SNRNP35 small nuclear ribonucleoprotein U11/U12 subunit 35

Information
Symbol
SNRNP35
Type
protein-coding
Description
small nuclear ribonucleoprotein U11/U12 subunit 35
Entrez Gene ID
11066
Genome
hg19
Position
chr12:123,944,070-123,950,846
Genome
hg38
Position
chr12:123,459,523-123,466,299
MIM
619631 OMIM
HGNC
HGNC:30852 HGNC
Ensembl
ENSG00000184209 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Uncertain significance 0 34
Ranking
ClinVar
0
0
0
36
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 HM-1
SYNONYM HM1
SYNONYM U1SNRNPBP
MIM 619631 OMIM
HGNC HGNC:30852 HGNC
Ensembl ENSG00000184209 Ensembl
AllianceGenome HGNC:30852
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000526639.3 hg38 chr12 123,458,139 123,466,936 8,798
ENST00000412157.2 hg38 chr12 123,459,523 123,466,299 6,777
ENST00000350887.5 hg38 chr12 123,464,506 123,466,390 1,885
ENST00000526639.3 hg19 chr12 123,942,686 123,951,483 8,798
ENST00000412157.2 hg19 chr12 123,944,070 123,950,846 6,777
ENST00000350887.5 hg19 chr12 123,949,053 123,950,937 1,885
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