| Entrez Gene ID | 153020 |
|---|---|
| Official Gene Symbol | RASGEF1B (GeneCards) |
| Full name | RasGEF domain family member 1B |
| Location | 4q21.21 |
| Other ids | Vega : OTTHUMG00000160890 MIM : 614532 HGNC : HGNC:24881 Ensembl : ENSG00000138670 |
| Other names | GPIG4 |
| Summary | None |
Found 15 variants in this database.
| Variant ID | Entrez Gene ID | Gene | Chromsome | Start | End | Disease | Method |
|---|---|---|---|---|---|---|---|
| 6084 | 153020 | RASGEF1B | 4 | 82946457 | 82946457 | Asymptomatic | HiSeq 2000 |
| 6239 | 153020 | RASGEF1B | 4 | 83032216 | 83032216 | Asymptomatic | HiSeq 2000 HiSeq X Ten |
| 6318 | 153020 | RASGEF1B | 4 | 82449558 | 82449558 | Asymptomatic | HiSeq 2000 HiSeq X Ten |
| 6627 | 153020 | RASGEF1B | 4 | 82923841 | 82923841 | Asymptomatic | HiSeq 2000 HiSeq X Ten |
| 7010 | 153020 | RASGEF1B | 4 | 83049398 | 83049398 | Asymptomatic | HiSeq 2000 HiSeq X Ten |
| 7039 | 153020 | RASGEF1B | 4 | 82956092 | 82956092 | Asymptomatic | HiSeq 2000 HiSeq X Ten |
| 7133 | 153020 | RASGEF1B | 4 | 82610730 | 82610730 | Cockayne syndrome | HiSeq 2000 HiSeq X Ten |
| 7170 | 153020 | RASGEF1B | 4 | 82907751 | 82907751 | Cockayne syndrome | HiSeq 2000 HiSeq X Ten |
| 7205 | 153020 | RASGEF1B | 4 | 83041872 | 83041872 | Cockayne syndrome | HiSeq 2000 HiSeq X Ten |
| 7221 | 153020 | RASGEF1B | 4 | 82864165 | 82864165 | Cockayne syndrome | HiSeq 2000 HiSeq X Ten |
| 7300 | 153020 | RASGEF1B | 4 | 82864758 | 82864758 | Cockayne syndrome | HiSeq 2000 HiSeq X Ten |
| 7359 | 153020 | RASGEF1B | 4 | 82717712 | 82717712 | Xeroderma Pigmentosum | HiSeq 2000 HiSeq X Ten |
| 7375 | 153020 | RASGEF1B | 4 | 82936940 | 82936940 | Xeroderma Pigmentosum | HiSeq 2000 HiSeq X Ten |
| 25667 | 153020 | RASGEF1B | 4 | 83016131 | 83016131 | Asymptomatic | HiSeq 2000 HiSeq X Ten Single cell Sequencing Cell cloning |
| 25712 | 153020 | RASGEF1B | 4 | 82938209 | 82938209 | Asymptomatic | HiSeq 2000 HiSeq X Ten Single cell Sequencing Cell cloning |