ClinVar Miner

List of variants in gene MED12 reported as likely benign for not provided

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Total variants: 13
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HGVS dbSNP
NM_005120.3(MED12):c.1113G>A (p.Leu371=)
NM_005120.3(MED12):c.1248+15T>C rs187377817
NM_005120.3(MED12):c.3355-16C>G
NM_005120.3(MED12):c.3785G>A (p.Arg1262Lys) rs202120461
NM_005120.3(MED12):c.3918C>T (p.Asp1306=)
NM_005120.3(MED12):c.4009G>A (p.Glu1337Lys) rs1057520129
NM_005120.3(MED12):c.4238C>A (p.Thr1413Asn) rs759532414
NM_005120.3(MED12):c.4428G>A (p.Leu1476=)
NM_005120.3(MED12):c.5709T>A (p.Pro1903=)
NM_005120.3(MED12):c.5711C>T (p.Ala1904Val) rs200663107
NM_005120.3(MED12):c.6045-24C>T rs140083803
NM_005120.3(MED12):c.6177_6182ACAGCA[1] (p.Gln2075_Gln2076del)
NM_005120.3(MED12):c.6309_6314ACAGCA[3] (p.Gln2114_Gln2115dup) rs764789036

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