SOX10 LOSS Detail (hg38) (SOX10)

Information

Genome

Assembly Position
hg19 chr22:38,368,307-38,380,544 View the variant detail on this assembly version.
hg38 chr22:37,972,300-37,984,537
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

ClinVar

Clinical Significance
Review star [No Data.]
Show details
Links
Type Database ID Link
Gene MIM 602229 OMIM
HGNC 11190 HGNC
Ensembl ENSG00000100146 Ensembl
NCBI NCBI
Gene Cards Gene Cards
OncoKB OncoKB
Type Database ID Link
Variant TogoVar
COSMIC
MONDO
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
Disease Drug EL ET ED CS VO TR Pubmed Links
melanoma Vemurafenib D Predictive Supports Resistance N/A 4 24670642 Detail
DisGeNET
[No Data.]
Annotation

Annotations

DescrptionSourceLinks
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
hg38
Position
chr22:37,972,300-37,984,537
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
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