ATF2 activating transcription factor 2
Information
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 4 |
| Likely benign | 0 | 2 |
| Uncertain significance | 0 | 36 |
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
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0 |
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42 |
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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
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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| 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 |
|---|---|
| SYNONYM | CRE-BP1 |
| SYNONYM | CREB-2 |
| SYNONYM | CREB2 |
| SYNONYM | HB16 |
| SYNONYM | TREB7 |
| MIM | 123811 OMIM |
| HGNC | HGNC:784 HGNC |
| Ensembl | ENSG00000115966 Ensembl |
| AllianceGenome | HGNC:784 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000426833.7 | hg38 | chr2 | 175,072,254 | 175,168,206 | 95,953 |
| ENST00000264110.7 | hg38 | chr2 | 175,072,259 | 175,168,203 | 95,945 |
| ENST00000392544.5 | hg38 | chr2 | 175,074,505 | 175,168,169 | 93,665 |
| ENST00000409499.5 | hg38 | chr2 | 175,074,505 | 175,168,169 | 93,665 |
| ENST00000345739.9 | hg38 | chr2 | 175,072,250 | 175,168,206 | 95,957 |
| ENST00000409635.5 | hg38 | chr2 | 175,074,280 | 175,168,203 | 93,924 |
| ENST00000409833.5 | hg38 | chr2 | 175,114,243 | 175,168,169 | 53,927 |
| ENST00000409437.5 | hg38 | chr2 | 175,072,265 | 175,151,082 | 78,818 |
| ENST00000345739.9 | hg19 | chr2 | 175,936,978 | 176,032,934 | 95,957 |
| ENST00000426833.7 | hg19 | chr2 | 175,936,982 | 176,032,934 | 95,953 |
| ENST00000264110.7 | hg19 | chr2 | 175,936,987 | 176,032,931 | 95,945 |
| ENST00000409499.5 | hg19 | chr2 | 175,939,233 | 176,032,897 | 93,665 |
| ENST00000409833.5 | hg19 | chr2 | 175,978,971 | 176,032,897 | 53,927 |
| ENST00000392544.5 | hg19 | chr2 | 175,939,233 | 176,032,897 | 93,665 |
| ENST00000409437.5 | hg19 | chr2 | 175,936,993 | 176,015,810 | 78,818 |
| ENST00000409635.5 | hg19 | chr2 | 175,939,008 | 176,032,931 | 93,924 |
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