NM_017837.4(PIGV):c.348G>A (p.Leu116=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Mar 29, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000455608.5
Allele description [Variation Report for NM_017837.4(PIGV):c.348G>A (p.Leu116=)]
NM_017837.4(PIGV):c.348G>A (p.Leu116=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Sep 1, 2024