NM_000038.6(APC):c.7589G>A (p.Arg2530Gln) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (2 submissions)
- Last evaluated:
- May 20, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000222733.18
Allele description [Variation Report for NM_000038.6(APC):c.7589G>A (p.Arg2530Gln)]
NM_000038.6(APC):c.7589G>A (p.Arg2530Gln)
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
-
Rattus norvegicus coiled-coil domain containing 69 (Ccdc69), mRNA
Rattus norvegicus coiled-coil domain containing 69 (Ccdc69), mRNAgi|157817331|ref|NM_001109031.1|Nucleotide
-
JGI_XZT19123.rev NIH_XGC_tropTad5 Xenopus tropicalis cDNA clone IMAGE:7595912 3'...
JGI_XZT19123.rev NIH_XGC_tropTad5 Xenopus tropicalis cDNA clone IMAGE:7595912 3', mRNA sequencegi|57072882|gnl|dbEST|26958274|gb|C 10.1|Nucleotide
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Sep 16, 2024