NM_178828.5(SPATA31E1):c.31G>A (p.Gly11Ser) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Nov 22, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004074847.1
Allele description [Variation Report for NM_178828.5(SPATA31E1):c.31G>A (p.Gly11Ser)]
NM_178828.5(SPATA31E1):c.31G>A (p.Gly11Ser)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Oct 13, 2024