NM_023067.4(FOXL2):c.994C>G (p.Pro332Ala) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 29, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002984021.2
Allele description [Variation Report for NM_023067.4(FOXL2):c.994C>G (p.Pro332Ala)]
NM_023067.4(FOXL2):c.994C>G (p.Pro332Ala)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
mitochondrial carnitine/acylcarnitine carrier-like protein [Vitis riparia]
mitochondrial carnitine/acylcarnitine carrier-like protein [Vitis riparia]gi|1847885025|ref|XP_034673314.1|Protein
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Last Updated: May 1, 2024