Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.129530975T>ACA354498371RHOc.461T>A (p.Ile154Asn)
3g.129530975T>CCA354498373RHOc.461T>C (p.Ile154Thr)
3g.129530975T>GCA354498375RHOc.461T>G (p.Ile154Ser)
3g.129530976C>ACA435643999RHOc.462C>A (p.Ile154=)
3g.129530976C>GCA354498376RHOc.462C>G (p.Ile154Met)
3g.129530976C>TCA435644002RHOc.462C>T (p.Ile154=)
gnomAD v4
3g.129530977A=CA1401209452RHOc.463A= (p.Met155=)
3g.129530977A>CCA354498379RHOc.463A>C (p.Met155Leu)
3g.129530977A>GCA2607162RHOc.463A>G (p.Met155Val)
dbSNP ExAC
3g.129530977A>TCA354498393RHOc.463A>T (p.Met155Leu)
3g.129530978T>ACA354498399RHOc.464T>A (p.Met155Lys)
3g.129530978T>CCA2607163RHOc.464T>C (p.Met155Thr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
3g.129530978T>GCA354498395RHOc.464T>G (p.Met155Arg)
3g.129530978T=CA1401209457RHOc.464T= (p.Met155=)
3g.129530979G>ACA354498402RHOc.465G>A (p.Met155Ile)
COSMIC
3g.129530979G>CCA354498404RHOc.465G>C (p.Met155Ile)
3g.129530979G>TCA354498406RHOc.465G>T (p.Met155Ile)
3g.129530980G>ACA354498408RHOc.466G>A (p.Gly156Ser)
gnomAD v4
3g.129530980G>CCA354498413RHOc.466G>C (p.Gly156Arg)
gnomAD v4
3g.129530980G>TCA354498415RHOc.466G>T (p.Gly156Cys)
3g.129530981G>ACA2607165RHOc.467G>A (p.Gly156Asp)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129530981G>CCA354498419RHOc.467G>C (p.Gly156Ala)
dbSNP gnomAD v2 gnomAD v4
3g.129530981G=CA1401209461RHOc.467G= (p.Gly156=)
3g.129530981G>TCA2607164RHOc.467G>T (p.Gly156Val)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
3g.129530982C>ACA435644023RHOc.468C>A (p.Gly156=)
3g.129530982C=CA1401209465RHOc.468C= (p.Gly156=)
3g.129530982C>GCA435644024RHOc.468C>G (p.Gly156=)
3g.129530982C>TCA2607166RHOc.468C>T (p.Gly156=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129530983G>ACA2607167RHOc.469G>A (p.Val157Ile)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129530983G>CCA354498423RHOc.469G>C (p.Val157Leu)
3g.129530983G=CA1401209468RHOc.469G= (p.Val157=)
3g.129530983G>TCA354498428RHOc.469G>T (p.Val157Phe)
3g.129530984T>ACA354498443RHOc.470T>A (p.Val157Asp)
3g.129530984T>CCA354498431RHOc.470T>C (p.Val157Ala)
3g.129530984T>GCA354498438RHOc.470T>G (p.Val157Gly)
3g.129530985T>ACA435644036RHOc.471T>A (p.Val157=)
3g.129530985T>CCA435644038RHOc.471T>C (p.Val157=)
3g.129530985T>GCA435644040RHOc.471T>G (p.Val157=)
dbSNP
3g.129530986G>ACA354498454RHOc.472G>A (p.Ala158Thr)
dbSNP
3g.129530986G>CCA354498455RHOc.472G>C (p.Ala158Pro)
3g.129530986G=CA1401209471RHOc.472G= (p.Ala158=)
3g.129530986G>TCA354498458RHOc.472G>T (p.Ala158Ser)
3g.129530987C>ACA354498460RHOc.473C>A (p.Ala158Asp)
3g.129530987C>GCA354498462RHOc.473C>G (p.Ala158Gly)
3g.129530987C>TCA354498463RHOc.473C>T (p.Ala158Val)
dbSNP
3g.129530988C>ACA435644049RHOc.474C>A (p.Ala158=)
3g.129530988C>GCA435644052RHOc.474C>G (p.Ala158=)
3g.129530988C>TCA435644054RHOc.474C>T (p.Ala158=)
3g.129530989T>ACA354498464RHOc.475T>A (p.Phe159Ile)
3g.129530989T>CCA354498465RHOc.475T>C (p.Phe159Leu)

Number of alleles fetched