SPRYD7 SPRY domain containing 7

Information
Symbol
SPRYD7
Type
protein-coding
Description
SPRY domain containing 7
Entrez Gene ID
57213
Genome
hg19
Position
chr13:50,486,838-50,510,476
Genome
hg38
Position
chr13:49,912,702-49,936,340
MIM
607866 OMIM
HGNC
HGNC:14297 HGNC
Ensembl
ENSG00000123178 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 14
Ranking
ClinVar
0
0
0
14
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
[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 C13orf1
SYNONYM CLLD6
MIM 607866 OMIM
HGNC HGNC:14297 HGNC
Ensembl ENSG00000123178 Ensembl
AllianceGenome HGNC:14297
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000361840.8 hg38 chr13 49,912,702 49,936,340 23,639
ENST00000378195.6 hg38 chr13 49,912,706 49,936,490 23,785
ENST00000361840.8 hg19 chr13 50,486,838 50,510,476 23,639
ENST00000378195.6 hg19 chr13 50,486,842 50,510,626 23,785
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