NM_014140.4(SMARCAL1):c.962G>A (p.Gly321Asp) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 16, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004020134.1
Allele description [Variation Report for NM_014140.4(SMARCAL1):c.962G>A (p.Gly321Asp)]
NM_014140.4(SMARCAL1):c.962G>A (p.Gly321Asp)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
UGT8 [Protobothrops mucrosquamatus]
UGT8 [Protobothrops mucrosquamatus]Gene ID:107296372Gene
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Last Updated: Oct 13, 2024