NM_018109.4(MTPAP):c.1478G>C (p.Ser493Thr) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 17, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002716239.2
Allele description [Variation Report for NM_018109.4(MTPAP):c.1478G>C (p.Ser493Thr)]
NM_018109.4(MTPAP):c.1478G>C (p.Ser493Thr)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: May 1, 2024