ClinVar Miner

List of variants in gene SAMD15 reported as uncertain significance

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Total variants: 41
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HGVS dbSNP gnomAD frequency
NM_001010860.4(SAMD15):c.849G>C (p.Glu283Asp) rs145730565 0.00036
NM_001010860.4(SAMD15):c.1415T>C (p.Ile472Thr) rs141444954 0.00032
NM_001010860.4(SAMD15):c.1843C>T (p.Arg615Cys) rs149116567 0.00027
NM_001010860.4(SAMD15):c.352T>G (p.Phe118Val) rs371745458 0.00015
NM_001010860.4(SAMD15):c.1177G>A (p.Glu393Lys) rs146296291 0.00013
NM_001010860.4(SAMD15):c.221A>T (p.Asn74Ile) rs371015537 0.00012
NM_001010860.4(SAMD15):c.112G>A (p.Asp38Asn) rs779375285 0.00005
NM_001010860.4(SAMD15):c.1813C>T (p.Leu605Phe) rs200429320 0.00005
NM_001010860.4(SAMD15):c.524C>G (p.Thr175Arg) rs369452640 0.00005
NM_001010860.4(SAMD15):c.1325G>A (p.Arg442His) rs749881791 0.00004
NM_001010860.4(SAMD15):c.758G>C (p.Arg253Thr) rs766095238 0.00004
NM_001010860.4(SAMD15):c.1522G>A (p.Val508Ile) rs148358741 0.00003
NM_001010860.4(SAMD15):c.170C>T (p.Pro57Leu) rs775931520 0.00003
NM_001010860.4(SAMD15):c.10G>T (p.Val4Phe) rs368880585 0.00002
NM_001010860.4(SAMD15):c.110C>T (p.Pro37Leu) rs1421067568 0.00001
NM_001010860.4(SAMD15):c.1535A>G (p.Glu512Gly) rs908791333 0.00001
NM_001010860.4(SAMD15):c.1024A>G (p.Arg342Gly)
NM_001010860.4(SAMD15):c.1301T>C (p.Val434Ala)
NM_001010860.4(SAMD15):c.130G>T (p.Asp44Tyr) rs1893856612
NM_001010860.4(SAMD15):c.1324C>T (p.Arg442Cys)
NM_001010860.4(SAMD15):c.134C>T (p.Ser45Leu) rs747132452
NM_001010860.4(SAMD15):c.1568G>A (p.Arg523Gln)
NM_001010860.4(SAMD15):c.1693T>G (p.Cys565Gly)
NM_001010860.4(SAMD15):c.1726C>T (p.Leu576Phe) rs2503534640
NM_001010860.4(SAMD15):c.1735G>A (p.Val579Ile)
NM_001010860.4(SAMD15):c.1877G>A (p.Gly626Asp) rs2503546360
NM_001010860.4(SAMD15):c.1984G>T (p.Ala662Ser)
NM_001010860.4(SAMD15):c.223G>A (p.Val75Met)
NM_001010860.4(SAMD15):c.256G>A (p.Gly86Arg) rs2503528364
NM_001010860.4(SAMD15):c.274A>C (p.Lys92Gln)
NM_001010860.4(SAMD15):c.289A>G (p.Ser97Gly) rs2503528453
NM_001010860.4(SAMD15):c.29C>G (p.Ser10Cys) rs2503527648
NM_001010860.4(SAMD15):c.318G>C (p.Glu106Asp)
NM_001010860.4(SAMD15):c.401A>C (p.Asp134Ala)
NM_001010860.4(SAMD15):c.556G>C (p.Glu186Gln)
NM_001010860.4(SAMD15):c.602A>G (p.His201Arg) rs2503529330
NM_001010860.4(SAMD15):c.712C>T (p.Pro238Ser) rs2503529631
NM_001010860.4(SAMD15):c.717G>T (p.Glu239Asp)
NM_001010860.4(SAMD15):c.74T>C (p.Leu25Pro)
NM_001010860.4(SAMD15):c.793C>A (p.Leu265Met) rs747476384
NM_001010860.4(SAMD15):c.865C>G (p.Pro289Ala) rs1277956337

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