NM_000744.7(CHRNA4):c.1454G>A (p.Arg485Gln) AND not provided
- Germline classification:
- Conflicting interpretations of pathogenicity (2 submissions)
- Last evaluated:
- Mar 16, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000724403.17
Allele description [Variation Report for NM_000744.7(CHRNA4):c.1454G>A (p.Arg485Gln)]
NM_000744.7(CHRNA4):c.1454G>A (p.Arg485Gln)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Apr 20, 2024