Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.6718331C>ACA403645200C3n.410G>T
c.226G>T (p.Val76Leu)
c.349G>T (p.Val117Leu)
19g.6718331C>GCA403645201C3n.410G>C
c.226G>C (p.Val76Leu)
c.349G>C (p.Val117Leu)
19g.6718331C>TCA403645202C3n.410G>A
c.226G>A (p.Val76Met)
c.349G>A (p.Val117Met)
19g.6718332C>ACA505125183C3n.409G>T
c.225G>T (p.Val75=)
c.348G>T (p.Val116=)
gnomAD v4
19g.6718332C>GCA505125181C3n.409G>C
c.225G>C (p.Val75=)
c.348G>C (p.Val116=)
19g.6718332C>TCA505125182C3n.409G>A
c.225G>A (p.Val75=)
c.348G>A (p.Val116=)
19g.6718333A>CCA403645203C3n.408T>G
c.224T>G (p.Val75Gly)
c.347T>G (p.Val116Gly)
19g.6718333A>GCA403645204C3n.408T>C
c.224T>C (p.Val75Ala)
c.347T>C (p.Val116Ala)
gnomAD v4
19g.6718333A>TCA403645205C3n.408T>A
c.224T>A (p.Val75Glu)
c.347T>A (p.Val116Glu)
19g.6718334C>ACA403645206C3n.407G>T
c.223G>T (p.Val75Leu)
c.346G>T (p.Val116Leu)
19g.6718334C>GCA403645207C3n.407G>C
c.223G>C (p.Val75Leu)
c.346G>C (p.Val116Leu)
19g.6718334C>TCA403645208C3n.407G>A
c.223G>A (p.Val75Met)
c.346G>A (p.Val116Met)
ClinVar
19g.6718335T>ACA403645209C3n.406A>T
c.222A>T (p.Gln74His)
c.345A>T (p.Gln115His)
gnomAD v4
19g.6718335T>CCA505125184C3n.406A>G
c.222A>G (p.Gln74=)
c.345A>G (p.Gln115=)
19g.6718335T>GCA403645210C3n.406A>C
c.222A>C (p.Gln74His)
c.345A>C (p.Gln115His)
19g.6718336T>ACA403645213C3n.405A>T
c.221A>T (p.Gln74Leu)
c.344A>T (p.Gln115Leu)
19g.6718336T>CCA403645212C3n.405A>G
c.221A>G (p.Gln74Arg)
c.344A>G (p.Gln115Arg)
19g.6718336T>GCA403645211C3n.405A>C
c.221A>C (p.Gln74Pro)
c.344A>C (p.Gln115Pro)
19g.6718337G>ACA403645214C3n.404C>T
c.220C>T (p.Gln74Ter)
c.343C>T (p.Gln115Ter)
19g.6718337G>CCA403645216C3n.404C>G
c.220C>G (p.Gln74Glu)
c.343C>G (p.Gln115Glu)
19g.6718337G=CA2320570628C3n.404C=
c.220C= (p.Gln74=)
c.343C= (p.Gln115=)
19g.6718337G>TCA403645215C3n.404C>A
c.220C>A (p.Gln74Lys)
c.343C>A (p.Gln115Lys)
dbSNP gnomAD v3 gnomAD v4
19g.6718338G>ACA505125185C3n.403C>T
c.219C>T (p.Thr73=)
c.342C>T (p.Thr114=)
dbSNP gnomAD v4
19g.6718338G>CCA505125186C3n.403C>G
c.219C>G (p.Thr73=)
c.342C>G (p.Thr114=)
gnomAD v4
19g.6718338G=CA2320570629C3n.403C=
c.219C= (p.Thr73=)
c.342C= (p.Thr114=)
19g.6718338G>TCA505125187C3n.403C>A
c.219C>A (p.Thr73=)
c.342C>A (p.Thr114=)
19g.6718339G>ACA9129842C3n.402C>T
c.218C>T (p.Thr73Ile)
c.341C>T (p.Thr114Ile)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.6718339G>CCA403645217C3n.402C>G
c.218C>G (p.Thr73Ser)
c.341C>G (p.Thr114Ser)
19g.6718339G=CA2320570630C3n.402C=
c.218C= (p.Thr73=)
c.341C= (p.Thr114=)
19g.6718339G>TCA403645218C3n.402C>A
c.218C>A (p.Thr73Asn)
c.341C>A (p.Thr114Asn)
dbSNP gnomAD v3 gnomAD v4
19g.6718340T>ACA403645219C3n.401A>T
c.217A>T (p.Thr73Ser)
c.340A>T (p.Thr114Ser)
19g.6718340T>CCA304803624C3n.401A>G
c.217A>G (p.Thr73Ala)
c.340A>G (p.Thr114Ala)
dbSNP gnomAD v4
19g.6718340T>GCA403645220C3n.401A>C
c.217A>C (p.Thr73Pro)
c.340A>C (p.Thr114Pro)
COSMIC
19g.6718340T=CA2320570631C3n.401A=
c.217A= (p.Thr73=)
c.340A= (p.Thr114=)
19g.6718341C>ACA505125188C3n.400G>T
c.216G>T (p.Gly72=)
c.339G>T (p.Gly113=)
19g.6718341C>GCA505125189C3n.400G>C
c.216G>C (p.Gly72=)
c.339G>C (p.Gly113=)
19g.6718341C>TCA505125190C3n.400G>A
c.216G>A (p.Gly72=)
c.339G>A (p.Gly113=)
19g.6718342C>ACA403645221C3n.399G>T
c.215G>T (p.Gly72Val)
c.338G>T (p.Gly113Val)
19g.6718342C>GCA403645222C3n.399G>C
c.215G>C (p.Gly72Ala)
c.338G>C (p.Gly113Ala)
19g.6718342C>TCA403645223C3n.399G>A
c.215G>A (p.Gly72Glu)
c.338G>A (p.Gly113Glu)
19g.6718343C>ACA403645224C3n.398G>T
c.214G>T (p.Gly72Trp)
c.337G>T (p.Gly113Trp)
19g.6718343C>GCA403645225C3n.398G>C
c.214G>C (p.Gly72Arg)
c.337G>C (p.Gly113Arg)
19g.6718343C>TCA403645226C3n.398G>A
c.214G>A (p.Gly72Arg)
c.337G>A (p.Gly113Arg)
19g.6718344G>ACA505125191C3n.397C>T
c.213C>T (p.Phe71=)
c.336C>T (p.Phe112=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.6718344G>CCA403645227C3n.397C>G
c.213C>G (p.Phe71Leu)
c.336C>G (p.Phe112Leu)
19g.6718344G=CA2320570632C3n.397C=
c.213C= (p.Phe71=)
c.336C= (p.Phe112=)
19g.6718344G>TCA403645228C3n.397C>A
c.213C>A (p.Phe71Leu)
c.336C>A (p.Phe112Leu)
19g.6718345A>CCA403645229C3n.396T>G
c.212T>G (p.Phe71Cys)
c.335T>G (p.Phe112Cys)
19g.6718345A>GCA403645230C3n.396T>C
c.212T>C (p.Phe71Ser)
c.335T>C (p.Phe112Ser)
19g.6718345A>TCA403645231C3n.396T>A
c.212T>A (p.Phe71Tyr)
c.335T>A (p.Phe112Tyr)

Number of alleles fetched