NM_001005484.2(OR4F5):c.655G>A (p.Val219Met) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jul 12, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004230996.1
Allele description [Variation Report for NM_001005484.2(OR4F5):c.655G>A (p.Val219Met)]
NM_001005484.2(OR4F5):c.655G>A (p.Val219Met)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
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See more...Assertion and evidence details
Last Updated: Oct 26, 2024