ClinVar Miner

List of variants in gene SMARCAL1 reported as uncertain significance by Invitae

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Total variants: 85
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HGVS dbSNP
NC_000002.12:g.(?_216416237)_(216416327_?)del
NM_014140.3(SMARCAL1):c.1001G>A (p.Arg334Gln) rs138575228
NM_014140.3(SMARCAL1):c.1030G>A (p.Glu344Lys) rs370663120
NM_014140.3(SMARCAL1):c.1297G>A (p.Val433Met) rs374696042
NM_014140.3(SMARCAL1):c.1317T>G (p.Phe439Leu) rs771757954
NM_014140.3(SMARCAL1):c.1375G>A (p.Asp459Asn) rs1574456732
NM_014140.3(SMARCAL1):c.1427G>A (p.Arg476Gln) rs142164846
NM_014140.3(SMARCAL1):c.1453G>T (p.Val485Leu) rs1574456834
NM_014140.3(SMARCAL1):c.1594C>T (p.Leu532Phe) rs968239393
NM_014140.3(SMARCAL1):c.1727T>C (p.Ile576Thr) rs138819354
NM_014140.3(SMARCAL1):c.1762G>A (p.Ala588Thr) rs769553029
NM_014140.3(SMARCAL1):c.1786G>A (p.Ala596Thr) rs143100109
NM_014140.3(SMARCAL1):c.179A>C (p.Glu60Ala) rs766086132
NM_014140.3(SMARCAL1):c.1993G>T (p.Ala665Ser) rs768868466
NM_014140.3(SMARCAL1):c.2009A>G (p.Asn670Ser) rs752621052
NM_014140.3(SMARCAL1):c.2114C>T (p.Thr705Ile) rs200644381
NM_014140.3(SMARCAL1):c.2141T>C (p.Ile714Thr) rs372158077
NM_014140.3(SMARCAL1):c.2225C>T (p.Thr742Met) rs2271336
NM_014140.3(SMARCAL1):c.2260C>T (p.Arg754Cys) rs1226816517
NM_014140.3(SMARCAL1):c.2401T>G (p.Phe801Val) rs200679534
NM_014140.3(SMARCAL1):c.2497G>A (p.Val833Met) rs756015461
NM_014140.3(SMARCAL1):c.2600C>T (p.Thr867Ile) rs752153044
NM_014140.3(SMARCAL1):c.2735C>T (p.Ser912Leu) rs763670564
NM_014140.3(SMARCAL1):c.2768G>A (p.Gly923Glu) rs1559140332
NM_014140.3(SMARCAL1):c.488C>A (p.Thr163Asn) rs748188404
NM_014140.3(SMARCAL1):c.506A>G (p.Lys169Arg) rs777999697
NM_014140.3(SMARCAL1):c.565A>G (p.Lys189Glu) rs754147208
NM_014140.3(SMARCAL1):c.734G>A (p.Gly245Asp) rs1574443795
NM_014140.3(SMARCAL1):c.735C>T (p.Gly245=) rs149510554
NM_014140.3(SMARCAL1):c.776T>C (p.Ile259Thr) rs750671325
NM_014140.3(SMARCAL1):c.836T>C (p.Phe279Ser) rs775057827
NM_014140.3(SMARCAL1):c.922A>G (p.Ser308Gly) rs1312214950
NM_014140.4(SMARCAL1):c.1031A>G (p.Glu344Gly)
NM_014140.4(SMARCAL1):c.1069T>A rs369180164
NM_014140.4(SMARCAL1):c.109A>G (p.Ser37Gly)
NM_014140.4(SMARCAL1):c.1369G>A (p.Ala457Thr)
NM_014140.4(SMARCAL1):c.1433A>G (p.Glu478Gly)
NM_014140.4(SMARCAL1):c.1439C>T (p.Pro480Leu)
NM_014140.4(SMARCAL1):c.1442T>C (p.Leu481Pro)
NM_014140.4(SMARCAL1):c.1468C>T (p.Arg490Cys)
NM_014140.4(SMARCAL1):c.1469G>A (p.Arg490His)
NM_014140.4(SMARCAL1):c.1552C>T (p.Arg518Cys)
NM_014140.4(SMARCAL1):c.1553G>A rs774075396
NM_014140.4(SMARCAL1):c.1622C>A (p.Thr541Asn)
NM_014140.4(SMARCAL1):c.1642A>G (p.Ile548Val)
NM_014140.4(SMARCAL1):c.1642_1644del (p.Ile548del)
NM_014140.4(SMARCAL1):c.1699C>A (p.Pro567Thr)
NM_014140.4(SMARCAL1):c.1750A>G (p.Met584Val)
NM_014140.4(SMARCAL1):c.1762G>T (p.Ala588Ser)
NM_014140.4(SMARCAL1):c.1975C>T (p.Arg659Cys)
NM_014140.4(SMARCAL1):c.2083A>C (p.Lys695Gln)
NM_014140.4(SMARCAL1):c.221A>G (p.Gln74Arg)
NM_014140.4(SMARCAL1):c.2243A>T (p.Lys748Met)
NM_014140.4(SMARCAL1):c.2245C>T (p.His749Tyr)
NM_014140.4(SMARCAL1):c.2263A>G (p.Ile755Val)
NM_014140.4(SMARCAL1):c.2341G>A (p.Val781Met)
NM_014140.4(SMARCAL1):c.2356G>A (p.Ala786Thr)
NM_014140.4(SMARCAL1):c.236C>T (p.Ser79Leu)
NM_014140.4(SMARCAL1):c.2389G>A (p.Asp797Asn)
NM_014140.4(SMARCAL1):c.2425G>A (p.Gly809Arg)
NM_014140.4(SMARCAL1):c.2512G>A (p.Ala838Thr)
NM_014140.4(SMARCAL1):c.2534T>A (p.Leu845Gln)
NM_014140.4(SMARCAL1):c.2644_2646del (p.Ile882del)
NM_014140.4(SMARCAL1):c.2650G>A (p.Asp884Asn)
NM_014140.4(SMARCAL1):c.2764A>G (p.Met922Val)
NM_014140.4(SMARCAL1):c.2765T>C rs200431186
NM_014140.4(SMARCAL1):c.2837A>C (p.Asn946Thr)
NM_014140.4(SMARCAL1):c.364A>G (p.Ile122Val)
NM_014140.4(SMARCAL1):c.379G>C (p.Ala127Pro)
NM_014140.4(SMARCAL1):c.422A>G (p.Tyr141Cys)
NM_014140.4(SMARCAL1):c.448G>T (p.Ala150Ser)
NM_014140.4(SMARCAL1):c.549G>T (p.Gln183His)
NM_014140.4(SMARCAL1):c.553C>T (p.Pro185Ser)
NM_014140.4(SMARCAL1):c.677C>T (p.Ser226Leu)
NM_014140.4(SMARCAL1):c.67C>T (p.Arg23Cys)
NM_014140.4(SMARCAL1):c.68G>A (p.Arg23His)
NM_014140.4(SMARCAL1):c.724G>A (p.Val242Ile)
NM_014140.4(SMARCAL1):c.767C>T (p.Ala256Val)
NM_014140.4(SMARCAL1):c.782T>A (p.Val261Glu)
NM_014140.4(SMARCAL1):c.811+6G>A
NM_014140.4(SMARCAL1):c.827C>T (p.Thr276Met)
NM_014140.4(SMARCAL1):c.841A>G (p.Met281Val)
NM_014140.4(SMARCAL1):c.866A>C (p.Lys289Thr)
NM_014140.4(SMARCAL1):c.888G>A (p.Thr296=)
NM_014140.4(SMARCAL1):c.92A>G (p.Glu31Gly)

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