NM_003172.4(SURF1):c.751+6T>C AND not specified
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Dec 27, 2013
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000128343.9
Allele description [Variation Report for NM_003172.4(SURF1):c.751+6T>C]
NM_003172.4(SURF1):c.751+6T>C
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Aug 18, 2024