NM_006218.4(PIK3CA):c.181C>T (p.Leu61Phe) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Mar 1, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002410330.2
Allele description [Variation Report for NM_006218.4(PIK3CA):c.181C>T (p.Leu61Phe)]
NM_006218.4(PIK3CA):c.181C>T (p.Leu61Phe)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
LOC109608421 [Aethina tumida]
LOC109608421 [Aethina tumida]Gene ID:109608421Gene
-
P2ry1 [Meriones unguiculatus]
P2ry1 [Meriones unguiculatus]Gene ID:110566209Gene
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: May 1, 2024