Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.129529062G>ACA256681RHOc.329G>A (p.Cys110Tyr)
ClinVar dbSNP
3g.129529062G>CCA354496916RHOc.329G>C (p.Cys110Ser)
3g.129529062G=CA1401206162RHOc.329G= (p.Cys110=)
3g.129529062G>TCA354496917RHOc.329G>T (p.Cys110Phe)
ClinVar
3g.129529063C>ACA354496919RHOc.330C>A (p.Cys110Ter)
gnomAD v4
3g.129529063C>GCA354496922RHOc.330C>G (p.Cys110Trp)
ClinVar
3g.129529063C>TCA435768812RHOc.330C>T (p.Cys110=)
dbSNP gnomAD v4
3g.129529064A>CCA354496926RHOc.331A>C (p.Asn111His)
3g.129529064A>GCA354496925RHOc.331A>G (p.Asn111Asp)
3g.129529064A>TCA354496923RHOc.331A>T (p.Asn111Tyr)
3g.129529065A=CA1401206167RHOc.332A= (p.Asn111=)
3g.129529065A>CCA354496927RHOc.332A>C (p.Asn111Thr)
3g.129529065A>GCA2607113RHOc.332A>G (p.Asn111Ser)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129529065A>TCA354496928RHOc.332A>T (p.Asn111Ile)
3g.129529066T>ACA354496930RHOc.333T>A (p.Asn111Lys)
3g.129529066T>CCA435768816RHOc.333T>C (p.Asn111=)
3g.129529066T>GCA354496931RHOc.333T>G (p.Asn111Lys)
3g.129529067T>ACA354496932RHOc.334T>A (p.Leu112Met)
3g.129529067T>CCA435768817RHOc.334T>C (p.Leu112=)
dbSNP gnomAD v4
3g.129529067T>GCA354496933RHOc.334T>G (p.Leu112Val)
3g.129529068T>ACA354496934RHOc.335T>A (p.Leu112Ter)
3g.129529068T>CCA82647073RHOc.335T>C (p.Leu112Ser)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.129529068T>GCA354496935RHOc.335T>G (p.Leu112Trp)
3g.129529068T=CA1401206172RHOc.335T= (p.Leu112=)
3g.129529069G>ACA435768818RHOc.336G>A (p.Leu112=)
gnomAD v4
3g.129529069G>CCA354496937RHOc.336G>C (p.Leu112Phe)
dbSNP
3g.129529069G>TCA354496939RHOc.336G>T (p.Leu112Phe)
3g.129529070G>ACA354496945RHOc.337G>A (p.Glu113Lys)
ClinVar dbSNP
3g.129529070G>CCA354496942RHOc.337G>C (p.Glu113Gln)
3g.129529070G>TCA354496941RHOc.337G>T (p.Glu113Ter)
3g.129529071A>CCA354496947RHOc.338A>C (p.Glu113Ala)
3g.129529071A>GCA354496950RHOc.338A>G (p.Glu113Gly)
3g.129529071A>TCA354496953RHOc.338A>T (p.Glu113Val)
3g.129529072G>ACA435768823RHOc.339G>A (p.Glu113=)
3g.129529072G>CCA354496954RHOc.339G>C (p.Glu113Asp)
3g.129529072G>TCA354496957RHOc.339G>T (p.Glu113Asp)
3g.129529073G>ACA354496961RHOc.340G>A (p.Gly114Ser)
3g.129529073G>CCA354496959RHOc.340G>C (p.Gly114Arg)
3g.129529073G>TCA354496958RHOc.340G>T (p.Gly114Cys)
3g.129529074G>ACA256688RHOc.341G>A (p.Gly114Asp)
ClinVar dbSNP gnomAD v4
3g.129529074G>CCA2607114RHOc.341G>C (p.Gly114Ala)
dbSNP ExAC gnomAD v2 gnomAD v4
3g.129529074G=CA1401206183RHOc.341G= (p.Gly114=)
3g.129529074G>TCA354496965RHOc.341G>T (p.Gly114Val)
ClinVar dbSNP
3g.129529075C>ACA435768827RHOc.342C>A (p.Gly114=)
3g.129529075C=CA1401206190RHOc.342C= (p.Gly114=)
3g.129529075C>GCA435768828RHOc.342C>G (p.Gly114=)
3g.129529075C>TCA435768829RHOc.342C>T (p.Gly114=)
dbSNP gnomAD v2 gnomAD v4
3g.129529076T>ACA354496967RHOc.343T>A (p.Phe115Ile)
3g.129529076T>CCA354496969RHOc.343T>C (p.Phe115Leu)
3g.129529076T>GCA354496970RHOc.343T>G (p.Phe115Val)

Number of alleles fetched