ClinVar Miner

List of variants in gene MT-TM studied for hereditary skeletal muscle disorder

Included ClinVar conditions (587):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 14
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HGVS dbSNP gnomAD frequency
NC_012920.1(MT-TM):m.4409T>C rs118203884
NC_012920.1(MT-TM):m.4417A>G rs1603219452
NC_012920.1(MT-TM):m.4418T>C rs1556422856
NC_012920.1(MT-TM):m.4429G>A rs1603219456
NC_012920.1(MT-TM):m.4435A>G rs878930498
NC_012920.1(MT-TM):m.4437C>T rs1603219459
NC_012920.1(MT-TM):m.4451T>G rs1603219461
NC_012920.1(MT-TM):m.4452T>C rs377043134
NC_012920.1(MT-TM):m.4454T>A rs11510098
NC_012920.1(MT-TM):m.4454T>C rs11510098
NC_012920.1(MT-TM):m.4455A>G rs878986264
NC_012920.1(MT-TM):m.4456C>T rs1603219465
NC_012920.1(MT-TM):m.4464G>A rs1603219466
NC_012920.1(MT-TM):m.4466A>G rs1603219467

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