NM_017739.4(POMGNT1):c.1456C>G (p.Arg486Gly) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jul 24, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002518155.9
Allele description [Variation Report for NM_017739.4(POMGNT1):c.1456C>G (p.Arg486Gly)]
NM_017739.4(POMGNT1):c.1456C>G (p.Arg486Gly)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
RecName: Full=Olfactory receptor 5H18; AltName: Full=Olfactory receptor 183-9; A...
RecName: Full=Olfactory receptor 5H18; AltName: Full=Olfactory receptor 183-9; AltName: Full=Olfactory receptor 186gi|81915282|sp|Q8VEX5.1|O5H18_MOUSEProtein
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Last Updated: Oct 13, 2024