ClinVar Miner

List of variants in gene GREM1 studied for Hereditary cancer-predisposing syndrome

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Gene type:
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Total variants: 191
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HGVS dbSNP gnomAD frequency
NM_013372.7(GREM1):c.103C>G (p.Pro35Ala) rs111262341 0.00259
NM_013372.7(GREM1):c.-1-797A>G rs183257520 0.00120
NM_013372.7(GREM1):c.-2+2056C>T rs146429140 0.00109
NM_013372.7(GREM1):c.309C>T (p.Ile103=) rs78005246 0.00012
NM_013372.7(GREM1):c.307A>G (p.Ile103Val) rs370674293 0.00008
NM_013372.7(GREM1):c.-2+1514T>G rs768670395 0.00006
NM_013372.7(GREM1):c.169A>C (p.Asn57His) rs754206331 0.00002
NM_013372.7(GREM1):c.105G>T (p.Pro35=) rs746525315 0.00001
NM_013372.7(GREM1):c.190C>T (p.Arg64Trp) rs750874632 0.00001
NM_013372.7(GREM1):c.103C>T (p.Pro35Ser)
NM_013372.7(GREM1):c.104C>A (p.Pro35Gln)
NM_013372.7(GREM1):c.104C>T (p.Pro35Leu)
NM_013372.7(GREM1):c.105G>A (p.Pro35=)
NM_013372.7(GREM1):c.10A>G (p.Thr4Ala)
NM_013372.7(GREM1):c.114G>A (p.Lys38=)
NM_013372.7(GREM1):c.115G>A (p.Ala39Thr)
NM_013372.7(GREM1):c.115G>T (p.Ala39Ser)
NM_013372.7(GREM1):c.116C>T (p.Ala39Val)
NM_013372.7(GREM1):c.120G>A (p.Gln40=)
NM_013372.7(GREM1):c.121C>A (p.His41Asn)
NM_013372.7(GREM1):c.122A>G (p.His41Arg)
NM_013372.7(GREM1):c.125A>G (p.Asn42Ser)
NM_013372.7(GREM1):c.127G>A (p.Asp43Asn)
NM_013372.7(GREM1):c.131C>T (p.Ser44Leu)
NM_013372.7(GREM1):c.132A>G (p.Ser44=)
NM_013372.7(GREM1):c.134A>G (p.Glu45Gly)
NM_013372.7(GREM1):c.137A>C (p.Gln46Pro)
NM_013372.7(GREM1):c.140C>G (p.Thr47Ser)
NM_013372.7(GREM1):c.140C>T (p.Thr47Ile)
NM_013372.7(GREM1):c.143A>C (p.Gln48Pro)
NM_013372.7(GREM1):c.143A>T (p.Gln48Leu)
NM_013372.7(GREM1):c.144G>T (p.Gln48His)
NM_013372.7(GREM1):c.147G>A (p.Ser49=)
NM_013372.7(GREM1):c.147G>T (p.Ser49=)
NM_013372.7(GREM1):c.148C>T (p.Pro50Ser)
NM_013372.7(GREM1):c.158C>G (p.Pro53Arg)
NM_013372.7(GREM1):c.159T>C (p.Pro53=)
NM_013372.7(GREM1):c.163T>C (p.Ser55Pro)
NM_013372.7(GREM1):c.172C>T (p.Arg58Trp)
NM_013372.7(GREM1):c.173G>C (p.Arg58Pro)
NM_013372.7(GREM1):c.175G>A (p.Gly59Arg)
NM_013372.7(GREM1):c.176G>A (p.Gly59Glu)
NM_013372.7(GREM1):c.17A>G (p.Tyr6Cys)
NM_013372.7(GREM1):c.185A>G (p.Gln62Arg)
NM_013372.7(GREM1):c.195C>T (p.Gly65=)
NM_013372.7(GREM1):c.205C>G (p.Pro69Ala)
NM_013372.7(GREM1):c.205C>T (p.Pro69Ser)
NM_013372.7(GREM1):c.208G>T (p.Gly70Trp)
NM_013372.7(GREM1):c.20C>T (p.Thr7Met)
NM_013372.7(GREM1):c.219G>C (p.Val73=)
NM_013372.7(GREM1):c.21G>A (p.Thr7=)
NM_013372.7(GREM1):c.21G>C (p.Thr7=)
NM_013372.7(GREM1):c.21G>T (p.Thr7=)
NM_013372.7(GREM1):c.220C>T (p.Leu74=)
NM_013372.7(GREM1):c.228C>T (p.Ser76=)
NM_013372.7(GREM1):c.229A>C (p.Ser77Arg)
NM_013372.7(GREM1):c.22G>A (p.Val8Met)
NM_013372.7(GREM1):c.230G>C (p.Ser77Thr)
NM_013372.7(GREM1):c.231C>G (p.Ser77Arg)
NM_013372.7(GREM1):c.233A>C (p.Gln78Pro)
NM_013372.7(GREM1):c.234A>G (p.Gln78=)
NM_013372.7(GREM1):c.238G>A (p.Ala80Thr)
NM_013372.7(GREM1):c.239C>T (p.Ala80Val)
NM_013372.7(GREM1):c.240C>A (p.Ala80=)
NM_013372.7(GREM1):c.241C>T (p.Leu81=)
NM_013372.7(GREM1):c.243G>A (p.Leu81=)
NM_013372.7(GREM1):c.245A>C (p.His82Pro)
NM_013372.7(GREM1):c.246T>A (p.His82Gln)
NM_013372.7(GREM1):c.246T>C (p.His82=)
NM_013372.7(GREM1):c.250A>G (p.Thr84Ala)
NM_013372.7(GREM1):c.251C>T (p.Thr84Met)
NM_013372.7(GREM1):c.252G>A (p.Thr84=)
NM_013372.7(GREM1):c.252G>C (p.Thr84=)
NM_013372.7(GREM1):c.256C>G (p.Arg86Gly)
NM_013372.7(GREM1):c.256C>T (p.Arg86Cys)
NM_013372.7(GREM1):c.261A>G (p.Lys87=)
NM_013372.7(GREM1):c.262T>C (p.Tyr88His)
NM_013372.7(GREM1):c.264C>T (p.Tyr88=)
NM_013372.7(GREM1):c.265C>T (p.Leu89=)
NM_013372.7(GREM1):c.269A>G (p.Lys90Arg)
NM_013372.7(GREM1):c.26G>A (p.Gly9Glu)
NM_013372.7(GREM1):c.272G>A (p.Arg91Gln)
NM_013372.7(GREM1):c.273A>G (p.Arg91=) rs869312795
NM_013372.7(GREM1):c.274G>A (p.Asp92Asn)
NM_013372.7(GREM1):c.276C>T (p.Asp92=)
NM_013372.7(GREM1):c.277T>G (p.Trp93Gly)
NM_013372.7(GREM1):c.27A>G (p.Gly9=)
NM_013372.7(GREM1):c.290A>G (p.Gln97Arg)
NM_013372.7(GREM1):c.294G>A (p.Pro98=)
NM_013372.7(GREM1):c.297T>G (p.Leu99=)
NM_013372.7(GREM1):c.303G>C (p.Gln101His)
NM_013372.7(GREM1):c.306C>G (p.Thr102=)
NM_013372.7(GREM1):c.309C>A (p.Ile103=)
NM_013372.7(GREM1):c.310C>A (p.His104Asn)
NM_013372.7(GREM1):c.312C>T (p.His104=)
NM_013372.7(GREM1):c.318A>G (p.Glu106=)
NM_013372.7(GREM1):c.31C>G (p.Leu11Val)
NM_013372.7(GREM1):c.31C>T (p.Leu11=)
NM_013372.7(GREM1):c.322T>A (p.Cys108Ser)
NM_013372.7(GREM1):c.323G>A (p.Cys108Tyr)
NM_013372.7(GREM1):c.324C>T (p.Cys108=)
NM_013372.7(GREM1):c.326A>G (p.Asn109Ser)
NM_013372.7(GREM1):c.330T>C (p.Ser110=)
NM_013372.7(GREM1):c.335C>G (p.Thr112Ser)
NM_013372.7(GREM1):c.33G>A (p.Leu11=)
NM_013372.7(GREM1):c.340A>G (p.Ile114Val)
NM_013372.7(GREM1):c.344A>T (p.Asn115Ile)
NM_013372.7(GREM1):c.345C>T (p.Asn115=)
NM_013372.7(GREM1):c.354T>C (p.Cys118=)
NM_013372.7(GREM1):c.357C>T (p.Tyr119=)
NM_013372.7(GREM1):c.363G>T (p.Gln121His)
NM_013372.7(GREM1):c.369C>A (p.Asn123Lys)
NM_013372.7(GREM1):c.369C>T (p.Asn123=)
NM_013372.7(GREM1):c.36T>A (p.Leu12=)
NM_013372.7(GREM1):c.372T>A (p.Ser124=)
NM_013372.7(GREM1):c.372T>C (p.Ser124=)
NM_013372.7(GREM1):c.381C>A (p.Ile127=)
NM_013372.7(GREM1):c.383C>T (p.Pro128Leu)
NM_013372.7(GREM1):c.384C>A (p.Pro128=) rs1595852343
NM_013372.7(GREM1):c.386G>A (p.Arg129Lys)
NM_013372.7(GREM1):c.387G>A (p.Arg129=)
NM_013372.7(GREM1):c.392T>G (p.Ile131Ser)
NM_013372.7(GREM1):c.393C>G (p.Ile131Met)
NM_013372.7(GREM1):c.393C>T (p.Ile131=)
NM_013372.7(GREM1):c.395G>A (p.Arg132Gln)
NM_013372.7(GREM1):c.396G>C (p.Arg132=)
NM_013372.7(GREM1):c.398A>G (p.Lys133Arg)
NM_013372.7(GREM1):c.39C>T (p.Leu13=) rs1595851879
NM_013372.7(GREM1):c.402G>A (p.Glu134=)
NM_013372.7(GREM1):c.406G>A (p.Gly136Ser)
NM_013372.7(GREM1):c.408T>C (p.Gly136=)
NM_013372.7(GREM1):c.411C>A (p.Ser137=)
NM_013372.7(GREM1):c.411C>T (p.Ser137=)
NM_013372.7(GREM1):c.417G>A (p.Gln139=) rs794727286
NM_013372.7(GREM1):c.425C>T (p.Ser142Phe)
NM_013372.7(GREM1):c.426C>T (p.Ser142=)
NM_013372.7(GREM1):c.429C>T (p.Phe143=)
NM_013372.7(GREM1):c.42C>T (p.Leu14=)
NM_013372.7(GREM1):c.435G>A (p.Lys145=)
NM_013372.7(GREM1):c.438C>T (p.Pro146=)
NM_013372.7(GREM1):c.439A>G (p.Lys147Glu)
NM_013372.7(GREM1):c.447C>G (p.Phe149Leu)
NM_013372.7(GREM1):c.447C>T (p.Phe149=)
NM_013372.7(GREM1):c.449C>G (p.Thr150Ser) rs202104240
NM_013372.7(GREM1):c.449C>T (p.Thr150Ile)
NM_013372.7(GREM1):c.450T>C (p.Thr150=)
NM_013372.7(GREM1):c.453C>G (p.Thr151=)
NM_013372.7(GREM1):c.453C>T (p.Thr151=)
NM_013372.7(GREM1):c.454A>G (p.Met152Val)
NM_013372.7(GREM1):c.456G>A (p.Met152Ile)
NM_013372.7(GREM1):c.456G>C (p.Met152Ile)
NM_013372.7(GREM1):c.459G>A (p.Met153Ile)
NM_013372.7(GREM1):c.463A>G (p.Thr155Ala)
NM_013372.7(GREM1):c.472T>A (p.Cys158Ser)
NM_013372.7(GREM1):c.483A>G (p.Leu161=)
NM_013372.7(GREM1):c.488C>T (p.Pro163Leu)
NM_013372.7(GREM1):c.48G>A (p.Gly16=)
NM_013372.7(GREM1):c.492T>C (p.Pro164=)
NM_013372.7(GREM1):c.495C>G (p.Thr165=)
NM_013372.7(GREM1):c.495C>T (p.Thr165=)
NM_013372.7(GREM1):c.498G>A (p.Lys166=)
NM_013372.7(GREM1):c.510C>G (p.Val170=)
NM_013372.7(GREM1):c.511A>G (p.Thr171Ala)
NM_013372.7(GREM1):c.514C>T (p.Arg172Cys)
NM_013372.7(GREM1):c.516T>C (p.Arg172=)
NM_013372.7(GREM1):c.522G>A (p.Lys174=)
NM_013372.7(GREM1):c.525G>C (p.Gln175His)
NM_013372.7(GREM1):c.534C>T (p.Cys178=)
NM_013372.7(GREM1):c.535A>G (p.Ile179Val)
NM_013372.7(GREM1):c.536T>C (p.Ile179Thr)
NM_013372.7(GREM1):c.539C>T (p.Ser180Phe)
NM_013372.7(GREM1):c.540C>T (p.Ser180=)
NM_013372.7(GREM1):c.541A>C (p.Ile181Leu)
NM_013372.7(GREM1):c.543C>T (p.Ile181=)
NM_013372.7(GREM1):c.551A>C (p.Asp184Ala)
NM_013372.7(GREM1):c.551A>G (p.Asp184Gly)
NM_013372.7(GREM1):c.55C>T (p.Leu19=)
NM_013372.7(GREM1):c.59C>A (p.Pro20Gln)
NM_013372.7(GREM1):c.60G>C (p.Pro20=)
NM_013372.7(GREM1):c.63T>G (p.Ala21=)
NM_013372.7(GREM1):c.65C>A (p.Ala22Asp)
NM_013372.7(GREM1):c.66T>C (p.Ala22=)
NM_013372.7(GREM1):c.68A>T (p.Glu23Val)
NM_013372.7(GREM1):c.69A>G (p.Glu23=)
NM_013372.7(GREM1):c.6C>T (p.Ser2=)
NM_013372.7(GREM1):c.76A>C (p.Lys26Gln)
NM_013372.7(GREM1):c.7C>T (p.Arg3Cys)
NM_013372.7(GREM1):c.87C>G (p.Ser29=)
NM_013372.7(GREM1):c.90A>G (p.Gln30=)
NM_013372.7(GREM1):c.93T>A (p.Gly31=)
NM_013372.7(GREM1):c.96C>T (p.Ala32=)

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