NM_000345.4(SNCA):c.*1287G>A AND Parkinson Disease, Dominant
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 13, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000405545.5
Allele description [Variation Report for NM_000345.4(SNCA):c.*1287G>A]
NM_000345.4(SNCA):c.*1287G>A
Condition(s)
- Name:
- Parkinson Disease, Dominant
- Identifiers:
- MedGen: CN239359
-
Homo sapiens chromosome 10 genomic scaffold, GRCh38.p14 Primary Assembly CEN10_4
Homo sapiens chromosome 10 genomic scaffold, GRCh38.p14 Primary Assembly CEN10_4gi|568815277|gnl|ASM:GCF_000001305. N10_4|ref|NT_187218.1||gpp|GPS_003205548.1|Nucleotide
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Last Updated: Dec 24, 2023