NM_001191016.2(CASP12):c.817+1A>G AND not specified
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Mar 28, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000455720.4
Allele description [Variation Report for NM_001191016.2(CASP12):c.817+1A>G]
NM_001191016.2(CASP12):c.817+1A>G
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Dec 24, 2023