chr12:7649400:> Detail (hg38)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chr12:7,801,996-7,818,504 |
| hg38 | chr12:7,649,400-7,665,908 |
HGVS
| Type | Transcript | Protein |
|---|---|---|
Summary
MGeND
| Clinical significance | |
| Variant entry | |
| GWAS entry | |
| Disease area statistics | Show details |
Frequency
[No Data.]
Prediction
[No Data.]
ClinVar
| Clinical Significance | |
| Review star | [No Data.] |
| Show details | |
Links
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
[No Data.]
DisGeNET
| Score | Disease name | Description | Source | Pubmed | Links |
|---|---|---|---|---|---|
| <0.001 | cerebral infarction | NA | BeFree | Detail | |
| 0.003 | cholelithiasis | NA | BeFree,GAD | Detail | |
| 0.080 | Colonic Neoplasms | NA | RGD | Detail | |
| <0.001 | colorectal carcinoma | NA | BeFree | Detail | |
| <0.001 | Gastrointestinal Neoplasms | NA | BeFree | Detail | |
| 0.002 | hepatitis C | NA | GAD | Detail | |
| <0.001 | HIV Infections | NA | BeFree | Detail | |
| <0.001 | Hypercholesterolemia | NA | BeFree | Detail | |
| 0.080 | Hyperlipidemia | NA | RGD | Detail | |
| <0.001 | Intestinal Neoplasms | NA | BeFree | Detail | |
| <0.001 | leukemia | NA | BeFree | Detail | |
| <0.001 | Liver neoplasms | NA | BeFree | Detail | |
| 0.003 | neurofibromatosis 1 | NA | BeFree,LHGDN | Detail | |
| 0.080 | obesity | This suggests that the APOBEC1 gene might be a novel target for obesity treatmen... | BeFree,RGD | 25216115 | Detail |
| <0.001 | Adenocarcinoma Of Esophagus | The RNA editing enzyme APOBEC1 induces somatic mutations and a compatible mutati... | BeFree | 25085003 | Detail |
| 0.001 | Carcinogenesis | APOBEC1 could be involved in cancer promotion at the very early stages of carcin... | BeFree | 25085003 | Detail |
| <0.001 | breast carcinoma | NA | BeFree | Detail | |
| <0.001 | colon carcinoma | NA | BeFree | Detail | |
| <0.001 | stomach carcinoma | NA | BeFree | Detail | |
| <0.001 | Middle Cerebral Artery Occlusion | NA | BeFree | Detail | |
| <0.001 | Cerebral Ischemia | NA | BeFree | Detail | |
| 0.003 | cholecystolithiasis | NA | BeFree,GAD | Detail | |
| <0.001 | Adenoma of small intestine | NA | BeFree | Detail | |
| <0.001 | colorectal cancer | NA | BeFree | Detail | |
| 0.001 | liver carcinoma | NA | BeFree | Detail | |
| <0.001 | adenoma | NA | BeFree | Detail | |
| <0.001 | arteriosclerosis | NA | BeFree | Detail | |
| <0.001 | atherosclerosis | NA | BeFree | Detail | |
| <0.001 | Barrett esophagus | APOBEC1 could be involved in cancer promotion at the very early stages of carcin... | BeFree | 25085003 | Detail |
| <0.001 | Malignant neoplasm of breast | NA | BeFree | Detail | |
| <0.001 | Malignant tumor of colon | NA | BeFree | Detail |
Annotation
Annotations
| Descrption | Source | Links |
|---|---|---|
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| This suggests that the APOBEC1 gene might be a novel target for obesity treatment. | DisGeNET | Detail |
| The RNA editing enzyme APOBEC1 induces somatic mutations and a compatible mutational signature is pr... | DisGeNET | Detail |
| APOBEC1 could be involved in cancer promotion at the very early stages of carcinogenesis, as it is h... | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| APOBEC1 could be involved in cancer promotion at the very early stages of carcinogenesis, as it is h... | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
Overlapped Transcript Coordinates
| Gene | Transcript ID | Exon Number | Chromosome | Start | Stop | Type | Amino Mutation | Transcript Position | Links |
|---|
Overlapped Transcript
| Gene | Transcript ID | Chromosome | Start | Stop | Links |
|---|
- Gene
- -
- Genome
- hg38
- Position
- chr12:7,649,400-7,665,908
- Variant Type
- snv
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