NM_005199.5(CHRNG):c.1141T>C (p.Trp381Arg) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 27, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003219764.2
Allele description [Variation Report for NM_005199.5(CHRNG):c.1141T>C (p.Trp381Arg)]
NM_005199.5(CHRNG):c.1141T>C (p.Trp381Arg)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
RPS3 ribosomal protein S3 [Homo sapiens]
RPS3 ribosomal protein S3 [Homo sapiens]Gene ID:6188Gene
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Last Updated: Sep 1, 2024