NM_005921.2(MAP3K1):c.3266C>G (p.Ser1089Cys) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 10, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002552861.2
Allele description [Variation Report for NM_005921.2(MAP3K1):c.3266C>G (p.Ser1089Cys)]
NM_005921.2(MAP3K1):c.3266C>G (p.Ser1089Cys)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
arginine N-methyltransferase 1 [Schistosoma japonicum]
arginine N-methyltransferase 1 [Schistosoma japonicum]gi|224813804|gb|ACN65119.1|Protein
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Last Updated: Sep 29, 2024