NM_001145860.2(POP1):c.2511G>A (p.Gln837=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Nov 18, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003701946.2
Allele description [Variation Report for NM_001145860.2(POP1):c.2511G>A (p.Gln837=)]
NM_001145860.2(POP1):c.2511G>A (p.Gln837=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024