NM_012210.4(TRIM32):c.1710G>A (p.Ser570=) AND not provided
- Germline classification:
- Uncertain significance (2 submissions)
- Last evaluated:
- Mar 4, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000726537.5
Allele description [Variation Report for NM_012210.4(TRIM32):c.1710G>A (p.Ser570=)]
NM_012210.4(TRIM32):c.1710G>A (p.Ser570=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Mar 10, 2024