NM_001369769.2(KIFC2):c.81G>C (p.Glu27Asp) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- May 25, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004244201.1
Allele description [Variation Report for NM_001369769.2(KIFC2):c.81G>C (p.Glu27Asp)]
NM_001369769.2(KIFC2):c.81G>C (p.Glu27Asp)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Aug 18, 2024