NM_182692.3(SRPK2):c.141T>A (p.Pro47=) AND SRPK2-related disorder
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Apr 17, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003983809.1
Allele description
NM_182692.3(SRPK2):c.141T>A (p.Pro47=)
Condition(s)
- Name:
- SRPK2-related disorder
- Synonyms:
- SRPK2-related condition
- Identifiers:
-
Homo sapiens UV radiation resistance associated (UVRAG), transcript variant 2, m...
Homo sapiens UV radiation resistance associated (UVRAG), transcript variant 2, mRNAgi|1519245328|ref|NM_003369.4|Nucleotide
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Last Updated: Sep 29, 2024