NM_022460.4(HS1BP3):c.814G>A (p.Gly272Ser) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 10, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004291797.1
Allele description [Variation Report for NM_022460.4(HS1BP3):c.814G>A (p.Gly272Ser)]
NM_022460.4(HS1BP3):c.814G>A (p.Gly272Ser)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Jun 9, 2024