NM_001146344.3(PRAMEF11):c.1010A>G (p.Asn337Ser) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 30, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004512558.1
Allele description [Variation Report for NM_001146344.3(PRAMEF11):c.1010A>G (p.Asn337Ser)]
NM_001146344.3(PRAMEF11):c.1010A>G (p.Asn337Ser)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: May 7, 2024