NM_152699.5(SENP5):c.437A>G (p.Asn146Ser) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Oct 4, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004159494.1
Allele description [Variation Report for NM_152699.5(SENP5):c.437A>G (p.Asn146Ser)]
NM_152699.5(SENP5):c.437A>G (p.Asn146Ser)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Jun 2, 2024