
17g.7673502T>CCA2733125421TP53c.993+33A>G (n.993+33A>G)
c.597+33A>G (n.597+33A>G)
c.714+33A>G (n.714+33A>G)
c.972+33A>G (n.972+33A>G)
c.782+679A>G (n.782+679A>G)
c.53+33A>G
c.876+33A>G (n.876+33A>G)
c.516+33A>G (n.516+33A>G)
c.960+33A>G (n.960+33A>G)
 dbSNP
17g.7673502T>GCA2733125445TP53c.993+33A>C (n.993+33A>C)
c.597+33A>C (n.597+33A>C)
c.714+33A>C (n.714+33A>C)
c.972+33A>C (n.972+33A>C)
c.782+679A>C (n.782+679A>C)
c.53+33A>C
c.876+33A>C (n.876+33A>C)
c.516+33A>C (n.516+33A>C)
c.960+33A>C (n.960+33A>C)
 dbSNP
17g.7673503T>ACA2635874022TP53c.993+32A>T (n.993+32A>T)
c.597+32A>T (n.597+32A>T)
c.714+32A>T (n.714+32A>T)
c.972+32A>T (n.972+32A>T)
c.782+678A>T (n.782+678A>T)
c.53+32A>T
c.876+32A>T (n.876+32A>T)
c.516+32A>T (n.516+32A>T)
c.960+32A>T (n.960+32A>T)
 gnomAD v4
17g.7673503T>CCA775168442TP53c.993+32A>G (n.993+32A>G)
c.597+32A>G (n.597+32A>G)
c.714+32A>G (n.714+32A>G)
c.972+32A>G (n.972+32A>G)
c.782+678A>G (n.782+678A>G)
c.53+32A>G
c.876+32A>G (n.876+32A>G)
c.516+32A>G (n.516+32A>G)
c.960+32A>G (n.960+32A>G)
 dbSNP
17g.7673503T=CA2245947244TP53c.993+32A= (n.993+32A=)
c.597+32A= (n.597+32A=)
c.714+32A= (n.714+32A=)
c.972+32A= (n.972+32A=)
c.782+678A= (n.782+678A=)
c.53+32A=
c.876+32A= (n.876+32A=)
c.516+32A= (n.516+32A=)
c.960+32A= (n.960+32A=)
17g.7673504C>ACA2733125473TP53c.993+31G>T (n.993+31G>T)
c.597+31G>T (n.597+31G>T)
c.714+31G>T (n.714+31G>T)
c.972+31G>T (n.972+31G>T)
c.782+677G>T (n.782+677G>T)
c.53+31G>T
c.876+31G>T (n.876+31G>T)
c.516+31G>T (n.516+31G>T)
c.960+31G>T (n.960+31G>T)
 dbSNP
17g.7673504C>TCA2733125471TP53c.993+31G>A (n.993+31G>A)
c.597+31G>A (n.597+31G>A)
c.714+31G>A (n.714+31G>A)
c.972+31G>A (n.972+31G>A)
c.782+677G>A (n.782+677G>A)
c.53+31G>A
c.876+31G>A (n.876+31G>A)
c.516+31G>A (n.516+31G>A)
c.960+31G>A (n.960+31G>A)
 dbSNP
17g.7673505C>ACA2732985595TP53c.993+30G>T (n.993+30G>T)
c.597+30G>T (n.597+30G>T)
c.714+30G>T (n.714+30G>T)
c.972+30G>T (n.972+30G>T)
c.782+676G>T (n.782+676G>T)
c.53+30G>T
c.876+30G>T (n.876+30G>T)
c.516+30G>T (n.516+30G>T)
c.960+30G>T (n.960+30G>T)
 dbSNP
17g.7673505C=CA2245947248TP53c.993+30G= (n.993+30G=)
c.597+30G= (n.597+30G=)
c.714+30G= (n.714+30G=)
c.972+30G= (n.972+30G=)
c.782+676G= (n.782+676G=)
c.53+30G=
c.876+30G= (n.876+30G=)
c.516+30G= (n.516+30G=)
c.960+30G= (n.960+30G=)
17g.7673505C>GCA2732985596TP53c.993+30G>C (n.993+30G>C)
c.597+30G>C (n.597+30G>C)
c.714+30G>C (n.714+30G>C)
c.972+30G>C (n.972+30G>C)
c.782+676G>C (n.782+676G>C)
c.53+30G>C
c.876+30G>C (n.876+30G>C)
c.516+30G>C (n.516+30G>C)
c.960+30G>C (n.960+30G>C)
 dbSNP
17g.7673505C>TCA981209202TP53c.993+30G>A (n.993+30G>A)
c.597+30G>A (n.597+30G>A)
c.714+30G>A (n.714+30G>A)
c.972+30G>A (n.972+30G>A)
c.782+676G>A (n.782+676G>A)
c.53+30G>A
c.876+30G>A (n.876+30G>A)
c.516+30G>A (n.516+30G>A)
c.960+30G>A (n.960+30G>A)
 dbSNP gnomAD v3 gnomAD v4
17g.7673506A>CCA2733125477TP53c.993+29T>G (n.993+29T>G)
c.597+29T>G (n.597+29T>G)
c.714+29T>G (n.714+29T>G)
c.972+29T>G (n.972+29T>G)
c.782+675T>G (n.782+675T>G)
c.53+29T>G
c.876+29T>G (n.876+29T>G)
c.516+29T>G (n.516+29T>G)
c.960+29T>G (n.960+29T>G)
 dbSNP
17g.7673506A>GCA2733125478TP53c.993+29T>C (n.993+29T>C)
c.597+29T>C (n.597+29T>C)
c.714+29T>C (n.714+29T>C)
c.972+29T>C (n.972+29T>C)
c.782+675T>C (n.782+675T>C)
c.53+29T>C
c.876+29T>C (n.876+29T>C)
c.516+29T>C (n.516+29T>C)
c.960+29T>C (n.960+29T>C)
 dbSNP
17g.7673506A>TCA2733125479TP53c.993+29T>A (n.993+29T>A)
c.597+29T>A (n.597+29T>A)
c.714+29T>A (n.714+29T>A)
c.972+29T>A (n.972+29T>A)
c.782+675T>A (n.782+675T>A)
c.53+29T>A
c.876+29T>A (n.876+29T>A)
c.516+29T>A (n.516+29T>A)
c.960+29T>A (n.960+29T>A)
 dbSNP
17g.7673507C>ACA2732954355TP53c.993+28G>T (n.993+28G>T)
c.597+28G>T (n.597+28G>T)
c.714+28G>T (n.714+28G>T)
c.972+28G>T (n.972+28G>T)
c.782+674G>T (n.782+674G>T)
c.53+28G>T
c.876+28G>T (n.876+28G>T)
c.516+28G>T (n.516+28G>T)
c.960+28G>T (n.960+28G>T)
 dbSNP
17g.7673507C=CA2245947251TP53c.993+28G= (n.993+28G=)
c.597+28G= (n.597+28G=)
c.714+28G= (n.714+28G=)
c.972+28G= (n.972+28G=)
c.782+674G= (n.782+674G=)
c.53+28G=
c.876+28G= (n.876+28G=)
c.516+28G= (n.516+28G=)
c.960+28G= (n.960+28G=)
17g.7673507C>GCA624865100TP53c.993+28G>C (n.993+28G>C)
c.597+28G>C (n.597+28G>C)
c.714+28G>C (n.714+28G>C)
c.972+28G>C (n.972+28G>C)
c.782+674G>C (n.782+674G>C)
c.53+28G>C
c.876+28G>C (n.876+28G>C)
c.516+28G>C (n.516+28G>C)
c.960+28G>C (n.960+28G>C)
 dbSNP gnomAD v2 gnomAD v4
17g.7673507C>TCA2732954353TP53c.993+28G>A (n.993+28G>A)
c.597+28G>A (n.597+28G>A)
c.714+28G>A (n.714+28G>A)
c.972+28G>A (n.972+28G>A)
c.782+674G>A (n.782+674G>A)
c.53+28G>A
c.876+28G>A (n.876+28G>A)
c.516+28G>A (n.516+28G>A)
c.960+28G>A (n.960+28G>A)
 dbSNP
17g.7673508T>ACA2732985603TP53c.993+27A>T (n.993+27A>T)
c.597+27A>T (n.597+27A>T)
c.714+27A>T (n.714+27A>T)
c.972+27A>T (n.972+27A>T)
c.782+673A>T (n.782+673A>T)
c.53+27A>T
c.876+27A>T (n.876+27A>T)
c.516+27A>T (n.516+27A>T)
c.960+27A>T (n.960+27A>T)
 dbSNP
17g.7673508T>CCA981209208TP53c.993+27A>G (n.993+27A>G)
c.597+27A>G (n.597+27A>G)
c.714+27A>G (n.714+27A>G)
c.972+27A>G (n.972+27A>G)
c.782+673A>G (n.782+673A>G)
c.53+27A>G
c.876+27A>G (n.876+27A>G)
c.516+27A>G (n.516+27A>G)
c.960+27A>G (n.960+27A>G)
 ClinVar dbSNP gnomAD v3 gnomAD v4
17g.7673508T=CA2245947256TP53c.993+27A= (n.993+27A=)
c.597+27A= (n.597+27A=)
c.714+27A= (n.714+27A=)
c.972+27A= (n.972+27A=)
c.782+673A= (n.782+673A=)
c.53+27A=
c.876+27A= (n.876+27A=)
c.516+27A= (n.516+27A=)
c.960+27A= (n.960+27A=)
17g.7673509T>ACA2732985604TP53c.993+26A>T (n.993+26A>T)
c.597+26A>T (n.597+26A>T)
c.714+26A>T (n.714+26A>T)
c.972+26A>T (n.972+26A>T)
c.782+672A>T (n.782+672A>T)
c.53+26A>T
c.876+26A>T (n.876+26A>T)
c.516+26A>T (n.516+26A>T)
c.960+26A>T (n.960+26A>T)
 dbSNP
17g.7673509T>CCA981209211TP53c.993+26A>G (n.993+26A>G)
c.597+26A>G (n.597+26A>G)
c.714+26A>G (n.714+26A>G)
c.972+26A>G (n.972+26A>G)
c.782+672A>G (n.782+672A>G)
c.53+26A>G
c.876+26A>G (n.876+26A>G)
c.516+26A>G (n.516+26A>G)
c.960+26A>G (n.960+26A>G)
 dbSNP gnomAD v3 gnomAD v4
17g.7673509T>GCA2566747584TP53c.993+26A>C (n.993+26A>C)
c.597+26A>C (n.597+26A>C)
c.714+26A>C (n.714+26A>C)
c.972+26A>C (n.972+26A>C)
c.782+672A>C (n.782+672A>C)
c.53+26A>C
c.876+26A>C (n.876+26A>C)
c.516+26A>C (n.516+26A>C)
c.960+26A>C (n.960+26A>C)
17g.7673509T=CA2245947259TP53c.993+26A= (n.993+26A=)
c.597+26A= (n.597+26A=)
c.714+26A= (n.714+26A=)
c.972+26A= (n.972+26A=)
c.782+672A= (n.782+672A=)
c.53+26A=
c.876+26A= (n.876+26A=)
c.516+26A= (n.516+26A=)
c.960+26A= (n.960+26A=)
17g.7673510G>ACA2733125482TP53c.993+25C>T (n.993+25C>T)
c.597+25C>T (n.597+25C>T)
c.714+25C>T (n.714+25C>T)
c.972+25C>T (n.972+25C>T)
c.782+671C>T (n.782+671C>T)
c.53+25C>T
c.876+25C>T (n.876+25C>T)
c.516+25C>T (n.516+25C>T)
c.960+25C>T (n.960+25C>T)
 dbSNP
17g.7673510G>CCA2733125502TP53c.993+25C>G (n.993+25C>G)
c.597+25C>G (n.597+25C>G)
c.714+25C>G (n.714+25C>G)
c.972+25C>G (n.972+25C>G)
c.782+671C>G (n.782+671C>G)
c.53+25C>G
c.876+25C>G (n.876+25C>G)
c.516+25C>G (n.516+25C>G)
c.960+25C>G (n.960+25C>G)
 dbSNP
17g.7673510G>TCA2733125584TP53c.993+25C>A (n.993+25C>A)
c.597+25C>A (n.597+25C>A)
c.714+25C>A (n.714+25C>A)
c.972+25C>A (n.972+25C>A)
c.782+671C>A (n.782+671C>A)
c.53+25C>A
c.876+25C>A (n.876+25C>A)
c.516+25C>A (n.516+25C>A)
c.960+25C>A (n.960+25C>A)
 dbSNP
17g.7673510_7673534delCA645587336TP53c.993+1_993+25del (n.993+1_993+25del)
c.597+1_597+25del (n.597+1_597+25del)
c.714+1_714+25del (n.714+1_714+25del)
c.972+1_972+25del (n.972+1_972+25del)
c.782+647_782+671del (n.782+647_782+671del)
c.53+1_53+25del
c.876+1_876+25del (n.876+1_876+25del)
c.516+1_516+25del (n.516+1_516+25del)
c.960+1_960+25del (n.960+1_960+25del)
 COSMIC COSMIC COSMIC COSMIC
17g.7673511A=CA2245947261TP53c.993+24T= (n.993+24T=)
c.597+24T= (n.597+24T=)
c.714+24T= (n.714+24T=)
c.972+24T= (n.972+24T=)
c.782+670T= (n.782+670T=)
c.53+24T=
c.876+24T= (n.876+24T=)
c.516+24T= (n.516+24T=)
c.960+24T= (n.960+24T=)
17g.7673511A>GCA287486485TP53c.993+24T>C (n.993+24T>C)
c.597+24T>C (n.597+24T>C)
c.714+24T>C (n.714+24T>C)
c.972+24T>C (n.972+24T>C)
c.782+670T>C (n.782+670T>C)
c.53+24T>C
c.876+24T>C (n.876+24T>C)
c.516+24T>C (n.516+24T>C)
c.960+24T>C (n.960+24T>C)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.7673511A>TCA2732942237TP53c.993+24T>A (n.993+24T>A)
c.597+24T>A (n.597+24T>A)
c.714+24T>A (n.714+24T>A)
c.972+24T>A (n.972+24T>A)
c.782+670T>A (n.782+670T>A)
c.53+24T>A
c.876+24T>A (n.876+24T>A)
c.516+24T>A (n.516+24T>A)
c.960+24T>A (n.960+24T>A)
 dbSNP
17g.7673512_7673515dupCA2635874035TP53c.993+20_993+23dup (n.993+20_993+23dup)
c.597+20_597+23dup (n.597+20_597+23dup)
c.714+20_714+23dup (n.714+20_714+23dup)
c.972+20_972+23dup (n.972+20_972+23dup)
c.782+666_782+669dup (n.782+666_782+669dup)
c.53+20_53+23dup
c.876+20_876+23dup (n.876+20_876+23dup)
c.516+20_516+23dup (n.516+20_516+23dup)
c.960+20_960+23dup (n.960+20_960+23dup)
 gnomAD v4
17g.7673513A>GCA2544471111TP53c.993+22T>C (n.993+22T>C)
c.597+22T>C (n.597+22T>C)
c.714+22T>C (n.714+22T>C)
c.972+22T>C (n.972+22T>C)
c.782+668T>C (n.782+668T>C)
c.53+22T>C
c.876+22T>C (n.876+22T>C)
c.516+22T>C (n.516+22T>C)
c.960+22T>C (n.960+22T>C)
 dbSNP
17g.7673513A>TCA2733125597TP53c.993+22T>A (n.993+22T>A)
c.597+22T>A (n.597+22T>A)
c.714+22T>A (n.714+22T>A)
c.972+22T>A (n.972+22T>A)
c.782+668T>A (n.782+668T>A)
c.53+22T>A
c.876+22T>A (n.876+22T>A)
c.516+22T>A (n.516+22T>A)
c.960+22T>A (n.960+22T>A)
 dbSNP
17g.7673514A>GCA2576230608TP53c.993+21T>C (n.993+21T>C)
c.597+21T>C (n.597+21T>C)
c.714+21T>C (n.714+21T>C)
c.972+21T>C (n.972+21T>C)
c.782+667T>C (n.782+667T>C)
c.53+21T>C
c.876+21T>C (n.876+21T>C)
c.516+21T>C (n.516+21T>C)
c.960+21T>C (n.960+21T>C)
 dbSNP
17g.7673514A>TCA2733125743TP53c.993+21T>A (n.993+21T>A)
c.597+21T>A (n.597+21T>A)
c.714+21T>A (n.714+21T>A)
c.972+21T>A (n.972+21T>A)
c.782+667T>A (n.782+667T>A)
c.53+21T>A
c.876+21T>A (n.876+21T>A)
c.516+21T>A (n.516+21T>A)
c.960+21T>A (n.960+21T>A)
 dbSNP
17g.7673515G>ACA2580094890TP53c.993+20C>T (n.993+20C>T)
c.597+20C>T (n.597+20C>T)
c.714+20C>T (n.714+20C>T)
c.972+20C>T (n.972+20C>T)
c.782+666C>T (n.782+666C>T)
c.53+20C>T
c.876+20C>T (n.876+20C>T)
c.516+20C>T (n.516+20C>T)
c.960+20C>T (n.960+20C>T)
 ClinVar dbSNP
17g.7673515G>CCA2245947265TP53c.993+20C>G (n.993+20C>G)
c.597+20C>G (n.597+20C>G)
c.714+20C>G (n.714+20C>G)
c.972+20C>G (n.972+20C>G)
c.782+666C>G (n.782+666C>G)
c.53+20C>G
c.876+20C>G (n.876+20C>G)
c.516+20C>G (n.516+20C>G)
c.960+20C>G (n.960+20C>G)
 dbSNP
17g.7673515G=CA2245947264TP53c.993+20C= (n.993+20C=)
c.597+20C= (n.597+20C=)
c.714+20C= (n.714+20C=)
c.972+20C= (n.972+20C=)
c.782+666C= (n.782+666C=)
c.53+20C=
c.876+20C= (n.876+20C=)
c.516+20C= (n.516+20C=)
c.960+20C= (n.960+20C=)
17g.7673515G>TCA2732985607TP53c.993+20C>A (n.993+20C>A)
c.597+20C>A (n.597+20C>A)
c.714+20C>A (n.714+20C>A)
c.972+20C>A (n.972+20C>A)
c.782+666C>A (n.782+666C>A)
c.53+20C>A
c.876+20C>A (n.876+20C>A)
c.516+20C>A (n.516+20C>A)
c.960+20C>A (n.960+20C>A)
 dbSNP
17g.7673516A=CA2245947269TP53c.993+19T= (n.993+19T=)
c.597+19T= (n.597+19T=)
c.714+19T= (n.714+19T=)
c.972+19T= (n.972+19T=)
c.782+665T= (n.782+665T=)
c.53+19T=
c.876+19T= (n.876+19T=)
c.516+19T= (n.516+19T=)
c.960+19T= (n.960+19T=)
17g.7673516A>GCA2732925963TP53c.993+19T>C (n.993+19T>C)
c.597+19T>C (n.597+19T>C)
c.714+19T>C (n.714+19T>C)
c.972+19T>C (n.972+19T>C)
c.782+665T>C (n.782+665T>C)
c.53+19T>C
c.876+19T>C (n.876+19T>C)
c.516+19T>C (n.516+19T>C)
c.960+19T>C (n.960+19T>C)
 dbSNP
17g.7673516A>TCA001165TP53c.993+19T>A (n.993+19T>A)
c.597+19T>A (n.597+19T>A)
c.714+19T>A (n.714+19T>A)
c.972+19T>A (n.972+19T>A)
c.782+665T>A (n.782+665T>A)
c.53+19T>A
c.876+19T>A (n.876+19T>A)
c.516+19T>A (n.516+19T>A)
c.960+19T>A (n.960+19T>A)
 ClinVar dbSNP ExAC gnomAD v2
17g.7673517G>ACA001171TP53c.993+18C>T (n.993+18C>T)
c.597+18C>T (n.597+18C>T)
c.714+18C>T (n.714+18C>T)
c.972+18C>T (n.972+18C>T)
c.782+664C>T (n.782+664C>T)
c.53+18C>T
c.876+18C>T (n.876+18C>T)
c.516+18C>T (n.516+18C>T)
c.960+18C>T (n.960+18C>T)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.7673517G>CCA2732926315TP53c.993+18C>G (n.993+18C>G)
c.597+18C>G (n.597+18C>G)
c.714+18C>G (n.714+18C>G)
c.972+18C>G (n.972+18C>G)
c.782+664C>G (n.782+664C>G)
c.53+18C>G
c.876+18C>G (n.876+18C>G)
c.516+18C>G (n.516+18C>G)
c.960+18C>G (n.960+18C>G)
 dbSNP
17g.7673517G=CA2245947274TP53c.993+18C= (n.993+18C=)
c.597+18C= (n.597+18C=)
c.714+18C= (n.714+18C=)
c.972+18C= (n.972+18C=)
c.782+664C= (n.782+664C=)
c.53+18C=
c.876+18C= (n.876+18C=)
c.516+18C= (n.516+18C=)
c.960+18C= (n.960+18C=)
17g.7673517G>TCA2695202234TP53c.993+18C>A (n.993+18C>A)
c.597+18C>A (n.597+18C>A)
c.714+18C>A (n.714+18C>A)
c.972+18C>A (n.972+18C>A)
c.782+664C>A (n.782+664C>A)
c.53+18C>A
c.876+18C>A (n.876+18C>A)
c.516+18C>A (n.516+18C>A)
c.960+18C>A (n.960+18C>A)
 dbSNP
17g.7673518G>ACA2580094892TP53c.993+17C>T (n.993+17C>T)
c.597+17C>T (n.597+17C>T)
c.714+17C>T (n.714+17C>T)
c.972+17C>T (n.972+17C>T)
c.782+663C>T (n.782+663C>T)
c.53+17C>T
c.876+17C>T (n.876+17C>T)
c.516+17C>T (n.516+17C>T)
c.960+17C>T (n.960+17C>T)
 ClinVar dbSNP
17g.7673518G>CCA2732931740TP53c.993+17C>G (n.993+17C>G)
c.597+17C>G (n.597+17C>G)
c.714+17C>G (n.714+17C>G)
c.972+17C>G (n.972+17C>G)
c.782+663C>G (n.782+663C>G)
c.53+17C>G
c.876+17C>G (n.876+17C>G)
c.516+17C>G (n.516+17C>G)
c.960+17C>G (n.960+17C>G)
 dbSNP
17g.7673518G=CA2245947277TP53c.993+17C= (n.993+17C=)
c.597+17C= (n.597+17C=)
c.714+17C= (n.714+17C=)
c.972+17C= (n.972+17C=)
c.782+663C= (n.782+663C=)
c.53+17C=
c.876+17C= (n.876+17C=)
c.516+17C= (n.516+17C=)
c.960+17C= (n.960+17C=)
17g.7673518G>TCA287486489TP53c.993+17C>A (n.993+17C>A)
c.597+17C>A (n.597+17C>A)
c.714+17C>A (n.714+17C>A)
c.972+17C>A (n.972+17C>A)
c.782+663C>A (n.782+663C>A)
c.53+17C>A
c.876+17C>A (n.876+17C>A)
c.516+17C>A (n.516+17C>A)
c.960+17C>A (n.960+17C>A)
 dbSNP
17g.7673519T>ACA2733125754TP53c.993+16A>T (n.993+16A>T)
c.597+16A>T (n.597+16A>T)
c.714+16A>T (n.714+16A>T)
c.972+16A>T (n.972+16A>T)
c.782+662A>T (n.782+662A>T)
c.53+16A>T
c.876+16A>T (n.876+16A>T)
c.516+16A>T (n.516+16A>T)
c.960+16A>T (n.960+16A>T)
 dbSNP
17g.7673519T>CCA2733125771TP53c.993+16A>G (n.993+16A>G)
c.597+16A>G (n.597+16A>G)
c.714+16A>G (n.714+16A>G)
c.972+16A>G (n.972+16A>G)
c.782+662A>G (n.782+662A>G)
c.53+16A>G
c.876+16A>G (n.876+16A>G)
c.516+16A>G (n.516+16A>G)
c.960+16A>G (n.960+16A>G)
 dbSNP
17g.7673519T>GCA2733125788TP53c.993+16A>C (n.993+16A>C)
c.597+16A>C (n.597+16A>C)
c.714+16A>C (n.714+16A>C)
c.972+16A>C (n.972+16A>C)
c.782+662A>C (n.782+662A>C)
c.53+16A>C
c.876+16A>C (n.876+16A>C)
c.516+16A>C (n.516+16A>C)
c.960+16A>C (n.960+16A>C)
 dbSNP
17g.7673520C>ACA658683979TP53c.993+15G>T (n.993+15G>T)
c.597+15G>T (n.597+15G>T)
c.714+15G>T (n.714+15G>T)
c.972+15G>T (n.972+15G>T)
c.782+661G>T (n.782+661G>T)
c.53+15G>T
c.876+15G>T (n.876+15G>T)
c.516+15G>T (n.516+15G>T)
c.960+15G>T (n.960+15G>T)
 ClinVar dbSNP
17g.7673520C=CA2245947284TP53c.993+15G= (n.993+15G=)
c.597+15G= (n.597+15G=)
c.714+15G= (n.714+15G=)
c.972+15G= (n.972+15G=)
c.782+661G= (n.782+661G=)
c.53+15G=
c.876+15G= (n.876+15G=)
c.516+15G= (n.516+15G=)
c.960+15G= (n.960+15G=)
17g.7673520C>GCA2635874040TP53c.993+15G>C (n.993+15G>C)
c.597+15G>C (n.597+15G>C)
c.714+15G>C (n.714+15G>C)
c.972+15G>C (n.972+15G>C)
c.782+661G>C (n.782+661G>C)
c.53+15G>C
c.876+15G>C (n.876+15G>C)
c.516+15G>C (n.516+15G>C)
c.960+15G>C (n.960+15G>C)
 ClinVar dbSNP gnomAD v4
17g.7673520C>TCA2732963321TP53c.993+15G>A (n.993+15G>A)
c.597+15G>A (n.597+15G>A)
c.714+15G>A (n.714+15G>A)
c.972+15G>A (n.972+15G>A)
c.782+661G>A (n.782+661G>A)
c.53+15G>A
c.876+15G>A (n.876+15G>A)
c.516+15G>A (n.516+15G>A)
c.960+15G>A (n.960+15G>A)
 ClinVar dbSNP
17g.7673521C>ACA2733125832TP53c.993+14G>T (n.993+14G>T)
c.597+14G>T (n.597+14G>T)
c.714+14G>T (n.714+14G>T)
c.972+14G>T (n.972+14G>T)
c.782+660G>T (n.782+660G>T)
c.53+14G>T
c.876+14G>T (n.876+14G>T)
c.516+14G>T (n.516+14G>T)
c.960+14G>T (n.960+14G>T)
 dbSNP
17g.7673521C>GCA2573154621TP53c.993+14G>C (n.993+14G>C)
c.597+14G>C (n.597+14G>C)
c.714+14G>C (n.714+14G>C)
c.972+14G>C (n.972+14G>C)
c.782+660G>C (n.782+660G>C)
c.53+14G>C
c.876+14G>C (n.876+14G>C)
c.516+14G>C (n.516+14G>C)
c.960+14G>C (n.960+14G>C)
 ClinVar dbSNP gnomAD v4
17g.7673521C>TCA2733125800TP53c.993+14G>A (n.993+14G>A)
c.597+14G>A (n.597+14G>A)
c.714+14G>A (n.714+14G>A)
c.972+14G>A (n.972+14G>A)
c.782+660G>A (n.782+660G>A)
c.53+14G>A
c.876+14G>A (n.876+14G>A)
c.516+14G>A (n.516+14G>A)
c.960+14G>A (n.960+14G>A)
 dbSNP
17g.7673522C>ACA2732925964TP53c.993+13G>T (n.993+13G>T)
c.597+13G>T (n.597+13G>T)
c.714+13G>T (n.714+13G>T)
c.972+13G>T (n.972+13G>T)
c.782+659G>T (n.782+659G>T)
c.53+13G>T
c.876+13G>T (n.876+13G>T)
c.516+13G>T (n.516+13G>T)
c.960+13G>T (n.960+13G>T)
 dbSNP
17g.7673522C=CA2245947294TP53c.993+13G= (n.993+13G=)
c.597+13G= (n.597+13G=)
c.714+13G= (n.714+13G=)
c.972+13G= (n.972+13G=)
c.782+659G= (n.782+659G=)
c.53+13G=
c.876+13G= (n.876+13G=)
c.516+13G= (n.516+13G=)
c.960+13G= (n.960+13G=)
17g.7673522C>GCA000522TP53c.993+13G>C (n.993+13G>C)
c.597+13G>C (n.597+13G>C)
c.714+13G>C (n.714+13G>C)
c.972+13G>C (n.972+13G>C)
c.782+659G>C (n.782+659G>C)
c.53+13G>C
c.876+13G>C (n.876+13G>C)
c.516+13G>C (n.516+13G>C)
c.960+13G>C (n.960+13G>C)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.7673522C>TCA2573154623TP53c.993+13G>A (n.993+13G>A)
c.597+13G>A (n.597+13G>A)
c.714+13G>A (n.714+13G>A)
c.972+13G>A (n.972+13G>A)
c.782+659G>A (n.782+659G>A)
c.53+13G>A
c.876+13G>A (n.876+13G>A)
c.516+13G>A (n.516+13G>A)
c.960+13G>A (n.960+13G>A)
 ClinVar dbSNP gnomAD v4
17g.7673522_7673523delinsTGCA2573154622TP53c.993+12_993+13delinsCA (n.993+12_993+13delinsCA)
c.597+12_597+13delinsCA (n.597+12_597+13delinsCA)
c.714+12_714+13delinsCA (n.714+12_714+13delinsCA)
c.972+12_972+13delinsCA (n.972+12_972+13delinsCA)
c.782+658_782+659delinsCA (n.782+658_782+659delinsCA)
c.53+12_53+13delinsCA
c.876+12_876+13delinsCA (n.876+12_876+13delinsCA)
c.516+12_516+13delinsCA (n.516+12_516+13delinsCA)
c.960+12_960+13delinsCA (n.960+12_960+13delinsCA)
 ClinVar
17g.7673523A=CA2245947305TP53c.993+12T= (n.993+12T=)
c.597+12T= (n.597+12T=)
c.714+12T= (n.714+12T=)
c.972+12T= (n.972+12T=)
c.782+658T= (n.782+658T=)
c.53+12T=
c.876+12T= (n.876+12T=)
c.516+12T= (n.516+12T=)
c.960+12T= (n.960+12T=)
17g.7673523A>CCA2580574841TP53c.993+12T>G (n.993+12T>G)
c.597+12T>G (n.597+12T>G)
c.714+12T>G (n.714+12T>G)
c.972+12T>G (n.972+12T>G)
c.782+658T>G (n.782+658T>G)
c.53+12T>G
c.876+12T>G (n.876+12T>G)
c.516+12T>G (n.516+12T>G)
c.960+12T>G (n.960+12T>G)
17g.7673523A>GCA000520TP53c.993+12T>C (n.993+12T>C)
c.597+12T>C (n.597+12T>C)
c.714+12T>C (n.714+12T>C)
c.972+12T>C (n.972+12T>C)
c.782+658T>C (n.782+658T>C)
c.53+12T>C
c.876+12T>C (n.876+12T>C)
c.516+12T>C (n.516+12T>C)
c.960+12T>C (n.960+12T>C)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.7673523A>TCA2580574842TP53c.993+12T>A (n.993+12T>A)
c.597+12T>A (n.597+12T>A)
c.714+12T>A (n.714+12T>A)
c.972+12T>A (n.972+12T>A)
c.782+658T>A (n.782+658T>A)
c.53+12T>A
c.876+12T>A (n.876+12T>A)
c.516+12T>A (n.516+12T>A)
c.960+12T>A (n.960+12T>A)
 dbSNP
17g.7673524A=CA2245947313TP53c.993+11T= (n.993+11T=)
c.597+11T= (n.597+11T=)
c.714+11T= (n.714+11T=)
c.972+11T= (n.972+11T=)
c.782+657T= (n.782+657T=)
c.53+11T=
c.876+11T= (n.876+11T=)
c.516+11T= (n.516+11T=)
c.960+11T= (n.960+11T=)
17g.7673524A>GCA001188TP53c.993+11T>C (n.993+11T>C)
c.597+11T>C (n.597+11T>C)
c.714+11T>C (n.714+11T>C)
c.972+11T>C (n.972+11T>C)
c.782+657T>C (n.782+657T>C)
c.53+11T>C
c.876+11T>C (n.876+11T>C)
c.516+11T>C (n.516+11T>C)
c.960+11T>C (n.960+11T>C)
 dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
17g.7673524A>TCA2732930950TP53c.993+11T>A (n.993+11T>A)
c.597+11T>A (n.597+11T>A)
c.714+11T>A (n.714+11T>A)
c.972+11T>A (n.972+11T>A)
c.782+657T>A (n.782+657T>A)
c.53+11T>A
c.876+11T>A (n.876+11T>A)
c.516+11T>A (n.516+11T>A)
c.960+11T>A (n.960+11T>A)
 dbSNP
17g.7673525G>ACA2733125845TP53c.993+10C>T (n.993+10C>T)
c.597+10C>T (n.597+10C>T)
c.714+10C>T (n.714+10C>T)
c.972+10C>T (n.972+10C>T)
c.782+656C>T (n.782+656C>T)
c.53+10C>T
c.876+10C>T (n.876+10C>T)
c.516+10C>T (n.516+10C>T)
c.960+10C>T (n.960+10C>T)
 dbSNP
17g.7673525G>CCA2635874081TP53c.993+10C>G (n.993+10C>G)
c.597+10C>G (n.597+10C>G)
c.714+10C>G (n.714+10C>G)
c.972+10C>G (n.972+10C>G)
c.782+656C>G (n.782+656C>G)
c.53+10C>G
c.876+10C>G (n.876+10C>G)
c.516+10C>G (n.516+10C>G)
c.960+10C>G (n.960+10C>G)
 dbSNP gnomAD v4
17g.7673525G>TCA2733125848TP53c.993+10C>A (n.993+10C>A)
c.597+10C>A (n.597+10C>A)
c.714+10C>A (n.714+10C>A)
c.972+10C>A (n.972+10C>A)
c.782+656C>A (n.782+656C>A)
c.53+10C>A
c.876+10C>A (n.876+10C>A)
c.516+10C>A (n.516+10C>A)
c.960+10C>A (n.960+10C>A)
 dbSNP
17g.7673525_7673526insGGTGCA2635874080TP53c.993+10_993+11insACCC (n.993+10_993+11insACCC)
c.597+10_597+11insACCC (n.597+10_597+11insACCC)
c.714+10_714+11insACCC (n.714+10_714+11insACCC)
c.972+10_972+11insACCC (n.972+10_972+11insACCC)
c.782+656_782+657insACCC (n.782+656_782+657insACCC)
c.53+10_53+11insACCC
c.876+10_876+11insACCC (n.876+10_876+11insACCC)
c.516+10_516+11insACCC (n.516+10_516+11insACCC)
c.960+10_960+11insACCC (n.960+10_960+11insACCC)
 gnomAD v4
17g.7673526A>GCA2576230614TP53c.993+9T>C (n.993+9T>C)
c.597+9T>C (n.597+9T>C)
c.714+9T>C (n.714+9T>C)
c.972+9T>C (n.972+9T>C)
c.782+655T>C (n.782+655T>C)
c.53+9T>C
c.876+9T>C (n.876+9T>C)
c.516+9T>C (n.516+9T>C)
c.960+9T>C (n.960+9T>C)
 ClinVar dbSNP
17g.7673526A>TCA2733125877TP53c.993+9T>A (n.993+9T>A)
c.597+9T>A (n.597+9T>A)
c.714+9T>A (n.714+9T>A)
c.972+9T>A (n.972+9T>A)
c.782+655T>A (n.782+655T>A)
c.53+9T>A
c.876+9T>A (n.876+9T>A)
c.516+9T>A (n.516+9T>A)
c.960+9T>A (n.960+9T>A)
 dbSNP
17g.7673527C>ACA2732943608TP53c.993+8G>T (n.993+8G>T)
c.597+8G>T (n.597+8G>T)
c.714+8G>T (n.714+8G>T)
c.972+8G>T (n.972+8G>T)
c.782+654G>T (n.782+654G>T)
c.53+8G>T
c.876+8G>T (n.876+8G>T)
c.516+8G>T (n.516+8G>T)
c.960+8G>T (n.960+8G>T)
 dbSNP
17g.7673527C=CA2245947326TP53c.993+8G= (n.993+8G=)
c.597+8G= (n.597+8G=)
c.714+8G= (n.714+8G=)
c.972+8G= (n.972+8G=)
c.782+654G= (n.782+654G=)
c.53+8G=
c.876+8G= (n.876+8G=)
c.516+8G= (n.516+8G=)
c.960+8G= (n.960+8G=)
17g.7673527C>GCA2576230615TP53c.993+8G>C (n.993+8G>C)
c.597+8G>C (n.597+8G>C)
c.714+8G>C (n.714+8G>C)
c.972+8G>C (n.972+8G>C)
c.782+654G>C (n.782+654G>C)
c.53+8G>C
c.876+8G>C (n.876+8G>C)
c.516+8G>C (n.516+8G>C)
c.960+8G>C (n.960+8G>C)
 ClinVar gnomAD v4
17g.7673527C>TCA16615685TP53c.993+8G>A (n.993+8G>A)
c.597+8G>A (n.597+8G>A)
c.714+8G>A (n.714+8G>A)
c.972+8G>A (n.972+8G>A)
c.782+654G>A (n.782+654G>A)
c.53+8G>A
c.876+8G>A (n.876+8G>A)
c.516+8G>A (n.516+8G>A)
c.960+8G>A (n.960+8G>A)
 ClinVar dbSNP
17g.7673527_7673529delCA2635874085TP53c.993+6_993+8del (n.993+6_993+8del)
c.597+6_597+8del (n.597+6_597+8del)
c.714+6_714+8del (n.714+6_714+8del)
c.972+6_972+8del (n.972+6_972+8del)
c.782+652_782+654del (n.782+652_782+654del)
c.53+6_53+8del
c.876+6_876+8del (n.876+6_876+8del)
c.516+6_516+8del (n.516+6_516+8del)
c.960+6_960+8del (n.960+6_960+8del)
 gnomAD v4
17g.7673528T>ACA2732941348TP53c.993+7A>T (n.993+7A>T)
c.597+7A>T (n.597+7A>T)
c.714+7A>T (n.714+7A>T)
c.972+7A>T (n.972+7A>T)
c.782+653A>T (n.782+653A>T)
c.53+7A>T
c.876+7A>T (n.876+7A>T)
c.516+7A>T (n.516+7A>T)
c.960+7A>T (n.960+7A>T)
 dbSNP
17g.7673528T>CCA287486495TP53c.993+7A>G (n.993+7A>G)
c.597+7A>G (n.597+7A>G)
c.714+7A>G (n.714+7A>G)
c.972+7A>G (n.972+7A>G)
c.782+653A>G (n.782+653A>G)
c.53+7A>G
c.876+7A>G (n.876+7A>G)
c.516+7A>G (n.516+7A>G)
c.960+7A>G (n.960+7A>G)
 ClinVar dbSNP gnomAD v4
17g.7673528T>GCA2732941347TP53c.993+7A>C (n.993+7A>C)
c.597+7A>C (n.597+7A>C)
c.714+7A>C (n.714+7A>C)
c.972+7A>C (n.972+7A>C)
c.782+653A>C (n.782+653A>C)
c.53+7A>C
c.876+7A>C (n.876+7A>C)
c.516+7A>C (n.516+7A>C)
c.960+7A>C (n.960+7A>C)
 dbSNP
17g.7673528T=CA2245947329TP53c.993+7A= (n.993+7A=)
c.597+7A= (n.597+7A=)
c.714+7A= (n.714+7A=)
c.972+7A= (n.972+7A=)
c.782+653A= (n.782+653A=)
c.53+7A=
c.876+7A= (n.876+7A=)
c.516+7A= (n.516+7A=)
c.960+7A= (n.960+7A=)
17g.7673529_7673532dupCA2573154625TP53c.993+4_993+7dup (n.993+4_993+7dup)
c.597+4_597+7dup (n.597+4_597+7dup)
c.714+4_714+7dup (n.714+4_714+7dup)
c.972+4_972+7dup (n.972+4_972+7dup)
c.782+650_782+653dup (n.782+650_782+653dup)
c.53+4_53+7dup
c.876+4_876+7dup (n.876+4_876+7dup)
c.516+4_516+7dup (n.516+4_516+7dup)
c.960+4_960+7dup (n.960+4_960+7dup)
 ClinVar dbSNP
17g.7673528_7673536delCA2573154624TP53c.992_993+7del
c.596_597+7del
c.713_714+7del
c.971_972+7del
c.782+645_782+653del (n.782+645_782+653del)
c.52_53+7del
c.875_876+7del
c.515_516+7del
c.959_960+7del
 dbSNP
17g.7673528_7673529insGCA2576230616TP53c.993+6_993+7insC (n.993+6_993+7insC)
c.597+6_597+7insC (n.597+6_597+7insC)
c.714+6_714+7insC (n.714+6_714+7insC)
c.972+6_972+7insC (n.972+6_972+7insC)
c.782+652_782+653insC (n.782+652_782+653insC)
c.53+6_53+7insC
c.876+6_876+7insC (n.876+6_876+7insC)
c.516+6_516+7insC (n.516+6_516+7insC)
c.960+6_960+7insC (n.960+6_960+7insC)
17g.7673529T>ACA2576230617TP53c.993+6A>T (n.993+6A>T)
c.597+6A>T (n.597+6A>T)
c.714+6A>T (n.714+6A>T)
c.972+6A>T (n.972+6A>T)
c.782+652A>T (n.782+652A>T)
c.53+6A>T
c.876+6A>T (n.876+6A>T)
c.516+6A>T (n.516+6A>T)
c.960+6A>T (n.960+6A>T)
17g.7673529T>CCA2573154626TP53c.993+6A>G (n.993+6A>G)
c.597+6A>G (n.597+6A>G)
c.714+6A>G (n.714+6A>G)
c.972+6A>G (n.972+6A>G)
c.782+652A>G (n.782+652A>G)
c.53+6A>G
c.876+6A>G (n.876+6A>G)
c.516+6A>G (n.516+6A>G)
c.960+6A>G (n.960+6A>G)
 ClinVar dbSNP gnomAD v4
17g.7673529T>GCA2733125928TP53c.993+6A>C (n.993+6A>C)
c.597+6A>C (n.597+6A>C)
c.714+6A>C (n.714+6A>C)
c.972+6A>C (n.972+6A>C)
c.782+652A>C (n.782+652A>C)
c.53+6A>C
c.876+6A>C (n.876+6A>C)
c.516+6A>C (n.516+6A>C)
c.960+6A>C (n.960+6A>C)
 dbSNP
17g.7673529_7673541delCA645587337TP53c.987_993+6del
c.591_597+6del
c.708_714+6del
c.966_972+6del
c.782+640_782+652del (n.782+640_782+652del)
c.47_53+6del
c.870_876+6del
c.510_516+6del
c.954_960+6del
 COSMIC COSMIC COSMIC COSMIC
17g.7673530A=CA2245947338TP53c.993+5T= (n.993+5T=)
c.597+5T= (n.597+5T=)
c.714+5T= (n.714+5T=)
c.972+5T= (n.972+5T=)
c.782+651T= (n.782+651T=)
c.53+5T=
c.876+5T= (n.876+5T=)
c.516+5T= (n.516+5T=)
c.960+5T= (n.960+5T=)
17g.7673530A>CCA915949513TP53c.993+5T>G (n.993+5T>G)
c.597+5T>G (n.597+5T>G)
c.714+5T>G (n.714+5T>G)
c.972+5T>G (n.972+5T>G)
c.782+651T>G (n.782+651T>G)
c.53+5T>G
c.876+5T>G (n.876+5T>G)
c.516+5T>G (n.516+5T>G)
c.960+5T>G (n.960+5T>G)
 ClinVar dbSNP gnomAD v4
17g.7673530A>GCA658656522TP53c.993+5T>C (n.993+5T>C)
c.597+5T>C (n.597+5T>C)
c.714+5T>C (n.714+5T>C)
c.972+5T>C (n.972+5T>C)
c.782+651T>C (n.782+651T>C)
c.53+5T>C
c.876+5T>C (n.876+5T>C)
c.516+5T>C (n.516+5T>C)
c.960+5T>C (n.960+5T>C)
 ClinVar dbSNP gnomAD v3 gnomAD v4
17g.7673530A>TCA2732953019TP53c.993+5T>A (n.993+5T>A)
c.597+5T>A (n.597+5T>A)
c.714+5T>A (n.714+5T>A)
c.972+5T>A (n.972+5T>A)
c.782+651T>A (n.782+651T>A)
c.53+5T>A
c.876+5T>A (n.876+5T>A)
c.516+5T>A (n.516+5T>A)
c.960+5T>A (n.960+5T>A)
 dbSNP
17g.7673530_7673531delinsAGCA2245947337TP53c.993+4_993+5delinsCT (n.993+4_993+5delinsCT)
c.597+4_597+5delinsCT (n.597+4_597+5delinsCT)
c.714+4_714+5delinsCT (n.714+4_714+5delinsCT)
c.972+4_972+5delinsCT (n.972+4_972+5delinsCT)
c.782+650_782+651delinsCT (n.782+650_782+651delinsCT)
c.53+4_53+5delinsCT
c.876+4_876+5delinsCT (n.876+4_876+5delinsCT)
c.516+4_516+5delinsCT (n.516+4_516+5delinsCT)
c.960+4_960+5delinsCT (n.960+4_960+5delinsCT)
17g.7673531delCA10580907TP53c.993+4del (n.993+4del)
c.597+4del (n.597+4del)
c.714+4del (n.714+4del)
c.972+4del (n.972+4del)
c.782+650del (n.782+650del)
c.53+4del
c.876+4del (n.876+4del)
c.516+4del (n.516+4del)
c.960+4del (n.960+4del)
 ClinVar dbSNP
17g.7673531G>ACA658798695TP53c.993+4C>T (n.993+4C>T)
c.597+4C>T (n.597+4C>T)
c.714+4C>T (n.714+4C>T)
c.972+4C>T (n.972+4C>T)
c.782+650C>T (n.782+650C>T)
c.53+4C>T
c.876+4C>T (n.876+4C>T)
c.516+4C>T (n.516+4C>T)
c.960+4C>T (n.960+4C>T)
 ClinVar dbSNP gnomAD v4
17g.7673531G>CCA913188777TP53c.993+4C>G (n.993+4C>G)
c.597+4C>G (n.597+4C>G)
c.714+4C>G (n.714+4C>G)
c.972+4C>G (n.972+4C>G)
c.782+650C>G (n.782+650C>G)
c.53+4C>G
c.876+4C>G (n.876+4C>G)
c.516+4C>G (n.516+4C>G)
c.960+4C>G (n.960+4C>G)
 ClinVar dbSNP
17g.7673531G=CA2245947358TP53c.993+4C= (n.993+4C=)
c.597+4C= (n.597+4C=)
c.714+4C= (n.714+4C=)
c.972+4C= (n.972+4C=)
c.782+650C= (n.782+650C=)
c.53+4C=
c.876+4C= (n.876+4C=)
c.516+4C= (n.516+4C=)
c.960+4C= (n.960+4C=)
17g.7673531G>TCA2732963322TP53c.993+4C>A (n.993+4C>A)
c.597+4C>A (n.597+4C>A)
c.714+4C>A (n.714+4C>A)
c.972+4C>A (n.972+4C>A)
c.782+650C>A (n.782+650C>A)
c.53+4C>A
c.876+4C>A (n.876+4C>A)
c.516+4C>A (n.516+4C>A)
c.960+4C>A (n.960+4C>A)
 dbSNP
17g.7673532_7673541delCA645587338TP53c.988_993+4del
c.592_597+4del
c.709_714+4del
c.967_972+4del
c.782+641_782+650del (n.782+641_782+650del)
c.48_53+4del
c.871_876+4del
c.511_516+4del
c.955_960+4del
 COSMIC COSMIC COSMIC COSMIC
17g.7673532T>ACA2573154627TP53c.993+3A>T (n.993+3A>T)
c.597+3A>T (n.597+3A>T)
c.714+3A>T (n.714+3A>T)
c.972+3A>T (n.972+3A>T)
c.782+649A>T (n.782+649A>T)
c.53+3A>T
c.876+3A>T (n.876+3A>T)
c.516+3A>T (n.516+3A>T)
c.960+3A>T (n.960+3A>T)
 ClinVar dbSNP gnomAD v4
17g.7673532T>CCA2733126018TP53c.993+3A>G (n.993+3A>G)
c.597+3A>G (n.597+3A>G)
c.714+3A>G (n.714+3A>G)
c.972+3A>G (n.972+3A>G)
c.782+649A>G (n.782+649A>G)
c.53+3A>G
c.876+3A>G (n.876+3A>G)
c.516+3A>G (n.516+3A>G)
c.960+3A>G (n.960+3A>G)
 dbSNP
17g.7673532T>GCA2733126009TP53c.993+3A>C (n.993+3A>C)
c.597+3A>C (n.597+3A>C)
c.714+3A>C (n.714+3A>C)
c.972+3A>C (n.972+3A>C)
c.782+649A>C (n.782+649A>C)
c.53+3A>C
c.876+3A>C (n.876+3A>C)
c.516+3A>C (n.516+3A>C)
c.960+3A>C (n.960+3A>C)
 dbSNP
17g.7673532_7673534delinsGCA645587339TP53c.993+1_993+3delinsC (n.993+1_993+3delinsC)
c.597+1_597+3delinsC (n.597+1_597+3delinsC)
c.714+1_714+3delinsC (n.714+1_714+3delinsC)
c.972+1_972+3delinsC (n.972+1_972+3delinsC)
c.782+647_782+649delinsC (n.782+647_782+649delinsC)
c.53+1_53+3delinsC
c.876+1_876+3delinsC (n.876+1_876+3delinsC)
c.516+1_516+3delinsC (n.516+1_516+3delinsC)
c.960+1_960+3delinsC (n.960+1_960+3delinsC)
 COSMIC
17g.7673533A=CA2245947371TP53c.993+2T= (n.993+2T=)
c.597+2T= (n.597+2T=)
c.714+2T= (n.714+2T=)
c.972+2T= (n.972+2T=)
c.782+648T= (n.782+648T=)
c.53+2T=
c.876+2T= (n.876+2T=)
c.516+2T= (n.516+2T=)
c.960+2T= (n.960+2T=)
17g.7673533A>CCA397835626TP53c.993+2T>G (n.993+2T>G)
c.597+2T>G (n.597+2T>G)
c.714+2T>G (n.714+2T>G)
c.972+2T>G (n.972+2T>G)
c.782+648T>G (n.782+648T>G)
c.53+2T>G
c.876+2T>G (n.876+2T>G)
c.516+2T>G (n.516+2T>G)
c.960+2T>G (n.960+2T>G)
 ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC
17g.7673533A>GCA397835629TP53c.993+2T>C (n.993+2T>C)
c.597+2T>C (n.597+2T>C)
c.714+2T>C (n.714+2T>C)
c.972+2T>C (n.972+2T>C)
c.782+648T>C (n.782+648T>C)
c.53+2T>C
c.876+2T>C (n.876+2T>C)
c.516+2T>C (n.516+2T>C)
c.960+2T>C (n.960+2T>C)
 ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC
17g.7673533A>TCA397835635TP53c.993+2T>A (n.993+2T>A)
c.597+2T>A (n.597+2T>A)
c.714+2T>A (n.714+2T>A)
c.972+2T>A (n.972+2T>A)
c.782+648T>A (n.782+648T>A)
c.53+2T>A
c.876+2T>A (n.876+2T>A)
c.516+2T>A (n.516+2T>A)
c.960+2T>A (n.960+2T>A)
 dbSNP COSMIC COSMIC COSMIC COSMIC
17g.7673533_7673534delinsACCA2245947369TP53c.993+1_993+2delinsGT (n.993+1_993+2delinsGT)
c.597+1_597+2delinsGT (n.597+1_597+2delinsGT)
c.714+1_714+2delinsGT (n.714+1_714+2delinsGT)
c.972+1_972+2delinsGT (n.972+1_972+2delinsGT)
c.782+647_782+648delinsGT (n.782+647_782+648delinsGT)
c.53+1_53+2delinsGT
c.876+1_876+2delinsGT (n.876+1_876+2delinsGT)
c.516+1_516+2delinsGT (n.516+1_516+2delinsGT)
c.960+1_960+2delinsGT (n.960+1_960+2delinsGT)
17g.7673533_7673541delinsTACA2580094895TP53c.987_993+2delinsTA
c.591_597+2delinsTA
c.708_714+2delinsTA
c.966_972+2delinsTA
c.782+640_782+648delinsTA (n.782+640_782+648delinsTA)
c.47_53+2delinsTA
c.870_876+2delinsTA
c.510_516+2delinsTA
c.954_960+2delinsTA
 ClinVar
17g.7673534C>ACA287486498TP53c.993+1G>T (n.993+1G>T)
c.597+1G>T (n.597+1G>T)
c.714+1G>T (n.714+1G>T)
c.972+1G>T (n.972+1G>T)
c.782+647G>T (n.782+647G>T)
c.53+1G>T
c.876+1G>T (n.876+1G>T)
c.516+1G>T (n.516+1G>T)
c.960+1G>T (n.960+1G>T)
 ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC
17g.7673534C=CA2245947398TP53c.993+1G= (n.993+1G=)
c.597+1G= (n.597+1G=)
c.714+1G= (n.714+1G=)
c.972+1G= (n.972+1G=)
c.782+647G= (n.782+647G=)
c.53+1G=
c.876+1G= (n.876+1G=)
c.516+1G= (n.516+1G=)
c.960+1G= (n.960+1G=)
17g.7673534C>GCA16607519TP53c.993+1G>C (n.993+1G>C)
c.597+1G>C (n.597+1G>C)
c.714+1G>C (n.714+1G>C)
c.972+1G>C (n.972+1G>C)
c.782+647G>C (n.782+647G>C)
c.53+1G>C
c.876+1G>C (n.876+1G>C)
c.516+1G>C (n.516+1G>C)
c.960+1G>C (n.960+1G>C)
 ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC
17g.7673534C>TCA397835645TP53c.993+1G>A (n.993+1G>A)
c.597+1G>A (n.597+1G>A)
c.714+1G>A (n.714+1G>A)
c.972+1G>A (n.972+1G>A)
c.782+647G>A (n.782+647G>A)
c.53+1G>A
c.876+1G>A (n.876+1G>A)
c.516+1G>A (n.516+1G>A)
c.960+1G>A (n.960+1G>A)
 ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC COSMIC COSMIC
17g.7673535delCA645369685TP53c.993+1del
c.597+1del
c.714+1del
c.972+1del
c.782+647del (n.782+647del)
c.53+1del
c.876+1del
c.516+1del
c.960+1del
 ClinVar dbSNP
17g.7673534_7673538delinsCCTGACA2245947390TP53c.990_993+1delinsTCAGG
c.594_597+1delinsTCAGG
c.711_714+1delinsTCAGG
c.969_972+1delinsTCAGG
c.782+643_782+647delinsTCAGG (n.782+643_782+647delinsTCAGG)
c.50_53+1delinsTCAGG
c.873_876+1delinsTCAGG
c.513_516+1delinsTCAGG
c.957_960+1delinsTCAGG
17g.7673535C>ACA287486501TP53c.993G>T (p.Gln331His)
c.597G>T (p.Gln199His)
c.714G>T (p.Gln238His)
c.972G>T (p.Gln324His)
c.782+646G>T (n.782+646G>T)
c.53G>T
c.876G>T (p.Gln292His)
c.516G>T (p.Gln172His)
c.960G>T (p.Gln320His)
 ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC
17g.7673535C=CA2245947419TP53c.993G= (p.Gln331=)
c.597G= (p.Gln199=)
c.714G= (p.Gln238=)
c.972G= (p.Gln324=)
c.782+646G= (n.782+646G=)
c.53G=
c.876G= (p.Gln292=)
c.516G= (p.Gln172=)
c.960G= (p.Gln320=)
17g.7673535C>GCA397835662TP53c.993G>C (p.Gln331His)
c.597G>C (p.Gln199His)
c.714G>C (p.Gln238His)
c.972G>C (p.Gln324His)
c.782+646G>C (n.782+646G>C)
c.53G>C
c.876G>C (p.Gln292His)
c.516G>C (p.Gln172His)
c.960G>C (p.Gln320His)
 ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC
17g.7673535C>TCA10590137TP53c.993G>A (p.Gln331=)
c.597G>A (p.Gln199=)
c.714G>A (p.Gln238=)
c.972G>A (p.Gln324=)
c.782+646G>A (n.782+646G>A)
c.53G>A
c.876G>A (p.Gln292=)
c.516G>A (p.Gln172=)
c.960G>A (p.Gln320=)
 ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC
17g.7673535_7673536delCA645587344TP53c.992_993del (p.Gln331HisfsTer5)
c.596_597del (p.Gln199HisfsTer5)
c.713_714del (p.Gln238HisfsTer5)
c.971_972del (p.Gln324HisfsTer5)
c.992_993del (p.Lys332AsnfsTer?)
c.782+645_782+646del (n.782+645_782+646del)
c.992_993del (p.Gln331ArgfsTer15)
c.992_993del (p.Gln331HisfsTer4)
c.596_597del (p.Gln199HisfsTer4)
c.596_597del (p.Gln199=)
c.596_597del (p.Gln199ArgfsTer15)
c.52_53del
c.875_876del (p.Gln292HisfsTer5)
c.875_876del (p.Gln292HisfsTer4)
c.515_516del (p.Gln172HisfsTer4)
c.959_960del (p.Gln320HisfsTer5)
c.515_516del (p.Gln172ArgfsTer15)
c.515_516del (p.Gln172HisfsTer5)
c.875_876del (p.Gln292ArgfsTer15)
 COSMIC
17g.7673535_7673536delinsTGCA645587342TP53c.992_993delinsCA (p.Gln331Pro)
c.596_597delinsCA (p.Gln199Pro)
c.713_714delinsCA (p.Gln238Pro)
c.971_972delinsCA (p.Gln324Pro)
c.782+645_782+646delinsCA (n.782+645_782+646delinsCA)
c.52_53delinsCA
c.875_876delinsCA (p.Gln292Pro)
c.515_516delinsCA (p.Gln172Pro)
c.959_960delinsCA (p.Gln320Pro)
 COSMIC
17g.7673535_7673538delCA658656523TP53c.990_993del (p.Gln331SerfsTer13)
c.594_597del (p.Gln199SerfsTer13)
c.711_714del (p.Gln238SerfsTer13)
c.969_972del (p.Gln324SerfsTer13)
c.990_993del (p.Gln331LysfsTer20)
c.782+643_782+646del (n.782+643_782+646del)
c.990_993del (p.Gln331ThrfsTer19)
c.990_993del (p.Gln331CysfsTer11)
c.594_597del (p.Gln199CysfsTer11)
c.594_597del (p.Leu198=)
c.594_597del (p.Gln199ThrfsTer19)
c.50_53del
c.873_876del (p.Gln292SerfsTer13)
c.873_876del (p.Gln292CysfsTer11)
c.513_516del (p.Gln172CysfsTer11)
c.957_960del (p.Gln320SerfsTer13)
c.513_516del (p.Gln172ThrfsTer19)
c.513_516del (p.Gln172SerfsTer13)
c.873_876del (p.Gln292ThrfsTer19)
 ClinVar dbSNP
17g.7673536T>ACA397835673TP53c.992A>T (p.Gln331Leu)
c.596A>T (p.Gln199Leu)
c.713A>T (p.Gln238Leu)
c.971A>T (p.Gln324Leu)
c.782+645A>T (n.782+645A>T)
c.52A>T
c.875A>T (p.Gln292Leu)
c.515A>T (p.Gln172Leu)
c.959A>T (p.Gln320Leu)
17g.7673536T>CCA16620611TP53c.992A>G (p.Gln331Arg)
c.596A>G (p.Gln199Arg)
c.713A>G (p.Gln238Arg)
c.971A>G (p.Gln324Arg)
c.782+645A>G (n.782+645A>G)
c.52A>G
c.875A>G (p.Gln292Arg)
c.515A>G (p.Gln172Arg)
c.959A>G (p.Gln320Arg)
 ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC
17g.7673536T>GCA397835672TP53c.992A>C (p.Gln331Pro)
c.596A>C (p.Gln199Pro)
c.713A>C (p.Gln238Pro)
c.971A>C (p.Gln324Pro)
c.782+645A>C (n.782+645A>C)
c.52A>C
c.875A>C (p.Gln292Pro)
c.515A>C (p.Gln172Pro)
c.959A>C (p.Gln320Pro)
 COSMIC
17g.7673536T=CA2245947430TP53c.992A= (p.Gln331=)
c.596A= (p.Gln199=)
c.713A= (p.Gln238=)
c.971A= (p.Gln324=)
c.782+645A= (n.782+645A=)
c.52A=
c.875A= (p.Gln292=)
c.515A= (p.Gln172=)
c.959A= (p.Gln320=)
17g.7673536_7673594dupCA2499224956TP53c.934_992dup (p.Ile332ProfsTer33)
c.538_596dup (p.Ile200ProfsTer33)
c.655_713dup (p.Ile239ProfsTer33)
c.913_971dup (p.Ile325ProfsTer33)
c.934_992dup (p.Lys332ProfsTer40)
c.782+587_782+645dup (n.782+587_782+645dup)
c.934_992dup (p.Asp332ProfsTer39)
c.934_992dup (p.Met332ProfsTer31)
c.538_596dup (p.Met200ProfsTer31)
c.538_596dup (p.Gln199=)
c.538_596dup (p.Asp200ProfsTer39)
c.817_875dup (p.Ile293ProfsTer33)
c.817_875dup (p.Met293ProfsTer31)
c.457_515dup (p.Met173ProfsTer31)
c.901_959dup (p.Ile321ProfsTer33)
c.457_515dup (p.Asp173ProfsTer39)
c.457_515dup (p.Ile173ProfsTer33)
c.817_875dup (p.Asp293ProfsTer39)
 ClinVar dbSNP
17g.7673537G>ACA397835674TP53c.991C>T (p.Gln331Ter)
c.595C>T (p.Gln199Ter)
c.712C>T (p.Gln238Ter)
c.970C>T (p.Gln324Ter)
c.782+644C>T (n.782+644C>T)
c.51C>T
c.874C>T (p.Gln292Ter)
c.514C>T (p.Gln172Ter)
c.958C>T (p.Gln320Ter)
 ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC
17g.7673537G>CCA397835677TP53c.991C>G (p.Gln331Glu)
c.595C>G (p.Gln199Glu)
c.712C>G (p.Gln238Glu)
c.970C>G (p.Gln324Glu)
c.782+644C>G (n.782+644C>G)
c.51C>G
c.874C>G (p.Gln292Glu)
c.514C>G (p.Gln172Glu)
c.958C>G (p.Gln320Glu)
 ClinVar
17g.7673537G=CA2245947449TP53c.991C= (p.Gln331=)
c.595C= (p.Gln199=)
c.712C= (p.Gln238=)
c.970C= (p.Gln324=)
c.782+644C= (n.782+644C=)
c.51C=
c.874C= (p.Gln292=)
c.514C= (p.Gln172=)
c.958C= (p.Gln320=)
17g.7673537G>TCA397835679TP53c.991C>A (p.Gln331Lys)
c.595C>A (p.Gln199Lys)
c.712C>A (p.Gln238Lys)
c.970C>A (p.Gln324Lys)
c.782+644C>A (n.782+644C>A)
c.51C>A
c.874C>A (p.Gln292Lys)
c.514C>A (p.Gln172Lys)
c.958C>A (p.Gln320Lys)
 ClinVar dbSNP
17g.7673538A>CCA497713725TP53c.990T>G (p.Leu330=)
c.594T>G (p.Leu198=)
c.711T>G (p.Leu237=)
c.969T>G (p.Leu323=)
c.782+643T>G (n.782+643T>G)
c.50T>G
c.873T>G (p.Leu291=)
c.513T>G (p.Leu171=)
c.957T>G (p.Leu319=)
 dbSNP
17g.7673538A>GCA497713729TP53c.990T>C (p.Leu330=)
c.594T>C (p.Leu198=)
c.711T>C (p.Leu237=)
c.969T>C (p.Leu323=)
c.782+643T>C (n.782+643T>C)
c.50T>C
c.873T>C (p.Leu291=)
c.513T>C (p.Leu171=)
c.957T>C (p.Leu319=)
 dbSNP
17g.7673538A>TCA497713734TP53c.990T>A (p.Leu330=)
c.594T>A (p.Leu198=)
c.711T>A (p.Leu237=)
c.969T>A (p.Leu323=)
c.782+643T>A (n.782+643T>A)
c.50T>A
c.873T>A (p.Leu291=)
c.513T>A (p.Leu171=)
c.957T>A (p.Leu319=)
 dbSNP
17g.7673539dupCA645587345TP53c.990dup (p.Gln331SerfsTer6)
c.594dup (p.Gln199SerfsTer6)
c.711dup (p.Gln238SerfsTer6)
c.969dup (p.Gln324SerfsTer6)
c.990dup (p.Gln331SerfsTer?)
c.782+643dup (n.782+643dup)
c.990dup (p.Gln331SerfsTer16)
c.990dup (p.Gln331SerfsTer5)
c.594dup (p.Gln199SerfsTer5)
c.594dup (p.Gln199SerfsTer?)
c.594dup (p.Gln199SerfsTer16)
c.50dup
c.873dup (p.Gln292SerfsTer6)
c.873dup (p.Gln292SerfsTer5)
c.513dup (p.Gln172SerfsTer5)
c.957dup (p.Gln320SerfsTer6)
c.513dup (p.Gln172SerfsTer16)
c.513dup (p.Gln172SerfsTer6)
c.873dup (p.Gln292SerfsTer16)
 COSMIC COSMIC
17g.7673539delCA497713744TP53c.990del (p.Gln331ArgfsTer14)
c.594del (p.Gln199ArgfsTer14)
c.711del (p.Gln238ArgfsTer14)
c.969del (p.Gln324ArgfsTer14)
c.990del (p.Gln331ArgfsTer21)
c.782+643del (n.782+643del)
c.990del (p.Gln331ArgfsTer20)
c.990del (p.Gln331ArgfsTer12)
c.594del (p.Gln199ArgfsTer12)
c.594del (p.Leu198=)
c.594del (p.Gln199ArgfsTer20)
c.50del
c.873del (p.Gln292ArgfsTer14)
c.873del (p.Gln292ArgfsTer12)
c.513del (p.Gln172ArgfsTer12)
c.957del (p.Gln320ArgfsTer14)
c.513del (p.Gln172ArgfsTer20)
c.513del (p.Gln172ArgfsTer14)
c.873del (p.Gln292ArgfsTer20)
 ClinVar dbSNP COSMIC
17g.7673538_7673539insTCA497713747TP53c.989_990insA (p.Gln331SerfsTer6)
c.593_594insA (p.Gln199SerfsTer6)
c.710_711insA (p.Gln238SerfsTer6)
c.968_969insA (p.Gln324SerfsTer6)
c.989_990insA (p.Gln331SerfsTer?)
c.782+642_782+643insA (n.782+642_782+643insA)
c.989_990insA (p.Gln331SerfsTer16)
c.989_990insA (p.Gln331SerfsTer5)
c.593_594insA (p.Gln199SerfsTer5)
c.593_594insA (p.Gln199SerfsTer?)
c.593_594insA (p.Gln199SerfsTer16)
c.49_50insA
c.872_873insA (p.Gln292SerfsTer6)
c.872_873insA (p.Gln292SerfsTer5)
c.512_513insA (p.Gln172SerfsTer5)
c.956_957insA (p.Gln320SerfsTer6)
c.512_513insA (p.Gln172SerfsTer16)
c.512_513insA (p.Gln172SerfsTer6)
c.872_873insA (p.Gln292SerfsTer16)
17g.7673539A=CA2245947462TP53c.989T= (p.Leu330=)
c.593T= (p.Leu198=)
c.710T= (p.Leu237=)
c.968T= (p.Leu323=)
c.782+642T= (n.782+642T=)
c.49T=
c.872T= (p.Leu291=)
c.512T= (p.Leu171=)
c.956T= (p.Leu319=)
17g.7673539A>CCA397835702TP53c.989T>G (p.Leu330Arg)
c.593T>G (p.Leu198Arg)
c.710T>G (p.Leu237Arg)
c.968T>G (p.Leu323Arg)
c.782+642T>G (n.782+642T>G)
c.49T>G
c.872T>G (p.Leu291Arg)
c.512T>G (p.Leu171Arg)
c.956T>G (p.Leu319Arg)
 ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC
17g.7673539A>GCA397835704TP53c.989T>C (p.Leu330Pro)
c.593T>C (p.Leu198Pro)
c.710T>C (p.Leu237Pro)
c.968T>C (p.Leu323Pro)
c.782+642T>C (n.782+642T>C)
c.49T>C
c.872T>C (p.Leu291Pro)
c.512T>C (p.Leu171Pro)
c.956T>C (p.Leu319Pro)
 ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC
17g.7673539A>TCA397835707TP53c.989T>A (p.Leu330His)
c.593T>A (p.Leu198His)
c.710T>A (p.Leu237His)
c.968T>A (p.Leu323His)
c.782+642T>A (n.782+642T>A)
c.49T>A
c.872T>A (p.Leu291His)
c.512T>A (p.Leu171His)
c.956T>A (p.Leu319His)
 ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC
17g.7673539_7673540delinsAGCA2245947468TP53c.988_989delinsCT (p.Leu330=)
c.592_593delinsCT (p.Leu198=)
c.709_710delinsCT (p.Leu237=)
c.967_968delinsCT (p.Leu323=)
c.782+641_782+642delinsCT (n.782+641_782+642delinsCT)
c.48_49delinsCT
c.871_872delinsCT (p.Leu291=)
c.511_512delinsCT (p.Leu171=)
c.955_956delinsCT (p.Leu319=)
17g.7673540G>ACA397835712TP53c.988C>T (p.Leu330Phe)
c.592C>T (p.Leu198Phe)
c.709C>T (p.Leu237Phe)
c.967C>T (p.Leu323Phe)
c.782+641C>T (n.782+641C>T)
c.48C>T
c.871C>T (p.Leu291Phe)
c.511C>T (p.Leu171Phe)
c.955C>T (p.Leu319Phe)
 ClinVar dbSNP
17g.7673540G>CCA397835714TP53c.988C>G (p.Leu330Val)
c.592C>G (p.Leu198Val)
c.709C>G (p.Leu237Val)
c.967C>G (p.Leu323Val)
c.782+641C>G (n.782+641C>G)
c.48C>G
c.871C>G (p.Leu291Val)
c.511C>G (p.Leu171Val)
c.955C>G (p.Leu319Val)
 dbSNP
17g.7673540G=CA2245947485TP53c.988C= (p.Leu330=)
c.592C= (p.Leu198=)
c.709C= (p.Leu237=)
c.967C= (p.Leu323=)
c.782+641C= (n.782+641C=)
c.48C=
c.871C= (p.Leu291=)
c.511C= (p.Leu171=)
c.955C= (p.Leu319=)
17g.7673540G>TCA397835718TP53c.988C>A (p.Leu330Ile)
c.592C>A (p.Leu198Ile)
c.709C>A (p.Leu237Ile)
c.967C>A (p.Leu323Ile)
c.782+641C>A (n.782+641C>A)
c.48C>A
c.871C>A (p.Leu291Ile)
c.511C>A (p.Leu171Ile)
c.955C>A (p.Leu319Ile)
 dbSNP
17g.7673542delCA497713751TP53c.988del (p.Leu330PhefsTer15)
c.592del (p.Leu198PhefsTer15)
c.709del (p.Leu237PhefsTer15)
c.967del (p.Leu323PhefsTer15)
c.988del (p.Leu330PhefsTer22)
c.782+641del (n.782+641del)
c.988del (p.Leu330PhefsTer21)
c.988del (p.Leu330PhefsTer13)
c.592del (p.Leu198PhefsTer13)
c.592del (p.Leu198PhefsTer?)
c.592del (p.Leu198PhefsTer21)
c.48del
c.871del (p.Leu291PhefsTer15)
c.871del (p.Leu291PhefsTer13)
c.511del (p.Leu171PhefsTer13)
c.955del (p.Leu319PhefsTer15)
c.511del (p.Leu171PhefsTer21)
c.511del (p.Leu171PhefsTer15)
c.871del (p.Leu291PhefsTer21)
 ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7673541G>ACA497713763TP53c.987C>T (p.Thr329=)
c.591C>T (p.Thr197=)
c.708C>T (p.Thr236=)
c.966C>T (p.Thr322=)
c.782+640C>T (n.782+640C>T)
c.47C>T
c.870C>T (p.Thr290=)
c.510C>T (p.Thr170=)
c.954C>T (p.Thr318=)
 ClinVar dbSNP gnomAD v4 COSMIC
17g.7673541G>CCA497713766TP53c.987C>G (p.Thr329=)
c.591C>G (p.Thr197=)
c.708C>G (p.Thr236=)
c.966C>G (p.Thr322=)
c.782+640C>G (n.782+640C>G)
c.47C>G
c.870C>G (p.Thr290=)
c.510C>G (p.Thr170=)
c.954C>G (p.Thr318=)
 dbSNP
17g.7673541G>TCA497713769TP53c.987C>A (p.Thr329=)
c.591C>A (p.Thr197=)
c.708C>A (p.Thr236=)
c.966C>A (p.Thr322=)
c.782+640C>A (n.782+640C>A)
c.47C>A
c.870C>A (p.Thr290=)
c.510C>A (p.Thr170=)
c.954C>A (p.Thr318=)
 ClinVar dbSNP COSMIC
17g.7673541_7673542delinsAACA645587346TP53c.986_987delinsTT (p.Thr329Ile)
c.590_591delinsTT (p.Thr197Ile)
c.707_708delinsTT (p.Thr236Ile)
c.965_966delinsTT (p.Thr322Ile)
c.782+639_782+640delinsTT (n.782+639_782+640delinsTT)
c.46_47delinsTT
c.869_870delinsTT (p.Thr290Ile)
c.509_510delinsTT (p.Thr170Ile)
c.953_954delinsTT (p.Thr318Ile)
 COSMIC COSMIC
17g.7673541_7673560delinsGGTGAAATATTCTCCATCCACA2245947495TP53c.968_987delinsTGGATGGAGAATATTTCACC (p.Leu323=)
c.572_591delinsTGGATGGAGAATATTTCACC (p.Leu191=)
c.689_708delinsTGGATGGAGAATATTTCACC (p.Leu230=)
c.947_966delinsTGGATGGAGAATATTTCACC (p.Leu316=)
c.782+621_782+640delinsTGGATGGAGAATATTTCACC (n.782+621_782+640delinsTGGATGGAGAATATTTCACC)
c.28_47delinsTGGATGGAGAATATTTCACC
c.851_870delinsTGGATGGAGAATATTTCACC (p.Leu284=)
c.491_510delinsTGGATGGAGAATATTTCACC (p.Leu164=)
c.935_954delinsTGGATGGAGAATATTTCACC (p.Leu312=)
17g.7673542G>ACA287486504TP53c.986C>T (p.Thr329Ile)
c.590C>T (p.Thr197Ile)
c.707C>T (p.Thr236Ile)
c.965C>T (p.Thr322Ile)
c.782+639C>T (n.782+639C>T)
c.46C>T
c.869C>T (p.Thr290Ile)
c.509C>T (p.Thr170Ile)
c.953C>T (p.Thr318Ile)
 ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC
17g.7673542G>CCA397835725TP53c.986C>G (p.Thr329Ser)
c.590C>G (p.Thr197Ser)
c.707C>G (p.Thr236Ser)
c.965C>G (p.Thr322Ser)
c.782+639C>G (n.782+639C>G)
c.46C>G
c.869C>G (p.Thr290Ser)
c.509C>G (p.Thr170Ser)
c.953C>G (p.Thr318Ser)
 dbSNP
17g.7673542G=CA2245947503TP53c.986C= (p.Thr329=)
c.590C= (p.Thr197=)
c.707C= (p.Thr236=)
c.965C= (p.Thr322=)
c.782+639C= (n.782+639C=)
c.46C=
c.869C= (p.Thr290=)
c.509C= (p.Thr170=)
c.953C= (p.Thr318=)
17g.7673542G>TCA397835730TP53c.986C>A (p.Thr329Asn)
c.590C>A (p.Thr197Asn)
c.707C>A (p.Thr236Asn)
c.965C>A (p.Thr322Asn)
c.782+639C>A (n.782+639C>A)
c.46C>A
c.869C>A (p.Thr290Asn)
c.509C>A (p.Thr170Asn)
c.953C>A (p.Thr318Asn)
 dbSNP
17g.7673545_7673563delCA913188778TP53c.968_986del (p.Leu323ProfsTer16)
c.572_590del (p.Leu191ProfsTer16)
c.689_707del (p.Leu230ProfsTer16)
c.947_965del (p.Leu316ProfsTer16)
c.968_986del (p.Leu323ProfsTer23)
c.782+621_782+639del (n.782+621_782+639del)
c.968_986del (p.Leu323ProfsTer22)
c.968_986del (p.Leu323ProfsTer14)
c.572_590del (p.Leu191ProfsTer14)
c.572_590del (p.Leu191ProfsTer?)
c.572_590del (p.Leu191ProfsTer22)
c.28_46del
c.851_869del (p.Leu284ProfsTer16)
c.851_869del (p.Leu284ProfsTer14)
c.491_509del (p.Leu164ProfsTer14)
c.935_953del (p.Leu312ProfsTer16)
c.491_509del (p.Leu164ProfsTer22)
c.491_509del (p.Leu164ProfsTer16)
c.851_869del (p.Leu284ProfsTer22)
 ClinVar dbSNP
17g.7673543T>ACA397835737TP53c.985A>T (p.Thr329Ser)
c.589A>T (p.Thr197Ser)
c.706A>T (p.Thr236Ser)
c.964A>T (p.Thr322Ser)
c.782+638A>T (n.782+638A>T)
c.45A>T
c.868A>T (p.Thr290Ser)
c.508A>T (p.Thr170Ser)
c.952A>T (p.Thr318Ser)
 dbSNP
17g.7673543T>CCA397835735TP53c.985A>G (p.Thr329Ala)
c.589A>G (p.Thr197Ala)
c.706A>G (p.Thr236Ala)
c.964A>G (p.Thr322Ala)
c.782+638A>G (n.782+638A>G)
c.45A>G
c.868A>G (p.Thr290Ala)
c.508A>G (p.Thr170Ala)
c.952A>G (p.Thr318Ala)
 ClinVar dbSNP gnomAD v4
17g.7673543T>GCA397835733TP53c.985A>C (p.Thr329Pro)
c.589A>C (p.Thr197Pro)
c.706A>C (p.Thr236Pro)
c.964A>C (p.Thr322Pro)
c.782+638A>C (n.782+638A>C)
c.45A>C
c.868A>C (p.Thr290Pro)
c.508A>C (p.Thr170Pro)
c.952A>C (p.Thr318Pro)
 dbSNP
17g.7673543T=CA2245947510TP53c.985A= (p.Thr329=)
c.589A= (p.Thr197=)
c.706A= (p.Thr236=)
c.964A= (p.Thr322=)
c.782+638A= (n.782+638A=)
c.45A=
c.868A= (p.Thr290=)
c.508A= (p.Thr170=)
c.952A= (p.Thr318=)
17g.7673544G>ACA16608656TP53c.984C>T (p.Phe328=)
c.588C>T (p.Phe196=)
c.705C>T (p.Phe235=)
c.963C>T (p.Phe321=)
c.782+637C>T (n.782+637C>T)
c.44C>T
c.867C>T (p.Phe289=)
c.507C>T (p.Phe169=)
c.951C>T (p.Phe317=)
 ClinVar dbSNP COSMIC
17g.7673544G>CCA397835743TP53c.984C>G (p.Phe328Leu)
c.588C>G (p.Phe196Leu)
c.705C>G (p.Phe235Leu)
c.963C>G (p.Phe321Leu)
c.782+637C>G (n.782+637C>G)
c.44C>G
c.867C>G (p.Phe289Leu)
c.507C>G (p.Phe169Leu)
c.951C>G (p.Phe317Leu)
 dbSNP
17g.7673544G=CA2245947520TP53c.984C= (p.Phe328=)
c.588C= (p.Phe196=)
c.705C= (p.Phe235=)
c.963C= (p.Phe321=)
c.782+637C= (n.782+637C=)
c.44C=
c.867C= (p.Phe289=)
c.507C= (p.Phe169=)
c.951C= (p.Phe317=)
17g.7673544G>TCA397835745TP53c.984C>A (p.Phe328Leu)
c.588C>A (p.Phe196Leu)
c.705C>A (p.Phe235Leu)
c.963C>A (p.Phe321Leu)
c.782+637C>A (n.782+637C>A)
c.44C>A
c.867C>A (p.Phe289Leu)
c.507C>A (p.Phe169Leu)
c.951C>A (p.Phe317Leu)
 dbSNP
17g.7673544_7673545insTCA645587347TP53c.983_984insA (p.Phe328LeufsTer9)
c.587_588insA (p.Phe196LeufsTer9)
c.704_705insA (p.Phe235LeufsTer9)
c.962_963insA (p.Phe321LeufsTer9)
c.983_984insA (p.Phe328LeufsTer?)
c.782+636_782+637insA (n.782+636_782+637insA)
c.983_984insA (p.Phe328LeufsTer19)
c.983_984insA (p.Phe328LeufsTer8)
c.587_588insA (p.Phe196LeufsTer8)
c.587_588insA (p.Phe196LeufsTer?)
c.587_588insA (p.Phe196LeufsTer19)
c.43_44insA
c.866_867insA (p.Phe289LeufsTer9)
c.866_867insA (p.Phe289LeufsTer8)
c.506_507insA (p.Phe169LeufsTer8)
c.950_951insA (p.Phe317LeufsTer9)
c.506_507insA (p.Phe169LeufsTer19)
c.506_507insA (p.Phe169LeufsTer9)
c.866_867insA (p.Phe289LeufsTer19)
 COSMIC
17g.7673545A=CA2245947539TP53c.983T= (p.Phe328=)
c.587T= (p.Phe196=)
c.704T= (p.Phe235=)
c.962T= (p.Phe321=)
c.782+636T= (n.782+636T=)
c.43T=
c.866T= (p.Phe289=)
c.506T= (p.Phe169=)
c.950T= (p.Phe317=)
17g.7673545A>CCA397835749TP53c.983T>G (p.Phe328Cys)
c.587T>G (p.Phe196Cys)
c.704T>G (p.Phe235Cys)
c.962T>G (p.Phe321Cys)
c.782+636T>G (n.782+636T>G)
c.43T>G
c.866T>G (p.Phe289Cys)
c.506T>G (p.Phe169Cys)
c.950T>G (p.Phe317Cys)
17g.7673545A>GCA397835751TP53c.983T>C (p.Phe328Ser)
c.587T>C (p.Phe196Ser)
c.704T>C (p.Phe235Ser)
c.962T>C (p.Phe321Ser)
c.782+636T>C (n.782+636T>C)
c.43T>C
c.866T>C (p.Phe289Ser)
c.506T>C (p.Phe169Ser)
c.950T>C (p.Phe317Ser)
 ClinVar dbSNP COSMIC
17g.7673545A>TCA397835754TP53c.983T>A (p.Phe328Tyr)
c.587T>A (p.Phe196Tyr)
c.704T>A (p.Phe235Tyr)
c.962T>A (p.Phe321Tyr)
c.782+636T>A (n.782+636T>A)
c.43T>A
c.866T>A (p.Phe289Tyr)
c.506T>A (p.Phe169Tyr)
c.950T>A (p.Phe317Tyr)
 dbSNP
17g.7673547dupCA10603410TP53c.983dup (p.Thr329HisfsTer8)
c.587dup (p.Thr197HisfsTer8)
c.704dup (p.Thr236HisfsTer8)
c.962dup (p.Thr322HisfsTer8)
c.983dup (p.Thr329HisfsTer?)
c.782+636dup (n.782+636dup)
c.983dup (p.Thr329HisfsTer18)
c.983dup (p.Thr329HisfsTer7)
c.587dup (p.Thr197HisfsTer7)
c.587dup (p.Thr197HisfsTer?)
c.587dup (p.Thr197HisfsTer18)
c.43dup
c.866dup (p.Thr290HisfsTer8)
c.866dup (p.Thr290HisfsTer7)
c.506dup (p.Thr170HisfsTer7)
c.950dup (p.Thr318HisfsTer8)
c.506dup (p.Thr170HisfsTer18)
c.506dup (p.Thr170HisfsTer8)
c.866dup (p.Thr290HisfsTer18)
 ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC
17g.7673546_7673547dupCA2573154629TP53c.982_983dup (p.Thr329SerfsTer17)
c.586_587dup (p.Thr197SerfsTer17)
c.703_704dup (p.Thr236SerfsTer17)
c.961_962dup (p.Thr322SerfsTer17)
c.982_983dup (p.Thr329SerfsTer24)
c.782+635_782+636dup (n.782+635_782+636dup)
c.982_983dup (p.Thr329SerfsTer23)
c.982_983dup (p.Thr329SerfsTer15)
c.586_587dup (p.Thr197SerfsTer15)
c.586_587dup (p.Thr197SerfsTer?)
c.586_587dup (p.Thr197SerfsTer23)
c.42_43dup
c.865_866dup (p.Thr290SerfsTer17)
c.865_866dup (p.Thr290SerfsTer15)
c.505_506dup (p.Thr170SerfsTer15)
c.949_950dup (p.Thr318SerfsTer17)
c.505_506dup (p.Thr170SerfsTer23)
c.505_506dup (p.Thr170SerfsTer17)
c.865_866dup (p.Thr290SerfsTer23)
 ClinVar dbSNP
17g.7673547delCA497713799TP53c.983del (p.Phe328SerfsTer17)
c.587del (p.Phe196SerfsTer17)
c.704del (p.Phe235SerfsTer17)
c.962del (p.Phe321SerfsTer17)
c.983del (p.Phe328SerfsTer24)
c.782+636del (n.782+636del)
c.983del (p.Phe328SerfsTer23)
c.983del (p.Phe328SerfsTer15)
c.587del (p.Phe196SerfsTer15)
c.587del (p.Phe196SerfsTer?)
c.587del (p.Phe196SerfsTer23)
c.43del
c.866del (p.Phe289SerfsTer17)
c.866del (p.Phe289SerfsTer15)
c.506del (p.Phe169SerfsTer15)
c.950del (p.Phe317SerfsTer17)
c.506del (p.Phe169SerfsTer23)
c.506del (p.Phe169SerfsTer17)
c.866del (p.Phe289SerfsTer23)
 COSMIC COSMIC COSMIC COSMIC
17g.7673545_7673546insTCA497713806TP53c.982_983insA (p.Phe328TyrfsTer9)
c.586_587insA (p.Phe196TyrfsTer9)
c.703_704insA (p.Phe235TyrfsTer9)
c.961_962insA (p.Phe321TyrfsTer9)
c.982_983insA (p.Phe328TyrfsTer?)
c.782+635_782+636insA (n.782+635_782+636insA)
c.982_983insA (p.Phe328TyrfsTer19)
c.982_983insA (p.Phe328TyrfsTer8)
c.586_587insA (p.Phe196TyrfsTer8)
c.586_587insA (p.Phe196TyrfsTer?)
c.586_587insA (p.Phe196TyrfsTer19)
c.42_43insA
c.865_866insA (p.Phe289TyrfsTer9)
c.865_866insA (p.Phe289TyrfsTer8)
c.505_506insA (p.Phe169TyrfsTer8)
c.949_950insA (p.Phe317TyrfsTer9)
c.505_506insA (p.Phe169TyrfsTer19)
c.505_506insA (p.Phe169TyrfsTer9)
c.865_866insA (p.Phe289TyrfsTer19)
17g.7673546A>CCA397835758TP53c.982T>G (p.Phe328Val)
c.586T>G (p.Phe196Val)
c.703T>G (p.Phe235Val)
c.961T>G (p.Phe321Val)
c.782+635T>G (n.782+635T>G)
c.42T>G
c.865T>G (p.Phe289Val)
c.505T>G (p.Phe169Val)
c.949T>G (p.Phe317Val)
 COSMIC
17g.7673546A>GCA397835759TP53c.982T>C (p.Phe328Leu)
c.586T>C (p.Phe196Leu)
c.703T>C (p.Phe235Leu)
c.961T>C (p.Phe321Leu)
c.782+635T>C (n.782+635T>C)
c.42T>C
c.865T>C (p.Phe289Leu)
c.505T>C (p.Phe169Leu)
c.949T>C (p.Phe317Leu)
17g.7673546A>TCA397835761TP53c.982T>A (p.Phe328Ile)
c.586T>A (p.Phe196Ile)
c.703T>A (p.Phe235Ile)
c.961T>A (p.Phe321Ile)
c.782+635T>A (n.782+635T>A)
c.42T>A
c.865T>A (p.Phe289Ile)
c.505T>A (p.Phe169Ile)
c.949T>A (p.Phe317Ile)
 dbSNP
17g.7673546_7673548delinsAATCA2245947548TP53c.980_982delinsATT (p.Tyr327=)
c.584_586delinsATT (p.Tyr195=)
c.701_703delinsATT (p.Tyr234=)
c.959_961delinsATT (p.Tyr320=)
c.782+633_782+635delinsATT (n.782+633_782+635delinsATT)
c.40_42delinsATT
c.863_865delinsATT (p.Tyr288=)
c.503_505delinsATT (p.Tyr168=)
c.947_949delinsATT (p.Tyr316=)
17g.7673547A=CA2245947559TP53c.981T= (p.Tyr327=)
c.585T= (p.Tyr195=)
c.702T= (p.Tyr234=)
c.960T= (p.Tyr320=)
c.782+634T= (n.782+634T=)
c.41T=
c.864T= (p.Tyr288=)
c.504T= (p.Tyr168=)
c.948T= (p.Tyr316=)
17g.7673547A>CCA10584585TP53c.981T>G (p.Tyr327Ter)
c.585T>G (p.Tyr195Ter)
c.702T>G (p.Tyr234Ter)
c.960T>G (p.Tyr320Ter)
c.782+634T>G (n.782+634T>G)
c.41T>G
c.864T>G (p.Tyr288Ter)
c.504T>G (p.Tyr168Ter)
c.948T>G (p.Tyr316Ter)
 ClinVar dbSNP COSMIC COSMIC
17g.7673547A>GCA497713821TP53c.981T>C (p.Tyr327=)
c.585T>C (p.Tyr195=)
c.702T>C (p.Tyr234=)
c.960T>C (p.Tyr320=)
c.782+634T>C (n.782+634T>C)
c.41T>C
c.864T>C (p.Tyr288=)
c.504T>C (p.Tyr168=)
c.948T>C (p.Tyr316=)
 dbSNP
17g.7673547A>TCA397835766TP53c.981T>A (p.Tyr327Ter)
c.585T>A (p.Tyr195Ter)
c.702T>A (p.Tyr234Ter)
c.960T>A (p.Tyr320Ter)
c.782+634T>A (n.782+634T>A)
c.41T>A
c.864T>A (p.Tyr288Ter)
c.504T>A (p.Tyr168Ter)
c.948T>A (p.Tyr316Ter)
 ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC
17g.7673549_7673550delCA645587348TP53c.980_981del (p.Tyr327PhefsTer9)
c.584_585del (p.Tyr195PhefsTer9)
c.701_702del (p.Tyr234PhefsTer9)
c.959_960del (p.Tyr320PhefsTer9)
c.980_981del (p.Tyr327PhefsTer?)
c.782+633_782+634del (n.782+633_782+634del)
c.980_981del (p.Tyr327PhefsTer19)
c.980_981del (p.Tyr327PhefsTer8)
c.584_585del (p.Tyr195PhefsTer8)
c.584_585del (p.Tyr195PhefsTer?)
c.584_585del (p.Tyr195PhefsTer19)
c.40_41del
c.863_864del (p.Tyr288PhefsTer9)
c.863_864del (p.Tyr288PhefsTer8)
c.503_504del (p.Tyr168PhefsTer8)
c.947_948del (p.Tyr316PhefsTer9)
c.503_504del (p.Tyr168PhefsTer19)
c.503_504del (p.Tyr168PhefsTer9)
c.863_864del (p.Tyr288PhefsTer19)
 ClinVar dbSNP COSMIC
17g.7673548T>ACA397835768TP53c.980A>T (p.Tyr327Phe)
c.584A>T (p.Tyr195Phe)
c.701A>T (p.Tyr234Phe)
c.959A>T (p.Tyr320Phe)
c.782+633A>T (n.782+633A>T)
c.40A>T
c.863A>T (p.Tyr288Phe)
c.503A>T (p.Tyr168Phe)
c.947A>T (p.Tyr316Phe)
 dbSNP
17g.7673548T>CCA397835771TP53c.980A>G (p.Tyr327Cys)
c.584A>G (p.Tyr195Cys)
c.701A>G (p.Tyr234Cys)
c.959A>G (p.Tyr320Cys)
c.782+633A>G (n.782+633A>G)
c.40A>G
c.863A>G (p.Tyr288Cys)
c.503A>G (p.Tyr168Cys)
c.947A>G (p.Tyr316Cys)
 ClinVar dbSNP
17g.7673548T>GCA397835778TP53c.980A>C (p.Tyr327Ser)
c.584A>C (p.Tyr195Ser)
c.701A>C (p.Tyr234Ser)
c.959A>C (p.Tyr320Ser)
c.782+633A>C (n.782+633A>C)
c.40A>C
c.863A>C (p.Tyr288Ser)
c.503A>C (p.Tyr168Ser)
c.947A>C (p.Tyr316Ser)
 dbSNP
17g.7673548_7673549insTTCA645587349TP53c.980_981insAA (p.Tyr327Ter)
c.584_585insAA (p.Tyr195Ter)
c.701_702insAA (p.Tyr234Ter)
c.959_960insAA (p.Tyr320Ter)
c.782+633_782+634insAA (n.782+633_782+634insAA)
c.40_41insAA
c.863_864insAA (p.Tyr288Ter)
c.503_504insAA (p.Tyr168Ter)
c.947_948insAA (p.Tyr316Ter)
 COSMIC
17g.7673549A>CCA397835781TP53c.979T>G (p.Tyr327Asp)
c.583T>G (p.Tyr195Asp)
c.700T>G (p.Tyr234Asp)
c.958T>G (p.Tyr320Asp)
c.782+632T>G (n.782+632T>G)
c.39T>G
c.862T>G (p.Tyr288Asp)
c.502T>G (p.Tyr168Asp)
c.946T>G (p.Tyr316Asp)
 dbSNP COSMIC
17g.7673549A>GCA397835786TP53c.979T>C (p.Tyr327His)
c.583T>C (p.Tyr195His)
c.700T>C (p.Tyr234His)
c.958T>C (p.Tyr320His)
c.782+632T>C (n.782+632T>C)
c.39T>C
c.862T>C (p.Tyr288His)
c.502T>C (p.Tyr168His)
c.946T>C (p.Tyr316His)
17g.7673549A>TCA397835783TP53c.979T>A (p.Tyr327Asn)
c.583T>A (p.Tyr195Asn)
c.700T>A (p.Tyr234Asn)
c.958T>A (p.Tyr320Asn)
c.782+632T>A (n.782+632T>A)
c.39T>A
c.862T>A (p.Tyr288Asn)
c.502T>A (p.Tyr168Asn)
c.946T>A (p.Tyr316Asn)
 dbSNP
17g.7673550T>ACA287486513TP53c.978A>T (p.Glu326Asp)
c.582A>T (p.Glu194Asp)
c.699A>T (p.Glu233Asp)
c.957A>T (p.Glu319Asp)
c.782+631A>T (n.782+631A>T)
c.38A>T
c.861A>T (p.Glu287Asp)
c.501A>T (p.Glu167Asp)
c.945A>T (p.Glu315Asp)
 ClinVar dbSNP gnomAD v4
17g.7673550T>CCA497713840TP53c.978A>G (p.Glu326=)
c.582A>G (p.Glu194=)
c.699A>G (p.Glu233=)
c.957A>G (p.Glu319=)
c.782+631A>G (n.782+631A>G)
c.38A>G
c.861A>G (p.Glu287=)
c.501A>G (p.Glu167=)
c.945A>G (p.Glu315=)
 ClinVar dbSNP
17g.7673550T>GCA397835791TP53c.978A>C (p.Glu326Asp)
c.582A>C (p.Glu194Asp)
c.699A>C (p.Glu233Asp)
c.957A>C (p.Glu319Asp)
c.782+631A>C (n.782+631A>C)
c.38A>C
c.861A>C (p.Glu287Asp)
c.501A>C (p.Glu167Asp)
c.945A>C (p.Glu315Asp)
 dbSNP gnomAD v2 gnomAD v4
17g.7673550T=CA2245947569TP53c.978A= (p.Glu326=)
c.582A= (p.Glu194=)
c.699A= (p.Glu233=)
c.957A= (p.Glu319=)
c.782+631A= (n.782+631A=)
c.38A=
c.861A= (p.Glu287=)
c.501A= (p.Glu167=)
c.945A= (p.Glu315=)
17g.7673551_7673553delCA2635874179TP53c.976_978del (p.Glu326del)
c.580_582del (p.Glu194del)
c.697_699del (p.Glu233del)
c.955_957del (p.Glu319del)
c.782+629_782+631del (n.782+629_782+631del)
c.36_38del
c.859_861del (p.Glu287del)
c.499_501del (p.Glu167del)
c.943_945del (p.Glu315del)
 gnomAD v4
17g.7673551T>ACA397835794TP53c.977A>T (p.Glu326Val)
c.581A>T (p.Glu194Val)
c.698A>T (p.Glu233Val)
c.956A>T (p.Glu319Val)
c.782+630A>T (n.782+630A>T)
c.37A>T
c.860A>T (p.Glu287Val)
c.500A>T (p.Glu167Val)
c.944A>T (p.Glu315Val)
 ClinVar dbSNP
17g.7673551T>CCA397835798TP53c.977A>G (p.Glu326Gly)
c.581A>G (p.Glu194Gly)
c.698A>G (p.Glu233Gly)
c.956A>G (p.Glu319Gly)
c.782+630A>G (n.782+630A>G)
c.37A>G
c.860A>G (p.Glu287Gly)
c.500A>G (p.Glu167Gly)
c.944A>G (p.Glu315Gly)
 dbSNP
17g.7673551T>GCA397835801TP53c.977A>C (p.Glu326Ala)
c.581A>C (p.Glu194Ala)
c.698A>C (p.Glu233Ala)
c.956A>C (p.Glu319Ala)
c.782+630A>C (n.782+630A>C)
c.37A>C
c.860A>C (p.Glu287Ala)
c.500A>C (p.Glu167Ala)
c.944A>C (p.Glu315Ala)
 dbSNP
17g.7673553_7673554dupCA915949514TP53c.976_977dup (p.Tyr327AsnfsTer19)
c.580_581dup (p.Tyr195AsnfsTer19)
c.697_698dup (p.Tyr234AsnfsTer19)
c.955_956dup (p.Tyr320AsnfsTer19)
c.976_977dup (p.Tyr327AsnfsTer26)
c.782+629_782+630dup (n.782+629_782+630dup)
c.976_977dup (p.Tyr327AsnfsTer25)
c.976_977dup (p.Tyr327AsnfsTer17)
c.580_581dup (p.Tyr195AsnfsTer17)
c.580_581dup (p.Tyr195AsnfsTer?)
c.580_581dup (p.Tyr195AsnfsTer25)
c.36_37dup
c.859_860dup (p.Tyr288AsnfsTer19)
c.859_860dup (p.Tyr288AsnfsTer17)
c.499_500dup (p.Tyr168AsnfsTer17)
c.943_944dup (p.Tyr316AsnfsTer19)
c.499_500dup (p.Tyr168AsnfsTer25)
c.499_500dup (p.Tyr168AsnfsTer19)
c.859_860dup (p.Tyr288AsnfsTer25)
 ClinVar dbSNP
17g.7673552C>ACA10580908TP53c.976G>T (p.Glu326Ter)
c.580G>T (p.Glu194Ter)
c.697G>T (p.Glu233Ter)
c.955G>T (p.Glu319Ter)
c.782+629G>T (n.782+629G>T)
c.36G>T
c.859G>T (p.Glu287Ter)
c.499G>T (p.Glu167Ter)
c.943G>T (p.Glu315Ter)
 ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC
17g.7673552C=CA2245947579TP53c.976G= (p.Glu326=)
c.580G= (p.Glu194=)
c.697G= (p.Glu233=)
c.955G= (p.Glu319=)
c.782+629G= (n.782+629G=)
c.36G=
c.859G= (p.Glu287=)
c.499G= (p.Glu167=)
c.943G= (p.Glu315=)
17g.7673552C>GCA397835806TP53c.976G>C (p.Glu326Gln)
c.580G>C (p.Glu194Gln)
c.697G>C (p.Glu233Gln)
c.955G>C (p.Glu319Gln)
c.782+629G>C (n.782+629G>C)
c.36G>C
c.859G>C (p.Glu287Gln)
c.499G>C (p.Glu167Gln)
c.943G>C (p.Glu315Gln)
 dbSNP
17g.7673552C>TCA397835809TP53c.976G>A (p.Glu326Lys)
c.580G>A (p.Glu194Lys)
c.697G>A (p.Glu233Lys)
c.955G>A (p.Glu319Lys)
c.782+629G>A (n.782+629G>A)
c.36G>A
c.859G>A (p.Glu287Lys)
c.499G>A (p.Glu167Lys)
c.943G>A (p.Glu315Lys)
 dbSNP COSMIC COSMIC COSMIC COSMIC
17g.7673553T>ACA497713884TP53c.975A>T (p.Gly325=)
c.579A>T (p.Gly193=)
c.696A>T (p.Gly232=)
c.954A>T (p.Gly318=)
c.782+628A>T (n.782+628A>T)
c.35A>T
c.858A>T (p.Gly286=)
c.498A>T (p.Gly166=)
c.942A>T (p.Gly314=)
17g.7673553T>CCA497713893TP53c.975A>G (p.Gly325=)
c.579A>G (p.Gly193=)
c.696A>G (p.Gly232=)
c.954A>G (p.Gly318=)
c.782+628A>G (n.782+628A>G)
c.35A>G
c.858A>G (p.Gly286=)
c.498A>G (p.Gly166=)
c.942A>G (p.Gly314=)
 ClinVar dbSNP gnomAD v2 gnomAD v4
17g.7673553T>GCA497713894TP53c.975A>C (p.Gly325=)
c.579A>C (p.Gly193=)
c.696A>C (p.Gly232=)
c.954A>C (p.Gly318=)
c.782+628A>C (n.782+628A>C)
c.35A>C
c.858A>C (p.Gly286=)
c.498A>C (p.Gly166=)
c.942A>C (p.Gly314=)
17g.7673553T=CA2245947582TP53c.975A= (p.Gly325=)
c.579A= (p.Gly193=)
c.696A= (p.Gly232=)
c.954A= (p.Gly318=)
c.782+628A= (n.782+628A=)
c.35A=
c.858A= (p.Gly286=)
c.498A= (p.Gly166=)
c.942A= (p.Gly314=)
17g.7673554C>ACA000516TP53c.974G>T (p.Gly325Val)
c.578G>T (p.Gly193Val)
c.695G>T (p.Gly232Val)
c.953G>T (p.Gly318Val)
c.782+627G>T (n.782+627G>T)
c.34G>T
c.857G>T (p.Gly286Val)
c.497G>T (p.Gly166Val)
c.941G>T (p.Gly314Val)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
17g.7673554C=CA2245947593TP53c.974G= (p.Gly325=)
c.578G= (p.Gly193=)
c.695G= (p.Gly232=)
c.953G= (p.Gly318=)
c.782+627G= (n.782+627G=)
c.34G=
c.857G= (p.Gly286=)
c.497G= (p.Gly166=)
c.941G= (p.Gly314=)
17g.7673554C>GCA397835813TP53c.974G>C (p.Gly325Ala)
c.578G>C (p.Gly193Ala)
c.695G>C (p.Gly232Ala)
c.953G>C (p.Gly318Ala)
c.782+627G>C (n.782+627G>C)
c.34G>C
c.857G>C (p.Gly286Ala)
c.497G>C (p.Gly166Ala)
c.941G>C (p.Gly314Ala)
 dbSNP COSMIC
17g.7673554C>TCA397835817TP53c.974G>A (p.Gly325Glu)
c.578G>A (p.Gly193Glu)
c.695G>A (p.Gly232Glu)
c.953G>A (p.Gly318Glu)
c.782+627G>A (n.782+627G>A)
c.34G>A
c.857G>A (p.Gly286Glu)
c.497G>A (p.Gly166Glu)
c.941G>A (p.Gly314Glu)
 ClinVar dbSNP COSMIC
17g.7673555C>ACA335679TP53c.973G>T (p.Gly325Ter)
c.577G>T (p.Gly193Ter)
c.694G>T (p.Gly232Ter)
c.952G>T (p.Gly318Ter)
c.782+626G>T (n.782+626G>T)
c.33G>T
c.856G>T (p.Gly286Ter)
c.496G>T (p.Gly166Ter)
c.940G>T (p.Gly314Ter)
 ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC
17g.7673555C=CA2245947602TP53c.973G= (p.Gly325=)
c.577G= (p.Gly193=)
c.694G= (p.Gly232=)
c.952G= (p.Gly318=)
c.782+626G= (n.782+626G=)
c.33G=
c.856G= (p.Gly286=)
c.496G= (p.Gly166=)
c.940G= (p.Gly314=)
17g.7673555C>GCA397835825TP53c.973G>C (p.Gly325Arg)
c.577G>C (p.Gly193Arg)
c.694G>C (p.Gly232Arg)
c.952G>C (p.Gly318Arg)
c.782+626G>C (n.782+626G>C)
c.33G>C
c.856G>C (p.Gly286Arg)
c.496G>C (p.Gly166Arg)
c.940G>C (p.Gly314Arg)
 dbSNP
17g.7673555C>TCA397835820TP53c.973G>A (p.Gly325Arg)
c.577G>A (p.Gly193Arg)
c.694G>A (p.Gly232Arg)
c.952G>A (p.Gly318Arg)
c.782+626G>A (n.782+626G>A)
c.33G>A
c.856G>A (p.Gly286Arg)
c.496G>A (p.Gly166Arg)
c.940G>A (p.Gly314Arg)
 ClinVar dbSNP
17g.7673556A>CCA397835833TP53c.972T>G (p.Asp324Glu)
c.576T>G (p.Asp192Glu)
c.693T>G (p.Asp231Glu)
c.951T>G (p.Asp317Glu)
c.782+625T>G (n.782+625T>G)
c.32T>G
c.855T>G (p.Asp285Glu)
c.495T>G (p.Asp165Glu)
c.939T>G (p.Asp313Glu)
 dbSNP COSMIC
17g.7673556A>GCA497713910TP53c.972T>C (p.Asp324=)
c.576T>C (p.Asp192=)
c.693T>C (p.Asp231=)
c.951T>C (p.Asp317=)
c.782+625T>C (n.782+625T>C)
c.32T>C
c.855T>C (p.Asp285=)
c.495T>C (p.Asp165=)
c.939T>C (p.Asp313=)
 dbSNP COSMIC
17g.7673556A>TCA397835829TP53c.972T>A (p.Asp324Glu)
c.576T>A (p.Asp192Glu)
c.693T>A (p.Asp231Glu)
c.951T>A (p.Asp317Glu)
c.782+625T>A (n.782+625T>A)
c.32T>A
c.855T>A (p.Asp285Glu)
c.495T>A (p.Asp165Glu)
c.939T>A (p.Asp313Glu)
 ClinVar dbSNP COSMIC
17g.7673557delCA497713915TP53c.971del (p.Asp324ValfsTer21)
c.575del (p.Asp192ValfsTer21)
c.692del (p.Asp231ValfsTer21)
c.950del (p.Asp317ValfsTer21)
c.971del (p.Asp324ValfsTer28)
c.782+624del (n.782+624del)
c.971del (p.Asp324ValfsTer27)
c.971del (p.Asp324ValfsTer19)
c.575del (p.Asp192ValfsTer19)
c.575del (p.Asp192ValfsTer?)
c.575del (p.Asp192ValfsTer27)
c.31del
c.854del (p.Asp285ValfsTer21)
c.854del (p.Asp285ValfsTer19)
c.494del (p.Asp165ValfsTer19)
c.938del (p.Asp313ValfsTer21)
c.494del (p.Asp165ValfsTer27)
c.494del (p.Asp165ValfsTer21)
c.854del (p.Asp285ValfsTer27)
 COSMIC
17g.7673557T>ACA397835834TP53c.971A>T (p.Asp324Val)
c.575A>T (p.Asp192Val)
c.692A>T (p.Asp231Val)
c.950A>T (p.Asp317Val)
c.782+624A>T (n.782+624A>T)
c.31A>T
c.854A>T (p.Asp285Val)
c.494A>T (p.Asp165Val)
c.938A>T (p.Asp313Val)
17g.7673557T>CCA397835837TP53c.971A>G (p.Asp324Gly)
c.575A>G (p.Asp192Gly)
c.692A>G (p.Asp231Gly)
c.950A>G (p.Asp317Gly)
c.782+624A>G (n.782+624A>G)
c.31A>G
c.854A>G (p.Asp285Gly)
c.494A>G (p.Asp165Gly)
c.938A>G (p.Asp313Gly)
 dbSNP gnomAD v2 gnomAD v4
17g.7673557T>GCA397835840TP53c.971A>C (p.Asp324Ala)
c.575A>C (p.Asp192Ala)
c.692A>C (p.Asp231Ala)
c.950A>C (p.Asp317Ala)
c.782+624A>C (n.782+624A>C)
c.31A>C
c.854A>C (p.Asp285Ala)
c.494A>C (p.Asp165Ala)
c.938A>C (p.Asp313Ala)
 dbSNP
17g.7673557T=CA2245947614TP53c.971A= (p.Asp324=)
c.575A= (p.Asp192=)
c.692A= (p.Asp231=)
c.950A= (p.Asp317=)
c.782+624A= (n.782+624A=)
c.31A=
c.854A= (p.Asp285=)
c.494A= (p.Asp165=)
c.938A= (p.Asp313=)
17g.7673557_7673558delinsCTCA645587350TP53c.970_971delinsAG (p.Asp324Ser)
c.574_575delinsAG (p.Asp192Ser)
c.691_692delinsAG (p.Asp231Ser)
c.949_950delinsAG (p.Asp317Ser)
c.782+623_782+624delinsAG (n.782+623_782+624delinsAG)
c.30_31delinsAG
c.853_854delinsAG (p.Asp285Ser)
c.493_494delinsAG (p.Asp165Ser)
c.937_938delinsAG (p.Asp313Ser)
 COSMIC
17g.7673557_7673558delinsTCCA2245947611TP53c.970_971delinsGA (p.Asp324=)
c.574_575delinsGA (p.Asp192=)
c.691_692delinsGA (p.Asp231=)
c.949_950delinsGA (p.Asp317=)
c.782+623_782+624delinsGA (n.782+623_782+624delinsGA)
c.30_31delinsGA
c.853_854delinsGA (p.Asp285=)
c.493_494delinsGA (p.Asp165=)
c.937_938delinsGA (p.Asp313=)
17g.7673558C>ACA397835843TP53c.970G>T (p.Asp324Tyr)
c.574G>T (p.Asp192Tyr)
c.691G>T (p.Asp231Tyr)
c.949G>T (p.Asp317Tyr)
c.782+623G>T (n.782+623G>T)
c.30G>T
c.853G>T (p.Asp285Tyr)
c.493G>T (p.Asp165Tyr)
c.937G>T (p.Asp313Tyr)
 ClinVar dbSNP
17g.7673558C=CA2245947625TP53c.970G= (p.Asp324=)
c.574G= (p.Asp192=)
c.691G= (p.Asp231=)
c.949G= (p.Asp317=)
c.782+623G= (n.782+623G=)
c.30G=
c.853G= (p.Asp285=)
c.493G= (p.Asp165=)
c.937G= (p.Asp313=)
17g.7673558C>GCA16620612TP53c.970G>C (p.Asp324His)
c.574G>C (p.Asp192His)
c.691G>C (p.Asp231His)
c.949G>C (p.Asp317His)
c.782+623G>C (n.782+623G>C)
c.30G>C
c.853G>C (p.Asp285His)
c.493G>C (p.Asp165His)
c.937G>C (p.Asp313His)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.7673558C>TCA397835847TP53c.970G>A (p.Asp324Asn)
c.574G>A (p.Asp192Asn)
c.691G>A (p.Asp231Asn)
c.949G>A (p.Asp317Asn)
c.782+623G>A (n.782+623G>A)
c.30G>A
c.853G>A (p.Asp285Asn)
c.493G>A (p.Asp165Asn)
c.937G>A (p.Asp313Asn)
 ClinVar dbSNP gnomAD v2 gnomAD v4
17g.7673559delCA658683980TP53c.970del (p.Asp324MetfsTer21)
c.574del (p.Asp192MetfsTer21)
c.691del (p.Asp231MetfsTer21)
c.949del (p.Asp317MetfsTer21)
c.970del (p.Asp324MetfsTer28)
c.782+623del (n.782+623del)
c.970del (p.Asp324MetfsTer27)
c.970del (p.Asp324MetfsTer19)
c.574del (p.Asp192MetfsTer19)
c.574del (p.Asp192MetfsTer?)
c.574del (p.Asp192MetfsTer27)
c.30del
c.853del (p.Asp285MetfsTer21)
c.853del (p.Asp285MetfsTer19)
c.493del (p.Asp165MetfsTer19)
c.937del (p.Asp313MetfsTer21)
c.493del (p.Asp165MetfsTer27)
c.493del (p.Asp165MetfsTer21)
c.853del (p.Asp285MetfsTer27)
 ClinVar dbSNP
17g.7673558_7673580dupCA645587351TP53c.948_970dup (p.Asp324AlafsTer29)
c.552_574dup (p.Asp192AlafsTer29)
c.669_691dup (p.Asp231AlafsTer29)
c.927_949dup (p.Asp317AlafsTer29)
c.948_970dup (p.Asp324AlafsTer36)
c.782+601_782+623dup (n.782+601_782+623dup)
c.948_970dup (p.Asp324AlafsTer35)
c.948_970dup (p.Asp324AlafsTer27)
c.552_574dup (p.Asp192AlafsTer27)
c.552_574dup (p.Asp192AlafsTer?)
c.552_574dup (p.Asp192AlafsTer35)
c.8_30dup
c.831_853dup (p.Asp285AlafsTer29)
c.831_853dup (p.Asp285AlafsTer27)
c.471_493dup (p.Asp165AlafsTer27)
c.915_937dup (p.Asp313AlafsTer29)
c.471_493dup (p.Asp165AlafsTer35)
c.471_493dup (p.Asp165AlafsTer29)
c.831_853dup (p.Asp285AlafsTer35)
 COSMIC
17g.7673559C>ACA497713919TP53c.969G>T (p.Leu323=)
c.573G>T (p.Leu191=)
c.690G>T (p.Leu230=)
c.948G>T (p.Leu316=)
c.782+622G>T (n.782+622G>T)
c.29G>T
c.852G>T (p.Leu284=)
c.492G>T (p.Leu164=)
c.936G>T (p.Leu312=)
 dbSNP
17g.7673559C=CA2245947634TP53c.969G= (p.Leu323=)
c.573G= (p.Leu191=)
c.690G= (p.Leu230=)
c.948G= (p.Leu316=)
c.782+622G= (n.782+622G=)
c.29G=
c.852G= (p.Leu284=)
c.492G= (p.Leu164=)
c.936G= (p.Leu312=)
17g.7673559C>GCA497713923TP53c.969G>C (p.Leu323=)
c.573G>C (p.Leu191=)
c.690G>C (p.Leu230=)
c.948G>C (p.Leu316=)
c.782+622G>C (n.782+622G>C)
c.29G>C
c.852G>C (p.Leu284=)
c.492G>C (p.Leu164=)
c.936G>C (p.Leu312=)
 ClinVar dbSNP
17g.7673559C>TCA000512TP53c.969G>A (p.Leu323=)
c.573G>A (p.Leu191=)
c.690G>A (p.Leu230=)
c.948G>A (p.Leu316=)
c.782+622G>A (n.782+622G>A)
c.29G>A
c.852G>A (p.Leu284=)
c.492G>A (p.Leu164=)
c.936G>A (p.Leu312=)
 ClinVar dbSNP gnomAD v3 gnomAD v4
17g.7673560A=CA2245947643TP53c.968T= (p.Leu323=)
c.572T= (p.Leu191=)
c.689T= (p.Leu230=)
c.947T= (p.Leu316=)
c.782+621T= (n.782+621T=)
c.28T=
c.851T= (p.Leu284=)
c.491T= (p.Leu164=)
c.935T= (p.Leu312=)
17g.7673560A>CCA397835852TP53c.968T>G (p.Leu323Arg)
c.572T>G (p.Leu191Arg)
c.689T>G (p.Leu230Arg)
c.947T>G (p.Leu316Arg)
c.782+621T>G (n.782+621T>G)
c.28T>G
c.851T>G (p.Leu284Arg)
c.491T>G (p.Leu164Arg)
c.935T>G (p.Leu312Arg)
 COSMIC
17g.7673560A>GCA397835853TP53c.968T>C (p.Leu323Pro)
c.572T>C (p.Leu191Pro)
c.689T>C (p.Leu230Pro)
c.947T>C (p.Leu316Pro)
c.782+621T>C (n.782+621T>C)
c.28T>C
c.851T>C (p.Leu284Pro)
c.491T>C (p.Leu164Pro)
c.935T>C (p.Leu312Pro)
 ClinVar dbSNP COSMIC
17g.7673560A>TCA397835857TP53c.968T>A (p.Leu323Gln)
c.572T>A (p.Leu191Gln)
c.689T>A (p.Leu230Gln)
c.947T>A (p.Leu316Gln)
c.782+621T>A (n.782+621T>A)
c.28T>A
c.851T>A (p.Leu284Gln)
c.491T>A (p.Leu164Gln)
c.935T>A (p.Leu312Gln)
 dbSNP
17g.7673560_7673561delinsCCCA645587352TP53c.967_968delinsGG (p.Leu323Gly)
c.571_572delinsGG (p.Leu191Gly)
c.688_689delinsGG (p.Leu230Gly)
c.946_947delinsGG (p.Leu316Gly)
c.782+620_782+621delinsGG (n.782+620_782+621delinsGG)
c.27_28delinsGG
c.850_851delinsGG (p.Leu284Gly)
c.490_491delinsGG (p.Leu164Gly)
c.934_935delinsGG (p.Leu312Gly)
 COSMIC
17g.7673562_7673586delCA645587353TP53c.944_968del (p.Ser315TrpfsTer22)
c.548_572del (p.Ser183TrpfsTer22)
c.665_689del (p.Ser222TrpfsTer22)
c.923_947del (p.Ser308TrpfsTer22)
c.944_968del (p.Ser315TrpfsTer29)
c.782+597_782+621del (n.782+597_782+621del)
c.944_968del (p.Ser315TrpfsTer28)
c.944_968del (p.Ser315TrpfsTer20)
c.548_572del (p.Ser183TrpfsTer20)
c.548_572del (p.Ser183TrpfsTer?)
c.548_572del (p.Ser183TrpfsTer28)
c.4_28del
c.827_851del (p.Ser276TrpfsTer22)
c.827_851del (p.Ser276TrpfsTer20)
c.467_491del (p.Ser156TrpfsTer20)
c.911_935del (p.Ser304TrpfsTer22)
c.467_491del (p.Ser156TrpfsTer28)
c.467_491del (p.Ser156TrpfsTer22)
c.827_851del (p.Ser276TrpfsTer28)
 COSMIC
17g.7673561delCA497713940TP53c.967del (p.Leu323TrpfsTer22)
c.571del (p.Leu191TrpfsTer22)
c.688del (p.Leu230TrpfsTer22)
c.946del (p.Leu316TrpfsTer22)
c.967del (p.Leu323TrpfsTer29)
c.782+620del (n.782+620del)
c.967del (p.Leu323TrpfsTer28)
c.967del (p.Leu323TrpfsTer20)
c.571del (p.Leu191TrpfsTer20)
c.571del (p.Leu191TrpfsTer?)
c.571del (p.Leu191TrpfsTer28)
c.27del
c.850del (p.Leu284TrpfsTer22)
c.850del (p.Leu284TrpfsTer20)
c.490del (p.Leu164TrpfsTer20)
c.934del (p.Leu312TrpfsTer22)
c.490del (p.Leu164TrpfsTer28)
c.490del (p.Leu164TrpfsTer22)
c.850del (p.Leu284TrpfsTer28)
 COSMIC
17g.7673561G>ACA497713934TP53c.967C>T (p.Leu323=)
c.571C>T (p.Leu191=)
c.688C>T (p.Leu230=)
c.946C>T (p.Leu316=)
c.782+620C>T (n.782+620C>T)
c.27C>T
c.850C>T (p.Leu284=)
c.490C>T (p.Leu164=)
c.934C>T (p.Leu312=)
 dbSNP
17g.7673561G>CCA397835860TP53c.967C>G (p.Leu323Val)
c.571C>G (p.Leu191Val)
c.688C>G (p.Leu230Val)
c.946C>G (p.Leu316Val)
c.782+620C>G (n.782+620C>G)
c.27C>G
c.850C>G (p.Leu284Val)
c.490C>G (p.Leu164Val)
c.934C>G (p.Leu312Val)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
17g.7673561G=CA2245947652TP53c.967C= (p.Leu323=)
c.571C= (p.Leu191=)
c.688C= (p.Leu230=)
c.946C= (p.Leu316=)
c.782+620C= (n.782+620C=)
c.27C=
c.850C= (p.Leu284=)
c.490C= (p.Leu164=)
c.934C= (p.Leu312=)
17g.7673561G>TCA397835867TP53c.967C>A (p.Leu323Met)
c.571C>A (p.Leu191Met)
c.688C>A (p.Leu230Met)
c.946C>A (p.Leu316Met)
c.782+620C>A (n.782+620C>A)
c.27C>A
c.850C>A (p.Leu284Met)
c.490C>A (p.Leu164Met)
c.934C>A (p.Leu312Met)
 dbSNP COSMIC
17g.7673562T>ACA497713943TP53c.966A>T (p.Pro322=)
c.570A>T (p.Pro190=)
c.687A>T (p.Pro229=)
c.945A>T (p.Pro315=)
c.782+619A>T (n.782+619A>T)
c.26A>T
c.849A>T (p.Pro283=)
c.489A>T (p.Pro163=)
c.933A>T (p.Pro311=)
17g.7673562T>CCA497713945TP53c.966A>G (p.Pro322=)
c.570A>G (p.Pro190=)
c.687A>G (p.Pro229=)
c.945A>G (p.Pro315=)
c.782+619A>G (n.782+619A>G)
c.26A>G
c.849A>G (p.Pro283=)
c.489A>G (p.Pro163=)
c.933A>G (p.Pro311=)
 ClinVar
17g.7673562T>GCA497713950TP53c.966A>C (p.Pro322=)
c.570A>C (p.Pro190=)
c.687A>C (p.Pro229=)
c.945A>C (p.Pro315=)
c.782+619A>C (n.782+619A>C)
c.26A>C
c.849A>C (p.Pro283=)
c.489A>C (p.Pro163=)
c.933A>C (p.Pro311=)
 ClinVar
17g.7673562dupCA2245947657TP53c.966dup (p.Leu323ThrfsTer14)
c.570dup (p.Leu191ThrfsTer14)
c.687dup (p.Leu230ThrfsTer14)
c.945dup (p.Leu316ThrfsTer14)
c.966dup (p.Leu323ThrfsTer?)
c.782+619dup (n.782+619dup)
c.966dup (p.Leu323ThrfsTer24)
c.966dup (p.Leu323ThrfsTer13)
c.570dup (p.Leu191ThrfsTer13)
c.570dup (p.Leu191ThrfsTer?)
c.570dup (p.Leu191ThrfsTer24)
c.26dup
c.849dup (p.Leu284ThrfsTer14)
c.849dup (p.Leu284ThrfsTer13)
c.489dup (p.Leu164ThrfsTer13)
c.933dup (p.Leu312ThrfsTer14)
c.489dup (p.Leu164ThrfsTer24)
c.489dup (p.Leu164ThrfsTer14)
c.849dup (p.Leu284ThrfsTer24)
 dbSNP
17g.7673563G>ACA397835873TP53c.965C>T (p.Pro322Leu)
c.569C>T (p.Pro190Leu)
c.686C>T (p.Pro229Leu)
c.944C>T (p.Pro315Leu)
c.782+618C>T (n.782+618C>T)
c.25C>T
c.848C>T (p.Pro283Leu)
c.488C>T (p.Pro163Leu)
c.932C>T (p.Pro311Leu)
 dbSNP COSMIC
17g.7673563G>CCA397835872TP53c.965C>G (p.Pro322Arg)
c.569C>G (p.Pro190Arg)
c.686C>G (p.Pro229Arg)
c.944C>G (p.Pro315Arg)
c.782+618C>G (n.782+618C>G)
c.25C>G
c.848C>G (p.Pro283Arg)
c.488C>G (p.Pro163Arg)
c.932C>G (p.Pro311Arg)
 ClinVar dbSNP COSMIC
17g.7673563G>TCA397835870TP53c.965C>A (p.Pro322Gln)
c.569C>A (p.Pro190Gln)
c.686C>A (p.Pro229Gln)
c.944C>A (p.Pro315Gln)
c.782+618C>A (n.782+618C>A)
c.25C>A
c.848C>A (p.Pro283Gln)
c.488C>A (p.Pro163Gln)
c.932C>A (p.Pro311Gln)
 dbSNP
17g.7673564delCA497713957TP53c.965del (p.Pro322HisfsTer23)
c.569del (p.Pro190HisfsTer23)
c.686del (p.Pro229HisfsTer23)
c.944del (p.Pro315HisfsTer23)
c.965del (p.Pro322HisfsTer30)
c.782+618del (n.782+618del)
c.965del (p.Pro322HisfsTer29)
c.965del (p.Pro322HisfsTer21)
c.569del (p.Pro190HisfsTer21)
c.569del (p.Pro190HisfsTer?)
c.569del (p.Pro190HisfsTer29)
c.25del
c.848del (p.Pro283HisfsTer23)
c.848del (p.Pro283HisfsTer21)
c.488del (p.Pro163HisfsTer21)
c.932del (p.Pro311HisfsTer23)
c.488del (p.Pro163HisfsTer29)
c.488del (p.Pro163HisfsTer23)
c.848del (p.Pro283HisfsTer29)
 ClinVar COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7673564G>ACA336073TP53c.964C>T (p.Pro322Ser)
c.568C>T (p.Pro190Ser)
c.685C>T (p.Pro229Ser)
c.943C>T (p.Pro315Ser)
c.782+617C>T (n.782+617C>T)
c.24C>T
c.847C>T (p.Pro283Ser)
c.487C>T (p.Pro163Ser)
c.931C>T (p.Pro311Ser)
 ClinVar dbSNP gnomAD v4
17g.7673564G>CCA397835876TP53c.964C>G (p.Pro322Ala)
c.568C>G (p.Pro190Ala)
c.685C>G (p.Pro229Ala)
c.943C>G (p.Pro315Ala)
c.782+617C>G (n.782+617C>G)
c.24C>G
c.847C>G (p.Pro283Ala)
c.487C>G (p.Pro163Ala)
c.931C>G (p.Pro311Ala)
 ClinVar dbSNP
17g.7673564G=CA2245947670TP53c.964C= (p.Pro322=)
c.568C= (p.Pro190=)
c.685C= (p.Pro229=)
c.943C= (p.Pro315=)
c.782+617C= (n.782+617C=)
c.24C=
c.847C= (p.Pro283=)
c.487C= (p.Pro163=)
c.931C= (p.Pro311=)
17g.7673564G>TCA10580909TP53c.964C>A (p.Pro322Thr)
c.568C>A (p.Pro190Thr)
c.685C>A (p.Pro229Thr)
c.943C>A (p.Pro315Thr)
c.782+617C>A (n.782+617C>A)
c.24C>A
c.847C>A (p.Pro283Thr)
c.487C>A (p.Pro163Thr)
c.931C>A (p.Pro311Thr)
 ClinVar dbSNP
17g.7673565T>ACA397835878TP53c.963A>T (p.Lys321Asn)
c.567A>T (p.Lys189Asn)
c.684A>T (p.Lys228Asn)
c.942A>T (p.Lys314Asn)
c.782+616A>T (n.782+616A>T)
c.23A>T
c.846A>T (p.Lys282Asn)
c.486A>T (p.Lys162Asn)
c.930A>T (p.Lys310Asn)
 dbSNP
17g.7673565T>CCA497713967TP53c.963A>G (p.Lys321=)
c.567A>G (p.Lys189=)
c.684A>G (p.Lys228=)
c.942A>G (p.Lys314=)
c.782+616A>G (n.782+616A>G)
c.23A>G
c.846A>G (p.Lys282=)
c.486A>G (p.Lys162=)
c.930A>G (p.Lys310=)
 ClinVar dbSNP COSMIC
17g.7673565T>GCA397835879TP53c.963A>C (p.Lys321Asn)
c.567A>C (p.Lys189Asn)
c.684A>C (p.Lys228Asn)
c.942A>C (p.Lys314Asn)
c.782+616A>C (n.782+616A>C)
c.23A>C
c.846A>C (p.Lys282Asn)
c.486A>C (p.Lys162Asn)
c.930A>C (p.Lys310Asn)
 dbSNP
17g.7673567dupCA645587355TP53c.963dup (p.Pro322ThrfsTer15)
c.567dup (p.Pro190ThrfsTer15)
c.684dup (p.Pro229ThrfsTer15)
c.942dup (p.Pro315ThrfsTer15)
c.963dup (p.Pro322ThrfsTer?)
c.782+616dup (n.782+616dup)
c.963dup (p.Pro322ThrfsTer25)
c.963dup (p.Pro322ThrfsTer14)
c.567dup (p.Pro190ThrfsTer14)
c.567dup (p.Pro190ThrfsTer?)
c.567dup (p.Pro190ThrfsTer25)
c.23dup
c.846dup (p.Pro283ThrfsTer15)
c.846dup (p.Pro283ThrfsTer14)
c.486dup (p.Pro163ThrfsTer14)
c.930dup (p.Pro311ThrfsTer15)
c.486dup (p.Pro163ThrfsTer25)
c.486dup (p.Pro163ThrfsTer15)
c.846dup (p.Pro283ThrfsTer25)
 COSMIC COSMIC COSMIC COSMIC
17g.7673567delCA497713971TP53c.963del (p.Lys321AsnfsTer24)
c.567del (p.Lys189AsnfsTer24)
c.684del (p.Lys228AsnfsTer24)
c.942del (p.Lys314AsnfsTer24)
c.963del (p.Lys321AsnfsTer?)
c.782+616del (n.782+616del)
c.963del (p.Lys321AsnfsTer30)
c.963del (p.Lys321AsnfsTer22)
c.567del (p.Lys189AsnfsTer22)
c.567del (p.Lys189AsnfsTer?)
c.567del (p.Lys189AsnfsTer30)
c.23del
c.846del (p.Lys282AsnfsTer24)
c.846del (p.Lys282AsnfsTer22)
c.486del (p.Lys162AsnfsTer22)
c.930del (p.Lys310AsnfsTer24)
c.486del (p.Lys162AsnfsTer30)
c.486del (p.Lys162AsnfsTer24)
c.846del (p.Lys282AsnfsTer30)
 COSMIC
17g.7673565_7673568delinsTTTCCA2245947676TP53c.960_963delinsGAAA (p.Lys320=)
c.564_567delinsGAAA (p.Lys188=)
c.681_684delinsGAAA (p.Lys227=)
c.939_942delinsGAAA (p.Lys313=)
c.782+613_782+616delinsGAAA (n.782+613_782+616delinsGAAA)
c.20_23delinsGAAA
c.843_846delinsGAAA (p.Lys281=)
c.483_486delinsGAAA (p.Lys161=)
c.927_930delinsGAAA (p.Lys309=)
17g.7673565_7673605delCA645587356TP53c.923_963del (p.Leu308ProfsTer15)
c.527_567del (p.Leu176ProfsTer15)
c.644_684del (p.Leu215ProfsTer15)
c.902_942del (p.Leu301ProfsTer15)
c.923_963del (p.Leu308ProfsTer?)
c.782+576_782+616del (n.782+576_782+616del)
c.923_963del (p.Leu308ProfsTer25)
c.923_963del (p.Leu308ProfsTer14)
c.527_567del (p.Leu176ProfsTer14)
c.527_567del (p.Leu176ProfsTer?)
c.527_567del (p.Leu176ProfsTer25)
c.806_846del (p.Leu269ProfsTer15)
c.806_846del (p.Leu269ProfsTer14)
c.446_486del (p.Leu149ProfsTer14)
c.890_930del (p.Leu297ProfsTer15)
c.446_486del (p.Leu149ProfsTer25)
c.446_486del (p.Leu149ProfsTer15)
c.806_846del (p.Leu269ProfsTer25)
 COSMIC
17g.7673566T>ACA397835881TP53c.962A>T (p.Lys321Ile)
c.566A>T (p.Lys189Ile)
c.683A>T (p.Lys228Ile)
c.941A>T (p.Lys314Ile)
c.782+615A>T (n.782+615A>T)
c.22A>T
c.845A>T (p.Lys282Ile)
c.485A>T (p.Lys162Ile)
c.929A>T (p.Lys310Ile)
 dbSNP
17g.7673566T>CCA397835882TP53c.962A>G (p.Lys321Arg)
c.566A>G (p.Lys189Arg)
c.683A>G (p.Lys228Arg)
c.941A>G (p.Lys314Arg)
c.782+615A>G (n.782+615A>G)
c.22A>G
c.845A>G (p.Lys282Arg)
c.485A>G (p.Lys162Arg)
c.929A>G (p.Lys310Arg)
 dbSNP
17g.7673566T>GCA397835886TP53c.962A>C (p.Lys321Thr)
c.566A>C (p.Lys189Thr)
c.683A>C (p.Lys228Thr)
c.941A>C (p.Lys314Thr)
c.782+615A>C (n.782+615A>C)
c.22A>C
c.845A>C (p.Lys282Thr)
c.485A>C (p.Lys162Thr)
c.929A>C (p.Lys310Thr)
 dbSNP
17g.7673571_7673573dupCA645587357TP53c.960_962dup (p.Lys321_Pro322insLys)
c.564_566dup (p.Lys189_Pro190insLys)
c.681_683dup (p.Lys228_Pro229insLys)
c.939_941dup (p.Lys314_Pro315insLys)
c.782+613_782+615dup (n.782+613_782+615dup)
c.20_22dup
c.843_845dup (p.Lys282_Pro283insLys)
c.483_485dup (p.Lys162_Pro163insLys)
c.927_929dup (p.Lys310_Pro311insLys)
 COSMIC COSMIC
17g.7673571_7673573delCA891844039TP53c.960_962del (p.Lys321del)
c.564_566del (p.Lys189del)
c.681_683del (p.Lys228del)
c.939_941del (p.Lys314del)
c.782+613_782+615del (n.782+613_782+615del)
c.20_22del
c.843_845del (p.Lys282del)
c.483_485del (p.Lys162del)
c.927_929del (p.Lys310del)
 ClinVar dbSNP
17g.7673567T>ACA397835889TP53c.961A>T (p.Lys321Ter)
c.565A>T (p.Lys189Ter)
c.682A>T (p.Lys228Ter)
c.940A>T (p.Lys314Ter)
c.782+614A>T (n.782+614A>T)
c.21A>T
c.844A>T (p.Lys282Ter)
c.484A>T (p.Lys162Ter)
c.928A>T (p.Lys310Ter)
 ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC
17g.7673567T>CCA397835893TP53c.961A>G (p.Lys321Glu)
c.565A>G (p.Lys189Glu)
c.682A>G (p.Lys228Glu)
c.940A>G (p.Lys314Glu)
c.782+614A>G (n.782+614A>G)
c.21A>G
c.844A>G (p.Lys282Glu)
c.484A>G (p.Lys162Glu)
c.928A>G (p.Lys310Glu)
17g.7673567T>GCA397835894TP53c.961A>C (p.Lys321Gln)
c.565A>C (p.Lys189Gln)
c.682A>C (p.Lys228Gln)
c.940A>C (p.Lys314Gln)
c.782+614A>C (n.782+614A>C)
c.21A>C
c.844A>C (p.Lys282Gln)
c.484A>C (p.Lys162Gln)
c.928A>C (p.Lys310Gln)
17g.7673567T=CA2245947687TP53c.961A= (p.Lys321=)
c.565A= (p.Lys189=)
c.682A= (p.Lys228=)
c.940A= (p.Lys314=)
c.782+614A= (n.782+614A=)
c.21A=
c.844A= (p.Lys282=)
c.484A= (p.Lys162=)
c.928A= (p.Lys310=)
17g.7673568delCA645587358TP53c.960del (p.Lys321AsnfsTer24)
c.564del (p.Lys189AsnfsTer24)
c.681del (p.Lys228AsnfsTer24)
c.939del (p.Lys314AsnfsTer24)
c.960del (p.Lys321AsnfsTer?)
c.782+613del (n.782+613del)
c.960del (p.Lys321AsnfsTer22)
c.564del (p.Lys189AsnfsTer22)
c.564del (p.Lys189AsnfsTer?)
c.20del
c.843del (p.Lys282AsnfsTer24)
c.843del (p.Lys282AsnfsTer22)
c.483del (p.Lys162AsnfsTer22)
c.927del (p.Lys310AsnfsTer24)
c.483del (p.Lys162AsnfsTer?)
c.483del (p.Lys162AsnfsTer24)
c.843del (p.Lys282AsnfsTer?)
 ClinVar COSMIC COSMIC COSMIC COSMIC
17g.7673568C>ACA397835895TP53c.960G>T (p.Lys320Asn)
c.564G>T (p.Lys188Asn)
c.681G>T (p.Lys227Asn)
c.939G>T (p.Lys313Asn)
c.782+613G>T (n.782+613G>T)
c.20G>T
c.843G>T (p.Lys281Asn)
c.483G>T (p.Lys161Asn)
c.927G>T (p.Lys309Asn)
 dbSNP
17g.7673568C>GCA397835897TP53c.960G>C (p.Lys320Asn)
c.564G>C (p.Lys188Asn)
c.681G>C (p.Lys227Asn)
c.939G>C (p.Lys313Asn)
c.782+613G>C (n.782+613G>C)
c.20G>C
c.843G>C (p.Lys281Asn)
c.483G>C (p.Lys161Asn)
c.927G>C (p.Lys309Asn)
 dbSNP COSMIC
17g.7673568C>TCA497713987TP53c.960G>A (p.Lys320=)
c.564G>A (p.Lys188=)
c.681G>A (p.Lys227=)
c.939G>A (p.Lys313=)
c.782+613G>A (n.782+613G>A)
c.20G>A
c.843G>A (p.Lys281=)
c.483G>A (p.Lys161=)
c.927G>A (p.Lys309=)
 dbSNP COSMIC COSMIC COSMIC COSMIC
17g.7673569T>ACA397835903TP53c.959A>T (p.Lys320Met)
c.563A>T (p.Lys188Met)
c.680A>T (p.Lys227Met)
c.938A>T (p.Lys313Met)
c.782+612A>T (n.782+612A>T)
c.19A>T
c.842A>T (p.Lys281Met)
c.482A>T (p.Lys161Met)
c.926A>T (p.Lys309Met)
 dbSNP
17g.7673569T>CCA397835905TP53c.959A>G (p.Lys320Arg)
c.563A>G (p.Lys188Arg)
c.680A>G (p.Lys227Arg)
c.938A>G (p.Lys313Arg)
c.782+612A>G (n.782+612A>G)
c.19A>G
c.842A>G (p.Lys281Arg)
c.482A>G (p.Lys161Arg)
c.926A>G (p.Lys309Arg)
 dbSNP
17g.7673569T>GCA397835900TP53c.959A>C (p.Lys320Thr)
c.563A>C (p.Lys188Thr)
c.680A>C (p.Lys227Thr)
c.938A>C (p.Lys313Thr)
c.782+612A>C (n.782+612A>C)
c.19A>C
c.842A>C (p.Lys281Thr)
c.482A>C (p.Lys161Thr)
c.926A>C (p.Lys309Thr)
17g.7673570delCA497714003TP53c.959del (p.Lys320ArgfsTer25)
c.563del (p.Lys188ArgfsTer25)
c.680del (p.Lys227ArgfsTer25)
c.938del (p.Lys313ArgfsTer25)
c.959del (p.Lys320ArgfsTer?)
c.782+612del (n.782+612del)
c.959del (p.Lys320ArgfsTer23)
c.563del (p.Lys188ArgfsTer23)
c.563del (p.Lys188ArgfsTer?)
c.19del
c.842del (p.Lys281ArgfsTer25)
c.842del (p.Lys281ArgfsTer23)
c.482del (p.Lys161ArgfsTer23)
c.926del (p.Lys309ArgfsTer25)
c.482del (p.Lys161ArgfsTer?)
c.482del (p.Lys161ArgfsTer25)
c.842del (p.Lys281ArgfsTer?)
 COSMIC
17g.7673570T>ACA397835908TP53c.958A>T (p.Lys320Ter)
c.562A>T (p.Lys188Ter)
c.679A>T (p.Lys227Ter)
c.937A>T (p.Lys313Ter)
c.782+611A>T (n.782+611A>T)
c.18A>T
c.841A>T (p.Lys281Ter)
c.481A>T (p.Lys161Ter)
c.925A>T (p.Lys309Ter)
 ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC
17g.7673570T>CCA397835912TP53c.958A>G (p.Lys320Glu)
c.562A>G (p.Lys188Glu)
c.679A>G (p.Lys227Glu)
c.937A>G (p.Lys313Glu)
c.782+611A>G (n.782+611A>G)
c.18A>G
c.841A>G (p.Lys281Glu)
c.481A>G (p.Lys161Glu)
c.925A>G (p.Lys309Glu)
 dbSNP
17g.7673570T>GCA397835915TP53c.958A>C (p.Lys320Gln)
c.562A>C (p.Lys188Gln)
c.679A>C (p.Lys227Gln)
c.937A>C (p.Lys313Gln)
c.782+611A>C (n.782+611A>C)
c.18A>C
c.841A>C (p.Lys281Gln)
c.481A>C (p.Lys161Gln)
c.925A>C (p.Lys309Gln)
17g.7673570_7673587delCA645587360TP53c.941_958del (p.Ser314Ter)
c.545_562del (p.Ser182Ter)
c.662_679del (p.Ser221Ter)
c.920_937del (p.Ser307Ter)
c.782+594_782+611del (n.782+594_782+611del)
c.1_18del
c.824_841del (p.Ser275Ter)
c.464_481del (p.Ser155Ter)
c.908_925del (p.Ser303Ter)
 COSMIC COSMIC COSMIC COSMIC
17g.7673570_7673588delCA645587363TP53c.940_958del (p.Ser314ArgfsTer25)
c.544_562del (p.Ser182ArgfsTer25)
c.661_679del (p.Ser221ArgfsTer25)
c.919_937del (p.Ser307ArgfsTer25)
c.940_958del (p.Ser314ArgfsTer?)
c.782+593_782+611del (n.782+593_782+611del)
c.940_958del (p.Ser314ArgfsTer23)
c.544_562del (p.Ser182ArgfsTer23)
c.544_562del (p.Ser182ArgfsTer?)
c.823_841del (p.Ser275ArgfsTer25)
c.823_841del (p.Ser275ArgfsTer23)
c.463_481del (p.Ser155ArgfsTer23)
c.907_925del (p.Ser303ArgfsTer25)
c.463_481del (p.Ser155ArgfsTer?)
c.463_481del (p.Ser155ArgfsTer25)
c.823_841del (p.Ser275ArgfsTer?)
 COSMIC
17g.7673571delCA645587364TP53c.957del (p.Lys320ArgfsTer25)
c.561del (p.Lys188ArgfsTer25)
c.678del (p.Lys227ArgfsTer25)
c.936del (p.Lys313ArgfsTer25)
c.957del (p.Lys320ArgfsTer?)
c.782+610del (n.782+610del)
c.957del (p.Lys320ArgfsTer23)
c.561del (p.Lys188ArgfsTer23)
c.561del (p.Lys188ArgfsTer?)
c.17del
c.840del (p.Lys281ArgfsTer25)
c.840del (p.Lys281ArgfsTer23)
c.480del (p.Lys161ArgfsTer23)
c.924del (p.Lys309ArgfsTer25)
c.480del (p.Lys161ArgfsTer?)
c.480del (p.Lys161ArgfsTer25)
c.840del (p.Lys281ArgfsTer?)
 COSMIC COSMIC COSMIC COSMIC
17g.7673571C>ACA397835919TP53c.957G>T (p.Lys319Asn)
c.561G>T (p.Lys187Asn)
c.678G>T (p.Lys226Asn)
c.936G>T (p.Lys312Asn)
c.782+610G>T (n.782+610G>T)
c.17G>T
c.840G>T (p.Lys280Asn)
c.480G>T (p.Lys160Asn)
c.924G>T (p.Lys308Asn)
 dbSNP COSMIC
17g.7673571C>GCA397835921TP53c.957G>C (p.Lys319Asn)
c.561G>C (p.Lys187Asn)
c.678G>C (p.Lys226Asn)
c.936G>C (p.Lys312Asn)
c.782+610G>C (n.782+610G>C)
c.17G>C
c.840G>C (p.Lys280Asn)
c.480G>C (p.Lys160Asn)
c.924G>C (p.Lys308Asn)
 dbSNP COSMIC COSMIC COSMIC COSMIC
17g.7673571C>TCA497714016TP53c.957G>A (p.Lys319=)
c.561G>A (p.Lys187=)
c.678G>A (p.Lys226=)
c.936G>A (p.Lys312=)
c.782+610G>A (n.782+610G>A)
c.17G>A
c.840G>A (p.Lys280=)
c.480G>A (p.Lys160=)
c.924G>A (p.Lys308=)
 dbSNP COSMIC
17g.7673572T>ACA397835924TP53c.956A>T (p.Lys319Met)
c.560A>T (p.Lys187Met)
c.677A>T (p.Lys226Met)
c.935A>T (p.Lys312Met)
c.782+609A>T (n.782+609A>T)
c.16A>T
c.839A>T (p.Lys280Met)
c.479A>T (p.Lys160Met)
c.923A>T (p.Lys308Met)
 dbSNP
17g.7673572T>CCA397835927TP53c.956A>G (p.Lys319Arg)
c.560A>G (p.Lys187Arg)
c.677A>G (p.Lys226Arg)
c.935A>G (p.Lys312Arg)
c.782+609A>G (n.782+609A>G)
c.16A>G
c.839A>G (p.Lys280Arg)
c.479A>G (p.Lys160Arg)
c.923A>G (p.Lys308Arg)
 dbSNP COSMIC
17g.7673572T>GCA397835930TP53c.956A>C (p.Lys319Thr)
c.560A>C (p.Lys187Thr)
c.677A>C (p.Lys226Thr)
c.935A>C (p.Lys312Thr)
c.782+609A>C (n.782+609A>C)
c.16A>C
c.839A>C (p.Lys280Thr)
c.479A>C (p.Lys160Thr)
c.923A>C (p.Lys308Thr)
17g.7673573T>ACA397835934TP53c.955A>T (p.Lys319Ter)
c.559A>T (p.Lys187Ter)
c.676A>T (p.Lys226Ter)
c.934A>T (p.Lys312Ter)
c.782+608A>T (n.782+608A>T)
c.15A>T
c.838A>T (p.Lys280Ter)
c.478A>T (p.Lys160Ter)
c.922A>T (p.Lys308Ter)
 dbSNP COSMIC COSMIC COSMIC COSMIC
17g.7673573T>CCA397835937TP53c.955A>G (p.Lys319Glu)
c.559A>G (p.Lys187Glu)
c.676A>G (p.Lys226Glu)
c.934A>G (p.Lys312Glu)
c.782+608A>G (n.782+608A>G)
c.15A>G
c.838A>G (p.Lys280Glu)
c.478A>G (p.Lys160Glu)
c.922A>G (p.Lys308Glu)
 COSMIC
17g.7673573T>GCA397835940TP53c.955A>C (p.Lys319Gln)
c.559A>C (p.Lys187Gln)
c.676A>C (p.Lys226Gln)
c.934A>C (p.Lys312Gln)
c.782+608A>C (n.782+608A>C)
c.15A>C
c.838A>C (p.Lys280Gln)
c.478A>C (p.Lys160Gln)
c.922A>C (p.Lys308Gln)
17g.7673573_7673577delinsTTGGCCA2245947690TP53c.951_955delinsGCCAA (p.Gln317=)
c.555_559delinsGCCAA (p.Gln185=)
c.672_676delinsGCCAA (p.Gln224=)
c.930_934delinsGCCAA (p.Gln310=)
c.782+604_782+608delinsGCCAA (n.782+604_782+608delinsGCCAA)
c.11_15delinsGCCAA
c.834_838delinsGCCAA (p.Gln278=)
c.474_478delinsGCCAA (p.Gln158=)
c.918_922delinsGCCAA (p.Gln306=)
17g.7673574T>ACA497714040TP53c.954A>T (p.Pro318=)
c.558A>T (p.Pro186=)
c.675A>T (p.Pro225=)
c.933A>T (p.Pro311=)
c.782+607A>T (n.782+607A>T)
c.14A>T
c.837A>T (p.Pro279=)
c.477A>T (p.Pro159=)
c.921A>T (p.Pro307=)
 ClinVar
17g.7673574T>CCA497714031TP53c.954A>G (p.Pro318=)
c.558A>G (p.Pro186=)
c.675A>G (p.Pro225=)
c.933A>G (p.Pro311=)
c.782+607A>G (n.782+607A>G)
c.14A>G
c.837A>G (p.Pro279=)
c.477A>G (p.Pro159=)
c.921A>G (p.Pro307=)
 ClinVar dbSNP
17g.7673574T>GCA001195TP53c.954A>C (p.Pro318=)
c.558A>C (p.Pro186=)
c.675A>C (p.Pro225=)
c.933A>C (p.Pro311=)
c.782+607A>C (n.782+607A>C)
c.14A>C
c.837A>C (p.Pro279=)
c.477A>C (p.Pro159=)
c.921A>C (p.Pro307=)
 dbSNP ExAC gnomAD v2 gnomAD v4
17g.7673574T=CA2245947701TP53c.954A= (p.Pro318=)
c.558A= (p.Pro186=)
c.675A= (p.Pro225=)
c.933A= (p.Pro311=)
c.782+607A= (n.782+607A=)
c.14A=
c.837A= (p.Pro279=)
c.477A= (p.Pro159=)
c.921A= (p.Pro307=)
17g.7673577_7673580dupCA645587367TP53c.951_954dup (p.Lys319AlafsTer19)
c.555_558dup (p.Lys187AlafsTer19)
c.672_675dup (p.Lys226AlafsTer19)
c.930_933dup (p.Lys312AlafsTer19)
c.951_954dup (p.Lys319AlafsTer?)
c.782+604_782+607dup (n.782+604_782+607dup)
c.951_954dup (p.Lys319AlafsTer29)
c.951_954dup (p.Lys319AlafsTer18)
c.555_558dup (p.Lys187AlafsTer18)
c.555_558dup (p.Lys187AlafsTer?)
c.555_558dup (p.Lys187AlafsTer29)
c.11_14dup
c.834_837dup (p.Lys280AlafsTer19)
c.834_837dup (p.Lys280AlafsTer18)
c.474_477dup (p.Lys160AlafsTer18)
c.918_921dup (p.Lys308AlafsTer19)
c.474_477dup (p.Lys160AlafsTer29)
c.474_477dup (p.Lys160AlafsTer19)
c.834_837dup (p.Lys280AlafsTer29)
 COSMIC COSMIC
17g.7673577_7673580delCA915949515TP53c.951_954del (p.Pro318ArgfsTer26)
c.555_558del (p.Pro186ArgfsTer26)
c.672_675del (p.Pro225ArgfsTer26)
c.930_933del (p.Pro311ArgfsTer26)
c.951_954del (p.Pro318ArgfsTer?)
c.782+604_782+607del (n.782+604_782+607del)
c.951_954del (p.Pro318ArgfsTer24)
c.555_558del (p.Pro186ArgfsTer24)
c.555_558del (p.Pro186ArgfsTer?)
c.11_14del
c.834_837del (p.Pro279ArgfsTer26)
c.834_837del (p.Pro279ArgfsTer24)
c.474_477del (p.Pro159ArgfsTer24)
c.918_921del (p.Pro307ArgfsTer26)
c.474_477del (p.Pro159ArgfsTer?)
c.474_477del (p.Pro159ArgfsTer26)
c.834_837del (p.Pro279ArgfsTer?)
 ClinVar dbSNP
17g.7673575G>ACA397835952TP53c.953C>T (p.Pro318Leu)
c.557C>T (p.Pro186Leu)
c.674C>T (p.Pro225Leu)
c.932C>T (p.Pro311Leu)
c.782+606C>T (n.782+606C>T)
c.13C>T
c.836C>T (p.Pro279Leu)
c.476C>T (p.Pro159Leu)
c.920C>T (p.Pro307Leu)
 ClinVar dbSNP gnomAD v4
17g.7673575G>CCA397835946TP53c.953C>G (p.Pro318Arg)
c.557C>G (p.Pro186Arg)
c.674C>G (p.Pro225Arg)
c.932C>G (p.Pro311Arg)
c.782+606C>G (n.782+606C>G)
c.13C>G
c.836C>G (p.Pro279Arg)
c.476C>G (p.Pro159Arg)
c.920C>G (p.Pro307Arg)
 ClinVar dbSNP
17g.7673575G=CA2245947708TP53c.953C= (p.Pro318=)
c.557C= (p.Pro186=)
c.674C= (p.Pro225=)
c.932C= (p.Pro311=)
c.782+606C= (n.782+606C=)
c.13C=
c.836C= (p.Pro279=)
c.476C= (p.Pro159=)
c.920C= (p.Pro307=)
17g.7673575G>TCA397835949TP53c.953C>A (p.Pro318Gln)
c.557C>A (p.Pro186Gln)
c.674C>A (p.Pro225Gln)
c.932C>A (p.Pro311Gln)
c.782+606C>A (n.782+606C>A)
c.13C>A
c.836C>A (p.Pro279Gln)
c.476C>A (p.Pro159Gln)
c.920C>A (p.Pro307Gln)
 dbSNP

Number of alleles fetched