NM_003977.4(AIP):c.508A>G (p.Met170Val) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Nov 16, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004516382.1
Allele description [Variation Report for NM_003977.4(AIP):c.508A>G (p.Met170Val)]
NM_003977.4(AIP):c.508A>G (p.Met170Val)
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
-
4-hydroxy-2-oxoglutarate aldolase, mitochondrial isoform X2 [Pongo abelii]
4-hydroxy-2-oxoglutarate aldolase, mitochondrial isoform X2 [Pongo abelii]gi|1351383083|ref|XP_024109456.1|Protein
-
SYPL1P1 synaptophysin like 1 pseudogene 1 [Homo sapiens]
SYPL1P1 synaptophysin like 1 pseudogene 1 [Homo sapiens]Gene ID:100130011Gene
-
SYPL1P1 AND (alive[prop]) (1)
Gene
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See more...Assertion and evidence details
Last Updated: May 7, 2024