NM_015466.4(PTPN23):c.2937G>C (p.Gln979His) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 8, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003111661.4
Allele description [Variation Report for NM_015466.4(PTPN23):c.2937G>C (p.Gln979His)]
NM_015466.4(PTPN23):c.2937G>C (p.Gln979His)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: May 1, 2024