NM_020361.5(CPA6):c.442T>C (p.Trp148Arg) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 7, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000596413.4
Allele description [Variation Report for NM_020361.5(CPA6):c.442T>C (p.Trp148Arg)]
NM_020361.5(CPA6):c.442T>C (p.Trp148Arg)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: May 1, 2024