NM_080680.3(COL11A2):c.2406C>G (p.Gly802=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 28, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002013594.6
Allele description [Variation Report for NM_080680.3(COL11A2):c.2406C>G (p.Gly802=)]
NM_080680.3(COL11A2):c.2406C>G (p.Gly802=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Homo sapiens calponin 3 (CNN3), transcript variant 2, mRNA
Homo sapiens calponin 3 (CNN3), transcript variant 2, mRNAgi|1890268646|ref|NM_001286055.2|Nucleotide
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Last Updated: Sep 29, 2024