NM_006567.5(FARS2):c.588C>T (p.Ala196=) AND Combined oxidative phosphorylation defect type 14
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 18, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000886872.9
Allele description [Variation Report for NM_006567.5(FARS2):c.588C>T (p.Ala196=)]
NM_006567.5(FARS2):c.588C>T (p.Ala196=)
Condition(s)
-
LOC112920550 [Vulpes vulpes]
LOC112920550 [Vulpes vulpes]Gene ID:112920550Gene
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See more...Assertion and evidence details
Last Updated: Aug 4, 2024