Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.25010273T>ACA412611732ARXc.1106A>T (p.Glu369Val)
Xg.25010273T>CCA412611733ARXc.1106A>G (p.Glu369Gly)
Xg.25010273T>GCA412611734ARXc.1106A>C (p.Glu369Ala)
Xg.25010274C>ACA121412ARXc.1105G>T (p.Glu369Ter)
ClinVar dbSNP gnomAD v4
Xg.25010274C=CA2420208036ARXc.1105G= (p.Glu369=)
Xg.25010274C>GCA412611735ARXc.1105G>C (p.Glu369Gln)
Xg.25010274C>TCA16608407ARXc.1105G>A (p.Glu369Lys)
ClinVar dbSNP
Xg.25010275G>ACA10373838ARXc.1104C>T (p.Thr368=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.25010275G>CCA515748679ARXc.1104C>G (p.Thr368=)
Xg.25010275G=CA2420208037ARXc.1104C= (p.Thr368=)
Xg.25010275G>TCA515748677ARXc.1104C>A (p.Thr368=)
dbSNP gnomAD v2 gnomAD v4
Xg.25010276G>ACA412611736ARXc.1103C>T (p.Thr368Ile)
Xg.25010276G>CCA412611737ARXc.1103C>G (p.Thr368Ser)
Xg.25010276G>TCA412611738ARXc.1103C>A (p.Thr368Asn)
Xg.25010277T>ACA412611739ARXc.1102A>T (p.Thr368Ser)
Xg.25010277T>CCA412611741ARXc.1102A>G (p.Thr368Ala)
Xg.25010277T>GCA412611740ARXc.1102A>C (p.Thr368Pro)
Xg.25010278C>ACA412611742ARXc.1101G>T (p.Leu367Phe)
Xg.25010278C>GCA412611743ARXc.1101G>C (p.Leu367Phe)
Xg.25010278C>TCA515748685ARXc.1101G>A (p.Leu367=)
Xg.25010279A>CCA412611744ARXc.1100T>G (p.Leu367Trp)
Xg.25010279A>GCA412611745ARXc.1100T>C (p.Leu367Ser)
Xg.25010279A>TCA412611746ARXc.1100T>A (p.Leu367Ter)
Xg.25010280A>CCA412611747ARXc.1099T>G (p.Leu367Val)
Xg.25010280A>GCA515748689ARXc.1099T>C (p.Leu367=)
Xg.25010280A>TCA412611748ARXc.1099T>A (p.Leu367Met)
Xg.25010281G>ACA515748691ARXc.1098C>T (p.Asp366=)
gnomAD v4
Xg.25010281G>CCA412611749ARXc.1098C>G (p.Asp366Glu)
Xg.25010281G>TCA412611750ARXc.1098C>A (p.Asp366Glu)
Xg.25010282T>ACA412611753ARXc.1097A>T (p.Asp366Val)
Xg.25010282T>CCA412611752ARXc.1097A>G (p.Asp366Gly)
Xg.25010282T>GCA412611751ARXc.1097A>C (p.Asp366Ala)
Xg.25010282_25010283delinsTCCA2420208038ARXc.1096_1097delinsGA (p.Asp366=)
Xg.25010283C>ACA412611754ARXc.1096G>T (p.Asp366Tyr)
Xg.25010283C>GCA412611755ARXc.1096G>C (p.Asp366His)
Xg.25010283C>TCA412611756ARXc.1096G>A (p.Asp366Asn)
Xg.25010284delCA213326ARXc.1096del (p.Asp366ThrfsTer2)
ClinVar dbSNP
Xg.25010284C>ACA515748698ARXc.1095G>T (p.Leu365=)
gnomAD v4
Xg.25010284C>GCA515748702ARXc.1095G>C (p.Leu365=)
Xg.25010284C>TCA515748700ARXc.1095G>A (p.Leu365=)
Xg.25010285A>CCA412611757ARXc.1094T>G (p.Leu365Arg)
Xg.25010285A>GCA412611758ARXc.1094T>C (p.Leu365Pro)
Xg.25010285A>TCA412611759ARXc.1094T>A (p.Leu365Gln)
Xg.25010286G>ACA515748705ARXc.1093C>T (p.Leu365=)
dbSNP
Xg.25010286G>CCA412611760ARXc.1093C>G (p.Leu365Val)
Xg.25010286G=CA2420208039ARXc.1093C= (p.Leu365=)
Xg.25010286G>TCA412611761ARXc.1093C>A (p.Leu365Met)
COSMIC
Xg.25010287C>ACA412611762ARXc.1092G>T (p.Arg364Ser)
Xg.25010287C>GCA412611763ARXc.1092G>C (p.Arg364Ser)
Xg.25010287C>TCA515748709ARXc.1092G>A (p.Arg364=)

Number of alleles fetched