NM_006846.4(SPINK5):c.1188T>C (p.His396=) AND not specified
- Germline classification:
- Benign (3 submissions)
- Last evaluated:
- Jan 24, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000243483.9
Allele description [Variation Report for NM_006846.4(SPINK5):c.1188T>C (p.His396=)]
NM_006846.4(SPINK5):c.1188T>C (p.His396=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Mar 10, 2024