Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 54756 |
|---|---|
| ensemblid | ENSG00000144730.19 |
| hgncid | 17616 |
| symbol | IL17RD |
| name | interleukin 17 receptor D |
| refseq_nuc | NM_017563.5 |
| refseq_prot | NP_060033.3 |
| ensembl_nuc | ENST00000296318.12 |
| ensembl_prot | ENSP00000296318.7 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 57089982 |
| end | 57165353 |
| strand | - |
| ver | v1.2 |
| region | chr3:57089982-57165353 |
| region5000 | chr3:57084982-57170353 |
| regionname0 | IL17RD_chr3_57089982_57165353 |
| regionname5000 | IL17RD_chr3_57084982_57170353 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 739 | 137 | 38 | 37 | 24 | 7 | 30 | 20 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0002 | 1/0 | 739 | 107 | 36 | 7 | 60 | 1 | 2 | 47 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0003 | 0/0 | 739 | 90 | 5 | 21 | 55 | 1 | 8 | 44 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0004 | 0/0 | 739 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0005 | 0/0 | 739 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0006 | 0/0 | 739 | 4 | 1 | 2 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0007 | 0/0 | 739 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0008 | 0/0 | 739 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0009 | 0/0 | 739 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0010 | 0/0 | 739 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0011 | 0/0 | 739 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 2220 | 130 | 32 | 37 | 24 | 7 | 29 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| c0002 | 0/0 | 2220 | 88 | 5 | 21 | 53 | 1 | 8 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| c0003 | 1/0 | 2220 | 82 | 20 | 4 | 56 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| c0004 | 0/0 | 2220 | 17 | 10 | 3 | 2 | 1 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| c0005 | 0/0 | 2220 | 6 | 6 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| c0006 | 0/0 | 2220 | 6 | 6 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| c0007 | 0/0 | 2220 | 6 | 6 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| c0008 | 0/0 | 2220 | 5 | 4 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| c0009 | 0/0 | 2220 | 4 | 1 | 2 | 0 | 1 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| c0010 | 0/0 | 2220 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| c0011 | 0/0 | 2220 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| c0012 | 0/0 | 2220 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| c0013 | 0/0 | 2220 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| c0014 | 0/0 | 2220 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| c0015 | 0/0 | 2220 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| c0016 | 0/0 | 2220 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| c0017 | 0/0 | 2220 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| c0018 | 0/0 | 2220 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| c0019 | 0/0 | 2220 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 6480 | 82 | 3 | 20 | 51 | 1 | 7 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| t0002 | 1/0 | 6479 | 62 | 2 | 1 | 57 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| t0003 | 0/0 | 6478 | 41 | 10 | 11 | 13 | 4 | 3 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| t0004 | 0/1 | 6478 | 30 | 7 | 12 | 2 | 1 | 7 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| t0005 | 0/0 | 6478 | 18 | 0 | 3 | 7 | 1 | 7 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| t0006 | 0/0 | 6478 | 14 | 13 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| t0007 | 0/0 | 6478 | 12 | 0 | 5 | 0 | 1 | 6 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| t0008 | 0/0 | 6479 | 7 | 0 | 3 | 2 | 1 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| t0009 | 0/0 | 6479 | 6 | 6 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| t0010 | 0/0 | 6478 | 6 | 6 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| t0011 | 0/0 | 6478 | 6 | 6 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| t0012 | 0/0 | 6479 | 5 | 4 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| t0013 | 0/0 | 6479 | 5 | 5 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| t0014 | 0/0 | 6478 | 4 | 3 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| t0015 | 0/0 | 6479 | 3 | 2 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| t0016 | 0/0 | 6479 | 3 | 3 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| t0017 | 0/0 | 6480 | 2 | 0 | 0 | 1 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| t0018 | 0/0 | 6478 | 2 | 2 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| t0019 | 0/0 | 6479 | 2 | 2 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| t0020 | 0/0 | 6478 | 2 | 0 | 1 | 0 | 1 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| t0021 | 0/0 | 6478 | 2 | 1 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| t0022 | 0/0 | 6479 | 2 | 2 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| t0023 | 0/0 | 6480 | 2 | 0 | 0 | 2 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| t0024 | 0/0 | 6478 | 2 | 1 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| t0025 | 0/0 | 6478 | 2 | 0 | 1 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| t0026 | 0/0 | 6478 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| t0027 | 0/0 | 6478 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| t0028 | 0/0 | 6478 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| t0029 | 0/0 | 6478 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| t0030 | 0/0 | 6479 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| t0031 | 0/0 | 6478 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| t0032 | 0/0 | 6480 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| t0033 | 0/0 | 6478 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| t0034 | 0/0 | 6478 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| t0035 | 0/0 | 6478 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| t0036 | 0/0 | 6478 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| t0037 | 0/0 | 6478 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| t0038 | 0/0 | 6478 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| t0039 | 0/0 | 6478 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| t0040 | 0/0 | 6479 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| t0041 | 0/0 | 6480 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| t0042 | 0/0 | 6478 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| t0043 | 0/0 | 6478 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| t0044 | 0/0 | 6478 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| t0045 | 0/0 | 6478 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| t0046 | 0/0 | 6478 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| t0047 | 0/0 | 6478 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| t0048 | 0/0 | 6479 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| t0049 | 0/0 | 6479 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| t0050 | 0/0 | 6479 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| t0051 | 0/0 | 6479 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| t0052 | 0/0 | 6478 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| t0053 | 0/0 | 6478 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| t0054 | 0/0 | 6479 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| t0055 | 0/0 | 6479 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| t0056 | 0/0 | 6478 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| t0057 | 0/0 | 6478 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0003 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0159 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0280 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2220 | 130 | 32 | 37 | 24 | 7 | 29 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0001c0006 | 0/0 | 2220 | 6 | 6 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0001c0013 | 0/0 | 2220 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0002c0003 | 1/0 | 2220 | 82 | 20 | 4 | 56 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0002c0004 | 0/0 | 2220 | 17 | 10 | 3 | 2 | 1 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0002c0007 | 0/0 | 2220 | 6 | 6 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0002c0012 | 0/0 | 2220 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0002c0015 | 0/0 | 2220 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0003c0002 | 0/0 | 2220 | 88 | 5 | 21 | 53 | 1 | 8 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0003c0010 | 0/0 | 2220 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0003c0011 | 0/0 | 2220 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0004c0005 | 0/0 | 2220 | 6 | 6 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0005c0008 | 0/0 | 2220 | 5 | 4 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0006c0009 | 0/0 | 2220 | 4 | 1 | 2 | 0 | 1 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0007c0018 | 0/0 | 2220 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0008c0014 | 0/0 | 2220 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0009c0016 | 0/0 | 2220 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0010c0017 | 0/0 | 2220 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0011c0019 | 0/0 | 2220 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0003 | 0/0 | 8697 | 35 | 8 | 9 | 12 | 3 | 3 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0001c0001t0004 | 0/1 | 8697 | 29 | 7 | 12 | 2 | 1 | 6 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0001c0001t0005 | 0/0 | 8697 | 18 | 0 | 3 | 7 | 1 | 7 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0001c0001t0006 | 0/0 | 8697 | 9 | 9 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0001c0001t0007 | 0/0 | 8697 | 12 | 0 | 5 | 0 | 1 | 6 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0001c0001t0018 | 0/0 | 8697 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0001c0001t0020 | 0/0 | 8697 | 2 | 0 | 1 | 0 | 1 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0001c0001t0024 | 0/0 | 8697 | 2 | 1 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0001c0001t0025 | 0/0 | 8697 | 2 | 0 | 1 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0001c0001t0026 | 0/0 | 8697 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0001c0001t0027 | 0/0 | 8697 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0001c0001t0028 | 0/0 | 8697 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0001c0001t0029 | 0/0 | 8697 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0001c0001t0033 | 0/0 | 8697 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0001c0001t0034 | 0/0 | 8697 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0001c0001t0035 | 0/0 | 8697 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0001c0001t0036 | 0/0 | 8697 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0001c0001t0037 | 0/0 | 8697 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0001c0001t0038 | 0/0 | 8697 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0001c0001t0039 | 0/0 | 8697 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0001c0001t0040 | 0/0 | 8698 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0001c0001t0042 | 0/0 | 8697 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0001c0001t0043 | 0/0 | 8697 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0001c0001t0044 | 0/0 | 8697 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0001c0001t0045 | 0/0 | 8697 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0001c0001t0046 | 0/0 | 8697 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0001c0001t0047 | 0/0 | 8697 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0001c0001t0052 | 0/0 | 8697 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0001c0001t0056 | 0/0 | 8697 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0001c0006t0011 | 0/0 | 8697 | 6 | 6 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0001c0013t0004 | 0/0 | 8697 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0002c0003t0002 | 1/0 | 8698 | 58 | 2 | 1 | 53 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0002c0003t0012 | 0/0 | 8698 | 5 | 4 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0002c0003t0013 | 0/0 | 8698 | 5 | 5 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0002c0003t0014 | 0/0 | 8697 | 4 | 3 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0002c0003t0021 | 0/0 | 8697 | 2 | 1 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0002c0003t0022 | 0/0 | 8698 | 2 | 2 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0002c0003t0030 | 0/0 | 8698 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0002c0003t0031 | 0/0 | 8697 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0002c0003t0032 | 0/0 | 8699 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0002c0003t0053 | 0/0 | 8697 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0002c0003t0054 | 0/0 | 8698 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0002c0003t0055 | 0/0 | 8698 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0002c0004t0008 | 0/0 | 8698 | 7 | 0 | 3 | 2 | 1 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0002c0004t0016 | 0/0 | 8698 | 3 | 3 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0002c0004t0019 | 0/0 | 8698 | 2 | 2 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0002c0004t0048 | 0/0 | 8698 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0002c0004t0049 | 0/0 | 8698 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0002c0004t0050 | 0/0 | 8698 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0002c0004t0051 | 0/0 | 8698 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0002c0004t0057 | 0/0 | 8697 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0002c0007t0009 | 0/0 | 8698 | 6 | 6 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0002c0012t0002 | 0/0 | 8698 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0002c0015t0002 | 0/0 | 8698 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0003c0002t0001 | 0/0 | 8699 | 81 | 3 | 20 | 50 | 1 | 7 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0003c0002t0015 | 0/0 | 8698 | 3 | 2 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0003c0002t0017 | 0/0 | 8699 | 2 | 0 | 0 | 1 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0003c0002t0023 | 0/0 | 8699 | 2 | 0 | 0 | 2 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0003c0010t0041 | 0/0 | 8699 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0003c0011t0001 | 0/0 | 8699 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0004c0005t0010 | 0/0 | 8697 | 6 | 6 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0005c0008t0006 | 0/0 | 8697 | 5 | 4 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0006c0009t0003 | 0/0 | 8697 | 4 | 1 | 2 | 0 | 1 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0007c0018t0003 | 0/0 | 8697 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0008c0014t0018 | 0/0 | 8697 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0009c0016t0002 | 0/0 | 8698 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0010c0017t0002 | 0/0 | 8698 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| a0011c0019t0003 | 0/0 | 8697 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | copy fasta | chr3 | 57084982 | 57170353 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0003g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0003g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0003g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0003g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0003g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0003g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0003g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0003g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0003g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0003g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0003g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0003g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0003g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0003g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0003g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0003g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0003g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0003g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0003g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0003g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0003g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0004g0003 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0004g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0004g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0004g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0004g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0004g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0004g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0004g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0004g0159 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0004g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0004g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0004g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0004g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0004g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0004g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0004g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0004g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0004g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0004g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0004g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0004g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0004g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0004g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0004g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0004g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0004g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0004g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0004g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0005g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0005g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0005g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0005g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0005g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0005g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0005g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0005g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0005g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0005g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0005g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0005g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0005g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0005g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0005g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0005g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0006g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0006g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0006g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0006g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0006g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0006g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0006g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0006g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0006g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0007g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0007g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0007g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0007g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0007g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0007g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0007g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0007g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0007g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0007g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0007g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0018g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0020g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0020g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0024g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0024g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0025g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0025g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0026g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0027g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0028g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0029g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0033g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0034g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0035g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0036g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0037g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0038g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0039g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0040g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0042g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0043g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0044g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0045g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0046g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0047g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0052g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0001t0056g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0006t0011g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0006t0011g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0006t0011g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0006t0011g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0006t0011g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0006t0011g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0001c0013t0004g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0002g0280 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0002g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0002g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0002g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0002g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0002g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0002g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0012g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0012g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0012g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0012g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0012g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0013g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0013g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0013g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0013g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0013g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0014g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0014g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0014g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0014g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0021g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0021g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0022g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0022g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0030g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0031g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0032g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0053g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0054g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0003t0055g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0004t0008g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0004t0008g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0004t0008g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0004t0008g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0004t0008g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0004t0008g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0004t0008g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0004t0016g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0004t0016g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0004t0016g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0004t0019g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0004t0019g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0004t0048g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0004t0049g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0004t0050g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0004t0051g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0004t0057g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0007t0009g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0007t0009g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0007t0009g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0007t0009g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0007t0009g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0007t0009g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0012t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0002c0015t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0015g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0015g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0015g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0017g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0017g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0002t0023g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0010t0041g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0003c0011t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0004c0005t0010g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0004c0005t0010g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0004c0005t0010g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0004c0005t0010g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0004c0005t0010g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0004c0005t0010g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0005c0008t0006g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0005c0008t0006g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0005c0008t0006g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0005c0008t0006g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0005c0008t0006g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0006c0009t0003g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0006c0009t0003g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0006c0009t0003g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0006c0009t0003g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0007c0018t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0008c0014t0018g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0009c0016t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0010c0017t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| a0011c0019t0003g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0004 | t0008 | g0310 | EUR | GBR | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0259 | EUR | GBR | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0277 | EUR | FIN | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG00280 | hp2 | a0001 | c0001 | t0007 | g0046 | EUR | FIN | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG00544 | hp1 | a0002 | c0003 | t0002 | g0100 | EAS | CHS | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG00544 | hp2 | a0002 | c0003 | t0002 | g0206 | EAS | CHS | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG00558 | hp1 | a0003 | c0002 | t0001 | g0182 | EAS | CHS | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG00558 | hp2 | a0002 | c0003 | t0032 | g0314 | EAS | CHS | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG00609 | hp1 | a0002 | c0012 | t0002 | g0241 | EAS | CHS | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG00609 | hp2 | a0001 | c0001 | t0003 | g0297 | EAS | CHS | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG00639 | hp1 | a0002 | c0004 | t0008 | g0177 | AMR | PUR | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG00639 | hp2 | a0003 | c0002 | t0001 | g0063 | AMR | PUR | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG00642 | hp1 | a0003 | c0002 | t0001 | g0220 | AMR | PUR | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0195 | AMR | PUR | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG00673 | hp1 | a0002 | c0003 | t0002 | g0034 | EAS | CHS | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG00673 | hp2 | a0003 | c0002 | t0001 | g0098 | EAS | CHS | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0260 | AMR | PUR | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG00738 | hp2 | a0001 | c0001 | t0004 | g0111 | AMR | PUR | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0258 | AMR | PUR | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG00741 | hp2 | a0001 | c0001 | t0004 | g0248 | AMR | PUR | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG01069 | hp1 | a0003 | c0002 | t0001 | g0070 | AMR | PUR | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG01069 | hp2 | a0001 | c0001 | t0026 | g0287 | AMR | PUR | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG01070 | hp1 | a0002 | c0003 | t0002 | g0307 | AMR | PUR | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG01070 | hp2 | a0001 | c0001 | t0004 | g0249 | AMR | PUR | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG01071 | hp1 | a0001 | c0001 | t0004 | g0003 | AMR | PUR | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG01071 | hp2 | a0003 | c0002 | t0001 | g0071 | AMR | PUR | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG01074 | hp1 | a0003 | c0002 | t0001 | g0141 | AMR | PUR | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG01074 | hp2 | a0006 | c0009 | t0003 | g0275 | AMR | PUR | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG01081 | hp1 | a0003 | c0002 | t0001 | g0084 | AMR | PUR | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG01081 | hp2 | a0001 | c0001 | t0047 | g0187 | AMR | PUR | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG01099 | hp1 | a0001 | c0001 | t0056 | g0273 | AMR | PUR | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG01099 | hp2 | a0002 | c0004 | t0008 | g0197 | AMR | PUR | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG01106 | hp1 | a0001 | c0001 | t0020 | g0021 | AMR | PUR | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG01106 | hp2 | a0003 | c0002 | t0001 | g0031 | AMR | PUR | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG01109 | hp1 | a0003 | c0002 | t0001 | g0225 | AMR | PUR | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG01109 | hp2 | a0002 | c0003 | t0014 | g0228 | AMR | PUR | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG01168 | hp1 | a0001 | c0001 | t0005 | g0246 | AMR | PUR | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0302 | AMR | PUR | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0301 | AMR | PUR | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG01169 | hp2 | a0003 | c0002 | t0015 | g0303 | AMR | PUR | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG01192 | hp1 | a0001 | c0001 | t0004 | g0151 | AMR | PUR | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG01192 | hp2 | a0003 | c0002 | t0001 | g0132 | AMR | PUR | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG01243 | hp1 | a0001 | c0001 | t0052 | g0311 | AMR | PUR | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG01243 | hp2 | a0005 | c0008 | t0006 | g0058 | AMR | PUR | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG01255 | hp1 | a0002 | c0003 | t0012 | g0146 | AMR | CLM | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG01255 | hp2 | a0001 | c0001 | t0004 | g0027 | AMR | CLM | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG01256 | hp1 | a0001 | c0001 | t0004 | g0110 | AMR | CLM | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG01256 | hp2 | a0003 | c0002 | t0001 | g0093 | AMR | CLM | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG01257 | hp1 | a0001 | c0001 | t0004 | g0305 | AMR | CLM | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG01257 | hp2 | a0001 | c0001 | t0025 | g0347 | AMR | CLM | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0057 | AMR | CLM | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG01258 | hp2 | a0001 | c0001 | t0004 | g0296 | AMR | CLM | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0211 | AMR | CLM | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG01261 | hp2 | a0001 | c0001 | t0007 | g0002 | AMR | CLM | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0014 | AMR | CLM | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG01346 | hp2 | a0002 | c0004 | t0008 | g0192 | AMR | CLM | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG01358 | hp1 | a0001 | c0001 | t0005 | g0035 | AMR | CLM | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG01358 | hp2 | a0001 | c0001 | t0007 | g0002 | AMR | CLM | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG01361 | hp1 | a0001 | c0001 | t0029 | g0221 | AMR | CLM | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG01361 | hp2 | a0001 | c0001 | t0004 | g0255 | AMR | CLM | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG01433 | hp1 | a0001 | c0001 | t0007 | g0060 | AMR | CLM | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG01433 | hp2 | a0006 | c0009 | t0003 | g0274 | AMR | CLM | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0304 | AMR | CLM | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG01496 | hp2 | a0003 | c0002 | t0001 | g0037 | AMR | CLM | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG01516 | hp1 | a0001 | c0001 | t0020 | g0250 | EUR | IBS | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG01516 | hp2 | a0001 | c0001 | t0004 | g0193 | EUR | IBS | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0283 | AFR | ACB | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG01884 | hp2 | a0002 | c0004 | t0048 | g0007 | AFR | ACB | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG01891 | hp1 | a0002 | c0003 | t0002 | g0105 | AFR | ACB | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG01891 | hp2 | a0002 | c0003 | t0012 | g0073 | AFR | ACB | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG01928 | hp1 | a0001 | c0001 | t0005 | g0219 | AMR | PEL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG01928 | hp2 | a0003 | c0002 | t0001 | g0131 | AMR | PEL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG01934 | hp1 | a0002 | c0003 | t0021 | g0332 | AMR | PEL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG01934 | hp2 | a0003 | c0002 | t0001 | g0065 | AMR | PEL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG01978 | hp1 | a0001 | c0001 | t0040 | g0183 | AMR | PEL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG01978 | hp2 | a0001 | c0001 | t0007 | g0026 | AMR | PEL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG01981 | hp1 | a0001 | c0001 | t0004 | g0240 | AMR | PEL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG01981 | hp2 | a0003 | c0002 | t0001 | g0127 | AMR | PEL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG02027 | hp1 | a0003 | c0002 | t0001 | g0039 | EAS | KHV | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG02027 | hp2 | a0003 | c0002 | t0001 | g0044 | EAS | KHV | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG02040 | hp1 | a0003 | c0002 | t0001 | g0216 | EAS | KHV | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG02040 | hp2 | a0001 | c0001 | t0004 | g0261 | EAS | KHV | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG02055 | hp1 | a0004 | c0005 | t0010 | g0076 | AFR | ACB | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG02055 | hp2 | a0006 | c0009 | t0003 | g0209 | AFR | ACB | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0269 | EAS | KHV | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG02074 | hp2 | a0003 | c0002 | t0001 | g0042 | EAS | KHV | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG02080 | hp1 | a0003 | c0002 | t0001 | g0030 | EAS | KHV | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG02080 | hp2 | a0002 | c0003 | t0002 | g0053 | EAS | KHV | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG02083 | hp1 | a0003 | c0010 | t0041 | g0129 | EAS | KHV | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0306 | EAS | KHV | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG02129 | hp1 | a0002 | c0003 | t0002 | g0056 | EAS | KHV | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG02129 | hp2 | a0003 | c0002 | t0001 | g0234 | EAS | KHV | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG02132 | hp1 | a0002 | c0003 | t0002 | g0189 | EAS | KHV | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG02132 | hp2 | a0002 | c0003 | t0002 | g0104 | EAS | KHV | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG02135 | hp1 | a0003 | c0002 | t0001 | g0040 | EAS | KHV | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG02135 | hp2 | a0002 | c0003 | t0002 | g0054 | EAS | KHV | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG02145 | hp1 | a0001 | c0001 | t0024 | g0346 | AFR | ACB | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG02145 | hp2 | a0001 | c0006 | t0011 | g0009 | AFR | ACB | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG02148 | hp1 | a0003 | c0002 | t0001 | g0023 | AMR | PEL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG02148 | hp2 | a0001 | c0001 | t0007 | g0025 | AMR | PEL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG02165 | hp1 | a0002 | c0003 | t0002 | g0299 | EAS | CDX | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG02165 | hp2 | a0002 | c0015 | t0002 | g0295 | EAS | CDX | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG02257 | hp1 | a0002 | c0004 | t0016 | g0343 | AFR | ACB | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0300 | AFR | ACB | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG02258 | hp1 | a0001 | c0001 | t0046 | g0318 | AFR | ACB | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0168 | AFR | ACB | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0281 | AFR | ACB | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0336 | AFR | ACB | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG02293 | hp1 | a0003 | c0002 | t0001 | g0068 | AMR | PEL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG02293 | hp2 | a0003 | c0002 | t0001 | g0101 | AMR | PEL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG02300 | hp1 | a0003 | c0002 | t0001 | g0134 | AMR | PEL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG02300 | hp2 | a0003 | c0002 | t0001 | g0308 | AMR | PEL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG02451 | hp1 | a0001 | c0001 | t0006 | g0161 | AFR | ACB | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG02451 | hp2 | a0002 | c0003 | t0013 | g0077 | AFR | ACB | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG02622 | hp1 | a0002 | c0003 | t0022 | g0107 | AFR | GWD | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG02622 | hp2 | a0002 | c0003 | t0014 | g0169 | AFR | GWD | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG02630 | hp1 | a0002 | c0003 | t0012 | g0048 | AFR | GWD | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG02630 | hp2 | a0002 | c0003 | t0055 | g0008 | AFR | GWD | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0174 | AFR | GWD | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG02647 | hp2 | a0002 | c0007 | t0009 | g0319 | AFR | GWD | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG02683 | hp1 | a0001 | c0001 | t0004 | g0003 | SAS | PJL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG02683 | hp2 | a0002 | c0003 | t0002 | g0312 | SAS | PJL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0238 | SAS | PJL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG02698 | hp2 | a0001 | c0001 | t0005 | g0016 | SAS | PJL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG02717 | hp1 | a0002 | c0003 | t0014 | g0226 | AFR | GWD | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG02717 | hp2 | a0002 | c0003 | t0013 | g0170 | AFR | GWD | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG02735 | hp1 | a0001 | c0001 | t0007 | g0239 | SAS | PJL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG02735 | hp2 | a0003 | c0002 | t0001 | g0120 | SAS | PJL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG02738 | hp1 | a0001 | c0001 | t0007 | g0217 | SAS | PJL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG02738 | hp2 | a0001 | c0001 | t0036 | g0029 | SAS | PJL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG02809 | hp1 | a0002 | c0007 | t0009 | g0205 | AFR | GWD | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG02809 | hp2 | a0001 | c0001 | t0018 | g0330 | AFR | GWD | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0333 | AFR | GWD | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG02818 | hp2 | a0002 | c0003 | t0022 | g0158 | AFR | GWD | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG02886 | hp1 | a0002 | c0004 | t0016 | g0335 | AFR | GWD | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG02886 | hp2 | a0002 | c0007 | t0009 | g0088 | AFR | GWD | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG02895 | hp1 | a0003 | c0002 | t0015 | g0172 | AFR | GWD | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG02895 | hp2 | a0001 | c0001 | t0006 | g0173 | AFR | GWD | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG02896 | hp1 | a0003 | c0002 | t0001 | g0140 | AFR | GWD | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG02896 | hp2 | a0001 | c0001 | t0006 | g0108 | AFR | GWD | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG02897 | hp1 | a0003 | c0002 | t0015 | g0139 | AFR | GWD | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG02897 | hp2 | a0003 | c0002 | t0001 | g0253 | AFR | GWD | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0322 | AFR | ESN | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG02922 | hp2 | a0002 | c0004 | t0019 | g0006 | AFR | ESN | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG02965 | hp1 | a0002 | c0003 | t0012 | g0074 | AFR | ESN | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG02965 | hp2 | a0004 | c0005 | t0010 | g0103 | AFR | ESN | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG02970 | hp1 | a0002 | c0003 | t0021 | g0342 | AFR | ESN | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG02970 | hp2 | a0002 | c0004 | t0016 | g0344 | AFR | ESN | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG02976 | hp1 | a0001 | c0006 | t0011 | g0010 | AFR | ESN | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG02976 | hp2 | a0002 | c0003 | t0053 | g0227 | AFR | ESN | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG03017 | hp1 | a0002 | c0004 | t0008 | g0324 | SAS | PJL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG03017 | hp2 | a0001 | c0001 | t0037 | g0055 | SAS | PJL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG03041 | hp1 | a0002 | c0004 | t0049 | g0224 | AFR | GWD | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG03041 | hp2 | a0011 | c0019 | t0003 | g0345 | AFR | GWD | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG03098 | hp1 | a0001 | c0001 | t0042 | g0018 | AFR | MSL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG03098 | hp2 | a0001 | c0001 | t0006 | g0162 | AFR | MSL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG03130 | hp1 | a0001 | c0001 | t0004 | g0176 | AFR | ESN | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG03130 | hp2 | a0001 | c0001 | t0027 | g0331 | AFR | ESN | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG03139 | hp1 | a0005 | c0008 | t0006 | g0213 | AFR | ESN | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0117 | AFR | ESN | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG03195 | hp1 | a0004 | c0005 | t0010 | g0334 | AFR | ESN | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG03195 | hp2 | a0001 | c0006 | t0011 | g0011 | AFR | ESN | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG03209 | hp1 | a0002 | c0003 | t0012 | g0254 | AFR | MSL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG03209 | hp2 | a0001 | c0001 | t0006 | g0263 | AFR | MSL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG03225 | hp1 | a0005 | c0008 | t0006 | g0090 | AFR | MSL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0257 | AFR | MSL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG03239 | hp1 | a0001 | c0001 | t0007 | g0045 | SAS | PJL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG03239 | hp2 | a0001 | c0001 | t0005 | g0222 | SAS | PJL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG03453 | hp1 | a0002 | c0004 | t0019 | g0005 | AFR | MSL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG03453 | hp2 | a0002 | c0003 | t0014 | g0150 | AFR | MSL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG03486 | hp1 | a0002 | c0007 | t0009 | g0148 | AFR | MSL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG03486 | hp2 | a0001 | c0006 | t0011 | g0013 | AFR | MSL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG03490 | hp1 | a0001 | c0001 | t0004 | g0264 | SAS | PJL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG03490 | hp2 | a0003 | c0002 | t0001 | g0094 | SAS | PJL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG03491 | hp1 | a0001 | c0001 | t0005 | g0326 | SAS | PJL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG03491 | hp2 | a0001 | c0001 | t0004 | g0247 | SAS | PJL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG03492 | hp1 | a0003 | c0002 | t0001 | g0061 | SAS | PJL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG03492 | hp2 | a0001 | c0001 | t0005 | g0327 | SAS | PJL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG03516 | hp1 | a0001 | c0001 | t0006 | g0113 | AFR | ESN | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG03516 | hp2 | a0002 | c0004 | t0057 | g0198 | AFR | ESN | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG03540 | hp1 | a0002 | c0003 | t0013 | g0092 | AFR | GWD | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG03540 | hp2 | a0001 | c0001 | t0039 | g0288 | AFR | GWD | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG03579 | hp1 | a0005 | c0008 | t0006 | g0320 | AFR | MSL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG03579 | hp2 | a0001 | c0001 | t0038 | g0049 | AFR | MSL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG03654 | hp1 | a0001 | c0001 | t0005 | g0328 | SAS | PJL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG03654 | hp2 | a0001 | c0001 | t0004 | g0271 | SAS | PJL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG03669 | hp1 | a0003 | c0002 | t0001 | g0137 | SAS | PJL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG03669 | hp2 | a0001 | c0013 | t0004 | g0136 | SAS | PJL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG03688 | hp1 | a0003 | c0002 | t0001 | g0184 | SAS | STU | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG03688 | hp2 | a0001 | c0001 | t0005 | g0181 | SAS | STU | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG03704 | hp1 | a0003 | c0002 | t0001 | g0064 | SAS | PJL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG03704 | hp2 | a0001 | c0001 | t0007 | g0143 | SAS | PJL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG03710 | hp1 | a0001 | c0001 | t0025 | g0349 | SAS | PJL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG03710 | hp2 | a0001 | c0001 | t0024 | g0348 | SAS | PJL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG03831 | hp1 | a0001 | c0001 | t0007 | g0142 | SAS | BEB | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0210 | SAS | BEB | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG03834 | hp1 | a0001 | c0001 | t0035 | g0215 | SAS | BEB | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG03834 | hp2 | a0001 | c0001 | t0005 | g0243 | SAS | BEB | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG03927 | hp1 | a0003 | c0002 | t0017 | g0180 | SAS | BEB | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG03927 | hp2 | a0001 | c0001 | t0033 | g0085 | SAS | BEB | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG04115 | hp1 | a0001 | c0001 | t0007 | g0124 | SAS | STU | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0175 | SAS | STU | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG04199 | hp1 | a0001 | c0001 | t0004 | g0059 | SAS | STU | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG04199 | hp2 | a0003 | c0002 | t0001 | g0179 | SAS | STU | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA18522 | hp1 | a0001 | c0001 | t0006 | g0160 | AFR | YRI | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA18522 | hp2 | a0002 | c0003 | t0013 | g0028 | AFR | YRI | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA18747 | hp1 | a0002 | c0003 | t0002 | g0153 | EAS | CHB | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA18747 | hp2 | a0003 | c0002 | t0001 | g0097 | EAS | CHB | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0149 | AFR | YRI | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA18906 | hp2 | a0005 | c0008 | t0006 | g0116 | AFR | YRI | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA18941 | hp1 | a0003 | c0002 | t0001 | g0231 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA18941 | hp2 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA18943 | hp1 | a0002 | c0003 | t0002 | g0196 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA18943 | hp2 | a0001 | c0001 | t0005 | g0188 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA18945 | hp1 | a0002 | c0003 | t0002 | g0082 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA18945 | hp2 | a0003 | c0002 | t0001 | g0121 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA18946 | hp1 | a0002 | c0004 | t0008 | g0091 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA18946 | hp2 | a0002 | c0003 | t0002 | g0200 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA18947 | hp1 | a0001 | c0001 | t0045 | g0185 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA18947 | hp2 | a0002 | c0004 | t0008 | g0323 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA18948 | hp1 | a0003 | c0002 | t0001 | g0041 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA18948 | hp2 | a0002 | c0003 | t0002 | g0256 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA18949 | hp1 | a0001 | c0001 | t0003 | g0289 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA18949 | hp2 | a0003 | c0002 | t0001 | g0126 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA18950 | hp1 | a0002 | c0003 | t0002 | g0201 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA18950 | hp2 | a0002 | c0003 | t0002 | g0106 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA18956 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA18956 | hp2 | a0003 | c0002 | t0001 | g0015 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA18957 | hp1 | a0003 | c0002 | t0001 | g0207 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0285 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA18959 | hp1 | a0001 | c0001 | t0003 | g0266 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA18959 | hp2 | a0002 | c0003 | t0002 | g0293 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA18961 | hp1 | a0002 | c0003 | t0002 | g0087 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA18961 | hp2 | a0003 | c0002 | t0001 | g0128 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0276 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA18962 | hp2 | a0003 | c0002 | t0001 | g0079 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA18964 | hp1 | a0003 | c0002 | t0001 | g0171 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA18964 | hp2 | a0002 | c0003 | t0002 | g0081 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0267 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA18970 | hp2 | a0003 | c0002 | t0001 | g0133 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA18971 | hp1 | a0003 | c0002 | t0001 | g0135 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA18971 | hp2 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA18973 | hp1 | a0002 | c0003 | t0002 | g0083 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA18973 | hp2 | a0003 | c0002 | t0001 | g0236 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA18974 | hp1 | a0002 | c0003 | t0002 | g0339 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA18974 | hp2 | a0003 | c0002 | t0001 | g0050 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA18975 | hp1 | a0002 | c0003 | t0002 | g0286 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA18975 | hp2 | a0003 | c0002 | t0001 | g0232 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA18977 | hp1 | a0003 | c0002 | t0001 | g0022 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA18977 | hp2 | a0002 | c0003 | t0002 | g0165 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA18978 | hp1 | a0002 | c0003 | t0002 | g0204 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA18978 | hp2 | a0003 | c0002 | t0001 | g0252 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA18980 | hp1 | a0003 | c0002 | t0001 | g0036 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA18980 | hp2 | a0002 | c0003 | t0002 | g0313 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA18982 | hp1 | a0002 | c0003 | t0031 | g0166 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA18982 | hp2 | a0002 | c0003 | t0002 | g0317 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA18984 | hp1 | a0003 | c0002 | t0001 | g0235 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA18984 | hp2 | a0010 | c0017 | t0002 | g0278 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA18989 | hp1 | a0001 | c0001 | t0028 | g0212 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA18989 | hp2 | a0003 | c0002 | t0001 | g0080 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA18990 | hp1 | a0002 | c0003 | t0002 | g0099 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA18990 | hp2 | a0001 | c0001 | t0004 | g0118 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA18992 | hp1 | a0002 | c0003 | t0002 | g0052 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA18992 | hp2 | a0003 | c0002 | t0001 | g0233 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA18993 | hp1 | a0003 | c0002 | t0023 | g0004 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA18993 | hp2 | a0001 | c0001 | t0003 | g0268 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA18995 | hp1 | a0002 | c0003 | t0002 | g0202 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0203 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA19000 | hp1 | a0003 | c0002 | t0001 | g0095 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA19000 | hp2 | a0002 | c0003 | t0002 | g0155 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA19001 | hp1 | a0003 | c0002 | t0001 | g0032 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA19001 | hp2 | a0002 | c0003 | t0002 | g0145 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA19002 | hp1 | a0003 | c0002 | t0023 | g0004 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA19002 | hp2 | a0002 | c0003 | t0002 | g0341 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA19004 | hp1 | a0002 | c0003 | t0002 | g0186 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA19004 | hp2 | a0003 | c0002 | t0001 | g0122 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA19005 | hp1 | a0003 | c0011 | t0001 | g0125 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA19005 | hp2 | a0002 | c0003 | t0002 | g0315 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA19006 | hp1 | a0003 | c0002 | t0001 | g0230 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA19006 | hp2 | a0002 | c0003 | t0002 | g0340 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA19007 | hp1 | a0001 | c0001 | t0005 | g0245 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA19007 | hp2 | a0002 | c0003 | t0002 | g0194 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA19009 | hp1 | a0003 | c0002 | t0001 | g0119 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA19009 | hp2 | a0002 | c0003 | t0002 | g0164 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA19010 | hp1 | a0002 | c0003 | t0002 | g0152 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0284 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA19011 | hp1 | a0002 | c0003 | t0002 | g0062 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA19011 | hp2 | a0003 | c0002 | t0001 | g0096 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA19012 | hp1 | a0002 | c0003 | t0002 | g0337 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA19012 | hp2 | a0003 | c0002 | t0001 | g0017 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA19030 | hp1 | a0001 | c0001 | t0034 | g0109 | AFR | LWK | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA19030 | hp2 | a0001 | c0001 | t0006 | g0112 | AFR | LWK | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA19054 | hp1 | a0001 | c0001 | t0003 | g0338 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA19054 | hp2 | a0002 | c0003 | t0002 | g0262 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA19056 | hp1 | a0002 | c0003 | t0002 | g0178 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA19056 | hp2 | a0003 | c0002 | t0001 | g0223 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA19057 | hp1 | a0002 | c0003 | t0002 | g0051 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA19057 | hp2 | a0003 | c0002 | t0001 | g0072 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA19063 | hp1 | a0002 | c0003 | t0002 | g0251 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA19063 | hp2 | a0001 | c0001 | t0005 | g0047 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA19064 | hp1 | a0001 | c0001 | t0005 | g0244 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA19064 | hp2 | a0002 | c0003 | t0002 | g0130 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA19065 | hp1 | a0003 | c0002 | t0001 | g0038 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA19065 | hp2 | a0003 | c0002 | t0001 | g0291 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA19066 | hp1 | a0002 | c0003 | t0002 | g0199 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA19066 | hp2 | a0009 | c0016 | t0002 | g0270 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA19067 | hp1 | a0002 | c0003 | t0030 | g0157 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA19067 | hp2 | a0003 | c0002 | t0001 | g0024 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA19068 | hp1 | a0002 | c0003 | t0002 | g0086 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA19068 | hp2 | a0003 | c0002 | t0001 | g0123 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA19075 | hp1 | a0003 | c0002 | t0001 | g0066 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA19075 | hp2 | a0002 | c0003 | t0002 | g0115 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA19079 | hp1 | a0001 | c0001 | t0044 | g0242 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA19079 | hp2 | a0003 | c0002 | t0001 | g0156 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA19084 | hp1 | a0002 | c0003 | t0002 | g0316 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA19084 | hp2 | a0003 | c0002 | t0001 | g0290 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA19085 | hp1 | a0002 | c0003 | t0002 | g0078 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA19085 | hp2 | a0003 | c0002 | t0001 | g0067 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA19086 | hp1 | a0002 | c0003 | t0002 | g0154 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA19086 | hp2 | a0003 | c0002 | t0017 | g0208 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA19087 | hp1 | a0002 | c0003 | t0002 | g0294 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA19087 | hp2 | a0003 | c0002 | t0001 | g0033 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA19088 | hp1 | a0003 | c0002 | t0001 | g0229 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA19088 | hp2 | a0002 | c0003 | t0002 | g0214 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA19090 | hp1 | a0007 | c0018 | t0003 | g0265 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA19090 | hp2 | a0003 | c0002 | t0001 | g0069 | EAS | JPT | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0282 | AFR | YRI | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA19240 | hp2 | a0002 | c0003 | t0013 | g0325 | AFR | YRI | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA20129 | hp1 | a0001 | c0006 | t0011 | g0147 | AFR | ASW | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA20129 | hp2 | a0002 | c0007 | t0009 | g0167 | AFR | ASW | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA20752 | hp1 | a0003 | c0002 | t0001 | g0309 | EUR | TSI | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA20752 | hp2 | a0006 | c0009 | t0003 | g0279 | EUR | TSI | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0237 | EUR | TSI | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA20805 | hp2 | a0001 | c0001 | t0005 | g0191 | EUR | TSI | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA20905 | hp1 | a0001 | c0001 | t0043 | g0144 | SAS | GIH | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA20905 | hp2 | a0001 | c0001 | t0004 | g0292 | SAS | GIH | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG01123 | hp1 | a0003 | c0002 | t0001 | g0043 | AMR | CLM | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG01123 | hp2 | a0001 | c0001 | t0004 | g0190 | AMR | CLM | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG02109 | hp1 | a0002 | c0007 | t0009 | g0089 | AFR | ACB | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG02109 | hp2 | a0002 | c0004 | t0051 | g0019 | AFR | ACB | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG02486 | hp1 | a0008 | c0014 | t0018 | g0329 | AFR | ACB | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0163 | AFR | ACB | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG02559 | hp1 | a0004 | c0005 | t0010 | g0102 | AFR | ACB | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG02559 | hp2 | a0002 | c0004 | t0050 | g0321 | AFR | ACB | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG03471 | hp1 | a0002 | c0003 | t0054 | g0020 | AFR | MSL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG03471 | hp2 | a0004 | c0005 | t0010 | g0218 | AFR | MSL | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG06807 | hp1 | a0001 | c0001 | t0006 | g0114 | AFR | USA | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| HG06807 | hp2 | a0003 | c0002 | t0001 | g0138 | AFR | USA | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA20300 | hp1 | a0002 | c0003 | t0002 | g0272 | AFR | USA | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA20300 | hp2 | a0001 | c0006 | t0011 | g0012 | AFR | USA | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA21309 | hp1 | a0001 | c0001 | t0004 | g0298 | AFR | LWK | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| NA21309 | hp2 | a0004 | c0005 | t0010 | g0075 | AFR | LWK | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0004 | g0159 | REF | REF | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| homoSapiens_grch38 | hp1 | a0002 | c0003 | t0002 | g0280 | REF | REF | IL17RD_chr3_57084982_57170353 | IL17RD | chr3 | 57084982 | 57170353 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:57097731
|
T | C | 1 | a0009 | 1 | NA19066.hp2 | missense_variant | MODERATE | c.1972A>G | p.Met658Val | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 12/13 | 2039/8698 | 1972/2220 | 658/739 | chr3 | 57097731 | ||
| chr3:57097779
|
C | G | 1 | a0004 | 6 | HG02055.hp1 HG02559.hp1 HG02965.hp2 others(3): Show |
missense_variant | MODERATE | c.1924G>C | p.Ala642Pro | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 12/13 | 1991/8698 | 1924/2220 | 642/739 | chr3 | 57097779 | ||
| chr3:57098006
|
G | A | 1 | a0005 | 5 | HG01243.hp2 HG03139.hp1 HG03225.hp1 others(2): Show |
missense_variant | MODERATE | c.1697C>T | p.Pro566Leu | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 12/13 | 1764/8698 | 1697/2220 | 566/739 | chr3 | 57098006 | ||
| chr3:57098007
|
G | A | 1 | a0006 | 4 | HG01074.hp2 HG01433.hp2 HG02055.hp2 others(1): Show |
missense_variant | MODERATE | c.1696C>T | p.Pro566Ser | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 12/13 | 1763/8698 | 1696/2220 | 566/739 | chr3 | 57098007 | ||
| chr3:57101356
|
T | C | 1 | a0010 | 1 | NA18984.hp2 | missense_variant | MODERATE | c.987A>G | p.Ile329Met | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 11/13 | 1054/8698 | 987/2220 | 329/739 | chr3 | 57101356 | ||
| chr3:57102557
|
C | T | 1 | a0003 | 90 | HG00558.hp1 HG00639.hp2 HG00642.hp1 others(87): Show |
missense_variant | MODERATE | c.901G>A | p.Val301Met | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 10/13 | 968/8698 | 901/2220 | 301/739 | chr3 | 57102557 | ||
| chr3:57102580
|
G | A | 1 | a0008 | 1 | HG02486.hp1 | missense_variant | MODERATE | c.878C>T | p.Pro293Leu | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 10/13 | 945/8698 | 878/2220 | 293/739 | chr3 | 57102580 | ||
| chr3:57104391
|
G | A | 7 | a0001a0004a0005others(4): Show | 155 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(152): Show |
missense_variant | MODERATE | c.764C>T | p.Thr255Met | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 8/13 | 831/8698 | 764/2220 | 255/739 | chr3 | 57104391 | ||
| chr3:57110263
|
G | A | 1 | a0007 | 1 | NA19090.hp1 | missense_variant | MODERATE | c.359C>T | p.Ser120Leu | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 4/13 | 426/8698 | 359/2220 | 120/739 | chr3 | 57110263 | ||
| chr3:57165283
|
C | A | 1 | a0011 | 1 | HG03041.hp2 | missense_variant | MODERATE | c.4G>T | p.Ala2Ser | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/13 | 71/8698 | 4/2220 | 2/739 | chr3 | 57165283 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:57096486
|
G | A | 1 | a0002c0015 | 1 | HG02165.hp2 | synonymous_variant | LOW | c.2127C>T | p.Ala709Ala | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 2194/8698 | 2127/2220 | 709/739 | chr3 | 57096486 | ||
| chr3:57097879
|
A | G | 1 | a0001c0013 | 1 | HG03669.hp2 | synonymous_variant | LOW | c.1824T>C | p.Ala608Ala | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 12/13 | 1891/8698 | 1824/2220 | 608/739 | chr3 | 57097879 | ||
| chr3:57098047
|
A | G | 1 | a0003c0010 | 1 | HG02083.hp1 | synonymous_variant | LOW | c.1656T>C | p.Phe552Phe | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 12/13 | 1723/8698 | 1656/2220 | 552/739 | chr3 | 57098047 | ||
| chr3:57098119
|
G | C | 1 | a0001c0006 | 6 | HG02145.hp2 HG02976.hp1 HG03195.hp2 others(3): Show |
synonymous_variant | LOW | c.1584C>G | p.Gly528Gly | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 12/13 | 1651/8698 | 1584/2220 | 528/739 | chr3 | 57098119 | ||
| chr3:57098158
|
G | A | 1 | a0002c0007 | 6 | HG02109.hp1 HG02647.hp2 HG02809.hp1 others(3): Show |
synonymous_variant | LOW | c.1545C>T | p.Asp515Asp | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 12/13 | 1612/8698 | 1545/2220 | 515/739 | chr3 | 57098158 | ||
| chr3:57098172
|
A | G | 13 | a0001c0001a0001c0006a0001c0013others(10): Show | 246 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(243): Show |
synonymous_variant | LOW | c.1531T>C | p.Leu511Leu | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 12/13 | 1598/8698 | 1531/2220 | 511/739 | chr3 | 57098172 | ||
| chr3:57098320
|
G | A | 1 | a0003c0011 | 1 | NA19005.hp1 | synonymous_variant | LOW | c.1383C>T | p.Leu461Leu | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 12/13 | 1450/8698 | 1383/2220 | 461/739 | chr3 | 57098320 | ||
| chr3:57105944
|
A | G | 14 | a0001c0001a0001c0006a0001c0013others(11): Show | 263 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(260): Show |
synonymous_variant | LOW | c.660T>C | p.His220His | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/13 | 727/8698 | 660/2220 | 220/739 | chr3 | 57105944 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:57090092
|
C | A | 1 | a0001c0001t0045 | 1 | NA18947.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6301G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 6301 | chr3 | 57090092 | |||||
| chr3:57090168
|
C | G | 1 | a0002c0004t0019 | 2 | HG02922.hp2 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6225G>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 6225 | chr3 | 57090168 | |||||
| chr3:57090245
|
C | T | 1 | a0001c0001t0039 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6148G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 6148 | chr3 | 57090245 | |||||
| chr3:57090333
|
A | G | 1 | a0002c0003t0012 | 5 | HG01255.hp1 HG01891.hp2 HG02630.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*6060T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 6060 | chr3 | 57090333 | |||||
| chr3:57090427
|
C | A | 1 | a0001c0006t0011 | 6 | HG02145.hp2 HG02976.hp1 HG03195.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5966G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 5966 | chr3 | 57090427 | |||||
| chr3:57090466
|
C | T | 1 | a0003c0002t0017 | 2 | HG03927.hp1 NA19086.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5927G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 5927 | chr3 | 57090466 | |||||
| chr3:57090490
|
C | T | 28 | a0001c0001t0003a0001c0001t0004a0001c0001t0007others(25): Show | 117 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(114): Show |
3_prime_UTR_variant | MODIFIER | c.*5903G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 5903 | chr3 | 57090490 | |||||
| chr3:57090531
|
G | A | 2 | a0001c0001t0046a0002c0003t0012 | 6 | HG01255.hp1 HG01891.hp2 HG02258.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5862C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 5862 | chr3 | 57090531 | |||||
| chr3:57090563
|
G | A | 28 | a0001c0001t0003a0001c0001t0004a0001c0001t0007others(25): Show | 117 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(114): Show |
3_prime_UTR_variant | MODIFIER | c.*5830C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 5830 | chr3 | 57090563 | |||||
| chr3:57090564
|
C | G | 1 | a0003c0010t0041 | 1 | HG02083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5829G>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 5829 | chr3 | 57090564 | |||||
| chr3:57090613
|
C | T | 1 | a0001c0001t0034 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5780G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 5780 | chr3 | 57090613 | |||||
| chr3:57090791
|
G | C | 1 | a0001c0006t0011 | 6 | HG02145.hp2 HG02976.hp1 HG03195.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5602C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 5602 | chr3 | 57090791 | |||||
| chr3:57090848
|
T | C | 1 | a0001c0001t0036 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5545A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 5545 | chr3 | 57090848 | |||||
| chr3:57091040
|
G | T | 3 | a0002c0004t0019a0002c0004t0049a0002c0004t0051 | 4 | HG02109.hp2 HG02922.hp2 HG03041.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5353C>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 5353 | chr3 | 57091040 | |||||
| chr3:57091073
|
A | C | 8 | a0001c0001t0037a0002c0004t0057a0003c0002t0001others(5): Show | 92 | HG00558.hp1 HG00639.hp2 HG00642.hp1 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*5320T>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 5320 | chr3 | 57091073 | |||||
| chr3:57091174
|
T | G | 14 | a0001c0001t0037a0002c0004t0008a0002c0004t0016others(11): Show | 107 | HG00099.hp1 HG00558.hp1 HG00639.hp1 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*5219A>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 5219 | chr3 | 57091174 | |||||
| chr3:57091178
|
A | G | 1 | a0001c0006t0011 | 6 | HG02145.hp2 HG02976.hp1 HG03195.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5215T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 5215 | chr3 | 57091178 | |||||
| chr3:57091252
|
G | A | 2 | a0002c0004t0019a0002c0004t0051 | 3 | HG02109.hp2 HG02922.hp2 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5141C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 5141 | chr3 | 57091252 | |||||
| chr3:57091352
|
C | T | 60 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(57): Show | 289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
3_prime_UTR_variant | MODIFIER | c.*5041G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 5041 | chr3 | 57091352 | |||||
| chr3:57091368
|
A | G | 1 | a0002c0003t0022 | 2 | HG02622.hp1 HG02818.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5025T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 5025 | chr3 | 57091368 | |||||
| chr3:57091371
|
GA | G | 2 | a0002c0003t0014a0002c0003t0053 | 5 | HG01109.hp2 HG02622.hp2 HG02717.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5021delT | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 5021 | chr3 | 57091371 | |||||
| chr3:57091396
|
G | A | 14 | a0001c0001t0037a0002c0004t0008a0002c0004t0016others(11): Show | 107 | HG00099.hp1 HG00558.hp1 HG00639.hp1 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*4997C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 4997 | chr3 | 57091396 | |||||
| chr3:57091402
|
G | A | 1 | a0001c0001t0038 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4991C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 4991 | chr3 | 57091402 | |||||
| chr3:57091493
|
G | A | 2 | a0002c0003t0022a0002c0003t0055 | 3 | HG02622.hp1 HG02630.hp2 HG02818.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4900C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 4900 | chr3 | 57091493 | |||||
| chr3:57091699
|
T | A | 17 | a0001c0001t0003a0001c0001t0006a0001c0001t0018others(14): Show | 72 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*4694A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 4694 | chr3 | 57091699 | |||||
| chr3:57091836
|
A | G | 6 | a0003c0002t0001a0003c0002t0015a0003c0002t0017others(3): Show | 90 | HG00558.hp1 HG00639.hp2 HG00642.hp1 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*4557T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 4557 | chr3 | 57091836 | |||||
| chr3:57092029
|
C | T | 1 | a0001c0001t0044 | 1 | NA19079.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4364G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 4364 | chr3 | 57092029 | |||||
| chr3:57092117
|
C | T | 1 | a0002c0003t0053 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4276G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 4276 | chr3 | 57092117 | |||||
| chr3:57092255
|
C | A | 1 | a0001c0001t0047 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4138G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 4138 | chr3 | 57092255 | |||||
| chr3:57092315
|
G | A | 1 | a0002c0004t0016 | 3 | HG02257.hp1 HG02886.hp1 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4078C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 4078 | chr3 | 57092315 | |||||
| chr3:57092333
|
A | T | 2 | a0002c0004t0048a0004c0005t0010 | 7 | HG01884.hp2 HG02055.hp1 HG02559.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4060T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 4060 | chr3 | 57092333 | |||||
| chr3:57092398
|
C | T | 1 | a0002c0004t0008 | 7 | HG00099.hp1 HG00639.hp1 HG01099.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3995G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 3995 | chr3 | 57092398 | |||||
| chr3:57092462
|
G | GC | 6 | a0002c0003t0032a0003c0002t0001a0003c0002t0017others(3): Show | 88 | HG00558.hp1 HG00558.hp2 HG00639.hp2 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*3930dupG | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 3930 | chr3 | 57092462 | |||||
| chr3:57092588
|
CA | C | 39 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(36): Show | 158 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*3804delT | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 3804 | chr3 | 57092588 | |||||
| chr3:57092753
|
G | T | 1 | a0001c0001t0033 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3640C>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 3640 | chr3 | 57092753 | |||||
| chr3:57092822
|
G | A | 1 | a0001c0001t0042 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3571C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 3571 | chr3 | 57092822 | |||||
| chr3:57093053
|
C | T | 1 | a0001c0001t0043 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3340G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 3340 | chr3 | 57093053 | |||||
| chr3:57093220
|
G | A | 3 | a0002c0003t0014a0002c0003t0053a0002c0003t0054 | 6 | HG01109.hp2 HG02622.hp2 HG02717.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3173C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 3173 | chr3 | 57093220 | |||||
| chr3:57093273
|
T | C | 1 | a0001c0001t0027 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3120A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 3120 | chr3 | 57093273 | |||||
| chr3:57093326
|
T | C | 2 | a0001c0001t0018a0008c0014t0018 | 2 | HG02486.hp1 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3067A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 3067 | chr3 | 57093326 | |||||
| chr3:57093428
|
A | T | 7 | a0002c0004t0016a0002c0004t0019a0002c0004t0048others(4): Show | 10 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2965T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 2965 | chr3 | 57093428 | |||||
| chr3:57093463
|
G | A | 2 | a0001c0001t0018a0008c0014t0018 | 2 | HG02486.hp1 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2930C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 2930 | chr3 | 57093463 | |||||
| chr3:57093541
|
A | G | 1 | a0002c0003t0030 | 1 | NA19067.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2852T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 2852 | chr3 | 57093541 | |||||
| chr3:57093963
|
G | A | 51 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(48): Show | 262 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(259): Show |
3_prime_UTR_variant | MODIFIER | c.*2430C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 2430 | chr3 | 57093963 | |||||
| chr3:57094183
|
G | A | 9 | a0001c0001t0005a0001c0001t0007a0001c0001t0028others(6): Show | 37 | HG00280.hp2 HG01081.hp2 HG01168.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*2210C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 2210 | chr3 | 57094183 | |||||
| chr3:57094186
|
T | C | 8 | a0002c0004t0008a0002c0004t0016a0002c0004t0019others(5): Show | 17 | HG00099.hp1 HG00639.hp1 HG01099.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*2207A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 2207 | chr3 | 57094186 | |||||
| chr3:57094231
|
T | G | 1 | a0001c0001t0052 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2162A>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 2162 | chr3 | 57094231 | |||||
| chr3:57094273
|
C | T | 1 | a0001c0001t0029 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2120G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 2120 | chr3 | 57094273 | |||||
| chr3:57094385
|
G | A | 1 | a0002c0004t0057 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2008C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 2008 | chr3 | 57094385 | |||||
| chr3:57094482
|
T | C | 3 | a0002c0003t0014a0002c0003t0053a0002c0003t0054 | 6 | HG01109.hp2 HG02622.hp2 HG02717.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1911A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 1911 | chr3 | 57094482 | |||||
| chr3:57094652
|
G | A | 1 | a0002c0003t0012 | 5 | HG01255.hp1 HG01891.hp2 HG02630.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1741C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 1741 | chr3 | 57094652 | |||||
| chr3:57094751
|
G | A | 3 | a0002c0003t0014a0002c0003t0053a0002c0003t0054 | 6 | HG01109.hp2 HG02622.hp2 HG02717.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1642C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 1642 | chr3 | 57094751 | |||||
| chr3:57094813
|
T | C | 1 | a0001c0001t0020 | 2 | HG01106.hp1 HG01516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1580A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 1580 | chr3 | 57094813 | |||||
| chr3:57094833
|
C | T | 1 | a0001c0001t0028 | 1 | NA18989.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1560G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 1560 | chr3 | 57094833 | |||||
| chr3:57094974
|
G | T | 1 | a0001c0001t0027 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1419C>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 1419 | chr3 | 57094974 | |||||
| chr3:57095121
|
C | A | 4 | a0002c0003t0013a0002c0003t0021a0002c0003t0022others(1): Show | 10 | HG01934.hp1 HG02451.hp2 HG02622.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1272G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 1272 | chr3 | 57095121 | |||||
| chr3:57095142
|
C | T | 1 | a0001c0001t0026 | 1 | HG01069.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1251G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 1251 | chr3 | 57095142 | |||||
| chr3:57095681
|
T | A | 1 | a0001c0001t0056 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*712A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 712 | chr3 | 57095681 | |||||
| chr3:57095810
|
T | C | 1 | a0002c0004t0008 | 7 | HG00099.hp1 HG00639.hp1 HG01099.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*583A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 583 | chr3 | 57095810 | |||||
| chr3:57096238
|
T | C | 1 | a0002c0004t0057 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*155A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 13/13 | 155 | chr3 | 57096238 | |||||
| chr3:57165312
|
G | A | 1 | a0003c0002t0023 | 2 | NA18993.hp1 NA19002.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-26C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/13 | chr3 | 57165312 | ||||||
| chr3:57165322
|
C | A | 2 | a0001c0001t0024a0001c0001t0025 | 4 | HG01257.hp2 HG02145.hp1 HG03710.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-36G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/13 | 36 | chr3 | 57165322 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:57096615
|
TA | T | 97 | a0001c0001t0004g0257a0001c0001t0038g0049a0001c0006t0011g0009others(94): Show | 98 | HG00558.hp1 HG00639.hp2 HG00642.hp1 others(95): Show |
intron_variant | MODIFIER | c.2108-111delT | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 12/12 | chr3 | 57096615 | ||||||
| chr3:57096631
|
C | T | 9 | a0002c0004t0016g0335a0002c0004t0016g0343a0002c0004t0016g0344others(6): Show | 9 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.2108-126G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 12/12 | chr3 | 57096631 | ||||||
| chr3:57096633
|
C | T | 5 | a0002c0003t0014g0150a0002c0003t0014g0169a0002c0003t0014g0226others(2): Show | 5 | HG01109.hp2 HG02622.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.2108-128G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 12/12 | chr3 | 57096633 | ||||||
| chr3:57096717
|
T | A | 1 | a0002c0003t0031g0166 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2108-212A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 12/12 | chr3 | 57096717 | ||||||
| chr3:57096860
|
A | C | 4 | a0002c0004t0008g0177a0002c0004t0008g0192a0002c0004t0008g0197others(1): Show | 4 | HG00099.hp1 HG00639.hp1 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.2108-355T>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 12/12 | chr3 | 57096860 | ||||||
| chr3:57096953
|
T | G | 89 | a0003c0002t0001g0015a0003c0002t0001g0017a0003c0002t0001g0022others(86): Show | 90 | HG00558.hp1 HG00639.hp2 HG00642.hp1 others(87): Show |
intron_variant | MODIFIER | c.2108-448A>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 12/12 | chr3 | 57096953 | ||||||
| chr3:57097004
|
C | CA | 11 | a0001c0001t0003g0266a0001c0001t0018g0330a0002c0003t0002g0034others(8): Show | 11 | HG00673.hp1 HG02109.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.2108-500dupT | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 12/12 | chr3 | 57097004 | ||||||
| chr3:57097004
|
CA | C | 104 | a0001c0001t0003g0302a0001c0001t0004g0257a0001c0001t0037g0055others(101): Show | 105 | HG00558.hp1 HG00642.hp1 HG00673.hp2 others(102): Show |
intron_variant | MODIFIER | c.2108-500delT | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 12/12 | chr3 | 57097004 | ||||||
| chr3:57097083
|
G | A | 17 | a0002c0004t0008g0091a0002c0004t0008g0177a0002c0004t0008g0192others(14): Show | 17 | HG00099.hp1 HG00639.hp1 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.2107+513C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 12/12 | chr3 | 57097083 | ||||||
| chr3:57097193
|
A | G | 1 | a0001c0001t0042g0018 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2107+403T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 12/12 | chr3 | 57097193 | ||||||
| chr3:57097365
|
C | A | 1 | a0002c0003t0012g0146 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2107+231G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 12/12 | chr3 | 57097365 | ||||||
| chr3:57097372
|
A | G | 1 | a0002c0003t0012g0074 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2107+224T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 12/12 | chr3 | 57097372 | ||||||
| chr3:57097501
|
A | C | 184 | a0001c0001t0003g0014a0001c0001t0003g0057a0001c0001t0003g0117others(181): Show | 188 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.2107+95T>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 12/12 | chr3 | 57097501 | ||||||
| chr3:57098666
|
A | G | 1 | a0002c0003t0021g0342 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1165-128T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 11/12 | chr3 | 57098666 | ||||||
| chr3:57098667
|
T | C | 2 | a0001c0001t0004g0118a0001c0001t0040g0183 | 2 | HG01978.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.1165-129A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 11/12 | chr3 | 57098667 | ||||||
| chr3:57098712
|
C | G | 1 | a0002c0004t0057g0198 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1165-174G>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 11/12 | chr3 | 57098712 | ||||||
| chr3:57099110
|
G | A | 151 | a0001c0001t0003g0014a0001c0001t0003g0057a0001c0001t0003g0117others(148): Show | 155 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.1165-572C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 11/12 | chr3 | 57099110 | ||||||
| chr3:57099117
|
T | C | 1 | a0002c0003t0031g0166 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1165-579A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 11/12 | chr3 | 57099117 | ||||||
| chr3:57099295
|
C | G | 1 | a0003c0002t0001g0068 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1165-757G>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 11/12 | chr3 | 57099295 | ||||||
| chr3:57099661
|
A | G | 5 | a0002c0003t0012g0048a0002c0003t0012g0073a0002c0003t0012g0074others(2): Show | 5 | HG01255.hp1 HG01891.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1165-1123T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 11/12 | chr3 | 57099661 | ||||||
| chr3:57099749
|
A | C | 1 | a0003c0002t0001g0309 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1165-1211T>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 11/12 | chr3 | 57099749 | ||||||
| chr3:57099922
|
C | T | 5 | a0002c0007t0009g0088a0002c0007t0009g0089a0002c0007t0009g0167others(2): Show | 5 | HG02109.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1164+1257G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 11/12 | chr3 | 57099922 | ||||||
| chr3:57100087
|
A | G | 242 | a0001c0001t0003g0014a0001c0001t0003g0057a0001c0001t0003g0117others(239): Show | 247 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.1164+1092T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 11/12 | chr3 | 57100087 | ||||||
| chr3:57100114
|
G | C | 3 | a0003c0002t0001g0041a0003c0002t0001g0065a0003c0002t0001g0101 | 3 | HG01934.hp2 HG02293.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.1164+1065C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 11/12 | chr3 | 57100114 | ||||||
| chr3:57100202
|
T | C | 262 | a0001c0001t0003g0014a0001c0001t0003g0057a0001c0001t0003g0117others(259): Show | 267 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.1164+977A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 11/12 | chr3 | 57100202 | ||||||
| chr3:57100218
|
C | T | 143 | a0001c0001t0003g0014a0001c0001t0003g0057a0001c0001t0003g0117others(140): Show | 147 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.1164+961G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 11/12 | chr3 | 57100218 | ||||||
| chr3:57100362
|
C | T | 1 | a0003c0002t0001g0084 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1164+817G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 11/12 | chr3 | 57100362 | ||||||
| chr3:57100768
|
G | A | 1 | a0001c0001t0007g0217 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1164+411C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 11/12 | chr3 | 57100768 | ||||||
| chr3:57100858
|
C | T | 1 | a0004c0005t0010g0334 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1164+321G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 11/12 | chr3 | 57100858 | ||||||
| chr3:57100940
|
CAAAGCTT others(1): Show |
C | 5 | a0002c0003t0014g0150a0002c0003t0014g0169a0002c0003t0014g0226others(2): Show | 5 | HG01109.hp2 HG02622.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1164+231_1164+238d others(10): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 11/12 | chr3 | 57100940 | ||||||
| chr3:57101034
|
G | A | 1 | a0003c0002t0001g0063 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1164+145C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 11/12 | chr3 | 57101034 | ||||||
| chr3:57101073
|
G | A | 1 | a0003c0002t0001g0033 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1164+106C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 11/12 | chr3 | 57101073 | ||||||
| chr3:57101379
|
A | T | 1 | a0001c0001t0003g0267 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.980-16T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 10/12 | chr3 | 57101379 | ||||||
| chr3:57101432
|
A | G | 2 | a0001c0001t0018g0330a0008c0014t0018g0329 | 2 | HG02486.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.980-69T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 10/12 | chr3 | 57101432 | ||||||
| chr3:57101488
|
C | T | 1 | a0001c0001t0034g0109 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.980-125G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 10/12 | chr3 | 57101488 | ||||||
| chr3:57101490
|
C | G | 241 | a0001c0001t0003g0014a0001c0001t0003g0057a0001c0001t0003g0117others(238): Show | 246 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.980-127G>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 10/12 | chr3 | 57101490 | ||||||
| chr3:57101633
|
G | A | 3 | a0002c0004t0016g0335a0002c0004t0016g0343a0002c0004t0016g0344 | 3 | HG02257.hp1 HG02886.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.980-270C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 10/12 | chr3 | 57101633 | ||||||
| chr3:57101707
|
C | G | 1 | a0001c0001t0027g0331 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.980-344G>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 10/12 | chr3 | 57101707 | ||||||
| chr3:57101723
|
T | A | 257 | a0001c0001t0003g0014a0001c0001t0003g0057a0001c0001t0003g0117others(254): Show | 262 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.980-360A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 10/12 | chr3 | 57101723 | ||||||
| chr3:57101907
|
A | G | 1 | a0003c0002t0001g0171 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.980-544T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 10/12 | chr3 | 57101907 | ||||||
| chr3:57101952
|
C | A | 284 | a0001c0001t0003g0014a0001c0001t0003g0057a0001c0001t0003g0117others(281): Show | 289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.979+527G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 10/12 | chr3 | 57101952 | ||||||
| chr3:57102013
|
AT | A | 257 | a0001c0001t0003g0014a0001c0001t0003g0057a0001c0001t0003g0117others(254): Show | 262 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.979+465delA | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 10/12 | chr3 | 57102013 | ||||||
| chr3:57102015
|
G | C | 257 | a0001c0001t0003g0014a0001c0001t0003g0057a0001c0001t0003g0117others(254): Show | 262 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.979+464C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 10/12 | chr3 | 57102015 | ||||||
| chr3:57102016
|
A | T | 257 | a0001c0001t0003g0014a0001c0001t0003g0057a0001c0001t0003g0117others(254): Show | 262 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.979+463T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 10/12 | chr3 | 57102016 | ||||||
| chr3:57102017
|
G | T | 257 | a0001c0001t0003g0014a0001c0001t0003g0057a0001c0001t0003g0117others(254): Show | 262 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.979+462C>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 10/12 | chr3 | 57102017 | ||||||
| chr3:57102018
|
A | T | 257 | a0001c0001t0003g0014a0001c0001t0003g0057a0001c0001t0003g0117others(254): Show | 262 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.979+461T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 10/12 | chr3 | 57102018 | ||||||
| chr3:57102114
|
T | C | 1 | a0002c0004t0049g0224 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.979+365A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 10/12 | chr3 | 57102114 | ||||||
| chr3:57102115
|
A | T | 7 | a0002c0003t0022g0107a0002c0003t0022g0158a0002c0003t0055g0008others(4): Show | 7 | HG01496.hp2 HG02559.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.979+364T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 10/12 | chr3 | 57102115 | ||||||
| chr3:57102278
|
G | A | 6 | a0002c0003t0014g0150a0002c0003t0014g0169a0002c0003t0014g0226others(3): Show | 6 | HG01109.hp2 HG02622.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.979+201C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 10/12 | chr3 | 57102278 | ||||||
| chr3:57102670
|
A | G | 1 | a0001c0001t0027g0331 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.869-81T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 9/12 | chr3 | 57102670 | ||||||
| chr3:57102685
|
G | C | 6 | a0004c0005t0010g0075a0004c0005t0010g0076a0004c0005t0010g0102others(3): Show | 6 | HG02055.hp1 HG02559.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.869-96C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 9/12 | chr3 | 57102685 | ||||||
| chr3:57102785
|
T | C | 5 | a0002c0003t0012g0048a0002c0003t0012g0073a0002c0003t0012g0074others(2): Show | 5 | HG01255.hp1 HG01891.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.869-196A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 9/12 | chr3 | 57102785 | ||||||
| chr3:57103062
|
A | G | 258 | a0001c0001t0003g0014a0001c0001t0003g0057a0001c0001t0003g0117others(255): Show | 263 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.868+29T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 9/12 | chr3 | 57103062 | ||||||
| chr3:57103204
|
GA | G | 89 | a0003c0002t0001g0015a0003c0002t0001g0017a0003c0002t0001g0022others(86): Show | 90 | HG00558.hp1 HG00639.hp2 HG00642.hp1 others(87): Show |
intron_variant | MODIFIER | c.814-60delT | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 8/12 | chr3 | 57103204 | ||||||
| chr3:57103265
|
G | A | 1 | a0002c0003t0002g0251 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.814-120C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 8/12 | chr3 | 57103265 | ||||||
| chr3:57103353
|
C | T | 1 | a0003c0002t0001g0015 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.814-208G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 8/12 | chr3 | 57103353 | ||||||
| chr3:57103433
|
C | A | 143 | a0001c0001t0003g0014a0001c0001t0003g0057a0001c0001t0003g0117others(140): Show | 147 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.814-288G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 8/12 | chr3 | 57103433 | ||||||
| chr3:57103495
|
G | A | 6 | a0002c0007t0009g0088a0002c0007t0009g0089a0002c0007t0009g0148others(3): Show | 6 | HG02109.hp1 HG02647.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.814-350C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 8/12 | chr3 | 57103495 | ||||||
| chr3:57103508
|
G | GT | 4 | a0002c0003t0014g0169a0002c0003t0014g0226a0002c0003t0014g0228others(1): Show | 4 | HG01109.hp2 HG02622.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.814-364dupA | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 8/12 | chr3 | 57103508 | ||||||
| chr3:57103568
|
A | C | 89 | a0003c0002t0001g0015a0003c0002t0001g0017a0003c0002t0001g0022others(86): Show | 90 | HG00558.hp1 HG00639.hp2 HG00642.hp1 others(87): Show |
intron_variant | MODIFIER | c.814-423T>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 8/12 | chr3 | 57103568 | ||||||
| chr3:57103744
|
A | G | 258 | a0001c0001t0003g0014a0001c0001t0003g0057a0001c0001t0003g0117others(255): Show | 263 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.813+598T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 8/12 | chr3 | 57103744 | ||||||
| chr3:57103783
|
C | G | 34 | a0001c0001t0005g0001a0001c0001t0005g0016a0001c0001t0005g0035others(31): Show | 37 | HG00280.hp2 HG01081.hp2 HG01168.hp1 others(34): Show |
intron_variant | MODIFIER | c.813+559G>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 8/12 | chr3 | 57103783 | ||||||
| chr3:57103864
|
CCAGCT | C | 4 | a0002c0004t0019g0005a0002c0004t0019g0006a0002c0004t0048g0007others(1): Show | 4 | HG01884.hp2 HG02109.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.813+473_813+477del others(5): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 8/12 | chr3 | 57103864 | ||||||
| chr3:57103870
|
A | T | 4 | a0002c0004t0019g0005a0002c0004t0019g0006a0002c0004t0048g0007others(1): Show | 4 | HG01884.hp2 HG02109.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.813+472T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 8/12 | chr3 | 57103870 | ||||||
| chr3:57103871
|
A | G | 4 | a0002c0004t0019g0005a0002c0004t0019g0006a0002c0004t0048g0007others(1): Show | 4 | HG01884.hp2 HG02109.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.813+471T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 8/12 | chr3 | 57103871 | ||||||
| chr3:57103939
|
T | C | 9 | a0001c0001t0004g0257a0001c0001t0004g0333a0001c0001t0038g0049others(6): Show | 9 | HG02145.hp2 HG02818.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.813+403A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 8/12 | chr3 | 57103939 | ||||||
| chr3:57104069
|
A | G | 1 | a0003c0002t0001g0041 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.813+273T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 8/12 | chr3 | 57104069 | ||||||
| chr3:57104200
|
T | A | 89 | a0003c0002t0001g0015a0003c0002t0001g0017a0003c0002t0001g0022others(86): Show | 90 | HG00558.hp1 HG00639.hp2 HG00642.hp1 others(87): Show |
intron_variant | MODIFIER | c.813+142A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 8/12 | chr3 | 57104200 | ||||||
| chr3:57104288
|
T | C | 2 | a0001c0001t0034g0109a0001c0001t0042g0018 | 2 | HG03098.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.813+54A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 8/12 | chr3 | 57104288 | ||||||
| chr3:57104695
|
C | T | 1 | a0002c0004t0057g0198 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.748-288G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57104695 | ||||||
| chr3:57104852
|
C | T | 1 | a0002c0003t0013g0028 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.748-445G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57104852 | ||||||
| chr3:57104947
|
G | A | 8 | a0001c0001t0004g0257a0001c0001t0038g0049a0001c0006t0011g0009others(5): Show | 8 | HG02145.hp2 HG02976.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.748-540C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57104947 | ||||||
| chr3:57104995
|
T | C | 6 | a0002c0007t0009g0088a0002c0007t0009g0089a0002c0007t0009g0148others(3): Show | 6 | HG02109.hp1 HG02647.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.748-588A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57104995 | ||||||
| chr3:57105180
|
T | C | 1 | a0002c0003t0002g0272 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.747+677A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105180 | ||||||
| chr3:57105303
|
C | T | 7 | a0001c0001t0004g0003a0001c0001t0004g0151a0001c0001t0004g0190others(4): Show | 8 | HG00741.hp2 HG01070.hp2 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.747+554G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105303 | ||||||
| chr3:57105397
|
T | C | 287 | a0001c0001t0003g0014a0001c0001t0003g0057a0001c0001t0003g0117others(284): Show | 292 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.747+460A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105397 | ||||||
| chr3:57105480
|
C | T | 17 | a0002c0004t0008g0091a0002c0004t0008g0177a0002c0004t0008g0192others(14): Show | 17 | HG00099.hp1 HG00639.hp1 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.747+377G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105480 | ||||||
| chr3:57105494
|
A | G | 1 | a0003c0002t0001g0131 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.747+363T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105494 | ||||||
| chr3:57105536
|
C | CA | 8 | a0003c0002t0001g0017a0003c0002t0001g0032a0003c0002t0001g0036others(5): Show | 8 | HG00639.hp2 NA18948.hp1 NA18971.hp1 others(5): Show |
intron_variant | MODIFIER | c.747+320dupT | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105536 | ||||||
| chr3:57105536
|
C | CAA | 60 | a0002c0003t0032g0314a0003c0002t0001g0022a0003c0002t0001g0024others(57): Show | 61 | HG00558.hp1 HG00558.hp2 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.747+319_747+320dup others(2): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105536 | ||||||
| chr3:57105536
|
C | CAAAAAAA others(5): Show |
1 | a0001c0001t0003g0175 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.747+309_747+320dup others(12): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105536 | ||||||
| chr3:57105536
|
C | CAAAAAAA others(6): Show |
3 | a0001c0001t0003g0237a0001c0001t0003g0304a0001c0001t0003g0306 | 3 | HG01496.hp1 HG02083.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.747+308_747+320dup others(13): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105536 | ||||||
| chr3:57105536
|
C | CAAAAAAA others(7): Show |
30 | a0001c0001t0003g0014a0001c0001t0003g0057a0001c0001t0003g0163others(27): Show | 30 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.747+307_747+320dup others(14): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105536 | ||||||
| chr3:57105536
|
C | CAAAAAAA others(8): Show |
2 | a0001c0001t0003g0195a0001c0001t0003g0300 | 2 | HG00642.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.747+306_747+320dup others(15): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105536 | ||||||
| chr3:57105548
|
AAAAAAT | A | 9 | a0002c0004t0016g0335a0002c0004t0016g0343a0002c0004t0016g0344others(6): Show | 9 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.747+303_747+308del others(6): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105548 | ||||||
| chr3:57105552
|
A | AAAAAAAA others(40): Show |
1 | a0002c0003t0012g0074 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.747+304_747+305ins others(47): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | ||||||
| chr3:57105552
|
A | AAAAAAAA others(42): Show |
1 | a0002c0003t0012g0254 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.747+304_747+305ins others(49): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | ||||||
| chr3:57105552
|
A | AAAAAAAA others(8): Show |
19 | a0001c0001t0004g0059a0001c0001t0004g0118a0001c0001t0004g0151others(16): Show | 19 | HG00741.hp2 HG01070.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.747+304_747+305ins others(15): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | ||||||
| chr3:57105552
|
A | AAAAAAAA others(10): Show |
1 | a0004c0005t0010g0076 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.747+304_747+305ins others(17): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | ||||||
| chr3:57105552
|
A | AAAAAAAA others(7): Show |
20 | a0001c0001t0003g0281a0001c0001t0003g0336a0001c0001t0004g0003others(17): Show | 21 | HG01071.hp1 HG01123.hp2 HG01257.hp1 others(18): Show |
intron_variant | MODIFIER | c.747+304_747+305ins others(14): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | ||||||
| chr3:57105552
|
A | AAAAAAAA others(9): Show |
1 | a0001c0001t0034g0109 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.747+304_747+305ins others(16): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | ||||||
| chr3:57105552
|
A | AAAAAAAA others(15): Show |
4 | a0002c0003t0013g0092a0002c0003t0013g0325a0002c0003t0021g0332others(1): Show | 4 | HG01934.hp1 HG02970.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.747+304_747+305ins others(22): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | ||||||
| chr3:57105552
|
A | AAAAAAAA others(33): Show |
1 | a0002c0003t0012g0048 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.747+304_747+305ins others(40): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | ||||||
| chr3:57105552
|
A | AAAAAAAA others(6): Show |
11 | a0001c0001t0004g0149a0001c0001t0004g0168a0001c0001t0004g0176others(8): Show | 11 | HG01069.hp2 HG01243.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.747+304_747+305ins others(13): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | ||||||
| chr3:57105552
|
A | AAAAAAAA others(8): Show |
12 | a0001c0001t0004g0027a0001c0001t0004g0110a0001c0001t0004g0111others(9): Show | 12 | HG00738.hp2 HG01106.hp1 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.747+304_747+305ins others(15): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | ||||||
| chr3:57105552
|
A | AAAAAAAA others(7): Show |
14 | a0001c0001t0003g0117a0001c0001t0003g0282a0001c0001t0003g0283others(11): Show | 16 | HG01168.hp1 HG01884.hp1 HG01928.hp1 others(13): Show |
intron_variant | MODIFIER | c.747+304_747+305ins others(14): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | ||||||
| chr3:57105552
|
A | AAAAAAAA others(9): Show |
1 | a0001c0001t0004g0240 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.747+304_747+305ins others(16): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | ||||||
| chr3:57105552
|
A | AAAAAAAA others(6): Show |
6 | a0001c0001t0005g0016a0001c0001t0005g0047a0001c0001t0005g0222others(3): Show | 6 | HG02698.hp2 HG02735.hp1 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.747+304_747+305ins others(13): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | ||||||
| chr3:57105552
|
A | AAAAAAAA others(8): Show |
5 | a0001c0001t0007g0026a0001c0001t0043g0144a0001c0001t0052g0311others(2): Show | 5 | HG01243.hp1 HG01978.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.747+304_747+305ins others(15): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | ||||||
| chr3:57105552
|
A | AAAAAAAA others(14): Show |
2 | a0002c0003t0013g0077a0002c0003t0013g0170 | 2 | HG02451.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.747+304_747+305ins others(21): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | ||||||
| chr3:57105552
|
A | AAAAAAAA others(5): Show |
1 | a0001c0001t0004g0333 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.747+304_747+305ins others(12): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | ||||||
| chr3:57105552
|
A | AAAAAAAA others(7): Show |
7 | a0001c0001t0005g0035a0001c0001t0005g0188a0001c0001t0005g0243others(4): Show | 7 | HG01081.hp2 HG01358.hp1 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.747+304_747+305ins others(14): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | ||||||
| chr3:57105552
|
A | AAAAAAAA others(15): Show |
1 | a0002c0003t0013g0028 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.747+304_747+305ins others(22): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | ||||||
| chr3:57105552
|
A | AAAAAAAA others(37): Show |
1 | a0002c0003t0012g0073 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.747+304_747+305ins others(44): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | ||||||
| chr3:57105552
|
A | AAAAAAAA others(6): Show |
4 | a0002c0003t0014g0169a0002c0003t0014g0226a0002c0003t0014g0228others(1): Show | 4 | HG01109.hp2 HG02622.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.747+304_747+305ins others(13): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | ||||||
| chr3:57105552
|
A | AAAAAAAA others(8): Show |
3 | a0001c0001t0007g0002a0001c0001t0007g0025a0001c0001t0007g0046 | 4 | HG00280.hp2 HG01261.hp2 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.747+304_747+305ins others(15): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | ||||||
| chr3:57105552
|
A | AAAAAAAA others(28): Show |
1 | a0002c0007t0009g0205 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.747+304_747+305ins others(35): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | ||||||
| chr3:57105552
|
A | AAAAAAAA others(5): Show |
1 | a0002c0003t0053g0227 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.747+304_747+305ins others(12): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | ||||||
| chr3:57105552
|
A | AAAAAAAA others(33): Show |
1 | a0002c0003t0012g0146 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.747+304_747+305ins others(40): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | ||||||
| chr3:57105552
|
A | AAAAAAAT others(6): Show |
1 | a0002c0003t0054g0020 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.747+304_747+305ins others(13): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | ||||||
| chr3:57105552
|
A | AAAAAAAT others(28): Show |
1 | a0002c0007t0009g0088 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.747+304_747+305ins others(35): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | ||||||
| chr3:57105552
|
A | AAAAAAAT others(32): Show |
1 | a0002c0007t0009g0319 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.747+304_747+305ins others(39): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | ||||||
| chr3:57105552
|
A | AAAAATAT others(6): Show |
1 | a0002c0003t0014g0150 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.747+304_747+305ins others(13): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | ||||||
| chr3:57105552
|
A | AAAAATAT others(8): Show |
1 | a0002c0007t0009g0148 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.747+304_747+305ins others(15): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | ||||||
| chr3:57105552
|
A | AAAATATA others(11): Show |
2 | a0002c0004t0008g0197a0002c0004t0008g0310 | 2 | HG00099.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.747+304_747+305ins others(18): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | ||||||
| chr3:57105552
|
A | AAAATATA others(13): Show |
1 | a0002c0004t0008g0177 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.747+304_747+305ins others(20): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | ||||||
| chr3:57105552
|
A | AAAATATA others(27): Show |
1 | a0002c0007t0009g0089 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.747+304_747+305ins others(34): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | ||||||
| chr3:57105552
|
A | AAAATATA others(33): Show |
1 | a0002c0003t0022g0158 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.747+304_747+305ins others(40): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | ||||||
| chr3:57105552
|
A | AAAATATA others(35): Show |
1 | a0002c0007t0009g0167 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.747+304_747+305ins others(42): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | ||||||
| chr3:57105552
|
A | AAATATAT others(4): Show |
1 | a0001c0006t0011g0012 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.747+304_747+305ins others(11): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | ||||||
| chr3:57105552
|
A | AAT | 11 | a0003c0002t0001g0023a0003c0002t0001g0070a0003c0002t0001g0071others(8): Show | 11 | HG01069.hp1 HG01071.hp2 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.747+303_747+304dup others(2): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | ||||||
| chr3:57105552
|
A | AATATATA others(3): Show |
1 | a0002c0004t0057g0198 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.747+295_747+304dup others(10): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | ||||||
| chr3:57105552
|
A | AATATATA others(11): Show |
1 | a0002c0004t0008g0192 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.747+287_747+304dup others(18): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | ||||||
| chr3:57105552
|
A | AATATATA others(31): Show |
1 | a0002c0003t0055g0008 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.747+304_747+305ins others(38): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | ||||||
| chr3:57105552
|
A | AT | 4 | a0002c0003t0002g0105a0002c0003t0002g0154a0003c0002t0001g0072others(1): Show | 4 | HG01891.hp1 HG06807.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.747+304_747+305ins others(1): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | ||||||
| chr3:57105552
|
A | ATATATAT others(2): Show |
3 | a0002c0004t0008g0091a0002c0004t0008g0323a0002c0004t0008g0324 | 3 | HG03017.hp1 NA18946.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.747+304_747+305ins others(9): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | ||||||
| chr3:57105552
|
A | ATATATAT others(28): Show |
1 | a0002c0003t0022g0107 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.747+304_747+305ins others(35): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | ||||||
| chr3:57105552
|
A | T | 12 | a0002c0003t0002g0078a0002c0003t0002g0104a0002c0003t0002g0145others(9): Show | 12 | HG01169.hp2 HG01928.hp2 HG01981.hp2 others(9): Show |
intron_variant | MODIFIER | c.747+305T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105552 | ||||||
| chr3:57105554
|
T | A | 2 | a0001c0001t0003g0259a0001c0001t0003g0260 | 2 | HG00099.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.747+303A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105554 | ||||||
| chr3:57105581
|
A | C | 1 | a0003c0002t0001g0067 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.747+276T>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105581 | ||||||
| chr3:57105701
|
T | C | 1 | a0003c0002t0001g0134 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.747+156A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105701 | ||||||
| chr3:57105805
|
G | A | 240 | a0001c0001t0003g0014a0001c0001t0003g0057a0001c0001t0003g0117others(237): Show | 245 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.747+52C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 7/12 | chr3 | 57105805 | ||||||
| chr3:57106057
|
C | G | 1 | a0001c0001t0003g0238 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.596-49G>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 6/12 | chr3 | 57106057 | ||||||
| chr3:57106080
|
G | A | 240 | a0001c0001t0003g0014a0001c0001t0003g0057a0001c0001t0003g0117others(237): Show | 245 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.595+30C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 6/12 | chr3 | 57106080 | ||||||
| chr3:57106167
|
TA | T | 3 | a0003c0002t0001g0253a0003c0002t0015g0172a0003c0002t0015g0303 | 3 | HG01169.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.551-14delT | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57106167 | ||||||
| chr3:57106339
|
T | C | 1 | a0001c0001t0003g0175 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.551-185A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57106339 | ||||||
| chr3:57106415
|
G | C | 7 | a0002c0004t0008g0091a0002c0004t0008g0177a0002c0004t0008g0192others(4): Show | 7 | HG00099.hp1 HG00639.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.551-261C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57106415 | ||||||
| chr3:57106420
|
G | A | 8 | a0001c0001t0004g0257a0001c0001t0038g0049a0001c0006t0011g0009others(5): Show | 8 | HG02145.hp2 HG02976.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.551-266C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57106420 | ||||||
| chr3:57106501
|
T | C | 1 | a0001c0001t0004g0333 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.551-347A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57106501 | ||||||
| chr3:57106766
|
A | G | 89 | a0003c0002t0001g0015a0003c0002t0001g0017a0003c0002t0001g0022others(86): Show | 90 | HG00558.hp1 HG00639.hp2 HG00642.hp1 others(87): Show |
intron_variant | MODIFIER | c.551-612T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57106766 | ||||||
| chr3:57106805
|
T | A | 9 | a0002c0004t0016g0335a0002c0004t0016g0343a0002c0004t0016g0344others(6): Show | 9 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.551-651A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57106805 | ||||||
| chr3:57106920
|
T | G | 1 | a0001c0001t0004g0333 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.551-766A>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57106920 | ||||||
| chr3:57106935
|
C | T | 3 | a0001c0001t0003g0258a0001c0001t0003g0259a0001c0001t0003g0260 | 3 | HG00099.hp2 HG00738.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.551-781G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57106935 | ||||||
| chr3:57106977
|
G | A | 1 | a0001c0001t0004g0298 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.551-823C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57106977 | ||||||
| chr3:57107035
|
T | C | 1 | a0001c0001t0038g0049 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.551-881A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57107035 | ||||||
| chr3:57107100
|
C | T | 1 | a0001c0001t0026g0287 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.551-946G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57107100 | ||||||
| chr3:57107101
|
G | A | 1 | a0002c0003t0002g0078 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.551-947C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57107101 | ||||||
| chr3:57107105
|
G | A | 1 | a0001c0001t0052g0311 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.551-951C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57107105 | ||||||
| chr3:57107149
|
C | T | 5 | a0002c0003t0012g0048a0002c0003t0012g0073a0002c0003t0012g0074others(2): Show | 5 | HG01255.hp1 HG01891.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.551-995G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57107149 | ||||||
| chr3:57107156
|
A | T | 1 | a0002c0003t0002g0051 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.551-1002T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57107156 | ||||||
| chr3:57107305
|
G | A | 7 | a0002c0004t0008g0091a0002c0004t0008g0177a0002c0004t0008g0192others(4): Show | 7 | HG00099.hp1 HG00639.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.551-1151C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57107305 | ||||||
| chr3:57107327
|
C | T | 7 | a0001c0001t0003g0014a0001c0001t0003g0057a0001c0001t0003g0211others(4): Show | 7 | HG01168.hp2 HG01169.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.551-1173G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57107327 | ||||||
| chr3:57107328
|
G | A | 6 | a0002c0003t0014g0150a0002c0003t0014g0169a0002c0003t0014g0226others(3): Show | 6 | HG01109.hp2 HG02622.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.551-1174C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57107328 | ||||||
| chr3:57107355
|
G | C | 1 | a0001c0001t0003g0175 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.551-1201C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57107355 | ||||||
| chr3:57107379
|
G | GA | 9 | a0001c0001t0004g0257a0001c0001t0038g0049a0001c0006t0011g0009others(6): Show | 9 | HG02145.hp2 HG03195.hp2 HG03225.hp2 others(6): Show |
intron_variant | MODIFIER | c.551-1226dupT | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57107379 | ||||||
| chr3:57107379
|
G | GAA | 87 | a0002c0003t0032g0314a0003c0002t0001g0015a0003c0002t0001g0017others(84): Show | 88 | HG00558.hp1 HG00558.hp2 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.551-1227_551-1226d others(4): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57107379 | ||||||
| chr3:57107385
|
A | AG | 159 | a0001c0001t0003g0014a0001c0001t0003g0057a0001c0001t0003g0117others(156): Show | 163 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.551-1232_551-1231i others(3): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57107385 | ||||||
| chr3:57107386
|
A | G | 2 | a0004c0005t0010g0102a0004c0005t0010g0103 | 2 | HG02559.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.551-1232T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57107386 | ||||||
| chr3:57107462
|
A | C | 160 | a0001c0001t0003g0014a0001c0001t0003g0057a0001c0001t0003g0117others(157): Show | 164 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.551-1308T>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57107462 | ||||||
| chr3:57107556
|
C | T | 10 | a0002c0003t0013g0028a0002c0003t0013g0077a0002c0003t0013g0092others(7): Show | 10 | HG01934.hp1 HG02451.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.551-1402G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57107556 | ||||||
| chr3:57107807
|
C | T | 1 | a0002c0003t0002g0199 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.551-1653G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57107807 | ||||||
| chr3:57107947
|
T | C | 1 | a0002c0003t0002g0034 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.550+1590A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57107947 | ||||||
| chr3:57108066
|
T | C | 63 | a0001c0001t0003g0014a0001c0001t0003g0057a0001c0001t0003g0117others(60): Show | 63 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.550+1471A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57108066 | ||||||
| chr3:57108148
|
C | T | 5 | a0002c0003t0012g0048a0002c0003t0012g0073a0002c0003t0012g0074others(2): Show | 5 | HG01255.hp1 HG01891.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.550+1389G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57108148 | ||||||
| chr3:57108305
|
C | T | 1 | a0001c0001t0004g0298 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.550+1232G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57108305 | ||||||
| chr3:57108317
|
T | G | 259 | a0001c0001t0003g0014a0001c0001t0003g0057a0001c0001t0003g0117others(256): Show | 264 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.550+1220A>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57108317 | ||||||
| chr3:57108509
|
C | CT | 158 | a0001c0001t0003g0014a0001c0001t0003g0117a0001c0001t0003g0175others(155): Show | 160 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.550+1027dupA | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57108509 | ||||||
| chr3:57108509
|
C | CTT | 40 | a0001c0001t0003g0057a0001c0001t0003g0163a0001c0001t0003g0174others(37): Show | 40 | HG00544.hp2 HG00609.hp1 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.550+1026_550+1027d others(4): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57108509 | ||||||
| chr3:57108509
|
C | CTTT | 8 | a0001c0001t0004g0149a0002c0003t0022g0107a0002c0003t0055g0008others(5): Show | 8 | HG01069.hp1 HG01169.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.550+1025_550+1027d others(5): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57108509 | ||||||
| chr3:57108509
|
C | CTTTT | 80 | a0002c0003t0013g0028a0002c0003t0013g0325a0002c0003t0014g0150others(77): Show | 81 | HG00558.hp2 HG00639.hp2 HG00642.hp1 others(78): Show |
intron_variant | MODIFIER | c.550+1024_550+1027d others(6): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57108509 | ||||||
| chr3:57108509
|
C | CTTTTT | 21 | a0002c0003t0014g0169a0002c0003t0014g0228a0002c0004t0008g0192others(18): Show | 21 | HG00099.hp1 HG01071.hp2 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.550+1023_550+1027d others(7): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57108509 | ||||||
| chr3:57108509
|
C | CTTTTTT | 9 | a0002c0004t0008g0091a0002c0004t0008g0177a0002c0004t0008g0197others(6): Show | 9 | HG00639.hp1 HG01099.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.550+1022_550+1027d others(8): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57108509 | ||||||
| chr3:57108576
|
C | T | 1 | a0001c0001t0004g0257 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.550+961G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57108576 | ||||||
| chr3:57108631
|
G | A | 143 | a0001c0001t0003g0014a0001c0001t0003g0057a0001c0001t0003g0117others(140): Show | 147 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.550+906C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57108631 | ||||||
| chr3:57108661
|
G | A | 1 | a0002c0004t0050g0321 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.550+876C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57108661 | ||||||
| chr3:57108670
|
G | T | 1 | a0001c0001t0027g0331 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.550+867C>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57108670 | ||||||
| chr3:57108734
|
T | G | 2 | a0001c0001t0018g0330a0008c0014t0018g0329 | 2 | HG02486.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.550+803A>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57108734 | ||||||
| chr3:57108741
|
A | C | 3 | a0001c0001t0004g0261a0001c0001t0004g0264a0001c0001t0004g0271 | 3 | HG02040.hp2 HG03490.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.550+796T>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57108741 | ||||||
| chr3:57108768
|
G | A | 1 | a0002c0003t0002g0206 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.550+769C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57108768 | ||||||
| chr3:57108807
|
C | T | 1 | a0001c0001t0004g0257 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.550+730G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57108807 | ||||||
| chr3:57108943
|
GGTAATGC others(23): Show |
G | 1 | a0002c0004t0057g0198 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.550+564_550+593del others(30): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57108943 | ||||||
| chr3:57109166
|
T | A | 1 | a0002c0003t0002g0286 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.550+371A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57109166 | ||||||
| chr3:57109220
|
C | T | 1 | a0001c0001t0004g0333 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.550+317G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57109220 | ||||||
| chr3:57109222
|
C | T | 1 | a0002c0004t0057g0198 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.550+315G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57109222 | ||||||
| chr3:57109348
|
T | C | 259 | a0001c0001t0003g0014a0001c0001t0003g0057a0001c0001t0003g0117others(256): Show | 264 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.550+189A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 5/12 | chr3 | 57109348 | ||||||
| chr3:57109822
|
G | C | 8 | a0001c0001t0004g0257a0001c0001t0038g0049a0001c0006t0011g0009others(5): Show | 8 | HG02145.hp2 HG02976.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.430-165C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 4/12 | chr3 | 57109822 | ||||||
| chr3:57109895
|
C | T | 3 | a0002c0004t0008g0091a0002c0004t0008g0323a0002c0004t0008g0324 | 3 | HG03017.hp1 NA18946.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.430-238G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 4/12 | chr3 | 57109895 | ||||||
| chr3:57109914
|
C | T | 94 | a0001c0001t0003g0268a0001c0001t0004g0149a0001c0001t0004g0168others(91): Show | 95 | HG00558.hp1 HG00639.hp2 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.430-257G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 4/12 | chr3 | 57109914 | ||||||
| chr3:57109931
|
T | C | 17 | a0002c0004t0008g0091a0002c0004t0008g0177a0002c0004t0008g0192others(14): Show | 17 | HG00099.hp1 HG00639.hp1 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.429+262A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 4/12 | chr3 | 57109931 | ||||||
| chr3:57109967
|
A | G | 143 | a0001c0001t0003g0014a0001c0001t0003g0057a0001c0001t0003g0117others(140): Show | 147 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.429+226T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 4/12 | chr3 | 57109967 | ||||||
| chr3:57109986
|
G | C | 1 | a0002c0004t0057g0198 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.429+207C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 4/12 | chr3 | 57109986 | ||||||
| chr3:57110000
|
C | T | 9 | a0001c0001t0004g0257a0001c0001t0038g0049a0001c0006t0011g0009others(6): Show | 9 | HG02145.hp2 HG02965.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.429+193G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 4/12 | chr3 | 57110000 | ||||||
| chr3:57110034
|
TG | T | 10 | a0002c0003t0013g0028a0002c0003t0013g0077a0002c0003t0013g0092others(7): Show | 10 | HG01934.hp1 HG02451.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.429+158delC | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 4/12 | chr3 | 57110034 | ||||||
| chr3:57110327
|
T | A | 1 | a0002c0003t0002g0337 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.311-16A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57110327 | ||||||
| chr3:57110628
|
A | G | 3 | a0003c0002t0001g0138a0003c0002t0001g0140a0003c0002t0015g0139 | 3 | HG02896.hp1 HG02897.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.311-317T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57110628 | ||||||
| chr3:57110642
|
T | C | 10 | a0002c0003t0013g0028a0002c0003t0013g0077a0002c0003t0013g0092others(7): Show | 10 | HG01934.hp1 HG02451.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.311-331A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57110642 | ||||||
| chr3:57110678
|
A | G | 6 | a0002c0003t0014g0150a0002c0003t0014g0169a0002c0003t0014g0226others(3): Show | 6 | HG01109.hp2 HG02622.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.311-367T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57110678 | ||||||
| chr3:57110771
|
T | C | 17 | a0002c0004t0008g0091a0002c0004t0008g0177a0002c0004t0008g0192others(14): Show | 17 | HG00099.hp1 HG00639.hp1 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.311-460A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57110771 | ||||||
| chr3:57110888
|
A | G | 1 | a0001c0001t0003g0210 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.311-577T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57110888 | ||||||
| chr3:57110944
|
G | A | 2 | a0004c0005t0010g0075a0004c0005t0010g0076 | 2 | HG02055.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.311-633C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57110944 | ||||||
| chr3:57110961
|
G | A | 1 | a0001c0001t0005g0035 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.311-650C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57110961 | ||||||
| chr3:57111132
|
G | A | 1 | a0002c0004t0057g0198 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.311-821C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57111132 | ||||||
| chr3:57111244
|
A | G | 1 | a0001c0001t0004g0247 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.311-933T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57111244 | ||||||
| chr3:57111279
|
G | C | 1 | a0002c0004t0057g0198 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.311-968C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57111279 | ||||||
| chr3:57111515
|
G | A | 10 | a0002c0003t0013g0028a0002c0003t0013g0077a0002c0003t0013g0092others(7): Show | 10 | HG01934.hp1 HG02451.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.311-1204C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57111515 | ||||||
| chr3:57111570
|
A | G | 2 | a0002c0003t0002g0315a0002c0003t0002g0317 | 2 | NA18982.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.311-1259T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57111570 | ||||||
| chr3:57111698
|
C | T | 84 | a0003c0002t0001g0015a0003c0002t0001g0022a0003c0002t0001g0023others(81): Show | 85 | HG00558.hp1 HG00639.hp2 HG00642.hp1 others(82): Show |
intron_variant | MODIFIER | c.311-1387G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57111698 | ||||||
| chr3:57111709
|
G | A | 34 | a0001c0001t0005g0001a0001c0001t0005g0016a0001c0001t0005g0035others(31): Show | 37 | HG00280.hp2 HG01081.hp2 HG01168.hp1 others(34): Show |
intron_variant | MODIFIER | c.311-1398C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57111709 | ||||||
| chr3:57111742
|
G | A | 1 | a0001c0001t0003g0297 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.311-1431C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57111742 | ||||||
| chr3:57111802
|
C | CA | 144 | a0001c0001t0003g0014a0001c0001t0003g0057a0001c0001t0003g0117others(141): Show | 148 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.311-1492dupT | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57111802 | ||||||
| chr3:57111864
|
A | C | 4 | a0001c0001t0004g0149a0001c0001t0004g0168a0001c0001t0004g0176others(1): Show | 4 | HG02258.hp2 HG02922.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.311-1553T>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57111864 | ||||||
| chr3:57111893
|
C | T | 5 | a0002c0003t0014g0150a0002c0003t0014g0169a0002c0003t0014g0226others(2): Show | 5 | HG01109.hp2 HG02622.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.311-1582G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57111893 | ||||||
| chr3:57111983
|
G | GA | 7 | a0001c0001t0004g0257a0001c0001t0038g0049a0001c0006t0011g0009others(4): Show | 7 | HG02145.hp2 HG02976.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.311-1673dupT | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57111983 | ||||||
| chr3:57111987
|
A | G | 6 | a0002c0007t0009g0088a0002c0007t0009g0089a0002c0007t0009g0148others(3): Show | 6 | HG02109.hp1 HG02647.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.311-1676T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57111987 | ||||||
| chr3:57112098
|
G | A | 1 | a0001c0001t0007g0217 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.311-1787C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57112098 | ||||||
| chr3:57112470
|
T | C | 6 | a0002c0007t0009g0088a0002c0007t0009g0089a0002c0007t0009g0148others(3): Show | 6 | HG02109.hp1 HG02647.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.311-2159A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57112470 | ||||||
| chr3:57112509
|
C | T | 10 | a0002c0003t0013g0028a0002c0003t0013g0077a0002c0003t0013g0092others(7): Show | 10 | HG01934.hp1 HG02451.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.310+2183G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57112509 | ||||||
| chr3:57112620
|
A | G | 1 | a0002c0004t0057g0198 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.310+2072T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57112620 | ||||||
| chr3:57112659
|
C | A | 6 | a0001c0001t0006g0108a0001c0001t0006g0112a0001c0001t0006g0113others(3): Show | 6 | HG02451.hp1 HG02895.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.310+2033G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57112659 | ||||||
| chr3:57112701
|
G | T | 7 | a0002c0004t0008g0091a0002c0004t0008g0177a0002c0004t0008g0192others(4): Show | 7 | HG00099.hp1 HG00639.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.310+1991C>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57112701 | ||||||
| chr3:57112702
|
TTAAAACC others(4): Show |
T | 7 | a0002c0004t0008g0091a0002c0004t0008g0177a0002c0004t0008g0192others(4): Show | 7 | HG00099.hp1 HG00639.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.310+1979_310+1989d others(13): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57112702 | ||||||
| chr3:57112743
|
A | G | 1 | a0002c0004t0008g0323 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.310+1949T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57112743 | ||||||
| chr3:57112880
|
G | A | 10 | a0002c0003t0013g0028a0002c0003t0013g0077a0002c0003t0013g0092others(7): Show | 10 | HG01934.hp1 HG02451.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.310+1812C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57112880 | ||||||
| chr3:57113011
|
T | C | 1 | a0002c0004t0057g0198 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.310+1681A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57113011 | ||||||
| chr3:57113101
|
A | G | 286 | a0001c0001t0003g0014a0001c0001t0003g0057a0001c0001t0003g0117others(283): Show | 291 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.310+1591T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57113101 | ||||||
| chr3:57113143
|
T | C | 1 | a0002c0004t0008g0091 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.310+1549A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57113143 | ||||||
| chr3:57113171
|
C | A | 6 | a0002c0003t0014g0150a0002c0003t0014g0169a0002c0003t0014g0226others(3): Show | 6 | HG01109.hp2 HG02622.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.310+1521G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57113171 | ||||||
| chr3:57113216
|
T | C | 2 | a0004c0005t0010g0102a0004c0005t0010g0103 | 2 | HG02559.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.310+1476A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57113216 | ||||||
| chr3:57113330
|
T | C | 1 | a0001c0001t0038g0049 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.310+1362A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57113330 | ||||||
| chr3:57113434
|
A | C | 2 | a0001c0001t0003g0276a0001c0001t0003g0285 | 2 | NA18957.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.310+1258T>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57113434 | ||||||
| chr3:57113445
|
C | G | 1 | a0002c0003t0002g0087 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.310+1247G>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57113445 | ||||||
| chr3:57113529
|
G | A | 9 | a0002c0004t0016g0335a0002c0004t0016g0343a0002c0004t0016g0344others(6): Show | 9 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.310+1163C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57113529 | ||||||
| chr3:57113536
|
C | T | 1 | a0002c0004t0057g0198 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.310+1156G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57113536 | ||||||
| chr3:57113561
|
G | A | 1 | a0002c0004t0057g0198 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.310+1131C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57113561 | ||||||
| chr3:57113950
|
C | T | 2 | a0003c0002t0001g0015a0003c0002t0001g0123 | 2 | NA18956.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.310+742G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57113950 | ||||||
| chr3:57114065
|
TC | T | 97 | a0001c0001t0004g0257a0001c0001t0038g0049a0001c0006t0011g0009others(94): Show | 98 | HG00558.hp1 HG00639.hp2 HG00642.hp1 others(95): Show |
intron_variant | MODIFIER | c.310+626delG | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57114065 | ||||||
| chr3:57114150
|
C | T | 1 | a0001c0001t0003g0210 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.310+542G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57114150 | ||||||
| chr3:57114183
|
CA | C | 91 | a0001c0001t0003g0266a0001c0001t0004g0257a0001c0001t0024g0348others(88): Show | 92 | HG00558.hp1 HG00639.hp2 HG00642.hp1 others(89): Show |
intron_variant | MODIFIER | c.310+508delT | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57114183 | ||||||
| chr3:57114243
|
C | T | 97 | a0001c0001t0004g0257a0001c0001t0038g0049a0001c0006t0011g0009others(94): Show | 98 | HG00558.hp1 HG00639.hp2 HG00642.hp1 others(95): Show |
intron_variant | MODIFIER | c.310+449G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57114243 | ||||||
| chr3:57114315
|
C | T | 1 | a0001c0001t0003g0203 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.310+377G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57114315 | ||||||
| chr3:57114346
|
C | T | 3 | a0003c0002t0001g0225a0003c0002t0017g0180a0003c0002t0017g0208 | 3 | HG01109.hp1 HG03927.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.310+346G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 3/12 | chr3 | 57114346 | ||||||
| chr3:57114827
|
A | AG | 6 | a0002c0003t0014g0150a0002c0003t0014g0169a0002c0003t0014g0226others(3): Show | 6 | HG01109.hp2 HG02622.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.185-11dupC | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57114827 | ||||||
| chr3:57114882
|
T | C | 1 | a0003c0002t0001g0066 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.185-65A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57114882 | ||||||
| chr3:57114940
|
C | A | 143 | a0001c0001t0003g0014a0001c0001t0003g0057a0001c0001t0003g0117others(140): Show | 147 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.185-123G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57114940 | ||||||
| chr3:57115166
|
T | G | 36 | a0001c0001t0004g0003a0001c0001t0004g0027a0001c0001t0004g0059others(33): Show | 37 | HG00738.hp2 HG00741.hp2 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.185-349A>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57115166 | ||||||
| chr3:57115185
|
T | C | 1 | a0002c0004t0057g0198 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.185-368A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57115185 | ||||||
| chr3:57115201
|
C | T | 151 | a0001c0001t0003g0014a0001c0001t0003g0057a0001c0001t0003g0117others(148): Show | 155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.185-384G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57115201 | ||||||
| chr3:57115219
|
G | A | 8 | a0001c0001t0004g0257a0001c0001t0038g0049a0001c0006t0011g0009others(5): Show | 8 | HG02145.hp2 HG02976.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.185-402C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57115219 | ||||||
| chr3:57115220
|
T | C | 1 | a0005c0008t0006g0320 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.185-403A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57115220 | ||||||
| chr3:57115287
|
T | G | 98 | a0001c0001t0004g0257a0001c0001t0038g0049a0001c0006t0011g0009others(95): Show | 99 | HG00558.hp1 HG00558.hp2 HG00639.hp2 others(96): Show |
intron_variant | MODIFIER | c.185-470A>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57115287 | ||||||
| chr3:57115397
|
T | A | 151 | a0001c0001t0003g0014a0001c0001t0003g0057a0001c0001t0003g0117others(148): Show | 155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.185-580A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57115397 | ||||||
| chr3:57115409
|
A | G | 1 | a0001c0001t0003g0282 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.185-592T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57115409 | ||||||
| chr3:57115581
|
C | T | 1 | a0001c0001t0004g0333 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.185-764G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57115581 | ||||||
| chr3:57115631
|
C | T | 151 | a0001c0001t0003g0014a0001c0001t0003g0057a0001c0001t0003g0117others(148): Show | 155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.185-814G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57115631 | ||||||
| chr3:57115699
|
G | C | 5 | a0002c0003t0012g0048a0002c0003t0012g0073a0002c0003t0012g0074others(2): Show | 5 | HG01255.hp1 HG01891.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.185-882C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57115699 | ||||||
| chr3:57115765
|
C | T | 98 | a0001c0001t0004g0257a0001c0001t0038g0049a0001c0006t0011g0009others(95): Show | 99 | HG00558.hp1 HG00558.hp2 HG00639.hp2 others(96): Show |
intron_variant | MODIFIER | c.185-948G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57115765 | ||||||
| chr3:57115896
|
A | G | 1 | a0003c0002t0001g0231 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.185-1079T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57115896 | ||||||
| chr3:57115941
|
T | C | 1 | a0001c0001t0004g0159 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.185-1124A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57115941 | ||||||
| chr3:57116000
|
A | G | 1 | a0001c0001t0007g0045 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.185-1183T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57116000 | ||||||
| chr3:57116095
|
T | A | 21 | a0001c0001t0005g0001a0001c0001t0005g0016a0001c0001t0005g0035others(18): Show | 23 | HG01081.hp2 HG01168.hp1 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.185-1278A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57116095 | ||||||
| chr3:57116162
|
T | C | 1 | a0002c0003t0014g0150 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.185-1345A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57116162 | ||||||
| chr3:57116244
|
T | C | 4 | a0001c0001t0004g0149a0001c0001t0004g0168a0001c0001t0004g0176others(1): Show | 4 | HG02258.hp2 HG02922.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.185-1427A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57116244 | ||||||
| chr3:57116282
|
C | CT | 7 | a0001c0001t0027g0331a0002c0003t0002g0145a0002c0003t0014g0150others(4): Show | 7 | HG02622.hp2 HG02717.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.185-1466dupA | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57116282 | ||||||
| chr3:57116282
|
CT | C | 252 | a0001c0001t0003g0014a0001c0001t0003g0057a0001c0001t0003g0117others(249): Show | 257 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.185-1466delA | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57116282 | ||||||
| chr3:57116282
|
CTT | C | 11 | a0001c0001t0005g0326a0001c0001t0006g0173a0001c0001t0007g0239others(8): Show | 11 | HG01074.hp1 HG02109.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.185-1467_185-1466d others(4): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57116282 | ||||||
| chr3:57116288
|
T | C | 8 | a0001c0001t0004g0257a0001c0001t0038g0049a0001c0006t0011g0009others(5): Show | 8 | HG02145.hp2 HG02976.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.185-1471A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57116288 | ||||||
| chr3:57116430
|
T | C | 2 | a0001c0001t0018g0330a0008c0014t0018g0329 | 2 | HG02486.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.185-1613A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57116430 | ||||||
| chr3:57116444
|
C | T | 1 | a0006c0009t0003g0279 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.185-1627G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57116444 | ||||||
| chr3:57116458
|
AT | A | 249 | a0001c0001t0003g0014a0001c0001t0003g0057a0001c0001t0003g0117others(246): Show | 254 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.185-1642delA | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57116458 | ||||||
| chr3:57116530
|
C | A | 8 | a0002c0003t0002g0130a0002c0003t0002g0200a0002c0003t0002g0201others(5): Show | 8 | NA18946.hp2 NA18950.hp1 NA18980.hp2 others(5): Show |
intron_variant | MODIFIER | c.185-1713G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57116530 | ||||||
| chr3:57116771
|
T | C | 1 | a0003c0002t0001g0044 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.185-1954A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57116771 | ||||||
| chr3:57116834
|
G | A | 1 | a0002c0003t0014g0150 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.185-2017C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57116834 | ||||||
| chr3:57116842
|
G | A | 4 | a0002c0003t0014g0169a0002c0003t0014g0226a0002c0003t0014g0228others(1): Show | 4 | HG01109.hp2 HG02622.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.185-2025C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57116842 | ||||||
| chr3:57116889
|
T | C | 8 | a0002c0004t0008g0091a0002c0004t0008g0177a0002c0004t0008g0192others(5): Show | 8 | HG00099.hp1 HG00639.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.185-2072A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57116889 | ||||||
| chr3:57116890
|
T | TA | 11 | a0002c0003t0002g0053a0002c0003t0002g0099a0002c0003t0002g0145others(8): Show | 11 | HG01255.hp1 HG01891.hp2 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.185-2074dupT | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57116890 | ||||||
| chr3:57116890
|
TA | T | 12 | a0001c0001t0005g0035a0002c0003t0002g0052a0002c0003t0002g0104others(9): Show | 12 | HG01358.hp1 HG02109.hp1 HG02132.hp2 others(9): Show |
intron_variant | MODIFIER | c.185-2074delT | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57116890 | ||||||
| chr3:57116890
|
TAA | T | 243 | a0001c0001t0003g0014a0001c0001t0003g0057a0001c0001t0003g0117others(240): Show | 248 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.185-2075_185-2074d others(4): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57116890 | ||||||
| chr3:57116939
|
ATATTTTG others(11): Show |
A | 1 | a0002c0003t0002g0052 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.185-2140_185-2123d others(20): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57116939 | ||||||
| chr3:57117103
|
A | C | 151 | a0001c0001t0003g0014a0001c0001t0003g0057a0001c0001t0003g0117others(148): Show | 155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.185-2286T>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57117103 | ||||||
| chr3:57117106
|
T | A | 1 | a0001c0001t0004g0333 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.185-2289A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57117106 | ||||||
| chr3:57117113
|
A | AT | 231 | a0001c0001t0003g0014a0001c0001t0003g0057a0001c0001t0003g0117others(228): Show | 236 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.185-2297dupA | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57117113 | ||||||
| chr3:57117113
|
A | ATT | 18 | a0001c0001t0003g0210a0001c0001t0004g0027a0001c0001t0005g0188others(15): Show | 18 | HG00558.hp2 HG00639.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.185-2298_185-2297d others(4): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57117113 | ||||||
| chr3:57117199
|
C | T | 1 | a0002c0003t0002g0104 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.185-2382G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57117199 | ||||||
| chr3:57117234
|
C | T | 3 | a0003c0002t0001g0138a0003c0002t0001g0140a0003c0002t0015g0139 | 3 | HG02896.hp1 HG02897.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.185-2417G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57117234 | ||||||
| chr3:57117339
|
C | G | 10 | a0002c0003t0013g0028a0002c0003t0013g0077a0002c0003t0013g0092others(7): Show | 10 | HG01934.hp1 HG02451.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.185-2522G>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57117339 | ||||||
| chr3:57117534
|
A | T | 1 | a0001c0001t0006g0112 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.185-2717T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57117534 | ||||||
| chr3:57117768
|
C | G | 6 | a0002c0007t0009g0088a0002c0007t0009g0089a0002c0007t0009g0148others(3): Show | 6 | HG02109.hp1 HG02647.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.184+2488G>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57117768 | ||||||
| chr3:57117784
|
G | A | 90 | a0002c0003t0032g0314a0003c0002t0001g0015a0003c0002t0001g0017others(87): Show | 91 | HG00558.hp1 HG00558.hp2 HG00639.hp2 others(88): Show |
intron_variant | MODIFIER | c.184+2472C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57117784 | ||||||
| chr3:57117978
|
A | G | 90 | a0002c0003t0032g0314a0003c0002t0001g0015a0003c0002t0001g0017others(87): Show | 91 | HG00558.hp1 HG00558.hp2 HG00639.hp2 others(88): Show |
intron_variant | MODIFIER | c.184+2278T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57117978 | ||||||
| chr3:57118013
|
C | T | 90 | a0002c0003t0032g0314a0003c0002t0001g0015a0003c0002t0001g0017others(87): Show | 91 | HG00558.hp1 HG00558.hp2 HG00639.hp2 others(88): Show |
intron_variant | MODIFIER | c.184+2243G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57118013 | ||||||
| chr3:57118231
|
A | C | 1 | a0002c0003t0002g0154 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.184+2025T>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57118231 | ||||||
| chr3:57118232
|
C | A | 1 | a0002c0003t0002g0154 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.184+2024G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57118232 | ||||||
| chr3:57118387
|
G | T | 4 | a0002c0003t0014g0169a0002c0003t0014g0226a0002c0003t0014g0228others(1): Show | 4 | HG01109.hp2 HG02622.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.184+1869C>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57118387 | ||||||
| chr3:57118440
|
C | A | 5 | a0002c0003t0012g0048a0002c0003t0012g0073a0002c0003t0012g0074others(2): Show | 5 | HG01255.hp1 HG01891.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.184+1816G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57118440 | ||||||
| chr3:57118503
|
C | A | 265 | a0001c0001t0003g0014a0001c0001t0003g0057a0001c0001t0003g0117others(262): Show | 270 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.184+1753G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57118503 | ||||||
| chr3:57118503
|
C | T | 1 | a0002c0003t0002g0294 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.184+1753G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57118503 | ||||||
| chr3:57118965
|
G | A | 1 | a0010c0017t0002g0278 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.184+1291C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57118965 | ||||||
| chr3:57119008
|
C | T | 1 | a0001c0001t0007g0217 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.184+1248G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57119008 | ||||||
| chr3:57119036
|
T | G | 9 | a0002c0004t0016g0335a0002c0004t0016g0343a0002c0004t0016g0344others(6): Show | 9 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.184+1220A>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57119036 | ||||||
| chr3:57119070
|
T | G | 1 | a0002c0003t0002g0154 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.184+1186A>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57119070 | ||||||
| chr3:57119078
|
C | T | 1 | a0001c0001t0004g0257 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.184+1178G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57119078 | ||||||
| chr3:57119080
|
C | T | 5 | a0002c0007t0009g0088a0002c0007t0009g0089a0002c0007t0009g0167others(2): Show | 5 | HG02109.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.184+1176G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57119080 | ||||||
| chr3:57119351
|
C | CA | 88 | a0001c0001t0004g0298a0001c0001t0005g0181a0001c0001t0046g0318others(85): Show | 89 | HG00558.hp1 HG00558.hp2 HG00642.hp1 others(86): Show |
intron_variant | MODIFIER | c.184+904dupT | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57119351 | ||||||
| chr3:57119360
|
C | A | 255 | a0001c0001t0003g0014a0001c0001t0003g0057a0001c0001t0003g0117others(252): Show | 260 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.184+896G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57119360 | ||||||
| chr3:57119418
|
G | A | 1 | a0003c0002t0001g0040 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.184+838C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57119418 | ||||||
| chr3:57119553
|
G | A | 249 | a0001c0001t0003g0014a0001c0001t0003g0057a0001c0001t0003g0117others(246): Show | 254 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.184+703C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57119553 | ||||||
| chr3:57119632
|
C | A | 7 | a0002c0004t0008g0091a0002c0004t0008g0177a0002c0004t0008g0192others(4): Show | 7 | HG00099.hp1 HG00639.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.184+624G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57119632 | ||||||
| chr3:57119653
|
G | GTTTCACA others(19): Show |
1 | a0002c0003t0014g0226 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.184+577_184+602dup others(26): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57119653 | ||||||
| chr3:57119653
|
GTTTCACA others(19): Show |
G | 170 | a0001c0001t0003g0014a0001c0001t0003g0057a0001c0001t0003g0117others(167): Show | 174 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.184+577_184+602del others(26): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57119653 | ||||||
| chr3:57119654
|
T | A | 90 | a0002c0003t0032g0314a0003c0002t0001g0015a0003c0002t0001g0017others(87): Show | 91 | HG00558.hp1 HG00558.hp2 HG00639.hp2 others(88): Show |
intron_variant | MODIFIER | c.184+602A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57119654 | ||||||
| chr3:57119680
|
T | A | 159 | a0001c0001t0003g0014a0001c0001t0003g0057a0001c0001t0003g0117others(156): Show | 163 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.184+576A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57119680 | ||||||
| chr3:57119841
|
C | T | 90 | a0002c0003t0032g0314a0003c0002t0001g0015a0003c0002t0001g0017others(87): Show | 91 | HG00558.hp1 HG00558.hp2 HG00639.hp2 others(88): Show |
intron_variant | MODIFIER | c.184+415G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57119841 | ||||||
| chr3:57119992
|
A | G | 5 | a0002c0003t0012g0048a0002c0003t0012g0073a0002c0003t0012g0074others(2): Show | 5 | HG01255.hp1 HG01891.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.184+264T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57119992 | ||||||
| chr3:57120156
|
C | A | 2 | a0002c0003t0013g0077a0002c0003t0013g0170 | 2 | HG02451.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.184+100G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 2/12 | chr3 | 57120156 | ||||||
| chr3:57120330
|
G | A | 1 | a0002c0003t0012g0146 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.127-17C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57120330 | ||||||
| chr3:57120637
|
C | T | 1 | a0002c0003t0002g0087 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.127-324G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57120637 | ||||||
| chr3:57120730
|
C | T | 7 | a0002c0004t0008g0091a0002c0004t0008g0177a0002c0004t0008g0192others(4): Show | 7 | HG00099.hp1 HG00639.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.127-417G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57120730 | ||||||
| chr3:57120794
|
A | G | 286 | a0001c0001t0003g0014a0001c0001t0003g0057a0001c0001t0003g0117others(283): Show | 291 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.127-481T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57120794 | ||||||
| chr3:57120850
|
C | T | 89 | a0003c0002t0001g0015a0003c0002t0001g0017a0003c0002t0001g0022others(86): Show | 90 | HG00558.hp1 HG00639.hp2 HG00642.hp1 others(87): Show |
intron_variant | MODIFIER | c.127-537G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57120850 | ||||||
| chr3:57121392
|
G | C | 4 | a0001c0006t0011g0009a0001c0006t0011g0010a0001c0006t0011g0011others(1): Show | 4 | HG02145.hp2 HG02976.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-1079C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57121392 | ||||||
| chr3:57121816
|
C | T | 3 | a0003c0002t0001g0037a0003c0002t0001g0308a0003c0002t0001g0309 | 3 | HG01496.hp2 HG02300.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.127-1503G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57121816 | ||||||
| chr3:57122014
|
G | T | 8 | a0001c0001t0004g0257a0001c0001t0038g0049a0001c0006t0011g0009others(5): Show | 8 | HG02145.hp2 HG02976.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.127-1701C>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57122014 | ||||||
| chr3:57122130
|
G | C | 1 | a0002c0004t0057g0198 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.127-1817C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57122130 | ||||||
| chr3:57122275
|
G | C | 9 | a0002c0004t0016g0335a0002c0004t0016g0343a0002c0004t0016g0344others(6): Show | 9 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.127-1962C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57122275 | ||||||
| chr3:57122338
|
C | T | 3 | a0002c0003t0002g0339a0002c0003t0002g0340a0002c0003t0002g0341 | 3 | NA18974.hp1 NA19002.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.127-2025G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57122338 | ||||||
| chr3:57122473
|
G | A | 1 | a0001c0001t0038g0049 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.127-2160C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57122473 | ||||||
| chr3:57122491
|
A | G | 7 | a0002c0004t0008g0091a0002c0004t0008g0177a0002c0004t0008g0192others(4): Show | 7 | HG00099.hp1 HG00639.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.127-2178T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57122491 | ||||||
| chr3:57122507
|
T | C | 267 | a0001c0001t0003g0014a0001c0001t0003g0057a0001c0001t0003g0117others(264): Show | 272 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.127-2194A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57122507 | ||||||
| chr3:57122740
|
C | CT | 34 | a0002c0003t0002g0204a0002c0003t0002g0214a0002c0003t0013g0028others(31): Show | 34 | HG01069.hp1 HG01081.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.127-2428dupA | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57122740 | ||||||
| chr3:57122740
|
C | CTT | 99 | a0001c0001t0003g0281a0001c0001t0003g0302a0001c0001t0004g0247others(96): Show | 100 | HG00280.hp2 HG00558.hp1 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.127-2429_127-2428d others(4): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57122740 | ||||||
| chr3:57122740
|
C | CTTT | 146 | a0001c0001t0003g0014a0001c0001t0003g0057a0001c0001t0003g0117others(143): Show | 150 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.127-2430_127-2428d others(5): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57122740 | ||||||
| chr3:57123128
|
G | C | 42 | a0001c0001t0003g0014a0001c0001t0003g0057a0001c0001t0003g0163others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.127-2815C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57123128 | ||||||
| chr3:57123128
|
G | T | 1 | a0003c0002t0001g0232 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.127-2815C>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57123128 | ||||||
| chr3:57123307
|
G | C | 1 | a0001c0001t0004g0333 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.127-2994C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57123307 | ||||||
| chr3:57123333
|
T | A | 1 | a0002c0007t0009g0319 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.127-3020A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57123333 | ||||||
| chr3:57123344
|
C | G | 2 | a0001c0001t0003g0163a0001c0001t0003g0174 | 2 | HG02486.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.127-3031G>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57123344 | ||||||
| chr3:57123493
|
C | T | 1 | a0002c0003t0002g0052 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.127-3180G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57123493 | ||||||
| chr3:57123496
|
T | C | 1 | a0002c0003t0002g0052 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.127-3183A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57123496 | ||||||
| chr3:57123499
|
C | T | 1 | a0002c0004t0057g0198 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.127-3186G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57123499 | ||||||
| chr3:57123688
|
G | A | 37 | a0001c0001t0004g0003a0001c0001t0004g0027a0001c0001t0004g0059others(34): Show | 38 | HG00544.hp1 HG00738.hp2 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.127-3375C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57123688 | ||||||
| chr3:57123950
|
C | T | 91 | a0001c0001t0004g0240a0001c0001t0045g0185a0003c0002t0001g0015others(88): Show | 92 | HG00558.hp1 HG00639.hp2 HG00642.hp1 others(89): Show |
intron_variant | MODIFIER | c.127-3637G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57123950 | ||||||
| chr3:57123951
|
G | A | 1 | a0001c0001t0004g0333 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.127-3638C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57123951 | ||||||
| chr3:57123999
|
C | T | 1 | a0002c0003t0012g0146 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.127-3686G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57123999 | ||||||
| chr3:57124156
|
A | G | 1 | a0001c0001t0018g0330 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.127-3843T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57124156 | ||||||
| chr3:57124168
|
C | T | 112 | a0001c0001t0003g0014a0001c0001t0003g0057a0001c0001t0003g0117others(109): Show | 115 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.127-3855G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57124168 | ||||||
| chr3:57124220
|
A | G | 120 | a0001c0001t0003g0014a0001c0001t0003g0057a0001c0001t0003g0117others(117): Show | 123 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.127-3907T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57124220 | ||||||
| chr3:57124309
|
G | C | 224 | a0001c0001t0003g0014a0001c0001t0003g0057a0001c0001t0003g0117others(221): Show | 228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.127-3996C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57124309 | ||||||
| chr3:57124350
|
T | C | 4 | a0002c0003t0002g0130a0002c0003t0002g0202a0002c0003t0002g0313others(1): Show | 4 | HG00558.hp2 NA18980.hp2 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-4037A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57124350 | ||||||
| chr3:57124364
|
C | T | 1 | a0002c0004t0008g0197 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.127-4051G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57124364 | ||||||
| chr3:57124525
|
GA | G | 199 | a0001c0001t0003g0014a0001c0001t0003g0057a0001c0001t0003g0163others(196): Show | 203 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.127-4213delT | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57124525 | ||||||
| chr3:57124558
|
G | A | 22 | a0001c0001t0003g0014a0001c0001t0003g0057a0001c0001t0003g0195others(19): Show | 22 | HG00099.hp2 HG00642.hp2 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.127-4245C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57124558 | ||||||
| chr3:57124657
|
C | T | 105 | a0001c0001t0003g0014a0001c0001t0003g0057a0001c0001t0003g0163others(102): Show | 108 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.127-4344G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57124657 | ||||||
| chr3:57124903
|
A | G | 3 | a0001c0001t0004g0240a0003c0002t0001g0084a0003c0002t0001g0184 | 3 | HG01081.hp1 HG01981.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.127-4590T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57124903 | ||||||
| chr3:57124991
|
A | G | 1 | a0001c0001t0003g0336 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.127-4678T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57124991 | ||||||
| chr3:57125116
|
A | G | 2 | a0001c0001t0006g0162a0002c0004t0057g0198 | 2 | HG03098.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.127-4803T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57125116 | ||||||
| chr3:57125119
|
T | C | 1 | a0002c0004t0051g0019 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.127-4806A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57125119 | ||||||
| chr3:57125224
|
T | C | 1 | a0001c0001t0005g0246 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.127-4911A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57125224 | ||||||
| chr3:57125236
|
G | A | 87 | a0001c0001t0004g0240a0001c0001t0020g0021a0001c0001t0020g0250others(84): Show | 88 | HG00558.hp1 HG00639.hp2 HG00673.hp2 others(85): Show |
intron_variant | MODIFIER | c.127-4923C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57125236 | ||||||
| chr3:57125268
|
G | T | 2 | a0002c0003t0014g0150a0002c0003t0054g0020 | 2 | HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.127-4955C>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57125268 | ||||||
| chr3:57125283
|
T | C | 11 | a0001c0001t0003g0117a0002c0007t0009g0088a0002c0007t0009g0089others(8): Show | 11 | HG01243.hp2 HG02109.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.127-4970A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57125283 | ||||||
| chr3:57125412
|
GA | G | 11 | a0002c0003t0002g0052a0002c0003t0002g0086a0002c0003t0013g0028others(8): Show | 11 | HG02622.hp1 HG02622.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.127-5100delT | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57125412 | ||||||
| chr3:57125434
|
A | G | 1 | a0002c0003t0002g0104 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.127-5121T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57125434 | ||||||
| chr3:57125944
|
T | C | 1 | a0004c0005t0010g0103 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.127-5631A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57125944 | ||||||
| chr3:57126089
|
C | T | 29 | a0002c0003t0002g0051a0002c0003t0002g0052a0002c0003t0002g0053others(26): Show | 29 | HG00544.hp1 HG00558.hp2 HG02080.hp2 others(26): Show |
intron_variant | MODIFIER | c.127-5776G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57126089 | ||||||
| chr3:57126123
|
G | A | 7 | a0001c0001t0003g0014a0001c0001t0003g0057a0001c0001t0003g0211others(4): Show | 7 | HG01168.hp2 HG01169.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.127-5810C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57126123 | ||||||
| chr3:57126284
|
T | C | 166 | a0001c0001t0003g0117a0001c0001t0004g0003a0001c0001t0004g0027others(163): Show | 168 | HG00558.hp1 HG00639.hp2 HG00673.hp2 others(165): Show |
intron_variant | MODIFIER | c.127-5971A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57126284 | ||||||
| chr3:57126430
|
C | A | 39 | a0001c0001t0003g0117a0001c0001t0004g0333a0001c0001t0027g0331others(36): Show | 39 | HG01243.hp2 HG01255.hp1 HG01884.hp2 others(36): Show |
intron_variant | MODIFIER | c.127-6117G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57126430 | ||||||
| chr3:57126443
|
C | A | 44 | a0001c0001t0003g0117a0001c0001t0004g0333a0001c0001t0027g0331others(41): Show | 44 | HG01109.hp2 HG01243.hp2 HG01255.hp1 others(41): Show |
intron_variant | MODIFIER | c.127-6130G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57126443 | ||||||
| chr3:57126454
|
C | T | 4 | a0002c0003t0012g0048a0002c0003t0012g0073a0002c0003t0012g0074others(1): Show | 4 | HG01255.hp1 HG01891.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-6141G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57126454 | ||||||
| chr3:57126538
|
C | A | 1 | a0002c0003t0022g0158 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.127-6225G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57126538 | ||||||
| chr3:57126774
|
GTGAACAG others(60): Show |
G | 1 | a0003c0002t0015g0172 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.127-6528_127-6462d others(69): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57126774 | ||||||
| chr3:57126950
|
G | A | 1 | a0001c0001t0005g0246 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.127-6637C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57126950 | ||||||
| chr3:57126975
|
C | G | 1 | a0001c0001t0004g0333 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.127-6662G>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57126975 | ||||||
| chr3:57127056
|
C | T | 1 | a0002c0003t0013g0092 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.127-6743G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127056 | ||||||
| chr3:57127181
|
C | CAT | 9 | a0001c0001t0005g0243a0001c0001t0018g0330a0002c0003t0002g0087others(6): Show | 9 | HG02486.hp1 HG02622.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.127-6870_127-6869d others(4): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127181 | ||||||
| chr3:57127181
|
C | CATAT | 29 | a0002c0003t0002g0051a0002c0003t0002g0052a0002c0003t0002g0053others(26): Show | 29 | HG00544.hp1 HG00558.hp2 HG02080.hp2 others(26): Show |
intron_variant | MODIFIER | c.127-6872_127-6869d others(6): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127181 | ||||||
| chr3:57127181
|
CAT | C | 5 | a0001c0001t0046g0318a0002c0004t0019g0005a0002c0004t0019g0006others(2): Show | 5 | HG01884.hp2 HG02109.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.127-6870_127-6869d others(4): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127181 | ||||||
| chr3:57127189
|
T | TATATATA others(15): Show |
1 | a0002c0003t0002g0196 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.127-6898_127-6877d others(24): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127189 | ||||||
| chr3:57127189
|
T | TATATATA others(25): Show |
1 | a0001c0001t0033g0085 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.127-6908_127-6877d others(34): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127189 | ||||||
| chr3:57127189
|
TATATATA others(37): Show |
T | 5 | a0002c0003t0013g0028a0002c0003t0013g0092a0002c0003t0013g0170others(2): Show | 5 | HG02622.hp2 HG02717.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.127-6920_127-6877d others(46): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127189 | ||||||
| chr3:57127197
|
T | A | 112 | a0001c0001t0003g0117a0001c0001t0004g0333a0001c0001t0020g0021others(109): Show | 113 | HG00558.hp1 HG00639.hp2 HG00673.hp2 others(110): Show |
intron_variant | MODIFIER | c.127-6884A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127197 | ||||||
| chr3:57127201
|
T | A | 13 | a0001c0001t0027g0331a0001c0001t0038g0049a0001c0006t0011g0009others(10): Show | 13 | HG01884.hp2 HG02109.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.127-6888A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127201 | ||||||
| chr3:57127207
|
TAA | T | 22 | a0001c0001t0003g0117a0001c0001t0004g0333a0002c0003t0013g0325others(19): Show | 22 | HG01109.hp2 HG01243.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.127-6896_127-6895d others(4): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127207 | ||||||
| chr3:57127209
|
A | T | 9 | a0001c0001t0027g0331a0001c0001t0038g0049a0001c0006t0011g0009others(6): Show | 9 | HG02145.hp2 HG02451.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.127-6896T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127209 | ||||||
| chr3:57127209
|
AAAATATA others(3): Show |
A | 1 | a0001c0001t0004g0248 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.127-6906_127-6897d others(12): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127209 | ||||||
| chr3:57127211
|
A | T | 4 | a0002c0003t0012g0048a0002c0003t0012g0073a0002c0003t0012g0074others(1): Show | 4 | HG01255.hp1 HG01891.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-6898T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127211 | ||||||
| chr3:57127219
|
T | A | 4 | a0002c0003t0012g0048a0002c0003t0012g0073a0002c0003t0012g0074others(1): Show | 4 | HG01255.hp1 HG01891.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-6906A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127219 | ||||||
| chr3:57127221
|
A | T | 4 | a0002c0003t0012g0048a0002c0003t0012g0073a0002c0003t0012g0074others(1): Show | 4 | HG01255.hp1 HG01891.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-6908T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127221 | ||||||
| chr3:57127233
|
A | AAT | 7 | a0002c0004t0008g0091a0002c0004t0008g0177a0002c0004t0008g0197others(4): Show | 7 | HG00099.hp1 HG00639.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.127-6922_127-6921d others(4): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127233 | ||||||
| chr3:57127233
|
A | AATATATA others(27): Show |
1 | a0002c0003t0002g0153 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.127-6921_127-6920i others(36): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127233 | ||||||
| chr3:57127233
|
A | T | 6 | a0002c0003t0012g0048a0002c0003t0012g0073a0002c0003t0012g0074others(3): Show | 6 | HG01109.hp1 HG01255.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-6920T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127233 | ||||||
| chr3:57127233
|
AATATATA others(5): Show |
A | 1 | a0001c0001t0004g0264 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.127-6932_127-6921d others(14): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127233 | ||||||
| chr3:57127239
|
T | TA | 4 | a0002c0003t0012g0048a0002c0003t0012g0073a0002c0003t0012g0074others(1): Show | 4 | HG01255.hp1 HG01891.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-6927dupT | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127239 | ||||||
| chr3:57127239
|
T | TATA | 35 | a0001c0001t0003g0117a0001c0001t0004g0333a0001c0001t0027g0331others(32): Show | 35 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.127-6927_127-6926i others(5): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127239 | ||||||
| chr3:57127243
|
T | A | 121 | a0001c0001t0020g0021a0001c0001t0020g0250a0002c0003t0002g0051others(118): Show | 122 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(119): Show |
intron_variant | MODIFIER | c.127-6930A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127243 | ||||||
| chr3:57127245
|
T | A | 83 | a0001c0001t0020g0021a0001c0001t0020g0250a0002c0003t0002g0099others(80): Show | 84 | HG00558.hp1 HG00639.hp2 HG00673.hp2 others(81): Show |
intron_variant | MODIFIER | c.127-6932A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127245 | ||||||
| chr3:57127251
|
T | A | 9 | a0001c0001t0037g0055a0002c0003t0002g0153a0002c0004t0008g0091others(6): Show | 9 | HG00099.hp1 HG00639.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.127-6938A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127251 | ||||||
| chr3:57127251
|
T | TAAAAATA others(17): Show |
28 | a0002c0003t0002g0051a0002c0003t0002g0052a0002c0003t0002g0053others(25): Show | 28 | HG00544.hp1 HG00558.hp2 HG02080.hp2 others(25): Show |
intron_variant | MODIFIER | c.127-6939_127-6938i others(26): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127251 | ||||||
| chr3:57127253
|
A | T | 1 | a0002c0003t0013g0325 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.127-6940T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127253 | ||||||
| chr3:57127257
|
T | A | 1 | a0002c0003t0013g0325 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.127-6944A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127257 | ||||||
| chr3:57127261
|
T | TA | 87 | a0001c0001t0020g0021a0001c0001t0020g0250a0002c0003t0002g0099others(84): Show | 88 | HG00558.hp1 HG00639.hp2 HG00673.hp2 others(85): Show |
intron_variant | MODIFIER | c.127-6949dupT | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127261 | ||||||
| chr3:57127263
|
AATATATA others(13): Show |
A | 1 | a0001c0001t0052g0311 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.127-6970_127-6951d others(22): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127263 | ||||||
| chr3:57127263
|
AATATATA others(39): Show |
A | 9 | a0002c0003t0012g0048a0002c0003t0012g0073a0002c0003t0012g0074others(6): Show | 9 | HG01255.hp1 HG01884.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.127-6996_127-6951d others(48): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127263 | ||||||
| chr3:57127263
|
AATATATA others(51): Show |
A | 29 | a0001c0001t0003g0117a0001c0001t0004g0333a0001c0001t0027g0331others(26): Show | 29 | HG01109.hp2 HG01243.hp2 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.127-7008_127-6951d others(60): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127263 | ||||||
| chr3:57127271
|
TA | T | 3 | a0002c0003t0002g0206a0002c0004t0049g0224a0003c0002t0001g0225 | 3 | HG00544.hp2 HG01109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.127-6959delT | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127271 | ||||||
| chr3:57127273
|
A | T | 88 | a0001c0001t0020g0021a0001c0001t0020g0250a0002c0003t0002g0099others(85): Show | 89 | HG00558.hp1 HG00639.hp2 HG00673.hp2 others(86): Show |
intron_variant | MODIFIER | c.127-6960T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127273 | ||||||
| chr3:57127273
|
AAAATATA others(3): Show |
A | 18 | a0001c0001t0003g0306a0001c0001t0004g0003a0001c0001t0004g0151others(15): Show | 19 | HG00741.hp2 HG01070.hp2 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.127-6970_127-6961d others(12): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127273 | ||||||
| chr3:57127275
|
A | T | 3 | a0002c0004t0049g0224a0002c0004t0057g0198a0003c0002t0001g0225 | 3 | HG01109.hp1 HG03041.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.127-6962T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127275 | ||||||
| chr3:57127283
|
T | A | 1 | a0002c0004t0057g0198 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.127-6970A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127283 | ||||||
| chr3:57127283
|
T | TAAATATA others(91): Show |
4 | a0002c0004t0008g0177a0002c0004t0008g0197a0002c0004t0008g0310others(1): Show | 4 | HG00099.hp1 HG00639.hp1 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-6971_127-6970i others(100): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127283 | ||||||
| chr3:57127285
|
A | T | 1 | a0001c0001t0004g0247 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.127-6972T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127285 | ||||||
| chr3:57127286
|
AT | A | 5 | a0002c0003t0013g0028a0002c0003t0013g0092a0002c0003t0013g0170others(2): Show | 5 | HG02622.hp2 HG02717.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.127-6974delA | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127286 | ||||||
| chr3:57127289
|
T | TAA | 87 | a0001c0001t0020g0021a0001c0001t0020g0250a0002c0003t0002g0099others(84): Show | 88 | HG00558.hp1 HG00639.hp2 HG00673.hp2 others(85): Show |
intron_variant | MODIFIER | c.127-6977_127-6976i others(4): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127289 | ||||||
| chr3:57127293
|
T | A | 1 | a0001c0001t0043g0144 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.127-6980A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127293 | ||||||
| chr3:57127295
|
A | T | 92 | a0001c0001t0020g0021a0001c0001t0020g0250a0002c0003t0002g0099others(89): Show | 93 | HG00558.hp1 HG00639.hp2 HG00673.hp2 others(90): Show |
intron_variant | MODIFIER | c.127-6982T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127295 | ||||||
| chr3:57127297
|
T | A | 22 | a0001c0001t0004g0027a0001c0001t0004g0059a0001c0001t0004g0110others(19): Show | 22 | HG00738.hp2 HG01255.hp2 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.127-6984A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127297 | ||||||
| chr3:57127297
|
TATATATA others(3): Show |
T | 4 | a0001c0001t0003g0282a0001c0001t0003g0283a0001c0001t0056g0273others(1): Show | 4 | HG01099.hp1 HG01884.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-6994_127-6985d others(12): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127297 | ||||||
| chr3:57127297
|
TATATATA others(55): Show |
T | 1 | a0002c0003t0013g0325 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.127-7046_127-6985d others(64): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127297 | ||||||
| chr3:57127299
|
T | A | 87 | a0001c0001t0020g0021a0001c0001t0020g0250a0002c0003t0002g0099others(84): Show | 88 | HG00558.hp1 HG00639.hp2 HG00673.hp2 others(85): Show |
intron_variant | MODIFIER | c.127-6986A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127299 | ||||||
| chr3:57127305
|
A | T | 111 | a0001c0001t0004g0027a0001c0001t0004g0059a0001c0001t0004g0110others(108): Show | 112 | HG00558.hp1 HG00639.hp2 HG00673.hp2 others(109): Show |
intron_variant | MODIFIER | c.127-6992T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127305 | ||||||
| chr3:57127305
|
AAAAT | A | 5 | a0002c0003t0013g0028a0002c0003t0013g0092a0002c0003t0013g0170others(2): Show | 5 | HG02622.hp2 HG02717.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.127-6996_127-6993d others(6): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127305 | ||||||
| chr3:57127307
|
A | T | 4 | a0002c0004t0008g0091a0002c0004t0008g0323a0002c0004t0049g0224others(1): Show | 4 | HG01109.hp1 HG03041.hp1 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-6994T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127307 | ||||||
| chr3:57127307
|
AATATATA others(15): Show |
A | 1 | a0002c0003t0002g0262 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.127-7016_127-6995d others(24): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127307 | ||||||
| chr3:57127313
|
TA | T | 87 | a0001c0001t0020g0021a0001c0001t0020g0250a0002c0003t0002g0099others(84): Show | 88 | HG00558.hp1 HG00639.hp2 HG00673.hp2 others(85): Show |
intron_variant | MODIFIER | c.127-7001delT | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127313 | ||||||
| chr3:57127315
|
A | T | 43 | a0001c0001t0004g0003a0001c0001t0004g0027a0001c0001t0004g0059others(40): Show | 44 | HG00738.hp2 HG00741.hp2 HG01070.hp2 others(41): Show |
intron_variant | MODIFIER | c.127-7002T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127315 | ||||||
| chr3:57127316
|
A | T | 87 | a0001c0001t0020g0021a0001c0001t0020g0250a0002c0003t0002g0099others(84): Show | 88 | HG00558.hp1 HG00639.hp2 HG00673.hp2 others(85): Show |
intron_variant | MODIFIER | c.127-7003T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127316 | ||||||
| chr3:57127317
|
A | T | 14 | a0002c0003t0012g0048a0002c0003t0012g0073a0002c0003t0012g0074others(11): Show | 14 | HG01255.hp1 HG01884.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.127-7004T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127317 | ||||||
| chr3:57127335
|
T | A | 87 | a0001c0001t0020g0021a0001c0001t0020g0250a0002c0003t0002g0099others(84): Show | 88 | HG00558.hp1 HG00639.hp2 HG00673.hp2 others(85): Show |
intron_variant | MODIFIER | c.127-7022A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127335 | ||||||
| chr3:57127335
|
TAAA | T | 14 | a0002c0003t0012g0048a0002c0003t0012g0073a0002c0003t0012g0074others(11): Show | 14 | HG01255.hp1 HG01884.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.127-7025_127-7023d others(5): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127335 | ||||||
| chr3:57127336
|
A | ATATAT | 87 | a0001c0001t0020g0021a0001c0001t0020g0250a0002c0003t0002g0099others(84): Show | 88 | HG00558.hp1 HG00639.hp2 HG00673.hp2 others(85): Show |
intron_variant | MODIFIER | c.127-7024_127-7023i others(7): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127336 | ||||||
| chr3:57127337
|
A | T | 31 | a0001c0001t0003g0117a0001c0001t0004g0333a0001c0001t0027g0331others(28): Show | 31 | HG01109.hp2 HG01243.hp2 HG02109.hp1 others(28): Show |
intron_variant | MODIFIER | c.127-7024T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127337 | ||||||
| chr3:57127338
|
A | T | 87 | a0001c0001t0020g0021a0001c0001t0020g0250a0002c0003t0002g0099others(84): Show | 88 | HG00558.hp1 HG00639.hp2 HG00673.hp2 others(85): Show |
intron_variant | MODIFIER | c.127-7025T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127338 | ||||||
| chr3:57127339
|
A | T | 2 | a0002c0004t0049g0224a0003c0002t0001g0225 | 2 | HG01109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.127-7026T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127339 | ||||||
| chr3:57127345
|
T | A | 2 | a0002c0004t0049g0224a0003c0002t0001g0225 | 2 | HG01109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.127-7032A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127345 | ||||||
| chr3:57127347
|
TA | T | 9 | a0001c0001t0003g0117a0001c0001t0027g0331a0001c0001t0038g0049others(6): Show | 9 | HG01243.hp2 HG02451.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.127-7035delT | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127347 | ||||||
| chr3:57127349
|
A | AT | 20 | a0001c0001t0004g0333a0001c0006t0011g0009a0001c0006t0011g0010others(17): Show | 20 | HG01109.hp2 HG02109.hp1 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.127-7037_127-7036i others(3): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127349 | ||||||
| chr3:57127355
|
T | TAA | 83 | a0001c0001t0020g0021a0001c0001t0020g0250a0002c0003t0002g0099others(80): Show | 84 | HG00558.hp1 HG00639.hp2 HG01069.hp1 others(81): Show |
intron_variant | MODIFIER | c.127-7043_127-7042i others(4): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127355 | ||||||
| chr3:57127355
|
TATAA | T | 13 | a0002c0003t0012g0048a0002c0003t0012g0073a0002c0003t0012g0074others(10): Show | 13 | HG01255.hp1 HG01884.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.127-7046_127-7043d others(6): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127355 | ||||||
| chr3:57127357
|
T | A | 23 | a0001c0001t0004g0333a0001c0006t0011g0009a0001c0006t0011g0010others(20): Show | 23 | HG00673.hp2 HG01109.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.127-7044A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127357 | ||||||
| chr3:57127359
|
A | T | 25 | a0001c0001t0004g0333a0001c0006t0011g0009a0001c0006t0011g0010others(22): Show | 25 | HG00673.hp2 HG01109.hp2 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.127-7046T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127359 | ||||||
| chr3:57127359
|
AATATAAA others(5): Show |
A | 2 | a0002c0004t0049g0224a0003c0002t0001g0225 | 2 | HG01109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.127-7058_127-7047d others(14): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127359 | ||||||
| chr3:57127361
|
T | A | 16 | a0002c0003t0002g0105a0002c0003t0012g0048a0002c0003t0012g0073others(13): Show | 16 | HG00673.hp2 HG01255.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.127-7048A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127361 | ||||||
| chr3:57127361
|
T | TATATATA others(266): Show |
1 | a0002c0004t0008g0323 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.127-7049_127-7048i others(275): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127361 | ||||||
| chr3:57127361
|
T | TATATATA others(266): Show |
1 | a0002c0004t0008g0091 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.127-7049_127-7048i others(275): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127361 | ||||||
| chr3:57127361
|
T | TATATATA others(148): Show |
4 | a0002c0004t0008g0177a0002c0004t0008g0197a0002c0004t0008g0310others(1): Show | 4 | HG00099.hp1 HG00639.hp1 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-7049_127-7048i others(157): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127361 | ||||||
| chr3:57127363
|
TAA | T | 9 | a0001c0001t0003g0117a0001c0001t0027g0331a0001c0001t0038g0049others(6): Show | 9 | HG01243.hp2 HG02451.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.127-7052_127-7051d others(4): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127363 | ||||||
| chr3:57127365
|
A | AATAT | 9 | a0001c0001t0007g0002a0001c0001t0007g0025a0001c0001t0007g0026others(6): Show | 10 | HG00280.hp2 HG01261.hp2 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.127-7056_127-7053d others(6): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127365 | ||||||
| chr3:57127365
|
A | T | 83 | a0001c0001t0020g0021a0001c0001t0020g0250a0002c0003t0002g0099others(80): Show | 84 | HG00558.hp1 HG00639.hp2 HG00673.hp2 others(81): Show |
intron_variant | MODIFIER | c.127-7052T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127365 | ||||||
| chr3:57127365
|
AAT | A | 3 | a0001c0001t0004g0264a0002c0003t0054g0020a0003c0002t0001g0121 | 3 | HG03471.hp1 HG03490.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.127-7054_127-7053d others(4): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127365 | ||||||
| chr3:57127365
|
AATAT | A | 5 | a0001c0001t0003g0163a0001c0001t0003g0174a0001c0001t0003g0336others(2): Show | 5 | HG01934.hp1 HG02280.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.127-7056_127-7053d others(6): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127365 | ||||||
| chr3:57127367
|
T | TAA | 81 | a0001c0001t0020g0021a0001c0001t0020g0250a0002c0003t0002g0099others(78): Show | 82 | HG00558.hp1 HG00639.hp2 HG01069.hp1 others(79): Show |
intron_variant | MODIFIER | c.127-7055_127-7054i others(4): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127367 | ||||||
| chr3:57127369
|
T | A | 30 | a0001c0001t0003g0117a0001c0001t0004g0333a0001c0001t0027g0331others(27): Show | 30 | HG01109.hp2 HG01243.hp2 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.127-7056A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127369 | ||||||
| chr3:57127369
|
T | TATATAAA others(58): Show |
30 | a0002c0003t0002g0051a0002c0003t0002g0052a0002c0003t0002g0053others(27): Show | 30 | HG00544.hp1 HG00558.hp2 HG02080.hp2 others(27): Show |
intron_variant | MODIFIER | c.127-7057_127-7056i others(67): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127369 | ||||||
| chr3:57127371
|
T | A | 19 | a0002c0003t0002g0105a0002c0003t0012g0048a0002c0003t0012g0073others(16): Show | 19 | HG00673.hp2 HG01255.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.127-7058A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127371 | ||||||
| chr3:57127373
|
T | A | 9 | a0001c0001t0003g0117a0001c0001t0027g0331a0001c0001t0038g0049others(6): Show | 9 | HG01243.hp2 HG02451.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.127-7060A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127373 | ||||||
| chr3:57127375
|
T | A | 125 | a0001c0001t0004g0333a0001c0001t0020g0021a0001c0001t0020g0250others(122): Show | 126 | HG00099.hp1 HG00558.hp1 HG00639.hp1 others(123): Show |
intron_variant | MODIFIER | c.127-7062A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127375 | ||||||
| chr3:57127375
|
TATAA | T | 12 | a0001c0001t0003g0210a0001c0001t0007g0002a0001c0001t0007g0025others(9): Show | 13 | HG00280.hp2 HG01261.hp2 HG01358.hp2 others(10): Show |
intron_variant | MODIFIER | c.127-7066_127-7063d others(6): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127375 | ||||||
| chr3:57127377
|
T | C | 1 | a0001c0001t0004g0240 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.127-7064A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127377 | ||||||
| chr3:57127379
|
A | T | 6 | a0002c0004t0008g0091a0002c0004t0008g0177a0002c0004t0008g0197others(3): Show | 6 | HG00099.hp1 HG00639.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-7066T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127379 | ||||||
| chr3:57127383
|
A | T | 30 | a0002c0003t0002g0051a0002c0003t0002g0052a0002c0003t0002g0053others(27): Show | 30 | HG00544.hp1 HG00558.hp2 HG02080.hp2 others(27): Show |
intron_variant | MODIFIER | c.127-7070T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127383 | ||||||
| chr3:57127387
|
A | T | 5 | a0002c0003t0013g0028a0002c0003t0013g0092a0002c0003t0013g0170others(2): Show | 5 | HG02622.hp2 HG02717.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.127-7074T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127387 | ||||||
| chr3:57127391
|
A | T | 17 | a0001c0001t0004g0333a0002c0003t0013g0028a0002c0003t0013g0092others(14): Show | 17 | HG01884.hp2 HG02109.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.127-7078T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127391 | ||||||
| chr3:57127395
|
A | AAT | 32 | a0001c0001t0004g0003a0001c0001t0004g0027a0001c0001t0004g0059others(29): Show | 33 | HG00741.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.127-7084_127-7083d others(4): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127395 | ||||||
| chr3:57127395
|
A | T | 46 | a0001c0001t0003g0117a0001c0001t0004g0111a0001c0001t0004g0333others(43): Show | 46 | HG00609.hp1 HG00738.hp2 HG01099.hp1 others(43): Show |
intron_variant | MODIFIER | c.127-7082T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127395 | ||||||
| chr3:57127395
|
AAT | A | 5 | a0002c0003t0014g0150a0002c0003t0014g0226a0002c0003t0053g0227others(2): Show | 5 | HG01109.hp1 HG02717.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.127-7084_127-7083d others(4): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127395 | ||||||
| chr3:57127399
|
T | A | 90 | a0001c0001t0003g0336a0001c0001t0020g0021a0001c0001t0020g0250others(87): Show | 91 | HG00099.hp1 HG00558.hp1 HG00639.hp1 others(88): Show |
intron_variant | MODIFIER | c.127-7086A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127399 | ||||||
| chr3:57127406
|
A | T | 1 | a0002c0007t0009g0148 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.127-7093T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127406 | ||||||
| chr3:57127408
|
A | AT | 3 | a0002c0003t0013g0028a0002c0003t0013g0170a0002c0003t0021g0342 | 3 | HG02717.hp2 HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.127-7096dupA | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127408 | ||||||
| chr3:57127408
|
A | T | 2 | a0002c0004t0019g0006a0002c0007t0009g0148 | 2 | HG02922.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.127-7095T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127408 | ||||||
| chr3:57127410
|
A | ATT | 4 | a0001c0001t0004g0190a0001c0001t0004g0292a0001c0001t0027g0331others(1): Show | 4 | HG01123.hp2 HG02109.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-7098_127-7097i others(4): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127410 | ||||||
| chr3:57127410
|
A | T | 20 | a0001c0001t0003g0203a0001c0001t0004g0333a0001c0001t0005g0191others(17): Show | 20 | HG00544.hp2 HG01884.hp2 HG02622.hp1 others(17): Show |
intron_variant | MODIFIER | c.127-7097T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127410 | ||||||
| chr3:57127411
|
TA | T | 7 | a0001c0006t0011g0009a0001c0006t0011g0010a0001c0006t0011g0011others(4): Show | 7 | HG01109.hp2 HG02145.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.127-7099delT | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127411 | ||||||
| chr3:57127412
|
A | ATATTTT | 27 | a0002c0003t0002g0051a0002c0003t0002g0052a0002c0003t0002g0053others(24): Show | 27 | HG00544.hp1 HG00558.hp2 HG02080.hp2 others(24): Show |
intron_variant | MODIFIER | c.127-7100_127-7099i others(8): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127412 | ||||||
| chr3:57127412
|
A | ATT | 9 | a0001c0001t0004g0149a0001c0001t0034g0109a0002c0007t0009g0088others(6): Show | 9 | HG02109.hp1 HG02559.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.127-7101_127-7100d others(4): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127412 | ||||||
| chr3:57127412
|
A | ATTTTTT | 6 | a0001c0001t0003g0117a0002c0003t0002g0062a0005c0008t0006g0058others(3): Show | 6 | HG01243.hp2 HG03139.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.127-7105_127-7100d others(8): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127412 | ||||||
| chr3:57127412
|
A | T | 142 | a0001c0001t0003g0014a0001c0001t0003g0057a0001c0001t0003g0174others(139): Show | 145 | HG00280.hp2 HG00544.hp2 HG00609.hp1 others(142): Show |
intron_variant | MODIFIER | c.127-7099T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127412 | ||||||
| chr3:57127412
|
AT | A | 91 | a0001c0001t0020g0021a0001c0001t0020g0250a0002c0003t0002g0099others(88): Show | 92 | HG00099.hp1 HG00558.hp1 HG00639.hp1 others(89): Show |
intron_variant | MODIFIER | c.127-7100delA | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127412 | ||||||
| chr3:57127414
|
T | A | 3 | a0001c0001t0004g0193a0001c0001t0004g0255a0001c0001t0037g0055 | 3 | HG01361.hp2 HG01516.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.127-7101A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127414 | ||||||
| chr3:57127415
|
T | A | 1 | a0003c0002t0001g0067 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.127-7102A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127415 | ||||||
| chr3:57127445
|
G | A | 1 | a0003c0002t0001g0131 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.127-7132C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127445 | ||||||
| chr3:57127551
|
G | A | 4 | a0002c0003t0012g0048a0002c0003t0012g0073a0002c0003t0012g0074others(1): Show | 4 | HG01255.hp1 HG01891.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-7238C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127551 | ||||||
| chr3:57127597
|
G | A | 1 | a0002c0004t0050g0321 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.127-7284C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127597 | ||||||
| chr3:57127859
|
C | A | 1 | a0001c0001t0034g0109 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.127-7546G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127859 | ||||||
| chr3:57127902
|
T | C | 2 | a0002c0004t0049g0224a0003c0002t0001g0225 | 2 | HG01109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.127-7589A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57127902 | ||||||
| chr3:57128144
|
T | C | 1 | a0002c0004t0050g0321 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.127-7831A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57128144 | ||||||
| chr3:57128146
|
T | C | 1 | a0002c0003t0054g0020 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.127-7833A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57128146 | ||||||
| chr3:57128147
|
G | A | 1 | a0002c0003t0012g0074 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.127-7834C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57128147 | ||||||
| chr3:57128250
|
G | A | 6 | a0002c0004t0008g0091a0002c0004t0008g0177a0002c0004t0008g0197others(3): Show | 6 | HG00099.hp1 HG00639.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-7937C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57128250 | ||||||
| chr3:57128338
|
A | G | 2 | a0001c0001t0003g0289a0001c0001t0003g0338 | 2 | NA18949.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.127-8025T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57128338 | ||||||
| chr3:57128431
|
G | A | 1 | a0002c0003t0002g0202 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.127-8118C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57128431 | ||||||
| chr3:57128443
|
G | A | 29 | a0002c0003t0002g0051a0002c0003t0002g0052a0002c0003t0002g0053others(26): Show | 29 | HG00544.hp1 HG00558.hp2 HG02080.hp2 others(26): Show |
intron_variant | MODIFIER | c.127-8130C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57128443 | ||||||
| chr3:57128448
|
C | T | 86 | a0001c0001t0020g0021a0001c0001t0020g0250a0002c0003t0002g0099others(83): Show | 87 | HG00558.hp1 HG00639.hp2 HG00673.hp2 others(84): Show |
intron_variant | MODIFIER | c.127-8135G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57128448 | ||||||
| chr3:57128449
|
G | A | 29 | a0002c0003t0002g0051a0002c0003t0002g0052a0002c0003t0002g0053others(26): Show | 29 | HG00544.hp1 HG00558.hp2 HG02080.hp2 others(26): Show |
intron_variant | MODIFIER | c.127-8136C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57128449 | ||||||
| chr3:57128530
|
C | T | 2 | a0003c0002t0001g0095a0003c0002t0001g0133 | 2 | NA18970.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.127-8217G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57128530 | ||||||
| chr3:57128551
|
C | CGAAATCC others(26): Show |
17 | a0002c0003t0002g0051a0002c0003t0002g0052a0002c0003t0002g0053others(14): Show | 17 | HG02080.hp2 HG02132.hp1 HG02135.hp2 others(14): Show |
intron_variant | MODIFIER | c.127-8271_127-8239d others(35): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57128551 | ||||||
| chr3:57128576
|
A | G | 2 | a0003c0002t0001g0216a0003c0002t0001g0291 | 2 | HG02040.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.127-8263T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57128576 | ||||||
| chr3:57128706
|
C | G | 4 | a0002c0004t0016g0335a0002c0004t0016g0343a0002c0004t0016g0344others(1): Show | 4 | HG02257.hp1 HG02559.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-8393G>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57128706 | ||||||
| chr3:57128715
|
A | G | 1 | a0002c0004t0057g0198 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.127-8402T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57128715 | ||||||
| chr3:57128812
|
C | A | 2 | a0002c0004t0049g0224a0003c0002t0001g0225 | 2 | HG01109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.127-8499G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57128812 | ||||||
| chr3:57128857
|
C | T | 2 | a0002c0004t0049g0224a0003c0002t0001g0225 | 2 | HG01109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.127-8544G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57128857 | ||||||
| chr3:57129144
|
A | T | 8 | a0001c0001t0052g0311a0002c0003t0012g0254a0004c0005t0010g0075others(5): Show | 8 | HG01243.hp1 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.127-8831T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57129144 | ||||||
| chr3:57129173
|
G | A | 2 | a0002c0004t0049g0224a0003c0002t0001g0225 | 2 | HG01109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.127-8860C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57129173 | ||||||
| chr3:57129303
|
C | T | 1 | a0002c0003t0002g0104 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.127-8990G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57129303 | ||||||
| chr3:57129367
|
A | G | 3 | a0003c0002t0001g0138a0003c0002t0001g0140a0003c0002t0015g0139 | 3 | HG02896.hp1 HG02897.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.127-9054T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57129367 | ||||||
| chr3:57129566
|
C | T | 2 | a0002c0003t0013g0170a0002c0003t0014g0169 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.127-9253G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57129566 | ||||||
| chr3:57129669
|
G | C | 6 | a0002c0004t0008g0091a0002c0004t0008g0177a0002c0004t0008g0197others(3): Show | 6 | HG00099.hp1 HG00639.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-9356C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57129669 | ||||||
| chr3:57129671
|
A | G | 6 | a0002c0003t0002g0099a0003c0002t0001g0024a0003c0002t0001g0050others(3): Show | 6 | NA18962.hp2 NA18974.hp2 NA18989.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-9358T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57129671 | ||||||
| chr3:57129723
|
T | C | 169 | a0001c0001t0003g0117a0001c0001t0004g0333a0001c0001t0020g0021others(166): Show | 170 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(167): Show |
intron_variant | MODIFIER | c.127-9410A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57129723 | ||||||
| chr3:57129737
|
C | T | 87 | a0001c0001t0020g0021a0001c0001t0020g0250a0002c0003t0002g0099others(84): Show | 88 | HG00558.hp1 HG00639.hp2 HG00673.hp2 others(85): Show |
intron_variant | MODIFIER | c.127-9424G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57129737 | ||||||
| chr3:57129859
|
G | T | 133 | a0001c0001t0003g0117a0001c0001t0004g0333a0001c0001t0020g0021others(130): Show | 134 | HG00558.hp1 HG00639.hp2 HG00673.hp2 others(131): Show |
intron_variant | MODIFIER | c.127-9546C>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57129859 | ||||||
| chr3:57129986
|
C | T | 1 | a0003c0002t0001g0138 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.127-9673G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57129986 | ||||||
| chr3:57129996
|
C | T | 1 | a0003c0002t0001g0156 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.127-9683G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57129996 | ||||||
| chr3:57130154
|
C | A | 1 | a0001c0001t0004g0176 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.127-9841G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57130154 | ||||||
| chr3:57130229
|
G | T | 2 | a0001c0001t0007g0142a0001c0001t0007g0239 | 2 | HG02735.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.127-9916C>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57130229 | ||||||
| chr3:57130334
|
C | T | 87 | a0001c0001t0020g0021a0001c0001t0020g0250a0002c0003t0002g0099others(84): Show | 88 | HG00558.hp1 HG00639.hp2 HG00673.hp2 others(85): Show |
intron_variant | MODIFIER | c.127-10021G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57130334 | ||||||
| chr3:57130380
|
A | T | 87 | a0001c0001t0020g0021a0001c0001t0020g0250a0002c0003t0002g0099others(84): Show | 88 | HG00558.hp1 HG00639.hp2 HG00673.hp2 others(85): Show |
intron_variant | MODIFIER | c.127-10067T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57130380 | ||||||
| chr3:57130562
|
G | A | 1 | a0002c0004t0057g0198 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.127-10249C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57130562 | ||||||
| chr3:57130578
|
G | C | 1 | a0002c0003t0002g0034 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.127-10265C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57130578 | ||||||
| chr3:57130597
|
G | A | 46 | a0001c0001t0003g0117a0001c0001t0004g0333a0001c0001t0027g0331others(43): Show | 46 | HG01109.hp1 HG01109.hp2 HG01243.hp2 others(43): Show |
intron_variant | MODIFIER | c.127-10284C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57130597 | ||||||
| chr3:57130667
|
C | G | 5 | a0002c0007t0009g0088a0002c0007t0009g0089a0002c0007t0009g0167others(2): Show | 5 | HG02109.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.127-10354G>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57130667 | ||||||
| chr3:57130670
|
G | A | 1 | a0001c0001t0003g0237 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.127-10357C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57130670 | ||||||
| chr3:57130771
|
T | C | 6 | a0002c0004t0008g0091a0002c0004t0008g0177a0002c0004t0008g0197others(3): Show | 6 | HG00099.hp1 HG00639.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-10458A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57130771 | ||||||
| chr3:57130821
|
T | A | 29 | a0002c0003t0002g0051a0002c0003t0002g0052a0002c0003t0002g0053others(26): Show | 29 | HG00544.hp1 HG00558.hp2 HG02080.hp2 others(26): Show |
intron_variant | MODIFIER | c.127-10508A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57130821 | ||||||
| chr3:57130901
|
G | A | 133 | a0001c0001t0003g0117a0001c0001t0004g0333a0001c0001t0020g0021others(130): Show | 134 | HG00558.hp1 HG00639.hp2 HG00673.hp2 others(131): Show |
intron_variant | MODIFIER | c.127-10588C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57130901 | ||||||
| chr3:57130931
|
C | T | 4 | a0001c0001t0004g0149a0001c0001t0004g0168a0001c0001t0004g0176others(1): Show | 4 | HG02258.hp2 HG02922.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-10618G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57130931 | ||||||
| chr3:57131055
|
G | A | 1 | a0003c0002t0001g0039 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.127-10742C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57131055 | ||||||
| chr3:57131055
|
G | C | 1 | a0001c0001t0005g0328 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.127-10742C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57131055 | ||||||
| chr3:57131063
|
G | C | 1 | a0002c0003t0002g0034 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.127-10750C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57131063 | ||||||
| chr3:57131216
|
T | C | 44 | a0001c0001t0003g0117a0001c0001t0004g0333a0001c0001t0027g0331others(41): Show | 44 | HG01109.hp2 HG01243.hp2 HG01255.hp1 others(41): Show |
intron_variant | MODIFIER | c.127-10903A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57131216 | ||||||
| chr3:57131232
|
T | C | 6 | a0002c0003t0013g0028a0002c0003t0013g0092a0002c0003t0013g0170others(3): Show | 6 | HG02622.hp2 HG02717.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.127-10919A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57131232 | ||||||
| chr3:57131278
|
G | A | 1 | a0001c0001t0039g0288 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.127-10965C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57131278 | ||||||
| chr3:57131279
|
C | T | 1 | a0001c0001t0025g0349 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.127-10966G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57131279 | ||||||
| chr3:57131282
|
C | A | 87 | a0001c0001t0020g0021a0001c0001t0020g0250a0002c0003t0002g0099others(84): Show | 88 | HG00558.hp1 HG00639.hp2 HG00673.hp2 others(85): Show |
intron_variant | MODIFIER | c.127-10969G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57131282 | ||||||
| chr3:57131329
|
C | G | 1 | a0003c0002t0001g0171 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.127-11016G>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57131329 | ||||||
| chr3:57131540
|
T | G | 1 | a0002c0003t0002g0199 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.127-11227A>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57131540 | ||||||
| chr3:57131627
|
C | T | 3 | a0002c0003t0014g0226a0002c0003t0014g0228a0002c0003t0053g0227 | 3 | HG01109.hp2 HG02717.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.127-11314G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57131627 | ||||||
| chr3:57131654
|
G | A | 1 | a0001c0001t0003g0175 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.127-11341C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57131654 | ||||||
| chr3:57131787
|
C | T | 2 | a0003c0002t0001g0140a0003c0002t0015g0139 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.127-11474G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57131787 | ||||||
| chr3:57131837
|
T | C | 1 | a0002c0003t0002g0340 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.127-11524A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57131837 | ||||||
| chr3:57131882
|
C | T | 1 | a0008c0014t0018g0329 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.127-11569G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57131882 | ||||||
| chr3:57132113
|
G | A | 1 | a0002c0003t0012g0074 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.127-11800C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57132113 | ||||||
| chr3:57132125
|
G | A | 3 | a0001c0001t0004g0193a0001c0001t0004g0255a0001c0001t0004g0292 | 3 | HG01361.hp2 HG01516.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.127-11812C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57132125 | ||||||
| chr3:57132195
|
G | A | 1 | a0002c0003t0014g0150 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.127-11882C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57132195 | ||||||
| chr3:57132198
|
C | T | 1 | a0001c0001t0052g0311 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.127-11885G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57132198 | ||||||
| chr3:57132300
|
C | CA | 9 | a0001c0001t0027g0331a0001c0001t0038g0049a0001c0006t0011g0009others(6): Show | 9 | HG02145.hp2 HG02451.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.127-11988dupT | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57132300 | ||||||
| chr3:57132320
|
C | T | 6 | a0002c0004t0008g0091a0002c0004t0008g0177a0002c0004t0008g0197others(3): Show | 6 | HG00099.hp1 HG00639.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-12007G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57132320 | ||||||
| chr3:57132352
|
C | T | 1 | a0001c0001t0004g0333 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.127-12039G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57132352 | ||||||
| chr3:57132353
|
G | A | 2 | a0001c0001t0005g0188a0001c0001t0005g0245 | 2 | NA18943.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.127-12040C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57132353 | ||||||
| chr3:57132415
|
G | A | 4 | a0002c0003t0012g0048a0002c0003t0012g0073a0002c0003t0012g0074others(1): Show | 4 | HG01255.hp1 HG01891.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-12102C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57132415 | ||||||
| chr3:57132587
|
T | C | 4 | a0002c0004t0019g0005a0002c0004t0019g0006a0002c0004t0048g0007others(1): Show | 4 | HG01884.hp2 HG02109.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-12274A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57132587 | ||||||
| chr3:57132604
|
T | C | 1 | a0001c0001t0003g0281 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.127-12291A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57132604 | ||||||
| chr3:57132929
|
G | A | 6 | a0002c0004t0008g0091a0002c0004t0008g0177a0002c0004t0008g0197others(3): Show | 6 | HG00099.hp1 HG00639.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-12616C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57132929 | ||||||
| chr3:57133111
|
A | T | 1 | a0002c0003t0012g0074 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.127-12798T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57133111 | ||||||
| chr3:57133112
|
C | G | 1 | a0002c0003t0012g0074 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.127-12799G>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57133112 | ||||||
| chr3:57133113
|
A | T | 1 | a0002c0003t0012g0074 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.127-12800T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57133113 | ||||||
| chr3:57133364
|
T | C | 44 | a0001c0001t0003g0117a0001c0001t0004g0333a0001c0001t0027g0331others(41): Show | 44 | HG01109.hp2 HG01243.hp2 HG01255.hp1 others(41): Show |
intron_variant | MODIFIER | c.127-13051A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57133364 | ||||||
| chr3:57133401
|
G | GCA | 3 | a0002c0003t0022g0107a0002c0003t0022g0158a0002c0003t0055g0008 | 3 | HG02622.hp1 HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.127-13090_127-1308 others(6): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57133401 | ||||||
| chr3:57133403
|
A | G | 1 | a0002c0003t0002g0082 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.127-13090T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57133403 | ||||||
| chr3:57133456
|
T | C | 1 | a0003c0002t0001g0119 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.127-13143A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57133456 | ||||||
| chr3:57133674
|
C | G | 3 | a0002c0004t0008g0177a0002c0004t0008g0197a0002c0004t0008g0310 | 3 | HG00099.hp1 HG00639.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.127-13361G>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57133674 | ||||||
| chr3:57133703
|
T | A | 2 | a0002c0004t0008g0323a0002c0004t0008g0324 | 2 | HG03017.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.127-13390A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57133703 | ||||||
| chr3:57133709
|
G | C | 5 | a0002c0003t0014g0150a0002c0003t0014g0226a0002c0003t0014g0228others(2): Show | 5 | HG01109.hp2 HG02717.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.127-13396C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57133709 | ||||||
| chr3:57133723
|
A | C | 1 | a0008c0014t0018g0329 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.127-13410T>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57133723 | ||||||
| chr3:57133915
|
G | T | 3 | a0003c0002t0001g0253a0003c0002t0015g0172a0003c0002t0015g0303 | 3 | HG01169.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.127-13602C>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57133915 | ||||||
| chr3:57133951
|
T | C | 1 | a0001c0001t0003g0266 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.127-13638A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57133951 | ||||||
| chr3:57134126
|
G | A | 6 | a0002c0004t0008g0091a0002c0004t0008g0177a0002c0004t0008g0197others(3): Show | 6 | HG00099.hp1 HG00639.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-13813C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57134126 | ||||||
| chr3:57134245
|
T | C | 169 | a0001c0001t0003g0117a0001c0001t0004g0333a0001c0001t0020g0021others(166): Show | 170 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(167): Show |
intron_variant | MODIFIER | c.127-13932A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57134245 | ||||||
| chr3:57134311
|
C | A | 1 | a0001c0001t0043g0144 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.127-13998G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57134311 | ||||||
| chr3:57134313
|
C | T | 134 | a0001c0001t0003g0117a0001c0001t0004g0333a0001c0001t0020g0021others(131): Show | 135 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(132): Show |
intron_variant | MODIFIER | c.127-14000G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57134313 | ||||||
| chr3:57134518
|
A | G | 4 | a0002c0003t0012g0048a0002c0003t0012g0073a0002c0003t0012g0074others(1): Show | 4 | HG01255.hp1 HG01891.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-14205T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57134518 | ||||||
| chr3:57134564
|
C | T | 4 | a0002c0003t0002g0105a0003c0002t0001g0253a0003c0002t0015g0172others(1): Show | 4 | HG01169.hp2 HG01891.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-14251G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57134564 | ||||||
| chr3:57134643
|
C | T | 4 | a0002c0003t0012g0048a0002c0003t0012g0073a0002c0003t0012g0074others(1): Show | 4 | HG01255.hp1 HG01891.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-14330G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57134643 | ||||||
| chr3:57134706
|
G | T | 1 | a0001c0001t0005g0243 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.127-14393C>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57134706 | ||||||
| chr3:57134765
|
G | A | 130 | a0001c0001t0003g0117a0001c0001t0004g0333a0001c0001t0020g0021others(127): Show | 131 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(128): Show |
intron_variant | MODIFIER | c.127-14452C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57134765 | ||||||
| chr3:57135118
|
AAAAC | A | 4 | a0002c0003t0002g0105a0003c0002t0001g0253a0003c0002t0015g0172others(1): Show | 4 | HG01169.hp2 HG01891.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-14809_127-1480 others(8): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57135118 | ||||||
| chr3:57135145
|
C | CA | 114 | a0001c0001t0004g0333a0001c0001t0020g0021a0001c0001t0020g0250others(111): Show | 115 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(112): Show |
intron_variant | MODIFIER | c.127-14833dupT | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57135145 | ||||||
| chr3:57135145
|
C | CAA | 10 | a0001c0001t0003g0117a0002c0007t0009g0088a0002c0007t0009g0089others(7): Show | 10 | HG01243.hp2 HG02109.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.127-14834_127-1483 others(6): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57135145 | ||||||
| chr3:57135146
|
A | AC | 5 | a0002c0003t0014g0150a0002c0003t0014g0226a0002c0003t0014g0228others(2): Show | 5 | HG01109.hp2 HG02717.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.127-14834_127-1483 others(5): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57135146 | ||||||
| chr3:57135185
|
C | T | 1 | a0003c0002t0001g0098 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.127-14872G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57135185 | ||||||
| chr3:57135206
|
C | G | 1 | a0003c0002t0001g0252 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.127-14893G>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57135206 | ||||||
| chr3:57135245
|
C | A | 1 | a0001c0001t0004g0118 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.127-14932G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57135245 | ||||||
| chr3:57135412
|
G | C | 8 | a0002c0003t0002g0186a0002c0003t0002g0286a0002c0003t0002g0299others(5): Show | 8 | HG02165.hp1 NA18974.hp1 NA18975.hp1 others(5): Show |
intron_variant | MODIFIER | c.127-15099C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57135412 | ||||||
| chr3:57135488
|
G | A | 1 | a0001c0001t0033g0085 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.127-15175C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57135488 | ||||||
| chr3:57135575
|
C | T | 1 | a0003c0002t0001g0093 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.127-15262G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57135575 | ||||||
| chr3:57135620
|
T | C | 93 | a0001c0001t0020g0021a0001c0001t0020g0250a0001c0001t0027g0331others(90): Show | 94 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.127-15307A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57135620 | ||||||
| chr3:57135742
|
C | T | 3 | a0002c0003t0002g0293a0002c0003t0002g0294a0002c0015t0002g0295 | 3 | HG02165.hp2 NA18959.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.127-15429G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57135742 | ||||||
| chr3:57135857
|
C | T | 1 | a0001c0001t0004g0248 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.127-15544G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57135857 | ||||||
| chr3:57135858
|
G | A | 1 | a0001c0001t0027g0331 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.127-15545C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57135858 | ||||||
| chr3:57135889
|
G | GTGTA | 134 | a0001c0001t0003g0117a0001c0001t0004g0333a0001c0001t0020g0021others(131): Show | 135 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(132): Show |
intron_variant | MODIFIER | c.127-15577_127-1557 others(8): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57135889 | ||||||
| chr3:57135963
|
C | T | 2 | a0002c0004t0049g0224a0003c0002t0001g0225 | 2 | HG01109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.127-15650G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57135963 | ||||||
| chr3:57136261
|
C | T | 7 | a0002c0003t0013g0028a0002c0003t0013g0092a0002c0003t0013g0170others(4): Show | 7 | HG01109.hp1 HG02622.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.127-15948G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57136261 | ||||||
| chr3:57136373
|
C | T | 1 | a0002c0004t0057g0198 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.127-16060G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57136373 | ||||||
| chr3:57136416
|
C | A | 6 | a0003c0002t0001g0023a0003c0002t0001g0127a0003c0002t0001g0131others(3): Show | 6 | HG01074.hp1 HG01192.hp2 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-16103G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57136416 | ||||||
| chr3:57136467
|
G | C | 132 | a0001c0001t0003g0117a0001c0001t0004g0333a0001c0001t0020g0021others(129): Show | 133 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(130): Show |
intron_variant | MODIFIER | c.127-16154C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57136467 | ||||||
| chr3:57136641
|
C | CA | 28 | a0001c0001t0003g0175a0001c0001t0003g0289a0001c0001t0003g0338others(25): Show | 29 | HG00741.hp2 HG01069.hp2 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.127-16329dupT | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57136641 | ||||||
| chr3:57136641
|
CA | C | 43 | a0001c0001t0003g0266a0001c0001t0003g0281a0001c0001t0004g0111others(40): Show | 44 | HG00544.hp1 HG00544.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.127-16329delT | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57136641 | ||||||
| chr3:57136641
|
CAA | C | 75 | a0001c0001t0020g0021a0001c0001t0020g0250a0001c0001t0027g0331others(72): Show | 75 | HG00558.hp1 HG00639.hp2 HG00673.hp2 others(72): Show |
intron_variant | MODIFIER | c.127-16330_127-1632 others(6): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57136641 | ||||||
| chr3:57136641
|
CAAA | C | 15 | a0002c0003t0002g0105a0002c0003t0012g0048a0002c0003t0012g0073others(12): Show | 15 | HG01255.hp1 HG01891.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.127-16331_127-1632 others(7): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57136641 | ||||||
| chr3:57136641
|
CAAAA | C | 34 | a0001c0001t0003g0117a0001c0001t0004g0333a0002c0003t0002g0154others(31): Show | 34 | HG00099.hp1 HG00639.hp1 HG01099.hp2 others(31): Show |
intron_variant | MODIFIER | c.127-16332_127-1632 others(8): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57136641 | ||||||
| chr3:57136641
|
CAAAAA | C | 25 | a0002c0003t0002g0051a0002c0003t0002g0052a0002c0003t0002g0053others(22): Show | 25 | HG00558.hp2 HG02080.hp2 HG02132.hp1 others(22): Show |
intron_variant | MODIFIER | c.127-16333_127-1632 others(9): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57136641 | ||||||
| chr3:57136712
|
C | T | 4 | a0002c0004t0016g0335a0002c0004t0016g0343a0002c0004t0016g0344others(1): Show | 4 | HG02257.hp1 HG02559.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-16399G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57136712 | ||||||
| chr3:57136716
|
T | C | 2 | a0001c0001t0003g0195a0001c0001t0026g0287 | 2 | HG00642.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.127-16403A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57136716 | ||||||
| chr3:57136738
|
T | G | 18 | a0002c0003t0002g0051a0002c0003t0002g0052a0002c0003t0002g0053others(15): Show | 18 | HG02080.hp2 HG02132.hp1 HG02135.hp2 others(15): Show |
intron_variant | MODIFIER | c.127-16425A>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57136738 | ||||||
| chr3:57136863
|
A | G | 6 | a0002c0004t0008g0091a0002c0004t0008g0177a0002c0004t0008g0197others(3): Show | 6 | HG00099.hp1 HG00639.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-16550T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57136863 | ||||||
| chr3:57136879
|
G | C | 128 | a0001c0001t0003g0117a0001c0001t0004g0333a0001c0001t0020g0021others(125): Show | 129 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(126): Show |
intron_variant | MODIFIER | c.127-16566C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57136879 | ||||||
| chr3:57136881
|
TAA | T | 28 | a0002c0003t0002g0051a0002c0003t0002g0052a0002c0003t0002g0053others(25): Show | 28 | HG00558.hp2 HG02080.hp2 HG02132.hp1 others(25): Show |
intron_variant | MODIFIER | c.127-16570_127-1656 others(6): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57136881 | ||||||
| chr3:57136924
|
A | T | 1 | a0002c0004t0057g0198 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.127-16611T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57136924 | ||||||
| chr3:57137048
|
C | T | 1 | a0002c0003t0002g0105 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.127-16735G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57137048 | ||||||
| chr3:57137062
|
G | T | 1 | a0002c0003t0002g0186 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.127-16749C>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57137062 | ||||||
| chr3:57137297
|
T | C | 5 | a0001c0001t0004g0257a0001c0001t0006g0162a0001c0001t0006g0263others(2): Show | 5 | HG03098.hp1 HG03098.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.127-16984A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57137297 | ||||||
| chr3:57137334
|
G | A | 1 | a0003c0002t0001g0068 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.127-17021C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57137334 | ||||||
| chr3:57137343
|
C | A | 1 | a0002c0007t0009g0088 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.127-17030G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57137343 | ||||||
| chr3:57137346
|
G | A | 1 | a0002c0007t0009g0088 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.127-17033C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57137346 | ||||||
| chr3:57137378
|
C | A | 33 | a0001c0001t0004g0003a0001c0001t0004g0027a0001c0001t0004g0059others(30): Show | 34 | HG00738.hp2 HG00741.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.127-17065G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57137378 | ||||||
| chr3:57137526
|
G | C | 93 | a0001c0001t0020g0021a0001c0001t0020g0250a0001c0001t0027g0331others(90): Show | 94 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.127-17213C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57137526 | ||||||
| chr3:57137646
|
C | A | 1 | a0002c0004t0057g0198 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.127-17333G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57137646 | ||||||
| chr3:57137674
|
A | G | 1 | a0001c0001t0052g0311 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.127-17361T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57137674 | ||||||
| chr3:57137777
|
G | A | 28 | a0002c0003t0002g0051a0002c0003t0002g0052a0002c0003t0002g0053others(25): Show | 28 | HG00558.hp2 HG02080.hp2 HG02132.hp1 others(25): Show |
intron_variant | MODIFIER | c.127-17464C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57137777 | ||||||
| chr3:57137805
|
C | T | 4 | a0002c0003t0014g0150a0002c0003t0014g0226a0002c0003t0014g0228others(1): Show | 4 | HG01109.hp2 HG02717.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-17492G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57137805 | ||||||
| chr3:57137874
|
T | C | 132 | a0001c0001t0003g0117a0001c0001t0004g0333a0001c0001t0020g0021others(129): Show | 133 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(130): Show |
intron_variant | MODIFIER | c.127-17561A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57137874 | ||||||
| chr3:57137967
|
A | C | 4 | a0002c0003t0002g0105a0003c0002t0001g0253a0003c0002t0015g0172others(1): Show | 4 | HG01169.hp2 HG01891.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-17654T>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57137967 | ||||||
| chr3:57138233
|
TA | T | 3 | a0002c0004t0016g0335a0002c0004t0016g0343a0002c0004t0016g0344 | 3 | HG02257.hp1 HG02886.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.127-17921delT | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57138233 | ||||||
| chr3:57138419
|
C | T | 28 | a0002c0003t0002g0051a0002c0003t0002g0052a0002c0003t0002g0053others(25): Show | 28 | HG00558.hp2 HG02080.hp2 HG02132.hp1 others(25): Show |
intron_variant | MODIFIER | c.127-18106G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57138419 | ||||||
| chr3:57138511
|
G | A | 1 | a0001c0001t0004g0059 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.127-18198C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57138511 | ||||||
| chr3:57138517
|
T | C | 1 | a0002c0003t0002g0105 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.127-18204A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57138517 | ||||||
| chr3:57138543
|
G | T | 4 | a0002c0003t0014g0150a0002c0003t0014g0226a0002c0003t0014g0228others(1): Show | 4 | HG01109.hp2 HG02717.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-18230C>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57138543 | ||||||
| chr3:57138582
|
A | G | 1 | a0002c0003t0014g0150 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.127-18269T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57138582 | ||||||
| chr3:57138614
|
C | T | 8 | a0001c0001t0003g0203a0001c0001t0003g0266a0001c0001t0003g0267others(5): Show | 10 | HG00609.hp2 NA18941.hp2 NA18956.hp1 others(7): Show |
intron_variant | MODIFIER | c.127-18301G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57138614 | ||||||
| chr3:57138865
|
G | A | 28 | a0002c0003t0002g0051a0002c0003t0002g0052a0002c0003t0002g0053others(25): Show | 28 | HG00558.hp2 HG02080.hp2 HG02132.hp1 others(25): Show |
intron_variant | MODIFIER | c.127-18552C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57138865 | ||||||
| chr3:57138939
|
C | CA | 24 | a0001c0001t0003g0211a0001c0001t0004g0168a0001c0001t0004g0247others(21): Show | 24 | HG00642.hp1 HG01109.hp1 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.127-18627dupT | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57138939 | ||||||
| chr3:57138939
|
CA | C | 11 | a0001c0001t0003g0203a0001c0001t0003g0266a0001c0001t0003g0267others(8): Show | 13 | HG00609.hp2 HG01074.hp2 HG03516.hp2 others(10): Show |
intron_variant | MODIFIER | c.127-18627delT | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57138939 | ||||||
| chr3:57138993
|
A | T | 129 | a0001c0001t0003g0117a0001c0001t0004g0333a0001c0001t0020g0021others(126): Show | 130 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(127): Show |
intron_variant | MODIFIER | c.127-18680T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57138993 | ||||||
| chr3:57139064
|
G | A | 11 | a0001c0001t0003g0117a0002c0007t0009g0088a0002c0007t0009g0089others(8): Show | 11 | HG01243.hp2 HG02109.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.127-18751C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57139064 | ||||||
| chr3:57139196
|
C | G | 1 | a0002c0003t0002g0105 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.127-18883G>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57139196 | ||||||
| chr3:57139236
|
C | T | 1 | a0002c0003t0002g0086 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.127-18923G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57139236 | ||||||
| chr3:57139322
|
G | A | 1 | a0001c0001t0027g0331 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.127-19009C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57139322 | ||||||
| chr3:57139515
|
CT | C | 119 | a0001c0001t0003g0117a0001c0001t0004g0333a0001c0001t0006g0114others(116): Show | 120 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(117): Show |
intron_variant | MODIFIER | c.127-19203delA | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57139515 | ||||||
| chr3:57139515
|
CTT | C | 11 | a0002c0003t0002g0105a0002c0003t0014g0150a0002c0003t0014g0226others(8): Show | 11 | HG00099.hp1 HG00639.hp1 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.127-19204_127-1920 others(6): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57139515 | ||||||
| chr3:57139887
|
T | C | 274 | a0001c0001t0003g0117a0001c0001t0003g0281a0001c0001t0003g0282others(271): Show | 277 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(274): Show |
intron_variant | MODIFIER | c.127-19574A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57139887 | ||||||
| chr3:57139933
|
G | C | 1 | a0002c0003t0002g0206 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.127-19620C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57139933 | ||||||
| chr3:57140246
|
T | C | 40 | a0001c0001t0005g0016a0001c0001t0005g0035a0001c0001t0005g0047others(37): Show | 41 | HG00280.hp2 HG00609.hp1 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.127-19933A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57140246 | ||||||
| chr3:57140259
|
A | G | 1 | a0002c0004t0057g0198 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.127-19946T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57140259 | ||||||
| chr3:57140449
|
A | T | 28 | a0002c0003t0002g0051a0002c0003t0002g0052a0002c0003t0002g0053others(25): Show | 28 | HG00558.hp2 HG02080.hp2 HG02132.hp1 others(25): Show |
intron_variant | MODIFIER | c.127-20136T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57140449 | ||||||
| chr3:57140608
|
C | T | 1 | a0002c0003t0002g0299 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.127-20295G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57140608 | ||||||
| chr3:57140785
|
G | T | 1 | a0003c0002t0001g0067 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.127-20472C>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57140785 | ||||||
| chr3:57140823
|
T | C | 1 | a0003c0002t0001g0135 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.127-20510A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57140823 | ||||||
| chr3:57140893
|
C | CT | 135 | a0001c0001t0020g0021a0001c0001t0020g0250a0001c0001t0027g0331others(132): Show | 136 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(133): Show |
intron_variant | MODIFIER | c.127-20581dupA | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57140893 | ||||||
| chr3:57140893
|
C | CTT | 11 | a0001c0001t0003g0117a0002c0007t0009g0088a0002c0007t0009g0089others(8): Show | 11 | HG01243.hp2 HG02109.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.127-20582_127-2058 others(6): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57140893 | ||||||
| chr3:57141087
|
A | G | 1 | a0002c0003t0054g0020 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.127-20774T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57141087 | ||||||
| chr3:57141104
|
G | A | 3 | a0002c0003t0013g0028a0002c0003t0013g0325a0002c0003t0021g0342 | 3 | HG02970.hp1 NA18522.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.127-20791C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57141104 | ||||||
| chr3:57141170
|
G | A | 6 | a0001c0001t0004g0193a0001c0001t0004g0255a0001c0001t0004g0261others(3): Show | 6 | HG01361.hp2 HG01516.hp2 HG02040.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-20857C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57141170 | ||||||
| chr3:57141426
|
A | G | 88 | a0001c0001t0020g0021a0001c0001t0020g0250a0002c0003t0002g0099others(85): Show | 89 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(86): Show |
intron_variant | MODIFIER | c.127-21113T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57141426 | ||||||
| chr3:57141512
|
A | G | 3 | a0002c0003t0002g0293a0002c0003t0002g0294a0002c0015t0002g0295 | 3 | HG02165.hp2 NA18959.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.127-21199T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57141512 | ||||||
| chr3:57141750
|
T | C | 6 | a0002c0003t0013g0028a0002c0003t0013g0092a0002c0003t0013g0170others(3): Show | 6 | HG02622.hp2 HG02717.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.127-21437A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57141750 | ||||||
| chr3:57141846
|
GA | G | 5 | a0002c0003t0014g0150a0002c0003t0014g0226a0002c0003t0014g0228others(2): Show | 5 | HG01109.hp2 HG02717.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.127-21534delT | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57141846 | ||||||
| chr3:57141860
|
T | C | 11 | a0001c0001t0003g0117a0002c0007t0009g0088a0002c0007t0009g0089others(8): Show | 11 | HG01243.hp2 HG02109.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.127-21547A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57141860 | ||||||
| chr3:57141945
|
A | G | 4 | a0002c0003t0012g0048a0002c0003t0012g0073a0002c0003t0012g0074others(1): Show | 4 | HG01255.hp1 HG01891.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-21632T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57141945 | ||||||
| chr3:57141951
|
G | A | 28 | a0002c0003t0002g0051a0002c0003t0002g0052a0002c0003t0002g0053others(25): Show | 28 | HG00558.hp2 HG02080.hp2 HG02132.hp1 others(25): Show |
intron_variant | MODIFIER | c.127-21638C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57141951 | ||||||
| chr3:57142049
|
C | T | 33 | a0001c0001t0004g0003a0001c0001t0004g0027a0001c0001t0004g0059others(30): Show | 34 | HG00738.hp2 HG00741.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.127-21736G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57142049 | ||||||
| chr3:57142056
|
C | G | 9 | a0001c0001t0027g0331a0001c0001t0038g0049a0001c0006t0011g0009others(6): Show | 9 | HG02145.hp2 HG02451.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.127-21743G>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57142056 | ||||||
| chr3:57142169
|
G | A | 132 | a0001c0001t0003g0117a0001c0001t0004g0333a0001c0001t0020g0021others(129): Show | 133 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(130): Show |
intron_variant | MODIFIER | c.127-21856C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57142169 | ||||||
| chr3:57142184
|
C | T | 1 | a0002c0003t0002g0105 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.127-21871G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57142184 | ||||||
| chr3:57142212
|
C | T | 1 | a0003c0002t0001g0232 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.127-21899G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57142212 | ||||||
| chr3:57142309
|
T | G | 4 | a0002c0003t0012g0048a0002c0003t0012g0073a0002c0003t0012g0074others(1): Show | 4 | HG01255.hp1 HG01891.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-21996A>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57142309 | ||||||
| chr3:57142361
|
T | C | 1 | a0002c0003t0054g0020 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.127-22048A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57142361 | ||||||
| chr3:57142474
|
C | T | 3 | a0001c0001t0003g0258a0001c0001t0003g0259a0001c0001t0003g0260 | 3 | HG00099.hp2 HG00738.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.127-22161G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57142474 | ||||||
| chr3:57142475
|
G | A | 28 | a0002c0003t0002g0051a0002c0003t0002g0052a0002c0003t0002g0053others(25): Show | 28 | HG00558.hp2 HG02080.hp2 HG02132.hp1 others(25): Show |
intron_variant | MODIFIER | c.127-22162C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57142475 | ||||||
| chr3:57142477
|
A | G | 132 | a0001c0001t0003g0117a0001c0001t0004g0333a0001c0001t0020g0021others(129): Show | 133 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(130): Show |
intron_variant | MODIFIER | c.127-22164T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57142477 | ||||||
| chr3:57142498
|
G | A | 1 | a0003c0002t0001g0308 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.127-22185C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57142498 | ||||||
| chr3:57142520
|
A | G | 11 | a0001c0001t0003g0117a0002c0007t0009g0088a0002c0007t0009g0089others(8): Show | 11 | HG01243.hp2 HG02109.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.127-22207T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57142520 | ||||||
| chr3:57142528
|
G | A | 9 | a0001c0001t0027g0331a0001c0001t0038g0049a0001c0006t0011g0009others(6): Show | 9 | HG02145.hp2 HG02451.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.127-22215C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57142528 | ||||||
| chr3:57142547
|
G | A | 6 | a0002c0004t0008g0091a0002c0004t0008g0177a0002c0004t0008g0197others(3): Show | 6 | HG00099.hp1 HG00639.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-22234C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57142547 | ||||||
| chr3:57142570
|
C | T | 1 | a0002c0003t0032g0314 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.127-22257G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57142570 | ||||||
| chr3:57142597
|
C | A | 1 | a0001c0001t0004g0176 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.127-22284G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57142597 | ||||||
| chr3:57142603
|
G | C | 1 | a0002c0004t0051g0019 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.127-22290C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57142603 | ||||||
| chr3:57142719
|
T | G | 4 | a0002c0003t0012g0048a0002c0003t0012g0073a0002c0003t0012g0074others(1): Show | 4 | HG01255.hp1 HG01891.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-22406A>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57142719 | ||||||
| chr3:57143068
|
A | C | 2 | a0001c0001t0003g0163a0001c0001t0003g0174 | 2 | HG02486.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.126+22093T>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57143068 | ||||||
| chr3:57143143
|
A | G | 88 | a0001c0001t0020g0021a0001c0001t0020g0250a0002c0003t0002g0099others(85): Show | 89 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(86): Show |
intron_variant | MODIFIER | c.126+22018T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57143143 | ||||||
| chr3:57143167
|
C | T | 167 | a0001c0001t0003g0117a0001c0001t0004g0333a0001c0001t0020g0021others(164): Show | 168 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(165): Show |
intron_variant | MODIFIER | c.126+21994G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57143167 | ||||||
| chr3:57143316
|
T | C | 1 | a0002c0003t0013g0077 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.126+21845A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57143316 | ||||||
| chr3:57143342
|
TGACAATC others(14): Show |
T | 1 | a0009c0016t0002g0270 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.126+21798_126+2181 others(25): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57143342 | ||||||
| chr3:57143380
|
G | T | 7 | a0001c0001t0004g0333a0002c0003t0013g0028a0002c0003t0013g0092others(4): Show | 7 | HG02622.hp2 HG02717.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.126+21781C>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57143380 | ||||||
| chr3:57143423
|
C | T | 6 | a0002c0003t0013g0028a0002c0003t0013g0092a0002c0003t0013g0170others(3): Show | 6 | HG02622.hp2 HG02717.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.126+21738G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57143423 | ||||||
| chr3:57143504
|
C | T | 1 | a0002c0003t0053g0227 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.126+21657G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57143504 | ||||||
| chr3:57143522
|
C | A | 3 | a0003c0002t0001g0120a0003c0002t0001g0121a0003c0002t0001g0122 | 3 | HG02735.hp2 NA18945.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.126+21639G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57143522 | ||||||
| chr3:57143615
|
C | T | 2 | a0001c0001t0003g0281a0011c0019t0003g0345 | 2 | HG02280.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.126+21546G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57143615 | ||||||
| chr3:57143688
|
T | C | 84 | a0001c0001t0020g0021a0001c0001t0020g0250a0002c0003t0002g0099others(81): Show | 85 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.126+21473A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57143688 | ||||||
| chr3:57143755
|
G | A | 1 | a0002c0004t0050g0321 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.126+21406C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57143755 | ||||||
| chr3:57143785
|
G | A | 1 | a0006c0009t0003g0279 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.126+21376C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57143785 | ||||||
| chr3:57143811
|
G | C | 1 | a0003c0002t0001g0184 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.126+21350C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57143811 | ||||||
| chr3:57143954
|
T | C | 1 | a0003c0002t0001g0137 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.126+21207A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57143954 | ||||||
| chr3:57144133
|
C | T | 1 | a0001c0001t0004g0333 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.126+21028G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57144133 | ||||||
| chr3:57144257
|
CCT | C | 44 | a0001c0001t0003g0117a0001c0001t0004g0333a0001c0001t0027g0331others(41): Show | 44 | HG01109.hp2 HG01243.hp2 HG01255.hp1 others(41): Show |
intron_variant | MODIFIER | c.126+20902_126+2090 others(6): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57144257 | ||||||
| chr3:57144265
|
C | T | 87 | a0001c0001t0020g0021a0001c0001t0020g0250a0002c0003t0002g0099others(84): Show | 88 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.126+20896G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57144265 | ||||||
| chr3:57144328
|
T | C | 1 | a0002c0003t0013g0092 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.126+20833A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57144328 | ||||||
| chr3:57144368
|
T | C | 11 | a0001c0001t0003g0117a0002c0007t0009g0088a0002c0007t0009g0089others(8): Show | 11 | HG01243.hp2 HG02109.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.126+20793A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57144368 | ||||||
| chr3:57144436
|
G | T | 2 | a0003c0002t0001g0043a0003c0002t0001g0101 | 2 | HG01123.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.126+20725C>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57144436 | ||||||
| chr3:57144670
|
A | C | 19 | a0001c0001t0003g0281a0001c0001t0003g0282a0001c0001t0003g0283others(16): Show | 19 | HG01099.hp1 HG01884.hp1 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.126+20491T>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57144670 | ||||||
| chr3:57144692
|
C | T | 1 | a0002c0003t0012g0254 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.126+20469G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57144692 | ||||||
| chr3:57144727
|
A | AGT | 347 | a0001c0001t0003g0014a0001c0001t0003g0057a0001c0001t0003g0117others(344): Show | 352 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(349): Show |
intron_variant | MODIFIER | c.126+20432_126+2043 others(6): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57144727 | ||||||
| chr3:57144773
|
G | C | 3 | a0003c0002t0001g0120a0003c0002t0001g0121a0003c0002t0001g0122 | 3 | HG02735.hp2 NA18945.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.126+20388C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57144773 | ||||||
| chr3:57144976
|
C | G | 1 | a0002c0003t0013g0170 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.126+20185G>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57144976 | ||||||
| chr3:57145045
|
C | G | 3 | a0002c0004t0016g0335a0002c0004t0016g0343a0002c0004t0016g0344 | 3 | HG02257.hp1 HG02886.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.126+20116G>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57145045 | ||||||
| chr3:57145140
|
G | A | 1 | a0002c0004t0057g0198 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.126+20021C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57145140 | ||||||
| chr3:57145218
|
T | A | 1 | a0003c0002t0001g0043 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.126+19943A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57145218 | ||||||
| chr3:57145233
|
C | G | 132 | a0001c0001t0003g0117a0001c0001t0004g0333a0001c0001t0020g0021others(129): Show | 133 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(130): Show |
intron_variant | MODIFIER | c.126+19928G>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57145233 | ||||||
| chr3:57145402
|
G | A | 8 | a0001c0001t0038g0049a0001c0006t0011g0009a0001c0006t0011g0010others(5): Show | 8 | HG02145.hp2 HG02451.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.126+19759C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57145402 | ||||||
| chr3:57145421
|
G | A | 1 | a0001c0001t0035g0215 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.126+19740C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57145421 | ||||||
| chr3:57145823
|
G | A | 4 | a0002c0003t0014g0150a0002c0003t0014g0226a0002c0003t0014g0228others(1): Show | 4 | HG01109.hp2 HG02717.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+19338C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57145823 | ||||||
| chr3:57145922
|
G | A | 1 | a0002c0004t0016g0335 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.126+19239C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57145922 | ||||||
| chr3:57145923
|
G | A | 1 | a0002c0003t0002g0105 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.126+19238C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57145923 | ||||||
| chr3:57145933
|
T | A | 1 | a0002c0004t0057g0198 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.126+19228A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57145933 | ||||||
| chr3:57146019
|
ACACACAC others(19): Show |
A | 1 | a0001c0001t0036g0029 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.126+19116_126+1914 others(30): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146019 | ||||||
| chr3:57146027
|
ACT | A | 4 | a0002c0004t0008g0091a0002c0004t0008g0177a0002c0004t0008g0310others(1): Show | 4 | HG00099.hp1 HG00639.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+19132_126+1913 others(6): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146027 | ||||||
| chr3:57146029
|
T | G | 2 | a0002c0004t0008g0197a0002c0004t0008g0323 | 2 | HG01099.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.126+19132A>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146029 | ||||||
| chr3:57146029
|
T | TCACGCG | 9 | a0001c0006t0011g0009a0001c0006t0011g0010a0002c0003t0012g0146others(6): Show | 9 | HG01109.hp2 HG01255.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.126+19126_126+1913 others(10): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146029 | ||||||
| chr3:57146031
|
A | ACG | 34 | a0001c0001t0003g0014a0001c0001t0003g0175a0001c0001t0003g0195others(31): Show | 34 | HG00544.hp2 HG00642.hp2 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.126+19128_126+1912 others(6): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146031 | ||||||
| chr3:57146031
|
A | ACGCGCAC others(3): Show |
1 | a0003c0002t0015g0303 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.126+19129_126+1913 others(14): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146031 | ||||||
| chr3:57146031
|
A | G | 6 | a0002c0004t0008g0091a0002c0004t0008g0177a0002c0004t0008g0197others(3): Show | 6 | HG00099.hp1 HG00639.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.126+19130T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146031 | ||||||
| chr3:57146033
|
G | GCGCA | 23 | a0001c0001t0003g0117a0001c0001t0027g0331a0001c0001t0038g0049others(20): Show | 23 | HG01243.hp2 HG01891.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.126+19127_126+1912 others(8): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146033 | ||||||
| chr3:57146035
|
G | GCACGCA | 11 | a0001c0001t0004g0333a0002c0003t0013g0028a0002c0003t0013g0092others(8): Show | 11 | HG01884.hp2 HG02109.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.126+19125_126+1912 others(10): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146035 | ||||||
| chr3:57146037
|
G | A | 82 | a0001c0001t0020g0021a0001c0001t0020g0250a0002c0003t0002g0099others(79): Show | 83 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.126+19124C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146037 | ||||||
| chr3:57146041
|
G | A | 2 | a0001c0001t0003g0237a0001c0001t0046g0318 | 2 | HG02258.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.126+19120C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146041 | ||||||
| chr3:57146042
|
C | T | 4 | a0002c0004t0019g0005a0002c0004t0019g0006a0002c0004t0048g0007others(1): Show | 4 | HG01884.hp2 HG02109.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+19119G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146042 | ||||||
| chr3:57146045
|
G | A | 48 | a0001c0001t0005g0016a0001c0001t0005g0035a0001c0001t0005g0047others(45): Show | 49 | HG00099.hp1 HG00280.hp2 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.126+19116C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146045 | ||||||
| chr3:57146045
|
G | GCACA | 5 | a0003c0002t0001g0015a0003c0002t0001g0022a0003c0002t0001g0080others(2): Show | 5 | HG02083.hp1 NA18956.hp2 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.126+19112_126+1911 others(8): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146045 | ||||||
| chr3:57146045
|
G | GCGCGCAC others(3): Show |
1 | a0002c0003t0054g0020 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.126+19115_126+1911 others(14): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146045 | ||||||
| chr3:57146045
|
G | GCGCGCAC others(5): Show |
1 | a0003c0002t0001g0229 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.126+19115_126+1911 others(16): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146045 | ||||||
| chr3:57146045
|
G | GCGCGCGC others(3): Show |
27 | a0001c0001t0020g0250a0003c0002t0001g0041a0003c0002t0001g0063others(24): Show | 27 | HG00558.hp1 HG00639.hp2 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.126+19115_126+1911 others(14): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146045 | ||||||
| chr3:57146045
|
G | GCGCGCGC others(5): Show |
3 | a0003c0002t0001g0017a0003c0002t0001g0135a0003c0002t0001g0291 | 3 | NA18971.hp1 NA19012.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.126+19115_126+1911 others(16): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146045 | ||||||
| chr3:57146045
|
G | GCGCGCGC others(7): Show |
1 | a0003c0002t0001g0032 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.126+19115_126+1911 others(18): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146045 | ||||||
| chr3:57146045
|
G | GCGCGCGC others(5): Show |
41 | a0001c0001t0020g0021a0002c0003t0002g0099a0002c0003t0002g0100others(38): Show | 42 | HG00544.hp1 HG00673.hp2 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.126+19115_126+1911 others(16): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146045 | ||||||
| chr3:57146045
|
G | GCGCGCGC others(7): Show |
4 | a0003c0002t0001g0036a0003c0002t0001g0042a0003c0002t0001g0069others(1): Show | 4 | HG02074.hp2 NA18980.hp1 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+19115_126+1911 others(18): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146045 | ||||||
| chr3:57146045
|
G | GCGCGCGC others(7): Show |
1 | a0003c0002t0001g0039 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.126+19115_126+1911 others(18): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146045 | ||||||
| chr3:57146045
|
G | GCTGCGCG others(6): Show |
1 | a0003c0002t0001g0252 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.126+19115_126+1911 others(17): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146045 | ||||||
| chr3:57146047
|
A | G | 1 | a0001c0001t0003g0174 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.126+19114T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146047 | ||||||
| chr3:57146132
|
G | C | 44 | a0001c0001t0003g0117a0001c0001t0004g0333a0001c0001t0027g0331others(41): Show | 44 | HG01109.hp2 HG01243.hp2 HG01255.hp1 others(41): Show |
intron_variant | MODIFIER | c.126+19029C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146132 | ||||||
| chr3:57146144
|
T | A | 35 | a0002c0003t0002g0051a0002c0003t0002g0052a0002c0003t0002g0053others(32): Show | 35 | HG00099.hp1 HG00558.hp2 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.126+19017A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146144 | ||||||
| chr3:57146302
|
G | A | 4 | a0002c0004t0016g0335a0002c0004t0016g0343a0002c0004t0016g0344others(1): Show | 4 | HG02257.hp1 HG02559.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+18859C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146302 | ||||||
| chr3:57146374
|
C | A | 122 | a0001c0001t0003g0117a0001c0001t0004g0333a0001c0001t0020g0021others(119): Show | 123 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(120): Show |
intron_variant | MODIFIER | c.126+18787G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146374 | ||||||
| chr3:57146406
|
T | A | 1 | a0001c0001t0005g0246 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.126+18755A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146406 | ||||||
| chr3:57146505
|
C | G | 6 | a0002c0003t0013g0028a0002c0003t0013g0092a0002c0003t0013g0170others(3): Show | 6 | HG02622.hp2 HG02717.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.126+18656G>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146505 | ||||||
| chr3:57146519
|
G | A | 1 | a0002c0003t0002g0105 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.126+18642C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146519 | ||||||
| chr3:57146639
|
A | G | 1 | a0002c0004t0051g0019 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.126+18522T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146639 | ||||||
| chr3:57146657
|
G | A | 28 | a0002c0003t0002g0051a0002c0003t0002g0052a0002c0003t0002g0053others(25): Show | 28 | HG00558.hp2 HG02080.hp2 HG02132.hp1 others(25): Show |
intron_variant | MODIFIER | c.126+18504C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146657 | ||||||
| chr3:57146749
|
C | CA | 9 | a0001c0001t0003g0014a0001c0001t0003g0057a0001c0001t0003g0211others(6): Show | 9 | HG01168.hp2 HG01169.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.126+18411dupT | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146749 | ||||||
| chr3:57146749
|
CA | C | 134 | a0001c0001t0004g0193a0001c0001t0004g0333a0001c0001t0020g0021others(131): Show | 134 | HG00099.hp1 HG00558.hp2 HG00639.hp1 others(131): Show |
intron_variant | MODIFIER | c.126+18411delT | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146749 | ||||||
| chr3:57146749
|
CAA | C | 17 | a0002c0003t0002g0100a0002c0003t0002g0105a0002c0003t0012g0048others(14): Show | 18 | HG00544.hp1 HG00558.hp1 HG00673.hp2 others(15): Show |
intron_variant | MODIFIER | c.126+18410_126+1841 others(6): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146749 | ||||||
| chr3:57146762
|
A | G | 1 | a0002c0003t0002g0105 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.126+18399T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146762 | ||||||
| chr3:57146797
|
T | C | 1 | a0002c0003t0002g0105 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.126+18364A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146797 | ||||||
| chr3:57146812
|
G | C | 1 | a0003c0002t0001g0120 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.126+18349C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146812 | ||||||
| chr3:57146820
|
C | CT | 139 | a0001c0001t0004g0333a0001c0001t0007g0026a0001c0001t0007g0217others(136): Show | 140 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(137): Show |
intron_variant | MODIFIER | c.126+18340dupA | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146820 | ||||||
| chr3:57146820
|
C | CTT | 12 | a0001c0001t0020g0021a0001c0006t0011g0009a0002c0003t0002g0155others(9): Show | 12 | HG01106.hp1 HG01884.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.126+18339_126+1834 others(6): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146820 | ||||||
| chr3:57146887
|
G | GC | 44 | a0001c0001t0003g0117a0001c0001t0004g0333a0001c0001t0027g0331others(41): Show | 44 | HG01109.hp2 HG01243.hp2 HG01255.hp1 others(41): Show |
intron_variant | MODIFIER | c.126+18273_126+1827 others(5): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146887 | ||||||
| chr3:57146890
|
T | TGCCATTG others(9): Show |
44 | a0001c0001t0003g0117a0001c0001t0004g0333a0001c0001t0027g0331others(41): Show | 44 | HG01109.hp2 HG01243.hp2 HG01255.hp1 others(41): Show |
intron_variant | MODIFIER | c.126+18270_126+1827 others(20): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146890 | ||||||
| chr3:57146989
|
A | AT | 10 | a0001c0001t0003g0175a0001c0001t0003g0210a0001c0001t0003g0258others(7): Show | 10 | HG00099.hp2 HG00738.hp1 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.126+18171dupA | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146989 | ||||||
| chr3:57146989
|
AT | A | 137 | a0001c0001t0003g0336a0001c0001t0020g0021a0001c0001t0020g0250others(134): Show | 138 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(135): Show |
intron_variant | MODIFIER | c.126+18171delA | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146989 | ||||||
| chr3:57146989
|
ATT | A | 31 | a0001c0001t0003g0117a0001c0001t0004g0333a0001c0001t0052g0311others(28): Show | 31 | HG01109.hp2 HG01243.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.126+18170_126+1817 others(6): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146989 | ||||||
| chr3:57146989
|
ATTT | A | 6 | a0004c0005t0010g0075a0004c0005t0010g0076a0004c0005t0010g0102others(3): Show | 6 | HG02055.hp1 HG02559.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.126+18169_126+1817 others(7): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57146989 | ||||||
| chr3:57147182
|
C | T | 2 | a0001c0001t0044g0242a0001c0001t0045g0185 | 2 | NA18947.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.126+17979G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57147182 | ||||||
| chr3:57147313
|
A | C | 4 | a0002c0003t0012g0048a0002c0003t0012g0073a0002c0003t0012g0074others(1): Show | 4 | HG01255.hp1 HG01891.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+17848T>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57147313 | ||||||
| chr3:57147603
|
T | C | 131 | a0001c0001t0003g0117a0001c0001t0004g0333a0001c0001t0020g0021others(128): Show | 132 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(129): Show |
intron_variant | MODIFIER | c.126+17558A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57147603 | ||||||
| chr3:57147729
|
T | C | 35 | a0001c0001t0003g0117a0001c0001t0004g0333a0001c0001t0027g0331others(32): Show | 35 | HG01243.hp2 HG01884.hp2 HG02109.hp1 others(32): Show |
intron_variant | MODIFIER | c.126+17432A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57147729 | ||||||
| chr3:57147776
|
A | G | 3 | a0003c0002t0001g0253a0003c0002t0015g0172a0003c0002t0015g0303 | 3 | HG01169.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.126+17385T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57147776 | ||||||
| chr3:57147781
|
T | TA | 44 | a0001c0001t0003g0117a0001c0001t0004g0333a0001c0001t0027g0331others(41): Show | 44 | HG01109.hp2 HG01243.hp2 HG01255.hp1 others(41): Show |
intron_variant | MODIFIER | c.126+17379dupT | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57147781 | ||||||
| chr3:57148044
|
C | T | 28 | a0002c0003t0002g0051a0002c0003t0002g0052a0002c0003t0002g0053others(25): Show | 28 | HG00558.hp2 HG02080.hp2 HG02132.hp1 others(25): Show |
intron_variant | MODIFIER | c.126+17117G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57148044 | ||||||
| chr3:57148088
|
T | TG | 55 | a0001c0001t0003g0163a0001c0001t0003g0175a0001c0001t0003g0210others(52): Show | 56 | HG00280.hp2 HG01069.hp2 HG01070.hp1 others(53): Show |
intron_variant | MODIFIER | c.126+17072dupC | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57148088 | ||||||
| chr3:57148088
|
TG | T | 68 | a0001c0001t0003g0057a0001c0001t0003g0203a0001c0001t0003g0297others(65): Show | 68 | HG00099.hp1 HG00558.hp2 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.126+17072delC | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57148088 | ||||||
| chr3:57148088
|
TGG | T | 29 | a0001c0001t0003g0266a0001c0001t0003g0267a0001c0001t0003g0268others(26): Show | 32 | HG01071.hp1 HG01256.hp1 HG01361.hp2 others(29): Show |
intron_variant | MODIFIER | c.126+17071_126+1707 others(6): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57148088 | ||||||
| chr3:57148092
|
G | A | 1 | a0001c0001t0043g0144 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.126+17069C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57148092 | ||||||
| chr3:57148092
|
G | T | 3 | a0002c0004t0008g0091a0002c0004t0008g0323a0002c0004t0008g0324 | 3 | HG03017.hp1 NA18946.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.126+17069C>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57148092 | ||||||
| chr3:57148098
|
G | A | 35 | a0002c0003t0002g0051a0002c0003t0002g0052a0002c0003t0002g0053others(32): Show | 35 | HG00099.hp1 HG00558.hp2 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.126+17063C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57148098 | ||||||
| chr3:57148099
|
G | C | 1 | a0003c0002t0001g0101 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.126+17062C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57148099 | ||||||
| chr3:57148102
|
G | A | 1 | a0004c0005t0010g0075 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.126+17059C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57148102 | ||||||
| chr3:57148102
|
G | GA | 5 | a0003c0002t0001g0033a0003c0002t0001g0253a0003c0002t0015g0172others(2): Show | 5 | HG01169.hp2 HG02055.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.126+17058_126+1705 others(5): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57148102 | ||||||
| chr3:57148104
|
G | C | 63 | a0001c0001t0006g0162a0001c0001t0042g0018a0002c0003t0002g0051others(60): Show | 63 | HG00099.hp1 HG00558.hp2 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.126+17057C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57148104 | ||||||
| chr3:57148104
|
G | GAGC | 17 | a0001c0001t0020g0250a0003c0002t0001g0017a0003c0002t0001g0038others(14): Show | 17 | HG01069.hp1 HG01074.hp1 HG01516.hp1 others(14): Show |
intron_variant | MODIFIER | c.126+17056_126+1705 others(7): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57148104 | ||||||
| chr3:57148104
|
G | GGAGC | 45 | a0001c0001t0020g0021a0002c0003t0002g0099a0002c0003t0002g0100others(42): Show | 46 | HG00544.hp1 HG00558.hp1 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.126+17056_126+1705 others(8): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57148104 | ||||||
| chr3:57148105
|
C | T | 1 | a0002c0004t0050g0321 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.126+17056G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57148105 | ||||||
| chr3:57148106
|
G | A | 6 | a0001c0001t0007g0002a0001c0001t0007g0025a0001c0001t0007g0026others(3): Show | 7 | HG00280.hp2 HG01261.hp2 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.126+17055C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57148106 | ||||||
| chr3:57148210
|
A | C | 2 | a0003c0002t0001g0043a0003c0002t0001g0101 | 2 | HG01123.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.126+16951T>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57148210 | ||||||
| chr3:57148240
|
G | A | 4 | a0001c0001t0003g0163a0001c0001t0003g0174a0001c0001t0003g0336others(1): Show | 4 | HG02280.hp2 HG02486.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+16921C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57148240 | ||||||
| chr3:57148278
|
T | G | 29 | a0002c0003t0002g0051a0002c0003t0002g0052a0002c0003t0002g0053others(26): Show | 29 | HG00558.hp2 HG02080.hp2 HG02132.hp1 others(26): Show |
intron_variant | MODIFIER | c.126+16883A>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57148278 | ||||||
| chr3:57148294
|
C | A | 47 | a0001c0001t0003g0117a0001c0001t0004g0333a0001c0001t0027g0331others(44): Show | 47 | HG01109.hp2 HG01243.hp2 HG01255.hp1 others(44): Show |
intron_variant | MODIFIER | c.126+16867G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57148294 | ||||||
| chr3:57148324
|
C | CA | 47 | a0001c0001t0003g0117a0001c0001t0004g0333a0001c0001t0026g0287others(44): Show | 47 | HG01069.hp2 HG01109.hp2 HG01243.hp2 others(44): Show |
intron_variant | MODIFIER | c.126+16836dupT | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57148324 | ||||||
| chr3:57148340
|
A | T | 1 | a0003c0002t0001g0182 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.126+16821T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57148340 | ||||||
| chr3:57148378
|
C | G | 47 | a0001c0001t0003g0117a0001c0001t0004g0333a0001c0001t0027g0331others(44): Show | 47 | HG01109.hp2 HG01243.hp2 HG01255.hp1 others(44): Show |
intron_variant | MODIFIER | c.126+16783G>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57148378 | ||||||
| chr3:57148468
|
T | C | 88 | a0001c0001t0007g0124a0001c0001t0020g0021a0001c0001t0020g0250others(85): Show | 89 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(86): Show |
intron_variant | MODIFIER | c.126+16693A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57148468 | ||||||
| chr3:57148635
|
G | A | 87 | a0001c0001t0020g0021a0001c0001t0020g0250a0002c0003t0002g0099others(84): Show | 88 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.126+16526C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57148635 | ||||||
| chr3:57148677
|
G | A | 1 | a0001c0001t0005g0246 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.126+16484C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57148677 | ||||||
| chr3:57149227
|
T | C | 9 | a0002c0003t0002g0199a0002c0003t0002g0200a0002c0003t0002g0201others(6): Show | 9 | HG00558.hp2 NA18946.hp2 NA18950.hp1 others(6): Show |
intron_variant | MODIFIER | c.126+15934A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57149227 | ||||||
| chr3:57149296
|
C | CA | 34 | a0001c0001t0003g0289a0001c0001t0004g0333a0001c0001t0039g0288others(31): Show | 34 | HG01109.hp2 HG01255.hp1 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.126+15864dupT | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57149296 | ||||||
| chr3:57149296
|
C | CAA | 9 | a0001c0001t0003g0117a0004c0005t0010g0075a0004c0005t0010g0076others(6): Show | 9 | HG01243.hp2 HG02055.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.126+15863_126+1586 others(6): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57149296 | ||||||
| chr3:57149296
|
CA | C | 28 | a0001c0001t0006g0173a0002c0003t0002g0051a0002c0003t0002g0052others(25): Show | 28 | HG00558.hp2 HG02080.hp2 HG02132.hp2 others(25): Show |
intron_variant | MODIFIER | c.126+15864delT | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57149296 | ||||||
| chr3:57149318
|
T | G | 4 | a0002c0004t0008g0091a0002c0004t0008g0177a0002c0004t0008g0323others(1): Show | 4 | HG00639.hp1 HG03017.hp1 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+15843A>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57149318 | ||||||
| chr3:57149399
|
T | C | 9 | a0001c0001t0027g0331a0001c0001t0038g0049a0001c0006t0011g0009others(6): Show | 9 | HG02145.hp2 HG02451.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.126+15762A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57149399 | ||||||
| chr3:57149458
|
C | T | 9 | a0001c0001t0027g0331a0001c0001t0038g0049a0001c0006t0011g0009others(6): Show | 9 | HG02145.hp2 HG02451.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.126+15703G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57149458 | ||||||
| chr3:57149559
|
G | A | 9 | a0001c0001t0027g0331a0001c0001t0038g0049a0001c0006t0011g0009others(6): Show | 9 | HG02145.hp2 HG02451.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.126+15602C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57149559 | ||||||
| chr3:57149735
|
G | A | 4 | a0002c0004t0008g0091a0002c0004t0008g0177a0002c0004t0008g0323others(1): Show | 4 | HG00639.hp1 HG03017.hp1 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+15426C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57149735 | ||||||
| chr3:57149849
|
T | C | 168 | a0001c0001t0003g0117a0001c0001t0004g0333a0001c0001t0007g0124others(165): Show | 169 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(166): Show |
intron_variant | MODIFIER | c.126+15312A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57149849 | ||||||
| chr3:57149930
|
G | C | 5 | a0002c0003t0002g0105a0002c0003t0012g0048a0002c0003t0012g0073others(2): Show | 5 | HG01255.hp1 HG01891.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.126+15231C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57149930 | ||||||
| chr3:57150013
|
A | C | 4 | a0002c0004t0019g0005a0002c0004t0019g0006a0002c0004t0048g0007others(1): Show | 4 | HG01884.hp2 HG02109.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+15148T>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57150013 | ||||||
| chr3:57150173
|
C | T | 1 | a0001c0001t0034g0109 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.126+14988G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57150173 | ||||||
| chr3:57150273
|
G | A | 5 | a0002c0007t0009g0088a0002c0007t0009g0089a0002c0007t0009g0167others(2): Show | 5 | HG02109.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.126+14888C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57150273 | ||||||
| chr3:57150302
|
C | G | 1 | a0003c0002t0023g0004 | 2 | NA18993.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.126+14859G>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57150302 | ||||||
| chr3:57150364
|
C | A | 29 | a0002c0003t0002g0051a0002c0003t0002g0052a0002c0003t0002g0053others(26): Show | 29 | HG00558.hp2 HG02080.hp2 HG02132.hp1 others(26): Show |
intron_variant | MODIFIER | c.126+14797G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57150364 | ||||||
| chr3:57150370
|
C | T | 3 | a0001c0001t0052g0311a0002c0003t0012g0254a0002c0004t0050g0321 | 3 | HG01243.hp1 HG02559.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.126+14791G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57150370 | ||||||
| chr3:57150437
|
C | T | 6 | a0004c0005t0010g0075a0004c0005t0010g0076a0004c0005t0010g0102others(3): Show | 6 | HG02055.hp1 HG02559.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.126+14724G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57150437 | ||||||
| chr3:57151561
|
T | A | 1 | a0002c0003t0014g0226 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.126+13600A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57151561 | ||||||
| chr3:57151631
|
A | G | 1 | a0001c0001t0004g0333 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.126+13530T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57151631 | ||||||
| chr3:57151755
|
T | C | 30 | a0002c0003t0002g0051a0002c0003t0002g0052a0002c0003t0002g0053others(27): Show | 30 | HG00558.hp2 HG02080.hp2 HG02132.hp1 others(27): Show |
intron_variant | MODIFIER | c.126+13406A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57151755 | ||||||
| chr3:57151785
|
C | T | 1 | a0002c0003t0002g0100 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.126+13376G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57151785 | ||||||
| chr3:57151821
|
C | G | 1 | a0002c0004t0048g0007 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.126+13340G>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57151821 | ||||||
| chr3:57151822
|
A | G | 3 | a0001c0001t0003g0258a0001c0001t0003g0259a0001c0001t0003g0260 | 3 | HG00099.hp2 HG00738.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.126+13339T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57151822 | ||||||
| chr3:57151923
|
A | C | 26 | a0001c0001t0027g0331a0001c0001t0038g0049a0001c0006t0011g0009others(23): Show | 26 | HG01109.hp1 HG01109.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.126+13238T>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57151923 | ||||||
| chr3:57151990
|
C | G | 3 | a0003c0002t0001g0253a0003c0002t0015g0172a0003c0002t0015g0303 | 3 | HG01169.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.126+13171G>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57151990 | ||||||
| chr3:57152007
|
A | C | 163 | a0001c0001t0004g0193a0001c0001t0004g0255a0001c0001t0004g0257others(160): Show | 165 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(162): Show |
intron_variant | MODIFIER | c.126+13154T>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57152007 | ||||||
| chr3:57152129
|
A | C | 5 | a0003c0002t0001g0061a0003c0002t0001g0094a0003c0002t0001g0138others(2): Show | 5 | HG02896.hp1 HG02897.hp1 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.126+13032T>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57152129 | ||||||
| chr3:57152131
|
A | G | 117 | a0001c0001t0004g0118a0001c0001t0004g0292a0001c0001t0004g0333others(114): Show | 118 | HG00558.hp1 HG00639.hp1 HG00639.hp2 others(115): Show |
intron_variant | MODIFIER | c.126+13030T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57152131 | ||||||
| chr3:57152156
|
G | A | 1 | a0002c0003t0012g0073 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.126+13005C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57152156 | ||||||
| chr3:57152196
|
G | C | 104 | a0001c0001t0004g0118a0001c0001t0004g0292a0001c0001t0005g0016others(101): Show | 105 | HG00544.hp1 HG00558.hp1 HG00639.hp1 others(102): Show |
intron_variant | MODIFIER | c.126+12965C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57152196 | ||||||
| chr3:57152236
|
C | A | 2 | a0003c0002t0001g0061a0003c0002t0001g0094 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.126+12925G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57152236 | ||||||
| chr3:57152260
|
C | T | 1 | a0002c0003t0002g0034 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.126+12901G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57152260 | ||||||
| chr3:57152291
|
A | G | 1 | a0001c0001t0003g0336 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.126+12870T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57152291 | ||||||
| chr3:57152303
|
G | A | 4 | a0002c0004t0008g0091a0002c0004t0008g0177a0002c0004t0008g0323others(1): Show | 4 | HG00639.hp1 HG03017.hp1 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+12858C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57152303 | ||||||
| chr3:57152305
|
T | C | 1 | a0002c0003t0021g0332 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.126+12856A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57152305 | ||||||
| chr3:57152334
|
A | G | 3 | a0003c0002t0001g0253a0003c0002t0015g0172a0003c0002t0015g0303 | 3 | HG01169.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.126+12827T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57152334 | ||||||
| chr3:57152372
|
A | G | 1 | a0002c0012t0002g0241 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.126+12789T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57152372 | ||||||
| chr3:57152433
|
C | A | 1 | a0002c0003t0002g0056 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.126+12728G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57152433 | ||||||
| chr3:57152552
|
A | C | 72 | a0001c0001t0003g0203a0001c0001t0004g0003a0001c0001t0004g0151others(69): Show | 74 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.126+12609T>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57152552 | ||||||
| chr3:57152567
|
T | G | 1 | a0002c0004t0008g0177 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.126+12594A>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57152567 | ||||||
| chr3:57152759
|
G | A | 6 | a0001c0006t0011g0009a0001c0006t0011g0010a0001c0006t0011g0011others(3): Show | 6 | HG02145.hp2 HG02976.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.126+12402C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57152759 | ||||||
| chr3:57152762
|
C | T | 2 | a0002c0004t0049g0224a0003c0002t0001g0225 | 2 | HG01109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.126+12399G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57152762 | ||||||
| chr3:57152810
|
A | G | 1 | a0002c0004t0057g0198 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.126+12351T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57152810 | ||||||
| chr3:57152928
|
C | T | 1 | a0001c0001t0004g0151 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.126+12233G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57152928 | ||||||
| chr3:57153008
|
A | G | 75 | a0001c0001t0004g0118a0001c0001t0007g0124a0001c0001t0035g0215others(72): Show | 76 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.126+12153T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57153008 | ||||||
| chr3:57153021
|
T | C | 2 | a0003c0002t0001g0043a0003c0002t0001g0101 | 2 | HG01123.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.126+12140A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57153021 | ||||||
| chr3:57153050
|
T | C | 130 | a0001c0001t0003g0117a0001c0001t0004g0118a0001c0001t0004g0149others(127): Show | 131 | HG00544.hp1 HG00558.hp1 HG00639.hp1 others(128): Show |
intron_variant | MODIFIER | c.126+12111A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57153050 | ||||||
| chr3:57153329
|
A | C | 1 | a0001c0001t0004g0240 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.126+11832T>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57153329 | ||||||
| chr3:57153468
|
G | A | 26 | a0001c0001t0003g0117a0001c0001t0004g0333a0002c0003t0002g0312others(23): Show | 26 | HG00639.hp1 HG01243.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.126+11693C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57153468 | ||||||
| chr3:57153532
|
A | G | 1 | a0003c0002t0001g0184 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.126+11629T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57153532 | ||||||
| chr3:57153789
|
G | A | 2 | a0001c0001t0038g0049a0002c0003t0013g0077 | 2 | HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.126+11372C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57153789 | ||||||
| chr3:57153812
|
C | T | 1 | a0001c0001t0007g0124 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.126+11349G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57153812 | ||||||
| chr3:57153913
|
G | A | 1 | a0002c0003t0002g0104 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.126+11248C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57153913 | ||||||
| chr3:57154052
|
C | T | 1 | a0001c0001t0004g0118 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.126+11109G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57154052 | ||||||
| chr3:57154259
|
A | T | 2 | a0001c0001t0018g0330a0008c0014t0018g0329 | 2 | HG02486.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.126+10902T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57154259 | ||||||
| chr3:57154260
|
T | TTA | 29 | a0001c0001t0003g0057a0001c0001t0003g0211a0001c0001t0003g0297others(26): Show | 29 | HG00099.hp1 HG00609.hp2 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.126+10899_126+1090 others(6): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57154260 | ||||||
| chr3:57154260
|
T | TTATA | 3 | a0001c0001t0005g0191a0001c0001t0027g0331a0002c0004t0008g0192 | 3 | HG01346.hp2 HG03130.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.126+10897_126+1090 others(8): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57154260 | ||||||
| chr3:57154260
|
T | TTATATAT others(5): Show |
2 | a0002c0004t0019g0006a0002c0004t0048g0007 | 2 | HG01884.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.126+10889_126+1090 others(16): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57154260 | ||||||
| chr3:57154260
|
T | TTATATAT others(7): Show |
2 | a0002c0004t0019g0005a0002c0004t0051g0019 | 2 | HG02109.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.126+10887_126+1090 others(18): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57154260 | ||||||
| chr3:57154260
|
TTA | T | 14 | a0001c0001t0004g0149a0002c0003t0002g0105a0002c0003t0012g0048others(11): Show | 14 | HG01255.hp1 HG01891.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.126+10899_126+1090 others(6): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57154260 | ||||||
| chr3:57154279
|
T | TACACACA others(13): Show |
2 | a0002c0003t0013g0170a0002c0003t0014g0169 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.126+10881_126+1088 others(24): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57154279 | ||||||
| chr3:57154279
|
T | TACACACA others(15): Show |
2 | a0001c0001t0004g0333a0002c0003t0013g0092 | 2 | HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.126+10881_126+1088 others(26): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57154279 | ||||||
| chr3:57154279
|
T | TACACACA others(17): Show |
3 | a0002c0003t0013g0028a0002c0003t0013g0325a0002c0003t0021g0342 | 3 | HG02970.hp1 NA18522.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.126+10881_126+1088 others(28): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57154279 | ||||||
| chr3:57154279
|
TATATACA others(5): Show |
T | 2 | a0003c0002t0001g0121a0003c0002t0001g0122 | 2 | NA18945.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.126+10870_126+1088 others(16): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57154279 | ||||||
| chr3:57154281
|
T | C | 7 | a0001c0001t0004g0333a0002c0003t0013g0028a0002c0003t0013g0092others(4): Show | 7 | HG02622.hp2 HG02717.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.126+10880A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57154281 | ||||||
| chr3:57154281
|
TATACACA others(3): Show |
T | 71 | a0001c0001t0004g0118a0001c0001t0007g0124a0001c0001t0035g0215others(68): Show | 72 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.126+10870_126+1087 others(14): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57154281 | ||||||
| chr3:57154283
|
T | C | 9 | a0001c0001t0004g0333a0002c0003t0013g0028a0002c0003t0013g0092others(6): Show | 9 | HG02559.hp2 HG02622.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.126+10878A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57154283 | ||||||
| chr3:57154283
|
T | TAC | 5 | a0002c0003t0002g0164a0002c0003t0002g0165a0002c0003t0022g0107others(2): Show | 5 | HG02622.hp1 HG02818.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.126+10876_126+1087 others(6): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57154283 | ||||||
| chr3:57154283
|
T | TACACATA others(9): Show |
3 | a0002c0004t0008g0091a0002c0004t0008g0323a0002c0004t0008g0324 | 3 | HG03017.hp1 NA18946.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.126+10877_126+1087 others(20): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57154283 | ||||||
| chr3:57154283
|
T | TATACACA others(11): Show |
3 | a0001c0001t0003g0117a0005c0008t0006g0058a0005c0008t0006g0116 | 3 | HG01243.hp2 HG03139.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.126+10877_126+1087 others(22): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57154283 | ||||||
| chr3:57154283
|
T | TATACACA others(11): Show |
1 | a0002c0004t0008g0177 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.126+10877_126+1087 others(22): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57154283 | ||||||
| chr3:57154283
|
T | TATATACA others(9): Show |
4 | a0002c0007t0009g0088a0002c0007t0009g0167a0002c0007t0009g0205others(1): Show | 4 | HG02647.hp2 HG02809.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+10877_126+1087 others(20): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57154283 | ||||||
| chr3:57154283
|
T | TATATACA others(11): Show |
1 | a0005c0008t0006g0090 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.126+10877_126+1087 others(22): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57154283 | ||||||
| chr3:57154283
|
T | TATATATA others(11): Show |
3 | a0002c0003t0055g0008a0002c0007t0009g0089a0005c0008t0006g0320 | 3 | HG02109.hp1 HG02630.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.126+10877_126+1087 others(22): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57154283 | ||||||
| chr3:57154283
|
T | TATATATA others(21): Show |
2 | a0002c0004t0016g0343a0002c0004t0016g0344 | 2 | HG02257.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.126+10877_126+1087 others(32): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57154283 | ||||||
| chr3:57154283
|
T | TATATATA others(33): Show |
1 | a0002c0003t0002g0312 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.126+10877_126+1087 others(44): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57154283 | ||||||
| chr3:57154285
|
C | T | 18 | a0001c0001t0038g0049a0001c0001t0046g0318a0001c0006t0011g0009others(15): Show | 18 | HG01109.hp1 HG01109.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.126+10876G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57154285 | ||||||
| chr3:57154287
|
C | T | 1 | a0002c0004t0019g0005 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.126+10874G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57154287 | ||||||
| chr3:57154303
|
T | C | 12 | a0001c0001t0003g0117a0002c0003t0002g0312a0002c0003t0055g0008others(9): Show | 12 | HG01243.hp2 HG02109.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.126+10858A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57154303 | ||||||
| chr3:57154418
|
T | TGC | 75 | a0001c0001t0004g0118a0001c0001t0007g0124a0001c0001t0035g0215others(72): Show | 76 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.126+10741_126+1074 others(6): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57154418 | ||||||
| chr3:57154649
|
T | C | 15 | a0001c0001t0027g0331a0001c0001t0038g0049a0001c0006t0011g0009others(12): Show | 15 | HG01109.hp1 HG01109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.126+10512A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57154649 | ||||||
| chr3:57154725
|
A | C | 1 | a0003c0011t0001g0125 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.126+10436T>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57154725 | ||||||
| chr3:57154818
|
C | T | 15 | a0001c0001t0027g0331a0001c0001t0038g0049a0001c0006t0011g0009others(12): Show | 15 | HG01109.hp1 HG01109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.126+10343G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57154818 | ||||||
| chr3:57155028
|
G | C | 1 | a0002c0004t0008g0177 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.126+10133C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57155028 | ||||||
| chr3:57155030
|
C | T | 2 | a0001c0001t0052g0311a0002c0003t0012g0254 | 2 | HG01243.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.126+10131G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57155030 | ||||||
| chr3:57155058
|
C | T | 1 | a0002c0004t0051g0019 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.126+10103G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57155058 | ||||||
| chr3:57155195
|
A | G | 3 | a0003c0002t0001g0253a0003c0002t0015g0172a0003c0002t0015g0303 | 3 | HG01169.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.126+9966T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57155195 | ||||||
| chr3:57155281
|
G | A | 2 | a0002c0004t0016g0343a0002c0004t0016g0344 | 2 | HG02257.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.126+9880C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57155281 | ||||||
| chr3:57155611
|
G | T | 2 | a0002c0003t0002g0251a0003c0002t0001g0252 | 2 | NA18978.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.126+9550C>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57155611 | ||||||
| chr3:57155792
|
T | C | 2 | a0002c0004t0049g0224a0003c0002t0001g0225 | 2 | HG01109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.126+9369A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57155792 | ||||||
| chr3:57155896
|
G | A | 6 | a0001c0006t0011g0009a0001c0006t0011g0010a0001c0006t0011g0011others(3): Show | 6 | HG02145.hp2 HG02976.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.126+9265C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57155896 | ||||||
| chr3:57155898
|
A | G | 1 | a0001c0001t0033g0085 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.126+9263T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57155898 | ||||||
| chr3:57155956
|
T | C | 4 | a0002c0004t0008g0091a0002c0004t0008g0177a0002c0004t0008g0323others(1): Show | 4 | HG00639.hp1 HG03017.hp1 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+9205A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57155956 | ||||||
| chr3:57156178
|
A | G | 6 | a0001c0006t0011g0009a0001c0006t0011g0010a0001c0006t0011g0011others(3): Show | 6 | HG02145.hp2 HG02976.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.126+8983T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57156178 | ||||||
| chr3:57156183
|
G | T | 130 | a0001c0001t0003g0117a0001c0001t0004g0118a0001c0001t0004g0149others(127): Show | 131 | HG00544.hp1 HG00558.hp1 HG00639.hp1 others(128): Show |
intron_variant | MODIFIER | c.126+8978C>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57156183 | ||||||
| chr3:57156191
|
A | G | 6 | a0001c0006t0011g0009a0001c0006t0011g0010a0001c0006t0011g0011others(3): Show | 6 | HG02145.hp2 HG02976.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.126+8970T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57156191 | ||||||
| chr3:57156218
|
A | G | 1 | a0001c0001t0004g0059 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.126+8943T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57156218 | ||||||
| chr3:57156275
|
C | CTT | 4 | a0002c0004t0008g0091a0002c0004t0008g0177a0002c0004t0008g0323others(1): Show | 4 | HG00639.hp1 HG03017.hp1 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+8885_126+8886i others(4): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57156275 | ||||||
| chr3:57156424
|
A | G | 130 | a0001c0001t0003g0117a0001c0001t0004g0118a0001c0001t0004g0149others(127): Show | 131 | HG00544.hp1 HG00558.hp1 HG00639.hp1 others(128): Show |
intron_variant | MODIFIER | c.126+8737T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57156424 | ||||||
| chr3:57156557
|
C | T | 11 | a0001c0001t0007g0002a0001c0001t0007g0025a0001c0001t0007g0026others(8): Show | 12 | HG00280.hp2 HG01261.hp2 HG01358.hp2 others(9): Show |
intron_variant | MODIFIER | c.126+8604G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57156557 | ||||||
| chr3:57156582
|
T | G | 1 | a0003c0002t0001g0044 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.126+8579A>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57156582 | ||||||
| chr3:57156669
|
C | T | 1 | a0002c0003t0002g0313 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.126+8492G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57156669 | ||||||
| chr3:57156777
|
T | C | 14 | a0001c0001t0027g0331a0001c0001t0038g0049a0001c0006t0011g0009others(11): Show | 14 | HG01109.hp1 HG01109.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.126+8384A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57156777 | ||||||
| chr3:57156783
|
G | C | 134 | a0001c0001t0003g0117a0001c0001t0004g0118a0001c0001t0004g0149others(131): Show | 135 | HG00544.hp1 HG00558.hp1 HG00639.hp1 others(132): Show |
intron_variant | MODIFIER | c.126+8378C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57156783 | ||||||
| chr3:57156796
|
C | T | 1 | a0001c0001t0007g0124 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.126+8365G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57156796 | ||||||
| chr3:57156844
|
C | G | 5 | a0001c0001t0018g0330a0002c0003t0022g0107a0002c0003t0022g0158others(2): Show | 5 | HG02486.hp1 HG02622.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.126+8317G>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57156844 | ||||||
| chr3:57156847
|
C | T | 1 | a0001c0001t0037g0055 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.126+8314G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57156847 | ||||||
| chr3:57156887
|
C | T | 2 | a0003c0002t0001g0061a0003c0002t0001g0094 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.126+8274G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57156887 | ||||||
| chr3:57157077
|
T | C | 1 | a0003c0002t0001g0119 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.126+8084A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57157077 | ||||||
| chr3:57157287
|
A | G | 4 | a0002c0004t0008g0091a0002c0004t0008g0177a0002c0004t0008g0323others(1): Show | 4 | HG00639.hp1 HG03017.hp1 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+7874T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57157287 | ||||||
| chr3:57157288
|
A | T | 4 | a0002c0004t0008g0091a0002c0004t0008g0177a0002c0004t0008g0323others(1): Show | 4 | HG00639.hp1 HG03017.hp1 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+7873T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57157288 | ||||||
| chr3:57157533
|
A | G | 4 | a0002c0004t0008g0091a0002c0004t0008g0177a0002c0004t0008g0323others(1): Show | 4 | HG00639.hp1 HG03017.hp1 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+7628T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57157533 | ||||||
| chr3:57157617
|
C | T | 2 | a0001c0001t0004g0059a0001c0001t0037g0055 | 2 | HG03017.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.126+7544G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57157617 | ||||||
| chr3:57157644
|
C | T | 1 | a0001c0001t0004g0333 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.126+7517G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57157644 | ||||||
| chr3:57157648
|
G | A | 1 | a0002c0004t0050g0321 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.126+7513C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57157648 | ||||||
| chr3:57157810
|
C | G | 1 | a0002c0004t0050g0321 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.126+7351G>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57157810 | ||||||
| chr3:57157812
|
A | T | 1 | a0001c0001t0005g0219 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.126+7349T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57157812 | ||||||
| chr3:57157830
|
C | T | 1 | a0003c0002t0001g0093 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.126+7331G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57157830 | ||||||
| chr3:57157850
|
C | T | 75 | a0001c0001t0004g0118a0001c0001t0007g0124a0001c0001t0035g0215others(72): Show | 76 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.126+7311G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57157850 | ||||||
| chr3:57157867
|
C | T | 75 | a0001c0001t0004g0118a0001c0001t0007g0124a0001c0001t0035g0215others(72): Show | 76 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.126+7294G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57157867 | ||||||
| chr3:57158016
|
G | A | 4 | a0002c0004t0008g0091a0002c0004t0008g0177a0002c0004t0008g0323others(1): Show | 4 | HG00639.hp1 HG03017.hp1 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+7145C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57158016 | ||||||
| chr3:57158018
|
T | C | 4 | a0002c0004t0008g0091a0002c0004t0008g0177a0002c0004t0008g0323others(1): Show | 4 | HG00639.hp1 HG03017.hp1 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+7143A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57158018 | ||||||
| chr3:57158072
|
T | C | 1 | a0003c0002t0001g0072 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.126+7089A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57158072 | ||||||
| chr3:57158197
|
A | G | 2 | a0001c0001t0018g0330a0008c0014t0018g0329 | 2 | HG02486.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.126+6964T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57158197 | ||||||
| chr3:57158266
|
G | T | 83 | a0001c0001t0003g0203a0001c0001t0004g0003a0001c0001t0004g0151others(80): Show | 85 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.126+6895C>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57158266 | ||||||
| chr3:57158380
|
T | C | 1 | a0002c0004t0057g0198 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.126+6781A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57158380 | ||||||
| chr3:57158512
|
G | A | 4 | a0001c0001t0003g0338a0002c0003t0002g0087a0002c0003t0002g0145others(1): Show | 4 | NA18961.hp1 NA18982.hp1 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+6649C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57158512 | ||||||
| chr3:57158548
|
A | G | 1 | a0002c0003t0002g0206 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.126+6613T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57158548 | ||||||
| chr3:57158560
|
C | A | 1 | a0001c0001t0003g0175 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.126+6601G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57158560 | ||||||
| chr3:57158693
|
G | T | 2 | a0003c0002t0001g0015a0003c0002t0001g0123 | 2 | NA18956.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.126+6468C>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57158693 | ||||||
| chr3:57158766
|
T | C | 2 | a0003c0002t0001g0121a0003c0002t0001g0122 | 2 | NA18945.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.126+6395A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57158766 | ||||||
| chr3:57158791
|
A | G | 1 | a0001c0001t0052g0311 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.126+6370T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57158791 | ||||||
| chr3:57158868
|
C | T | 6 | a0002c0003t0013g0028a0002c0003t0013g0092a0002c0003t0013g0170others(3): Show | 6 | HG02622.hp2 HG02717.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.126+6293G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57158868 | ||||||
| chr3:57158899
|
A | G | 75 | a0001c0001t0004g0118a0001c0001t0007g0124a0001c0001t0035g0215others(72): Show | 76 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.126+6262T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57158899 | ||||||
| chr3:57158972
|
G | C | 2 | a0003c0002t0001g0121a0003c0002t0001g0122 | 2 | NA18945.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.126+6189C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57158972 | ||||||
| chr3:57159054
|
T | C | 4 | a0002c0004t0019g0005a0002c0004t0019g0006a0002c0004t0048g0007others(1): Show | 4 | HG01884.hp2 HG02109.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+6107A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57159054 | ||||||
| chr3:57159112
|
C | T | 4 | a0002c0004t0008g0091a0002c0004t0008g0177a0002c0004t0008g0323others(1): Show | 4 | HG00639.hp1 HG03017.hp1 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+6049G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57159112 | ||||||
| chr3:57159123
|
CT | C | 126 | a0001c0001t0003g0117a0001c0001t0003g0304a0001c0001t0003g0306others(123): Show | 127 | HG00544.hp1 HG00558.hp1 HG00639.hp1 others(124): Show |
intron_variant | MODIFIER | c.126+6037delA | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57159123 | ||||||
| chr3:57159474
|
C | T | 1 | a0002c0004t0050g0321 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.126+5687G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57159474 | ||||||
| chr3:57159487
|
T | A | 4 | a0002c0004t0008g0310a0003c0002t0001g0037a0003c0002t0001g0308others(1): Show | 4 | HG00099.hp1 HG01496.hp2 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+5674A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57159487 | ||||||
| chr3:57159526
|
G | A | 5 | a0001c0001t0038g0049a0002c0003t0013g0077a0002c0003t0014g0226others(2): Show | 5 | HG01109.hp2 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.126+5635C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57159526 | ||||||
| chr3:57159549
|
C | T | 2 | a0001c0001t0003g0237a0001c0001t0003g0238 | 2 | HG02698.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.126+5612G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57159549 | ||||||
| chr3:57159641
|
G | GC | 10 | a0001c0001t0003g0117a0002c0007t0009g0088a0002c0007t0009g0089others(7): Show | 10 | HG01243.hp2 HG02109.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.126+5519dupG | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57159641 | ||||||
| chr3:57159695
|
TG | T | 5 | a0002c0007t0009g0088a0002c0007t0009g0089a0002c0007t0009g0167others(2): Show | 5 | HG02109.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.126+5465delC | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57159695 | ||||||
| chr3:57159735
|
G | C | 1 | a0001c0001t0005g0016 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.126+5426C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57159735 | ||||||
| chr3:57159863
|
C | CAG | 11 | a0001c0001t0003g0117a0002c0003t0055g0008a0002c0007t0009g0088others(8): Show | 11 | HG01243.hp2 HG02109.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.126+5296_126+5297d others(4): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57159863 | ||||||
| chr3:57160244
|
C | T | 130 | a0001c0001t0003g0117a0001c0001t0004g0118a0001c0001t0004g0149others(127): Show | 131 | HG00544.hp1 HG00558.hp1 HG00639.hp1 others(128): Show |
intron_variant | MODIFIER | c.126+4917G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57160244 | ||||||
| chr3:57160312
|
G | GA | 8 | a0001c0001t0007g0002a0001c0001t0007g0025a0001c0001t0007g0026others(5): Show | 9 | HG00280.hp2 HG01243.hp1 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.126+4848dupT | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57160312 | ||||||
| chr3:57160312
|
G | GAA | 22 | a0001c0001t0003g0117a0001c0001t0004g0333a0002c0003t0002g0312others(19): Show | 22 | HG01243.hp2 HG02109.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.126+4847_126+4848d others(4): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57160312 | ||||||
| chr3:57160398
|
G | T | 75 | a0001c0001t0004g0118a0001c0001t0007g0124a0001c0001t0035g0215others(72): Show | 76 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.126+4763C>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57160398 | ||||||
| chr3:57160489
|
A | C | 4 | a0002c0004t0008g0091a0002c0004t0008g0177a0002c0004t0008g0323others(1): Show | 4 | HG00639.hp1 HG03017.hp1 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+4672T>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57160489 | ||||||
| chr3:57160552
|
T | A | 1 | a0002c0003t0002g0312 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.126+4609A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57160552 | ||||||
| chr3:57160642
|
T | C | 2 | a0001c0001t0018g0330a0008c0014t0018g0329 | 2 | HG02486.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.126+4519A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57160642 | ||||||
| chr3:57160763
|
A | G | 1 | a0001c0001t0005g0047 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.126+4398T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57160763 | ||||||
| chr3:57160806
|
A | G | 1 | a0003c0002t0001g0229 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.126+4355T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57160806 | ||||||
| chr3:57160935
|
A | G | 3 | a0003c0002t0001g0120a0003c0002t0001g0121a0003c0002t0001g0122 | 3 | HG02735.hp2 NA18945.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.126+4226T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57160935 | ||||||
| chr3:57161015
|
C | T | 1 | a0003c0002t0001g0119 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.126+4146G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57161015 | ||||||
| chr3:57161034
|
C | G | 4 | a0002c0004t0008g0091a0002c0004t0008g0177a0002c0004t0008g0323others(1): Show | 4 | HG00639.hp1 HG03017.hp1 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+4127G>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57161034 | ||||||
| chr3:57161248
|
C | G | 25 | a0001c0001t0003g0117a0001c0001t0004g0333a0002c0003t0013g0028others(22): Show | 25 | HG00639.hp1 HG01243.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.126+3913G>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57161248 | ||||||
| chr3:57161339
|
C | T | 1 | a0002c0004t0050g0321 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.126+3822G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57161339 | ||||||
| chr3:57161446
|
A | G | 8 | a0001c0001t0027g0331a0001c0001t0038g0049a0002c0003t0013g0077others(5): Show | 8 | HG01109.hp1 HG01109.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.126+3715T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57161446 | ||||||
| chr3:57161514
|
C | T | 1 | a0003c0002t0001g0223 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.126+3647G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57161514 | ||||||
| chr3:57161647
|
G | C | 4 | a0002c0004t0008g0091a0002c0004t0008g0177a0002c0004t0008g0323others(1): Show | 4 | HG00639.hp1 HG03017.hp1 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+3514C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57161647 | ||||||
| chr3:57161764
|
G | A | 2 | a0001c0001t0005g0001a0001c0001t0028g0212 | 4 | NA18941.hp2 NA18956.hp1 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+3397C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57161764 | ||||||
| chr3:57161840
|
GGT | G | 4 | a0002c0004t0008g0091a0002c0004t0008g0177a0002c0004t0008g0323others(1): Show | 4 | HG00639.hp1 HG03017.hp1 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+3319_126+3320d others(4): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57161840 | ||||||
| chr3:57161982
|
A | C | 1 | a0002c0003t0002g0104 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.126+3179T>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57161982 | ||||||
| chr3:57162022
|
T | C | 10 | a0001c0001t0003g0203a0002c0003t0002g0199a0002c0003t0002g0200others(7): Show | 10 | HG00558.hp2 NA18946.hp2 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.126+3139A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57162022 | ||||||
| chr3:57162142
|
T | C | 25 | a0001c0001t0003g0117a0001c0001t0004g0333a0002c0003t0013g0028others(22): Show | 25 | HG00639.hp1 HG01243.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.126+3019A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57162142 | ||||||
| chr3:57162209
|
G | C | 25 | a0001c0001t0003g0117a0001c0001t0004g0333a0002c0003t0013g0028others(22): Show | 25 | HG00639.hp1 HG01243.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.126+2952C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57162209 | ||||||
| chr3:57162230
|
T | C | 4 | a0002c0004t0008g0091a0002c0004t0008g0177a0002c0004t0008g0323others(1): Show | 4 | HG00639.hp1 HG03017.hp1 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+2931A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57162230 | ||||||
| chr3:57162335
|
C | T | 1 | a0001c0001t0007g0060 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.126+2826G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57162335 | ||||||
| chr3:57162356
|
A | G | 7 | a0001c0001t0005g0016a0001c0001t0005g0035a0001c0001t0005g0219others(4): Show | 7 | HG00642.hp1 HG01106.hp2 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.126+2805T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57162356 | ||||||
| chr3:57162361
|
C | T | 3 | a0002c0003t0012g0048a0002c0003t0012g0073a0002c0003t0012g0146 | 3 | HG01255.hp1 HG01891.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.126+2800G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57162361 | ||||||
| chr3:57162378
|
T | C | 1 | a0001c0001t0003g0336 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.126+2783A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57162378 | ||||||
| chr3:57162383
|
C | T | 1 | a0001c0001t0005g0181 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.126+2778G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57162383 | ||||||
| chr3:57162608
|
C | T | 11 | a0001c0006t0011g0147a0002c0003t0012g0048a0002c0003t0012g0073others(8): Show | 11 | HG01255.hp1 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.126+2553G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57162608 | ||||||
| chr3:57162811
|
T | C | 1 | a0002c0003t0002g0204 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.126+2350A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57162811 | ||||||
| chr3:57162820
|
A | G | 75 | a0001c0001t0005g0047a0001c0001t0007g0002a0001c0001t0007g0025others(72): Show | 76 | HG00280.hp2 HG00544.hp1 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.126+2341T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57162820 | ||||||
| chr3:57162882
|
G | A | 1 | a0001c0001t0046g0318 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.126+2279C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57162882 | ||||||
| chr3:57162983
|
G | C | 1 | a0002c0004t0008g0177 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.126+2178C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57162983 | ||||||
| chr3:57162990
|
G | A | 21 | a0001c0001t0003g0117a0001c0001t0004g0333a0002c0003t0013g0028others(18): Show | 21 | HG01243.hp2 HG02109.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.126+2171C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57162990 | ||||||
| chr3:57163090
|
G | A | 2 | a0001c0001t0004g0333a0002c0004t0050g0321 | 2 | HG02559.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.126+2071C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57163090 | ||||||
| chr3:57163142
|
G | A | 1 | a0001c0001t0004g0059 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.126+2019C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57163142 | ||||||
| chr3:57163223
|
C | G | 4 | a0002c0004t0008g0091a0002c0004t0008g0177a0002c0004t0008g0323others(1): Show | 4 | HG00639.hp1 HG03017.hp1 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+1938G>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57163223 | ||||||
| chr3:57163246
|
C | G | 4 | a0002c0004t0008g0091a0002c0004t0008g0177a0002c0004t0008g0323others(1): Show | 4 | HG00639.hp1 HG03017.hp1 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+1915G>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57163246 | ||||||
| chr3:57163246
|
C | T | 75 | a0001c0001t0007g0002a0001c0001t0007g0025a0001c0001t0007g0026others(72): Show | 76 | HG00280.hp2 HG00544.hp1 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.126+1915G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57163246 | ||||||
| chr3:57163255
|
G | A | 1 | a0002c0003t0002g0206 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.126+1906C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57163255 | ||||||
| chr3:57163300
|
C | G | 2 | a0002c0003t0002g0178a0002c0003t0002g0214 | 2 | NA19056.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.126+1861G>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57163300 | ||||||
| chr3:57163426
|
G | A | 3 | a0001c0001t0004g0168a0001c0001t0004g0176a0001c0001t0004g0322 | 3 | HG02258.hp2 HG02922.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.126+1735C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57163426 | ||||||
| chr3:57163446
|
C | T | 1 | a0005c0008t0006g0213 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.126+1715G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57163446 | ||||||
| chr3:57163467
|
G | C | 1 | a0001c0001t0018g0330 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.126+1694C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57163467 | ||||||
| chr3:57163521
|
C | A | 11 | a0001c0001t0004g0118a0002c0003t0013g0028a0002c0003t0013g0092others(8): Show | 11 | HG00639.hp1 HG02622.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.126+1640G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57163521 | ||||||
| chr3:57163542
|
T | A | 3 | a0001c0001t0005g0326a0001c0001t0005g0327a0001c0001t0005g0328 | 3 | HG03491.hp1 HG03492.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.126+1619A>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57163542 | ||||||
| chr3:57163555
|
C | A | 1 | a0001c0001t0003g0014 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.126+1606G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57163555 | ||||||
| chr3:57163785
|
C | CG | 37 | a0001c0001t0003g0117a0001c0001t0003g0210a0001c0001t0003g0211others(34): Show | 37 | HG00544.hp1 HG00673.hp1 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.126+1375dupC | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57163785 | ||||||
| chr3:57163785
|
C | CGG | 33 | a0001c0001t0007g0060a0001c0001t0033g0085a0002c0003t0002g0062others(30): Show | 33 | HG00639.hp2 HG01069.hp1 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.126+1374_126+1375d others(4): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57163785 | ||||||
| chr3:57163785
|
C | CGGG | 24 | a0001c0001t0003g0057a0001c0001t0004g0059a0001c0001t0005g0047others(21): Show | 24 | HG00280.hp2 HG01123.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.126+1373_126+1375d others(5): Show |
IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57163785 | ||||||
| chr3:57163792
|
GC | G | 9 | a0001c0001t0003g0174a0001c0001t0003g0175a0001c0001t0004g0176others(6): Show | 9 | HG00639.hp1 HG02647.hp1 HG02698.hp2 others(6): Show |
intron_variant | MODIFIER | c.126+1368delG | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57163792 | ||||||
| chr3:57163793
|
C | CG | 29 | a0001c0001t0003g0195a0001c0001t0003g0203a0001c0001t0004g0190others(26): Show | 29 | HG00544.hp2 HG00558.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.126+1367dupC | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57163793 | ||||||
| chr3:57163793
|
C | G | 149 | a0001c0001t0003g0057a0001c0001t0003g0117a0001c0001t0003g0163others(146): Show | 150 | HG00280.hp2 HG00544.hp1 HG00639.hp2 others(147): Show |
intron_variant | MODIFIER | c.126+1368G>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57163793 | ||||||
| chr3:57163794
|
G | C | 1 | a0002c0003t0021g0342 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.126+1367C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57163794 | ||||||
| chr3:57163800
|
G | A | 3 | a0001c0001t0018g0330a0002c0003t0021g0342a0008c0014t0018g0329 | 3 | HG02486.hp1 HG02809.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.126+1361C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57163800 | ||||||
| chr3:57163803
|
A | AG | 5 | a0001c0001t0005g0035a0002c0003t0002g0034a0003c0002t0001g0033others(2): Show | 5 | HG00673.hp1 HG01358.hp1 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.126+1357dupC | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57163803 | ||||||
| chr3:57163803
|
A | G | 12 | a0001c0001t0004g0027a0001c0001t0007g0025a0001c0001t0007g0026others(9): Show | 12 | HG01106.hp2 HG01255.hp2 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.126+1358T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57163803 | ||||||
| chr3:57163808
|
GT | G | 8 | a0001c0001t0003g0336a0001c0006t0011g0009a0001c0006t0011g0010others(5): Show | 8 | HG02145.hp2 HG02280.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.126+1352delA | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57163808 | ||||||
| chr3:57163809
|
T | G | 3 | a0001c0001t0004g0333a0001c0001t0027g0331a0002c0003t0021g0332 | 3 | HG01934.hp1 HG02818.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.126+1352A>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57163809 | ||||||
| chr3:57163843
|
G | A | 1 | a0002c0003t0002g0337 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.126+1318C>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57163843 | ||||||
| chr3:57163910
|
C | T | 1 | a0001c0001t0020g0021 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.126+1251G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57163910 | ||||||
| chr3:57164039
|
T | C | 1 | a0001c0001t0003g0338 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.126+1122A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57164039 | ||||||
| chr3:57164092
|
A | C | 3 | a0002c0003t0054g0020a0002c0004t0016g0343a0002c0004t0016g0344 | 3 | HG02257.hp1 HG02970.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.126+1069T>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57164092 | ||||||
| chr3:57164190
|
C | T | 1 | a0002c0004t0051g0019 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.126+971G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57164190 | ||||||
| chr3:57164215
|
C | T | 1 | a0001c0001t0042g0018 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.126+946G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57164215 | ||||||
| chr3:57164234
|
G | T | 1 | a0003c0002t0001g0017 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.126+927C>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57164234 | ||||||
| chr3:57164336
|
G | C | 3 | a0002c0003t0002g0339a0002c0003t0002g0340a0002c0003t0002g0341 | 3 | NA18974.hp1 NA19002.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.126+825C>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57164336 | ||||||
| chr3:57164717
|
A | T | 1 | a0001c0001t0005g0016 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.126+444T>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57164717 | ||||||
| chr3:57164769
|
C | T | 1 | a0003c0002t0001g0015 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.126+392G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57164769 | ||||||
| chr3:57164775
|
C | A | 1 | a0002c0003t0021g0342 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.126+386G>T | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57164775 | ||||||
| chr3:57164940
|
A | G | 1 | a0001c0001t0003g0014 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.126+221T>C | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57164940 | ||||||
| chr3:57165051
|
C | T | 2 | a0002c0004t0016g0343a0002c0004t0016g0344 | 2 | HG02257.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.126+110G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57165051 | ||||||
| chr3:57165110
|
T | C | 2 | a0002c0004t0016g0343a0002c0004t0016g0344 | 2 | HG02257.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.126+51A>G | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57165110 | ||||||
| chr3:57165115
|
C | T | 9 | a0001c0006t0011g0009a0001c0006t0011g0010a0001c0006t0011g0011others(6): Show | 9 | HG01884.hp2 HG02145.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.126+46G>A | IL17RD | ENSG00000144730.19 | transcript | ENST00000296318.12 | protein_coding | 1/12 | chr3 | 57165115 |