NM_152783.5(D2HGDH):c.1083G>A (p.Ala361=) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 6, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003293897.2
Allele description [Variation Report for NM_152783.5(D2HGDH):c.1083G>A (p.Ala361=)]
NM_152783.5(D2HGDH):c.1083G>A (p.Ala361=)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
PREDICTED: methyltransferase-like protein 23 isoform X2 [Odobenus rosmarus diver...
PREDICTED: methyltransferase-like protein 23 isoform X2 [Odobenus rosmarus divergens]gi|472349287|ref|XP_004394344.1|Protein
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Last Updated: Sep 29, 2024