NM_024867.4(SPEF2):c.1355+150G>A AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- May 17, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001679250.1
Allele description [Variation Report for NM_024867.4(SPEF2):c.1355+150G>A]
NM_024867.4(SPEF2):c.1355+150G>A
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
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Last Updated: Dec 24, 2023