NM_001039762.3(INSYN2A):c.122G>A (p.Arg41Gln) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 16, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004289490.1
Allele description [Variation Report for NM_001039762.3(INSYN2A):c.122G>A (p.Arg41Gln)]
NM_001039762.3(INSYN2A):c.122G>A (p.Arg41Gln)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
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Last Updated: Jun 2, 2024