Chr Mutation (hg38) CAid Gene Transcript Linkouts
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)
3g.129532728G=CA1401212016RHOc.892G= (p.Ala298=)
3g.129532728G>TCA354470827RHOc.892G>T (p.Ala298Ser)
dbSNP gnomAD v2 gnomAD v4
3g.129532729C>ACA354470834RHOc.893C>A (p.Ala298Asp)
dbSNP
3g.129532729C=CA1401212023RHOc.893C= (p.Ala298=)
3g.129532729C>GCA354470839RHOc.893C>G (p.Ala298Gly)
COSMIC
3g.129532729C>TCA354470836RHOc.893C>T (p.Ala298Val)
ClinVar
3g.129532730C>ACA435769223RHOc.894C>A (p.Ala298=)
3g.129532730C=CA1401212027RHOc.894C= (p.Ala298=)
3g.129532730C>GCA2607304RHOc.894C>G (p.Ala298=)
dbSNP ExAC gnomAD v2 gnomAD v4
3g.129532730C>TCA2607303RHOc.894C>T (p.Ala298=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129532731G>ACA2607306RHOc.895G>A (p.Ala299Thr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129532731G>CCA354470847RHOc.895G>C (p.Ala299Pro)
3g.129532731G=CA1401212032RHOc.895G= (p.Ala299=)
3g.129532731G>TCA2607305RHOc.895G>T (p.Ala299Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.129532732C>ACA354470851RHOc.896C>A (p.Ala299Asp)
3g.129532732C>GCA354470854RHOc.896C>G (p.Ala299Gly)
3g.129532732C>TCA354470856RHOc.896C>T (p.Ala299Val)
3g.129532733C>ACA435769224RHOc.897C>A (p.Ala299=)
3g.129532733C=CA1401212038RHOc.897C= (p.Ala299=)
3g.129532733C>GCA435769225RHOc.897C>G (p.Ala299=)
3g.129532733C>TCA435769226RHOc.897C>T (p.Ala299=)
dbSNP gnomAD v3 gnomAD v4
3g.129532734A=CA1401212046RHOc.898A= (p.Ile300=)
3g.129532734A>CCA354470859RHOc.898A>C (p.Ile300Leu)
3g.129532734A>GCA354470862RHOc.898A>G (p.Ile300Val)
3g.129532734A>TCA2607307RHOc.898A>T (p.Ile300Phe)
dbSNP ExAC gnomAD v2 gnomAD v4
3g.129532735T>ACA354470867RHOc.899T>A (p.Ile300Asn)
3g.129532735T>CCA354470870RHOc.899T>C (p.Ile300Thr)

Number of alleles fetched