NM_002755.4(MAP2K1):c.39G>A (p.Pro13=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Mar 12, 2015
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000221741.4
Allele description [Variation Report for NM_002755.4(MAP2K1):c.39G>A (p.Pro13=)]
NM_002755.4(MAP2K1):c.39G>A (p.Pro13=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Feb 20, 2024