NM_001130438.3(SPTAN1):c.2753A>G (p.Tyr918Cys) AND Inborn genetic diseases
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Nov 26, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002433857.9
Allele description [Variation Report for NM_001130438.3(SPTAN1):c.2753A>G (p.Tyr918Cys)]
NM_001130438.3(SPTAN1):c.2753A>G (p.Tyr918Cys)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
forkhead box protein F1 [Pan troglodytes]
forkhead box protein F1 [Pan troglodytes]gi|2468531451|ref|XP_523449.6|Protein
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Oct 13, 2024