Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 1540 |
| ensemblid | ENSG00000083799.18 |
| hgncid | 2584 |
| symbol | CYLD |
| name | CYLD lysine 63 deubiquitinase |
| refseq_nuc | NM_001378743.1 |
| refseq_prot | NP_001365672.1 |
| ensembl_nuc | ENST00000427738.8 |
| ensembl_prot | ENSP00000392025.3 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 50742086 |
| end | 50801935 |
| strand | + |
| ver | v1.2 |
| region | chr16:50742086-50801935 |
| region5000 | chr16:50737086-50806935 |
| regionname0 | CYLD_chr16_50742086_50801935 |
| regionname5000 | CYLD_chr16_50737086_50806935 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 956 | 301 | 84 | 56 | 121 | 12 | 26 | 99 | CYLD_chr16_50737086_50806935 | CYLD | MSSGL others(951): Show |
chr16 | 50737086 | 50806935 |
| a0002 | 0/0 | 956 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CYLD_chr16_50737086_50806935 | CYLD | MSSGL others(951): Show |
chr16 | 50737086 | 50806935 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2868 | 258 | 73 | 48 | 103 | 12 | 20 | CYLD_chr16_50737086_50806935 | CYLD | ATGAG others(2863): Show |
chr16 | 50737086 | 50806935 | ||
| a0001c0002 | 0/0 | 2868 | 33 | 3 | 7 | 17 | 0 | 6 | CYLD_chr16_50737086_50806935 | CYLD | ATGAG others(2863): Show |
chr16 | 50737086 | 50806935 | ||
| a0001c0003 | 0/0 | 2868 | 7 | 7 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | ATGAG others(2863): Show |
chr16 | 50737086 | 50806935 | ||
| a0001c0005 | 0/0 | 2868 | 1 | 0 | 1 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | ATGAG others(2863): Show |
chr16 | 50737086 | 50806935 | ||
| a0001c0006 | 0/0 | 2868 | 1 | 1 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | ATGAG others(2863): Show |
chr16 | 50737086 | 50806935 | ||
| a0001c0007 | 0/0 | 2868 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | ATGAG others(2863): Show |
chr16 | 50737086 | 50806935 | ||
| a0002c0004 | 0/0 | 2868 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | ATGAG others(2863): Show |
chr16 | 50737086 | 50806935 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 8540 | 193 | 41 | 39 | 81 | 10 | 20 | CYLD_chr16_50737086_50806935 | CYLD | AGGTA others(8535): Show |
chr16 | 50737086 | 50806935 |
| a0001c0001t0003 | 0/0 | 8537 | 22 | 15 | 0 | 7 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | AGGTA others(8532): Show |
chr16 | 50737086 | 50806935 |
| a0001c0001t0004 | 0/0 | 8539 | 10 | 2 | 6 | 1 | 1 | 0 | CYLD_chr16_50737086_50806935 | CYLD | AGGTA others(8534): Show |
chr16 | 50737086 | 50806935 |
| a0001c0001t0006 | 0/0 | 8540 | 6 | 0 | 0 | 6 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | AGGTA others(8535): Show |
chr16 | 50737086 | 50806935 |
| a0001c0001t0007 | 0/0 | 8539 | 4 | 4 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | AGGTA others(8534): Show |
chr16 | 50737086 | 50806935 |
| a0001c0001t0008 | 0/0 | 8539 | 4 | 4 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | AGGTA others(8534): Show |
chr16 | 50737086 | 50806935 |
| a0001c0001t0009 | 0/0 | 8539 | 3 | 3 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | AGGTA others(8534): Show |
chr16 | 50737086 | 50806935 |
| a0001c0001t0011 | 0/0 | 8540 | 2 | 1 | 1 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | AGGTA others(8535): Show |
chr16 | 50737086 | 50806935 |
| a0001c0001t0013 | 0/0 | 8540 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | AGGTA others(8535): Show |
chr16 | 50737086 | 50806935 |
| a0001c0001t0014 | 0/0 | 8540 | 1 | 1 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | AGGTA others(8535): Show |
chr16 | 50737086 | 50806935 |
| a0001c0001t0015 | 0/0 | 8539 | 1 | 0 | 1 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | AGGTA others(8534): Show |
chr16 | 50737086 | 50806935 |
| a0001c0001t0016 | 0/0 | 8540 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | AGGTA others(8535): Show |
chr16 | 50737086 | 50806935 |
| a0001c0001t0017 | 0/0 | 8540 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | AGGTA others(8535): Show |
chr16 | 50737086 | 50806935 |
| a0001c0001t0018 | 0/0 | 8540 | 1 | 0 | 1 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | AGGTA others(8535): Show |
chr16 | 50737086 | 50806935 |
| a0001c0001t0019 | 0/0 | 8540 | 1 | 0 | 0 | 0 | 1 | 0 | CYLD_chr16_50737086_50806935 | CYLD | AGGTA others(8535): Show |
chr16 | 50737086 | 50806935 |
| a0001c0001t0020 | 0/0 | 8540 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | AGGTA others(8535): Show |
chr16 | 50737086 | 50806935 |
| a0001c0001t0021 | 0/0 | 8540 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | AGGTA others(8535): Show |
chr16 | 50737086 | 50806935 |
| a0001c0001t0022 | 0/0 | 8537 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | AGGTA others(8532): Show |
chr16 | 50737086 | 50806935 |
| a0001c0001t0024 | 0/0 | 8540 | 1 | 1 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | AGGTA others(8535): Show |
chr16 | 50737086 | 50806935 |
| a0001c0001t0025 | 0/0 | 8537 | 1 | 1 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | AGGTA others(8532): Show |
chr16 | 50737086 | 50806935 |
| a0001c0001t0026 | 0/0 | 8540 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | AGGTA others(8535): Show |
chr16 | 50737086 | 50806935 |
| a0001c0001t0027 | 0/0 | 8540 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | AGGTA others(8535): Show |
chr16 | 50737086 | 50806935 |
| a0001c0002t0002 | 0/0 | 8539 | 28 | 2 | 6 | 14 | 0 | 6 | CYLD_chr16_50737086_50806935 | CYLD | AGGTA others(8534): Show |
chr16 | 50737086 | 50806935 |
| a0001c0002t0010 | 0/0 | 8540 | 2 | 1 | 1 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | AGGTA others(8535): Show |
chr16 | 50737086 | 50806935 |
| a0001c0002t0012 | 0/0 | 8539 | 2 | 0 | 0 | 2 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | AGGTA others(8534): Show |
chr16 | 50737086 | 50806935 |
| a0001c0002t0023 | 0/0 | 8539 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | AGGTA others(8534): Show |
chr16 | 50737086 | 50806935 |
| a0001c0003t0005 | 0/0 | 8539 | 7 | 7 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | AGGTA others(8534): Show |
chr16 | 50737086 | 50806935 |
| a0001c0005t0001 | 0/0 | 8540 | 1 | 0 | 1 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | AGGTA others(8535): Show |
chr16 | 50737086 | 50806935 |
| a0001c0006t0001 | 0/0 | 8540 | 1 | 1 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | AGGTA others(8535): Show |
chr16 | 50737086 | 50806935 |
| a0001c0007t0001 | 0/0 | 8540 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | AGGTA others(8535): Show |
chr16 | 50737086 | 50806935 |
| a0002c0004t0001 | 0/0 | 8540 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | AGGTA others(8535): Show |
chr16 | 50737086 | 50806935 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0002 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0007 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0060 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0260 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0003g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0003g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0003g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0003g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0003g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0003g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0003g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0003g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0003g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0003g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0003g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0003g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0003g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0003g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0004g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0004g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0004g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0004g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0004g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0004g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0004g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0004g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0004g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0004g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0006g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0006g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0006g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0006g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0006g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0006g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0007g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0007g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0007g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0007g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0008g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0008g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0008g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0008g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0009g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0009g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0009g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0011g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0011g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0013g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0014g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0015g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0016g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0017g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0018g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0019g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0020g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0021g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0022g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0024g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0025g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0026g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0001t0027g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0002t0002g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0002t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0002t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0002t0002g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0002t0002g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0002t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0002t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0002t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0002t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0002t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0002t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0002t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0002t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0002t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0002t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0002t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0002t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0002t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0002t0010g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0002t0010g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0002t0012g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0002t0012g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0002t0023g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0003t0005g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0003t0005g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0003t0005g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0003t0005g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0003t0005g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0005t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0006t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0001c0007t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| a0002c0004t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0181 | EUR | GBR | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0202 | EUR | GBR | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0099 | EUR | FIN | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0186 | EUR | FIN | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0020 | EUR | FIN | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0038 | EUR | FIN | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | CHS | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | CHS | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | CHS | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | CHS | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG00735 | hp1 | a0001 | c0002 | t0002 | g0030 | AMR | PUR | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG00738 | hp2 | a0001 | c0002 | t0002 | g0017 | AMR | PUR | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG01070 | hp2 | a0001 | c0005 | t0001 | g0102 | AMR | PUR | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG01074 | hp2 | a0001 | c0001 | t0015 | g0003 | AMR | PUR | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG01081 | hp1 | a0001 | c0001 | t0004 | g0191 | AMR | PUR | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG01099 | hp1 | a0001 | c0001 | t0004 | g0192 | AMR | PUR | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG01109 | hp2 | a0001 | c0001 | t0011 | g0106 | AMR | PUR | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG01167 | hp1 | a0001 | c0001 | t0004 | g0221 | AMR | PUR | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG01175 | hp2 | a0001 | c0002 | t0002 | g0143 | AMR | PUR | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | CLM | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG01255 | hp2 | a0001 | c0001 | t0004 | g0039 | AMR | CLM | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG01256 | hp1 | a0001 | c0002 | t0002 | g0147 | AMR | CLM | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG01256 | hp2 | a0001 | c0001 | t0004 | g0001 | AMR | CLM | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG01258 | hp2 | a0001 | c0002 | t0002 | g0037 | AMR | CLM | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG01346 | hp2 | a0001 | c0002 | t0002 | g0017 | AMR | CLM | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | CLM | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG01433 | hp2 | a0001 | c0002 | t0010 | g0029 | AMR | CLM | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0110 | EUR | IBS | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG01516 | hp2 | a0001 | c0001 | t0019 | g0061 | EUR | IBS | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG01884 | hp2 | a0001 | c0001 | t0007 | g0130 | AFR | ACB | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG01891 | hp1 | a0001 | c0003 | t0005 | g0008 | AFR | ACB | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PEL | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG01928 | hp2 | a0001 | c0001 | t0018 | g0187 | AMR | PEL | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PEL | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PEL | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | KHV | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG02055 | hp1 | a0001 | c0002 | t0010 | g0146 | AFR | ACB | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | ACB | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG02056 | hp1 | a0001 | c0002 | t0002 | g0245 | EAS | KHV | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | KHV | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG02080 | hp2 | a0001 | c0001 | t0017 | g0083 | EAS | KHV | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG02132 | hp1 | a0001 | c0001 | t0004 | g0007 | EAS | KHV | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG02135 | hp1 | a0001 | c0002 | t0002 | g0244 | EAS | KHV | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG02135 | hp2 | a0001 | c0001 | t0016 | g0247 | EAS | KHV | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0257 | AFR | ACB | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0258 | AFR | ACB | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG02257 | hp1 | a0001 | c0001 | t0008 | g0223 | AFR | ACB | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PEL | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PEL | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG02280 | hp1 | a0001 | c0001 | t0009 | g0131 | AFR | ACB | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0261 | AMR | PEL | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | ACB | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | KHV | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | GWD | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0236 | AFR | GWD | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG02615 | hp1 | a0001 | c0001 | t0025 | g0250 | AFR | GWD | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0264 | AFR | GWD | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG02622 | hp1 | a0001 | c0001 | t0008 | g0135 | AFR | GWD | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG02622 | hp2 | a0001 | c0001 | t0007 | g0129 | AFR | GWD | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG02630 | hp1 | a0001 | c0001 | t0007 | g0132 | AFR | GWD | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0231 | AFR | GWD | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0238 | AFR | GWD | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0255 | AFR | GWD | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG02717 | hp2 | a0001 | c0003 | t0005 | g0242 | AFR | GWD | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG02723 | hp1 | a0001 | c0001 | t0007 | g0128 | AFR | GWD | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | GWD | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG02738 | hp1 | a0001 | c0002 | t0002 | g0229 | SAS | PJL | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG02809 | hp1 | a0001 | c0001 | t0024 | g0003 | AFR | GWD | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | GWD | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG02895 | hp2 | a0001 | c0003 | t0005 | g0243 | AFR | GWD | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | GWD | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG02922 | hp2 | a0001 | c0002 | t0002 | g0034 | AFR | ESN | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | ESN | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0232 | AFR | ESN | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ESN | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG03017 | hp1 | a0001 | c0002 | t0002 | g0033 | SAS | PJL | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG03041 | hp1 | a0001 | c0001 | t0008 | g0136 | AFR | GWD | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | GWD | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG03098 | hp1 | a0001 | c0001 | t0009 | g0222 | AFR | MSL | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | MSL | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG03130 | hp1 | a0001 | c0003 | t0005 | g0008 | AFR | ESN | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | ESN | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0220 | AFR | ESN | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | ESN | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG03195 | hp1 | a0001 | c0001 | t0011 | g0200 | AFR | ESN | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | MSL | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0251 | AFR | MSL | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG03453 | hp1 | a0001 | c0003 | t0005 | g0241 | AFR | MSL | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG03453 | hp2 | a0001 | c0001 | t0008 | g0134 | AFR | MSL | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | ESN | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | ESN | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0239 | AFR | GWD | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | MSL | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | MSL | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0201 | SAS | PJL | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | STU | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG03688 | hp2 | a0001 | c0002 | t0002 | g0140 | SAS | STU | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG03927 | hp1 | a0001 | c0002 | t0002 | g0144 | SAS | BEB | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0163 | SAS | BEB | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | STU | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0211 | SAS | STU | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | STU | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0167 | SAS | STU | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG04228 | hp2 | a0001 | c0002 | t0002 | g0228 | SAS | STU | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | CHB | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0235 | AFR | YRI | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0249 | AFR | YRI | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA18940 | hp1 | a0001 | c0001 | t0006 | g0113 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA18942 | hp2 | a0001 | c0002 | t0012 | g0036 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA18943 | hp2 | a0001 | c0001 | t0003 | g0227 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA18947 | hp1 | a0001 | c0002 | t0002 | g0031 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA18947 | hp2 | a0001 | c0001 | t0006 | g0198 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA18951 | hp1 | a0001 | c0002 | t0012 | g0145 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA18952 | hp2 | a0001 | c0002 | t0002 | g0018 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0234 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA18956 | hp2 | a0001 | c0002 | t0002 | g0016 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA18959 | hp1 | a0001 | c0001 | t0026 | g0103 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA18960 | hp1 | a0001 | c0007 | t0001 | g0004 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA18963 | hp2 | a0002 | c0004 | t0001 | g0121 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA18965 | hp1 | a0001 | c0001 | t0003 | g0237 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA18967 | hp1 | a0001 | c0001 | t0013 | g0180 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA18967 | hp2 | a0001 | c0001 | t0003 | g0252 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA18972 | hp1 | a0001 | c0001 | t0022 | g0096 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA18972 | hp2 | a0001 | c0001 | t0003 | g0226 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA18984 | hp2 | a0001 | c0001 | t0020 | g0071 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA18985 | hp2 | a0001 | c0001 | t0021 | g0206 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA18986 | hp1 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA18992 | hp1 | a0001 | c0001 | t0003 | g0254 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA19002 | hp2 | a0001 | c0001 | t0006 | g0179 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA19009 | hp1 | a0001 | c0002 | t0002 | g0182 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA19009 | hp2 | a0001 | c0001 | t0027 | g0063 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA19010 | hp2 | a0001 | c0002 | t0002 | g0028 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | LWK | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | LWK | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0240 | AFR | LWK | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | LWK | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA19054 | hp1 | a0001 | c0002 | t0002 | g0016 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA19057 | hp2 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA19060 | hp2 | a0001 | c0002 | t0023 | g0009 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA19067 | hp1 | a0001 | c0002 | t0002 | g0246 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA19080 | hp1 | a0001 | c0001 | t0006 | g0123 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA19081 | hp1 | a0001 | c0001 | t0003 | g0233 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA19082 | hp2 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA19083 | hp1 | a0001 | c0001 | t0006 | g0197 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA19083 | hp2 | a0001 | c0002 | t0002 | g0142 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA19084 | hp1 | a0001 | c0001 | t0006 | g0115 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA19091 | hp1 | a0001 | c0002 | t0002 | g0018 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0024 | AFR | YRI | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA19240 | hp2 | a0001 | c0001 | t0004 | g0127 | AFR | YRI | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | ASW | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | ASW | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0161 | EUR | TSI | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0139 | EUR | TSI | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA20805 | hp1 | a0001 | c0001 | t0004 | g0107 | EUR | TSI | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0168 | EUR | TSI | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | GIH | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA20905 | hp2 | a0001 | c0002 | t0002 | g0141 | SAS | GIH | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | CLM | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG01123 | hp2 | a0001 | c0001 | t0004 | g0002 | AMR | CLM | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ACB | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0024 | AFR | ACB | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG02486 | hp1 | a0001 | c0001 | t0009 | g0133 | AFR | ACB | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG02486 | hp2 | a0001 | c0006 | t0001 | g0267 | AFR | ACB | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | MSL | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | MSL | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG06807 | hp1 | a0001 | c0001 | t0014 | g0069 | AFR | USA | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| HG06807 | hp2 | a0001 | c0003 | t0005 | g0008 | AFR | USA | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA20300 | hp1 | a0001 | c0003 | t0005 | g0259 | AFR | USA | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0253 | AFR | USA | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | LWK | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| NA21309 | hp2 | a0001 | c0002 | t0002 | g0035 | AFR | LWK | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0260 | REF | REF | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0060 | REF | REF | CYLD_chr16_50737086_50806935 | CYLD | chr16 | 50737086 | 50806935 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:50779698 | T | C | 1 | a0002 | 1 | NA18963.hp2 | missense_variant | MODERATE | c.1172T>C | p.Ile391Thr | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 9/19 | 1414/8540 | 1172/2871 | 391/956 | chr16 | 50779698 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:50749785 | C | T | 1 | a0001c0003 | 7 | HG01891.hp1 HG02717.hp2 HG02895.hp2 others(4): Show |
synonymous_variant | LOW | c.87C>T | p.Ser29Ser | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 3/19 | 329/8540 | 87/2871 | 29/956 | chr16 | 50749785 | |||
| chr16:50751774 | C | T | 1 | a0001c0007 | 1 | NA18960.hp1 | synonymous_variant | LOW | c.675C>T | p.Val225Val | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 4/19 | 917/8540 | 675/2871 | 225/956 | chr16 | 50751774 | |||
| chr16:50779999 | C | T | 1 | a0001c0006 | 1 | HG02486.hp2 | synonymous_variant | LOW | c.1473C>T | p.Ile491Ile | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 9/19 | 1715/8540 | 1473/2871 | 491/956 | chr16 | 50779999 | |||
| chr16:50784422 | G | A | 1 | a0001c0005 | 1 | HG01070.hp2 | synonymous_variant | LOW | c.1920G>A | p.Leu640Leu | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 12/19 | 2162/8540 | 1920/2871 | 640/956 | chr16 | 50784422 | |||
| chr16:50793607 | C | T | 1 | a0001c0002 | 33 | HG00735.hp1 HG00738.hp2 HG01175.hp2 others(30): Show |
synonymous_variant | LOW | c.2412C>T | p.Asp804Asp | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 17/19 | 2654/8540 | 2412/2871 | 804/956 | chr16 | 50793607 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:50742113 | C | G | 1 | a0001c0001t0027 | 1 | NA19009.hp2 | 5_prime_UTR_variant | MODIFIER | c.-215C>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 1/19 | 7586 | chr16 | 50742113 | ||||||
| chr16:50796606 | G | A | 1 | a0001c0001t0013 | 1 | NA18967.hp1 | 3_prime_UTR_variant | MODIFIER | c.*98G>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 19/19 | 98 | chr16 | 50796606 | ||||||
| chr16:50796744 | A | G | 1 | a0001c0001t0026 | 1 | NA18959.hp1 | 3_prime_UTR_variant | MODIFIER | c.*236A>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 19/19 | 236 | chr16 | 50796744 | ||||||
| chr16:50797339 | C | T | 1 | a0001c0002t0012 | 2 | NA18942.hp2 NA18951.hp1 |
3_prime_UTR_variant | MODIFIER | c.*831C>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 19/19 | 831 | chr16 | 50797339 | ||||||
| chr16:50797345 | A | G | 2 | a0001c0001t0003 a0001c0001t0025 |
23 | HG02109.hp2 HG02145.hp1 HG02145.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*837A>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 19/19 | 837 | chr16 | 50797345 | ||||||
| chr16:50797630 | A | G | 1 | a0001c0001t0011 | 2 | HG01109.hp2 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1122A>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 19/19 | 1122 | chr16 | 50797630 | ||||||
| chr16:50797849 | T | G | 1 | a0001c0001t0006 | 6 | NA18940.hp1 NA18947.hp2 NA19002.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1341T>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 19/19 | 1341 | chr16 | 50797849 | ||||||
| chr16:50797865 | G | T | 1 | a0001c0001t0024 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1357G>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 19/19 | 1357 | chr16 | 50797865 | ||||||
| chr16:50798307 | C | T | 1 | a0001c0003t0005 | 7 | HG01891.hp1 HG02717.hp2 HG02895.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1799C>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 19/19 | 1799 | chr16 | 50798307 | ||||||
| chr16:50798497 | C | T | 1 | a0001c0001t0025 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1989C>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 19/19 | 1989 | chr16 | 50798497 | ||||||
| chr16:50798614 | GA | G | 11 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0007 others(8): Show |
83 | HG00735.hp1 HG00738.hp2 HG01081.hp1 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*2122delA | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 19/19 | 2122 | INFO_REALIGN_3_PRIME | chr16 | 50798614 | |||||
| chr16:50798668 | A | C | 1 | a0001c0001t0013 | 1 | NA18967.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2160A>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 19/19 | 2160 | chr16 | 50798668 | ||||||
| chr16:50798669 | C | A | 1 | a0001c0001t0013 | 1 | NA18967.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2161C>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 19/19 | 2161 | chr16 | 50798669 | ||||||
| chr16:50798670 | A | C | 1 | a0001c0002t0023 | 1 | NA19060.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2162A>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 19/19 | 2162 | chr16 | 50798670 | ||||||
| chr16:50798744 | C | T | 1 | a0001c0001t0008 | 4 | HG02257.hp1 HG02622.hp1 HG03041.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2236C>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 19/19 | 2236 | chr16 | 50798744 | ||||||
| chr16:50798813 | A | T | 1 | a0001c0001t0021 | 1 | NA18985.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2305A>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 19/19 | 2305 | chr16 | 50798813 | ||||||
| chr16:50798843 | T | C | 1 | a0001c0001t0014 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2335T>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 19/19 | 2335 | chr16 | 50798843 | ||||||
| chr16:50798877 | G | A | 2 | a0001c0001t0007 a0001c0001t0009 |
7 | HG01884.hp2 HG02280.hp1 HG02486.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2369G>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 19/19 | 2369 | chr16 | 50798877 | ||||||
| chr16:50799908 | C | T | 1 | a0001c0001t0020 | 1 | NA18984.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3400C>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 19/19 | 3400 | chr16 | 50799908 | ||||||
| chr16:50799931 | A | G | 1 | a0001c0001t0019 | 1 | HG01516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3423A>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 19/19 | 3423 | chr16 | 50799931 | ||||||
| chr16:50800247 | C | G | 2 | a0001c0001t0007 a0001c0001t0009 |
7 | HG01884.hp2 HG02280.hp1 HG02486.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3739C>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 19/19 | 3739 | chr16 | 50800247 | ||||||
| chr16:50800282 | C | T | 1 | a0001c0001t0018 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3774C>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 19/19 | 3774 | chr16 | 50800282 | ||||||
| chr16:50801069 | G | A | 4 | a0001c0002t0002 a0001c0002t0010 a0001c0002t0012 others(1): Show |
33 | HG00735.hp1 HG00738.hp2 HG01175.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*4561G>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 19/19 | 4561 | chr16 | 50801069 | ||||||
| chr16:50801075 | C | T | 1 | a0001c0001t0009 | 3 | HG02280.hp1 HG02486.hp1 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4567C>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 19/19 | 4567 | chr16 | 50801075 | ||||||
| chr16:50801395 | CAT | C | 3 | a0001c0001t0003 a0001c0001t0022 a0001c0001t0025 |
24 | HG02109.hp2 HG02145.hp1 HG02145.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*4888_*4889delAT | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 19/19 | 4888 | chr16 | 50801395 | ||||||
| chr16:50801515 | A | T | 1 | a0001c0001t0017 | 1 | HG02080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5007A>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 19/19 | 5007 | chr16 | 50801515 | ||||||
| chr16:50801594 | A | G | 1 | a0001c0001t0016 | 1 | HG02135.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5086A>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 19/19 | 5086 | chr16 | 50801594 | ||||||
| chr16:50801685 | T | A | 1 | a0001c0001t0015 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5177T>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 19/19 | 5177 | chr16 | 50801685 | ||||||
| chr16:50801686 | C | T | 1 | a0001c0001t0015 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5178C>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 19/19 | 5178 | chr16 | 50801686 | ||||||
| chr16:50801687 | ATTTTCTA others(56): Show |
A | 1 | a0001c0001t0015 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5180_*5242delTTTT others(59): Show |
CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 19/19 | 5180 | chr16 | 50801687 | ||||||
| chr16:50801751 | G | A | 1 | a0001c0001t0015 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5243G>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 19/19 | 5243 | chr16 | 50801751 | ||||||
| chr16:50801752 | C | A | 1 | a0001c0001t0015 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5244C>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 19/19 | 5244 | chr16 | 50801752 | ||||||
| chr16:50801761 | C | CACAGAAA others(55): Show |
1 | a0001c0001t0015 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5253_*5254insACAG others(58): Show |
CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 19/19 | 5254 | chr16 | 50801761 | ||||||
| chr16:50801763 | A | G | 1 | a0001c0001t0015 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5255A>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 19/19 | 5255 | chr16 | 50801763 | ||||||
| chr16:50801766 | T | G | 1 | a0001c0001t0015 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5258T>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 19/19 | 5258 | chr16 | 50801766 | ||||||
| chr16:50801769 | A | T | 1 | a0001c0001t0015 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5261A>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 19/19 | 5261 | chr16 | 50801769 | ||||||
| chr16:50801772 | A | T | 1 | a0001c0001t0015 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5264A>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 19/19 | 5264 | chr16 | 50801772 | ||||||
| chr16:50801778 | T | A | 1 | a0001c0001t0015 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5270T>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 19/19 | 5270 | chr16 | 50801778 | ||||||
| chr16:50801780 | C | T | 1 | a0001c0001t0015 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5272C>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 19/19 | 5272 | chr16 | 50801780 | ||||||
| chr16:50801785 | A | T | 1 | a0001c0001t0015 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5277A>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 19/19 | 5277 | chr16 | 50801785 | ||||||
| chr16:50801786 | G | T | 1 | a0001c0001t0015 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5278G>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 19/19 | 5278 | chr16 | 50801786 | ||||||
| chr16:50801787 | A | G | 1 | a0001c0001t0015 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5279A>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 19/19 | 5279 | chr16 | 50801787 | ||||||
| chr16:50801793 | A | T | 1 | a0001c0001t0015 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5285A>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 19/19 | 5285 | chr16 | 50801793 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:50742256 | C | T | 6 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0264 others(3): Show |
6 | HG02486.hp2 HG02572.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-204+132C>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 1/18 | chr16 | 50742256 | |||||||
| chr16:50742313 | A | T | 1 | a0001c0001t0001g0261 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-204+189A>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 1/18 | chr16 | 50742313 | |||||||
| chr16:50742402 | T | TC | 36 | a0001c0001t0001g0230 a0001c0001t0001g0248 a0001c0001t0001g0256 others(33): Show |
39 | HG00639.hp2 HG01891.hp1 HG02056.hp1 others(36): Show |
intron_variant | MODIFIER | c.-204+287dupC | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr16 | 50742402 | ||||||
| chr16:50742546 | G | GC | 121 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0019 others(118): Show |
135 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.-203-210dupC | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr16 | 50742546 | ||||||
| chr16:50742671 | C | G | 1 | a0001c0001t0001g0224 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-203-91C>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 1/18 | chr16 | 50742671 | |||||||
| chr16:50742671 | C | T | 1 | a0001c0001t0001g0225 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-203-91C>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 1/18 | chr16 | 50742671 | |||||||
| chr16:50742911 | G | A | 2 | a0001c0001t0003g0226 a0001c0001t0003g0227 |
2 | NA18943.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.-124+70G>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 2/18 | chr16 | 50742911 | |||||||
| chr16:50743286 | C | T | 5 | a0001c0003t0005g0008 a0001c0003t0005g0241 a0001c0003t0005g0242 others(2): Show |
7 | HG01891.hp1 HG02717.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-124+445C>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 2/18 | chr16 | 50743286 | |||||||
| chr16:50743391 | C | T | 31 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0216 others(28): Show |
33 | HG01167.hp1 HG01884.hp2 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.-124+550C>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 2/18 | chr16 | 50743391 | |||||||
| chr16:50743423 | A | G | 1 | a0001c0001t0001g0215 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-124+582A>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 2/18 | chr16 | 50743423 | |||||||
| chr16:50743545 | A | T | 31 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0216 others(28): Show |
33 | HG01167.hp1 HG01884.hp2 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.-124+704A>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 2/18 | chr16 | 50743545 | |||||||
| chr16:50743668 | T | C | 2 | a0001c0001t0001g0025 a0001c0001t0001g0137 |
2 | HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-124+827T>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 2/18 | chr16 | 50743668 | |||||||
| chr16:50743837 | A | G | 4 | a0001c0001t0008g0134 a0001c0001t0008g0135 a0001c0001t0008g0136 others(1): Show |
4 | HG02257.hp1 HG02622.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-124+996A>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 2/18 | chr16 | 50743837 | |||||||
| chr16:50743853 | T | C | 3 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0138 |
3 | HG02451.hp1 HG02809.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-124+1012T>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 2/18 | chr16 | 50743853 | |||||||
| chr16:50744096 | T | C | 9 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0216 others(6): Show |
9 | HG01167.hp1 HG02055.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.-124+1255T>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 2/18 | chr16 | 50744096 | |||||||
| chr16:50744306 | A | T | 1 | a0001c0006t0001g0267 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-124+1465A>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 2/18 | chr16 | 50744306 | |||||||
| chr16:50744453 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-124+1612C>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 2/18 | chr16 | 50744453 | |||||||
| chr16:50744678 | G | A | 4 | a0001c0001t0008g0134 a0001c0001t0008g0135 a0001c0001t0008g0136 others(1): Show |
4 | HG02257.hp1 HG02622.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-124+1837G>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 2/18 | chr16 | 50744678 | |||||||
| chr16:50744700 | T | C | 1 | a0001c0003t0005g0241 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-124+1859T>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 2/18 | chr16 | 50744700 | |||||||
| chr16:50744966 | G | A | 1 | a0001c0001t0001g0139 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-124+2125G>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 2/18 | chr16 | 50744966 | |||||||
| chr16:50745139 | C | T | 2 | a0001c0001t0001g0124 a0001c0001t0001g0213 |
2 | NA19000.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.-124+2298C>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 2/18 | chr16 | 50745139 | |||||||
| chr16:50745199 | T | C | 4 | a0001c0002t0002g0009 a0001c0002t0002g0016 a0001c0002t0002g0028 others(1): Show |
5 | NA18956.hp2 NA19010.hp2 NA19054.hp1 others(2): Show |
intron_variant | MODIFIER | c.-124+2358T>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 2/18 | chr16 | 50745199 | |||||||
| chr16:50745292 | A | C | 23 | a0001c0001t0001g0256 a0001c0001t0003g0024 a0001c0001t0003g0226 others(20): Show |
24 | HG00639.hp2 HG02109.hp2 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.-124+2451A>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 2/18 | chr16 | 50745292 | |||||||
| chr16:50745362 | G | GT | 86 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(83): Show |
99 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.-124+2544dupT | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr16 | 50745362 | ||||||
| chr16:50745362 | G | GTT | 23 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0125 others(20): Show |
25 | HG01167.hp1 HG01884.hp1 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.-124+2543_-124+254 others(6): Show |
CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr16 | 50745362 | ||||||
| chr16:50745362 | G | GTTT | 6 | a0001c0001t0001g0263 a0001c0001t0001g0264 a0001c0001t0001g0265 others(3): Show |
6 | HG02486.hp1 HG02486.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-124+2542_-124+254 others(7): Show |
CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr16 | 50745362 | ||||||
| chr16:50745362 | G | GTTTT | 6 | a0001c0001t0001g0266 a0001c0001t0009g0222 a0001c0003t0005g0008 others(3): Show |
8 | HG01891.hp1 HG02572.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.-124+2541_-124+254 others(8): Show |
CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr16 | 50745362 | ||||||
| chr16:50745428 | T | C | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(146): Show |
170 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.-124+2587T>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 2/18 | chr16 | 50745428 | |||||||
| chr16:50745527 | C | G | 1 | a0001c0001t0001g0104 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-124+2686C>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 2/18 | chr16 | 50745527 | |||||||
| chr16:50745984 | C | T | 54 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0216 others(51): Show |
57 | HG00639.hp2 HG01167.hp1 HG01884.hp2 others(54): Show |
intron_variant | MODIFIER | c.-124+3143C>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 2/18 | chr16 | 50745984 | |||||||
| chr16:50746092 | C | T | 2 | a0001c0001t0001g0202 a0001c0001t0001g0203 |
2 | HG00099.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.-124+3251C>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 2/18 | chr16 | 50746092 | |||||||
| chr16:50746600 | C | G | 6 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0264 others(3): Show |
6 | HG02486.hp2 HG02572.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-123-2976C>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 2/18 | chr16 | 50746600 | |||||||
| chr16:50746641 | C | T | 65 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(62): Show |
79 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.-123-2935C>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 2/18 | chr16 | 50746641 | |||||||
| chr16:50746909 | T | C | 4 | a0001c0001t0003g0231 a0001c0001t0003g0232 a0001c0001t0003g0249 others(1): Show |
4 | HG02145.hp1 HG02630.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-123-2667T>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 2/18 | chr16 | 50746909 | |||||||
| chr16:50747004 | G | T | 1 | a0001c0001t0026g0103 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-123-2572G>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 2/18 | chr16 | 50747004 | |||||||
| chr16:50747206 | G | A | 32 | a0001c0001t0001g0032 a0001c0001t0001g0041 a0001c0001t0001g0149 others(29): Show |
36 | HG00735.hp1 HG00738.hp2 HG01175.hp2 others(33): Show |
intron_variant | MODIFIER | c.-123-2370G>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 2/18 | chr16 | 50747206 | |||||||
| chr16:50747221 | T | C | 2 | a0001c0001t0001g0120 a0001c0001t0001g0150 |
2 | NA18945.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.-123-2355T>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 2/18 | chr16 | 50747221 | |||||||
| chr16:50747437 | C | G | 1 | a0001c0001t0004g0221 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-123-2139C>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 2/18 | chr16 | 50747437 | |||||||
| chr16:50747523 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-123-2053A>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 2/18 | chr16 | 50747523 | |||||||
| chr16:50747593 | G | C | 1 | a0001c0001t0001g0150 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-123-1983G>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 2/18 | chr16 | 50747593 | |||||||
| chr16:50747685 | T | C | 1 | a0001c0001t0001g0125 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.-123-1891T>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 2/18 | chr16 | 50747685 | |||||||
| chr16:50747687 | G | C | 1 | a0001c0001t0001g0125 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.-123-1889G>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 2/18 | chr16 | 50747687 | |||||||
| chr16:50747688 | A | C | 1 | a0001c0001t0001g0125 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.-123-1888A>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 2/18 | chr16 | 50747688 | |||||||
| chr16:50747689 | G | T | 1 | a0001c0001t0001g0125 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.-123-1887G>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 2/18 | chr16 | 50747689 | |||||||
| chr16:50747693 | T | G | 1 | a0001c0001t0001g0125 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.-123-1883T>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 2/18 | chr16 | 50747693 | |||||||
| chr16:50747891 | T | C | 71 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(68): Show |
86 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.-123-1685T>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 2/18 | chr16 | 50747891 | |||||||
| chr16:50747956 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-123-1620G>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 2/18 | chr16 | 50747956 | |||||||
| chr16:50748046 | A | C | 5 | a0001c0003t0005g0008 a0001c0003t0005g0241 a0001c0003t0005g0242 others(2): Show |
7 | HG01891.hp1 HG02717.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-123-1530A>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 2/18 | chr16 | 50748046 | |||||||
| chr16:50748509 | A | G | 1 | a0001c0001t0001g0262 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-123-1067A>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 2/18 | chr16 | 50748509 | |||||||
| chr16:50748877 | G | A | 1 | a0001c0001t0001g0045 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-123-699G>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 2/18 | chr16 | 50748877 | |||||||
| chr16:50748927 | C | A | 5 | a0001c0001t0001g0263 a0001c0001t0001g0264 a0001c0001t0001g0265 others(2): Show |
5 | HG02486.hp2 HG02572.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-123-649C>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 2/18 | chr16 | 50748927 | |||||||
| chr16:50749227 | A | T | 23 | a0001c0001t0001g0256 a0001c0001t0003g0024 a0001c0001t0003g0226 others(20): Show |
24 | HG00639.hp2 HG02109.hp2 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.-123-349A>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 2/18 | chr16 | 50749227 | |||||||
| chr16:50749259 | C | T | 2 | a0001c0001t0001g0181 a0001c0005t0001g0102 |
2 | HG00099.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.-123-317C>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 2/18 | chr16 | 50749259 | |||||||
| chr16:50749475 | AT | A | 4 | a0001c0001t0007g0128 a0001c0001t0007g0129 a0001c0001t0007g0130 others(1): Show |
4 | HG01884.hp2 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.-123-97delT | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr16 | 50749475 | ||||||
| chr16:50749517 | A | G | 13 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0216 others(10): Show |
13 | HG01167.hp1 HG02055.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.-123-59A>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 2/18 | chr16 | 50749517 | |||||||
| chr16:50750625 | G | A | 2 | a0001c0001t0001g0152 a0001c0001t0001g0153 |
2 | HG01106.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.504+423G>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 3/18 | chr16 | 50750625 | |||||||
| chr16:50750897 | T | C | 4 | a0001c0001t0007g0128 a0001c0001t0007g0129 a0001c0001t0007g0130 others(1): Show |
4 | HG01884.hp2 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.504+695T>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 3/18 | chr16 | 50750897 | |||||||
| chr16:50751124 | C | T | 1 | a0001c0001t0007g0132 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.505-480C>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 3/18 | chr16 | 50751124 | |||||||
| chr16:50751188 | A | G | 1 | a0001c0001t0001g0256 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.505-416A>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 3/18 | chr16 | 50751188 | |||||||
| chr16:50751309 | A | G | 1 | a0001c0001t0001g0101 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.505-295A>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 3/18 | chr16 | 50751309 | |||||||
| chr16:50751575 | A | C | 1 | a0001c0001t0013g0180 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.505-29A>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 3/18 | chr16 | 50751575 | |||||||
| chr16:50751979 | AACATATA others(7): Show |
A | 152 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(149): Show |
173 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.807+98_807+111delA others(13): Show |
CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr16 | 50751979 | ||||||
| chr16:50752075 | C | G | 7 | a0001c0001t0007g0128 a0001c0001t0007g0129 a0001c0001t0007g0130 others(4): Show |
7 | HG01884.hp2 HG02280.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.807+169C>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 4/18 | chr16 | 50752075 | |||||||
| chr16:50752220 | G | A | 1 | a0001c0001t0001g0046 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.807+314G>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 4/18 | chr16 | 50752220 | |||||||
| chr16:50752261 | GACAAA | G | 64 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(61): Show |
78 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.807+365_807+369del others(5): Show |
CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr16 | 50752261 | ||||||
| chr16:50752647 | C | G | 1 | a0001c0001t0001g0256 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.807+741C>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 4/18 | chr16 | 50752647 | |||||||
| chr16:50752966 | GA | G | 4 | a0001c0001t0007g0128 a0001c0001t0007g0129 a0001c0001t0007g0130 others(1): Show |
4 | HG01884.hp2 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.807+1062delA | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr16 | 50752966 | ||||||
| chr16:50753236 | G | A | 152 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(149): Show |
173 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.808-1083G>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 4/18 | chr16 | 50753236 | |||||||
| chr16:50753256 | A | G | 1 | a0001c0001t0003g0227 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.808-1063A>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 4/18 | chr16 | 50753256 | |||||||
| chr16:50753441 | G | A | 23 | a0001c0001t0001g0256 a0001c0001t0003g0024 a0001c0001t0003g0226 others(20): Show |
24 | HG00639.hp2 HG02109.hp2 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.808-878G>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 4/18 | chr16 | 50753441 | |||||||
| chr16:50753515 | C | T | 3 | a0001c0001t0003g0239 a0001c0001t0003g0240 a0001c0001t0003g0258 |
3 | HG02145.hp2 HG03540.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.808-804C>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 4/18 | chr16 | 50753515 | |||||||
| chr16:50753572 | A | G | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(150): Show |
174 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.808-747A>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 4/18 | chr16 | 50753572 | |||||||
| chr16:50753746 | A | G | 9 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0216 others(6): Show |
9 | HG01167.hp1 HG02055.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.808-573A>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 4/18 | chr16 | 50753746 | |||||||
| chr16:50754111 | T | C | 4 | a0001c0001t0008g0134 a0001c0001t0008g0135 a0001c0001t0008g0136 others(1): Show |
4 | HG02257.hp1 HG02622.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.808-208T>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 4/18 | chr16 | 50754111 | |||||||
| chr16:50754214 | C | T | 1 | a0001c0001t0001g0208 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.808-105C>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 4/18 | chr16 | 50754214 | |||||||
| chr16:50754234 | T | G | 1 | a0001c0001t0001g0047 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.808-85T>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 4/18 | chr16 | 50754234 | |||||||
| chr16:50754455 | G | A | 5 | a0001c0001t0003g0231 a0001c0001t0003g0232 a0001c0001t0003g0249 others(2): Show |
5 | HG02145.hp1 HG02615.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.913+31G>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50754455 | |||||||
| chr16:50754750 | A | G | 1 | a0001c0001t0001g0201 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.913+326A>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50754750 | |||||||
| chr16:50754773 | G | A | 1 | a0001c0001t0001g0048 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.913+349G>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50754773 | |||||||
| chr16:50754826 | G | A | 4 | a0001c0001t0001g0126 a0001c0001t0001g0216 a0001c0001t0001g0217 others(1): Show |
4 | HG02055.hp2 HG03225.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.913+402G>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50754826 | |||||||
| chr16:50754873 | A | ATG | 6 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0264 others(3): Show |
6 | HG02486.hp2 HG02572.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.913+451_913+452dup others(2): Show |
CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr16 | 50754873 | ||||||
| chr16:50754875 | G | GTA | 37 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0216 others(34): Show |
40 | HG00639.hp2 HG01167.hp1 HG01891.hp1 others(37): Show |
intron_variant | MODIFIER | c.913+462_913+463dup others(2): Show |
CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr16 | 50754875 | ||||||
| chr16:50754875 | G | GTATA | 4 | a0001c0001t0008g0134 a0001c0001t0008g0135 a0001c0001t0008g0136 others(1): Show |
4 | HG02257.hp1 HG02622.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.913+460_913+463dup others(4): Show |
CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr16 | 50754875 | ||||||
| chr16:50754875 | GTA | G | 6 | a0001c0001t0001g0047 a0001c0001t0001g0049 a0001c0001t0001g0050 others(3): Show |
6 | NA18941.hp1 NA18959.hp2 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.913+462_913+463del others(2): Show |
CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr16 | 50754875 | ||||||
| chr16:50754886 | TAC | T | 3 | a0001c0001t0009g0131 a0001c0001t0009g0133 a0001c0001t0009g0222 |
3 | HG02280.hp1 HG02486.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.913+463_913+464del others(2): Show |
CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50754886 | |||||||
| chr16:50754888 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.913+464C>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50754888 | |||||||
| chr16:50754909 | A | T | 5 | a0001c0003t0005g0008 a0001c0003t0005g0241 a0001c0003t0005g0242 others(2): Show |
7 | HG01891.hp1 HG02717.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.913+485A>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50754909 | |||||||
| chr16:50754927 | A | G | 1 | a0001c0001t0001g0100 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.913+503A>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50754927 | |||||||
| chr16:50754951 | A | G | 7 | a0001c0001t0007g0128 a0001c0001t0007g0129 a0001c0001t0007g0130 others(4): Show |
7 | HG01884.hp2 HG02280.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.913+527A>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50754951 | |||||||
| chr16:50754952 | T | C | 1 | a0001c0001t0001g0072 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.913+528T>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50754952 | |||||||
| chr16:50754975 | GTATACAT others(1): Show |
G | 4 | a0001c0001t0001g0263 a0001c0001t0001g0264 a0001c0001t0001g0265 others(1): Show |
4 | HG02572.hp1 HG02615.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.913+564_913+571del others(8): Show |
CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr16 | 50754975 | ||||||
| chr16:50754975 | GTATACAT others(37): Show |
G | 3 | a0001c0001t0001g0248 a0001c0001t0001g0262 a0001c0006t0001g0267 |
3 | HG02056.hp2 HG02486.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.913+564_913+607del others(44): Show |
CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr16 | 50754975 | ||||||
| chr16:50754975 | GTATACAT others(73): Show |
G | 1 | a0001c0001t0001g0055 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.913+562_913+641del others(80): Show |
CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr16 | 50754975 | ||||||
| chr16:50754980 | C | CATATATA others(11): Show |
4 | a0001c0001t0001g0046 a0001c0001t0001g0081 a0001c0001t0001g0181 others(1): Show |
4 | HG00099.hp1 HG01070.hp2 NA18943.hp1 others(1): Show |
intron_variant | MODIFIER | c.913+624_913+641dup others(18): Show |
CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr16 | 50754980 | ||||||
| chr16:50754980 | CATATATA others(11): Show |
C | 5 | a0001c0001t0001g0072 a0001c0001t0001g0101 a0001c0001t0001g0105 others(2): Show |
5 | HG02040.hp1 HG04204.hp1 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.913+624_913+641del others(18): Show |
CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr16 | 50754980 | ||||||
| chr16:50754980 | CATATATA others(29): Show |
C | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(160): Show |
182 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.913+606_913+641del others(36): Show |
CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr16 | 50754980 | ||||||
| chr16:50754980 | CATATATA others(47): Show |
C | 4 | a0001c0001t0001g0091 a0001c0001t0001g0094 a0001c0001t0003g0238 others(1): Show |
4 | HG00544.hp2 HG02647.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.913+588_913+641del others(54): Show |
CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr16 | 50754980 | ||||||
| chr16:50754986 | T | C | 3 | a0001c0001t0001g0049 a0001c0001t0001g0053 a0001c0001t0001g0054 |
3 | HG01069.hp2 NA18951.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.913+562T>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50754986 | |||||||
| chr16:50754988 | CATATATA others(57): Show |
C | 30 | a0001c0001t0001g0032 a0001c0002t0002g0009 a0001c0002t0002g0010 others(27): Show |
34 | HG00735.hp1 HG00738.hp2 HG01175.hp2 others(31): Show |
intron_variant | MODIFIER | c.913+572_913+635del others(64): Show |
CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr16 | 50754988 | ||||||
| chr16:50754990 | T | C | 3 | a0001c0001t0001g0049 a0001c0001t0001g0053 a0001c0001t0001g0054 |
3 | HG01069.hp2 NA18951.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.913+566T>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50754990 | |||||||
| chr16:50755006 | CATATATA others(31): Show |
C | 5 | a0001c0003t0005g0008 a0001c0003t0005g0241 a0001c0003t0005g0242 others(2): Show |
7 | HG01891.hp1 HG02717.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.913+589_913+626del others(38): Show |
CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr16 | 50755006 | ||||||
| chr16:50755030 | T | G | 10 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0216 others(7): Show |
10 | HG01167.hp1 HG02055.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.913+606T>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50755030 | |||||||
| chr16:50755033 | G | A | 9 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0216 others(6): Show |
9 | HG01167.hp1 HG02055.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.913+609G>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50755033 | |||||||
| chr16:50755035 | A | G | 9 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0216 others(6): Show |
9 | HG01167.hp1 HG02055.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.913+611A>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50755035 | |||||||
| chr16:50755037 | A | G | 1 | a0001c0001t0025g0250 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.913+613A>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50755037 | |||||||
| chr16:50755040 | T | C | 10 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0216 others(7): Show |
10 | HG01167.hp1 HG02055.hp2 HG02897.hp2 others(7): Show |
intron_variant | MODIFIER | c.913+616T>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50755040 | |||||||
| chr16:50755042 | C | T | 9 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0216 others(6): Show |
9 | HG01167.hp1 HG02055.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.913+618C>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50755042 | |||||||
| chr16:50755046 | T | C | 9 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0216 others(6): Show |
9 | HG01167.hp1 HG02055.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.913+622T>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50755046 | |||||||
| chr16:50755048 | T | C | 1 | a0001c0001t0025g0250 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.913+624T>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50755048 | |||||||
| chr16:50755050 | T | C | 10 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0216 others(7): Show |
10 | HG01167.hp1 HG02055.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.913+626T>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50755050 | |||||||
| chr16:50755051 | G | A | 10 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0216 others(7): Show |
10 | HG01167.hp1 HG02055.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.913+627G>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50755051 | |||||||
| chr16:50755052 | T | C | 1 | a0001c0001t0025g0250 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.913+628T>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50755052 | |||||||
| chr16:50755057 | A | G | 7 | a0001c0001t0007g0128 a0001c0001t0007g0129 a0001c0001t0007g0130 others(4): Show |
7 | HG01884.hp2 HG02280.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.913+633A>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50755057 | |||||||
| chr16:50755058 | T | C | 9 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0216 others(6): Show |
9 | HG01167.hp1 HG02055.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.913+634T>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50755058 | |||||||
| chr16:50755060 | CATATAGA others(5): Show |
C | 1 | a0001c0001t0025g0250 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.913+640_913+651del others(12): Show |
CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr16 | 50755060 | ||||||
| chr16:50755062 | T | C | 1 | a0001c0001t0001g0118 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.913+638T>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50755062 | |||||||
| chr16:50755064 | T | C | 1 | a0001c0001t0001g0118 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.913+640T>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50755064 | |||||||
| chr16:50755066 | G | C | 9 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0216 others(6): Show |
9 | HG01167.hp1 HG02055.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.913+642G>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50755066 | |||||||
| chr16:50755066 | G | T | 1 | a0001c0001t0001g0118 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.913+642G>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50755066 | |||||||
| chr16:50755068 | T | C | 1 | a0001c0001t0001g0262 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.913+644T>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50755068 | |||||||
| chr16:50755071 | G | A | 1 | a0001c0001t0001g0118 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.913+647G>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50755071 | |||||||
| chr16:50755072 | T | C | 1 | a0001c0001t0001g0118 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.913+648T>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50755072 | |||||||
| chr16:50755073 | A | G | 9 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0216 others(6): Show |
9 | HG01167.hp1 HG02055.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.913+649A>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50755073 | |||||||
| chr16:50755076 | C | T | 9 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0216 others(6): Show |
9 | HG01167.hp1 HG02055.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.913+652C>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50755076 | |||||||
| chr16:50755080 | T | C | 7 | a0001c0001t0007g0128 a0001c0001t0007g0129 a0001c0001t0007g0130 others(4): Show |
7 | HG01884.hp2 HG02280.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.913+656T>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50755080 | |||||||
| chr16:50755082 | C | T | 2 | a0001c0001t0001g0118 a0001c0001t0025g0250 |
2 | HG02615.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.913+658C>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50755082 | |||||||
| chr16:50755092 | T | C | 9 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0216 others(6): Show |
9 | HG01167.hp1 HG02055.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.913+668T>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50755092 | |||||||
| chr16:50755095 | ATACATAT others(71): Show |
A | 9 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0216 others(6): Show |
9 | HG01167.hp1 HG02055.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.913+673_913+750del others(78): Show |
CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr16 | 50755095 | ||||||
| chr16:50755110 | C | T | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(135): Show |
159 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.913+686C>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50755110 | |||||||
| chr16:50755114 | T | C | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(135): Show |
159 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.913+690T>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50755114 | |||||||
| chr16:50755116 | C | T | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(135): Show |
159 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.913+692C>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50755116 | |||||||
| chr16:50755119 | ATGTGTAT others(25): Show |
A | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(135): Show |
159 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.913+697_913+728del others(32): Show |
CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr16 | 50755119 | ||||||
| chr16:50755125 | A | G | 1 | a0001c0001t0001g0170 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.913+701A>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50755125 | |||||||
| chr16:50755125 | ATATATAC others(47): Show |
A | 1 | a0001c0001t0001g0118 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.913+729_913+782del others(54): Show |
CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr16 | 50755125 | ||||||
| chr16:50755142 | CATATGTG others(49): Show |
C | 1 | a0001c0001t0025g0250 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.913+721_913+776del others(56): Show |
CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr16 | 50755142 | ||||||
| chr16:50755145 | ATGTGTGT others(21): Show |
A | 1 | a0001c0001t0006g0179 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.913+783_913+810del others(28): Show |
CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr16 | 50755145 | ||||||
| chr16:50755163 | G | A | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(135): Show |
159 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.913+739G>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50755163 | |||||||
| chr16:50755165 | G | A | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(135): Show |
159 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.913+741G>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50755165 | |||||||
| chr16:50755168 | CAT | C | 6 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0264 others(3): Show |
6 | HG02486.hp2 HG02572.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.913+747_913+748del others(2): Show |
CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr16 | 50755168 | ||||||
| chr16:50755170 | T | C | 131 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(128): Show |
152 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.913+746T>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50755170 | |||||||
| chr16:50755171 | ATG | A | 132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(129): Show |
153 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.913+755_913+756del others(2): Show |
CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr16 | 50755171 | ||||||
| chr16:50755172 | T | C | 6 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0264 others(3): Show |
6 | HG02486.hp2 HG02572.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.913+748T>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50755172 | |||||||
| chr16:50755174 | T | C | 1 | a0001c0001t0011g0106 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.913+750T>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50755174 | |||||||
| chr16:50755179 | G | A | 147 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(144): Show |
168 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.913+755G>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50755179 | |||||||
| chr16:50755184 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.913+760T>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50755184 | |||||||
| chr16:50755217 | A | G | 1 | a0001c0001t0001g0099 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.913+793A>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50755217 | |||||||
| chr16:50755269 | C | T | 6 | a0001c0001t0009g0222 a0001c0003t0005g0008 a0001c0003t0005g0241 others(3): Show |
8 | HG01891.hp1 HG02717.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.913+845C>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50755269 | |||||||
| chr16:50755329 | T | G | 4 | a0001c0001t0001g0015 a0001c0001t0001g0184 a0001c0001t0001g0209 others(1): Show |
5 | HG01884.hp1 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.913+905T>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50755329 | |||||||
| chr16:50755339 | G | C | 67 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(64): Show |
81 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.913+915G>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50755339 | |||||||
| chr16:50755364 | A | G | 13 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0216 others(10): Show |
13 | HG01167.hp1 HG02055.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.913+940A>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50755364 | |||||||
| chr16:50755482 | A | G | 1 | a0001c0001t0001g0150 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.913+1058A>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50755482 | |||||||
| chr16:50755564 | G | A | 1 | a0001c0001t0001g0056 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.913+1140G>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50755564 | |||||||
| chr16:50755647 | C | G | 1 | a0001c0001t0001g0117 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.913+1223C>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50755647 | |||||||
| chr16:50755757 | A | C | 5 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0264 others(2): Show |
5 | HG02572.hp1 HG02615.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.913+1333A>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50755757 | |||||||
| chr16:50755757 | A | T | 1 | a0001c0006t0001g0267 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.913+1333A>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50755757 | |||||||
| chr16:50755788 | T | A | 13 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0264 others(10): Show |
13 | HG01884.hp2 HG02280.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.913+1364T>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50755788 | |||||||
| chr16:50755908 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.913+1484G>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50755908 | |||||||
| chr16:50756155 | A | G | 2 | a0001c0002t0002g0037 a0001c0002t0002g0147 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.913+1731A>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50756155 | |||||||
| chr16:50756247 | A | C | 2 | a0001c0001t0001g0178 a0001c0001t0001g0207 |
2 | HG01255.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.913+1823A>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50756247 | |||||||
| chr16:50756271 | C | T | 5 | a0001c0003t0005g0008 a0001c0003t0005g0241 a0001c0003t0005g0242 others(2): Show |
7 | HG01891.hp1 HG02717.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.913+1847C>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50756271 | |||||||
| chr16:50756493 | A | T | 1 | a0001c0001t0021g0206 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.913+2069A>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50756493 | |||||||
| chr16:50756788 | A | G | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(148): Show |
172 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.913+2364A>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50756788 | |||||||
| chr16:50756830 | G | A | 4 | a0001c0001t0008g0134 a0001c0001t0008g0135 a0001c0001t0008g0136 others(1): Show |
4 | HG02257.hp1 HG02622.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.913+2406G>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50756830 | |||||||
| chr16:50756980 | A | G | 44 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0019 others(41): Show |
47 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.913+2556A>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50756980 | |||||||
| chr16:50757094 | A | C | 2 | a0001c0001t0001g0202 a0001c0001t0001g0203 |
2 | HG00099.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.913+2670A>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50757094 | |||||||
| chr16:50757103 | T | C | 1 | a0001c0001t0001g0184 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.913+2679T>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50757103 | |||||||
| chr16:50757339 | T | G | 52 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(49): Show |
65 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.913+2915T>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50757339 | |||||||
| chr16:50757543 | A | AT | 52 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(49): Show |
65 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.913+3130dupT | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr16 | 50757543 | ||||||
| chr16:50757556 | A | T | 5 | a0001c0001t0003g0231 a0001c0001t0003g0232 a0001c0001t0003g0249 others(2): Show |
5 | HG02145.hp1 HG02615.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.913+3132A>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50757556 | |||||||
| chr16:50757787 | C | A | 1 | a0001c0001t0001g0057 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.913+3363C>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50757787 | |||||||
| chr16:50757827 | C | T | 1 | a0001c0001t0001g0098 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.913+3403C>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50757827 | |||||||
| chr16:50758357 | C | T | 64 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(61): Show |
78 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.913+3933C>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50758357 | |||||||
| chr16:50758569 | C | G | 13 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0216 others(10): Show |
13 | HG01167.hp1 HG02055.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.913+4145C>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50758569 | |||||||
| chr16:50758735 | C | T | 8 | a0001c0001t0001g0262 a0001c0001t0007g0128 a0001c0001t0007g0129 others(5): Show |
8 | HG01884.hp2 HG02280.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.913+4311C>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50758735 | |||||||
| chr16:50758791 | G | A | 1 | a0001c0001t0017g0083 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.913+4367G>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50758791 | |||||||
| chr16:50758793 | C | G | 84 | a0001c0001t0001g0032 a0001c0001t0001g0125 a0001c0001t0001g0126 others(81): Show |
91 | HG00639.hp2 HG00735.hp1 HG00738.hp2 others(88): Show |
intron_variant | MODIFIER | c.913+4369C>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50758793 | |||||||
| chr16:50759065 | C | A | 5 | a0001c0001t0001g0263 a0001c0001t0001g0264 a0001c0001t0001g0265 others(2): Show |
5 | HG02486.hp2 HG02572.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.913+4641C>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50759065 | |||||||
| chr16:50759481 | C | A | 18 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0216 others(15): Show |
20 | HG01167.hp1 HG01891.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.913+5057C>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50759481 | |||||||
| chr16:50759700 | C | T | 4 | a0001c0001t0008g0134 a0001c0001t0008g0135 a0001c0001t0008g0136 others(1): Show |
4 | HG02257.hp1 HG02622.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.913+5276C>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50759700 | |||||||
| chr16:50759720 | C | T | 30 | a0001c0001t0001g0032 a0001c0002t0002g0009 a0001c0002t0002g0010 others(27): Show |
34 | HG00735.hp1 HG00738.hp2 HG01175.hp2 others(31): Show |
intron_variant | MODIFIER | c.913+5296C>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50759720 | |||||||
| chr16:50759863 | G | A | 1 | a0001c0001t0001g0224 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.913+5439G>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50759863 | |||||||
| chr16:50760110 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.913+5686G>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50760110 | |||||||
| chr16:50760374 | C | A | 7 | a0001c0001t0007g0128 a0001c0001t0007g0129 a0001c0001t0007g0130 others(4): Show |
7 | HG01884.hp2 HG02280.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.913+5950C>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50760374 | |||||||
| chr16:50760389 | T | C | 2 | a0001c0001t0001g0058 a0001c0001t0001g0155 |
2 | HG03710.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.913+5965T>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50760389 | |||||||
| chr16:50760796 | GATAT | G | 84 | a0001c0001t0001g0032 a0001c0001t0001g0125 a0001c0001t0001g0126 others(81): Show |
91 | HG00639.hp2 HG00735.hp1 HG00738.hp2 others(88): Show |
intron_variant | MODIFIER | c.913+6379_913+6382d others(6): Show |
CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr16 | 50760796 | ||||||
| chr16:50760997 | G | A | 1 | a0001c0001t0001g0219 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.913+6573G>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50760997 | |||||||
| chr16:50761244 | T | A | 23 | a0001c0001t0001g0256 a0001c0001t0003g0024 a0001c0001t0003g0226 others(20): Show |
24 | HG00639.hp2 HG02109.hp2 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.913+6820T>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50761244 | |||||||
| chr16:50761245 | A | T | 5 | a0001c0003t0005g0008 a0001c0003t0005g0241 a0001c0003t0005g0242 others(2): Show |
7 | HG01891.hp1 HG02717.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.913+6821A>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50761245 | |||||||
| chr16:50761388 | T | G | 4 | a0001c0001t0007g0128 a0001c0001t0007g0129 a0001c0001t0007g0130 others(1): Show |
4 | HG01884.hp2 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.913+6964T>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50761388 | |||||||
| chr16:50761389 | C | T | 1 | a0001c0001t0001g0041 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.913+6965C>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50761389 | |||||||
| chr16:50761610 | T | A | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(148): Show |
172 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.913+7186T>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50761610 | |||||||
| chr16:50761650 | A | T | 54 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0216 others(51): Show |
57 | HG00639.hp2 HG01167.hp1 HG01884.hp2 others(54): Show |
intron_variant | MODIFIER | c.913+7226A>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50761650 | |||||||
| chr16:50761705 | G | A | 3 | a0001c0001t0001g0015 a0001c0001t0001g0209 a0001c0001t0001g0210 |
4 | HG01884.hp1 HG01891.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.913+7281G>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50761705 | |||||||
| chr16:50761746 | A | ATATCTAT others(1): Show |
7 | a0001c0001t0001g0021 a0001c0001t0001g0062 a0001c0001t0001g0100 others(4): Show |
8 | HG01070.hp1 HG01167.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.913+7346_913+7353d others(10): Show |
CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr16 | 50761746 | ||||||
| chr16:50761746 | A | ATATCTAT others(5): Show |
44 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0032 others(41): Show |
49 | HG00544.hp1 HG00735.hp1 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.913+7342_913+7353d others(14): Show |
CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr16 | 50761746 | ||||||
| chr16:50761746 | A | ATATCTAT others(9): Show |
100 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(97): Show |
110 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.913+7338_913+7353d others(18): Show |
CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr16 | 50761746 | ||||||
| chr16:50761746 | A | ATATCTAT others(13): Show |
79 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(76): Show |
87 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.913+7334_913+7353d others(22): Show |
CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr16 | 50761746 | ||||||
| chr16:50761746 | A | ATATCTAT others(17): Show |
35 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0040 others(32): Show |
38 | HG00423.hp1 HG01106.hp2 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.913+7330_913+7353d others(26): Show |
CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr16 | 50761746 | ||||||
| chr16:50761746 | A | ATATCTAT others(21): Show |
1 | a0001c0001t0001g0218 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.913+7326_913+7353d others(30): Show |
CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr16 | 50761746 | ||||||
| chr16:50761751 | T | TATCTATC others(16): Show |
1 | a0001c0001t0001g0085 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.913+7328_913+7350d others(25): Show |
CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr16 | 50761751 | ||||||
| chr16:50761848 | C | A | 2 | a0001c0001t0001g0120 a0001c0001t0001g0150 |
2 | NA18945.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.913+7424C>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50761848 | |||||||
| chr16:50761887 | A | G | 1 | a0001c0001t0001g0077 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.913+7463A>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50761887 | |||||||
| chr16:50761952 | G | C | 18 | a0001c0001t0001g0256 a0001c0001t0003g0024 a0001c0001t0003g0226 others(15): Show |
19 | HG00639.hp2 HG02109.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.913+7528G>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50761952 | |||||||
| chr16:50761983 | T | C | 84 | a0001c0001t0001g0032 a0001c0001t0001g0125 a0001c0001t0001g0126 others(81): Show |
91 | HG00639.hp2 HG00735.hp1 HG00738.hp2 others(88): Show |
intron_variant | MODIFIER | c.913+7559T>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50761983 | |||||||
| chr16:50761988 | C | T | 3 | a0001c0001t0001g0090 a0001c0001t0001g0219 a0001c0001t0004g0221 |
3 | HG01167.hp1 HG03516.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.913+7564C>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50761988 | |||||||
| chr16:50762165 | C | T | 1 | a0001c0001t0001g0041 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.913+7741C>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50762165 | |||||||
| chr16:50762166 | G | A | 7 | a0001c0001t0007g0128 a0001c0001t0007g0129 a0001c0001t0007g0130 others(4): Show |
7 | HG01884.hp2 HG02280.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.913+7742G>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50762166 | |||||||
| chr16:50762212 | G | A | 6 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0264 others(3): Show |
6 | HG02486.hp2 HG02572.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.913+7788G>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50762212 | |||||||
| chr16:50762471 | C | T | 54 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0216 others(51): Show |
57 | HG00639.hp2 HG01167.hp1 HG01884.hp2 others(54): Show |
intron_variant | MODIFIER | c.913+8047C>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50762471 | |||||||
| chr16:50762538 | T | A | 5 | a0001c0003t0005g0008 a0001c0003t0005g0241 a0001c0003t0005g0242 others(2): Show |
7 | HG01891.hp1 HG02717.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.913+8114T>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50762538 | |||||||
| chr16:50762971 | A | G | 1 | a0001c0003t0005g0243 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.913+8547A>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50762971 | |||||||
| chr16:50763274 | A | G | 1 | a0001c0001t0001g0062 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.913+8850A>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50763274 | |||||||
| chr16:50763283 | G | C | 7 | a0001c0001t0007g0128 a0001c0001t0007g0129 a0001c0001t0007g0130 others(4): Show |
7 | HG01884.hp2 HG02280.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.913+8859G>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50763283 | |||||||
| chr16:50763324 | A | G | 5 | a0001c0001t0001g0089 a0001c0001t0001g0094 a0001c0001t0001g0099 others(2): Show |
5 | HG00280.hp1 HG00544.hp2 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.913+8900A>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50763324 | |||||||
| chr16:50763403 | A | G | 84 | a0001c0001t0001g0032 a0001c0001t0001g0125 a0001c0001t0001g0126 others(81): Show |
91 | HG00639.hp2 HG00735.hp1 HG00738.hp2 others(88): Show |
intron_variant | MODIFIER | c.913+8979A>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50763403 | |||||||
| chr16:50763955 | G | A | 30 | a0001c0001t0001g0032 a0001c0002t0002g0009 a0001c0002t0002g0010 others(27): Show |
34 | HG00735.hp1 HG00738.hp2 HG01175.hp2 others(31): Show |
intron_variant | MODIFIER | c.913+9531G>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50763955 | |||||||
| chr16:50763972 | A | G | 1 | a0001c0001t0001g0111 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.913+9548A>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50763972 | |||||||
| chr16:50763986 | A | G | 13 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0216 others(10): Show |
13 | HG01167.hp1 HG02055.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.913+9562A>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50763986 | |||||||
| chr16:50764027 | A | T | 1 | a0001c0001t0013g0180 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.913+9603A>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50764027 | |||||||
| chr16:50764045 | A | G | 5 | a0001c0003t0005g0008 a0001c0003t0005g0241 a0001c0003t0005g0242 others(2): Show |
7 | HG01891.hp1 HG02717.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.913+9621A>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50764045 | |||||||
| chr16:50764225 | A | G | 1 | a0001c0002t0002g0229 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.913+9801A>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50764225 | |||||||
| chr16:50764296 | A | G | 84 | a0001c0001t0001g0032 a0001c0001t0001g0125 a0001c0001t0001g0126 others(81): Show |
91 | HG00639.hp2 HG00735.hp1 HG00738.hp2 others(88): Show |
intron_variant | MODIFIER | c.913+9872A>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50764296 | |||||||
| chr16:50764544 | A | G | 18 | a0001c0001t0001g0013 a0001c0001t0001g0084 a0001c0001t0001g0087 others(15): Show |
19 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(16): Show |
intron_variant | MODIFIER | c.913+10120A>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50764544 | |||||||
| chr16:50765018 | A | G | 67 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(64): Show |
81 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.914-10148A>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50765018 | |||||||
| chr16:50765052 | T | C | 1 | a0001c0001t0001g0161 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.914-10114T>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50765052 | |||||||
| chr16:50765512 | A | G | 23 | a0001c0001t0001g0256 a0001c0001t0003g0024 a0001c0001t0003g0226 others(20): Show |
24 | HG00639.hp2 HG02109.hp2 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.914-9654A>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50765512 | |||||||
| chr16:50765613 | C | T | 1 | a0001c0001t0001g0262 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.914-9553C>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50765613 | |||||||
| chr16:50765801 | C | T | 5 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0068 others(2): Show |
5 | HG00741.hp1 HG01099.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.914-9365C>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50765801 | |||||||
| chr16:50765851 | G | GT | 224 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(221): Show |
249 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.914-9315_914-9314i others(3): Show |
CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50765851 | |||||||
| chr16:50765958 | G | T | 31 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0216 others(28): Show |
33 | HG01167.hp1 HG01884.hp2 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.914-9208G>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50765958 | |||||||
| chr16:50766182 | C | T | 23 | a0001c0001t0001g0256 a0001c0001t0003g0024 a0001c0001t0003g0226 others(20): Show |
24 | HG00639.hp2 HG02109.hp2 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.914-8984C>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50766182 | |||||||
| chr16:50766353 | T | C | 30 | a0001c0001t0001g0032 a0001c0002t0002g0009 a0001c0002t0002g0010 others(27): Show |
34 | HG00735.hp1 HG00738.hp2 HG01175.hp2 others(31): Show |
intron_variant | MODIFIER | c.914-8813T>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50766353 | |||||||
| chr16:50766517 | A | C | 7 | a0001c0001t0007g0128 a0001c0001t0007g0129 a0001c0001t0007g0130 others(4): Show |
7 | HG01884.hp2 HG02280.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.914-8649A>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50766517 | |||||||
| chr16:50766556 | G | C | 5 | a0001c0003t0005g0008 a0001c0003t0005g0241 a0001c0003t0005g0242 others(2): Show |
7 | HG01891.hp1 HG02717.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.914-8610G>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50766556 | |||||||
| chr16:50766639 | A | G | 1 | a0001c0001t0001g0032 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.914-8527A>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50766639 | |||||||
| chr16:50766653 | G | C | 1 | a0001c0001t0001g0159 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.914-8513G>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50766653 | |||||||
| chr16:50766736 | T | G | 52 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(49): Show |
65 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.914-8430T>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50766736 | |||||||
| chr16:50766782 | G | T | 31 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0216 others(28): Show |
33 | HG01167.hp1 HG01884.hp2 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.914-8384G>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50766782 | |||||||
| chr16:50766784 | T | C | 2 | a0001c0001t0007g0129 a0001c0001t0007g0130 |
2 | HG01884.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.914-8382T>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50766784 | |||||||
| chr16:50767127 | A | G | 3 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0138 |
3 | HG02451.hp1 HG02809.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.914-8039A>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50767127 | |||||||
| chr16:50767466 | A | AT | 85 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(82): Show |
101 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.914-7686dupT | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr16 | 50767466 | ||||||
| chr16:50767466 | A | ATT | 10 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0216 others(7): Show |
10 | HG01109.hp2 HG02055.hp2 HG02897.hp2 others(7): Show |
intron_variant | MODIFIER | c.914-7687_914-7686d others(4): Show |
CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr16 | 50767466 | ||||||
| chr16:50767530 | G | A | 5 | a0001c0001t0001g0263 a0001c0001t0001g0264 a0001c0001t0001g0265 others(2): Show |
5 | HG02486.hp2 HG02572.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.914-7636G>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50767530 | |||||||
| chr16:50767634 | G | T | 1 | a0001c0001t0025g0250 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.914-7532G>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50767634 | |||||||
| chr16:50767731 | G | C | 1 | a0001c0001t0001g0058 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.914-7435G>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50767731 | |||||||
| chr16:50767791 | T | G | 31 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0216 others(28): Show |
33 | HG01167.hp1 HG01884.hp2 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.914-7375T>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50767791 | |||||||
| chr16:50767867 | C | A | 84 | a0001c0001t0001g0032 a0001c0001t0001g0125 a0001c0001t0001g0126 others(81): Show |
91 | HG00639.hp2 HG00735.hp1 HG00738.hp2 others(88): Show |
intron_variant | MODIFIER | c.914-7299C>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50767867 | |||||||
| chr16:50767986 | G | A | 1 | a0002c0004t0001g0121 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.914-7180G>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50767986 | |||||||
| chr16:50768002 | T | A | 84 | a0001c0001t0001g0032 a0001c0001t0001g0125 a0001c0001t0001g0126 others(81): Show |
91 | HG00639.hp2 HG00735.hp1 HG00738.hp2 others(88): Show |
intron_variant | MODIFIER | c.914-7164T>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50768002 | |||||||
| chr16:50768330 | T | G | 1 | a0001c0001t0001g0181 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.914-6836T>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50768330 | |||||||
| chr16:50768356 | A | G | 3 | a0001c0002t0002g0034 a0001c0002t0002g0035 a0001c0002t0010g0146 |
3 | HG02055.hp1 HG02922.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.914-6810A>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50768356 | |||||||
| chr16:50768518 | T | A | 1 | a0001c0001t0001g0262 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.914-6648T>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50768518 | |||||||
| chr16:50768553 | G | A | 9 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0216 others(6): Show |
9 | HG01167.hp1 HG02055.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.914-6613G>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50768553 | |||||||
| chr16:50768743 | G | T | 2 | a0001c0001t0001g0263 a0001c0001t0001g0265 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.914-6423G>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50768743 | |||||||
| chr16:50768784 | GT | G | 6 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0264 others(3): Show |
6 | HG02486.hp2 HG02572.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.914-6375delT | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr16 | 50768784 | ||||||
| chr16:50768804 | G | A | 84 | a0001c0001t0001g0032 a0001c0001t0001g0125 a0001c0001t0001g0126 others(81): Show |
91 | HG00639.hp2 HG00735.hp1 HG00738.hp2 others(88): Show |
intron_variant | MODIFIER | c.914-6362G>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50768804 | |||||||
| chr16:50769052 | T | C | 1 | a0001c0001t0001g0211 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.914-6114T>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50769052 | |||||||
| chr16:50769346 | C | T | 31 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0216 others(28): Show |
33 | HG01167.hp1 HG01884.hp2 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.914-5820C>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50769346 | |||||||
| chr16:50769466 | T | C | 1 | a0001c0001t0001g0225 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.914-5700T>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50769466 | |||||||
| chr16:50769547 | A | G | 3 | a0001c0001t0009g0131 a0001c0001t0009g0133 a0001c0001t0009g0222 |
3 | HG02280.hp1 HG02486.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.914-5619A>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50769547 | |||||||
| chr16:50769650 | A | T | 1 | a0001c0006t0001g0267 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.914-5516A>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50769650 | |||||||
| chr16:50769661 | C | T | 2 | a0001c0001t0001g0183 a0001c0001t0001g0185 |
2 | HG02886.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.914-5505C>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50769661 | |||||||
| chr16:50769845 | G | C | 84 | a0001c0001t0001g0032 a0001c0001t0001g0125 a0001c0001t0001g0126 others(81): Show |
91 | HG00639.hp2 HG00735.hp1 HG00738.hp2 others(88): Show |
intron_variant | MODIFIER | c.914-5321G>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50769845 | |||||||
| chr16:50769970 | A | G | 5 | a0001c0001t0001g0263 a0001c0001t0001g0264 a0001c0001t0001g0265 others(2): Show |
5 | HG02486.hp2 HG02572.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.914-5196A>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50769970 | |||||||
| chr16:50770376 | A | G | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(148): Show |
172 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.914-4790A>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50770376 | |||||||
| chr16:50770468 | G | A | 1 | a0001c0001t0025g0250 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.914-4698G>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50770468 | |||||||
| chr16:50770520 | G | A | 70 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(67): Show |
84 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.914-4646G>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50770520 | |||||||
| chr16:50770599 | C | T | 31 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0216 others(28): Show |
33 | HG01167.hp1 HG01884.hp2 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.914-4567C>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50770599 | |||||||
| chr16:50770623 | G | C | 1 | a0001c0001t0001g0162 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.914-4543G>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50770623 | |||||||
| chr16:50770999 | G | A | 4 | a0001c0001t0008g0134 a0001c0001t0008g0135 a0001c0001t0008g0136 others(1): Show |
4 | HG02257.hp1 HG02622.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.914-4167G>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50770999 | |||||||
| chr16:50771022 | C | T | 30 | a0001c0001t0001g0032 a0001c0002t0002g0009 a0001c0002t0002g0010 others(27): Show |
34 | HG00735.hp1 HG00738.hp2 HG01175.hp2 others(31): Show |
intron_variant | MODIFIER | c.914-4144C>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50771022 | |||||||
| chr16:50771044 | C | T | 1 | a0001c0001t0001g0089 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.914-4122C>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50771044 | |||||||
| chr16:50771058 | TCTC | T | 3 | a0001c0002t0002g0017 a0001c0002t0002g0030 a0001c0002t0002g0228 |
4 | HG00735.hp1 HG00738.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.914-4105_914-4103d others(5): Show |
CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr16 | 50771058 | ||||||
| chr16:50771216 | C | G | 9 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0216 others(6): Show |
9 | HG01167.hp1 HG02055.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.914-3950C>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50771216 | |||||||
| chr16:50771343 | T | A | 1 | a0001c0001t0004g0107 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.914-3823T>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50771343 | |||||||
| chr16:50771436 | T | A | 1 | a0001c0001t0003g0238 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.914-3730T>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50771436 | |||||||
| chr16:50771531 | A | G | 23 | a0001c0001t0001g0256 a0001c0001t0003g0024 a0001c0001t0003g0226 others(20): Show |
24 | HG00639.hp2 HG02109.hp2 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.914-3635A>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50771531 | |||||||
| chr16:50771642 | T | A | 84 | a0001c0001t0001g0032 a0001c0001t0001g0125 a0001c0001t0001g0126 others(81): Show |
91 | HG00639.hp2 HG00735.hp1 HG00738.hp2 others(88): Show |
intron_variant | MODIFIER | c.914-3524T>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50771642 | |||||||
| chr16:50771765 | T | A | 8 | a0001c0001t0007g0128 a0001c0001t0007g0129 a0001c0001t0007g0130 others(5): Show |
8 | HG01884.hp2 HG02280.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.914-3401T>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50771765 | |||||||
| chr16:50771775 | A | G | 1 | a0001c0001t0025g0250 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.914-3391A>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50771775 | |||||||
| chr16:50771890 | T | C | 1 | a0001c0001t0013g0180 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.914-3276T>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50771890 | |||||||
| chr16:50771977 | A | G | 30 | a0001c0001t0001g0032 a0001c0002t0002g0009 a0001c0002t0002g0010 others(27): Show |
34 | HG00735.hp1 HG00738.hp2 HG01175.hp2 others(31): Show |
intron_variant | MODIFIER | c.914-3189A>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50771977 | |||||||
| chr16:50772223 | T | C | 2 | a0001c0001t0001g0089 a0001c0001t0001g0177 |
2 | NA18957.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.914-2943T>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50772223 | |||||||
| chr16:50772283 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.914-2883G>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50772283 | |||||||
| chr16:50772292 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.914-2874G>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50772292 | |||||||
| chr16:50772726 | C | CTAGGCCA others(7): Show |
84 | a0001c0001t0001g0032 a0001c0001t0001g0125 a0001c0001t0001g0126 others(81): Show |
91 | HG00639.hp2 HG00735.hp1 HG00738.hp2 others(88): Show |
intron_variant | MODIFIER | c.914-2438_914-2437i others(16): Show |
CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr16 | 50772726 | ||||||
| chr16:50772920 | C | A | 1 | a0001c0001t0001g0074 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.914-2246C>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50772920 | |||||||
| chr16:50772955 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.914-2211A>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50772955 | |||||||
| chr16:50773096 | T | C | 31 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0216 others(28): Show |
33 | HG01167.hp1 HG01884.hp2 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.914-2070T>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50773096 | |||||||
| chr16:50773160 | T | G | 2 | a0001c0001t0001g0183 a0001c0001t0001g0185 |
2 | HG02886.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.914-2006T>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50773160 | |||||||
| chr16:50773615 | T | A | 41 | a0001c0001t0001g0256 a0001c0001t0001g0262 a0001c0001t0001g0263 others(38): Show |
44 | HG00639.hp2 HG01884.hp2 HG01891.hp1 others(41): Show |
intron_variant | MODIFIER | c.914-1551T>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50773615 | |||||||
| chr16:50773868 | C | T | 65 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(62): Show |
79 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.914-1298C>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50773868 | |||||||
| chr16:50774069 | G | A | 1 | a0001c0001t0001g0190 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.914-1097G>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50774069 | |||||||
| chr16:50774122 | T | G | 6 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0264 others(3): Show |
6 | HG02486.hp2 HG02572.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.914-1044T>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50774122 | |||||||
| chr16:50774391 | G | A | 147 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(144): Show |
167 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.914-775G>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50774391 | |||||||
| chr16:50774635 | T | A | 2 | a0001c0001t0001g0078 a0001c0001t0001g0166 |
2 | HG02027.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.914-531T>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50774635 | |||||||
| chr16:50774672 | C | T | 3 | a0001c0002t0002g0034 a0001c0002t0002g0035 a0001c0002t0010g0146 |
3 | HG02055.hp1 HG02922.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.914-494C>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50774672 | |||||||
| chr16:50774697 | T | C | 7 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0216 others(4): Show |
7 | HG01167.hp1 HG02055.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.914-469T>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50774697 | |||||||
| chr16:50774715 | T | C | 2 | a0001c0001t0004g0127 a0001c0001t0004g0220 |
2 | HG03139.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.914-451T>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50774715 | |||||||
| chr16:50774815 | G | A | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(121): Show |
143 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.914-351G>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50774815 | |||||||
| chr16:50774877 | A | G | 2 | a0001c0001t0001g0181 a0001c0005t0001g0102 |
2 | HG00099.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.914-289A>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50774877 | |||||||
| chr16:50775005 | A | G | 7 | a0001c0001t0007g0128 a0001c0001t0007g0129 a0001c0001t0007g0130 others(4): Show |
7 | HG01884.hp2 HG02280.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.914-161A>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 5/18 | chr16 | 50775005 | |||||||
| chr16:50775520 | T | G | 23 | a0001c0001t0001g0256 a0001c0001t0003g0024 a0001c0001t0003g0226 others(20): Show |
24 | HG00639.hp2 HG02109.hp2 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.922+346T>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 6/18 | chr16 | 50775520 | |||||||
| chr16:50775625 | T | C | 2 | a0001c0001t0001g0186 a0001c0001t0001g0224 |
2 | HG00280.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.922+451T>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 6/18 | chr16 | 50775625 | |||||||
| chr16:50775991 | C | G | 23 | a0001c0001t0001g0256 a0001c0001t0003g0024 a0001c0001t0003g0226 others(20): Show |
24 | HG00639.hp2 HG02109.hp2 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.923-188C>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 6/18 | chr16 | 50775991 | |||||||
| chr16:50776011 | A | G | 1 | a0001c0001t0001g0041 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.923-168A>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 6/18 | chr16 | 50776011 | |||||||
| chr16:50776486 | A | G | 1 | a0001c0001t0008g0135 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1021+209A>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 7/18 | chr16 | 50776486 | |||||||
| chr16:50776547 | A | G | 1 | a0001c0001t0001g0194 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1021+270A>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 7/18 | chr16 | 50776547 | |||||||
| chr16:50776743 | G | C | 1 | a0001c0001t0001g0170 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1021+466G>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 7/18 | chr16 | 50776743 | |||||||
| chr16:50776861 | A | C | 1 | a0001c0001t0001g0110 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1021+584A>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 7/18 | chr16 | 50776861 | |||||||
| chr16:50776954 | G | C | 2 | a0001c0001t0004g0127 a0001c0001t0004g0220 |
2 | HG03139.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1021+677G>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 7/18 | chr16 | 50776954 | |||||||
| chr16:50777062 | T | G | 1 | a0001c0001t0001g0032 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1022-763T>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 7/18 | chr16 | 50777062 | |||||||
| chr16:50777207 | T | C | 77 | a0001c0001t0001g0032 a0001c0001t0001g0256 a0001c0001t0001g0262 others(74): Show |
84 | HG00639.hp2 HG00735.hp1 HG00738.hp2 others(81): Show |
intron_variant | MODIFIER | c.1022-618T>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 7/18 | chr16 | 50777207 | |||||||
| chr16:50777248 | A | G | 6 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0264 others(3): Show |
6 | HG02486.hp2 HG02572.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1022-577A>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 7/18 | chr16 | 50777248 | |||||||
| chr16:50777250 | G | T | 4 | a0001c0001t0003g0231 a0001c0001t0003g0232 a0001c0001t0003g0249 others(1): Show |
4 | HG02145.hp1 HG02630.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1022-575G>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 7/18 | chr16 | 50777250 | |||||||
| chr16:50777426 | A | T | 7 | a0001c0001t0007g0128 a0001c0001t0007g0129 a0001c0001t0007g0130 others(4): Show |
7 | HG01884.hp2 HG02280.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1022-399A>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 7/18 | chr16 | 50777426 | |||||||
| chr16:50777561 | T | A | 30 | a0001c0001t0001g0032 a0001c0002t0002g0009 a0001c0002t0002g0010 others(27): Show |
34 | HG00735.hp1 HG00738.hp2 HG01175.hp2 others(31): Show |
intron_variant | MODIFIER | c.1022-264T>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 7/18 | chr16 | 50777561 | |||||||
| chr16:50777596 | G | A | 11 | a0001c0001t0004g0127 a0001c0001t0004g0220 a0001c0001t0008g0134 others(8): Show |
13 | HG01891.hp1 HG02257.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.1022-229G>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 7/18 | chr16 | 50777596 | |||||||
| chr16:50778053 | G | A | 47 | a0001c0001t0001g0256 a0001c0001t0001g0262 a0001c0001t0001g0263 others(44): Show |
50 | HG00639.hp2 HG01884.hp2 HG01891.hp1 others(47): Show |
intron_variant | MODIFIER | c.1138+112G>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 8/18 | chr16 | 50778053 | |||||||
| chr16:50778324 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1138+383G>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 8/18 | chr16 | 50778324 | |||||||
| chr16:50778798 | G | A | 1 | a0001c0001t0001g0116 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1138+857G>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 8/18 | chr16 | 50778798 | |||||||
| chr16:50778856 | T | A | 1 | a0001c0001t0003g0240 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1139-809T>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 8/18 | chr16 | 50778856 | |||||||
| chr16:50778856 | T | TA | 21 | a0001c0001t0001g0256 a0001c0001t0003g0024 a0001c0001t0003g0226 others(18): Show |
22 | HG00639.hp2 HG02109.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.1139-804dupA | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr16 | 50778856 | ||||||
| chr16:50779180 | T | G | 1 | a0001c0001t0001g0075 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1139-485T>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 8/18 | chr16 | 50779180 | |||||||
| chr16:50779241 | T | C | 271 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(268): Show |
299 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.1139-424T>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 8/18 | chr16 | 50779241 | |||||||
| chr16:50779300 | G | A | 4 | a0001c0001t0008g0134 a0001c0001t0008g0135 a0001c0001t0008g0136 others(1): Show |
4 | HG02257.hp1 HG02622.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1139-365G>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 8/18 | chr16 | 50779300 | |||||||
| chr16:50779355 | G | C | 1 | a0001c0001t0001g0171 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1139-310G>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 8/18 | chr16 | 50779355 | |||||||
| chr16:50780086 | G | A | 29 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0016 others(26): Show |
33 | HG00735.hp1 HG00738.hp2 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.1518+42G>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 9/18 | chr16 | 50780086 | |||||||
| chr16:50780118 | C | G | 1 | a0001c0001t0004g0127 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1518+74C>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 9/18 | chr16 | 50780118 | |||||||
| chr16:50780247 | G | A | 4 | a0001c0001t0008g0134 a0001c0001t0008g0135 a0001c0001t0008g0136 others(1): Show |
4 | HG02257.hp1 HG02622.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1518+203G>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 9/18 | chr16 | 50780247 | |||||||
| chr16:50780332 | A | T | 2 | a0001c0001t0006g0197 a0001c0001t0006g0198 |
2 | NA18947.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.1518+288A>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 9/18 | chr16 | 50780332 | |||||||
| chr16:50780582 | G | A | 2 | a0001c0001t0004g0127 a0001c0001t0004g0220 |
2 | HG03139.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1518+538G>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 9/18 | chr16 | 50780582 | |||||||
| chr16:50780745 | C | A | 1 | a0001c0002t0002g0140 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1519-501C>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 9/18 | chr16 | 50780745 | |||||||
| chr16:50780834 | CT | C | 23 | a0001c0001t0001g0014 a0001c0001t0001g0026 a0001c0001t0001g0118 others(20): Show |
25 | HG00639.hp2 HG02109.hp2 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.1519-399delT | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr16 | 50780834 | ||||||
| chr16:50780960 | A | T | 24 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0264 others(21): Show |
26 | HG01884.hp2 HG01891.hp1 HG02257.hp1 others(23): Show |
intron_variant | MODIFIER | c.1519-286A>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 9/18 | chr16 | 50780960 | |||||||
| chr16:50781521 | C | T | 29 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0016 others(26): Show |
33 | HG00735.hp1 HG00738.hp2 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.1684+110C>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 10/18 | chr16 | 50781521 | |||||||
| chr16:50781772 | T | C | 7 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0216 others(4): Show |
7 | HG01167.hp1 HG02055.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1684+361T>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 10/18 | chr16 | 50781772 | |||||||
| chr16:50781845 | C | T | 1 | a0001c0001t0008g0135 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1684+434C>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 10/18 | chr16 | 50781845 | |||||||
| chr16:50781924 | T | C | 1 | a0001c0001t0001g0094 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1685-401T>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 10/18 | chr16 | 50781924 | |||||||
| chr16:50782092 | A | G | 3 | a0001c0001t0001g0088 a0001c0001t0001g0176 a0001c0001t0001g0248 |
3 | HG02027.hp2 HG02056.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.1685-233A>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 10/18 | chr16 | 50782092 | |||||||
| chr16:50782210 | A | C | 7 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0216 others(4): Show |
7 | HG01167.hp1 HG02055.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1685-115A>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 10/18 | chr16 | 50782210 | |||||||
| chr16:50782239 | A | G | 7 | a0001c0001t0007g0128 a0001c0001t0007g0129 a0001c0001t0007g0130 others(4): Show |
7 | HG01884.hp2 HG02280.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1685-86A>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 10/18 | chr16 | 50782239 | |||||||
| chr16:50782524 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1826+58C>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 11/18 | chr16 | 50782524 | |||||||
| chr16:50782525 | G | GGT | 29 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0016 others(26): Show |
33 | HG00735.hp1 HG00738.hp2 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.1826+75_1826+76dup others(2): Show |
CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr16 | 50782525 | ||||||
| chr16:50782749 | C | T | 68 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(65): Show |
82 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.1826+283C>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 11/18 | chr16 | 50782749 | |||||||
| chr16:50782836 | C | T | 1 | a0001c0001t0003g0255 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1826+370C>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 11/18 | chr16 | 50782836 | |||||||
| chr16:50782907 | C | A | 1 | a0001c0001t0001g0095 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1826+441C>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 11/18 | chr16 | 50782907 | |||||||
| chr16:50782916 | A | AT | 53 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0026 others(50): Show |
55 | HG00323.hp2 HG00423.hp1 HG01123.hp1 others(52): Show |
intron_variant | MODIFIER | c.1826+476dupT | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr16 | 50782916 | ||||||
| chr16:50782916 | A | ATT | 51 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(48): Show |
62 | HG00099.hp2 HG00280.hp2 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.1826+475_1826+476d others(4): Show |
CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr16 | 50782916 | ||||||
| chr16:50782916 | A | ATTT | 25 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0109 others(22): Show |
28 | HG00423.hp2 HG01167.hp1 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.1826+474_1826+476d others(5): Show |
CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr16 | 50782916 | ||||||
| chr16:50782916 | AT | A | 10 | a0001c0001t0001g0157 a0001c0001t0001g0262 a0001c0001t0004g0220 others(7): Show |
10 | HG02280.hp1 HG02486.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1826+476delT | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr16 | 50782916 | ||||||
| chr16:50782916 | ATT | A | 34 | a0001c0001t0008g0134 a0001c0001t0008g0135 a0001c0001t0008g0136 others(31): Show |
40 | HG00735.hp1 HG00738.hp2 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.1826+475_1826+476d others(4): Show |
CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr16 | 50782916 | ||||||
| chr16:50782982 | C | T | 18 | a0001c0001t0001g0256 a0001c0001t0003g0024 a0001c0001t0003g0226 others(15): Show |
19 | HG00639.hp2 HG02109.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.1826+516C>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 11/18 | chr16 | 50782982 | |||||||
| chr16:50783028 | G | A | 23 | a0001c0001t0001g0256 a0001c0001t0003g0024 a0001c0001t0003g0226 others(20): Show |
24 | HG00639.hp2 HG02109.hp2 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.1826+562G>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 11/18 | chr16 | 50783028 | |||||||
| chr16:50783119 | C | T | 2 | a0001c0001t0001g0152 a0001c0001t0001g0153 |
2 | HG01106.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1826+653C>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 11/18 | chr16 | 50783119 | |||||||
| chr16:50783133 | C | T | 68 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(65): Show |
82 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.1826+667C>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 11/18 | chr16 | 50783133 | |||||||
| chr16:50783145 | T | C | 2 | a0001c0001t0004g0191 a0001c0001t0004g0192 |
2 | HG01081.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.1826+679T>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 11/18 | chr16 | 50783145 | |||||||
| chr16:50783178 | C | T | 5 | a0001c0001t0001g0072 a0001c0001t0001g0101 a0001c0001t0001g0104 others(2): Show |
5 | HG02040.hp1 NA18989.hp2 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.1826+712C>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 11/18 | chr16 | 50783178 | |||||||
| chr16:50783308 | A | G | 52 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(49): Show |
64 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.1826+842A>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 11/18 | chr16 | 50783308 | |||||||
| chr16:50783555 | T | C | 1 | a0001c0001t0001g0051 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1827-774T>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 11/18 | chr16 | 50783555 | |||||||
| chr16:50783563 | G | A | 4 | a0001c0001t0001g0263 a0001c0001t0001g0264 a0001c0001t0001g0265 others(1): Show |
4 | HG02572.hp1 HG02615.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1827-766G>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 11/18 | chr16 | 50783563 | |||||||
| chr16:50783578 | G | A | 29 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0016 others(26): Show |
33 | HG00735.hp1 HG00738.hp2 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.1827-751G>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 11/18 | chr16 | 50783578 | |||||||
| chr16:50783599 | C | T | 1 | a0001c0001t0001g0098 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1827-730C>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 11/18 | chr16 | 50783599 | |||||||
| chr16:50783638 | A | C | 76 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(73): Show |
90 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.1827-691A>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 11/18 | chr16 | 50783638 | |||||||
| chr16:50783920 | G | A | 1 | a0001c0001t0011g0200 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1827-409G>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 11/18 | chr16 | 50783920 | |||||||
| chr16:50784021 | A | G | 76 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(73): Show |
90 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.1827-308A>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 11/18 | chr16 | 50784021 | |||||||
| chr16:50784474 | T | C | 1 | a0001c0001t0004g0107 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1949+23T>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 12/18 | chr16 | 50784474 | |||||||
| chr16:50784551 | G | A | 1 | a0001c0001t0001g0201 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1949+100G>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 12/18 | chr16 | 50784551 | |||||||
| chr16:50784586 | C | T | 1 | a0001c0001t0001g0264 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1949+135C>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 12/18 | chr16 | 50784586 | |||||||
| chr16:50784917 | G | A | 1 | a0001c0001t0001g0082 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1949+466G>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 12/18 | chr16 | 50784917 | |||||||
| chr16:50784961 | G | A | 1 | a0001c0001t0001g0066 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1949+510G>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 12/18 | chr16 | 50784961 | |||||||
| chr16:50785049 | C | T | 2 | a0001c0001t0004g0127 a0001c0001t0004g0220 |
2 | HG03139.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1949+598C>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 12/18 | chr16 | 50785049 | |||||||
| chr16:50785201 | A | G | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(145): Show |
169 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.1949+750A>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 12/18 | chr16 | 50785201 | |||||||
| chr16:50785201 | A | T | 4 | a0001c0001t0001g0263 a0001c0001t0001g0264 a0001c0001t0001g0265 others(1): Show |
4 | HG02572.hp1 HG02615.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1949+750A>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 12/18 | chr16 | 50785201 | |||||||
| chr16:50785409 | A | G | 1 | a0001c0002t0012g0036 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1949+958A>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 12/18 | chr16 | 50785409 | |||||||
| chr16:50785559 | T | C | 1 | a0001c0002t0002g0228 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1949+1108T>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 12/18 | chr16 | 50785559 | |||||||
| chr16:50785604 | C | T | 1 | a0001c0002t0002g0140 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1949+1153C>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 12/18 | chr16 | 50785604 | |||||||
| chr16:50785644 | C | A | 23 | a0001c0001t0001g0256 a0001c0001t0003g0024 a0001c0001t0003g0226 others(20): Show |
24 | HG00639.hp2 HG02109.hp2 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.1949+1193C>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 12/18 | chr16 | 50785644 | |||||||
| chr16:50785655 | G | A | 137 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(134): Show |
158 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.1950-1200G>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 12/18 | chr16 | 50785655 | |||||||
| chr16:50785836 | A | G | 1 | a0001c0001t0007g0129 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1950-1019A>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 12/18 | chr16 | 50785836 | |||||||
| chr16:50785999 | C | T | 143 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(140): Show |
164 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.1950-856C>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 12/18 | chr16 | 50785999 | |||||||
| chr16:50786022 | T | C | 1 | a0001c0001t0001g0173 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1950-833T>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 12/18 | chr16 | 50786022 | |||||||
| chr16:50786053 | T | C | 1 | a0001c0001t0001g0056 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1950-802T>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 12/18 | chr16 | 50786053 | |||||||
| chr16:50786167 | C | T | 74 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(71): Show |
88 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.1950-688C>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 12/18 | chr16 | 50786167 | |||||||
| chr16:50786352 | A | G | 76 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(73): Show |
90 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.1950-503A>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 12/18 | chr16 | 50786352 | |||||||
| chr16:50786495 | C | T | 76 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(73): Show |
90 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.1950-360C>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 12/18 | chr16 | 50786495 | |||||||
| chr16:50786522 | G | GGCCGAGG others(1): Show |
76 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(73): Show |
90 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.1950-331_1950-324d others(10): Show |
CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr16 | 50786522 | ||||||
| chr16:50786761 | C | CA | 35 | a0001c0001t0001g0256 a0001c0001t0001g0262 a0001c0001t0001g0263 others(32): Show |
36 | HG00639.hp2 HG01884.hp2 HG02109.hp2 others(33): Show |
intron_variant | MODIFIER | c.1950-82dupA | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr16 | 50786761 | ||||||
| chr16:50787056 | G | A | 23 | a0001c0001t0001g0256 a0001c0001t0003g0024 a0001c0001t0003g0226 others(20): Show |
24 | HG00639.hp2 HG02109.hp2 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.2041+110G>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 13/18 | chr16 | 50787056 | |||||||
| chr16:50787220 | G | C | 2 | a0001c0001t0001g0014 a0001c0001t0001g0118 |
3 | HG02257.hp2 HG02976.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2041+274G>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 13/18 | chr16 | 50787220 | |||||||
| chr16:50787301 | A | T | 1 | a0001c0001t0001g0080 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2041+355A>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 13/18 | chr16 | 50787301 | |||||||
| chr16:50787682 | G | T | 1 | a0001c0001t0001g0204 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.2042-104G>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 13/18 | chr16 | 50787682 | |||||||
| chr16:50787736 | G | A | 5 | a0001c0003t0005g0008 a0001c0003t0005g0241 a0001c0003t0005g0242 others(2): Show |
7 | HG01891.hp1 HG02717.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.2042-50G>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 13/18 | chr16 | 50787736 | |||||||
| chr16:50787903 | T | C | 1 | a0001c0001t0001g0184 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2108+51T>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 14/18 | chr16 | 50787903 | |||||||
| chr16:50788246 | T | G | 13 | a0001c0001t0003g0239 a0001c0001t0007g0128 a0001c0001t0007g0129 others(10): Show |
15 | HG01884.hp2 HG01891.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.2108+394T>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 14/18 | chr16 | 50788246 | |||||||
| chr16:50788676 | A | G | 2 | a0001c0001t0001g0163 a0001c0001t0001g0167 |
2 | HG03927.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.2108+824A>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 14/18 | chr16 | 50788676 | |||||||
| chr16:50788804 | G | A | 5 | a0001c0003t0005g0008 a0001c0003t0005g0241 a0001c0003t0005g0242 others(2): Show |
7 | HG01891.hp1 HG02717.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.2108+952G>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 14/18 | chr16 | 50788804 | |||||||
| chr16:50789053 | A | C | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(147): Show |
171 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.2108+1201A>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 14/18 | chr16 | 50789053 | |||||||
| chr16:50789145 | A | G | 1 | a0001c0001t0001g0043 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.2108+1293A>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 14/18 | chr16 | 50789145 | |||||||
| chr16:50789338 | G | A | 7 | a0001c0001t0007g0128 a0001c0001t0007g0129 a0001c0001t0007g0130 others(4): Show |
7 | HG01884.hp2 HG02280.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.2108+1486G>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 14/18 | chr16 | 50789338 | |||||||
| chr16:50789374 | G | A | 7 | a0001c0001t0007g0128 a0001c0001t0007g0129 a0001c0001t0007g0130 others(4): Show |
7 | HG01884.hp2 HG02280.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.2108+1522G>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 14/18 | chr16 | 50789374 | |||||||
| chr16:50789791 | T | C | 1 | a0001c0001t0001g0125 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.2109-1767T>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 14/18 | chr16 | 50789791 | |||||||
| chr16:50790710 | G | GT | 29 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0016 others(26): Show |
33 | HG00735.hp1 HG00738.hp2 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.2109-836dupT | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr16 | 50790710 | ||||||
| chr16:50790920 | T | C | 29 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0016 others(26): Show |
33 | HG00735.hp1 HG00738.hp2 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.2109-638T>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 14/18 | chr16 | 50790920 | |||||||
| chr16:50791000 | T | A | 29 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0016 others(26): Show |
33 | HG00735.hp1 HG00738.hp2 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.2109-558T>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 14/18 | chr16 | 50791000 | |||||||
| chr16:50791434 | A | G | 1 | a0001c0001t0001g0262 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2109-124A>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 14/18 | chr16 | 50791434 | |||||||
| chr16:50791548 | G | A | 19 | a0001c0001t0001g0262 a0001c0001t0004g0127 a0001c0001t0004g0220 others(16): Show |
21 | HG01884.hp2 HG01891.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.2109-10G>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 14/18 | chr16 | 50791548 | |||||||
| chr16:50791731 | T | A | 7 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0216 others(4): Show |
7 | HG01167.hp1 HG02055.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.2241+41T>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 15/18 | chr16 | 50791731 | |||||||
| chr16:50792039 | C | A | 19 | a0001c0001t0001g0262 a0001c0001t0004g0127 a0001c0001t0004g0220 others(16): Show |
21 | HG01884.hp2 HG01891.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.2241+349C>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 15/18 | chr16 | 50792039 | |||||||
| chr16:50792100 | T | C | 1 | a0001c0001t0001g0157 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2241+410T>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 15/18 | chr16 | 50792100 | |||||||
| chr16:50792112 | T | C | 8 | a0001c0001t0001g0262 a0001c0001t0007g0128 a0001c0001t0007g0129 others(5): Show |
8 | HG01884.hp2 HG02280.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.2241+422T>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 15/18 | chr16 | 50792112 | |||||||
| chr16:50792458 | G | A | 2 | a0001c0001t0003g0238 a0001c0001t0003g0255 |
2 | HG02647.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.2242-139G>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 15/18 | chr16 | 50792458 | |||||||
| chr16:50792551 | G | T | 48 | a0001c0001t0001g0262 a0001c0001t0004g0127 a0001c0001t0004g0220 others(45): Show |
54 | HG00735.hp1 HG00738.hp2 HG01175.hp2 others(51): Show |
intron_variant | MODIFIER | c.2242-46G>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 15/18 | chr16 | 50792551 | |||||||
| chr16:50792766 | C | T | 4 | a0001c0001t0008g0134 a0001c0001t0008g0135 a0001c0001t0008g0136 others(1): Show |
4 | HG02257.hp1 HG02622.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.2350+61C>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 16/18 | chr16 | 50792766 | |||||||
| chr16:50792938 | A | G | 1 | a0001c0001t0001g0095 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2350+233A>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 16/18 | chr16 | 50792938 | |||||||
| chr16:50793031 | G | A | 1 | a0001c0001t0001g0032 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2350+326G>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 16/18 | chr16 | 50793031 | |||||||
| chr16:50793086 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2350+381C>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 16/18 | chr16 | 50793086 | |||||||
| chr16:50793111 | CAT | C | 11 | a0001c0002t0002g0009 a0001c0002t0002g0016 a0001c0002t0002g0028 others(8): Show |
12 | HG02135.hp1 HG02738.hp1 HG03927.hp1 others(9): Show |
intron_variant | MODIFIER | c.2350+410_2350+411d others(4): Show |
CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr16 | 50793111 | ||||||
| chr16:50793113 | T | TACACACA others(3): Show |
2 | a0001c0001t0001g0014 a0001c0001t0001g0118 |
2 | HG02976.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2350+409_2350+410i others(12): Show |
CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr16 | 50793113 | ||||||
| chr16:50793113 | TATAC | T | 5 | a0001c0002t0002g0010 a0001c0002t0002g0018 a0001c0002t0002g0031 others(2): Show |
7 | NA18947.hp1 NA18952.hp2 NA18986.hp1 others(4): Show |
intron_variant | MODIFIER | c.2350+410_2350+413d others(6): Show |
CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr16 | 50793113 | ||||||
| chr16:50793115 | T | C | 7 | a0001c0001t0001g0014 a0001c0001t0001g0108 a0001c0001t0001g0118 others(4): Show |
8 | HG01074.hp1 HG02257.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.2350+410T>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 16/18 | chr16 | 50793115 | |||||||
| chr16:50793115 | T | TAC | 19 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0032 others(16): Show |
19 | HG00099.hp1 HG00735.hp2 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.2351-399_2351-398d others(4): Show |
CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr16 | 50793115 | ||||||
| chr16:50793115 | TAC | T | 18 | a0001c0001t0001g0064 a0001c0001t0001g0125 a0001c0001t0001g0126 others(15): Show |
18 | HG01433.hp2 HG01884.hp2 HG01943.hp2 others(15): Show |
intron_variant | MODIFIER | c.2351-399_2351-398d others(4): Show |
CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr16 | 50793115 | ||||||
| chr16:50793115 | TACAC | T | 15 | a0001c0001t0001g0041 a0001c0001t0001g0149 a0001c0001t0004g0127 others(12): Show |
16 | HG00735.hp1 HG00738.hp2 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.2351-401_2351-398d others(6): Show |
CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr16 | 50793115 | ||||||
| chr16:50793115 | TACACAC | T | 28 | a0001c0001t0001g0262 a0001c0001t0003g0024 a0001c0001t0003g0226 others(25): Show |
31 | HG01891.hp1 HG02109.hp2 HG02257.hp1 others(28): Show |
intron_variant | MODIFIER | c.2351-403_2351-398d others(8): Show |
CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr16 | 50793115 | ||||||
| chr16:50793119 | C | T | 4 | a0001c0001t0007g0128 a0001c0001t0007g0129 a0001c0001t0007g0130 others(1): Show |
4 | HG01884.hp2 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.2350+414C>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 16/18 | chr16 | 50793119 | |||||||
| chr16:50793121 | C | T | 3 | a0001c0001t0004g0127 a0001c0001t0004g0220 a0001c0001t0009g0222 |
3 | HG03098.hp1 HG03139.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2350+416C>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 16/18 | chr16 | 50793121 | |||||||
| chr16:50793123 | C | T | 10 | a0001c0001t0001g0262 a0001c0001t0008g0134 a0001c0001t0008g0135 others(7): Show |
12 | HG01891.hp1 HG02257.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.2350+418C>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 16/18 | chr16 | 50793123 | |||||||
| chr16:50793306 | A | G | 19 | a0001c0001t0001g0262 a0001c0001t0004g0127 a0001c0001t0004g0220 others(16): Show |
21 | HG01884.hp2 HG01891.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.2351-240A>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 16/18 | chr16 | 50793306 | |||||||
| chr16:50793690 | A | G | 226 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(223): Show |
250 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.2469+26A>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 17/18 | chr16 | 50793690 | |||||||
| chr16:50793737 | C | T | 1 | a0001c0001t0001g0169 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2469+73C>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 17/18 | chr16 | 50793737 | |||||||
| chr16:50793794 | T | C | 2 | a0001c0001t0004g0191 a0001c0001t0004g0192 |
2 | HG01081.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.2469+130T>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 17/18 | chr16 | 50793794 | |||||||
| chr16:50793898 | T | C | 3 | a0001c0002t0002g0017 a0001c0002t0002g0030 a0001c0002t0002g0228 |
4 | HG00735.hp1 HG00738.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.2469+234T>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 17/18 | chr16 | 50793898 | |||||||
| chr16:50793920 | A | AT | 123 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(120): Show |
139 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.2470-273dupT | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr16 | 50793920 | ||||||
| chr16:50793920 | A | ATT | 6 | a0001c0001t0001g0014 a0001c0001t0001g0114 a0001c0001t0001g0118 others(3): Show |
7 | HG01175.hp1 HG02257.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.2469+274_2470-273d others(4): Show |
CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr16 | 50793920 | ||||||
| chr16:50793970 | C | T | 4 | a0001c0001t0001g0085 a0001c0001t0001g0090 a0001c0001t0001g0170 others(1): Show |
4 | NA18952.hp1 NA18965.hp2 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.2470-242C>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 17/18 | chr16 | 50793970 | |||||||
| chr16:50794013 | C | T | 1 | a0001c0001t0001g0262 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2470-199C>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 17/18 | chr16 | 50794013 | |||||||
| chr16:50794161 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2470-51C>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 17/18 | chr16 | 50794161 | |||||||
| chr16:50794619 | G | GT | 131 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(128): Show |
151 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.2686+202dupT | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr16 | 50794619 | ||||||
| chr16:50794619 | G | GTT | 24 | a0001c0001t0001g0264 a0001c0001t0003g0024 a0001c0001t0003g0226 others(21): Show |
25 | HG02109.hp2 HG02145.hp1 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.2686+201_2686+202d others(4): Show |
CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr16 | 50794619 | ||||||
| chr16:50794958 | T | A | 1 | a0001c0001t0001g0213 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2686+530T>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 18/18 | chr16 | 50794958 | |||||||
| chr16:50795008 | C | A | 1 | a0001c0001t0008g0134 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2686+580C>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 18/18 | chr16 | 50795008 | |||||||
| chr16:50795252 | T | C | 1 | a0001c0006t0001g0267 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2686+824T>C | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 18/18 | chr16 | 50795252 | |||||||
| chr16:50795253 | G | A | 1 | a0001c0006t0001g0267 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2686+825G>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 18/18 | chr16 | 50795253 | |||||||
| chr16:50795651 | A | G | 1 | a0001c0001t0001g0262 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2687-673A>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 18/18 | chr16 | 50795651 | |||||||
| chr16:50795697 | T | A | 1 | a0001c0001t0001g0087 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.2687-627T>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 18/18 | chr16 | 50795697 | |||||||
| chr16:50795796 | A | G | 3 | a0001c0001t0001g0088 a0001c0001t0001g0176 a0001c0001t0001g0248 |
3 | HG02027.hp2 HG02056.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.2687-528A>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 18/18 | chr16 | 50795796 | |||||||
| chr16:50795866 | A | G | 1 | a0001c0001t0001g0185 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2687-458A>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 18/18 | chr16 | 50795866 | |||||||
| chr16:50795924 | G | A | 1 | a0001c0001t0001g0172 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.2687-400G>A | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 18/18 | chr16 | 50795924 | |||||||
| chr16:50795942 | A | T | 75 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(72): Show |
89 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.2687-382A>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 18/18 | chr16 | 50795942 | |||||||
| chr16:50795975 | C | G | 4 | a0001c0001t0008g0134 a0001c0001t0008g0135 a0001c0001t0008g0136 others(1): Show |
4 | HG02257.hp1 HG02622.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.2687-349C>G | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 18/18 | chr16 | 50795975 | |||||||
| chr16:50796100 | C | T | 1 | a0001c0001t0004g0107 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2687-224C>T | CYLD | ENSG00000083799.18 | transcript | ENST00000427738.8 | protein_coding | 18/18 | chr16 | 50796100 |