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.7673802_7674193delCA645588414TP53c.772_820del
c.376_424del
c.493_541del
c.751_799del
c.772_782+381del
c.655_703del
c.295_343del
c.739_787del
 COSMIC
17g.7674105_7674106delinsGTCA2245950832TP53c.782+75_782+76delinsAC (n.782+75_782+76delinsAC)
c.386+75_386+76delinsAC (n.386+75_386+76delinsAC)
c.503+75_503+76delinsAC (n.503+75_503+76delinsAC)
c.761+75_761+76delinsAC (n.761+75_761+76delinsAC)
c.665+75_665+76delinsAC (n.665+75_665+76delinsAC)
c.305+75_305+76delinsAC (n.305+75_305+76delinsAC)
c.749+75_749+76delinsAC (n.749+75_749+76delinsAC)
17g.7674106delCA981209627TP53c.782+75del (n.782+75del)
c.386+75del (n.386+75del)
c.503+75del (n.503+75del)
c.761+75del (n.761+75del)
c.665+75del (n.665+75del)
c.305+75del (n.305+75del)
c.749+75del (n.749+75del)
 dbSNP gnomAD v3 gnomAD v4
17g.7674106T>ACA2635875779TP53c.782+75A>T (n.782+75A>T)
c.386+75A>T (n.386+75A>T)
c.503+75A>T (n.503+75A>T)
c.761+75A>T (n.761+75A>T)
c.665+75A>T (n.665+75A>T)
c.305+75A>T (n.305+75A>T)
c.749+75A>T (n.749+75A>T)
 gnomAD v4
17g.7674106T>CCA2635875782TP53c.782+75A>G (n.782+75A>G)
c.386+75A>G (n.386+75A>G)
c.503+75A>G (n.503+75A>G)
c.761+75A>G (n.761+75A>G)
c.665+75A>G (n.665+75A>G)
c.305+75A>G (n.305+75A>G)
c.749+75A>G (n.749+75A>G)
 gnomAD v4
17g.7674107G>ACA2245950836TP53c.782+74C>T (n.782+74C>T)
c.386+74C>T (n.386+74C>T)
c.503+74C>T (n.503+74C>T)
c.761+74C>T (n.761+74C>T)
c.665+74C>T (n.665+74C>T)
c.305+74C>T (n.305+74C>T)
c.749+74C>T (n.749+74C>T)
 dbSNP gnomAD v4
17g.7674107G=CA2245950835TP53c.782+74C= (n.782+74C=)
c.386+74C= (n.386+74C=)
c.503+74C= (n.503+74C=)
c.761+74C= (n.761+74C=)
c.665+74C= (n.665+74C=)
c.305+74C= (n.305+74C=)
c.749+74C= (n.749+74C=)
17g.7674107G>TCA2808380456TP53c.782+74C>A (n.782+74C>A)
c.386+74C>A (n.386+74C>A)
c.503+74C>A (n.503+74C>A)
c.761+74C>A (n.761+74C>A)
c.665+74C>A (n.665+74C>A)
c.305+74C>A (n.305+74C>A)
c.749+74C>A (n.749+74C>A)
17g.7674109delCA2576230632TP53c.782+74del (n.782+74del)
c.386+74del (n.386+74del)
c.503+74del (n.503+74del)
c.761+74del (n.761+74del)
c.665+74del (n.665+74del)
c.305+74del (n.305+74del)
c.749+74del (n.749+74del)
 gnomAD v4
17g.7674109G>ACA16534633TP53c.782+72C>T (n.782+72C>T)
c.386+72C>T (n.386+72C>T)
c.503+72C>T (n.503+72C>T)
c.761+72C>T (n.761+72C>T)
c.665+72C>T (n.665+72C>T)
c.305+72C>T (n.305+72C>T)
c.749+72C>T (n.749+72C>T)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.7674109G>CCA2580576600TP53c.782+72C>G (n.782+72C>G)
c.386+72C>G (n.386+72C>G)
c.503+72C>G (n.503+72C>G)
c.761+72C>G (n.761+72C>G)
c.665+72C>G (n.665+72C>G)
c.305+72C>G (n.305+72C>G)
c.749+72C>G (n.749+72C>G)
17g.7674109G=CA2245950840TP53c.782+72C= (n.782+72C=)
c.386+72C= (n.386+72C=)
c.503+72C= (n.503+72C=)
c.761+72C= (n.761+72C=)
c.665+72C= (n.665+72C=)
c.305+72C= (n.305+72C=)
c.749+72C= (n.749+72C=)
17g.7674109G>TCA2576230633TP53c.782+72C>A (n.782+72C>A)
c.386+72C>A (n.386+72C>A)
c.503+72C>A (n.503+72C>A)
c.761+72C>A (n.761+72C>A)
c.665+72C>A (n.665+72C>A)
c.305+72C>A (n.305+72C>A)
c.749+72C>A (n.749+72C>A)
 gnomAD v4
17g.7674110C>ACA2635875790TP53c.782+71G>T (n.782+71G>T)
c.386+71G>T (n.386+71G>T)
c.503+71G>T (n.503+71G>T)
c.761+71G>T (n.761+71G>T)
c.665+71G>T (n.665+71G>T)
c.305+71G>T (n.305+71G>T)
c.749+71G>T (n.749+71G>T)
 gnomAD v4
17g.7674110C=CA2245950843TP53c.782+71G= (n.782+71G=)
c.386+71G= (n.386+71G=)
c.503+71G= (n.503+71G=)
c.761+71G= (n.761+71G=)
c.665+71G= (n.665+71G=)
c.305+71G= (n.305+71G=)
c.749+71G= (n.749+71G=)
17g.7674110C>GCA2245950844TP53c.782+71G>C (n.782+71G>C)
c.386+71G>C (n.386+71G>C)
c.503+71G>C (n.503+71G>C)
c.761+71G>C (n.761+71G>C)
c.665+71G>C (n.665+71G>C)
c.305+71G>C (n.305+71G>C)
c.749+71G>C (n.749+71G>C)
 dbSNP gnomAD v4
17g.7674110C>TCA656753452TP53c.782+71G>A (n.782+71G>A)
c.386+71G>A (n.386+71G>A)
c.503+71G>A (n.503+71G>A)
c.761+71G>A (n.761+71G>A)
c.665+71G>A (n.665+71G>A)
c.305+71G>A (n.305+71G>A)
c.749+71G>A (n.749+71G>A)
 dbSNP gnomAD v3 gnomAD v4 COSMIC
17g.7674112delCA2576230634TP53c.782+71del (n.782+71del)
c.386+71del (n.386+71del)
c.503+71del (n.503+71del)
c.761+71del (n.761+71del)
c.665+71del (n.665+71del)
c.305+71del (n.305+71del)
c.749+71del (n.749+71del)
17g.7674111C>ACA2635875791TP53c.782+70G>T (n.782+70G>T)
c.386+70G>T (n.386+70G>T)
c.503+70G>T (n.503+70G>T)
c.761+70G>T (n.761+70G>T)
c.665+70G>T (n.665+70G>T)
c.305+70G>T (n.305+70G>T)
c.749+70G>T (n.749+70G>T)
 gnomAD v4
17g.7674111C=CA2245950846TP53c.782+70G= (n.782+70G=)
c.386+70G= (n.386+70G=)
c.503+70G= (n.503+70G=)
c.761+70G= (n.761+70G=)
c.665+70G= (n.665+70G=)
c.305+70G= (n.305+70G=)
c.749+70G= (n.749+70G=)
17g.7674111C>GCA2245950847TP53c.782+70G>C (n.782+70G>C)
c.386+70G>C (n.386+70G>C)
c.503+70G>C (n.503+70G>C)
c.761+70G>C (n.761+70G>C)
c.665+70G>C (n.665+70G>C)
c.305+70G>C (n.305+70G>C)
c.749+70G>C (n.749+70G>C)
 dbSNP gnomAD v4
17g.7674111C>TCA2635875792TP53c.782+70G>A (n.782+70G>A)
c.386+70G>A (n.386+70G>A)
c.503+70G>A (n.503+70G>A)
c.761+70G>A (n.761+70G>A)
c.665+70G>A (n.665+70G>A)
c.305+70G>A (n.305+70G>A)
c.749+70G>A (n.749+70G>A)
 gnomAD v4
17g.7674112C>ACA2635875793TP53c.782+69G>T (n.782+69G>T)
c.386+69G>T (n.386+69G>T)
c.503+69G>T (n.503+69G>T)
c.761+69G>T (n.761+69G>T)
c.665+69G>T (n.665+69G>T)
c.305+69G>T (n.305+69G>T)
c.749+69G>T (n.749+69G>T)
 gnomAD v4
17g.7674113A>GCA2635875794TP53c.782+68T>C (n.782+68T>C)
c.386+68T>C (n.386+68T>C)
c.503+68T>C (n.503+68T>C)
c.761+68T>C (n.761+68T>C)
c.665+68T>C (n.665+68T>C)
c.305+68T>C (n.305+68T>C)
c.749+68T>C (n.749+68T>C)
 gnomAD v4
17g.7674114G>CCA2635875795TP53c.782+67C>G (n.782+67C>G)
c.386+67C>G (n.386+67C>G)
c.503+67C>G (n.503+67C>G)
c.761+67C>G (n.761+67C>G)
c.665+67C>G (n.665+67C>G)
c.305+67C>G (n.305+67C>G)
c.749+67C>G (n.749+67C>G)
 gnomAD v4
17g.7674114G>TCA2635875796TP53c.782+67C>A (n.782+67C>A)
c.386+67C>A (n.386+67C>A)
c.503+67C>A (n.503+67C>A)
c.761+67C>A (n.761+67C>A)
c.665+67C>A (n.665+67C>A)
c.305+67C>A (n.305+67C>A)
c.749+67C>A (n.749+67C>A)
 gnomAD v4
17g.7674115G>ACA2635875797TP53c.782+66C>T (n.782+66C>T)
c.386+66C>T (n.386+66C>T)
c.503+66C>T (n.503+66C>T)
c.761+66C>T (n.761+66C>T)
c.665+66C>T (n.665+66C>T)
c.305+66C>T (n.305+66C>T)
c.749+66C>T (n.749+66C>T)
 gnomAD v4
17g.7674115G>TCA2635875798TP53c.782+66C>A (n.782+66C>A)
c.386+66C>A (n.386+66C>A)
c.503+66C>A (n.503+66C>A)
c.761+66C>A (n.761+66C>A)
c.665+66C>A (n.665+66C>A)
c.305+66C>A (n.305+66C>A)
c.749+66C>A (n.749+66C>A)
 gnomAD v4
17g.7674116G>ACA2635875801TP53c.782+65C>T (n.782+65C>T)
c.386+65C>T (n.386+65C>T)
c.503+65C>T (n.503+65C>T)
c.761+65C>T (n.761+65C>T)
c.665+65C>T (n.665+65C>T)
c.305+65C>T (n.305+65C>T)
c.749+65C>T (n.749+65C>T)
 gnomAD v4
17g.7674116G>CCA775170098TP53c.782+65C>G (n.782+65C>G)
c.386+65C>G (n.386+65C>G)
c.503+65C>G (n.503+65C>G)
c.761+65C>G (n.761+65C>G)
c.665+65C>G (n.665+65C>G)
c.305+65C>G (n.305+65C>G)
c.749+65C>G (n.749+65C>G)
 dbSNP
17g.7674116G=CA2245950849TP53c.782+65C= (n.782+65C=)
c.386+65C= (n.386+65C=)
c.503+65C= (n.503+65C=)
c.761+65C= (n.761+65C=)
c.665+65C= (n.665+65C=)
c.305+65C= (n.305+65C=)
c.749+65C= (n.749+65C=)
17g.7674116G>TCA2635875804TP53c.782+65C>A (n.782+65C>A)
c.386+65C>A (n.386+65C>A)
c.503+65C>A (n.503+65C>A)
c.761+65C>A (n.761+65C>A)
c.665+65C>A (n.665+65C>A)
c.305+65C>A (n.305+65C>A)
c.749+65C>A (n.749+65C>A)
 gnomAD v4
17g.7674117G>ACA2635875805TP53c.782+64C>T (n.782+64C>T)
c.386+64C>T (n.386+64C>T)
c.503+64C>T (n.503+64C>T)
c.761+64C>T (n.761+64C>T)
c.665+64C>T (n.665+64C>T)
c.305+64C>T (n.305+64C>T)
c.749+64C>T (n.749+64C>T)
 gnomAD v4
17g.7674117G>TCA2635875806TP53c.782+64C>A (n.782+64C>A)
c.386+64C>A (n.386+64C>A)
c.503+64C>A (n.503+64C>A)
c.761+64C>A (n.761+64C>A)
c.665+64C>A (n.665+64C>A)
c.305+64C>A (n.305+64C>A)
c.749+64C>A (n.749+64C>A)
 gnomAD v4
17g.7674119C>ACA2635875808TP53c.782+62G>T (n.782+62G>T)
c.386+62G>T (n.386+62G>T)
c.503+62G>T (n.503+62G>T)
c.761+62G>T (n.761+62G>T)
c.665+62G>T (n.665+62G>T)
c.305+62G>T (n.305+62G>T)
c.749+62G>T (n.749+62G>T)
 gnomAD v4
17g.7674119C>TCA2576230635TP53c.782+62G>A (n.782+62G>A)
c.386+62G>A (n.386+62G>A)
c.503+62G>A (n.503+62G>A)
c.761+62G>A (n.761+62G>A)
c.665+62G>A (n.665+62G>A)
c.305+62G>A (n.305+62G>A)
c.749+62G>A (n.749+62G>A)
 gnomAD v4
17g.7674126_7674135delCA2733136085TP53c.782+53_782+62del (n.782+53_782+62del)
c.386+53_386+62del (n.386+53_386+62del)
c.503+53_503+62del (n.503+53_503+62del)
c.761+53_761+62del (n.761+53_761+62del)
c.665+53_665+62del (n.665+53_665+62del)
c.305+53_305+62del (n.305+53_305+62del)
c.749+53_749+62del (n.749+53_749+62del)
 dbSNP
17g.7674120A>GCA2635875810TP53c.782+61T>C (n.782+61T>C)
c.386+61T>C (n.386+61T>C)
c.503+61T>C (n.503+61T>C)
c.761+61T>C (n.761+61T>C)
c.665+61T>C (n.665+61T>C)
c.305+61T>C (n.305+61T>C)
c.749+61T>C (n.749+61T>C)
 gnomAD v4
17g.7674121G>CCA2245950852TP53c.782+60C>G (n.782+60C>G)
c.386+60C>G (n.386+60C>G)
c.503+60C>G (n.503+60C>G)
c.761+60C>G (n.761+60C>G)
c.665+60C>G (n.665+60C>G)
c.305+60C>G (n.305+60C>G)
c.749+60C>G (n.749+60C>G)
 dbSNP
17g.7674121G=CA2245950850TP53c.782+60C= (n.782+60C=)
c.386+60C= (n.386+60C=)
c.503+60C= (n.503+60C=)
c.761+60C= (n.761+60C=)
c.665+60C= (n.665+60C=)
c.305+60C= (n.305+60C=)
c.749+60C= (n.749+60C=)
17g.7674121G>TCA2635875814TP53c.782+60C>A (n.782+60C>A)
c.386+60C>A (n.386+60C>A)
c.503+60C>A (n.503+60C>A)
c.761+60C>A (n.761+60C>A)
c.665+60C>A (n.665+60C>A)
c.305+60C>A (n.305+60C>A)
c.749+60C>A (n.749+60C>A)
 gnomAD v4
17g.7674122A=CA2245950853TP53c.782+59T= (n.782+59T=)
c.386+59T= (n.386+59T=)
c.503+59T= (n.503+59T=)
c.761+59T= (n.761+59T=)
c.665+59T= (n.665+59T=)
c.305+59T= (n.305+59T=)
c.749+59T= (n.749+59T=)
17g.7674122A>CCA287486762TP53c.782+59T>G (n.782+59T>G)
c.386+59T>G (n.386+59T>G)
c.503+59T>G (n.503+59T>G)
c.761+59T>G (n.761+59T>G)
c.665+59T>G (n.665+59T>G)
c.305+59T>G (n.305+59T>G)
c.749+59T>G (n.749+59T>G)
 dbSNP
17g.7674122A>GCA2580574843TP53c.782+59T>C (n.782+59T>C)
c.386+59T>C (n.386+59T>C)
c.503+59T>C (n.503+59T>C)
c.761+59T>C (n.761+59T>C)
c.665+59T>C (n.665+59T>C)
c.305+59T>C (n.305+59T>C)
c.749+59T>C (n.749+59T>C)
 gnomAD v4
17g.7674122A>TCA2580574844TP53c.782+59T>A (n.782+59T>A)
c.386+59T>A (n.386+59T>A)
c.503+59T>A (n.503+59T>A)
c.761+59T>A (n.761+59T>A)
c.665+59T>A (n.665+59T>A)
c.305+59T>A (n.305+59T>A)
c.749+59T>A (n.749+59T>A)
 gnomAD v4
17g.7674123G>ACA287486764TP53c.782+58C>T (n.782+58C>T)
c.386+58C>T (n.386+58C>T)
c.503+58C>T (n.503+58C>T)
c.761+58C>T (n.761+58C>T)
c.665+58C>T (n.665+58C>T)
c.305+58C>T (n.305+58C>T)
c.749+58C>T (n.749+58C>T)
 dbSNP gnomAD v3 gnomAD v4
17g.7674123G>CCA2635875818TP53c.782+58C>G (n.782+58C>G)
c.386+58C>G (n.386+58C>G)
c.503+58C>G (n.503+58C>G)
c.761+58C>G (n.761+58C>G)
c.665+58C>G (n.665+58C>G)
c.305+58C>G (n.305+58C>G)
c.749+58C>G (n.749+58C>G)
 gnomAD v4
17g.7674123G=CA2245950854TP53c.782+58C= (n.782+58C=)
c.386+58C= (n.386+58C=)
c.503+58C= (n.503+58C=)
c.761+58C= (n.761+58C=)
c.665+58C= (n.665+58C=)
c.305+58C= (n.305+58C=)
c.749+58C= (n.749+58C=)
17g.7674123G>TCA2635875819TP53c.782+58C>A (n.782+58C>A)
c.386+58C>A (n.386+58C>A)
c.503+58C>A (n.503+58C>A)
c.761+58C>A (n.761+58C>A)
c.665+58C>A (n.665+58C>A)
c.305+58C>A (n.305+58C>A)
c.749+58C>A (n.749+58C>A)
 gnomAD v4
17g.7674124G>ACA2635875824TP53c.782+57C>T (n.782+57C>T)
c.386+57C>T (n.386+57C>T)
c.503+57C>T (n.503+57C>T)
c.761+57C>T (n.761+57C>T)
c.665+57C>T (n.665+57C>T)
c.305+57C>T (n.305+57C>T)
c.749+57C>T (n.749+57C>T)
 gnomAD v4
17g.7674124G>TCA2635875821TP53c.782+57C>A (n.782+57C>A)
c.386+57C>A (n.386+57C>A)
c.503+57C>A (n.503+57C>A)
c.761+57C>A (n.761+57C>A)
c.665+57C>A (n.665+57C>A)
c.305+57C>A (n.305+57C>A)
c.749+57C>A (n.749+57C>A)
 gnomAD v4
17g.7674125delCA2635875830TP53c.782+56del (n.782+56del)
c.386+56del (n.386+56del)
c.503+56del (n.503+56del)
c.761+56del (n.761+56del)
c.665+56del (n.665+56del)
c.305+56del (n.305+56del)
c.749+56del (n.749+56del)
 gnomAD v4
17g.7674125C>ACA2635875831TP53c.782+56G>T (n.782+56G>T)
c.386+56G>T (n.386+56G>T)
c.503+56G>T (n.503+56G>T)
c.761+56G>T (n.761+56G>T)
c.665+56G>T (n.665+56G>T)
c.305+56G>T (n.305+56G>T)
c.749+56G>T (n.749+56G>T)
 gnomAD v4
17g.7674125C>TCA2576230636TP53c.782+56G>A (n.782+56G>A)
c.386+56G>A (n.386+56G>A)
c.503+56G>A (n.503+56G>A)
c.761+56G>A (n.761+56G>A)
c.665+56G>A (n.665+56G>A)
c.305+56G>A (n.305+56G>A)
c.749+56G>A (n.749+56G>A)
 dbSNP gnomAD v4
17g.7674126A>TCA2635875834TP53c.782+55T>A (n.782+55T>A)
c.386+55T>A (n.386+55T>A)
c.503+55T>A (n.503+55T>A)
c.761+55T>A (n.761+55T>A)
c.665+55T>A (n.665+55T>A)
c.305+55T>A (n.305+55T>A)
c.749+55T>A (n.749+55T>A)
 dbSNP gnomAD v4
17g.7674128G>ACA2635875864TP53c.782+53C>T (n.782+53C>T)
c.386+53C>T (n.386+53C>T)
c.503+53C>T (n.503+53C>T)
c.761+53C>T (n.761+53C>T)
c.665+53C>T (n.665+53C>T)
c.305+53C>T (n.305+53C>T)
c.749+53C>T (n.749+53C>T)
 dbSNP gnomAD v4
17g.7674128G>TCA2576230637TP53c.782+53C>A (n.782+53C>A)
c.386+53C>A (n.386+53C>A)
c.503+53C>A (n.503+53C>A)
c.761+53C>A (n.761+53C>A)
c.665+53C>A (n.665+53C>A)
c.305+53C>A (n.305+53C>A)
c.749+53C>A (n.749+53C>A)
 gnomAD v4
17g.7674128_7674129delinsGCCA2245950858TP53c.782+52_782+53delinsGC (n.782+52_782+53delinsGC)
c.386+52_386+53delinsGC (n.386+52_386+53delinsGC)
c.503+52_503+53delinsGC (n.503+52_503+53delinsGC)
c.761+52_761+53delinsGC (n.761+52_761+53delinsGC)
c.665+52_665+53delinsGC (n.665+52_665+53delinsGC)
c.305+52_305+53delinsGC (n.305+52_305+53delinsGC)
c.749+52_749+53delinsGC (n.749+52_749+53delinsGC)
17g.7674129delCA919785709TP53c.782+52del (n.782+52del)
c.386+52del (n.386+52del)
c.503+52del (n.503+52del)
c.761+52del (n.761+52del)
c.665+52del (n.665+52del)
c.305+52del (n.305+52del)
c.749+52del (n.749+52del)
 dbSNP gnomAD v3 gnomAD v4
17g.7674129C>ACA2635875868TP53c.782+52G>T (n.782+52G>T)
c.386+52G>T (n.386+52G>T)
c.503+52G>T (n.503+52G>T)
c.761+52G>T (n.761+52G>T)
c.665+52G>T (n.665+52G>T)
c.305+52G>T (n.305+52G>T)
c.749+52G>T (n.749+52G>T)
 dbSNP gnomAD v4
17g.7674129C>GCA2733136087TP53c.782+52G>C (n.782+52G>C)
c.386+52G>C (n.386+52G>C)
c.503+52G>C (n.503+52G>C)
c.761+52G>C (n.761+52G>C)
c.665+52G>C (n.665+52G>C)
c.305+52G>C (n.305+52G>C)
c.749+52G>C (n.749+52G>C)
 dbSNP
17g.7674129C>TCA2500519498TP53c.782+52G>A (n.782+52G>A)
c.386+52G>A (n.386+52G>A)
c.503+52G>A (n.503+52G>A)
c.761+52G>A (n.761+52G>A)
c.665+52G>A (n.665+52G>A)
c.305+52G>A (n.305+52G>A)
c.749+52G>A (n.749+52G>A)
 dbSNP
17g.7674130A>GCA2576230638TP53c.782+51T>C (n.782+51T>C)
c.386+51T>C (n.386+51T>C)
c.503+51T>C (n.503+51T>C)
c.761+51T>C (n.761+51T>C)
c.665+51T>C (n.665+51T>C)
c.305+51T>C (n.305+51T>C)
c.749+51T>C (n.749+51T>C)
 gnomAD v4
17g.7674131G>ACA287486767TP53c.782+50C>T (n.782+50C>T)
c.386+50C>T (n.386+50C>T)
c.503+50C>T (n.503+50C>T)
c.761+50C>T (n.761+50C>T)
c.665+50C>T (n.665+50C>T)
c.305+50C>T (n.305+50C>T)
c.749+50C>T (n.749+50C>T)
 dbSNP
17g.7674131G=CA2245950861TP53c.782+50C= (n.782+50C=)
c.386+50C= (n.386+50C=)
c.503+50C= (n.503+50C=)
c.761+50C= (n.761+50C=)
c.665+50C= (n.665+50C=)
c.305+50C= (n.305+50C=)
c.749+50C= (n.749+50C=)
17g.7674131G>TCA2576230639TP53c.782+50C>A (n.782+50C>A)
c.386+50C>A (n.386+50C>A)
c.503+50C>A (n.503+50C>A)
c.761+50C>A (n.761+50C>A)
c.665+50C>A (n.665+50C>A)
c.305+50C>A (n.305+50C>A)
c.749+50C>A (n.749+50C>A)
17g.7674132A>GCA2576230640TP53c.782+49T>C (n.782+49T>C)
c.386+49T>C (n.386+49T>C)
c.503+49T>C (n.503+49T>C)
c.761+49T>C (n.761+49T>C)
c.665+49T>C (n.665+49T>C)
c.305+49T>C (n.305+49T>C)
c.749+49T>C (n.749+49T>C)
 dbSNP gnomAD v4
17g.7674132A>TCA2733136088TP53c.782+49T>A (n.782+49T>A)
c.386+49T>A (n.386+49T>A)
c.503+49T>A (n.503+49T>A)
c.761+49T>A (n.761+49T>A)
c.665+49T>A (n.665+49T>A)
c.305+49T>A (n.305+49T>A)
c.749+49T>A (n.749+49T>A)
 dbSNP
17g.7674133G>ACA001654TP53c.782+48C>T (n.782+48C>T)
c.386+48C>T (n.386+48C>T)
c.503+48C>T (n.503+48C>T)
c.761+48C>T (n.761+48C>T)
c.665+48C>T (n.665+48C>T)
c.305+48C>T (n.305+48C>T)
c.749+48C>T (n.749+48C>T)
 dbSNP ExAC gnomAD v2 gnomAD v4
17g.7674133G>CCA2635875877TP53c.782+48C>G (n.782+48C>G)
c.386+48C>G (n.386+48C>G)
c.503+48C>G (n.503+48C>G)
c.761+48C>G (n.761+48C>G)
c.665+48C>G (n.665+48C>G)
c.305+48C>G (n.305+48C>G)
c.749+48C>G (n.749+48C>G)
 gnomAD v4
17g.7674133G=CA2245950865TP53c.782+48C= (n.782+48C=)
c.386+48C= (n.386+48C=)
c.503+48C= (n.503+48C=)
c.761+48C= (n.761+48C=)
c.665+48C= (n.665+48C=)
c.305+48C= (n.305+48C=)
c.749+48C= (n.749+48C=)
17g.7674133G>TCA2635875878TP53c.782+48C>A (n.782+48C>A)
c.386+48C>A (n.386+48C>A)
c.503+48C>A (n.503+48C>A)
c.761+48C>A (n.761+48C>A)
c.665+48C>A (n.665+48C>A)
c.305+48C>A (n.305+48C>A)
c.749+48C>A (n.749+48C>A)
 dbSNP gnomAD v4
17g.7674134delCA2576230641TP53c.782+48del (n.782+48del)
c.386+48del (n.386+48del)
c.503+48del (n.503+48del)
c.761+48del (n.761+48del)
c.665+48del (n.665+48del)
c.305+48del (n.305+48del)
c.749+48del (n.749+48del)
17g.7674134G>ACA2733136092TP53c.782+47C>T (n.782+47C>T)
c.386+47C>T (n.386+47C>T)
c.503+47C>T (n.503+47C>T)
c.761+47C>T (n.761+47C>T)
c.665+47C>T (n.665+47C>T)
c.305+47C>T (n.305+47C>T)
c.749+47C>T (n.749+47C>T)
 dbSNP
17g.7674134G>TCA2576230642TP53c.782+47C>A (n.782+47C>A)
c.386+47C>A (n.386+47C>A)
c.503+47C>A (n.503+47C>A)
c.761+47C>A (n.761+47C>A)
c.665+47C>A (n.665+47C>A)
c.305+47C>A (n.305+47C>A)
c.749+47C>A (n.749+47C>A)
 gnomAD v4
17g.7674135C>ACA2733136094TP53c.782+46G>T (n.782+46G>T)
c.386+46G>T (n.386+46G>T)
c.503+46G>T (n.503+46G>T)
c.761+46G>T (n.761+46G>T)
c.665+46G>T (n.665+46G>T)
c.305+46G>T (n.305+46G>T)
c.749+46G>T (n.749+46G>T)
 dbSNP
17g.7674135C>GCA2733136093TP53c.782+46G>C (n.782+46G>C)
c.386+46G>C (n.386+46G>C)
c.503+46G>C (n.503+46G>C)
c.761+46G>C (n.761+46G>C)
c.665+46G>C (n.665+46G>C)
c.305+46G>C (n.305+46G>C)
c.749+46G>C (n.749+46G>C)
 dbSNP
17g.7674135C>TCA645588468TP53c.782+46G>A (n.782+46G>A)
c.386+46G>A (n.386+46G>A)
c.503+46G>A (n.503+46G>A)
c.761+46G>A (n.761+46G>A)
c.665+46G>A (n.665+46G>A)
c.305+46G>A (n.305+46G>A)
c.749+46G>A (n.749+46G>A)
 dbSNP COSMIC
17g.7674136delCA2741514599TP53c.782+45del (n.782+45del)
c.386+45del (n.386+45del)
c.503+45del (n.503+45del)
c.761+45del (n.761+45del)
c.665+45del (n.665+45del)
c.305+45del (n.305+45del)
c.749+45del (n.749+45del)
17g.7674136T>CCA2635875880TP53c.782+45A>G (n.782+45A>G)
c.386+45A>G (n.386+45A>G)
c.503+45A>G (n.503+45A>G)
c.761+45A>G (n.761+45A>G)
c.665+45A>G (n.665+45A>G)
c.305+45A>G (n.305+45A>G)
c.749+45A>G (n.749+45A>G)
 gnomAD v4
17g.7674137G>ACA287486770TP53c.782+44C>T (n.782+44C>T)
c.386+44C>T (n.386+44C>T)
c.503+44C>T (n.503+44C>T)
c.761+44C>T (n.761+44C>T)
c.665+44C>T (n.665+44C>T)
c.305+44C>T (n.305+44C>T)
c.749+44C>T (n.749+44C>T)
 dbSNP
17g.7674137G=CA2245950866TP53c.782+44C= (n.782+44C=)
c.386+44C= (n.386+44C=)
c.503+44C= (n.503+44C=)
c.761+44C= (n.761+44C=)
c.665+44C= (n.665+44C=)
c.305+44C= (n.305+44C=)
c.749+44C= (n.749+44C=)
17g.7674137G>TCA2576230643TP53c.782+44C>A (n.782+44C>A)
c.386+44C>A (n.386+44C>A)
c.503+44C>A (n.503+44C>A)
c.761+44C>A (n.761+44C>A)
c.665+44C>A (n.665+44C>A)
c.305+44C>A (n.305+44C>A)
c.749+44C>A (n.749+44C>A)
 gnomAD v4
17g.7674140delCA2635875883TP53c.782+44del (n.782+44del)
c.386+44del (n.386+44del)
c.503+44del (n.503+44del)
c.761+44del (n.761+44del)
c.665+44del (n.665+44del)
c.305+44del (n.305+44del)
c.749+44del (n.749+44del)
 gnomAD v4
17g.7674138G>ACA2245950870TP53c.782+43C>T (n.782+43C>T)
c.386+43C>T (n.386+43C>T)
c.503+43C>T (n.503+43C>T)
c.761+43C>T (n.761+43C>T)
c.665+43C>T (n.665+43C>T)
c.305+43C>T (n.305+43C>T)
c.749+43C>T (n.749+43C>T)
 dbSNP
17g.7674138G>CCA2732985645TP53c.782+43C>G (n.782+43C>G)
c.386+43C>G (n.386+43C>G)
c.503+43C>G (n.503+43C>G)
c.761+43C>G (n.761+43C>G)
c.665+43C>G (n.665+43C>G)
c.305+43C>G (n.305+43C>G)
c.749+43C>G (n.749+43C>G)
 dbSNP
17g.7674138G=CA2245950869TP53c.782+43C= (n.782+43C=)
c.386+43C= (n.386+43C=)
c.503+43C= (n.503+43C=)
c.761+43C= (n.761+43C=)
c.665+43C= (n.665+43C=)
c.305+43C= (n.305+43C=)
c.749+43C= (n.749+43C=)
17g.7674138G>TCA2576230644TP53c.782+43C>A (n.782+43C>A)
c.386+43C>A (n.386+43C>A)
c.503+43C>A (n.503+43C>A)
c.761+43C>A (n.761+43C>A)
c.665+43C>A (n.665+43C>A)
c.305+43C>A (n.305+43C>A)
c.749+43C>A (n.749+43C>A)
 dbSNP gnomAD v4
17g.7674139G>ACA624865111TP53c.782+42C>T (n.782+42C>T)
c.386+42C>T (n.386+42C>T)
c.503+42C>T (n.503+42C>T)
c.761+42C>T (n.761+42C>T)
c.665+42C>T (n.665+42C>T)
c.305+42C>T (n.305+42C>T)
c.749+42C>T (n.749+42C>T)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
17g.7674139G=CA2245950871TP53c.782+42C= (n.782+42C=)
c.386+42C= (n.386+42C=)
c.503+42C= (n.503+42C=)
c.761+42C= (n.761+42C=)
c.665+42C= (n.665+42C=)
c.305+42C= (n.305+42C=)
c.749+42C= (n.749+42C=)
17g.7674139G>TCA2635875892TP53c.782+42C>A (n.782+42C>A)
c.386+42C>A (n.386+42C>A)
c.503+42C>A (n.503+42C>A)
c.761+42C>A (n.761+42C>A)
c.665+42C>A (n.665+42C>A)
c.305+42C>A (n.305+42C>A)
c.749+42C>A (n.749+42C>A)
 dbSNP gnomAD v4
17g.7674140G>ACA001660TP53c.782+41C>T (n.782+41C>T)
c.386+41C>T (n.386+41C>T)
c.503+41C>T (n.503+41C>T)
c.761+41C>T (n.761+41C>T)
c.665+41C>T (n.665+41C>T)
c.305+41C>T (n.305+41C>T)
c.749+41C>T (n.749+41C>T)
 dbSNP ExAC gnomAD v2 gnomAD v4
17g.7674140G>CCA2732930579TP53c.782+41C>G (n.782+41C>G)
c.386+41C>G (n.386+41C>G)
c.503+41C>G (n.503+41C>G)
c.761+41C>G (n.761+41C>G)
c.665+41C>G (n.665+41C>G)
c.305+41C>G (n.305+41C>G)
c.749+41C>G (n.749+41C>G)
 dbSNP
17g.7674140G=CA2245950873TP53c.782+41C= (n.782+41C=)
c.386+41C= (n.386+41C=)
c.503+41C= (n.503+41C=)
c.761+41C= (n.761+41C=)
c.665+41C= (n.665+41C=)
c.305+41C= (n.305+41C=)
c.749+41C= (n.749+41C=)
17g.7674140G>TCA2635875895TP53c.782+41C>A (n.782+41C>A)
c.386+41C>A (n.386+41C>A)
c.503+41C>A (n.503+41C>A)
c.761+41C>A (n.761+41C>A)
c.665+41C>A (n.665+41C>A)
c.305+41C>A (n.305+41C>A)
c.749+41C>A (n.749+41C>A)
 gnomAD v4
17g.7674141C=CA2245950877TP53c.782+40G= (n.782+40G=)
c.386+40G= (n.386+40G=)
c.503+40G= (n.503+40G=)
c.761+40G= (n.761+40G=)
c.665+40G= (n.665+40G=)
c.305+40G= (n.305+40G=)
c.749+40G= (n.749+40G=)
17g.7674141C>GCA2245950879TP53c.782+40G>C (n.782+40G>C)
c.386+40G>C (n.386+40G>C)
c.503+40G>C (n.503+40G>C)
c.761+40G>C (n.761+40G>C)
c.665+40G>C (n.665+40G>C)
c.305+40G>C (n.305+40G>C)
c.749+40G>C (n.749+40G>C)
 dbSNP gnomAD v4
17g.7674142A>CCA2733136095TP53c.782+39T>G (n.782+39T>G)
c.386+39T>G (n.386+39T>G)
c.503+39T>G (n.503+39T>G)
c.761+39T>G (n.761+39T>G)
c.665+39T>G (n.665+39T>G)
c.305+39T>G (n.305+39T>G)
c.749+39T>G (n.749+39T>G)
 dbSNP
17g.7674142A>GCA2635875899TP53c.782+39T>C (n.782+39T>C)
c.386+39T>C (n.386+39T>C)
c.503+39T>C (n.503+39T>C)
c.761+39T>C (n.761+39T>C)
c.665+39T>C (n.665+39T>C)
c.305+39T>C (n.305+39T>C)
c.749+39T>C (n.749+39T>C)
 gnomAD v4
17g.7674142A>TCA2576230645TP53c.782+39T>A (n.782+39T>A)
c.386+39T>A (n.386+39T>A)
c.503+39T>A (n.503+39T>A)
c.761+39T>A (n.761+39T>A)
c.665+39T>A (n.665+39T>A)
c.305+39T>A (n.305+39T>A)
c.749+39T>A (n.749+39T>A)
 dbSNP
17g.7674143C>ACA2733136096TP53c.782+38G>T (n.782+38G>T)
c.386+38G>T (n.386+38G>T)
c.503+38G>T (n.503+38G>T)
c.761+38G>T (n.761+38G>T)
c.665+38G>T (n.665+38G>T)
c.305+38G>T (n.305+38G>T)
c.749+38G>T (n.749+38G>T)
 dbSNP
17g.7674143C>GCA2733136097TP53c.782+38G>C (n.782+38G>C)
c.386+38G>C (n.386+38G>C)
c.503+38G>C (n.503+38G>C)
c.761+38G>C (n.761+38G>C)
c.665+38G>C (n.665+38G>C)
c.305+38G>C (n.305+38G>C)
c.749+38G>C (n.749+38G>C)
 dbSNP
17g.7674144A>TCA645588469TP53c.782+37T>A (n.782+37T>A)
c.386+37T>A (n.386+37T>A)
c.503+37T>A (n.503+37T>A)
c.761+37T>A (n.761+37T>A)
c.665+37T>A (n.665+37T>A)
c.305+37T>A (n.305+37T>A)
c.749+37T>A (n.749+37T>A)
 dbSNP COSMIC
17g.7674145G>ACA2635875902TP53c.782+36C>T (n.782+36C>T)
c.386+36C>T (n.386+36C>T)
c.503+36C>T (n.503+36C>T)
c.761+36C>T (n.761+36C>T)
c.665+36C>T (n.665+36C>T)
c.305+36C>T (n.305+36C>T)
c.749+36C>T (n.749+36C>T)
 dbSNP gnomAD v4
17g.7674145G>CCA2733136099TP53c.782+36C>G (n.782+36C>G)
c.386+36C>G (n.386+36C>G)
c.503+36C>G (n.503+36C>G)
c.761+36C>G (n.761+36C>G)
c.665+36C>G (n.665+36C>G)
c.305+36C>G (n.305+36C>G)
c.749+36C>G (n.749+36C>G)
 dbSNP
17g.7674145G>TCA2576230646TP53c.782+36C>A (n.782+36C>A)
c.386+36C>A (n.386+36C>A)
c.503+36C>A (n.503+36C>A)
c.761+36C>A (n.761+36C>A)
c.665+36C>A (n.665+36C>A)
c.305+36C>A (n.305+36C>A)
c.749+36C>A (n.749+36C>A)
 gnomAD v4
17g.7674146C>ACA624865112TP53c.782+35G>T (n.782+35G>T)
c.386+35G>T (n.386+35G>T)
c.503+35G>T (n.503+35G>T)
c.761+35G>T (n.761+35G>T)
c.665+35G>T (n.665+35G>T)
c.305+35G>T (n.305+35G>T)
c.749+35G>T (n.749+35G>T)
 dbSNP gnomAD v2 gnomAD v4
17g.7674146C=CA2245950883TP53c.782+35G= (n.782+35G=)
c.386+35G= (n.386+35G=)
c.503+35G= (n.503+35G=)
c.761+35G= (n.761+35G=)
c.665+35G= (n.665+35G=)
c.305+35G= (n.305+35G=)
c.749+35G= (n.749+35G=)
17g.7674146C>GCA2732951162TP53c.782+35G>C (n.782+35G>C)
c.386+35G>C (n.386+35G>C)
c.503+35G>C (n.503+35G>C)
c.761+35G>C (n.761+35G>C)
c.665+35G>C (n.665+35G>C)
c.305+35G>C (n.305+35G>C)
c.749+35G>C (n.749+35G>C)
 dbSNP
17g.7674146C>TCA2732951161TP53c.782+35G>A (n.782+35G>A)
c.386+35G>A (n.386+35G>A)
c.503+35G>A (n.503+35G>A)
c.761+35G>A (n.761+35G>A)
c.665+35G>A (n.665+35G>A)
c.305+35G>A (n.305+35G>A)
c.749+35G>A (n.749+35G>A)
 dbSNP
17g.7674146dupCA2635875906TP53c.782+35dup (n.782+35dup)
c.386+35dup (n.386+35dup)
c.503+35dup (n.503+35dup)
c.761+35dup (n.761+35dup)
c.665+35dup (n.665+35dup)
c.305+35dup (n.305+35dup)
c.749+35dup (n.749+35dup)
 gnomAD v4
17g.7674147A>GCA2733136108TP53c.782+34T>C (n.782+34T>C)
c.386+34T>C (n.386+34T>C)
c.503+34T>C (n.503+34T>C)
c.761+34T>C (n.761+34T>C)
c.665+34T>C (n.665+34T>C)
c.305+34T>C (n.305+34T>C)
c.749+34T>C (n.749+34T>C)
 dbSNP
17g.7674147A>TCA2733136100TP53c.782+34T>A (n.782+34T>A)
c.386+34T>A (n.386+34T>A)
c.503+34T>A (n.503+34T>A)
c.761+34T>A (n.761+34T>A)
c.665+34T>A (n.665+34T>A)
c.305+34T>A (n.305+34T>A)
c.749+34T>A (n.749+34T>A)
 dbSNP
17g.7674148G>ACA287486777TP53c.782+33C>T (n.782+33C>T)
c.386+33C>T (n.386+33C>T)
c.503+33C>T (n.503+33C>T)
c.761+33C>T (n.761+33C>T)
c.665+33C>T (n.665+33C>T)
c.305+33C>T (n.305+33C>T)
c.749+33C>T (n.749+33C>T)
 dbSNP gnomAD v3 gnomAD v4
17g.7674148G>CCA624865113TP53c.782+33C>G (n.782+33C>G)
c.386+33C>G (n.386+33C>G)
c.503+33C>G (n.503+33C>G)
c.761+33C>G (n.761+33C>G)
c.665+33C>G (n.665+33C>G)
c.305+33C>G (n.305+33C>G)
c.749+33C>G (n.749+33C>G)
 dbSNP gnomAD v2 gnomAD v4
17g.7674148G=CA2245950885TP53c.782+33C= (n.782+33C=)
c.386+33C= (n.386+33C=)
c.503+33C= (n.503+33C=)
c.761+33C= (n.761+33C=)
c.665+33C= (n.665+33C=)
c.305+33C= (n.305+33C=)
c.749+33C= (n.749+33C=)
17g.7674148G>TCA2635875910TP53c.782+33C>A (n.782+33C>A)
c.386+33C>A (n.386+33C>A)
c.503+33C>A (n.503+33C>A)
c.761+33C>A (n.761+33C>A)
c.665+33C>A (n.665+33C>A)
c.305+33C>A (n.305+33C>A)
c.749+33C>A (n.749+33C>A)
 gnomAD v4
17g.7674149G>ACA001666TP53c.782+32C>T (n.782+32C>T)
c.386+32C>T (n.386+32C>T)
c.503+32C>T (n.503+32C>T)
c.761+32C>T (n.761+32C>T)
c.665+32C>T (n.665+32C>T)
c.305+32C>T (n.305+32C>T)
c.749+32C>T (n.749+32C>T)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.7674149G>CCA2245950887TP53c.782+32C>G (n.782+32C>G)
c.386+32C>G (n.386+32C>G)
c.503+32C>G (n.503+32C>G)
c.761+32C>G (n.761+32C>G)
c.665+32C>G (n.665+32C>G)
c.305+32C>G (n.305+32C>G)
c.749+32C>G (n.749+32C>G)
 dbSNP
17g.7674149G=CA2245950886TP53c.782+32C= (n.782+32C=)
c.386+32C= (n.386+32C=)
c.503+32C= (n.503+32C=)
c.761+32C= (n.761+32C=)
c.665+32C= (n.665+32C=)
c.305+32C= (n.305+32C=)
c.749+32C= (n.749+32C=)
17g.7674149G>TCA624865114TP53c.782+32C>A (n.782+32C>A)
c.386+32C>A (n.386+32C>A)
c.503+32C>A (n.503+32C>A)
c.761+32C>A (n.761+32C>A)
c.665+32C>A (n.665+32C>A)
c.305+32C>A (n.305+32C>A)
c.749+32C>A (n.749+32C>A)
 dbSNP gnomAD v2 gnomAD v4
17g.7674150C>ACA2732932589TP53c.782+31G>T (n.782+31G>T)
c.386+31G>T (n.386+31G>T)
c.503+31G>T (n.503+31G>T)
c.761+31G>T (n.761+31G>T)
c.665+31G>T (n.665+31G>T)
c.305+31G>T (n.305+31G>T)
c.749+31G>T (n.749+31G>T)
 dbSNP
17g.7674150C=CA2245950890TP53c.782+31G= (n.782+31G=)
c.386+31G= (n.386+31G=)
c.503+31G= (n.503+31G=)
c.761+31G= (n.761+31G=)
c.665+31G= (n.665+31G=)
c.305+31G= (n.305+31G=)
c.749+31G= (n.749+31G=)
17g.7674150C>GCA287486785TP53c.782+31G>C (n.782+31G>C)
c.386+31G>C (n.386+31G>C)
c.503+31G>C (n.503+31G>C)
c.761+31G>C (n.761+31G>C)
c.665+31G>C (n.665+31G>C)
c.305+31G>C (n.305+31G>C)
c.749+31G>C (n.749+31G>C)
 dbSNP
17g.7674150C>TCA624865115TP53c.782+31G>A (n.782+31G>A)
c.386+31G>A (n.386+31G>A)
c.503+31G>A (n.503+31G>A)
c.761+31G>A (n.761+31G>A)
c.665+31G>A (n.665+31G>A)
c.305+31G>A (n.305+31G>A)
c.749+31G>A (n.749+31G>A)
 dbSNP gnomAD v2 gnomAD v4 COSMIC
17g.7674158_7674198delCA2695202190TP53c.773_782+31del
c.377_386+31del
c.494_503+31del
c.752_761+31del
c.656_665+31del
c.296_305+31del
c.740_749+31del
17g.7674151C>ACA2732985647TP53c.782+30G>T (n.782+30G>T)
c.386+30G>T (n.386+30G>T)
c.503+30G>T (n.503+30G>T)
c.761+30G>T (n.761+30G>T)
c.665+30G>T (n.665+30G>T)
c.305+30G>T (n.305+30G>T)
c.749+30G>T (n.749+30G>T)
 dbSNP
17g.7674151C=CA2245950894TP53c.782+30G= (n.782+30G=)
c.386+30G= (n.386+30G=)
c.503+30G= (n.503+30G=)
c.761+30G= (n.761+30G=)
c.665+30G= (n.665+30G=)
c.305+30G= (n.305+30G=)
c.749+30G= (n.749+30G=)
17g.7674151C>GCA2732985648TP53c.782+30G>C (n.782+30G>C)
c.386+30G>C (n.386+30G>C)
c.503+30G>C (n.503+30G>C)
c.761+30G>C (n.761+30G>C)
c.665+30G>C (n.665+30G>C)
c.305+30G>C (n.305+30G>C)
c.749+30G>C (n.749+30G>C)
 dbSNP
17g.7674151C>TCA2245950897TP53c.782+30G>A (n.782+30G>A)
c.386+30G>A (n.386+30G>A)
c.503+30G>A (n.503+30G>A)
c.761+30G>A (n.761+30G>A)
c.665+30G>A (n.665+30G>A)
c.305+30G>A (n.305+30G>A)
c.749+30G>A (n.749+30G>A)
 dbSNP gnomAD v4
17g.7674152A>GCA2733136124TP53c.782+29T>C (n.782+29T>C)
c.386+29T>C (n.386+29T>C)
c.503+29T>C (n.503+29T>C)
c.761+29T>C (n.761+29T>C)
c.665+29T>C (n.665+29T>C)
c.305+29T>C (n.305+29T>C)
c.749+29T>C (n.749+29T>C)
 dbSNP
17g.7674152A>TCA2733136110TP53c.782+29T>A (n.782+29T>A)
c.386+29T>A (n.386+29T>A)
c.503+29T>A (n.503+29T>A)
c.761+29T>A (n.761+29T>A)
c.665+29T>A (n.665+29T>A)
c.305+29T>A (n.305+29T>A)
c.749+29T>A (n.749+29T>A)
 dbSNP
17g.7674153G>ACA2733136127TP53c.782+28C>T (n.782+28C>T)
c.386+28C>T (n.386+28C>T)
c.503+28C>T (n.503+28C>T)
c.761+28C>T (n.761+28C>T)
c.665+28C>T (n.665+28C>T)
c.305+28C>T (n.305+28C>T)
c.749+28C>T (n.749+28C>T)
 dbSNP
17g.7674153G>CCA2635875919TP53c.782+28C>G (n.782+28C>G)
c.386+28C>G (n.386+28C>G)
c.503+28C>G (n.503+28C>G)
c.761+28C>G (n.761+28C>G)
c.665+28C>G (n.665+28C>G)
c.305+28C>G (n.305+28C>G)
c.749+28C>G (n.749+28C>G)
 gnomAD v4
17g.7674153G>TCA2635875920TP53c.782+28C>A (n.782+28C>A)
c.386+28C>A (n.386+28C>A)
c.503+28C>A (n.503+28C>A)
c.761+28C>A (n.761+28C>A)
c.665+28C>A (n.665+28C>A)
c.305+28C>A (n.305+28C>A)
c.749+28C>A (n.749+28C>A)
 gnomAD v4
17g.7674154T>CCA001673TP53c.782+27A>G (n.782+27A>G)
c.386+27A>G (n.386+27A>G)
c.503+27A>G (n.503+27A>G)
c.761+27A>G (n.761+27A>G)
c.665+27A>G (n.665+27A>G)
c.305+27A>G (n.305+27A>G)
c.749+27A>G (n.749+27A>G)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.7674154T=CA2245950898TP53c.782+27A= (n.782+27A=)
c.386+27A= (n.386+27A=)
c.503+27A= (n.503+27A=)
c.761+27A= (n.761+27A=)
c.665+27A= (n.665+27A=)
c.305+27A= (n.305+27A=)
c.749+27A= (n.749+27A=)
17g.7674155G>ACA2733136128TP53c.782+26C>T (n.782+26C>T)
c.386+26C>T (n.386+26C>T)
c.503+26C>T (n.503+26C>T)
c.761+26C>T (n.761+26C>T)
c.665+26C>T (n.665+26C>T)
c.305+26C>T (n.305+26C>T)
c.749+26C>T (n.749+26C>T)
 dbSNP
17g.7674155G>CCA2733136129TP53c.782+26C>G (n.782+26C>G)
c.386+26C>G (n.386+26C>G)
c.503+26C>G (n.503+26C>G)
c.761+26C>G (n.761+26C>G)
c.665+26C>G (n.665+26C>G)
c.305+26C>G (n.305+26C>G)
c.749+26C>G (n.749+26C>G)
 dbSNP
17g.7674155G>TCA2635875924TP53c.782+26C>A (n.782+26C>A)
c.386+26C>A (n.386+26C>A)
c.503+26C>A (n.503+26C>A)
c.761+26C>A (n.761+26C>A)
c.665+26C>A (n.665+26C>A)
c.305+26C>A (n.305+26C>A)
c.749+26C>A (n.749+26C>A)
 gnomAD v4
17g.7674156T>ACA2733136130TP53c.782+25A>T (n.782+25A>T)
c.386+25A>T (n.386+25A>T)
c.503+25A>T (n.503+25A>T)
c.761+25A>T (n.761+25A>T)
c.665+25A>T (n.665+25A>T)
c.305+25A>T (n.305+25A>T)
c.749+25A>T (n.749+25A>T)
 dbSNP
17g.7674156T>GCA2733136131TP53c.782+25A>C (n.782+25A>C)
c.386+25A>C (n.386+25A>C)
c.503+25A>C (n.503+25A>C)
c.761+25A>C (n.761+25A>C)
c.665+25A>C (n.665+25A>C)
c.305+25A>C (n.305+25A>C)
c.749+25A>C (n.749+25A>C)
 dbSNP
17g.7674157G>ACA2733136132TP53c.782+24C>T (n.782+24C>T)
c.386+24C>T (n.386+24C>T)
c.503+24C>T (n.503+24C>T)
c.761+24C>T (n.761+24C>T)
c.665+24C>T (n.665+24C>T)
c.305+24C>T (n.305+24C>T)
c.749+24C>T (n.749+24C>T)
 dbSNP
17g.7674157G>CCA645588470TP53c.782+24C>G (n.782+24C>G)
c.386+24C>G (n.386+24C>G)
c.503+24C>G (n.503+24C>G)
c.761+24C>G (n.761+24C>G)
c.665+24C>G (n.665+24C>G)
c.305+24C>G (n.305+24C>G)
c.749+24C>G (n.749+24C>G)
 COSMIC
17g.7674157G>TCA645588471TP53c.782+24C>A (n.782+24C>A)
c.386+24C>A (n.386+24C>A)
c.503+24C>A (n.503+24C>A)
c.761+24C>A (n.761+24C>A)
c.665+24C>A (n.665+24C>A)
c.305+24C>A (n.305+24C>A)
c.749+24C>A (n.749+24C>A)
 gnomAD v4 COSMIC
17g.7674158C>ACA2733136137TP53c.782+23G>T (n.782+23G>T)
c.386+23G>T (n.386+23G>T)
c.503+23G>T (n.503+23G>T)
c.761+23G>T (n.761+23G>T)
c.665+23G>T (n.665+23G>T)
c.305+23G>T (n.305+23G>T)
c.749+23G>T (n.749+23G>T)
 dbSNP
17g.7674158C>GCA2733136138TP53c.782+23G>C (n.782+23G>C)
c.386+23G>C (n.386+23G>C)
c.503+23G>C (n.503+23G>C)
c.761+23G>C (n.761+23G>C)
c.665+23G>C (n.665+23G>C)
c.305+23G>C (n.305+23G>C)
c.749+23G>C (n.749+23G>C)
 dbSNP
17g.7674158C>TCA2576230647TP53c.782+23G>A (n.782+23G>A)
c.386+23G>A (n.386+23G>A)
c.503+23G>A (n.503+23G>A)
c.761+23G>A (n.761+23G>A)
c.665+23G>A (n.665+23G>A)
c.305+23G>A (n.305+23G>A)
c.749+23G>A (n.749+23G>A)
 dbSNP gnomAD v4
17g.7674159A=CA2245950901TP53c.782+22T= (n.782+22T=)
c.386+22T= (n.386+22T=)
c.503+22T= (n.503+22T=)
c.761+22T= (n.761+22T=)
c.665+22T= (n.665+22T=)
c.305+22T= (n.305+22T=)
c.749+22T= (n.749+22T=)
17g.7674159A>CCA2733136141TP53c.782+22T>G (n.782+22T>G)
c.386+22T>G (n.386+22T>G)
c.503+22T>G (n.503+22T>G)
c.761+22T>G (n.761+22T>G)
c.665+22T>G (n.665+22T>G)
c.305+22T>G (n.305+22T>G)
c.749+22T>G (n.749+22T>G)
 dbSNP
17g.7674159A>GCA2733136140TP53c.782+22T>C (n.782+22T>C)
c.386+22T>C (n.386+22T>C)
c.503+22T>C (n.503+22T>C)
c.761+22T>C (n.761+22T>C)
c.665+22T>C (n.665+22T>C)
c.305+22T>C (n.305+22T>C)
c.749+22T>C (n.749+22T>C)
 dbSNP
17g.7674159A>TCA2733136139TP53c.782+22T>A (n.782+22T>A)
c.386+22T>A (n.386+22T>A)
c.503+22T>A (n.503+22T>A)
c.761+22T>A (n.761+22T>A)
c.665+22T>A (n.665+22T>A)
c.305+22T>A (n.305+22T>A)
c.749+22T>A (n.749+22T>A)
 dbSNP
17g.7674160G>ACA2245950908TP53c.782+21C>T (n.782+21C>T)
c.386+21C>T (n.386+21C>T)
c.503+21C>T (n.503+21C>T)
c.761+21C>T (n.761+21C>T)
c.665+21C>T (n.665+21C>T)
c.305+21C>T (n.305+21C>T)
c.749+21C>T (n.749+21C>T)
 dbSNP
17g.7674160G>CCA287486797TP53c.782+21C>G (n.782+21C>G)
c.386+21C>G (n.386+21C>G)
c.503+21C>G (n.503+21C>G)
c.761+21C>G (n.761+21C>G)
c.665+21C>G (n.665+21C>G)
c.305+21C>G (n.305+21C>G)
c.749+21C>G (n.749+21C>G)
 dbSNP gnomAD v3 gnomAD v4
17g.7674160G=CA2245950907TP53c.782+21C= (n.782+21C=)
c.386+21C= (n.386+21C=)
c.503+21C= (n.503+21C=)
c.761+21C= (n.761+21C=)
c.665+21C= (n.665+21C=)
c.305+21C= (n.305+21C=)
c.749+21C= (n.749+21C=)
17g.7674160G>TCA001679TP53c.782+21C>A (n.782+21C>A)
c.386+21C>A (n.386+21C>A)
c.503+21C>A (n.503+21C>A)
c.761+21C>A (n.761+21C>A)
c.665+21C>A (n.665+21C>A)
c.305+21C>A (n.305+21C>A)
c.749+21C>A (n.749+21C>A)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.7674161_7674237dupCA913190585TP53c.727_782+21dup
c.331_386+21dup
c.448_503+21dup
c.706_761+21dup
c.610_665+21dup
c.250_305+21dup
c.694_749+21dup
 ClinVar dbSNP
17g.7674161G>ACA656753453TP53c.782+20C>T (n.782+20C>T)
c.386+20C>T (n.386+20C>T)
c.503+20C>T (n.503+20C>T)
c.761+20C>T (n.761+20C>T)
c.665+20C>T (n.665+20C>T)
c.305+20C>T (n.305+20C>T)
c.749+20C>T (n.749+20C>T)
 dbSNP COSMIC
17g.7674161G>TCA2576230648TP53c.782+20C>A (n.782+20C>A)
c.386+20C>A (n.386+20C>A)
c.503+20C>A (n.503+20C>A)
c.761+20C>A (n.761+20C>A)
c.665+20C>A (n.665+20C>A)
c.305+20C>A (n.305+20C>A)
c.749+20C>A (n.749+20C>A)
 dbSNP gnomAD v4
17g.7674162G>ACA2590177398TP53c.782+19C>T (n.782+19C>T)
c.386+19C>T (n.386+19C>T)
c.503+19C>T (n.503+19C>T)
c.761+19C>T (n.761+19C>T)
c.665+19C>T (n.665+19C>T)
c.305+19C>T (n.305+19C>T)
c.749+19C>T (n.749+19C>T)
 dbSNP gnomAD v3 gnomAD v4
17g.7674162G>CCA645588472TP53c.782+19C>G (n.782+19C>G)
c.386+19C>G (n.386+19C>G)
c.503+19C>G (n.503+19C>G)
c.761+19C>G (n.761+19C>G)
c.665+19C>G (n.665+19C>G)
c.305+19C>G (n.305+19C>G)
c.749+19C>G (n.749+19C>G)
 dbSNP COSMIC
17g.7674162G>TCA2635875939TP53c.782+19C>A (n.782+19C>A)
c.386+19C>A (n.386+19C>A)
c.503+19C>A (n.503+19C>A)
c.761+19C>A (n.761+19C>A)
c.665+19C>A (n.665+19C>A)
c.305+19C>A (n.305+19C>A)
c.749+19C>A (n.749+19C>A)
 gnomAD v4
17g.7674163T>ACA645588473TP53c.782+18A>T (n.782+18A>T)
c.386+18A>T (n.386+18A>T)
c.503+18A>T (n.503+18A>T)
c.761+18A>T (n.761+18A>T)
c.665+18A>T (n.665+18A>T)
c.305+18A>T (n.305+18A>T)
c.749+18A>T (n.749+18A>T)
 COSMIC
17g.7674163T>CCA2573154649TP53c.782+18A>G (n.782+18A>G)
c.386+18A>G (n.386+18A>G)
c.503+18A>G (n.503+18A>G)
c.761+18A>G (n.761+18A>G)
c.665+18A>G (n.665+18A>G)
c.305+18A>G (n.305+18A>G)
c.749+18A>G (n.749+18A>G)
 ClinVar dbSNP
17g.7674163T>GCA2245950913TP53c.782+18A>C (n.782+18A>C)
c.386+18A>C (n.386+18A>C)
c.503+18A>C (n.503+18A>C)
c.761+18A>C (n.761+18A>C)
c.665+18A>C (n.665+18A>C)
c.305+18A>C (n.305+18A>C)
c.749+18A>C (n.749+18A>C)
 dbSNP
17g.7674163T=CA2245950912TP53c.782+18A= (n.782+18A=)
c.386+18A= (n.386+18A=)
c.503+18A= (n.503+18A=)
c.761+18A= (n.761+18A=)
c.665+18A= (n.665+18A=)
c.305+18A= (n.305+18A=)
c.749+18A= (n.749+18A=)
17g.7674164G>ACA000413TP53c.782+17C>T (n.782+17C>T)
c.386+17C>T (n.386+17C>T)
c.503+17C>T (n.503+17C>T)
c.761+17C>T (n.761+17C>T)
c.665+17C>T (n.665+17C>T)
c.305+17C>T (n.305+17C>T)
c.749+17C>T (n.749+17C>T)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.7674164G=CA2245950917TP53c.782+17C= (n.782+17C=)
c.386+17C= (n.386+17C=)
c.503+17C= (n.503+17C=)
c.761+17C= (n.761+17C=)
c.665+17C= (n.665+17C=)
c.305+17C= (n.305+17C=)
c.749+17C= (n.749+17C=)
17g.7674164G>TCA645588474TP53c.782+17C>A (n.782+17C>A)
c.386+17C>A (n.386+17C>A)
c.503+17C>A (n.503+17C>A)
c.761+17C>A (n.761+17C>A)
c.665+17C>A (n.665+17C>A)
c.305+17C>A (n.305+17C>A)
c.749+17C>A (n.749+17C>A)
 gnomAD v4 COSMIC
17g.7674165G>ACA2635875947TP53c.782+16C>T (n.782+16C>T)
c.386+16C>T (n.386+16C>T)
c.503+16C>T (n.503+16C>T)
c.761+16C>T (n.761+16C>T)
c.665+16C>T (n.665+16C>T)
c.305+16C>T (n.305+16C>T)
c.749+16C>T (n.749+16C>T)
 dbSNP gnomAD v4
17g.7674165G>TCA2635875949TP53c.782+16C>A (n.782+16C>A)
c.386+16C>A (n.386+16C>A)
c.503+16C>A (n.503+16C>A)
c.761+16C>A (n.761+16C>A)
c.665+16C>A (n.665+16C>A)
c.305+16C>A (n.305+16C>A)
c.749+16C>A (n.749+16C>A)
 gnomAD v4
17g.7674166C>ACA2733136143TP53c.782+15G>T (n.782+15G>T)
c.386+15G>T (n.386+15G>T)
c.503+15G>T (n.503+15G>T)
c.761+15G>T (n.761+15G>T)
c.665+15G>T (n.665+15G>T)
c.305+15G>T (n.305+15G>T)
c.749+15G>T (n.749+15G>T)
 dbSNP
17g.7674166C>GCA2733136144TP53c.782+15G>C (n.782+15G>C)
c.386+15G>C (n.386+15G>C)
c.503+15G>C (n.503+15G>C)
c.761+15G>C (n.761+15G>C)
c.665+15G>C (n.665+15G>C)
c.305+15G>C (n.305+15G>C)
c.749+15G>C (n.749+15G>C)
 dbSNP
17g.7674166C>TCA2733136142TP53c.782+15G>A (n.782+15G>A)
c.386+15G>A (n.386+15G>A)
c.503+15G>A (n.503+15G>A)
c.761+15G>A (n.761+15G>A)
c.665+15G>A (n.665+15G>A)
c.305+15G>A (n.305+15G>A)
c.749+15G>A (n.749+15G>A)
 dbSNP
17g.7674167A=CA2245950920TP53c.782+14T= (n.782+14T=)
c.386+14T= (n.386+14T=)
c.503+14T= (n.503+14T=)
c.761+14T= (n.761+14T=)
c.665+14T= (n.665+14T=)
c.305+14T= (n.305+14T=)
c.749+14T= (n.749+14T=)
17g.7674167A>CCA624865116TP53c.782+14T>G (n.782+14T>G)
c.386+14T>G (n.386+14T>G)
c.503+14T>G (n.503+14T>G)
c.761+14T>G (n.761+14T>G)
c.665+14T>G (n.665+14T>G)
c.305+14T>G (n.305+14T>G)
c.749+14T>G (n.749+14T>G)
 ClinVar dbSNP gnomAD v2 gnomAD v4
17g.7674167A>TCA775170127TP53c.782+14T>A (n.782+14T>A)
c.386+14T>A (n.386+14T>A)
c.503+14T>A (n.503+14T>A)
c.761+14T>A (n.761+14T>A)
c.665+14T>A (n.665+14T>A)
c.305+14T>A (n.305+14T>A)
c.749+14T>A (n.749+14T>A)
 dbSNP
17g.7674168A>GCA2733136146TP53c.782+13T>C (n.782+13T>C)
c.386+13T>C (n.386+13T>C)
c.503+13T>C (n.503+13T>C)
c.761+13T>C (n.761+13T>C)
c.665+13T>C (n.665+13T>C)
c.305+13T>C (n.305+13T>C)
c.749+13T>C (n.749+13T>C)
 dbSNP
17g.7674168A>TCA2733136145TP53c.782+13T>A (n.782+13T>A)
c.386+13T>A (n.386+13T>A)
c.503+13T>A (n.503+13T>A)
c.761+13T>A (n.761+13T>A)
c.665+13T>A (n.665+13T>A)
c.305+13T>A (n.305+13T>A)
c.749+13T>A (n.749+13T>A)
 dbSNP
17g.7674171_7674187delCA2695200374TP53c.779_782+13del
c.383_386+13del
c.500_503+13del
c.758_761+13del
c.662_665+13del
c.302_305+13del
c.746_749+13del
 ClinVar
17g.7674169G>ACA000411TP53c.782+12C>T (n.782+12C>T)
c.386+12C>T (n.386+12C>T)
c.503+12C>T (n.503+12C>T)
c.761+12C>T (n.761+12C>T)
c.665+12C>T (n.665+12C>T)
c.305+12C>T (n.305+12C>T)
c.749+12C>T (n.749+12C>T)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
17g.7674169G>CCA2732922985TP53c.782+12C>G (n.782+12C>G)
c.386+12C>G (n.386+12C>G)
c.503+12C>G (n.503+12C>G)
c.761+12C>G (n.761+12C>G)
c.665+12C>G (n.665+12C>G)
c.305+12C>G (n.305+12C>G)
c.749+12C>G (n.749+12C>G)
 dbSNP
17g.7674169G=CA2245950923TP53c.782+12C= (n.782+12C=)
c.386+12C= (n.386+12C=)
c.503+12C= (n.503+12C=)
c.761+12C= (n.761+12C=)
c.665+12C= (n.665+12C=)
c.305+12C= (n.305+12C=)
c.749+12C= (n.749+12C=)
17g.7674170T>ACA645588475TP53c.782+11A>T (n.782+11A>T)
c.386+11A>T (n.386+11A>T)
c.503+11A>T (n.503+11A>T)
c.761+11A>T (n.761+11A>T)
c.665+11A>T (n.665+11A>T)
c.305+11A>T (n.305+11A>T)
c.749+11A>T (n.749+11A>T)
 dbSNP COSMIC
17g.7674170T>CCA2733136147TP53c.782+11A>G (n.782+11A>G)
c.386+11A>G (n.386+11A>G)
c.503+11A>G (n.503+11A>G)
c.761+11A>G (n.761+11A>G)
c.665+11A>G (n.665+11A>G)
c.305+11A>G (n.305+11A>G)
c.749+11A>G (n.749+11A>G)
 dbSNP
17g.7674170T>GCA2635875966TP53c.782+11A>C (n.782+11A>C)
c.386+11A>C (n.386+11A>C)
c.503+11A>C (n.503+11A>C)
c.761+11A>C (n.761+11A>C)
c.665+11A>C (n.665+11A>C)
c.305+11A>C (n.305+11A>C)
c.749+11A>C (n.749+11A>C)
 dbSNP gnomAD v4
17g.7674170_7674179delCA645588476TP53c.782+2_782+11del (n.782+2_782+11del)
c.386+2_386+11del (n.386+2_386+11del)
c.503+2_503+11del (n.503+2_503+11del)
c.761+2_761+11del (n.761+2_761+11del)
c.665+2_665+11del (n.665+2_665+11del)
c.305+2_305+11del (n.305+2_305+11del)
c.749+2_749+11del (n.749+2_749+11del)
 COSMIC
17g.7674171G>ACA001695TP53c.782+10C>T (n.782+10C>T)
c.386+10C>T (n.386+10C>T)
c.503+10C>T (n.503+10C>T)
c.761+10C>T (n.761+10C>T)
c.665+10C>T (n.665+10C>T)
c.305+10C>T (n.305+10C>T)
c.749+10C>T (n.749+10C>T)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.7674171G=CA2245950927TP53c.782+10C= (n.782+10C=)
c.386+10C= (n.386+10C=)
c.503+10C= (n.503+10C=)
c.761+10C= (n.761+10C=)
c.665+10C= (n.665+10C=)
c.305+10C= (n.305+10C=)
c.749+10C= (n.749+10C=)
17g.7674171G>TCA497716655TP53c.782+10C>A (n.782+10C>A)
c.386+10C>A (n.386+10C>A)
c.503+10C>A (n.503+10C>A)
c.761+10C>A (n.761+10C>A)
c.665+10C>A (n.665+10C>A)
c.305+10C>A (n.305+10C>A)
c.749+10C>A (n.749+10C>A)
 ClinVar gnomAD v4 COSMIC
17g.7674172G>ACA2733136149TP53c.782+9C>T (n.782+9C>T)
c.386+9C>T (n.386+9C>T)
c.503+9C>T (n.503+9C>T)
c.761+9C>T (n.761+9C>T)
c.665+9C>T (n.665+9C>T)
c.305+9C>T (n.305+9C>T)
c.749+9C>T (n.749+9C>T)
 dbSNP
17g.7674172G>CCA2733136148TP53c.782+9C>G (n.782+9C>G)
c.386+9C>G (n.386+9C>G)
c.503+9C>G (n.503+9C>G)
c.761+9C>G (n.761+9C>G)
c.665+9C>G (n.665+9C>G)
c.305+9C>G (n.305+9C>G)
c.749+9C>G (n.749+9C>G)
 dbSNP
17g.7674172G>TCA2635875975TP53c.782+9C>A (n.782+9C>A)
c.386+9C>A (n.386+9C>A)
c.503+9C>A (n.503+9C>A)
c.761+9C>A (n.761+9C>A)
c.665+9C>A (n.665+9C>A)
c.305+9C>A (n.305+9C>A)
c.749+9C>A (n.749+9C>A)
 ClinVar gnomAD v4
17g.7674172_7674176delCA624865117TP53c.782+5_782+9del (n.782+5_782+9del)
c.386+5_386+9del (n.386+5_386+9del)
c.503+5_503+9del (n.503+5_503+9del)
c.761+5_761+9del (n.761+5_761+9del)
c.665+5_665+9del (n.665+5_665+9del)
c.305+5_305+9del (n.305+5_305+9del)
c.749+5_749+9del (n.749+5_749+9del)
 gnomAD v2
17g.7674173C>ACA915949525TP53c.782+8G>T (n.782+8G>T)
c.386+8G>T (n.386+8G>T)
c.503+8G>T (n.503+8G>T)
c.761+8G>T (n.761+8G>T)
c.665+8G>T (n.665+8G>T)
c.305+8G>T (n.305+8G>T)
c.749+8G>T (n.749+8G>T)
 ClinVar dbSNP
17g.7674173C=CA2245950933TP53c.782+8G= (n.782+8G=)
c.386+8G= (n.386+8G=)
c.503+8G= (n.503+8G=)
c.761+8G= (n.761+8G=)
c.665+8G= (n.665+8G=)
c.305+8G= (n.305+8G=)
c.749+8G= (n.749+8G=)
17g.7674173C>GCA2499224963TP53c.782+8G>C (n.782+8G>C)
c.386+8G>C (n.386+8G>C)
c.503+8G>C (n.503+8G>C)
c.761+8G>C (n.761+8G>C)
c.665+8G>C (n.665+8G>C)
c.305+8G>C (n.305+8G>C)
c.749+8G>C (n.749+8G>C)
 ClinVar dbSNP
17g.7674173C>TCA2732965399TP53c.782+8G>A (n.782+8G>A)
c.386+8G>A (n.386+8G>A)
c.503+8G>A (n.503+8G>A)
c.761+8G>A (n.761+8G>A)
c.665+8G>A (n.665+8G>A)
c.305+8G>A (n.305+8G>A)
c.749+8G>A (n.749+8G>A)
 dbSNP
17g.7674173_7674182delCA2580094824TP53c.781_782+8del
c.385_386+8del
c.502_503+8del
c.760_761+8del
c.664_665+8del
c.304_305+8del
c.748_749+8del
 ClinVar
17g.7674174T>ACA2580094825TP53c.782+7A>T (n.782+7A>T)
c.386+7A>T (n.386+7A>T)
c.503+7A>T (n.503+7A>T)
c.761+7A>T (n.761+7A>T)
c.665+7A>T (n.665+7A>T)
c.305+7A>T (n.305+7A>T)
c.749+7A>T (n.749+7A>T)
 ClinVar dbSNP
17g.7674174T>CCA2733136150TP53c.782+7A>G (n.782+7A>G)
c.386+7A>G (n.386+7A>G)
c.503+7A>G (n.503+7A>G)
c.761+7A>G (n.761+7A>G)
c.665+7A>G (n.665+7A>G)
c.305+7A>G (n.305+7A>G)
c.749+7A>G (n.749+7A>G)
 dbSNP
17g.7674174_7674175delinsTCCA2245950935TP53c.782+6_782+7delinsGA (n.782+6_782+7delinsGA)
c.386+6_386+7delinsGA (n.386+6_386+7delinsGA)
c.503+6_503+7delinsGA (n.503+6_503+7delinsGA)
c.761+6_761+7delinsGA (n.761+6_761+7delinsGA)
c.665+6_665+7delinsGA (n.665+6_665+7delinsGA)
c.305+6_305+7delinsGA (n.305+6_305+7delinsGA)
c.749+6_749+7delinsGA (n.749+6_749+7delinsGA)
17g.7674174_7674179delinsTCCTGACA2245950936TP53c.782+2_782+7delinsTCAGGA (n.782+2_782+7delinsTCAGGA)
c.386+2_386+7delinsTCAGGA (n.386+2_386+7delinsTCAGGA)
c.503+2_503+7delinsTCAGGA (n.503+2_503+7delinsTCAGGA)
c.761+2_761+7delinsTCAGGA (n.761+2_761+7delinsTCAGGA)
c.665+2_665+7delinsTCAGGA (n.665+2_665+7delinsTCAGGA)
c.305+2_305+7delinsTCAGGA (n.305+2_305+7delinsTCAGGA)
c.749+2_749+7delinsTCAGGA (n.749+2_749+7delinsTCAGGA)
17g.7674174_7674182delCA645588477TP53c.781_782+7del
c.385_386+7del
c.502_503+7del
c.760_761+7del
c.664_665+7del
c.304_305+7del
c.748_749+7del
 COSMIC
17g.7674175C>ACA2635875981TP53c.782+6G>T (n.782+6G>T)
c.386+6G>T (n.386+6G>T)
c.503+6G>T (n.503+6G>T)
c.761+6G>T (n.761+6G>T)
c.665+6G>T (n.665+6G>T)
c.305+6G>T (n.305+6G>T)
c.749+6G>T (n.749+6G>T)
 gnomAD v4
17g.7674175C=CA2245950942TP53c.782+6G= (n.782+6G=)
c.386+6G= (n.386+6G=)
c.503+6G= (n.503+6G=)
c.761+6G= (n.761+6G=)
c.665+6G= (n.665+6G=)
c.305+6G= (n.305+6G=)
c.749+6G= (n.749+6G=)
17g.7674175C>GCA2573154650TP53c.782+6G>C (n.782+6G>C)
c.386+6G>C (n.386+6G>C)
c.503+6G>C (n.503+6G>C)
c.761+6G>C (n.761+6G>C)
c.665+6G>C (n.665+6G>C)
c.305+6G>C (n.305+6G>C)
c.749+6G>C (n.749+6G>C)
 ClinVar dbSNP
17g.7674175C>TCA287486810TP53c.782+6G>A (n.782+6G>A)
c.386+6G>A (n.386+6G>A)
c.503+6G>A (n.503+6G>A)
c.761+6G>A (n.761+6G>A)
c.665+6G>A (n.665+6G>A)
c.305+6G>A (n.305+6G>A)
c.749+6G>A (n.749+6G>A)
 ClinVar dbSNP gnomAD v2 gnomAD v4
17g.7674176delCA348096TP53c.782+6del (n.782+6del)
c.386+6del (n.386+6del)
c.503+6del (n.503+6del)
c.761+6del (n.761+6del)
c.665+6del (n.665+6del)
c.305+6del (n.305+6del)
c.749+6del (n.749+6del)
 ClinVar dbSNP
17g.7674179_7674183delCA891844044TP53c.782+2_782+6del
c.386+2_386+6del
c.503+2_503+6del
c.761+2_761+6del
c.665+2_665+6del
c.305+2_305+6del
c.749+2_749+6del
 ClinVar dbSNP
17g.7674176C>ACA2733136151TP53c.782+5G>T (n.782+5G>T)
c.386+5G>T (n.386+5G>T)
c.503+5G>T (n.503+5G>T)
c.761+5G>T (n.761+5G>T)
c.665+5G>T (n.665+5G>T)
c.305+5G>T (n.305+5G>T)
c.749+5G>T (n.749+5G>T)
 dbSNP
17g.7674176C>GCA2580094827TP53c.782+5G>C (n.782+5G>C)
c.386+5G>C (n.386+5G>C)
c.503+5G>C (n.503+5G>C)
c.761+5G>C (n.761+5G>C)
c.665+5G>C (n.665+5G>C)
c.305+5G>C (n.305+5G>C)
c.749+5G>C (n.749+5G>C)
 ClinVar dbSNP
17g.7674176C>TCA891842238TP53c.782+5G>A (n.782+5G>A)
c.386+5G>A (n.386+5G>A)
c.503+5G>A (n.503+5G>A)
c.761+5G>A (n.761+5G>A)
c.665+5G>A (n.665+5G>A)
c.305+5G>A (n.305+5G>A)
c.749+5G>A (n.749+5G>A)
 ClinVar dbSNP gnomAD v4
17g.7674177T>ACA2733136152TP53c.782+4A>T (n.782+4A>T)
c.386+4A>T (n.386+4A>T)
c.503+4A>T (n.503+4A>T)
c.761+4A>T (n.761+4A>T)
c.665+4A>T (n.665+4A>T)
c.305+4A>T (n.305+4A>T)
c.749+4A>T (n.749+4A>T)
 dbSNP
17g.7674177T>CCA2733136153TP53c.782+4A>G (n.782+4A>G)
c.386+4A>G (n.386+4A>G)
c.503+4A>G (n.503+4A>G)
c.761+4A>G (n.761+4A>G)
c.665+4A>G (n.665+4A>G)
c.305+4A>G (n.305+4A>G)
c.749+4A>G (n.749+4A>G)
 dbSNP
17g.7674177T>GCA2580094828TP53c.782+4A>C (n.782+4A>C)
c.386+4A>C (n.386+4A>C)
c.503+4A>C (n.503+4A>C)
c.761+4A>C (n.761+4A>C)
c.665+4A>C (n.665+4A>C)
c.305+4A>C (n.305+4A>C)
c.749+4A>C (n.749+4A>C)
 ClinVar gnomAD v4
17g.7674178G>ACA891844045TP53c.782+3C>T (n.782+3C>T)
c.386+3C>T (n.386+3C>T)
c.503+3C>T (n.503+3C>T)
c.761+3C>T (n.761+3C>T)
c.665+3C>T (n.665+3C>T)
c.305+3C>T (n.305+3C>T)
c.749+3C>T (n.749+3C>T)
 ClinVar dbSNP gnomAD v4
17g.7674178G>CCA497716669TP53c.782+3C>G (n.782+3C>G)
c.386+3C>G (n.386+3C>G)
c.503+3C>G (n.503+3C>G)
c.761+3C>G (n.761+3C>G)
c.665+3C>G (n.665+3C>G)
c.305+3C>G (n.305+3C>G)
c.749+3C>G (n.749+3C>G)
 dbSNP COSMIC
17g.7674178G=CA2245950952TP53c.782+3C= (n.782+3C=)
c.386+3C= (n.386+3C=)
c.503+3C= (n.503+3C=)
c.761+3C= (n.761+3C=)
c.665+3C= (n.665+3C=)
c.305+3C= (n.305+3C=)
c.749+3C= (n.749+3C=)
17g.7674178G>TCA658656542TP53c.782+3C>A (n.782+3C>A)
c.386+3C>A (n.386+3C>A)
c.503+3C>A (n.503+3C>A)
c.761+3C>A (n.761+3C>A)
c.665+3C>A (n.665+3C>A)
c.305+3C>A (n.305+3C>A)
c.749+3C>A (n.749+3C>A)
 ClinVar dbSNP gnomAD v4
17g.7674178_7674180delinsGACCA2245950948TP53c.782+1_782+3delinsGTC (n.782+1_782+3delinsGTC)
c.386+1_386+3delinsGTC (n.386+1_386+3delinsGTC)
c.503+1_503+3delinsGTC (n.503+1_503+3delinsGTC)
c.761+1_761+3delinsGTC (n.761+1_761+3delinsGTC)
c.665+1_665+3delinsGTC (n.665+1_665+3delinsGTC)
c.305+1_305+3delinsGTC (n.305+1_305+3delinsGTC)
c.749+1_749+3delinsGTC (n.749+1_749+3delinsGTC)
17g.7674180_7674185delCA2580094829TP53c.780_782+3del
c.384_386+3del
c.501_503+3del
c.759_761+3del
c.663_665+3del
c.303_305+3del
c.747_749+3del
 ClinVar
17g.7674179delCA2635876057TP53c.782+2del (n.782+2del)
c.386+2del (n.386+2del)
c.503+2del (n.503+2del)
c.761+2del (n.761+2del)
c.665+2del (n.665+2del)
c.305+2del (n.305+2del)
c.749+2del (n.749+2del)
 gnomAD v4
17g.7674179A=CA2245950961TP53c.782+2T= (n.782+2T=)
c.386+2T= (n.386+2T=)
c.503+2T= (n.503+2T=)
c.761+2T= (n.761+2T=)
c.665+2T= (n.665+2T=)
c.305+2T= (n.305+2T=)
c.749+2T= (n.749+2T=)
17g.7674179A>CCA10580920TP53c.782+2T>G (n.782+2T>G)
c.386+2T>G (n.386+2T>G)
c.503+2T>G (n.503+2T>G)
c.761+2T>G (n.761+2T>G)
c.665+2T>G (n.665+2T>G)
c.305+2T>G (n.305+2T>G)
c.749+2T>G (n.749+2T>G)
 ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7674179A>GCA397837521TP53c.782+2T>C (n.782+2T>C)
c.386+2T>C (n.386+2T>C)
c.503+2T>C (n.503+2T>C)
c.761+2T>C (n.761+2T>C)
c.665+2T>C (n.665+2T>C)
c.305+2T>C (n.305+2T>C)
c.749+2T>C (n.749+2T>C)
 ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7674179A>TCA397837526TP53c.782+2T>A (n.782+2T>A)
c.386+2T>A (n.386+2T>A)
c.503+2T>A (n.503+2T>A)
c.761+2T>A (n.761+2T>A)
c.665+2T>A (n.665+2T>A)
c.305+2T>A (n.305+2T>A)
c.749+2T>A (n.749+2T>A)
 ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7674179_7674180delCA624865118TP53c.782+1_782+2del (n.782+1_782+2del)
c.386+1_386+2del (n.386+1_386+2del)
c.503+1_503+2del (n.503+1_503+2del)
c.761+1_761+2del (n.761+1_761+2del)
c.665+1_665+2del (n.665+1_665+2del)
c.305+1_305+2del (n.305+1_305+2del)
c.749+1_749+2del (n.749+1_749+2del)
 dbSNP gnomAD v2
17g.7674180C>ACA397837531TP53c.782+1G>T (n.782+1G>T)
c.386+1G>T (n.386+1G>T)
c.503+1G>T (n.503+1G>T)
c.761+1G>T (n.761+1G>T)
c.665+1G>T (n.665+1G>T)
c.305+1G>T (n.305+1G>T)
c.749+1G>T (n.749+1G>T)
 ClinVar dbSNP
17g.7674180C=CA2245950970TP53c.782+1G= (n.782+1G=)
c.386+1G= (n.386+1G=)
c.503+1G= (n.503+1G=)
c.761+1G= (n.761+1G=)
c.665+1G= (n.665+1G=)
c.305+1G= (n.305+1G=)
c.749+1G= (n.749+1G=)
17g.7674180C>GCA397837534TP53c.782+1G>C (n.782+1G>C)
c.386+1G>C (n.386+1G>C)
c.503+1G>C (n.503+1G>C)
c.761+1G>C (n.761+1G>C)
c.665+1G>C (n.665+1G>C)
c.305+1G>C (n.305+1G>C)
c.749+1G>C (n.749+1G>C)
 COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7674180C>TCA10575449TP53c.782+1G>A (n.782+1G>A)
c.386+1G>A (n.386+1G>A)
c.503+1G>A (n.503+1G>A)
c.761+1G>A (n.761+1G>A)
c.665+1G>A (n.665+1G>A)
c.305+1G>A (n.305+1G>A)
c.749+1G>A (n.749+1G>A)
 ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7674180_7674181delinsTTCA645588480TP53c.782_782+1delinsAA
c.386_386+1delinsAA
c.503_503+1delinsAA
c.761_761+1delinsAA
c.665_665+1delinsAA
c.305_305+1delinsAA
c.749_749+1delinsAA
 COSMIC
17g.7674181delCA645588479TP53c.782+1del
c.386+1del
c.503+1del
c.761+1del
c.665+1del
c.305+1del
c.749+1del
 COSMIC
17g.7674182_7674192delCA645588478TP53c.773_782+1del
c.377_386+1del
c.494_503+1del
c.752_761+1del
c.656_665+1del
c.296_305+1del
c.740_749+1del
 COSMIC
17g.7674181C>ACA397837540TP53c.782G>T (p.Ser261Ile)
c.386G>T (p.Ser129Ile)
c.503G>T (p.Ser168Ile)
c.761G>T (p.Ser254Ile)
c.782G>T (p.Arg261Met)
c.665G>T (p.Ser222Ile)
c.305G>T (p.Ser102Ile)
c.749G>T (p.Ser250Ile)
 dbSNP
17g.7674181C=CA2245950981TP53c.782G= (p.Ser261=)
c.386G= (p.Ser129=)
c.503G= (p.Ser168=)
c.761G= (p.Ser254=)
c.782G= (p.Arg261=)
c.665G= (p.Ser222=)
c.305G= (p.Ser102=)
c.749G= (p.Ser250=)
17g.7674181C>GCA000415TP53c.782G>C (p.Ser261Thr)
c.386G>C (p.Ser129Thr)
c.503G>C (p.Ser168Thr)
c.761G>C (p.Ser254Thr)
c.782G>C (p.Arg261Thr)
c.665G>C (p.Ser222Thr)
c.305G>C (p.Ser102Thr)
c.749G>C (p.Ser250Thr)
 ClinVar dbSNP COSMIC COSMIC COSMIC
17g.7674181C>TCA397837548TP53c.782G>A (p.Ser261Asn)
c.386G>A (p.Ser129Asn)
c.503G>A (p.Ser168Asn)
c.761G>A (p.Ser254Asn)
c.782G>A (p.Arg261Lys)
c.665G>A (p.Ser222Asn)
c.305G>A (p.Ser102Asn)
c.749G>A (p.Ser250Asn)
 dbSNP COSMIC
17g.7674181_7674186delCA645588481TP53c.777_782del (p.Ser260_Ser261del)
c.381_386del (p.Ser128_Ser129del)
c.498_503del (p.Ser167_Ser168del)
c.756_761del (p.Ser253_Ser254del)
c.777_782del (p.Asp259_Arg261delinsGlu)
c.660_665del (p.Ser221_Ser222del)
c.300_305del (p.Ser101_Ser102del)
c.744_749del (p.Ser249_Ser250del)
 COSMIC
17g.7674181_7674182insAGGGCA624865119TP53c.781_782insCCCT (p.Ser261ThrfsTer4)
c.385_386insCCCT (p.Ser129ThrfsTer4)
c.502_503insCCCT (p.Ser168ThrfsTer4)
c.760_761insCCCT (p.Ser254ThrfsTer4)
c.781_782insCCCT (p.Arg261ThrfsTer?)
c.664_665insCCCT (p.Ser222ThrfsTer4)
c.304_305insCCCT (p.Ser102ThrfsTer4)
c.748_749insCCCT (p.Ser250ThrfsTer4)
 dbSNP gnomAD v2
17g.7674182delCA497716702TP53c.781del (p.Ser261ValfsTer?)
c.385del (p.Ser129ValfsTer?)
c.502del (p.Ser168ValfsTer?)
c.760del (p.Ser254ValfsTer?)
c.781del (p.Arg261GlyfsTer8)
c.664del (p.Ser222ValfsTer?)
c.304del (p.Ser102ValfsTer?)
c.748del (p.Ser250ValfsTer?)
 ClinVar COSMIC
17g.7674182T>ACA397837563TP53c.781A>T (p.Ser261Cys)
c.385A>T (p.Ser129Cys)
c.502A>T (p.Ser168Cys)
c.760A>T (p.Ser254Cys)
c.781A>T (p.Arg261Trp)
c.664A>T (p.Ser222Cys)
c.304A>T (p.Ser102Cys)
c.748A>T (p.Ser250Cys)
 COSMIC
17g.7674182T>CCA397837559TP53c.781A>G (p.Ser261Gly)
c.385A>G (p.Ser129Gly)
c.502A>G (p.Ser168Gly)
c.760A>G (p.Ser254Gly)
c.781A>G (p.Arg261Gly)
c.664A>G (p.Ser222Gly)
c.304A>G (p.Ser102Gly)
c.748A>G (p.Ser250Gly)
 ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7674182T>GCA397837554TP53c.781A>C (p.Ser261Arg)
c.385A>C (p.Ser129Arg)
c.502A>C (p.Ser168Arg)
c.760A>C (p.Ser254Arg)
c.781A>C (p.Arg261=)
c.664A>C (p.Ser222Arg)
c.304A>C (p.Ser102Arg)
c.748A>C (p.Ser250Arg)
 COSMIC
17g.7674182_7674183delinsTGCA2245950983TP53c.780_781delinsCA (p.Ser260=)
c.384_385delinsCA (p.Ser128=)
c.501_502delinsCA (p.Ser167=)
c.759_760delinsCA (p.Ser253=)
c.663_664delinsCA (p.Ser221=)
c.303_304delinsCA (p.Ser101=)
c.747_748delinsCA (p.Ser249=)
17g.7674182_7674184delCA2697552063TP53c.779_781del (p.Ser260_Ser261delinsCys)
c.383_385del (p.Ser128_Ser129delinsCys)
c.500_502del (p.Ser167_Ser168delinsCys)
c.758_760del (p.Ser253_Ser254delinsCys)
c.779_781del (p.Ser260_Arg261delinsTrp)
c.662_664del (p.Ser221_Ser222delinsCys)
c.302_304del (p.Ser101_Ser102delinsCys)
c.746_748del (p.Ser249_Ser250delinsCys)
 ClinVar
17g.7674182_7674183insACA645588482TP53c.780_781insT (p.Ser261Ter)
c.384_385insT (p.Ser129Ter)
c.501_502insT (p.Ser168Ter)
c.759_760insT (p.Ser254Ter)
c.780_781insT (p.Arg261Ter)
c.663_664insT (p.Ser222Ter)
c.303_304insT (p.Ser102Ter)
c.747_748insT (p.Ser250Ter)
 COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7674183G>ACA287486813TP53c.780C>T (p.Ser260=)
c.384C>T (p.Ser128=)
c.501C>T (p.Ser167=)
c.759C>T (p.Ser253=)
c.663C>T (p.Ser221=)
c.303C>T (p.Ser101=)
c.747C>T (p.Ser249=)
 dbSNP COSMIC
17g.7674183G>CCA497716707TP53c.780C>G (p.Ser260=)
c.384C>G (p.Ser128=)
c.501C>G (p.Ser167=)
c.759C>G (p.Ser253=)
c.663C>G (p.Ser221=)
c.303C>G (p.Ser101=)
c.747C>G (p.Ser249=)
 dbSNP
17g.7674183G=CA2245950987TP53c.780C= (p.Ser260=)
c.384C= (p.Ser128=)
c.501C= (p.Ser167=)
c.759C= (p.Ser253=)
c.663C= (p.Ser221=)
c.303C= (p.Ser101=)
c.747C= (p.Ser249=)
17g.7674183G>TCA497716711TP53c.780C>A (p.Ser260=)
c.384C>A (p.Ser128=)
c.501C>A (p.Ser167=)
c.759C>A (p.Ser253=)
c.663C>A (p.Ser221=)
c.303C>A (p.Ser101=)
c.747C>A (p.Ser249=)
17g.7674184delCA497716715TP53c.780del (p.Ser261ValfsTer?)
c.384del (p.Ser129ValfsTer?)
c.501del (p.Ser168ValfsTer?)
c.759del (p.Ser254ValfsTer?)
c.780del (p.Arg261GlyfsTer8)
c.663del (p.Ser222ValfsTer?)
c.303del (p.Ser102ValfsTer?)
c.747del (p.Ser250ValfsTer?)
 dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7674184_7674186delCA645588483TP53c.778_780del (p.Ser260del)
c.382_384del (p.Ser128del)
c.499_501del (p.Ser167del)
c.757_759del (p.Ser253del)
c.661_663del (p.Ser221del)
c.301_303del (p.Ser101del)
c.745_747del (p.Ser249del)
 COSMIC
17g.7674183_7674191delCA645588484TP53c.772_780del (p.Glu258_Ser260del)
c.376_384del (p.Glu126_Ser128del)
c.493_501del (p.Glu165_Ser167del)
c.751_759del (p.Glu251_Ser253del)
c.655_663del (p.Glu219_Ser221del)
c.295_303del (p.Glu99_Ser101del)
c.739_747del (p.Glu247_Ser249del)
 COSMIC
17g.7674184G>ACA397837574TP53c.779C>T (p.Ser260Phe)
c.383C>T (p.Ser128Phe)
c.500C>T (p.Ser167Phe)
c.758C>T (p.Ser253Phe)
c.662C>T (p.Ser221Phe)
c.302C>T (p.Ser101Phe)
c.746C>T (p.Ser249Phe)
 ClinVar dbSNP COSMIC
17g.7674184G>CCA397837584TP53c.779C>G (p.Ser260Cys)
c.383C>G (p.Ser128Cys)
c.500C>G (p.Ser167Cys)
c.758C>G (p.Ser253Cys)
c.662C>G (p.Ser221Cys)
c.302C>G (p.Ser101Cys)
c.746C>G (p.Ser249Cys)
 dbSNP COSMIC
17g.7674184G=CA2245950989TP53c.779C= (p.Ser260=)
c.383C= (p.Ser128=)
c.500C= (p.Ser167=)
c.758C= (p.Ser253=)
c.662C= (p.Ser221=)
c.302C= (p.Ser101=)
c.746C= (p.Ser249=)
17g.7674184G>TCA10580921TP53c.779C>A (p.Ser260Tyr)
c.383C>A (p.Ser128Tyr)
c.500C>A (p.Ser167Tyr)
c.758C>A (p.Ser253Tyr)
c.662C>A (p.Ser221Tyr)
c.302C>A (p.Ser101Tyr)
c.746C>A (p.Ser249Tyr)
 ClinVar dbSNP gnomAD v4 COSMIC
17g.7674185_7674186delCA645588487TP53c.778_779del (p.Ser260GlnfsTer3)
c.382_383del (p.Ser128GlnfsTer3)
c.499_500del (p.Ser167GlnfsTer3)
c.757_758del (p.Ser253GlnfsTer3)
c.778_779del (p.Ser260GlnfsTer?)
c.661_662del (p.Ser221GlnfsTer3)
c.301_302del (p.Ser101GlnfsTer3)
c.745_746del (p.Ser249GlnfsTer3)
 COSMIC
17g.7674185_7674194delCA645588485TP53c.770_779del (p.Leu257ProfsTer?)
c.374_383del (p.Leu125ProfsTer?)
c.491_500del (p.Leu164ProfsTer?)
c.749_758del (p.Leu250ProfsTer?)
c.770_779del (p.Leu257ProfsTer9)
c.653_662del (p.Leu218ProfsTer?)
c.293_302del (p.Leu98ProfsTer?)
c.737_746del (p.Leu246ProfsTer?)
 COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7674187_7674209delCA645588486TP53c.757_779del (p.Thr253GlnfsTer3)
c.361_383del (p.Thr121GlnfsTer3)
c.478_500del (p.Thr160GlnfsTer3)
c.736_758del (p.Thr246GlnfsTer3)
c.757_779del (p.Thr253GlnfsTer?)
c.640_662del (p.Thr214GlnfsTer3)
c.280_302del (p.Thr94GlnfsTer3)
c.724_746del (p.Thr242GlnfsTer3)
 COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7674184_7674185insCACA624865120TP53c.778_779insTG (p.Ser260LeufsTer?)
c.382_383insTG (p.Ser128LeufsTer?)
c.499_500insTG (p.Ser167LeufsTer?)
c.757_758insTG (p.Ser253LeufsTer?)
c.778_779insTG (p.Ser260LeufsTer10)
c.661_662insTG (p.Ser221LeufsTer?)
c.301_302insTG (p.Ser101LeufsTer?)
c.745_746insTG (p.Ser249LeufsTer?)
 dbSNP gnomAD v2
17g.7674185delCA497716729TP53c.778del (p.Ser260ProfsTer?)
c.382del (p.Ser128ProfsTer?)
c.499del (p.Ser167ProfsTer?)
c.757del (p.Ser253ProfsTer?)
c.778del (p.Ser260ProfsTer9)
c.661del (p.Ser221ProfsTer?)
c.301del (p.Ser101ProfsTer?)
c.745del (p.Ser249ProfsTer?)
 COSMIC
17g.7674185A>CCA397837593TP53c.778T>G (p.Ser260Ala)
c.382T>G (p.Ser128Ala)
c.499T>G (p.Ser167Ala)
c.757T>G (p.Ser253Ala)
c.661T>G (p.Ser221Ala)
c.301T>G (p.Ser101Ala)
c.745T>G (p.Ser249Ala)
 COSMIC
17g.7674185A>GCA397837596TP53c.778T>C (p.Ser260Pro)
c.382T>C (p.Ser128Pro)
c.499T>C (p.Ser167Pro)
c.757T>C (p.Ser253Pro)
c.661T>C (p.Ser221Pro)
c.301T>C (p.Ser101Pro)
c.745T>C (p.Ser249Pro)
 dbSNP COSMIC
17g.7674185A>TCA397837600TP53c.778T>A (p.Ser260Thr)
c.382T>A (p.Ser128Thr)
c.499T>A (p.Ser167Thr)
c.757T>A (p.Ser253Thr)
c.661T>A (p.Ser221Thr)
c.301T>A (p.Ser101Thr)
c.745T>A (p.Ser249Thr)
 dbSNP
17g.7674185dupCA2635876077TP53c.778dup (p.Ser260PhefsTer4)
c.382dup (p.Ser128PhefsTer4)
c.499dup (p.Ser167PhefsTer4)
c.757dup (p.Ser253PhefsTer4)
c.778dup (p.Ser260PhefsTer?)
c.661dup (p.Ser221PhefsTer4)
c.301dup (p.Ser101PhefsTer4)
c.745dup (p.Ser249PhefsTer4)
 gnomAD v4
17g.7674185_7674191delCA645588488TP53c.772_778del (p.Glu258ProfsTer?)
c.376_382del (p.Glu126ProfsTer?)
c.493_499del (p.Glu165ProfsTer?)
c.751_757del (p.Glu251ProfsTer?)
c.772_778del (p.Glu258ProfsTer9)
c.655_661del (p.Glu219ProfsTer?)
c.295_301del (p.Glu99ProfsTer?)
c.739_745del (p.Glu247ProfsTer?)
 COSMIC
17g.7674186delCA497716735TP53c.777del (p.Ser260ProfsTer?)
c.381del (p.Ser128ProfsTer?)
c.498del (p.Ser167ProfsTer?)
c.756del (p.Ser253ProfsTer?)
c.777del (p.Ser260ProfsTer9)
c.660del (p.Ser221ProfsTer?)
c.300del (p.Ser101ProfsTer?)
c.744del (p.Ser249ProfsTer?)
 COSMIC
17g.7674186G>ACA497716739TP53c.777C>T (p.Asp259=)
c.381C>T (p.Asp127=)
c.498C>T (p.Asp166=)
c.756C>T (p.Asp252=)
c.660C>T (p.Asp220=)
c.300C>T (p.Asp100=)
c.744C>T (p.Asp248=)
 COSMIC
17g.7674186G>CCA397837612TP53c.777C>G (p.Asp259Glu)
c.381C>G (p.Asp127Glu)
c.498C>G (p.Asp166Glu)
c.756C>G (p.Asp252Glu)
c.660C>G (p.Asp220Glu)
c.300C>G (p.Asp100Glu)
c.744C>G (p.Asp248Glu)
 dbSNP
17g.7674186G>TCA397837614TP53c.777C>A (p.Asp259Glu)
c.381C>A (p.Asp127Glu)
c.498C>A (p.Asp166Glu)
c.756C>A (p.Asp252Glu)
c.660C>A (p.Asp220Glu)
c.300C>A (p.Asp100Glu)
c.744C>A (p.Asp248Glu)
 gnomAD v4 COSMIC
17g.7674186_7674187delinsAACA645588489TP53c.776_777delinsTT (p.Asp259Val)
c.380_381delinsTT (p.Asp127Val)
c.497_498delinsTT (p.Asp166Val)
c.755_756delinsTT (p.Asp252Val)
c.659_660delinsTT (p.Asp220Val)
c.299_300delinsTT (p.Asp100Val)
c.743_744delinsTT (p.Asp248Val)
 COSMIC
17g.7674187delCA645588491TP53c.776del (p.Asp259AlafsTer?)
c.380del (p.Asp127AlafsTer?)
c.497del (p.Asp166AlafsTer?)
c.755del (p.Asp252AlafsTer?)
c.776del (p.Asp259AlafsTer10)
c.659del (p.Asp220AlafsTer?)
c.299del (p.Asp100AlafsTer?)
c.743del (p.Asp248AlafsTer?)
 COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7674187T>ACA397837621TP53c.776A>T (p.Asp259Val)
c.380A>T (p.Asp127Val)
c.497A>T (p.Asp166Val)
c.755A>T (p.Asp252Val)
c.659A>T (p.Asp220Val)
c.299A>T (p.Asp100Val)
c.743A>T (p.Asp248Val)
 ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7674187T>CCA000408TP53c.776A>G (p.Asp259Gly)
c.380A>G (p.Asp127Gly)
c.497A>G (p.Asp166Gly)
c.755A>G (p.Asp252Gly)
c.659A>G (p.Asp220Gly)
c.299A>G (p.Asp100Gly)
c.743A>G (p.Asp248Gly)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
17g.7674187T>GCA397837636TP53c.776A>C (p.Asp259Ala)
c.380A>C (p.Asp127Ala)
c.497A>C (p.Asp166Ala)
c.755A>C (p.Asp252Ala)
c.659A>C (p.Asp220Ala)
c.299A>C (p.Asp100Ala)
c.743A>C (p.Asp248Ala)
 ClinVar dbSNP
17g.7674187T=CA2245950995TP53c.776A= (p.Asp259=)
c.380A= (p.Asp127=)
c.497A= (p.Asp166=)
c.755A= (p.Asp252=)
c.659A= (p.Asp220=)
c.299A= (p.Asp100=)
c.743A= (p.Asp248=)
17g.7674187_7674188delinsCTCA645588492TP53c.775_776delinsAG (p.Asp259Ser)
c.379_380delinsAG (p.Asp127Ser)
c.496_497delinsAG (p.Asp166Ser)
c.754_755delinsAG (p.Asp252Ser)
c.658_659delinsAG (p.Asp220Ser)
c.298_299delinsAG (p.Asp100Ser)
c.742_743delinsAG (p.Asp248Ser)
 COSMIC
17g.7674189_7674191delCA645588490TP53c.774_776del (p.Glu258del)
c.378_380del (p.Glu126del)
c.495_497del (p.Glu165del)
c.753_755del (p.Glu251del)
c.657_659del (p.Glu219del)
c.297_299del (p.Glu99del)
c.741_743del (p.Glu247del)
 COSMIC
17g.7674188delCA497716755TP53c.775del (p.Asp259ThrfsTer?)
c.379del (p.Asp127ThrfsTer?)
c.496del (p.Asp166ThrfsTer?)
c.754del (p.Asp252ThrfsTer?)
c.775del (p.Asp259ThrfsTer10)
c.658del (p.Asp220ThrfsTer?)
c.298del (p.Asp100ThrfsTer?)
c.742del (p.Asp248ThrfsTer?)
 COSMIC
17g.7674188C>ACA397837654TP53c.775G>T (p.Asp259Tyr)
c.379G>T (p.Asp127Tyr)
c.496G>T (p.Asp166Tyr)
c.754G>T (p.Asp252Tyr)
c.658G>T (p.Asp220Tyr)
c.298G>T (p.Asp100Tyr)
c.742G>T (p.Asp248Tyr)
 ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7674188C=CA2245950998TP53c.775G= (p.Asp259=)
c.379G= (p.Asp127=)
c.496G= (p.Asp166=)
c.754G= (p.Asp252=)
c.658G= (p.Asp220=)
c.298G= (p.Asp100=)
c.742G= (p.Asp248=)
17g.7674188C>GCA397837641TP53c.775G>C (p.Asp259His)
c.379G>C (p.Asp127His)
c.496G>C (p.Asp166His)
c.754G>C (p.Asp252His)
c.658G>C (p.Asp220His)
c.298G>C (p.Asp100His)
c.742G>C (p.Asp248His)
 ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7674188C>TCA397837639TP53c.775G>A (p.Asp259Asn)
c.379G>A (p.Asp127Asn)
c.496G>A (p.Asp166Asn)
c.754G>A (p.Asp252Asn)
c.658G>A (p.Asp220Asn)
c.298G>A (p.Asp100Asn)
c.742G>A (p.Asp248Asn)
 dbSNP gnomAD v4 COSMIC
17g.7674189_7674192delCA2573334898TP53c.772_775del (p.Glu258ThrfsTer?)
c.376_379del (p.Glu126ThrfsTer?)
c.493_496del (p.Glu165ThrfsTer?)
c.751_754del (p.Glu251ThrfsTer?)
c.772_775del (p.Glu258ThrfsTer10)
c.655_658del (p.Glu219ThrfsTer?)
c.295_298del (p.Glu99ThrfsTer?)
c.739_742del (p.Glu247ThrfsTer?)
17g.7674189T>ACA397837660TP53c.774A>T (p.Glu258Asp)
c.378A>T (p.Glu126Asp)
c.495A>T (p.Glu165Asp)
c.753A>T (p.Glu251Asp)
c.657A>T (p.Glu219Asp)
c.297A>T (p.Glu99Asp)
c.741A>T (p.Glu247Asp)
 dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7674189T>CCA497716762TP53c.774A>G (p.Glu258=)
c.378A>G (p.Glu126=)
c.495A>G (p.Glu165=)
c.753A>G (p.Glu251=)
c.657A>G (p.Glu219=)
c.297A>G (p.Glu99=)
c.741A>G (p.Glu247=)
 dbSNP
17g.7674189T>GCA397837662TP53c.774A>C (p.Glu258Asp)
c.378A>C (p.Glu126Asp)
c.495A>C (p.Glu165Asp)
c.753A>C (p.Glu251Asp)
c.657A>C (p.Glu219Asp)
c.297A>C (p.Glu99Asp)
c.741A>C (p.Glu247Asp)
 ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7674189T=CA2245951004TP53c.774A= (p.Glu258=)
c.378A= (p.Glu126=)
c.495A= (p.Glu165=)
c.753A= (p.Glu251=)
c.657A= (p.Glu219=)
c.297A= (p.Glu99=)
c.741A= (p.Glu247=)
17g.7674190delCA497716765TP53c.774del (p.Asp259ThrfsTer?)
c.378del (p.Asp127ThrfsTer?)
c.495del (p.Asp166ThrfsTer?)
c.753del (p.Asp252ThrfsTer?)
c.774del (p.Asp259ThrfsTer10)
c.657del (p.Asp220ThrfsTer?)
c.297del (p.Asp100ThrfsTer?)
c.741del (p.Asp248ThrfsTer?)
 COSMIC
17g.7674190_7674212delCA2695239762TP53c.752_774del (p.Ile251ArgfsTer5)
c.356_378del (p.Ile119ArgfsTer5)
c.473_495del (p.Ile158ArgfsTer5)
c.731_753del (p.Ile244ArgfsTer5)
c.752_774del (p.Ile251ArgfsTer?)
c.635_657del (p.Ile212ArgfsTer5)
c.275_297del (p.Ile92ArgfsTer5)
c.719_741del (p.Ile240ArgfsTer5)
17g.7674190T>ACA397837670TP53c.773A>T (p.Glu258Val)
c.377A>T (p.Glu126Val)
c.494A>T (p.Glu165Val)
c.752A>T (p.Glu251Val)
c.656A>T (p.Glu219Val)
c.296A>T (p.Glu99Val)
c.740A>T (p.Glu247Val)
 ClinVar dbSNP COSMIC
17g.7674190T>CCA16615703TP53c.773A>G (p.Glu258Gly)
c.377A>G (p.Glu126Gly)
c.494A>G (p.Glu165Gly)
c.752A>G (p.Glu251Gly)
c.656A>G (p.Glu219Gly)
c.296A>G (p.Glu99Gly)
c.740A>G (p.Glu247Gly)
 ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7674190T>GCA397837678TP53c.773A>C (p.Glu258Ala)
c.377A>C (p.Glu126Ala)
c.494A>C (p.Glu165Ala)
c.752A>C (p.Glu251Ala)
c.656A>C (p.Glu219Ala)
c.296A>C (p.Glu99Ala)
c.740A>C (p.Glu247Ala)
 ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7674190T=CA2245951014TP53c.773A= (p.Glu258=)
c.377A= (p.Glu126=)
c.494A= (p.Glu165=)
c.752A= (p.Glu251=)
c.656A= (p.Glu219=)
c.296A= (p.Glu99=)
c.740A= (p.Glu247=)
17g.7674190_7674191delinsAACA645588494TP53c.772_773delinsTT (p.Glu258Leu)
c.376_377delinsTT (p.Glu126Leu)
c.493_494delinsTT (p.Glu165Leu)
c.751_752delinsTT (p.Glu251Leu)
c.655_656delinsTT (p.Glu219Leu)
c.295_296delinsTT (p.Glu99Leu)
c.739_740delinsTT (p.Glu247Leu)
 COSMIC
17g.7674191_7674197delCA645588493TP53c.767_773del (p.Thr256LysfsTer?)
c.371_377del (p.Thr124LysfsTer?)
c.488_494del (p.Thr163LysfsTer?)
c.746_752del (p.Thr249LysfsTer?)
c.767_773del (p.Thr256LysfsTer11)
c.650_656del (p.Thr217LysfsTer?)
c.290_296del (p.Thr97LysfsTer?)
c.734_740del (p.Thr245LysfsTer?)
 COSMIC
17g.7674191C>ACA397837685TP53c.772G>T (p.Glu258Ter)
c.376G>T (p.Glu126Ter)
c.493G>T (p.Glu165Ter)
c.751G>T (p.Glu251Ter)
c.655G>T (p.Glu219Ter)
c.295G>T (p.Glu99Ter)
c.739G>T (p.Glu247Ter)
 ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7674191C=CA2245951025TP53c.772G= (p.Glu258=)
c.376G= (p.Glu126=)
c.493G= (p.Glu165=)
c.751G= (p.Glu251=)
c.655G= (p.Glu219=)
c.295G= (p.Glu99=)
c.739G= (p.Glu247=)
17g.7674191C>GCA397837688TP53c.772G>C (p.Glu258Gln)
c.376G>C (p.Glu126Gln)
c.493G>C (p.Glu165Gln)
c.751G>C (p.Glu251Gln)
c.655G>C (p.Glu219Gln)
c.295G>C (p.Glu99Gln)
c.739G>C (p.Glu247Gln)
 dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7674191C>TCA000406TP53c.772G>A (p.Glu258Lys)
c.376G>A (p.Glu126Lys)
c.493G>A (p.Glu165Lys)
c.751G>A (p.Glu251Lys)
c.655G>A (p.Glu219Lys)
c.295G>A (p.Glu99Lys)
c.739G>A (p.Glu247Lys)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
17g.7674191_7674192delinsTTCA645588496TP53c.771_772delinsAA (p.Glu258Lys)
c.375_376delinsAA (p.Glu126Lys)
c.492_493delinsAA (p.Glu165Lys)
c.750_751delinsAA (p.Glu251Lys)
c.654_655delinsAA (p.Glu219Lys)
c.294_295delinsAA (p.Glu99Lys)
c.738_739delinsAA (p.Glu247Lys)
 COSMIC
17g.7674192dupCA645588495TP53c.772dup (p.Glu258GlyfsTer6)
c.376dup (p.Glu126GlyfsTer6)
c.493dup (p.Glu165GlyfsTer6)
c.751dup (p.Glu251GlyfsTer6)
c.772dup (p.Glu258GlyfsTer?)
c.655dup (p.Glu219GlyfsTer6)
c.295dup (p.Glu99GlyfsTer6)
c.739dup (p.Glu247GlyfsTer6)
 COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7674192delCA497716781TP53c.772del (p.Glu258LysfsTer?)
c.376del (p.Glu126LysfsTer?)
c.493del (p.Glu165LysfsTer?)
c.751del (p.Glu251LysfsTer?)
c.772del (p.Glu258LysfsTer11)
c.655del (p.Glu219LysfsTer?)
c.295del (p.Glu99LysfsTer?)
c.739del (p.Glu247LysfsTer?)
 COSMIC
17g.7674191_7674198delCA891842239TP53c.765_772del (p.Thr256ArgfsTer5)
c.369_376del (p.Thr124ArgfsTer5)
c.486_493del (p.Thr163ArgfsTer5)
c.744_751del (p.Thr249ArgfsTer5)
c.765_772del (p.Thr256ArgfsTer?)
c.648_655del (p.Thr217ArgfsTer5)
c.288_295del (p.Thr97ArgfsTer5)
c.732_739del (p.Thr245ArgfsTer5)
17g.7674191_7674204delCA2580094835TP53c.759_772del (p.Ile254ArgfsTer5)
c.363_376del (p.Ile122ArgfsTer5)
c.480_493del (p.Ile161ArgfsTer5)
c.738_751del (p.Ile247ArgfsTer5)
c.759_772del (p.Ile254ArgfsTer?)
c.642_655del (p.Ile215ArgfsTer5)
c.282_295del (p.Ile95ArgfsTer5)
c.726_739del (p.Ile243ArgfsTer5)
 ClinVar
17g.7674192C>ACA497716787TP53c.771G>T (p.Leu257=)
c.375G>T (p.Leu125=)
c.492G>T (p.Leu164=)
c.750G>T (p.Leu250=)
c.654G>T (p.Leu218=)
c.294G>T (p.Leu98=)
c.738G>T (p.Leu246=)
 COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7674192C>GCA497716789TP53c.771G>C (p.Leu257=)
c.375G>C (p.Leu125=)
c.492G>C (p.Leu164=)
c.750G>C (p.Leu250=)
c.654G>C (p.Leu218=)
c.294G>C (p.Leu98=)
c.738G>C (p.Leu246=)
 dbSNP
17g.7674192C>TCA497716791TP53c.771G>A (p.Leu257=)
c.375G>A (p.Leu125=)
c.492G>A (p.Leu164=)
c.750G>A (p.Leu250=)
c.654G>A (p.Leu218=)
c.294G>A (p.Leu98=)
c.738G>A (p.Leu246=)
 ClinVar dbSNP COSMIC
17g.7674192_7674193delCA645588497TP53c.770_771del (p.Leu257ArgfsTer6)
c.374_375del (p.Leu125ArgfsTer6)
c.491_492del (p.Leu164ArgfsTer6)
c.749_750del (p.Leu250ArgfsTer6)
c.770_771del (p.Leu257ArgfsTer?)
c.653_654del (p.Leu218ArgfsTer6)
c.293_294del (p.Leu98ArgfsTer6)
c.737_738del (p.Leu246ArgfsTer6)
 COSMIC
17g.7674192_7674197delinsCAGTGTCA2245951029TP53c.766_771delinsACACTG (p.Thr256=)
c.370_375delinsACACTG (p.Thr124=)
c.487_492delinsACACTG (p.Thr163=)
c.745_750delinsACACTG (p.Thr249=)
c.649_654delinsACACTG (p.Thr217=)
c.289_294delinsACACTG (p.Thr97=)
c.733_738delinsACACTG (p.Thr245=)
17g.7674193delCA1139768484TP53c.770del (p.Leu257ArgfsTer?)
c.374del (p.Leu125ArgfsTer?)
c.491del (p.Leu164ArgfsTer?)
c.749del (p.Leu250ArgfsTer?)
c.770del (p.Leu257ArgfsTer12)
c.653del (p.Leu218ArgfsTer?)
c.293del (p.Leu98ArgfsTer?)
c.737del (p.Leu246ArgfsTer?)
17g.7674193A=CA2245951034TP53c.770T= (p.Leu257=)
c.374T= (p.Leu125=)
c.491T= (p.Leu164=)
c.749T= (p.Leu250=)
c.653T= (p.Leu218=)
c.293T= (p.Leu98=)
c.737T= (p.Leu246=)
17g.7674193A>CCA000404TP53c.770T>G (p.Leu257Arg)
c.374T>G (p.Leu125Arg)
c.491T>G (p.Leu164Arg)
c.749T>G (p.Leu250Arg)
c.653T>G (p.Leu218Arg)
c.293T>G (p.Leu98Arg)
c.737T>G (p.Leu246Arg)
 ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7674193A>GCA397837703TP53c.770T>C (p.Leu257Pro)
c.374T>C (p.Leu125Pro)
c.491T>C (p.Leu164Pro)
c.749T>C (p.Leu250Pro)
c.653T>C (p.Leu218Pro)
c.293T>C (p.Leu98Pro)
c.737T>C (p.Leu246Pro)
 ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7674193A>TCA000402TP53c.770T>A (p.Leu257Gln)
c.374T>A (p.Leu125Gln)
c.491T>A (p.Leu164Gln)
c.749T>A (p.Leu250Gln)
c.653T>A (p.Leu218Gln)
c.293T>A (p.Leu98Gln)
c.737T>A (p.Leu246Gln)
 ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7674193_7674197delinsTGGATGTCCTGACCTGCA10580922TP53c.766_770delinsCAGGTCAGGACATCCA (p.Thr256GlnfsTer?)
c.370_374delinsCAGGTCAGGACATCCA (p.Thr124GlnfsTer?)
c.487_491delinsCAGGTCAGGACATCCA (p.Thr163GlnfsTer?)
c.745_749delinsCAGGTCAGGACATCCA (p.Thr249GlnfsTer?)
c.766_770delinsCAGGTCAGGACATCCA (p.Thr256GlnfsTer17)
c.649_653delinsCAGGTCAGGACATCCA (p.Thr217GlnfsTer?)
c.289_293delinsCAGGTCAGGACATCCA (p.Thr97GlnfsTer?)
c.733_737delinsCAGGTCAGGACATCCA (p.Thr245GlnfsTer?)
 ClinVar dbSNP
17g.7674194delCA497716803TP53c.769del (p.Leu257TrpfsTer?)
c.373del (p.Leu125TrpfsTer?)
c.490del (p.Leu164TrpfsTer?)
c.748del (p.Leu250TrpfsTer?)
c.769del (p.Leu257TrpfsTer12)
c.652del (p.Leu218TrpfsTer?)
c.292del (p.Leu98TrpfsTer?)
c.736del (p.Leu246TrpfsTer?)
 COSMIC
17g.7674194G>ACA001712TP53c.769C>T (p.Leu257=)
c.373C>T (p.Leu125=)
c.490C>T (p.Leu164=)
c.748C>T (p.Leu250=)
c.652C>T (p.Leu218=)
c.292C>T (p.Leu98=)
c.736C>T (p.Leu246=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.7674194G>CCA397837734TP53c.769C>G (p.Leu257Val)
c.373C>G (p.Leu125Val)
c.490C>G (p.Leu164Val)
c.748C>G (p.Leu250Val)
c.652C>G (p.Leu218Val)
c.292C>G (p.Leu98Val)
c.736C>G (p.Leu246Val)
 ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7674194G=CA2245951041TP53c.769C= (p.Leu257=)
c.373C= (p.Leu125=)
c.490C= (p.Leu164=)
c.748C= (p.Leu250=)
c.652C= (p.Leu218=)
c.292C= (p.Leu98=)
c.736C= (p.Leu246=)
17g.7674194G>TCA397837730TP53c.769C>A (p.Leu257Met)
c.373C>A (p.Leu125Met)
c.490C>A (p.Leu164Met)
c.748C>A (p.Leu250Met)
c.652C>A (p.Leu218Met)
c.292C>A (p.Leu98Met)
c.736C>A (p.Leu246Met)
17g.7674194_7674196delCA645588499TP53c.767_769del (p.Thr256_Leu257delinsMet)
c.371_373del (p.Thr124_Leu125delinsMet)
c.488_490del (p.Thr163_Leu164delinsMet)
c.746_748del (p.Thr249_Leu250delinsMet)
c.650_652del (p.Thr217_Leu218delinsMet)
c.290_292del (p.Thr97_Leu98delinsMet)
c.734_736del (p.Thr245_Leu246delinsMet)
 COSMIC COSMIC COSMIC
17g.7674197_7674198delCA645588498TP53c.768_769del (p.Leu257GlyfsTer6)
c.372_373del (p.Leu125GlyfsTer6)
c.489_490del (p.Leu164GlyfsTer6)
c.747_748del (p.Leu250GlyfsTer6)
c.768_769del (p.Leu257GlyfsTer?)
c.651_652del (p.Leu218GlyfsTer6)
c.291_292del (p.Leu98GlyfsTer6)
c.735_736del (p.Leu246GlyfsTer6)
 ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7674195T>ACA497716817TP53c.768A>T (p.Thr256=)
c.372A>T (p.Thr124=)
c.489A>T (p.Thr163=)
c.747A>T (p.Thr249=)
c.651A>T (p.Thr217=)
c.291A>T (p.Thr97=)
c.735A>T (p.Thr245=)
 ClinVar dbSNP
17g.7674195T>CCA000400TP53c.768A>G (p.Thr256=)
c.372A>G (p.Thr124=)
c.489A>G (p.Thr163=)
c.747A>G (p.Thr249=)
c.651A>G (p.Thr217=)
c.291A>G (p.Thr97=)
c.735A>G (p.Thr245=)
 ClinVar dbSNP gnomAD v4 COSMIC
17g.7674195T>GCA497716815TP53c.768A>C (p.Thr256=)
c.372A>C (p.Thr124=)
c.489A>C (p.Thr163=)
c.747A>C (p.Thr249=)
c.651A>C (p.Thr217=)
c.291A>C (p.Thr97=)
c.735A>C (p.Thr245=)
 ClinVar
17g.7674195T=CA2245951047TP53c.768A= (p.Thr256=)
c.372A= (p.Thr124=)
c.489A= (p.Thr163=)
c.747A= (p.Thr249=)
c.651A= (p.Thr217=)
c.291A= (p.Thr97=)
c.735A= (p.Thr245=)
17g.7674195_7674197delCA2635876158TP53c.766_768del (p.Thr256del)
c.370_372del (p.Thr124del)
c.487_489del (p.Thr163del)
c.745_747del (p.Thr249del)
c.649_651del (p.Thr217del)
c.289_291del (p.Thr97del)
c.733_735del (p.Thr245del)
 gnomAD v4
17g.7674197_7674204delCA645588501TP53c.761_768del (p.Ile254ThrfsTer7)
c.365_372del (p.Ile122ThrfsTer7)
c.482_489del (p.Ile161ThrfsTer7)
c.740_747del (p.Ile247ThrfsTer7)
c.761_768del (p.Ile254ThrfsTer?)
c.644_651del (p.Ile215ThrfsTer7)
c.284_291del (p.Ile95ThrfsTer7)
c.728_735del (p.Ile243ThrfsTer7)
 COSMIC
17g.7674195_7674218delCA645588500TP53c.745_768del (p.Arg249_Thr256del)
c.349_372del (p.Arg117_Thr124del)
c.466_489del (p.Arg156_Thr163del)
c.724_747del (p.Arg242_Thr249del)
c.628_651del (p.Arg210_Thr217del)
c.268_291del (p.Arg90_Thr97del)
c.712_735del (p.Arg238_Thr245del)
 COSMIC
17g.7674195_7674196insCACA2635876168TP53c.767_768insTG (p.Leu257AspfsTer?)
c.371_372insTG (p.Leu125AspfsTer?)
c.488_489insTG (p.Leu164AspfsTer?)
c.746_747insTG (p.Leu250AspfsTer?)
c.767_768insTG (p.Leu257AspfsTer13)
c.650_651insTG (p.Leu218AspfsTer?)
c.290_291insTG (p.Leu98AspfsTer?)
c.734_735insTG (p.Leu246AspfsTer?)
 gnomAD v4
17g.7674196delCA497716826TP53c.767del (p.Thr256AsnfsTer?)
c.371del (p.Thr124AsnfsTer?)
c.488del (p.Thr163AsnfsTer?)
c.746del (p.Thr249AsnfsTer?)
c.767del (p.Thr256AsnfsTer13)
c.650del (p.Thr217AsnfsTer?)
c.290del (p.Thr97AsnfsTer?)
c.734del (p.Thr245AsnfsTer?)
 COSMIC
17g.7674196G>ACA397837735TP53c.767C>T (p.Thr256Ile)
c.371C>T (p.Thr124Ile)
c.488C>T (p.Thr163Ile)
c.746C>T (p.Thr249Ile)
c.650C>T (p.Thr217Ile)
c.290C>T (p.Thr97Ile)
c.734C>T (p.Thr245Ile)
 ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7674196G>CCA397837737TP53c.767C>G (p.Thr256Arg)
c.371C>G (p.Thr124Arg)
c.488C>G (p.Thr163Arg)
c.746C>G (p.Thr249Arg)
c.650C>G (p.Thr217Arg)
c.290C>G (p.Thr97Arg)
c.734C>G (p.Thr245Arg)
17g.7674196G=CA2245951060TP53c.767C= (p.Thr256=)
c.371C= (p.Thr124=)
c.488C= (p.Thr163=)
c.746C= (p.Thr249=)
c.650C= (p.Thr217=)
c.290C= (p.Thr97=)
c.734C= (p.Thr245=)
17g.7674196G>TCA397837739TP53c.767C>A (p.Thr256Lys)
c.371C>A (p.Thr124Lys)
c.488C>A (p.Thr163Lys)
c.746C>A (p.Thr249Lys)
c.650C>A (p.Thr217Lys)
c.290C>A (p.Thr97Lys)
c.734C>A (p.Thr245Lys)
 ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7674196_7674198delCA645588502TP53c.765_767del (p.Thr256del)
c.369_371del (p.Thr124del)
c.486_488del (p.Thr163del)
c.744_746del (p.Thr249del)
c.648_650del (p.Thr217del)
c.288_290del (p.Thr97del)
c.732_734del (p.Thr245del)
 COSMIC COSMIC COSMIC
17g.7674196_7674199delinsGTGACA2245951058TP53c.764_767delinsTCAC (p.Ile255=)
c.368_371delinsTCAC (p.Ile123=)
c.485_488delinsTCAC (p.Ile162=)
c.743_746delinsTCAC (p.Ile248=)
c.647_650delinsTCAC (p.Ile216=)
c.287_290delinsTCAC (p.Ile96=)
c.731_734delinsTCAC (p.Ile244=)
17g.7674200_7674208delCA645588503TP53c.759_767del (p.Ile254_Thr256del)
c.363_371del (p.Ile122_Thr124del)
c.480_488del (p.Ile161_Thr163del)
c.738_746del (p.Ile247_Thr249del)
c.642_650del (p.Ile215_Thr217del)
c.282_290del (p.Ile95_Thr97del)
c.726_734del (p.Ile243_Thr245del)
 ClinVar COSMIC COSMIC
17g.7674197delCA497716837TP53c.766del (p.Thr256HisfsTer?)
c.370del (p.Thr124HisfsTer?)
c.487del (p.Thr163HisfsTer?)
c.745del (p.Thr249HisfsTer?)
c.766del (p.Thr256HisfsTer13)
c.649del (p.Thr217HisfsTer?)
c.289del (p.Thr97HisfsTer?)
c.733del (p.Thr245HisfsTer?)
 COSMIC
17g.7674197T>ACA397837740TP53c.766A>T (p.Thr256Ser)
c.370A>T (p.Thr124Ser)
c.487A>T (p.Thr163Ser)
c.745A>T (p.Thr249Ser)
c.649A>T (p.Thr217Ser)
c.289A>T (p.Thr97Ser)
c.733A>T (p.Thr245Ser)
 COSMIC
17g.7674197T>CCA000399TP53c.766A>G (p.Thr256Ala)
c.370A>G (p.Thr124Ala)
c.487A>G (p.Thr163Ala)
c.745A>G (p.Thr249Ala)
c.649A>G (p.Thr217Ala)
c.289A>G (p.Thr97Ala)
c.733A>G (p.Thr245Ala)
 ClinVar dbSNP gnomAD v4 COSMIC
17g.7674197T>GCA397837741TP53c.766A>C (p.Thr256Pro)
c.370A>C (p.Thr124Pro)
c.487A>C (p.Thr163Pro)
c.745A>C (p.Thr249Pro)
c.649A>C (p.Thr217Pro)
c.289A>C (p.Thr97Pro)
c.733A>C (p.Thr245Pro)
 ClinVar dbSNP COSMIC
17g.7674197T=CA2245951095TP53c.766A= (p.Thr256=)
c.370A= (p.Thr124=)
c.487A= (p.Thr163=)
c.745A= (p.Thr249=)
c.649A= (p.Thr217=)
c.289A= (p.Thr97=)
c.733A= (p.Thr245=)
17g.7674197dupCA645588504TP53c.766dup (p.Thr256AsnfsTer8)
c.370dup (p.Thr124AsnfsTer8)
c.487dup (p.Thr163AsnfsTer8)
c.745dup (p.Thr249AsnfsTer8)
c.766dup (p.Thr256AsnfsTer?)
c.649dup (p.Thr217AsnfsTer8)
c.289dup (p.Thr97AsnfsTer8)
c.733dup (p.Thr245AsnfsTer8)
 ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7674197_7674198delinsACA2795330543TP53c.765_766delinsT (p.Thr256HisfsTer?)
c.369_370delinsT (p.Thr124HisfsTer?)
c.486_487delinsT (p.Thr163HisfsTer?)
c.744_745delinsT (p.Thr249HisfsTer?)
c.765_766delinsT (p.Thr256HisfsTer13)
c.648_649delinsT (p.Thr217HisfsTer?)
c.288_289delinsT (p.Thr97HisfsTer?)
c.732_733delinsT (p.Thr245HisfsTer?)
17g.7674197_7674200delCA2635876178TP53c.763_766del (p.Ile255HisfsTer?)
c.367_370del (p.Ile123HisfsTer?)
c.484_487del (p.Ile162HisfsTer?)
c.742_745del (p.Ile248HisfsTer?)
c.763_766del (p.Ile255HisfsTer13)
c.646_649del (p.Ile216HisfsTer?)
c.286_289del (p.Ile96HisfsTer?)
c.730_733del (p.Ile244HisfsTer?)
 gnomAD v4
17g.7674202_7674204delCA16620619TP53c.764_766del (p.Ile255del)
c.368_370del (p.Ile123del)
c.485_487del (p.Ile162del)
c.743_745del (p.Ile248del)
c.647_649del (p.Ile216del)
c.287_289del (p.Ile96del)
c.731_733del (p.Ile244del)
 ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7674197_7674198insACA497716846TP53c.765_766insT (p.Thr256TyrfsTer8)
c.369_370insT (p.Thr124TyrfsTer8)
c.486_487insT (p.Thr163TyrfsTer8)
c.744_745insT (p.Thr249TyrfsTer8)
c.765_766insT (p.Thr256TyrfsTer?)
c.648_649insT (p.Thr217TyrfsTer8)
c.288_289insT (p.Thr97TyrfsTer8)
c.732_733insT (p.Thr245TyrfsTer8)
17g.7674198G>ACA497716845TP53c.765C>T (p.Ile255=)
c.369C>T (p.Ile123=)
c.486C>T (p.Ile162=)
c.744C>T (p.Ile248=)
c.648C>T (p.Ile216=)
c.288C>T (p.Ile96=)
c.732C>T (p.Ile244=)
 ClinVar dbSNP COSMIC
17g.7674198G>CCA397837742TP53c.765C>G (p.Ile255Met)
c.369C>G (p.Ile123Met)
c.486C>G (p.Ile162Met)
c.744C>G (p.Ile248Met)
c.648C>G (p.Ile216Met)
c.288C>G (p.Ile96Met)
c.732C>G (p.Ile244Met)
 COSMIC
17g.7674198G>TCA497716844TP53c.765C>A (p.Ile255=)
c.369C>A (p.Ile123=)
c.486C>A (p.Ile162=)
c.744C>A (p.Ile248=)
c.648C>A (p.Ile216=)
c.288C>A (p.Ile96=)
c.732C>A (p.Ile244=)
 gnomAD v4 COSMIC
17g.7674199_7674222delCA2733136155TP53c.742_765del (p.Arg248_Ile255del)
c.346_369del (p.Arg116_Ile123del)
c.463_486del (p.Arg155_Ile162del)
c.721_744del (p.Arg241_Ile248del)
c.625_648del (p.Arg209_Ile216del)
c.265_288del (p.Arg89_Ile96del)
c.709_732del (p.Arg237_Ile244del)
 dbSNP
17g.7674199A=CA2245951109TP53c.764T= (p.Ile255=)
c.368T= (p.Ile123=)
c.485T= (p.Ile162=)
c.743T= (p.Ile248=)
c.647T= (p.Ile216=)
c.287T= (p.Ile96=)
c.731T= (p.Ile244=)
17g.7674199A>CCA16603042TP53c.764T>G (p.Ile255Ser)
c.368T>G (p.Ile123Ser)
c.485T>G (p.Ile162Ser)
c.743T>G (p.Ile248Ser)
c.647T>G (p.Ile216Ser)
c.287T>G (p.Ile96Ser)
c.731T>G (p.Ile244Ser)
 ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7674199A>GCA16603043TP53c.764T>C (p.Ile255Thr)
c.368T>C (p.Ile123Thr)
c.485T>C (p.Ile162Thr)
c.743T>C (p.Ile248Thr)
c.647T>C (p.Ile216Thr)
c.287T>C (p.Ile96Thr)
c.731T>C (p.Ile244Thr)
 ClinVar dbSNP gnomAD v4
17g.7674199A>TCA10580923TP53c.764T>A (p.Ile255Asn)
c.368T>A (p.Ile123Asn)
c.485T>A (p.Ile162Asn)
c.743T>A (p.Ile248Asn)
c.647T>A (p.Ile216Asn)
c.287T>A (p.Ile96Asn)
c.731T>A (p.Ile244Asn)
 ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7674199_7674200delCA645588506TP53c.763_764del (p.Ile255HisfsTer8)
c.367_368del (p.Ile123HisfsTer8)
c.484_485del (p.Ile162HisfsTer8)
c.742_743del (p.Ile248HisfsTer8)
c.763_764del (p.Ile255HisfsTer?)
c.646_647del (p.Ile216HisfsTer8)
c.286_287del (p.Ile96HisfsTer8)
c.730_731del (p.Ile244HisfsTer8)
 COSMIC
17g.7674199_7674203delCA645588505TP53c.760_764del (p.Ile254HisfsTer8)
c.364_368del (p.Ile122HisfsTer8)
c.481_485del (p.Ile161HisfsTer8)
c.739_743del (p.Ile247HisfsTer8)
c.760_764del (p.Ile254HisfsTer?)
c.643_647del (p.Ile215HisfsTer8)
c.283_287del (p.Ile95HisfsTer8)
c.727_731del (p.Ile243HisfsTer8)
 COSMIC COSMIC COSMIC
17g.7674200delCA497716862TP53c.763del (p.Ile255SerfsTer?)
c.367del (p.Ile123SerfsTer?)
c.484del (p.Ile162SerfsTer?)
c.742del (p.Ile248SerfsTer?)
c.763del (p.Ile255SerfsTer14)
c.646del (p.Ile216SerfsTer?)
c.286del (p.Ile96SerfsTer?)
c.730del (p.Ile244SerfsTer?)
 COSMIC
17g.7674200T>ACA16603041TP53c.763A>T (p.Ile255Phe)
c.367A>T (p.Ile123Phe)
c.484A>T (p.Ile162Phe)
c.742A>T (p.Ile248Phe)
c.646A>T (p.Ile216Phe)
c.286A>T (p.Ile96Phe)
c.730A>T (p.Ile244Phe)
 ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7674200T>CCA397837750TP53c.763A>G (p.Ile255Val)
c.367A>G (p.Ile123Val)
c.484A>G (p.Ile162Val)
c.742A>G (p.Ile248Val)
c.646A>G (p.Ile216Val)
c.286A>G (p.Ile96Val)
c.730A>G (p.Ile244Val)
 COSMIC
17g.7674200T>GCA397837752TP53c.763A>C (p.Ile255Leu)
c.367A>C (p.Ile123Leu)
c.484A>C (p.Ile162Leu)
c.742A>C (p.Ile248Leu)
c.646A>C (p.Ile216Leu)
c.286A>C (p.Ile96Leu)
c.730A>C (p.Ile244Leu)
17g.7674200T=CA2245951126TP53c.763A= (p.Ile255=)
c.367A= (p.Ile123=)
c.484A= (p.Ile162=)
c.742A= (p.Ile248=)
c.646A= (p.Ile216=)
c.286A= (p.Ile96=)
c.730A= (p.Ile244=)
17g.7674200_7674209delinsTGATGGTGAGCA2245951132TP53c.754_763delinsCTCACCATCA (p.Leu252=)
c.358_367delinsCTCACCATCA (p.Leu120=)
c.475_484delinsCTCACCATCA (p.Leu159=)
c.733_742delinsCTCACCATCA (p.Leu245=)
c.637_646delinsCTCACCATCA (p.Leu213=)
c.277_286delinsCTCACCATCA (p.Leu93=)
c.721_730delinsCTCACCATCA (p.Leu241=)
17g.7674200_7674201insCACA2576230649TP53c.762_763insTG (p.Ile255Ter)
c.366_367insTG (p.Ile123Ter)
c.483_484insTG (p.Ile162Ter)
c.741_742insTG (p.Ile248Ter)
c.645_646insTG (p.Ile216Ter)
c.285_286insTG (p.Ile96Ter)
c.729_730insTG (p.Ile244Ter)
17g.7674201delCA497716869TP53c.762del (p.Ile255SerfsTer?)
c.366del (p.Ile123SerfsTer?)
c.483del (p.Ile162SerfsTer?)
c.741del (p.Ile248SerfsTer?)
c.762del (p.Ile255SerfsTer14)
c.645del (p.Ile216SerfsTer?)
c.285del (p.Ile96SerfsTer?)
c.729del (p.Ile244SerfsTer?)
 COSMIC
17g.7674201G>ACA497716865TP53c.762C>T (p.Ile254=)
c.366C>T (p.Ile122=)
c.483C>T (p.Ile161=)
c.741C>T (p.Ile247=)
c.645C>T (p.Ile215=)
c.285C>T (p.Ile95=)
c.729C>T (p.Ile243=)
 ClinVar dbSNP
17g.7674201G>CCA397837754TP53c.762C>G (p.Ile254Met)
c.366C>G (p.Ile122Met)
c.483C>G (p.Ile161Met)
c.741C>G (p.Ile247Met)
c.645C>G (p.Ile215Met)
c.285C>G (p.Ile95Met)
c.729C>G (p.Ile243Met)
 ClinVar dbSNP
17g.7674201G=CA2245951138TP53c.762C= (p.Ile254=)
c.366C= (p.Ile122=)
c.483C= (p.Ile161=)
c.741C= (p.Ile247=)
c.645C= (p.Ile215=)
c.285C= (p.Ile95=)
c.729C= (p.Ile243=)
17g.7674201G>TCA497716866TP53c.762C>A (p.Ile254=)
c.366C>A (p.Ile122=)
c.483C>A (p.Ile161=)
c.741C>A (p.Ile247=)
c.645C>A (p.Ile215=)
c.285C>A (p.Ile95=)
c.729C>A (p.Ile243=)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
17g.7674201_7674202delinsATCA2739265546TP53c.761_762delinsAT (p.Ile254Asn)
c.365_366delinsAT (p.Ile122Asn)
c.482_483delinsAT (p.Ile161Asn)
c.740_741delinsAT (p.Ile247Asn)
c.644_645delinsAT (p.Ile215Asn)
c.284_285delinsAT (p.Ile95Asn)
c.728_729delinsAT (p.Ile243Asn)
 ClinVar
17g.7674206_7674214delCA645588507TP53c.754_762del (p.Leu252_Ile254del)
c.358_366del (p.Leu120_Ile122del)
c.475_483del (p.Leu159_Ile161del)
c.733_741del (p.Leu245_Ile247del)
c.637_645del (p.Leu213_Ile215del)
c.277_285del (p.Leu93_Ile95del)
c.721_729del (p.Leu241_Ile243del)
 ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7674202A=CA2245951151TP53c.761T= (p.Ile254=)
c.365T= (p.Ile122=)
c.482T= (p.Ile161=)
c.740T= (p.Ile247=)
c.644T= (p.Ile215=)
c.284T= (p.Ile95=)
c.728T= (p.Ile243=)
17g.7674202A>CCA397837758TP53c.761T>G (p.Ile254Ser)
c.365T>G (p.Ile122Ser)
c.482T>G (p.Ile161Ser)
c.740T>G (p.Ile247Ser)
c.644T>G (p.Ile215Ser)
c.284T>G (p.Ile95Ser)
c.728T>G (p.Ile243Ser)
 ClinVar dbSNP gnomAD v2 COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7674202A>GCA397837761TP53c.761T>C (p.Ile254Thr)
c.365T>C (p.Ile122Thr)
c.482T>C (p.Ile161Thr)
c.740T>C (p.Ile247Thr)
c.644T>C (p.Ile215Thr)
c.284T>C (p.Ile95Thr)
c.728T>C (p.Ile243Thr)
 ClinVar COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7674202A>TCA397837760TP53c.761T>A (p.Ile254Asn)
c.365T>A (p.Ile122Asn)
c.482T>A (p.Ile161Asn)
c.740T>A (p.Ile247Asn)
c.644T>A (p.Ile215Asn)
c.284T>A (p.Ile95Asn)
c.728T>A (p.Ile243Asn)
 ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC
17g.7674202_7674203delinsATCA2245951157TP53c.760_761delinsAT (p.Ile254=)
c.364_365delinsAT (p.Ile122=)
c.481_482delinsAT (p.Ile161=)
c.739_740delinsAT (p.Ile247=)
c.643_644delinsAT (p.Ile215=)
c.283_284delinsAT (p.Ile95=)
c.727_728delinsAT (p.Ile243=)
17g.7674202_7674203delinsTCCA645588508TP53c.760_761delinsGA (p.Ile254Asp)
c.364_365delinsGA (p.Ile122Asp)
c.481_482delinsGA (p.Ile161Asp)
c.739_740delinsGA (p.Ile247Asp)
c.643_644delinsGA (p.Ile215Asp)
c.283_284delinsGA (p.Ile95Asp)
c.727_728delinsGA (p.Ile243Asp)
 COSMIC
17g.7674203delCA497716879TP53c.760del (p.Ile254SerfsTer?)
c.364del (p.Ile122SerfsTer?)
c.481del (p.Ile161SerfsTer?)
c.739del (p.Ile247SerfsTer?)
c.760del (p.Ile254SerfsTer15)
c.643del (p.Ile215SerfsTer?)
c.283del (p.Ile95SerfsTer?)
c.727del (p.Ile243SerfsTer?)
 dbSNP COSMIC
17g.7674203T>ACA397837763TP53c.760A>T (p.Ile254Phe)
c.364A>T (p.Ile122Phe)
c.481A>T (p.Ile161Phe)
c.739A>T (p.Ile247Phe)
c.643A>T (p.Ile215Phe)
c.283A>T (p.Ile95Phe)
c.727A>T (p.Ile243Phe)
 COSMIC
17g.7674203T>CCA001720TP53c.760A>G (p.Ile254Val)
c.364A>G (p.Ile122Val)
c.481A>G (p.Ile161Val)
c.739A>G (p.Ile247Val)
c.643A>G (p.Ile215Val)
c.283A>G (p.Ile95Val)
c.727A>G (p.Ile243Val)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.7674203T>GCA397837772TP53c.760A>C (p.Ile254Leu)
c.364A>C (p.Ile122Leu)
c.481A>C (p.Ile161Leu)
c.739A>C (p.Ile247Leu)
c.643A>C (p.Ile215Leu)
c.283A>C (p.Ile95Leu)
c.727A>C (p.Ile243Leu)
 COSMIC COSMIC COSMIC
17g.7674203T=CA2245951174TP53c.760A= (p.Ile254=)
c.364A= (p.Ile122=)
c.481A= (p.Ile161=)
c.739A= (p.Ile247=)
c.643A= (p.Ile215=)
c.283A= (p.Ile95=)
c.727A= (p.Ile243=)
17g.7674203_7674204delinsTGCA2245951167TP53c.759_760delinsCA (p.Thr253=)
c.363_364delinsCA (p.Thr121=)
c.480_481delinsCA (p.Thr160=)
c.738_739delinsCA (p.Thr246=)
c.642_643delinsCA (p.Thr214=)
c.282_283delinsCA (p.Thr94=)
c.726_727delinsCA (p.Thr242=)
17g.7674203_7674206delCA645588510TP53c.757_760del (p.Thr253SerfsTer?)
c.361_364del (p.Thr121SerfsTer?)
c.478_481del (p.Thr160SerfsTer?)
c.736_739del (p.Thr246SerfsTer?)
c.757_760del (p.Thr253SerfsTer15)
c.640_643del (p.Thr214SerfsTer?)
c.280_283del (p.Thr94SerfsTer?)
c.724_727del (p.Thr242SerfsTer?)
 COSMIC
17g.7674205_7674207dupCA915949526TP53c.758_760dup (p.Thr253_Ile254insThr)
c.362_364dup (p.Thr121_Ile122insThr)
c.479_481dup (p.Thr160_Ile161insThr)
c.737_739dup (p.Thr246_Ile247insThr)
c.641_643dup (p.Thr214_Ile215insThr)
c.281_283dup (p.Thr94_Ile95insThr)
c.725_727dup (p.Thr242_Ile243insThr)
 ClinVar dbSNP
17g.7674205_7674207delCA645588509TP53c.758_760del (p.Thr253del)
c.362_364del (p.Thr121del)
c.479_481del (p.Thr160del)
c.737_739del (p.Thr246del)
c.641_643del (p.Thr214del)
c.281_283del (p.Thr94del)
c.725_727del (p.Thr242del)
 COSMIC
17g.7674204G>ACA497717194TP53c.759C>T (p.Thr253=)
c.363C>T (p.Thr121=)
c.480C>T (p.Thr160=)
c.738C>T (p.Thr246=)
c.642C>T (p.Thr214=)
c.282C>T (p.Thr94=)
c.726C>T (p.Thr242=)
 ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7674204G>CCA497717196TP53c.759C>G (p.Thr253=)
c.363C>G (p.Thr121=)
c.480C>G (p.Thr160=)
c.738C>G (p.Thr246=)
c.642C>G (p.Thr214=)
c.282C>G (p.Thr94=)
c.726C>G (p.Thr242=)
17g.7674204G=CA2245951185TP53c.759C= (p.Thr253=)
c.363C= (p.Thr121=)
c.480C= (p.Thr160=)
c.738C= (p.Thr246=)
c.642C= (p.Thr214=)
c.282C= (p.Thr94=)
c.726C= (p.Thr242=)
17g.7674204G>TCA497717200TP53c.759C>A (p.Thr253=)
c.363C>A (p.Thr121=)
c.480C>A (p.Thr160=)
c.738C>A (p.Thr246=)
c.642C>A (p.Thr214=)
c.282C>A (p.Thr94=)
c.726C>A (p.Thr242=)
17g.7674205delCA645588511TP53c.759del (p.Ile254SerfsTer?)
c.363del (p.Ile122SerfsTer?)
c.480del (p.Ile161SerfsTer?)
c.738del (p.Ile247SerfsTer?)
c.759del (p.Ile254SerfsTer15)
c.642del (p.Ile215SerfsTer?)
c.282del (p.Ile95SerfsTer?)
c.726del (p.Ile243SerfsTer?)
 ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7674205_7674210delCA645588514TP53c.754_759del (p.Leu252_Thr253del)
c.358_363del (p.Leu120_Thr121del)
c.475_480del (p.Leu159_Thr160del)
c.733_738del (p.Leu245_Thr246del)
c.637_642del (p.Leu213_Thr214del)
c.277_282del (p.Leu93_Thr94del)
c.721_726del (p.Leu241_Thr242del)
 COSMIC
17g.7674204_7674215delCA645588512TP53c.748_759del (p.Pro250_Thr253del)
c.352_363del (p.Pro118_Thr121del)
c.469_480del (p.Pro157_Thr160del)
c.727_738del (p.Pro243_Thr246del)
c.631_642del (p.Pro211_Thr214del)
c.271_282del (p.Pro91_Thr94del)
c.715_726del (p.Pro239_Thr242del)
 COSMIC
17g.7674204_7674225delCA645588513TP53c.738_759del (p.Met246IlefsTer?)
c.342_363del (p.Met114IlefsTer?)
c.459_480del (p.Met153IlefsTer?)
c.717_738del (p.Met239IlefsTer?)
c.738_759del (p.Met246IlefsTer16)
c.621_642del (p.Met207IlefsTer?)
c.261_282del (p.Met87IlefsTer?)
c.705_726del (p.Met235IlefsTer?)
 COSMIC COSMIC COSMIC COSMIC
17g.7674205G>ACA397838857TP53c.758C>T (p.Thr253Ile)
c.362C>T (p.Thr121Ile)
c.479C>T (p.Thr160Ile)
c.737C>T (p.Thr246Ile)
c.641C>T (p.Thr214Ile)
c.281C>T (p.Thr94Ile)
c.725C>T (p.Thr242Ile)
 ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7674205G>CCA397838858TP53c.758C>G (p.Thr253Ser)
c.362C>G (p.Thr121Ser)
c.479C>G (p.Thr160Ser)
c.737C>G (p.Thr246Ser)
c.641C>G (p.Thr214Ser)
c.281C>G (p.Thr94Ser)
c.725C>G (p.Thr242Ser)
 dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7674205G=CA2245951191TP53c.758C= (p.Thr253=)
c.362C= (p.Thr121=)
c.479C= (p.Thr160=)
c.737C= (p.Thr246=)
c.641C= (p.Thr214=)
c.281C= (p.Thr94=)
c.725C= (p.Thr242=)
17g.7674205G>TCA397838859TP53c.758C>A (p.Thr253Asn)
c.362C>A (p.Thr121Asn)
c.479C>A (p.Thr160Asn)
c.737C>A (p.Thr246Asn)
c.641C>A (p.Thr214Asn)
c.281C>A (p.Thr94Asn)
c.725C>A (p.Thr242Asn)
 ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7674206_7674221delCA645588517TP53c.743_758del (p.Arg248ProfsTer?)
c.347_362del (p.Arg116ProfsTer?)
c.464_479del (p.Arg155ProfsTer?)
c.722_737del (p.Arg241ProfsTer?)
c.743_758del (p.Arg248ProfsTer16)
c.626_641del (p.Arg209ProfsTer?)
c.266_281del (p.Arg89ProfsTer?)
c.710_725del (p.Arg237ProfsTer?)
 COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7674206T>ACA397838861TP53c.757A>T (p.Thr253Ser)
c.361A>T (p.Thr121Ser)
c.478A>T (p.Thr160Ser)
c.736A>T (p.Thr246Ser)
c.640A>T (p.Thr214Ser)
c.280A>T (p.Thr94Ser)
c.724A>T (p.Thr242Ser)
 dbSNP COSMIC
17g.7674206T>CCA397838863TP53c.757A>G (p.Thr253Ala)
c.361A>G (p.Thr121Ala)
c.478A>G (p.Thr160Ala)
c.736A>G (p.Thr246Ala)
c.640A>G (p.Thr214Ala)
c.280A>G (p.Thr94Ala)
c.724A>G (p.Thr242Ala)
 ClinVar dbSNP COSMIC
17g.7674206T>GCA397838866TP53c.757A>C (p.Thr253Pro)
c.361A>C (p.Thr121Pro)
c.478A>C (p.Thr160Pro)
c.736A>C (p.Thr246Pro)
c.640A>C (p.Thr214Pro)
c.280A>C (p.Thr94Pro)
c.724A>C (p.Thr242Pro)
 COSMIC
17g.7674206T=CA2245951201TP53c.757A= (p.Thr253=)
c.361A= (p.Thr121=)
c.478A= (p.Thr160=)
c.736A= (p.Thr246=)
c.640A= (p.Thr214=)
c.280A= (p.Thr94=)
c.724A= (p.Thr242=)
17g.7674206_7674207insATCA645588518TP53c.757_758insTA (p.Thr253IlefsTer?)
c.361_362insTA (p.Thr121IlefsTer?)
c.478_479insTA (p.Thr160IlefsTer?)
c.736_737insTA (p.Thr246IlefsTer?)
c.757_758insTA (p.Thr253IlefsTer17)
c.640_641insTA (p.Thr214IlefsTer?)
c.280_281insTA (p.Thr94IlefsTer?)
c.724_725insTA (p.Thr242IlefsTer?)
 COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7674206dupCA2580094854TP53c.757dup (p.Thr253AsnfsTer11)
c.361dup (p.Thr121AsnfsTer11)
c.478dup (p.Thr160AsnfsTer11)
c.736dup (p.Thr246AsnfsTer11)
c.757dup (p.Thr253AsnfsTer?)
c.640dup (p.Thr214AsnfsTer11)
c.280dup (p.Thr94AsnfsTer11)
c.724dup (p.Thr242AsnfsTer11)
 ClinVar
17g.7674206_7674209delinsTGAGCA2245951204TP53c.754_757delinsCTCA (p.Leu252=)
c.358_361delinsCTCA (p.Leu120=)
c.475_478delinsCTCA (p.Leu159=)
c.733_736delinsCTCA (p.Leu245=)
c.637_640delinsCTCA (p.Leu213=)
c.277_280delinsCTCA (p.Leu93=)
c.721_724delinsCTCA (p.Leu241=)

Number of alleles fetched