NM_000136.3(FANCC):c.90C>G (p.Thr30=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Feb 9, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000611416.1
Allele description [Variation Report for NM_000136.3(FANCC):c.90C>G (p.Thr30=)]
NM_000136.3(FANCC):c.90C>G (p.Thr30=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
Rattus norvegicus synaptojanin 2 (Synj2), transcript variant 1, mRNA
Rattus norvegicus synaptojanin 2 (Synj2), transcript variant 1, mRNAgi|164565434|ref|NM_001113371.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024