NM_003810.4(TNFSF10):c.758A>G (p.Asn253Ser) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 23, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004473219.1
Allele description [Variation Report for NM_003810.4(TNFSF10):c.758A>G (p.Asn253Ser)]
NM_003810.4(TNFSF10):c.758A>G (p.Asn253Ser)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: May 7, 2024