NM_014495.4(ANGPTL3):c.291G>T (p.Lys97Asn) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 25, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004414974.1
Allele description [Variation Report for NM_014495.4(ANGPTL3):c.291G>T (p.Lys97Asn)]
NM_014495.4(ANGPTL3):c.291G>T (p.Lys97Asn)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
tail-specific protease [Flavivirga eckloniae]
tail-specific protease [Flavivirga eckloniae]gi|1329927918|gnl|PRJNA428941|C1H87 5|gb|AUP81562.1|Protein
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Sep 1, 2024