NM_000038.6(APC):c.7703G>C (p.Gly2568Ala) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Nov 29, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001026735.11
Allele description [Variation Report for NM_000038.6(APC):c.7703G>C (p.Gly2568Ala)]
NM_000038.6(APC):c.7703G>C (p.Gly2568Ala)
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
-
Mus musculus hemoglobin Z, beta-like embryonic chain (Hbb-bh1), mRNA
Mus musculus hemoglobin Z, beta-like embryonic chain (Hbb-bh1), mRNAgi|6680178|ref|NM_008219.1|Nucleotide
-
Rattus norvegicus ribophorin II (Rpn2), mRNA
Rattus norvegicus ribophorin II (Rpn2), mRNAgi|13928973|ref|NM_031698.1|Nucleotide
-
Mus musculus EGF-like-domain, multiple 6, mRNA (cDNA clone MGC:141463 IMAGE:4006...
Mus musculus EGF-like-domain, multiple 6, mRNA (cDNA clone MGC:141463 IMAGE:40062530), complete cdsgi|115528504|gb|BC117702.2|Nucleotide
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Sep 16, 2024