NM_000113.3(TOR1A):c.470G>A (p.Gly157Asp) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Mar 31, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003250090.2
Allele description [Variation Report for NM_000113.3(TOR1A):c.470G>A (p.Gly157Asp)]
NM_000113.3(TOR1A):c.470G>A (p.Gly157Asp)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
uncharacterized protein LOC21388281 [Morus notabilis]
uncharacterized protein LOC21388281 [Morus notabilis]gi|703073465|ref|XP_010089554.1|Protein
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See more...Assertion and evidence details
Last Updated: May 1, 2024