NM_000038.6(APC):c.7412C>T (p.Pro2471Leu) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 19, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000216831.11
Allele description [Variation Report for NM_000038.6(APC):c.7412C>T (p.Pro2471Leu)]
NM_000038.6(APC):c.7412C>T (p.Pro2471Leu)
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 olfactomedin 2 (Olfm2), mRNA
Rattus norvegicus olfactomedin 2 (Olfm2), mRNAgi|62543528|ref|NM_001015017.1|Nucleotide
-
Hyperglycinuria
HyperglycinuriaMedGen
-
(107456[MIM]) OR (107456[UID]) (1)
MedGen
-
pomgnt2 [Cyclopterus lumpus]
pomgnt2 [Cyclopterus lumpus]Gene ID:117728303Gene
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See more...Assertion and evidence details
Last Updated: Oct 26, 2024