NM_000487.6(ARSA):c.802G>A (p.Gly268Arg) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Feb 6, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004044053.1
Allele description [Variation Report for NM_000487.6(ARSA):c.802G>A (p.Gly268Arg)]
NM_000487.6(ARSA):c.802G>A (p.Gly268Arg)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
TSA: Thaumetopoea pityocampa isotig02752 transcribed RNA sequence
TSA: Thaumetopoea pityocampa isotig02752 transcribed RNA sequencegi|759179947|gb|GBYZ01001449.1||gnl GBYZ01|isotig02752Nucleotide
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024