NM_006907.4(PYCR1):c.922C>G (p.Leu308Val) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 1, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002974934.2
Allele description [Variation Report for NM_006907.4(PYCR1):c.922C>G (p.Leu308Val)]
NM_006907.4(PYCR1):c.922C>G (p.Leu308Val)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024