NM_012193.4(FZD4):c.421G>C (p.Glu141Gln) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Nov 22, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002550355.2
Allele description [Variation Report for NM_012193.4(FZD4):c.421G>C (p.Glu141Gln)]
NM_012193.4(FZD4):c.421G>C (p.Glu141Gln)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
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Homo sapiens solute carrier family 30 member 8 (SLC30A8), transcript variant 1, ...
Homo sapiens solute carrier family 30 member 8 (SLC30A8), transcript variant 1, mRNAgi|64762488|ref|NM_173851.2|Nucleotide
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Leviprora inops
Leviprora inopsLeviprora inops (Longhead Flathead), fLevIno1, sequence dataBioProject
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Last Updated: Sep 29, 2024