SUGP2 SURP and G-patch domain containing 2

Information
Symbol
SUGP2
Type
protein-coding
Description
SURP and G-patch domain containing 2
Entrez Gene ID
10147
Genome
hg19
Position
chr19:19,103,734-19,144,348
Genome
hg38
Position
chr19:18,992,925-19,033,539
MIM
607993 OMIM
HGNC
HGNC:18641 HGNC
Ensembl
ENSG00000064607 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 6
Uncertain significance 0 106
Ranking
ClinVar
0
0
0
112
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 :
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 SFRS14
SYNONYM SRFS14
MIM 607993 OMIM
HGNC HGNC:18641 HGNC
Ensembl ENSG00000064607 Ensembl
AllianceGenome HGNC:18641
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000601879.5 hg38 chr19 18,992,367 19,034,023 41,657
ENST00000600377.1 hg38 chr19 18,992,925 19,033,539 40,615
ENST00000452918.7 hg38 chr19 18,990,893 19,033,517 42,625
ENST00000337018.10 hg38 chr19 18,990,893 19,033,559 42,667
ENST00000452918.7 hg19 chr19 19,101,702 19,144,326 42,625
ENST00000337018.10 hg19 chr19 19,101,702 19,144,368 42,667
ENST00000601879.5 hg19 chr19 19,103,176 19,144,832 41,657
ENST00000600377.1 hg19 chr19 19,103,734 19,144,348 40,615
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