NM_002972.4(SBF1):c.4612G>A (p.Gly1538Ser) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Mar 28, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004032938.1
Allele description [Variation Report for NM_002972.4(SBF1):c.4612G>A (p.Gly1538Ser)]
NM_002972.4(SBF1):c.4612G>A (p.Gly1538Ser)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Oct 26, 2024