NM_000349.3(STAR):c.481G>A (p.Gly161Arg) AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 30, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000904441.7
Allele description [Variation Report for NM_000349.3(STAR):c.481G>A (p.Gly161Arg)]
NM_000349.3(STAR):c.481G>A (p.Gly161Arg)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
GOLGA2 golgin A2 [Homo sapiens]
GOLGA2 golgin A2 [Homo sapiens]Gene ID:2801Gene
-
Gene Links for GEO Profiles (Select 42582225) (1)
Gene
-
Profile neighbors for GEO Profiles (Select 126294821) (200)
GEO Profiles
-
txid1835370[Organism:noexp] (2)
PMC
-
Gene Links for GEO Profiles (Select 126307318) (1)
Gene
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See more...Assertion and evidence details
Last Updated: Feb 20, 2024