NM_152732.5(RSPH9):c.263C>T (p.Ala88Val) AND not specified
- Germline classification:
- Benign (1 submission)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000252936.13
Allele description [Variation Report for NM_152732.5(RSPH9):c.263C>T (p.Ala88Val)]
NM_152732.5(RSPH9):c.263C>T (p.Ala88Val)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Sep 29, 2024