NM_001001671.4(MAP3K15):c.2978C>T (p.Ser993Leu) AND MAP3K15-related disorder
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jul 1, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003916776.2
Allele description [Variation Report for NM_001001671.4(MAP3K15):c.2978C>T (p.Ser993Leu)]
NM_001001671.4(MAP3K15):c.2978C>T (p.Ser993Leu)
Condition(s)
- Name:
- MAP3K15-related disorder
- Synonyms:
- MAP3K15-related condition
- Identifiers:
Assertion and evidence details
Last Updated: Oct 13, 2024