Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.129528866T>ACA354495882RHOc.133T>A (p.Phe45Ile)
3g.129528866T>CCA256666RHOc.133T>C (p.Phe45Leu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129528866T>GCA354495884RHOc.133T>G (p.Phe45Val)
3g.129528866T=CA1401205403RHOc.133T= (p.Phe45=)
3g.129528867T>ACA354495886RHOc.134T>A (p.Phe45Tyr)
3g.129528867T>CCA354495888RHOc.134T>C (p.Phe45Ser)
3g.129528867T>GCA354495889RHOc.134T>G (p.Phe45Cys)
3g.129528868T>ACA354495891RHOc.135T>A (p.Phe45Leu)
3g.129528868T>CCA435768908RHOc.135T>C (p.Phe45=)
dbSNP
3g.129528868T>GCA354495894RHOc.135T>G (p.Phe45Leu)
3g.129528869C>ACA354495899RHOc.136C>A (p.Leu46Met)
3g.129528869C>GCA354495902RHOc.136C>G (p.Leu46Val)
3g.129528869C>TCA435768909RHOc.136C>T (p.Leu46=)
3g.129528870T>ACA354495903RHOc.137T>A (p.Leu46Gln)
3g.129528870T>CCA354495904RHOc.137T>C (p.Leu46Pro)
3g.129528870T>GCA354495905RHOc.137T>G (p.Leu46Arg)
ClinVar dbSNP
3g.129528870T=CA1401205410RHOc.137T= (p.Leu46=)
3g.129528871G>ACA435768910RHOc.138G>A (p.Leu46=)
gnomAD v4
3g.129528871G>CCA435768911RHOc.138G>C (p.Leu46=)
3g.129528871G>TCA435768912RHOc.138G>T (p.Leu46=)
3g.129528872C>ACA354495906RHOc.139C>A (p.Leu47Met)
3g.129528872C=CA1401205415RHOc.139C= (p.Leu47=)
3g.129528872C>GCA354495907RHOc.139C>G (p.Leu47Val)
3g.129528872C>TCA435768914RHOc.139C>T (p.Leu47=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.129528873T>ACA354495908RHOc.140T>A (p.Leu47Gln)
3g.129528873T>CCA354495909RHOc.140T>C (p.Leu47Pro)
3g.129528873T>GCA354495910RHOc.140T>G (p.Leu47Arg)
3g.129528874G>ACA435768915RHOc.141G>A (p.Leu47=)
3g.129528874G>CCA435768916RHOc.141G>C (p.Leu47=)
dbSNP
3g.129528874G>TCA435768917RHOc.141G>T (p.Leu47=)
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=)

Number of alleles fetched