NM_001198800.3(ASCC1):c.626+134C>T AND not provided
- Germline classification:
- Benign (2 submissions)
- Last evaluated:
- May 10, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001654588.3
Allele description [Variation Report for NM_001198800.3(ASCC1):c.626+134C>T]
NM_001198800.3(ASCC1):c.626+134C>T
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024