Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.129528875A>CCA354495911RHOc.142A>C (p.Ile48Leu)
3g.129528875A>GCA354495913RHOc.142A>G (p.Ile48Val)
3g.129528875A>TCA354495914RHOc.142A>T (p.Ile48Phe)
3g.129528876T>ACA354495915RHOc.143T>A (p.Ile48Asn)
3g.129528876T>CCA354495918RHOc.143T>C (p.Ile48Thr)
COSMIC
3g.129528876T>GCA354495916RHOc.143T>G (p.Ile48Ser)
3g.129528877C>ACA435768919RHOc.144C>A (p.Ile48=)
gnomAD v4
3g.129528877C=CA1401205420RHOc.144C= (p.Ile48=)
3g.129528877C>GCA354495921RHOc.144C>G (p.Ile48Met)
gnomAD v4
3g.129528877C>TCA2607068RHOc.144C>T (p.Ile48=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
3g.129528878G>ACA2607069RHOc.145G>A (p.Val49Met)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129528878G>CCA354495924RHOc.145G>C (p.Val49Leu)
3g.129528878G=CA1401205426RHOc.145G= (p.Val49=)
3g.129528878G>TCA354495926RHOc.145G>T (p.Val49Leu)
3g.129528879T>ACA354495928RHOc.146T>A (p.Val49Glu)
3g.129528879T>CCA354495929RHOc.146T>C (p.Val49Ala)
3g.129528879T>GCA354495931RHOc.146T>G (p.Val49Gly)
3g.129528880G>ACA435768922RHOc.147G>A (p.Val49=)
3g.129528880G>CCA435768923RHOc.147G>C (p.Val49=)
3g.129528880G>TCA435768924RHOc.147G>T (p.Val49=)
3g.129528881C>ACA354495932RHOc.148C>A (p.Leu50Met)
3g.129528881C>GCA354495933RHOc.148C>G (p.Leu50Val)
3g.129528881C>TCA435768925RHOc.148C>T (p.Leu50=)
gnomAD v4
3g.129528882T>ACA354495935RHOc.149T>A (p.Leu50Gln)
3g.129528882T>CCA354495937RHOc.149T>C (p.Leu50Pro)
dbSNP
3g.129528882T>GCA354495941RHOc.149T>G (p.Leu50Arg)
3g.129528882T=CA1401205436RHOc.149T= (p.Leu50=)
3g.129528883G>ACA435768927RHOc.150G>A (p.Leu50=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.129528883G>CCA435768928RHOc.150G>C (p.Leu50=)
3g.129528883G=CA1401205443RHOc.150G= (p.Leu50=)
3g.129528883G>TCA435768929RHOc.150G>T (p.Leu50=)
3g.129528884G>ACA354495942RHOc.151G>A (p.Gly51Ser)
3g.129528884G>CCA256687RHOc.151G>C (p.Gly51Arg)
ClinVar dbSNP gnomAD v4
3g.129528884G=CA1401205449RHOc.151G= (p.Gly51=)
3g.129528884G>TCA354495943RHOc.151G>T (p.Gly51Cys)
dbSNP
3g.129528885G>ACA354495946RHOc.152G>A (p.Gly51Asp)
3g.129528885G>CCA2607070RHOc.152G>C (p.Gly51Ala)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129528885G=CA1401205458RHOc.152G= (p.Gly51=)
3g.129528885G>TCA354495947RHOc.152G>T (p.Gly51Val)
ClinVar dbSNP gnomAD v3 gnomAD v4
3g.129528886C>ACA435768930RHOc.153C>A (p.Gly51=)
3g.129528886C>GCA435768931RHOc.153C>G (p.Gly51=)
3g.129528886C>TCA435768932RHOc.153C>T (p.Gly51=)
gnomAD v4
3g.129528887T>ACA354495948RHOc.154T>A (p.Phe52Ile)
3g.129528887T>CCA82646800RHOc.154T>C (p.Phe52Leu)
dbSNP
3g.129528887T>GCA354495950RHOc.154T>G (p.Phe52Val)
3g.129528887T=CA1401205473RHOc.154T= (p.Phe52=)
3g.129528888T>ACA354495952RHOc.155T>A (p.Phe52Tyr)
gnomAD v4
3g.129528888T>CCA354495954RHOc.155T>C (p.Phe52Ser)
3g.129528888T>GCA354495955RHOc.155T>G (p.Phe52Cys)
3g.129528889C>ACA354495958RHOc.156C>A (p.Phe52Leu)

Number of alleles fetched