OSM oncostatin M
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 12 |
Uncertain significance | 0 | 54 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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66 |
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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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Target data | : |
MGeND data only
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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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MGeND data only
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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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Target data | : |
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 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000403389.1 | hg38 | chr22 | 30,263,868 | 30,265,818 | 1,951 |
ENST00000403463.1 | hg38 | chr22 | 30,264,075 | 30,266,839 | 2,765 |
ENST00000215781.3 | hg38 | chr22 | 30,262,829 | 30,266,851 | 4,023 |
ENST00000215781.3 | hg19 | chr22 | 30,658,818 | 30,662,840 | 4,023 |
ENST00000403389.1 | hg19 | chr22 | 30,659,857 | 30,661,807 | 1,951 |
ENST00000403463.1 | hg19 | chr22 | 30,660,064 | 30,662,828 | 2,765 |
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