NM_207309.3(UAP1L1):c.1117C>T (p.Pro373Ser) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jul 14, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004084823.1
Allele description [Variation Report for NM_207309.3(UAP1L1):c.1117C>T (p.Pro373Ser)]
NM_207309.3(UAP1L1):c.1117C>T (p.Pro373Ser)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Oct 26, 2024