NM_000136.3(FANCC):c.1501G>A (p.Gly501Ser) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 8, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002395843.3
Allele description [Variation Report for NM_000136.3(FANCC):c.1501G>A (p.Gly501Ser)]
NM_000136.3(FANCC):c.1501G>A (p.Gly501Ser)
Condition(s)
- Name:
- Hereditary cancer-predisposing syndrome
- Synonyms:
- Neoplastic Syndromes, Hereditary; Tumor predisposition; Cancer predisposition; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0015356; MeSH: D009386; MedGen: C0027672
-
Cpgi7465 AND (alive[prop]) (0)
Gene
-
SLIC-CAGE of paired-end sequencing data in mouse islets
SLIC-CAGE of paired-end sequencing data in mouse isletsSLIC-CAGE of paired-end sequencing data in mouse isletsBioProject
-
Clostridiales bacterium VE202-06
Clostridiales bacterium VE202-06Clostridiales bacterium VE202-06 Genome sequencingBioProject
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See more...Assertion and evidence details
Last Updated: Jul 23, 2024