NM_006058.5(TNIP1):c.1746G>A (p.Pro582=) AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Dec 31, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000955346.4
Allele description [Variation Report for NM_006058.5(TNIP1):c.1746G>A (p.Pro582=)]
NM_006058.5(TNIP1):c.1746G>A (p.Pro582=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Dec 24, 2023