ClinVar Miner

Submissions for variant NM_014555.4(TRPM5):c.1365C>T (p.Pro455=)

gnomAD frequency: 0.00327  dbSNP: rs200801959
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000897295 SCV001041434 benign not provided 2018-08-16 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000897295 SCV002544485 likely benign not provided 2022-05-01 criteria provided, single submitter clinical testing TRPM5: BP4, BP7

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