Search by Gene
| Item | Value |
|---|---|
| geneid | 25 |
| ensemblid | ENSG00000097007.20 |
| hgncid | 76 |
| symbol | ABL1 |
| name | ABL proto-oncogene 1, non-receptor tyrosine kinase |
| refseq_nuc | NM_005157.6 |
| refseq_prot | NP_005148.2 |
| ensembl_nuc | ENST00000318560.6 |
| ensembl_prot | ENSP00000323315.5 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 130835254 |
| end | 130887675 |
| strand | + |
| ver | v1.2 |
| region | chr9:130835254-130887675 |
| region5000 | chr9:130830254-130892675 |
| regionname0 | ABL1_chr9_130835254_130887675 |
| regionname5000 | ABL1_chr9_130830254_130892675 |
Multiple Alignments (by translate haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
Multiple Alignments (by aa haplotype frequency)
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1130 | 265 | 85 | 61 | 81 | 8 | 28 | ABL1_chr9_130830254_130892675 | ABL1 | MLEIC others(1125): Show |
chr9 | 130830254 | 130892675 |
| a0002 | 0/0 | 1130 | 6 | 3 | 3 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | MLEIC others(1125): Show |
chr9 | 130830254 | 130892675 |
| a0003 | 0/0 | 1130 | 2 | 0 | 2 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | MLEIC others(1125): Show |
chr9 | 130830254 | 130892675 |
| a0004 | 0/0 | 1130 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | MLEIC others(1125): Show |
chr9 | 130830254 | 130892675 |
| a0005 | 0/0 | 1130 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | MLEIC others(1125): Show |
chr9 | 130830254 | 130892675 |
| a0006 | 0/0 | 1130 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | MLEIC others(1125): Show |
chr9 | 130830254 | 130892675 |
| a0007 | 0/0 | 1130 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | MLEIC others(1125): Show |
chr9 | 130830254 | 130892675 |
| a0008 | 0/0 | 1130 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | MLEIC others(1125): Show |
chr9 | 130830254 | 130892675 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 3390 | 133 | 31 | 38 | 48 | 5 | 11 | ABL1_chr9_130830254_130892675 | ABL1 | ATGTT others(3385): Show |
chr9 | 130830254 | 130892675 | ||
| a0001c0002 | 1/1 | 3390 | 65 | 8 | 11 | 29 | 2 | 13 | ABL1_chr9_130830254_130892675 | ABL1 | ATGTT others(3385): Show |
chr9 | 130830254 | 130892675 | ||
| a0001c0003 | 0/0 | 3390 | 28 | 21 | 5 | 0 | 1 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | ATGTT others(3385): Show |
chr9 | 130830254 | 130892675 | ||
| a0001c0004 | 0/0 | 3390 | 8 | 6 | 1 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | ATGTT others(3385): Show |
chr9 | 130830254 | 130892675 | ||
| a0001c0006 | 0/0 | 3390 | 5 | 5 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | ATGTT others(3385): Show |
chr9 | 130830254 | 130892675 | ||
| a0001c0007 | 0/0 | 3390 | 5 | 0 | 5 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | ATGTT others(3385): Show |
chr9 | 130830254 | 130892675 | ||
| a0001c0008 | 0/0 | 3390 | 3 | 3 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | ATGTT others(3385): Show |
chr9 | 130830254 | 130892675 | ||
| a0001c0009 | 0/0 | 3390 | 3 | 3 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | ATGTT others(3385): Show |
chr9 | 130830254 | 130892675 | ||
| a0001c0010 | 0/0 | 3390 | 3 | 0 | 1 | 2 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | ATGTT others(3385): Show |
chr9 | 130830254 | 130892675 | ||
| a0001c0011 | 0/0 | 3390 | 3 | 2 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | ATGTT others(3385): Show |
chr9 | 130830254 | 130892675 | ||
| a0001c0013 | 0/0 | 3390 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | ATGTT others(3385): Show |
chr9 | 130830254 | 130892675 | ||
| a0001c0018 | 0/0 | 3390 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | ATGTT others(3385): Show |
chr9 | 130830254 | 130892675 | ||
| a0001c0019 | 0/0 | 3390 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | ATGTT others(3385): Show |
chr9 | 130830254 | 130892675 | ||
| a0001c0020 | 0/0 | 3390 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | ATGTT others(3385): Show |
chr9 | 130830254 | 130892675 | ||
| a0001c0021 | 0/0 | 3390 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | ATGTT others(3385): Show |
chr9 | 130830254 | 130892675 | ||
| a0001c0023 | 0/0 | 3390 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | ATGTT others(3385): Show |
chr9 | 130830254 | 130892675 | ||
| a0001c0024 | 0/0 | 3390 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | ATGTT others(3385): Show |
chr9 | 130830254 | 130892675 | ||
| a0001c0025 | 0/0 | 3390 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | ATGTT others(3385): Show |
chr9 | 130830254 | 130892675 | ||
| a0001c0026 | 0/0 | 3390 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | ATGTT others(3385): Show |
chr9 | 130830254 | 130892675 | ||
| a0002c0005 | 0/0 | 3390 | 6 | 3 | 3 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | ATGTT others(3385): Show |
chr9 | 130830254 | 130892675 | ||
| a0003c0012 | 0/0 | 3390 | 2 | 0 | 2 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | ATGTT others(3385): Show |
chr9 | 130830254 | 130892675 | ||
| a0004c0017 | 0/0 | 3390 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | ATGTT others(3385): Show |
chr9 | 130830254 | 130892675 | ||
| a0005c0022 | 0/0 | 3390 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | ATGTT others(3385): Show |
chr9 | 130830254 | 130892675 | ||
| a0006c0015 | 0/0 | 3390 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | ATGTT others(3385): Show |
chr9 | 130830254 | 130892675 | ||
| a0007c0014 | 0/0 | 3390 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | ATGTT others(3385): Show |
chr9 | 130830254 | 130892675 | ||
| a0008c0016 | 0/0 | 3390 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | ATGTT others(3385): Show |
chr9 | 130830254 | 130892675 |
| acthapid | grch38/chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5578 | 77 | 8 | 24 | 35 | 3 | 7 | ABL1_chr9_130830254_130892675 | ABL1 | GTTAA others(5573): Show |
chr9 | 130830254 | 130892675 |
| a0001c0001t0002 | 0/0 | 5578 | 27 | 0 | 11 | 12 | 2 | 2 | ABL1_chr9_130830254_130892675 | ABL1 | GTTAA others(5573): Show |
chr9 | 130830254 | 130892675 |
| a0001c0001t0004 | 0/0 | 5578 | 2 | 1 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | GTTAA others(5573): Show |
chr9 | 130830254 | 130892675 |
| a0001c0001t0006 | 0/0 | 5578 | 4 | 3 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | GTTAA others(5573): Show |
chr9 | 130830254 | 130892675 |
| a0001c0001t0007 | 0/0 | 5578 | 7 | 7 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | GTTAA others(5573): Show |
chr9 | 130830254 | 130892675 |
| a0001c0001t0008 | 0/0 | 5578 | 4 | 4 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | GTTAA others(5573): Show |
chr9 | 130830254 | 130892675 |
| a0001c0001t0010 | 0/0 | 5578 | 3 | 3 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | GTTAA others(5573): Show |
chr9 | 130830254 | 130892675 |
| a0001c0001t0011 | 0/0 | 5578 | 2 | 2 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | GTTAA others(5573): Show |
chr9 | 130830254 | 130892675 |
| a0001c0001t0012 | 0/0 | 5578 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | GTTAA others(5573): Show |
chr9 | 130830254 | 130892675 |
| a0001c0001t0015 | 0/0 | 5559 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | GTTAA others(5554): Show |
chr9 | 130830254 | 130892675 |
| a0001c0001t0021 | 0/0 | 5578 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | GTTAA others(5573): Show |
chr9 | 130830254 | 130892675 |
| a0001c0001t0024 | 0/0 | 5578 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | GTTAA others(5573): Show |
chr9 | 130830254 | 130892675 |
| a0001c0001t0025 | 0/0 | 5578 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | GTTAA others(5573): Show |
chr9 | 130830254 | 130892675 |
| a0001c0001t0026 | 0/0 | 5578 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | GTTAA others(5573): Show |
chr9 | 130830254 | 130892675 |
| a0001c0001t0033 | 0/0 | 5578 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | GTTAA others(5573): Show |
chr9 | 130830254 | 130892675 |
| a0001c0002t0001 | 1/0 | 5578 | 60 | 5 | 10 | 29 | 2 | 13 | ABL1_chr9_130830254_130892675 | ABL1 | GTTAA others(5573): Show |
chr9 | 130830254 | 130892675 |
| a0001c0002t0009 | 0/0 | 5578 | 2 | 2 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | GTTAA others(5573): Show |
chr9 | 130830254 | 130892675 |
| a0001c0002t0014 | 0/1 | 5581 | 1 | 0 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | GTTAA others(5576): Show |
chr9 | 130830254 | 130892675 |
| a0001c0002t0019 | 0/0 | 5578 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | GTTAA others(5573): Show |
chr9 | 130830254 | 130892675 |
| a0001c0002t0032 | 0/0 | 5578 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | GTTAA others(5573): Show |
chr9 | 130830254 | 130892675 |
| a0001c0003t0003 | 0/0 | 5578 | 19 | 18 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | GTTAA others(5573): Show |
chr9 | 130830254 | 130892675 |
| a0001c0003t0005 | 0/0 | 5578 | 7 | 1 | 4 | 0 | 1 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | GTTAA others(5573): Show |
chr9 | 130830254 | 130892675 |
| a0001c0003t0016 | 0/0 | 5559 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | GTTAA others(5554): Show |
chr9 | 130830254 | 130892675 |
| a0001c0003t0020 | 0/0 | 5578 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | GTTAA others(5573): Show |
chr9 | 130830254 | 130892675 |
| a0001c0004t0004 | 0/0 | 5578 | 6 | 4 | 1 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | GTTAA others(5573): Show |
chr9 | 130830254 | 130892675 |
| a0001c0004t0017 | 0/0 | 5578 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | GTTAA others(5573): Show |
chr9 | 130830254 | 130892675 |
| a0001c0004t0022 | 0/0 | 5578 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | GTTAA others(5573): Show |
chr9 | 130830254 | 130892675 |
| a0001c0006t0005 | 0/0 | 5578 | 5 | 5 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | GTTAA others(5573): Show |
chr9 | 130830254 | 130892675 |
| a0001c0007t0005 | 0/0 | 5578 | 4 | 0 | 4 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | GTTAA others(5573): Show |
chr9 | 130830254 | 130892675 |
| a0001c0007t0023 | 0/0 | 5578 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | GTTAA others(5573): Show |
chr9 | 130830254 | 130892675 |
| a0001c0008t0012 | 0/0 | 5578 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | GTTAA others(5573): Show |
chr9 | 130830254 | 130892675 |
| a0001c0008t0030 | 0/0 | 5578 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | GTTAA others(5573): Show |
chr9 | 130830254 | 130892675 |
| a0001c0008t0031 | 0/0 | 5578 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | GTTAA others(5573): Show |
chr9 | 130830254 | 130892675 |
| a0001c0009t0006 | 0/0 | 5578 | 3 | 3 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | GTTAA others(5573): Show |
chr9 | 130830254 | 130892675 |
| a0001c0010t0001 | 0/0 | 5578 | 3 | 0 | 1 | 2 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | GTTAA others(5573): Show |
chr9 | 130830254 | 130892675 |
| a0001c0011t0002 | 0/0 | 5578 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | GTTAA others(5573): Show |
chr9 | 130830254 | 130892675 |
| a0001c0011t0013 | 0/0 | 5578 | 2 | 2 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | GTTAA others(5573): Show |
chr9 | 130830254 | 130892675 |
| a0001c0013t0027 | 0/0 | 5578 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | GTTAA others(5573): Show |
chr9 | 130830254 | 130892675 |
| a0001c0018t0009 | 0/0 | 5578 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | GTTAA others(5573): Show |
chr9 | 130830254 | 130892675 |
| a0001c0019t0001 | 0/0 | 5578 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | GTTAA others(5573): Show |
chr9 | 130830254 | 130892675 |
| a0001c0020t0004 | 0/0 | 5578 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | GTTAA others(5573): Show |
chr9 | 130830254 | 130892675 |
| a0001c0021t0001 | 0/0 | 5578 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | GTTAA others(5573): Show |
chr9 | 130830254 | 130892675 |
| a0001c0023t0028 | 0/0 | 5578 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | GTTAA others(5573): Show |
chr9 | 130830254 | 130892675 |
| a0001c0024t0001 | 0/0 | 5578 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | GTTAA others(5573): Show |
chr9 | 130830254 | 130892675 |
| a0001c0025t0018 | 0/0 | 5578 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | GTTAA others(5573): Show |
chr9 | 130830254 | 130892675 |
| a0001c0026t0029 | 0/0 | 5562 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | GTTAA others(5557): Show |
chr9 | 130830254 | 130892675 |
| a0002c0005t0004 | 0/0 | 5578 | 6 | 3 | 3 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | GTTAA others(5573): Show |
chr9 | 130830254 | 130892675 |
| a0003c0012t0004 | 0/0 | 5578 | 2 | 0 | 2 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | GTTAA others(5573): Show |
chr9 | 130830254 | 130892675 |
| a0004c0017t0001 | 0/0 | 5578 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | GTTAA others(5573): Show |
chr9 | 130830254 | 130892675 |
| a0005c0022t0001 | 0/0 | 5578 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | GTTAA others(5573): Show |
chr9 | 130830254 | 130892675 |
| a0006c0015t0004 | 0/0 | 5578 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | GTTAA others(5573): Show |
chr9 | 130830254 | 130892675 |
| a0007c0014t0008 | 0/0 | 5578 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | GTTAA others(5573): Show |
chr9 | 130830254 | 130892675 |
| a0008c0016t0001 | 0/0 | 5578 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | GTTAA others(5573): Show |
chr9 | 130830254 | 130892675 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 5 | 0 | 4 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0001g0006 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0002g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0004g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0006g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0006g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0006g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0006g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0007g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0007g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0007g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0007g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0007g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0007g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0007g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0008g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0008g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0008g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0010g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0010g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0011g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0011g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0012g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0015g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0021g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0024g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0025g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0026g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0001t0033g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0002t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0002t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0002t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0002t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0002t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0002t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0002t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0002t0001g0251 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0002t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0002t0009g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0002t0009g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0002t0014g0121 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0002t0019g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0002t0032g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0003t0003g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0003t0003g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0003t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0003t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0003t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0003t0003g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0003t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0003t0003g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0003t0003g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0003t0003g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0003t0003g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0003t0003g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0003t0003g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0003t0003g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0003t0003g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0003t0003g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0003t0003g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0003t0003g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0003t0005g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0003t0005g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0003t0005g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0003t0005g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0003t0005g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0003t0005g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0003t0005g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0003t0016g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0003t0020g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0004t0004g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0004t0004g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0004t0004g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0004t0004g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0004t0004g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0004t0017g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0004t0022g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0006t0005g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0006t0005g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0006t0005g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0006t0005g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0006t0005g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0007t0005g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0007t0005g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0007t0005g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0007t0023g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0008t0012g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0008t0030g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0008t0031g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0009t0006g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0009t0006g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0009t0006g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0010t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0010t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0010t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0011t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0011t0013g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0011t0013g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0013t0027g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0018t0009g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0019t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0020t0004g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0021t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0023t0028g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0024t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0025t0018g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0001c0026t0029g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0002c0005t0004g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0002c0005t0004g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0002c0005t0004g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0002c0005t0004g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0002c0005t0004g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0003c0012t0004g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0003c0012t0004g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0004c0017t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0005c0022t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0006c0015t0004g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0007c0014t0008g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| a0008c0016t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0002 | t0001 | g0094 | EUR | FIN | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0102 | EUR | FIN | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0228 | EUR | FIN | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0156 | EUR | FIN | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0079 | EAS | CHS | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | CHS | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG00423 | hp1 | a0001 | c0002 | t0001 | g0172 | EAS | CHS | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | CHS | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG00438 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | CHS | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0064 | EAS | CHS | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | CHS | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0174 | EAS | CHS | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | CHS | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG00639 | hp1 | a0002 | c0005 | t0004 | g0189 | AMR | PUR | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0146 | AMR | PUR | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0060 | AMR | PUR | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG00673 | hp1 | a0001 | c0002 | t0001 | g0120 | EAS | CHS | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | CHS | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0116 | AMR | PUR | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0010 | AMR | PUR | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG01074 | hp2 | a0001 | c0007 | t0023 | g0002 | AMR | PUR | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG01081 | hp1 | a0001 | c0003 | t0005 | g0254 | AMR | PUR | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG01099 | hp1 | a0001 | c0007 | t0005 | g0243 | AMR | PUR | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG01106 | hp1 | a0001 | c0001 | t0024 | g0226 | AMR | PUR | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0142 | AMR | PUR | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG01109 | hp1 | a0001 | c0001 | t0004 | g0105 | AMR | PUR | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG01109 | hp2 | a0004 | c0017 | t0001 | g0110 | AMR | PUR | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG01167 | hp1 | a0001 | c0003 | t0003 | g0241 | AMR | PUR | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0139 | AMR | PUR | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG01175 | hp1 | a0001 | c0003 | t0005 | g0253 | AMR | PUR | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0010 | AMR | PUR | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0023 | AMR | PUR | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0111 | AMR | PUR | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG01243 | hp2 | a0001 | c0001 | t0006 | g0018 | AMR | PUR | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG01255 | hp1 | a0001 | c0007 | t0005 | g0002 | AMR | CLM | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0203 | AMR | CLM | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG01256 | hp2 | a0001 | c0002 | t0001 | g0188 | AMR | CLM | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG01257 | hp1 | a0001 | c0002 | t0032 | g0112 | AMR | CLM | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG01257 | hp2 | a0001 | c0007 | t0005 | g0002 | AMR | CLM | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0202 | AMR | CLM | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG01258 | hp2 | a0001 | c0007 | t0005 | g0200 | AMR | CLM | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | CLM | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG01361 | hp1 | a0001 | c0003 | t0005 | g0247 | AMR | CLM | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG01361 | hp2 | a0003 | c0012 | t0004 | g0003 | AMR | CLM | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0092 | AMR | CLM | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG01433 | hp2 | a0002 | c0005 | t0004 | g0214 | AMR | CLM | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG01496 | hp1 | a0001 | c0004 | t0004 | g0027 | AMR | CLM | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG01496 | hp2 | a0001 | c0003 | t0005 | g0246 | AMR | CLM | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0123 | EUR | IBS | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG01515 | hp2 | a0001 | c0003 | t0005 | g0252 | EUR | IBS | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG01884 | hp1 | a0001 | c0002 | t0019 | g0048 | AFR | ACB | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG01884 | hp2 | a0001 | c0004 | t0004 | g0009 | AFR | ACB | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0106 | AFR | ACB | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG01891 | hp2 | a0001 | c0003 | t0003 | g0173 | AFR | ACB | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PEL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0021 | AMR | PEL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG01943 | hp2 | a0003 | c0012 | t0004 | g0213 | AMR | PEL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0104 | AMR | PEL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PEL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0201 | AMR | PEL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | PEL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG01993 | hp1 | a0001 | c0010 | t0001 | g0163 | AMR | PEL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PEL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | KHV | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG02027 | hp2 | a0001 | c0002 | t0001 | g0128 | EAS | KHV | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG02055 | hp1 | a0001 | c0002 | t0009 | g0044 | AFR | ACB | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG02055 | hp2 | a0001 | c0003 | t0005 | g0217 | AFR | ACB | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0157 | EAS | KHV | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | KHV | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG02135 | hp1 | a0001 | c0021 | t0001 | g0050 | EAS | KHV | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG02145 | hp1 | a0001 | c0004 | t0022 | g0020 | AFR | ACB | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG02145 | hp2 | a0001 | c0001 | t0006 | g0255 | AFR | ACB | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0022 | AMR | PEL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG02258 | hp1 | a0001 | c0003 | t0003 | g0148 | AFR | ACB | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG02258 | hp2 | a0001 | c0001 | t0006 | g0256 | AFR | ACB | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0238 | AMR | PEL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG02280 | hp1 | a0001 | c0008 | t0030 | g0040 | AFR | ACB | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG02280 | hp2 | a0001 | c0003 | t0003 | g0219 | AFR | ACB | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PEL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0237 | AMR | PEL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG02451 | hp1 | a0001 | c0003 | t0003 | g0208 | AFR | ACB | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | KHV | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | GWD | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG02572 | hp2 | a0001 | c0001 | t0007 | g0056 | AFR | GWD | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG02615 | hp1 | a0002 | c0005 | t0004 | g0003 | AFR | GWD | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG02615 | hp2 | a0001 | c0002 | t0001 | g0195 | AFR | GWD | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG02630 | hp1 | a0001 | c0008 | t0012 | g0036 | AFR | GWD | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG02630 | hp2 | a0001 | c0006 | t0005 | g0154 | AFR | GWD | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG02647 | hp1 | a0001 | c0006 | t0005 | g0171 | AFR | GWD | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG02647 | hp2 | a0001 | c0003 | t0003 | g0204 | AFR | GWD | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG02698 | hp2 | a0001 | c0002 | t0001 | g0081 | SAS | PJL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG02717 | hp1 | a0001 | c0003 | t0016 | g0192 | AFR | GWD | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG02717 | hp2 | a0006 | c0015 | t0004 | g0199 | AFR | GWD | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG02723 | hp1 | a0001 | c0025 | t0018 | g0047 | AFR | GWD | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG02723 | hp2 | a0001 | c0006 | t0005 | g0153 | AFR | GWD | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0232 | SAS | PJL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG02738 | hp2 | a0001 | c0004 | t0004 | g0091 | SAS | PJL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG02809 | hp1 | a0001 | c0009 | t0006 | g0175 | AFR | GWD | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG02809 | hp2 | a0001 | c0001 | t0010 | g0043 | AFR | GWD | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG02818 | hp1 | a0001 | c0003 | t0003 | g0245 | AFR | GWD | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG02818 | hp2 | a0001 | c0004 | t0004 | g0107 | AFR | GWD | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG02895 | hp1 | a0001 | c0001 | t0011 | g0042 | AFR | GWD | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG02895 | hp2 | a0001 | c0002 | t0001 | g0258 | AFR | GWD | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG02897 | hp1 | a0001 | c0001 | t0011 | g0041 | AFR | GWD | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG02897 | hp2 | a0001 | c0003 | t0003 | g0147 | AFR | GWD | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG02922 | hp1 | a0001 | c0003 | t0003 | g0012 | AFR | ESN | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG02922 | hp2 | a0001 | c0003 | t0003 | g0216 | AFR | ESN | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG02965 | hp1 | a0001 | c0003 | t0003 | g0190 | AFR | ESN | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG02965 | hp2 | a0001 | c0001 | t0008 | g0016 | AFR | ESN | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG02970 | hp1 | a0001 | c0006 | t0005 | g0152 | AFR | ESN | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG02970 | hp2 | a0001 | c0003 | t0003 | g0240 | AFR | ESN | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0169 | SAS | PJL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0109 | SAS | PJL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG03041 | hp1 | a0001 | c0002 | t0009 | g0046 | AFR | GWD | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG03041 | hp2 | a0001 | c0001 | t0007 | g0207 | AFR | GWD | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG03098 | hp1 | a0001 | c0001 | t0015 | g0193 | AFR | MSL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG03098 | hp2 | a0001 | c0020 | t0004 | g0134 | AFR | MSL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG03130 | hp1 | a0001 | c0001 | t0004 | g0054 | AFR | ESN | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG03130 | hp2 | a0001 | c0003 | t0003 | g0248 | AFR | ESN | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG03139 | hp1 | a0001 | c0001 | t0007 | g0206 | AFR | ESN | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG03139 | hp2 | a0001 | c0003 | t0020 | g0218 | AFR | ESN | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG03195 | hp1 | a0001 | c0009 | t0006 | g0211 | AFR | ESN | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | ESN | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG03209 | hp1 | a0001 | c0011 | t0013 | g0039 | AFR | MSL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG03209 | hp2 | a0001 | c0001 | t0026 | g0024 | AFR | MSL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG03225 | hp1 | a0001 | c0001 | t0012 | g0149 | AFR | MSL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG03225 | hp2 | a0001 | c0026 | t0029 | g0250 | AFR | MSL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG03239 | hp1 | a0001 | c0024 | t0001 | g0090 | SAS | PJL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG03239 | hp2 | a0001 | c0003 | t0005 | g0244 | SAS | PJL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG03453 | hp1 | a0001 | c0018 | t0009 | g0045 | AFR | MSL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | MSL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG03486 | hp1 | a0001 | c0002 | t0001 | g0057 | AFR | MSL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG03486 | hp2 | a0001 | c0001 | t0010 | g0005 | AFR | MSL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0084 | SAS | PJL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG03492 | hp2 | a0001 | c0001 | t0033 | g0131 | SAS | PJL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG03516 | hp1 | a0001 | c0003 | t0003 | g0182 | AFR | ESN | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG03516 | hp2 | a0001 | c0001 | t0008 | g0017 | AFR | ESN | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG03540 | hp1 | a0001 | c0001 | t0007 | g0205 | AFR | GWD | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG03540 | hp2 | a0002 | c0005 | t0004 | g0242 | AFR | GWD | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG03579 | hp1 | a0001 | c0001 | t0010 | g0005 | AFR | MSL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG03579 | hp2 | a0007 | c0014 | t0008 | g0037 | AFR | MSL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG03654 | hp1 | a0001 | c0001 | t0025 | g0222 | SAS | PJL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG03654 | hp2 | a0001 | c0002 | t0001 | g0177 | SAS | PJL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0086 | SAS | PJL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0135 | SAS | PJL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0141 | SAS | BEB | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG03834 | hp2 | a0001 | c0019 | t0001 | g0129 | SAS | BEB | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | BEB | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0233 | SAS | BEB | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0230 | SAS | BEB | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0179 | SAS | BEB | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG04115 | hp1 | a0001 | c0002 | t0001 | g0137 | SAS | STU | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | STU | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | STU | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0065 | SAS | STU | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA18522 | hp1 | a0001 | c0004 | t0004 | g0108 | AFR | YRI | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA18522 | hp2 | a0001 | c0011 | t0013 | g0215 | AFR | YRI | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | YRI | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA18906 | hp2 | a0001 | c0001 | t0008 | g0004 | AFR | YRI | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA18941 | hp1 | a0001 | c0002 | t0001 | g0140 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA18942 | hp1 | a0001 | c0002 | t0001 | g0162 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA18945 | hp1 | a0001 | c0002 | t0001 | g0035 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA18954 | hp2 | a0001 | c0002 | t0001 | g0136 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA18963 | hp1 | a0001 | c0011 | t0002 | g0249 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0151 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA18977 | hp1 | a0001 | c0002 | t0001 | g0034 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA18978 | hp1 | a0001 | c0002 | t0001 | g0181 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA18990 | hp1 | a0001 | c0002 | t0001 | g0031 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA18990 | hp2 | a0001 | c0002 | t0001 | g0115 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA18995 | hp2 | a0001 | c0002 | t0001 | g0029 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA18998 | hp2 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA19000 | hp2 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA19001 | hp1 | a0001 | c0002 | t0001 | g0164 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA19001 | hp2 | a0001 | c0002 | t0001 | g0103 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA19011 | hp2 | a0001 | c0002 | t0001 | g0234 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA19012 | hp2 | a0001 | c0002 | t0001 | g0159 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA19030 | hp1 | a0001 | c0003 | t0003 | g0130 | AFR | LWK | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA19030 | hp2 | a0001 | c0001 | t0007 | g0210 | AFR | LWK | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA19043 | hp1 | a0001 | c0001 | t0008 | g0004 | AFR | LWK | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA19043 | hp2 | a0001 | c0003 | t0003 | g0160 | AFR | LWK | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA19065 | hp2 | a0001 | c0002 | t0001 | g0168 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA19066 | hp1 | a0001 | c0010 | t0001 | g0165 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA19066 | hp2 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA19072 | hp1 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA19078 | hp1 | a0001 | c0010 | t0001 | g0170 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA19078 | hp2 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA19085 | hp1 | a0001 | c0001 | t0021 | g0187 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA19088 | hp1 | a0008 | c0016 | t0001 | g0155 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA19091 | hp1 | a0001 | c0002 | t0001 | g0052 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | YRI | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA19240 | hp2 | a0001 | c0003 | t0003 | g0138 | AFR | YRI | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | ASW | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA20129 | hp2 | a0001 | c0003 | t0003 | g0012 | AFR | ASW | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0125 | EUR | TSI | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0113 | EUR | TSI | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0144 | SAS | GIH | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | GIH | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG01123 | hp1 | a0005 | c0022 | t0001 | g0011 | AMR | CLM | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG01123 | hp2 | a0002 | c0005 | t0004 | g0212 | AMR | CLM | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG02109 | hp1 | a0001 | c0006 | t0005 | g0055 | AFR | ACB | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG02109 | hp2 | a0001 | c0003 | t0003 | g0183 | AFR | ACB | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG02486 | hp1 | a0001 | c0009 | t0006 | g0145 | AFR | ACB | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG02486 | hp2 | a0001 | c0001 | t0007 | g0194 | AFR | ACB | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG02559 | hp1 | a0001 | c0001 | t0007 | g0176 | AFR | ACB | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG02559 | hp2 | a0001 | c0001 | t0006 | g0257 | AFR | ACB | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG03471 | hp1 | a0001 | c0004 | t0004 | g0009 | AFR | MSL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG03471 | hp2 | a0001 | c0004 | t0017 | g0049 | AFR | MSL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG06807 | hp1 | a0001 | c0008 | t0031 | g0038 | AFR | USA | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| HG06807 | hp2 | a0001 | c0023 | t0028 | g0059 | AFR | USA | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA20300 | hp1 | a0002 | c0005 | t0004 | g0003 | AFR | USA | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | USA | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA21309 | hp1 | a0001 | c0002 | t0001 | g0025 | AFR | LWK | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| NA21309 | hp2 | a0001 | c0013 | t0027 | g0150 | AFR | LWK | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0014 | g0121 | REF | REF | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0251 | REF | REF | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
| view | chr:pos | ref | alt | # # of ahapid:amio-acid(protein) level
|
ahapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:130854112 | G | A | 1 | a0003 | 2 | HG01361.hp2 HG01943.hp2 |
missense_variant | MODERATE | c.128G>A | p.Ser43Asn | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 2/11 | 321/5578 | 128/3393 | 43/1130 | chr9 | 130854112 | |||
| chr9:130878562 | G | A | 1 | a0007 | 1 | HG03579.hp2 | missense_variant | MODERATE | c.1418G>A | p.Arg473Gln | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 8/11 | 1611/5578 | 1418/3393 | 473/1130 | chr9 | 130878562 | |||
| chr9:130884323 | G | A | 1 | a0008 | 1 | NA19088.hp1 | missense_variant | MODERATE | c.2033G>A | p.Gly678Asp | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 2226/5578 | 2033/3393 | 678/1130 | chr9 | 130884323 | |||
| chr9:130884325 | T | G | 1 | a0004 | 1 | HG01109.hp2 | missense_variant | MODERATE | c.2035T>G | p.Ser679Ala | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 2228/5578 | 2035/3393 | 679/1130 | chr9 | 130884325 | |||
| chr9:130884388 | A | G | 1 | a0006 | 1 | HG02717.hp2 | missense_variant | MODERATE | c.2098A>G | p.Thr700Ala | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 2291/5578 | 2098/3393 | 700/1130 | chr9 | 130884388 | |||
| chr9:130884719 | C | T | 1 | a0005 | 1 | HG01123.hp1 | missense_variant | MODERATE | c.2429C>T | p.Pro810Leu | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 2622/5578 | 2429/3393 | 810/1130 | chr9 | 130884719 | |||
| chr9:130885205 | C | T | 2 | a0002a0003 | 8 | HG00639.hp1 HG01123.hp2 HG01361.hp2 others(5): Show |
missense_variant | MODERATE | c.2915C>T | p.Ser972Leu | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 3108/5578 | 2915/3393 | 972/1130 | chr9 | 130885205 |
| view | chr:pos | ref | alt | # # of chapid
|
chapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:130854967 | G | A | 1 | a0001c0013 | 1 | NA21309.hp2 | synonymous_variant | LOW | c.420G>A | p.Leu140Leu | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/11 | 613/5578 | 420/3393 | 140/1130 | chr9 | 130854967 | |||
| chr9:130862933 | G | A | 2 | a0001c0008a0007c0014 | 4 | HG02280.hp1 HG02630.hp1 HG03579.hp2 others(1): Show |
synonymous_variant | LOW | c.720G>A | p.Thr240Thr | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/11 | 913/5578 | 720/3393 | 240/1130 | chr9 | 130862933 | |||
| chr9:130880141 | A | G | 2 | a0001c0003a0001c0007 | 33 | HG01074.hp2 HG01081.hp1 HG01099.hp1 others(30): Show |
synonymous_variant | LOW | c.1497A>G | p.Glu499Glu | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 9/11 | 1690/5578 | 1497/3393 | 499/1130 | chr9 | 130880141 | |||
| chr9:130880156 | C | T | 1 | a0001c0026 | 1 | HG03225.hp2 | splice_region_variant&synonymous_variant | LOW | c.1512C>T | p.Asp504Asp | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 9/11 | 1705/5578 | 1512/3393 | 504/1130 | chr9 | 130880156 | |||
| chr9:130880663 | C | T | 1 | a0001c0025 | 1 | HG02723.hp1 | splice_region_variant&synonymous_variant | LOW | c.1677C>T | p.Ser559Ser | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/11 | 1870/5578 | 1677/3393 | 559/1130 | chr9 | 130880663 | |||
| chr9:130884159 | G | A | 3 | a0002c0005a0003c0012a0006c0015 | 9 | HG00639.hp1 HG01123.hp2 HG01361.hp2 others(6): Show |
synonymous_variant | LOW | c.1869G>A | p.Glu623Glu | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 2062/5578 | 1869/3393 | 623/1130 | chr9 | 130884159 | |||
| chr9:130884189 | C | T | 1 | a0001c0011 | 3 | HG03209.hp1 NA18522.hp2 NA18963.hp1 |
synonymous_variant | LOW | c.1899C>T | p.Ala633Ala | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 2092/5578 | 1899/3393 | 633/1130 | chr9 | 130884189 | |||
| chr9:130884390 | C | T | 1 | a0001c0024 | 1 | HG03239.hp1 | synonymous_variant | LOW | c.2100C>T | p.Thr700Thr | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 2293/5578 | 2100/3393 | 700/1130 | chr9 | 130884390 | |||
| chr9:130884477 | G | A | 1 | a0001c0018 | 1 | HG03453.hp1 | synonymous_variant | LOW | c.2187G>A | p.Thr729Thr | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 2380/5578 | 2187/3393 | 729/1130 | chr9 | 130884477 | |||
| chr9:130884642 | C | G | 4 | a0001c0003a0001c0006a0001c0007others(1): Show | 39 | HG01074.hp2 HG01081.hp1 HG01099.hp1 others(36): Show |
synonymous_variant | LOW | c.2352C>G | p.Pro784Pro | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 2545/5578 | 2352/3393 | 784/1130 | chr9 | 130884642 | |||
| chr9:130885077 | C | T | 1 | a0001c0021 | 1 | HG02135.hp1 | synonymous_variant | LOW | c.2787C>T | p.Gly929Gly | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 2980/5578 | 2787/3393 | 929/1130 | chr9 | 130885077 | |||
| chr9:130885206 | G | A | 1 | a0001c0023 | 1 | HG06807.hp2 | synonymous_variant | LOW | c.2916G>A | p.Ser972Ser | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 3109/5578 | 2916/3393 | 972/1130 | chr9 | 130885206 | |||
| chr9:130885230 | C | T | 4 | a0001c0004a0001c0007a0001c0020others(1): Show | 15 | HG01074.hp2 HG01099.hp1 HG01255.hp1 others(12): Show |
synonymous_variant | LOW | c.2940C>T | p.Pro980Pro | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 3133/5578 | 2940/3393 | 980/1130 | chr9 | 130885230 | |||
| chr9:130885248 | A | G | 1 | a0001c0010 | 3 | HG01993.hp1 NA19066.hp1 NA19078.hp1 |
synonymous_variant | LOW | c.2958A>G | p.Pro986Pro | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 3151/5578 | 2958/3393 | 986/1130 | chr9 | 130885248 | |||
| chr9:130885281 | G | A | 1 | a0001c0019 | 1 | HG03834.hp2 | synonymous_variant | LOW | c.2991G>A | p.Pro997Pro | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 3184/5578 | 2991/3393 | 997/1130 | chr9 | 130885281 | |||
| chr9:130885290 | C | T | 1 | a0001c0009 | 3 | HG02486.hp1 HG02809.hp1 HG03195.hp1 |
synonymous_variant | LOW | c.3000C>T | p.Thr1000Thr | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 3193/5578 | 3000/3393 | 1000/1130 | chr9 | 130885290 | |||
| chr9:130885558 | C | T | 1 | a0001c0020 | 1 | HG03098.hp2 | synonymous_variant | LOW | c.3268C>T | p.Leu1090Leu | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 3461/5578 | 3268/3393 | 1090/1130 | chr9 | 130885558 | |||
| chr9:130885614 | A | G | 18 | a0001c0001a0001c0003a0001c0004others(15): Show | 204 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(201): Show |
synonymous_variant | LOW | c.3324A>G | p.Pro1108Pro | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 3517/5578 | 3324/3393 | 1108/1130 | chr9 | 130885614 |
| view | chr:pos | ref | alt | # # of thapid:transcript level
|
thapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:130835296 | C | T | 1 | a0001c0001t0033 | 1 | HG03492.hp2 | 5_prime_UTR_variant | MODIFIER | c.-151C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/11 | 151 | chr9 | 130835296 | ||||||
| chr9:130835348 | GGGGCGCC others(12): Show |
G | 2 | a0001c0001t0015a0001c0003t0016 | 2 | HG02717.hp1 HG03098.hp1 |
5_prime_UTR_variant | MODIFIER | c.-94_-76delGCCGGGGG others(11): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/11 | 76 | INFO_REALIGN_3_PRIME | chr9 | 130835348 | |||||
| chr9:130835353 | G | GC | 49 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(46): Show | 264 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(261): Show |
5_prime_UTR_variant | MODIFIER | c.-92dupC | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/11 | 91 | INFO_REALIGN_3_PRIME | chr9 | 130835353 | |||||
| chr9:130835353 | G | GT | 4 | a0001c0001t0007a0001c0009t0006a0002c0005t0004others(1): Show | 9 | HG01123.hp2 HG01361.hp2 HG01433.hp2 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-94_-93insT | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/11 | 93 | chr9 | 130835353 | ||||||
| chr9:130835368 | G | A | 7 | a0001c0001t0010a0001c0001t0011a0001c0002t0009others(4): Show | 11 | HG01884.hp1 HG02055.hp1 HG02723.hp1 others(8): Show |
5_prime_UTR_variant | MODIFIER | c.-79G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/11 | 79 | chr9 | 130835368 | ||||||
| chr9:130835377 | C | A | 1 | a0001c0003t0020 | 1 | HG03139.hp2 | 5_prime_UTR_variant | MODIFIER | c.-70C>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/11 | 70 | chr9 | 130835377 | ||||||
| chr9:130835377 | C | T | 1 | a0001c0002t0032 | 1 | HG01257.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-70C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/11 | chr9 | 130835377 | |||||||
| chr9:130835388 | C | A | 1 | a0001c0001t0021 | 1 | NA19085.hp1 | 5_prime_UTR_variant | MODIFIER | c.-59C>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/11 | 59 | chr9 | 130835388 | ||||||
| chr9:130835394 | C | G | 2 | a0001c0001t0015a0001c0003t0016 | 2 | HG02717.hp1 HG03098.hp1 |
5_prime_UTR_variant | MODIFIER | c.-53C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/11 | 53 | chr9 | 130835394 | ||||||
| chr9:130885752 | G | A | 2 | a0001c0001t0006a0001c0009t0006 | 7 | HG01243.hp2 HG02145.hp2 HG02258.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*69G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 69 | chr9 | 130885752 | ||||||
| chr9:130885796 | A | G | 1 | a0001c0002t0019 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*113A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 113 | chr9 | 130885796 | ||||||
| chr9:130885820 | G | C | 2 | a0001c0004t0017a0001c0004t0022 | 2 | HG02145.hp1 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*137G>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 137 | chr9 | 130885820 | ||||||
| chr9:130885874 | G | A | 1 | a0001c0007t0023 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*191G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 191 | chr9 | 130885874 | ||||||
| chr9:130886169 | G | A | 2 | a0001c0001t0012a0001c0008t0012 | 2 | HG02630.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*486G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 486 | chr9 | 130886169 | ||||||
| chr9:130886202 | C | T | 1 | a0001c0004t0022 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*519C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 519 | chr9 | 130886202 | ||||||
| chr9:130886229 | C | T | 2 | a0001c0008t0030a0001c0008t0031 | 2 | HG02280.hp1 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*546C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 546 | chr9 | 130886229 | ||||||
| chr9:130886288 | C | T | 3 | a0001c0003t0003a0001c0003t0016a0001c0003t0020 | 21 | HG01167.hp1 HG01891.hp2 HG02109.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*605C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 605 | chr9 | 130886288 | ||||||
| chr9:130886496 | T | C | 4 | a0001c0001t0002a0001c0001t0024a0001c0001t0025others(1): Show | 30 | HG00323.hp1 HG00323.hp2 HG01069.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*813T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 813 | chr9 | 130886496 | ||||||
| chr9:130886505 | C | T | 1 | a0001c0008t0031 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*822C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 822 | chr9 | 130886505 | ||||||
| chr9:130886527 | TGGAGGCA others(9): Show |
T | 1 | a0001c0026t0029 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*853_*868delGGGACA others(10): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 853 | INFO_REALIGN_3_PRIME | chr9 | 130886527 | |||||
| chr9:130886605 | G | C | 8 | a0001c0001t0002a0001c0001t0008a0001c0001t0011others(5): Show | 38 | HG00323.hp1 HG00323.hp2 HG01069.hp2 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*922G>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 922 | chr9 | 130886605 | ||||||
| chr9:130886732 | C | G | 1 | a0001c0001t0007 | 7 | HG02486.hp2 HG02559.hp1 HG02572.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1049C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 1049 | chr9 | 130886732 | ||||||
| chr9:130886900 | C | G | 1 | a0001c0001t0015 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1217C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 1217 | chr9 | 130886900 | ||||||
| chr9:130887017 | G | A | 1 | a0001c0013t0027 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1334G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 1334 | chr9 | 130887017 | ||||||
| chr9:130887046 | G | A | 4 | a0001c0001t0002a0001c0001t0024a0001c0001t0025others(1): Show | 30 | HG00323.hp1 HG00323.hp2 HG01069.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*1363G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 1363 | chr9 | 130887046 | ||||||
| chr9:130887107 | C | T | 1 | a0001c0001t0007 | 7 | HG02486.hp2 HG02559.hp1 HG02572.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1424C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 1424 | chr9 | 130887107 | ||||||
| chr9:130887113 | C | T | 1 | a0001c0001t0025 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1430C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 1430 | chr9 | 130887113 | ||||||
| chr9:130887128 | C | G | 1 | a0001c0023t0028 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1445C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 1445 | chr9 | 130887128 | ||||||
| chr9:130887128 | C | T | 1 | a0001c0001t0024 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1445C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 1445 | chr9 | 130887128 | ||||||
| chr9:130887166 | A | G | 30 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(27): Show | 117 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(114): Show |
3_prime_UTR_variant | MODIFIER | c.*1483A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 1483 | chr9 | 130887166 | ||||||
| chr9:130887171 | T | C | 17 | a0001c0001t0004a0001c0001t0010a0001c0003t0003others(14): Show | 63 | HG00639.hp1 HG01074.hp2 HG01081.hp1 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*1488T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 1488 | chr9 | 130887171 | ||||||
| chr9:130887203 | G | A | 10 | a0001c0001t0010a0001c0003t0003a0001c0003t0005others(7): Show | 44 | HG01074.hp2 HG01081.hp1 HG01099.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*1520G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 1520 | chr9 | 130887203 | ||||||
| chr9:130887439 | C | T | 8 | a0001c0003t0003a0001c0003t0005a0001c0003t0016others(5): Show | 39 | HG01074.hp2 HG01081.hp1 HG01099.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*1756C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 1756 | chr9 | 130887439 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level
|
ghapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:130835658 | CCTCTT | C | 199 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(196): Show | 212 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(209): Show |
intron_variant | MODIFIER | c.79+150_79+154delTC others(3): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130835658 | ||||||
| chr9:130835669 | C | T | 4 | a0001c0001t0006g0255a0001c0001t0006g0256a0001c0001t0006g0257others(1): Show | 4 | HG02145.hp2 HG02258.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.79+144C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130835669 | |||||||
| chr9:130835681 | G | A | 6 | a0001c0001t0001g0019a0001c0001t0006g0018a0001c0001t0008g0004others(3): Show | 7 | HG00735.hp1 HG01243.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.79+156G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130835681 | |||||||
| chr9:130835726 | C | G | 1 | a0006c0015t0004g0199 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.79+201C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130835726 | |||||||
| chr9:130835736 | C | A | 3 | a0001c0007t0005g0002a0001c0007t0005g0200a0001c0007t0023g0002 | 4 | HG01074.hp2 HG01255.hp1 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.79+211C>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130835736 | |||||||
| chr9:130835751 | T | TTTTCTC | 173 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(170): Show | 185 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.79+228_79+233dupTT others(4): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130835751 | ||||||
| chr9:130835753 | TTCTC | T | 3 | a0001c0003t0005g0252a0001c0003t0005g0253a0001c0003t0005g0254 | 3 | HG01081.hp1 HG01175.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.79+236_79+239delCT others(2): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130835753 | ||||||
| chr9:130835848 | A | T | 1 | a0001c0001t0001g0198 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.79+323A>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130835848 | |||||||
| chr9:130835849 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.79+324C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130835849 | |||||||
| chr9:130835876 | G | A | 63 | a0001c0001t0001g0209a0001c0001t0001g0221a0001c0001t0001g0224others(60): Show | 67 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(64): Show |
intron_variant | MODIFIER | c.79+351G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130835876 | |||||||
| chr9:130835979 | C | T | 2 | a0001c0001t0001g0013a0001c0001t0001g0197 | 3 | HG02572.hp1 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.79+454C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130835979 | |||||||
| chr9:130835987 | T | G | 4 | a0001c0001t0002g0014a0001c0001t0002g0201a0001c0001t0002g0202others(1): Show | 5 | HG01069.hp2 HG01071.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.79+462T>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130835987 | |||||||
| chr9:130836016 | A | G | 1 | a0006c0015t0004g0199 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.79+491A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130836016 | |||||||
| chr9:130836108 | C | T | 1 | a0001c0001t0001g0196 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.79+583C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130836108 | |||||||
| chr9:130836163 | G | A | 10 | a0001c0001t0010g0005a0001c0001t0010g0043a0001c0001t0011g0041others(7): Show | 11 | HG01884.hp1 HG02055.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.79+638G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130836163 | |||||||
| chr9:130836194 | G | A | 5 | a0001c0001t0007g0205a0001c0001t0007g0206a0001c0001t0007g0207others(2): Show | 5 | HG02451.hp1 HG02647.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.79+669G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130836194 | |||||||
| chr9:130836242 | C | G | 1 | a0001c0008t0030g0040 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.79+717C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130836242 | |||||||
| chr9:130836465 | G | A | 6 | a0001c0001t0001g0019a0001c0001t0006g0018a0001c0001t0008g0004others(3): Show | 7 | HG00735.hp1 HG01243.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.79+940G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130836465 | |||||||
| chr9:130836482 | G | C | 1 | a0001c0001t0006g0255 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.79+957G>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130836482 | |||||||
| chr9:130836824 | C | CA | 8 | a0001c0001t0001g0051a0001c0001t0001g0053a0001c0001t0004g0054others(5): Show | 8 | HG00673.hp2 HG02109.hp1 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.79+1321dupA | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130836824 | ||||||
| chr9:130836824 | CA | C | 16 | a0001c0001t0001g0191a0001c0001t0007g0194a0001c0001t0010g0005others(13): Show | 17 | HG00558.hp1 HG00639.hp1 HG01256.hp2 others(14): Show |
intron_variant | MODIFIER | c.79+1321delA | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130836824 | ||||||
| chr9:130836824 | CAAAA | C | 14 | a0001c0001t0007g0210a0001c0002t0001g0026a0001c0003t0003g0204others(11): Show | 15 | HG01123.hp2 HG01361.hp2 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.79+1318_79+1321del others(4): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130836824 | ||||||
| chr9:130836824 | CAAAAA | C | 68 | a0001c0001t0001g0019a0001c0001t0001g0221a0001c0001t0001g0224others(65): Show | 72 | HG00323.hp1 HG00735.hp1 HG01069.hp2 others(69): Show |
intron_variant | MODIFIER | c.79+1317_79+1321del others(5): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130836824 | ||||||
| chr9:130836843 | A | G | 5 | a0001c0001t0007g0194a0001c0001t0015g0193a0001c0002t0001g0195others(2): Show | 5 | HG02486.hp2 HG02615.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.79+1318A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130836843 | |||||||
| chr9:130836854 | A | G | 1 | a0001c0026t0029g0250 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.79+1329A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130836854 | |||||||
| chr9:130836875 | A | G | 10 | a0001c0001t0010g0005a0001c0001t0010g0043a0001c0001t0011g0041others(7): Show | 11 | HG01884.hp1 HG02055.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.79+1350A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130836875 | |||||||
| chr9:130837016 | A | G | 2 | a0001c0003t0003g0204a0001c0003t0003g0208 | 2 | HG02451.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.79+1491A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130837016 | |||||||
| chr9:130837017 | T | C | 85 | a0001c0001t0001g0019a0001c0001t0001g0221a0001c0001t0001g0224others(82): Show | 90 | HG00323.hp1 HG00735.hp1 HG01069.hp2 others(87): Show |
intron_variant | MODIFIER | c.79+1492T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130837017 | |||||||
| chr9:130837072 | G | T | 10 | a0001c0001t0010g0005a0001c0001t0010g0043a0001c0001t0011g0041others(7): Show | 11 | HG01884.hp1 HG02055.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.79+1547G>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130837072 | |||||||
| chr9:130837340 | G | A | 2 | a0001c0001t0007g0194a0001c0002t0001g0195 | 2 | HG02486.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.79+1815G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130837340 | |||||||
| chr9:130837352 | G | A | 2 | a0001c0001t0001g0058a0001c0002t0001g0057 | 2 | HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.79+1827G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130837352 | |||||||
| chr9:130837414 | T | G | 86 | a0001c0001t0001g0019a0001c0001t0001g0221a0001c0001t0001g0224others(83): Show | 91 | HG00323.hp1 HG00735.hp1 HG01069.hp2 others(88): Show |
intron_variant | MODIFIER | c.79+1889T>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130837414 | |||||||
| chr9:130837513 | G | A | 1 | a0001c0002t0001g0060 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.79+1988G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130837513 | |||||||
| chr9:130837549 | CA | C | 65 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0221others(62): Show | 69 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(66): Show |
intron_variant | MODIFIER | c.79+2038delA | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130837549 | ||||||
| chr9:130837813 | C | G | 2 | a0001c0001t0026g0024a0001c0002t0001g0025 | 2 | HG03209.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.79+2288C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130837813 | |||||||
| chr9:130837914 | T | C | 1 | a0001c0004t0004g0027 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.79+2389T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130837914 | |||||||
| chr9:130838056 | A | G | 6 | a0001c0001t0007g0194a0001c0001t0015g0193a0001c0002t0001g0195others(3): Show | 6 | HG02486.hp2 HG02615.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.79+2531A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130838056 | |||||||
| chr9:130838065 | A | G | 1 | a0001c0002t0001g0060 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.79+2540A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130838065 | |||||||
| chr9:130838120 | T | C | 86 | a0001c0001t0001g0019a0001c0001t0001g0221a0001c0001t0001g0224others(83): Show | 91 | HG00323.hp1 HG00735.hp1 HG01069.hp2 others(88): Show |
intron_variant | MODIFIER | c.79+2595T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130838120 | |||||||
| chr9:130838273 | A | ATTGTGAC others(4): Show |
91 | a0001c0001t0001g0019a0001c0001t0001g0221a0001c0001t0001g0224others(88): Show | 96 | HG00323.hp1 HG00735.hp1 HG01069.hp2 others(93): Show |
intron_variant | MODIFIER | c.79+2749_79+2750ins others(11): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130838273 | ||||||
| chr9:130838311 | A | G | 1 | a0001c0011t0002g0249 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.79+2786A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130838311 | |||||||
| chr9:130838529 | G | A | 1 | a0001c0001t0001g0061 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.79+3004G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130838529 | |||||||
| chr9:130838576 | TTTA | T | 85 | a0001c0001t0001g0019a0001c0001t0001g0221a0001c0001t0001g0224others(82): Show | 90 | HG00323.hp1 HG00735.hp1 HG01069.hp2 others(87): Show |
intron_variant | MODIFIER | c.79+3056_79+3058del others(3): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130838576 | ||||||
| chr9:130838647 | C | T | 1 | a0001c0002t0001g0025 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.79+3122C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130838647 | |||||||
| chr9:130838669 | A | G | 1 | a0001c0003t0003g0183 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.79+3144A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130838669 | |||||||
| chr9:130839077 | A | AT | 6 | a0001c0001t0001g0180a0001c0001t0015g0193a0001c0002t0001g0025others(3): Show | 6 | HG02717.hp1 HG03098.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.79+3568dupT | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130839077 | ||||||
| chr9:130839078 | T | A | 74 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(71): Show | 82 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.79+3553T>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130839078 | |||||||
| chr9:130839079 | T | A | 1 | a0001c0001t0001g0062 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.79+3554T>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130839079 | |||||||
| chr9:130839127 | G | T | 2 | a0001c0001t0011g0041a0001c0001t0011g0042 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.79+3602G>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130839127 | |||||||
| chr9:130839379 | T | G | 53 | a0001c0001t0001g0019a0001c0001t0001g0221a0001c0001t0001g0224others(50): Show | 56 | HG00323.hp1 HG00735.hp1 HG01069.hp2 others(53): Show |
intron_variant | MODIFIER | c.79+3854T>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130839379 | |||||||
| chr9:130839819 | C | G | 85 | a0001c0001t0001g0019a0001c0001t0001g0221a0001c0001t0001g0224others(82): Show | 90 | HG00323.hp1 HG00735.hp1 HG01069.hp2 others(87): Show |
intron_variant | MODIFIER | c.79+4294C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130839819 | |||||||
| chr9:130839904 | T | C | 92 | a0001c0001t0001g0019a0001c0001t0001g0102a0001c0001t0001g0221others(89): Show | 97 | HG00280.hp2 HG00323.hp1 HG00735.hp1 others(94): Show |
intron_variant | MODIFIER | c.79+4379T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130839904 | |||||||
| chr9:130839952 | C | T | 1 | a0001c0001t0001g0101 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.79+4427C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130839952 | |||||||
| chr9:130840065 | A | C | 1 | a0001c0002t0001g0179 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.79+4540A>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130840065 | |||||||
| chr9:130840185 | C | T | 10 | a0001c0001t0010g0005a0001c0001t0010g0043a0001c0001t0011g0041others(7): Show | 11 | HG01884.hp1 HG02055.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.79+4660C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130840185 | |||||||
| chr9:130840203 | C | T | 101 | a0001c0001t0001g0019a0001c0001t0001g0221a0001c0001t0001g0224others(98): Show | 107 | HG00323.hp1 HG00735.hp1 HG01069.hp2 others(104): Show |
intron_variant | MODIFIER | c.79+4678C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130840203 | |||||||
| chr9:130840242 | A | G | 1 | a0001c0001t0001g0178 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.79+4717A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130840242 | |||||||
| chr9:130840266 | T | C | 9 | a0001c0002t0001g0026a0001c0002t0001g0028a0001c0002t0001g0029others(6): Show | 9 | NA18945.hp1 NA18977.hp1 NA18990.hp1 others(6): Show |
intron_variant | MODIFIER | c.79+4741T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130840266 | |||||||
| chr9:130840314 | G | A | 1 | a0001c0001t0010g0043 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.79+4789G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130840314 | |||||||
| chr9:130840322 | T | C | 1 | a0001c0002t0001g0103 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.79+4797T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130840322 | |||||||
| chr9:130840349 | A | G | 1 | a0001c0002t0001g0177 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.79+4824A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130840349 | |||||||
| chr9:130840410 | C | T | 1 | a0001c0023t0028g0059 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.79+4885C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130840410 | |||||||
| chr9:130840657 | T | C | 2 | a0001c0003t0003g0240a0001c0003t0003g0241 | 2 | HG01167.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.79+5132T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130840657 | |||||||
| chr9:130840709 | GGGTCTCA others(16): Show |
G | 2 | a0001c0001t0001g0053a0001c0002t0001g0052 | 2 | HG03927.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.79+5192_79+5214del others(23): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130840709 | ||||||
| chr9:130840758 | A | G | 1 | a0001c0001t0001g0100 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.79+5233A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130840758 | |||||||
| chr9:130840847 | A | G | 1 | a0001c0023t0028g0059 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.79+5322A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130840847 | |||||||
| chr9:130840877 | T | A | 3 | a0001c0001t0015g0193a0001c0003t0016g0192a0001c0023t0028g0059 | 3 | HG02717.hp1 HG03098.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.79+5352T>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130840877 | |||||||
| chr9:130841187 | G | A | 1 | a0001c0003t0005g0252 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.79+5662G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130841187 | |||||||
| chr9:130841223 | C | G | 1 | a0001c0004t0004g0027 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.79+5698C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130841223 | |||||||
| chr9:130841228 | A | G | 9 | a0001c0002t0001g0026a0001c0002t0001g0028a0001c0002t0001g0029others(6): Show | 9 | NA18945.hp1 NA18977.hp1 NA18990.hp1 others(6): Show |
intron_variant | MODIFIER | c.79+5703A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130841228 | |||||||
| chr9:130841248 | C | T | 3 | a0001c0001t0007g0194a0001c0002t0001g0195a0006c0015t0004g0199 | 3 | HG02486.hp2 HG02615.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.79+5723C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130841248 | |||||||
| chr9:130841292 | C | T | 1 | a0001c0001t0015g0193 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.79+5767C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130841292 | |||||||
| chr9:130841307 | C | G | 1 | a0001c0003t0005g0252 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.79+5782C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130841307 | |||||||
| chr9:130841415 | T | C | 92 | a0001c0001t0001g0019a0001c0001t0001g0102a0001c0001t0001g0221others(89): Show | 97 | HG00280.hp2 HG00323.hp1 HG00735.hp1 others(94): Show |
intron_variant | MODIFIER | c.79+5890T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130841415 | |||||||
| chr9:130841475 | A | G | 1 | a0001c0023t0028g0059 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.79+5950A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130841475 | |||||||
| chr9:130841539 | C | T | 2 | a0001c0001t0007g0176a0001c0009t0006g0175 | 2 | HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.79+6014C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130841539 | |||||||
| chr9:130841738 | G | A | 1 | a0001c0002t0001g0104 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.79+6213G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130841738 | |||||||
| chr9:130841822 | G | A | 8 | a0001c0001t0007g0210a0001c0009t0006g0211a0002c0005t0004g0003others(5): Show | 9 | HG01123.hp2 HG01361.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.79+6297G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130841822 | |||||||
| chr9:130841883 | G | T | 1 | a0001c0003t0003g0219 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.79+6358G>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130841883 | |||||||
| chr9:130841888 | T | G | 2 | a0001c0001t0001g0006a0001c0001t0001g0063 | 3 | HG02451.hp2 HG02523.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.79+6363T>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130841888 | |||||||
| chr9:130841924 | G | A | 4 | a0001c0001t0004g0054a0001c0001t0004g0105a0001c0002t0001g0106others(1): Show | 5 | HG01109.hp1 HG01884.hp2 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.79+6399G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130841924 | |||||||
| chr9:130841936 | T | TAGAG | 101 | a0001c0001t0001g0019a0001c0001t0001g0102a0001c0001t0001g0221others(98): Show | 107 | HG00280.hp2 HG00323.hp1 HG00735.hp1 others(104): Show |
intron_variant | MODIFIER | c.79+6422_79+6425dup others(4): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130841936 | ||||||
| chr9:130841976 | G | T | 1 | a0001c0001t0001g0051 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.79+6451G>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130841976 | |||||||
| chr9:130841998 | C | A | 23 | a0001c0001t0001g0019a0001c0001t0006g0018a0001c0001t0008g0004others(20): Show | 24 | HG00735.hp1 HG01243.hp2 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.79+6473C>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130841998 | |||||||
| chr9:130842004 | G | A | 86 | a0001c0001t0001g0019a0001c0001t0001g0102a0001c0001t0001g0221others(83): Show | 91 | HG00280.hp2 HG00323.hp1 HG00735.hp1 others(88): Show |
intron_variant | MODIFIER | c.79+6479G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130842004 | |||||||
| chr9:130842121 | G | A | 2 | a0001c0004t0004g0107a0001c0004t0004g0108 | 2 | HG02818.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.79+6596G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130842121 | |||||||
| chr9:130842175 | A | C | 1 | a0001c0002t0001g0174 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.79+6650A>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130842175 | |||||||
| chr9:130842358 | A | G | 5 | a0001c0008t0012g0036a0001c0008t0030g0040a0001c0008t0031g0038others(2): Show | 5 | HG02280.hp1 HG02630.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.79+6833A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130842358 | |||||||
| chr9:130842423 | A | G | 1 | a0001c0001t0002g0239 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.79+6898A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130842423 | |||||||
| chr9:130842494 | C | T | 92 | a0001c0001t0001g0019a0001c0001t0001g0102a0001c0001t0001g0221others(89): Show | 97 | HG00280.hp2 HG00323.hp1 HG00735.hp1 others(94): Show |
intron_variant | MODIFIER | c.79+6969C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130842494 | |||||||
| chr9:130842774 | A | G | 3 | a0001c0001t0001g0008a0001c0001t0001g0099a0001c0021t0001g0050 | 4 | HG01934.hp1 HG02135.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.79+7249A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130842774 | |||||||
| chr9:130842818 | T | G | 1 | a0001c0002t0001g0179 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.79+7293T>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130842818 | |||||||
| chr9:130842855 | G | T | 92 | a0001c0001t0001g0019a0001c0001t0001g0102a0001c0001t0001g0221others(89): Show | 97 | HG00280.hp2 HG00323.hp1 HG00735.hp1 others(94): Show |
intron_variant | MODIFIER | c.79+7330G>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130842855 | |||||||
| chr9:130843038 | A | C | 1 | a0001c0002t0001g0172 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.79+7513A>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130843038 | |||||||
| chr9:130843137 | A | G | 1 | a0001c0001t0001g0098 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.79+7612A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130843137 | |||||||
| chr9:130843248 | AC | A | 2 | a0001c0002t0001g0010a0001c0002t0001g0109 | 3 | HG01071.hp2 HG01192.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.79+7727delC | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130843248 | ||||||
| chr9:130843254 | G | A | 2 | a0001c0001t0007g0210a0001c0009t0006g0211 | 2 | HG03195.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.79+7729G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130843254 | |||||||
| chr9:130843310 | G | A | 1 | a0001c0002t0001g0028 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.79+7785G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130843310 | |||||||
| chr9:130843869 | T | A | 90 | a0001c0001t0001g0019a0001c0001t0001g0102a0001c0001t0001g0221others(87): Show | 95 | HG00280.hp2 HG00323.hp1 HG00735.hp1 others(92): Show |
intron_variant | MODIFIER | c.79+8344T>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130843869 | |||||||
| chr9:130844034 | A | G | 3 | a0001c0001t0007g0194a0001c0002t0001g0195a0006c0015t0004g0199 | 3 | HG02486.hp2 HG02615.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.79+8509A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130844034 | |||||||
| chr9:130844135 | G | A | 3 | a0001c0001t0007g0194a0001c0002t0001g0195a0006c0015t0004g0199 | 3 | HG02486.hp2 HG02615.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.79+8610G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130844135 | |||||||
| chr9:130844153 | A | G | 90 | a0001c0001t0001g0019a0001c0001t0001g0102a0001c0001t0001g0221others(87): Show | 95 | HG00280.hp2 HG00323.hp1 HG00735.hp1 others(92): Show |
intron_variant | MODIFIER | c.79+8628A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130844153 | |||||||
| chr9:130844159 | T | C | 1 | a0001c0011t0013g0215 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.79+8634T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130844159 | |||||||
| chr9:130844165 | C | A | 10 | a0001c0001t0010g0005a0001c0001t0010g0043a0001c0001t0011g0041others(7): Show | 11 | HG01884.hp1 HG02055.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.79+8640C>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130844165 | |||||||
| chr9:130844257 | G | A | 1 | a0001c0001t0008g0016 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.79+8732G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130844257 | |||||||
| chr9:130844363 | A | G | 10 | a0001c0001t0010g0005a0001c0001t0010g0043a0001c0001t0011g0041others(7): Show | 11 | HG01884.hp1 HG02055.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.79+8838A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130844363 | |||||||
| chr9:130844491 | AT | A | 109 | a0001c0001t0001g0019a0001c0001t0001g0102a0001c0001t0001g0114others(106): Show | 114 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.79+8978delT | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130844491 | ||||||
| chr9:130844491 | ATT | A | 5 | a0001c0003t0005g0244a0001c0007t0005g0002a0001c0007t0005g0200others(2): Show | 6 | HG01074.hp2 HG01099.hp1 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.79+8977_79+8978del others(2): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130844491 | ||||||
| chr9:130844795 | C | T | 2 | a0001c0001t0001g0096a0001c0001t0001g0097 | 2 | NA18979.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.80-9269C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130844795 | |||||||
| chr9:130845014 | C | G | 1 | a0001c0001t0001g0095 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.80-9050C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130845014 | |||||||
| chr9:130845034 | A | G | 5 | a0001c0008t0012g0036a0001c0008t0030g0040a0001c0008t0031g0038others(2): Show | 5 | HG02280.hp1 HG02630.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.80-9030A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130845034 | |||||||
| chr9:130845477 | G | T | 3 | a0001c0001t0001g0236a0001c0001t0002g0237a0001c0001t0002g0238 | 3 | HG01981.hp2 HG02273.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.80-8587G>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130845477 | |||||||
| chr9:130845490 | C | T | 63 | a0001c0001t0001g0102a0001c0001t0001g0221a0001c0001t0001g0224others(60): Show | 67 | HG00280.hp2 HG00323.hp1 HG01069.hp2 others(64): Show |
intron_variant | MODIFIER | c.80-8574C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130845490 | |||||||
| chr9:130845498 | C | T | 3 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126 | 3 | HG01981.hp1 HG04115.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.80-8566C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130845498 | |||||||
| chr9:130845589 | C | T | 15 | a0001c0001t0006g0255a0001c0001t0006g0256a0001c0001t0006g0257others(12): Show | 16 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.80-8475C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130845589 | |||||||
| chr9:130845601 | C | T | 1 | a0001c0001t0015g0193 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.80-8463C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130845601 | |||||||
| chr9:130845788 | T | C | 3 | a0001c0001t0007g0194a0001c0002t0001g0195a0006c0015t0004g0199 | 3 | HG02486.hp2 HG02615.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.80-8276T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130845788 | |||||||
| chr9:130845859 | T | TA | 64 | a0001c0001t0001g0102a0001c0001t0001g0221a0001c0001t0001g0224others(61): Show | 68 | HG00280.hp2 HG00323.hp1 HG01069.hp2 others(65): Show |
intron_variant | MODIFIER | c.80-8192dupA | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130845859 | ||||||
| chr9:130845859 | TA | T | 6 | a0001c0001t0006g0255a0001c0001t0006g0256a0001c0001t0006g0257others(3): Show | 6 | HG02145.hp2 HG02258.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.80-8192delA | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130845859 | ||||||
| chr9:130845891 | C | G | 1 | a0001c0023t0028g0059 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.80-8173C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130845891 | |||||||
| chr9:130845960 | G | A | 1 | a0001c0003t0003g0216 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.80-8104G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130845960 | |||||||
| chr9:130846081 | C | CTG | 17 | a0001c0001t0001g0058a0001c0001t0001g0093a0001c0001t0001g0122others(14): Show | 17 | HG00280.hp1 HG00438.hp2 HG00639.hp1 others(14): Show |
intron_variant | MODIFIER | c.80-7956_80-7955dup others(2): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130846081 | ||||||
| chr9:130846081 | C | CTGTGTGT others(1): Show |
10 | a0001c0002t0001g0026a0001c0002t0001g0028a0001c0002t0001g0029others(7): Show | 10 | HG03209.hp1 NA18945.hp1 NA18977.hp1 others(7): Show |
intron_variant | MODIFIER | c.80-7962_80-7955dup others(8): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130846081 | ||||||
| chr9:130846081 | CTG | C | 4 | a0001c0001t0002g0184a0001c0003t0005g0244a0001c0004t0017g0049others(1): Show | 4 | HG03239.hp2 HG03471.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.80-7956_80-7955del others(2): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130846081 | ||||||
| chr9:130846081 | CTGTG | C | 64 | a0001c0001t0001g0102a0001c0001t0001g0221a0001c0001t0001g0224others(61): Show | 68 | HG00280.hp2 HG00323.hp1 HG01069.hp2 others(65): Show |
intron_variant | MODIFIER | c.80-7958_80-7955del others(4): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130846081 | ||||||
| chr9:130846081 | CTGTGTG | C | 17 | a0001c0001t0006g0255a0001c0001t0006g0256a0001c0001t0006g0257others(14): Show | 18 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.80-7960_80-7955del others(6): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130846081 | ||||||
| chr9:130846081 | CTGTGTGT others(3): Show |
C | 1 | a0001c0001t0015g0193 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.80-7964_80-7955del others(10): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130846081 | ||||||
| chr9:130846095 | GTGTGTGT others(9): Show |
G | 2 | a0001c0002t0001g0010a0001c0002t0001g0109 | 3 | HG01071.hp2 HG01192.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.80-7954_80-7939del others(16): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130846095 | ||||||
| chr9:130846108 | T | C | 1 | a0001c0001t0001g0117 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.80-7956T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130846108 | |||||||
| chr9:130846509 | T | C | 1 | a0001c0023t0028g0059 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.80-7555T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130846509 | |||||||
| chr9:130847022 | A | G | 1 | a0001c0004t0022g0020 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.80-7042A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130847022 | |||||||
| chr9:130847078 | G | A | 2 | a0001c0001t0001g0053a0001c0002t0001g0052 | 2 | HG03927.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.80-6986G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130847078 | |||||||
| chr9:130847235 | G | A | 1 | a0001c0008t0012g0036 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.80-6829G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130847235 | |||||||
| chr9:130847349 | G | T | 15 | a0001c0001t0006g0255a0001c0001t0006g0256a0001c0001t0006g0257others(12): Show | 16 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.80-6715G>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130847349 | |||||||
| chr9:130847409 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.80-6655G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130847409 | |||||||
| chr9:130847566 | A | G | 3 | a0001c0001t0007g0194a0001c0002t0001g0195a0006c0015t0004g0199 | 3 | HG02486.hp2 HG02615.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.80-6498A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130847566 | |||||||
| chr9:130847594 | C | G | 1 | a0001c0001t0001g0089 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.80-6470C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130847594 | |||||||
| chr9:130847844 | T | C | 1 | a0001c0024t0001g0090 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.80-6220T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130847844 | |||||||
| chr9:130847897 | C | A | 1 | a0001c0002t0001g0128 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.80-6167C>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130847897 | |||||||
| chr9:130848017 | G | A | 3 | a0001c0001t0007g0194a0001c0002t0001g0195a0006c0015t0004g0199 | 3 | HG02486.hp2 HG02615.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.80-6047G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130848017 | |||||||
| chr9:130848075 | C | A | 1 | a0001c0001t0015g0193 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.80-5989C>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130848075 | |||||||
| chr9:130848086 | A | G | 1 | a0001c0002t0001g0103 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.80-5978A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130848086 | |||||||
| chr9:130848150 | G | C | 1 | a0001c0023t0028g0059 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.80-5914G>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130848150 | |||||||
| chr9:130848151 | A | T | 1 | a0001c0023t0028g0059 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.80-5913A>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130848151 | |||||||
| chr9:130848207 | A | G | 56 | a0001c0001t0001g0221a0001c0001t0001g0224a0001c0001t0001g0225others(53): Show | 59 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.80-5857A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130848207 | |||||||
| chr9:130848210 | T | G | 2 | a0001c0002t0001g0065a0001c0019t0001g0129 | 2 | HG03834.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.80-5854T>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130848210 | |||||||
| chr9:130848345 | G | GA | 66 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(63): Show | 73 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.80-5697dupA | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130848345 | ||||||
| chr9:130848345 | G | GAA | 10 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0127others(7): Show | 10 | HG00621.hp1 HG01243.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.80-5698_80-5697dup others(2): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130848345 | ||||||
| chr9:130848345 | GA | G | 59 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0236others(56): Show | 63 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(60): Show |
intron_variant | MODIFIER | c.80-5697delA | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130848345 | ||||||
| chr9:130848517 | C | CA | 7 | a0001c0001t0001g0013a0001c0001t0001g0096a0001c0001t0001g0180others(4): Show | 8 | HG02572.hp1 HG02738.hp2 HG03942.hp2 others(5): Show |
intron_variant | MODIFIER | c.80-5528dupA | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130848517 | ||||||
| chr9:130848517 | CA | C | 76 | a0001c0001t0001g0080a0001c0001t0001g0124a0001c0001t0001g0209others(73): Show | 81 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(78): Show |
intron_variant | MODIFIER | c.80-5528delA | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130848517 | ||||||
| chr9:130848517 | CAA | C | 6 | a0001c0001t0002g0235a0001c0001t0006g0255a0001c0001t0006g0256others(3): Show | 6 | HG02027.hp1 HG02145.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.80-5529_80-5528del others(2): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130848517 | ||||||
| chr9:130848529 | A | G | 2 | a0001c0001t0001g0087a0001c0001t0001g0088 | 2 | HG01074.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.80-5535A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130848529 | |||||||
| chr9:130848666 | G | A | 1 | a0001c0001t0002g0139 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.80-5398G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130848666 | |||||||
| chr9:130848677 | C | T | 2 | a0001c0001t0001g0096a0001c0001t0001g0097 | 2 | NA18979.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.80-5387C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130848677 | |||||||
| chr9:130848766 | A | G | 3 | a0001c0008t0030g0040a0001c0008t0031g0038a0007c0014t0008g0037 | 3 | HG02280.hp1 HG03579.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.80-5298A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130848766 | |||||||
| chr9:130848896 | G | A | 1 | a0001c0001t0001g0007 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.80-5168G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130848896 | |||||||
| chr9:130848985 | A | G | 4 | a0001c0001t0001g0221a0001c0001t0002g0015a0001c0001t0002g0235others(1): Show | 5 | HG02027.hp1 NA18962.hp1 NA19011.hp2 others(2): Show |
intron_variant | MODIFIER | c.80-5079A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130848985 | |||||||
| chr9:130849032 | G | A | 3 | a0001c0001t0007g0194a0001c0002t0001g0195a0006c0015t0004g0199 | 3 | HG02486.hp2 HG02615.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.80-5032G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130849032 | |||||||
| chr9:130849071 | T | C | 2 | a0001c0001t0001g0196a0001c0002t0001g0140 | 2 | NA18941.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.80-4993T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130849071 | |||||||
| chr9:130849244 | G | A | 2 | a0001c0004t0004g0027a0001c0011t0013g0039 | 2 | HG01496.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.80-4820G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130849244 | |||||||
| chr9:130849277 | A | G | 1 | a0001c0002t0001g0233 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.80-4787A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130849277 | |||||||
| chr9:130849528 | G | T | 64 | a0001c0001t0001g0221a0001c0001t0001g0224a0001c0001t0001g0225others(61): Show | 68 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(65): Show |
intron_variant | MODIFIER | c.80-4536G>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130849528 | |||||||
| chr9:130849528 | GT | G | 22 | a0001c0001t0006g0255a0001c0001t0006g0256a0001c0001t0006g0257others(19): Show | 23 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.80-4527delT | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130849528 | ||||||
| chr9:130849529 | T | G | 64 | a0001c0001t0001g0221a0001c0001t0001g0224a0001c0001t0001g0225others(61): Show | 68 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(65): Show |
intron_variant | MODIFIER | c.80-4535T>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130849529 | |||||||
| chr9:130849548 | C | G | 3 | a0001c0001t0001g0178a0001c0002t0001g0137a0001c0002t0001g0169 | 3 | HG03017.hp1 HG04115.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.80-4516C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130849548 | |||||||
| chr9:130849572 | G | A | 1 | a0001c0001t0015g0193 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.80-4492G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130849572 | |||||||
| chr9:130849637 | A | G | 1 | a0001c0002t0001g0168 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.80-4427A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130849637 | |||||||
| chr9:130849771 | C | A | 1 | a0001c0001t0015g0193 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.80-4293C>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130849771 | |||||||
| chr9:130850086 | C | G | 2 | a0001c0003t0003g0216a0001c0003t0020g0218 | 2 | HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.80-3978C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130850086 | |||||||
| chr9:130850125 | A | G | 1 | a0001c0001t0015g0193 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.80-3939A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130850125 | |||||||
| chr9:130850362 | C | CT | 65 | a0001c0001t0001g0102a0001c0001t0001g0221a0001c0001t0001g0224others(62): Show | 69 | HG00280.hp2 HG00323.hp1 HG01069.hp2 others(66): Show |
intron_variant | MODIFIER | c.80-3699dupT | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130850362 | ||||||
| chr9:130850380 | G | A | 65 | a0001c0001t0001g0102a0001c0001t0001g0221a0001c0001t0001g0224others(62): Show | 69 | HG00280.hp2 HG00323.hp1 HG01069.hp2 others(66): Show |
intron_variant | MODIFIER | c.80-3684G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130850380 | |||||||
| chr9:130850443 | T | C | 87 | a0001c0001t0001g0102a0001c0001t0001g0221a0001c0001t0001g0224others(84): Show | 92 | HG00280.hp2 HG00323.hp1 HG01069.hp2 others(89): Show |
intron_variant | MODIFIER | c.80-3621T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130850443 | |||||||
| chr9:130850505 | G | A | 1 | a0001c0023t0028g0059 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.80-3559G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130850505 | |||||||
| chr9:130850608 | G | A | 3 | a0001c0001t0007g0194a0001c0002t0001g0195a0006c0015t0004g0199 | 3 | HG02486.hp2 HG02615.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.80-3456G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130850608 | |||||||
| chr9:130850650 | G | A | 15 | a0001c0001t0006g0255a0001c0001t0006g0256a0001c0001t0006g0257others(12): Show | 16 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.80-3414G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130850650 | |||||||
| chr9:130850670 | C | A | 1 | a0001c0002t0001g0177 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.80-3394C>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130850670 | |||||||
| chr9:130850696 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.80-3368G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130850696 | |||||||
| chr9:130850796 | C | T | 1 | a0001c0002t0001g0172 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.80-3268C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130850796 | |||||||
| chr9:130850798 | C | T | 2 | a0001c0001t0015g0193a0001c0023t0028g0059 | 2 | HG03098.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.80-3266C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130850798 | |||||||
| chr9:130850893 | G | A | 1 | a0001c0025t0018g0047 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.80-3171G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130850893 | |||||||
| chr9:130850910 | GTTTTTGT others(5): Show |
G | 33 | a0001c0001t0001g0068a0001c0001t0001g0102a0001c0001t0001g0221others(30): Show | 35 | HG00280.hp2 HG00323.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.80-3152_80-3141del others(12): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130850910 | ||||||
| chr9:130851025 | G | A | 1 | a0001c0001t0015g0193 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.80-3039G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130851025 | |||||||
| chr9:130851072 | C | T | 3 | a0001c0001t0007g0194a0001c0002t0001g0195a0006c0015t0004g0199 | 3 | HG02486.hp2 HG02615.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.80-2992C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130851072 | |||||||
| chr9:130851125 | C | T | 1 | a0001c0023t0028g0059 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.80-2939C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130851125 | |||||||
| chr9:130851382 | T | C | 1 | a0001c0006t0005g0055 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.80-2682T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130851382 | |||||||
| chr9:130851428 | G | A | 1 | a0001c0001t0001g0101 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.80-2636G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130851428 | |||||||
| chr9:130851569 | A | T | 84 | a0001c0001t0001g0221a0001c0001t0001g0224a0001c0001t0001g0225others(81): Show | 89 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(86): Show |
intron_variant | MODIFIER | c.80-2495A>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130851569 | |||||||
| chr9:130851607 | T | G | 15 | a0001c0001t0006g0255a0001c0001t0006g0256a0001c0001t0006g0257others(12): Show | 16 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.80-2457T>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130851607 | |||||||
| chr9:130851766 | C | CT | 6 | a0001c0001t0001g0019a0001c0001t0001g0167a0001c0001t0001g0180others(3): Show | 6 | HG00735.hp1 HG00735.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.80-2280dupT | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130851766 | ||||||
| chr9:130851766 | CT | C | 76 | a0001c0001t0001g0221a0001c0001t0001g0224a0001c0001t0001g0225others(73): Show | 81 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(78): Show |
intron_variant | MODIFIER | c.80-2280delT | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130851766 | ||||||
| chr9:130851766 | CTT | C | 16 | a0001c0001t0002g0223a0001c0001t0006g0255a0001c0001t0006g0256others(13): Show | 17 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.80-2281_80-2280del others(2): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130851766 | ||||||
| chr9:130851869 | A | C | 1 | a0001c0003t0003g0248 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.80-2195A>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130851869 | |||||||
| chr9:130851912 | C | T | 15 | a0001c0001t0006g0255a0001c0001t0006g0256a0001c0001t0006g0257others(12): Show | 16 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.80-2152C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130851912 | |||||||
| chr9:130851915 | G | A | 21 | a0001c0001t0001g0019a0001c0001t0006g0018a0001c0001t0008g0004others(18): Show | 22 | HG00735.hp1 HG01243.hp2 HG01496.hp1 others(19): Show |
intron_variant | MODIFIER | c.80-2149G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130851915 | |||||||
| chr9:130852066 | T | A | 86 | a0001c0001t0001g0221a0001c0001t0001g0224a0001c0001t0001g0225others(83): Show | 91 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(88): Show |
intron_variant | MODIFIER | c.80-1998T>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130852066 | |||||||
| chr9:130852071 | G | A | 1 | a0001c0002t0001g0028 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.80-1993G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130852071 | |||||||
| chr9:130852100 | A | C | 3 | a0001c0002t0001g0030a0001c0002t0001g0031a0001c0002t0001g0035 | 3 | NA18945.hp1 NA18990.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.80-1964A>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130852100 | |||||||
| chr9:130852106 | A | T | 1 | a0001c0001t0007g0207 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.80-1958A>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130852106 | |||||||
| chr9:130852272 | C | T | 5 | a0001c0008t0012g0036a0001c0008t0030g0040a0001c0008t0031g0038others(2): Show | 5 | HG02280.hp1 HG02630.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.80-1792C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130852272 | |||||||
| chr9:130852290 | A | G | 13 | a0001c0001t0007g0210a0001c0003t0003g0173a0001c0003t0003g0216others(10): Show | 14 | HG01123.hp2 HG01361.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.80-1774A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130852290 | |||||||
| chr9:130852470 | A | G | 4 | a0001c0008t0030g0040a0001c0008t0031g0038a0001c0011t0013g0039others(1): Show | 4 | HG02280.hp1 HG03209.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.80-1594A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130852470 | |||||||
| chr9:130852664 | G | A | 5 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0002t0001g0109others(2): Show | 5 | HG00639.hp1 HG01109.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.80-1400G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130852664 | |||||||
| chr9:130852756 | T | C | 5 | a0001c0001t0001g0019a0001c0001t0006g0018a0001c0001t0008g0004others(2): Show | 6 | HG00735.hp1 HG01243.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.80-1308T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130852756 | |||||||
| chr9:130852936 | GGT | G | 16 | a0001c0001t0007g0056a0001c0001t0007g0194a0001c0001t0010g0005others(13): Show | 17 | HG01884.hp1 HG02055.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.80-1123_80-1122del others(2): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130852936 | ||||||
| chr9:130853015 | C | T | 31 | a0001c0001t0001g0221a0001c0001t0001g0224a0001c0001t0001g0225others(28): Show | 33 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.80-1049C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130853015 | |||||||
| chr9:130853019 | T | C | 1 | a0001c0001t0001g0069 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.80-1045T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130853019 | |||||||
| chr9:130853170 | C | CT | 165 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(162): Show | 178 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.80-871dupT | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130853170 | ||||||
| chr9:130853170 | C | CTT | 35 | a0001c0001t0001g0058a0001c0001t0001g0180a0001c0001t0001g0224others(32): Show | 36 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.80-872_80-871dupTT | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130853170 | ||||||
| chr9:130853170 | C | CTTT | 15 | a0001c0001t0001g0221a0001c0001t0002g0023a0001c0001t0002g0232others(12): Show | 16 | HG01192.hp2 HG01884.hp1 HG02027.hp1 others(13): Show |
intron_variant | MODIFIER | c.80-873_80-871dupTT others(1): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130853170 | ||||||
| chr9:130853175 | T | C | 1 | a0001c0001t0001g0178 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.80-889T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130853175 | |||||||
| chr9:130853176 | T | C | 5 | a0001c0001t0001g0019a0001c0001t0006g0018a0001c0001t0008g0004others(2): Show | 6 | HG00735.hp1 HG01243.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.80-888T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130853176 | |||||||
| chr9:130853387 | G | A | 1 | a0001c0009t0006g0145 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.80-677G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130853387 | |||||||
| chr9:130853389 | T | C | 1 | a0001c0010t0001g0170 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.80-675T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130853389 | |||||||
| chr9:130853424 | G | A | 10 | a0001c0001t0010g0005a0001c0001t0010g0043a0001c0001t0011g0041others(7): Show | 11 | HG01884.hp1 HG02055.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.80-640G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130853424 | |||||||
| chr9:130853503 | C | T | 63 | a0001c0001t0001g0221a0001c0001t0001g0236a0001c0001t0002g0014others(60): Show | 67 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(64): Show |
intron_variant | MODIFIER | c.80-561C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130853503 | |||||||
| chr9:130853564 | G | A | 1 | a0001c0002t0001g0146 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.80-500G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130853564 | |||||||
| chr9:130853595 | A | G | 2 | a0001c0001t0001g0019a0001c0001t0006g0018 | 2 | HG00735.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.80-469A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130853595 | |||||||
| chr9:130853704 | C | T | 9 | a0001c0001t0001g0191a0001c0001t0002g0166a0001c0002t0001g0136others(6): Show | 9 | HG00558.hp1 HG01993.hp1 NA18942.hp1 others(6): Show |
intron_variant | MODIFIER | c.80-360C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130853704 | |||||||
| chr9:130853711 | G | A | 1 | a0001c0003t0003g0240 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.80-353G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130853711 | |||||||
| chr9:130853889 | G | C | 1 | a0001c0002t0001g0179 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.80-175G>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130853889 | |||||||
| chr9:130854361 | A | G | 2 | a0001c0001t0011g0041a0001c0001t0011g0042 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.253+124A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 2/10 | chr9 | 130854361 | |||||||
| chr9:130854386 | G | A | 1 | a0001c0002t0001g0025 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.253+149G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 2/10 | chr9 | 130854386 | |||||||
| chr9:130854488 | C | T | 4 | a0001c0001t0006g0255a0001c0001t0006g0256a0001c0001t0006g0257others(1): Show | 4 | HG02145.hp2 HG02258.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.253+251C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 2/10 | chr9 | 130854488 | |||||||
| chr9:130854507 | A | G | 1 | a0001c0004t0022g0020 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.253+270A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 2/10 | chr9 | 130854507 | |||||||
| chr9:130854507 | A | T | 1 | a0001c0001t0007g0056 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.253+270A>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 2/10 | chr9 | 130854507 | |||||||
| chr9:130854751 | G | A | 4 | a0001c0001t0006g0255a0001c0001t0006g0256a0001c0001t0006g0257others(1): Show | 4 | HG02145.hp2 HG02258.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.254-50G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 2/10 | chr9 | 130854751 | |||||||
| chr9:130855122 | T | C | 1 | a0001c0001t0001g0178 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.549+26T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130855122 | |||||||
| chr9:130855205 | A | G | 1 | a0001c0010t0001g0170 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.549+109A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130855205 | |||||||
| chr9:130855277 | T | C | 2 | a0001c0001t0015g0193a0001c0023t0028g0059 | 2 | HG03098.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.549+181T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130855277 | |||||||
| chr9:130855398 | C | T | 1 | a0001c0009t0006g0145 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.549+302C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130855398 | |||||||
| chr9:130855405 | TA | T | 104 | a0001c0001t0001g0019a0001c0001t0001g0221a0001c0001t0001g0236others(101): Show | 110 | HG00323.hp1 HG00735.hp1 HG01069.hp2 others(107): Show |
intron_variant | MODIFIER | c.549+317delA | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr9 | 130855405 | ||||||
| chr9:130855444 | G | A | 10 | a0001c0001t0010g0005a0001c0001t0010g0043a0001c0001t0011g0041others(7): Show | 11 | HG01884.hp1 HG02055.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.549+348G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130855444 | |||||||
| chr9:130855469 | C | T | 11 | a0001c0001t0007g0056a0001c0001t0010g0005a0001c0001t0010g0043others(8): Show | 12 | HG01884.hp1 HG02055.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.549+373C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130855469 | |||||||
| chr9:130855797 | T | C | 62 | a0001c0001t0001g0102a0001c0001t0001g0221a0001c0001t0001g0236others(59): Show | 66 | HG00280.hp2 HG00323.hp1 HG01069.hp2 others(63): Show |
intron_variant | MODIFIER | c.549+701T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130855797 | |||||||
| chr9:130855910 | ATGTT | A | 11 | a0001c0001t0007g0056a0001c0001t0010g0005a0001c0001t0010g0043others(8): Show | 12 | HG01884.hp1 HG02055.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.549+832_549+835del others(4): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr9 | 130855910 | ||||||
| chr9:130855979 | G | A | 3 | a0001c0001t0007g0194a0001c0002t0001g0195a0006c0015t0004g0199 | 3 | HG02486.hp2 HG02615.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.549+883G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130855979 | |||||||
| chr9:130856113 | A | G | 11 | a0001c0001t0007g0056a0001c0001t0010g0005a0001c0001t0010g0043others(8): Show | 12 | HG01884.hp1 HG02055.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.549+1017A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130856113 | |||||||
| chr9:130856145 | A | G | 2 | a0001c0002t0001g0025a0001c0004t0022g0020 | 2 | HG02145.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.549+1049A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130856145 | |||||||
| chr9:130856158 | G | A | 1 | a0001c0002t0001g0064 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.549+1062G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130856158 | |||||||
| chr9:130856181 | C | T | 1 | a0001c0001t0002g0184 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.549+1085C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130856181 | |||||||
| chr9:130856380 | G | A | 1 | a0001c0002t0001g0116 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.549+1284G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130856380 | |||||||
| chr9:130856461 | A | G | 1 | a0001c0002t0019g0048 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.549+1365A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130856461 | |||||||
| chr9:130856466 | C | T | 2 | a0001c0001t0015g0193a0001c0023t0028g0059 | 2 | HG03098.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.549+1370C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130856466 | |||||||
| chr9:130856521 | C | G | 1 | a0001c0001t0001g0058 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.549+1425C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130856521 | |||||||
| chr9:130857252 | C | G | 1 | a0001c0008t0012g0036 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.549+2156C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130857252 | |||||||
| chr9:130857311 | G | A | 28 | a0001c0001t0001g0221a0001c0001t0001g0236a0001c0001t0002g0014others(25): Show | 30 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.549+2215G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130857311 | |||||||
| chr9:130857365 | C | T | 27 | a0001c0001t0007g0176a0001c0001t0007g0205a0001c0001t0007g0206others(24): Show | 28 | HG01074.hp2 HG01081.hp1 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.549+2269C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130857365 | |||||||
| chr9:130857537 | G | T | 1 | a0001c0001t0001g0058 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.549+2441G>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130857537 | |||||||
| chr9:130857624 | C | A | 1 | a0001c0001t0024g0226 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.549+2528C>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130857624 | |||||||
| chr9:130857633 | C | CT | 38 | a0001c0001t0007g0056a0001c0001t0007g0176a0001c0001t0007g0194others(35): Show | 40 | HG01074.hp2 HG01081.hp1 HG01099.hp1 others(37): Show |
intron_variant | MODIFIER | c.549+2550dupT | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr9 | 130857633 | ||||||
| chr9:130857642 | T | G | 10 | a0001c0001t0010g0005a0001c0001t0010g0043a0001c0001t0011g0041others(7): Show | 11 | HG01884.hp1 HG02055.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.549+2546T>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130857642 | |||||||
| chr9:130857778 | G | A | 1 | a0001c0003t0003g0173 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.549+2682G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130857778 | |||||||
| chr9:130857851 | G | A | 9 | a0001c0001t0001g0167a0001c0003t0003g0130a0001c0003t0003g0138others(6): Show | 9 | HG02258.hp1 HG02486.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.549+2755G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130857851 | |||||||
| chr9:130857933 | C | G | 1 | a0001c0002t0001g0028 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.549+2837C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130857933 | |||||||
| chr9:130858015 | T | G | 4 | a0001c0001t0004g0054a0001c0001t0004g0105a0001c0002t0001g0106others(1): Show | 5 | HG01109.hp1 HG01884.hp2 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.549+2919T>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130858015 | |||||||
| chr9:130858574 | A | G | 88 | a0001c0001t0001g0221a0001c0001t0001g0236a0001c0001t0002g0014others(85): Show | 94 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(91): Show |
intron_variant | MODIFIER | c.549+3478A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130858574 | |||||||
| chr9:130858645 | G | A | 2 | a0001c0003t0003g0240a0001c0003t0003g0241 | 2 | HG01167.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.549+3549G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130858645 | |||||||
| chr9:130858688 | C | T | 78 | a0001c0001t0001g0221a0001c0001t0001g0236a0001c0001t0002g0014others(75): Show | 83 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(80): Show |
intron_variant | MODIFIER | c.549+3592C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130858688 | |||||||
| chr9:130858877 | C | G | 1 | a0001c0002t0001g0025 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.549+3781C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130858877 | |||||||
| chr9:130858924 | C | T | 11 | a0001c0001t0007g0056a0001c0001t0010g0005a0001c0001t0010g0043others(8): Show | 12 | HG01884.hp1 HG02055.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.549+3828C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130858924 | |||||||
| chr9:130858971 | G | A | 5 | a0001c0001t0001g0019a0001c0001t0006g0018a0001c0001t0008g0004others(2): Show | 6 | HG00735.hp1 HG01243.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.550-3792G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130858971 | |||||||
| chr9:130859007 | G | A | 1 | a0001c0002t0001g0141 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.550-3756G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130859007 | |||||||
| chr9:130859386 | C | G | 1 | a0001c0002t0001g0135 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.550-3377C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130859386 | |||||||
| chr9:130859388 | G | A | 3 | a0001c0001t0007g0194a0001c0002t0001g0195a0006c0015t0004g0199 | 3 | HG02486.hp2 HG02615.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.550-3375G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130859388 | |||||||
| chr9:130859475 | T | C | 4 | a0001c0008t0030g0040a0001c0008t0031g0038a0001c0023t0028g0059others(1): Show | 4 | HG02280.hp1 HG03579.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.550-3288T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130859475 | |||||||
| chr9:130859525 | G | A | 2 | a0001c0001t0007g0210a0001c0009t0006g0211 | 2 | HG03195.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.550-3238G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130859525 | |||||||
| chr9:130859668 | CTTTCTTT others(13): Show |
C | 1 | a0001c0004t0022g0020 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.550-3091_550-3072d others(22): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr9 | 130859668 | ||||||
| chr9:130859672 | C | CT | 29 | a0001c0001t0001g0102a0001c0001t0001g0236a0001c0001t0002g0014others(26): Show | 31 | HG00280.hp2 HG00323.hp1 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.550-3088dupT | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr9 | 130859672 | ||||||
| chr9:130859672 | CTTTCCTT others(3): Show |
C | 1 | a0001c0003t0003g0204 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.550-3087_550-3078d others(12): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr9 | 130859672 | ||||||
| chr9:130859672 | CTTTCCTT others(4): Show |
C | 1 | a0001c0003t0003g0012 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.550-3087_550-3077d others(13): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr9 | 130859672 | ||||||
| chr9:130859672 | CTTTCCTT others(6): Show |
C | 1 | a0001c0003t0005g0244 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.550-3087_550-3075d others(15): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr9 | 130859672 | ||||||
| chr9:130859672 | CTTTCCTT others(7): Show |
C | 1 | a0001c0001t0015g0193 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.550-3087_550-3074d others(16): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr9 | 130859672 | ||||||
| chr9:130859672 | CTTTCCTT others(9): Show |
C | 15 | a0001c0001t0001g0019a0001c0001t0006g0018a0001c0001t0008g0004others(12): Show | 17 | HG00735.hp1 HG01243.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.550-3087_550-3072d others(18): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr9 | 130859672 | ||||||
| chr9:130859675 | TCC | T | 12 | a0001c0001t0007g0210a0001c0008t0012g0036a0001c0008t0030g0040others(9): Show | 12 | HG01123.hp2 HG01361.hp2 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.550-3087_550-3086d others(4): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130859675 | |||||||
| chr9:130859676 | C | T | 41 | a0001c0001t0001g0167a0001c0001t0002g0201a0001c0001t0002g0230others(38): Show | 41 | HG01081.hp1 HG01167.hp1 HG01175.hp1 others(38): Show |
intron_variant | MODIFIER | c.550-3087C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130859676 | |||||||
| chr9:130859677 | C | CT | 53 | a0001c0001t0001g0001a0001c0001t0001g0066a0001c0001t0001g0067others(50): Show | 56 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(53): Show |
intron_variant | MODIFIER | c.550-3057dupT | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr9 | 130859677 | ||||||
| chr9:130859677 | C | CTT | 9 | a0001c0001t0001g0096a0001c0001t0002g0232a0001c0002t0001g0157others(6): Show | 9 | HG01081.hp1 HG01175.hp1 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.550-3058_550-3057d others(4): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr9 | 130859677 | ||||||
| chr9:130859677 | C | CTTT | 18 | a0001c0001t0002g0230a0001c0001t0007g0176a0001c0001t0007g0205others(15): Show | 18 | HG01167.hp1 HG01891.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.550-3059_550-3057d others(5): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr9 | 130859677 | ||||||
| chr9:130859677 | C | T | 29 | a0001c0001t0001g0102a0001c0001t0001g0236a0001c0001t0002g0014others(26): Show | 31 | HG00280.hp2 HG00323.hp1 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.550-3086C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130859677 | |||||||
| chr9:130859677 | CT | C | 15 | a0001c0001t0001g0101a0001c0001t0001g0118a0001c0002t0001g0025others(12): Show | 15 | HG02698.hp2 HG02818.hp2 HG03704.hp2 others(12): Show |
intron_variant | MODIFIER | c.550-3057delT | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr9 | 130859677 | ||||||
| chr9:130859677 | CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0001g0080 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.550-3068_550-3057d others(14): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr9 | 130859677 | ||||||
| chr9:130859679 | T | C | 12 | a0001c0001t0007g0210a0001c0008t0012g0036a0001c0008t0030g0040others(9): Show | 12 | HG01123.hp2 HG01361.hp2 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.550-3084T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130859679 | |||||||
| chr9:130859684 | T | C | 2 | a0001c0002t0001g0195a0006c0015t0004g0199 | 2 | HG02615.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.550-3079T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130859684 | |||||||
| chr9:130859685 | T | C | 2 | a0001c0001t0007g0194a0001c0023t0028g0059 | 2 | HG02486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.550-3078T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130859685 | |||||||
| chr9:130859687 | T | C | 1 | a0001c0003t0003g0204 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.550-3076T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130859687 | |||||||
| chr9:130859688 | T | C | 1 | a0001c0003t0003g0012 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.550-3075T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130859688 | |||||||
| chr9:130859690 | T | C | 1 | a0001c0003t0005g0244 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.550-3073T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130859690 | |||||||
| chr9:130859691 | T | C | 1 | a0001c0001t0015g0193 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.550-3072T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130859691 | |||||||
| chr9:130859693 | T | C | 16 | a0001c0001t0001g0019a0001c0001t0006g0018a0001c0001t0008g0004others(13): Show | 18 | HG00735.hp1 HG01243.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.550-3070T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130859693 | |||||||
| chr9:130859779 | C | T | 1 | a0001c0002t0001g0025 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.550-2984C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130859779 | |||||||
| chr9:130859947 | G | C | 1 | a0001c0001t0007g0056 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.550-2816G>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130859947 | |||||||
| chr9:130859959 | G | A | 2 | a0001c0001t0002g0022a0001c0003t0003g0248 | 2 | HG02148.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.550-2804G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130859959 | |||||||
| chr9:130859963 | G | A | 1 | a0001c0001t0002g0022 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.550-2800G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130859963 | |||||||
| chr9:130859971 | T | A | 1 | a0001c0002t0001g0162 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.550-2792T>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130859971 | |||||||
| chr9:130860082 | C | G | 2 | a0001c0001t0011g0041a0001c0001t0011g0042 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.550-2681C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130860082 | |||||||
| chr9:130860112 | A | G | 3 | a0001c0001t0015g0193a0001c0008t0012g0036a0001c0020t0004g0134 | 3 | HG02630.hp1 HG03098.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.550-2651A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130860112 | |||||||
| chr9:130860130 | CT | C | 6 | a0001c0001t0001g0019a0001c0001t0006g0018a0001c0001t0008g0004others(3): Show | 7 | HG00735.hp1 HG01243.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.550-2632delT | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130860130 | |||||||
| chr9:130860177 | G | T | 2 | a0001c0001t0001g0096a0001c0001t0001g0161 | 2 | NA18977.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.550-2586G>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130860177 | |||||||
| chr9:130860245 | T | C | 13 | a0001c0001t0007g0176a0001c0001t0007g0194a0001c0001t0007g0205others(10): Show | 14 | HG01123.hp2 HG01361.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.550-2518T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130860245 | |||||||
| chr9:130860254 | A | T | 4 | a0001c0003t0003g0216a0001c0003t0020g0218a0001c0004t0004g0027others(1): Show | 4 | HG01496.hp1 HG02922.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.550-2509A>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130860254 | |||||||
| chr9:130860257 | A | G | 198 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(195): Show | 212 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.550-2506A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130860257 | |||||||
| chr9:130860355 | A | C | 4 | a0001c0001t0006g0255a0001c0001t0006g0256a0001c0001t0006g0257others(1): Show | 4 | HG02145.hp2 HG02258.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.550-2408A>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130860355 | |||||||
| chr9:130860394 | A | G | 1 | a0001c0004t0004g0107 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.550-2369A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130860394 | |||||||
| chr9:130860426 | C | T | 4 | a0001c0001t0006g0255a0001c0001t0006g0256a0001c0001t0006g0257others(1): Show | 4 | HG02145.hp2 HG02258.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.550-2337C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130860426 | |||||||
| chr9:130860599 | T | C | 1 | a0001c0001t0001g0053 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.550-2164T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130860599 | |||||||
| chr9:130860709 | T | G | 1 | a0001c0001t0026g0024 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.550-2054T>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130860709 | |||||||
| chr9:130860729 | A | G | 113 | a0001c0001t0001g0102a0001c0001t0001g0221a0001c0001t0002g0014others(110): Show | 121 | HG00280.hp2 HG00323.hp1 HG01069.hp2 others(118): Show |
intron_variant | MODIFIER | c.550-2034A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130860729 | |||||||
| chr9:130860853 | G | A | 3 | a0001c0001t0001g0127a0001c0001t0001g0224a0001c0001t0001g0225 | 3 | HG00621.hp1 NA18966.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.550-1910G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130860853 | |||||||
| chr9:130860977 | G | A | 1 | a0002c0005t0004g0212 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.550-1786G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130860977 | |||||||
| chr9:130860983 | G | A | 4 | a0001c0001t0006g0255a0001c0001t0006g0256a0001c0001t0006g0257others(1): Show | 4 | HG02145.hp2 HG02258.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.550-1780G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130860983 | |||||||
| chr9:130861009 | T | C | 1 | a0001c0010t0001g0163 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.550-1754T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130861009 | |||||||
| chr9:130861142 | C | T | 4 | a0001c0001t0011g0041a0001c0001t0011g0042a0001c0002t0001g0195others(1): Show | 4 | HG02615.hp2 HG02717.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.550-1621C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130861142 | |||||||
| chr9:130861224 | TC | T | 4 | a0001c0001t0006g0018a0001c0001t0008g0004a0001c0001t0008g0016others(1): Show | 5 | HG01243.hp2 HG02965.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.550-1538delC | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130861224 | |||||||
| chr9:130861324 | A | G | 4 | a0001c0001t0006g0255a0001c0001t0006g0256a0001c0001t0006g0257others(1): Show | 4 | HG02145.hp2 HG02258.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.550-1439A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130861324 | |||||||
| chr9:130861380 | C | T | 3 | a0001c0001t0008g0004a0001c0001t0008g0016a0001c0001t0008g0017 | 4 | HG02965.hp2 HG03516.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.550-1383C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130861380 | |||||||
| chr9:130861390 | T | C | 1 | a0001c0026t0029g0250 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.550-1373T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130861390 | |||||||
| chr9:130861424 | G | A | 1 | a0001c0003t0003g0138 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.550-1339G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130861424 | |||||||
| chr9:130861471 | A | C | 11 | a0001c0001t0004g0054a0001c0001t0004g0105a0001c0002t0001g0086others(8): Show | 12 | HG01109.hp1 HG01496.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.550-1292A>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130861471 | |||||||
| chr9:130861583 | A | G | 1 | a0001c0001t0001g0085 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.550-1180A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130861583 | |||||||
| chr9:130861847 | C | G | 1 | a0001c0003t0003g0245 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.550-916C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130861847 | |||||||
| chr9:130861996 | C | T | 5 | a0001c0001t0006g0018a0001c0001t0008g0004a0001c0001t0008g0016others(2): Show | 6 | HG01243.hp2 HG02965.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.550-767C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130861996 | |||||||
| chr9:130862022 | G | A | 1 | a0001c0003t0003g0160 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.550-741G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130862022 | |||||||
| chr9:130862036 | C | T | 1 | a0001c0001t0015g0193 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.550-727C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130862036 | |||||||
| chr9:130862070 | G | A | 11 | a0001c0001t0007g0056a0001c0001t0007g0210a0001c0004t0017g0049others(8): Show | 12 | HG01123.hp2 HG01361.hp2 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.550-693G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130862070 | |||||||
| chr9:130862098 | C | G | 2 | a0001c0001t0011g0041a0001c0001t0011g0042 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.550-665C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130862098 | |||||||
| chr9:130862132 | A | G | 11 | a0001c0001t0004g0054a0001c0001t0004g0105a0001c0002t0001g0086others(8): Show | 12 | HG01109.hp1 HG01496.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.550-631A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130862132 | |||||||
| chr9:130862248 | A | G | 8 | a0001c0001t0010g0005a0001c0001t0010g0043a0001c0002t0001g0025others(5): Show | 9 | HG01884.hp1 HG02055.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.550-515A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130862248 | |||||||
| chr9:130862262 | G | A | 40 | a0001c0001t0004g0054a0001c0001t0004g0105a0001c0001t0006g0018others(37): Show | 43 | HG01109.hp1 HG01123.hp2 HG01243.hp2 others(40): Show |
intron_variant | MODIFIER | c.550-501G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130862262 | |||||||
| chr9:130862419 | T | C | 7 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0023others(4): Show | 7 | HG01106.hp1 HG01192.hp2 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.550-344T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130862419 | |||||||
| chr9:130862474 | G | A | 1 | a0001c0008t0012g0036 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.550-289G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130862474 | |||||||
| chr9:130862625 | AAC | A | 9 | a0001c0001t0006g0255a0001c0001t0006g0256a0001c0001t0006g0257others(6): Show | 9 | HG02145.hp2 HG02258.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.550-135_550-134del others(2): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr9 | 130862625 | ||||||
| chr9:130862687 | C | T | 4 | a0001c0001t0006g0018a0001c0001t0008g0004a0001c0001t0008g0016others(1): Show | 5 | HG01243.hp2 HG02965.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.550-76C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130862687 | |||||||
| chr9:130862702 | A | C | 1 | a0001c0002t0001g0060 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.550-61A>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130862702 | |||||||
| chr9:130863051 | C | G | 1 | a0001c0001t0001g0085 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.822+16C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130863051 | |||||||
| chr9:130863145 | C | T | 1 | a0001c0025t0018g0047 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.822+110C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130863145 | |||||||
| chr9:130863222 | C | T | 24 | a0001c0001t0001g0133a0001c0001t0001g0158a0001c0001t0001g0191others(21): Show | 24 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(21): Show |
intron_variant | MODIFIER | c.822+187C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130863222 | |||||||
| chr9:130863237 | A | G | 3 | a0001c0003t0003g0012a0001c0003t0003g0160a0001c0003t0016g0192 | 4 | HG02717.hp1 HG02922.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.822+202A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130863237 | |||||||
| chr9:130863604 | C | T | 1 | a0001c0026t0029g0250 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.822+569C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130863604 | |||||||
| chr9:130863633 | C | G | 4 | a0001c0008t0012g0036a0001c0008t0030g0040a0001c0008t0031g0038others(1): Show | 4 | HG02280.hp1 HG02630.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.822+598C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130863633 | |||||||
| chr9:130864158 | C | T | 1 | a0008c0016t0001g0155 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.822+1123C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130864158 | |||||||
| chr9:130864223 | C | T | 2 | a0001c0001t0010g0005a0001c0001t0010g0043 | 3 | HG02809.hp2 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.822+1188C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130864223 | |||||||
| chr9:130864224 | C | G | 8 | a0001c0001t0010g0005a0001c0001t0010g0043a0001c0002t0001g0025others(5): Show | 9 | HG01884.hp1 HG02055.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.822+1189C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130864224 | |||||||
| chr9:130864247 | T | A | 1 | a0001c0001t0001g0221 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.822+1212T>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130864247 | |||||||
| chr9:130864348 | G | T | 32 | a0001c0001t0007g0176a0001c0001t0007g0194a0001c0001t0007g0205others(29): Show | 34 | HG01074.hp2 HG01081.hp1 HG01175.hp1 others(31): Show |
intron_variant | MODIFIER | c.822+1313G>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130864348 | |||||||
| chr9:130864394 | G | A | 1 | a0001c0001t0015g0193 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.822+1359G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130864394 | |||||||
| chr9:130864465 | A | G | 1 | a0001c0001t0002g0238 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.822+1430A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130864465 | |||||||
| chr9:130864591 | C | G | 1 | a0001c0001t0021g0187 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.822+1556C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130864591 | |||||||
| chr9:130864744 | G | A | 34 | a0001c0001t0001g0007a0001c0001t0001g0062a0001c0001t0001g0067others(31): Show | 36 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(33): Show |
intron_variant | MODIFIER | c.822+1709G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130864744 | |||||||
| chr9:130864862 | C | G | 10 | a0001c0001t0004g0054a0001c0001t0004g0105a0001c0002t0001g0106others(7): Show | 11 | HG01109.hp1 HG01496.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.822+1827C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130864862 | |||||||
| chr9:130864879 | T | C | 1 | a0001c0002t0001g0111 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.822+1844T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130864879 | |||||||
| chr9:130864896 | C | T | 4 | a0001c0008t0012g0036a0001c0008t0030g0040a0001c0008t0031g0038others(1): Show | 4 | HG02280.hp1 HG02630.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.822+1861C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130864896 | |||||||
| chr9:130864980 | G | A | 2 | a0001c0001t0002g0227a0001c0002t0001g0026 | 2 | NA18978.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.822+1945G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130864980 | |||||||
| chr9:130865002 | T | C | 1 | a0001c0023t0028g0059 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.822+1967T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130865002 | |||||||
| chr9:130865230 | G | A | 1 | a0001c0001t0001g0051 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.822+2195G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130865230 | |||||||
| chr9:130865238 | G | A | 2 | a0001c0001t0001g0133a0001c0002t0001g0157 | 2 | HG02074.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.822+2203G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130865238 | |||||||
| chr9:130865270 | A | G | 2 | a0001c0001t0011g0041a0001c0001t0011g0042 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.822+2235A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130865270 | |||||||
| chr9:130865327 | G | A | 5 | a0001c0001t0006g0255a0001c0001t0006g0256a0001c0001t0006g0257others(2): Show | 5 | HG02145.hp2 HG02258.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.822+2292G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130865327 | |||||||
| chr9:130865549 | C | A | 1 | a0001c0001t0001g0209 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.822+2514C>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130865549 | |||||||
| chr9:130865576 | G | A | 1 | a0001c0023t0028g0059 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.822+2541G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130865576 | |||||||
| chr9:130865676 | G | T | 2 | a0001c0001t0010g0005a0001c0001t0010g0043 | 3 | HG02809.hp2 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.822+2641G>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130865676 | |||||||
| chr9:130865746 | C | CA | 76 | a0001c0001t0001g0066a0001c0001t0001g0075a0001c0001t0001g0099others(73): Show | 81 | HG00280.hp2 HG00323.hp1 HG01071.hp2 others(78): Show |
intron_variant | MODIFIER | c.822+2733dupA | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr9 | 130865746 | ||||||
| chr9:130865746 | C | CAA | 14 | a0001c0001t0002g0166a0001c0001t0002g0220a0001c0001t0002g0232others(11): Show | 14 | HG01167.hp1 HG01175.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.822+2732_822+2733d others(4): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr9 | 130865746 | ||||||
| chr9:130865746 | CA | C | 11 | a0001c0001t0002g0203a0001c0001t0004g0054a0001c0001t0004g0105others(8): Show | 12 | HG01109.hp1 HG01256.hp1 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.822+2733delA | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr9 | 130865746 | ||||||
| chr9:130865845 | G | T | 1 | a0001c0002t0001g0028 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.822+2810G>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130865845 | |||||||
| chr9:130865873 | G | A | 5 | a0001c0001t0006g0255a0001c0001t0006g0256a0001c0001t0006g0257others(2): Show | 5 | HG02145.hp2 HG02258.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.822+2838G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130865873 | |||||||
| chr9:130865908 | C | G | 1 | a0001c0001t0001g0085 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.822+2873C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130865908 | |||||||
| chr9:130865999 | T | G | 1 | a0001c0001t0015g0193 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.822+2964T>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130865999 | |||||||
| chr9:130866239 | T | C | 58 | a0001c0001t0004g0054a0001c0001t0004g0105a0001c0001t0007g0176others(55): Show | 62 | HG01074.hp2 HG01081.hp1 HG01099.hp1 others(59): Show |
intron_variant | MODIFIER | c.822+3204T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130866239 | |||||||
| chr9:130866617 | T | C | 6 | a0001c0002t0001g0025a0001c0002t0009g0044a0001c0002t0009g0046others(3): Show | 6 | HG01884.hp1 HG02055.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.822+3582T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130866617 | |||||||
| chr9:130866699 | A | T | 2 | a0001c0001t0015g0193a0001c0011t0013g0215 | 2 | HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.822+3664A>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130866699 | |||||||
| chr9:130866713 | T | G | 2 | a0001c0001t0011g0041a0001c0001t0011g0042 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.822+3678T>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130866713 | |||||||
| chr9:130867165 | T | C | 15 | a0001c0001t0004g0054a0001c0001t0004g0105a0001c0001t0006g0255others(12): Show | 16 | HG01109.hp1 HG01496.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.822+4130T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130867165 | |||||||
| chr9:130867383 | C | A | 1 | a0001c0001t0002g0227 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.822+4348C>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130867383 | |||||||
| chr9:130867549 | T | C | 5 | a0001c0001t0006g0255a0001c0001t0006g0256a0001c0001t0006g0257others(2): Show | 5 | HG02145.hp2 HG02258.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.822+4514T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130867549 | |||||||
| chr9:130867648 | T | C | 15 | a0001c0001t0004g0054a0001c0001t0004g0105a0001c0001t0006g0255others(12): Show | 16 | HG01109.hp1 HG01496.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.823-4481T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130867648 | |||||||
| chr9:130867712 | G | T | 1 | a0001c0026t0029g0250 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.823-4417G>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130867712 | |||||||
| chr9:130867937 | G | GT | 82 | a0001c0001t0001g0102a0001c0001t0001g0221a0001c0001t0002g0014others(79): Show | 87 | HG00280.hp2 HG00323.hp1 HG00735.hp2 others(84): Show |
intron_variant | MODIFIER | c.823-4179dupT | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr9 | 130867937 | ||||||
| chr9:130867937 | G | GTT | 9 | a0001c0001t0010g0005a0001c0001t0010g0043a0001c0001t0011g0041others(6): Show | 10 | HG01884.hp1 HG02055.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.823-4180_823-4179d others(4): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr9 | 130867937 | ||||||
| chr9:130868001 | C | G | 5 | a0001c0001t0006g0255a0001c0001t0006g0256a0001c0001t0006g0257others(2): Show | 5 | HG02145.hp2 HG02258.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.823-4128C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130868001 | |||||||
| chr9:130868029 | G | A | 14 | a0001c0001t0004g0054a0001c0001t0004g0105a0001c0001t0006g0255others(11): Show | 15 | HG01109.hp1 HG01496.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.823-4100G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130868029 | |||||||
| chr9:130868082 | C | T | 16 | a0001c0001t0004g0054a0001c0001t0004g0105a0001c0001t0006g0255others(13): Show | 17 | HG01109.hp1 HG01496.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.823-4047C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130868082 | |||||||
| chr9:130868149 | A | G | 1 | a0001c0002t0001g0128 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.823-3980A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130868149 | |||||||
| chr9:130868179 | C | T | 23 | a0001c0001t0001g0133a0001c0001t0001g0158a0001c0002t0001g0064others(20): Show | 23 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(20): Show |
intron_variant | MODIFIER | c.823-3950C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130868179 | |||||||
| chr9:130868246 | C | T | 3 | a0001c0001t0007g0056a0001c0001t0026g0024a0007c0014t0008g0037 | 3 | HG02572.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.823-3883C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130868246 | |||||||
| chr9:130868267 | G | A | 111 | a0001c0001t0001g0221a0001c0001t0002g0014a0001c0001t0002g0015others(108): Show | 119 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(116): Show |
intron_variant | MODIFIER | c.823-3862G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130868267 | |||||||
| chr9:130868306 | G | T | 10 | a0001c0001t0007g0210a0001c0004t0017g0049a0001c0004t0022g0020others(7): Show | 11 | HG01123.hp2 HG01361.hp2 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.823-3823G>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130868306 | |||||||
| chr9:130868438 | G | T | 4 | a0001c0001t0006g0018a0001c0001t0008g0004a0001c0001t0008g0016others(1): Show | 5 | HG01243.hp2 HG02965.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.823-3691G>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130868438 | |||||||
| chr9:130868520 | C | CT | 17 | a0001c0001t0001g0073a0001c0001t0001g0096a0001c0001t0001g0101others(14): Show | 18 | HG01109.hp1 HG01258.hp2 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.823-3588dupT | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr9 | 130868520 | ||||||
| chr9:130868520 | CT | C | 47 | a0001c0001t0001g0066a0001c0001t0002g0228a0001c0001t0006g0018others(44): Show | 50 | HG00323.hp1 HG01167.hp1 HG01243.hp2 others(47): Show |
intron_variant | MODIFIER | c.823-3588delT | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr9 | 130868520 | ||||||
| chr9:130868520 | CTTTTTTT others(3): Show |
C | 14 | a0001c0001t0007g0210a0001c0003t0003g0173a0001c0003t0003g0216others(11): Show | 15 | HG01123.hp2 HG01361.hp2 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.823-3597_823-3588d others(12): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr9 | 130868520 | ||||||
| chr9:130868526 | T | C | 1 | a0001c0001t0007g0056 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.823-3603T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130868526 | |||||||
| chr9:130868527 | T | C | 7 | a0001c0001t0007g0176a0001c0001t0007g0194a0001c0001t0007g0205others(4): Show | 7 | HG02486.hp2 HG02559.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.823-3602T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130868527 | |||||||
| chr9:130868541 | T | C | 10 | a0001c0001t0001g0161a0001c0001t0010g0005a0001c0001t0010g0043others(7): Show | 11 | HG01884.hp1 HG02055.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.823-3588T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130868541 | |||||||
| chr9:130868579 | A | G | 2 | a0001c0001t0015g0193a0001c0011t0013g0215 | 2 | HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.823-3550A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130868579 | |||||||
| chr9:130868591 | T | C | 1 | a0001c0023t0028g0059 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.823-3538T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130868591 | |||||||
| chr9:130868605 | C | T | 2 | a0001c0003t0003g0216a0001c0003t0020g0218 | 2 | HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.823-3524C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130868605 | |||||||
| chr9:130868644 | C | T | 1 | a0001c0002t0001g0104 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.823-3485C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130868644 | |||||||
| chr9:130868645 | T | C | 112 | a0001c0001t0001g0167a0001c0001t0001g0221a0001c0001t0002g0014others(109): Show | 120 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(117): Show |
intron_variant | MODIFIER | c.823-3484T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130868645 | |||||||
| chr9:130868730 | G | A | 1 | a0001c0010t0001g0170 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.823-3399G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130868730 | |||||||
| chr9:130868833 | C | T | 1 | a0001c0010t0001g0165 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.823-3296C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130868833 | |||||||
| chr9:130868845 | G | T | 13 | a0001c0003t0003g0012a0001c0003t0003g0130a0001c0003t0003g0138others(10): Show | 14 | HG01167.hp1 HG02258.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.823-3284G>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130868845 | |||||||
| chr9:130869028 | G | A | 15 | a0001c0001t0010g0005a0001c0001t0010g0043a0001c0001t0011g0041others(12): Show | 16 | HG01884.hp1 HG02055.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.823-3101G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130869028 | |||||||
| chr9:130869040 | G | T | 4 | a0001c0001t0006g0018a0001c0001t0008g0004a0001c0001t0008g0016others(1): Show | 5 | HG01243.hp2 HG02965.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.823-3089G>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130869040 | |||||||
| chr9:130869051 | C | T | 1 | a0001c0003t0003g0130 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.823-3078C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130869051 | |||||||
| chr9:130869099 | G | A | 1 | a0001c0001t0008g0016 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.823-3030G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130869099 | |||||||
| chr9:130869116 | G | A | 97 | a0001c0001t0001g0221a0001c0001t0002g0014a0001c0001t0002g0015others(94): Show | 104 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(101): Show |
intron_variant | MODIFIER | c.823-3013G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130869116 | |||||||
| chr9:130869121 | C | T | 1 | a0001c0001t0001g0082 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.823-3008C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130869121 | |||||||
| chr9:130869123 | C | T | 5 | a0001c0001t0007g0176a0001c0001t0007g0194a0001c0001t0007g0205others(2): Show | 5 | HG02486.hp2 HG02559.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.823-3006C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130869123 | |||||||
| chr9:130869166 | CA | C | 111 | a0001c0001t0001g0221a0001c0001t0002g0014a0001c0001t0002g0015others(108): Show | 119 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(116): Show |
intron_variant | MODIFIER | c.823-2952delA | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr9 | 130869166 | ||||||
| chr9:130869176 | A | G | 1 | a0001c0011t0013g0215 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.823-2953A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130869176 | |||||||
| chr9:130869275 | C | T | 4 | a0001c0001t0006g0018a0001c0001t0008g0004a0001c0001t0008g0016others(1): Show | 5 | HG01243.hp2 HG02965.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.823-2854C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130869275 | |||||||
| chr9:130869285 | G | A | 97 | a0001c0001t0001g0221a0001c0001t0002g0014a0001c0001t0002g0015others(94): Show | 104 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(101): Show |
intron_variant | MODIFIER | c.823-2844G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130869285 | |||||||
| chr9:130869337 | C | T | 14 | a0001c0001t0007g0210a0001c0003t0003g0173a0001c0003t0003g0216others(11): Show | 15 | HG01123.hp2 HG01361.hp2 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.823-2792C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130869337 | |||||||
| chr9:130869524 | G | A | 80 | a0001c0001t0001g0221a0001c0001t0002g0014a0001c0001t0002g0015others(77): Show | 86 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(83): Show |
intron_variant | MODIFIER | c.823-2605G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130869524 | |||||||
| chr9:130869537 | T | C | 9 | a0001c0001t0010g0005a0001c0001t0010g0043a0001c0002t0001g0025others(6): Show | 10 | HG01884.hp1 HG02055.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.823-2592T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130869537 | |||||||
| chr9:130869814 | T | C | 3 | a0001c0001t0007g0056a0001c0001t0026g0024a0007c0014t0008g0037 | 3 | HG02572.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.823-2315T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130869814 | |||||||
| chr9:130870053 | G | A | 1 | a0001c0019t0001g0129 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.823-2076G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130870053 | |||||||
| chr9:130870100 | A | G | 81 | a0001c0001t0001g0221a0001c0001t0002g0014a0001c0001t0002g0015others(78): Show | 87 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(84): Show |
intron_variant | MODIFIER | c.823-2029A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130870100 | |||||||
| chr9:130870172 | C | A | 1 | a0001c0002t0001g0106 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.823-1957C>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130870172 | |||||||
| chr9:130870283 | A | G | 9 | a0001c0001t0004g0054a0001c0001t0004g0105a0001c0002t0001g0106others(6): Show | 10 | HG01109.hp1 HG01496.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.823-1846A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130870283 | |||||||
| chr9:130870296 | AT | A | 3 | a0001c0001t0007g0056a0001c0001t0026g0024a0007c0014t0008g0037 | 3 | HG02572.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.823-1832delT | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130870296 | |||||||
| chr9:130870386 | G | A | 1 | a0001c0007t0005g0243 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.823-1743G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130870386 | |||||||
| chr9:130870478 | C | T | 1 | a0002c0005t0004g0214 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.823-1651C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130870478 | |||||||
| chr9:130870524 | A | C | 1 | a0001c0023t0028g0059 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.823-1605A>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130870524 | |||||||
| chr9:130870528 | C | A | 8 | a0001c0001t0004g0054a0001c0002t0001g0106a0001c0004t0004g0009others(5): Show | 9 | HG01496.hp1 HG01884.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.823-1601C>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130870528 | |||||||
| chr9:130870544 | G | A | 1 | a0001c0002t0001g0128 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.823-1585G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130870544 | |||||||
| chr9:130870635 | G | A | 2 | a0001c0001t0015g0193a0001c0011t0013g0215 | 2 | HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.823-1494G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130870635 | |||||||
| chr9:130870673 | G | A | 50 | a0001c0001t0001g0221a0001c0001t0002g0014a0001c0001t0002g0015others(47): Show | 54 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(51): Show |
intron_variant | MODIFIER | c.823-1456G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130870673 | |||||||
| chr9:130870730 | T | C | 92 | a0001c0001t0001g0221a0001c0001t0002g0014a0001c0001t0002g0015others(89): Show | 99 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(96): Show |
intron_variant | MODIFIER | c.823-1399T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130870730 | |||||||
| chr9:130870804 | G | A | 1 | a0001c0001t0025g0222 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.823-1325G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130870804 | |||||||
| chr9:130870983 | G | A | 7 | a0001c0001t0011g0041a0001c0001t0011g0042a0001c0001t0012g0149others(4): Show | 7 | HG02280.hp1 HG02630.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.823-1146G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130870983 | |||||||
| chr9:130871184 | C | T | 5 | a0001c0006t0005g0055a0001c0006t0005g0152a0001c0006t0005g0153others(2): Show | 5 | HG02109.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.823-945C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130871184 | |||||||
| chr9:130871198 | C | T | 1 | a0001c0002t0001g0094 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.823-931C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130871198 | |||||||
| chr9:130871395 | G | A | 1 | a0001c0002t0001g0032 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.823-734G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130871395 | |||||||
| chr9:130871404 | C | T | 5 | a0001c0001t0007g0176a0001c0001t0007g0194a0001c0001t0007g0205others(2): Show | 5 | HG02486.hp2 HG02559.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.823-725C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130871404 | |||||||
| chr9:130871532 | T | A | 1 | a0001c0002t0001g0111 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.823-597T>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130871532 | |||||||
| chr9:130871570 | C | G | 1 | a0001c0001t0001g0133 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.823-559C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130871570 | |||||||
| chr9:130871778 | T | C | 1 | a0001c0002t0001g0169 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.823-351T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130871778 | |||||||
| chr9:130871915 | G | A | 10 | a0001c0001t0001g0007a0001c0001t0001g0067a0001c0001t0001g0071others(7): Show | 11 | HG00280.hp2 HG00558.hp1 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.823-214G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130871915 | |||||||
| chr9:130872027 | C | T | 4 | a0001c0001t0006g0018a0001c0001t0008g0004a0001c0001t0008g0016others(1): Show | 5 | HG01243.hp2 HG02965.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.823-102C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130872027 | |||||||
| chr9:130872070 | C | T | 4 | a0001c0001t0006g0018a0001c0001t0008g0004a0001c0001t0008g0016others(1): Show | 5 | HG01243.hp2 HG02965.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.823-59C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130872070 | |||||||
| chr9:130872275 | G | A | 2 | a0001c0001t0011g0041a0001c0001t0011g0042 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.907+62G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 5/10 | chr9 | 130872275 | |||||||
| chr9:130872287 | G | A | 12 | a0001c0001t0006g0018a0001c0001t0007g0176a0001c0001t0007g0194others(9): Show | 13 | HG01243.hp2 HG02109.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.907+74G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 5/10 | chr9 | 130872287 | |||||||
| chr9:130872290 | C | T | 2 | a0001c0001t0012g0149a0001c0008t0012g0036 | 2 | HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.907+77C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 5/10 | chr9 | 130872290 | |||||||
| chr9:130872291 | G | A | 5 | a0001c0001t0002g0074a0001c0001t0002g0220a0001c0001t0002g0229others(2): Show | 5 | NA18963.hp1 NA18971.hp1 NA19065.hp1 others(2): Show |
intron_variant | MODIFIER | c.907+78G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 5/10 | chr9 | 130872291 | |||||||
| chr9:130872311 | C | T | 2 | a0001c0002t0001g0113a0001c0002t0001g0188 | 2 | HG01256.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.907+98C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 5/10 | chr9 | 130872311 | |||||||
| chr9:130872336 | C | T | 2 | a0001c0001t0012g0149a0001c0008t0012g0036 | 2 | HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.907+123C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 5/10 | chr9 | 130872336 | |||||||
| chr9:130872337 | G | A | 1 | a0001c0026t0029g0250 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.907+124G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 5/10 | chr9 | 130872337 | |||||||
| chr9:130872347 | C | T | 36 | a0001c0001t0001g0221a0001c0001t0002g0014a0001c0001t0002g0015others(33): Show | 39 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.907+134C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 5/10 | chr9 | 130872347 | |||||||
| chr9:130872409 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.907+196G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 5/10 | chr9 | 130872409 | |||||||
| chr9:130872685 | A | G | 3 | a0001c0001t0002g0227a0001c0002t0001g0026a0001c0002t0001g0034 | 3 | NA18977.hp1 NA18978.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.908-175A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 5/10 | chr9 | 130872685 | |||||||
| chr9:130872696 | A | G | 54 | a0001c0001t0001g0221a0001c0001t0002g0014a0001c0001t0002g0015others(51): Show | 58 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(55): Show |
intron_variant | MODIFIER | c.908-164A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 5/10 | chr9 | 130872696 | |||||||
| chr9:130872815 | T | C | 7 | a0001c0001t0006g0255a0001c0001t0006g0256a0001c0001t0006g0257others(4): Show | 7 | HG02145.hp2 HG02258.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.908-45T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 5/10 | chr9 | 130872815 | |||||||
| chr9:130873196 | C | T | 3 | a0001c0001t0007g0056a0001c0001t0026g0024a0007c0014t0008g0037 | 3 | HG02572.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1085+159C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 6/10 | chr9 | 130873196 | |||||||
| chr9:130873252 | C | G | 1 | a0001c0001t0001g0063 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1085+215C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 6/10 | chr9 | 130873252 | |||||||
| chr9:130873286 | G | T | 3 | a0001c0001t0007g0056a0001c0001t0026g0024a0007c0014t0008g0037 | 3 | HG02572.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1085+249G>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 6/10 | chr9 | 130873286 | |||||||
| chr9:130873418 | G | A | 2 | a0001c0004t0004g0107a0001c0004t0004g0108 | 2 | HG02818.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1085+381G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 6/10 | chr9 | 130873418 | |||||||
| chr9:130873440 | C | T | 1 | a0001c0001t0006g0018 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1085+403C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 6/10 | chr9 | 130873440 | |||||||
| chr9:130873778 | C | T | 2 | a0001c0001t0015g0193a0001c0011t0013g0215 | 2 | HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1085+741C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 6/10 | chr9 | 130873778 | |||||||
| chr9:130874120 | C | G | 1 | a0001c0001t0001g0167 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1086-748C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 6/10 | chr9 | 130874120 | |||||||
| chr9:130874170 | G | A | 5 | a0001c0001t0006g0255a0001c0001t0006g0256a0001c0001t0006g0257others(2): Show | 5 | HG02145.hp2 HG02258.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1086-698G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 6/10 | chr9 | 130874170 | |||||||
| chr9:130874195 | C | A | 4 | a0001c0001t0006g0018a0001c0001t0008g0004a0001c0001t0008g0016others(1): Show | 5 | HG01243.hp2 HG02965.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1086-673C>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 6/10 | chr9 | 130874195 | |||||||
| chr9:130874362 | C | A | 2 | a0001c0002t0001g0092a0001c0002t0001g0094 | 2 | HG00280.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.1086-506C>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 6/10 | chr9 | 130874362 | |||||||
| chr9:130874379 | C | T | 29 | a0001c0001t0006g0018a0001c0001t0007g0210a0001c0001t0008g0004others(26): Show | 32 | HG01123.hp2 HG01243.hp2 HG01361.hp2 others(29): Show |
intron_variant | MODIFIER | c.1086-489C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 6/10 | chr9 | 130874379 | |||||||
| chr9:130874461 | C | T | 112 | a0001c0001t0001g0221a0001c0001t0002g0014a0001c0001t0002g0015others(109): Show | 120 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(117): Show |
intron_variant | MODIFIER | c.1086-407C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 6/10 | chr9 | 130874461 | |||||||
| chr9:130874502 | C | T | 1 | a0001c0001t0007g0194 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1086-366C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 6/10 | chr9 | 130874502 | |||||||
| chr9:130874541 | C | A | 2 | a0001c0001t0015g0193a0001c0011t0013g0215 | 2 | HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1086-327C>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 6/10 | chr9 | 130874541 | |||||||
| chr9:130874594 | G | C | 4 | a0001c0001t0006g0018a0001c0001t0008g0004a0001c0001t0008g0016others(1): Show | 5 | HG01243.hp2 HG02965.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1086-274G>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 6/10 | chr9 | 130874594 | |||||||
| chr9:130875092 | A | G | 1 | a0001c0002t0001g0146 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1270+40A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130875092 | |||||||
| chr9:130875152 | G | GT | 8 | a0001c0001t0007g0176a0001c0001t0007g0194a0001c0001t0007g0205others(5): Show | 8 | HG02109.hp2 HG02451.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1270+107dupT | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 130875152 | ||||||
| chr9:130875163 | A | G | 2 | a0001c0001t0002g0139a0001c0001t0002g0156 | 2 | HG00323.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1270+111A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130875163 | |||||||
| chr9:130875165 | G | A | 34 | a0001c0001t0006g0018a0001c0001t0007g0210a0001c0001t0008g0004others(31): Show | 37 | HG01123.hp2 HG01243.hp2 HG01361.hp2 others(34): Show |
intron_variant | MODIFIER | c.1270+113G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130875165 | |||||||
| chr9:130875203 | G | A | 2 | a0001c0001t0012g0149a0001c0008t0012g0036 | 2 | HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1270+151G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130875203 | |||||||
| chr9:130875220 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1270+168C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130875220 | |||||||
| chr9:130875244 | C | T | 23 | a0001c0001t0001g0133a0001c0001t0001g0158a0001c0002t0001g0064others(20): Show | 23 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(20): Show |
intron_variant | MODIFIER | c.1270+192C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130875244 | |||||||
| chr9:130875446 | CT | C | 95 | a0001c0001t0001g0075a0001c0001t0001g0143a0001c0001t0001g0221others(92): Show | 102 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(99): Show |
intron_variant | MODIFIER | c.1270+410delT | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 130875446 | ||||||
| chr9:130875446 | CTT | C | 5 | a0001c0001t0006g0255a0001c0001t0006g0256a0001c0001t0006g0257others(2): Show | 5 | HG02145.hp2 HG02258.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1270+409_1270+410d others(4): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 130875446 | ||||||
| chr9:130875451 | T | C | 14 | a0001c0001t0007g0210a0001c0003t0003g0173a0001c0003t0003g0216others(11): Show | 15 | HG01123.hp2 HG01361.hp2 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.1270+399T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130875451 | |||||||
| chr9:130875452 | T | C | 93 | a0001c0001t0001g0221a0001c0001t0002g0014a0001c0001t0002g0015others(90): Show | 100 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(97): Show |
intron_variant | MODIFIER | c.1270+400T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130875452 | |||||||
| chr9:130875536 | C | A | 7 | a0001c0001t0002g0014a0001c0001t0002g0201a0001c0001t0002g0202others(4): Show | 8 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1270+484C>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130875536 | |||||||
| chr9:130875596 | G | A | 1 | a0001c0006t0005g0055 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1270+544G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130875596 | |||||||
| chr9:130875641 | A | G | 1 | a0001c0004t0017g0049 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1270+589A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130875641 | |||||||
| chr9:130875846 | C | T | 5 | a0001c0001t0012g0149a0001c0008t0012g0036a0001c0008t0030g0040others(2): Show | 5 | HG02280.hp1 HG02630.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1270+794C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130875846 | |||||||
| chr9:130875931 | G | A | 4 | a0001c0001t0007g0056a0001c0001t0010g0043a0001c0001t0026g0024others(1): Show | 4 | HG02572.hp2 HG02809.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1270+879G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130875931 | |||||||
| chr9:130875987 | CCGGCTAA others(21): Show |
C | 1 | a0001c0001t0001g0119 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1270+939_1270+966d others(30): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 130875987 | ||||||
| chr9:130876015 | A | G | 17 | a0001c0001t0006g0255a0001c0001t0006g0256a0001c0001t0006g0257others(14): Show | 18 | HG01123.hp2 HG01361.hp2 HG01433.hp2 others(15): Show |
intron_variant | MODIFIER | c.1270+963A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130876015 | |||||||
| chr9:130876139 | T | C | 29 | a0001c0001t0001g0221a0001c0001t0002g0014a0001c0001t0002g0015others(26): Show | 31 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.1270+1087T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130876139 | |||||||
| chr9:130876162 | G | GT | 10 | a0001c0002t0001g0026a0001c0002t0001g0028a0001c0002t0001g0031others(7): Show | 10 | HG00642.hp1 HG02698.hp2 HG04199.hp2 others(7): Show |
intron_variant | MODIFIER | c.1270+1119dupT | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 130876162 | ||||||
| chr9:130876323 | C | T | 1 | a0006c0015t0004g0199 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1270+1271C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130876323 | |||||||
| chr9:130876353 | G | A | 2 | a0001c0001t0001g0008a0001c0001t0001g0099 | 3 | HG01934.hp1 HG02148.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1270+1301G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130876353 | |||||||
| chr9:130876411 | C | CTTTTCT | 35 | a0001c0001t0006g0018a0001c0001t0006g0255a0001c0001t0006g0256others(32): Show | 38 | HG01123.hp2 HG01243.hp2 HG01361.hp2 others(35): Show |
intron_variant | MODIFIER | c.1270+1363_1270+136 others(10): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 130876411 | ||||||
| chr9:130876411 | C | CTTTTT | 37 | a0001c0001t0004g0054a0001c0001t0004g0105a0001c0002t0001g0106others(34): Show | 40 | HG01074.hp2 HG01081.hp1 HG01099.hp1 others(37): Show |
intron_variant | MODIFIER | c.1270+1367_1270+137 others(9): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 130876411 | ||||||
| chr9:130876411 | C | CTTTTTT | 32 | a0001c0001t0001g0221a0001c0001t0002g0014a0001c0001t0002g0015others(29): Show | 34 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.1270+1366_1270+137 others(10): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 130876411 | ||||||
| chr9:130876411 | C | CTTTTTTT others(1): Show |
8 | a0001c0001t0007g0176a0001c0001t0007g0194a0001c0001t0007g0205others(5): Show | 8 | HG02109.hp2 HG02451.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1270+1364_1270+137 others(12): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 130876411 | ||||||
| chr9:130876585 | A | AT | 9 | a0001c0001t0004g0054a0001c0001t0004g0105a0001c0002t0001g0106others(6): Show | 10 | HG01109.hp1 HG01496.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.1270+1540dupT | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 130876585 | ||||||
| chr9:130876594 | T | C | 23 | a0001c0001t0004g0054a0001c0001t0004g0105a0001c0001t0006g0255others(20): Show | 25 | HG00639.hp1 HG01109.hp1 HG01123.hp2 others(22): Show |
intron_variant | MODIFIER | c.1270+1542T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130876594 | |||||||
| chr9:130876666 | C | G | 1 | a0001c0001t0008g0016 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1270+1614C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130876666 | |||||||
| chr9:130876701 | G | A | 1 | a0001c0002t0001g0109 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1270+1649G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130876701 | |||||||
| chr9:130876733 | C | CT | 47 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0061others(44): Show | 52 | HG00639.hp2 HG00735.hp1 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.1271-1659dupT | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 130876733 | ||||||
| chr9:130876733 | C | CTTTTT | 24 | a0001c0003t0003g0012a0001c0003t0003g0138a0001c0003t0003g0147others(21): Show | 26 | HG01074.hp2 HG01099.hp1 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.1271-1663_1271-165 others(9): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 130876733 | ||||||
| chr9:130876733 | C | CTTTTTTT others(4): Show |
1 | a0001c0011t0013g0215 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1271-1669_1271-165 others(15): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 130876733 | ||||||
| chr9:130876733 | CT | C | 21 | a0001c0001t0001g0191a0001c0001t0004g0054a0001c0001t0004g0105others(18): Show | 23 | HG00558.hp1 HG00639.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.1271-1659delT | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 130876733 | ||||||
| chr9:130876733 | CTT | C | 7 | a0001c0001t0001g0209a0001c0001t0006g0018a0001c0001t0007g0056others(4): Show | 8 | HG01243.hp2 HG02572.hp2 HG02698.hp1 others(5): Show |
intron_variant | MODIFIER | c.1271-1660_1271-165 others(6): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 130876733 | ||||||
| chr9:130876733 | CTTTT | C | 6 | a0001c0001t0007g0176a0001c0001t0007g0194a0001c0001t0007g0205others(3): Show | 6 | HG02486.hp2 HG02559.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1271-1662_1271-165 others(8): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 130876733 | ||||||
| chr9:130876733 | CTTTTTTT others(3): Show |
C | 1 | a0001c0002t0001g0081 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1271-1668_1271-165 others(14): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 130876733 | ||||||
| chr9:130876738 | T | C | 1 | a0001c0018t0009g0045 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1271-1677T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130876738 | |||||||
| chr9:130876746 | TTTTTTTT others(1055): Show |
T | 6 | a0001c0003t0003g0130a0001c0003t0003g0183a0001c0003t0003g0219others(3): Show | 6 | HG01081.hp1 HG01175.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1271-1658_1271-597 others(3): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 130876746 | ||||||
| chr9:130876775 | C | T | 5 | a0001c0001t0007g0176a0001c0001t0007g0194a0001c0001t0007g0205others(2): Show | 5 | HG02486.hp2 HG02559.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1271-1640C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130876775 | |||||||
| chr9:130876782 | GCTGGAGT others(1063): Show |
G | 24 | a0001c0003t0003g0012a0001c0003t0003g0138a0001c0003t0003g0147others(21): Show | 26 | HG01074.hp2 HG01099.hp1 HG01255.hp1 others(23): Show |
intron_variant | MODIFIER | c.1271-1617_1271-548 others(3): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 130876782 | ||||||
| chr9:130876798 | A | G | 1 | a0001c0001t0006g0256 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1271-1617A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130876798 | |||||||
| chr9:130876798 | A | T | 2 | a0001c0003t0003g0240a0001c0003t0003g0241 | 2 | HG01167.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1271-1617A>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130876798 | |||||||
| chr9:130876805 | C | T | 2 | a0001c0003t0003g0240a0001c0003t0003g0241 | 2 | HG01167.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1271-1610C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130876805 | |||||||
| chr9:130876806 | A | G | 2 | a0001c0003t0003g0240a0001c0003t0003g0241 | 2 | HG01167.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1271-1609A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130876806 | |||||||
| chr9:130876871 | A | G | 1 | a0001c0001t0001g0185 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1271-1544A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130876871 | |||||||
| chr9:130876877 | T | C | 1 | a0001c0001t0001g0185 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1271-1538T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130876877 | |||||||
| chr9:130876966 | G | C | 1 | a0001c0026t0029g0250 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1271-1449G>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130876966 | |||||||
| chr9:130877175 | A | T | 5 | a0001c0001t0012g0149a0001c0008t0012g0036a0001c0008t0030g0040others(2): Show | 5 | HG02280.hp1 HG02630.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1271-1240A>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130877175 | |||||||
| chr9:130877182 | A | G | 5 | a0001c0001t0012g0149a0001c0008t0012g0036a0001c0008t0030g0040others(2): Show | 5 | HG02280.hp1 HG02630.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1271-1233A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130877182 | |||||||
| chr9:130877188 | T | A | 1 | a0001c0001t0006g0256 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1271-1227T>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130877188 | |||||||
| chr9:130877214 | T | A | 5 | a0001c0001t0007g0176a0001c0001t0007g0194a0001c0001t0007g0205others(2): Show | 5 | HG02486.hp2 HG02559.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1271-1201T>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130877214 | |||||||
| chr9:130877224 | G | A | 41 | a0001c0001t0001g0221a0001c0001t0002g0014a0001c0001t0002g0015others(38): Show | 44 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(41): Show |
intron_variant | MODIFIER | c.1271-1191G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130877224 | |||||||
| chr9:130877362 | A | G | 1 | a0001c0004t0017g0049 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1271-1053A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130877362 | |||||||
| chr9:130877559 | C | G | 1 | a0001c0001t0001g0119 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1271-856C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130877559 | |||||||
| chr9:130877560 | A | AGGGGGGG others(23): Show |
1 | a0001c0001t0001g0119 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1271-852_1271-851i others(32): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 130877560 | ||||||
| chr9:130877564 | T | G | 1 | a0001c0001t0001g0119 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1271-851T>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130877564 | |||||||
| chr9:130877565 | C | G | 1 | a0001c0001t0001g0119 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1271-850C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130877565 | |||||||
| chr9:130877566 | T | G | 1 | a0001c0001t0001g0119 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1271-849T>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130877566 | |||||||
| chr9:130877568 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1271-847A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130877568 | |||||||
| chr9:130877569 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1271-846A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130877569 | |||||||
| chr9:130877570 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1271-845A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130877570 | |||||||
| chr9:130877571 | C | G | 1 | a0001c0001t0001g0119 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1271-844C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130877571 | |||||||
| chr9:130877603 | G | A | 5 | a0001c0001t0007g0176a0001c0001t0007g0194a0001c0001t0007g0205others(2): Show | 5 | HG02486.hp2 HG02559.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1271-812G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130877603 | |||||||
| chr9:130877607 | A | G | 3 | a0001c0001t0001g0127a0001c0001t0001g0224a0001c0001t0001g0225 | 3 | HG00621.hp1 NA18966.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.1271-808A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130877607 | |||||||
| chr9:130877726 | C | T | 60 | a0001c0001t0001g0221a0001c0001t0002g0014a0001c0001t0002g0015others(57): Show | 64 | HG00323.hp1 HG00323.hp2 HG01069.hp2 others(61): Show |
intron_variant | MODIFIER | c.1271-689C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130877726 | |||||||
| chr9:130877727 | G | C | 6 | a0001c0001t0006g0018a0001c0006t0005g0055a0001c0006t0005g0152others(3): Show | 6 | HG01243.hp2 HG02109.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1271-688G>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130877727 | |||||||
| chr9:130877808 | A | AT | 11 | a0001c0001t0004g0054a0001c0001t0004g0105a0001c0002t0001g0181others(8): Show | 12 | HG01109.hp1 HG01496.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1271-591dupT | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 130877808 | ||||||
| chr9:130877808 | ATTT | A | 34 | a0001c0001t0001g0221a0001c0001t0002g0014a0001c0001t0002g0015others(31): Show | 37 | HG00323.hp1 HG00323.hp2 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.1271-593_1271-591d others(5): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 130877808 | ||||||
| chr9:130877828 | ATG | A | 6 | a0001c0003t0003g0130a0001c0003t0003g0183a0001c0003t0003g0219others(3): Show | 6 | HG01081.hp1 HG01175.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1271-586_1271-585d others(4): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130877828 | |||||||
| chr9:130877831 | G | C | 6 | a0001c0003t0003g0130a0001c0003t0003g0183a0001c0003t0003g0219others(3): Show | 6 | HG01081.hp1 HG01175.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1271-584G>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130877831 | |||||||
| chr9:130877831 | G | T | 4 | a0001c0001t0010g0005a0001c0001t0010g0043a0001c0011t0013g0215others(1): Show | 5 | HG02809.hp2 HG03225.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1271-584G>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130877831 | |||||||
| chr9:130877838 | G | A | 6 | a0001c0003t0003g0130a0001c0003t0003g0183a0001c0003t0003g0219others(3): Show | 6 | HG01081.hp1 HG01175.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1271-577G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130877838 | |||||||
| chr9:130877846 | A | G | 6 | a0001c0003t0003g0130a0001c0003t0003g0183a0001c0003t0003g0219others(3): Show | 6 | HG01081.hp1 HG01175.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1271-569A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130877846 | |||||||
| chr9:130877852 | C | G | 6 | a0001c0003t0003g0130a0001c0003t0003g0183a0001c0003t0003g0219others(3): Show | 6 | HG01081.hp1 HG01175.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1271-563C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130877852 | |||||||
| chr9:130877961 | T | C | 116 | a0001c0001t0001g0221a0001c0001t0002g0014a0001c0001t0002g0015others(113): Show | 124 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(121): Show |
intron_variant | MODIFIER | c.1271-454T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130877961 | |||||||
| chr9:130877973 | C | T | 1 | a0001c0001t0008g0016 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1271-442C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130877973 | |||||||
| chr9:130877979 | ATT | A | 60 | a0001c0001t0001g0221a0001c0001t0002g0014a0001c0001t0002g0015others(57): Show | 64 | HG00323.hp1 HG00323.hp2 HG01069.hp2 others(61): Show |
intron_variant | MODIFIER | c.1271-430_1271-429d others(4): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 130877979 | ||||||
| chr9:130878011 | C | T | 1 | a0001c0003t0003g0148 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1271-404C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130878011 | |||||||
| chr9:130878022 | C | G | 66 | a0001c0001t0001g0221a0001c0001t0002g0014a0001c0001t0002g0015others(63): Show | 70 | HG00323.hp1 HG00323.hp2 HG01069.hp2 others(67): Show |
intron_variant | MODIFIER | c.1271-393C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130878022 | |||||||
| chr9:130878060 | G | A | 1 | a0001c0002t0001g0128 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1271-355G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130878060 | |||||||
| chr9:130878065 | G | A | 1 | a0001c0001t0007g0194 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1271-350G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130878065 | |||||||
| chr9:130878097 | G | A | 1 | a0001c0001t0026g0024 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1271-318G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130878097 | |||||||
| chr9:130878131 | A | T | 5 | a0001c0001t0012g0149a0001c0008t0012g0036a0001c0008t0030g0040others(2): Show | 5 | HG02280.hp1 HG02630.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1271-284A>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130878131 | |||||||
| chr9:130878147 | C | T | 5 | a0001c0001t0006g0255a0001c0001t0006g0256a0001c0001t0006g0257others(2): Show | 5 | HG02145.hp2 HG02258.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1271-268C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130878147 | |||||||
| chr9:130878148 | G | A | 1 | a0001c0002t0001g0146 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1271-267G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130878148 | |||||||
| chr9:130878593 | C | G | 2 | a0001c0001t0001g0075a0001c0001t0001g0085 | 2 | NA18941.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.1423+26C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 8/10 | chr9 | 130878593 | |||||||
| chr9:130878645 | A | G | 31 | a0001c0003t0003g0012a0001c0003t0003g0130a0001c0003t0003g0138others(28): Show | 33 | HG01074.hp2 HG01081.hp1 HG01099.hp1 others(30): Show |
intron_variant | MODIFIER | c.1423+78A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 8/10 | chr9 | 130878645 | |||||||
| chr9:130878712 | C | A | 44 | a0001c0001t0004g0054a0001c0001t0004g0105a0001c0001t0010g0005others(41): Show | 48 | HG01074.hp2 HG01081.hp1 HG01099.hp1 others(45): Show |
intron_variant | MODIFIER | c.1423+145C>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 8/10 | chr9 | 130878712 | |||||||
| chr9:130878768 | G | A | 7 | a0001c0001t0001g0008a0001c0001t0001g0051a0001c0001t0001g0070others(4): Show | 8 | HG00423.hp2 HG00621.hp2 HG00673.hp2 others(5): Show |
intron_variant | MODIFIER | c.1423+201G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 8/10 | chr9 | 130878768 | |||||||
| chr9:130878769 | C | G | 1 | a0001c0002t0001g0188 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1423+202C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 8/10 | chr9 | 130878769 | |||||||
| chr9:130878833 | T | C | 105 | a0001c0001t0001g0221a0001c0001t0002g0014a0001c0001t0002g0015others(102): Show | 112 | HG00323.hp1 HG00323.hp2 HG01069.hp2 others(109): Show |
intron_variant | MODIFIER | c.1423+266T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 8/10 | chr9 | 130878833 | |||||||
| chr9:130878871 | G | A | 1 | a0001c0001t0006g0257 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1423+304G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 8/10 | chr9 | 130878871 | |||||||
| chr9:130878874 | A | AT | 32 | a0001c0001t0001g0013a0001c0001t0001g0124a0001c0001t0001g0125others(29): Show | 34 | HG01175.hp1 HG01496.hp1 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.1423+327dupT | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr9 | 130878874 | ||||||
| chr9:130878874 | AT | A | 28 | a0001c0001t0001g0006a0001c0001t0001g0058a0001c0001t0001g0063others(25): Show | 29 | HG01074.hp1 HG01106.hp1 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.1423+327delT | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr9 | 130878874 | ||||||
| chr9:130878939 | G | A | 41 | a0001c0001t0001g0221a0001c0001t0002g0014a0001c0001t0002g0015others(38): Show | 44 | HG00323.hp1 HG00323.hp2 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.1423+372G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 8/10 | chr9 | 130878939 | |||||||
| chr9:130879034 | C | T | 5 | a0001c0001t0007g0176a0001c0001t0007g0194a0001c0001t0007g0205others(2): Show | 5 | HG02486.hp2 HG02559.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1423+467C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 8/10 | chr9 | 130879034 | |||||||
| chr9:130879035 | G | T | 1 | a0001c0001t0001g0058 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1423+468G>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 8/10 | chr9 | 130879035 | |||||||
| chr9:130879038 | C | T | 1 | a0001c0003t0005g0254 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1423+471C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 8/10 | chr9 | 130879038 | |||||||
| chr9:130879089 | C | T | 4 | a0001c0001t0010g0005a0001c0001t0010g0043a0001c0011t0013g0215others(1): Show | 5 | HG02809.hp2 HG03225.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1423+522C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 8/10 | chr9 | 130879089 | |||||||
| chr9:130879137 | A | G | 1 | a0001c0001t0007g0176 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1423+570A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 8/10 | chr9 | 130879137 | |||||||
| chr9:130879157 | G | A | 5 | a0001c0001t0007g0176a0001c0001t0007g0194a0001c0001t0007g0205others(2): Show | 5 | HG02486.hp2 HG02559.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1423+590G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 8/10 | chr9 | 130879157 | |||||||
| chr9:130879199 | G | A | 1 | a0001c0001t0001g0161 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1423+632G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 8/10 | chr9 | 130879199 | |||||||
| chr9:130879398 | G | A | 11 | a0001c0001t0006g0018a0001c0001t0006g0255a0001c0001t0006g0256others(8): Show | 11 | HG01243.hp2 HG02109.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1424-670G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 8/10 | chr9 | 130879398 | |||||||
| chr9:130879481 | G | A | 5 | a0001c0001t0006g0255a0001c0001t0006g0256a0001c0001t0006g0257others(2): Show | 5 | HG02145.hp2 HG02258.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1424-587G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 8/10 | chr9 | 130879481 | |||||||
| chr9:130879668 | T | C | 11 | a0001c0001t0006g0018a0001c0001t0006g0255a0001c0001t0006g0256others(8): Show | 11 | HG01243.hp2 HG02109.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1424-400T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 8/10 | chr9 | 130879668 | |||||||
| chr9:130879718 | A | T | 5 | a0001c0001t0007g0176a0001c0001t0007g0194a0001c0001t0007g0205others(2): Show | 5 | HG02486.hp2 HG02559.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1424-350A>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 8/10 | chr9 | 130879718 | |||||||
| chr9:130879895 | T | G | 32 | a0001c0003t0003g0012a0001c0003t0003g0130a0001c0003t0003g0138others(29): Show | 34 | HG01074.hp2 HG01081.hp1 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.1424-173T>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 8/10 | chr9 | 130879895 | |||||||
| chr9:130879906 | A | G | 11 | a0001c0001t0006g0018a0001c0001t0006g0255a0001c0001t0006g0256others(8): Show | 11 | HG01243.hp2 HG02109.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1424-162A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 8/10 | chr9 | 130879906 | |||||||
| chr9:130880163 | G | T | 1 | a0001c0001t0001g0191 | 1 | HG00558.hp1 | splice_region_variant&intron_variant | LOW | c.1513+6G>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 9/10 | chr9 | 130880163 | |||||||
| chr9:130880249 | A | C | 9 | a0001c0001t0004g0054a0001c0001t0004g0105a0001c0004t0004g0009others(6): Show | 10 | HG01109.hp1 HG01496.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.1513+92A>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 9/10 | chr9 | 130880249 | |||||||
| chr9:130880300 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1513+143G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 9/10 | chr9 | 130880300 | |||||||
| chr9:130880367 | T | C | 117 | a0001c0001t0001g0221a0001c0001t0002g0014a0001c0001t0002g0015others(114): Show | 125 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(122): Show |
intron_variant | MODIFIER | c.1514-133T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 9/10 | chr9 | 130880367 | |||||||
| chr9:130880374 | G | A | 1 | a0001c0002t0001g0195 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1514-126G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 9/10 | chr9 | 130880374 | |||||||
| chr9:130880732 | C | G | 1 | a0001c0001t0001g0080 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1678+68C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | chr9 | 130880732 | |||||||
| chr9:130880742 | C | T | 1 | a0001c0001t0015g0193 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1678+78C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | chr9 | 130880742 | |||||||
| chr9:130880793 | A | G | 2 | a0001c0001t0001g0076a0001c0001t0001g0143 | 2 | NA18963.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.1678+129A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | chr9 | 130880793 | |||||||
| chr9:130880843 | A | G | 1 | a0001c0011t0013g0215 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1678+179A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | chr9 | 130880843 | |||||||
| chr9:130880960 | C | T | 7 | a0001c0001t0004g0054a0001c0001t0004g0105a0001c0004t0004g0009others(4): Show | 8 | HG01109.hp1 HG01884.hp2 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.1678+296C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | chr9 | 130880960 | |||||||
| chr9:130881083 | C | T | 8 | a0001c0001t0004g0054a0001c0001t0004g0105a0001c0004t0004g0009others(5): Show | 9 | HG01109.hp1 HG01496.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.1678+419C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | chr9 | 130881083 | |||||||
| chr9:130881249 | CTCTGT | C | 3 | a0001c0001t0015g0193a0001c0009t0006g0145a0001c0009t0006g0175 | 3 | HG02486.hp1 HG02809.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1678+589_1678+593d others(7): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 130881249 | ||||||
| chr9:130881323 | T | C | 8 | a0001c0001t0007g0056a0001c0001t0007g0176a0001c0001t0007g0194others(5): Show | 8 | HG02486.hp2 HG02559.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1678+659T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | chr9 | 130881323 | |||||||
| chr9:130881340 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1678+676C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | chr9 | 130881340 | |||||||
| chr9:130881406 | T | C | 258 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(255): Show | 275 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(272): Show |
intron_variant | MODIFIER | c.1678+742T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | chr9 | 130881406 | |||||||
| chr9:130881449 | C | A | 5 | a0002c0005t0004g0003a0002c0005t0004g0212a0002c0005t0004g0242others(2): Show | 6 | HG01123.hp2 HG01361.hp2 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.1678+785C>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | chr9 | 130881449 | |||||||
| chr9:130881501 | G | T | 7 | a0001c0006t0005g0153a0002c0005t0004g0003a0002c0005t0004g0212others(4): Show | 8 | HG01123.hp2 HG01361.hp2 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.1678+837G>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | chr9 | 130881501 | |||||||
| chr9:130881568 | A | C | 1 | a0001c0001t0008g0016 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1678+904A>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | chr9 | 130881568 | |||||||
| chr9:130881569 | T | C | 5 | a0001c0006t0005g0055a0001c0006t0005g0152a0001c0006t0005g0153others(2): Show | 5 | HG02109.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1678+905T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | chr9 | 130881569 | |||||||
| chr9:130881670 | C | T | 7 | a0002c0005t0004g0003a0002c0005t0004g0189a0002c0005t0004g0212others(4): Show | 8 | HG00639.hp1 HG01123.hp2 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.1678+1006C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | chr9 | 130881670 | |||||||
| chr9:130881693 | G | A | 59 | a0001c0001t0004g0054a0001c0001t0004g0105a0001c0001t0007g0056others(56): Show | 64 | HG00639.hp1 HG01074.hp2 HG01081.hp1 others(61): Show |
intron_variant | MODIFIER | c.1678+1029G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | chr9 | 130881693 | |||||||
| chr9:130881715 | C | T | 112 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0021others(109): Show | 120 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(117): Show |
intron_variant | MODIFIER | c.1678+1051C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | chr9 | 130881715 | |||||||
| chr9:130881765 | A | G | 9 | a0001c0001t0004g0054a0001c0001t0004g0105a0001c0004t0004g0009others(6): Show | 10 | HG01109.hp1 HG01496.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.1678+1101A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | chr9 | 130881765 | |||||||
| chr9:130881773 | C | T | 1 | a0001c0001t0004g0054 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1678+1109C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | chr9 | 130881773 | |||||||
| chr9:130881855 | T | TTTTC | 107 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0021others(104): Show | 115 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(112): Show |
intron_variant | MODIFIER | c.1678+1194_1678+119 others(8): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 130881855 | ||||||
| chr9:130881877 | T | TA | 30 | a0001c0001t0004g0054a0001c0001t0004g0105a0001c0001t0007g0056others(27): Show | 33 | HG00639.hp1 HG01109.hp1 HG01123.hp2 others(30): Show |
intron_variant | MODIFIER | c.1678+1223dupA | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 130881877 | ||||||
| chr9:130881877 | TA | T | 5 | a0001c0006t0005g0055a0001c0006t0005g0152a0001c0006t0005g0153others(2): Show | 5 | HG02109.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1678+1223delA | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 130881877 | ||||||
| chr9:130881886 | AAC | A | 32 | a0001c0003t0003g0012a0001c0003t0003g0130a0001c0003t0003g0138others(29): Show | 34 | HG01074.hp2 HG01081.hp1 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.1678+1224_1678+122 others(6): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 130881886 | ||||||
| chr9:130881888 | C | A | 1 | a0001c0001t0001g0158 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1678+1224C>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | chr9 | 130881888 | |||||||
| chr9:130881935 | G | A | 1 | a0001c0026t0029g0250 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1678+1271G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | chr9 | 130881935 | |||||||
| chr9:130881949 | G | A | 1 | a0001c0001t0001g0008 | 2 | HG01934.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1678+1285G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | chr9 | 130881949 | |||||||
| chr9:130882134 | G | A | 1 | a0001c0024t0001g0090 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1678+1470G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | chr9 | 130882134 | |||||||
| chr9:130882239 | G | C | 2 | a0001c0002t0001g0079a0001c0002t0001g0172 | 2 | HG00408.hp1 HG00423.hp1 |
intron_variant | MODIFIER | c.1678+1575G>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | chr9 | 130882239 | |||||||
| chr9:130882308 | G | A | 42 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0021others(39): Show | 45 | HG00323.hp1 HG00323.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.1678+1644G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | chr9 | 130882308 | |||||||
| chr9:130882356 | A | C | 5 | a0001c0006t0005g0055a0001c0006t0005g0152a0001c0006t0005g0153others(2): Show | 5 | HG02109.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1679-1613A>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | chr9 | 130882356 | |||||||
| chr9:130882398 | G | A | 42 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0021others(39): Show | 45 | HG00323.hp1 HG00323.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.1679-1571G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | chr9 | 130882398 | |||||||
| chr9:130882504 | T | C | 8 | a0002c0005t0004g0003a0002c0005t0004g0189a0002c0005t0004g0212others(5): Show | 9 | HG00639.hp1 HG01123.hp2 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.1679-1465T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | chr9 | 130882504 | |||||||
| chr9:130882734 | T | C | 258 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(255): Show | 275 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(272): Show |
intron_variant | MODIFIER | c.1679-1235T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | chr9 | 130882734 | |||||||
| chr9:130882777 | G | A | 1 | a0001c0026t0029g0250 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1679-1192G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | chr9 | 130882777 | |||||||
| chr9:130882791 | C | T | 1 | a0001c0008t0031g0038 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1679-1178C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | chr9 | 130882791 | |||||||
| chr9:130882850 | A | T | 1 | a0001c0001t0002g0228 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1679-1119A>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | chr9 | 130882850 | |||||||
| chr9:130883061 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1679-908G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | chr9 | 130883061 | |||||||
| chr9:130883324 | C | T | 9 | a0001c0001t0004g0054a0001c0001t0004g0105a0001c0004t0004g0009others(6): Show | 10 | HG01109.hp1 HG01496.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.1679-645C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | chr9 | 130883324 | |||||||
| chr9:130883429 | G | A | 1 | a0003c0012t0004g0213 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1679-540G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | chr9 | 130883429 | |||||||
| chr9:130883451 | C | T | 115 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0021others(112): Show | 123 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(120): Show |
intron_variant | MODIFIER | c.1679-518C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | chr9 | 130883451 | |||||||
| chr9:130883495 | C | CA | 54 | a0001c0001t0001g0087a0001c0001t0001g0096a0001c0001t0001g0125others(51): Show | 57 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.1679-459dupA | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 130883495 | ||||||
| chr9:130883649 | C | T | 1 | a0001c0004t0004g0027 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1679-320C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | chr9 | 130883649 | |||||||
| chr9:130883716 | A | G | 1 | a0001c0001t0007g0206 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1679-253A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | chr9 | 130883716 | |||||||
| chr9:130883850 | T | C | 1 | a0001c0001t0012g0149 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1679-119T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | chr9 | 130883850 |