GTF2I-AS1 GTF2I antisense RNA 1
Information
- Symbol
- GTF2I-AS1
- Type
- ncRNA
- Description
- GTF2I antisense RNA 1
- Entrez Gene ID
- 101926943
- Genome
- hg19
- Position
- chr7:74,113,790-74,143,187
- Genome
- hg38
- Position
- chr7:74,699,460-74,728,849
- HGNC
- HGNC:55572 HGNC
- Ensembl
- ENSG00000232729 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| not provided | 3 | 0 |
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
Locus Zoom
Variants
Search Word
| Target data | : |
MGeND data only
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| 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
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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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| 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 | |||||||||||||||
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000669011.1 | hg38 | chr7 | 74,688,864 | 74,727,886 | 39,023 |
| ENST00000434256.5 | hg38 | chr7 | 74,699,460 | 74,728,849 | 29,390 |
| ENST00000595409.1 | hg38 | chr7 | 74,726,950 | 74,727,883 | 934 |
| ENST00000669011.1 | hg19 | chr7 | 74,103,198 | 74,142,224 | 39,027 |
| ENST00000434256.5 | hg19 | chr7 | 74,113,790 | 74,143,187 | 29,398 |
| ENST00000595409.1 | hg19 | chr7 | 74,141,288 | 74,142,221 | 934 |
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