SOX10 LOSS Detail (hg19) (SOX10)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr22:38,368,307-38,380,544 |
hg38 | chr22:37,972,300-37,984,537 View the variant detail on this assembly version. |
Summary
MGeND
Clinical significance | |
Variant entry | |
GWAS entry | |
Disease area statistics | Show details |
ClinVar
Clinical Significance | |
Review star | [No Data.] |
Show details |
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
DisGeNET
[No Data.]
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
FACS-assisted shRNA genetic screen identified SOX10 as a determinant of vemurafenib resistance. Supp... | CIViC Evidence | Detail |
Overlapped Transcript Coordinates
Gene | Transcript ID | Exon Number | Chromosome | Start | Stop | Type | Amino Mutation | Transcript Position | Links |
---|
Overlapped Transcript
Gene | Transcript ID | Chromosome | Start | Stop | Links |
---|
- Gene
- SOX10
- Genome
- hg19
- Position
- chr22:38,368,307-38,380,544
- Variant Type
- cnv
- Variant (CIViC) (CIViC Variant)
- LOSS
- Transcript 1 (CIViC Variant)
- ENST00000396884.2
- Variant URL (CIViC Variant)
- https://civic.genome.wustl.edu/links/variants/672
Genome browser