NM_000251.3(MSH2):c.227A>C (p.Gln76Pro) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 2, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001788459.2
Allele description [Variation Report for NM_000251.3(MSH2):c.227A>C (p.Gln76Pro)]
NM_000251.3(MSH2):c.227A>C (p.Gln76Pro)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Homo sapiens chitinase domain containing 1 (CHID1), transcript variant 3, mRNA
Homo sapiens chitinase domain containing 1 (CHID1), transcript variant 3, mRNAgi|1653961341|ref|NM_023947.4|Nucleotide
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Last Updated: Feb 20, 2024