ClinVar Miner

List of variants reported as likely pathogenic by Reproductive Endocrine Unit, Massachusetts General Hospital

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Total variants: 46
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HGVS dbSNP gnomAD frequency
NM_023110.3(FGFR1):c.1409G>T (p.Arg470Leu) rs121909637 0.00010
NM_001030055.2(ARHGAP5):c.2366dup (p.Phe790fs)
NM_004491.5(ARHGAP35):c.1800_1803del (p.Val601fs)
NM_004491.5(ARHGAP35):c.2565C>A (p.Tyr855Ter)
NM_004491.5(ARHGAP35):c.325C>T (p.Arg109Ter)
NM_004491.5(ARHGAP35):c.3283_3286delinsT (p.Val1095_Lys1096delinsTer)
NM_004491.5(ARHGAP35):c.345del (p.Tyr116fs)
NM_004491.5(ARHGAP35):c.352A>T (p.Lys118Ter)
NM_004491.5(ARHGAP35):c.3569_3570del (p.Glu1190fs)
NM_004491.5(ARHGAP35):c.3850C>T (p.Arg1284Trp)
NM_004491.5(ARHGAP35):c.516del (p.Asn173fs)
NM_012414.4(RAB3GAP2):c.1283C>A (p.Ala428Glu) rs1658614059
NM_012414.4(RAB3GAP2):c.387-2A>G rs769114540
NM_023110.3(FGFR1):c.1018A>G (p.Thr340Ala)
NM_023110.3(FGFR1):c.1025T>C (p.Leu342Ser) rs121909638
NM_023110.3(FGFR1):c.1028C>T (p.Ala343Val) rs1818935081
NM_023110.3(FGFR1):c.1097C>T (p.Pro366Leu) rs121909641
NM_023110.3(FGFR1):c.1286T>A (p.Val429Glu)
NM_023110.3(FGFR1):c.1552+1G>T
NM_023110.3(FGFR1):c.1829G>A (p.Gly610Asp)
NM_023110.3(FGFR1):c.1854G>T (p.Lys618Asn)
NM_023110.3(FGFR1):c.1977+1G>A rs876661334
NM_023110.3(FGFR1):c.1977+1G>T
NM_023110.3(FGFR1):c.1982G>A (p.Arg661Gln) rs1257312391
NM_023110.3(FGFR1):c.2011G>C (p.Ala671Pro)
NM_023110.3(FGFR1):c.2057T>C (p.Phe686Ser)
NM_023110.3(FGFR1):c.2075A>G (p.Glu692Gly) rs397515445
NM_023110.3(FGFR1):c.2107G>A (p.Gly703Ser)
NM_023110.3(FGFR1):c.2152C>T (p.Arg718Cys)
NM_023110.3(FGFR1):c.2165C>A (p.Pro722His) rs267606805
NM_023110.3(FGFR1):c.2172C>G (p.Asn724Lys) rs267606806
NM_023110.3(FGFR1):c.2209T>C (p.Trp737Arg) rs727505377
NM_023110.3(FGFR1):c.2231G>T (p.Arg744Ile)
NM_023110.3(FGFR1):c.2233C>T (p.Pro745Ser)
NM_023110.3(FGFR1):c.2235_2238dup (p.Phe747fs)
NM_023110.3(FGFR1):c.2241C>A (p.Phe747Leu)
NM_023110.3(FGFR1):c.232C>T (p.Arg78Cys) rs1554570706
NM_023110.3(FGFR1):c.289G>A (p.Gly97Ser)
NM_023110.3(FGFR1):c.670G>C (p.Asp224His)
NM_023110.3(FGFR1):c.677G>A (p.Gly226Asp) rs1246231808
NM_023110.3(FGFR1):c.682T>G (p.Tyr228Asp)
NM_023110.3(FGFR1):c.709G>A (p.Gly237Ser) rs121909635
NM_023110.3(FGFR1):c.716T>C (p.Ile239Thr)
NM_023110.3(FGFR1):c.760C>T (p.Arg254Trp)
NM_023110.3(FGFR1):c.761G>A (p.Arg254Gln)
NM_023110.3(FGFR1):c.797C>T (p.Thr266Ile)

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