NM_015386.3(COG4):c.1827+12G>C AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Mar 31, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000437221.1
Allele description [Variation Report for NM_015386.3(COG4):c.1827+12G>C]
NM_015386.3(COG4):c.1827+12G>C
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Feb 28, 2024