NM_015726.4(DCAF8):c.959+4A>C AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Oct 3, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002470165.1
Allele description [Variation Report for NM_015726.4(DCAF8):c.959+4A>C]
NM_015726.4(DCAF8):c.959+4A>C
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
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Last Updated: Dec 24, 2022