NM_001099289.3(SH3RF3):c.2362A>T (p.Met788Leu) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jul 26, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004154547.1
Allele description [Variation Report for NM_001099289.3(SH3RF3):c.2362A>T (p.Met788Leu)]
NM_001099289.3(SH3RF3):c.2362A>T (p.Met788Leu)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Jun 2, 2024