NM_016729.3(FOLR1):c.501C>T (p.Asn167=) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Sep 29, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002343140.2
Allele description [Variation Report for NM_016729.3(FOLR1):c.501C>T (p.Asn167=)]
NM_016729.3(FOLR1):c.501C>T (p.Asn167=)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Roseobacter sp. HKCCD7120 NODE_1, whole genome shotgun sequence
Roseobacter sp. HKCCD7120 NODE_1, whole genome shotgun sequencegi|1847009789|ref|NZ_WVNU01000001.1 |WGS:NZ_WVNU01|NODE_1Nucleotide
-
Plekhh3 pleckstrin homology domain containing, family H (with MyTH4 domain) memb...
Plekhh3 pleckstrin homology domain containing, family H (with MyTH4 domain) member 3 [Mus musculus]Gene ID:217198Gene
-
217198[uid] AND (alive[prop]) (1)
Gene
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Last Updated: May 1, 2024