SRSF7 serine and arginine rich splicing factor 7

Information
Symbol
SRSF7
Type
protein-coding
Description
serine and arginine rich splicing factor 7
Entrez Gene ID
6432
Genome
hg19
Position
chr2:38,970,741-38,978,503
Genome
hg38
Position
chr2:38,743,599-38,751,361
MIM
600572 OMIM
HGNC
HGNC:10789 HGNC
Ensembl
ENSG00000115875 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
not provided 0 2
Uncertain significance 0 8
Ranking
ClinVar
0
0
0
6
2
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
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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 9G8
SYNONYM AAG3
SYNONYM SFRS7
MIM 600572 OMIM
HGNC HGNC:10789 HGNC
Ensembl ENSG00000115875 Ensembl
AllianceGenome HGNC:10789
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000409276.5 hg38 chr2 38,744,893 38,751,358 6,466
ENST00000446327.6 hg38 chr2 38,743,599 38,751,494 7,896
ENST00000313117.11 hg38 chr2 38,743,599 38,751,361 7,763
ENST00000313117.11 hg19 chr2 38,970,741 38,978,503 7,763
ENST00000446327.6 hg19 chr2 38,970,741 38,978,636 7,896
ENST00000409276.5 hg19 chr2 38,972,035 38,978,500 6,466
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