ClinVar Miner

List of variants in gene TPM3 reported as likely benign for childhood-onset nemaline myopathy

Included ClinVar conditions (12):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 3
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NM_152263.4(TPM3):c.144G>A (p.Gln48=) rs765923858
NM_152263.4(TPM3):c.483G>A (p.Arg161=) rs150586027
NM_152263.4(TPM3):c.706-9T>A rs931328025

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