NM_001371596.2(MFSD8):c.935T>C (p.Ile312Thr) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jul 31, 2015
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000194054.7
Allele description [Variation Report for NM_001371596.2(MFSD8):c.935T>C (p.Ile312Thr)]
NM_001371596.2(MFSD8):c.935T>C (p.Ile312Thr)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Dec 24, 2023