Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.25010263G>ACA515748642ARXc.1116C>T (p.Val372=)
Xg.25010263G>CCA515748639ARXc.1116C>G (p.Val372=)
Xg.25010263G=CA2420208033ARXc.1116C= (p.Val372=)
Xg.25010263G>TCA515748640ARXc.1116C>A (p.Val372=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
Xg.25010264A>CCA412611714ARXc.1115T>G (p.Val372Gly)
Xg.25010264A>GCA412611715ARXc.1115T>C (p.Val372Ala)
Xg.25010264A>TCA412611716ARXc.1115T>A (p.Val372Asp)
Xg.25010265C>ACA412611717ARXc.1114G>T (p.Val372Phe)
Xg.25010265C>GCA412611718ARXc.1114G>C (p.Val372Leu)
Xg.25010265C>TCA412611719ARXc.1114G>A (p.Val372Ile)
Xg.25010266T>ACA515748649ARXc.1113A>T (p.Arg371=)
Xg.25010266T>CCA515748651ARXc.1113A>G (p.Arg371=)
Xg.25010266T>GCA515748653ARXc.1113A>C (p.Arg371=)
Xg.25010267C>ACA412611720ARXc.1112G>T (p.Arg371Leu)
Xg.25010267C>GCA412611721ARXc.1112G>C (p.Arg371Pro)
Xg.25010267C>TCA412611722ARXc.1112G>A (p.Arg371Gln)
ClinVar dbSNP
Xg.25010268G>ACA233280ARXc.1111C>T (p.Arg371Ter)
ClinVar dbSNP gnomAD v2
Xg.25010268G>CCA412611723ARXc.1111C>G (p.Arg371Gly)
Xg.25010268G=CA2420208034ARXc.1111C= (p.Arg371=)
Xg.25010268G>TCA515748657ARXc.1111C>A (p.Arg371=)
COSMIC
Xg.25010270delCA2580100526ARXc.1111del (p.Arg371GlufsTer?)
ClinVar
Xg.25010269G>ACA515748662ARXc.1110C>T (p.Ala370=)
Xg.25010269G>CCA515748661ARXc.1110C>G (p.Ala370=)
Xg.25010269G>TCA515748664ARXc.1110C>A (p.Ala370=)
Xg.25010270G>ACA412611724ARXc.1109C>T (p.Ala370Val)
gnomAD v4
Xg.25010270G>CCA412611726ARXc.1109C>G (p.Ala370Gly)
Xg.25010270G>TCA412611725ARXc.1109C>A (p.Ala370Asp)
Xg.25010271C>ACA412611727ARXc.1108G>T (p.Ala370Ser)
Xg.25010271C>GCA412611729ARXc.1108G>C (p.Ala370Pro)
Xg.25010271C>TCA412611728ARXc.1108G>A (p.Ala370Thr)
Xg.25010272C>ACA412611730ARXc.1107G>T (p.Glu369Asp)
Xg.25010272C=CA2420208035ARXc.1107G= (p.Glu369=)
Xg.25010272C>GCA412611731ARXc.1107G>C (p.Glu369Asp)
Xg.25010272C>TCA10373837ARXc.1107G>A (p.Glu369=)
dbSNP ExAC gnomAD v2 gnomAD v4
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)

Number of alleles fetched