NM_001330239.4(TJP1):c.5042T>C (p.Ile1681Thr) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 2, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004356854.1
Allele description [Variation Report for NM_001330239.4(TJP1):c.5042T>C (p.Ile1681Thr)]
NM_001330239.4(TJP1):c.5042T>C (p.Ile1681Thr)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Jul 7, 2024