NM_032635.4(TMEM147):c.632G>A (p.Ser211Asn) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 21, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003345109.1
Allele description [Variation Report for NM_032635.4(TMEM147):c.632G>A (p.Ser211Asn)]
NM_032635.4(TMEM147):c.632G>A (p.Ser211Asn)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: Oct 28, 2023