NM_018699.4(PRDM5):c.1283-5C>T AND Ehlers-Danlos syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Nov 30, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002278567.4
Allele description [Variation Report for NM_018699.4(PRDM5):c.1283-5C>T]
NM_018699.4(PRDM5):c.1283-5C>T
Condition(s)
-
Homo sapiens stathmin 1 (STMN1), transcript variant 3, mRNA
Homo sapiens stathmin 1 (STMN1), transcript variant 3, mRNAgi|1519245806|ref|NM_005563.4|Nucleotide
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Last Updated: Aug 4, 2024