NM_001371596.2(MFSD8):c.54T>G (p.Pro18=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Mar 5, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000868738.7
Allele description [Variation Report for NM_001371596.2(MFSD8):c.54T>G (p.Pro18=)]
NM_001371596.2(MFSD8):c.54T>G (p.Pro18=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024