NM_000168.6(GLI3):c.506C>T (p.Pro169Leu) AND multiple conditions
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Apr 11, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001034454.8
Allele description [Variation Report for NM_000168.6(GLI3):c.506C>T (p.Pro169Leu)]
NM_000168.6(GLI3):c.506C>T (p.Pro169Leu)
Condition(s)
-
Homo sapiens cDNA clone IMAGE:9051927
Homo sapiens cDNA clone IMAGE:9051927gi|219517831|gb|BC143419.1|Nucleotide
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Sep 29, 2024