ClinVar Miner

List of variants in gene MSH2 reported as not provided for not specified

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Gene type:
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Total variants: 19
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HGVS dbSNP gnomAD frequency
NM_000251.3(MSH2):c.380A>G (p.Asn127Ser) rs17217772 0.02317
NM_000251.3(MSH2):c.965G>A (p.Gly322Asp) rs4987188 0.01714
NM_000251.3(MSH2):c.23C>T (p.Thr8Met) rs17217716 0.00184
NC_000002.12:g.47678259C>A rs182017009 0.00074
NM_000251.3(MSH2):c.1886A>G (p.Gln629Arg) rs61756468 0.00042
NM_000251.3(MSH2):c.1168C>T (p.Leu390Phe) rs17224367 0.00039
NM_000251.3(MSH2):c.1255C>A (p.Gln419Lys) rs63750006 0.00019
NM_000251.3(MSH2):c.138C>G (p.His46Gln) rs33946261 0.00019
NM_000251.3(MSH2):c.2425G>A (p.Glu809Lys) rs202145681 0.00013
NM_000251.3(MSH2):c.1601G>A (p.Arg534His) rs587778523 0.00004
NM_000251.3(MSH2):c.208G>A (p.Ala70Thr) rs587778522 0.00001
NM_000251.3(MSH2):c.220A>C (p.Asn74His) rs150548839 0.00001
NM_000251.3(MSH2):c.2545C>G (p.Leu849Val) rs587778527 0.00001
NM_000251.3(MSH2):c.5C>T (p.Ala2Val) rs587778521 0.00001
NC_000002.12:g.47678251C>A rs17036817
NC_000002.12:g.47678251C>G rs17036817
NM_000251.3(MSH2):c.1631T>C (p.Ile544Thr) rs587778524
NM_000251.3(MSH2):c.1662C>T (p.Ser554=) rs587778525
NM_000251.3(MSH2):c.1798G>T (p.Ala600Ser) rs587778526

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