NM_014363.6(SACS):c.9076T>A (p.Phe3026Ile) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Oct 4, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002897587.2
Allele description [Variation Report for NM_014363.6(SACS):c.9076T>A (p.Phe3026Ile)]
NM_014363.6(SACS):c.9076T>A (p.Phe3026Ile)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
mitochondrial arginine transporter BAC1-like isoform X1 [Glycine max]
mitochondrial arginine transporter BAC1-like isoform X1 [Glycine max]gi|955326078|ref|XP_014632278.1|Protein
-
Hcf [Leptopilina heterotoma]
Hcf [Leptopilina heterotoma]Gene ID:122511068Gene
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Last Updated: May 1, 2024