NM_001379200.1(TBX1):c.1165G>A (p.Gly389Ser) AND DiGeorge syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Oct 23, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003856443.2
Allele description [Variation Report for NM_001379200.1(TBX1):c.1165G>A (p.Gly389Ser)]
NM_001379200.1(TBX1):c.1165G>A (p.Gly389Ser)
Condition(s)
- Name:
- DiGeorge syndrome
- Synonyms:
- Hypoplasia of thymus and parathyroid; Third and fourth pharyngeal pouch syndrome; DiGeorge anomaly; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0008564; MedGen: C0012236; Orphanet: 567; OMIM: 188400
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Last Updated: Sep 29, 2024