NM_017837.4(PIGV):c.111T>C (p.His37=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Nov 3, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000433638.1
Allele description [Variation Report for NM_017837.4(PIGV):c.111T>C (p.His37=)]
NM_017837.4(PIGV):c.111T>C (p.His37=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Apr 23, 2022