Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.129528902C>ACA354496028RHOc.169C>A (p.Leu57Ile)
3g.129528902C>GCA354496029RHOc.169C>G (p.Leu57Val)
3g.129528902C>TCA354496030RHOc.169C>T (p.Leu57Phe)
dbSNP
3g.129528903T>ACA354496032RHOc.170T>A (p.Leu57His)
3g.129528903T>CCA354496033RHOc.170T>C (p.Leu57Pro)
3g.129528903T>GCA354496031RHOc.170T>G (p.Leu57Arg)
3g.129528904C>ACA435768946RHOc.171C>A (p.Leu57=)
3g.129528904C=CA1401205493RHOc.171C= (p.Leu57=)
3g.129528904C>GCA435768948RHOc.171C>G (p.Leu57=)
3g.129528904C>TCA2607072RHOc.171C>T (p.Leu57=)
dbSNP ExAC gnomAD v2 gnomAD v4
3g.129528905A>CCA354496036RHOc.172A>C (p.Thr58Pro)
3g.129528905A>GCA354496037RHOc.172A>G (p.Thr58Ala)
3g.129528905A>TCA354496040RHOc.172A>T (p.Thr58Ser)
3g.129528905_129528906delinsACCA1401205498RHOc.172_173delinsAC (p.Thr58=)
3g.129528905_129528906delinsTACA916082603RHOc.172_173delinsTA (p.Thr58Ter)
ClinVar dbSNP
3g.129528906C>ACA354496045RHOc.173C>A (p.Thr58Lys)
gnomAD v4
3g.129528906C=CA1401205509RHOc.173C= (p.Thr58=)
3g.129528906C>GCA256664RHOc.173C>G (p.Thr58Arg)
ClinVar dbSNP gnomAD v4
3g.129528906C>TCA2607073RHOc.173C>T (p.Thr58Met)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
3g.129528907G>ACA2607074RHOc.174G>A (p.Thr58=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129528907G>CCA435768949RHOc.174G>C (p.Thr58=)
3g.129528907G=CA1401205513RHOc.174G= (p.Thr58=)
3g.129528907G>TCA435768950RHOc.174G>T (p.Thr58=)
3g.129528908C>ACA354496050RHOc.175C>A (p.Leu59Ile)
dbSNP
3g.129528908C=CA1401205519RHOc.175C= (p.Leu59=)
3g.129528908C>GCA354496054RHOc.175C>G (p.Leu59Val)
3g.129528908C>TCA2607075RHOc.175C>T (p.Leu59Phe)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129528909T>ACA354496057RHOc.176T>A (p.Leu59His)
ClinVar dbSNP
3g.129528909T>CCA354496058RHOc.176T>C (p.Leu59Pro)
3g.129528909T>GCA354496062RHOc.176T>G (p.Leu59Arg)
ClinVar dbSNP
3g.129528910C>ACA435768952RHOc.177C>A (p.Leu59=)
3g.129528910C=CA1401205523RHOc.177C= (p.Leu59=)
3g.129528910C>GCA2607076RHOc.177C>G (p.Leu59=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
3g.129528910C>TCA435768953RHOc.177C>T (p.Leu59=)
3g.129528911T>ACA354496067RHOc.178T>A (p.Tyr60Asn)
3g.129528911T>CCA2607077RHOc.178T>C (p.Tyr60His)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129528911T>GCA354496079RHOc.178T>G (p.Tyr60Asp)
3g.129528911T=CA1401205528RHOc.178T= (p.Tyr60=)
3g.129528912A>CCA354496080RHOc.179A>C (p.Tyr60Ser)
3g.129528912A>GCA354496082RHOc.179A>G (p.Tyr60Cys)
3g.129528912A>TCA354496085RHOc.179A>T (p.Tyr60Phe)
3g.129528913C>ACA270021RHOc.180C>A (p.Tyr60Ter)
ClinVar dbSNP
3g.129528913C=CA1401205532RHOc.180C= (p.Tyr60=)
3g.129528913C>GCA354496086RHOc.180C>G (p.Tyr60Ter)
ClinVar dbSNP gnomAD v4
3g.129528913C>TCA435768956RHOc.180C>T (p.Tyr60=)
ClinVar dbSNP gnomAD v4
3g.129528914G>ACA2607078RHOc.181G>A (p.Val61Ile)
dbSNP ExAC gnomAD v2 gnomAD v4
3g.129528914G>CCA354496087RHOc.181G>C (p.Val61Leu)
3g.129528914G=CA1401205542RHOc.181G= (p.Val61=)
3g.129528914G>TCA354496088RHOc.181G>T (p.Val61Phe)
3g.129528915T>ACA354496091RHOc.182T>A (p.Val61Asp)

Number of alleles fetched