Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.129532713T>ACA354470726RHOc.877T>A (p.Phe293Ile)
3g.129532713T>CCA354470728RHOc.877T>C (p.Phe293Leu)
3g.129532713T>GCA354470731RHOc.877T>G (p.Phe293Val)
3g.129532714T>ACA354470735RHOc.878T>A (p.Phe293Tyr)
3g.129532714T>CCA354470736RHOc.878T>C (p.Phe293Ser)
3g.129532714T>GCA354470739RHOc.878T>G (p.Phe293Cys)
3g.129532715C>ACA354470743RHOc.879C>A (p.Phe293Leu)
3g.129532715C>GCA354470745RHOc.879C>G (p.Phe293Leu)
3g.129532715C>TCA435769217RHOc.879C>T (p.Phe293=)
COSMIC
3g.129532716T>ACA354470754RHOc.880T>A (p.Phe294Ile)
3g.129532716T>CCA354470751RHOc.880T>C (p.Phe294Leu)
3g.129532716T>GCA354470747RHOc.880T>G (p.Phe294Val)
3g.129532717T>ACA354470757RHOc.881T>A (p.Phe294Tyr)
3g.129532717T>CCA354470759RHOc.881T>C (p.Phe294Ser)
3g.129532717T>GCA354470762RHOc.881T>G (p.Phe294Cys)
3g.129532718T>ACA354470764RHOc.882T>A (p.Phe294Leu)
3g.129532718T>CCA435769218RHOc.882T>C (p.Phe294=)
3g.129532718T>GCA354470766RHOc.882T>G (p.Phe294Leu)
3g.129532719G>ACA354470776RHOc.883G>A (p.Ala295Thr)
gnomAD v4
3g.129532719G>CCA354470772RHOc.883G>C (p.Ala295Pro)
3g.129532719G>TCA354470771RHOc.883G>T (p.Ala295Ser)
3g.129532720C>ACA354470780RHOc.884C>A (p.Ala295Asp)
3g.129532720C>GCA354470782RHOc.884C>G (p.Ala295Gly)
3g.129532720C>TCA354470783RHOc.884C>T (p.Ala295Val)
3g.129532721C>ACA435769219RHOc.885C>A (p.Ala295=)
3g.129532721C>GCA435769220RHOc.885C>G (p.Ala295=)
3g.129532721C>TCA435769221RHOc.885C>T (p.Ala295=)
3g.129532722A=CA1401211987RHOc.886A= (p.Lys296=)
3g.129532722A>CCA354470787RHOc.886A>C (p.Lys296Gln)
ClinVar dbSNP
3g.129532722A>GCA256677RHOc.886A>G (p.Lys296Glu)
ClinVar dbSNP
3g.129532722A>TCA354470792RHOc.886A>T (p.Lys296Ter)
3g.129532723A>CCA354470793RHOc.887A>C (p.Lys296Thr)
3g.129532723A>GCA354470798RHOc.887A>G (p.Lys296Arg)
3g.129532723A>TCA354470795RHOc.887A>T (p.Lys296Met)
3g.129532724G>ACA435769222RHOc.888G>A (p.Lys296=)
ClinVar gnomAD v4
3g.129532724G>CCA354470800RHOc.888G>C (p.Lys296Asn)
ClinVar dbSNP
3g.129532724G=CA1401211995RHOc.888G= (p.Lys296=)
3g.129532724G>TCA354470802RHOc.888G>T (p.Lys296Asn)
ClinVar
3g.129532725A>CCA354470804RHOc.889A>C (p.Ser297Arg)
ClinVar
3g.129532725A>GCA354470806RHOc.889A>G (p.Ser297Gly)
3g.129532725A>TCA354470808RHOc.889A>T (p.Ser297Cys)
3g.129532726G>ACA354470810RHOc.890G>A (p.Ser297Asn)
3g.129532726G>CCA354470812RHOc.890G>C (p.Ser297Thr)
3g.129532726G>TCA354470815RHOc.890G>T (p.Ser297Ile)
3g.129532727C>ACA354470817RHOc.891C>A (p.Ser297Arg)
3g.129532727C=CA1401212009RHOc.891C= (p.Ser297=)
3g.129532727C>GCA354470820RHOc.891C>G (p.Ser297Arg)
ClinVar dbSNP
3g.129532727C>TCA232817RHOc.891C>T (p.Ser297=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129532728G>ACA2607302RHOc.892G>A (p.Ala298Thr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
3g.129532728G>CCA354470829RHOc.892G>C (p.Ala298Pro)

Number of alleles fetched