NM_002755.4(MAP2K1):c.156C>T (p.Ala52=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Mar 19, 2012
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000151007.4
Allele description [Variation Report for NM_002755.4(MAP2K1):c.156C>T (p.Ala52=)]
NM_002755.4(MAP2K1):c.156C>T (p.Ala52=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
Profile neighbors for GEO Profiles (Select 132373091) (200)
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Profile neighbors for GEO Profiles (Select 132378249) (200)
GEO Profiles
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Last Updated: Sep 29, 2024