ClinVar Miner

Submissions for variant NM_017636.4(TRPM4):c.3288C>T (p.Pro1096=)

dbSNP: rs1847604099
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002219086 SCV002377089 likely benign Progressive familial heart block type IB 2021-09-23 criteria provided, single submitter clinical testing
Ambry Genetics RCV002443146 SCV002611559 likely benign Cardiovascular phenotype 2021-05-18 criteria provided, single submitter clinical testing This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity.

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