NM_014777.4(URB2):c.3362G>C (p.Ser1121Thr) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Oct 19, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004225709.1
Allele description [Variation Report for NM_014777.4(URB2):c.3362G>C (p.Ser1121Thr)]
NM_014777.4(URB2):c.3362G>C (p.Ser1121Thr)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Aug 11, 2024