NM_024782.3(NHEJ1):c.707-7A>T AND not provided
- Germline classification:
- Likely benign (2 submissions)
- Last evaluated:
- Sep 1, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000840974.18
Allele description [Variation Report for NM_024782.3(NHEJ1):c.707-7A>T]
NM_024782.3(NHEJ1):c.707-7A>T
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Oct 8, 2024