NM_002755.4(MAP2K1):c.693+10G>A AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 15, 2015
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000157671.7
Allele description [Variation Report for NM_002755.4(MAP2K1):c.693+10G>A]
NM_002755.4(MAP2K1):c.693+10G>A
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Mar 5, 2024