Chr Mutation (hg38) CAid Gene Transcript Linkouts
13g.48381248_48381444delCA645578673RB1c.1500_1695+1del
c.1239_1434+1del
COSMIC
13g.48381313A=CA2089972404RB1c.1565A= (p.Asn522=)
c.64A=
c.1304A= (p.Asn435=)
13g.48381313A>CCA388163538RB1c.1565A>C (p.Asn522Thr)
c.64A>C
c.1304A>C (p.Asn435Thr)
13g.48381313A>GCA388163540RB1c.1565A>G (p.Asn522Ser)
c.64A>G
c.1304A>G (p.Asn435Ser)
13g.48381313A>TCA388163541RB1c.1565A>T (p.Asn522Ile)
c.64A>T
c.1304A>T (p.Asn435Ile)
13g.48381314T>ACA388163544RB1c.1566T>A (p.Asn522Lys)
c.65T>A
c.1305T>A (p.Asn435Lys)
dbSNP
13g.48381314T>CCA483559459RB1c.1566T>C (p.Asn522=)
c.65T>C
c.1305T>C (p.Asn435=)
13g.48381314T>GCA388163543RB1c.1566T>G (p.Asn522Lys)
c.65T>G
c.1305T>G (p.Asn435Lys)
13g.48381315_48381316dupCA916081694RB1c.1567_1568dup (p.Leu523PhefsTer2)
c.66_67dup
c.1306_1307dup (p.Leu436PhefsTer2)
ClinVar dbSNP
13g.48381315T>ACA388163545RB1c.1567T>A (p.Leu523Ile)
c.66T>A
c.1306T>A (p.Leu436Ile)
13g.48381315T>CCA483559461RB1c.1567T>C (p.Leu523=)
c.66T>C
c.1306T>C (p.Leu436=)
13g.48381315T>GCA388163547RB1c.1567T>G (p.Leu523Val)
c.66T>G
c.1306T>G (p.Leu436Val)
13g.48381316T>ACA388163549RB1c.1568T>A (p.Leu523Ter)
c.67T>A
c.1307T>A (p.Leu436Ter)
ClinVar dbSNP
13g.48381316T>CCA388163551RB1c.1568T>C (p.Leu523Ser)
c.67T>C
c.1307T>C (p.Leu436Ser)
13g.48381316T>GCA388163553RB1c.1568T>G (p.Leu523Ter)
c.67T>G
c.1307T>G (p.Leu436Ter)
ClinVar
13g.48381316_48381319dupCA2695218497RB1c.1568_1571dup (p.Lys524AsnfsTer5)
c.67_70dup
c.1307_1310dup (p.Lys437AsnfsTer5)
13g.48381317A>CCA388163555RB1c.1569A>C (p.Leu523Phe)
c.68A>C
c.1308A>C (p.Leu436Phe)
13g.48381317A>GCA483559463RB1c.1569A>G (p.Leu523=)
c.68A>G
c.1308A>G (p.Leu436=)
13g.48381317A>TCA388163556RB1c.1569A>T (p.Leu523Phe)
c.68A>T
c.1308A>T (p.Leu436Phe)
dbSNP
13g.48381320dupCA2580087605RB1c.1572dup (p.Ala525SerfsTer3)
c.71dup
c.1311dup (p.Ala438SerfsTer3)
ClinVar
13g.48381319_48381320dupCA2695218498RB1c.1571_1572dup (p.Ala525LysfsTer8)
c.70_71dup
c.1310_1311dup (p.Ala438LysfsTer8)
13g.48381320delCA2499222454RB1c.1572del (p.Ala525ProfsTer7)
c.71del
c.1311del (p.Ala438ProfsTer7)
ClinVar dbSNP
13g.48381318A>CCA388163559RB1c.1570A>C (p.Lys524Gln)
c.69A>C
c.1309A>C (p.Lys437Gln)
dbSNP
13g.48381318A>GCA388163561RB1c.1570A>G (p.Lys524Glu)
c.69A>G
c.1309A>G (p.Lys437Glu)
13g.48381318A>TCA388163562RB1c.1570A>T (p.Lys524Ter)
c.69A>T
c.1309A>T (p.Lys437Ter)
dbSNP
13g.48381319A>CCA388163565RB1c.1571A>C (p.Lys524Thr)
c.70A>C
c.1310A>C (p.Lys437Thr)
13g.48381319A>GCA388163567RB1c.1571A>G (p.Lys524Arg)
c.70A>G
c.1310A>G (p.Lys437Arg)
13g.48381319A>TCA388163569RB1c.1571A>T (p.Lys524Ile)
c.70A>T
c.1310A>T (p.Lys437Ile)
13g.48381319_48381321delCA2695218499RB1c.1571_1573del (p.Lys524_Ala525delinsThr)
c.70_72del
c.1310_1312del (p.Lys437_Ala438delinsThr)
13g.48381319_48381326delCA645578677RB1c.1571_1578del (p.Lys524ArgfsTer28)
c.70_77del
c.1310_1317del (p.Lys437ArgfsTer28)
COSMIC COSMIC
13g.48381320A>CCA388163570RB1c.1572A>C (p.Lys524Asn)
c.71A>C
c.1311A>C (p.Lys437Asn)
13g.48381320A>GCA483559465RB1c.1572A>G (p.Lys524=)
c.71A>G
c.1311A>G (p.Lys437=)
13g.48381320A>TCA388163572RB1c.1572A>T (p.Lys524Asn)
c.71A>T
c.1311A>T (p.Lys437Asn)
dbSNP
13g.48381321G>ACA026380RB1c.1573G>A (p.Ala525Thr)
c.72G>A
c.1312G>A (p.Ala438Thr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
13g.48381321G>CCA388163576RB1c.1573G>C (p.Ala525Pro)
c.72G>C
c.1312G>C (p.Ala438Pro)
dbSNP
13g.48381321G=CA2089972414RB1c.1573G= (p.Ala525=)
c.72G=
c.1312G= (p.Ala438=)
13g.48381321G>TCA388163575RB1c.1573G>T (p.Ala525Ser)
c.72G>T
c.1312G>T (p.Ala438Ser)
13g.48381321_48381322delinsGCCA2089972417RB1c.1573_1574delinsGC (p.Ala525=)
c.72_73delinsGC
c.1312_1313delinsGC (p.Ala438=)
13g.48381322C>ACA388163580RB1c.1574C>A (p.Ala525Asp)
c.73C>A
c.1313C>A (p.Ala438Asp)
ClinVar dbSNP gnomAD v4
13g.48381322C=CA2089972425RB1c.1574C= (p.Ala525=)
c.73C=
c.1313C= (p.Ala438=)
13g.48381322C>GCA026381RB1c.1574C>G (p.Ala525Gly)
c.73C>G
c.1313C>G (p.Ala438Gly)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.48381322C>TCA388163584RB1c.1574C>T (p.Ala525Val)
c.73C>T
c.1313C>T (p.Ala438Val)
ClinVar dbSNP gnomAD v3 gnomAD v4
13g.48381323delCA483559467RB1c.1575del (p.Phe526LeufsTer6)
c.74del
c.1314del (p.Phe439LeufsTer6)
ClinVar dbSNP COSMIC COSMIC
13g.48381323C>ACA483559468RB1c.1575C>A (p.Ala525=)
c.74C>A
c.1314C>A (p.Ala438=)
dbSNP
13g.48381323C>GCA483559469RB1c.1575C>G (p.Ala525=)
c.74C>G
c.1314C>G (p.Ala438=)
ClinVar dbSNP
13g.48381323C>TCA483559470RB1c.1575C>T (p.Ala525=)
c.74C>T
c.1314C>T (p.Ala438=)
dbSNP gnomAD v4 COSMIC
13g.48381324T>ACA388163586RB1c.1576T>A (p.Phe526Ile)
c.75T>A
c.1315T>A (p.Phe439Ile)
dbSNP
13g.48381324T>CCA388163588RB1c.1576T>C (p.Phe526Leu)
c.75T>C
c.1315T>C (p.Phe439Leu)
ClinVar dbSNP
13g.48381324T>GCA388163589RB1c.1576T>G (p.Phe526Val)
c.75T>G
c.1315T>G (p.Phe439Val)
dbSNP gnomAD v2 gnomAD v4
13g.48381324T=CA2089972431RB1c.1576T= (p.Phe526=)
c.75T=
c.1315T= (p.Phe439=)

Number of alleles fetched