NM_001482.3(GATM):c.48G>T (p.Ala16=) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- May 31, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002316371.9
Allele description [Variation Report for NM_001482.3(GATM):c.48G>T (p.Ala16=)]
NM_001482.3(GATM):c.48G>T (p.Ala16=)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
[Ruminococcus] torques strain DFI.4.27 HOGILOJC_192, whole genome shotgun sequen...
[Ruminococcus] torques strain DFI.4.27 HOGILOJC_192, whole genome shotgun sequencegi|2192625923|ref|NZ_JAKNFB01000019 gnl|WGS:NZ_JAKNFB01|HOGILOJC_192Nucleotide
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Last Updated: Jun 2, 2024