NM_001395207.1(SORBS2):c.836C>T (p.Pro279Leu) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 9, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004464878.1
Allele description [Variation Report for NM_001395207.1(SORBS2):c.836C>T (p.Pro279Leu)]
NM_001395207.1(SORBS2):c.836C>T (p.Pro279Leu)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: May 7, 2024