Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 89910 |
| ensemblid | ENSG00000151148.14 |
| hgncid | 13478 |
| symbol | UBE3B |
| name | ubiquitin protein ligase E3B |
| refseq_nuc | NM_130466.4 |
| refseq_prot | NP_569733.2 |
| ensembl_nuc | ENST00000342494.8 |
| ensembl_prot | ENSP00000340596.3 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 109477634 |
| end | 109536702 |
| strand | + |
| ver | v1.2 |
| region | chr12:109477634-109536702 |
| region5000 | chr12:109472634-109541702 |
| regionname0 | UBE3B_chr12_109477634_109536702 |
| regionname5000 | UBE3B_chr12_109472634_109541702 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 1068 | 177 | 64 | 32 | 55 | 10 | 15 | 46 | UBE3B_chr12_109472634_109541702 | UBE3B | MFTLS others(1063): Show |
chr12 | 109472634 | 109541702 |
| a0002 | 1/0 | 1068 | 146 | 23 | 27 | 69 | 6 | 20 | 52 | UBE3B_chr12_109472634_109541702 | UBE3B | MFTLS others(1063): Show |
chr12 | 109472634 | 109541702 |
| a0003 | 0/0 | 1068 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | MFTLS others(1063): Show |
chr12 | 109472634 | 109541702 |
| a0004 | 0/0 | 1068 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | MFTLS others(1063): Show |
chr12 | 109472634 | 109541702 |
| a0005 | 0/0 | 1068 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | MFTLS others(1063): Show |
chr12 | 109472634 | 109541702 |
| a0006 | 0/0 | 1068 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | MFTLS others(1063): Show |
chr12 | 109472634 | 109541702 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002 | 0/1 | 3204 | 119 | 39 | 25 | 33 | 9 | 12 | UBE3B_chr12_109472634_109541702 | UBE3B | ATGTT others(3199): Show |
chr12 | 109472634 | 109541702 | ||
| a0001c0003 | 0/0 | 3204 | 38 | 16 | 7 | 14 | 1 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | ATGTT others(3199): Show |
chr12 | 109472634 | 109541702 | ||
| a0001c0004 | 0/0 | 3204 | 13 | 5 | 0 | 6 | 0 | 2 | UBE3B_chr12_109472634_109541702 | UBE3B | ATGTT others(3199): Show |
chr12 | 109472634 | 109541702 | ||
| a0001c0006 | 0/0 | 3204 | 2 | 2 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | ATGTT others(3199): Show |
chr12 | 109472634 | 109541702 | ||
| a0001c0007 | 0/0 | 3204 | 2 | 2 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | ATGTT others(3199): Show |
chr12 | 109472634 | 109541702 | ||
| a0001c0011 | 0/0 | 3204 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | ATGTT others(3199): Show |
chr12 | 109472634 | 109541702 | ||
| a0001c0013 | 0/0 | 3204 | 1 | 0 | 0 | 0 | 0 | 1 | UBE3B_chr12_109472634_109541702 | UBE3B | ATGTT others(3199): Show |
chr12 | 109472634 | 109541702 | ||
| a0001c0016 | 0/0 | 3204 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | ATGTT others(3199): Show |
chr12 | 109472634 | 109541702 | ||
| a0002c0001 | 1/0 | 3204 | 142 | 22 | 26 | 67 | 6 | 20 | UBE3B_chr12_109472634_109541702 | UBE3B | ATGTT others(3199): Show |
chr12 | 109472634 | 109541702 | ||
| a0002c0008 | 0/0 | 3204 | 2 | 1 | 1 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | ATGTT others(3199): Show |
chr12 | 109472634 | 109541702 | ||
| a0002c0014 | 0/0 | 3204 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | ATGTT others(3199): Show |
chr12 | 109472634 | 109541702 | ||
| a0002c0015 | 0/0 | 3204 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | ATGTT others(3199): Show |
chr12 | 109472634 | 109541702 | ||
| a0003c0005 | 0/0 | 3204 | 2 | 0 | 2 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | ATGTT others(3199): Show |
chr12 | 109472634 | 109541702 | ||
| a0004c0012 | 0/0 | 3204 | 1 | 0 | 1 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | ATGTT others(3199): Show |
chr12 | 109472634 | 109541702 | ||
| a0005c0009 | 0/0 | 3204 | 1 | 1 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | ATGTT others(3199): Show |
chr12 | 109472634 | 109541702 | ||
| a0006c0010 | 0/0 | 3204 | 1 | 0 | 0 | 0 | 0 | 1 | UBE3B_chr12_109472634_109541702 | UBE3B | ATGTT others(3199): Show |
chr12 | 109472634 | 109541702 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0002 | 0/0 | 5730 | 40 | 2 | 9 | 17 | 6 | 6 | UBE3B_chr12_109472634_109541702 | UBE3B | GAACA others(5725): Show |
chr12 | 109472634 | 109541702 |
| a0001c0002t0004 | 0/0 | 5727 | 20 | 9 | 4 | 5 | 0 | 2 | UBE3B_chr12_109472634_109541702 | UBE3B | GAACA others(5722): Show |
chr12 | 109472634 | 109541702 |
| a0001c0002t0006 | 0/0 | 5730 | 12 | 12 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | GAACA others(5725): Show |
chr12 | 109472634 | 109541702 |
| a0001c0002t0007 | 0/0 | 5730 | 11 | 0 | 2 | 9 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | GAACA others(5725): Show |
chr12 | 109472634 | 109541702 |
| a0001c0002t0008 | 0/1 | 5727 | 10 | 1 | 4 | 0 | 1 | 3 | UBE3B_chr12_109472634_109541702 | UBE3B | GAACA others(5722): Show |
chr12 | 109472634 | 109541702 |
| a0001c0002t0010 | 0/0 | 5727 | 6 | 3 | 2 | 0 | 1 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | GAACA others(5722): Show |
chr12 | 109472634 | 109541702 |
| a0001c0002t0011 | 0/0 | 5727 | 4 | 0 | 2 | 0 | 1 | 1 | UBE3B_chr12_109472634_109541702 | UBE3B | GAACA others(5722): Show |
chr12 | 109472634 | 109541702 |
| a0001c0002t0012 | 0/0 | 5730 | 4 | 4 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | GAACA others(5725): Show |
chr12 | 109472634 | 109541702 |
| a0001c0002t0015 | 0/0 | 5727 | 2 | 2 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | GAACA others(5722): Show |
chr12 | 109472634 | 109541702 |
| a0001c0002t0016 | 0/0 | 5730 | 2 | 2 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | GAACA others(5725): Show |
chr12 | 109472634 | 109541702 |
| a0001c0002t0020 | 0/0 | 5727 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | GAACA others(5722): Show |
chr12 | 109472634 | 109541702 |
| a0001c0002t0021 | 0/0 | 5727 | 1 | 1 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | GAACA others(5722): Show |
chr12 | 109472634 | 109541702 |
| a0001c0002t0022 | 0/0 | 5727 | 1 | 1 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | GAACA others(5722): Show |
chr12 | 109472634 | 109541702 |
| a0001c0002t0032 | 0/0 | 5727 | 1 | 0 | 1 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | GAACA others(5722): Show |
chr12 | 109472634 | 109541702 |
| a0001c0002t0033 | 0/0 | 5730 | 1 | 1 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | GAACA others(5725): Show |
chr12 | 109472634 | 109541702 |
| a0001c0002t0034 | 0/0 | 5730 | 1 | 1 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | GAACA others(5725): Show |
chr12 | 109472634 | 109541702 |
| a0001c0002t0035 | 0/0 | 5730 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | GAACA others(5725): Show |
chr12 | 109472634 | 109541702 |
| a0001c0002t0036 | 0/0 | 5730 | 1 | 0 | 1 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | GAACA others(5725): Show |
chr12 | 109472634 | 109541702 |
| a0001c0003t0003 | 0/0 | 5727 | 28 | 6 | 7 | 14 | 1 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | GAACA others(5722): Show |
chr12 | 109472634 | 109541702 |
| a0001c0003t0009 | 0/0 | 5727 | 8 | 8 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | GAACA others(5722): Show |
chr12 | 109472634 | 109541702 |
| a0001c0003t0023 | 0/0 | 5727 | 1 | 1 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | GAACA others(5722): Show |
chr12 | 109472634 | 109541702 |
| a0001c0003t0029 | 0/0 | 5727 | 1 | 1 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | GAACA others(5722): Show |
chr12 | 109472634 | 109541702 |
| a0001c0004t0005 | 0/0 | 5730 | 13 | 5 | 0 | 6 | 0 | 2 | UBE3B_chr12_109472634_109541702 | UBE3B | GAACA others(5725): Show |
chr12 | 109472634 | 109541702 |
| a0001c0006t0027 | 0/0 | 5727 | 1 | 1 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | GAACA others(5722): Show |
chr12 | 109472634 | 109541702 |
| a0001c0006t0028 | 0/0 | 5727 | 1 | 1 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | GAACA others(5722): Show |
chr12 | 109472634 | 109541702 |
| a0001c0007t0003 | 0/0 | 5727 | 2 | 2 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | GAACA others(5722): Show |
chr12 | 109472634 | 109541702 |
| a0001c0011t0004 | 0/0 | 5727 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | GAACA others(5722): Show |
chr12 | 109472634 | 109541702 |
| a0001c0013t0011 | 0/0 | 5727 | 1 | 0 | 0 | 0 | 0 | 1 | UBE3B_chr12_109472634_109541702 | UBE3B | GAACA others(5722): Show |
chr12 | 109472634 | 109541702 |
| a0001c0016t0002 | 0/0 | 5730 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | GAACA others(5725): Show |
chr12 | 109472634 | 109541702 |
| a0002c0001t0001 | 1/0 | 5730 | 128 | 22 | 23 | 58 | 6 | 18 | UBE3B_chr12_109472634_109541702 | UBE3B | GAACA others(5725): Show |
chr12 | 109472634 | 109541702 |
| a0002c0001t0013 | 0/0 | 5729 | 3 | 0 | 0 | 3 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | GAACA others(5724): Show |
chr12 | 109472634 | 109541702 |
| a0002c0001t0014 | 0/0 | 5730 | 2 | 0 | 0 | 2 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | GAACA others(5725): Show |
chr12 | 109472634 | 109541702 |
| a0002c0001t0017 | 0/0 | 5730 | 2 | 0 | 0 | 0 | 0 | 2 | UBE3B_chr12_109472634_109541702 | UBE3B | GAACA others(5725): Show |
chr12 | 109472634 | 109541702 |
| a0002c0001t0018 | 0/0 | 5730 | 2 | 0 | 0 | 2 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | GAACA others(5725): Show |
chr12 | 109472634 | 109541702 |
| a0002c0001t0019 | 0/0 | 5730 | 2 | 0 | 2 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | GAACA others(5725): Show |
chr12 | 109472634 | 109541702 |
| a0002c0001t0025 | 0/0 | 5730 | 1 | 0 | 1 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | GAACA others(5725): Show |
chr12 | 109472634 | 109541702 |
| a0002c0001t0030 | 0/0 | 5730 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | GAACA others(5725): Show |
chr12 | 109472634 | 109541702 |
| a0002c0001t0031 | 0/0 | 5730 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | GAACA others(5725): Show |
chr12 | 109472634 | 109541702 |
| a0002c0008t0001 | 0/0 | 5730 | 2 | 1 | 1 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | GAACA others(5725): Show |
chr12 | 109472634 | 109541702 |
| a0002c0014t0001 | 0/0 | 5730 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | GAACA others(5725): Show |
chr12 | 109472634 | 109541702 |
| a0002c0015t0001 | 0/0 | 5730 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | GAACA others(5725): Show |
chr12 | 109472634 | 109541702 |
| a0003c0005t0004 | 0/0 | 5727 | 2 | 0 | 2 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | GAACA others(5722): Show |
chr12 | 109472634 | 109541702 |
| a0004c0012t0024 | 0/0 | 5727 | 1 | 0 | 1 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | GAACA others(5722): Show |
chr12 | 109472634 | 109541702 |
| a0005c0009t0026 | 0/0 | 5730 | 1 | 1 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | GAACA others(5725): Show |
chr12 | 109472634 | 109541702 |
| a0006c0010t0004 | 0/0 | 5727 | 1 | 0 | 0 | 0 | 0 | 1 | UBE3B_chr12_109472634_109541702 | UBE3B | GAACA others(5722): Show |
chr12 | 109472634 | 109541702 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0002g0003 | 0/0 | 8 | 2 | 2 | 4 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0002g0007 | 0/0 | 5 | 0 | 3 | 0 | 2 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0002g0036 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0004g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0004g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0004g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0004g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0004g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0004g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0004g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0004g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0004g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0004g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0004g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0004g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0004g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0004g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0004g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0004g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0006g0006 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0006g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0006g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0006g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0006g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0006g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0006g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0007g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0007g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0007g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0007g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0007g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0007g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0007g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0007g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0007g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0007g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0008g0010 | 0/0 | 4 | 1 | 1 | 0 | 0 | 2 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0008g0018 | 0/1 | 3 | 0 | 2 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0008g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0008g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0008g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0010g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0010g0022 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0010g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0010g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0011g0017 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0011g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0012g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0012g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0012g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0015g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0015g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0016g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0016g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0020g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0021g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0022g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0032g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0033g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0034g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0035g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0002t0036g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0003t0003g0002 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0003t0003g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0003t0003g0016 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0003t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0003t0003g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0003t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0003t0003g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0003t0003g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0003t0003g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0003t0003g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0003t0003g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0003t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0003t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0003t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0003t0009g0009 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0003t0009g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0003t0009g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0003t0009g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0003t0009g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0003t0023g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0003t0029g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0004t0005g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0004t0005g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0004t0005g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0004t0005g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0004t0005g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0004t0005g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0004t0005g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0004t0005g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0004t0005g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0006t0027g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0006t0028g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0007t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0007t0003g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0011t0004g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0013t0011g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0001c0016t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0001 | 1/0 | 9 | 4 | 0 | 3 | 0 | 1 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0004 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0011 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0013 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0026 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0013g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0013g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0014g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0017g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0018g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0018g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0019g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0025g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0030g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0001t0031g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0008t0001g0033 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0014t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0002c0015t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0003c0005t0004g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0004c0012t0024g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0005c0009t0026g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| a0006c0010t0004g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0002 | g0036 | EUR | GBR | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG00099 | hp2 | a0001 | c0003 | t0003 | g0152 | EUR | GBR | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG00140 | hp1 | a0001 | c0002 | t0011 | g0017 | EUR | GBR | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG00140 | hp2 | a0001 | c0002 | t0002 | g0169 | EUR | GBR | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG00323 | hp1 | a0001 | c0002 | t0002 | g0168 | EUR | FIN | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG00323 | hp2 | a0002 | c0001 | t0001 | g0098 | EUR | FIN | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG00408 | hp1 | a0002 | c0001 | t0001 | g0132 | EAS | CHS | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG00408 | hp2 | a0002 | c0001 | t0018 | g0104 | EAS | CHS | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG00423 | hp1 | a0001 | c0003 | t0003 | g0002 | EAS | CHS | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG00423 | hp2 | a0002 | c0001 | t0001 | g0004 | EAS | CHS | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG00597 | hp1 | a0001 | c0002 | t0002 | g0184 | EAS | CHS | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG00597 | hp2 | a0002 | c0001 | t0001 | g0127 | EAS | CHS | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG00609 | hp1 | a0001 | c0002 | t0007 | g0003 | EAS | CHS | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG00609 | hp2 | a0002 | c0001 | t0001 | g0085 | EAS | CHS | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG00621 | hp1 | a0002 | c0001 | t0001 | g0012 | EAS | CHS | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG00621 | hp2 | a0001 | c0002 | t0002 | g0167 | EAS | CHS | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG00639 | hp1 | a0001 | c0002 | t0002 | g0171 | AMR | PUR | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG00639 | hp2 | a0001 | c0002 | t0008 | g0018 | AMR | PUR | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG00642 | hp1 | a0002 | c0001 | t0001 | g0095 | AMR | PUR | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG00642 | hp2 | a0001 | c0002 | t0008 | g0018 | AMR | PUR | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG00673 | hp1 | a0002 | c0001 | t0001 | g0076 | EAS | CHS | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG00673 | hp2 | a0002 | c0001 | t0001 | g0136 | EAS | CHS | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG00733 | hp1 | a0001 | c0002 | t0002 | g0036 | AMR | PUR | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG00733 | hp2 | a0002 | c0001 | t0001 | g0011 | AMR | PUR | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG00738 | hp1 | a0002 | c0001 | t0001 | g0011 | AMR | PUR | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG00738 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG01070 | hp1 | a0002 | c0001 | t0001 | g0086 | AMR | PUR | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG01070 | hp2 | a0002 | c0001 | t0001 | g0031 | AMR | PUR | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG01071 | hp1 | a0002 | c0001 | t0001 | g0031 | AMR | PUR | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG01071 | hp2 | a0001 | c0002 | t0004 | g0020 | AMR | PUR | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG01074 | hp1 | a0002 | c0001 | t0001 | g0129 | AMR | PUR | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG01074 | hp2 | a0002 | c0001 | t0001 | g0091 | AMR | PUR | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG01081 | hp1 | a0002 | c0001 | t0025 | g0004 | AMR | PUR | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG01081 | hp2 | a0001 | c0002 | t0002 | g0193 | AMR | PUR | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG01099 | hp1 | a0001 | c0003 | t0003 | g0016 | AMR | PUR | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG01099 | hp2 | a0001 | c0002 | t0008 | g0010 | AMR | PUR | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG01106 | hp1 | a0002 | c0001 | t0001 | g0026 | AMR | PUR | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG01106 | hp2 | a0001 | c0002 | t0004 | g0048 | AMR | PUR | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG01109 | hp1 | a0002 | c0001 | t0001 | g0109 | AMR | PUR | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG01109 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG01167 | hp1 | a0002 | c0001 | t0019 | g0001 | AMR | PUR | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG01167 | hp2 | a0001 | c0003 | t0003 | g0148 | AMR | PUR | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG01168 | hp1 | a0001 | c0002 | t0002 | g0007 | AMR | PUR | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG01168 | hp2 | a0002 | c0001 | t0001 | g0030 | AMR | PUR | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG01169 | hp1 | a0002 | c0001 | t0001 | g0030 | AMR | PUR | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG01169 | hp2 | a0002 | c0001 | t0019 | g0001 | AMR | PUR | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG01243 | hp1 | a0002 | c0008 | t0001 | g0033 | AMR | PUR | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG01243 | hp2 | a0001 | c0002 | t0010 | g0055 | AMR | PUR | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG01255 | hp1 | a0001 | c0002 | t0036 | g0192 | AMR | CLM | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG01255 | hp2 | a0001 | c0002 | t0032 | g0225 | AMR | CLM | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG01257 | hp1 | a0002 | c0001 | t0001 | g0023 | AMR | CLM | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG01257 | hp2 | a0003 | c0005 | t0004 | g0044 | AMR | CLM | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG01258 | hp1 | a0001 | c0002 | t0008 | g0163 | AMR | CLM | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG01258 | hp2 | a0003 | c0005 | t0004 | g0044 | AMR | CLM | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG01346 | hp1 | a0001 | c0002 | t0004 | g0020 | AMR | CLM | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG01346 | hp2 | a0001 | c0002 | t0011 | g0017 | AMR | CLM | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG01358 | hp1 | a0001 | c0002 | t0011 | g0156 | AMR | CLM | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG01358 | hp2 | a0002 | c0001 | t0001 | g0023 | AMR | CLM | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG01361 | hp1 | a0001 | c0002 | t0010 | g0053 | AMR | CLM | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG01361 | hp2 | a0001 | c0002 | t0002 | g0007 | AMR | CLM | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG01433 | hp1 | a0002 | c0001 | t0001 | g0099 | AMR | CLM | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG01433 | hp2 | a0004 | c0012 | t0024 | g0161 | AMR | CLM | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG01496 | hp1 | a0002 | c0001 | t0001 | g0102 | AMR | CLM | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG01496 | hp2 | a0002 | c0001 | t0001 | g0094 | AMR | CLM | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG01515 | hp1 | a0002 | c0001 | t0001 | g0011 | EUR | IBS | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG01515 | hp2 | a0001 | c0002 | t0002 | g0007 | EUR | IBS | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG01516 | hp1 | a0002 | c0001 | t0001 | g0027 | EUR | IBS | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG01516 | hp2 | a0001 | c0002 | t0010 | g0022 | EUR | IBS | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG01517 | hp1 | a0002 | c0001 | t0001 | g0027 | EUR | IBS | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG01517 | hp2 | a0001 | c0002 | t0002 | g0007 | EUR | IBS | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG01884 | hp1 | a0001 | c0002 | t0016 | g0208 | AFR | ACB | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG01884 | hp2 | a0001 | c0003 | t0029 | g0141 | AFR | ACB | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG01891 | hp1 | a0001 | c0002 | t0033 | g0219 | AFR | ACB | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG01891 | hp2 | a0002 | c0001 | t0001 | g0112 | AFR | ACB | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG01928 | hp1 | a0001 | c0003 | t0003 | g0149 | AMR | PEL | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG01928 | hp2 | a0002 | c0001 | t0001 | g0103 | AMR | PEL | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG01934 | hp1 | a0002 | c0001 | t0001 | g0063 | AMR | PEL | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG01934 | hp2 | a0001 | c0002 | t0007 | g0170 | AMR | PEL | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG01943 | hp1 | a0001 | c0002 | t0002 | g0205 | AMR | PEL | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG01943 | hp2 | a0001 | c0002 | t0004 | g0159 | AMR | PEL | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG01952 | hp1 | a0002 | c0001 | t0001 | g0013 | AMR | PEL | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG01952 | hp2 | a0002 | c0001 | t0001 | g0101 | AMR | PEL | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG01978 | hp1 | a0002 | c0001 | t0001 | g0013 | AMR | PEL | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG01978 | hp2 | a0001 | c0003 | t0003 | g0150 | AMR | PEL | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG01981 | hp1 | a0001 | c0003 | t0003 | g0016 | AMR | PEL | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG01981 | hp2 | a0001 | c0002 | t0007 | g0179 | AMR | PEL | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG02040 | hp1 | a0001 | c0003 | t0003 | g0153 | EAS | KHV | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG02040 | hp2 | a0002 | c0001 | t0013 | g0034 | EAS | KHV | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG02056 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | KHV | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG02056 | hp2 | a0001 | c0011 | t0004 | g0224 | EAS | KHV | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG02083 | hp1 | a0002 | c0001 | t0013 | g0034 | EAS | KHV | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG02083 | hp2 | a0001 | c0003 | t0003 | g0002 | EAS | KHV | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG02132 | hp1 | a0001 | c0002 | t0002 | g0172 | EAS | KHV | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG02132 | hp2 | a0002 | c0001 | t0001 | g0075 | EAS | KHV | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG02135 | hp1 | a0002 | c0014 | t0001 | g0005 | EAS | KHV | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG02135 | hp2 | a0002 | c0001 | t0001 | g0093 | EAS | KHV | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG02145 | hp1 | a0001 | c0002 | t0002 | g0003 | AFR | ACB | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG02145 | hp2 | a0002 | c0008 | t0001 | g0033 | AFR | ACB | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG02148 | hp1 | a0002 | c0001 | t0001 | g0013 | AMR | PEL | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG02148 | hp2 | a0001 | c0003 | t0003 | g0016 | AMR | PEL | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG02257 | hp1 | a0001 | c0002 | t0034 | g0202 | AFR | ACB | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG02257 | hp2 | a0001 | c0002 | t0010 | g0021 | AFR | ACB | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG02258 | hp1 | a0001 | c0002 | t0002 | g0003 | AFR | ACB | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG02258 | hp2 | a0001 | c0002 | t0006 | g0188 | AFR | ACB | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG02280 | hp1 | a0001 | c0006 | t0028 | g0216 | AFR | ACB | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG02280 | hp2 | a0001 | c0002 | t0012 | g0203 | AFR | ACB | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG02451 | hp1 | a0001 | c0002 | t0008 | g0010 | AFR | ACB | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG02451 | hp2 | a0001 | c0004 | t0005 | g0215 | AFR | ACB | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG02523 | hp1 | a0002 | c0001 | t0001 | g0008 | EAS | KHV | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG02523 | hp2 | a0002 | c0001 | t0001 | g0005 | EAS | KHV | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG02572 | hp1 | a0002 | c0001 | t0001 | g0001 | AFR | GWD | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG02572 | hp2 | a0001 | c0002 | t0006 | g0186 | AFR | GWD | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG02615 | hp1 | a0001 | c0002 | t0010 | g0022 | AFR | GWD | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG02615 | hp2 | a0001 | c0002 | t0004 | g0035 | AFR | GWD | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG02622 | hp1 | a0001 | c0002 | t0004 | g0059 | AFR | GWD | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG02622 | hp2 | a0002 | c0001 | t0001 | g0029 | AFR | GWD | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG02630 | hp1 | a0001 | c0002 | t0006 | g0190 | AFR | GWD | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG02630 | hp2 | a0001 | c0002 | t0004 | g0035 | AFR | GWD | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG02647 | hp1 | a0001 | c0002 | t0006 | g0187 | AFR | GWD | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG02647 | hp2 | a0001 | c0003 | t0009 | g0143 | AFR | GWD | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG02683 | hp1 | a0001 | c0002 | t0011 | g0017 | SAS | PJL | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG02683 | hp2 | a0002 | c0001 | t0001 | g0011 | SAS | PJL | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG02698 | hp1 | a0002 | c0001 | t0001 | g0114 | SAS | PJL | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG02698 | hp2 | a0001 | c0013 | t0011 | g0157 | SAS | PJL | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG02723 | hp1 | a0001 | c0002 | t0021 | g0054 | AFR | GWD | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG02723 | hp2 | a0002 | c0001 | t0001 | g0060 | AFR | GWD | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG02735 | hp1 | a0002 | c0001 | t0001 | g0116 | SAS | PJL | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG02735 | hp2 | a0001 | c0002 | t0004 | g0221 | SAS | PJL | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG02738 | hp1 | a0002 | c0001 | t0001 | g0026 | SAS | PJL | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG02738 | hp2 | a0002 | c0001 | t0001 | g0118 | SAS | PJL | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG02809 | hp1 | a0002 | c0001 | t0001 | g0131 | AFR | GWD | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG02809 | hp2 | a0002 | c0001 | t0001 | g0014 | AFR | GWD | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG02818 | hp1 | a0001 | c0002 | t0006 | g0006 | AFR | GWD | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG02818 | hp2 | a0002 | c0001 | t0001 | g0111 | AFR | GWD | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG02886 | hp1 | a0001 | c0002 | t0006 | g0185 | AFR | GWD | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG02886 | hp2 | a0001 | c0002 | t0022 | g0217 | AFR | GWD | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG02896 | hp1 | a0001 | c0003 | t0003 | g0139 | AFR | GWD | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG02896 | hp2 | a0001 | c0002 | t0004 | g0165 | AFR | GWD | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG02897 | hp1 | a0001 | c0003 | t0009 | g0145 | AFR | GWD | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG02897 | hp2 | a0001 | c0002 | t0004 | g0164 | AFR | GWD | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG02922 | hp1 | a0001 | c0004 | t0005 | g0214 | AFR | ESN | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG02922 | hp2 | a0002 | c0001 | t0001 | g0064 | AFR | ESN | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG02965 | hp1 | a0002 | c0001 | t0001 | g0014 | AFR | ESN | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG02965 | hp2 | a0001 | c0002 | t0016 | g0209 | AFR | ESN | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG02970 | hp1 | a0002 | c0001 | t0001 | g0124 | AFR | ESN | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG02970 | hp2 | a0001 | c0003 | t0003 | g0015 | AFR | ESN | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG03017 | hp1 | a0002 | c0001 | t0001 | g0079 | SAS | PJL | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG03017 | hp2 | a0001 | c0004 | t0005 | g0040 | SAS | PJL | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG03041 | hp1 | a0001 | c0002 | t0006 | g0006 | AFR | GWD | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG03041 | hp2 | a0001 | c0004 | t0005 | g0039 | AFR | GWD | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG03098 | hp1 | a0002 | c0001 | t0001 | g0110 | AFR | MSL | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG03098 | hp2 | a0001 | c0003 | t0003 | g0015 | AFR | MSL | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG03130 | hp1 | a0001 | c0003 | t0003 | g0146 | AFR | ESN | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG03130 | hp2 | a0001 | c0002 | t0006 | g0006 | AFR | ESN | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG03139 | hp1 | a0001 | c0002 | t0006 | g0189 | AFR | ESN | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG03139 | hp2 | a0001 | c0003 | t0009 | g0009 | AFR | ESN | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG03195 | hp1 | a0001 | c0007 | t0003 | g0046 | AFR | ESN | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG03195 | hp2 | a0001 | c0003 | t0003 | g0015 | AFR | ESN | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG03209 | hp1 | a0001 | c0002 | t0012 | g0049 | AFR | MSL | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG03209 | hp2 | a0002 | c0001 | t0001 | g0088 | AFR | MSL | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG03225 | hp1 | a0005 | c0009 | t0026 | g0061 | AFR | MSL | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG03225 | hp2 | a0001 | c0003 | t0009 | g0144 | AFR | MSL | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG03239 | hp1 | a0002 | c0001 | t0001 | g0089 | SAS | PJL | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG03239 | hp2 | a0001 | c0002 | t0008 | g0162 | SAS | PJL | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG03453 | hp1 | a0002 | c0001 | t0001 | g0014 | AFR | MSL | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG03453 | hp2 | a0001 | c0002 | t0004 | g0160 | AFR | MSL | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG03490 | hp1 | a0001 | c0002 | t0002 | g0174 | SAS | PJL | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG03490 | hp2 | a0002 | c0001 | t0001 | g0001 | SAS | PJL | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG03491 | hp1 | a0001 | c0004 | t0005 | g0040 | SAS | PJL | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG03491 | hp2 | a0002 | c0001 | t0017 | g0025 | SAS | PJL | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG03492 | hp1 | a0002 | c0001 | t0017 | g0025 | SAS | PJL | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG03492 | hp2 | a0001 | c0002 | t0002 | g0180 | SAS | PJL | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG03516 | hp1 | a0001 | c0003 | t0003 | g0147 | AFR | ESN | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG03516 | hp2 | a0001 | c0002 | t0006 | g0006 | AFR | ESN | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG03540 | hp1 | a0002 | c0001 | t0001 | g0001 | AFR | GWD | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG03540 | hp2 | a0001 | c0002 | t0004 | g0056 | AFR | GWD | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG03579 | hp1 | a0002 | c0001 | t0001 | g0096 | AFR | MSL | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG03579 | hp2 | a0002 | c0001 | t0001 | g0106 | AFR | MSL | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG03654 | hp1 | a0001 | c0002 | t0002 | g0037 | SAS | PJL | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG03654 | hp2 | a0001 | c0002 | t0002 | g0196 | SAS | PJL | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG03831 | hp1 | a0002 | c0001 | t0001 | g0087 | SAS | BEB | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG03831 | hp2 | a0001 | c0002 | t0008 | g0010 | SAS | BEB | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG03927 | hp1 | a0002 | c0001 | t0001 | g0083 | SAS | BEB | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG03927 | hp2 | a0001 | c0002 | t0002 | g0199 | SAS | BEB | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG03942 | hp1 | a0002 | c0001 | t0001 | g0069 | SAS | BEB | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG03942 | hp2 | a0002 | c0001 | t0001 | g0115 | SAS | BEB | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG04115 | hp1 | a0001 | c0002 | t0008 | g0010 | SAS | STU | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG04115 | hp2 | a0001 | c0002 | t0004 | g0222 | SAS | STU | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG04184 | hp1 | a0001 | c0002 | t0002 | g0176 | SAS | BEB | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG04184 | hp2 | a0002 | c0001 | t0001 | g0068 | SAS | BEB | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG04199 | hp1 | a0002 | c0001 | t0001 | g0072 | SAS | STU | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG04199 | hp2 | a0002 | c0001 | t0001 | g0119 | SAS | STU | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG04228 | hp1 | a0002 | c0001 | t0001 | g0130 | SAS | STU | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG04228 | hp2 | a0002 | c0001 | t0001 | g0080 | SAS | STU | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA18522 | hp1 | a0001 | c0002 | t0006 | g0006 | AFR | YRI | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA18522 | hp2 | a0001 | c0002 | t0010 | g0021 | AFR | YRI | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA18612 | hp1 | a0002 | c0001 | t0001 | g0005 | EAS | CHB | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA18612 | hp2 | a0001 | c0003 | t0003 | g0002 | EAS | CHB | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA18906 | hp1 | a0002 | c0001 | t0001 | g0097 | AFR | YRI | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA18906 | hp2 | a0001 | c0002 | t0015 | g0058 | AFR | YRI | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA18941 | hp1 | a0001 | c0002 | t0004 | g0041 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA18941 | hp2 | a0002 | c0001 | t0031 | g0050 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA18942 | hp1 | a0001 | c0003 | t0003 | g0002 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA18942 | hp2 | a0001 | c0002 | t0002 | g0194 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA18945 | hp1 | a0002 | c0001 | t0001 | g0004 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA18945 | hp2 | a0001 | c0002 | t0002 | g0200 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA18946 | hp1 | a0002 | c0001 | t0001 | g0012 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA18946 | hp2 | a0001 | c0004 | t0005 | g0019 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA18950 | hp1 | a0001 | c0002 | t0002 | g0198 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA18950 | hp2 | a0002 | c0001 | t0001 | g0004 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA18951 | hp1 | a0001 | c0002 | t0002 | g0177 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA18951 | hp2 | a0002 | c0001 | t0001 | g0077 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA18952 | hp1 | a0001 | c0003 | t0003 | g0002 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA18952 | hp2 | a0002 | c0001 | t0001 | g0134 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA18953 | hp1 | a0001 | c0004 | t0005 | g0019 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA18953 | hp2 | a0001 | c0002 | t0004 | g0042 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA18957 | hp1 | a0002 | c0001 | t0001 | g0090 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA18957 | hp2 | a0001 | c0002 | t0035 | g0178 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA18959 | hp1 | a0002 | c0001 | t0001 | g0125 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA18959 | hp2 | a0001 | c0002 | t0020 | g0220 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA18960 | hp1 | a0001 | c0003 | t0003 | g0155 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA18960 | hp2 | a0002 | c0001 | t0001 | g0105 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA18963 | hp1 | a0002 | c0001 | t0001 | g0066 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA18963 | hp2 | a0001 | c0003 | t0003 | g0002 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA18964 | hp1 | a0002 | c0001 | t0001 | g0122 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA18964 | hp2 | a0002 | c0001 | t0001 | g0082 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA18967 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA18967 | hp2 | a0001 | c0004 | t0005 | g0210 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA18969 | hp1 | a0002 | c0001 | t0001 | g0120 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA18969 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA18973 | hp1 | a0001 | c0002 | t0007 | g0181 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA18973 | hp2 | a0002 | c0001 | t0001 | g0138 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA18974 | hp1 | a0002 | c0001 | t0001 | g0008 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA18974 | hp2 | a0001 | c0002 | t0002 | g0175 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA18980 | hp1 | a0002 | c0001 | t0001 | g0133 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA18980 | hp2 | a0001 | c0003 | t0003 | g0002 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA18983 | hp1 | a0002 | c0001 | t0001 | g0005 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA18983 | hp2 | a0002 | c0001 | t0013 | g0135 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA18984 | hp1 | a0001 | c0003 | t0003 | g0002 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA18984 | hp2 | a0002 | c0001 | t0001 | g0121 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA18985 | hp1 | a0001 | c0002 | t0007 | g0166 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA18985 | hp2 | a0002 | c0001 | t0014 | g0028 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA18986 | hp1 | a0001 | c0002 | t0007 | g0051 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA18986 | hp2 | a0002 | c0001 | t0001 | g0100 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA18987 | hp1 | a0002 | c0001 | t0018 | g0073 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA18987 | hp2 | a0002 | c0001 | t0001 | g0005 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA18990 | hp1 | a0001 | c0002 | t0004 | g0042 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA18990 | hp2 | a0002 | c0001 | t0001 | g0108 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA18993 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA18993 | hp2 | a0002 | c0001 | t0001 | g0062 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA18995 | hp1 | a0001 | c0003 | t0003 | g0002 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA18995 | hp2 | a0002 | c0001 | t0001 | g0071 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA18998 | hp1 | a0002 | c0001 | t0001 | g0004 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA18998 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA18999 | hp1 | a0002 | c0001 | t0001 | g0004 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA18999 | hp2 | a0001 | c0002 | t0004 | g0043 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA19000 | hp1 | a0001 | c0003 | t0003 | g0154 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA19000 | hp2 | a0002 | c0001 | t0030 | g0084 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA19003 | hp1 | a0001 | c0002 | t0002 | g0201 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA19003 | hp2 | a0002 | c0001 | t0001 | g0065 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA19004 | hp1 | a0002 | c0001 | t0001 | g0004 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA19004 | hp2 | a0001 | c0003 | t0003 | g0002 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA19007 | hp1 | a0002 | c0001 | t0001 | g0004 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA19007 | hp2 | a0002 | c0001 | t0001 | g0126 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA19009 | hp1 | a0001 | c0002 | t0004 | g0041 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA19009 | hp2 | a0001 | c0002 | t0007 | g0037 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA19010 | hp1 | a0002 | c0015 | t0001 | g0074 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA19010 | hp2 | a0002 | c0001 | t0001 | g0005 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA19011 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA19011 | hp2 | a0002 | c0001 | t0014 | g0028 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA19030 | hp1 | a0001 | c0003 | t0009 | g0009 | AFR | LWK | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA19030 | hp2 | a0001 | c0002 | t0004 | g0223 | AFR | LWK | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA19043 | hp1 | a0001 | c0007 | t0003 | g0045 | AFR | LWK | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA19043 | hp2 | a0001 | c0006 | t0027 | g0218 | AFR | LWK | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA19055 | hp1 | a0002 | c0001 | t0001 | g0107 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA19055 | hp2 | a0001 | c0004 | t0005 | g0019 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA19060 | hp1 | a0001 | c0002 | t0007 | g0003 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA19060 | hp2 | a0002 | c0001 | t0001 | g0123 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA19062 | hp1 | a0001 | c0016 | t0002 | g0195 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA19062 | hp2 | a0002 | c0001 | t0001 | g0067 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA19064 | hp1 | a0001 | c0003 | t0003 | g0002 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA19064 | hp2 | a0002 | c0001 | t0001 | g0012 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA19066 | hp1 | a0002 | c0001 | t0001 | g0078 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA19066 | hp2 | a0002 | c0001 | t0001 | g0092 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA19072 | hp1 | a0002 | c0001 | t0001 | g0117 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA19072 | hp2 | a0001 | c0002 | t0007 | g0173 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA19074 | hp1 | a0002 | c0001 | t0001 | g0070 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA19074 | hp2 | a0001 | c0002 | t0002 | g0182 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA19078 | hp1 | a0001 | c0002 | t0002 | g0191 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA19078 | hp2 | a0002 | c0001 | t0001 | g0047 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA19082 | hp1 | a0001 | c0002 | t0007 | g0207 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA19082 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA19083 | hp1 | a0001 | c0004 | t0005 | g0211 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA19083 | hp2 | a0002 | c0001 | t0001 | g0024 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA19087 | hp1 | a0001 | c0004 | t0005 | g0213 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA19087 | hp2 | a0002 | c0001 | t0001 | g0024 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA19088 | hp1 | a0002 | c0001 | t0001 | g0008 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA19088 | hp2 | a0001 | c0002 | t0002 | g0197 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA19089 | hp1 | a0002 | c0001 | t0001 | g0137 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA19089 | hp2 | a0001 | c0002 | t0007 | g0204 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA19091 | hp1 | a0002 | c0001 | t0001 | g0008 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA19091 | hp2 | a0001 | c0002 | t0002 | g0183 | EAS | JPT | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA19240 | hp1 | a0002 | c0001 | t0001 | g0032 | AFR | YRI | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA19240 | hp2 | a0001 | c0003 | t0009 | g0009 | AFR | YRI | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA20129 | hp1 | a0002 | c0001 | t0001 | g0029 | AFR | ASW | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA20129 | hp2 | a0001 | c0004 | t0005 | g0039 | AFR | ASW | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA20752 | hp1 | a0001 | c0002 | t0002 | g0206 | EUR | TSI | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA20752 | hp2 | a0002 | c0001 | t0001 | g0128 | EUR | TSI | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA20805 | hp1 | a0001 | c0002 | t0008 | g0158 | EUR | TSI | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA20805 | hp2 | a0002 | c0001 | t0001 | g0081 | EUR | TSI | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA20905 | hp1 | a0002 | c0001 | t0001 | g0113 | SAS | GIH | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA20905 | hp2 | a0006 | c0010 | t0004 | g0043 | SAS | GIH | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG01123 | hp1 | a0001 | c0002 | t0002 | g0007 | AMR | CLM | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG01123 | hp2 | a0001 | c0003 | t0003 | g0151 | AMR | CLM | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG02109 | hp1 | a0001 | c0002 | t0006 | g0006 | AFR | ACB | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG02109 | hp2 | a0001 | c0003 | t0009 | g0140 | AFR | ACB | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG02486 | hp1 | a0001 | c0002 | t0015 | g0052 | AFR | ACB | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG02486 | hp2 | a0002 | c0001 | t0001 | g0032 | AFR | ACB | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG02559 | hp1 | a0001 | c0004 | t0005 | g0212 | AFR | ACB | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG02559 | hp2 | a0001 | c0002 | t0012 | g0038 | AFR | ACB | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG03471 | hp1 | a0001 | c0002 | t0004 | g0057 | AFR | MSL | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG03471 | hp2 | a0001 | c0003 | t0023 | g0142 | AFR | MSL | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG06807 | hp1 | a0001 | c0002 | t0012 | g0038 | AFR | USA | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| HG06807 | hp2 | a0002 | c0001 | t0001 | g0001 | AFR | USA | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA21309 | hp1 | a0001 | c0003 | t0009 | g0009 | AFR | LWK | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| NA21309 | hp2 | a0002 | c0001 | t0001 | g0001 | AFR | LWK | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0008 | g0018 | REF | REF | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| homoSapiens | grch38p0 | a0002 | c0001 | t0001 | g0001 | REF | REF | UBE3B_chr12_109472634_109541702 | UBE3B | chr12 | 109472634 | 109541702 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:109486017 | T | G | 1 | a0005 | 1 | HG03225.hp1 | missense_variant | MODERATE | c.288T>G | p.Phe96Leu | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 5/28 | 891/5730 | 288/3207 | 96/1068 | chr12 | 109486017 | |||
| chr12:109491100 | T | C | 1 | a0006 | 1 | NA20905.hp2 | missense_variant | MODERATE | c.686T>C | p.Leu229Ser | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 9/28 | 1289/5730 | 686/3207 | 229/1068 | chr12 | 109491100 | |||
| chr12:109498251 | T | C | 1 | a0003 | 2 | HG01257.hp2 HG01258.hp2 |
missense_variant | MODERATE | c.838T>C | p.Ser280Pro | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 11/28 | 1441/5730 | 838/3207 | 280/1068 | chr12 | 109498251 | |||
| chr12:109499729 | G | A | 5 | a0001 a0003 a0004 others(2): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
missense_variant | MODERATE | c.1037G>A | p.Arg346Gln | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 12/28 | 1640/5730 | 1037/3207 | 346/1068 | chr12 | 109499729 | |||
| chr12:109530647 | A | G | 1 | a0004 | 1 | HG01433.hp2 | missense_variant | MODERATE | c.2911A>G | p.Met971Val | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 26/28 | 3514/5730 | 2911/3207 | 971/1068 | chr12 | 109530647 |
| 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 cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:109483590 | C | T | 1 | a0001c0016 | 1 | NA19062.hp1 | synonymous_variant | LOW | c.39C>T | p.Ile13Ile | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 3/28 | 642/5730 | 39/3207 | 13/1068 | chr12 | 109483590 | |||
| chr12:109483918 | A | C | 1 | a0001c0004 | 13 | HG02451.hp2 HG02559.hp1 HG02922.hp1 others(10): Show |
synonymous_variant | LOW | c.219A>C | p.Ala73Ala | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 4/28 | 822/5730 | 219/3207 | 73/1068 | chr12 | 109483918 | |||
| chr12:109490001 | G | C | 1 | a0001c0004 | 13 | HG02451.hp2 HG02559.hp1 HG02922.hp1 others(10): Show |
synonymous_variant | LOW | c.627G>C | p.Leu209Leu | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 8/28 | 1230/5730 | 627/3207 | 209/1068 | chr12 | 109490001 | |||
| chr12:109501437 | G | C | 1 | a0002c0008 | 2 | HG01243.hp1 HG02145.hp2 |
synonymous_variant | LOW | c.1185G>C | p.Arg395Arg | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 13/28 | 1788/5730 | 1185/3207 | 395/1068 | chr12 | 109501437 | |||
| chr12:109507628 | C | T | 1 | a0001c0007 | 2 | HG03195.hp1 NA19043.hp1 |
synonymous_variant | LOW | c.1515C>T | p.His505His | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 15/28 | 2118/5730 | 1515/3207 | 505/1068 | chr12 | 109507628 | |||
| chr12:109511237 | C | T | 1 | a0002c0015 | 1 | NA19010.hp1 | synonymous_variant | LOW | c.1890C>T | p.Leu630Leu | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 18/28 | 2493/5730 | 1890/3207 | 630/1068 | chr12 | 109511237 | |||
| chr12:109521255 | C | T | 1 | a0005c0009 | 1 | HG03225.hp1 | synonymous_variant | LOW | c.2184C>T | p.Asp728Asp | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 20/28 | 2787/5730 | 2184/3207 | 728/1068 | chr12 | 109521255 | |||
| chr12:109524043 | C | T | 1 | a0001c0013 | 1 | HG02698.hp2 | synonymous_variant | LOW | c.2430C>T | p.Ser810Ser | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 22/28 | 3033/5730 | 2430/3207 | 810/1068 | chr12 | 109524043 | |||
| chr12:109524473 | G | A | 1 | a0002c0014 | 1 | HG02135.hp1 | synonymous_variant | LOW | c.2538G>A | p.Thr846Thr | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 23/28 | 3141/5730 | 2538/3207 | 846/1068 | chr12 | 109524473 | |||
| chr12:109526387 | G | A | 1 | a0001c0011 | 1 | HG02056.hp2 | synonymous_variant | LOW | c.2598G>A | p.Gly866Gly | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 24/28 | 3201/5730 | 2598/3207 | 866/1068 | chr12 | 109526387 | |||
| chr12:109530040 | C | T | 1 | a0001c0006 | 2 | HG02280.hp1 NA19043.hp2 |
synonymous_variant | LOW | c.2778C>T | p.Gly926Gly | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 25/28 | 3381/5730 | 2778/3207 | 926/1068 | chr12 | 109530040 | |||
| chr12:109530622 | C | T | 2 | a0001c0003 a0001c0007 |
40 | HG00099.hp2 HG00423.hp1 HG01099.hp1 others(37): Show |
synonymous_variant | LOW | c.2886C>T | p.Ser962Ser | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 26/28 | 3489/5730 | 2886/3207 | 962/1068 | chr12 | 109530622 |
| 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 cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:109477662 | G | C | 1 | a0001c0002t0020 | 1 | NA18959.hp2 | 5_prime_UTR_variant | MODIFIER | c.-575G>C | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 1/28 | 5890 | chr12 | 109477662 | ||||||
| chr12:109477688 | A | G | 1 | a0001c0003t0009 | 8 | HG02109.hp2 HG02647.hp2 HG02897.hp1 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-549A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 1/28 | 5864 | chr12 | 109477688 | ||||||
| chr12:109477765 | G | A | 1 | a0002c0001t0014 | 2 | NA18985.hp2 NA19011.hp2 |
5_prime_UTR_variant | MODIFIER | c.-472G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 1/28 | 5787 | chr12 | 109477765 | ||||||
| chr12:109477795 | C | A | 1 | a0001c0002t0021 | 1 | HG02723.hp1 | 5_prime_UTR_variant | MODIFIER | c.-442C>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 1/28 | 5757 | chr12 | 109477795 | ||||||
| chr12:109477922 | G | T | 9 | a0001c0002t0002 a0001c0002t0006 a0001c0002t0007 others(6): Show |
72 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(69): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-315G>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 1/28 | chr12 | 109477922 | |||||||
| chr12:109478067 | T | C | 1 | a0001c0002t0033 | 1 | HG01891.hp1 | 5_prime_UTR_variant | MODIFIER | c.-170T>C | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 1/28 | 5485 | chr12 | 109478067 | ||||||
| chr12:109481675 | C | T | 2 | a0001c0002t0010 a0001c0002t0021 |
7 | HG01243.hp2 HG01361.hp1 HG01516.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-89C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 2/28 | 1877 | chr12 | 109481675 | ||||||
| chr12:109481682 | G | A | 1 | a0001c0002t0022 | 1 | HG02886.hp2 | 5_prime_UTR_variant | MODIFIER | c.-82G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 2/28 | 1870 | chr12 | 109481682 | ||||||
| chr12:109481734 | G | T | 1 | a0001c0002t0032 | 1 | HG01255.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-30G>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 2/28 | chr12 | 109481734 | |||||||
| chr12:109535323 | A | G | 1 | a0002c0001t0019 | 2 | HG01167.hp1 HG01169.hp2 |
3_prime_UTR_variant | MODIFIER | c.*541A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 28/28 | 541 | chr12 | 109535323 | ||||||
| chr12:109535341 | C | T | 1 | a0001c0002t0036 | 1 | HG01255.hp1 | 3_prime_UTR_variant | MODIFIER | c.*559C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 28/28 | 559 | chr12 | 109535341 | ||||||
| chr12:109535364 | A | G | 1 | a0001c0002t0035 | 1 | NA18957.hp2 | 3_prime_UTR_variant | MODIFIER | c.*582A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 28/28 | 582 | chr12 | 109535364 | ||||||
| chr12:109535373 | G | A | 3 | a0001c0002t0008 a0001c0003t0023 a0004c0012t0024 |
11 | HG00639.hp2 HG00642.hp2 HG01099.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*591G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 28/28 | 591 | chr12 | 109535373 | ||||||
| chr12:109535451 | G | A | 1 | a0002c0001t0025 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*669G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 28/28 | 669 | chr12 | 109535451 | ||||||
| chr12:109535468 | T | C | 33 | a0001c0002t0002 a0001c0002t0004 a0001c0002t0006 others(30): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
3_prime_UTR_variant | MODIFIER | c.*686T>C | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 28/28 | 686 | chr12 | 109535468 | ||||||
| chr12:109535487 | G | T | 2 | a0001c0002t0011 a0001c0013t0011 |
5 | HG00140.hp1 HG01346.hp2 HG01358.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*705G>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 28/28 | 705 | chr12 | 109535487 | ||||||
| chr12:109535492 | A | G | 8 | a0001c0002t0002 a0001c0002t0006 a0001c0002t0007 others(5): Show |
71 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*710A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 28/28 | 710 | chr12 | 109535492 | ||||||
| chr12:109535594 | C | T | 1 | a0001c0003t0029 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*812C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 28/28 | 812 | chr12 | 109535594 | ||||||
| chr12:109535691 | G | A | 1 | a0001c0002t0015 | 2 | HG02486.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*909G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 28/28 | 909 | chr12 | 109535691 | ||||||
| chr12:109535712 | C | A | 1 | a0005c0009t0026 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*930C>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 28/28 | 930 | chr12 | 109535712 | ||||||
| chr12:109535747 | C | T | 1 | a0002c0001t0031 | 1 | NA18941.hp2 | 3_prime_UTR_variant | MODIFIER | c.*965C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 28/28 | 965 | chr12 | 109535747 | ||||||
| chr12:109535776 | G | A | 1 | a0001c0002t0034 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*994G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 28/28 | 994 | chr12 | 109535776 | ||||||
| chr12:109535869 | C | A | 3 | a0001c0004t0005 a0002c0001t0017 a0005c0009t0026 |
16 | HG02451.hp2 HG02559.hp1 HG02922.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1087C>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 28/28 | 1087 | chr12 | 109535869 | ||||||
| chr12:109535925 | G | A | 1 | a0002c0001t0018 | 2 | HG00408.hp2 NA18987.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1143G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 28/28 | 1143 | chr12 | 109535925 | ||||||
| chr12:109535946 | C | T | 1 | a0004c0012t0024 | 1 | HG01433.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1164C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 28/28 | 1164 | chr12 | 109535946 | ||||||
| chr12:109535960 | C | G | 1 | a0005c0009t0026 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1178C>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 28/28 | 1178 | chr12 | 109535960 | ||||||
| chr12:109536024 | C | T | 2 | a0001c0002t0012 a0001c0002t0034 |
5 | HG02257.hp1 HG02280.hp2 HG02559.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1242C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 28/28 | 1242 | chr12 | 109536024 | ||||||
| chr12:109536143 | AC | A | 1 | a0002c0001t0013 | 3 | HG02040.hp2 HG02083.hp1 NA18983.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1364delC | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 28/28 | 1364 | INFO_REALIGN_3_PRIME | chr12 | 109536143 | |||||
| chr12:109536174 | G | C | 32 | a0001c0002t0002 a0001c0002t0004 a0001c0002t0006 others(29): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
3_prime_UTR_variant | MODIFIER | c.*1392G>C | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 28/28 | 1392 | chr12 | 109536174 | ||||||
| chr12:109536176 | G | A | 8 | a0001c0002t0002 a0001c0002t0006 a0001c0002t0007 others(5): Show |
71 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*1394G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 28/28 | 1394 | chr12 | 109536176 | ||||||
| chr12:109536224 | A | G | 8 | a0001c0002t0022 a0001c0003t0003 a0001c0003t0009 others(5): Show |
43 | HG00099.hp2 HG00423.hp1 HG01099.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*1442A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 28/28 | 1442 | chr12 | 109536224 | ||||||
| chr12:109536295 | C | T | 1 | a0001c0006t0028 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1513C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 28/28 | 1513 | chr12 | 109536295 | ||||||
| chr12:109536297 | G | A | 1 | a0002c0001t0030 | 1 | NA19000.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1515G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 28/28 | 1515 | chr12 | 109536297 | ||||||
| chr12:109536346 | C | T | 9 | a0001c0002t0002 a0001c0002t0006 a0001c0002t0007 others(6): Show |
72 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*1564C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 28/28 | 1564 | chr12 | 109536346 | ||||||
| chr12:109536386 | A | G | 8 | a0001c0002t0002 a0001c0002t0006 a0001c0002t0007 others(5): Show |
71 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*1604A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 28/28 | 1604 | chr12 | 109536386 | ||||||
| chr12:109536389 | T | A | 3 | a0001c0002t0022 a0001c0006t0027 a0001c0006t0028 |
3 | HG02280.hp1 HG02886.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1607T>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 28/28 | 1607 | chr12 | 109536389 | ||||||
| chr12:109536459 | G | A | 5 | a0001c0002t0002 a0001c0002t0007 a0001c0002t0035 others(2): Show |
54 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*1677G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 28/28 | 1677 | chr12 | 109536459 | ||||||
| chr12:109536490 | CAAG | C | 21 | a0001c0002t0004 a0001c0002t0008 a0001c0002t0010 others(18): Show |
93 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*1709_*1711delAAG | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 28/28 | 1709 | chr12 | 109536490 | ||||||
| chr12:109536592 | C | T | 3 | a0001c0002t0007 a0001c0002t0035 a0001c0002t0036 |
13 | HG00609.hp1 HG01255.hp1 HG01934.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1810C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 28/28 | 1810 | chr12 | 109536592 |
| 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 cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:109478124 | C | G | 11 | a0001c0002t0004g0041 a0001c0002t0004g0042 a0001c0002t0004g0043 others(8): Show |
14 | HG01255.hp2 HG01257.hp2 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.-128+15C>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 1/27 | chr12 | 109478124 | |||||||
| chr12:109478150 | G | A | 2 | a0001c0007t0003g0045 a0001c0007t0003g0046 |
2 | HG03195.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-128+41G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 1/27 | chr12 | 109478150 | |||||||
| chr12:109478321 | G | A | 1 | a0002c0001t0001g0047 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-128+212G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 1/27 | chr12 | 109478321 | |||||||
| chr12:109478480 | A | G | 1 | a0001c0002t0033g0219 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-128+371A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 1/27 | chr12 | 109478480 | |||||||
| chr12:109478657 | T | A | 2 | a0001c0002t0004g0020 a0001c0002t0004g0048 |
3 | HG01071.hp2 HG01106.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.-128+548T>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 1/27 | chr12 | 109478657 | |||||||
| chr12:109478848 | A | G | 3 | a0001c0002t0022g0217 a0001c0006t0027g0218 a0001c0006t0028g0216 |
3 | HG02280.hp1 HG02886.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-128+739A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 1/27 | chr12 | 109478848 | |||||||
| chr12:109478896 | C | G | 9 | a0001c0004t0005g0019 a0001c0004t0005g0039 a0001c0004t0005g0040 others(6): Show |
13 | HG02451.hp2 HG02559.hp1 HG02922.hp1 others(10): Show |
intron_variant | MODIFIER | c.-128+787C>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 1/27 | chr12 | 109478896 | |||||||
| chr12:109478985 | T | C | 1 | a0001c0002t0012g0049 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-128+876T>C | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 1/27 | chr12 | 109478985 | |||||||
| chr12:109479010 | C | G | 1 | a0001c0002t0033g0219 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-128+901C>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 1/27 | chr12 | 109479010 | |||||||
| chr12:109479101 | C | T | 2 | a0001c0002t0016g0208 a0001c0002t0016g0209 |
2 | HG01884.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-128+992C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 1/27 | chr12 | 109479101 | |||||||
| chr12:109479140 | C | A | 3 | a0001c0002t0004g0041 a0001c0002t0004g0042 a0001c0002t0020g0220 |
5 | NA18941.hp1 NA18953.hp2 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.-128+1031C>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 1/27 | chr12 | 109479140 | |||||||
| chr12:109479191 | C | T | 1 | a0001c0006t0027g0218 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-128+1082C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 1/27 | chr12 | 109479191 | |||||||
| chr12:109479481 | A | G | 1 | a0001c0002t0007g0207 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-128+1372A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 1/27 | chr12 | 109479481 | |||||||
| chr12:109479806 | G | C | 1 | a0002c0001t0031g0050 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-128+1697G>C | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 1/27 | chr12 | 109479806 | |||||||
| chr12:109480172 | G | A | 1 | a0001c0002t0007g0051 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-127-1465G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 1/27 | chr12 | 109480172 | |||||||
| chr12:109480212 | G | T | 1 | a0001c0002t0002g0206 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-127-1425G>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 1/27 | chr12 | 109480212 | |||||||
| chr12:109480298 | G | A | 12 | a0001c0002t0004g0020 a0001c0002t0004g0048 a0001c0002t0004g0056 others(9): Show |
15 | HG01071.hp2 HG01106.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.-127-1339G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 1/27 | chr12 | 109480298 | |||||||
| chr12:109480406 | G | T | 1 | a0002c0001t0001g0011 | 4 | HG00733.hp2 HG00738.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.-127-1231G>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 1/27 | chr12 | 109480406 | |||||||
| chr12:109480456 | A | G | 1 | a0001c0002t0022g0217 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-127-1181A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 1/27 | chr12 | 109480456 | |||||||
| chr12:109480600 | A | G | 52 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0036 others(49): Show |
71 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.-127-1037A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 1/27 | chr12 | 109480600 | |||||||
| chr12:109480650 | T | TA | 52 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0036 others(49): Show |
71 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.-127-973dupA | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 109480650 | ||||||
| chr12:109480650 | TAA | T | 23 | a0001c0002t0004g0020 a0001c0002t0004g0035 a0001c0002t0004g0048 others(20): Show |
31 | HG00639.hp2 HG00642.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-127-974_-127-973d others(4): Show |
UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 109480650 | ||||||
| chr12:109480669 | T | TA | 4 | a0001c0002t0022g0217 a0001c0006t0027g0218 a0001c0006t0028g0216 others(1): Show |
4 | HG02280.hp1 HG02886.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-127-967dupA | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 109480669 | ||||||
| chr12:109480776 | A | G | 3 | a0001c0002t0011g0017 a0001c0002t0011g0156 a0001c0013t0011g0157 |
5 | HG00140.hp1 HG01346.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.-127-861A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 1/27 | chr12 | 109480776 | |||||||
| chr12:109481029 | C | T | 23 | a0001c0003t0003g0002 a0001c0003t0003g0015 a0001c0003t0003g0016 others(20): Show |
40 | HG00099.hp2 HG00423.hp1 HG01099.hp1 others(37): Show |
intron_variant | MODIFIER | c.-127-608C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 1/27 | chr12 | 109481029 | |||||||
| chr12:109481036 | C | T | 1 | a0001c0002t0032g0225 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-127-601C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 1/27 | chr12 | 109481036 | |||||||
| chr12:109481062 | G | A | 3 | a0001c0002t0011g0017 a0001c0002t0011g0156 a0001c0013t0011g0157 |
5 | HG00140.hp1 HG01346.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.-127-575G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 1/27 | chr12 | 109481062 | |||||||
| chr12:109481104 | C | CA | 8 | a0001c0002t0002g0036 a0001c0002t0007g0166 a0001c0002t0008g0158 others(5): Show |
10 | HG00099.hp1 HG00733.hp1 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-127-516dupA | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 109481104 | ||||||
| chr12:109481104 | CA | C | 10 | a0001c0002t0016g0209 a0002c0001t0001g0008 a0002c0001t0001g0132 others(7): Show |
14 | HG00408.hp1 HG00673.hp2 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.-127-516delA | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 109481104 | ||||||
| chr12:109481129 | C | T | 52 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0036 others(49): Show |
71 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.-127-508C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 1/27 | chr12 | 109481129 | |||||||
| chr12:109481275 | C | T | 9 | a0001c0004t0005g0019 a0001c0004t0005g0039 a0001c0004t0005g0040 others(6): Show |
13 | HG02451.hp2 HG02559.hp1 HG02922.hp1 others(10): Show |
intron_variant | MODIFIER | c.-127-362C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 1/27 | chr12 | 109481275 | |||||||
| chr12:109481313 | C | CA | 9 | a0001c0004t0005g0019 a0001c0004t0005g0039 a0001c0004t0005g0040 others(6): Show |
13 | HG02451.hp2 HG02559.hp1 HG02922.hp1 others(10): Show |
intron_variant | MODIFIER | c.-127-310dupA | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 109481313 | ||||||
| chr12:109481313 | C | CAA | 4 | a0001c0002t0011g0017 a0001c0002t0011g0156 a0001c0004t0005g0211 others(1): Show |
6 | HG00140.hp1 HG01346.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.-127-311_-127-310d others(4): Show |
UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 109481313 | ||||||
| chr12:109481532 | C | A | 34 | a0001c0002t0004g0020 a0001c0002t0004g0035 a0001c0002t0004g0041 others(31): Show |
45 | HG00639.hp2 HG00642.hp2 HG01071.hp2 others(42): Show |
intron_variant | MODIFIER | c.-127-105C>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 1/27 | chr12 | 109481532 | |||||||
| chr12:109481804 | G | A | 2 | a0001c0006t0027g0218 a0001c0006t0028g0216 |
2 | HG02280.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-22+62G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 2/27 | chr12 | 109481804 | |||||||
| chr12:109482117 | A | G | 2 | a0001c0002t0016g0208 a0001c0002t0016g0209 |
2 | HG01884.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-22+375A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 2/27 | chr12 | 109482117 | |||||||
| chr12:109482148 | G | A | 2 | a0001c0002t0016g0208 a0001c0002t0016g0209 |
2 | HG01884.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-22+406G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 2/27 | chr12 | 109482148 | |||||||
| chr12:109482160 | A | C | 51 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0036 others(48): Show |
70 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.-22+418A>C | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 2/27 | chr12 | 109482160 | |||||||
| chr12:109482266 | G | T | 128 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0036 others(125): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.-22+524G>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 2/27 | chr12 | 109482266 | |||||||
| chr12:109482358 | A | G | 36 | a0001c0002t0022g0217 a0001c0003t0003g0002 a0001c0003t0003g0015 others(33): Show |
57 | HG00099.hp2 HG00423.hp1 HG01099.hp1 others(54): Show |
intron_variant | MODIFIER | c.-22+616A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 2/27 | chr12 | 109482358 | |||||||
| chr12:109482473 | C | G | 13 | a0001c0002t0022g0217 a0001c0004t0005g0019 a0001c0004t0005g0039 others(10): Show |
17 | HG02280.hp1 HG02451.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.-22+731C>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 2/27 | chr12 | 109482473 | |||||||
| chr12:109482611 | C | A | 1 | a0002c0001t0001g0024 | 2 | NA19083.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.-22+869C>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 2/27 | chr12 | 109482611 | |||||||
| chr12:109482683 | C | T | 3 | a0002c0001t0001g0032 a0002c0001t0001g0131 a0002c0008t0001g0033 |
5 | HG01243.hp1 HG02145.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-21-848C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 2/27 | chr12 | 109482683 | |||||||
| chr12:109482695 | C | T | 1 | a0002c0001t0001g0130 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-21-836C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 2/27 | chr12 | 109482695 | |||||||
| chr12:109482696 | T | C | 27 | a0001c0002t0022g0217 a0001c0003t0003g0002 a0001c0003t0003g0015 others(24): Show |
44 | HG00099.hp2 HG00423.hp1 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.-21-835T>C | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 2/27 | chr12 | 109482696 | |||||||
| chr12:109482697 | G | A | 1 | a0005c0009t0026g0061 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-21-834G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 2/27 | chr12 | 109482697 | |||||||
| chr12:109482702 | C | CT | 52 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0036 others(49): Show |
71 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.-21-826dupT | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr12 | 109482702 | ||||||
| chr12:109482766 | C | A | 1 | a0001c0002t0033g0219 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-21-765C>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 2/27 | chr12 | 109482766 | |||||||
| chr12:109482806 | G | A | 1 | a0001c0002t0022g0217 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-21-725G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 2/27 | chr12 | 109482806 | |||||||
| chr12:109482959 | A | T | 1 | a0002c0001t0001g0024 | 2 | NA19083.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.-21-572A>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 2/27 | chr12 | 109482959 | |||||||
| chr12:109483188 | T | C | 3 | a0001c0002t0022g0217 a0001c0006t0027g0218 a0001c0006t0028g0216 |
3 | HG02280.hp1 HG02886.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-21-343T>C | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 2/27 | chr12 | 109483188 | |||||||
| chr12:109483278 | C | G | 1 | a0001c0002t0022g0217 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-21-253C>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 2/27 | chr12 | 109483278 | |||||||
| chr12:109483286 | T | C | 2 | a0002c0001t0001g0130 a0002c0001t0017g0025 |
3 | HG03491.hp2 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.-21-245T>C | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 2/27 | chr12 | 109483286 | |||||||
| chr12:109483356 | A | T | 11 | a0001c0002t0004g0035 a0001c0002t0004g0159 a0001c0002t0004g0160 others(8): Show |
16 | HG00639.hp2 HG00642.hp2 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.-21-175A>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 2/27 | chr12 | 109483356 | |||||||
| chr12:109483453 | C | T | 23 | a0001c0003t0003g0002 a0001c0003t0003g0015 a0001c0003t0003g0016 others(20): Show |
40 | HG00099.hp2 HG00423.hp1 HG01099.hp1 others(37): Show |
intron_variant | MODIFIER | c.-21-78C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 2/27 | chr12 | 109483453 | |||||||
| chr12:109484004 | G | T | 1 | a0001c0002t0004g0042 | 2 | NA18953.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.282+23G>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 4/27 | chr12 | 109484004 | |||||||
| chr12:109484060 | A | T | 1 | a0001c0002t0012g0203 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.282+79A>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 4/27 | chr12 | 109484060 | |||||||
| chr12:109484081 | T | C | 23 | a0001c0003t0003g0002 a0001c0003t0003g0015 a0001c0003t0003g0016 others(20): Show |
40 | HG00099.hp2 HG00423.hp1 HG01099.hp1 others(37): Show |
intron_variant | MODIFIER | c.282+100T>C | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 4/27 | chr12 | 109484081 | |||||||
| chr12:109484234 | T | TA | 11 | a0001c0002t0004g0041 a0001c0002t0004g0042 a0001c0002t0004g0043 others(8): Show |
14 | HG01255.hp2 HG01257.hp2 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.282+261dupA | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr12 | 109484234 | ||||||
| chr12:109484356 | C | T | 9 | a0001c0003t0003g0002 a0001c0003t0003g0016 a0001c0003t0003g0149 others(6): Show |
21 | HG00099.hp2 HG00423.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.282+375C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 4/27 | chr12 | 109484356 | |||||||
| chr12:109484459 | T | A | 2 | a0001c0002t0004g0159 a0001c0002t0004g0160 |
2 | HG01943.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.282+478T>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 4/27 | chr12 | 109484459 | |||||||
| chr12:109484502 | C | T | 3 | a0001c0003t0003g0002 a0001c0003t0003g0154 a0001c0003t0003g0155 |
13 | HG00423.hp1 HG02083.hp2 NA18612.hp2 others(10): Show |
intron_variant | MODIFIER | c.282+521C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 4/27 | chr12 | 109484502 | |||||||
| chr12:109484538 | C | T | 3 | a0001c0002t0011g0017 a0001c0002t0011g0156 a0001c0013t0011g0157 |
5 | HG00140.hp1 HG01346.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.282+557C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 4/27 | chr12 | 109484538 | |||||||
| chr12:109484694 | AT | A | 7 | a0001c0002t0004g0159 a0001c0002t0007g0204 a0001c0002t0015g0052 others(4): Show |
7 | HG01891.hp1 HG01943.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.282+731delT | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr12 | 109484694 | ||||||
| chr12:109484929 | G | A | 5 | a0001c0002t0010g0021 a0001c0002t0010g0022 a0001c0002t0010g0053 others(2): Show |
7 | HG01243.hp2 HG01361.hp1 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.282+948G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 4/27 | chr12 | 109484929 | |||||||
| chr12:109485070 | T | A | 1 | a0001c0002t0002g0168 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.283-942T>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 4/27 | chr12 | 109485070 | |||||||
| chr12:109485119 | G | A | 1 | a0001c0002t0004g0221 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.283-893G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 4/27 | chr12 | 109485119 | |||||||
| chr12:109485137 | G | A | 1 | a0002c0001t0001g0068 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.283-875G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 4/27 | chr12 | 109485137 | |||||||
| chr12:109485207 | A | G | 1 | a0001c0003t0003g0155 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.283-805A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 4/27 | chr12 | 109485207 | |||||||
| chr12:109485241 | T | A | 1 | a0001c0002t0020g0220 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.283-771T>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 4/27 | chr12 | 109485241 | |||||||
| chr12:109485333 | C | G | 2 | a0002c0001t0001g0128 a0002c0001t0001g0129 |
2 | HG01074.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.283-679C>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 4/27 | chr12 | 109485333 | |||||||
| chr12:109485402 | G | A | 52 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0036 others(49): Show |
71 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.283-610G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 4/27 | chr12 | 109485402 | |||||||
| chr12:109485439 | A | G | 52 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0036 others(49): Show |
71 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.283-573A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 4/27 | chr12 | 109485439 | |||||||
| chr12:109486219 | C | G | 1 | a0001c0002t0012g0203 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.342+148C>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 5/27 | chr12 | 109486219 | |||||||
| chr12:109486448 | A | G | 1 | a0002c0001t0001g0130 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.343-23A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 5/27 | chr12 | 109486448 | |||||||
| chr12:109486580 | C | CA | 10 | a0001c0002t0010g0053 a0002c0001t0001g0026 a0002c0001t0001g0047 others(7): Show |
11 | HG01106.hp1 HG01361.hp1 HG02132.hp2 others(8): Show |
intron_variant | MODIFIER | c.447+28dupA | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr12 | 109486580 | ||||||
| chr12:109486580 | CA | C | 42 | a0001c0002t0004g0035 a0001c0002t0004g0056 a0001c0002t0004g0057 others(39): Show |
69 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.447+28delA | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr12 | 109486580 | ||||||
| chr12:109486580 | CAA | C | 9 | a0001c0002t0002g0037 a0001c0002t0002g0206 a0001c0002t0004g0059 others(6): Show |
9 | HG01167.hp2 HG01934.hp2 HG01943.hp2 others(6): Show |
intron_variant | MODIFIER | c.447+27_447+28delAA | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr12 | 109486580 | ||||||
| chr12:109486580 | CAAA | C | 49 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0036 others(46): Show |
68 | HG00099.hp1 HG00323.hp1 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.447+26_447+28delAA others(1): Show |
UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr12 | 109486580 | ||||||
| chr12:109486580 | CAAAAAAA others(1): Show |
C | 12 | a0001c0002t0004g0041 a0001c0002t0004g0042 a0001c0002t0004g0043 others(9): Show |
15 | HG00597.hp2 HG01255.hp2 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.447+21_447+28delAA others(6): Show |
UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr12 | 109486580 | ||||||
| chr12:109486721 | A | G | 1 | a0001c0002t0010g0055 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.447+146A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 6/27 | chr12 | 109486721 | |||||||
| chr12:109486723 | T | G | 53 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0036 others(50): Show |
72 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.447+148T>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 6/27 | chr12 | 109486723 | |||||||
| chr12:109486724 | C | G | 1 | a0001c0006t0027g0218 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.447+149C>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 6/27 | chr12 | 109486724 | |||||||
| chr12:109486780 | C | T | 1 | a0001c0006t0027g0218 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.447+205C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 6/27 | chr12 | 109486780 | |||||||
| chr12:109486863 | T | A | 1 | a0002c0001t0001g0132 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.447+288T>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 6/27 | chr12 | 109486863 | |||||||
| chr12:109486901 | C | T | 27 | a0001c0002t0022g0217 a0001c0003t0003g0002 a0001c0003t0003g0015 others(24): Show |
44 | HG00099.hp2 HG00423.hp1 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.447+326C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 6/27 | chr12 | 109486901 | |||||||
| chr12:109486902 | G | A | 2 | a0001c0002t0016g0208 a0001c0002t0016g0209 |
2 | HG01884.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.447+327G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 6/27 | chr12 | 109486902 | |||||||
| chr12:109486974 | G | A | 4 | a0001c0002t0022g0217 a0001c0006t0027g0218 a0001c0006t0028g0216 others(1): Show |
4 | HG02280.hp1 HG02886.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.447+399G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 6/27 | chr12 | 109486974 | |||||||
| chr12:109487006 | C | G | 1 | a0001c0002t0004g0160 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.447+431C>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 6/27 | chr12 | 109487006 | |||||||
| chr12:109487043 | C | G | 1 | a0002c0001t0001g0124 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.447+468C>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 6/27 | chr12 | 109487043 | |||||||
| chr12:109487066 | TTCCTGCT others(4): Show |
T | 1 | a0002c0001t0001g0133 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.447+494_447+504del others(11): Show |
UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr12 | 109487066 | ||||||
| chr12:109487156 | A | G | 1 | a0001c0002t0033g0219 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.447+581A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 6/27 | chr12 | 109487156 | |||||||
| chr12:109487162 | C | T | 1 | a0001c0002t0033g0219 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.447+587C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 6/27 | chr12 | 109487162 | |||||||
| chr12:109487297 | C | A | 1 | a0001c0002t0033g0219 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.447+722C>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 6/27 | chr12 | 109487297 | |||||||
| chr12:109487679 | G | A | 1 | a0002c0001t0001g0076 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.448-893G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 6/27 | chr12 | 109487679 | |||||||
| chr12:109487684 | A | G | 128 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0036 others(125): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.448-888A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 6/27 | chr12 | 109487684 | |||||||
| chr12:109487866 | A | G | 1 | a0001c0004t0005g0040 | 2 | HG03017.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.448-706A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 6/27 | chr12 | 109487866 | |||||||
| chr12:109487917 | A | G | 23 | a0001c0002t0004g0020 a0001c0002t0004g0035 a0001c0002t0004g0048 others(20): Show |
31 | HG00639.hp2 HG00642.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.448-655A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 6/27 | chr12 | 109487917 | |||||||
| chr12:109487949 | C | T | 1 | a0005c0009t0026g0061 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.448-623C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 6/27 | chr12 | 109487949 | |||||||
| chr12:109488060 | C | T | 52 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0036 others(49): Show |
71 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.448-512C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 6/27 | chr12 | 109488060 | |||||||
| chr12:109488402 | A | AT | 11 | a0001c0002t0004g0041 a0001c0002t0004g0042 a0001c0002t0004g0043 others(8): Show |
14 | HG01255.hp2 HG01257.hp2 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.448-167dupT | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr12 | 109488402 | ||||||
| chr12:109488402 | A | G | 52 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0036 others(49): Show |
71 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.448-170A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 6/27 | chr12 | 109488402 | |||||||
| chr12:109488455 | A | T | 2 | a0001c0007t0003g0045 a0001c0007t0003g0046 |
2 | HG03195.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.448-117A>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 6/27 | chr12 | 109488455 | |||||||
| chr12:109488491 | T | C | 7 | a0002c0001t0001g0004 a0002c0001t0001g0062 a0002c0001t0001g0066 others(4): Show |
13 | HG00423.hp2 HG01081.hp1 NA18945.hp1 others(10): Show |
intron_variant | MODIFIER | c.448-81T>C | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 6/27 | chr12 | 109488491 | |||||||
| chr12:109489090 | A | G | 1 | a0001c0002t0008g0163 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.544+422A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 7/27 | chr12 | 109489090 | |||||||
| chr12:109489237 | A | G | 1 | a0001c0002t0015g0058 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.544+569A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 7/27 | chr12 | 109489237 | |||||||
| chr12:109489506 | C | A | 1 | a0002c0001t0001g0069 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.545-413C>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 7/27 | chr12 | 109489506 | |||||||
| chr12:109489613 | G | T | 1 | a0002c0001t0001g0138 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.545-306G>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 7/27 | chr12 | 109489613 | |||||||
| chr12:109489803 | G | A | 1 | a0001c0002t0002g0171 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.545-116G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 7/27 | chr12 | 109489803 | |||||||
| chr12:109489811 | G | T | 1 | a0001c0002t0015g0058 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.545-108G>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 7/27 | chr12 | 109489811 | |||||||
| chr12:109489882 | A | T | 24 | a0002c0001t0001g0005 a0002c0001t0001g0031 a0002c0001t0001g0065 others(21): Show |
30 | HG00673.hp1 HG01070.hp2 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.545-37A>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 7/27 | chr12 | 109489882 | |||||||
| chr12:109490022 | C | A | 3 | a0001c0002t0011g0017 a0001c0002t0011g0156 a0001c0013t0011g0157 |
5 | HG00140.hp1 HG01346.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.630+18C>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 8/27 | chr12 | 109490022 | |||||||
| chr12:109490150 | C | T | 7 | a0002c0001t0001g0014 a0002c0001t0001g0029 a0002c0001t0001g0030 others(4): Show |
11 | HG01168.hp2 HG01169.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.630+146C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 8/27 | chr12 | 109490150 | |||||||
| chr12:109490208 | C | T | 52 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0036 others(49): Show |
71 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.630+204C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 8/27 | chr12 | 109490208 | |||||||
| chr12:109490326 | A | G | 1 | a0001c0002t0033g0219 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.630+322A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 8/27 | chr12 | 109490326 | |||||||
| chr12:109490841 | A | C | 1 | a0002c0001t0001g0024 | 2 | NA19083.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.631-204A>C | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 8/27 | chr12 | 109490841 | |||||||
| chr12:109490919 | G | A | 9 | a0001c0004t0005g0019 a0001c0004t0005g0039 a0001c0004t0005g0040 others(6): Show |
13 | HG02451.hp2 HG02559.hp1 HG02922.hp1 others(10): Show |
intron_variant | MODIFIER | c.631-126G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 8/27 | chr12 | 109490919 | |||||||
| chr12:109490923 | C | T | 4 | a0001c0002t0012g0038 a0001c0002t0012g0049 a0001c0002t0012g0203 others(1): Show |
5 | HG02257.hp1 HG02280.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.631-122C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 8/27 | chr12 | 109490923 | |||||||
| chr12:109491700 | C | G | 8 | a0001c0002t0002g0194 a0001c0002t0002g0196 a0001c0002t0002g0197 others(5): Show |
8 | HG03654.hp2 HG03927.hp2 NA18942.hp2 others(5): Show |
intron_variant | MODIFIER | c.713+573C>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 9/27 | chr12 | 109491700 | |||||||
| chr12:109491797 | C | T | 1 | a0001c0002t0022g0217 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.713+670C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 9/27 | chr12 | 109491797 | |||||||
| chr12:109492013 | A | C | 5 | a0001c0002t0010g0021 a0001c0002t0010g0022 a0001c0002t0010g0053 others(2): Show |
7 | HG01243.hp2 HG01361.hp1 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.713+886A>C | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 9/27 | chr12 | 109492013 | |||||||
| chr12:109492045 | A | G | 2 | a0001c0002t0004g0164 a0001c0002t0004g0165 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.713+918A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 9/27 | chr12 | 109492045 | |||||||
| chr12:109492088 | G | A | 1 | a0002c0001t0001g0130 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.713+961G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 9/27 | chr12 | 109492088 | |||||||
| chr12:109492132 | G | T | 1 | a0001c0002t0002g0193 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.713+1005G>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 9/27 | chr12 | 109492132 | |||||||
| chr12:109492185 | C | T | 4 | a0001c0002t0012g0038 a0001c0002t0012g0049 a0001c0002t0012g0203 others(1): Show |
5 | HG02257.hp1 HG02280.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.713+1058C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 9/27 | chr12 | 109492185 | |||||||
| chr12:109492317 | A | G | 1 | a0001c0002t0033g0219 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.713+1190A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 9/27 | chr12 | 109492317 | |||||||
| chr12:109492356 | T | C | 1 | a0001c0002t0002g0194 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.713+1229T>C | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 9/27 | chr12 | 109492356 | |||||||
| chr12:109492356 | T | TAGAAAAC others(309): Show |
3 | a0001c0002t0011g0017 a0001c0002t0011g0156 a0001c0013t0011g0157 |
5 | HG00140.hp1 HG01346.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.713+1239_713+1240i others(318): Show |
UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 9/27 | INFO_REALIGN_3_PRIME | chr12 | 109492356 | ||||||
| chr12:109492461 | G | T | 1 | a0002c0001t0013g0034 | 2 | HG02040.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.713+1334G>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 9/27 | chr12 | 109492461 | |||||||
| chr12:109492506 | C | T | 1 | a0002c0001t0001g0109 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.713+1379C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 9/27 | chr12 | 109492506 | |||||||
| chr12:109492519 | A | G | 7 | a0002c0001t0001g0014 a0002c0001t0001g0029 a0002c0001t0001g0030 others(4): Show |
11 | HG01168.hp2 HG01169.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.713+1392A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 9/27 | chr12 | 109492519 | |||||||
| chr12:109492687 | G | A | 1 | a0001c0002t0033g0219 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.713+1560G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 9/27 | chr12 | 109492687 | |||||||
| chr12:109492692 | G | A | 54 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0036 others(51): Show |
73 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.713+1565G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 9/27 | chr12 | 109492692 | |||||||
| chr12:109492700 | G | A | 1 | a0002c0001t0001g0068 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.713+1573G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 9/27 | chr12 | 109492700 | |||||||
| chr12:109492737 | CA | C | 73 | a0001c0002t0004g0020 a0001c0002t0004g0035 a0001c0002t0004g0041 others(70): Show |
106 | HG00099.hp2 HG00423.hp1 HG00639.hp2 others(103): Show |
intron_variant | MODIFIER | c.713+1626delA | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 9/27 | INFO_REALIGN_3_PRIME | chr12 | 109492737 | ||||||
| chr12:109492737 | CAA | C | 53 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0036 others(50): Show |
72 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.713+1625_713+1626d others(4): Show |
UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 9/27 | INFO_REALIGN_3_PRIME | chr12 | 109492737 | ||||||
| chr12:109492944 | G | T | 1 | a0001c0002t0015g0058 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.713+1817G>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 9/27 | chr12 | 109492944 | |||||||
| chr12:109493100 | C | G | 52 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0036 others(49): Show |
71 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.713+1973C>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 9/27 | chr12 | 109493100 | |||||||
| chr12:109493324 | G | T | 3 | a0002c0001t0001g0047 a0002c0001t0001g0107 a0002c0001t0001g0108 |
3 | NA18990.hp2 NA19055.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.713+2197G>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 9/27 | chr12 | 109493324 | |||||||
| chr12:109493336 | C | G | 1 | a0001c0002t0033g0219 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.713+2209C>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 9/27 | chr12 | 109493336 | |||||||
| chr12:109493368 | A | G | 1 | a0001c0002t0008g0158 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.713+2241A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 9/27 | chr12 | 109493368 | |||||||
| chr12:109493416 | T | C | 1 | a0001c0002t0002g0172 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.713+2289T>C | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 9/27 | chr12 | 109493416 | |||||||
| chr12:109493565 | C | T | 23 | a0001c0003t0003g0002 a0001c0003t0003g0015 a0001c0003t0003g0016 others(20): Show |
40 | HG00099.hp2 HG00423.hp1 HG01099.hp1 others(37): Show |
intron_variant | MODIFIER | c.713+2438C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 9/27 | chr12 | 109493565 | |||||||
| chr12:109493632 | T | C | 1 | a0002c0001t0001g0079 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.713+2505T>C | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 9/27 | chr12 | 109493632 | |||||||
| chr12:109493648 | T | G | 9 | a0001c0004t0005g0019 a0001c0004t0005g0039 a0001c0004t0005g0040 others(6): Show |
13 | HG02451.hp2 HG02559.hp1 HG02922.hp1 others(10): Show |
intron_variant | MODIFIER | c.713+2521T>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 9/27 | chr12 | 109493648 | |||||||
| chr12:109493699 | C | T | 1 | a0001c0007t0003g0046 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.713+2572C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 9/27 | chr12 | 109493699 | |||||||
| chr12:109493700 | G | A | 2 | a0001c0002t0002g0036 a0001c0002t0010g0053 |
3 | HG00099.hp1 HG00733.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.713+2573G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 9/27 | chr12 | 109493700 | |||||||
| chr12:109493783 | T | C | 1 | a0001c0004t0005g0212 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.713+2656T>C | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 9/27 | chr12 | 109493783 | |||||||
| chr12:109493789 | G | A | 52 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0036 others(49): Show |
71 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.713+2662G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 9/27 | chr12 | 109493789 | |||||||
| chr12:109493825 | G | A | 53 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0036 others(50): Show |
72 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.713+2698G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 9/27 | chr12 | 109493825 | |||||||
| chr12:109493854 | C | T | 3 | a0001c0002t0011g0017 a0001c0002t0011g0156 a0001c0013t0011g0157 |
5 | HG00140.hp1 HG01346.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.713+2727C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 9/27 | chr12 | 109493854 | |||||||
| chr12:109493872 | G | T | 1 | a0001c0006t0027g0218 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.713+2745G>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 9/27 | chr12 | 109493872 | |||||||
| chr12:109493936 | C | T | 52 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0036 others(49): Show |
71 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.713+2809C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 9/27 | chr12 | 109493936 | |||||||
| chr12:109494026 | A | G | 1 | a0001c0002t0012g0049 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.713+2899A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 9/27 | chr12 | 109494026 | |||||||
| chr12:109494085 | C | T | 1 | a0001c0002t0007g0051 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.713+2958C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 9/27 | chr12 | 109494085 | |||||||
| chr12:109494230 | T | C | 1 | a0001c0004t0005g0215 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.713+3103T>C | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 9/27 | chr12 | 109494230 | |||||||
| chr12:109494242 | G | T | 1 | a0002c0001t0001g0106 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.713+3115G>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 9/27 | chr12 | 109494242 | |||||||
| chr12:109494380 | C | T | 1 | a0001c0006t0027g0218 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.713+3253C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 9/27 | chr12 | 109494380 | |||||||
| chr12:109494638 | G | C | 2 | a0001c0002t0015g0052 a0001c0002t0015g0058 |
2 | HG02486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.714-3180G>C | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 9/27 | chr12 | 109494638 | |||||||
| chr12:109494643 | A | G | 2 | a0001c0002t0016g0208 a0001c0002t0016g0209 |
2 | HG01884.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.714-3175A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 9/27 | chr12 | 109494643 | |||||||
| chr12:109494780 | C | T | 52 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0036 others(49): Show |
71 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.714-3038C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 9/27 | chr12 | 109494780 | |||||||
| chr12:109494781 | CA | C | 9 | a0001c0003t0003g0002 a0001c0003t0003g0016 a0001c0003t0003g0149 others(6): Show |
21 | HG00099.hp2 HG00423.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.714-3034delA | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 9/27 | INFO_REALIGN_3_PRIME | chr12 | 109494781 | ||||||
| chr12:109494829 | C | T | 3 | a0002c0001t0001g0014 a0002c0001t0001g0111 a0002c0001t0001g0112 |
5 | HG01891.hp2 HG02809.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.714-2989C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 9/27 | chr12 | 109494829 | |||||||
| chr12:109495175 | A | T | 24 | a0001c0003t0003g0002 a0001c0003t0003g0015 a0001c0003t0003g0016 others(21): Show |
41 | HG00099.hp2 HG00423.hp1 HG01099.hp1 others(38): Show |
intron_variant | MODIFIER | c.714-2643A>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 9/27 | chr12 | 109495175 | |||||||
| chr12:109495179 | C | G | 24 | a0001c0003t0003g0002 a0001c0003t0003g0015 a0001c0003t0003g0016 others(21): Show |
41 | HG00099.hp2 HG00423.hp1 HG01099.hp1 others(38): Show |
intron_variant | MODIFIER | c.714-2639C>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 9/27 | chr12 | 109495179 | |||||||
| chr12:109495290 | G | A | 1 | a0001c0002t0022g0217 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.714-2528G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 9/27 | chr12 | 109495290 | |||||||
| chr12:109495318 | T | C | 1 | a0001c0002t0004g0041 | 2 | NA18941.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.714-2500T>C | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 9/27 | chr12 | 109495318 | |||||||
| chr12:109495355 | A | G | 1 | a0002c0015t0001g0074 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.714-2463A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 9/27 | chr12 | 109495355 | |||||||
| chr12:109495413 | A | G | 1 | a0001c0003t0003g0147 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.714-2405A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 9/27 | chr12 | 109495413 | |||||||
| chr12:109495472 | A | G | 4 | a0001c0002t0012g0038 a0001c0002t0012g0049 a0001c0002t0012g0203 others(1): Show |
5 | HG02257.hp1 HG02280.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.714-2346A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 9/27 | chr12 | 109495472 | |||||||
| chr12:109495518 | C | T | 2 | a0001c0007t0003g0045 a0001c0007t0003g0046 |
2 | HG03195.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.714-2300C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 9/27 | chr12 | 109495518 | |||||||
| chr12:109495695 | C | T | 1 | a0002c0001t0001g0105 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.714-2123C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 9/27 | chr12 | 109495695 | |||||||
| chr12:109495717 | G | A | 24 | a0001c0003t0003g0002 a0001c0003t0003g0015 a0001c0003t0003g0016 others(21): Show |
41 | HG00099.hp2 HG00423.hp1 HG01099.hp1 others(38): Show |
intron_variant | MODIFIER | c.714-2101G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 9/27 | chr12 | 109495717 | |||||||
| chr12:109495721 | G | A | 1 | a0001c0006t0027g0218 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.714-2097G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 9/27 | chr12 | 109495721 | |||||||
| chr12:109495769 | C | G | 1 | a0001c0002t0012g0049 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.714-2049C>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 9/27 | chr12 | 109495769 | |||||||
| chr12:109495920 | C | T | 1 | a0001c0003t0003g0153 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.714-1898C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 9/27 | chr12 | 109495920 | |||||||
| chr12:109496029 | C | T | 1 | a0001c0002t0036g0192 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.714-1789C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 9/27 | chr12 | 109496029 | |||||||
| chr12:109496077 | C | T | 1 | a0001c0003t0003g0146 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.714-1741C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 9/27 | chr12 | 109496077 | |||||||
| chr12:109496183 | C | G | 2 | a0001c0002t0004g0020 a0001c0002t0004g0048 |
3 | HG01071.hp2 HG01106.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.714-1635C>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 9/27 | chr12 | 109496183 | |||||||
| chr12:109496248 | C | A | 1 | a0001c0003t0003g0139 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.714-1570C>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 9/27 | chr12 | 109496248 | |||||||
| chr12:109496324 | T | C | 3 | a0001c0002t0011g0017 a0001c0002t0011g0156 a0001c0013t0011g0157 |
5 | HG00140.hp1 HG01346.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.714-1494T>C | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 9/27 | chr12 | 109496324 | |||||||
| chr12:109496581 | G | A | 1 | a0001c0002t0004g0020 | 2 | HG01071.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.714-1237G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 9/27 | chr12 | 109496581 | |||||||
| chr12:109496585 | C | G | 53 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0036 others(50): Show |
72 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.714-1233C>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 9/27 | chr12 | 109496585 | |||||||
| chr12:109496638 | G | C | 1 | a0001c0003t0003g0149 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.714-1180G>C | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 9/27 | chr12 | 109496638 | |||||||
| chr12:109496895 | A | G | 52 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0036 others(49): Show |
71 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.714-923A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 9/27 | chr12 | 109496895 | |||||||
| chr12:109497276 | G | A | 34 | a0001c0002t0004g0020 a0001c0002t0004g0035 a0001c0002t0004g0041 others(31): Show |
45 | HG00639.hp2 HG00642.hp2 HG01071.hp2 others(42): Show |
intron_variant | MODIFIER | c.714-542G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 9/27 | chr12 | 109497276 | |||||||
| chr12:109497364 | A | G | 1 | a0005c0009t0026g0061 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.714-454A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 9/27 | chr12 | 109497364 | |||||||
| chr12:109497571 | A | C | 1 | a0002c0001t0001g0123 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.714-247A>C | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 9/27 | chr12 | 109497571 | |||||||
| chr12:109497600 | C | G | 2 | a0002c0001t0018g0073 a0002c0001t0018g0104 |
2 | HG00408.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.714-218C>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 9/27 | chr12 | 109497600 | |||||||
| chr12:109497626 | G | A | 1 | a0001c0002t0011g0156 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.714-192G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 9/27 | chr12 | 109497626 | |||||||
| chr12:109497640 | A | G | 1 | a0002c0001t0001g0103 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.714-178A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 9/27 | chr12 | 109497640 | |||||||
| chr12:109497670 | C | T | 53 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0036 others(50): Show |
72 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.714-148C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 9/27 | chr12 | 109497670 | |||||||
| chr12:109497684 | A | C | 1 | a0002c0001t0001g0102 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.714-134A>C | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 9/27 | chr12 | 109497684 | |||||||
| chr12:109497723 | T | C | 9 | a0001c0004t0005g0019 a0001c0004t0005g0039 a0001c0004t0005g0040 others(6): Show |
13 | HG02451.hp2 HG02559.hp1 HG02922.hp1 others(10): Show |
intron_variant | MODIFIER | c.714-95T>C | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 9/27 | chr12 | 109497723 | |||||||
| chr12:109498055 | G | A | 1 | a0001c0002t0020g0220 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.819+132G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 10/27 | chr12 | 109498055 | |||||||
| chr12:109498083 | A | G | 1 | a0001c0002t0022g0217 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.820-150A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 10/27 | chr12 | 109498083 | |||||||
| chr12:109498084 | A | G | 1 | a0001c0002t0022g0217 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.820-149A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 10/27 | chr12 | 109498084 | |||||||
| chr12:109498089 | G | C | 53 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0036 others(50): Show |
72 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.820-144G>C | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 10/27 | chr12 | 109498089 | |||||||
| chr12:109498406 | G | A | 53 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0036 others(50): Show |
72 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.940+53G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 11/27 | chr12 | 109498406 | |||||||
| chr12:109498433 | G | T | 3 | a0001c0002t0011g0017 a0001c0002t0011g0156 a0001c0013t0011g0157 |
5 | HG00140.hp1 HG01346.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.940+80G>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 11/27 | chr12 | 109498433 | |||||||
| chr12:109498449 | G | T | 4 | a0002c0001t0001g0075 a0002c0001t0001g0120 a0002c0001t0001g0121 others(1): Show |
4 | HG02132.hp2 NA18964.hp1 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.940+96G>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 11/27 | chr12 | 109498449 | |||||||
| chr12:109498586 | G | A | 1 | a0002c0001t0001g0027 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.940+233G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 11/27 | chr12 | 109498586 | |||||||
| chr12:109498698 | A | C | 1 | a0003c0005t0004g0044 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.940+345A>C | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 11/27 | chr12 | 109498698 | |||||||
| chr12:109498699 | G | C | 1 | a0003c0005t0004g0044 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.940+346G>C | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 11/27 | chr12 | 109498699 | |||||||
| chr12:109498748 | G | A | 1 | a0001c0002t0033g0219 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.940+395G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 11/27 | chr12 | 109498748 | |||||||
| chr12:109498829 | G | T | 1 | a0001c0002t0002g0191 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.940+476G>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 11/27 | chr12 | 109498829 | |||||||
| chr12:109499070 | G | A | 1 | a0001c0002t0033g0219 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.941-563G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 11/27 | chr12 | 109499070 | |||||||
| chr12:109499143 | C | T | 52 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0036 others(49): Show |
71 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.941-490C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 11/27 | chr12 | 109499143 | |||||||
| chr12:109499191 | A | G | 1 | a0001c0002t0033g0219 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.941-442A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 11/27 | chr12 | 109499191 | |||||||
| chr12:109499287 | A | G | 11 | a0001c0002t0004g0041 a0001c0002t0004g0042 a0001c0002t0004g0043 others(8): Show |
14 | HG01255.hp2 HG01257.hp2 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.941-346A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 11/27 | chr12 | 109499287 | |||||||
| chr12:109499359 | A | G | 8 | a0001c0002t0002g0194 a0001c0002t0002g0196 a0001c0002t0002g0197 others(5): Show |
8 | HG03654.hp2 HG03927.hp2 NA18942.hp2 others(5): Show |
intron_variant | MODIFIER | c.941-274A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 11/27 | chr12 | 109499359 | |||||||
| chr12:109499438 | C | G | 7 | a0001c0002t0006g0006 a0001c0002t0006g0185 a0001c0002t0006g0186 others(4): Show |
12 | HG02109.hp1 HG02258.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.941-195C>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 11/27 | chr12 | 109499438 | |||||||
| chr12:109499577 | G | A | 2 | a0001c0003t0009g0140 a0002c0015t0001g0074 |
2 | HG02109.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.941-56G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 11/27 | chr12 | 109499577 | |||||||
| chr12:109499606 | A | C | 1 | a0001c0002t0008g0162 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.941-27A>C | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 11/27 | chr12 | 109499606 | |||||||
| chr12:109500102 | C | T | 125 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0036 others(122): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.1118+292C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 12/27 | chr12 | 109500102 | |||||||
| chr12:109500271 | A | C | 20 | a0002c0001t0001g0005 a0002c0001t0001g0031 a0002c0001t0001g0065 others(17): Show |
26 | HG00673.hp1 HG01070.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.1118+461A>C | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 12/27 | chr12 | 109500271 | |||||||
| chr12:109500512 | A | G | 1 | a0002c0001t0001g0031 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1118+702A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 12/27 | chr12 | 109500512 | |||||||
| chr12:109500569 | G | A | 1 | a0001c0016t0002g0195 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1118+759G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 12/27 | chr12 | 109500569 | |||||||
| chr12:109500660 | A | T | 11 | a0001c0002t0004g0041 a0001c0002t0004g0042 a0001c0002t0004g0043 others(8): Show |
14 | HG01255.hp2 HG01257.hp2 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.1119-711A>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 12/27 | chr12 | 109500660 | |||||||
| chr12:109500832 | G | A | 2 | a0001c0002t0022g0217 a0001c0006t0027g0218 |
2 | HG02886.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1119-539G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 12/27 | chr12 | 109500832 | |||||||
| chr12:109500846 | C | T | 3 | a0001c0002t0002g0193 a0001c0002t0004g0020 a0001c0002t0004g0048 |
4 | HG01071.hp2 HG01081.hp2 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.1119-525C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 12/27 | chr12 | 109500846 | |||||||
| chr12:109500856 | C | T | 2 | a0001c0002t0004g0159 a0001c0002t0004g0160 |
2 | HG01943.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1119-515C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 12/27 | chr12 | 109500856 | |||||||
| chr12:109501028 | C | A | 11 | a0001c0002t0004g0035 a0001c0002t0004g0159 a0001c0002t0004g0160 others(8): Show |
16 | HG00639.hp2 HG00642.hp2 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.1119-343C>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 12/27 | chr12 | 109501028 | |||||||
| chr12:109501052 | A | G | 126 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0036 others(123): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.1119-319A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 12/27 | chr12 | 109501052 | |||||||
| chr12:109501244 | C | T | 3 | a0002c0001t0001g0032 a0002c0001t0001g0131 a0002c0008t0001g0033 |
5 | HG01243.hp1 HG02145.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1119-127C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 12/27 | chr12 | 109501244 | |||||||
| chr12:109501543 | C | T | 9 | a0001c0004t0005g0019 a0001c0004t0005g0039 a0001c0004t0005g0040 others(6): Show |
13 | HG02451.hp2 HG02559.hp1 HG02922.hp1 others(10): Show |
intron_variant | MODIFIER | c.1282+9C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 13/27 | chr12 | 109501543 | |||||||
| chr12:109501614 | C | T | 23 | a0001c0003t0003g0002 a0001c0003t0003g0015 a0001c0003t0003g0016 others(20): Show |
40 | HG00099.hp2 HG00423.hp1 HG01099.hp1 others(37): Show |
intron_variant | MODIFIER | c.1282+80C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 13/27 | chr12 | 109501614 | |||||||
| chr12:109501821 | AT | A | 12 | a0001c0002t0002g0174 a0001c0002t0002g0175 a0001c0002t0002g0193 others(9): Show |
12 | HG01081.hp2 HG01255.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1282+302delT | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr12 | 109501821 | ||||||
| chr12:109501836 | T | A | 127 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0036 others(124): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.1282+302T>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 13/27 | chr12 | 109501836 | |||||||
| chr12:109502035 | A | G | 1 | a0002c0001t0001g0106 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1282+501A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 13/27 | chr12 | 109502035 | |||||||
| chr12:109502398 | T | C | 1 | a0001c0003t0003g0147 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1283-625T>C | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 13/27 | chr12 | 109502398 | |||||||
| chr12:109502492 | T | A | 1 | a0002c0001t0001g0083 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1283-531T>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 13/27 | chr12 | 109502492 | |||||||
| chr12:109502504 | C | T | 1 | a0001c0002t0008g0010 | 4 | HG01099.hp2 HG02451.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.1283-519C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 13/27 | chr12 | 109502504 | |||||||
| chr12:109502595 | A | G | 1 | a0001c0006t0027g0218 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1283-428A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 13/27 | chr12 | 109502595 | |||||||
| chr12:109502762 | A | G | 1 | a0001c0006t0028g0216 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1283-261A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 13/27 | chr12 | 109502762 | |||||||
| chr12:109502940 | T | C | 1 | a0001c0002t0002g0176 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1283-83T>C | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 13/27 | chr12 | 109502940 | |||||||
| chr12:109503194 | C | G | 1 | a0002c0001t0001g0101 | 1 | HG01952.hp2 | splice_region_variant&intron_variant | LOW | c.1450+4C>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 14/27 | chr12 | 109503194 | |||||||
| chr12:109503498 | G | A | 53 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0036 others(50): Show |
72 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.1450+308G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 14/27 | chr12 | 109503498 | |||||||
| chr12:109503645 | T | A | 52 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0036 others(49): Show |
71 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.1450+455T>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 14/27 | chr12 | 109503645 | |||||||
| chr12:109503646 | C | T | 52 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0036 others(49): Show |
71 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.1450+456C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 14/27 | chr12 | 109503646 | |||||||
| chr12:109503666 | G | T | 5 | a0001c0002t0010g0021 a0001c0002t0010g0022 a0001c0002t0010g0053 others(2): Show |
7 | HG01243.hp2 HG01361.hp1 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.1450+476G>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 14/27 | chr12 | 109503666 | |||||||
| chr12:109503700 | C | T | 2 | a0001c0006t0027g0218 a0001c0006t0028g0216 |
2 | HG02280.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1450+510C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 14/27 | chr12 | 109503700 | |||||||
| chr12:109503752 | T | C | 1 | a0001c0002t0006g0185 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1450+562T>C | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 14/27 | chr12 | 109503752 | |||||||
| chr12:109503779 | G | A | 1 | a0002c0001t0030g0084 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1450+589G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 14/27 | chr12 | 109503779 | |||||||
| chr12:109504009 | C | T | 1 | a0002c0001t0018g0073 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1450+819C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 14/27 | chr12 | 109504009 | |||||||
| chr12:109504414 | G | A | 23 | a0001c0003t0003g0002 a0001c0003t0003g0015 a0001c0003t0003g0016 others(20): Show |
40 | HG00099.hp2 HG00423.hp1 HG01099.hp1 others(37): Show |
intron_variant | MODIFIER | c.1450+1224G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 14/27 | chr12 | 109504414 | |||||||
| chr12:109504806 | CT | C | 51 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0036 others(48): Show |
70 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.1450+1631delT | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr12 | 109504806 | ||||||
| chr12:109504823 | G | A | 10 | a0001c0004t0005g0019 a0001c0004t0005g0039 a0001c0004t0005g0040 others(7): Show |
14 | HG02451.hp2 HG02559.hp1 HG02922.hp1 others(11): Show |
intron_variant | MODIFIER | c.1450+1633G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 14/27 | chr12 | 109504823 | |||||||
| chr12:109504880 | A | G | 1 | a0005c0009t0026g0061 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1450+1690A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 14/27 | chr12 | 109504880 | |||||||
| chr12:109504883 | G | T | 1 | a0005c0009t0026g0061 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1450+1693G>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 14/27 | chr12 | 109504883 | |||||||
| chr12:109504972 | A | AT | 26 | a0001c0003t0003g0002 a0001c0003t0003g0015 a0001c0003t0003g0016 others(23): Show |
45 | HG00099.hp2 HG00423.hp1 HG01099.hp1 others(42): Show |
intron_variant | MODIFIER | c.1450+1792dupT | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr12 | 109504972 | ||||||
| chr12:109505010 | T | A | 1 | a0001c0003t0003g0150 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1450+1820T>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 14/27 | chr12 | 109505010 | |||||||
| chr12:109505050 | T | C | 1 | a0002c0001t0001g0083 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1450+1860T>C | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 14/27 | chr12 | 109505050 | |||||||
| chr12:109505104 | C | T | 34 | a0001c0002t0004g0020 a0001c0002t0004g0035 a0001c0002t0004g0041 others(31): Show |
45 | HG00639.hp2 HG00642.hp2 HG01071.hp2 others(42): Show |
intron_variant | MODIFIER | c.1450+1914C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 14/27 | chr12 | 109505104 | |||||||
| chr12:109505213 | C | T | 2 | a0002c0001t0001g0066 a0002c0001t0001g0078 |
2 | NA18963.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.1450+2023C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 14/27 | chr12 | 109505213 | |||||||
| chr12:109505215 | C | T | 26 | a0001c0003t0003g0002 a0001c0003t0003g0015 a0001c0003t0003g0016 others(23): Show |
45 | HG00099.hp2 HG00423.hp1 HG01099.hp1 others(42): Show |
intron_variant | MODIFIER | c.1450+2025C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 14/27 | chr12 | 109505215 | |||||||
| chr12:109505335 | C | T | 9 | a0001c0003t0003g0002 a0001c0003t0003g0016 a0001c0003t0003g0149 others(6): Show |
21 | HG00099.hp2 HG00423.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.1450+2145C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 14/27 | chr12 | 109505335 | |||||||
| chr12:109505537 | T | G | 1 | a0001c0002t0002g0177 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1451-2027T>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 14/27 | chr12 | 109505537 | |||||||
| chr12:109505734 | C | A | 1 | a0002c0001t0001g0029 | 2 | HG02622.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1451-1830C>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 14/27 | chr12 | 109505734 | |||||||
| chr12:109505833 | C | T | 2 | a0001c0007t0003g0045 a0001c0007t0003g0046 |
2 | HG03195.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1451-1731C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 14/27 | chr12 | 109505833 | |||||||
| chr12:109506226 | G | A | 1 | a0001c0003t0003g0147 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1451-1338G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 14/27 | chr12 | 109506226 | |||||||
| chr12:109506237 | A | G | 1 | a0001c0003t0003g0139 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1451-1327A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 14/27 | chr12 | 109506237 | |||||||
| chr12:109506322 | A | G | 1 | a0002c0001t0001g0100 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1451-1242A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 14/27 | chr12 | 109506322 | |||||||
| chr12:109506336 | G | GTTTTGT | 5 | a0001c0002t0004g0020 a0001c0002t0004g0048 a0001c0002t0004g0056 others(2): Show |
7 | HG01071.hp2 HG01106.hp2 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1451-1204_1451-119 others(10): Show |
UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr12 | 109506336 | ||||||
| chr12:109506449 | A | G | 3 | a0001c0002t0002g0198 a0001c0002t0002g0199 a0001c0002t0002g0200 |
3 | HG03927.hp2 NA18945.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.1451-1115A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 14/27 | chr12 | 109506449 | |||||||
| chr12:109506509 | C | T | 1 | a0001c0002t0022g0217 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1451-1055C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 14/27 | chr12 | 109506509 | |||||||
| chr12:109506611 | A | G | 10 | a0001c0003t0003g0015 a0001c0003t0003g0139 a0001c0003t0003g0146 others(7): Show |
15 | HG01167.hp2 HG01884.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1451-953A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 14/27 | chr12 | 109506611 | |||||||
| chr12:109506636 | C | G | 11 | a0001c0002t0004g0041 a0001c0002t0004g0042 a0001c0002t0004g0043 others(8): Show |
14 | HG01255.hp2 HG01257.hp2 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.1451-928C>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 14/27 | chr12 | 109506636 | |||||||
| chr12:109506881 | A | G | 3 | a0001c0002t0011g0017 a0001c0002t0011g0156 a0001c0013t0011g0157 |
5 | HG00140.hp1 HG01346.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.1451-683A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 14/27 | chr12 | 109506881 | |||||||
| chr12:109506892 | G | C | 1 | a0002c0001t0001g0030 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1451-672G>C | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 14/27 | chr12 | 109506892 | |||||||
| chr12:109507025 | C | G | 1 | a0001c0003t0023g0142 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1451-539C>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 14/27 | chr12 | 109507025 | |||||||
| chr12:109507398 | G | A | 31 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0037 others(28): Show |
43 | HG00140.hp2 HG00323.hp1 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.1451-166G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 14/27 | chr12 | 109507398 | |||||||
| chr12:109507413 | A | T | 13 | a0001c0002t0022g0217 a0001c0004t0005g0019 a0001c0004t0005g0039 others(10): Show |
17 | HG02280.hp1 HG02451.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.1451-151A>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 14/27 | chr12 | 109507413 | |||||||
| chr12:109507458 | A | G | 1 | a0005c0009t0026g0061 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1451-106A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 14/27 | chr12 | 109507458 | |||||||
| chr12:109507533 | T | A | 1 | a0005c0009t0026g0061 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1451-31T>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 14/27 | chr12 | 109507533 | |||||||
| chr12:109507893 | T | C | 1 | a0005c0009t0026g0061 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1622+158T>C | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 15/27 | chr12 | 109507893 | |||||||
| chr12:109507960 | G | A | 1 | a0001c0002t0022g0217 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1622+225G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 15/27 | chr12 | 109507960 | |||||||
| chr12:109508093 | A | G | 1 | a0001c0006t0027g0218 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1622+358A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 15/27 | chr12 | 109508093 | |||||||
| chr12:109508116 | G | A | 1 | a0002c0001t0001g0069 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1622+381G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 15/27 | chr12 | 109508116 | |||||||
| chr12:109508128 | G | A | 1 | a0001c0004t0005g0215 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1622+393G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 15/27 | chr12 | 109508128 | |||||||
| chr12:109508207 | G | A | 52 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0036 others(49): Show |
71 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.1622+472G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 15/27 | chr12 | 109508207 | |||||||
| chr12:109508231 | A | G | 10 | a0001c0004t0005g0019 a0001c0004t0005g0039 a0001c0004t0005g0040 others(7): Show |
14 | HG02451.hp2 HG02559.hp1 HG02922.hp1 others(11): Show |
intron_variant | MODIFIER | c.1622+496A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 15/27 | chr12 | 109508231 | |||||||
| chr12:109508617 | A | G | 2 | a0001c0002t0016g0208 a0001c0002t0016g0209 |
2 | HG01884.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1622+882A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 15/27 | chr12 | 109508617 | |||||||
| chr12:109508946 | T | A | 52 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0036 others(49): Show |
71 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.1623-650T>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 15/27 | chr12 | 109508946 | |||||||
| chr12:109508947 | G | C | 23 | a0001c0002t0004g0020 a0001c0002t0004g0035 a0001c0002t0004g0048 others(20): Show |
31 | HG00639.hp2 HG00642.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.1623-649G>C | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 15/27 | chr12 | 109508947 | |||||||
| chr12:109509002 | C | G | 1 | a0001c0002t0022g0217 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1623-594C>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 15/27 | chr12 | 109509002 | |||||||
| chr12:109509069 | T | G | 1 | a0001c0002t0012g0049 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1623-527T>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 15/27 | chr12 | 109509069 | |||||||
| chr12:109509220 | A | G | 1 | a0002c0001t0017g0025 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1623-376A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 15/27 | chr12 | 109509220 | |||||||
| chr12:109509234 | C | T | 2 | a0002c0001t0001g0072 a0002c0001t0001g0119 |
2 | HG04199.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1623-362C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 15/27 | chr12 | 109509234 | |||||||
| chr12:109509389 | A | G | 3 | a0001c0002t0002g0007 a0001c0002t0002g0171 a0001c0002t0002g0205 |
7 | HG00639.hp1 HG01123.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.1623-207A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 15/27 | chr12 | 109509389 | |||||||
| chr12:109509426 | C | T | 1 | a0002c0001t0001g0027 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1623-170C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 15/27 | chr12 | 109509426 | |||||||
| chr12:109509429 | T | C | 9 | a0001c0003t0003g0002 a0001c0003t0003g0016 a0001c0003t0003g0149 others(6): Show |
21 | HG00099.hp2 HG00423.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.1623-167T>C | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 15/27 | chr12 | 109509429 | |||||||
| chr12:109509453 | T | C | 1 | a0002c0001t0014g0028 | 2 | NA18985.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.1623-143T>C | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 15/27 | chr12 | 109509453 | |||||||
| chr12:109509460 | T | A | 10 | a0001c0004t0005g0019 a0001c0004t0005g0039 a0001c0004t0005g0040 others(7): Show |
14 | HG02451.hp2 HG02559.hp1 HG02922.hp1 others(11): Show |
intron_variant | MODIFIER | c.1623-136T>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 15/27 | chr12 | 109509460 | |||||||
| chr12:109509482 | T | C | 10 | a0001c0004t0005g0019 a0001c0004t0005g0039 a0001c0004t0005g0040 others(7): Show |
14 | HG02451.hp2 HG02559.hp1 HG02922.hp1 others(11): Show |
intron_variant | MODIFIER | c.1623-114T>C | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 15/27 | chr12 | 109509482 | |||||||
| chr12:109509552 | C | CT | 23 | a0001c0003t0003g0002 a0001c0003t0003g0015 a0001c0003t0003g0016 others(20): Show |
40 | HG00099.hp2 HG00423.hp1 HG01099.hp1 others(37): Show |
intron_variant | MODIFIER | c.1623-38dupT | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr12 | 109509552 | ||||||
| chr12:109510087 | A | G | 1 | a0001c0002t0022g0217 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1742-257A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 16/27 | chr12 | 109510087 | |||||||
| chr12:109510100 | C | T | 92 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0036 others(89): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.1742-244C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 16/27 | chr12 | 109510100 | |||||||
| chr12:109510140 | A | G | 1 | a0001c0002t0032g0225 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1742-204A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 16/27 | chr12 | 109510140 | |||||||
| chr12:109510268 | G | A | 1 | a0001c0002t0008g0162 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1742-76G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 16/27 | chr12 | 109510268 | |||||||
| chr12:109510310 | C | T | 1 | a0002c0001t0001g0099 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1742-34C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 16/27 | chr12 | 109510310 | |||||||
| chr12:109510665 | A | C | 1 | a0002c0001t0001g0098 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1856+207A>C | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 17/27 | chr12 | 109510665 | |||||||
| chr12:109510736 | T | C | 23 | a0001c0003t0003g0002 a0001c0003t0003g0015 a0001c0003t0003g0016 others(20): Show |
40 | HG00099.hp2 HG00423.hp1 HG01099.hp1 others(37): Show |
intron_variant | MODIFIER | c.1856+278T>C | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 17/27 | chr12 | 109510736 | |||||||
| chr12:109511099 | C | T | 1 | a0001c0002t0033g0219 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1857-105C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 17/27 | chr12 | 109511099 | |||||||
| chr12:109511329 | C | T | 52 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0036 others(49): Show |
71 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.1956+26C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 18/27 | chr12 | 109511329 | |||||||
| chr12:109511343 | A | G | 4 | a0001c0002t0012g0038 a0001c0002t0012g0049 a0001c0002t0012g0203 others(1): Show |
5 | HG02257.hp1 HG02280.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.1956+40A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 18/27 | chr12 | 109511343 | |||||||
| chr12:109511353 | G | A | 1 | a0001c0013t0011g0157 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1956+50G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 18/27 | chr12 | 109511353 | |||||||
| chr12:109511530 | C | T | 1 | a0001c0002t0022g0217 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1956+227C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 18/27 | chr12 | 109511530 | |||||||
| chr12:109511544 | G | T | 1 | a0001c0011t0004g0224 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1956+241G>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 18/27 | chr12 | 109511544 | |||||||
| chr12:109511643 | A | G | 3 | a0001c0002t0011g0017 a0001c0002t0011g0156 a0001c0013t0011g0157 |
5 | HG00140.hp1 HG01346.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.1956+340A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 18/27 | chr12 | 109511643 | |||||||
| chr12:109511756 | T | C | 6 | a0001c0002t0008g0010 a0001c0002t0008g0018 a0001c0002t0008g0158 others(3): Show |
10 | HG00639.hp2 HG00642.hp2 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.1956+453T>C | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 18/27 | chr12 | 109511756 | |||||||
| chr12:109511770 | G | A | 3 | a0001c0002t0004g0056 a0001c0002t0004g0057 a0001c0002t0004g0059 |
3 | HG02622.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1956+467G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 18/27 | chr12 | 109511770 | |||||||
| chr12:109511777 | T | C | 4 | a0002c0001t0001g0070 a0002c0001t0001g0085 a0002c0001t0001g0105 others(1): Show |
4 | HG00597.hp2 HG00609.hp2 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.1956+474T>C | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 18/27 | chr12 | 109511777 | |||||||
| chr12:109511837 | G | A | 11 | a0001c0002t0004g0035 a0001c0002t0004g0159 a0001c0002t0004g0160 others(8): Show |
16 | HG00639.hp2 HG00642.hp2 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.1956+534G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 18/27 | chr12 | 109511837 | |||||||
| chr12:109511944 | G | A | 1 | a0001c0002t0004g0222 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1956+641G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 18/27 | chr12 | 109511944 | |||||||
| chr12:109512185 | C | T | 1 | a0002c0001t0001g0130 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1956+882C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 18/27 | chr12 | 109512185 | |||||||
| chr12:109512339 | A | G | 126 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0036 others(123): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.1956+1036A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 18/27 | chr12 | 109512339 | |||||||
| chr12:109512848 | G | A | 23 | a0001c0003t0003g0002 a0001c0003t0003g0015 a0001c0003t0003g0016 others(20): Show |
40 | HG00099.hp2 HG00423.hp1 HG01099.hp1 others(37): Show |
intron_variant | MODIFIER | c.1956+1545G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 18/27 | chr12 | 109512848 | |||||||
| chr12:109513007 | A | G | 1 | a0001c0002t0002g0197 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1956+1704A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 18/27 | chr12 | 109513007 | |||||||
| chr12:109513286 | C | T | 1 | a0002c0001t0001g0097 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1956+1983C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 18/27 | chr12 | 109513286 | |||||||
| chr12:109513344 | G | A | 1 | a0001c0002t0006g0186 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1956+2041G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 18/27 | chr12 | 109513344 | |||||||
| chr12:109513380 | C | T | 1 | a0001c0006t0028g0216 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1956+2077C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 18/27 | chr12 | 109513380 | |||||||
| chr12:109513630 | G | A | 2 | a0001c0002t0016g0208 a0001c0002t0016g0209 |
2 | HG01884.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1956+2327G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 18/27 | chr12 | 109513630 | |||||||
| chr12:109513689 | A | AT | 41 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0036 others(38): Show |
54 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(51): Show |
intron_variant | MODIFIER | c.1956+2396dupT | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 18/27 | INFO_REALIGN_3_PRIME | chr12 | 109513689 | ||||||
| chr12:109513689 | AT | A | 7 | a0001c0002t0006g0006 a0001c0002t0006g0185 a0001c0002t0006g0186 others(4): Show |
12 | HG02109.hp1 HG02258.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.1956+2396delT | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 18/27 | INFO_REALIGN_3_PRIME | chr12 | 109513689 | ||||||
| chr12:109513875 | G | A | 2 | a0001c0002t0016g0208 a0001c0002t0016g0209 |
2 | HG01884.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1956+2572G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 18/27 | chr12 | 109513875 | |||||||
| chr12:109514086 | C | A | 5 | a0001c0003t0009g0009 a0001c0003t0009g0140 a0001c0003t0009g0143 others(2): Show |
8 | HG02109.hp2 HG02647.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1957-2679C>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 18/27 | chr12 | 109514086 | |||||||
| chr12:109514098 | G | A | 9 | a0001c0004t0005g0019 a0001c0004t0005g0039 a0001c0004t0005g0040 others(6): Show |
13 | HG02451.hp2 HG02559.hp1 HG02922.hp1 others(10): Show |
intron_variant | MODIFIER | c.1957-2667G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 18/27 | chr12 | 109514098 | |||||||
| chr12:109514102 | A | G | 1 | a0001c0002t0002g0200 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1957-2663A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 18/27 | chr12 | 109514102 | |||||||
| chr12:109514127 | A | G | 1 | a0005c0009t0026g0061 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1957-2638A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 18/27 | chr12 | 109514127 | |||||||
| chr12:109514681 | A | G | 1 | a0001c0002t0033g0219 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1957-2084A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 18/27 | chr12 | 109514681 | |||||||
| chr12:109514757 | A | G | 1 | a0001c0002t0033g0219 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1957-2008A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 18/27 | chr12 | 109514757 | |||||||
| chr12:109514776 | C | G | 1 | a0001c0002t0004g0057 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1957-1989C>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 18/27 | chr12 | 109514776 | |||||||
| chr12:109514789 | C | T | 10 | a0001c0004t0005g0019 a0001c0004t0005g0039 a0001c0004t0005g0040 others(7): Show |
14 | HG02451.hp2 HG02559.hp1 HG02922.hp1 others(11): Show |
intron_variant | MODIFIER | c.1957-1976C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 18/27 | chr12 | 109514789 | |||||||
| chr12:109514902 | C | T | 1 | a0001c0002t0033g0219 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1957-1863C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 18/27 | chr12 | 109514902 | |||||||
| chr12:109514974 | C | T | 2 | a0001c0006t0027g0218 a0001c0006t0028g0216 |
2 | HG02280.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1957-1791C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 18/27 | chr12 | 109514974 | |||||||
| chr12:109515009 | G | T | 1 | a0001c0002t0033g0219 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1957-1756G>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 18/27 | chr12 | 109515009 | |||||||
| chr12:109515015 | G | A | 6 | a0001c0002t0008g0010 a0001c0002t0008g0018 a0001c0002t0008g0158 others(3): Show |
10 | HG00639.hp2 HG00642.hp2 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.1957-1750G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 18/27 | chr12 | 109515015 | |||||||
| chr12:109515120 | A | C | 59 | a0001c0002t0004g0020 a0001c0002t0004g0035 a0001c0002t0004g0048 others(56): Show |
88 | HG00099.hp2 HG00423.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.1957-1645A>C | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 18/27 | chr12 | 109515120 | |||||||
| chr12:109515159 | C | T | 1 | a0002c0001t0001g0100 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1957-1606C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 18/27 | chr12 | 109515159 | |||||||
| chr12:109515182 | G | T | 46 | a0001c0002t0004g0020 a0001c0002t0004g0035 a0001c0002t0004g0048 others(43): Show |
71 | HG00099.hp2 HG00423.hp1 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.1957-1583G>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 18/27 | chr12 | 109515182 | |||||||
| chr12:109515217 | C | A | 1 | a0001c0003t0009g0143 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1957-1548C>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 18/27 | chr12 | 109515217 | |||||||
| chr12:109515316 | C | G | 2 | a0001c0006t0027g0218 a0001c0006t0028g0216 |
2 | HG02280.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1957-1449C>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 18/27 | chr12 | 109515316 | |||||||
| chr12:109515359 | GT | G | 113 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0036 others(110): Show |
163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.1957-1399delT | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 18/27 | INFO_REALIGN_3_PRIME | chr12 | 109515359 | ||||||
| chr12:109515366 | TG | T | 12 | a0001c0002t0004g0041 a0001c0002t0004g0042 a0001c0002t0004g0043 others(9): Show |
15 | HG01255.hp2 HG01257.hp2 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1957-1398delG | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 18/27 | chr12 | 109515366 | |||||||
| chr12:109515367 | G | T | 12 | a0001c0002t0016g0208 a0001c0002t0016g0209 a0001c0002t0022g0217 others(9): Show |
15 | HG01074.hp1 HG01516.hp1 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.1957-1398G>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 18/27 | chr12 | 109515367 | |||||||
| chr12:109515370 | G | T | 2 | a0002c0001t0001g0128 a0002c0001t0001g0129 |
2 | HG01074.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1957-1395G>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 18/27 | chr12 | 109515370 | |||||||
| chr12:109515455 | C | T | 1 | a0001c0002t0033g0219 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1957-1310C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 18/27 | chr12 | 109515455 | |||||||
| chr12:109515526 | C | T | 48 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0036 others(45): Show |
66 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.1957-1239C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 18/27 | chr12 | 109515526 | |||||||
| chr12:109515612 | A | G | 128 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0036 others(125): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.1957-1153A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 18/27 | chr12 | 109515612 | |||||||
| chr12:109515685 | G | T | 1 | a0001c0002t0033g0219 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1957-1080G>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 18/27 | chr12 | 109515685 | |||||||
| chr12:109515869 | A | AC | 8 | a0001c0003t0003g0002 a0001c0003t0003g0016 a0001c0003t0003g0149 others(5): Show |
20 | HG00423.hp1 HG01099.hp1 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.1957-896_1957-895i others(3): Show |
UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 18/27 | chr12 | 109515869 | |||||||
| chr12:109516167 | CT | C | 80 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0036 others(77): Show |
111 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.1957-576delT | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 18/27 | INFO_REALIGN_3_PRIME | chr12 | 109516167 | ||||||
| chr12:109516167 | CTT | C | 24 | a0001c0002t0002g0205 a0001c0002t0006g0006 a0001c0002t0006g0185 others(21): Show |
34 | HG01891.hp1 HG01943.hp1 HG02109.hp1 others(31): Show |
intron_variant | MODIFIER | c.1957-577_1957-576d others(4): Show |
UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 18/27 | INFO_REALIGN_3_PRIME | chr12 | 109516167 | ||||||
| chr12:109516279 | C | G | 5 | a0001c0002t0010g0021 a0001c0002t0010g0022 a0001c0002t0010g0053 others(2): Show |
7 | HG01243.hp2 HG01361.hp1 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.1957-486C>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 18/27 | chr12 | 109516279 | |||||||
| chr12:109516339 | T | G | 1 | a0002c0001t0001g0098 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1957-426T>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 18/27 | chr12 | 109516339 | |||||||
| chr12:109516405 | G | C | 2 | a0001c0002t0007g0207 a0001c0002t0035g0178 |
2 | NA18957.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1957-360G>C | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 18/27 | chr12 | 109516405 | |||||||
| chr12:109516425 | C | T | 1 | a0002c0001t0001g0069 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1957-340C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 18/27 | chr12 | 109516425 | |||||||
| chr12:109516446 | G | A | 9 | a0001c0003t0003g0002 a0001c0003t0003g0016 a0001c0003t0003g0149 others(6): Show |
21 | HG00099.hp2 HG00423.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.1957-319G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 18/27 | chr12 | 109516446 | |||||||
| chr12:109516457 | G | A | 4 | a0001c0004t0005g0019 a0001c0004t0005g0210 a0001c0004t0005g0211 others(1): Show |
6 | NA18946.hp2 NA18953.hp1 NA18967.hp2 others(3): Show |
intron_variant | MODIFIER | c.1957-308G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 18/27 | chr12 | 109516457 | |||||||
| chr12:109516468 | C | T | 21 | a0001c0003t0003g0002 a0001c0003t0003g0015 a0001c0003t0003g0016 others(18): Show |
38 | HG00099.hp2 HG00423.hp1 HG01099.hp1 others(35): Show |
intron_variant | MODIFIER | c.1957-297C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 18/27 | chr12 | 109516468 | |||||||
| chr12:109516594 | C | A | 3 | a0001c0002t0004g0056 a0001c0002t0004g0057 a0001c0002t0004g0059 |
3 | HG02622.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1957-171C>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 18/27 | chr12 | 109516594 | |||||||
| chr12:109517172 | C | G | 1 | a0001c0002t0002g0193 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2076+288C>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 19/27 | chr12 | 109517172 | |||||||
| chr12:109517512 | C | T | 52 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0036 others(49): Show |
71 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.2076+628C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 19/27 | chr12 | 109517512 | |||||||
| chr12:109517751 | C | T | 2 | a0001c0002t0010g0053 a0001c0002t0021g0054 |
2 | HG01361.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.2076+867C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 19/27 | chr12 | 109517751 | |||||||
| chr12:109517903 | A | C | 23 | a0001c0002t0004g0020 a0001c0002t0004g0035 a0001c0002t0004g0048 others(20): Show |
31 | HG00639.hp2 HG00642.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.2076+1019A>C | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 19/27 | chr12 | 109517903 | |||||||
| chr12:109518099 | C | A | 1 | a0002c0001t0001g0086 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2076+1215C>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 19/27 | chr12 | 109518099 | |||||||
| chr12:109518111 | G | A | 4 | a0001c0002t0012g0038 a0001c0002t0012g0049 a0001c0002t0012g0203 others(1): Show |
5 | HG02257.hp1 HG02280.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.2076+1227G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 19/27 | chr12 | 109518111 | |||||||
| chr12:109518289 | C | T | 3 | a0001c0002t0011g0017 a0001c0002t0011g0156 a0001c0013t0011g0157 |
5 | HG00140.hp1 HG01346.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.2076+1405C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 19/27 | chr12 | 109518289 | |||||||
| chr12:109518379 | C | A | 1 | a0002c0001t0001g0134 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.2076+1495C>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 19/27 | chr12 | 109518379 | |||||||
| chr12:109518549 | C | T | 1 | a0001c0002t0033g0219 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2076+1665C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 19/27 | chr12 | 109518549 | |||||||
| chr12:109518890 | C | T | 1 | a0002c0001t0001g0096 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2076+2006C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 19/27 | chr12 | 109518890 | |||||||
| chr12:109518997 | T | G | 1 | a0002c0001t0001g0131 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2076+2113T>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 19/27 | chr12 | 109518997 | |||||||
| chr12:109519103 | T | A | 9 | a0001c0004t0005g0019 a0001c0004t0005g0039 a0001c0004t0005g0040 others(6): Show |
13 | HG02451.hp2 HG02559.hp1 HG02922.hp1 others(10): Show |
intron_variant | MODIFIER | c.2077-2045T>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 19/27 | chr12 | 109519103 | |||||||
| chr12:109519197 | A | T | 1 | a0001c0002t0004g0020 | 2 | HG01071.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.2077-1951A>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 19/27 | chr12 | 109519197 | |||||||
| chr12:109519220 | G | A | 1 | a0001c0002t0010g0021 | 2 | HG02257.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2077-1928G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 19/27 | chr12 | 109519220 | |||||||
| chr12:109519281 | G | A | 1 | a0001c0004t0005g0040 | 2 | HG03017.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.2077-1867G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 19/27 | chr12 | 109519281 | |||||||
| chr12:109519326 | A | G | 1 | a0001c0016t0002g0195 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2077-1822A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 19/27 | chr12 | 109519326 | |||||||
| chr12:109519327 | G | A | 3 | a0001c0002t0011g0017 a0001c0002t0011g0156 a0001c0013t0011g0157 |
5 | HG00140.hp1 HG01346.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.2077-1821G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 19/27 | chr12 | 109519327 | |||||||
| chr12:109519426 | G | A | 1 | a0001c0002t0022g0217 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2077-1722G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 19/27 | chr12 | 109519426 | |||||||
| chr12:109519470 | C | A | 1 | a0001c0002t0033g0219 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2077-1678C>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 19/27 | chr12 | 109519470 | |||||||
| chr12:109519640 | G | A | 1 | a0001c0002t0002g0196 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2077-1508G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 19/27 | chr12 | 109519640 | |||||||
| chr12:109519702 | C | T | 1 | a0001c0002t0022g0217 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2077-1446C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 19/27 | chr12 | 109519702 | |||||||
| chr12:109519779 | CCTT | C | 9 | a0001c0004t0005g0019 a0001c0004t0005g0039 a0001c0004t0005g0040 others(6): Show |
13 | HG02451.hp2 HG02559.hp1 HG02922.hp1 others(10): Show |
intron_variant | MODIFIER | c.2077-1366_2077-136 others(7): Show |
UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 19/27 | INFO_REALIGN_3_PRIME | chr12 | 109519779 | ||||||
| chr12:109519881 | C | T | 1 | a0002c0001t0001g0095 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2077-1267C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 19/27 | chr12 | 109519881 | |||||||
| chr12:109519888 | T | TAAGATTC | 128 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0036 others(125): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.2077-1260_2077-125 others(11): Show |
UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 19/27 | chr12 | 109519888 | |||||||
| chr12:109519889 | C | A | 128 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0036 others(125): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.2077-1259C>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 19/27 | chr12 | 109519889 | |||||||
| chr12:109519941 | G | A | 1 | a0002c0001t0001g0087 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2077-1207G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 19/27 | chr12 | 109519941 | |||||||
| chr12:109520082 | T | C | 1 | a0001c0002t0033g0219 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2077-1066T>C | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 19/27 | chr12 | 109520082 | |||||||
| chr12:109520410 | C | T | 1 | a0002c0001t0001g0126 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.2077-738C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 19/27 | chr12 | 109520410 | |||||||
| chr12:109520411 | A | G | 1 | a0001c0002t0006g0190 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2077-737A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 19/27 | chr12 | 109520411 | |||||||
| chr12:109520542 | A | C | 1 | a0005c0009t0026g0061 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2077-606A>C | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 19/27 | chr12 | 109520542 | |||||||
| chr12:109520743 | AT | A | 62 | a0001c0002t0004g0020 a0001c0002t0004g0035 a0001c0002t0004g0048 others(59): Show |
92 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.2077-391delT | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 19/27 | INFO_REALIGN_3_PRIME | chr12 | 109520743 | ||||||
| chr12:109520743 | ATT | A | 57 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0036 others(54): Show |
77 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.2077-392_2077-391d others(4): Show |
UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 19/27 | INFO_REALIGN_3_PRIME | chr12 | 109520743 | ||||||
| chr12:109520743 | ATTT | A | 12 | a0001c0002t0004g0041 a0001c0002t0004g0042 a0001c0002t0004g0043 others(9): Show |
15 | HG01255.hp2 HG01257.hp2 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.2077-393_2077-391d others(5): Show |
UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 19/27 | INFO_REALIGN_3_PRIME | chr12 | 109520743 | ||||||
| chr12:109520778 | T | C | 1 | a0005c0009t0026g0061 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2077-370T>C | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 19/27 | chr12 | 109520778 | |||||||
| chr12:109520779 | G | A | 2 | a0002c0001t0018g0073 a0002c0001t0018g0104 |
2 | HG00408.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.2077-369G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 19/27 | chr12 | 109520779 | |||||||
| chr12:109520982 | C | G | 1 | a0001c0002t0033g0219 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2077-166C>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 19/27 | chr12 | 109520982 | |||||||
| chr12:109521026 | C | T | 1 | a0002c0001t0001g0094 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2077-122C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 19/27 | chr12 | 109521026 | |||||||
| chr12:109521070 | G | A | 1 | a0001c0002t0006g0188 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2077-78G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 19/27 | chr12 | 109521070 | |||||||
| chr12:109521389 | G | T | 2 | a0001c0007t0003g0045 a0001c0007t0003g0046 |
2 | HG03195.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2254-52G>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 20/27 | chr12 | 109521389 | |||||||
| chr12:109521560 | G | GT | 3 | a0001c0002t0011g0017 a0001c0002t0011g0156 a0001c0013t0011g0157 |
5 | HG00140.hp1 HG01346.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.2364+11dupT | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 109521560 | ||||||
| chr12:109521584 | TA | T | 52 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0036 others(49): Show |
71 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.2364+37delA | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 109521584 | ||||||
| chr12:109521668 | G | A | 1 | a0001c0002t0033g0219 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2364+117G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 21/27 | chr12 | 109521668 | |||||||
| chr12:109521702 | C | A | 1 | a0001c0003t0023g0142 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2364+151C>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 21/27 | chr12 | 109521702 | |||||||
| chr12:109522082 | T | C | 2 | a0002c0001t0001g0088 a0002c0001t0001g0096 |
2 | HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2364+531T>C | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 21/27 | chr12 | 109522082 | |||||||
| chr12:109522254 | A | G | 1 | a0002c0001t0001g0068 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2364+703A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 21/27 | chr12 | 109522254 | |||||||
| chr12:109522411 | A | T | 1 | a0001c0002t0002g0183 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.2364+860A>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 21/27 | chr12 | 109522411 | |||||||
| chr12:109522424 | G | A | 1 | a0001c0003t0003g0147 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2364+873G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 21/27 | chr12 | 109522424 | |||||||
| chr12:109522478 | G | T | 11 | a0001c0002t0004g0041 a0001c0002t0004g0042 a0001c0002t0004g0043 others(8): Show |
14 | HG01255.hp2 HG01257.hp2 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.2364+927G>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 21/27 | chr12 | 109522478 | |||||||
| chr12:109522482 | G | C | 1 | a0001c0002t0033g0219 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2364+931G>C | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 21/27 | chr12 | 109522482 | |||||||
| chr12:109522576 | C | CTGGAGAA others(10): Show |
1 | a0001c0002t0007g0173 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.2364+1027_2364+104 others(21): Show |
UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 109522576 | ||||||
| chr12:109522584 | G | A | 6 | a0002c0001t0001g0014 a0002c0001t0001g0030 a0002c0001t0001g0064 others(3): Show |
9 | HG01168.hp2 HG01169.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.2364+1033G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 21/27 | chr12 | 109522584 | |||||||
| chr12:109522585 | C | T | 21 | a0001c0003t0003g0002 a0001c0003t0003g0015 a0001c0003t0003g0016 others(18): Show |
38 | HG00099.hp2 HG00423.hp1 HG01099.hp1 others(35): Show |
intron_variant | MODIFIER | c.2364+1034C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 21/27 | chr12 | 109522585 | |||||||
| chr12:109522620 | G | A | 9 | a0001c0004t0005g0019 a0001c0004t0005g0039 a0001c0004t0005g0040 others(6): Show |
13 | HG02451.hp2 HG02559.hp1 HG02922.hp1 others(10): Show |
intron_variant | MODIFIER | c.2364+1069G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 21/27 | chr12 | 109522620 | |||||||
| chr12:109522702 | A | G | 1 | a0001c0002t0034g0202 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2364+1151A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 21/27 | chr12 | 109522702 | |||||||
| chr12:109523047 | T | A | 2 | a0001c0002t0004g0159 a0001c0002t0004g0160 |
2 | HG01943.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2365-931T>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 21/27 | chr12 | 109523047 | |||||||
| chr12:109523146 | C | G | 2 | a0002c0001t0001g0077 a0002c0001t0001g0125 |
2 | NA18951.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.2365-832C>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 21/27 | chr12 | 109523146 | |||||||
| chr12:109523154 | A | T | 1 | a0001c0002t0015g0058 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2365-824A>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 21/27 | chr12 | 109523154 | |||||||
| chr12:109523157 | T | C | 126 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0036 others(123): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.2365-821T>C | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 21/27 | chr12 | 109523157 | |||||||
| chr12:109523317 | C | T | 12 | a0001c0002t0004g0041 a0001c0002t0004g0042 a0001c0002t0004g0043 others(9): Show |
15 | HG01255.hp2 HG01257.hp2 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.2365-661C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 21/27 | chr12 | 109523317 | |||||||
| chr12:109523539 | C | T | 2 | a0001c0002t0004g0020 a0001c0002t0004g0048 |
3 | HG01071.hp2 HG01106.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.2365-439C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 21/27 | chr12 | 109523539 | |||||||
| chr12:109523630 | G | A | 1 | a0001c0002t0033g0219 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2365-348G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 21/27 | chr12 | 109523630 | |||||||
| chr12:109523679 | G | GC | 51 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0036 others(48): Show |
70 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.2365-293dupC | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 109523679 | ||||||
| chr12:109523727 | G | A | 1 | a0002c0001t0001g0101 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2365-251G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 21/27 | chr12 | 109523727 | |||||||
| chr12:109523763 | C | T | 1 | a0002c0001t0001g0119 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2365-215C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 21/27 | chr12 | 109523763 | |||||||
| chr12:109524332 | GCCATGGG others(6): Show |
G | 7 | a0001c0002t0006g0006 a0001c0002t0006g0185 a0001c0002t0006g0186 others(4): Show |
12 | HG02109.hp1 HG02258.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.2503-104_2503-92de others(14): Show |
UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr12 | 109524332 | ||||||
| chr12:109524512 | G | A | 1 | a0002c0001t0001g0119 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2568+9G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 23/27 | chr12 | 109524512 | |||||||
| chr12:109524713 | C | T | 11 | a0001c0002t0004g0041 a0001c0002t0004g0042 a0001c0002t0004g0043 others(8): Show |
14 | HG01255.hp2 HG01257.hp2 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.2568+210C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 23/27 | chr12 | 109524713 | |||||||
| chr12:109524798 | C | T | 1 | a0001c0003t0003g0151 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2568+295C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 23/27 | chr12 | 109524798 | |||||||
| chr12:109524814 | T | G | 1 | a0001c0002t0016g0208 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2568+311T>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 23/27 | chr12 | 109524814 | |||||||
| chr12:109524907 | C | T | 1 | a0002c0001t0001g0115 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2568+404C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 23/27 | chr12 | 109524907 | |||||||
| chr12:109524925 | G | T | 2 | a0002c0001t0001g0131 a0002c0008t0001g0033 |
3 | HG01243.hp1 HG02145.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.2568+422G>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 23/27 | chr12 | 109524925 | |||||||
| chr12:109524990 | G | C | 123 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0036 others(120): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.2568+487G>C | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 23/27 | chr12 | 109524990 | |||||||
| chr12:109525015 | G | A | 1 | a0004c0012t0024g0161 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2568+512G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 23/27 | chr12 | 109525015 | |||||||
| chr12:109525062 | G | A | 1 | a0002c0001t0030g0084 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2568+559G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 23/27 | chr12 | 109525062 | |||||||
| chr12:109525171 | A | G | 20 | a0001c0003t0003g0002 a0001c0003t0003g0015 a0001c0003t0003g0016 others(17): Show |
37 | HG00099.hp2 HG00423.hp1 HG01099.hp1 others(34): Show |
intron_variant | MODIFIER | c.2568+668A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 23/27 | chr12 | 109525171 | |||||||
| chr12:109525220 | G | A | 1 | a0001c0002t0033g0219 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2568+717G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 23/27 | chr12 | 109525220 | |||||||
| chr12:109525376 | C | T | 1 | a0002c0001t0001g0099 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2568+873C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 23/27 | chr12 | 109525376 | |||||||
| chr12:109525378 | C | T | 1 | a0001c0002t0033g0219 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2568+875C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 23/27 | chr12 | 109525378 | |||||||
| chr12:109525384 | C | T | 1 | a0001c0002t0012g0049 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2568+881C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 23/27 | chr12 | 109525384 | |||||||
| chr12:109525441 | G | T | 12 | a0002c0001t0001g0008 a0002c0001t0001g0082 a0002c0001t0001g0092 others(9): Show |
16 | HG00408.hp1 HG00673.hp2 HG02040.hp2 others(13): Show |
intron_variant | MODIFIER | c.2569-917G>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 23/27 | chr12 | 109525441 | |||||||
| chr12:109525648 | C | T | 1 | a0001c0016t0002g0195 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2569-710C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 23/27 | chr12 | 109525648 | |||||||
| chr12:109525720 | C | T | 3 | a0001c0004t0005g0039 a0001c0004t0005g0214 a0001c0004t0005g0215 |
4 | HG02451.hp2 HG02922.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.2569-638C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 23/27 | chr12 | 109525720 | |||||||
| chr12:109525842 | C | T | 3 | a0002c0001t0001g0047 a0002c0001t0001g0107 a0002c0001t0001g0108 |
3 | NA18990.hp2 NA19055.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.2569-516C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 23/27 | chr12 | 109525842 | |||||||
| chr12:109526012 | T | C | 1 | a0002c0001t0001g0080 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2569-346T>C | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 23/27 | chr12 | 109526012 | |||||||
| chr12:109526042 | A | G | 1 | a0001c0002t0022g0217 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2569-316A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 23/27 | chr12 | 109526042 | |||||||
| chr12:109526067 | C | T | 6 | a0002c0001t0001g0023 a0002c0001t0001g0063 a0002c0001t0001g0081 others(3): Show |
7 | HG00323.hp2 HG01074.hp2 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.2569-291C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 23/27 | chr12 | 109526067 | |||||||
| chr12:109526096 | A | G | 6 | a0001c0002t0008g0010 a0001c0002t0008g0018 a0001c0002t0008g0158 others(3): Show |
10 | HG00639.hp2 HG00642.hp2 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.2569-262A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 23/27 | chr12 | 109526096 | |||||||
| chr12:109526297 | C | T | 51 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0036 others(48): Show |
70 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.2569-61C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 23/27 | chr12 | 109526297 | |||||||
| chr12:109526303 | G | A | 1 | a0005c0009t0026g0061 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2569-55G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 23/27 | chr12 | 109526303 | |||||||
| chr12:109526335 | A | AT | 4 | a0001c0002t0012g0038 a0001c0002t0012g0049 a0001c0002t0012g0203 others(1): Show |
5 | HG02257.hp1 HG02280.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.2569-21dupT | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr12 | 109526335 | ||||||
| chr12:109526591 | G | A | 4 | a0001c0002t0012g0038 a0001c0002t0012g0049 a0001c0002t0012g0203 others(1): Show |
5 | HG02257.hp1 HG02280.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.2627+175G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 24/27 | chr12 | 109526591 | |||||||
| chr12:109526612 | C | A | 2 | a0001c0002t0002g0174 a0001c0002t0002g0180 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.2627+196C>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 24/27 | chr12 | 109526612 | |||||||
| chr12:109526643 | C | A | 1 | a0001c0002t0033g0219 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2627+227C>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 24/27 | chr12 | 109526643 | |||||||
| chr12:109526664 | A | T | 12 | a0001c0002t0004g0041 a0001c0002t0004g0042 a0001c0002t0004g0043 others(9): Show |
15 | HG01255.hp2 HG01257.hp2 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.2627+248A>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 24/27 | chr12 | 109526664 | |||||||
| chr12:109526730 | G | A | 2 | a0001c0006t0027g0218 a0001c0006t0028g0216 |
2 | HG02280.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2627+314G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 24/27 | chr12 | 109526730 | |||||||
| chr12:109526818 | C | T | 1 | a0001c0002t0033g0219 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2627+402C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 24/27 | chr12 | 109526818 | |||||||
| chr12:109526861 | A | G | 2 | a0002c0001t0001g0093 a0002c0001t0001g0136 |
2 | HG00673.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.2627+445A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 24/27 | chr12 | 109526861 | |||||||
| chr12:109526870 | C | CA | 50 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0036 others(47): Show |
69 | HG00099.hp1 HG00140.hp2 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.2627+469dupA | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr12 | 109526870 | ||||||
| chr12:109526870 | C | CAA | 39 | a0001c0002t0002g0191 a0001c0002t0002g0199 a0001c0002t0007g0207 others(36): Show |
62 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.2627+468_2627+469d others(4): Show |
UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr12 | 109526870 | ||||||
| chr12:109526883 | A | AAT | 36 | a0001c0002t0004g0020 a0001c0002t0004g0035 a0001c0002t0004g0041 others(33): Show |
47 | HG00639.hp2 HG00642.hp2 HG01071.hp2 others(44): Show |
intron_variant | MODIFIER | c.2627+468_2627+469i others(4): Show |
UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr12 | 109526883 | ||||||
| chr12:109526925 | G | A | 2 | a0002c0001t0001g0012 a0002c0001t0001g0024 |
5 | HG00621.hp1 NA18946.hp1 NA19064.hp2 others(2): Show |
intron_variant | MODIFIER | c.2627+509G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 24/27 | chr12 | 109526925 | |||||||
| chr12:109527024 | C | T | 1 | a0001c0002t0006g0189 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2627+608C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 24/27 | chr12 | 109527024 | |||||||
| chr12:109527091 | T | C | 1 | a0002c0001t0001g0133 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.2627+675T>C | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 24/27 | chr12 | 109527091 | |||||||
| chr12:109527151 | A | G | 4 | a0001c0002t0012g0038 a0001c0002t0012g0049 a0001c0002t0012g0203 others(1): Show |
5 | HG02257.hp1 HG02280.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.2627+735A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 24/27 | chr12 | 109527151 | |||||||
| chr12:109527162 | G | A | 1 | a0002c0001t0001g0089 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2627+746G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 24/27 | chr12 | 109527162 | |||||||
| chr12:109527201 | C | G | 52 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0036 others(49): Show |
71 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.2627+785C>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 24/27 | chr12 | 109527201 | |||||||
| chr12:109527278 | A | T | 1 | a0001c0002t0015g0052 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2627+862A>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 24/27 | chr12 | 109527278 | |||||||
| chr12:109527483 | A | G | 1 | a0001c0002t0033g0219 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2627+1067A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 24/27 | chr12 | 109527483 | |||||||
| chr12:109527494 | G | A | 1 | a0001c0002t0002g0193 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2627+1078G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 24/27 | chr12 | 109527494 | |||||||
| chr12:109527707 | C | G | 125 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0036 others(122): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.2627+1291C>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 24/27 | chr12 | 109527707 | |||||||
| chr12:109527729 | A | C | 1 | a0001c0002t0002g0200 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2627+1313A>C | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 24/27 | chr12 | 109527729 | |||||||
| chr12:109527734 | CAG | C | 34 | a0001c0002t0004g0020 a0001c0002t0004g0035 a0001c0002t0004g0041 others(31): Show |
45 | HG00639.hp2 HG00642.hp2 HG01071.hp2 others(42): Show |
intron_variant | MODIFIER | c.2627+1327_2627+132 others(6): Show |
UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr12 | 109527734 | ||||||
| chr12:109527780 | G | A | 1 | a0002c0001t0001g0083 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2627+1364G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 24/27 | chr12 | 109527780 | |||||||
| chr12:109527852 | G | A | 13 | a0001c0002t0022g0217 a0001c0004t0005g0019 a0001c0004t0005g0039 others(10): Show |
17 | HG02280.hp1 HG02451.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.2627+1436G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 24/27 | chr12 | 109527852 | |||||||
| chr12:109527854 | G | A | 13 | a0001c0002t0022g0217 a0001c0004t0005g0019 a0001c0004t0005g0039 others(10): Show |
17 | HG02280.hp1 HG02451.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.2627+1438G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 24/27 | chr12 | 109527854 | |||||||
| chr12:109527982 | A | T | 1 | a0001c0002t0004g0048 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2627+1566A>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 24/27 | chr12 | 109527982 | |||||||
| chr12:109528080 | C | T | 48 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0036 others(45): Show |
66 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.2627+1664C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 24/27 | chr12 | 109528080 | |||||||
| chr12:109528266 | G | A | 1 | a0001c0002t0004g0057 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2628-1624G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 24/27 | chr12 | 109528266 | |||||||
| chr12:109528338 | T | C | 1 | a0002c0001t0001g0128 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2628-1552T>C | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 24/27 | chr12 | 109528338 | |||||||
| chr12:109528393 | G | A | 9 | a0001c0003t0003g0002 a0001c0003t0003g0016 a0001c0003t0003g0149 others(6): Show |
21 | HG00099.hp2 HG00423.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.2628-1497G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 24/27 | chr12 | 109528393 | |||||||
| chr12:109528488 | T | C | 1 | a0001c0002t0033g0219 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2628-1402T>C | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 24/27 | chr12 | 109528488 | |||||||
| chr12:109528600 | T | A | 1 | a0001c0002t0004g0160 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2628-1290T>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 24/27 | chr12 | 109528600 | |||||||
| chr12:109528683 | G | A | 11 | a0001c0002t0004g0035 a0001c0002t0004g0159 a0001c0002t0004g0160 others(8): Show |
16 | HG00639.hp2 HG00642.hp2 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.2628-1207G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 24/27 | chr12 | 109528683 | |||||||
| chr12:109528704 | A | C | 1 | a0005c0009t0026g0061 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2628-1186A>C | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 24/27 | chr12 | 109528704 | |||||||
| chr12:109528803 | C | T | 3 | a0001c0002t0011g0017 a0001c0002t0011g0156 a0001c0013t0011g0157 |
5 | HG00140.hp1 HG01346.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.2628-1087C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 24/27 | chr12 | 109528803 | |||||||
| chr12:109528857 | AAAAG | A | 51 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0036 others(48): Show |
70 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.2628-1029_2628-102 others(8): Show |
UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr12 | 109528857 | ||||||
| chr12:109528941 | C | T | 3 | a0002c0001t0001g0092 a0002c0001t0013g0034 a0002c0001t0013g0135 |
4 | HG02040.hp2 HG02083.hp1 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.2628-949C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 24/27 | chr12 | 109528941 | |||||||
| chr12:109528946 | G | A | 1 | a0002c0001t0001g0128 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2628-944G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 24/27 | chr12 | 109528946 | |||||||
| chr12:109528963 | A | G | 2 | a0002c0001t0001g0116 a0002c0001t0001g0118 |
2 | HG02735.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.2628-927A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 24/27 | chr12 | 109528963 | |||||||
| chr12:109529127 | C | T | 34 | a0001c0002t0004g0020 a0001c0002t0004g0035 a0001c0002t0004g0041 others(31): Show |
45 | HG00639.hp2 HG00642.hp2 HG01071.hp2 others(42): Show |
intron_variant | MODIFIER | c.2628-763C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 24/27 | chr12 | 109529127 | |||||||
| chr12:109529128 | T | A | 1 | a0001c0002t0002g0196 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2628-762T>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 24/27 | chr12 | 109529128 | |||||||
| chr12:109529259 | T | A | 21 | a0001c0003t0003g0002 a0001c0003t0003g0015 a0001c0003t0003g0016 others(18): Show |
38 | HG00099.hp2 HG00423.hp1 HG01099.hp1 others(35): Show |
intron_variant | MODIFIER | c.2628-631T>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 24/27 | chr12 | 109529259 | |||||||
| chr12:109529388 | C | T | 3 | a0001c0002t0002g0172 a0001c0002t0002g0175 a0001c0002t0002g0182 |
3 | HG02132.hp1 NA18974.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.2628-502C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 24/27 | chr12 | 109529388 | |||||||
| chr12:109529603 | T | C | 1 | a0001c0002t0022g0217 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2628-287T>C | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 24/27 | chr12 | 109529603 | |||||||
| chr12:109529607 | C | T | 3 | a0001c0002t0011g0017 a0001c0002t0011g0156 a0001c0013t0011g0157 |
5 | HG00140.hp1 HG01346.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.2628-283C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 24/27 | chr12 | 109529607 | |||||||
| chr12:109529608 | G | A | 1 | a0001c0002t0033g0219 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2628-282G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 24/27 | chr12 | 109529608 | |||||||
| chr12:109530086 | G | C | 4 | a0001c0003t0003g0002 a0001c0003t0003g0153 a0001c0003t0003g0154 others(1): Show |
14 | HG00423.hp1 HG02040.hp1 HG02083.hp2 others(11): Show |
intron_variant | MODIFIER | c.2810+14G>C | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 25/27 | chr12 | 109530086 | |||||||
| chr12:109530167 | G | T | 1 | a0001c0002t0008g0158 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2810+95G>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 25/27 | chr12 | 109530167 | |||||||
| chr12:109530287 | T | C | 1 | a0001c0006t0027g0218 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2810+215T>C | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 25/27 | chr12 | 109530287 | |||||||
| chr12:109530342 | G | T | 1 | a0001c0006t0027g0218 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2811-205G>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 25/27 | chr12 | 109530342 | |||||||
| chr12:109530384 | G | A | 2 | a0002c0001t0018g0073 a0002c0001t0018g0104 |
2 | HG00408.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.2811-163G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 25/27 | chr12 | 109530384 | |||||||
| chr12:109530444 | G | T | 1 | a0001c0002t0033g0219 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2811-103G>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 25/27 | chr12 | 109530444 | |||||||
| chr12:109530981 | T | C | 5 | a0001c0002t0007g0170 a0001c0002t0007g0179 a0001c0002t0007g0207 others(2): Show |
5 | HG01255.hp1 HG01934.hp2 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.2922+323T>C | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 26/27 | chr12 | 109530981 | |||||||
| chr12:109531041 | T | C | 6 | a0002c0001t0001g0013 a0002c0001t0001g0086 a0002c0001t0001g0094 others(3): Show |
8 | HG01070.hp1 HG01433.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.2922+383T>C | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 26/27 | chr12 | 109531041 | |||||||
| chr12:109531043 | T | C | 41 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0036 others(38): Show |
54 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(51): Show |
intron_variant | MODIFIER | c.2922+385T>C | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 26/27 | chr12 | 109531043 | |||||||
| chr12:109531100 | C | G | 1 | a0001c0002t0033g0219 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2922+442C>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 26/27 | chr12 | 109531100 | |||||||
| chr12:109531108 | G | A | 91 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0036 others(88): Show |
133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.2922+450G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 26/27 | chr12 | 109531108 | |||||||
| chr12:109531269 | T | C | 1 | a0001c0002t0033g0219 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2922+611T>C | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 26/27 | chr12 | 109531269 | |||||||
| chr12:109531349 | C | T | 1 | a0002c0001t0017g0025 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2922+691C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 26/27 | chr12 | 109531349 | |||||||
| chr12:109531370 | C | T | 1 | a0001c0002t0011g0017 | 3 | HG00140.hp1 HG01346.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.2922+712C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 26/27 | chr12 | 109531370 | |||||||
| chr12:109531457 | A | G | 3 | a0001c0002t0011g0017 a0001c0002t0011g0156 a0001c0013t0011g0157 |
5 | HG00140.hp1 HG01346.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.2922+799A>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 26/27 | chr12 | 109531457 | |||||||
| chr12:109531473 | G | A | 2 | a0001c0006t0027g0218 a0001c0006t0028g0216 |
2 | HG02280.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2922+815G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 26/27 | chr12 | 109531473 | |||||||
| chr12:109531881 | C | T | 23 | a0001c0002t0004g0020 a0001c0002t0004g0035 a0001c0002t0004g0048 others(20): Show |
31 | HG00639.hp2 HG00642.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.2922+1223C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 26/27 | chr12 | 109531881 | |||||||
| chr12:109532106 | C | T | 1 | a0005c0009t0026g0061 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2923-1360C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 26/27 | chr12 | 109532106 | |||||||
| chr12:109532165 | G | A | 4 | a0001c0002t0011g0017 a0001c0002t0011g0156 a0001c0004t0005g0213 others(1): Show |
6 | HG00140.hp1 HG01346.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.2923-1301G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 26/27 | chr12 | 109532165 | |||||||
| chr12:109532259 | A | C | 21 | a0001c0003t0003g0002 a0001c0003t0003g0015 a0001c0003t0003g0016 others(18): Show |
38 | HG00099.hp2 HG00423.hp1 HG01099.hp1 others(35): Show |
intron_variant | MODIFIER | c.2923-1207A>C | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 26/27 | chr12 | 109532259 | |||||||
| chr12:109532296 | T | C | 4 | a0001c0002t0012g0038 a0001c0002t0012g0049 a0001c0002t0012g0203 others(1): Show |
5 | HG02257.hp1 HG02280.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.2923-1170T>C | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 26/27 | chr12 | 109532296 | |||||||
| chr12:109532298 | T | C | 2 | a0001c0002t0012g0038 a0001c0002t0034g0202 |
3 | HG02257.hp1 HG02559.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2923-1168T>C | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 26/27 | chr12 | 109532298 | |||||||
| chr12:109532300 | G | A | 1 | a0001c0003t0023g0142 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2923-1166G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 26/27 | chr12 | 109532300 | |||||||
| chr12:109532446 | T | C | 52 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0036 others(49): Show |
71 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.2923-1020T>C | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 26/27 | chr12 | 109532446 | |||||||
| chr12:109532682 | C | T | 1 | a0002c0001t0001g0075 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2923-784C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 26/27 | chr12 | 109532682 | |||||||
| chr12:109532695 | G | T | 10 | a0001c0003t0003g0015 a0001c0003t0003g0139 a0001c0003t0003g0146 others(7): Show |
15 | HG01167.hp2 HG01884.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.2923-771G>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 26/27 | chr12 | 109532695 | |||||||
| chr12:109532762 | TTGGGCTG others(30): Show |
T | 1 | a0001c0002t0002g0197 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.2923-700_2923-664d others(39): Show |
UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 26/27 | INFO_REALIGN_3_PRIME | chr12 | 109532762 | ||||||
| chr12:109532772 | G | A | 1 | a0001c0002t0002g0196 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2923-694G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 26/27 | chr12 | 109532772 | |||||||
| chr12:109532824 | A | T | 1 | a0001c0006t0028g0216 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2923-642A>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 26/27 | chr12 | 109532824 | |||||||
| chr12:109532828 | T | G | 1 | a0001c0006t0028g0216 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2923-638T>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 26/27 | chr12 | 109532828 | |||||||
| chr12:109532858 | G | T | 1 | a0002c0001t0001g0137 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.2923-608G>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 26/27 | chr12 | 109532858 | |||||||
| chr12:109532953 | C | G | 1 | a0001c0002t0033g0219 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2923-513C>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 26/27 | chr12 | 109532953 | |||||||
| chr12:109533047 | G | A | 1 | a0002c0015t0001g0074 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.2923-419G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 26/27 | chr12 | 109533047 | |||||||
| chr12:109533081 | C | A | 1 | a0002c0001t0001g0090 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.2923-385C>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 26/27 | chr12 | 109533081 | |||||||
| chr12:109533148 | G | A | 1 | a0002c0001t0001g0111 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2923-318G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 26/27 | chr12 | 109533148 | |||||||
| chr12:109533229 | C | G | 1 | a0001c0002t0007g0181 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.2923-237C>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 26/27 | chr12 | 109533229 | |||||||
| chr12:109533295 | C | T | 35 | a0001c0002t0004g0020 a0001c0002t0004g0035 a0001c0002t0004g0041 others(32): Show |
46 | HG00639.hp2 HG00642.hp2 HG01071.hp2 others(43): Show |
intron_variant | MODIFIER | c.2923-171C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 26/27 | chr12 | 109533295 | |||||||
| chr12:109533366 | C | T | 3 | a0001c0002t0004g0056 a0001c0002t0004g0057 a0001c0002t0004g0059 |
3 | HG02622.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2923-100C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 26/27 | chr12 | 109533366 | |||||||
| chr12:109533388 | G | A | 1 | a0002c0015t0001g0074 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.2923-78G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 26/27 | chr12 | 109533388 | |||||||
| chr12:109533410 | C | T | 52 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0036 others(49): Show |
71 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.2923-56C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 26/27 | chr12 | 109533410 | |||||||
| chr12:109533411 | G | A | 1 | a0001c0002t0033g0219 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2923-55G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 26/27 | chr12 | 109533411 | |||||||
| chr12:109533676 | C | G | 35 | a0001c0002t0004g0020 a0001c0002t0004g0035 a0001c0002t0004g0041 others(32): Show |
46 | HG00639.hp2 HG00642.hp2 HG01071.hp2 others(43): Show |
intron_variant | MODIFIER | c.3015+118C>G | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 27/27 | chr12 | 109533676 | |||||||
| chr12:109533956 | C | A | 2 | a0001c0007t0003g0045 a0001c0007t0003g0046 |
2 | HG03195.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.3015+398C>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 27/27 | chr12 | 109533956 | |||||||
| chr12:109534005 | C | T | 1 | a0001c0003t0023g0142 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3015+447C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 27/27 | chr12 | 109534005 | |||||||
| chr12:109534018 | G | A | 10 | a0001c0002t0002g0036 a0001c0002t0002g0193 a0001c0002t0002g0194 others(7): Show |
11 | HG00099.hp1 HG00733.hp1 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.3015+460G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 27/27 | chr12 | 109534018 | |||||||
| chr12:109534045 | C | T | 1 | a0002c0001t0030g0084 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.3015+487C>T | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 27/27 | chr12 | 109534045 | |||||||
| chr12:109534096 | G | A | 1 | a0002c0001t0001g0110 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3016-495G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 27/27 | chr12 | 109534096 | |||||||
| chr12:109534173 | G | A | 2 | a0001c0003t0009g0009 a0001c0003t0009g0140 |
5 | HG02109.hp2 HG03139.hp2 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.3016-418G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 27/27 | chr12 | 109534173 | |||||||
| chr12:109534232 | G | A | 53 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0036 others(50): Show |
72 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.3016-359G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 27/27 | chr12 | 109534232 | |||||||
| chr12:109534333 | G | A | 1 | a0002c0001t0001g0117 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.3016-258G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 27/27 | chr12 | 109534333 | |||||||
| chr12:109534466 | G | A | 2 | a0002c0001t0001g0093 a0002c0001t0001g0136 |
2 | HG00673.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.3016-125G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 27/27 | chr12 | 109534466 | |||||||
| chr12:109534576 | G | A | 1 | a0002c0001t0001g0097 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3016-15G>A | UBE3B | ENSG00000151148.14 | transcript | ENST00000342494.8 | protein_coding | 27/27 | chr12 | 109534576 |