NM_031462.4(CD99L2):c.782G>A (p.Arg261Gln) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 11, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000943131.3
Allele description [Variation Report for NM_031462.4(CD99L2):c.782G>A (p.Arg261Gln)]
NM_031462.4(CD99L2):c.782G>A (p.Arg261Gln)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
eggc.vipT0G (0)
BioProject
-
Embryonic V6.5 stem cell differentiation in vitro (MG-430B)
Embryonic V6.5 stem cell differentiation in vitro (MG-430B)Accession: GDS2672GEO DataSets
-
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GEO DataSets
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See more...Assertion and evidence details
Last Updated: Dec 24, 2023