SOCS2 suppressor of cytokine signaling 2
Information
Clinical Significance
MGeND | ClinVar | |
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Uncertain significance | 0 | 26 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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26 |
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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
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Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
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MGeND data only
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Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Type | ID |
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SYNONYM | CIS2 |
SYNONYM | Cish2 |
SYNONYM | SOCS-2 |
SYNONYM | SSI-2 |
SYNONYM | SSI2 |
SYNONYM | STATI2 |
MIM | 605117 OMIM |
HGNC | HGNC:19382 HGNC |
Ensembl | ENSG00000120833 Ensembl |
AllianceGenome | HGNC:19382 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000548537.1 | hg38 | chr12 | 93,571,704 | 93,576,206 | 4,503 |
ENST00000622746.4 | hg38 | chr12 | 93,571,681 | 93,576,744 | 5,064 |
ENST00000549122.5 | hg38 | chr12 | 93,571,361 | 93,576,206 | 4,846 |
ENST00000340600.6 | hg38 | chr12 | 93,569,814 | 93,576,745 | 6,932 |
ENST00000551556.2 | hg38 | chr12 | 93,572,675 | 93,576,745 | 4,071 |
ENST00000536696.6 | hg38 | chr12 | 93,570,980 | 93,575,197 | 4,218 |
ENST00000549206.5 | hg38 | chr12 | 93,570,399 | 93,576,174 | 5,776 |
ENST00000340600.6 | hg19 | chr12 | 93,963,590 | 93,970,521 | 6,932 |
ENST00000549206.5 | hg19 | chr12 | 93,964,175 | 93,969,950 | 5,776 |
ENST00000536696.6 | hg19 | chr12 | 93,964,756 | 93,968,973 | 4,218 |
ENST00000549122.5 | hg19 | chr12 | 93,965,137 | 93,969,982 | 4,846 |
ENST00000622746.4 | hg19 | chr12 | 93,965,457 | 93,970,520 | 5,064 |
ENST00000548537.1 | hg19 | chr12 | 93,965,480 | 93,969,982 | 4,503 |
ENST00000551556.2 | hg19 | chr12 | 93,966,451 | 93,970,521 | 4,071 |
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