SF3B6 splicing factor 3b subunit 6

Information
Symbol
SF3B6
Type
protein-coding
Description
splicing factor 3b subunit 6
Entrez Gene ID
51639
Genome
hg19
Position
chr2:24,290,456-24,299,196
Genome
hg38
Position
chr2:24,067,586-24,076,326
MIM
607835 OMIM
HGNC
HGNC:30096 HGNC
Ensembl
ENSG00000115128 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 4
Likely benign 0 2
not provided 2 0
Uncertain significance 0 2
Ranking
ClinVar
0
0
2
4
0
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Variant name Gene AA change CDS Japanese
frequency		 TogoVar MGeND Genome ClinVar CIViC evidence DisGeNET entry COSMIC
occurrence		 Prediction
Entry Origin Type Annotation Entry Origin Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Gene symbol Chromosome Genomic start Genomic stop Strand Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
TypeID
SYNONYM CGI-110
SYNONYM HSPC175
SYNONYM Ht006
SYNONYM P14
SYNONYM SAP14
SYNONYM SAP14a
SYNONYM SF3B14
SYNONYM SF3B14a
MIM 607835 OMIM
HGNC HGNC:30096 HGNC
Ensembl ENSG00000115128 Ensembl
AllianceGenome HGNC:30096
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000233468.5 hg38 chr2 24,067,586 24,076,326 8,741
ENST00000233468.5 hg19 chr2 24,290,456 24,299,196 8,741
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