NM_017694.4(MFSD6):c.1216G>T (p.Val406Leu) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 28, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004343965.1
Allele description [Variation Report for NM_017694.4(MFSD6):c.1216G>T (p.Val406Leu)]
NM_017694.4(MFSD6):c.1216G>T (p.Val406Leu)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: May 19, 2024