Chr Mutation (hg38) CAid Gene Transcript Linkouts
9g.130873024A>CCA375249696ABL1c.1129A>C (p.Asn377His)
c.1072A>C (p.Asn358His)
9g.130873024A>GCA375249697ABL1c.1129A>G (p.Asn377Asp)
c.1072A>G (p.Asn358Asp)
9g.130873024A>TCA375249698ABL1c.1129A>T (p.Asn377Tyr)
c.1072A>T (p.Asn358Tyr)
9g.130873025A>CCA375249699ABL1c.1130A>C (p.Asn377Thr)
c.1073A>C (p.Asn358Thr)
ClinVar
9g.130873025A>GCA375249700ABL1c.1130A>G (p.Asn377Ser)
c.1073A>G (p.Asn358Ser)
9g.130873025A>TCA375249701ABL1c.1130A>T (p.Asn377Ile)
c.1073A>T (p.Asn358Ile)
9g.130873026C>ACA375249702ABL1c.1131C>A (p.Asn377Lys)
c.1074C>A (p.Asn358Lys)
9g.130873026C>GCA375249703ABL1c.1131C>G (p.Asn377Lys)
c.1074C>G (p.Asn358Lys)
9g.130873026C>TCA467395212ABL1c.1131C>T (p.Asn377=)
c.1074C>T (p.Asn358=)
9g.130873027T>ACA16602580ABL1c.1132T>A (p.Phe378Ile)
c.1075T>A (p.Phe359Ile)
ClinVar dbSNP COSMIC
9g.130873027T>CCA16602581ABL1c.1132T>C (p.Phe378Leu)
c.1075T>C (p.Phe359Leu)
ClinVar dbSNP
9g.130873027T>GCA16602557ABL1c.1132T>G (p.Phe378Val)
c.1075T>G (p.Phe359Val)
ClinVar dbSNP COSMIC
9g.130873027T=CA1881476182ABL1c.1132T= (p.Phe378=)
c.1075T= (p.Phe359=)
9g.130873028T>ACA375249705ABL1c.1133T>A (p.Phe378Tyr)
c.1076T>A (p.Phe359Tyr)
9g.130873028T>CCA375249704ABL1c.1133T>C (p.Phe378Ser)
c.1076T>C (p.Phe359Ser)
9g.130873028T>GCA16602582ABL1c.1133T>G (p.Phe378Cys)
c.1076T>G (p.Phe359Cys)
ClinVar dbSNP COSMIC
9g.130873028T=CA1881476202ABL1c.1133T= (p.Phe378=)
c.1076T= (p.Phe359=)
9g.130873029C>ACA375249706ABL1c.1134C>A (p.Phe378Leu)
c.1077C>A (p.Phe359Leu)
9g.130873029C>GCA375249707ABL1c.1134C>G (p.Phe378Leu)
c.1077C>G (p.Phe359Leu)
9g.130873029C>TCA467395214ABL1c.1134C>T (p.Phe378=)
c.1077C>T (p.Phe359=)
COSMIC COSMIC COSMIC
9g.130873030A>CCA375249708ABL1c.1135A>C (p.Ile379Leu)
c.1078A>C (p.Ile360Leu)
9g.130873030A>GCA375249709ABL1c.1135A>G (p.Ile379Val)
c.1078A>G (p.Ile360Val)
9g.130873030A>TCA375249710ABL1c.1135A>T (p.Ile379Phe)
c.1078A>T (p.Ile360Phe)
9g.130873031T>ACA375249711ABL1c.1136T>A (p.Ile379Asn)
c.1079T>A (p.Ile360Asn)
9g.130873031T>CCA375249712ABL1c.1136T>C (p.Ile379Thr)
c.1079T>C (p.Ile360Thr)
dbSNP
9g.130873031T>GCA375249713ABL1c.1136T>G (p.Ile379Ser)
c.1079T>G (p.Ile360Ser)
9g.130873032C>ACA467395217ABL1c.1137C>A (p.Ile379=)
c.1080C>A (p.Ile360=)
9g.130873032C>GCA375249714ABL1c.1137C>G (p.Ile379Met)
c.1080C>G (p.Ile360Met)
9g.130873032C>TCA467395218ABL1c.1137C>T (p.Ile379=)
c.1080C>T (p.Ile360=)
9g.130873033C>ACA375249715ABL1c.1138C>A (p.His380Asn)
c.1081C>A (p.His361Asn)
9g.130873033C>GCA375249716ABL1c.1138C>G (p.His380Asp)
c.1081C>G (p.His361Asp)
9g.130873033C>TCA375249717ABL1c.1138C>T (p.His380Tyr)
c.1081C>T (p.His361Tyr)
9g.130873034A>CCA375249720ABL1c.1139A>C (p.His380Pro)
c.1082A>C (p.His361Pro)
9g.130873034A>GCA375249718ABL1c.1139A>G (p.His380Arg)
c.1082A>G (p.His361Arg)
dbSNP
9g.130873034A>TCA375249719ABL1c.1139A>T (p.His380Leu)
c.1082A>T (p.His361Leu)
9g.130873035C>ACA375249721ABL1c.1140C>A (p.His380Gln)
c.1083C>A (p.His361Gln)
9g.130873035C=CA1881476206ABL1c.1140C= (p.His380=)
c.1083C= (p.His361=)
9g.130873035C>GCA375249722ABL1c.1140C>G (p.His380Gln)
c.1083C>G (p.His361Gln)
9g.130873035C>TCA5285370ABL1c.1140C>T (p.His380=)
c.1083C>T (p.His361=)
dbSNP ExAC gnomAD v2 gnomAD v4
9g.130873036A>CCA467395220ABL1c.1141A>C (p.Arg381=)
c.1084A>C (p.Arg362=)
9g.130873036A>GCA375249723ABL1c.1141A>G (p.Arg381Gly)
c.1084A>G (p.Arg362Gly)
9g.130873036A>TCA375249724ABL1c.1141A>T (p.Arg381Ter)
c.1084A>T (p.Arg362Ter)
9g.130873036_130873037delCA645556987ABL1c.1141_1142del (p.Asp382SerfsTer18)
c.1084_1085del (p.Asp363SerfsTer18)
COSMIC COSMIC COSMIC
9g.130873037G>ACA375249725ABL1c.1142G>A (p.Arg381Lys)
c.1085G>A (p.Arg362Lys)
dbSNP COSMIC COSMIC COSMIC
9g.130873037G>CCA375249726ABL1c.1142G>C (p.Arg381Thr)
c.1085G>C (p.Arg362Thr)
9g.130873037G>TCA375249727ABL1c.1142G>T (p.Arg381Ile)
c.1085G>T (p.Arg362Ile)
9g.130873037_130878415delCA658820873ABL1c.1142_1328del
c.1085_1271del
9g.130873038G>ACA375249728ABL1c.1142+1G>A (n.1142+1G>A)
c.1085+1G>A (n.1085+1G>A)
9g.130873038G>CCA375249729ABL1c.1142+1G>C (n.1142+1G>C)
c.1085+1G>C (n.1085+1G>C)
9g.130873038G>TCA375249730ABL1c.1142+1G>T (n.1142+1G>T)
c.1085+1G>T (n.1085+1G>T)

Number of alleles fetched