NM_000136.3(FANCC):c.1329+1del AND Fanconi anemia complementation group C
- Germline classification:
- Likely pathogenic (1 submission)
- Last evaluated:
- Jan 19, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003460187.1
Allele description [Variation Report for NM_000136.3(FANCC):c.1329+1del]
NM_000136.3(FANCC):c.1329+1del
Condition(s)
-
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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See more...Assertion and evidence details
Last Updated: Dec 30, 2023