Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.129530876G>ACA354497828RHOc.362G>A (p.Gly121Asp)
3g.129530876G>CCA354497832RHOc.362G>C (p.Gly121Ala)
3g.129530876G=CA1401209185RHOc.362G= (p.Gly121=)
3g.129530876G>TCA354497833RHOc.362G>T (p.Gly121Val)
ClinVar dbSNP gnomAD v4
3g.129530877T>ACA435643710RHOc.363T>A (p.Gly121=)
3g.129530877T>CCA435643711RHOc.363T>C (p.Gly121=)
3g.129530877T>GCA435643712RHOc.363T>G (p.Gly121=)
3g.129530878G>ACA2607145RHOc.364G>A (p.Glu122Lys)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129530878G>CCA354497836RHOc.364G>C (p.Glu122Gln)
3g.129530878G=CA1401209190RHOc.364G= (p.Glu122=)
3g.129530878G>TCA354497834RHOc.364G>T (p.Glu122Ter)
ClinVar
3g.129530879A=CA1401209195RHOc.365A= (p.Glu122=)
3g.129530879A>CCA354497843RHOc.365A>C (p.Glu122Ala)
3g.129530879A>GCA2607146RHOc.365A>G (p.Glu122Gly)
dbSNP ExAC gnomAD v2 gnomAD v4
3g.129530879A>TCA354497846RHOc.365A>T (p.Glu122Val)
3g.129530880A=CA1401209199RHOc.366A= (p.Glu122=)
3g.129530880A>CCA354497849RHOc.366A>C (p.Glu122Asp)
3g.129530880A>GCA435643713RHOc.366A>G (p.Glu122=)
dbSNP gnomAD v4
3g.129530880A>TCA354497851RHOc.366A>T (p.Glu122Asp)
3g.129530881A>CCA354497854RHOc.367A>C (p.Ile123Leu)
3g.129530881A>GCA354497855RHOc.367A>G (p.Ile123Val)
3g.129530881A>TCA354497858RHOc.367A>T (p.Ile123Phe)
3g.129530882T>ACA354497860RHOc.368T>A (p.Ile123Asn)
3g.129530882T>CCA354497862RHOc.368T>C (p.Ile123Thr)
gnomAD v4
3g.129530882T>GCA354497864RHOc.368T>G (p.Ile123Ser)
3g.129530883T>ACA435643714RHOc.369T>A (p.Ile123=)
3g.129530883T>CCA435643715RHOc.369T>C (p.Ile123=)
gnomAD v4
3g.129530883T>GCA354497867RHOc.369T>G (p.Ile123Met)
3g.129530884G>ACA354497881RHOc.370G>A (p.Ala124Thr)
gnomAD v4
3g.129530884G>CCA354497872RHOc.370G>C (p.Ala124Pro)
3g.129530884G=CA1401209202RHOc.370G= (p.Ala124=)
3g.129530884G>TCA354497883RHOc.370G>T (p.Ala124Ser)
dbSNP COSMIC
3g.129530885C>ACA354497886RHOc.371C>A (p.Ala124Asp)
3g.129530885C=CA1401209206RHOc.371C= (p.Ala124=)
3g.129530885C>GCA354497888RHOc.371C>G (p.Ala124Gly)
3g.129530885C>TCA82648458RHOc.371C>T (p.Ala124Val)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.129530886C>ACA435643716RHOc.372C>A (p.Ala124=)
3g.129530886C=CA1401209209RHOc.372C= (p.Ala124=)
3g.129530886C>GCA435643717RHOc.372C>G (p.Ala124=)
3g.129530886C>TCA435643718RHOc.372C>T (p.Ala124=)
dbSNP gnomAD v2 gnomAD v4
3g.129530887C>ACA354497889RHOc.373C>A (p.Leu125Met)
3g.129530887C>GCA354497891RHOc.373C>G (p.Leu125Val)
3g.129530887C>TCA435643719RHOc.373C>T (p.Leu125=)
3g.129530888T>ACA354497893RHOc.374T>A (p.Leu125Gln)
3g.129530888T>CCA354497896RHOc.374T>C (p.Leu125Pro)
dbSNP gnomAD v2 gnomAD v4
3g.129530888T>GCA354497898RHOc.374T>G (p.Leu125Arg)
ClinVar
3g.129530888T=CA1401209212RHOc.374T= (p.Leu125=)
3g.129530889G>ACA435643720RHOc.375G>A (p.Leu125=)
3g.129530889G>CCA435643721RHOc.375G>C (p.Leu125=)
3g.129530889G>TCA435643722RHOc.375G>T (p.Leu125=)

Number of alleles fetched