NM_000015.3(NAT2):c.749C>A (p.Thr250Lys) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Mar 21, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004291910.1
Allele description [Variation Report for NM_000015.3(NAT2):c.749C>A (p.Thr250Lys)]
NM_000015.3(NAT2):c.749C>A (p.Thr250Lys)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Aug 25, 2024