NM_001039762.3(INSYN2A):c.863G>A (p.Arg288Gln) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 11, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004398333.1
Allele description [Variation Report for NM_001039762.3(INSYN2A):c.863G>A (p.Arg288Gln)]
NM_001039762.3(INSYN2A):c.863G>A (p.Arg288Gln)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
Homo sapiens DDB1 and CUL4 associated factor 17 (DCAF17), transcript variant 1, ...
Homo sapiens DDB1 and CUL4 associated factor 17 (DCAF17), transcript variant 1, mRNAgi|1519242207|ref|NM_025000.4|Nucleotide
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Last Updated: Sep 1, 2024