SOCS2-AS1 SOCS2 antisense RNA 1
Clinical Significance
| MGeND | ClinVar |
|---|
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
0 |
 |
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
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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
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| 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
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| Category | : |
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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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Type | ID |
|---|---|
| MIM | 617269 OMIM |
| HGNC | HGNC:27054 HGNC |
| Ensembl | ENSG00000246985 Ensembl |
| AllianceGenome | HGNC:27054 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000499137.6 | hg38 | chr12 | 93,542,463 | 93,571,768 | 29,306 |
| ENST00000500986.6 | hg38 | chr12 | 93,542,022 | 93,571,768 | 29,747 |
| ENST00000662875.1 | hg38 | chr12 | 93,542,820 | 93,570,854 | 28,035 |
| ENST00000668485.1 | hg38 | chr12 | 93,542,463 | 93,570,961 | 28,499 |
| ENST00000551626.1 | hg38 | chr12 | 93,565,584 | 93,571,398 | 5,815 |
| ENST00000500986.6 | hg19 | chr12 | 93,935,798 | 93,965,544 | 29,747 |
| ENST00000668485.1 | hg19 | chr12 | 93,936,239 | 93,964,737 | 28,499 |
| ENST00000499137.6 | hg19 | chr12 | 93,936,239 | 93,965,544 | 29,306 |
| ENST00000662875.1 | hg19 | chr12 | 93,936,596 | 93,964,630 | 28,035 |
| ENST00000551626.1 | hg19 | chr12 | 93,959,360 | 93,965,174 | 5,815 |
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