Chr Mutation (hg38) CAid Gene Transcript Linkouts
9g.130872905T>ACA375249435ABL1c.1010T>A (p.Met337Lys)
c.953T>A (p.Met318Lys)
9g.130872905T>CCA375249436ABL1c.1010T>C (p.Met337Thr)
c.953T>C (p.Met318Thr)
9g.130872905T>GCA375249437ABL1c.1010T>G (p.Met337Arg)
c.953T>G (p.Met318Arg)
9g.130872906G>ACA375249438ABL1c.1011G>A (p.Met337Ile)
c.954G>A (p.Met318Ile)
gnomAD v4 COSMIC
9g.130872906G>CCA375249439ABL1c.1011G>C (p.Met337Ile)
c.954G>C (p.Met318Ile)
dbSNP
9g.130872906G>TCA375249440ABL1c.1011G>T (p.Met337Ile)
c.954G>T (p.Met318Ile)
9g.130872907A>CCA375249441ABL1c.1012A>C (p.Thr338Pro)
c.955A>C (p.Thr319Pro)
9g.130872907A>GCA375249442ABL1c.1012A>G (p.Thr338Ala)
c.955A>G (p.Thr319Ala)
9g.130872907A>TCA375249443ABL1c.1012A>T (p.Thr338Ser)
c.955A>T (p.Thr319Ser)
9g.130872908C>ACA375249444ABL1c.1013C>A (p.Thr338Asn)
c.956C>A (p.Thr319Asn)
9g.130872908C>GCA375249446ABL1c.1013C>G (p.Thr338Ser)
c.956C>G (p.Thr319Ser)
9g.130872908C>TCA375249445ABL1c.1013C>T (p.Thr338Ile)
c.956C>T (p.Thr319Ile)
gnomAD v4 COSMIC
9g.130872909C>ACA467395085ABL1c.1014C>A (p.Thr338=)
c.957C>A (p.Thr319=)
9g.130872909C=CA1881476039ABL1c.1014C= (p.Thr338=)
c.957C= (p.Thr319=)
9g.130872909C>GCA467395083ABL1c.1014C>G (p.Thr338=)
c.957C>G (p.Thr319=)
9g.130872909C>TCA5285351ABL1c.1014C>T (p.Thr338=)
c.957C>T (p.Thr319=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.130872910T>ACA375249447ABL1c.1015T>A (p.Tyr339Asn)
c.958T>A (p.Tyr320Asn)
gnomAD v4
9g.130872910T>CCA375249448ABL1c.1015T>C (p.Tyr339His)
c.958T>C (p.Tyr320His)
9g.130872910T>GCA375249449ABL1c.1015T>G (p.Tyr339Asp)
c.958T>G (p.Tyr320Asp)
9g.130872911A=CA1881476042ABL1c.1016A= (p.Tyr339=)
c.959A= (p.Tyr320=)
9g.130872911A>CCA375249450ABL1c.1016A>C (p.Tyr339Ser)
c.959A>C (p.Tyr320Ser)
9g.130872911A>GCA5285352ABL1c.1016A>G (p.Tyr339Cys)
c.959A>G (p.Tyr320Cys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.130872911A>TCA375249451ABL1c.1016A>T (p.Tyr339Phe)
c.959A>T (p.Tyr320Phe)
9g.130872912C>ACA375249452ABL1c.1017C>A (p.Tyr339Ter)
c.960C>A (p.Tyr320Ter)
gnomAD v4
9g.130872912C=CA1881476044ABL1c.1017C= (p.Tyr339=)
c.960C= (p.Tyr320=)
9g.130872912C>GCA375249453ABL1c.1017C>G (p.Tyr339Ter)
c.960C>G (p.Tyr320Ter)
9g.130872912C>TCA467395087ABL1c.1017C>T (p.Tyr339=)
c.960C>T (p.Tyr320=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
9g.130872913G>ACA375249454ABL1c.1018G>A (p.Gly340Arg)
c.961G>A (p.Gly321Arg)
dbSNP gnomAD v4 COSMIC COSMIC COSMIC
9g.130872913G>CCA375249455ABL1c.1018G>C (p.Gly340Arg)
c.961G>C (p.Gly321Arg)
9g.130872913G>TCA375249456ABL1c.1018G>T (p.Gly340Trp)
c.961G>T (p.Gly321Trp)
9g.130872914G>ACA375249459ABL1c.1019G>A (p.Gly340Glu)
c.962G>A (p.Gly321Glu)
9g.130872914G>CCA375249457ABL1c.1019G>C (p.Gly340Ala)
c.962G>C (p.Gly321Ala)
9g.130872914G>TCA375249458ABL1c.1019G>T (p.Gly340Val)
c.962G>T (p.Gly321Val)
9g.130872915G>ACA467395090ABL1c.1020G>A (p.Gly340=)
c.963G>A (p.Gly321=)
9g.130872915G>CCA467395091ABL1c.1020G>C (p.Gly340=)
c.963G>C (p.Gly321=)
9g.130872915G>TCA467395092ABL1c.1020G>T (p.Gly340=)
c.963G>T (p.Gly321=)
9g.130872916A=CA1881476046ABL1c.1021A= (p.Asn341=)
c.964A= (p.Asn322=)
9g.130872916A>CCA375249460ABL1c.1021A>C (p.Asn341His)
c.964A>C (p.Asn322His)
9g.130872916A>GCA375249461ABL1c.1021A>G (p.Asn341Asp)
c.964A>G (p.Asn322Asp)
dbSNP gnomAD v2 gnomAD v4
9g.130872916A>TCA375249462ABL1c.1021A>T (p.Asn341Tyr)
c.964A>T (p.Asn322Tyr)
9g.130872917A>CCA375249463ABL1c.1022A>C (p.Asn341Thr)
c.965A>C (p.Asn322Thr)
9g.130872917A>GCA375249464ABL1c.1022A>G (p.Asn341Ser)
c.965A>G (p.Asn322Ser)
9g.130872917A>TCA375249465ABL1c.1022A>T (p.Asn341Ile)
c.965A>T (p.Asn322Ile)
9g.130872918C>ACA5285353ABL1c.1023C>A (p.Asn341Lys)
c.966C>A (p.Asn322Lys)
dbSNP ExAC gnomAD v3 gnomAD v4
9g.130872918C=CA1881476048ABL1c.1023C= (p.Asn341=)
c.966C= (p.Asn322=)
9g.130872918C>GCA375249466ABL1c.1023C>G (p.Asn341Lys)
c.966C>G (p.Asn322Lys)
9g.130872918C>TCA467395093ABL1c.1023C>T (p.Asn341=)
c.966C>T (p.Asn322=)
gnomAD v4
9g.130872919C>ACA375249467ABL1c.1024C>A (p.Leu342Ile)
c.967C>A (p.Leu323Ile)
9g.130872919C>GCA375249468ABL1c.1024C>G (p.Leu342Val)
c.967C>G (p.Leu323Val)
9g.130872919C>TCA375249469ABL1c.1024C>T (p.Leu342Phe)
c.967C>T (p.Leu323Phe)

Number of alleles fetched