Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.59443626T>ACA380773983OR5A1c.458T>A (p.Val153Asp)
11g.59443626T>CCA380773986OR5A1c.458T>C (p.Val153Ala)
11g.59443626T>GCA380773989OR5A1c.458T>G (p.Val153Gly)
11g.59443627T>ACA474822927OR5A1c.459T>A (p.Val153=)
11g.59443627T>CCA474822929OR5A1c.459T>C (p.Val153=)
11g.59443627T>GCA474822931OR5A1c.459T>G (p.Val153=)
dbSNP gnomAD v4
11g.59443627T=CA1976398968OR5A1c.459T= (p.Val153=)
11g.59443628G>ACA380773998OR5A1c.460G>A (p.Gly154Ser)
11g.59443628G>CCA380774001OR5A1c.460G>C (p.Gly154Arg)
11g.59443628G>TCA380774025OR5A1c.460G>T (p.Gly154Cys)
gnomAD v4
11g.59443629G>ACA6018362OR5A1c.461G>A (p.Gly154Asp)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
11g.59443629G>CCA380774050OR5A1c.461G>C (p.Gly154Ala)
gnomAD v4
11g.59443629G=CA1976398972OR5A1c.461G= (p.Gly154=)
11g.59443629G>TCA6018363OR5A1c.461G>T (p.Gly154Val)
dbSNP ExAC gnomAD v2 gnomAD v4
11g.59443630T>ACA474822939OR5A1c.462T>A (p.Gly154=)
11g.59443630T>CCA474822940OR5A1c.462T>C (p.Gly154=)
11g.59443630T>GCA474822941OR5A1c.462T>G (p.Gly154=)
11g.59443631G>ACA380774057OR5A1c.463G>A (p.Gly155Ser)
11g.59443631G>CCA380774061OR5A1c.463G>C (p.Gly155Arg)
gnomAD v4
11g.59443631G>TCA380774081OR5A1c.463G>T (p.Gly155Cys)
11g.59443632G>ACA380774084OR5A1c.464G>A (p.Gly155Asp)
COSMIC
11g.59443632G>CCA380774083OR5A1c.464G>C (p.Gly155Ala)
11g.59443632G>TCA380774082OR5A1c.464G>T (p.Gly155Val)
11g.59443633C>ACA474822946OR5A1c.465C>A (p.Gly155=)
11g.59443633C=CA1976398975OR5A1c.465C= (p.Gly155=)
11g.59443633C>GCA474822948OR5A1c.465C>G (p.Gly155=)
11g.59443633C>TCA6018364OR5A1c.465C>T (p.Gly155=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.59443634T>ACA380774089OR5A1c.466T>A (p.Phe156Ile)
11g.59443634T>CCA380774091OR5A1c.466T>C (p.Phe156Leu)
gnomAD v4
11g.59443634T>GCA380774093OR5A1c.466T>G (p.Phe156Val)
11g.59443635T>ACA380774098OR5A1c.467T>A (p.Phe156Tyr)
11g.59443635T>CCA380774102OR5A1c.467T>C (p.Phe156Ser)
11g.59443635T>GCA380774105OR5A1c.467T>G (p.Phe156Cys)
11g.59443636C>ACA380774109OR5A1c.468C>A (p.Phe156Leu)
11g.59443636C>GCA380774119OR5A1c.468C>G (p.Phe156Leu)
11g.59443636C>TCA474822954OR5A1c.468C>T (p.Phe156=)
11g.59443637C>ACA380774121OR5A1c.469C>A (p.Leu157Met)
11g.59443637C=CA1976398979OR5A1c.469C= (p.Leu157=)
11g.59443637C>GCA380774125OR5A1c.469C>G (p.Leu157Val)
dbSNP gnomAD v2 gnomAD v4
11g.59443637C>TCA223220657OR5A1c.469C>T (p.Leu157=)
dbSNP
11g.59443638T>ACA380774129OR5A1c.470T>A (p.Leu157Gln)
11g.59443638T>CCA380774128OR5A1c.470T>C (p.Leu157Pro)
ClinVar dbSNP gnomAD v2 gnomAD v4
11g.59443638T>GCA380774127OR5A1c.470T>G (p.Leu157Arg)
11g.59443638T=CA1976398984OR5A1c.470T= (p.Leu157=)
11g.59443639G>ACA6018365OR5A1c.471G>A (p.Leu157=)
dbSNP ExAC gnomAD v2 gnomAD v4
11g.59443639G>CCA474822964OR5A1c.471G>C (p.Leu157=)
11g.59443639G=CA1976398988OR5A1c.471G= (p.Leu157=)
11g.59443639G>TCA474822965OR5A1c.471G>T (p.Leu157=)
11g.59443640A>CCA380774136OR5A1c.472A>C (p.Ser158Arg)
11g.59443640A>GCA380774137OR5A1c.472A>G (p.Ser158Gly)
dbSNP

Number of alleles fetched