NM_001145860.2(POP1):c.2984C>T (p.Ser995Phe) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jul 19, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001894192.5
Allele description [Variation Report for NM_001145860.2(POP1):c.2984C>T (p.Ser995Phe)]
NM_001145860.2(POP1):c.2984C>T (p.Ser995Phe)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 14, 2024