NM_000168.6(GLI3):c.1525G>A (p.Glu509Lys) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 16, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001771209.3
Allele description [Variation Report for NM_000168.6(GLI3):c.1525G>A (p.Glu509Lys)]
NM_000168.6(GLI3):c.1525G>A (p.Glu509Lys)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
PREDICTED: Homo sapiens SURP and G-patch domain containing 2 (SUGP2), transcript...
PREDICTED: Homo sapiens SURP and G-patch domain containing 2 (SUGP2), transcript variant X24, misc_RNAgi|2462562258|ref|XR_008485058.1|Nucleotide
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: May 1, 2024