ClinVar Miner

List of variants in gene MTM1 reported as likely benign for X-linked disease

Included ClinVar conditions (313):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 9
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HGVS dbSNP
NM_000252.2(MTM1):c.1119G>A (p.Val373=) rs941979306
NM_000252.2(MTM1):c.232-7A>G rs373045797
NM_000252.2(MTM1):c.423G>A (p.Ala141=) rs377311110
NM_000252.3(MTM1):c.1131C>T (p.Asp377=) rs1557414507
NM_000252.3(MTM1):c.1376A>G (p.Asn459Ser) rs587783785
NM_000252.3(MTM1):c.1578C>T (p.Ala526=) rs1603208507
NM_000252.3(MTM1):c.1692C>T (p.Arg564=) rs1557415136
NM_000252.3(MTM1):c.64-9T>C rs189752798
NM_000252.3(MTM1):c.954G>C (p.Arg318=) rs1557414126

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