NM_003506.4(FZD6):c.1900G>A (p.Asp634Asn) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 22, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003374322.2
Allele description [Variation Report for NM_003506.4(FZD6):c.1900G>A (p.Asp634Asn)]
NM_003506.4(FZD6):c.1900G>A (p.Asp634Asn)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
PDGFRL platelet derived growth factor receptor like [Homo sapiens]
PDGFRL platelet derived growth factor receptor like [Homo sapiens]Gene ID:5157Gene
-
Gene Links for GEO Profiles (Select 74659436) (1)
Gene
-
PMC Links for Protein (Select 1314817946) (3)
PMC
-
Taxonomy Links for Nucleotide (Select 846338223) (1)
Taxonomy
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Last Updated: May 1, 2024