Chr Mutation (hg38) CAid Gene Transcript Linkouts
6g.49451683_49451706delCA913110642MMUTc.1092_1115del (p.Tyr364Ter)
6g.49451683_49451706delinsATTGCAGTACGGACAATATTATTGCA1627389369MMUTc.1092_1115delinsCAATAATATTGTCCGTACTGCAAT (p.Tyr364=)
6g.49451685_49451707delCA567155986MMUTc.1092_1114del (p.Asn365ArgfsTer19)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
6g.49451693G>ACA347895MMUTc.1105C>T (p.Arg369Cys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.49451693G>CCA364399134MMUTc.1105C>G (p.Arg369Gly)
6g.49451693G=CA1627389374MMUTc.1105C= (p.Arg369=)
6g.49451693G>TCA364399136MMUTc.1105C>A (p.Arg369Ser)
6g.49451694G>ACA450606661MMUTc.1104C>T (p.Val368=)
6g.49451694G>CCA450606662MMUTc.1104C>G (p.Val368=)
6g.49451694G>TCA450606663MMUTc.1104C>A (p.Val368=)
6g.49451695A>CCA364399139MMUTc.1103T>G (p.Val368Gly)
6g.49451695A>GCA364399140MMUTc.1103T>C (p.Val368Ala)
gnomAD v4
6g.49451695A>TCA364399141MMUTc.1103T>A (p.Val368Asp)
6g.49451695_49451696delinsACCA1627389375MMUTc.1102_1103delinsGT (p.Val368=)
6g.49451696delCA1139659594MMUTc.1102del (p.Val368SerfsTer5)
ClinVar dbSNP
6g.49451696C>ACA364399142MMUTc.1102G>T (p.Val368Phe)
6g.49451696C=CA1627389376MMUTc.1102G= (p.Val368=)
6g.49451696C>GCA364399144MMUTc.1102G>C (p.Val368Leu)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
6g.49451696C>TCA364399145MMUTc.1102G>A (p.Val368Ile)
6g.49451697A=CA1627389377MMUTc.1101T= (p.Ile367=)
6g.49451697A>CCA364399146MMUTc.1101T>G (p.Ile367Met)
6g.49451697A>GCA450606664MMUTc.1101T>C (p.Ile367=)
ClinVar dbSNP gnomAD v2 gnomAD v4
6g.49451697A>TCA450606665MMUTc.1101T>A (p.Ile367=)
6g.49451698A>CCA364399152MMUTc.1100T>G (p.Ile367Ser)
6g.49451698A>GCA364399151MMUTc.1100T>C (p.Ile367Thr)
gnomAD v4
6g.49451698A>TCA364399149MMUTc.1100T>A (p.Ile367Asn)
6g.49451699T>ACA364399153MMUTc.1099A>T (p.Ile367Phe)
6g.49451699T>CCA364399154MMUTc.1099A>G (p.Ile367Val)
6g.49451699T>GCA364399155MMUTc.1099A>C (p.Ile367Leu)
6g.49451700A=CA1627389378MMUTc.1098T= (p.Asn366=)
6g.49451700A>CCA364399156MMUTc.1098T>G (p.Asn366Lys)
6g.49451700A>GCA450606666MMUTc.1098T>C (p.Asn366=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
6g.49451700A>TCA364399159MMUTc.1098T>A (p.Asn366Lys)
6g.49451701T>ACA364399161MMUTc.1097A>T (p.Asn366Ile)
6g.49451701T>CCA347901MMUTc.1097A>G (p.Asn366Ser)
ClinVar dbSNP
6g.49451701T>GCA364399163MMUTc.1097A>C (p.Asn366Thr)
6g.49451701T=CA1627389379MMUTc.1097A= (p.Asn366=)
6g.49451702T>ACA364399165MMUTc.1096A>T (p.Asn366Tyr)
6g.49451702T>CCA364399166MMUTc.1096A>G (p.Asn366Asp)
6g.49451702T>GCA364399167MMUTc.1096A>C (p.Asn366His)
6g.49451703A>CCA364399169MMUTc.1095T>G (p.Asn365Lys)
6g.49451703A>GCA450606667MMUTc.1095T>C (p.Asn365=)
6g.49451703A>TCA364399171MMUTc.1095T>A (p.Asn365Lys)
6g.49451704T>ACA364399175MMUTc.1094A>T (p.Asn365Ile)
6g.49451704T>CCA364399176MMUTc.1094A>G (p.Asn365Ser)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
6g.49451704T>GCA364399174MMUTc.1094A>C (p.Asn365Thr)
6g.49451704T=CA1627389380MMUTc.1094A= (p.Asn365=)
6g.49451705T>ACA364399177MMUTc.1093A>T (p.Asn365Tyr)
6g.49451705T>CCA3846958MMUTc.1093A>G (p.Asn365Asp)
dbSNP ExAC gnomAD v2
6g.49451705T>GCA364399179MMUTc.1093A>C (p.Asn365His)
dbSNP gnomAD v3 gnomAD v4

Number of alleles fetched