NM_003977.4(AIP):c.23T>G (p.Leu8Arg) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Apr 22, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002431998.2
Allele description [Variation Report for NM_003977.4(AIP):c.23T>G (p.Leu8Arg)]
NM_003977.4(AIP):c.23T>G (p.Leu8Arg)
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
-
CHN2 chimerin 2 [Homo sapiens]
CHN2 chimerin 2 [Homo sapiens]Gene ID:1124Gene
-
Gene Links for GEO Profiles (Select 120446829) (1)
Gene
-
Profile neighbors for GEO Profiles (Select 120440811) (200)
GEO Profiles
-
CPVL-AS2 CPVL antisense RNA 2 [Homo sapiens]
CPVL-AS2 CPVL antisense RNA 2 [Homo sapiens]Gene ID:100506497Gene
-
Gene Links for GEO Profiles (Select 120433542) (1)
Gene
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See more...Assertion and evidence details
Last Updated: May 1, 2024