NM_145886.4(PIDD1):c.2226G>T (p.Arg742Ser) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Nov 9, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003479488.1
Allele description [Variation Report for NM_145886.4(PIDD1):c.2226G>T (p.Arg742Ser)]
NM_145886.4(PIDD1):c.2226G>T (p.Arg742Ser)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: May 1, 2024