NM_000038.6(APC):c.1313-15G>T AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 3, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001192159.9
Allele description [Variation Report for NM_000038.6(APC):c.1313-15G>T]
NM_000038.6(APC):c.1313-15G>T
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
-
Drosophila melanogaster chitinase 12 (Cht12), mRNA
Drosophila melanogaster chitinase 12 (Cht12), mRNAgi|320544194|ref|NM_166420.2|Nucleotide
-
Homo sapiens mRNA for FLJ00001 protein, partial cds
Homo sapiens mRNA for FLJ00001 protein, partial cdsgi|7209302|dbj|AK000001.1|Nucleotide
-
Primary peritoneal serous/papillary carcinoma
Primary peritoneal serous/papillary carcinomaMedGen
-
C1368918[conceptid] (1)
MedGen
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See more...Assertion and evidence details
Last Updated: Oct 13, 2024