Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.59443616G>ACA380773892OR5A1c.448G>A (p.Gly150Arg)
11g.59443616G>CCA380773909OR5A1c.448G>C (p.Gly150Arg)
dbSNP
11g.59443616G=CA1976398953OR5A1c.448G= (p.Gly150=)
11g.59443616G>TCA380773910OR5A1c.448G>T (p.Gly150Trp)
11g.59443617G>ACA380773917OR5A1c.449G>A (p.Gly150Glu)
11g.59443617G>CCA380773924OR5A1c.449G>C (p.Gly150Ala)
11g.59443617G>TCA380773913OR5A1c.449G>T (p.Gly150Val)
11g.59443618G>ACA474822905OR5A1c.450G>A (p.Gly150=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.59443618G>CCA474822903OR5A1c.450G>C (p.Gly150=)
gnomAD v4
11g.59443618G=CA1976398958OR5A1c.450G= (p.Gly150=)
11g.59443618G>TCA474822901OR5A1c.450G>T (p.Gly150=)
11g.59443619G>ACA380773930OR5A1c.451G>A (p.Ala151Thr)
11g.59443619G>CCA380773946OR5A1c.451G>C (p.Ala151Pro)
11g.59443619G>TCA380773934OR5A1c.451G>T (p.Ala151Ser)
COSMIC
11g.59443620C>ACA380773950OR5A1c.452C>A (p.Ala151Glu)
11g.59443620C>GCA380773956OR5A1c.452C>G (p.Ala151Gly)
11g.59443620C>TCA380773959OR5A1c.452C>T (p.Ala151Val)
gnomAD v4 COSMIC
11g.59443621A=CA1976398960OR5A1c.453A= (p.Ala151=)
11g.59443621A>CCA223220615OR5A1c.453A>C (p.Ala151=)
dbSNP
11g.59443621A>GCA474822914OR5A1c.453A>G (p.Ala151=)
11g.59443621A>TCA474822911OR5A1c.453A>T (p.Ala151=)
gnomAD v4
11g.59443622T>ACA380773962OR5A1c.454T>A (p.Tyr152Asn)
11g.59443622T>CCA380773964OR5A1c.454T>C (p.Tyr152His)
11g.59443622T>GCA380773966OR5A1c.454T>G (p.Tyr152Asp)
11g.59443623A>CCA380773970OR5A1c.455A>C (p.Tyr152Ser)
11g.59443623A>GCA380773971OR5A1c.455A>G (p.Tyr152Cys)
COSMIC
11g.59443623A>TCA380773972OR5A1c.455A>T (p.Tyr152Phe)
COSMIC
11g.59443624T>ACA6018361OR5A1c.456T>A (p.Tyr152Ter)
dbSNP ExAC gnomAD v2 gnomAD v4
11g.59443624T>CCA474822922OR5A1c.456T>C (p.Tyr152=)
11g.59443624T>GCA380773974OR5A1c.456T>G (p.Tyr152Ter)
11g.59443624T=CA1976398964OR5A1c.456T= (p.Tyr152=)
11g.59443625G>ACA380773982OR5A1c.457G>A (p.Val153Ile)
dbSNP gnomAD v4
11g.59443625G>CCA380773981OR5A1c.457G>C (p.Val153Leu)
11g.59443625G=CA1976398966OR5A1c.457G= (p.Val153=)
11g.59443625G>TCA380773980OR5A1c.457G>T (p.Val153Phe)
gnomAD v4
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=)

Number of alleles fetched