ClinVar Miner

List of variants in gene MLH3 reported as uncertain significance for not provided

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Total variants: 17
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HGVS dbSNP gnomAD frequency
NM_001040108.2(MLH3):c.1939C>T (p.Arg647Cys) rs28756987 0.00171
NM_001040108.2(MLH3):c.3488G>A (p.Gly1163Asp) rs28757011 0.00100
NM_001040108.2(MLH3):c.2911G>A (p.Val971Ile) rs41555714 0.00048
NM_001040108.2(MLH3):c.3440A>T (p.Asn1147Ile) rs142124529 0.00035
NM_001040108.2(MLH3):c.1637G>T (p.Arg546Ile) rs55725216 0.00034
NM_001040108.2(MLH3):c.2638C>G (p.Leu880Val) rs201453923 0.00010
NM_001040108.2(MLH3):c.3455G>A (p.Arg1152His) rs374041909 0.00006
NM_001040108.2(MLH3):c.2126T>C (p.Ile709Thr) rs750178172 0.00004
NM_001040108.2(MLH3):c.962T>C (p.Met321Thr) rs1004768761 0.00002
NM_001040108.2(MLH3):c.1384G>A (p.Asp462Asn) rs369525473 0.00001
NM_001040108.2(MLH3):c.2344C>G (p.Leu782Val) rs772267556 0.00001
NM_001040108.2(MLH3):c.1768T>C (p.Cys590Arg) rs2139576463
NM_001040108.2(MLH3):c.2299C>T (p.Pro767Ser) rs2139565569
NM_001040108.2(MLH3):c.2793_2794del (p.Asn932fs) rs754716792
NM_001040108.2(MLH3):c.3793A>G (p.Ile1265Val)
NM_001040108.2(MLH3):c.536C>T (p.Ser179Leu) rs2139603869
NM_001040108.2(MLH3):c.602T>G (p.Leu201Arg)

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