NM_006068.5(TLR6):c.938C>T (p.Thr313Met) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Nov 17, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004220129.1
Allele description [Variation Report for NM_006068.5(TLR6):c.938C>T (p.Thr313Met)]
NM_006068.5(TLR6):c.938C>T (p.Thr313Met)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: May 26, 2024