NM_001482.3(GATM):c.1269C>G (p.Asp423Glu) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 12, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002317623.9
Allele description [Variation Report for NM_001482.3(GATM):c.1269C>G (p.Asp423Glu)]
NM_001482.3(GATM):c.1269C>G (p.Asp423Glu)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Abcg4 ATP binding cassette subfamily G member 4 [Mus musculus]
Abcg4 ATP binding cassette subfamily G member 4 [Mus musculus]Gene ID:192663Gene
-
192663[uid] AND (alive[prop]) (1)
Gene
-
LOC110716483 [Chenopodium quinoa]
LOC110716483 [Chenopodium quinoa]Gene ID:110716483Gene
-
esv3573452 (1)
dbVar
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Last Updated: Oct 26, 2024