Chr Mutation (hg38) CAid Gene Transcript Linkouts
6g.49451568_49451570delCA1627389324MMUTc.1233_1235del (p.Ile412del)
ClinVar dbSNP
6g.49451565_49451570delCA2499218330MMUTc.1230_1235del (p.Ile411_Ile412del)
ClinVar dbSNP
6g.49451568G>ACA450606394MMUTc.1230C>T (p.Ile410=)
6g.49451568G>CCA364398843MMUTc.1230C>G (p.Ile410Met)
6g.49451568G>TCA450606391MMUTc.1230C>A (p.Ile410=)
6g.49451569A>CCA364398844MMUTc.1229T>G (p.Ile410Ser)
6g.49451569A>GCA364398845MMUTc.1229T>C (p.Ile410Thr)
6g.49451569A>TCA364398846MMUTc.1229T>A (p.Ile410Asn)
6g.49451570T>ACA364398849MMUTc.1228A>T (p.Ile410Phe)
6g.49451570T>CCA364398847MMUTc.1228A>G (p.Ile410Val)
6g.49451570T>GCA364398848MMUTc.1228A>C (p.Ile410Leu)
6g.49451571T>ACA364398850MMUTc.1227A>T (p.Gln409His)
6g.49451571T>CCA450606402MMUTc.1227A>G (p.Gln409=)
6g.49451571T>GCA364398851MMUTc.1227A>C (p.Gln409His)
6g.49451572T>ACA364398852MMUTc.1226A>T (p.Gln409Leu)
6g.49451572T>CCA364398853MMUTc.1226A>G (p.Gln409Arg)
6g.49451572T>GCA364398854MMUTc.1226A>C (p.Gln409Pro)
6g.49451573G>ACA364398855MMUTc.1225C>T (p.Gln409Ter)
gnomAD v4
6g.49451573G>CCA364398857MMUTc.1225C>G (p.Gln409Glu)
6g.49451573G>TCA364398856MMUTc.1225C>A (p.Gln409Lys)
6g.49451574T>ACA450606411MMUTc.1224A>T (p.Thr408=)
6g.49451574T>CCA450606413MMUTc.1224A>G (p.Thr408=)
gnomAD v4
6g.49451574T>GCA450606412MMUTc.1224A>C (p.Thr408=)
6g.49451575G>ACA364398858MMUTc.1223C>T (p.Thr408Ile)
gnomAD v4
6g.49451575G>CCA364398859MMUTc.1223C>G (p.Thr408Arg)
6g.49451575G>TCA364398860MMUTc.1223C>A (p.Thr408Lys)
6g.49451576T>ACA3846937MMUTc.1222A>T (p.Thr408Ser)
dbSNP ExAC gnomAD v2 gnomAD v4
6g.49451576T>CCA364398861MMUTc.1222A>G (p.Thr408Ala)
6g.49451576T>GCA364398862MMUTc.1222A>C (p.Thr408Pro)
6g.49451576T=CA1627389327MMUTc.1222A= (p.Thr408=)
6g.49451577G>ACA450606421MMUTc.1221C>T (p.Asn407=)
6g.49451577G>CCA364398863MMUTc.1221C>G (p.Asn407Lys)
6g.49451577G>TCA364398864MMUTc.1221C>A (p.Asn407Lys)
6g.49451578T>ACA364398865MMUTc.1220A>T (p.Asn407Ile)
6g.49451578T>CCA3846938MMUTc.1220A>G (p.Asn407Ser)
dbSNP ExAC gnomAD v2 gnomAD v4
6g.49451578T>GCA364398866MMUTc.1220A>C (p.Asn407Thr)
6g.49451578T=CA1627389328MMUTc.1220A= (p.Asn407=)
6g.49451579T>ACA3846939MMUTc.1219A>T (p.Asn407Tyr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.49451579T>CCA364398868MMUTc.1219A>G (p.Asn407Asp)
6g.49451579T>GCA364398867MMUTc.1219A>C (p.Asn407His)
6g.49451579T=CA1627389330MMUTc.1219A= (p.Asn407=)
6g.49451579_49451580delinsTCCA1627389329MMUTc.1218_1219delinsGA (p.Arg406=)
6g.49451580C>ACA364398869MMUTc.1218G>T (p.Arg406Ser)
6g.49451580C>GCA364398870MMUTc.1218G>C (p.Arg406Ser)
6g.49451580C>TCA450606432MMUTc.1218G>A (p.Arg406=)
6g.49451581delCA138796356MMUTc.1218del (p.Asn407ThrfsTer24)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
6g.49451581C>ACA364398871MMUTc.1217G>T (p.Arg406Met)
6g.49451581C>GCA364398872MMUTc.1217G>C (p.Arg406Thr)
6g.49451581C>TCA364398873MMUTc.1217G>A (p.Arg406Lys)
COSMIC
6g.49451582T>ACA364398874MMUTc.1216A>T (p.Arg406Trp)

Number of alleles fetched