NM_198904.4(GABRG2):c.1087C>T (p.Arg363Trp) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 23, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002317098.9
Allele description [Variation Report for NM_198904.4(GABRG2):c.1087C>T (p.Arg363Trp)]
NM_198904.4(GABRG2):c.1087C>T (p.Arg363Trp)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Purpureocillium takamizusanense uncharacterized protein (JDV02_006844), mRNA
Purpureocillium takamizusanense uncharacterized protein (JDV02_006844), mRNAgi|2234671833|ref|XM_047988275.1|Nucleotide
-
Gm28311 AND (alive[prop]) (0)
Gene
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Last Updated: Oct 13, 2024