NM_001363764.2(TEPSIN):c.784G>A (p.Gly262Ser) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 17, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004222224.1
Allele description [Variation Report for NM_001363764.2(TEPSIN):c.784G>A (p.Gly262Ser)]
NM_001363764.2(TEPSIN):c.784G>A (p.Gly262Ser)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Jun 2, 2024