| geneid | 114088 |
|---|---|
| ensemblid | ENSG00000100505.14 |
| hgncid | 16288 |
| symbol | TRIM9 |
| name | tripartite motif containing 9 |
| refseq_nuc | NM_001387360.1 |
| refseq_prot | NP_001374289.1 |
| ensembl_nuc | ENST00000684578.1 |
| ensembl_prot | ENSP00000507131.1 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 50975266 |
| end | 51095105 |
| strand | - |
| ver | v1.2 |
| region | chr14:50975266-51095105 |
| region5000 | chr14:50970266-51100105 |
| regionname0 | TRIM9_chr14_50975266_51095105 |
| regionname5000 | TRIM9_chr14_50970266_51100105 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 795 | 186 | 35 | 42 | 84 | 7 | 18 | 63 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| a0002 | 1/1 | 795 | 150 | 52 | 25 | 50 | 5 | 16 | 39 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| a0003 | 0/0 | 795 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| a0004 | 0/0 | 795 | 2 | 0 | 0 | 0 | 2 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| a0005 | 0/0 | 795 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 2388 | 175 | 31 | 40 | 79 | 7 | 18 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| c0002 | 1/1 | 2388 | 140 | 44 | 24 | 49 | 5 | 16 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| c0003 | 0/0 | 2388 | 5 | 4 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| c0004 | 0/0 | 2388 | 5 | 5 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| c0005 | 0/0 | 2388 | 4 | 0 | 0 | 4 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| c0006 | 0/0 | 2388 | 3 | 0 | 3 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| c0007 | 0/0 | 2388 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| c0008 | 0/0 | 2388 | 2 | 0 | 0 | 0 | 2 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| c0009 | 0/0 | 2388 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| c0010 | 0/0 | 2388 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| c0011 | 0/0 | 2388 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| c0012 | 0/0 | 2388 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| c0013 | 0/0 | 2388 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| c0014 | 0/0 | 2388 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 2192 | 117 | 38 | 23 | 36 | 5 | 13 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| t0002 | 0/0 | 2192 | 80 | 2 | 21 | 40 | 4 | 13 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| t0003 | 0/0 | 2192 | 76 | 9 | 15 | 43 | 4 | 5 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| t0004 | 0/0 | 2192 | 19 | 10 | 5 | 3 | 1 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| t0005 | 0/0 | 2192 | 13 | 12 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| t0006 | 0/0 | 2192 | 12 | 0 | 0 | 9 | 0 | 3 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| t0007 | 0/0 | 2192 | 3 | 2 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| t0008 | 0/0 | 2192 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| t0009 | 0/0 | 2192 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| t0010 | 0/0 | 2192 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| t0011 | 0/0 | 2192 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| t0012 | 0/0 | 2192 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| t0013 | 0/0 | 2192 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| t0014 | 0/0 | 2192 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| t0015 | 0/0 | 2192 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| t0016 | 0/0 | 2192 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| t0017 | 0/0 | 2192 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| t0018 | 0/0 | 2192 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| t0019 | 0/0 | 2192 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0005 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0067 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0279 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2388 | 175 | 31 | 40 | 79 | 7 | 18 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| a0001c0003 | 0/0 | 2388 | 5 | 4 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| a0001c0005 | 0/0 | 2388 | 4 | 0 | 0 | 4 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| a0001c0009 | 0/0 | 2388 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| a0001c0014 | 0/0 | 2388 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| a0002c0002 | 1/1 | 2388 | 140 | 44 | 24 | 49 | 5 | 16 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| a0002c0004 | 0/0 | 2388 | 5 | 5 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| a0002c0007 | 0/0 | 2388 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| a0002c0010 | 0/0 | 2388 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| a0002c0012 | 0/0 | 2388 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| a0002c0013 | 0/0 | 2388 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| a0003c0006 | 0/0 | 2388 | 3 | 0 | 3 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| a0004c0008 | 0/0 | 2388 | 2 | 0 | 0 | 0 | 2 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| a0005c0011 | 0/0 | 2388 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4579 | 17 | 10 | 3 | 4 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| a0001c0001t0002 | 0/0 | 4579 | 72 | 2 | 19 | 34 | 4 | 13 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| a0001c0001t0003 | 0/0 | 4579 | 57 | 2 | 12 | 36 | 2 | 5 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| a0001c0001t0004 | 0/0 | 4579 | 15 | 6 | 5 | 3 | 1 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| a0001c0001t0005 | 0/0 | 4579 | 5 | 5 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| a0001c0001t0009 | 0/0 | 4579 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| a0001c0001t0010 | 0/0 | 4579 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| a0001c0001t0012 | 0/0 | 4579 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| a0001c0001t0015 | 0/0 | 4579 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| a0001c0001t0017 | 0/0 | 4579 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| a0001c0001t0019 | 0/0 | 4579 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| a0001c0003t0001 | 0/0 | 4579 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| a0001c0003t0007 | 0/0 | 4579 | 3 | 2 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| a0001c0005t0002 | 0/0 | 4579 | 4 | 0 | 0 | 4 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| a0001c0009t0002 | 0/0 | 4579 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| a0001c0014t0002 | 0/0 | 4579 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| a0002c0002t0001 | 1/1 | 4579 | 91 | 24 | 18 | 31 | 3 | 13 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| a0002c0002t0002 | 0/0 | 4579 | 2 | 0 | 1 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| a0002c0002t0003 | 0/0 | 4579 | 19 | 7 | 3 | 7 | 2 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| a0002c0002t0004 | 0/0 | 4579 | 4 | 4 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| a0002c0002t0005 | 0/0 | 4579 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| a0002c0002t0006 | 0/0 | 4579 | 12 | 0 | 0 | 9 | 0 | 3 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| a0002c0002t0008 | 0/0 | 4579 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| a0002c0002t0010 | 0/0 | 4579 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| a0002c0002t0011 | 0/0 | 4579 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| a0002c0002t0013 | 0/0 | 4579 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| a0002c0002t0014 | 0/0 | 4579 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| a0002c0002t0016 | 0/0 | 4579 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| a0002c0004t0005 | 0/0 | 4579 | 5 | 5 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| a0002c0007t0001 | 0/0 | 4579 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| a0002c0007t0011 | 0/0 | 4579 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| a0002c0010t0005 | 0/0 | 4579 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| a0002c0012t0005 | 0/0 | 4579 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| a0002c0013t0001 | 0/0 | 4579 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| a0003c0006t0001 | 0/0 | 4579 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| a0003c0006t0018 | 0/0 | 4579 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| a0004c0008t0001 | 0/0 | 4579 | 2 | 0 | 0 | 0 | 2 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| a0005c0011t0001 | 0/0 | 4579 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | copy fasta | chr14 | 50970266 | 51100105 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0003g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0003g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0003g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0003g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0003g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0003g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0003g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0003g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0003g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0003g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0003g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0004g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0004g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0004g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0004g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0004g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0004g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0004g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0004g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0004g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0004g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0004g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0004g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0004g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0004g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0004g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0005g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0005g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0005g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0005g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0005g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0009g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0009g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0009g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0010g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0012g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0012g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0015g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0017g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0019g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0003t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0003t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0003t0007g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0003t0007g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0003t0007g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0005t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0005t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0005t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0005t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0009t0002g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0014t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0067 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0279 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0003g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0003g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0003g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0003g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0003g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0003g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0003g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0003g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0004g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0004g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0004g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0004g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0005g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0006g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0006g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0006g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0006g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0006g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0006g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0006g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0006g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0006g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0006g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0006g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0008g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0008g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0008g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0010g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0010g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0011g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0013g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0013g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0014g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0016g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0004t0005g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0004t0005g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0004t0005g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0004t0005g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0004t0005g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0007t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0007t0011g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0010t0005g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0012t0005g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0013t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0003c0006t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0003c0006t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0003c0006t0018g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0004c0008t0001g0005 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0005c0011t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0002 | c0002 | t0003 | g0239 | EUR | GBR | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0049 | EUR | GBR | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG00280 | hp1 | a0002 | c0002 | t0001 | g0158 | EUR | FIN | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG00280 | hp2 | a0001 | c0001 | t0004 | g0232 | EUR | FIN | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG00408 | hp1 | a0001 | c0014 | t0002 | g0328 | EAS | CHS | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0183 | EAS | CHS | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0163 | EAS | CHS | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0095 | EAS | CHS | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG00438 | hp1 | a0002 | c0002 | t0001 | g0203 | EAS | CHS | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0273 | EAS | CHS | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG00544 | hp1 | a0001 | c0005 | t0002 | g0226 | EAS | CHS | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG00544 | hp2 | a0002 | c0002 | t0001 | g0263 | EAS | CHS | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG00597 | hp1 | a0002 | c0002 | t0001 | g0162 | EAS | CHS | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | CHS | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | CHS | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0318 | EAS | CHS | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0299 | AMR | PUR | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0202 | AMR | PUR | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG00642 | hp1 | a0002 | c0002 | t0001 | g0230 | AMR | PUR | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0300 | AMR | PUR | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0058 | AMR | PUR | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG00733 | hp2 | a0002 | c0002 | t0003 | g0281 | AMR | PUR | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG00735 | hp1 | a0001 | c0009 | t0002 | g0009 | AMR | PUR | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG00735 | hp2 | a0002 | c0002 | t0001 | g0231 | AMR | PUR | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0130 | AMR | PUR | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0210 | AMR | PUR | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0309 | AMR | PUR | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0208 | AMR | PUR | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01069 | hp1 | a0002 | c0002 | t0003 | g0066 | AMR | PUR | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01069 | hp2 | a0002 | c0002 | t0001 | g0236 | AMR | PUR | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0219 | AMR | PUR | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01070 | hp2 | a0001 | c0001 | t0015 | g0240 | AMR | PUR | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0218 | AMR | PUR | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01071 | hp2 | a0002 | c0002 | t0003 | g0065 | AMR | PUR | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0257 | AMR | PUR | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01074 | hp2 | a0002 | c0002 | t0001 | g0137 | AMR | PUR | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0308 | AMR | PUR | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01081 | hp2 | a0002 | c0002 | t0001 | g0007 | AMR | PUR | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01099 | hp1 | a0003 | c0006 | t0001 | g0142 | AMR | PUR | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01099 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0133 | AMR | PUR | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01109 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01167 | hp1 | a0002 | c0002 | t0001 | g0227 | AMR | PUR | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0156 | AMR | PUR | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0215 | AMR | PUR | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01168 | hp2 | a0001 | c0001 | t0004 | g0241 | AMR | PUR | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0214 | AMR | PUR | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01169 | hp2 | a0002 | c0002 | t0001 | g0007 | AMR | PUR | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01175 | hp1 | a0002 | c0002 | t0001 | g0234 | AMR | PUR | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01175 | hp2 | a0003 | c0006 | t0018 | g0151 | AMR | PUR | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0316 | AMR | PUR | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01243 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01255 | hp1 | a0002 | c0002 | t0001 | g0238 | AMR | CLM | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0129 | AMR | CLM | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0111 | AMR | CLM | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0139 | AMR | CLM | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0154 | AMR | CLM | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01257 | hp2 | a0002 | c0002 | t0014 | g0008 | AMR | CLM | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0110 | AMR | CLM | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01258 | hp2 | a0002 | c0002 | t0014 | g0008 | AMR | CLM | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01261 | hp1 | a0001 | c0001 | t0004 | g0099 | AMR | CLM | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0153 | AMR | CLM | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0121 | AMR | CLM | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01346 | hp2 | a0001 | c0001 | t0004 | g0064 | AMR | CLM | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | CLM | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0187 | AMR | CLM | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0322 | AMR | CLM | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01361 | hp2 | a0001 | c0001 | t0004 | g0323 | AMR | CLM | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01433 | hp1 | a0001 | c0003 | t0007 | g0011 | AMR | CLM | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01433 | hp2 | a0002 | c0002 | t0001 | g0131 | AMR | CLM | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01496 | hp1 | a0002 | c0012 | t0005 | g0161 | AMR | CLM | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01496 | hp2 | a0002 | c0002 | t0001 | g0237 | AMR | CLM | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0019 | EUR | IBS | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0059 | EUR | IBS | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01516 | hp1 | a0004 | c0008 | t0001 | g0005 | EUR | IBS | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0271 | EUR | IBS | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0060 | EUR | IBS | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01517 | hp2 | a0004 | c0008 | t0001 | g0005 | EUR | IBS | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01884 | hp1 | a0002 | c0002 | t0001 | g0039 | AFR | ACB | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01884 | hp2 | a0002 | c0002 | t0001 | g0025 | AFR | ACB | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01891 | hp1 | a0001 | c0001 | t0005 | g0027 | AFR | ACB | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01891 | hp2 | a0002 | c0002 | t0001 | g0093 | AFR | ACB | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0157 | AMR | PEL | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0222 | AMR | PEL | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0150 | AMR | PEL | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01943 | hp2 | a0001 | c0001 | t0004 | g0138 | AMR | PEL | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01975 | hp1 | a0002 | c0002 | t0002 | g0233 | AMR | PEL | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0192 | AMR | PEL | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01981 | hp1 | a0002 | c0002 | t0001 | g0145 | AMR | PEL | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0054 | AMR | PEL | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0209 | AMR | PEL | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PEL | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02027 | hp1 | a0002 | c0002 | t0001 | g0174 | EAS | KHV | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02027 | hp2 | a0001 | c0001 | t0003 | g0083 | EAS | KHV | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02055 | hp1 | a0002 | c0002 | t0004 | g0046 | AFR | ACB | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02055 | hp2 | a0002 | c0002 | t0003 | g0044 | AFR | ACB | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | KHV | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02056 | hp2 | a0001 | c0001 | t0003 | g0063 | EAS | KHV | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0167 | EAS | KHV | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02074 | hp2 | a0002 | c0002 | t0001 | g0128 | EAS | KHV | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0165 | EAS | KHV | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | KHV | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02129 | hp1 | a0001 | c0001 | t0004 | g0314 | EAS | KHV | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0195 | EAS | KHV | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02135 | hp1 | a0002 | c0002 | t0001 | g0294 | EAS | KHV | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0296 | EAS | KHV | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02145 | hp1 | a0002 | c0002 | t0001 | g0326 | AFR | ACB | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02145 | hp2 | a0002 | c0002 | t0004 | g0321 | AFR | ACB | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0069 | EAS | CDX | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02155 | hp2 | a0002 | c0002 | t0006 | g0079 | EAS | CDX | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0213 | EAS | CDX | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02165 | hp2 | a0002 | c0002 | t0016 | g0076 | EAS | CDX | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02257 | hp1 | a0001 | c0001 | t0019 | g0331 | AFR | ACB | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02257 | hp2 | a0001 | c0001 | t0009 | g0301 | AFR | ACB | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02273 | hp1 | a0003 | c0006 | t0001 | g0140 | AMR | PEL | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02273 | hp2 | a0001 | c0001 | t0003 | g0160 | AMR | PEL | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02280 | hp1 | a0002 | c0002 | t0013 | g0035 | AFR | ACB | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02280 | hp2 | a0002 | c0002 | t0001 | g0041 | AFR | ACB | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0061 | AMR | PEL | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PEL | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02451 | hp1 | a0001 | c0001 | t0004 | g0148 | AFR | ACB | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | ACB | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02523 | hp1 | a0002 | c0002 | t0003 | g0050 | EAS | KHV | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0269 | EAS | KHV | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02572 | hp1 | a0002 | c0002 | t0003 | g0029 | AFR | GWD | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02572 | hp2 | a0001 | c0001 | t0004 | g0100 | AFR | GWD | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0220 | SAS | PJL | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02602 | hp2 | a0002 | c0002 | t0001 | g0188 | SAS | PJL | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02615 | hp1 | a0001 | c0001 | t0005 | g0026 | AFR | GWD | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02615 | hp2 | a0001 | c0001 | t0004 | g0126 | AFR | GWD | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02622 | hp1 | a0002 | c0007 | t0001 | g0017 | AFR | GWD | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02622 | hp2 | a0001 | c0001 | t0004 | g0105 | AFR | GWD | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02630 | hp1 | a0001 | c0001 | t0010 | g0329 | AFR | GWD | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02630 | hp2 | a0002 | c0002 | t0001 | g0228 | AFR | GWD | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02647 | hp1 | a0002 | c0002 | t0003 | g0106 | AFR | GWD | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02647 | hp2 | a0001 | c0003 | t0001 | g0010 | AFR | GWD | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02683 | hp1 | a0002 | c0002 | t0001 | g0125 | SAS | PJL | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0200 | SAS | PJL | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02717 | hp1 | a0005 | c0011 | t0001 | g0315 | AFR | GWD | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02717 | hp2 | a0002 | c0002 | t0008 | g0040 | AFR | GWD | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02723 | hp1 | a0001 | c0001 | t0005 | g0305 | AFR | GWD | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02723 | hp2 | a0001 | c0003 | t0001 | g0014 | AFR | GWD | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0107 | SAS | PJL | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0068 | SAS | PJL | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02738 | hp1 | a0002 | c0002 | t0001 | g0146 | SAS | PJL | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0136 | SAS | PJL | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02809 | hp1 | a0002 | c0002 | t0010 | g0332 | AFR | GWD | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0310 | AFR | GWD | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02818 | hp1 | a0002 | c0002 | t0001 | g0307 | AFR | GWD | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02818 | hp2 | a0002 | c0002 | t0001 | g0295 | AFR | GWD | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02886 | hp1 | a0002 | c0002 | t0013 | g0250 | AFR | GWD | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02886 | hp2 | a0002 | c0002 | t0001 | g0288 | AFR | GWD | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02895 | hp1 | a0001 | c0001 | t0005 | g0033 | AFR | GWD | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02895 | hp2 | a0002 | c0002 | t0001 | g0022 | AFR | GWD | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02897 | hp1 | a0001 | c0001 | t0005 | g0032 | AFR | GWD | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02922 | hp1 | a0002 | c0002 | t0001 | g0104 | AFR | ESN | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02922 | hp2 | a0002 | c0002 | t0011 | g0034 | AFR | ESN | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02970 | hp1 | a0002 | c0002 | t0001 | g0246 | AFR | ESN | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02970 | hp2 | a0002 | c0002 | t0001 | g0021 | AFR | ESN | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02976 | hp1 | a0002 | c0002 | t0001 | g0248 | AFR | ESN | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02976 | hp2 | a0002 | c0002 | t0001 | g0207 | AFR | ESN | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG03041 | hp1 | a0002 | c0002 | t0008 | g0306 | AFR | GWD | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG03041 | hp2 | a0002 | c0004 | t0005 | g0311 | AFR | GWD | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG03098 | hp1 | a0001 | c0001 | t0009 | g0038 | AFR | MSL | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG03098 | hp2 | a0002 | c0002 | t0001 | g0313 | AFR | MSL | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG03130 | hp1 | a0002 | c0002 | t0004 | g0212 | AFR | ESN | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0324 | AFR | ESN | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG03139 | hp1 | a0002 | c0002 | t0001 | g0247 | AFR | ESN | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG03139 | hp2 | a0002 | c0002 | t0008 | g0325 | AFR | ESN | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG03195 | hp1 | a0002 | c0002 | t0003 | g0172 | AFR | ESN | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG03195 | hp2 | a0002 | c0004 | t0005 | g0256 | AFR | ESN | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG03209 | hp1 | a0002 | c0002 | t0001 | g0092 | AFR | MSL | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG03209 | hp2 | a0002 | c0002 | t0001 | g0303 | AFR | MSL | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG03225 | hp1 | a0002 | c0002 | t0003 | g0098 | AFR | MSL | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG03225 | hp2 | a0001 | c0001 | t0017 | g0036 | AFR | MSL | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG03453 | hp1 | a0002 | c0002 | t0010 | g0330 | AFR | MSL | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG03453 | hp2 | a0002 | c0007 | t0011 | g0013 | AFR | MSL | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG03486 | hp1 | a0001 | c0001 | t0009 | g0096 | AFR | MSL | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0101 | AFR | MSL | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0186 | SAS | PJL | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0006 | SAS | PJL | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0006 | SAS | PJL | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0152 | SAS | PJL | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG03516 | hp1 | a0002 | c0002 | t0004 | g0304 | AFR | ESN | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG03516 | hp2 | a0002 | c0002 | t0003 | g0249 | AFR | ESN | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | MSL | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG03579 | hp2 | a0001 | c0003 | t0007 | g0015 | AFR | MSL | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0108 | SAS | PJL | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0147 | SAS | PJL | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG03669 | hp1 | a0002 | c0002 | t0001 | g0123 | SAS | PJL | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0196 | SAS | PJL | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG03704 | hp1 | a0002 | c0002 | t0001 | g0047 | SAS | PJL | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0155 | SAS | PJL | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0056 | SAS | PJL | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG03710 | hp2 | a0002 | c0002 | t0006 | g0018 | SAS | PJL | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG03834 | hp1 | a0002 | c0002 | t0001 | g0243 | SAS | BEB | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0159 | SAS | BEB | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG03927 | hp1 | a0002 | c0002 | t0001 | g0135 | SAS | BEB | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG03927 | hp2 | a0002 | c0002 | t0001 | g0189 | SAS | BEB | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG03942 | hp1 | a0002 | c0002 | t0001 | g0124 | SAS | BEB | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG03942 | hp2 | a0002 | c0002 | t0006 | g0191 | SAS | BEB | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG04115 | hp1 | a0002 | c0002 | t0001 | g0181 | SAS | STU | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0045 | SAS | STU | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0176 | SAS | BEB | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG04184 | hp2 | a0002 | c0002 | t0001 | g0024 | SAS | BEB | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG04204 | hp1 | a0002 | c0002 | t0006 | g0144 | SAS | STU | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0193 | SAS | STU | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18522 | hp1 | a0002 | c0002 | t0003 | g0177 | AFR | YRI | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18522 | hp2 | a0002 | c0002 | t0001 | g0030 | AFR | YRI | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18612 | hp1 | a0002 | c0002 | t0001 | g0072 | EAS | CHB | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | CHB | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18906 | hp1 | a0002 | c0010 | t0005 | g0016 | AFR | YRI | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18906 | hp2 | a0002 | c0002 | t0005 | g0302 | AFR | YRI | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18939 | hp2 | a0002 | c0002 | t0001 | g0264 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18941 | hp1 | a0002 | c0002 | t0001 | g0089 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18942 | hp2 | a0001 | c0001 | t0003 | g0194 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0320 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18943 | hp2 | a0002 | c0002 | t0006 | g0292 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18944 | hp1 | a0002 | c0002 | t0001 | g0190 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18944 | hp2 | a0002 | c0002 | t0001 | g0114 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18946 | hp1 | a0002 | c0002 | t0006 | g0224 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18949 | hp1 | a0002 | c0002 | t0001 | g0164 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18949 | hp2 | a0001 | c0001 | t0012 | g0276 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18951 | hp2 | a0001 | c0001 | t0003 | g0260 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18954 | hp1 | a0001 | c0005 | t0002 | g0251 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18954 | hp2 | a0002 | c0002 | t0001 | g0120 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18956 | hp1 | a0002 | c0002 | t0001 | g0262 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18956 | hp2 | a0001 | c0001 | t0003 | g0169 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18957 | hp1 | a0002 | c0013 | t0001 | g0327 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18961 | hp1 | a0001 | c0001 | t0004 | g0266 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0198 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0074 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18963 | hp2 | a0002 | c0002 | t0003 | g0109 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0197 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18969 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18973 | hp1 | a0002 | c0002 | t0001 | g0175 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18973 | hp2 | a0001 | c0005 | t0002 | g0252 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18974 | hp1 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0084 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18980 | hp1 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18980 | hp2 | a0002 | c0002 | t0001 | g0185 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18981 | hp2 | a0001 | c0001 | t0003 | g0080 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18983 | hp1 | a0002 | c0002 | t0001 | g0091 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18984 | hp1 | a0001 | c0005 | t0002 | g0255 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18984 | hp2 | a0002 | c0002 | t0003 | g0117 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18991 | hp2 | a0002 | c0002 | t0006 | g0004 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18992 | hp1 | a0002 | c0002 | t0001 | g0085 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18992 | hp2 | a0001 | c0001 | t0003 | g0221 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18993 | hp1 | a0001 | c0001 | t0003 | g0094 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18993 | hp2 | a0002 | c0002 | t0006 | g0223 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18998 | hp1 | a0002 | c0002 | t0001 | g0265 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18998 | hp2 | a0002 | c0002 | t0003 | g0242 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0168 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA19000 | hp2 | a0002 | c0002 | t0001 | g0051 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA19002 | hp1 | a0002 | c0002 | t0001 | g0184 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA19003 | hp1 | a0002 | c0002 | t0001 | g0166 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA19004 | hp1 | a0002 | c0002 | t0003 | g0112 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA19004 | hp2 | a0001 | c0001 | t0003 | g0057 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA19005 | hp1 | a0002 | c0002 | t0001 | g0115 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA19007 | hp1 | a0002 | c0002 | t0006 | g0004 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA19007 | hp2 | a0002 | c0002 | t0001 | g0280 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA19010 | hp1 | a0002 | c0002 | t0003 | g0113 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0297 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0170 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA19011 | hp2 | a0002 | c0002 | t0001 | g0090 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA19012 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA19030 | hp1 | a0002 | c0002 | t0001 | g0245 | AFR | LWK | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | LWK | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA19054 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA19056 | hp2 | a0002 | c0002 | t0002 | g0225 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA19057 | hp1 | a0002 | c0002 | t0001 | g0204 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA19058 | hp1 | a0002 | c0002 | t0006 | g0078 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA19058 | hp2 | a0001 | c0001 | t0004 | g0253 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA19060 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA19065 | hp1 | a0002 | c0002 | t0003 | g0118 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA19066 | hp1 | a0001 | c0001 | t0003 | g0254 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA19066 | hp2 | a0002 | c0002 | t0006 | g0081 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA19074 | hp2 | a0002 | c0002 | t0001 | g0116 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA19078 | hp1 | a0001 | c0001 | t0003 | g0258 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA19078 | hp2 | a0002 | c0002 | t0006 | g0077 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA19079 | hp1 | a0001 | c0001 | t0012 | g0291 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA19079 | hp2 | a0002 | c0002 | t0001 | g0319 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA19081 | hp1 | a0001 | c0001 | t0003 | g0082 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA19084 | hp2 | a0001 | c0001 | t0003 | g0180 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA19087 | hp2 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | YRI | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | YRI | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA20129 | hp1 | a0001 | c0001 | t0004 | g0102 | AFR | ASW | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0143 | AFR | ASW | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0235 | EUR | TSI | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA20752 | hp2 | a0002 | c0002 | t0003 | g0282 | EUR | TSI | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0119 | EUR | TSI | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA20805 | hp2 | a0002 | c0002 | t0001 | g0244 | EUR | TSI | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0229 | SAS | GIH | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0286 | SAS | GIH | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02109 | hp1 | a0002 | c0004 | t0005 | g0149 | AFR | ACB | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02109 | hp2 | a0002 | c0002 | t0001 | g0134 | AFR | ACB | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0037 | AFR | ACB | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0287 | AFR | ACB | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | MSL | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0317 | AFR | MSL | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG06807 | hp1 | a0001 | c0003 | t0007 | g0012 | AFR | USA | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG06807 | hp2 | a0002 | c0002 | t0001 | g0097 | AFR | USA | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0289 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA20300 | hp1 | a0002 | c0004 | t0005 | g0312 | AFR | USA | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0141 | AFR | USA | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA21309 | hp1 | a0002 | c0002 | t0001 | g0020 | AFR | LWK | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA21309 | hp2 | a0002 | c0004 | t0005 | g0298 | AFR | LWK | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0001 | g0279 | REF | REF | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| homoSapiens_grch38 | hp1 | a0002 | c0002 | t0001 | g0067 | REF | REF | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:50979498
|
T | G | 2 | a0001a0003 | 189 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(186): Show |
missense_variant | MODERATE | c.2214A>C | p.Leu738Phe | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 12/13 | 2380/4579 | 2214/2388 | 738/795 | chr14 | 50979498 | ||
| chr14:50986099
|
T | C | 1 | a0005 | 1 | HG02717.hp1 | missense_variant | MODERATE | c.1649A>G | p.Glu550Gly | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 8/13 | 1815/4579 | 1649/2388 | 550/795 | chr14 | 50986099 | ||
| chr14:51022864
|
C | T | 1 | a0003 | 3 | HG01099.hp1 HG01175.hp2 HG02273.hp1 |
missense_variant | MODERATE | c.1012G>A | p.Val338Ile | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/13 | 1178/4579 | 1012/2388 | 338/795 | chr14 | 51022864 | ||
| chr14:51025336
|
C | T | 1 | a0004 | 2 | HG01516.hp1 HG01517.hp2 |
missense_variant | MODERATE | c.847G>A | p.Gly283Arg | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 2/13 | 1013/4579 | 847/2388 | 283/795 | chr14 | 51025336 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:50981811
|
C | A | 1 | a0001c0005 | 4 | HG00544.hp1 NA18954.hp1 NA18973.hp2 others(1): Show |
synonymous_variant | LOW | c.2151G>T | p.Ser717Ser | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 11/13 | 2317/4579 | 2151/2388 | 717/795 | chr14 | 50981811 | ||
| chr14:50981934
|
G | A | 3 | a0002c0004a0002c0010a0002c0012 | 7 | HG01496.hp1 HG02109.hp1 HG03041.hp2 others(4): Show |
synonymous_variant | LOW | c.2028C>T | p.His676His | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 11/13 | 2194/4579 | 2028/2388 | 676/795 | chr14 | 50981934 | ||
| chr14:51009174
|
T | A | 1 | a0002c0012 | 1 | HG01496.hp1 | synonymous_variant | LOW | c.1212A>T | p.Thr404Thr | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/13 | 1378/4579 | 1212/2388 | 404/795 | chr14 | 51009174 | ||
| chr14:51094139
|
C | T | 3 | a0001c0003a0002c0007a0002c0010 | 8 | HG01433.hp1 HG02622.hp1 HG02647.hp2 others(5): Show |
synonymous_variant | LOW | c.801G>A | p.Gly267Gly | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/13 | 967/4579 | 801/2388 | 267/795 | chr14 | 51094139 | ||
| chr14:51094310
|
C | T | 1 | a0001c0009 | 1 | HG00735.hp1 | synonymous_variant | LOW | c.630G>A | p.Val210Val | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/13 | 796/4579 | 630/2388 | 210/795 | chr14 | 51094310 | ||
| chr14:51094343
|
C | A | 1 | a0002c0013 | 1 | NA18957.hp1 | synonymous_variant | LOW | c.597G>T | p.Pro199Pro | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/13 | 763/4579 | 597/2388 | 199/795 | chr14 | 51094343 | ||
| chr14:51094907
|
G | C | 1 | a0001c0014 | 1 | HG00408.hp1 | synonymous_variant | LOW | c.33C>G | p.Pro11Pro | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/13 | 199/4579 | 33/2388 | 11/795 | chr14 | 51094907 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:50975349
|
T | G | 1 | a0001c0001t0017 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1942A>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 13/13 | 1942 | chr14 | 50975349 | |||||
| chr14:50975436
|
C | T | 1 | a0002c0002t0016 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1855G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 13/13 | 1855 | chr14 | 50975436 | |||||
| chr14:50975773
|
T | C | 1 | a0002c0002t0006 | 12 | HG02155.hp2 HG03710.hp2 HG03942.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1518A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 13/13 | 1518 | chr14 | 50975773 | |||||
| chr14:50975912
|
G | A | 6 | a0001c0001t0004a0001c0001t0009a0002c0002t0004others(3): Show | 36 | HG00280.hp2 HG01168.hp2 HG01261.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*1379C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 13/13 | 1379 | chr14 | 50975912 | |||||
| chr14:50975952
|
A | G | 4 | a0001c0001t0003a0001c0001t0012a0002c0002t0003others(1): Show | 79 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*1339T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 13/13 | 1339 | chr14 | 50975952 | |||||
| chr14:50976419
|
C | T | 1 | a0002c0002t0008 | 3 | HG02717.hp2 HG03041.hp1 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*872G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 13/13 | 872 | chr14 | 50976419 | |||||
| chr14:50976594
|
G | A | 2 | a0002c0002t0011a0002c0007t0011 | 2 | HG02922.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*697C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 13/13 | 697 | chr14 | 50976594 | |||||
| chr14:50976642
|
A | G | 6 | a0001c0001t0002a0001c0001t0012a0001c0005t0002others(3): Show | 82 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*649T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 13/13 | 649 | chr14 | 50976642 | |||||
| chr14:50976797
|
G | A | 1 | a0003c0006t0018 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*494C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 13/13 | 494 | chr14 | 50976797 | |||||
| chr14:50976815
|
G | A | 6 | a0001c0001t0004a0002c0002t0004a0002c0002t0006others(3): Show | 35 | HG00280.hp2 HG01168.hp2 HG01261.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*476C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 13/13 | 476 | chr14 | 50976815 | |||||
| chr14:50976980
|
C | T | 2 | a0002c0002t0011a0002c0007t0011 | 2 | HG02922.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*311G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 13/13 | 311 | chr14 | 50976980 | |||||
| chr14:50976987
|
A | G | 3 | a0001c0001t0019a0001c0003t0007a0002c0002t0006 | 16 | HG01433.hp1 HG02155.hp2 HG02257.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*304T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 13/13 | 304 | chr14 | 50976987 | |||||
| chr14:50977250
|
C | T | 1 | a0001c0001t0015 | 1 | HG01070.hp2 | 3_prime_UTR_variant | MODIFIER | c.*41G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 13/13 | 41 | chr14 | 50977250 | |||||
| chr14:50977274
|
G | A | 5 | a0001c0001t0005a0002c0002t0005a0002c0004t0005others(2): Show | 13 | HG01496.hp1 HG01891.hp1 HG02109.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*17C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 13/13 | 17 | chr14 | 50977274 | |||||
| chr14:51094946
|
C | A | 3 | a0001c0001t0010a0001c0001t0019a0002c0002t0010 | 4 | HG02257.hp1 HG02630.hp1 HG02809.hp1 others(1): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-7G>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/13 | chr14 | 51094946 | ||||||
| chr14:51095093
|
G | A | 1 | a0002c0002t0014 | 2 | HG01257.hp2 HG01258.hp2 |
5_prime_UTR_variant | MODIFIER | c.-154C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/13 | 154 | chr14 | 51095093 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:50977395
|
C | T | 1 | a0001c0001t0001g0287 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2326-42G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 12/12 | chr14 | 50977395 | ||||||
| chr14:50977491
|
C | T | 1 | a0002c0002t0001g0246 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2326-138G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 12/12 | chr14 | 50977491 | ||||||
| chr14:50977515
|
A | G | 3 | a0002c0002t0003g0172a0002c0002t0003g0177a0002c0002t0003g0249 | 3 | HG03195.hp1 HG03516.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2326-162T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 12/12 | chr14 | 50977515 | ||||||
| chr14:50977581
|
G | A | 1 | a0002c0002t0001g0228 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2326-228C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 12/12 | chr14 | 50977581 | ||||||
| chr14:50977618
|
G | A | 1 | a0001c0001t0002g0285 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.2326-265C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 12/12 | chr14 | 50977618 | ||||||
| chr14:50977656
|
T | C | 2 | a0002c0002t0013g0035a0002c0002t0013g0250 | 2 | HG02280.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.2326-303A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 12/12 | chr14 | 50977656 | ||||||
| chr14:50977677
|
C | T | 1 | a0001c0001t0002g0202 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2326-324G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 12/12 | chr14 | 50977677 | ||||||
| chr14:50977847
|
C | T | 28 | a0001c0001t0004g0099a0001c0001t0004g0100a0001c0001t0004g0101others(25): Show | 29 | HG01261.hp1 HG02145.hp2 HG02155.hp2 others(26): Show |
intron_variant | MODIFIER | c.2326-494G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 12/12 | chr14 | 50977847 | ||||||
| chr14:50977910
|
A | G | 28 | a0001c0001t0004g0099a0001c0001t0004g0100a0001c0001t0004g0101others(25): Show | 29 | HG01261.hp1 HG02145.hp2 HG02155.hp2 others(26): Show |
intron_variant | MODIFIER | c.2326-557T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 12/12 | chr14 | 50977910 | ||||||
| chr14:50977944
|
A | G | 8 | a0001c0001t0009g0038a0001c0001t0009g0096a0001c0001t0009g0301others(5): Show | 8 | HG02145.hp2 HG02257.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.2326-591T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 12/12 | chr14 | 50977944 | ||||||
| chr14:50978200
|
A | G | 123 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0042others(120): Show | 126 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.2326-847T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 12/12 | chr14 | 50978200 | ||||||
| chr14:50978261
|
C | T | 146 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0042others(143): Show | 150 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.2326-908G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 12/12 | chr14 | 50978261 | ||||||
| chr14:50978296
|
T | C | 2 | a0002c0002t0011g0034a0002c0007t0011g0013 | 2 | HG02922.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2326-943A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 12/12 | chr14 | 50978296 | ||||||
| chr14:50978616
|
C | T | 2 | a0001c0001t0009g0096a0001c0001t0009g0301 | 2 | HG02257.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2325+771G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 12/12 | chr14 | 50978616 | ||||||
| chr14:50978691
|
T | G | 2 | a0002c0002t0013g0035a0002c0002t0013g0250 | 2 | HG02280.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.2325+696A>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 12/12 | chr14 | 50978691 | ||||||
| chr14:50978758
|
G | GTT | 109 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0042others(106): Show | 112 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.2325+627_2325+628d others(4): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 12/12 | chr14 | 50978758 | ||||||
| chr14:50978766
|
G | GT | 62 | a0001c0001t0001g0206a0001c0001t0001g0287a0001c0001t0001g0310others(59): Show | 63 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.2325+620dupA | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 12/12 | chr14 | 50978766 | ||||||
| chr14:50978843
|
T | C | 18 | a0001c0001t0001g0028a0001c0001t0001g0042a0001c0001t0001g0062others(15): Show | 18 | HG01070.hp2 HG01099.hp1 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.2325+544A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 12/12 | chr14 | 50978843 | ||||||
| chr14:50978893
|
G | A | 220 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0042others(217): Show | 224 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(221): Show |
intron_variant | MODIFIER | c.2325+494C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 12/12 | chr14 | 50978893 | ||||||
| chr14:50978910
|
G | A | 4 | a0001c0001t0002g0061a0001c0001t0002g0141a0001c0001t0002g0218others(1): Show | 4 | HG01070.hp1 HG01071.hp1 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.2325+477C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 12/12 | chr14 | 50978910 | ||||||
| chr14:50978934
|
A | T | 3 | a0001c0001t0001g0287a0001c0001t0001g0310a0001c0003t0001g0010 | 3 | HG02486.hp2 HG02647.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.2325+453T>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 12/12 | chr14 | 50978934 | ||||||
| chr14:50978988
|
A | T | 2 | a0002c0002t0011g0034a0002c0007t0011g0013 | 2 | HG02922.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2325+399T>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 12/12 | chr14 | 50978988 | ||||||
| chr14:50979140
|
T | C | 1 | a0001c0001t0004g0266 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2325+247A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 12/12 | chr14 | 50979140 | ||||||
| chr14:50979143
|
A | G | 4 | a0001c0001t0019g0331a0001c0003t0007g0011a0001c0003t0007g0012others(1): Show | 4 | HG01433.hp1 HG02257.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2325+244T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 12/12 | chr14 | 50979143 | ||||||
| chr14:50979213
|
C | T | 2 | a0002c0002t0011g0034a0002c0007t0011g0013 | 2 | HG02922.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2325+174G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 12/12 | chr14 | 50979213 | ||||||
| chr14:50979251
|
C | G | 35 | a0001c0001t0002g0023a0001c0001t0002g0045a0001c0001t0002g0053others(32): Show | 36 | HG00544.hp1 HG00597.hp2 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.2325+136G>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 12/12 | chr14 | 50979251 | ||||||
| chr14:50979336
|
T | G | 3 | a0002c0002t0004g0212a0002c0002t0004g0304a0002c0002t0004g0321 | 3 | HG02145.hp2 HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2325+51A>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 12/12 | chr14 | 50979336 | ||||||
| chr14:50979376
|
A | G | 1 | a0001c0001t0004g0266 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2325+11T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 12/12 | chr14 | 50979376 | ||||||
| chr14:50979572
|
G | T | 68 | a0001c0001t0001g0179a0001c0001t0003g0001a0001c0001t0003g0006others(65): Show | 71 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.2163-23C>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 11/12 | chr14 | 50979572 | ||||||
| chr14:50979639
|
C | G | 78 | a0001c0001t0001g0179a0001c0001t0003g0001a0001c0001t0003g0006others(75): Show | 81 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.2163-90G>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 11/12 | chr14 | 50979639 | ||||||
| chr14:50979647
|
T | C | 1 | a0001c0001t0009g0301 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2163-98A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 11/12 | chr14 | 50979647 | ||||||
| chr14:50979669
|
G | T | 70 | a0001c0001t0001g0179a0001c0001t0003g0001a0001c0001t0003g0006others(67): Show | 73 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.2163-120C>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 11/12 | chr14 | 50979669 | ||||||
| chr14:50979978
|
T | C | 1 | a0001c0001t0002g0273 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2163-429A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 11/12 | chr14 | 50979978 | ||||||
| chr14:50980053
|
T | G | 45 | a0001c0001t0001g0028a0001c0001t0001g0042a0001c0001t0001g0062others(42): Show | 46 | HG01099.hp1 HG01358.hp1 HG01496.hp1 others(43): Show |
intron_variant | MODIFIER | c.2163-504A>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 11/12 | chr14 | 50980053 | ||||||
| chr14:50980071
|
T | C | 27 | a0001c0001t0005g0026a0001c0001t0005g0027a0001c0001t0005g0032others(24): Show | 28 | HG01496.hp1 HG01891.hp1 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.2163-522A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 11/12 | chr14 | 50980071 | ||||||
| chr14:50980111
|
A | C | 54 | a0001c0001t0001g0287a0001c0001t0001g0310a0001c0001t0002g0056others(51): Show | 54 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.2163-562T>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 11/12 | chr14 | 50980111 | ||||||
| chr14:50980304
|
T | C | 12 | a0002c0002t0002g0225a0002c0002t0006g0004a0002c0002t0006g0018others(9): Show | 13 | HG02155.hp2 HG03710.hp2 HG03942.hp2 others(10): Show |
intron_variant | MODIFIER | c.2163-755A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 11/12 | chr14 | 50980304 | ||||||
| chr14:50980372
|
T | C | 5 | a0001c0001t0002g0045a0001c0001t0002g0108a0001c0001t0002g0110others(2): Show | 5 | HG01256.hp1 HG01258.hp1 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.2163-823A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 11/12 | chr14 | 50980372 | ||||||
| chr14:50980382
|
A | G | 4 | a0001c0001t0009g0096a0002c0002t0004g0212a0002c0002t0004g0304others(1): Show | 4 | HG02145.hp2 HG03130.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2163-833T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 11/12 | chr14 | 50980382 | ||||||
| chr14:50980593
|
C | T | 7 | a0002c0004t0005g0149a0002c0004t0005g0256a0002c0004t0005g0298others(4): Show | 7 | HG01496.hp1 HG02109.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.2163-1044G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 11/12 | chr14 | 50980593 | ||||||
| chr14:50980625
|
T | C | 1 | a0002c0002t0001g0166 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2163-1076A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 11/12 | chr14 | 50980625 | ||||||
| chr14:50980643
|
C | T | 1 | a0001c0001t0004g0241 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2163-1094G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 11/12 | chr14 | 50980643 | ||||||
| chr14:50980670
|
A | G | 40 | a0001c0001t0001g0287a0001c0001t0001g0310a0001c0001t0002g0056others(37): Show | 40 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.2163-1121T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 11/12 | chr14 | 50980670 | ||||||
| chr14:50980721
|
G | A | 150 | a0001c0001t0001g0028a0001c0001t0001g0042a0001c0001t0001g0062others(147): Show | 155 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.2162+1079C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 11/12 | chr14 | 50980721 | ||||||
| chr14:50980841
|
A | G | 1 | a0002c0002t0013g0035 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2162+959T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 11/12 | chr14 | 50980841 | ||||||
| chr14:50980951
|
T | C | 57 | a0001c0001t0001g0205a0001c0001t0003g0129a0001c0001t0003g0130others(54): Show | 61 | HG00280.hp1 HG00438.hp1 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.2162+849A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 11/12 | chr14 | 50980951 | ||||||
| chr14:50980980
|
A | AT | 9 | a0001c0001t0002g0056a0001c0001t0003g0001a0001c0001t0003g0054others(6): Show | 11 | HG01074.hp1 HG01256.hp2 HG01981.hp2 others(8): Show |
intron_variant | MODIFIER | c.2162+819dupA | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 11/12 | chr14 | 50980980 | ||||||
| chr14:50980980
|
AT | A | 21 | a0001c0001t0001g0031a0001c0001t0002g0058a0001c0001t0002g0060others(18): Show | 21 | HG00280.hp2 HG00642.hp2 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.2162+819delA | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 11/12 | chr14 | 50980980 | ||||||
| chr14:50980994
|
T | C | 5 | a0001c0001t0005g0027a0001c0001t0005g0305a0002c0002t0003g0172others(2): Show | 5 | HG01891.hp1 HG02723.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2162+806A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 11/12 | chr14 | 50980994 | ||||||
| chr14:50981007
|
T | C | 1 | a0001c0001t0002g0087 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.2162+793A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 11/12 | chr14 | 50981007 | ||||||
| chr14:50981289
|
C | T | 1 | a0001c0001t0002g0182 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.2162+511G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 11/12 | chr14 | 50981289 | ||||||
| chr14:50981293
|
A | C | 1 | a0001c0001t0009g0038 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2162+507T>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 11/12 | chr14 | 50981293 | ||||||
| chr14:50981313
|
G | A | 1 | a0001c0001t0005g0305 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2162+487C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 11/12 | chr14 | 50981313 | ||||||
| chr14:50981323
|
G | A | 12 | a0002c0002t0002g0225a0002c0002t0006g0004a0002c0002t0006g0018others(9): Show | 13 | HG02155.hp2 HG03710.hp2 HG03942.hp2 others(10): Show |
intron_variant | MODIFIER | c.2162+477C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 11/12 | chr14 | 50981323 | ||||||
| chr14:50981380
|
A | C | 94 | a0001c0001t0001g0206a0001c0001t0001g0277a0001c0001t0002g0023others(91): Show | 94 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.2162+420T>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 11/12 | chr14 | 50981380 | ||||||
| chr14:50981398
|
C | G | 1 | a0001c0001t0003g0209 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2162+402G>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 11/12 | chr14 | 50981398 | ||||||
| chr14:50981470
|
A | T | 1 | a0002c0002t0001g0124 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2162+330T>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 11/12 | chr14 | 50981470 | ||||||
| chr14:50981604
|
C | T | 1 | a0002c0004t0005g0311 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2162+196G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 11/12 | chr14 | 50981604 | ||||||
| chr14:50981646
|
C | T | 137 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0277others(134): Show | 138 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.2162+154G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 11/12 | chr14 | 50981646 | ||||||
| chr14:50981661
|
T | C | 2 | a0001c0001t0003g0208a0001c0001t0003g0210 | 2 | HG00738.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.2162+139A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 11/12 | chr14 | 50981661 | ||||||
| chr14:50981695
|
T | C | 166 | a0001c0001t0001g0028a0001c0001t0001g0042a0001c0001t0001g0062others(163): Show | 171 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(168): Show |
intron_variant | MODIFIER | c.2162+105A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 11/12 | chr14 | 50981695 | ||||||
| chr14:50981709
|
T | C | 1 | a0002c0002t0001g0307 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2162+91A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 11/12 | chr14 | 50981709 | ||||||
| chr14:50982114
|
C | T | 1 | a0002c0002t0001g0307 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1859-11G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 10/12 | chr14 | 50982114 | ||||||
| chr14:50982156
|
C | G | 1 | a0002c0002t0001g0245 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1859-53G>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 10/12 | chr14 | 50982156 | ||||||
| chr14:50982210
|
C | T | 12 | a0002c0002t0002g0225a0002c0002t0006g0004a0002c0002t0006g0018others(9): Show | 13 | HG02155.hp2 HG03710.hp2 HG03942.hp2 others(10): Show |
intron_variant | MODIFIER | c.1859-107G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 10/12 | chr14 | 50982210 | ||||||
| chr14:50982551
|
C | T | 1 | a0001c0001t0002g0056 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1858+391G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 10/12 | chr14 | 50982551 | ||||||
| chr14:50982592
|
G | C | 1 | a0002c0002t0001g0134 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1858+350C>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 10/12 | chr14 | 50982592 | ||||||
| chr14:50982592
|
G | T | 4 | a0001c0001t0003g0048a0001c0001t0003g0057a0001c0001t0003g0094others(1): Show | 4 | NA18962.hp1 NA18980.hp1 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.1858+350C>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 10/12 | chr14 | 50982592 | ||||||
| chr14:50982593
|
G | T | 1 | a0002c0002t0001g0134 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1858+349C>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 10/12 | chr14 | 50982593 | ||||||
| chr14:50982800
|
C | T | 1 | a0002c0002t0004g0321 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1858+142G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 10/12 | chr14 | 50982800 | ||||||
| chr14:50982860
|
T | C | 1 | a0002c0002t0001g0207 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1858+82A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 10/12 | chr14 | 50982860 | ||||||
| chr14:50982928
|
A | C | 1 | a0001c0001t0002g0127 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1858+14T>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 10/12 | chr14 | 50982928 | ||||||
| chr14:50983022
|
T | C | 1 | a0001c0001t0002g0272 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1835-57A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 9/12 | chr14 | 50983022 | ||||||
| chr14:50983156
|
C | T | 171 | a0001c0001t0001g0028a0001c0001t0001g0042a0001c0001t0001g0062others(168): Show | 172 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.1835-191G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 9/12 | chr14 | 50983156 | ||||||
| chr14:50983188
|
G | C | 270 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0042others(267): Show | 275 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(272): Show |
intron_variant | MODIFIER | c.1834+192C>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 9/12 | chr14 | 50983188 | ||||||
| chr14:50983210
|
C | T | 9 | a0001c0001t0001g0324a0001c0001t0005g0026a0001c0001t0005g0027others(6): Show | 9 | HG01891.hp1 HG02615.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.1834+170G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 9/12 | chr14 | 50983210 | ||||||
| chr14:50983230
|
T | C | 1 | a0002c0002t0001g0134 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1834+150A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 9/12 | chr14 | 50983230 | ||||||
| chr14:50983488
|
C | T | 4 | a0001c0001t0001g0122a0001c0001t0001g0132a0001c0001t0001g0178others(1): Show | 4 | HG01358.hp1 HG02630.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1793-67G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 8/12 | chr14 | 50983488 | ||||||
| chr14:50983569
|
G | T | 12 | a0001c0001t0004g0099a0001c0001t0004g0100a0001c0001t0004g0101others(9): Show | 12 | HG01261.hp1 HG02145.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1793-148C>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 8/12 | chr14 | 50983569 | ||||||
| chr14:50983877
|
A | G | 1 | a0001c0001t0004g0314 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1793-456T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 8/12 | chr14 | 50983877 | ||||||
| chr14:50984006
|
G | A | 1 | a0002c0002t0011g0034 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1793-585C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 8/12 | chr14 | 50984006 | ||||||
| chr14:50984084
|
T | C | 12 | a0002c0002t0002g0225a0002c0002t0006g0004a0002c0002t0006g0018others(9): Show | 13 | HG02155.hp2 HG03710.hp2 HG03942.hp2 others(10): Show |
intron_variant | MODIFIER | c.1793-663A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 8/12 | chr14 | 50984084 | ||||||
| chr14:50984260
|
T | C | 34 | a0001c0001t0001g0028a0001c0001t0001g0042a0001c0001t0001g0062others(31): Show | 34 | HG01099.hp1 HG01175.hp2 HG01358.hp1 others(31): Show |
intron_variant | MODIFIER | c.1793-839A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 8/12 | chr14 | 50984260 | ||||||
| chr14:50984505
|
C | A | 3 | a0002c0002t0001g0089a0002c0002t0001g0090a0002c0002t0001g0091 | 3 | NA18941.hp1 NA18983.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.1793-1084G>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 8/12 | chr14 | 50984505 | ||||||
| chr14:50984548
|
C | G | 170 | a0001c0001t0001g0031a0001c0001t0001g0206a0001c0001t0001g0277others(167): Show | 174 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(171): Show |
intron_variant | MODIFIER | c.1793-1127G>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 8/12 | chr14 | 50984548 | ||||||
| chr14:50984812
|
G | A | 183 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0042others(180): Show | 188 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(185): Show |
intron_variant | MODIFIER | c.1792+1144C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 8/12 | chr14 | 50984812 | ||||||
| chr14:50984831
|
G | A | 181 | a0001c0001t0001g0028a0001c0001t0001g0042a0001c0001t0001g0062others(178): Show | 182 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(179): Show |
intron_variant | MODIFIER | c.1792+1125C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 8/12 | chr14 | 50984831 | ||||||
| chr14:50985154
|
G | T | 2 | a0002c0002t0001g0095a0002c0002t0001g0174 | 2 | HG00423.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.1792+802C>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 8/12 | chr14 | 50985154 | ||||||
| chr14:50985194
|
T | A | 87 | a0001c0001t0001g0206a0001c0001t0001g0277a0001c0001t0002g0023others(84): Show | 87 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.1792+762A>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 8/12 | chr14 | 50985194 | ||||||
| chr14:50985568
|
G | A | 1 | a0002c0002t0001g0115 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1792+388C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 8/12 | chr14 | 50985568 | ||||||
| chr14:50985809
|
G | A | 6 | a0001c0001t0004g0099a0001c0001t0004g0100a0001c0001t0004g0101others(3): Show | 6 | HG01261.hp1 HG02451.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1792+147C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 8/12 | chr14 | 50985809 | ||||||
| chr14:50985847
|
T | C | 24 | a0001c0001t0001g0028a0001c0001t0001g0042a0001c0001t0001g0062others(21): Show | 24 | HG01099.hp1 HG01175.hp2 HG01358.hp1 others(21): Show |
intron_variant | MODIFIER | c.1792+109A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 8/12 | chr14 | 50985847 | ||||||
| chr14:50985861
|
C | A | 9 | a0001c0001t0001g0324a0001c0001t0005g0026a0001c0001t0005g0027others(6): Show | 9 | HG01891.hp1 HG02615.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.1792+95G>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 8/12 | chr14 | 50985861 | ||||||
| chr14:50985868
|
C | CA | 4 | a0001c0001t0002g0199a0001c0001t0002g0283a0001c0001t0002g0284others(1): Show | 4 | NA18974.hp2 NA18983.hp2 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.1792+87dupT | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 8/12 | chr14 | 50985868 | ||||||
| chr14:50986245
|
C | G | 1 | a0001c0001t0002g0052 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1604-101G>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50986245 | ||||||
| chr14:50986532
|
C | T | 1 | a0001c0001t0003g0006 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1604-388G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50986532 | ||||||
| chr14:50986594
|
T | C | 1 | a0002c0002t0003g0044 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1604-450A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50986594 | ||||||
| chr14:50986597
|
C | G | 24 | a0001c0001t0001g0028a0001c0001t0001g0042a0001c0001t0001g0062others(21): Show | 24 | HG01099.hp1 HG01175.hp2 HG01358.hp1 others(21): Show |
intron_variant | MODIFIER | c.1604-453G>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50986597 | ||||||
| chr14:50986887
|
T | C | 10 | a0001c0001t0001g0324a0001c0001t0005g0026a0001c0001t0005g0027others(7): Show | 10 | HG01891.hp1 HG02615.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1604-743A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50986887 | ||||||
| chr14:50987013
|
A | G | 3 | a0002c0002t0001g0041a0002c0002t0001g0313a0002c0002t0003g0106 | 3 | HG02280.hp2 HG02647.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1604-869T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50987013 | ||||||
| chr14:50987035
|
G | A | 2 | a0002c0002t0003g0044a0002c0002t0003g0098 | 2 | HG02055.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1604-891C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50987035 | ||||||
| chr14:50987063
|
C | T | 11 | a0002c0002t0002g0225a0002c0002t0006g0004a0002c0002t0006g0018others(8): Show | 12 | HG02155.hp2 HG03710.hp2 HG03942.hp2 others(9): Show |
intron_variant | MODIFIER | c.1604-919G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50987063 | ||||||
| chr14:50987281
|
T | C | 331 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0042others(328): Show | 341 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.1604-1137A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50987281 | ||||||
| chr14:50987380
|
T | C | 11 | a0002c0002t0002g0225a0002c0002t0006g0004a0002c0002t0006g0018others(8): Show | 12 | HG02155.hp2 HG03710.hp2 HG03942.hp2 others(9): Show |
intron_variant | MODIFIER | c.1604-1236A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50987380 | ||||||
| chr14:50987416
|
T | C | 60 | a0001c0001t0001g0179a0001c0001t0002g0171a0001c0001t0002g0173others(57): Show | 65 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.1604-1272A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50987416 | ||||||
| chr14:50987594
|
C | T | 60 | a0001c0001t0001g0287a0001c0001t0001g0310a0001c0001t0002g0056others(57): Show | 63 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.1604-1450G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50987594 | ||||||
| chr14:50987707
|
A | C | 11 | a0002c0002t0002g0225a0002c0002t0006g0004a0002c0002t0006g0018others(8): Show | 12 | HG02155.hp2 HG03710.hp2 HG03942.hp2 others(9): Show |
intron_variant | MODIFIER | c.1604-1563T>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50987707 | ||||||
| chr14:50987743
|
C | T | 60 | a0001c0001t0001g0287a0001c0001t0001g0310a0001c0001t0002g0056others(57): Show | 63 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.1604-1599G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50987743 | ||||||
| chr14:50987760
|
A | G | 78 | a0001c0001t0001g0206a0001c0001t0001g0277a0001c0001t0002g0023others(75): Show | 78 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.1604-1616T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50987760 | ||||||
| chr14:50987879
|
G | A | 1 | a0002c0002t0001g0137 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1604-1735C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50987879 | ||||||
| chr14:50987945
|
C | T | 26 | a0001c0001t0001g0028a0001c0001t0001g0042a0001c0001t0001g0062others(23): Show | 26 | HG01099.hp1 HG01175.hp2 HG01358.hp1 others(23): Show |
intron_variant | MODIFIER | c.1604-1801G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50987945 | ||||||
| chr14:50988098
|
G | A | 60 | a0001c0001t0001g0287a0001c0001t0001g0310a0001c0001t0002g0056others(57): Show | 63 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.1604-1954C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50988098 | ||||||
| chr14:50988179
|
A | G | 2 | a0002c0002t0006g0144a0002c0002t0006g0191 | 2 | HG03942.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1604-2035T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50988179 | ||||||
| chr14:50988259
|
G | C | 1 | a0002c0002t0001g0133 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1604-2115C>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50988259 | ||||||
| chr14:50988338
|
T | C | 84 | a0001c0001t0001g0031a0001c0001t0001g0287a0001c0001t0001g0310others(81): Show | 88 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.1604-2194A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50988338 | ||||||
| chr14:50988384
|
A | G | 270 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0042others(267): Show | 275 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(272): Show |
intron_variant | MODIFIER | c.1604-2240T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50988384 | ||||||
| chr14:50988448
|
T | C | 84 | a0001c0001t0001g0031a0001c0001t0001g0287a0001c0001t0001g0310others(81): Show | 88 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.1604-2304A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50988448 | ||||||
| chr14:50988574
|
CT | C | 53 | a0001c0001t0001g0324a0001c0001t0002g0111a0001c0001t0002g0127others(50): Show | 54 | HG00639.hp1 HG01069.hp1 HG01256.hp1 others(51): Show |
intron_variant | MODIFIER | c.1604-2431delA | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50988574 | ||||||
| chr14:50988574
|
CTT | C | 25 | a0001c0001t0001g0028a0001c0001t0001g0042a0001c0001t0001g0062others(22): Show | 25 | HG01099.hp1 HG01175.hp2 HG01358.hp1 others(22): Show |
intron_variant | MODIFIER | c.1604-2432_1604-243 others(6): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50988574 | ||||||
| chr14:50988574
|
CTTTTT | C | 60 | a0001c0001t0001g0287a0001c0001t0001g0310a0001c0001t0002g0056others(57): Show | 63 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.1604-2435_1604-243 others(9): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50988574 | ||||||
| chr14:50988754
|
T | C | 13 | a0001c0001t0001g0031a0001c0001t0002g0058a0001c0001t0002g0059others(10): Show | 13 | HG00280.hp2 HG00642.hp2 HG00733.hp1 others(10): Show |
intron_variant | MODIFIER | c.1604-2610A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50988754 | ||||||
| chr14:50988789
|
G | A | 9 | a0002c0002t0001g0041a0002c0002t0001g0313a0002c0002t0003g0106others(6): Show | 9 | HG01496.hp1 HG02109.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1604-2645C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50988789 | ||||||
| chr14:50988877
|
G | A | 60 | a0001c0001t0001g0287a0001c0001t0001g0310a0001c0001t0002g0056others(57): Show | 63 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.1604-2733C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50988877 | ||||||
| chr14:50989027
|
T | C | 29 | a0001c0001t0001g0277a0001c0001t0002g0023a0001c0001t0002g0045others(26): Show | 29 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(26): Show |
intron_variant | MODIFIER | c.1604-2883A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50989027 | ||||||
| chr14:50989029
|
G | A | 1 | a0002c0002t0001g0124 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1604-2885C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50989029 | ||||||
| chr14:50989322
|
A | C | 1 | a0001c0001t0001g0211 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1604-3178T>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50989322 | ||||||
| chr14:50989922
|
T | G | 1 | a0002c0002t0001g0295 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1604-3778A>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50989922 | ||||||
| chr14:50990111
|
G | A | 6 | a0002c0002t0001g0051a0002c0002t0001g0089a0002c0002t0001g0090others(3): Show | 6 | NA18939.hp2 NA18941.hp1 NA18943.hp2 others(3): Show |
intron_variant | MODIFIER | c.1604-3967C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50990111 | ||||||
| chr14:50990191
|
T | A | 1 | a0001c0001t0003g0136 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1604-4047A>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50990191 | ||||||
| chr14:50990242
|
C | T | 76 | a0001c0001t0001g0206a0001c0001t0001g0277a0001c0001t0002g0023others(73): Show | 76 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.1604-4098G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50990242 | ||||||
| chr14:50990295
|
G | A | 60 | a0001c0001t0001g0287a0001c0001t0001g0310a0001c0001t0002g0056others(57): Show | 63 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.1604-4151C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50990295 | ||||||
| chr14:50990408
|
A | G | 4 | a0001c0001t0009g0096a0002c0002t0004g0212a0002c0002t0004g0304others(1): Show | 4 | HG02145.hp2 HG03130.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1604-4264T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50990408 | ||||||
| chr14:50990626
|
T | C | 11 | a0002c0002t0002g0225a0002c0002t0006g0004a0002c0002t0006g0018others(8): Show | 12 | HG02155.hp2 HG03710.hp2 HG03942.hp2 others(9): Show |
intron_variant | MODIFIER | c.1604-4482A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50990626 | ||||||
| chr14:50990728
|
C | T | 60 | a0001c0001t0001g0287a0001c0001t0001g0310a0001c0001t0002g0056others(57): Show | 63 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.1604-4584G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50990728 | ||||||
| chr14:50990789
|
G | A | 5 | a0002c0002t0001g0131a0002c0002t0001g0133a0002c0002t0001g0207others(2): Show | 5 | HG00639.hp1 HG01109.hp1 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.1604-4645C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50990789 | ||||||
| chr14:50990904
|
C | T | 1 | a0001c0001t0017g0036 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1604-4760G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50990904 | ||||||
| chr14:50990954
|
C | T | 1 | a0001c0014t0002g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1604-4810G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50990954 | ||||||
| chr14:50990977
|
G | A | 51 | a0001c0001t0001g0205a0001c0001t0003g0129a0001c0001t0003g0130others(48): Show | 52 | HG00280.hp1 HG00438.hp1 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.1604-4833C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50990977 | ||||||
| chr14:50990995
|
G | C | 172 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0042others(169): Show | 177 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(174): Show |
intron_variant | MODIFIER | c.1604-4851C>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50990995 | ||||||
| chr14:50991192
|
C | A | 1 | a0001c0001t0017g0036 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1604-5048G>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50991192 | ||||||
| chr14:50991526
|
G | C | 1 | a0001c0001t0002g0055 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1604-5382C>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50991526 | ||||||
| chr14:50991707
|
T | C | 1 | a0002c0002t0001g0231 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1604-5563A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50991707 | ||||||
| chr14:50991743
|
CT | C | 3 | a0002c0002t0004g0212a0002c0002t0004g0304a0002c0002t0004g0321 | 3 | HG02145.hp2 HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1604-5600delA | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50991743 | ||||||
| chr14:50991747
|
T | A | 3 | a0002c0002t0004g0212a0002c0002t0004g0304a0002c0002t0004g0321 | 3 | HG02145.hp2 HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1604-5603A>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50991747 | ||||||
| chr14:50991748
|
T | G | 3 | a0002c0002t0004g0212a0002c0002t0004g0304a0002c0002t0004g0321 | 3 | HG02145.hp2 HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1604-5604A>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50991748 | ||||||
| chr14:50991838
|
A | G | 2 | a0001c0001t0001g0205a0002c0002t0001g0024 | 2 | HG04184.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.1604-5694T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50991838 | ||||||
| chr14:50992007
|
C | A | 1 | a0001c0001t0017g0036 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1604-5863G>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50992007 | ||||||
| chr14:50992010
|
G | C | 73 | a0001c0001t0001g0031a0001c0001t0001g0287a0001c0001t0001g0310others(70): Show | 76 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.1604-5866C>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50992010 | ||||||
| chr14:50992067
|
T | C | 260 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0042others(257): Show | 265 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.1604-5923A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50992067 | ||||||
| chr14:50992076
|
G | C | 51 | a0001c0001t0001g0205a0001c0001t0003g0129a0001c0001t0003g0130others(48): Show | 52 | HG00280.hp1 HG00438.hp1 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.1604-5932C>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50992076 | ||||||
| chr14:50992171
|
T | C | 24 | a0001c0001t0001g0031a0001c0001t0002g0058a0001c0001t0002g0059others(21): Show | 25 | HG00280.hp2 HG00642.hp2 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.1603+5879A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50992171 | ||||||
| chr14:50992205
|
C | T | 1 | a0001c0001t0004g0232 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1603+5845G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50992205 | ||||||
| chr14:50992367
|
C | T | 25 | a0001c0001t0001g0028a0001c0001t0001g0042a0001c0001t0001g0062others(22): Show | 25 | HG01099.hp1 HG01175.hp2 HG01358.hp1 others(22): Show |
intron_variant | MODIFIER | c.1603+5683G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50992367 | ||||||
| chr14:50992372
|
G | A | 6 | a0001c0001t0004g0099a0001c0001t0004g0100a0001c0001t0004g0101others(3): Show | 6 | HG01261.hp1 HG02451.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1603+5678C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50992372 | ||||||
| chr14:50992416
|
GA | G | 60 | a0001c0001t0001g0287a0001c0001t0001g0310a0001c0001t0002g0056others(57): Show | 63 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.1603+5633delT | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50992416 | ||||||
| chr14:50992418
|
A | G | 60 | a0001c0001t0001g0287a0001c0001t0001g0310a0001c0001t0002g0056others(57): Show | 63 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.1603+5632T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50992418 | ||||||
| chr14:50992527
|
C | T | 60 | a0001c0001t0001g0287a0001c0001t0001g0310a0001c0001t0002g0056others(57): Show | 63 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.1603+5523G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50992527 | ||||||
| chr14:50992581
|
AAATG | A | 110 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0042others(107): Show | 114 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(111): Show |
intron_variant | MODIFIER | c.1603+5465_1603+546 others(8): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50992581 | ||||||
| chr14:50992775
|
T | C | 1 | a0001c0001t0002g0308 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1603+5275A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50992775 | ||||||
| chr14:50992848
|
A | G | 3 | a0002c0004t0005g0256a0002c0004t0005g0312a0002c0010t0005g0016 | 3 | HG03195.hp2 NA18906.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1603+5202T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50992848 | ||||||
| chr14:50992959
|
A | G | 7 | a0001c0001t0002g0037a0001c0001t0002g0147a0001c0001t0002g0155others(4): Show | 7 | HG00735.hp1 HG01167.hp2 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.1603+5091T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50992959 | ||||||
| chr14:50993008
|
G | A | 1 | a0002c0002t0001g0025 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1603+5042C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50993008 | ||||||
| chr14:50993086
|
T | C | 1 | a0002c0012t0005g0161 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1603+4964A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50993086 | ||||||
| chr14:50993123
|
A | G | 78 | a0001c0001t0001g0031a0001c0001t0001g0287a0001c0001t0001g0310others(75): Show | 81 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.1603+4927T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50993123 | ||||||
| chr14:50993158
|
C | T | 1 | a0001c0001t0001g0216 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1603+4892G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50993158 | ||||||
| chr14:50993219
|
T | C | 77 | a0001c0001t0001g0206a0001c0001t0001g0277a0001c0001t0002g0023others(74): Show | 77 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.1603+4831A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50993219 | ||||||
| chr14:50993357
|
T | C | 73 | a0001c0001t0001g0031a0001c0001t0001g0287a0001c0001t0001g0310others(70): Show | 76 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.1603+4693A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50993357 | ||||||
| chr14:50993371
|
C | CT | 12 | a0001c0001t0001g0031a0001c0001t0002g0058a0001c0001t0002g0059others(9): Show | 12 | HG00280.hp2 HG00642.hp2 HG00733.hp1 others(9): Show |
intron_variant | MODIFIER | c.1603+4678dupA | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50993371 | ||||||
| chr14:50993436
|
T | G | 1 | a0002c0002t0001g0307 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1603+4614A>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50993436 | ||||||
| chr14:50993451
|
C | T | 1 | a0002c0002t0003g0098 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1603+4599G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50993451 | ||||||
| chr14:50993618
|
A | G | 35 | a0001c0001t0001g0028a0001c0001t0001g0042a0001c0001t0001g0062others(32): Show | 35 | HG01099.hp1 HG01175.hp2 HG01358.hp1 others(32): Show |
intron_variant | MODIFIER | c.1603+4432T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50993618 | ||||||
| chr14:50993687
|
C | T | 2 | a0002c0002t0003g0044a0002c0002t0003g0098 | 2 | HG02055.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1603+4363G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50993687 | ||||||
| chr14:50993809
|
G | A | 12 | a0001c0001t0004g0099a0001c0001t0004g0100a0001c0001t0004g0101others(9): Show | 12 | HG01261.hp1 HG02145.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1603+4241C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50993809 | ||||||
| chr14:50993828
|
C | T | 11 | a0002c0002t0001g0002a0002c0002t0001g0121a0002c0002t0001g0137others(8): Show | 13 | HG00642.hp1 HG00735.hp2 HG01069.hp2 others(10): Show |
intron_variant | MODIFIER | c.1603+4222G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50993828 | ||||||
| chr14:50993829
|
G | A | 1 | a0001c0001t0002g0173 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1603+4221C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50993829 | ||||||
| chr14:50993940
|
T | A | 9 | a0001c0001t0001g0324a0001c0001t0005g0026a0001c0001t0005g0027others(6): Show | 9 | HG01891.hp1 HG02615.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.1603+4110A>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50993940 | ||||||
| chr14:50993988
|
C | G | 4 | a0001c0001t0009g0096a0002c0002t0004g0212a0002c0002t0004g0304others(1): Show | 4 | HG02145.hp2 HG03130.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1603+4062G>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50993988 | ||||||
| chr14:50994041
|
T | G | 90 | a0001c0001t0001g0031a0001c0001t0001g0206a0001c0001t0001g0277others(87): Show | 90 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.1603+4009A>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50994041 | ||||||
| chr14:50994054
|
A | G | 13 | a0001c0001t0001g0031a0001c0001t0002g0058a0001c0001t0002g0059others(10): Show | 13 | HG00280.hp2 HG00642.hp2 HG00733.hp1 others(10): Show |
intron_variant | MODIFIER | c.1603+3996T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50994054 | ||||||
| chr14:50994284
|
G | A | 25 | a0001c0001t0001g0028a0001c0001t0001g0042a0001c0001t0001g0062others(22): Show | 25 | HG01099.hp1 HG01175.hp2 HG01358.hp1 others(22): Show |
intron_variant | MODIFIER | c.1603+3766C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50994284 | ||||||
| chr14:50994400
|
T | C | 1 | a0002c0002t0001g0326 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1603+3650A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50994400 | ||||||
| chr14:50994456
|
G | C | 1 | a0002c0002t0001g0025 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1603+3594C>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50994456 | ||||||
| chr14:50994483
|
C | A | 1 | a0002c0002t0013g0035 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1603+3567G>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50994483 | ||||||
| chr14:50994664
|
TCA | T | 3 | a0002c0002t0001g0041a0002c0002t0001g0313a0002c0002t0003g0106 | 3 | HG02280.hp2 HG02647.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1603+3384_1603+338 others(6): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50994664 | ||||||
| chr14:50994880
|
A | G | 13 | a0001c0001t0001g0031a0001c0001t0002g0058a0001c0001t0002g0059others(10): Show | 13 | HG00280.hp2 HG00642.hp2 HG00733.hp1 others(10): Show |
intron_variant | MODIFIER | c.1603+3170T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50994880 | ||||||
| chr14:50995130
|
G | T | 2 | a0002c0002t0003g0044a0002c0002t0003g0098 | 2 | HG02055.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1603+2920C>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50995130 | ||||||
| chr14:50995211
|
T | C | 270 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0042others(267): Show | 275 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(272): Show |
intron_variant | MODIFIER | c.1603+2839A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50995211 | ||||||
| chr14:50995216
|
C | T | 13 | a0001c0001t0001g0031a0001c0001t0002g0058a0001c0001t0002g0059others(10): Show | 13 | HG00280.hp2 HG00642.hp2 HG00733.hp1 others(10): Show |
intron_variant | MODIFIER | c.1603+2834G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50995216 | ||||||
| chr14:50995268
|
G | T | 122 | a0001c0001t0001g0028a0001c0001t0001g0042a0001c0001t0001g0062others(119): Show | 123 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.1603+2782C>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50995268 | ||||||
| chr14:50995286
|
C | G | 1 | a0002c0002t0001g0189 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1603+2764G>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50995286 | ||||||
| chr14:50995337
|
C | G | 1 | a0001c0001t0004g0099 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1603+2713G>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50995337 | ||||||
| chr14:50995519
|
A | G | 10 | a0001c0001t0001g0324a0001c0001t0005g0026a0001c0001t0005g0027others(7): Show | 10 | HG01891.hp1 HG02615.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1603+2531T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50995519 | ||||||
| chr14:50995655
|
T | C | 1 | a0001c0001t0017g0036 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1603+2395A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50995655 | ||||||
| chr14:50995773
|
G | GA | 13 | a0001c0001t0001g0031a0001c0001t0002g0058a0001c0001t0002g0059others(10): Show | 13 | HG00280.hp2 HG00642.hp2 HG00733.hp1 others(10): Show |
intron_variant | MODIFIER | c.1603+2276dupT | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50995773 | ||||||
| chr14:50995773
|
GA | G | 6 | a0001c0001t0003g0080a0001c0001t0009g0038a0002c0002t0010g0330others(3): Show | 6 | HG01496.hp1 HG02109.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1603+2276delT | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50995773 | ||||||
| chr14:50995909
|
GAT | G | 3 | a0002c0002t0001g0041a0002c0002t0001g0313a0002c0002t0003g0106 | 3 | HG02280.hp2 HG02647.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1603+2139_1603+214 others(6): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50995909 | ||||||
| chr14:50996362
|
T | C | 3 | a0002c0004t0005g0149a0002c0004t0005g0298a0002c0012t0005g0161 | 3 | HG01496.hp1 HG02109.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1603+1688A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50996362 | ||||||
| chr14:50996364
|
A | T | 3 | a0002c0004t0005g0149a0002c0004t0005g0298a0002c0012t0005g0161 | 3 | HG01496.hp1 HG02109.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1603+1686T>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50996364 | ||||||
| chr14:50996507
|
C | T | 4 | a0002c0004t0005g0256a0002c0004t0005g0311a0002c0004t0005g0312others(1): Show | 4 | HG03041.hp2 HG03195.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1603+1543G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50996507 | ||||||
| chr14:50996604
|
A | G | 35 | a0001c0001t0001g0287a0001c0001t0001g0310a0001c0001t0002g0056others(32): Show | 35 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.1603+1446T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50996604 | ||||||
| chr14:50996632
|
G | T | 1 | a0001c0001t0002g0087 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1603+1418C>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50996632 | ||||||
| chr14:50996640
|
C | T | 4 | a0002c0002t0001g0007a0002c0002t0001g0227a0002c0002t0001g0237others(1): Show | 5 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.1603+1410G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50996640 | ||||||
| chr14:50996656
|
G | C | 3 | a0003c0006t0001g0140a0003c0006t0001g0142a0003c0006t0018g0151 | 3 | HG01099.hp1 HG01175.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.1603+1394C>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50996656 | ||||||
| chr14:50997105
|
G | C | 125 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0042others(122): Show | 126 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.1603+945C>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50997105 | ||||||
| chr14:50997133
|
C | T | 2 | a0002c0004t0005g0149a0002c0004t0005g0298 | 2 | HG02109.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1603+917G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50997133 | ||||||
| chr14:50997365
|
C | A | 48 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0042others(45): Show | 49 | HG00280.hp2 HG00642.hp2 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.1603+685G>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50997365 | ||||||
| chr14:50997484
|
C | T | 2 | a0002c0002t0001g0237a0002c0002t0001g0238 | 2 | HG01255.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.1603+566G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50997484 | ||||||
| chr14:50997554
|
G | A | 25 | a0001c0001t0001g0028a0001c0001t0001g0042a0001c0001t0001g0103others(22): Show | 25 | HG01099.hp1 HG01175.hp2 HG01358.hp1 others(22): Show |
intron_variant | MODIFIER | c.1603+496C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50997554 | ||||||
| chr14:50997570
|
A | T | 6 | a0001c0001t0001g0062a0001c0001t0002g0173a0001c0001t0003g0208others(3): Show | 6 | HG00621.hp1 HG00738.hp2 HG00741.hp2 others(3): Show |
intron_variant | MODIFIER | c.1603+480T>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50997570 | ||||||
| chr14:50997822
|
G | A | 1 | a0002c0002t0001g0264 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1603+228C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50997822 | ||||||
| chr14:50997983
|
C | T | 1 | a0002c0002t0001g0184 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1603+67G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50997983 | ||||||
| chr14:50997992
|
C | T | 1 | a0002c0002t0001g0248 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1603+58G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 7/12 | chr14 | 50997992 | ||||||
| chr14:50998200
|
C | T | 1 | a0001c0001t0002g0053 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1465-12G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 6/12 | chr14 | 50998200 | ||||||
| chr14:50998241
|
C | T | 11 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0122others(8): Show | 11 | HG01099.hp1 HG01175.hp2 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.1465-53G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 6/12 | chr14 | 50998241 | ||||||
| chr14:50998333
|
T | C | 96 | a0001c0001t0001g0206a0001c0001t0001g0277a0001c0001t0002g0023others(93): Show | 96 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.1465-145A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 6/12 | chr14 | 50998333 | ||||||
| chr14:50998573
|
C | T | 35 | a0001c0001t0001g0287a0001c0001t0001g0310a0001c0001t0002g0056others(32): Show | 35 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.1465-385G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 6/12 | chr14 | 50998573 | ||||||
| chr14:50998592
|
A | G | 1 | a0001c0001t0002g0150 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1465-404T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 6/12 | chr14 | 50998592 | ||||||
| chr14:50998604
|
T | C | 2 | a0001c0001t0017g0036a0002c0002t0001g0307 | 2 | HG02818.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1465-416A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 6/12 | chr14 | 50998604 | ||||||
| chr14:50998919
|
T | A | 110 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0122others(107): Show | 110 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.1465-731A>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 6/12 | chr14 | 50998919 | ||||||
| chr14:50999173
|
G | C | 1 | a0001c0001t0017g0036 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1465-985C>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 6/12 | chr14 | 50999173 | ||||||
| chr14:50999211
|
A | G | 12 | a0001c0001t0001g0042a0001c0001t0001g0103a0001c0001t0001g0216others(9): Show | 12 | HG02055.hp2 HG02145.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1465-1023T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 6/12 | chr14 | 50999211 | ||||||
| chr14:50999237
|
C | T | 5 | a0001c0001t0002g0058a0001c0001t0002g0059a0001c0001t0002g0060others(2): Show | 5 | HG00642.hp2 HG00733.hp1 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.1465-1049G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 6/12 | chr14 | 50999237 | ||||||
| chr14:50999248
|
C | T | 1 | a0001c0001t0001g0205 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1465-1060G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 6/12 | chr14 | 50999248 | ||||||
| chr14:50999308
|
C | A | 15 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0122others(12): Show | 15 | HG01099.hp1 HG01175.hp2 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.1465-1120G>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 6/12 | chr14 | 50999308 | ||||||
| chr14:50999330
|
A | G | 11 | a0002c0002t0002g0225a0002c0002t0006g0004a0002c0002t0006g0018others(8): Show | 12 | HG02155.hp2 HG03710.hp2 HG03942.hp2 others(9): Show |
intron_variant | MODIFIER | c.1465-1142T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 6/12 | chr14 | 50999330 | ||||||
| chr14:50999365
|
A | AAC | 45 | a0001c0001t0001g0132a0001c0001t0001g0287a0001c0001t0001g0310others(42): Show | 45 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.1465-1179_1465-117 others(6): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 6/12 | chr14 | 50999365 | ||||||
| chr14:50999366
|
ACACACAC others(11): Show |
A | 1 | a0001c0001t0004g0100 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1465-1196_1465-117 others(22): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 6/12 | chr14 | 50999366 | ||||||
| chr14:50999373
|
C | G | 1 | a0001c0001t0002g0296 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1465-1185G>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 6/12 | chr14 | 50999373 | ||||||
| chr14:50999541
|
A | C | 257 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0042others(254): Show | 262 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(259): Show |
intron_variant | MODIFIER | c.1464+1142T>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 6/12 | chr14 | 50999541 | ||||||
| chr14:50999602
|
G | T | 1 | a0001c0001t0017g0036 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1464+1081C>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 6/12 | chr14 | 50999602 | ||||||
| chr14:50999682
|
G | T | 11 | a0001c0001t0002g0058a0001c0001t0002g0059a0001c0001t0002g0060others(8): Show | 11 | HG00280.hp2 HG00642.hp2 HG00733.hp1 others(8): Show |
intron_variant | MODIFIER | c.1464+1001C>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 6/12 | chr14 | 50999682 | ||||||
| chr14:50999716
|
A | C | 1 | a0002c0002t0001g0135 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1464+967T>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 6/12 | chr14 | 50999716 | ||||||
| chr14:50999738
|
G | T | 1 | a0002c0002t0003g0106 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1464+945C>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 6/12 | chr14 | 50999738 | ||||||
| chr14:50999748
|
C | T | 11 | a0002c0002t0002g0225a0002c0002t0006g0004a0002c0002t0006g0018others(8): Show | 12 | HG02155.hp2 HG03710.hp2 HG03942.hp2 others(9): Show |
intron_variant | MODIFIER | c.1464+935G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 6/12 | chr14 | 50999748 | ||||||
| chr14:50999756
|
C | T | 14 | a0001c0001t0001g0028a0001c0001t0001g0122a0001c0001t0001g0178others(11): Show | 14 | HG01099.hp1 HG01175.hp2 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.1464+927G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 6/12 | chr14 | 50999756 | ||||||
| chr14:50999766
|
G | T | 28 | a0001c0001t0003g0271a0001c0001t0003g0317a0001c0001t0009g0096others(25): Show | 31 | HG00642.hp1 HG00735.hp2 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.1464+917C>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 6/12 | chr14 | 50999766 | ||||||
| chr14:50999778
|
A | G | 1 | a0002c0002t0013g0035 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1464+905T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 6/12 | chr14 | 50999778 | ||||||
| chr14:50999863
|
G | C | 99 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0122others(96): Show | 99 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.1464+820C>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 6/12 | chr14 | 50999863 | ||||||
| chr14:50999923
|
T | C | 260 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0042others(257): Show | 265 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.1464+760A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 6/12 | chr14 | 50999923 | ||||||
| chr14:50999997
|
T | C | 2 | a0001c0001t0002g0152a0001c0001t0002g0316 | 2 | HG01243.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1464+686A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 6/12 | chr14 | 50999997 | ||||||
| chr14:51000144
|
C | T | 18 | a0001c0001t0001g0042a0001c0001t0001g0103a0001c0001t0004g0099others(15): Show | 18 | HG01261.hp1 HG01496.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.1464+539G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 6/12 | chr14 | 51000144 | ||||||
| chr14:51000169
|
G | A | 24 | a0001c0001t0003g0271a0001c0001t0003g0317a0001c0001t0015g0240others(21): Show | 27 | HG00642.hp1 HG00735.hp2 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.1464+514C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 6/12 | chr14 | 51000169 | ||||||
| chr14:51000243
|
A | G | 1 | a0001c0001t0002g0217 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1464+440T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 6/12 | chr14 | 51000243 | ||||||
| chr14:51000309
|
C | T | 26 | a0001c0001t0002g0056a0001c0001t0002g0073a0002c0002t0001g0047others(23): Show | 26 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(23): Show |
intron_variant | MODIFIER | c.1464+374G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 6/12 | chr14 | 51000309 | ||||||
| chr14:51000454
|
C | T | 1 | a0002c0002t0006g0224 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1464+229G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 6/12 | chr14 | 51000454 | ||||||
| chr14:51000564
|
C | T | 1 | a0005c0011t0001g0315 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1464+119G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 6/12 | chr14 | 51000564 | ||||||
| chr14:51000605
|
G | A | 1 | a0001c0001t0003g0074 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1464+78C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 6/12 | chr14 | 51000605 | ||||||
| chr14:51000914
|
C | T | 3 | a0002c0004t0005g0298a0002c0004t0005g0311a0002c0012t0005g0161 | 3 | HG01496.hp1 HG03041.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1307-74G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51000914 | ||||||
| chr14:51000960
|
G | A | 1 | a0002c0002t0011g0034 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1307-120C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51000960 | ||||||
| chr14:51001123
|
T | C | 3 | a0002c0004t0005g0298a0002c0004t0005g0311a0002c0012t0005g0161 | 3 | HG01496.hp1 HG03041.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1307-283A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51001123 | ||||||
| chr14:51001130
|
C | T | 6 | a0001c0001t0001g0216a0002c0002t0003g0044a0002c0002t0003g0098others(3): Show | 6 | HG02055.hp2 HG02145.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1307-290G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51001130 | ||||||
| chr14:51001228
|
A | AT | 15 | a0001c0001t0003g0006a0001c0001t0003g0168a0001c0001t0003g0254others(12): Show | 17 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.1307-389dupA | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51001228 | ||||||
| chr14:51001228
|
AT | A | 158 | a0001c0001t0001g0028a0001c0001t0001g0042a0001c0001t0001g0103others(155): Show | 160 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.1307-389delA | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51001228 | ||||||
| chr14:51001228
|
ATT | A | 18 | a0001c0001t0001g0031a0001c0001t0001g0122a0001c0001t0001g0178others(15): Show | 18 | HG01099.hp1 HG01168.hp2 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.1307-390_1307-389d others(4): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51001228 | ||||||
| chr14:51001261
|
G | T | 10 | a0002c0002t0002g0225a0002c0002t0006g0004a0002c0002t0006g0018others(7): Show | 11 | HG02155.hp2 HG03710.hp2 HG04204.hp1 others(8): Show |
intron_variant | MODIFIER | c.1307-421C>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51001261 | ||||||
| chr14:51001276
|
T | C | 3 | a0002c0002t0001g0072a0002c0002t0001g0263a0002c0002t0001g0319 | 3 | HG00544.hp2 NA18612.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.1307-436A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51001276 | ||||||
| chr14:51001331
|
A | G | 2 | a0001c0001t0003g0168a0001c0001t0003g0169 | 2 | NA18956.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.1307-491T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51001331 | ||||||
| chr14:51001337
|
C | G | 1 | a0002c0002t0001g0264 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1307-497G>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51001337 | ||||||
| chr14:51001347
|
A | G | 105 | a0001c0001t0001g0206a0001c0001t0001g0277a0001c0001t0002g0023others(102): Show | 106 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.1307-507T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51001347 | ||||||
| chr14:51001408
|
T | G | 1 | a0002c0002t0001g0030 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1307-568A>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51001408 | ||||||
| chr14:51001430
|
T | C | 1 | a0001c0001t0002g0200 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1307-590A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51001430 | ||||||
| chr14:51001431
|
G | A | 1 | a0001c0001t0002g0200 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1307-591C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51001431 | ||||||
| chr14:51001594
|
C | G | 24 | a0001c0001t0001g0042a0001c0001t0001g0103a0001c0001t0001g0216others(21): Show | 24 | HG01261.hp1 HG01496.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.1307-754G>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51001594 | ||||||
| chr14:51001733
|
G | GATC | 12 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0122others(9): Show | 12 | HG01099.hp1 HG01175.hp2 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.1307-894_1307-893i others(5): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51001733 | ||||||
| chr14:51001923
|
C | T | 1 | a0002c0002t0001g0166 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1307-1083G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51001923 | ||||||
| chr14:51002105
|
TTG | T | 163 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0042others(160): Show | 167 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(164): Show |
intron_variant | MODIFIER | c.1307-1267_1307-126 others(6): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51002105 | ||||||
| chr14:51002105
|
TTGTG | T | 9 | a0002c0002t0002g0225a0002c0002t0006g0004a0002c0002t0006g0018others(6): Show | 10 | HG02155.hp2 HG03710.hp2 HG04204.hp1 others(7): Show |
intron_variant | MODIFIER | c.1307-1269_1307-126 others(8): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51002105 | ||||||
| chr14:51002125
|
G | T | 13 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0122others(10): Show | 13 | HG01099.hp1 HG01175.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.1307-1285C>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51002125 | ||||||
| chr14:51002130
|
T | C | 1 | a0002c0002t0006g0077 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1307-1290A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51002130 | ||||||
| chr14:51002131
|
C | T | 3 | a0001c0001t0009g0038a0002c0002t0006g0077a0002c0002t0010g0330 | 3 | HG03098.hp1 HG03453.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.1307-1291G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51002131 | ||||||
| chr14:51002144
|
C | T | 2 | a0001c0001t0001g0028a0005c0011t0001g0315 | 2 | HG02717.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1307-1304G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51002144 | ||||||
| chr14:51002146
|
C | G | 103 | a0001c0001t0001g0206a0001c0001t0001g0277a0001c0001t0002g0023others(100): Show | 104 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.1307-1306G>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51002146 | ||||||
| chr14:51002247
|
G | A | 9 | a0001c0001t0005g0027a0001c0001t0005g0032a0001c0001t0005g0033others(6): Show | 9 | HG01891.hp1 HG02280.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1307-1407C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51002247 | ||||||
| chr14:51002267
|
C | A | 143 | a0001c0001t0001g0206a0001c0001t0001g0277a0001c0001t0001g0287others(140): Show | 144 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.1307-1427G>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51002267 | ||||||
| chr14:51002288
|
A | AT | 31 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0122others(28): Show | 32 | HG00639.hp1 HG01099.hp1 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.1307-1449dupA | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51002288 | ||||||
| chr14:51002288
|
A | ATT | 91 | a0001c0001t0001g0206a0001c0001t0001g0277a0001c0001t0002g0023others(88): Show | 91 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.1307-1450_1307-144 others(6): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51002288 | ||||||
| chr14:51002288
|
AT | A | 25 | a0001c0001t0003g0271a0001c0001t0003g0317a0001c0001t0015g0240others(22): Show | 28 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.1307-1449delA | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51002288 | ||||||
| chr14:51002324
|
C | T | 1 | a0002c0002t0011g0034 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1307-1484G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51002324 | ||||||
| chr14:51002335
|
C | T | 39 | a0001c0001t0001g0205a0001c0001t0003g0129a0001c0001t0003g0130others(36): Show | 40 | HG00280.hp1 HG00438.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.1307-1495G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51002335 | ||||||
| chr14:51002350
|
G | A | 5 | a0001c0001t0002g0058a0001c0001t0002g0059a0001c0001t0002g0060others(2): Show | 5 | HG00642.hp2 HG00733.hp1 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.1307-1510C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51002350 | ||||||
| chr14:51002351
|
G | T | 9 | a0001c0001t0005g0027a0001c0001t0005g0032a0001c0001t0005g0033others(6): Show | 9 | HG01891.hp1 HG02280.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1307-1511C>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51002351 | ||||||
| chr14:51002423
|
C | T | 1 | a0002c0002t0008g0325 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1307-1583G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51002423 | ||||||
| chr14:51002547
|
TCCAGGGA others(7): Show |
T | 1 | a0002c0002t0011g0034 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1307-1721_1307-170 others(18): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51002547 | ||||||
| chr14:51002683
|
C | T | 5 | a0002c0002t0002g0225a0002c0002t0006g0018a0002c0002t0006g0144others(2): Show | 5 | HG03710.hp2 HG04204.hp1 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.1307-1843G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51002683 | ||||||
| chr14:51002767
|
C | T | 13 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0122others(10): Show | 13 | HG01099.hp1 HG01175.hp2 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.1307-1927G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51002767 | ||||||
| chr14:51002778
|
C | T | 40 | a0001c0001t0001g0287a0001c0001t0001g0310a0001c0001t0002g0056others(37): Show | 40 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.1307-1938G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51002778 | ||||||
| chr14:51003033
|
T | C | 40 | a0001c0001t0001g0287a0001c0001t0001g0310a0001c0001t0002g0056others(37): Show | 40 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.1307-2193A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51003033 | ||||||
| chr14:51003177
|
T | C | 12 | a0001c0001t0001g0042a0001c0001t0001g0103a0001c0001t0001g0216others(9): Show | 12 | HG02055.hp2 HG02145.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1307-2337A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51003177 | ||||||
| chr14:51003295
|
C | T | 1 | a0001c0001t0002g0199 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1307-2455G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51003295 | ||||||
| chr14:51003301
|
G | C | 1 | a0001c0001t0002g0199 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1307-2461C>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51003301 | ||||||
| chr14:51003420
|
T | G | 98 | a0001c0001t0001g0206a0001c0001t0001g0277a0001c0001t0002g0023others(95): Show | 99 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.1307-2580A>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51003420 | ||||||
| chr14:51003705
|
AC | A | 11 | a0001c0001t0002g0058a0001c0001t0002g0059a0001c0001t0002g0060others(8): Show | 11 | HG00280.hp2 HG00642.hp2 HG00733.hp1 others(8): Show |
intron_variant | MODIFIER | c.1307-2866delG | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51003705 | ||||||
| chr14:51003868
|
G | A | 254 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0042others(251): Show | 259 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.1307-3028C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51003868 | ||||||
| chr14:51004043
|
T | A | 1 | a0001c0001t0002g0199 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1307-3203A>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51004043 | ||||||
| chr14:51004086
|
G | A | 40 | a0001c0001t0001g0287a0001c0001t0001g0310a0001c0001t0002g0056others(37): Show | 40 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.1307-3246C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51004086 | ||||||
| chr14:51004101
|
C | T | 40 | a0001c0001t0001g0287a0001c0001t0001g0310a0001c0001t0002g0056others(37): Show | 40 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.1307-3261G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51004101 | ||||||
| chr14:51004130
|
A | ATTTTTAC others(338): Show |
1 | a0001c0001t0002g0023 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1307-3291_1307-329 others(349): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51004130 | ||||||
| chr14:51004220
|
T | A | 1 | a0001c0001t0002g0199 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1307-3380A>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51004220 | ||||||
| chr14:51004304
|
C | T | 15 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0122others(12): Show | 15 | HG01099.hp1 HG01175.hp2 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.1307-3464G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51004304 | ||||||
| chr14:51004315
|
C | G | 93 | a0001c0001t0001g0206a0001c0001t0001g0277a0001c0001t0002g0023others(90): Show | 93 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.1307-3475G>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51004315 | ||||||
| chr14:51004317
|
G | A | 9 | a0001c0001t0001g0324a0001c0001t0005g0027a0001c0001t0005g0032others(6): Show | 9 | HG01891.hp1 HG02723.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.1307-3477C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51004317 | ||||||
| chr14:51004372
|
T | G | 1 | a0001c0001t0002g0199 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1307-3532A>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51004372 | ||||||
| chr14:51004437
|
A | T | 4 | a0001c0001t0002g0088a0001c0001t0003g0254a0001c0001t0003g0289others(1): Show | 4 | HG00621.hp2 NA18942.hp1 NA18955.hp1 others(1): Show |
intron_variant | MODIFIER | c.1307-3597T>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51004437 | ||||||
| chr14:51004874
|
A | G | 73 | a0001c0001t0001g0042a0001c0001t0001g0103a0001c0001t0001g0132others(70): Show | 74 | HG00280.hp1 HG00438.hp1 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.1307-4034T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51004874 | ||||||
| chr14:51005009
|
C | T | 2 | a0001c0001t0002g0153a0001c0001t0002g0154 | 2 | HG01257.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.1306+4071G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51005009 | ||||||
| chr14:51005127
|
G | T | 150 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0122others(147): Show | 150 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.1306+3953C>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51005127 | ||||||
| chr14:51005147
|
C | T | 1 | a0002c0002t0001g0137 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1306+3933G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51005147 | ||||||
| chr14:51005401
|
T | C | 5 | a0001c0001t0002g0045a0001c0001t0002g0108a0001c0001t0002g0110others(2): Show | 5 | HG01256.hp1 HG01258.hp1 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.1306+3679A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51005401 | ||||||
| chr14:51005417
|
C | T | 4 | a0001c0001t0009g0096a0002c0002t0001g0247a0002c0002t0008g0306others(1): Show | 4 | HG03041.hp1 HG03139.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1306+3663G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51005417 | ||||||
| chr14:51005472
|
A | G | 24 | a0001c0001t0003g0271a0001c0001t0003g0317a0001c0001t0015g0240others(21): Show | 27 | HG00642.hp1 HG00735.hp2 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.1306+3608T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51005472 | ||||||
| chr14:51005475
|
T | C | 1 | a0001c0001t0004g0253 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1306+3605A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51005475 | ||||||
| chr14:51005555
|
CCAAA | C | 4 | a0001c0001t0009g0096a0002c0002t0001g0247a0002c0002t0008g0306others(1): Show | 4 | HG03041.hp1 HG03139.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1306+3521_1306+352 others(8): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51005555 | ||||||
| chr14:51005750
|
G | T | 1 | a0001c0001t0003g0043 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1306+3330C>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51005750 | ||||||
| chr14:51005792
|
A | T | 10 | a0002c0002t0002g0225a0002c0002t0006g0004a0002c0002t0006g0018others(7): Show | 11 | HG02155.hp2 HG03710.hp2 HG04204.hp1 others(8): Show |
intron_variant | MODIFIER | c.1306+3288T>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51005792 | ||||||
| chr14:51005892
|
G | C | 1 | a0001c0001t0003g0221 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1306+3188C>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51005892 | ||||||
| chr14:51005906
|
G | T | 119 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0042others(116): Show | 121 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.1306+3174C>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51005906 | ||||||
| chr14:51005990
|
G | A | 47 | a0001c0001t0001g0132a0001c0001t0001g0205a0001c0001t0003g0129others(44): Show | 48 | HG00280.hp1 HG00438.hp1 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.1306+3090C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51005990 | ||||||
| chr14:51006011
|
T | TCAA | 4 | a0001c0001t0004g0126a0001c0001t0004g0232a0001c0001t0004g0241others(1): Show | 4 | HG00280.hp2 HG01168.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.1306+3066_1306+306 others(7): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51006011 | ||||||
| chr14:51006132
|
G | T | 1 | a0002c0002t0011g0034 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1306+2948C>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51006132 | ||||||
| chr14:51006164
|
T | G | 22 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0042others(19): Show | 22 | HG01099.hp1 HG01175.hp2 HG01358.hp1 others(19): Show |
intron_variant | MODIFIER | c.1306+2916A>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51006164 | ||||||
| chr14:51006253
|
C | T | 1 | a0001c0001t0002g0186 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1306+2827G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51006253 | ||||||
| chr14:51006264
|
A | G | 22 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0042others(19): Show | 22 | HG01099.hp1 HG01175.hp2 HG01358.hp1 others(19): Show |
intron_variant | MODIFIER | c.1306+2816T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51006264 | ||||||
| chr14:51006272
|
T | C | 22 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0042others(19): Show | 22 | HG01099.hp1 HG01175.hp2 HG01358.hp1 others(19): Show |
intron_variant | MODIFIER | c.1306+2808A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51006272 | ||||||
| chr14:51006367
|
C | A | 1 | a0002c0002t0011g0034 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1306+2713G>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51006367 | ||||||
| chr14:51006380
|
G | A | 51 | a0001c0001t0001g0287a0001c0001t0001g0310a0001c0001t0002g0056others(48): Show | 52 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.1306+2700C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51006380 | ||||||
| chr14:51006400
|
G | A | 18 | a0001c0001t0003g0271a0001c0001t0015g0240a0002c0002t0001g0002others(15): Show | 21 | HG00642.hp1 HG00735.hp2 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.1306+2680C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51006400 | ||||||
| chr14:51006512
|
T | A | 3 | a0002c0002t0001g0041a0002c0002t0001g0313a0002c0002t0003g0106 | 3 | HG02280.hp2 HG02647.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1306+2568A>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51006512 | ||||||
| chr14:51006659
|
A | T | 1 | a0001c0001t0002g0165 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1306+2421T>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51006659 | ||||||
| chr14:51006939
|
C | T | 3 | a0002c0002t0004g0212a0002c0002t0004g0304a0002c0002t0004g0321 | 3 | HG02145.hp2 HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1306+2141G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51006939 | ||||||
| chr14:51006951
|
A | G | 4 | a0001c0001t0001g0211a0003c0006t0001g0140a0003c0006t0001g0142others(1): Show | 4 | HG01099.hp1 HG01175.hp2 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.1306+2129T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51006951 | ||||||
| chr14:51007048
|
A | G | 16 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0122others(13): Show | 16 | HG01099.hp1 HG01175.hp2 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.1306+2032T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51007048 | ||||||
| chr14:51007632
|
T | C | 10 | a0002c0002t0002g0225a0002c0002t0006g0004a0002c0002t0006g0018others(7): Show | 11 | HG02155.hp2 HG03710.hp2 HG04204.hp1 others(8): Show |
intron_variant | MODIFIER | c.1306+1448A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51007632 | ||||||
| chr14:51007746
|
T | C | 24 | a0001c0001t0003g0271a0001c0001t0003g0317a0001c0001t0015g0240others(21): Show | 27 | HG00642.hp1 HG00735.hp2 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.1306+1334A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51007746 | ||||||
| chr14:51007800
|
CA | C | 144 | a0001c0001t0001g0042a0001c0001t0001g0062a0001c0001t0001g0103others(141): Show | 146 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(143): Show |
intron_variant | MODIFIER | c.1306+1279delT | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51007800 | ||||||
| chr14:51007800
|
CAA | C | 95 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0122others(92): Show | 101 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.1306+1278_1306+127 others(6): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51007800 | ||||||
| chr14:51007882
|
G | A | 2 | a0002c0002t0001g0131a0002c0002t0001g0133 | 2 | HG01109.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.1306+1198C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51007882 | ||||||
| chr14:51007954
|
T | A | 24 | a0001c0001t0003g0271a0001c0001t0003g0317a0001c0001t0015g0240others(21): Show | 27 | HG00642.hp1 HG00735.hp2 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.1306+1126A>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51007954 | ||||||
| chr14:51008012
|
G | T | 24 | a0001c0001t0003g0271a0001c0001t0003g0317a0001c0001t0015g0240others(21): Show | 27 | HG00642.hp1 HG00735.hp2 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.1306+1068C>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51008012 | ||||||
| chr14:51008034
|
G | A | 3 | a0002c0002t0001g0041a0002c0002t0001g0313a0002c0002t0003g0106 | 3 | HG02280.hp2 HG02647.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1306+1046C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51008034 | ||||||
| chr14:51008189
|
A | T | 1 | a0001c0001t0001g0205 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1306+891T>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51008189 | ||||||
| chr14:51008223
|
T | C | 8 | a0001c0001t0001g0132a0001c0001t0019g0331a0002c0002t0001g0131others(5): Show | 8 | HG00639.hp1 HG01109.hp1 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.1306+857A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51008223 | ||||||
| chr14:51008281
|
G | A | 5 | a0001c0001t0002g0058a0001c0001t0002g0059a0001c0001t0002g0060others(2): Show | 5 | HG00642.hp2 HG00733.hp1 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.1306+799C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51008281 | ||||||
| chr14:51008379
|
C | T | 1 | a0002c0002t0001g0246 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1306+701G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51008379 | ||||||
| chr14:51008398
|
G | C | 258 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0042others(255): Show | 263 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.1306+682C>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51008398 | ||||||
| chr14:51008403
|
A | C | 10 | a0002c0002t0002g0225a0002c0002t0006g0004a0002c0002t0006g0018others(7): Show | 11 | HG02155.hp2 HG03710.hp2 HG04204.hp1 others(8): Show |
intron_variant | MODIFIER | c.1306+677T>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51008403 | ||||||
| chr14:51008587
|
A | G | 1 | a0001c0001t0002g0157 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1306+493T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51008587 | ||||||
| chr14:51008810
|
C | G | 2 | a0001c0001t0002g0023a0001c0001t0002g0261 | 2 | HG00597.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.1306+270G>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51008810 | ||||||
| chr14:51008967
|
T | C | 1 | a0002c0002t0016g0076 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1306+113A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51008967 | ||||||
| chr14:51009045
|
T | C | 1 | a0002c0002t0013g0035 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1306+35A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51009045 | ||||||
| chr14:51009076
|
A | T | 219 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0062others(216): Show | 223 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(220): Show |
splice_region_variant&intron_variant | LOW | c.1306+4T>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 5/12 | chr14 | 51009076 | ||||||
| chr14:51009274
|
C | T | 20 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0122others(17): Show | 20 | HG00639.hp1 HG01099.hp1 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.1153-41G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 4/12 | chr14 | 51009274 | ||||||
| chr14:51009332
|
C | T | 1 | a0001c0001t0002g0270 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1153-99G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 4/12 | chr14 | 51009332 | ||||||
| chr14:51009694
|
C | T | 1 | a0001c0001t0003g0269 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1153-461G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 4/12 | chr14 | 51009694 | ||||||
| chr14:51009747
|
C | G | 1 | a0002c0002t0013g0035 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1153-514G>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 4/12 | chr14 | 51009747 | ||||||
| chr14:51009786
|
G | C | 18 | a0001c0001t0002g0058a0001c0001t0002g0059a0001c0001t0002g0060others(15): Show | 18 | HG00280.hp2 HG00642.hp2 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.1153-553C>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 4/12 | chr14 | 51009786 | ||||||
| chr14:51009790
|
A | C | 82 | a0001c0001t0001g0206a0001c0001t0001g0277a0001c0001t0002g0023others(79): Show | 82 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.1153-557T>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 4/12 | chr14 | 51009790 | ||||||
| chr14:51009977
|
A | T | 8 | a0001c0001t0001g0132a0001c0001t0019g0331a0002c0002t0001g0131others(5): Show | 8 | HG00639.hp1 HG01109.hp1 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.1152+407T>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 4/12 | chr14 | 51009977 | ||||||
| chr14:51009987
|
C | T | 3 | a0001c0001t0001g0216a0002c0002t0003g0044a0002c0002t0003g0098 | 3 | HG02055.hp2 HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1152+397G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 4/12 | chr14 | 51009987 | ||||||
| chr14:51010130
|
G | GA | 246 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0042others(243): Show | 251 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(248): Show |
intron_variant | MODIFIER | c.1152+253dupT | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 4/12 | chr14 | 51010130 | ||||||
| chr14:51010135
|
A | AT | 4 | a0001c0001t0009g0096a0002c0002t0001g0247a0002c0002t0008g0306others(1): Show | 4 | HG03041.hp1 HG03139.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1152+248_1152+249i others(3): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 4/12 | chr14 | 51010135 | ||||||
| chr14:51010170
|
C | T | 9 | a0002c0002t0002g0225a0002c0002t0006g0004a0002c0002t0006g0018others(6): Show | 10 | HG02155.hp2 HG03710.hp2 NA18946.hp1 others(7): Show |
intron_variant | MODIFIER | c.1152+214G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 4/12 | chr14 | 51010170 | ||||||
| chr14:51010232
|
G | A | 11 | a0001c0001t0001g0324a0001c0001t0005g0027a0001c0001t0005g0032others(8): Show | 11 | HG01891.hp1 HG02280.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.1152+152C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 4/12 | chr14 | 51010232 | ||||||
| chr14:51010361
|
C | T | 4 | a0001c0001t0009g0096a0002c0002t0001g0247a0002c0002t0008g0306others(1): Show | 4 | HG03041.hp1 HG03139.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1152+23G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 4/12 | chr14 | 51010361 | ||||||
| chr14:51010564
|
T | C | 1 | a0002c0002t0003g0098 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1042-70A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51010564 | ||||||
| chr14:51010565
|
T | C | 1 | a0002c0002t0003g0098 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1042-71A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51010565 | ||||||
| chr14:51010780
|
A | G | 1 | a0001c0001t0017g0036 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1042-286T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51010780 | ||||||
| chr14:51010819
|
C | T | 1 | a0001c0001t0002g0296 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1042-325G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51010819 | ||||||
| chr14:51010960
|
T | C | 1 | a0002c0004t0005g0256 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1042-466A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51010960 | ||||||
| chr14:51011012
|
C | A | 5 | a0001c0001t0002g0058a0001c0001t0002g0059a0001c0001t0002g0060others(2): Show | 5 | HG00642.hp2 HG00733.hp1 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.1042-518G>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51011012 | ||||||
| chr14:51011015
|
T | C | 9 | a0002c0002t0002g0225a0002c0002t0006g0004a0002c0002t0006g0018others(6): Show | 10 | HG02155.hp2 HG03710.hp2 NA18946.hp1 others(7): Show |
intron_variant | MODIFIER | c.1042-521A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51011015 | ||||||
| chr14:51011035
|
G | A | 256 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0042others(253): Show | 261 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(258): Show |
intron_variant | MODIFIER | c.1042-541C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51011035 | ||||||
| chr14:51011036
|
G | T | 3 | a0002c0002t0004g0212a0002c0002t0004g0304a0002c0002t0004g0321 | 3 | HG02145.hp2 HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1042-542C>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51011036 | ||||||
| chr14:51011053
|
G | A | 27 | a0001c0001t0002g0058a0001c0001t0002g0059a0001c0001t0002g0060others(24): Show | 28 | HG00280.hp2 HG00642.hp2 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.1042-559C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51011053 | ||||||
| chr14:51011102
|
C | T | 1 | a0002c0002t0001g0134 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1042-608G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51011102 | ||||||
| chr14:51011143
|
C | T | 2 | a0002c0002t0001g0120a0002c0013t0001g0327 | 2 | NA18954.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.1042-649G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51011143 | ||||||
| chr14:51011290
|
C | A | 256 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0042others(253): Show | 261 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(258): Show |
intron_variant | MODIFIER | c.1042-796G>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51011290 | ||||||
| chr14:51011319
|
T | A | 256 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0042others(253): Show | 261 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(258): Show |
intron_variant | MODIFIER | c.1042-825A>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51011319 | ||||||
| chr14:51011325
|
C | T | 1 | a0002c0002t0003g0282 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1042-831G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51011325 | ||||||
| chr14:51011454
|
T | C | 7 | a0001c0001t0004g0099a0001c0001t0004g0100a0001c0001t0004g0101others(4): Show | 7 | HG01261.hp1 HG02451.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1042-960A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51011454 | ||||||
| chr14:51011507
|
A | G | 41 | a0001c0001t0001g0062a0001c0001t0001g0287a0001c0001t0001g0310others(38): Show | 41 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.1042-1013T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51011507 | ||||||
| chr14:51011618
|
G | T | 1 | a0002c0002t0006g0223 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1042-1124C>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51011618 | ||||||
| chr14:51011675
|
T | C | 256 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0042others(253): Show | 261 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(258): Show |
intron_variant | MODIFIER | c.1042-1181A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51011675 | ||||||
| chr14:51011734
|
T | C | 1 | a0002c0002t0001g0307 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1042-1240A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51011734 | ||||||
| chr14:51011905
|
T | C | 108 | a0001c0001t0001g0206a0001c0001t0001g0277a0001c0001t0002g0023others(105): Show | 109 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.1042-1411A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51011905 | ||||||
| chr14:51011964
|
C | A | 1 | a0002c0002t0011g0034 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1042-1470G>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51011964 | ||||||
| chr14:51012054
|
T | C | 1 | a0001c0001t0001g0031 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1042-1560A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51012054 | ||||||
| chr14:51012110
|
A | G | 54 | a0001c0001t0001g0042a0001c0001t0001g0062a0001c0001t0001g0103others(51): Show | 54 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.1042-1616T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51012110 | ||||||
| chr14:51012494
|
C | T | 1 | a0002c0012t0005g0161 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1042-2000G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51012494 | ||||||
| chr14:51012718
|
T | G | 6 | a0001c0001t0004g0099a0001c0001t0004g0100a0001c0001t0004g0101others(3): Show | 6 | HG01261.hp1 HG02572.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1042-2224A>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51012718 | ||||||
| chr14:51012839
|
C | T | 12 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0122others(9): Show | 12 | HG01099.hp1 HG01175.hp2 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.1042-2345G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51012839 | ||||||
| chr14:51012853
|
C | G | 258 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0042others(255): Show | 263 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.1042-2359G>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51012853 | ||||||
| chr14:51012897
|
T | C | 1 | a0002c0002t0001g0307 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1042-2403A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51012897 | ||||||
| chr14:51012971
|
T | C | 108 | a0001c0001t0001g0206a0001c0001t0001g0277a0001c0001t0002g0023others(105): Show | 109 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.1042-2477A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51012971 | ||||||
| chr14:51013080
|
T | C | 1 | a0001c0001t0004g0266 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1042-2586A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51013080 | ||||||
| chr14:51013162
|
A | G | 108 | a0001c0001t0001g0206a0001c0001t0001g0277a0001c0001t0002g0023others(105): Show | 109 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.1042-2668T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51013162 | ||||||
| chr14:51013226
|
A | AT | 53 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0122others(50): Show | 54 | HG00280.hp1 HG00438.hp1 HG00738.hp1 others(51): Show |
intron_variant | MODIFIER | c.1042-2733dupA | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51013226 | ||||||
| chr14:51013226
|
AT | A | 18 | a0001c0001t0001g0103a0001c0001t0009g0096a0001c0003t0001g0014others(15): Show | 19 | HG02155.hp2 HG02451.hp2 HG02723.hp2 others(16): Show |
intron_variant | MODIFIER | c.1042-2733delA | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51013226 | ||||||
| chr14:51013226
|
ATT | A | 148 | a0001c0001t0001g0042a0001c0001t0001g0062a0001c0001t0001g0206others(145): Show | 148 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.1042-2734_1042-273 others(6): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51013226 | ||||||
| chr14:51013330
|
A | C | 4 | a0001c0001t0009g0096a0002c0002t0001g0247a0002c0002t0008g0306others(1): Show | 4 | HG03041.hp1 HG03139.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1042-2836T>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51013330 | ||||||
| chr14:51013346
|
A | G | 108 | a0001c0001t0001g0206a0001c0001t0001g0277a0001c0001t0002g0023others(105): Show | 109 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.1042-2852T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51013346 | ||||||
| chr14:51013424
|
T | C | 8 | a0001c0001t0001g0132a0001c0001t0019g0331a0002c0002t0001g0131others(5): Show | 8 | HG00639.hp1 HG01109.hp1 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.1042-2930A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51013424 | ||||||
| chr14:51013613
|
A | G | 8 | a0001c0001t0001g0324a0001c0001t0005g0027a0001c0001t0005g0032others(5): Show | 8 | HG01891.hp1 HG02723.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1042-3119T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51013613 | ||||||
| chr14:51013738
|
G | A | 4 | a0001c0001t0009g0096a0002c0002t0001g0247a0002c0002t0008g0306others(1): Show | 4 | HG03041.hp1 HG03139.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1042-3244C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51013738 | ||||||
| chr14:51013782
|
A | G | 3 | a0002c0002t0004g0212a0002c0002t0004g0304a0002c0002t0004g0321 | 3 | HG02145.hp2 HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1042-3288T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51013782 | ||||||
| chr14:51014148
|
T | C | 1 | a0002c0002t0003g0282 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1042-3654A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51014148 | ||||||
| chr14:51014152
|
T | C | 1 | a0002c0012t0005g0161 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1042-3658A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51014152 | ||||||
| chr14:51014173
|
A | C | 12 | a0001c0001t0001g0042a0001c0001t0001g0103a0001c0001t0001g0216others(9): Show | 12 | HG02055.hp2 HG02145.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1042-3679T>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51014173 | ||||||
| chr14:51014459
|
A | G | 2 | a0002c0002t0003g0065a0002c0002t0003g0066 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1042-3965T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51014459 | ||||||
| chr14:51014592
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1042-4098G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51014592 | ||||||
| chr14:51014655
|
C | G | 104 | a0001c0001t0001g0028a0001c0001t0001g0122a0001c0001t0001g0132others(101): Show | 108 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.1042-4161G>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51014655 | ||||||
| chr14:51014703
|
C | G | 18 | a0001c0001t0001g0287a0001c0001t0001g0310a0001c0001t0002g0058others(15): Show | 18 | HG00642.hp2 HG00733.hp1 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.1042-4209G>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51014703 | ||||||
| chr14:51014783
|
C | A | 11 | a0001c0001t0001g0028a0001c0001t0004g0126a0001c0001t0004g0232others(8): Show | 11 | HG00280.hp2 HG01168.hp2 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.1042-4289G>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51014783 | ||||||
| chr14:51014854
|
G | A | 24 | a0001c0001t0003g0271a0001c0001t0003g0317a0001c0001t0010g0329others(21): Show | 27 | HG00642.hp1 HG00735.hp2 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.1042-4360C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51014854 | ||||||
| chr14:51014883
|
T | G | 13 | a0001c0001t0001g0042a0001c0001t0001g0103a0001c0001t0001g0216others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.1042-4389A>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51014883 | ||||||
| chr14:51015023
|
G | T | 4 | a0001c0001t0009g0096a0002c0002t0001g0247a0002c0002t0008g0306others(1): Show | 4 | HG03041.hp1 HG03139.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1042-4529C>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51015023 | ||||||
| chr14:51015024
|
C | T | 6 | a0001c0001t0001g0216a0002c0002t0003g0044a0002c0002t0003g0098others(3): Show | 6 | HG02055.hp2 HG02145.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1042-4530G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51015024 | ||||||
| chr14:51015042
|
C | T | 1 | a0002c0002t0006g0223 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1042-4548G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51015042 | ||||||
| chr14:51015156
|
T | G | 92 | a0001c0001t0001g0028a0001c0001t0001g0122a0001c0001t0001g0132others(89): Show | 96 | HG00280.hp1 HG00438.hp1 HG00639.hp1 others(93): Show |
intron_variant | MODIFIER | c.1042-4662A>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51015156 | ||||||
| chr14:51015162
|
G | T | 140 | a0001c0001t0001g0062a0001c0001t0001g0206a0001c0001t0001g0287others(137): Show | 141 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.1042-4668C>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51015162 | ||||||
| chr14:51015194
|
T | C | 160 | a0001c0001t0001g0031a0001c0001t0001g0042a0001c0001t0001g0062others(157): Show | 161 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.1042-4700A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51015194 | ||||||
| chr14:51015239
|
G | A | 3 | a0001c0003t0007g0011a0001c0003t0007g0012a0001c0003t0007g0015 | 3 | HG01433.hp1 HG03579.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1042-4745C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51015239 | ||||||
| chr14:51015338
|
C | T | 7 | a0001c0001t0001g0031a0001c0001t0005g0032a0001c0001t0005g0033others(4): Show | 7 | HG02895.hp1 HG02897.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.1042-4844G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51015338 | ||||||
| chr14:51015354
|
A | C | 5 | a0001c0001t0002g0058a0001c0001t0002g0059a0001c0001t0002g0060others(2): Show | 5 | HG00642.hp2 HG00733.hp1 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.1042-4860T>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51015354 | ||||||
| chr14:51015379
|
A | G | 1 | a0002c0002t0011g0034 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1042-4885T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51015379 | ||||||
| chr14:51015381
|
G | T | 141 | a0001c0001t0001g0062a0001c0001t0001g0206a0001c0001t0001g0287others(138): Show | 142 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.1042-4887C>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51015381 | ||||||
| chr14:51015415
|
A | G | 12 | a0001c0001t0001g0042a0001c0001t0001g0103a0001c0001t0001g0216others(9): Show | 12 | HG02055.hp2 HG02145.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1042-4921T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51015415 | ||||||
| chr14:51015445
|
G | A | 31 | a0001c0001t0001g0062a0001c0001t0002g0037a0001c0001t0002g0056others(28): Show | 31 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.1042-4951C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51015445 | ||||||
| chr14:51015505
|
C | CT | 16 | a0001c0001t0001g0324a0001c0001t0003g0043a0001c0001t0003g0048others(13): Show | 16 | HG01099.hp1 HG01891.hp1 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.1042-5012dupA | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51015505 | ||||||
| chr14:51015505
|
C | CTT | 10 | a0001c0001t0001g0122a0001c0001t0001g0178a0001c0001t0001g0211others(7): Show | 10 | HG01175.hp2 HG01358.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1042-5013_1042-501 others(6): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51015505 | ||||||
| chr14:51015505
|
C | CTTTTCTT others(8): Show |
1 | a0001c0001t0001g0031 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1042-5012_1042-501 others(19): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51015505 | ||||||
| chr14:51015505
|
C | CTTTTTTT others(3): Show |
6 | a0001c0001t0001g0042a0001c0001t0001g0103a0001c0003t0001g0014others(3): Show | 6 | HG02145.hp2 HG02451.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1042-5021_1042-501 others(14): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51015505 | ||||||
| chr14:51015505
|
C | CTTTTTTT others(4): Show |
2 | a0002c0007t0001g0017a0002c0007t0011g0013 | 2 | HG02622.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1042-5022_1042-501 others(15): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51015505 | ||||||
| chr14:51015505
|
C | CTTTTTTT others(5): Show |
2 | a0001c0001t0001g0216a0002c0002t0003g0044 | 2 | HG02055.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1042-5023_1042-501 others(16): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51015505 | ||||||
| chr14:51015505
|
C | CTTTTTTT others(6): Show |
1 | a0002c0002t0003g0098 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1042-5024_1042-501 others(17): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51015505 | ||||||
| chr14:51015505
|
C | CTTTTTTT others(9): Show |
3 | a0001c0001t0005g0032a0001c0001t0005g0033a0002c0002t0008g0306 | 3 | HG02895.hp1 HG02897.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1042-5027_1042-501 others(20): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51015505 | ||||||
| chr14:51015505
|
C | CTTTTTTT others(12): Show |
1 | a0002c0002t0008g0325 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1042-5030_1042-501 others(23): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51015505 | ||||||
| chr14:51015505
|
C | CTTTTTTT others(14): Show |
1 | a0002c0002t0001g0247 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1042-5032_1042-501 others(25): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51015505 | ||||||
| chr14:51015505
|
C | CTTTTTTT others(19): Show |
1 | a0001c0001t0009g0096 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1042-5037_1042-501 others(30): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51015505 | ||||||
| chr14:51015505
|
CT | C | 40 | a0001c0001t0001g0132a0001c0001t0001g0205a0001c0001t0002g0073others(37): Show | 41 | HG00280.hp1 HG00438.hp1 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.1042-5012delA | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51015505 | ||||||
| chr14:51015505
|
CTTT | C | 38 | a0001c0001t0001g0062a0001c0001t0002g0037a0001c0001t0002g0052others(35): Show | 38 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.1042-5014_1042-501 others(7): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51015505 | ||||||
| chr14:51015505
|
CTTTT | C | 77 | a0001c0001t0001g0206a0001c0001t0001g0287a0001c0001t0002g0023others(74): Show | 77 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.1042-5015_1042-501 others(8): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51015505 | ||||||
| chr14:51015505
|
CTTTTT | C | 9 | a0001c0001t0002g0070a0001c0001t0002g0075a0001c0001t0002g0215others(6): Show | 10 | HG01168.hp1 HG02155.hp2 HG03710.hp2 others(7): Show |
intron_variant | MODIFIER | c.1042-5016_1042-501 others(9): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51015505 | ||||||
| chr14:51015505
|
CTTTTTTT others(4): Show |
C | 14 | a0001c0001t0002g0058a0001c0001t0002g0059a0001c0001t0002g0060others(11): Show | 14 | HG00642.hp2 HG00733.hp1 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.1042-5022_1042-501 others(15): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51015505 | ||||||
| chr14:51015510
|
T | C | 1 | a0002c0002t0001g0288 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1042-5016A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51015510 | ||||||
| chr14:51015781
|
C | T | 1 | a0001c0001t0001g0031 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1042-5287G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51015781 | ||||||
| chr14:51015842
|
T | A | 104 | a0001c0001t0001g0206a0001c0001t0001g0287a0001c0001t0002g0023others(101): Show | 104 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.1042-5348A>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51015842 | ||||||
| chr14:51015948
|
T | C | 26 | a0001c0001t0001g0310a0001c0001t0003g0271a0001c0001t0009g0301others(23): Show | 29 | HG00642.hp1 HG00735.hp2 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.1042-5454A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51015948 | ||||||
| chr14:51016013
|
C | T | 10 | a0001c0001t0001g0028a0001c0001t0001g0122a0001c0001t0001g0178others(7): Show | 10 | HG01099.hp1 HG01175.hp2 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.1042-5519G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51016013 | ||||||
| chr14:51016014
|
A | G | 1 | a0002c0002t0003g0106 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1042-5520T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51016014 | ||||||
| chr14:51016019
|
T | C | 146 | a0001c0001t0001g0062a0001c0001t0001g0206a0001c0001t0001g0287others(143): Show | 147 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.1042-5525A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51016019 | ||||||
| chr14:51016129
|
C | T | 1 | a0002c0002t0001g0024 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1042-5635G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51016129 | ||||||
| chr14:51016153
|
C | A | 1 | a0002c0002t0001g0072 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1042-5659G>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51016153 | ||||||
| chr14:51016165
|
A | G | 1 | a0002c0002t0001g0085 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1042-5671T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51016165 | ||||||
| chr14:51016263
|
G | A | 92 | a0001c0001t0001g0028a0001c0001t0001g0122a0001c0001t0001g0132others(89): Show | 96 | HG00280.hp1 HG00438.hp1 HG00639.hp1 others(93): Show |
intron_variant | MODIFIER | c.1042-5769C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51016263 | ||||||
| chr14:51016339
|
A | T | 1 | a0002c0002t0011g0034 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1042-5845T>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51016339 | ||||||
| chr14:51016373
|
C | T | 2 | a0001c0001t0004g0232a0002c0002t0013g0035 | 2 | HG00280.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.1042-5879G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51016373 | ||||||
| chr14:51016424
|
T | G | 2 | a0001c0001t0002g0052a0001c0001t0002g0270 | 2 | NA18941.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.1042-5930A>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51016424 | ||||||
| chr14:51016556
|
G | A | 258 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0042others(255): Show | 263 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.1042-6062C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51016556 | ||||||
| chr14:51016674
|
G | A | 1 | a0001c0001t0003g0309 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1041+6161C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51016674 | ||||||
| chr14:51016754
|
C | G | 142 | a0001c0001t0001g0062a0001c0001t0001g0206a0001c0001t0001g0287others(139): Show | 143 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.1041+6081G>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51016754 | ||||||
| chr14:51016886
|
C | T | 6 | a0002c0002t0006g0004a0002c0002t0006g0018a0002c0002t0006g0077others(3): Show | 7 | HG02155.hp2 HG03710.hp2 NA18991.hp2 others(4): Show |
intron_variant | MODIFIER | c.1041+5949G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51016886 | ||||||
| chr14:51017009
|
A | G | 3 | a0001c0001t0001g0103a0002c0002t0001g0303a0002c0007t0011g0013 | 3 | HG02451.hp2 HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1041+5826T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51017009 | ||||||
| chr14:51017512
|
G | A | 1 | a0002c0002t0001g0190 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1041+5323C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51017512 | ||||||
| chr14:51017587
|
G | A | 4 | a0001c0001t0003g0043a0001c0001t0003g0054a0001c0001t0003g0192others(1): Show | 4 | HG01975.hp2 HG01981.hp2 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.1041+5248C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51017587 | ||||||
| chr14:51017651
|
G | C | 4 | a0001c0001t0003g0043a0001c0001t0003g0054a0001c0001t0003g0192others(1): Show | 4 | HG01975.hp2 HG01981.hp2 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.1041+5184C>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51017651 | ||||||
| chr14:51017803
|
G | C | 1 | a0001c0001t0001g0031 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1041+5032C>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51017803 | ||||||
| chr14:51017886
|
C | T | 1 | a0002c0002t0001g0229 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1041+4949G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51017886 | ||||||
| chr14:51018000
|
TG | T | 92 | a0001c0001t0001g0028a0001c0001t0001g0122a0001c0001t0001g0132others(89): Show | 96 | HG00280.hp1 HG00438.hp1 HG00639.hp1 others(93): Show |
intron_variant | MODIFIER | c.1041+4834delC | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51018000 | ||||||
| chr14:51018097
|
G | A | 92 | a0001c0001t0001g0028a0001c0001t0001g0122a0001c0001t0001g0132others(89): Show | 96 | HG00280.hp1 HG00438.hp1 HG00639.hp1 others(93): Show |
intron_variant | MODIFIER | c.1041+4738C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51018097 | ||||||
| chr14:51018114
|
G | C | 2 | a0001c0001t0017g0036a0002c0002t0001g0307 | 2 | HG02818.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1041+4721C>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51018114 | ||||||
| chr14:51018336
|
TTCCTTCT others(5): Show |
T | 1 | a0002c0002t0001g0307 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1041+4487_1041+449 others(16): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51018336 | ||||||
| chr14:51018472
|
C | T | 4 | a0001c0001t0004g0126a0001c0001t0004g0232a0001c0001t0004g0241others(1): Show | 4 | HG00280.hp2 HG01168.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.1041+4363G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51018472 | ||||||
| chr14:51018477
|
C | T | 26 | a0001c0001t0001g0310a0001c0001t0003g0271a0001c0001t0009g0301others(23): Show | 29 | HG00642.hp1 HG00735.hp2 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.1041+4358G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51018477 | ||||||
| chr14:51018575
|
T | C | 56 | a0001c0001t0001g0132a0001c0001t0001g0205a0001c0001t0001g0324others(53): Show | 57 | HG00280.hp1 HG00438.hp1 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.1041+4260A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51018575 | ||||||
| chr14:51018581
|
G | T | 10 | a0001c0001t0001g0028a0001c0001t0001g0122a0001c0001t0001g0178others(7): Show | 10 | HG01099.hp1 HG01175.hp2 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.1041+4254C>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51018581 | ||||||
| chr14:51018692
|
G | A | 26 | a0001c0001t0001g0310a0001c0001t0003g0271a0001c0001t0009g0301others(23): Show | 29 | HG00642.hp1 HG00735.hp2 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.1041+4143C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51018692 | ||||||
| chr14:51018696
|
G | A | 1 | a0002c0002t0001g0184 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1041+4139C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51018696 | ||||||
| chr14:51018697
|
C | T | 146 | a0001c0001t0001g0062a0001c0001t0001g0206a0001c0001t0001g0287others(143): Show | 147 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.1041+4138G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51018697 | ||||||
| chr14:51018736
|
C | T | 4 | a0001c0001t0002g0037a0002c0004t0005g0256a0002c0004t0005g0312others(1): Show | 4 | HG02486.hp1 HG03195.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1041+4099G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51018736 | ||||||
| chr14:51018963
|
C | T | 1 | a0001c0001t0017g0036 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1041+3872G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51018963 | ||||||
| chr14:51018976
|
T | A | 146 | a0001c0001t0001g0062a0001c0001t0001g0206a0001c0001t0001g0287others(143): Show | 147 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.1041+3859A>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51018976 | ||||||
| chr14:51018990
|
A | G | 1 | a0002c0002t0001g0125 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1041+3845T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51018990 | ||||||
| chr14:51019064
|
T | C | 146 | a0001c0001t0001g0062a0001c0001t0001g0206a0001c0001t0001g0287others(143): Show | 147 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.1041+3771A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51019064 | ||||||
| chr14:51019205
|
G | A | 1 | a0002c0002t0001g0164 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1041+3630C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51019205 | ||||||
| chr14:51019220
|
G | A | 1 | a0001c0001t0002g0150 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1041+3615C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51019220 | ||||||
| chr14:51019223
|
C | G | 260 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0042others(257): Show | 265 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.1041+3612G>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51019223 | ||||||
| chr14:51019369
|
T | C | 1 | a0001c0001t0004g0253 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1041+3466A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51019369 | ||||||
| chr14:51019405
|
A | G | 146 | a0001c0001t0001g0062a0001c0001t0001g0206a0001c0001t0001g0287others(143): Show | 147 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.1041+3430T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51019405 | ||||||
| chr14:51019566
|
T | C | 2 | a0001c0001t0009g0038a0002c0002t0010g0330 | 2 | HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1041+3269A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51019566 | ||||||
| chr14:51019674
|
A | G | 6 | a0001c0001t0005g0032a0001c0001t0005g0033a0001c0001t0009g0096others(3): Show | 6 | HG02895.hp1 HG02897.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1041+3161T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51019674 | ||||||
| chr14:51019889
|
C | T | 1 | a0001c0001t0002g0235 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1041+2946G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51019889 | ||||||
| chr14:51019970
|
C | T | 248 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0062others(245): Show | 253 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(250): Show |
intron_variant | MODIFIER | c.1041+2865G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51019970 | ||||||
| chr14:51020286
|
C | T | 138 | a0001c0001t0001g0062a0001c0001t0001g0206a0001c0001t0001g0287others(135): Show | 139 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.1041+2549G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51020286 | ||||||
| chr14:51020426
|
G | A | 1 | a0001c0001t0001g0031 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1041+2409C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51020426 | ||||||
| chr14:51020466
|
T | C | 1 | a0002c0002t0001g0185 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1041+2369A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51020466 | ||||||
| chr14:51020534
|
G | A | 1 | a0001c0001t0003g0082 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1041+2301C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51020534 | ||||||
| chr14:51020636
|
C | T | 42 | a0001c0001t0001g0062a0001c0001t0002g0037a0001c0001t0002g0056others(39): Show | 43 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.1041+2199G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51020636 | ||||||
| chr14:51020781
|
G | C | 30 | a0001c0001t0001g0062a0001c0001t0002g0037a0001c0001t0002g0056others(27): Show | 30 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(27): Show |
intron_variant | MODIFIER | c.1041+2054C>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51020781 | ||||||
| chr14:51020890
|
C | T | 42 | a0001c0001t0001g0062a0001c0001t0002g0037a0001c0001t0002g0056others(39): Show | 43 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.1041+1945G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51020890 | ||||||
| chr14:51020973
|
G | T | 1 | a0002c0002t0001g0039 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1041+1862C>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51020973 | ||||||
| chr14:51021125
|
T | C | 6 | a0001c0001t0004g0099a0001c0001t0004g0100a0001c0001t0004g0101others(3): Show | 6 | HG01261.hp1 HG02572.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1041+1710A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51021125 | ||||||
| chr14:51021227
|
G | A | 1 | a0001c0001t0002g0023 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1041+1608C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51021227 | ||||||
| chr14:51021296
|
C | T | 1 | a0001c0001t0004g0138 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1041+1539G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51021296 | ||||||
| chr14:51021387
|
C | T | 4 | a0001c0001t0004g0126a0001c0001t0004g0232a0001c0001t0004g0241others(1): Show | 4 | HG00280.hp2 HG01168.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.1041+1448G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51021387 | ||||||
| chr14:51021412
|
C | T | 2 | a0002c0002t0003g0117a0002c0002t0003g0118 | 2 | NA18984.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.1041+1423G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51021412 | ||||||
| chr14:51021633
|
T | G | 1 | a0002c0002t0001g0024 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1041+1202A>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51021633 | ||||||
| chr14:51021848
|
G | T | 1 | a0002c0002t0016g0076 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1041+987C>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51021848 | ||||||
| chr14:51021992
|
AT | A | 42 | a0001c0001t0001g0062a0001c0001t0002g0037a0001c0001t0002g0056others(39): Show | 43 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.1041+842delA | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51021992 | ||||||
| chr14:51022068
|
C | A | 42 | a0001c0001t0001g0062a0001c0001t0002g0037a0001c0001t0002g0056others(39): Show | 43 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.1041+767G>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51022068 | ||||||
| chr14:51022243
|
T | C | 56 | a0001c0001t0001g0132a0001c0001t0001g0205a0001c0001t0001g0324others(53): Show | 57 | HG00280.hp1 HG00438.hp1 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.1041+592A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51022243 | ||||||
| chr14:51022313
|
T | A | 1 | a0002c0002t0001g0243 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1041+522A>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51022313 | ||||||
| chr14:51022314
|
T | G | 1 | a0002c0002t0001g0003 | 2 | NA18969.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.1041+521A>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51022314 | ||||||
| chr14:51022724
|
G | A | 42 | a0001c0001t0001g0062a0001c0001t0002g0037a0001c0001t0002g0056others(39): Show | 43 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.1041+111C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51022724 | ||||||
| chr14:51022735
|
C | T | 1 | a0002c0002t0016g0076 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1041+100G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 3/12 | chr14 | 51022735 | ||||||
| chr14:51023160
|
T | C | 2 | a0001c0001t0001g0028a0005c0011t0001g0315 | 2 | HG02717.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.919-203A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 2/12 | chr14 | 51023160 | ||||||
| chr14:51023169
|
C | T | 46 | a0001c0001t0001g0062a0001c0001t0002g0037a0001c0001t0002g0056others(43): Show | 47 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.919-212G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 2/12 | chr14 | 51023169 | ||||||
| chr14:51023494
|
A | G | 6 | a0001c0001t0005g0032a0001c0001t0005g0033a0001c0001t0009g0096others(3): Show | 6 | HG02895.hp1 HG02897.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.919-537T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 2/12 | chr14 | 51023494 | ||||||
| chr14:51023555
|
C | G | 6 | a0001c0001t0005g0032a0001c0001t0005g0033a0001c0001t0009g0096others(3): Show | 6 | HG02895.hp1 HG02897.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.919-598G>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 2/12 | chr14 | 51023555 | ||||||
| chr14:51023632
|
C | A | 30 | a0001c0001t0001g0062a0001c0001t0002g0037a0001c0001t0002g0056others(27): Show | 30 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(27): Show |
intron_variant | MODIFIER | c.919-675G>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 2/12 | chr14 | 51023632 | ||||||
| chr14:51023944
|
T | A | 1 | a0002c0002t0011g0034 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.919-987A>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 2/12 | chr14 | 51023944 | ||||||
| chr14:51023971
|
G | A | 1 | a0001c0001t0002g0023 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.919-1014C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 2/12 | chr14 | 51023971 | ||||||
| chr14:51024049
|
G | A | 44 | a0001c0001t0001g0028a0001c0001t0001g0122a0001c0001t0001g0178others(41): Show | 47 | HG00642.hp1 HG00735.hp2 HG01069.hp2 others(44): Show |
intron_variant | MODIFIER | c.919-1092C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 2/12 | chr14 | 51024049 | ||||||
| chr14:51024171
|
T | G | 1 | a0002c0002t0001g0207 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.918+1094A>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 2/12 | chr14 | 51024171 | ||||||
| chr14:51024223
|
G | A | 3 | a0002c0002t0003g0172a0002c0002t0003g0177a0002c0002t0003g0249 | 3 | HG03195.hp1 HG03516.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.918+1042C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 2/12 | chr14 | 51024223 | ||||||
| chr14:51024226
|
C | T | 42 | a0001c0001t0001g0062a0001c0001t0002g0037a0001c0001t0002g0056others(39): Show | 43 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.918+1039G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 2/12 | chr14 | 51024226 | ||||||
| chr14:51024285
|
T | C | 2 | a0001c0001t0003g0049a0001c0001t0003g0068 | 2 | HG00140.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.918+980A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 2/12 | chr14 | 51024285 | ||||||
| chr14:51024536
|
G | C | 1 | a0001c0001t0001g0031 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.918+729C>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 2/12 | chr14 | 51024536 | ||||||
| chr14:51024691
|
A | G | 45 | a0001c0001t0001g0178a0001c0001t0001g0205a0001c0001t0001g0324others(42): Show | 46 | HG00438.hp1 HG00639.hp1 HG01109.hp1 others(43): Show |
intron_variant | MODIFIER | c.918+574T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 2/12 | chr14 | 51024691 | ||||||
| chr14:51024738
|
T | C | 46 | a0001c0001t0001g0178a0001c0001t0001g0205a0001c0001t0001g0324others(43): Show | 47 | HG00438.hp1 HG00639.hp1 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.918+527A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 2/12 | chr14 | 51024738 | ||||||
| chr14:51024919
|
T | G | 2 | a0001c0001t0001g0216a0002c0002t0003g0044 | 2 | HG02055.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.918+346A>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 2/12 | chr14 | 51024919 | ||||||
| chr14:51024930
|
A | G | 68 | a0001c0001t0001g0062a0001c0001t0001g0122a0001c0001t0001g0132others(65): Show | 68 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.918+335T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 2/12 | chr14 | 51024930 | ||||||
| chr14:51024979
|
G | T | 2 | a0001c0001t0009g0096a0002c0002t0001g0307 | 2 | HG02818.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.918+286C>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 2/12 | chr14 | 51024979 | ||||||
| chr14:51025128
|
T | A | 1 | a0001c0001t0003g0170 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.918+137A>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 2/12 | chr14 | 51025128 | ||||||
| chr14:51025221
|
G | A | 1 | a0002c0002t0001g0003 | 2 | NA18969.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.918+44C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 2/12 | chr14 | 51025221 | ||||||
| chr14:51025238
|
T | C | 143 | a0001c0001t0001g0062a0001c0001t0001g0132a0001c0001t0001g0206others(140): Show | 143 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.918+27A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 2/12 | chr14 | 51025238 | ||||||
| chr14:51025417
|
C | CCACACAG others(7): Show |
254 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0042others(251): Show | 258 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(255): Show |
intron_variant | MODIFIER | c.823-58_823-57insAA others(12): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51025417 | ||||||
| chr14:51025426
|
C | T | 1 | a0002c0002t0008g0325 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.823-66G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51025426 | ||||||
| chr14:51025698
|
T | C | 1 | a0002c0002t0003g0098 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.823-338A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51025698 | ||||||
| chr14:51025759
|
G | GAT | 131 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0042others(128): Show | 134 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(131): Show |
intron_variant | MODIFIER | c.823-400_823-399ins others(2): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51025759 | ||||||
| chr14:51025773
|
A | G | 1 | a0001c0001t0001g0031 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.823-413T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51025773 | ||||||
| chr14:51025810
|
T | C | 81 | a0001c0001t0001g0042a0001c0001t0001g0062a0001c0001t0001g0103others(78): Show | 81 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.823-450A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51025810 | ||||||
| chr14:51025871
|
C | T | 3 | a0002c0002t0004g0212a0002c0002t0004g0304a0002c0002t0004g0321 | 3 | HG02145.hp2 HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.823-511G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51025871 | ||||||
| chr14:51025886
|
C | T | 1 | a0002c0002t0001g0021 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.823-526G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51025886 | ||||||
| chr14:51025946
|
T | C | 247 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0042others(244): Show | 251 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(248): Show |
intron_variant | MODIFIER | c.823-586A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51025946 | ||||||
| chr14:51025952
|
G | A | 1 | a0002c0002t0001g0124 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.823-592C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51025952 | ||||||
| chr14:51025967
|
G | T | 14 | a0001c0001t0001g0122a0001c0001t0001g0178a0001c0001t0001g0287others(11): Show | 14 | HG01099.hp1 HG01358.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.823-607C>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51025967 | ||||||
| chr14:51026012
|
A | T | 2 | a0002c0004t0005g0298a0002c0004t0005g0311 | 2 | HG03041.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.823-652T>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51026012 | ||||||
| chr14:51026053
|
T | C | 255 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0042others(252): Show | 259 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.823-693A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51026053 | ||||||
| chr14:51026085
|
C | T | 1 | a0001c0001t0004g0314 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.823-725G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51026085 | ||||||
| chr14:51026104
|
C | T | 1 | a0001c0001t0002g0087 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.823-744G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51026104 | ||||||
| chr14:51026108
|
C | T | 1 | a0002c0002t0010g0330 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.823-748G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51026108 | ||||||
| chr14:51026111
|
C | G | 248 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0042others(245): Show | 252 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(249): Show |
intron_variant | MODIFIER | c.823-751G>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51026111 | ||||||
| chr14:51026214
|
C | A | 1 | a0002c0002t0006g0018 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.823-854G>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51026214 | ||||||
| chr14:51026218
|
A | T | 3 | a0002c0002t0003g0172a0002c0002t0003g0177a0002c0002t0003g0249 | 3 | HG03195.hp1 HG03516.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.823-858T>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51026218 | ||||||
| chr14:51026243
|
C | T | 241 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0062others(238): Show | 245 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(242): Show |
intron_variant | MODIFIER | c.823-883G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51026243 | ||||||
| chr14:51026618
|
C | G | 1 | a0001c0001t0002g0272 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.823-1258G>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51026618 | ||||||
| chr14:51026666
|
T | A | 17 | a0001c0001t0001g0103a0001c0001t0001g0205a0001c0001t0002g0187others(14): Show | 17 | HG01261.hp1 HG01358.hp2 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.823-1306A>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51026666 | ||||||
| chr14:51026686
|
G | A | 14 | a0001c0001t0001g0103a0001c0001t0001g0205a0001c0001t0002g0187others(11): Show | 14 | HG01261.hp1 HG01358.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.823-1326C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51026686 | ||||||
| chr14:51026704
|
TATGCACA others(4): Show |
T | 1 | a0001c0001t0001g0031 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.823-1355_823-1345d others(13): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51026704 | ||||||
| chr14:51026754
|
T | C | 4 | a0001c0001t0002g0199a0001c0001t0002g0283a0001c0001t0002g0284others(1): Show | 4 | NA18974.hp2 NA18983.hp2 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.823-1394A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51026754 | ||||||
| chr14:51026757
|
G | GC | 14 | a0001c0001t0001g0042a0001c0001t0001g0216a0001c0001t0001g0287others(11): Show | 14 | HG01884.hp1 HG02055.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.823-1398_823-1397i others(3): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51026757 | ||||||
| chr14:51026844
|
G | A | 10 | a0001c0001t0002g0159a0001c0001t0003g0257a0001c0001t0003g0271others(7): Show | 12 | HG00140.hp1 HG00733.hp2 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.823-1484C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51026844 | ||||||
| chr14:51026854
|
C | T | 12 | a0001c0001t0001g0132a0001c0001t0004g0126a0001c0001t0004g0241others(9): Show | 12 | HG01168.hp2 HG01361.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.823-1494G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51026854 | ||||||
| chr14:51026871
|
T | C | 1 | a0001c0001t0005g0027 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.823-1511A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51026871 | ||||||
| chr14:51026944
|
T | A | 152 | a0001c0001t0001g0103a0001c0001t0001g0205a0001c0001t0001g0206others(149): Show | 157 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.823-1584A>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51026944 | ||||||
| chr14:51027106
|
C | T | 83 | a0001c0001t0001g0031a0001c0001t0001g0042a0001c0001t0001g0103others(80): Show | 84 | HG00438.hp1 HG01256.hp1 HG01258.hp1 others(81): Show |
intron_variant | MODIFIER | c.823-1746G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51027106 | ||||||
| chr14:51027132
|
CT | C | 25 | a0001c0001t0001g0211a0001c0001t0002g0055a0001c0001t0002g0153others(22): Show | 26 | HG00597.hp1 HG00621.hp1 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.823-1773delA | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51027132 | ||||||
| chr14:51027132
|
CTT | C | 15 | a0001c0001t0002g0141a0001c0001t0002g0154a0001c0001t0002g0187others(12): Show | 15 | HG00438.hp2 HG00738.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.823-1774_823-1773d others(4): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51027132 | ||||||
| chr14:51027132
|
CTTT | C | 75 | a0001c0001t0001g0062a0001c0001t0001g0179a0001c0001t0001g0206others(72): Show | 76 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.823-1775_823-1773d others(5): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51027132 | ||||||
| chr14:51027132
|
CTTTT | C | 25 | a0001c0001t0001g0028a0001c0001t0001g0178a0001c0001t0002g0052others(22): Show | 25 | HG00639.hp1 HG00642.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.823-1776_823-1773d others(6): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51027132 | ||||||
| chr14:51027132
|
CTTTTT | C | 43 | a0001c0001t0001g0132a0001c0001t0002g0053a0001c0001t0002g0056others(40): Show | 43 | HG00280.hp2 HG00544.hp2 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.823-1777_823-1773d others(7): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51027132 | ||||||
| chr14:51027132
|
CTTTTTTT others(2): Show |
C | 114 | a0001c0001t0001g0031a0001c0001t0001g0042a0001c0001t0001g0103others(111): Show | 121 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.823-1781_823-1773d others(11): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51027132 | ||||||
| chr14:51027132
|
CTTTTTTT others(3): Show |
C | 14 | a0001c0001t0001g0216a0001c0001t0003g0317a0001c0001t0005g0033others(11): Show | 14 | HG01891.hp2 HG02145.hp2 HG02895.hp1 others(11): Show |
intron_variant | MODIFIER | c.823-1782_823-1773d others(12): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51027132 | ||||||
| chr14:51027132
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0003g0297 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.823-1783_823-1773d others(13): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51027132 | ||||||
| chr14:51027139
|
T | A | 1 | a0002c0002t0003g0098 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.823-1779A>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51027139 | ||||||
| chr14:51027243
|
A | G | 219 | a0001c0001t0001g0031a0001c0001t0001g0042a0001c0001t0001g0062others(216): Show | 225 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.823-1883T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51027243 | ||||||
| chr14:51027261
|
A | C | 220 | a0001c0001t0001g0031a0001c0001t0001g0042a0001c0001t0001g0062others(217): Show | 226 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.823-1901T>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51027261 | ||||||
| chr14:51027262
|
G | A | 1 | a0002c0002t0003g0029 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.823-1902C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51027262 | ||||||
| chr14:51027303
|
C | T | 6 | a0001c0001t0005g0026a0002c0002t0001g0313a0002c0002t0003g0106others(3): Show | 6 | HG02615.hp1 HG02647.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.823-1943G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51027303 | ||||||
| chr14:51027510
|
G | A | 48 | a0001c0001t0002g0023a0001c0001t0002g0070a0001c0001t0002g0075others(45): Show | 51 | HG00280.hp2 HG00408.hp2 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.823-2150C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51027510 | ||||||
| chr14:51027580
|
T | C | 331 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0042others(328): Show | 341 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.823-2220A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51027580 | ||||||
| chr14:51027682
|
T | C | 1 | a0001c0003t0007g0012 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.823-2322A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51027682 | ||||||
| chr14:51027727
|
C | A | 1 | a0002c0002t0001g0295 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.823-2367G>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51027727 | ||||||
| chr14:51027732
|
G | C | 2 | a0001c0001t0002g0316a0002c0002t0001g0307 | 2 | HG01243.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.823-2372C>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51027732 | ||||||
| chr14:51027781
|
T | A | 133 | a0001c0001t0001g0028a0001c0001t0001g0042a0001c0001t0001g0103others(130): Show | 137 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.823-2421A>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51027781 | ||||||
| chr14:51027837
|
C | CT | 129 | a0001c0001t0001g0028a0001c0001t0001g0042a0001c0001t0001g0103others(126): Show | 133 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.823-2478dupA | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51027837 | ||||||
| chr14:51027905
|
C | G | 1 | a0002c0010t0005g0016 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.823-2545G>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51027905 | ||||||
| chr14:51027936
|
A | C | 70 | a0001c0001t0001g0103a0001c0001t0001g0205a0001c0001t0001g0216others(67): Show | 73 | HG00280.hp2 HG00408.hp2 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.823-2576T>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51027936 | ||||||
| chr14:51027950
|
A | G | 133 | a0001c0001t0001g0028a0001c0001t0001g0042a0001c0001t0001g0103others(130): Show | 137 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.823-2590T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51027950 | ||||||
| chr14:51027987
|
C | G | 1 | a0001c0001t0001g0277 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.823-2627G>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51027987 | ||||||
| chr14:51028252
|
T | TA | 144 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0042others(141): Show | 149 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(146): Show |
intron_variant | MODIFIER | c.823-2893dupT | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51028252 | ||||||
| chr14:51028330
|
T | C | 3 | a0002c0002t0001g0123a0002c0002t0001g0124a0002c0002t0001g0188 | 3 | HG02602.hp2 HG03669.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.823-2970A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51028330 | ||||||
| chr14:51028349
|
A | G | 34 | a0001c0001t0001g0028a0001c0001t0001g0103a0001c0001t0001g0178others(31): Show | 34 | HG01261.hp1 HG01433.hp1 HG01496.hp1 others(31): Show |
intron_variant | MODIFIER | c.823-2989T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51028349 | ||||||
| chr14:51028403
|
T | A | 129 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0103others(126): Show | 134 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.823-3043A>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51028403 | ||||||
| chr14:51028413
|
A | G | 129 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0103others(126): Show | 134 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.823-3053T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51028413 | ||||||
| chr14:51028680
|
G | A | 240 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0042others(237): Show | 247 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.823-3320C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51028680 | ||||||
| chr14:51028714
|
A | G | 1 | a0002c0002t0001g0134 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.823-3354T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51028714 | ||||||
| chr14:51028721
|
T | C | 149 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0042others(146): Show | 154 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.823-3361A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51028721 | ||||||
| chr14:51028803
|
A | G | 124 | a0001c0001t0001g0028a0001c0001t0001g0122a0001c0001t0001g0178others(121): Show | 128 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.823-3443T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51028803 | ||||||
| chr14:51028818
|
G | A | 12 | a0001c0001t0001g0031a0001c0001t0002g0141a0001c0001t0003g0006others(9): Show | 13 | HG00738.hp1 HG01099.hp1 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.823-3458C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51028818 | ||||||
| chr14:51028856
|
A | G | 22 | a0001c0001t0001g0031a0001c0001t0002g0141a0001c0001t0003g0006others(19): Show | 23 | HG00738.hp1 HG01099.hp1 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.823-3496T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51028856 | ||||||
| chr14:51028956
|
A | G | 48 | a0001c0001t0001g0042a0001c0001t0001g0122a0001c0001t0002g0037others(45): Show | 49 | HG00438.hp1 HG01256.hp1 HG01258.hp1 others(46): Show |
intron_variant | MODIFIER | c.823-3596T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51028956 | ||||||
| chr14:51028980
|
C | G | 253 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0042others(250): Show | 260 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.823-3620G>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51028980 | ||||||
| chr14:51029082
|
T | C | 241 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0042others(238): Show | 248 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.823-3722A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51029082 | ||||||
| chr14:51029098
|
A | C | 1 | a0001c0001t0003g0309 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.823-3738T>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51029098 | ||||||
| chr14:51029148
|
T | C | 1 | a0002c0002t0001g0051 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.823-3788A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51029148 | ||||||
| chr14:51029168
|
T | G | 4 | a0001c0001t0001g0216a0001c0001t0002g0316a0002c0002t0001g0307others(1): Show | 4 | HG01243.hp1 HG02818.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.823-3808A>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51029168 | ||||||
| chr14:51029178
|
C | A | 157 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0042others(154): Show | 162 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.823-3818G>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51029178 | ||||||
| chr14:51029239
|
C | A | 1 | a0001c0001t0002g0217 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.823-3879G>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51029239 | ||||||
| chr14:51029303
|
T | C | 117 | a0001c0001t0001g0028a0001c0001t0001g0178a0001c0001t0001g0179others(114): Show | 119 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.823-3943A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51029303 | ||||||
| chr14:51029386
|
T | G | 44 | a0001c0001t0001g0031a0001c0001t0001g0122a0001c0001t0002g0045others(41): Show | 46 | HG00438.hp1 HG00738.hp1 HG01099.hp1 others(43): Show |
intron_variant | MODIFIER | c.823-4026A>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51029386 | ||||||
| chr14:51029453
|
A | G | 6 | a0001c0001t0001g0216a0001c0001t0002g0316a0001c0001t0009g0096others(3): Show | 6 | HG01243.hp1 HG02572.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.823-4093T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51029453 | ||||||
| chr14:51029484
|
T | C | 46 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0178others(43): Show | 47 | HG00738.hp1 HG01099.hp1 HG01255.hp2 others(44): Show |
intron_variant | MODIFIER | c.823-4124A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51029484 | ||||||
| chr14:51029493
|
T | C | 10 | a0001c0001t0004g0148a0001c0001t0009g0096a0002c0002t0001g0288others(7): Show | 10 | HG02109.hp1 HG02451.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.823-4133A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51029493 | ||||||
| chr14:51029564
|
T | A | 3 | a0001c0001t0002g0259a0001c0001t0002g0273a0002c0002t0001g0128 | 3 | HG00438.hp2 HG02074.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.823-4204A>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51029564 | ||||||
| chr14:51029624
|
G | GTGTAAGC others(16): Show |
4 | a0001c0001t0001g0216a0001c0001t0002g0316a0002c0002t0001g0307others(1): Show | 4 | HG01243.hp1 HG02818.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.823-4287_823-4265d others(25): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51029624 | ||||||
| chr14:51029627
|
T | C | 1 | a0001c0001t0003g0084 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.823-4267A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51029627 | ||||||
| chr14:51029776
|
CT | C | 83 | a0001c0001t0001g0179a0001c0001t0001g0206a0001c0001t0001g0277others(80): Show | 85 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.823-4417delA | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51029776 | ||||||
| chr14:51029803
|
C | T | 44 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0178others(41): Show | 45 | HG00738.hp1 HG01099.hp1 HG01255.hp2 others(42): Show |
intron_variant | MODIFIER | c.823-4443G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51029803 | ||||||
| chr14:51029866
|
A | C | 13 | a0001c0001t0001g0042a0001c0001t0002g0037a0001c0001t0009g0038others(10): Show | 13 | HG01891.hp2 HG02145.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.823-4506T>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51029866 | ||||||
| chr14:51029873
|
G | C | 2 | a0001c0001t0004g0232a0002c0002t0001g0236 | 2 | HG00280.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.823-4513C>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51029873 | ||||||
| chr14:51030242
|
T | C | 1 | a0001c0001t0003g0170 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.823-4882A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51030242 | ||||||
| chr14:51030274
|
G | A | 7 | a0001c0001t0001g0103a0001c0001t0004g0099a0001c0001t0004g0100others(4): Show | 7 | HG01261.hp1 HG02451.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.823-4914C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51030274 | ||||||
| chr14:51030480
|
C | T | 3 | a0002c0002t0001g0123a0002c0002t0001g0124a0002c0002t0001g0188 | 3 | HG02602.hp2 HG03669.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.823-5120G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51030480 | ||||||
| chr14:51030583
|
T | A | 1 | a0002c0002t0003g0281 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.823-5223A>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51030583 | ||||||
| chr14:51030586
|
G | GGT | 12 | a0001c0001t0001g0031a0001c0001t0002g0141a0001c0001t0003g0006others(9): Show | 13 | HG00738.hp1 HG01099.hp1 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.823-5228_823-5227d others(4): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51030586 | ||||||
| chr14:51030610
|
T | C | 12 | a0001c0001t0001g0031a0001c0001t0002g0141a0001c0001t0003g0006others(9): Show | 13 | HG00738.hp1 HG01099.hp1 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.823-5250A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51030610 | ||||||
| chr14:51030636
|
T | C | 1 | a0001c0001t0002g0150 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.823-5276A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51030636 | ||||||
| chr14:51030698
|
T | C | 12 | a0001c0001t0001g0031a0001c0001t0002g0141a0001c0001t0003g0006others(9): Show | 13 | HG00738.hp1 HG01099.hp1 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.823-5338A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51030698 | ||||||
| chr14:51030927
|
A | G | 1 | a0002c0002t0001g0263 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.823-5567T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51030927 | ||||||
| chr14:51031021
|
G | A | 1 | a0002c0002t0001g0295 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.823-5661C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51031021 | ||||||
| chr14:51031111
|
G | C | 1 | a0002c0002t0001g0190 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.823-5751C>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51031111 | ||||||
| chr14:51031125
|
G | C | 1 | a0002c0002t0001g0190 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.823-5765C>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51031125 | ||||||
| chr14:51031147
|
C | CA | 176 | a0001c0001t0001g0042a0001c0001t0001g0062a0001c0001t0001g0103others(173): Show | 183 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(180): Show |
intron_variant | MODIFIER | c.823-5788dupT | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51031147 | ||||||
| chr14:51031147
|
C | CAA | 92 | a0001c0001t0001g0179a0001c0001t0001g0206a0001c0001t0001g0277others(89): Show | 95 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.823-5789_823-5788d others(4): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51031147 | ||||||
| chr14:51031166
|
G | A | 1 | a0001c0001t0001g0211 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.823-5806C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51031166 | ||||||
| chr14:51031167
|
A | G | 1 | a0001c0001t0001g0211 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.823-5807T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51031167 | ||||||
| chr14:51031175
|
G | A | 1 | a0001c0001t0001g0211 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.823-5815C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51031175 | ||||||
| chr14:51031176
|
A | AAAAG | 7 | a0001c0001t0002g0070a0001c0001t0002g0075a0001c0001t0003g0006others(4): Show | 8 | HG00738.hp1 HG01255.hp2 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.823-5820_823-5817d others(6): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51031176 | ||||||
| chr14:51031176
|
A | G | 1 | a0001c0001t0001g0211 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.823-5816T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51031176 | ||||||
| chr14:51031213
|
A | T | 4 | a0001c0001t0001g0122a0002c0002t0001g0021a0002c0002t0001g0022others(1): Show | 4 | HG01358.hp1 HG02895.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.823-5853T>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51031213 | ||||||
| chr14:51031233
|
G | A | 10 | a0001c0001t0001g0103a0001c0001t0001g0310a0001c0001t0004g0099others(7): Show | 10 | HG01261.hp1 HG02451.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.823-5873C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51031233 | ||||||
| chr14:51031381
|
C | T | 247 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0042others(244): Show | 254 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.823-6021G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51031381 | ||||||
| chr14:51031759
|
A | G | 18 | a0001c0001t0001g0324a0001c0001t0002g0283a0001c0001t0002g0284others(15): Show | 18 | HG00423.hp2 HG02135.hp1 HG02723.hp1 others(15): Show |
intron_variant | MODIFIER | c.823-6399T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51031759 | ||||||
| chr14:51031819
|
G | A | 33 | a0001c0001t0001g0122a0001c0001t0002g0045a0001c0001t0002g0108others(30): Show | 34 | HG00408.hp2 HG00438.hp1 HG01256.hp1 others(31): Show |
intron_variant | MODIFIER | c.823-6459C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51031819 | ||||||
| chr14:51031908
|
C | G | 32 | a0001c0001t0002g0070a0001c0001t0002g0075a0001c0001t0002g0087others(29): Show | 35 | HG00280.hp2 HG00642.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.823-6548G>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51031908 | ||||||
| chr14:51031909
|
T | TATTAGTA | 32 | a0001c0001t0002g0070a0001c0001t0002g0075a0001c0001t0002g0087others(29): Show | 35 | HG00280.hp2 HG00642.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.823-6550_823-6549i others(9): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51031909 | ||||||
| chr14:51031910
|
C | T | 32 | a0001c0001t0002g0070a0001c0001t0002g0075a0001c0001t0002g0087others(29): Show | 35 | HG00280.hp2 HG00642.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.823-6550G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51031910 | ||||||
| chr14:51031961
|
G | A | 1 | a0001c0001t0004g0126 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.823-6601C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51031961 | ||||||
| chr14:51032009
|
C | T | 1 | a0001c0001t0001g0211 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.823-6649G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51032009 | ||||||
| chr14:51032012
|
T | C | 1 | a0001c0001t0001g0211 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.823-6652A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51032012 | ||||||
| chr14:51032113
|
T | G | 2 | a0001c0001t0009g0096a0002c0002t0003g0029 | 2 | HG02572.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.823-6753A>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51032113 | ||||||
| chr14:51032136
|
T | G | 1 | a0002c0002t0006g0018 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.823-6776A>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51032136 | ||||||
| chr14:51032158
|
G | T | 2 | a0001c0001t0002g0156a0001c0001t0002g0157 | 2 | HG01167.hp2 HG01928.hp1 |
intron_variant | MODIFIER | c.823-6798C>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51032158 | ||||||
| chr14:51032247
|
A | C | 1 | a0002c0002t0001g0025 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.823-6887T>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51032247 | ||||||
| chr14:51032440
|
C | A | 1 | a0001c0001t0001g0211 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.823-7080G>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51032440 | ||||||
| chr14:51032626
|
C | A | 32 | a0001c0001t0002g0070a0001c0001t0002g0075a0001c0001t0002g0087others(29): Show | 35 | HG00280.hp2 HG00642.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.823-7266G>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51032626 | ||||||
| chr14:51032685
|
G | A | 4 | a0001c0001t0005g0032a0001c0001t0005g0033a0002c0002t0008g0325others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.823-7325C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51032685 | ||||||
| chr14:51032839
|
C | T | 2 | a0001c0001t0005g0026a0002c0002t0003g0098 | 2 | HG02615.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.823-7479G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51032839 | ||||||
| chr14:51033016
|
A | T | 2 | a0001c0001t0002g0176a0001c0001t0002g0186 | 2 | HG03490.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.823-7656T>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51033016 | ||||||
| chr14:51033047
|
C | T | 2 | a0001c0001t0002g0165a0002c0002t0001g0243 | 2 | HG02080.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.823-7687G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51033047 | ||||||
| chr14:51033217
|
T | C | 2 | a0001c0001t0009g0096a0002c0002t0003g0029 | 2 | HG02572.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.823-7857A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51033217 | ||||||
| chr14:51033241
|
T | C | 240 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0042others(237): Show | 247 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.823-7881A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51033241 | ||||||
| chr14:51033322
|
A | G | 32 | a0001c0001t0001g0122a0001c0001t0002g0108a0001c0001t0002g0110others(29): Show | 33 | HG00408.hp2 HG00438.hp1 HG01256.hp1 others(30): Show |
intron_variant | MODIFIER | c.823-7962T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51033322 | ||||||
| chr14:51033335
|
C | T | 1 | a0002c0002t0003g0098 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.823-7975G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51033335 | ||||||
| chr14:51033342
|
C | T | 1 | a0002c0002t0001g0162 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.823-7982G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51033342 | ||||||
| chr14:51033359
|
G | A | 18 | a0001c0001t0001g0324a0001c0001t0002g0283a0001c0001t0002g0284others(15): Show | 18 | HG00423.hp2 HG02135.hp1 HG02723.hp1 others(15): Show |
intron_variant | MODIFIER | c.823-7999C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51033359 | ||||||
| chr14:51033434
|
A | G | 1 | a0002c0002t0006g0018 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.823-8074T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51033434 | ||||||
| chr14:51033542
|
C | G | 1 | a0002c0002t0001g0114 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.823-8182G>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51033542 | ||||||
| chr14:51033619
|
C | T | 32 | a0001c0001t0001g0122a0001c0001t0002g0108a0001c0001t0002g0110others(29): Show | 33 | HG00408.hp2 HG00438.hp1 HG01256.hp1 others(30): Show |
intron_variant | MODIFIER | c.823-8259G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51033619 | ||||||
| chr14:51034147
|
G | T | 28 | a0001c0001t0002g0108a0001c0001t0002g0110a0001c0001t0002g0111others(25): Show | 29 | HG00408.hp2 HG00438.hp1 HG01256.hp1 others(26): Show |
intron_variant | MODIFIER | c.823-8787C>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51034147 | ||||||
| chr14:51034601
|
G | A | 3 | a0001c0001t0009g0096a0002c0002t0001g0166a0002c0002t0003g0029 | 3 | HG02572.hp1 HG03486.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.823-9241C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51034601 | ||||||
| chr14:51034725
|
C | T | 1 | a0001c0001t0009g0038 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.823-9365G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51034725 | ||||||
| chr14:51034899
|
T | C | 1 | a0002c0002t0006g0081 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.823-9539A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51034899 | ||||||
| chr14:51034945
|
C | A | 1 | a0001c0001t0002g0108 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.823-9585G>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51034945 | ||||||
| chr14:51034990
|
A | AG | 6 | a0001c0001t0002g0037a0001c0001t0002g0259a0001c0001t0002g0316others(3): Show | 6 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.823-9631dupC | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51034990 | ||||||
| chr14:51035042
|
TGAAAA | T | 32 | a0001c0001t0002g0070a0001c0001t0002g0075a0001c0001t0002g0087others(29): Show | 35 | HG00280.hp2 HG00642.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.823-9687_823-9683d others(7): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51035042 | ||||||
| chr14:51035051
|
C | G | 105 | a0001c0001t0001g0179a0001c0001t0001g0206a0001c0001t0001g0216others(102): Show | 108 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.823-9691G>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51035051 | ||||||
| chr14:51035091
|
T | C | 1 | a0002c0002t0006g0018 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.823-9731A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51035091 | ||||||
| chr14:51035295
|
C | A | 2 | a0002c0002t0001g0326a0002c0002t0002g0233 | 2 | HG01975.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.823-9935G>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51035295 | ||||||
| chr14:51035352
|
A | G | 189 | a0001c0001t0001g0122a0001c0001t0001g0179a0001c0001t0001g0206others(186): Show | 196 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.823-9992T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51035352 | ||||||
| chr14:51035563
|
G | GT | 4 | a0001c0001t0005g0032a0001c0001t0005g0033a0002c0002t0008g0325others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.823-10204dupA | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51035563 | ||||||
| chr14:51035583
|
G | A | 1 | a0001c0001t0002g0193 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.823-10223C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51035583 | ||||||
| chr14:51035612
|
C | T | 11 | a0001c0001t0002g0141a0001c0001t0003g0006a0001c0001t0003g0054others(8): Show | 12 | HG00738.hp1 HG01099.hp1 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.823-10252G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51035612 | ||||||
| chr14:51035623
|
C | G | 11 | a0001c0001t0001g0031a0001c0001t0001g0205a0001c0001t0001g0287others(8): Show | 11 | HG01433.hp1 HG01884.hp2 HG02129.hp2 others(8): Show |
intron_variant | MODIFIER | c.823-10263G>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51035623 | ||||||
| chr14:51035730
|
G | A | 11 | a0001c0001t0002g0141a0001c0001t0003g0006a0001c0001t0003g0054others(8): Show | 12 | HG00738.hp1 HG01099.hp1 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.823-10370C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51035730 | ||||||
| chr14:51035744
|
G | C | 2 | a0001c0001t0002g0308a0001c0001t0003g0309 | 2 | HG00741.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.823-10384C>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51035744 | ||||||
| chr14:51035875
|
C | T | 22 | a0001c0001t0001g0028a0001c0001t0001g0178a0001c0001t0002g0165others(19): Show | 22 | HG00639.hp1 HG00642.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.823-10515G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51035875 | ||||||
| chr14:51035933
|
A | G | 239 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0042others(236): Show | 246 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.823-10573T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51035933 | ||||||
| chr14:51036123
|
C | T | 331 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0042others(328): Show | 341 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.823-10763G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51036123 | ||||||
| chr14:51036266
|
T | G | 3 | a0001c0001t0009g0096a0002c0002t0003g0029a0002c0002t0006g0018 | 3 | HG02572.hp1 HG03486.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.823-10906A>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51036266 | ||||||
| chr14:51036295
|
T | C | 18 | a0001c0001t0001g0324a0001c0001t0002g0283a0001c0001t0002g0284others(15): Show | 18 | HG00423.hp2 HG02135.hp1 HG02723.hp1 others(15): Show |
intron_variant | MODIFIER | c.823-10935A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51036295 | ||||||
| chr14:51036320
|
G | A | 2 | a0001c0001t0004g0148a0002c0004t0005g0149 | 2 | HG02109.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.823-10960C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51036320 | ||||||
| chr14:51036335
|
C | T | 18 | a0001c0001t0001g0324a0001c0001t0002g0283a0001c0001t0002g0284others(15): Show | 18 | HG00423.hp2 HG02135.hp1 HG02723.hp1 others(15): Show |
intron_variant | MODIFIER | c.823-10975G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51036335 | ||||||
| chr14:51036581
|
T | C | 11 | a0001c0001t0002g0141a0001c0001t0003g0006a0001c0001t0003g0054others(8): Show | 12 | HG00738.hp1 HG01099.hp1 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.823-11221A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51036581 | ||||||
| chr14:51036866
|
C | T | 30 | a0001c0001t0001g0277a0001c0001t0002g0023a0001c0001t0002g0159others(27): Show | 32 | HG00140.hp1 HG00597.hp2 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.823-11506G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51036866 | ||||||
| chr14:51036871
|
A | G | 1 | a0002c0002t0006g0018 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.823-11511T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51036871 | ||||||
| chr14:51037129
|
C | G | 1 | a0002c0002t0003g0242 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.823-11769G>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51037129 | ||||||
| chr14:51037132
|
C | T | 86 | a0001c0001t0001g0179a0001c0001t0001g0206a0001c0001t0001g0216others(83): Show | 88 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.823-11772G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51037132 | ||||||
| chr14:51037297
|
G | A | 4 | a0002c0002t0001g0313a0002c0002t0003g0106a0002c0004t0005g0311others(1): Show | 4 | HG02647.hp1 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.823-11937C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51037297 | ||||||
| chr14:51037407
|
G | A | 18 | a0001c0001t0001g0324a0001c0001t0002g0283a0001c0001t0002g0284others(15): Show | 18 | HG00423.hp2 HG02135.hp1 HG02723.hp1 others(15): Show |
intron_variant | MODIFIER | c.823-12047C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51037407 | ||||||
| chr14:51037491
|
A | G | 1 | a0001c0001t0002g0308 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.823-12131T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51037491 | ||||||
| chr14:51037702
|
T | C | 32 | a0001c0001t0002g0070a0001c0001t0002g0075a0001c0001t0002g0087others(29): Show | 35 | HG00280.hp2 HG00642.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.823-12342A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51037702 | ||||||
| chr14:51037857
|
A | T | 2 | a0001c0001t0002g0218a0001c0001t0002g0219 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.823-12497T>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51037857 | ||||||
| chr14:51037858
|
G | A | 2 | a0001c0001t0009g0096a0002c0002t0003g0029 | 2 | HG02572.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.823-12498C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51037858 | ||||||
| chr14:51037921
|
T | C | 3 | a0002c0002t0001g0114a0002c0002t0001g0115a0002c0002t0001g0116 | 3 | NA18944.hp2 NA19005.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.823-12561A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51037921 | ||||||
| chr14:51038063
|
C | G | 6 | a0001c0001t0004g0148a0002c0002t0001g0313a0002c0002t0003g0106others(3): Show | 6 | HG02109.hp1 HG02451.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.823-12703G>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51038063 | ||||||
| chr14:51038130
|
A | T | 7 | a0001c0001t0001g0062a0001c0001t0002g0073a0002c0002t0006g0004others(4): Show | 8 | HG02004.hp2 HG02155.hp2 NA18951.hp1 others(5): Show |
intron_variant | MODIFIER | c.823-12770T>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51038130 | ||||||
| chr14:51038164
|
T | C | 38 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0178others(35): Show | 38 | HG00639.hp1 HG00642.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.823-12804A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51038164 | ||||||
| chr14:51038399
|
T | C | 11 | a0001c0001t0001g0031a0001c0001t0001g0205a0001c0001t0001g0287others(8): Show | 11 | HG01433.hp1 HG01884.hp2 HG02129.hp2 others(8): Show |
intron_variant | MODIFIER | c.823-13039A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51038399 | ||||||
| chr14:51038535
|
A | C | 3 | a0001c0001t0009g0096a0002c0002t0003g0029a0002c0002t0006g0018 | 3 | HG02572.hp1 HG03486.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.823-13175T>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51038535 | ||||||
| chr14:51038598
|
A | G | 87 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0178others(84): Show | 91 | HG00280.hp2 HG00639.hp1 HG00642.hp1 others(88): Show |
intron_variant | MODIFIER | c.823-13238T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51038598 | ||||||
| chr14:51038654
|
T | G | 1 | a0002c0002t0001g0207 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.823-13294A>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51038654 | ||||||
| chr14:51038862
|
T | C | 1 | a0001c0001t0001g0122 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.823-13502A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51038862 | ||||||
| chr14:51038868
|
A | G | 49 | a0001c0001t0002g0070a0001c0001t0002g0075a0001c0001t0002g0087others(46): Show | 53 | HG00280.hp2 HG00642.hp1 HG00735.hp2 others(50): Show |
intron_variant | MODIFIER | c.823-13508T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51038868 | ||||||
| chr14:51039077
|
C | T | 11 | a0001c0001t0002g0037a0001c0001t0009g0038a0001c0001t0017g0036others(8): Show | 11 | HG02145.hp2 HG02280.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.823-13717G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51039077 | ||||||
| chr14:51039201
|
G | C | 1 | a0001c0001t0002g0023 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.823-13841C>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51039201 | ||||||
| chr14:51039212
|
C | A | 2 | a0001c0001t0009g0096a0002c0002t0003g0029 | 2 | HG02572.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.823-13852G>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51039212 | ||||||
| chr14:51039384
|
T | C | 18 | a0001c0001t0001g0324a0001c0001t0002g0283a0001c0001t0002g0284others(15): Show | 18 | HG00423.hp2 HG02135.hp1 HG02723.hp1 others(15): Show |
intron_variant | MODIFIER | c.823-14024A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51039384 | ||||||
| chr14:51039570
|
A | G | 4 | a0001c0001t0001g0179a0001c0001t0003g0063a0001c0001t0003g0180others(1): Show | 4 | HG02056.hp2 NA18964.hp1 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.823-14210T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51039570 | ||||||
| chr14:51039693
|
A | C | 1 | a0002c0002t0001g0019 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.823-14333T>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51039693 | ||||||
| chr14:51039755
|
C | CT | 49 | a0001c0001t0002g0070a0001c0001t0002g0075a0001c0001t0002g0087others(46): Show | 53 | HG00280.hp2 HG00642.hp1 HG00735.hp2 others(50): Show |
intron_variant | MODIFIER | c.823-14396dupA | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51039755 | ||||||
| chr14:51039806
|
G | A | 25 | a0001c0001t0001g0028a0001c0001t0001g0178a0001c0001t0002g0300others(22): Show | 25 | HG00639.hp1 HG00642.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.823-14446C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51039806 | ||||||
| chr14:51039839
|
C | T | 1 | a0002c0002t0010g0332 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.823-14479G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51039839 | ||||||
| chr14:51040075
|
A | G | 49 | a0001c0001t0002g0070a0001c0001t0002g0075a0001c0001t0002g0087others(46): Show | 53 | HG00280.hp2 HG00642.hp1 HG00735.hp2 others(50): Show |
intron_variant | MODIFIER | c.823-14715T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51040075 | ||||||
| chr14:51040116
|
G | A | 61 | a0001c0001t0001g0122a0001c0001t0001g0324a0001c0001t0002g0037others(58): Show | 62 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.823-14756C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51040116 | ||||||
| chr14:51040118
|
G | A | 1 | a0002c0002t0004g0046 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.823-14758C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51040118 | ||||||
| chr14:51040173
|
C | T | 50 | a0001c0001t0001g0122a0001c0001t0001g0324a0001c0001t0002g0108others(47): Show | 51 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.823-14813G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51040173 | ||||||
| chr14:51040223
|
C | T | 1 | a0002c0002t0003g0242 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.823-14863G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51040223 | ||||||
| chr14:51040254
|
C | T | 1 | a0002c0002t0006g0018 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.823-14894G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51040254 | ||||||
| chr14:51040297
|
C | T | 11 | a0001c0001t0002g0141a0001c0001t0003g0006a0001c0001t0003g0054others(8): Show | 12 | HG00738.hp1 HG01099.hp1 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.823-14937G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51040297 | ||||||
| chr14:51040500
|
A | G | 1 | a0001c0001t0002g0023 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.823-15140T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51040500 | ||||||
| chr14:51040504
|
C | T | 101 | a0001c0001t0001g0179a0001c0001t0001g0206a0001c0001t0001g0211others(98): Show | 103 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.823-15144G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51040504 | ||||||
| chr14:51040532
|
C | G | 1 | a0001c0001t0003g0222 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.823-15172G>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51040532 | ||||||
| chr14:51040576
|
T | C | 49 | a0001c0001t0002g0070a0001c0001t0002g0075a0001c0001t0002g0087others(46): Show | 53 | HG00280.hp2 HG00642.hp1 HG00735.hp2 others(50): Show |
intron_variant | MODIFIER | c.823-15216A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51040576 | ||||||
| chr14:51040771
|
T | C | 11 | a0001c0001t0002g0037a0001c0001t0009g0038a0001c0001t0017g0036others(8): Show | 11 | HG02145.hp2 HG02280.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.823-15411A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51040771 | ||||||
| chr14:51040808
|
C | G | 1 | a0001c0001t0002g0150 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.823-15448G>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51040808 | ||||||
| chr14:51040875
|
A | T | 32 | a0001c0001t0001g0122a0001c0001t0002g0108a0001c0001t0002g0110others(29): Show | 33 | HG00408.hp2 HG00438.hp1 HG01256.hp1 others(30): Show |
intron_variant | MODIFIER | c.823-15515T>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51040875 | ||||||
| chr14:51040890
|
T | C | 1 | a0001c0001t0003g0163 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.823-15530A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51040890 | ||||||
| chr14:51041011
|
G | A | 18 | a0001c0001t0001g0324a0001c0001t0002g0283a0001c0001t0002g0284others(15): Show | 18 | HG00423.hp2 HG02135.hp1 HG02723.hp1 others(15): Show |
intron_variant | MODIFIER | c.823-15651C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51041011 | ||||||
| chr14:51041067
|
G | A | 1 | a0001c0001t0001g0028 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.823-15707C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51041067 | ||||||
| chr14:51041240
|
A | G | 151 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0122others(148): Show | 156 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.823-15880T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51041240 | ||||||
| chr14:51041281
|
T | C | 11 | a0001c0001t0001g0031a0001c0001t0001g0205a0001c0001t0001g0287others(8): Show | 11 | HG01433.hp1 HG01884.hp2 HG02129.hp2 others(8): Show |
intron_variant | MODIFIER | c.823-15921A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51041281 | ||||||
| chr14:51041804
|
TAA | T | 11 | a0001c0001t0002g0141a0001c0001t0003g0006a0001c0001t0003g0054others(8): Show | 12 | HG00738.hp1 HG01099.hp1 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.823-16446_823-1644 others(6): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51041804 | ||||||
| chr14:51041807
|
G | C | 25 | a0001c0001t0001g0028a0001c0001t0001g0178a0001c0001t0002g0300others(22): Show | 25 | HG00639.hp1 HG00642.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.823-16447C>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51041807 | ||||||
| chr14:51042148
|
C | T | 32 | a0001c0001t0002g0070a0001c0001t0002g0075a0001c0001t0002g0087others(29): Show | 35 | HG00280.hp2 HG00642.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.823-16788G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51042148 | ||||||
| chr14:51042232
|
G | A | 252 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0122others(249): Show | 259 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.823-16872C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51042232 | ||||||
| chr14:51042347
|
T | C | 1 | a0002c0002t0006g0018 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.823-16987A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51042347 | ||||||
| chr14:51042425
|
T | C | 32 | a0001c0001t0002g0070a0001c0001t0002g0075a0001c0001t0002g0087others(29): Show | 35 | HG00280.hp2 HG00642.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.823-17065A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51042425 | ||||||
| chr14:51042735
|
G | T | 1 | a0002c0002t0001g0190 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.823-17375C>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51042735 | ||||||
| chr14:51042771
|
T | C | 3 | a0001c0001t0009g0096a0002c0002t0003g0029a0002c0002t0006g0018 | 3 | HG02572.hp1 HG03486.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.823-17411A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51042771 | ||||||
| chr14:51042806
|
G | A | 3 | a0001c0001t0002g0023a0001c0001t0002g0261a0001c0001t0002g0270 | 3 | HG00597.hp2 NA18941.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.823-17446C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51042806 | ||||||
| chr14:51042898
|
C | T | 1 | a0001c0001t0002g0316 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.823-17538G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51042898 | ||||||
| chr14:51042925
|
T | C | 1 | a0001c0001t0002g0267 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.823-17565A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51042925 | ||||||
| chr14:51042958
|
A | T | 4 | a0001c0001t0005g0032a0001c0001t0005g0033a0002c0002t0008g0325others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.823-17598T>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51042958 | ||||||
| chr14:51042963
|
T | C | 51 | a0001c0001t0001g0122a0001c0001t0001g0324a0001c0001t0002g0108others(48): Show | 52 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.823-17603A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51042963 | ||||||
| chr14:51043061
|
T | C | 2 | a0001c0001t0005g0026a0001c0001t0005g0027 | 2 | HG01891.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.823-17701A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51043061 | ||||||
| chr14:51043124
|
T | C | 1 | a0002c0002t0006g0018 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.823-17764A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51043124 | ||||||
| chr14:51043309
|
A | G | 37 | a0001c0001t0002g0070a0001c0001t0002g0075a0001c0001t0002g0087others(34): Show | 40 | HG00280.hp2 HG00642.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.823-17949T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51043309 | ||||||
| chr14:51043325
|
C | G | 37 | a0001c0001t0002g0070a0001c0001t0002g0075a0001c0001t0002g0087others(34): Show | 40 | HG00280.hp2 HG00642.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.823-17965G>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51043325 | ||||||
| chr14:51043473
|
C | T | 1 | a0005c0011t0001g0315 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.823-18113G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51043473 | ||||||
| chr14:51043567
|
T | C | 32 | a0001c0001t0002g0070a0001c0001t0002g0075a0001c0001t0002g0087others(29): Show | 35 | HG00280.hp2 HG00642.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.823-18207A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51043567 | ||||||
| chr14:51043799
|
T | C | 32 | a0001c0001t0002g0070a0001c0001t0002g0075a0001c0001t0002g0087others(29): Show | 35 | HG00280.hp2 HG00642.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.823-18439A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51043799 | ||||||
| chr14:51043835
|
CA | C | 32 | a0001c0001t0002g0070a0001c0001t0002g0075a0001c0001t0002g0087others(29): Show | 35 | HG00280.hp2 HG00642.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.823-18476delT | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51043835 | ||||||
| chr14:51043897
|
G | A | 1 | a0002c0002t0001g0181 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.823-18537C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51043897 | ||||||
| chr14:51044033
|
C | T | 1 | a0002c0002t0001g0307 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.823-18673G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51044033 | ||||||
| chr14:51044108
|
T | G | 1 | a0001c0001t0001g0206 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.823-18748A>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51044108 | ||||||
| chr14:51044113
|
C | T | 2 | a0001c0001t0005g0026a0001c0001t0005g0027 | 2 | HG01891.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.823-18753G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51044113 | ||||||
| chr14:51044124
|
C | T | 134 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0122others(131): Show | 138 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.823-18764G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51044124 | ||||||
| chr14:51044128
|
A | G | 1 | a0002c0002t0003g0112 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.823-18768T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51044128 | ||||||
| chr14:51044386
|
A | G | 101 | a0001c0001t0001g0179a0001c0001t0001g0206a0001c0001t0001g0211others(98): Show | 103 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.823-19026T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51044386 | ||||||
| chr14:51044392
|
T | C | 1 | a0002c0002t0001g0262 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.823-19032A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51044392 | ||||||
| chr14:51044429
|
T | C | 1 | a0002c0002t0002g0233 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.823-19069A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51044429 | ||||||
| chr14:51044469
|
A | T | 1 | a0002c0002t0001g0207 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.823-19109T>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51044469 | ||||||
| chr14:51044526
|
T | G | 1 | a0002c0002t0006g0018 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.823-19166A>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51044526 | ||||||
| chr14:51044648
|
A | C | 2 | a0001c0001t0009g0096a0002c0002t0003g0029 | 2 | HG02572.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.823-19288T>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51044648 | ||||||
| chr14:51044820
|
A | G | 1 | a0001c0001t0005g0026 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.823-19460T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51044820 | ||||||
| chr14:51045041
|
G | A | 32 | a0001c0001t0002g0070a0001c0001t0002g0075a0001c0001t0002g0087others(29): Show | 35 | HG00280.hp2 HG00642.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.823-19681C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51045041 | ||||||
| chr14:51045057
|
G | GA | 33 | a0001c0001t0001g0122a0001c0001t0002g0045a0001c0001t0002g0110others(30): Show | 34 | HG00408.hp2 HG00438.hp1 HG01256.hp1 others(31): Show |
intron_variant | MODIFIER | c.823-19698dupT | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51045057 | ||||||
| chr14:51045057
|
GA | G | 101 | a0001c0001t0001g0179a0001c0001t0001g0206a0001c0001t0001g0211others(98): Show | 103 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.823-19698delT | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51045057 | ||||||
| chr14:51045115
|
G | T | 135 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0122others(132): Show | 139 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.823-19755C>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51045115 | ||||||
| chr14:51045151
|
C | G | 4 | a0002c0002t0001g0313a0002c0002t0003g0106a0002c0004t0005g0311others(1): Show | 4 | HG02647.hp1 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.823-19791G>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51045151 | ||||||
| chr14:51045167
|
G | A | 1 | a0002c0002t0003g0029 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.823-19807C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51045167 | ||||||
| chr14:51045191
|
C | T | 1 | a0001c0001t0002g0056 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.823-19831G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51045191 | ||||||
| chr14:51045311
|
T | G | 1 | a0001c0001t0004g0105 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.823-19951A>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51045311 | ||||||
| chr14:51045338
|
A | C | 1 | a0001c0001t0002g0217 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.823-19978T>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51045338 | ||||||
| chr14:51045390
|
G | A | 32 | a0001c0001t0002g0070a0001c0001t0002g0075a0001c0001t0002g0087others(29): Show | 35 | HG00280.hp2 HG00642.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.823-20030C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51045390 | ||||||
| chr14:51045400
|
T | C | 32 | a0001c0001t0002g0070a0001c0001t0002g0075a0001c0001t0002g0087others(29): Show | 35 | HG00280.hp2 HG00642.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.823-20040A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51045400 | ||||||
| chr14:51045617
|
A | G | 32 | a0001c0001t0002g0070a0001c0001t0002g0075a0001c0001t0002g0087others(29): Show | 35 | HG00280.hp2 HG00642.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.823-20257T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51045617 | ||||||
| chr14:51045782
|
T | G | 11 | a0001c0001t0001g0031a0001c0001t0001g0205a0001c0001t0001g0287others(8): Show | 11 | HG01433.hp1 HG01884.hp2 HG02129.hp2 others(8): Show |
intron_variant | MODIFIER | c.823-20422A>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51045782 | ||||||
| chr14:51045912
|
C | G | 32 | a0001c0001t0002g0070a0001c0001t0002g0075a0001c0001t0002g0087others(29): Show | 35 | HG00280.hp2 HG00642.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.823-20552G>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51045912 | ||||||
| chr14:51046132
|
G | C | 1 | a0002c0002t0006g0018 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.823-20772C>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51046132 | ||||||
| chr14:51046199
|
T | G | 32 | a0001c0001t0002g0070a0001c0001t0002g0075a0001c0001t0002g0087others(29): Show | 35 | HG00280.hp2 HG00642.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.823-20839A>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51046199 | ||||||
| chr14:51046232
|
G | A | 2 | a0001c0001t0003g0258a0001c0001t0003g0260 | 2 | NA18951.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.823-20872C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51046232 | ||||||
| chr14:51046441
|
C | T | 3 | a0001c0001t0002g0176a0001c0001t0002g0186a0002c0002t0003g0239 | 3 | HG00140.hp1 HG03490.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.823-21081G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51046441 | ||||||
| chr14:51046460
|
G | C | 1 | a0001c0001t0003g0043 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.823-21100C>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51046460 | ||||||
| chr14:51046531
|
G | A | 32 | a0001c0001t0002g0070a0001c0001t0002g0075a0001c0001t0002g0087others(29): Show | 35 | HG00280.hp2 HG00642.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.823-21171C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51046531 | ||||||
| chr14:51046584
|
C | T | 1 | a0002c0004t0005g0312 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.823-21224G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51046584 | ||||||
| chr14:51046599
|
G | A | 2 | a0001c0001t0009g0096a0002c0002t0003g0029 | 2 | HG02572.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.823-21239C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51046599 | ||||||
| chr14:51046739
|
G | A | 1 | a0002c0002t0013g0035 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.823-21379C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51046739 | ||||||
| chr14:51046752
|
C | A | 2 | a0001c0001t0004g0148a0002c0004t0005g0149 | 2 | HG02109.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.823-21392G>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51046752 | ||||||
| chr14:51046840
|
C | T | 1 | a0001c0001t0003g0071 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.823-21480G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51046840 | ||||||
| chr14:51047042
|
C | T | 4 | a0001c0001t0001g0042a0002c0002t0001g0039a0002c0002t0001g0041others(1): Show | 4 | HG01884.hp1 HG02280.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.823-21682G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51047042 | ||||||
| chr14:51047121
|
T | G | 32 | a0001c0001t0002g0070a0001c0001t0002g0075a0001c0001t0002g0087others(29): Show | 35 | HG00280.hp2 HG00642.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.823-21761A>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51047121 | ||||||
| chr14:51047133
|
T | C | 4 | a0001c0001t0005g0032a0001c0001t0005g0033a0002c0002t0008g0325others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.823-21773A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51047133 | ||||||
| chr14:51047338
|
A | G | 101 | a0001c0001t0001g0179a0001c0001t0001g0206a0001c0001t0001g0211others(98): Show | 103 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.823-21978T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51047338 | ||||||
| chr14:51047649
|
CA | C | 11 | a0001c0001t0002g0141a0001c0001t0003g0006a0001c0001t0003g0054others(8): Show | 12 | HG00738.hp1 HG01099.hp1 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.823-22290delT | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51047649 | ||||||
| chr14:51047751
|
C | A | 32 | a0001c0001t0002g0070a0001c0001t0002g0075a0001c0001t0002g0087others(29): Show | 35 | HG00280.hp2 HG00642.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.823-22391G>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51047751 | ||||||
| chr14:51047924
|
C | T | 21 | a0001c0001t0001g0028a0001c0001t0001g0178a0001c0001t0002g0300others(18): Show | 21 | HG00639.hp1 HG00642.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.823-22564G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51047924 | ||||||
| chr14:51047942
|
A | G | 17 | a0001c0001t0003g0183a0002c0002t0001g0003a0002c0002t0001g0114others(14): Show | 18 | HG00408.hp2 HG00438.hp1 HG02027.hp1 others(15): Show |
intron_variant | MODIFIER | c.823-22582T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51047942 | ||||||
| chr14:51047952
|
C | A | 1 | a0001c0001t0003g0269 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.823-22592G>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51047952 | ||||||
| chr14:51047952
|
C | G | 1 | a0001c0001t0002g0261 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.823-22592G>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51047952 | ||||||
| chr14:51047959
|
C | CA | 6 | a0001c0001t0002g0055a0001c0001t0002g0056a0001c0001t0004g0241others(3): Show | 6 | HG01168.hp2 HG01361.hp2 HG03710.hp1 others(3): Show |
intron_variant | MODIFIER | c.823-22600dupT | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51047959 | ||||||
| chr14:51047959
|
CA | C | 190 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0103others(187): Show | 193 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(190): Show |
intron_variant | MODIFIER | c.823-22600delT | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51047959 | ||||||
| chr14:51047959
|
CAA | C | 30 | a0001c0001t0002g0070a0001c0001t0002g0075a0001c0001t0002g0087others(27): Show | 33 | HG00280.hp2 HG00642.hp1 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.823-22601_823-2260 others(6): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51047959 | ||||||
| chr14:51047966
|
A | C | 1 | a0001c0001t0010g0329 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.823-22606T>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51047966 | ||||||
| chr14:51047996
|
G | A | 1 | a0001c0014t0002g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.823-22636C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51047996 | ||||||
| chr14:51048101
|
A | G | 330 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0042others(327): Show | 340 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.823-22741T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51048101 | ||||||
| chr14:51048220
|
C | T | 101 | a0001c0001t0001g0179a0001c0001t0001g0206a0001c0001t0001g0211others(98): Show | 103 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.823-22860G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51048220 | ||||||
| chr14:51048300
|
T | C | 32 | a0001c0001t0002g0070a0001c0001t0002g0075a0001c0001t0002g0087others(29): Show | 35 | HG00280.hp2 HG00642.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.823-22940A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51048300 | ||||||
| chr14:51048358
|
T | C | 32 | a0001c0001t0002g0070a0001c0001t0002g0075a0001c0001t0002g0087others(29): Show | 35 | HG00280.hp2 HG00642.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.823-22998A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51048358 | ||||||
| chr14:51048395
|
C | T | 1 | a0001c0001t0002g0056 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.823-23035G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51048395 | ||||||
| chr14:51048449
|
C | A | 4 | a0001c0001t0005g0032a0001c0001t0005g0033a0002c0002t0008g0325others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.823-23089G>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51048449 | ||||||
| chr14:51048508
|
G | T | 2 | a0001c0001t0002g0037a0001c0001t0009g0038 | 2 | HG02486.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.823-23148C>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51048508 | ||||||
| chr14:51048510
|
T | C | 21 | a0001c0001t0001g0028a0001c0001t0001g0178a0001c0001t0002g0300others(18): Show | 21 | HG00639.hp1 HG00642.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.823-23150A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51048510 | ||||||
| chr14:51048521
|
T | G | 32 | a0001c0001t0002g0070a0001c0001t0002g0075a0001c0001t0002g0087others(29): Show | 35 | HG00280.hp2 HG00642.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.823-23161A>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51048521 | ||||||
| chr14:51048572
|
C | CAGAAGAG others(4): Show |
230 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0122others(227): Show | 236 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.823-23213_823-2321 others(15): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51048572 | ||||||
| chr14:51048629
|
G | A | 2 | a0001c0001t0002g0037a0001c0001t0009g0038 | 2 | HG02486.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.823-23269C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51048629 | ||||||
| chr14:51048679
|
T | C | 1 | a0001c0001t0002g0086 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.823-23319A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51048679 | ||||||
| chr14:51048706
|
C | T | 21 | a0001c0001t0001g0028a0001c0001t0001g0178a0001c0001t0002g0300others(18): Show | 21 | HG00639.hp1 HG00642.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.823-23346G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51048706 | ||||||
| chr14:51048744
|
G | A | 3 | a0001c0001t0002g0086a0001c0001t0003g0048a0002c0002t0001g0166 | 3 | NA18980.hp1 NA19003.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.823-23384C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51048744 | ||||||
| chr14:51048745
|
A | G | 133 | a0001c0001t0001g0179a0001c0001t0001g0206a0001c0001t0001g0211others(130): Show | 138 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.823-23385T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51048745 | ||||||
| chr14:51048948
|
C | T | 1 | a0001c0001t0002g0173 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.823-23588G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51048948 | ||||||
| chr14:51048978
|
C | T | 2 | a0001c0001t0002g0156a0001c0001t0002g0157 | 2 | HG01167.hp2 HG01928.hp1 |
intron_variant | MODIFIER | c.823-23618G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51048978 | ||||||
| chr14:51048980
|
T | A | 32 | a0001c0001t0002g0070a0001c0001t0002g0075a0001c0001t0002g0087others(29): Show | 35 | HG00280.hp2 HG00642.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.823-23620A>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51048980 | ||||||
| chr14:51048983
|
C | CA | 7 | a0001c0001t0004g0148a0002c0002t0001g0313a0002c0002t0003g0106others(4): Show | 7 | HG02109.hp1 HG02451.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.823-23624dupT | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51048983 | ||||||
| chr14:51048983
|
CA | C | 23 | a0001c0001t0001g0028a0001c0001t0001g0178a0001c0001t0002g0300others(20): Show | 23 | HG00639.hp1 HG00642.hp2 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.823-23624delT | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51048983 | ||||||
| chr14:51049296
|
A | G | 32 | a0001c0001t0002g0070a0001c0001t0002g0075a0001c0001t0002g0087others(29): Show | 35 | HG00280.hp2 HG00642.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.823-23936T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51049296 | ||||||
| chr14:51049302
|
T | C | 30 | a0001c0001t0001g0277a0001c0001t0002g0023a0001c0001t0002g0159others(27): Show | 32 | HG00140.hp1 HG00597.hp2 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.823-23942A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51049302 | ||||||
| chr14:51049373
|
G | C | 4 | a0001c0001t0002g0141a0001c0001t0003g0054a0003c0006t0001g0140others(1): Show | 4 | HG01099.hp1 HG01981.hp2 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.823-24013C>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51049373 | ||||||
| chr14:51049416
|
A | G | 21 | a0001c0001t0001g0028a0001c0001t0001g0178a0001c0001t0002g0300others(18): Show | 21 | HG00639.hp1 HG00642.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.823-24056T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51049416 | ||||||
| chr14:51049514
|
G | A | 4 | a0002c0002t0001g0313a0002c0002t0003g0106a0002c0004t0005g0311others(1): Show | 4 | HG02647.hp1 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.823-24154C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51049514 | ||||||
| chr14:51049549
|
C | T | 2 | a0001c0001t0002g0108a0001c0001t0003g0082 | 2 | HG03654.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.823-24189G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51049549 | ||||||
| chr14:51049550
|
G | A | 2 | a0001c0001t0009g0096a0002c0002t0003g0029 | 2 | HG02572.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.823-24190C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51049550 | ||||||
| chr14:51049579
|
G | C | 32 | a0001c0001t0002g0070a0001c0001t0002g0075a0001c0001t0002g0087others(29): Show | 35 | HG00280.hp2 HG00642.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.823-24219C>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51049579 | ||||||
| chr14:51049584
|
T | C | 7 | a0001c0001t0001g0103a0001c0001t0004g0099a0001c0001t0004g0100others(4): Show | 7 | HG01261.hp1 HG02451.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.823-24224A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51049584 | ||||||
| chr14:51049601
|
G | C | 2 | a0001c0001t0002g0056a0001c0001t0003g0080 | 2 | HG03710.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.823-24241C>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51049601 | ||||||
| chr14:51049603
|
G | T | 1 | a0001c0001t0002g0056 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.823-24243C>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51049603 | ||||||
| chr14:51049651
|
C | T | 1 | a0001c0001t0001g0206 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.823-24291G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51049651 | ||||||
| chr14:51049652
|
G | C | 32 | a0001c0001t0002g0070a0001c0001t0002g0075a0001c0001t0002g0087others(29): Show | 35 | HG00280.hp2 HG00642.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.823-24292C>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51049652 | ||||||
| chr14:51049687
|
G | A | 4 | a0002c0002t0001g0313a0002c0002t0003g0106a0002c0004t0005g0311others(1): Show | 4 | HG02647.hp1 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.823-24327C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51049687 | ||||||
| chr14:51049770
|
A | G | 1 | a0001c0001t0002g0261 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.823-24410T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51049770 | ||||||
| chr14:51049824
|
C | CA | 24 | a0001c0001t0002g0045a0001c0001t0003g0080a0001c0001t0003g0258others(21): Show | 25 | HG00438.hp1 HG02027.hp1 HG02572.hp1 others(22): Show |
intron_variant | MODIFIER | c.823-24465dupT | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51049824 | ||||||
| chr14:51049835
|
AT | A | 5 | a0001c0001t0005g0032a0001c0001t0005g0033a0002c0002t0006g0018others(2): Show | 5 | HG02895.hp1 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.823-24476delA | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51049835 | ||||||
| chr14:51049915
|
G | A | 1 | a0002c0002t0001g0279 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.823-24555C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51049915 | ||||||
| chr14:51049950
|
A | G | 37 | a0001c0001t0001g0324a0001c0001t0002g0070a0001c0001t0002g0075others(34): Show | 40 | HG00280.hp2 HG00639.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.823-24590T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51049950 | ||||||
| chr14:51049954
|
A | T | 1 | a0001c0001t0002g0037 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.823-24594T>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51049954 | ||||||
| chr14:51050030
|
C | T | 98 | a0001c0001t0001g0179a0001c0001t0001g0206a0001c0001t0001g0211others(95): Show | 100 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.823-24670G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51050030 | ||||||
| chr14:51050031
|
G | A | 17 | a0001c0001t0002g0141a0001c0001t0003g0006a0001c0001t0003g0054others(14): Show | 18 | HG00738.hp1 HG01099.hp1 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.823-24671C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51050031 | ||||||
| chr14:51050426
|
C | T | 1 | a0001c0001t0003g0317 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.823-25066G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51050426 | ||||||
| chr14:51050498
|
T | A | 1 | a0001c0001t0002g0056 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.823-25138A>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51050498 | ||||||
| chr14:51050539
|
G | T | 1 | a0001c0001t0002g0056 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.823-25179C>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51050539 | ||||||
| chr14:51050594
|
T | C | 2 | a0002c0002t0006g0018a0002c0002t0006g0223 | 2 | HG03710.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.823-25234A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51050594 | ||||||
| chr14:51050671
|
C | T | 15 | a0001c0001t0002g0087a0001c0001t0002g0316a0001c0001t0003g0071others(12): Show | 15 | HG01243.hp1 HG02630.hp2 HG02886.hp1 others(12): Show |
intron_variant | MODIFIER | c.823-25311G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51050671 | ||||||
| chr14:51050676
|
T | C | 52 | a0001c0001t0001g0132a0001c0001t0001g0205a0001c0001t0001g0206others(49): Show | 52 | HG00741.hp1 HG01081.hp1 HG01256.hp1 others(49): Show |
intron_variant | MODIFIER | c.823-25316A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51050676 | ||||||
| chr14:51050731
|
T | C | 1 | a0001c0001t0001g0028 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.823-25371A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51050731 | ||||||
| chr14:51050936
|
T | C | 1 | a0001c0001t0003g0222 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.823-25576A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51050936 | ||||||
| chr14:51050983
|
T | C | 40 | a0001c0001t0002g0108a0001c0001t0002g0110a0001c0001t0002g0111others(37): Show | 42 | HG00408.hp2 HG00438.hp1 HG01256.hp1 others(39): Show |
intron_variant | MODIFIER | c.823-25623A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51050983 | ||||||
| chr14:51051207
|
C | G | 1 | a0002c0002t0001g0107 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.823-25847G>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51051207 | ||||||
| chr14:51051218
|
C | T | 1 | a0002c0002t0006g0018 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.823-25858G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51051218 | ||||||
| chr14:51051232
|
A | G | 26 | a0001c0001t0001g0206a0001c0001t0001g0324a0001c0001t0002g0283others(23): Show | 26 | HG00741.hp1 HG01081.hp1 HG02135.hp1 others(23): Show |
intron_variant | MODIFIER | c.823-25872T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51051232 | ||||||
| chr14:51051438
|
A | G | 4 | a0001c0001t0005g0032a0001c0001t0005g0033a0002c0002t0008g0325others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.823-26078T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51051438 | ||||||
| chr14:51051462
|
A | C | 4 | a0001c0001t0005g0032a0001c0001t0005g0033a0002c0002t0008g0325others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.823-26102T>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51051462 | ||||||
| chr14:51051570
|
T | C | 330 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0042others(327): Show | 340 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.823-26210A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51051570 | ||||||
| chr14:51051590
|
A | C | 4 | a0001c0001t0005g0032a0001c0001t0005g0033a0002c0002t0008g0325others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.823-26230T>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51051590 | ||||||
| chr14:51051632
|
C | T | 2 | a0001c0001t0002g0283a0001c0001t0002g0284 | 2 | NA18983.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.823-26272G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51051632 | ||||||
| chr14:51051737
|
C | T | 4 | a0001c0001t0001g0042a0002c0002t0001g0039a0002c0002t0001g0041others(1): Show | 4 | HG01884.hp1 HG02280.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.823-26377G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51051737 | ||||||
| chr14:51051863
|
A | G | 1 | a0001c0001t0002g0220 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.823-26503T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51051863 | ||||||
| chr14:51051943
|
G | A | 5 | a0001c0001t0002g0283a0001c0001t0002g0284a0001c0001t0002g0285others(2): Show | 5 | HG02135.hp1 NA18983.hp2 NA19054.hp2 others(2): Show |
intron_variant | MODIFIER | c.823-26583C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51051943 | ||||||
| chr14:51051997
|
C | G | 4 | a0001c0001t0005g0032a0001c0001t0005g0033a0002c0002t0008g0325others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.823-26637G>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51051997 | ||||||
| chr14:51052042
|
AAGAAG | A | 85 | a0001c0001t0001g0028a0001c0001t0001g0122a0001c0001t0001g0310others(82): Show | 90 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.823-26687_823-2668 others(9): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51052042 | ||||||
| chr14:51052050
|
A | AAGAGAAG others(18): Show |
1 | a0001c0001t0003g0286 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.823-26715_823-2669 others(29): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51052050 | ||||||
| chr14:51052102
|
G | A | 4 | a0001c0001t0005g0032a0001c0001t0005g0033a0002c0002t0008g0325others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.823-26742C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51052102 | ||||||
| chr14:51052207
|
T | C | 24 | a0001c0001t0001g0132a0001c0001t0001g0205a0001c0001t0001g0287others(21): Show | 25 | HG00738.hp1 HG01074.hp2 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.823-26847A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51052207 | ||||||
| chr14:51052215
|
C | T | 4 | a0001c0001t0005g0032a0001c0001t0005g0033a0002c0002t0008g0325others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.823-26855G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51052215 | ||||||
| chr14:51052272
|
C | T | 4 | a0001c0001t0005g0032a0001c0001t0005g0033a0002c0002t0008g0325others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.823-26912G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51052272 | ||||||
| chr14:51052320
|
A | G | 1 | a0001c0001t0001g0031 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.823-26960T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51052320 | ||||||
| chr14:51052454
|
C | T | 4 | a0001c0001t0005g0032a0001c0001t0005g0033a0002c0002t0008g0325others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.823-27094G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51052454 | ||||||
| chr14:51052476
|
G | A | 4 | a0001c0001t0005g0032a0001c0001t0005g0033a0002c0002t0008g0325others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.823-27116C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51052476 | ||||||
| chr14:51052503
|
A | G | 13 | a0001c0001t0001g0310a0001c0001t0002g0037a0001c0001t0009g0038others(10): Show | 13 | HG02145.hp2 HG02280.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.823-27143T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51052503 | ||||||
| chr14:51052514
|
C | T | 5 | a0001c0001t0004g0148a0001c0001t0005g0026a0001c0001t0005g0027others(2): Show | 5 | HG01884.hp2 HG01891.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.823-27154G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51052514 | ||||||
| chr14:51052631
|
T | G | 4 | a0001c0001t0005g0032a0001c0001t0005g0033a0002c0002t0008g0325others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.823-27271A>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51052631 | ||||||
| chr14:51052754
|
G | A | 2 | a0001c0001t0003g0129a0001c0001t0003g0130 | 2 | HG00738.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.823-27394C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51052754 | ||||||
| chr14:51052875
|
G | T | 5 | a0001c0001t0004g0148a0001c0001t0005g0026a0001c0001t0005g0027others(2): Show | 5 | HG01884.hp2 HG01891.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.823-27515C>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51052875 | ||||||
| chr14:51052904
|
C | T | 1 | a0002c0002t0001g0145 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.823-27544G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51052904 | ||||||
| chr14:51053030
|
G | A | 1 | a0002c0002t0006g0081 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.823-27670C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51053030 | ||||||
| chr14:51053141
|
C | T | 1 | a0002c0002t0001g0188 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.823-27781G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51053141 | ||||||
| chr14:51053159
|
C | CA | 143 | a0001c0001t0001g0122a0001c0001t0001g0178a0001c0001t0001g0179others(140): Show | 146 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.823-27800dupT | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51053159 | ||||||
| chr14:51053159
|
CA | C | 39 | a0001c0001t0002g0235a0001c0001t0002g0300a0001c0001t0003g0254others(36): Show | 42 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.823-27800delT | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51053159 | ||||||
| chr14:51053172
|
A | G | 17 | a0001c0001t0001g0132a0001c0001t0002g0141a0001c0001t0002g0147others(14): Show | 18 | HG00738.hp1 HG01074.hp2 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.823-27812T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51053172 | ||||||
| chr14:51053232
|
A | C | 1 | a0001c0001t0002g0150 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.823-27872T>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51053232 | ||||||
| chr14:51053424
|
C | G | 2 | a0001c0001t0002g0176a0001c0001t0002g0186 | 2 | HG03490.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.823-28064G>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51053424 | ||||||
| chr14:51053426
|
C | T | 4 | a0001c0001t0005g0032a0001c0001t0005g0033a0002c0002t0008g0325others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.823-28066G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51053426 | ||||||
| chr14:51053495
|
TCAGAACA others(311): Show |
T | 4 | a0001c0001t0005g0032a0001c0001t0005g0033a0002c0002t0008g0325others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.823-28453_823-2813 others(4): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51053495 | ||||||
| chr14:51053509
|
C | CT | 11 | a0001c0001t0001g0031a0001c0001t0002g0088a0001c0001t0004g0138others(8): Show | 11 | HG01069.hp1 HG01071.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.823-28150dupA | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51053509 | ||||||
| chr14:51053509
|
CT | C | 10 | a0001c0001t0001g0103a0001c0001t0003g0143a0001c0001t0004g0099others(7): Show | 10 | HG01261.hp1 HG02165.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.823-28150delA | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51053509 | ||||||
| chr14:51053509
|
CTT | C | 63 | a0001c0001t0001g0205a0001c0001t0001g0287a0001c0001t0001g0310others(60): Show | 66 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.823-28151_823-2815 others(6): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51053509 | ||||||
| chr14:51053509
|
CTTT | C | 104 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0206others(101): Show | 105 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.823-28152_823-2815 others(7): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51053509 | ||||||
| chr14:51053509
|
CTTTT | C | 59 | a0001c0001t0001g0122a0001c0001t0001g0324a0001c0001t0002g0108others(56): Show | 61 | HG00408.hp2 HG00438.hp1 HG00741.hp1 others(58): Show |
intron_variant | MODIFIER | c.823-28153_823-2815 others(8): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51053509 | ||||||
| chr14:51053509
|
CTTTTT | C | 18 | a0001c0001t0001g0132a0001c0001t0002g0141a0001c0001t0002g0147others(15): Show | 19 | HG00738.hp1 HG01074.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.823-28154_823-2815 others(9): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51053509 | ||||||
| chr14:51053523
|
T | C | 34 | a0001c0001t0001g0122a0001c0001t0002g0108a0001c0001t0002g0110others(31): Show | 36 | HG00408.hp2 HG00438.hp1 HG01256.hp1 others(33): Show |
intron_variant | MODIFIER | c.823-28163A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51053523 | ||||||
| chr14:51053529
|
T | A | 1 | a0002c0002t0003g0249 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.823-28169A>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51053529 | ||||||
| chr14:51053556
|
TA | T | 19 | a0001c0001t0002g0316a0001c0001t0003g0183a0001c0001t0003g0317others(16): Show | 20 | HG00408.hp2 HG00438.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.823-28197delT | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51053556 | ||||||
| chr14:51053557
|
A | T | 12 | a0001c0001t0002g0108a0001c0001t0002g0110a0001c0001t0002g0111others(9): Show | 13 | HG01256.hp1 HG01258.hp1 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.823-28197T>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51053557 | ||||||
| chr14:51053561
|
T | A | 56 | a0001c0001t0001g0031a0001c0001t0001g0132a0001c0001t0001g0310others(53): Show | 57 | HG00544.hp1 HG00597.hp1 HG00738.hp1 others(54): Show |
intron_variant | MODIFIER | c.823-28201A>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51053561 | ||||||
| chr14:51053580
|
C | CT | 20 | a0001c0001t0002g0141a0001c0001t0002g0147a0001c0001t0003g0129others(17): Show | 21 | HG00733.hp2 HG00738.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.823-28221dupA | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51053580 | ||||||
| chr14:51053580
|
CT | C | 26 | a0001c0001t0001g0028a0001c0001t0001g0103a0001c0001t0001g0179others(23): Show | 26 | HG00639.hp1 HG00642.hp2 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.823-28221delA | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51053580 | ||||||
| chr14:51053593
|
T | A | 6 | a0001c0001t0002g0300a0002c0002t0001g0236a0002c0002t0001g0243others(3): Show | 6 | HG00639.hp1 HG00642.hp2 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.823-28233A>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51053593 | ||||||
| chr14:51053593
|
T | TA | 35 | a0001c0001t0002g0235a0001c0001t0003g0254a0001c0001t0004g0232others(32): Show | 38 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.823-28234dupT | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51053593 | ||||||
| chr14:51053594
|
A | T | 39 | a0001c0001t0001g0324a0001c0001t0002g0141a0001c0001t0002g0147others(36): Show | 40 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(37): Show |
intron_variant | MODIFIER | c.823-28234T>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51053594 | ||||||
| chr14:51053595
|
A | T | 21 | a0001c0001t0001g0324a0001c0001t0002g0159a0001c0001t0002g0283others(18): Show | 21 | HG00741.hp1 HG01074.hp2 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.823-28235T>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51053595 | ||||||
| chr14:51053595
|
AT | A | 61 | a0001c0001t0002g0055a0001c0001t0002g0059a0001c0001t0002g0060others(58): Show | 64 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.823-28236delA | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51053595 | ||||||
| chr14:51053596
|
T | A | 46 | a0001c0001t0001g0031a0001c0001t0001g0122a0001c0001t0001g0132others(43): Show | 47 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.823-28236A>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51053596 | ||||||
| chr14:51053597
|
T | A | 25 | a0001c0001t0001g0324a0001c0001t0002g0283a0001c0001t0002g0284others(22): Show | 25 | HG00741.hp1 HG01074.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.823-28237A>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51053597 | ||||||
| chr14:51053598
|
T | A | 1 | a0002c0002t0001g0307 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.823-28238A>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51053598 | ||||||
| chr14:51053670
|
A | G | 17 | a0001c0001t0001g0132a0001c0001t0002g0141a0001c0001t0002g0147others(14): Show | 18 | HG00738.hp1 HG01074.hp2 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.823-28310T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51053670 | ||||||
| chr14:51053686
|
C | T | 1 | a0002c0002t0006g0224 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.823-28326G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51053686 | ||||||
| chr14:51053687
|
G | A | 1 | a0002c0002t0001g0307 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.823-28327C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51053687 | ||||||
| chr14:51053734
|
C | T | 1 | a0001c0001t0002g0088 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.823-28374G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51053734 | ||||||
| chr14:51053746
|
G | C | 36 | a0001c0001t0001g0122a0001c0001t0002g0108a0001c0001t0002g0110others(33): Show | 38 | HG00408.hp2 HG00438.hp1 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.823-28386C>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51053746 | ||||||
| chr14:51053757
|
C | G | 2 | a0002c0002t0001g0288a0002c0004t0005g0298 | 2 | HG02886.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.823-28397G>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51053757 | ||||||
| chr14:51053952
|
A | G | 4 | a0001c0001t0005g0032a0001c0001t0005g0033a0002c0002t0008g0325others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.823-28592T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51053952 | ||||||
| chr14:51054017
|
T | C | 4 | a0001c0001t0001g0179a0001c0001t0002g0171a0001c0001t0003g0180others(1): Show | 4 | NA18964.hp1 NA18969.hp1 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.823-28657A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51054017 | ||||||
| chr14:51054084
|
C | A | 36 | a0001c0001t0001g0122a0001c0001t0002g0108a0001c0001t0002g0110others(33): Show | 38 | HG00408.hp2 HG00438.hp1 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.823-28724G>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51054084 | ||||||
| chr14:51054094
|
T | C | 1 | a0002c0002t0003g0239 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.823-28734A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51054094 | ||||||
| chr14:51054122
|
G | A | 4 | a0001c0001t0005g0032a0001c0001t0005g0033a0002c0002t0008g0325others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.823-28762C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51054122 | ||||||
| chr14:51054134
|
T | C | 4 | a0001c0001t0005g0032a0001c0001t0005g0033a0002c0002t0008g0325others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.823-28774A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51054134 | ||||||
| chr14:51054297
|
T | TTTGTTGT others(2): Show |
190 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0205others(187): Show | 194 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.823-28946_823-2893 others(13): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51054297 | ||||||
| chr14:51054297
|
T | TTTGTTGT others(5): Show |
17 | a0001c0001t0001g0132a0001c0001t0002g0141a0001c0001t0002g0147others(14): Show | 18 | HG00738.hp1 HG01074.hp2 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.823-28949_823-2893 others(16): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51054297 | ||||||
| chr14:51054319
|
C | A | 2 | a0002c0002t0001g0092a0002c0002t0001g0093 | 2 | HG01891.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.823-28959G>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51054319 | ||||||
| chr14:51054447
|
AT | A | 254 | a0001c0001t0001g0122a0001c0001t0001g0132a0001c0001t0001g0178others(251): Show | 261 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.823-29088delA | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51054447 | ||||||
| chr14:51054547
|
A | G | 1 | a0001c0001t0003g0130 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.823-29187T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51054547 | ||||||
| chr14:51054568
|
C | G | 123 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0206others(120): Show | 124 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.823-29208G>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51054568 | ||||||
| chr14:51054605
|
G | A | 4 | a0001c0001t0001g0310a0002c0002t0001g0030a0002c0002t0001g0245others(1): Show | 4 | HG02809.hp2 HG02970.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.823-29245C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51054605 | ||||||
| chr14:51054629
|
G | A | 1 | a0002c0002t0001g0265 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.823-29269C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51054629 | ||||||
| chr14:51054711
|
C | G | 7 | a0001c0001t0004g0148a0001c0001t0005g0026a0001c0001t0005g0027others(4): Show | 7 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.823-29351G>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51054711 | ||||||
| chr14:51054731
|
G | A | 116 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0206others(113): Show | 117 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.823-29371C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51054731 | ||||||
| chr14:51054805
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.823-29445G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51054805 | ||||||
| chr14:51054963
|
G | A | 115 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0206others(112): Show | 116 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.823-29603C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51054963 | ||||||
| chr14:51054979
|
G | A | 1 | a0001c0001t0003g0080 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.823-29619C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51054979 | ||||||
| chr14:51054997
|
T | C | 1 | a0001c0001t0001g0132 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.823-29637A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51054997 | ||||||
| chr14:51055016
|
A | G | 1 | a0001c0001t0004g0148 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.823-29656T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51055016 | ||||||
| chr14:51055073
|
C | T | 1 | a0001c0001t0002g0165 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.823-29713G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51055073 | ||||||
| chr14:51055102
|
G | A | 1 | a0001c0001t0003g0163 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.823-29742C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51055102 | ||||||
| chr14:51055486
|
T | C | 1 | a0001c0001t0004g0266 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.823-30126A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51055486 | ||||||
| chr14:51055678
|
T | C | 131 | a0001c0001t0001g0122a0001c0001t0001g0132a0001c0001t0001g0324others(128): Show | 137 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.823-30318A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51055678 | ||||||
| chr14:51055767
|
T | C | 131 | a0001c0001t0001g0122a0001c0001t0001g0132a0001c0001t0001g0324others(128): Show | 137 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.823-30407A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51055767 | ||||||
| chr14:51055839
|
C | G | 131 | a0001c0001t0001g0122a0001c0001t0001g0132a0001c0001t0001g0324others(128): Show | 137 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.823-30479G>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51055839 | ||||||
| chr14:51056042
|
C | T | 7 | a0001c0001t0004g0148a0001c0001t0005g0026a0001c0001t0005g0027others(4): Show | 7 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.823-30682G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51056042 | ||||||
| chr14:51056117
|
G | A | 138 | a0001c0001t0001g0122a0001c0001t0001g0132a0001c0001t0001g0205others(135): Show | 144 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.823-30757C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51056117 | ||||||
| chr14:51056170
|
T | C | 1 | a0001c0001t0005g0026 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.823-30810A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51056170 | ||||||
| chr14:51056237
|
T | C | 138 | a0001c0001t0001g0122a0001c0001t0001g0132a0001c0001t0001g0205others(135): Show | 144 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.823-30877A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51056237 | ||||||
| chr14:51056436
|
T | C | 138 | a0001c0001t0001g0122a0001c0001t0001g0132a0001c0001t0001g0205others(135): Show | 144 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.823-31076A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51056436 | ||||||
| chr14:51056481
|
CCAGAGCT others(13): Show |
C | 15 | a0001c0001t0001g0324a0001c0001t0002g0283a0001c0001t0002g0284others(12): Show | 15 | HG00741.hp1 HG01081.hp1 HG02135.hp1 others(12): Show |
intron_variant | MODIFIER | c.823-31141_823-3112 others(24): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51056481 | ||||||
| chr14:51056701
|
T | C | 94 | a0001c0001t0001g0122a0001c0001t0001g0132a0001c0001t0001g0205others(91): Show | 97 | HG00408.hp2 HG00438.hp1 HG00738.hp1 others(94): Show |
intron_variant | MODIFIER | c.823-31341A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51056701 | ||||||
| chr14:51056845
|
C | T | 1 | a0001c0001t0001g0031 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.823-31485G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51056845 | ||||||
| chr14:51057005
|
C | T | 94 | a0001c0001t0001g0122a0001c0001t0001g0132a0001c0001t0001g0205others(91): Show | 97 | HG00408.hp2 HG00438.hp1 HG00738.hp1 others(94): Show |
intron_variant | MODIFIER | c.823-31645G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51057005 | ||||||
| chr14:51057101
|
G | A | 2 | a0002c0002t0001g0228a0002c0002t0013g0250 | 2 | HG02630.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.823-31741C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51057101 | ||||||
| chr14:51057500
|
G | A | 94 | a0001c0001t0001g0122a0001c0001t0001g0132a0001c0001t0001g0205others(91): Show | 97 | HG00408.hp2 HG00438.hp1 HG00738.hp1 others(94): Show |
intron_variant | MODIFIER | c.823-32140C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51057500 | ||||||
| chr14:51057521
|
A | G | 116 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0206others(113): Show | 117 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.823-32161T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51057521 | ||||||
| chr14:51057524
|
A | C | 4 | a0001c0001t0005g0032a0001c0001t0005g0033a0002c0002t0008g0325others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.823-32164T>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51057524 | ||||||
| chr14:51057698
|
T | G | 1 | a0002c0002t0003g0044 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.823-32338A>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51057698 | ||||||
| chr14:51057734
|
A | G | 94 | a0001c0001t0001g0122a0001c0001t0001g0132a0001c0001t0001g0205others(91): Show | 97 | HG00408.hp2 HG00438.hp1 HG00738.hp1 others(94): Show |
intron_variant | MODIFIER | c.823-32374T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51057734 | ||||||
| chr14:51057771
|
C | G | 94 | a0001c0001t0001g0122a0001c0001t0001g0132a0001c0001t0001g0205others(91): Show | 97 | HG00408.hp2 HG00438.hp1 HG00738.hp1 others(94): Show |
intron_variant | MODIFIER | c.823-32411G>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51057771 | ||||||
| chr14:51057806
|
C | T | 94 | a0001c0001t0001g0122a0001c0001t0001g0132a0001c0001t0001g0205others(91): Show | 97 | HG00408.hp2 HG00438.hp1 HG00738.hp1 others(94): Show |
intron_variant | MODIFIER | c.823-32446G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51057806 | ||||||
| chr14:51057952
|
T | C | 254 | a0001c0001t0001g0122a0001c0001t0001g0132a0001c0001t0001g0178others(251): Show | 261 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.823-32592A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51057952 | ||||||
| chr14:51058166
|
G | C | 1 | a0001c0001t0003g0170 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.823-32806C>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51058166 | ||||||
| chr14:51058208
|
G | T | 1 | a0002c0002t0004g0046 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.823-32848C>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51058208 | ||||||
| chr14:51058211
|
T | C | 94 | a0001c0001t0001g0122a0001c0001t0001g0132a0001c0001t0001g0205others(91): Show | 97 | HG00408.hp2 HG00438.hp1 HG00738.hp1 others(94): Show |
intron_variant | MODIFIER | c.823-32851A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51058211 | ||||||
| chr14:51058288
|
C | T | 1 | a0001c0001t0012g0291 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.823-32928G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51058288 | ||||||
| chr14:51058344
|
C | T | 1 | a0002c0012t0005g0161 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.823-32984G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51058344 | ||||||
| chr14:51058456
|
C | A | 98 | a0001c0001t0001g0122a0001c0001t0001g0132a0001c0001t0001g0205others(95): Show | 101 | HG00408.hp2 HG00438.hp1 HG00639.hp1 others(98): Show |
intron_variant | MODIFIER | c.823-33096G>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51058456 | ||||||
| chr14:51058479
|
A | G | 98 | a0001c0001t0001g0122a0001c0001t0001g0132a0001c0001t0001g0205others(95): Show | 101 | HG00408.hp2 HG00438.hp1 HG00639.hp1 others(98): Show |
intron_variant | MODIFIER | c.823-33119T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51058479 | ||||||
| chr14:51058561
|
G | A | 74 | a0001c0001t0001g0122a0001c0001t0001g0324a0001c0001t0002g0108others(71): Show | 76 | HG00408.hp2 HG00438.hp1 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.823-33201C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51058561 | ||||||
| chr14:51058606
|
C | T | 5 | a0001c0001t0001g0122a0002c0002t0001g0020a0002c0002t0001g0021others(2): Show | 5 | HG01358.hp1 HG02895.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.823-33246G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51058606 | ||||||
| chr14:51058647
|
ACAGCTGC | A | 40 | a0001c0001t0002g0235a0001c0001t0003g0254a0001c0001t0004g0232others(37): Show | 43 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.823-33294_823-3328 others(11): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51058647 | ||||||
| chr14:51058739
|
C | A | 4 | a0001c0001t0005g0032a0001c0001t0005g0033a0002c0002t0008g0325others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.823-33379G>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51058739 | ||||||
| chr14:51058755
|
A | G | 98 | a0001c0001t0001g0122a0001c0001t0001g0132a0001c0001t0001g0205others(95): Show | 101 | HG00408.hp2 HG00438.hp1 HG00639.hp1 others(98): Show |
intron_variant | MODIFIER | c.823-33395T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51058755 | ||||||
| chr14:51058818
|
G | A | 1 | a0002c0002t0001g0181 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.823-33458C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51058818 | ||||||
| chr14:51058923
|
T | C | 1 | a0001c0001t0009g0096 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.823-33563A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51058923 | ||||||
| chr14:51058968
|
C | T | 98 | a0001c0001t0001g0122a0001c0001t0001g0132a0001c0001t0001g0205others(95): Show | 101 | HG00408.hp2 HG00438.hp1 HG00639.hp1 others(98): Show |
intron_variant | MODIFIER | c.823-33608G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51058968 | ||||||
| chr14:51059036
|
G | A | 1 | a0002c0002t0014g0008 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.823-33676C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51059036 | ||||||
| chr14:51059076
|
T | C | 98 | a0001c0001t0001g0122a0001c0001t0001g0132a0001c0001t0001g0205others(95): Show | 101 | HG00408.hp2 HG00438.hp1 HG00639.hp1 others(98): Show |
intron_variant | MODIFIER | c.823-33716A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51059076 | ||||||
| chr14:51059083
|
C | G | 1 | a0001c0001t0002g0316 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.823-33723G>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51059083 | ||||||
| chr14:51059365
|
C | G | 98 | a0001c0001t0001g0122a0001c0001t0001g0132a0001c0001t0001g0205others(95): Show | 101 | HG00408.hp2 HG00438.hp1 HG00639.hp1 others(98): Show |
intron_variant | MODIFIER | c.823-34005G>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51059365 | ||||||
| chr14:51059466
|
A | G | 31 | a0001c0001t0001g0324a0001c0001t0002g0283a0001c0001t0002g0284others(28): Show | 31 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.823-34106T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51059466 | ||||||
| chr14:51059480
|
A | AAAAAC | 24 | a0001c0001t0001g0132a0001c0001t0001g0205a0001c0001t0001g0287others(21): Show | 25 | HG00738.hp1 HG01074.hp2 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.823-34125_823-3412 others(9): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51059480 | ||||||
| chr14:51059623
|
C | T | 2 | a0001c0001t0002g0218a0001c0001t0002g0219 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.823-34263G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51059623 | ||||||
| chr14:51059647
|
A | C | 1 | a0001c0001t0002g0187 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.823-34287T>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51059647 | ||||||
| chr14:51059713
|
G | A | 1 | a0001c0001t0003g0198 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.823-34353C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51059713 | ||||||
| chr14:51059741
|
T | C | 1 | a0001c0001t0001g0287 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.822+34377A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51059741 | ||||||
| chr14:51059797
|
C | CA | 131 | a0001c0001t0001g0132a0001c0001t0001g0178a0001c0001t0001g0179others(128): Show | 133 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(130): Show |
intron_variant | MODIFIER | c.822+34320dupT | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51059797 | ||||||
| chr14:51059797
|
C | CAA | 7 | a0001c0001t0002g0147a0001c0001t0002g0152a0001c0001t0002g0199others(4): Show | 7 | HG00280.hp1 HG01981.hp1 HG03492.hp2 others(4): Show |
intron_variant | MODIFIER | c.822+34319_822+3432 others(6): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51059797 | ||||||
| chr14:51059843
|
A | G | 40 | a0001c0001t0002g0235a0001c0001t0003g0254a0001c0001t0004g0232others(37): Show | 43 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.822+34275T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51059843 | ||||||
| chr14:51059856
|
C | G | 36 | a0001c0001t0001g0122a0001c0001t0002g0108a0001c0001t0002g0110others(33): Show | 38 | HG00408.hp2 HG00438.hp1 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.822+34262G>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51059856 | ||||||
| chr14:51059915
|
C | T | 1 | a0002c0002t0013g0035 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.822+34203G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51059915 | ||||||
| chr14:51059977
|
T | C | 2 | a0001c0001t0002g0316a0001c0001t0003g0317 | 2 | HG01243.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.822+34141A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51059977 | ||||||
| chr14:51060018
|
T | C | 1 | a0001c0005t0002g0255 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.822+34100A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51060018 | ||||||
| chr14:51060071
|
A | G | 118 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0206others(115): Show | 119 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.822+34047T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51060071 | ||||||
| chr14:51060072
|
T | C | 27 | a0001c0001t0001g0324a0001c0001t0002g0283a0001c0001t0002g0284others(24): Show | 27 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.822+34046A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51060072 | ||||||
| chr14:51060082
|
A | C | 147 | a0001c0001t0001g0132a0001c0001t0001g0178a0001c0001t0001g0179others(144): Show | 149 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(146): Show |
intron_variant | MODIFIER | c.822+34036T>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51060082 | ||||||
| chr14:51060106
|
T | C | 3 | a0001c0001t0002g0058a0001c0001t0002g0059a0001c0001t0002g0060 | 3 | HG00733.hp1 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.822+34012A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51060106 | ||||||
| chr14:51060324
|
T | C | 1 | a0002c0010t0005g0016 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.822+33794A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51060324 | ||||||
| chr14:51060456
|
C | A | 116 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0206others(113): Show | 117 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.822+33662G>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51060456 | ||||||
| chr14:51060511
|
G | A | 2 | a0001c0001t0015g0240a0002c0002t0003g0239 | 2 | HG00140.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.822+33607C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51060511 | ||||||
| chr14:51060553
|
A | G | 116 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0206others(113): Show | 117 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.822+33565T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51060553 | ||||||
| chr14:51060626
|
C | T | 116 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0206others(113): Show | 117 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.822+33492G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51060626 | ||||||
| chr14:51060657
|
C | T | 7 | a0001c0001t0002g0153a0001c0001t0002g0154a0001c0001t0002g0155others(4): Show | 7 | HG00735.hp1 HG01167.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.822+33461G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51060657 | ||||||
| chr14:51060719
|
G | A | 7 | a0001c0001t0001g0205a0001c0001t0001g0287a0001c0003t0001g0014others(4): Show | 7 | HG01433.hp1 HG02486.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.822+33399C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51060719 | ||||||
| chr14:51060847
|
A | G | 40 | a0001c0001t0002g0235a0001c0001t0003g0254a0001c0001t0004g0232others(37): Show | 43 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.822+33271T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51060847 | ||||||
| chr14:51060980
|
G | A | 40 | a0001c0001t0002g0235a0001c0001t0003g0254a0001c0001t0004g0232others(37): Show | 43 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.822+33138C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51060980 | ||||||
| chr14:51061239
|
C | T | 2 | a0001c0001t0002g0316a0001c0001t0003g0317 | 2 | HG01243.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.822+32879G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51061239 | ||||||
| chr14:51061300
|
C | A | 40 | a0001c0001t0002g0235a0001c0001t0003g0254a0001c0001t0004g0232others(37): Show | 43 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.822+32818G>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51061300 | ||||||
| chr14:51061344
|
C | T | 2 | a0001c0001t0002g0176a0001c0001t0002g0186 | 2 | HG03490.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.822+32774G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51061344 | ||||||
| chr14:51061392
|
G | A | 7 | a0001c0001t0004g0148a0001c0001t0005g0026a0001c0001t0005g0027others(4): Show | 7 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.822+32726C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51061392 | ||||||
| chr14:51061415
|
G | GA | 99 | a0001c0001t0001g0122a0001c0001t0001g0132a0001c0001t0001g0205others(96): Show | 102 | HG00408.hp2 HG00438.hp1 HG00639.hp1 others(99): Show |
intron_variant | MODIFIER | c.822+32702dupT | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51061415 | ||||||
| chr14:51061415
|
G | GAA | 8 | a0001c0001t0003g0254a0001c0001t0004g0253a0001c0005t0002g0251others(5): Show | 8 | HG01167.hp1 HG03834.hp1 NA18954.hp1 others(5): Show |
intron_variant | MODIFIER | c.822+32701_822+3270 others(6): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51061415 | ||||||
| chr14:51061415
|
G | GAAA | 32 | a0001c0001t0002g0235a0001c0001t0004g0232a0001c0001t0010g0329others(29): Show | 35 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.822+32700_822+3270 others(7): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51061415 | ||||||
| chr14:51061457
|
G | A | 2 | a0001c0001t0002g0316a0001c0001t0003g0317 | 2 | HG01243.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.822+32661C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51061457 | ||||||
| chr14:51061815
|
T | C | 14 | a0001c0001t0002g0283a0001c0001t0002g0284a0001c0001t0002g0285others(11): Show | 14 | HG00741.hp1 HG01081.hp1 HG02135.hp1 others(11): Show |
intron_variant | MODIFIER | c.822+32303A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51061815 | ||||||
| chr14:51061833
|
TTCATCTT others(3): Show |
T | 1 | a0002c0002t0006g0018 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.822+32275_822+3228 others(14): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51061833 | ||||||
| chr14:51061955
|
G | A | 1 | a0002c0002t0001g0030 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.822+32163C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51061955 | ||||||
| chr14:51062026
|
G | A | 1 | a0001c0001t0003g0163 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.822+32092C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51062026 | ||||||
| chr14:51062102
|
ATTAT | A | 40 | a0001c0001t0002g0235a0001c0001t0003g0254a0001c0001t0004g0232others(37): Show | 43 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.822+32012_822+3201 others(8): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51062102 | ||||||
| chr14:51062124
|
C | CT | 24 | a0001c0001t0001g0132a0001c0001t0001g0205a0001c0001t0001g0287others(21): Show | 25 | HG00738.hp1 HG01074.hp2 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.822+31993dupA | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51062124 | ||||||
| chr14:51062300
|
T | A | 1 | a0002c0002t0001g0288 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.822+31818A>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51062300 | ||||||
| chr14:51062303
|
C | T | 1 | a0001c0001t0001g0031 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.822+31815G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51062303 | ||||||
| chr14:51062304
|
G | A | 40 | a0001c0001t0002g0235a0001c0001t0003g0254a0001c0001t0004g0232others(37): Show | 43 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.822+31814C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51062304 | ||||||
| chr14:51062358
|
A | T | 31 | a0001c0001t0001g0324a0001c0001t0002g0283a0001c0001t0002g0284others(28): Show | 31 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.822+31760T>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51062358 | ||||||
| chr14:51062404
|
G | A | 7 | a0001c0001t0004g0148a0001c0001t0005g0026a0001c0001t0005g0027others(4): Show | 7 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.822+31714C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51062404 | ||||||
| chr14:51062425
|
C | G | 1 | a0001c0001t0002g0056 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.822+31693G>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51062425 | ||||||
| chr14:51062511
|
T | G | 24 | a0001c0001t0001g0132a0001c0001t0001g0205a0001c0001t0001g0287others(21): Show | 25 | HG00738.hp1 HG01074.hp2 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.822+31607A>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51062511 | ||||||
| chr14:51062619
|
T | C | 138 | a0001c0001t0001g0122a0001c0001t0001g0132a0001c0001t0001g0205others(135): Show | 144 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.822+31499A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51062619 | ||||||
| chr14:51062695
|
G | C | 2 | a0002c0002t0003g0117a0002c0002t0003g0118 | 2 | NA18984.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.822+31423C>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51062695 | ||||||
| chr14:51062831
|
A | G | 1 | a0001c0001t0003g0063 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.822+31287T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51062831 | ||||||
| chr14:51062840
|
T | A | 40 | a0001c0001t0002g0235a0001c0001t0003g0254a0001c0001t0004g0232others(37): Show | 43 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.822+31278A>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51062840 | ||||||
| chr14:51063112
|
G | A | 1 | a0002c0002t0006g0223 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.822+31006C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51063112 | ||||||
| chr14:51063252
|
C | T | 24 | a0001c0001t0001g0132a0001c0001t0001g0205a0001c0001t0001g0287others(21): Show | 25 | HG00738.hp1 HG01074.hp2 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.822+30866G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51063252 | ||||||
| chr14:51063253
|
G | A | 7 | a0001c0001t0004g0148a0001c0001t0005g0026a0001c0001t0005g0027others(4): Show | 7 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.822+30865C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51063253 | ||||||
| chr14:51063267
|
G | A | 3 | a0001c0001t0001g0216a0002c0002t0001g0175a0002c0002t0004g0212 | 3 | HG03130.hp1 HG03579.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.822+30851C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51063267 | ||||||
| chr14:51063272
|
G | A | 7 | a0001c0001t0004g0148a0001c0001t0005g0026a0001c0001t0005g0027others(4): Show | 7 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.822+30846C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51063272 | ||||||
| chr14:51063355
|
C | T | 7 | a0001c0001t0004g0148a0001c0001t0005g0026a0001c0001t0005g0027others(4): Show | 7 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.822+30763G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51063355 | ||||||
| chr14:51063461
|
T | G | 7 | a0001c0001t0004g0148a0001c0001t0005g0026a0001c0001t0005g0027others(4): Show | 7 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.822+30657A>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51063461 | ||||||
| chr14:51063481
|
C | CAAG | 138 | a0001c0001t0001g0122a0001c0001t0001g0132a0001c0001t0001g0205others(135): Show | 144 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.822+30634_822+3063 others(7): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51063481 | ||||||
| chr14:51063673
|
G | A | 7 | a0001c0001t0004g0148a0001c0001t0005g0026a0001c0001t0005g0027others(4): Show | 7 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.822+30445C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51063673 | ||||||
| chr14:51063701
|
A | C | 1 | a0001c0001t0002g0322 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.822+30417T>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51063701 | ||||||
| chr14:51063742
|
T | A | 24 | a0001c0001t0001g0132a0001c0001t0001g0205a0001c0001t0001g0287others(21): Show | 25 | HG00738.hp1 HG01074.hp2 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.822+30376A>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51063742 | ||||||
| chr14:51063791
|
T | C | 7 | a0001c0001t0004g0148a0001c0001t0005g0026a0001c0001t0005g0027others(4): Show | 7 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.822+30327A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51063791 | ||||||
| chr14:51063818
|
T | C | 7 | a0001c0001t0004g0148a0001c0001t0005g0026a0001c0001t0005g0027others(4): Show | 7 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.822+30300A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51063818 | ||||||
| chr14:51063859
|
G | A | 40 | a0001c0001t0002g0235a0001c0001t0003g0254a0001c0001t0004g0232others(37): Show | 43 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.822+30259C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51063859 | ||||||
| chr14:51063909
|
C | A | 1 | a0001c0001t0002g0165 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.822+30209G>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51063909 | ||||||
| chr14:51063916
|
G | A | 1 | a0002c0002t0003g0281 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.822+30202C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51063916 | ||||||
| chr14:51063944
|
G | A | 1 | a0001c0001t0002g0201 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.822+30174C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51063944 | ||||||
| chr14:51064003
|
T | C | 1 | a0001c0001t0003g0129 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.822+30115A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51064003 | ||||||
| chr14:51064135
|
T | A | 107 | a0001c0001t0001g0122a0001c0001t0001g0132a0001c0001t0001g0205others(104): Show | 113 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.822+29983A>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51064135 | ||||||
| chr14:51064165
|
T | TA | 7 | a0001c0001t0004g0148a0001c0001t0005g0026a0001c0001t0005g0027others(4): Show | 7 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.822+29952dupT | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51064165 | ||||||
| chr14:51064179
|
T | A | 2 | a0001c0001t0003g0129a0001c0001t0003g0130 | 2 | HG00738.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.822+29939A>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51064179 | ||||||
| chr14:51064179
|
T | C | 98 | a0001c0001t0001g0122a0001c0001t0001g0132a0001c0001t0001g0205others(95): Show | 104 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.822+29939A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51064179 | ||||||
| chr14:51064266
|
A | T | 1 | a0001c0001t0002g0316 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.822+29852T>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51064266 | ||||||
| chr14:51064310
|
T | C | 1 | a0001c0001t0002g0127 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.822+29808A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51064310 | ||||||
| chr14:51064404
|
G | C | 7 | a0001c0001t0004g0148a0001c0001t0005g0026a0001c0001t0005g0027others(4): Show | 7 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.822+29714C>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51064404 | ||||||
| chr14:51064439
|
C | T | 7 | a0001c0001t0004g0148a0001c0001t0005g0026a0001c0001t0005g0027others(4): Show | 7 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.822+29679G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51064439 | ||||||
| chr14:51064468
|
C | T | 1 | a0002c0002t0001g0024 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.822+29650G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51064468 | ||||||
| chr14:51064508
|
A | AAAGT | 107 | a0001c0001t0001g0122a0001c0001t0001g0132a0001c0001t0001g0205others(104): Show | 113 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.822+29609_822+2961 others(8): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51064508 | ||||||
| chr14:51064560
|
G | C | 1 | a0001c0001t0004g0064 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.822+29558C>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51064560 | ||||||
| chr14:51064679
|
A | C | 75 | a0001c0001t0001g0122a0001c0001t0001g0310a0001c0001t0002g0108others(72): Show | 80 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.822+29439T>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51064679 | ||||||
| chr14:51064726
|
T | G | 24 | a0001c0001t0001g0132a0001c0001t0001g0205a0001c0001t0001g0287others(21): Show | 25 | HG00738.hp1 HG01074.hp2 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.822+29392A>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51064726 | ||||||
| chr14:51064924
|
A | G | 7 | a0001c0001t0004g0148a0001c0001t0005g0026a0001c0001t0005g0027others(4): Show | 7 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.822+29194T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51064924 | ||||||
| chr14:51064971
|
C | T | 1 | a0002c0002t0003g0109 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.822+29147G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51064971 | ||||||
| chr14:51065031
|
A | T | 36 | a0001c0001t0001g0122a0001c0001t0002g0108a0001c0001t0002g0110others(33): Show | 38 | HG00408.hp2 HG00438.hp1 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.822+29087T>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51065031 | ||||||
| chr14:51065418
|
A | T | 7 | a0001c0001t0004g0148a0001c0001t0005g0026a0001c0001t0005g0027others(4): Show | 7 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.822+28700T>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51065418 | ||||||
| chr14:51065433
|
C | A | 7 | a0001c0001t0004g0148a0001c0001t0005g0026a0001c0001t0005g0027others(4): Show | 7 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.822+28685G>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51065433 | ||||||
| chr14:51065452
|
T | C | 7 | a0001c0001t0004g0148a0001c0001t0005g0026a0001c0001t0005g0027others(4): Show | 7 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.822+28666A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51065452 | ||||||
| chr14:51065569
|
A | C | 1 | a0002c0002t0004g0046 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.822+28549T>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51065569 | ||||||
| chr14:51065611
|
T | C | 7 | a0001c0001t0004g0148a0001c0001t0005g0026a0001c0001t0005g0027others(4): Show | 7 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.822+28507A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51065611 | ||||||
| chr14:51065848
|
A | G | 139 | a0001c0001t0001g0122a0001c0001t0001g0132a0001c0001t0001g0205others(136): Show | 145 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.822+28270T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51065848 | ||||||
| chr14:51066020
|
T | C | 4 | a0001c0001t0005g0032a0001c0001t0005g0033a0002c0002t0008g0325others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.822+28098A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51066020 | ||||||
| chr14:51066025
|
G | A | 40 | a0001c0001t0002g0235a0001c0001t0003g0254a0001c0001t0004g0232others(37): Show | 43 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.822+28093C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51066025 | ||||||
| chr14:51066052
|
A | AGAAG | 5 | a0001c0001t0001g0031a0001c0001t0001g0062a0001c0001t0002g0087others(2): Show | 5 | HG02004.hp2 NA18961.hp2 NA18992.hp1 others(2): Show |
intron_variant | MODIFIER | c.822+28062_822+2806 others(8): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51066052 | ||||||
| chr14:51066052
|
AGAAGGAA others(1): Show |
A | 119 | a0001c0001t0001g0122a0001c0001t0001g0178a0001c0001t0001g0179others(116): Show | 120 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.822+28058_822+2806 others(12): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51066052 | ||||||
| chr14:51066052
|
AGAAGGAA others(5): Show |
A | 1 | a0002c0002t0001g0207 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.822+28054_822+2806 others(16): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51066052 | ||||||
| chr14:51066083
|
A | G | 97 | a0001c0001t0001g0122a0001c0001t0001g0132a0001c0001t0001g0205others(94): Show | 100 | HG00408.hp2 HG00438.hp1 HG00639.hp1 others(97): Show |
intron_variant | MODIFIER | c.822+28035T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51066083 | ||||||
| chr14:51066087
|
A | AGGAAGGA others(5): Show |
4 | a0001c0001t0005g0026a0002c0002t0001g0025a0002c0002t0001g0092others(1): Show | 4 | HG01884.hp2 HG01891.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.822+28030_822+2803 others(16): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51066087 | ||||||
| chr14:51066087
|
A | AGGAGGGA others(5): Show |
1 | a0001c0001t0005g0027 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.822+28019_822+2803 others(16): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51066087 | ||||||
| chr14:51066087
|
A | G | 132 | a0001c0001t0001g0122a0001c0001t0001g0132a0001c0001t0001g0205others(129): Show | 138 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.822+28031T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51066087 | ||||||
| chr14:51066099
|
G | A | 2 | a0001c0001t0003g0129a0001c0001t0003g0130 | 2 | HG00738.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.822+28019C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51066099 | ||||||
| chr14:51066125
|
G | T | 1 | a0001c0001t0004g0323 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.822+27993C>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51066125 | ||||||
| chr14:51066273
|
A | G | 255 | a0001c0001t0001g0031a0001c0001t0001g0122a0001c0001t0001g0132others(252): Show | 262 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(259): Show |
intron_variant | MODIFIER | c.822+27845T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51066273 | ||||||
| chr14:51066337
|
C | T | 7 | a0001c0001t0004g0148a0001c0001t0005g0026a0001c0001t0005g0027others(4): Show | 7 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.822+27781G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51066337 | ||||||
| chr14:51066488
|
G | A | 7 | a0001c0001t0004g0148a0001c0001t0005g0026a0001c0001t0005g0027others(4): Show | 7 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.822+27630C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51066488 | ||||||
| chr14:51066725
|
A | T | 20 | a0001c0001t0001g0062a0001c0001t0002g0055a0001c0001t0002g0070others(17): Show | 21 | HG00423.hp2 HG01256.hp2 HG01346.hp2 others(18): Show |
intron_variant | MODIFIER | c.822+27393T>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51066725 | ||||||
| chr14:51066831
|
G | C | 1 | a0002c0012t0005g0161 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.822+27287C>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51066831 | ||||||
| chr14:51066924
|
T | C | 1 | a0001c0001t0002g0200 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.822+27194A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51066924 | ||||||
| chr14:51067139
|
T | C | 1 | a0002c0002t0001g0025 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.822+26979A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51067139 | ||||||
| chr14:51067170
|
T | C | 7 | a0001c0001t0004g0148a0001c0001t0005g0026a0001c0001t0005g0027others(4): Show | 7 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.822+26948A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51067170 | ||||||
| chr14:51067223
|
G | A | 31 | a0001c0001t0001g0324a0001c0001t0002g0283a0001c0001t0002g0284others(28): Show | 31 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.822+26895C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51067223 | ||||||
| chr14:51067233
|
C | T | 24 | a0001c0001t0001g0132a0001c0001t0002g0141a0001c0001t0002g0147others(21): Show | 25 | HG00738.hp1 HG01074.hp2 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.822+26885G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51067233 | ||||||
| chr14:51067336
|
C | T | 34 | a0001c0001t0001g0122a0001c0001t0002g0108a0001c0001t0002g0110others(31): Show | 36 | HG00408.hp2 HG00438.hp1 HG01256.hp1 others(33): Show |
intron_variant | MODIFIER | c.822+26782G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51067336 | ||||||
| chr14:51067388
|
G | A | 8 | a0001c0001t0004g0064a0001c0001t0004g0148a0001c0001t0005g0026others(5): Show | 8 | HG01346.hp2 HG01884.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.822+26730C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51067388 | ||||||
| chr14:51067413
|
T | C | 7 | a0001c0001t0004g0148a0001c0001t0005g0026a0001c0001t0005g0027others(4): Show | 7 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.822+26705A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51067413 | ||||||
| chr14:51067723
|
A | G | 1 | a0001c0001t0002g0272 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.822+26395T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51067723 | ||||||
| chr14:51067780
|
T | C | 113 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0206others(110): Show | 115 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.822+26338A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51067780 | ||||||
| chr14:51067859
|
GTTTAT | G | 40 | a0001c0001t0002g0235a0001c0001t0003g0254a0001c0001t0004g0232others(37): Show | 43 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.822+26254_822+2625 others(9): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51067859 | ||||||
| chr14:51067931
|
G | A | 42 | a0001c0001t0002g0235a0001c0001t0003g0254a0001c0001t0004g0232others(39): Show | 45 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.822+26187C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51067931 | ||||||
| chr14:51068171
|
T | C | 1 | a0001c0001t0003g0317 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.822+25947A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51068171 | ||||||
| chr14:51068280
|
G | C | 42 | a0001c0001t0002g0235a0001c0001t0003g0254a0001c0001t0004g0232others(39): Show | 45 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.822+25838C>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51068280 | ||||||
| chr14:51068292
|
G | C | 7 | a0001c0001t0004g0148a0001c0001t0005g0026a0001c0001t0005g0027others(4): Show | 7 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.822+25826C>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51068292 | ||||||
| chr14:51068349
|
A | AAAC | 42 | a0001c0001t0002g0235a0001c0001t0003g0254a0001c0001t0004g0232others(39): Show | 45 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.822+25766_822+2576 others(7): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51068349 | ||||||
| chr14:51068473
|
A | C | 42 | a0001c0001t0002g0235a0001c0001t0003g0254a0001c0001t0004g0232others(39): Show | 45 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.822+25645T>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51068473 | ||||||
| chr14:51068489
|
G | A | 1 | a0002c0002t0006g0018 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.822+25629C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51068489 | ||||||
| chr14:51068494
|
G | A | 1 | a0002c0002t0006g0018 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.822+25624C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51068494 | ||||||
| chr14:51068549
|
A | T | 42 | a0001c0001t0002g0235a0001c0001t0003g0254a0001c0001t0004g0232others(39): Show | 45 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.822+25569T>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51068549 | ||||||
| chr14:51068711
|
T | A | 42 | a0001c0001t0002g0235a0001c0001t0003g0254a0001c0001t0004g0232others(39): Show | 45 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.822+25407A>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51068711 | ||||||
| chr14:51068720
|
A | G | 42 | a0001c0001t0002g0235a0001c0001t0003g0254a0001c0001t0004g0232others(39): Show | 45 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.822+25398T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51068720 | ||||||
| chr14:51068734
|
G | A | 2 | a0001c0001t0002g0053a0001c0001t0003g0043 | 2 | NA18964.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.822+25384C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51068734 | ||||||
| chr14:51068757
|
C | T | 3 | a0001c0001t0010g0329a0001c0001t0019g0331a0002c0002t0010g0330 | 3 | HG02257.hp1 HG02630.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.822+25361G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51068757 | ||||||
| chr14:51068758
|
A | G | 1 | a0002c0002t0001g0229 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.822+25360T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51068758 | ||||||
| chr14:51068760
|
G | A | 4 | a0001c0001t0002g0322a0001c0001t0004g0241a0001c0001t0004g0323others(1): Show | 4 | HG01168.hp2 HG01361.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.822+25358C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51068760 | ||||||
| chr14:51068979
|
A | G | 241 | a0001c0001t0001g0103a0001c0001t0001g0122a0001c0001t0001g0132others(238): Show | 247 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.822+25139T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51068979 | ||||||
| chr14:51069043
|
T | C | 1 | a0001c0001t0002g0217 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.822+25075A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51069043 | ||||||
| chr14:51069060
|
A | T | 2 | a0001c0001t0002g0316a0001c0001t0003g0317 | 2 | HG01243.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.822+25058T>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51069060 | ||||||
| chr14:51069124
|
C | G | 4 | a0001c0001t0005g0032a0001c0001t0005g0033a0002c0002t0008g0325others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.822+24994G>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51069124 | ||||||
| chr14:51069181
|
C | T | 1 | a0001c0001t0002g0272 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.822+24937G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51069181 | ||||||
| chr14:51069283
|
G | A | 4 | a0001c0001t0005g0032a0001c0001t0005g0033a0002c0002t0008g0325others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.822+24835C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51069283 | ||||||
| chr14:51069345
|
T | C | 1 | a0001c0001t0002g0171 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.822+24773A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51069345 | ||||||
| chr14:51069404
|
A | T | 1 | a0001c0001t0002g0182 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.822+24714T>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51069404 | ||||||
| chr14:51069428
|
A | G | 122 | a0001c0001t0001g0103a0001c0001t0001g0122a0001c0001t0001g0132others(119): Show | 126 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(123): Show |
intron_variant | MODIFIER | c.822+24690T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51069428 | ||||||
| chr14:51069553
|
C | T | 42 | a0001c0001t0002g0235a0001c0001t0003g0254a0001c0001t0004g0232others(39): Show | 45 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.822+24565G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51069553 | ||||||
| chr14:51069671
|
T | C | 1 | a0002c0002t0006g0018 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.822+24447A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51069671 | ||||||
| chr14:51070071
|
A | G | 1 | a0002c0004t0005g0298 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.822+24047T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51070071 | ||||||
| chr14:51070086
|
T | C | 1 | a0001c0001t0002g0201 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.822+24032A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51070086 | ||||||
| chr14:51070111
|
T | G | 21 | a0001c0001t0001g0205a0001c0001t0002g0141a0001c0001t0002g0147others(18): Show | 22 | HG00738.hp1 HG01074.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.822+24007A>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51070111 | ||||||
| chr14:51070169
|
T | C | 1 | a0002c0002t0006g0018 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.822+23949A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51070169 | ||||||
| chr14:51070516
|
A | AT | 60 | a0001c0001t0001g0132a0001c0001t0001g0310a0001c0001t0001g0324others(57): Show | 61 | HG00639.hp1 HG00642.hp2 HG00738.hp1 others(58): Show |
intron_variant | MODIFIER | c.822+23601dupA | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51070516 | ||||||
| chr14:51070516
|
A | ATT | 22 | a0001c0001t0001g0103a0001c0001t0001g0122a0001c0001t0001g0287others(19): Show | 22 | HG01261.hp1 HG01358.hp1 HG02451.hp2 others(19): Show |
intron_variant | MODIFIER | c.822+23600_822+2360 others(6): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51070516 | ||||||
| chr14:51070550
|
A | G | 31 | a0001c0001t0001g0287a0001c0001t0001g0324a0001c0001t0002g0283others(28): Show | 31 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.822+23568T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51070550 | ||||||
| chr14:51070684
|
G | T | 1 | a0001c0001t0003g0049 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.822+23434C>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51070684 | ||||||
| chr14:51070778
|
A | T | 1 | a0001c0001t0005g0026 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.822+23340T>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51070778 | ||||||
| chr14:51070780
|
T | A | 1 | a0001c0001t0005g0026 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.822+23338A>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51070780 | ||||||
| chr14:51070839
|
T | C | 60 | a0001c0001t0001g0132a0001c0001t0001g0287a0001c0001t0001g0310others(57): Show | 61 | HG00639.hp1 HG00642.hp2 HG00738.hp1 others(58): Show |
intron_variant | MODIFIER | c.822+23279A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51070839 | ||||||
| chr14:51070975
|
T | C | 85 | a0001c0001t0001g0132a0001c0001t0001g0277a0001c0001t0001g0287others(82): Show | 86 | HG00438.hp2 HG00544.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.822+23143A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51070975 | ||||||
| chr14:51071034
|
C | T | 1 | a0002c0002t0001g0326 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.822+23084G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51071034 | ||||||
| chr14:51071093
|
G | A | 7 | a0001c0001t0001g0310a0001c0001t0002g0037a0001c0001t0009g0038others(4): Show | 7 | HG02145.hp2 HG02280.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.822+23025C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51071093 | ||||||
| chr14:51071253
|
G | A | 31 | a0001c0001t0001g0287a0001c0001t0001g0324a0001c0001t0002g0283others(28): Show | 31 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.822+22865C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51071253 | ||||||
| chr14:51071259
|
C | T | 60 | a0001c0001t0001g0132a0001c0001t0001g0287a0001c0001t0001g0310others(57): Show | 61 | HG00639.hp1 HG00642.hp2 HG00738.hp1 others(58): Show |
intron_variant | MODIFIER | c.822+22859G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51071259 | ||||||
| chr14:51071268
|
C | A | 2 | a0002c0002t0001g0007a0002c0002t0001g0227 | 3 | HG01081.hp2 HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.822+22850G>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51071268 | ||||||
| chr14:51071324
|
C | T | 8 | a0001c0001t0002g0283a0001c0001t0002g0284a0001c0001t0002g0285others(5): Show | 8 | HG02135.hp1 NA18955.hp1 NA18983.hp2 others(5): Show |
intron_variant | MODIFIER | c.822+22794G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51071324 | ||||||
| chr14:51071375
|
TAAAAAAA others(10): Show |
T | 1 | a0001c0001t0003g0006 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.822+22726_822+2274 others(21): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51071375 | ||||||
| chr14:51071387
|
G | GA | 12 | a0001c0001t0001g0028a0001c0001t0002g0268a0001c0003t0001g0010others(9): Show | 12 | HG01433.hp1 HG02055.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.822+22730dupT | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51071387 | ||||||
| chr14:51071387
|
GA | G | 42 | a0001c0001t0001g0310a0001c0001t0002g0073a0001c0001t0002g0235others(39): Show | 45 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(42): Show |
intron_variant | MODIFIER | c.822+22730delT | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51071387 | ||||||
| chr14:51071387
|
GAA | G | 68 | a0001c0001t0001g0132a0001c0001t0001g0205a0001c0001t0001g0287others(65): Show | 70 | HG00639.hp1 HG00642.hp2 HG00738.hp1 others(67): Show |
intron_variant | MODIFIER | c.822+22729_822+2273 others(6): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51071387 | ||||||
| chr14:51071388
|
A | G | 1 | a0001c0001t0003g0221 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.822+22730T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51071388 | ||||||
| chr14:51071441
|
T | C | 27 | a0001c0001t0001g0287a0001c0001t0001g0324a0001c0001t0002g0283others(24): Show | 27 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.822+22677A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51071441 | ||||||
| chr14:51071513
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.822+22605C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51071513 | ||||||
| chr14:51071646
|
T | C | 1 | a0002c0002t0001g0030 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.822+22472A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51071646 | ||||||
| chr14:51071660
|
A | C | 4 | a0001c0001t0002g0023a0001c0001t0002g0261a0001c0001t0002g0270others(1): Show | 4 | HG00597.hp2 HG02523.hp2 NA18941.hp2 others(1): Show |
intron_variant | MODIFIER | c.822+22458T>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51071660 | ||||||
| chr14:51071811
|
T | C | 50 | a0001c0001t0001g0205a0001c0001t0002g0235a0001c0001t0003g0254others(47): Show | 53 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.822+22307A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51071811 | ||||||
| chr14:51071955
|
C | A | 50 | a0001c0001t0001g0205a0001c0001t0002g0235a0001c0001t0003g0254others(47): Show | 53 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.822+22163G>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51071955 | ||||||
| chr14:51071970
|
G | A | 38 | a0001c0001t0001g0287a0001c0001t0001g0310a0001c0001t0001g0324others(35): Show | 38 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.822+22148C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51071970 | ||||||
| chr14:51072014
|
A | G | 1 | a0002c0002t0006g0018 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.822+22104T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51072014 | ||||||
| chr14:51072034
|
T | C | 74 | a0001c0001t0001g0103a0001c0001t0001g0122a0001c0001t0001g0132others(71): Show | 75 | HG00639.hp1 HG00642.hp2 HG00738.hp1 others(72): Show |
intron_variant | MODIFIER | c.822+22084A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51072034 | ||||||
| chr14:51072161
|
C | G | 1 | a0002c0002t0006g0018 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.822+21957G>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51072161 | ||||||
| chr14:51072655
|
CT | C | 77 | a0001c0001t0001g0103a0001c0001t0001g0122a0001c0001t0001g0132others(74): Show | 78 | HG00639.hp1 HG00642.hp2 HG00733.hp1 others(75): Show |
intron_variant | MODIFIER | c.822+21462delA | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51072655 | ||||||
| chr14:51072655
|
CTT | C | 58 | a0001c0001t0001g0205a0001c0001t0002g0235a0001c0001t0003g0254others(55): Show | 61 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.822+21461_822+2146 others(6): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51072655 | ||||||
| chr14:51072855
|
G | A | 1 | a0001c0001t0002g0202 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.822+21263C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51072855 | ||||||
| chr14:51072992
|
A | AT | 18 | a0001c0001t0001g0132a0001c0001t0002g0141a0001c0001t0002g0147others(15): Show | 19 | HG00738.hp1 HG01074.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.822+21125dupA | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51072992 | ||||||
| chr14:51072992
|
AT | A | 16 | a0001c0001t0002g0108a0001c0001t0002g0110a0001c0001t0002g0111others(13): Show | 17 | HG01256.hp1 HG01258.hp1 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.822+21125delA | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51072992 | ||||||
| chr14:51073048
|
T | C | 242 | a0001c0001t0001g0103a0001c0001t0001g0122a0001c0001t0001g0132others(239): Show | 248 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.822+21070A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51073048 | ||||||
| chr14:51073358
|
T | C | 1 | a0002c0002t0001g0203 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.822+20760A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51073358 | ||||||
| chr14:51073454
|
A | G | 58 | a0001c0001t0001g0205a0001c0001t0002g0235a0001c0001t0003g0254others(55): Show | 61 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.822+20664T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51073454 | ||||||
| chr14:51073500
|
G | A | 7 | a0002c0002t0001g0228a0002c0002t0001g0245a0002c0002t0001g0246others(4): Show | 7 | HG02630.hp2 HG02886.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.822+20618C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51073500 | ||||||
| chr14:51073501
|
T | G | 1 | a0004c0008t0001g0005 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.822+20617A>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51073501 | ||||||
| chr14:51073642
|
G | A | 29 | a0001c0001t0001g0132a0001c0001t0001g0310a0001c0001t0002g0037others(26): Show | 30 | HG00738.hp1 HG01074.hp2 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.822+20476C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51073642 | ||||||
| chr14:51073753
|
T | A | 6 | a0001c0001t0003g0254a0001c0001t0004g0253a0001c0005t0002g0251others(3): Show | 6 | NA18954.hp1 NA18973.hp2 NA18984.hp1 others(3): Show |
intron_variant | MODIFIER | c.822+20365A>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51073753 | ||||||
| chr14:51073789
|
A | C | 31 | a0001c0001t0001g0287a0001c0001t0001g0324a0001c0001t0002g0283others(28): Show | 31 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.822+20329T>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51073789 | ||||||
| chr14:51074105
|
C | T | 9 | a0001c0001t0001g0103a0001c0001t0004g0099a0001c0001t0004g0100others(6): Show | 9 | HG01261.hp1 HG02451.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.822+20013G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51074105 | ||||||
| chr14:51074106
|
G | C | 4 | a0001c0001t0010g0329a0001c0001t0019g0331a0002c0002t0010g0330others(1): Show | 4 | HG02257.hp1 HG02630.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.822+20012C>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51074106 | ||||||
| chr14:51074247
|
C | T | 2 | a0002c0002t0001g0092a0002c0002t0001g0093 | 2 | HG01891.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.822+19871G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51074247 | ||||||
| chr14:51074334
|
A | G | 18 | a0001c0001t0001g0062a0001c0001t0002g0055a0001c0001t0002g0061others(15): Show | 19 | HG00423.hp2 HG01346.hp2 HG01981.hp2 others(16): Show |
intron_variant | MODIFIER | c.822+19784T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51074334 | ||||||
| chr14:51074625
|
C | T | 31 | a0001c0001t0001g0287a0001c0001t0001g0324a0001c0001t0002g0283others(28): Show | 31 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.822+19493G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51074625 | ||||||
| chr14:51074728
|
G | A | 48 | a0001c0001t0001g0205a0001c0001t0002g0235a0001c0001t0003g0254others(45): Show | 51 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(48): Show |
intron_variant | MODIFIER | c.822+19390C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51074728 | ||||||
| chr14:51074836
|
C | T | 108 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0206others(105): Show | 110 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.822+19282G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51074836 | ||||||
| chr14:51074890
|
A | G | 181 | a0001c0001t0001g0103a0001c0001t0001g0122a0001c0001t0001g0178others(178): Show | 186 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.822+19228T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51074890 | ||||||
| chr14:51074935
|
A | G | 1 | a0002c0002t0006g0018 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.822+19183T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51074935 | ||||||
| chr14:51074990
|
C | A | 2 | a0001c0001t0009g0301a0002c0002t0005g0302 | 2 | HG02257.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.822+19128G>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51074990 | ||||||
| chr14:51075010
|
T | C | 1 | a0001c0014t0002g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.822+19108A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51075010 | ||||||
| chr14:51075233
|
A | G | 4 | a0001c0003t0001g0014a0001c0003t0007g0011a0001c0003t0007g0012others(1): Show | 4 | HG01433.hp1 HG02723.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.822+18885T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51075233 | ||||||
| chr14:51075244
|
G | A | 6 | a0001c0001t0002g0037a0001c0001t0009g0038a0001c0001t0017g0036others(3): Show | 6 | HG02145.hp2 HG02280.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.822+18874C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51075244 | ||||||
| chr14:51075399
|
G | T | 2 | a0001c0001t0002g0322a0001c0001t0004g0323 | 2 | HG01361.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.822+18719C>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51075399 | ||||||
| chr14:51075424
|
G | C | 1 | a0001c0001t0015g0240 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.822+18694C>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51075424 | ||||||
| chr14:51075461
|
T | C | 72 | a0001c0001t0001g0103a0001c0001t0001g0122a0001c0001t0001g0205others(69): Show | 75 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.822+18657A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51075461 | ||||||
| chr14:51075715
|
G | A | 1 | a0002c0002t0006g0018 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.822+18403C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51075715 | ||||||
| chr14:51075763
|
T | C | 4 | a0001c0001t0001g0277a0001c0001t0003g0258a0001c0001t0003g0260others(1): Show | 4 | NA18612.hp2 NA18949.hp2 NA18951.hp2 others(1): Show |
intron_variant | MODIFIER | c.822+18355A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51075763 | ||||||
| chr14:51075835
|
G | A | 2 | a0002c0002t0001g0288a0002c0004t0005g0298 | 2 | HG02886.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.822+18283C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51075835 | ||||||
| chr14:51076160
|
C | A | 10 | a0001c0001t0002g0037a0001c0001t0005g0032a0001c0001t0005g0033others(7): Show | 10 | HG02145.hp2 HG02280.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.822+17958G>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51076160 | ||||||
| chr14:51076160
|
C | T | 20 | a0001c0001t0001g0132a0001c0001t0002g0141a0001c0001t0002g0147others(17): Show | 21 | HG00738.hp1 HG01074.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.822+17958G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51076160 | ||||||
| chr14:51076461
|
A | G | 244 | a0001c0001t0001g0103a0001c0001t0001g0122a0001c0001t0001g0132others(241): Show | 249 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.822+17657T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51076461 | ||||||
| chr14:51076553
|
G | C | 2 | a0001c0001t0003g0168a0001c0001t0003g0169 | 2 | NA18956.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.822+17565C>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51076553 | ||||||
| chr14:51076721
|
G | A | 57 | a0001c0001t0001g0310a0001c0001t0002g0235a0001c0001t0003g0254others(54): Show | 60 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(57): Show |
intron_variant | MODIFIER | c.822+17397C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51076721 | ||||||
| chr14:51076755
|
C | T | 3 | a0001c0003t0001g0010a0002c0007t0001g0017a0002c0007t0011g0013 | 3 | HG02622.hp1 HG02647.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.822+17363G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51076755 | ||||||
| chr14:51076769
|
A | G | 3 | a0001c0003t0001g0010a0002c0007t0001g0017a0002c0007t0011g0013 | 3 | HG02622.hp1 HG02647.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.822+17349T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51076769 | ||||||
| chr14:51076794
|
A | G | 1 | a0002c0002t0003g0098 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.822+17324T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51076794 | ||||||
| chr14:51076827
|
C | A | 1 | a0002c0002t0006g0081 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.822+17291G>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51076827 | ||||||
| chr14:51077016
|
G | A | 1 | a0002c0004t0005g0311 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.822+17102C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51077016 | ||||||
| chr14:51077042
|
A | G | 1 | a0001c0001t0002g0173 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.822+17076T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51077042 | ||||||
| chr14:51077185
|
C | G | 33 | a0001c0001t0002g0045a0001c0001t0002g0052a0001c0001t0002g0053others(30): Show | 36 | HG00733.hp1 HG01168.hp2 HG01515.hp2 others(33): Show |
intron_variant | MODIFIER | c.822+16933G>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51077185 | ||||||
| chr14:51077205
|
A | G | 1 | a0002c0012t0005g0161 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.822+16913T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51077205 | ||||||
| chr14:51077217
|
C | A | 1 | a0001c0001t0001g0206 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.822+16901G>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51077217 | ||||||
| chr14:51077375
|
T | A | 8 | a0001c0003t0001g0010a0001c0003t0001g0014a0001c0003t0007g0011others(5): Show | 8 | HG01433.hp1 HG02622.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.822+16743A>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51077375 | ||||||
| chr14:51077386
|
G | GT | 54 | a0001c0001t0001g0028a0001c0001t0001g0122a0001c0001t0001g0132others(51): Show | 55 | HG00639.hp1 HG00642.hp2 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.822+16731dupA | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51077386 | ||||||
| chr14:51077386
|
G | GTT | 68 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0216others(65): Show | 68 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.822+16730_822+1673 others(6): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51077386 | ||||||
| chr14:51077386
|
G | GTTT | 47 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0211others(44): Show | 48 | HG00438.hp2 HG00544.hp2 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.822+16729_822+1673 others(7): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51077386 | ||||||
| chr14:51077386
|
G | GTTTT | 7 | a0001c0001t0003g0208a0001c0001t0003g0258a0001c0001t0003g0318others(4): Show | 7 | HG00621.hp2 HG00741.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.822+16728_822+1673 others(8): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51077386 | ||||||
| chr14:51077386
|
GT | G | 27 | a0001c0001t0002g0070a0001c0001t0002g0108a0001c0001t0002g0110others(24): Show | 28 | HG01099.hp1 HG01256.hp1 HG01256.hp2 others(25): Show |
intron_variant | MODIFIER | c.822+16731delA | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51077386 | ||||||
| chr14:51077386
|
GTTT | G | 13 | a0001c0001t0004g0148a0001c0001t0005g0026a0001c0003t0001g0010others(10): Show | 13 | HG01433.hp1 HG01884.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.822+16729_822+1673 others(7): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51077386 | ||||||
| chr14:51077386
|
GTTTTTTT others(4): Show |
G | 36 | a0001c0001t0002g0235a0001c0001t0003g0254a0001c0001t0004g0232others(33): Show | 39 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(36): Show |
intron_variant | MODIFIER | c.822+16721_822+1673 others(15): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51077386 | ||||||
| chr14:51077397
|
T | G | 2 | a0001c0001t0009g0096a0002c0002t0003g0029 | 2 | HG02572.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.822+16721A>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51077397 | ||||||
| chr14:51077616
|
T | A | 134 | a0001c0001t0001g0103a0001c0001t0001g0122a0001c0001t0001g0132others(131): Show | 138 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.822+16502A>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51077616 | ||||||
| chr14:51077646
|
G | A | 4 | a0001c0001t0001g0310a0002c0002t0001g0313a0002c0004t0005g0311others(1): Show | 4 | HG02809.hp2 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.822+16472C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51077646 | ||||||
| chr14:51077675
|
T | C | 1 | a0004c0008t0001g0005 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.822+16443A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51077675 | ||||||
| chr14:51077905
|
C | T | 41 | a0001c0001t0001g0310a0001c0001t0002g0235a0001c0001t0003g0254others(38): Show | 44 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(41): Show |
intron_variant | MODIFIER | c.822+16213G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51077905 | ||||||
| chr14:51078133
|
T | C | 34 | a0001c0001t0001g0103a0001c0001t0001g0122a0001c0001t0001g0132others(31): Show | 35 | HG00738.hp1 HG01074.hp2 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.822+15985A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51078133 | ||||||
| chr14:51078187
|
T | C | 3 | a0001c0001t0004g0126a0002c0002t0001g0019a0002c0002t0001g0125 | 3 | HG01515.hp1 HG02615.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.822+15931A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51078187 | ||||||
| chr14:51078205
|
G | A | 8 | a0001c0001t0004g0148a0001c0001t0005g0026a0001c0001t0005g0027others(5): Show | 8 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.822+15913C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51078205 | ||||||
| chr14:51078312
|
T | A | 1 | a0001c0001t0003g0143 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.822+15806A>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51078312 | ||||||
| chr14:51078642
|
C | T | 8 | a0001c0001t0004g0148a0001c0001t0005g0026a0001c0001t0005g0027others(5): Show | 8 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.822+15476G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51078642 | ||||||
| chr14:51078677
|
T | G | 20 | a0001c0001t0001g0132a0001c0001t0002g0141a0001c0001t0002g0147others(17): Show | 21 | HG00738.hp1 HG01074.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.822+15441A>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51078677 | ||||||
| chr14:51078883
|
T | A | 1 | a0002c0002t0001g0313 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.822+15235A>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51078883 | ||||||
| chr14:51079010
|
A | G | 1 | a0002c0002t0006g0018 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.822+15108T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51079010 | ||||||
| chr14:51079049
|
A | G | 1 | a0002c0002t0001g0025 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.822+15069T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51079049 | ||||||
| chr14:51079145
|
T | C | 8 | a0001c0001t0004g0148a0001c0001t0005g0026a0001c0001t0005g0027others(5): Show | 8 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.822+14973A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51079145 | ||||||
| chr14:51079149
|
A | G | 8 | a0001c0001t0004g0148a0001c0001t0005g0026a0001c0001t0005g0027others(5): Show | 8 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.822+14969T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51079149 | ||||||
| chr14:51079150
|
T | C | 2 | a0001c0001t0003g0082a0001c0001t0003g0084 | 2 | NA18979.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.822+14968A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51079150 | ||||||
| chr14:51079273
|
T | C | 1 | a0002c0002t0006g0018 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.822+14845A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51079273 | ||||||
| chr14:51079301
|
G | A | 1 | a0002c0007t0001g0017 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.822+14817C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51079301 | ||||||
| chr14:51079423
|
C | T | 9 | a0001c0001t0002g0267a0001c0001t0002g0268a0001c0001t0003g0318others(6): Show | 9 | HG00544.hp2 HG00621.hp2 NA18939.hp2 others(6): Show |
intron_variant | MODIFIER | c.822+14695G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51079423 | ||||||
| chr14:51079510
|
AT | A | 246 | a0001c0001t0001g0031a0001c0001t0001g0103a0001c0001t0001g0122others(243): Show | 251 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.822+14607delA | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51079510 | ||||||
| chr14:51079751
|
T | G | 20 | a0001c0001t0001g0132a0001c0001t0002g0141a0001c0001t0002g0147others(17): Show | 21 | HG00738.hp1 HG01074.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.822+14367A>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51079751 | ||||||
| chr14:51079818
|
C | T | 1 | a0001c0001t0002g0322 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.822+14300G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51079818 | ||||||
| chr14:51079936
|
G | A | 1 | a0002c0002t0001g0024 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.822+14182C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51079936 | ||||||
| chr14:51079989
|
G | T | 30 | a0001c0001t0001g0287a0001c0001t0001g0324a0001c0001t0002g0283others(27): Show | 30 | HG00639.hp1 HG00642.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.822+14129C>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51079989 | ||||||
| chr14:51080112
|
A | G | 8 | a0001c0001t0004g0148a0001c0001t0005g0026a0001c0001t0005g0027others(5): Show | 8 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.822+14006T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51080112 | ||||||
| chr14:51080226
|
TA | T | 29 | a0001c0001t0001g0287a0001c0001t0001g0324a0001c0001t0002g0283others(26): Show | 29 | HG00639.hp1 HG00642.hp2 HG02129.hp1 others(26): Show |
intron_variant | MODIFIER | c.822+13891delT | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51080226 | ||||||
| chr14:51080368
|
T | C | 2 | a0001c0001t0009g0096a0002c0002t0003g0029 | 2 | HG02572.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.822+13750A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51080368 | ||||||
| chr14:51080386
|
A | ATG | 8 | a0001c0001t0004g0148a0001c0001t0005g0026a0001c0001t0005g0027others(5): Show | 8 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.822+13730_822+1373 others(6): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51080386 | ||||||
| chr14:51080436
|
A | AAC | 4 | a0001c0001t0003g0048a0001c0001t0003g0049a0002c0002t0001g0039others(1): Show | 4 | HG00140.hp2 HG01884.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.822+13680_822+1368 others(6): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51080436 | ||||||
| chr14:51080436
|
AAC | A | 23 | a0001c0001t0001g0042a0001c0001t0002g0073a0001c0001t0002g0108others(20): Show | 23 | HG00738.hp1 HG01361.hp1 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.822+13680_822+1368 others(6): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51080436 | ||||||
| chr14:51080436
|
AACAC | A | 50 | a0001c0001t0001g0132a0001c0001t0001g0287a0001c0001t0002g0075others(47): Show | 55 | HG01109.hp1 HG01243.hp1 HG01256.hp1 others(52): Show |
intron_variant | MODIFIER | c.822+13678_822+1368 others(8): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51080436 | ||||||
| chr14:51080436
|
AACACAC | A | 110 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0205others(107): Show | 111 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.822+13676_822+1368 others(10): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51080436 | ||||||
| chr14:51080436
|
AACACACA others(1): Show |
A | 46 | a0001c0001t0001g0031a0001c0001t0001g0211a0001c0001t0001g0216others(43): Show | 46 | HG00738.hp2 HG00741.hp2 HG01099.hp1 others(43): Show |
intron_variant | MODIFIER | c.822+13674_822+1368 others(12): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51080436 | ||||||
| chr14:51080436
|
AACACACA others(3): Show |
A | 31 | a0001c0001t0002g0165a0001c0001t0002g0218a0001c0001t0002g0219others(28): Show | 34 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.822+13672_822+1368 others(14): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51080436 | ||||||
| chr14:51080436
|
AACACACA others(5): Show |
A | 18 | a0001c0001t0001g0310a0001c0001t0003g0254a0001c0001t0004g0253others(15): Show | 18 | HG00408.hp1 HG02809.hp2 HG02886.hp1 others(15): Show |
intron_variant | MODIFIER | c.822+13670_822+1368 others(16): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51080436 | ||||||
| chr14:51080436
|
AACACACA others(7): Show |
A | 3 | a0002c0002t0001g0313a0002c0004t0005g0311a0002c0004t0005g0312 | 3 | HG03041.hp2 HG03098.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.822+13668_822+1368 others(18): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51080436 | ||||||
| chr14:51080436
|
AACACACA others(9): Show |
A | 13 | a0001c0001t0001g0103a0001c0001t0001g0122a0001c0001t0004g0099others(10): Show | 13 | HG01261.hp1 HG01358.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.822+13666_822+1368 others(20): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51080436 | ||||||
| chr14:51080536
|
T | TA | 18 | a0001c0001t0001g0103a0001c0001t0001g0122a0001c0001t0001g0310others(15): Show | 18 | HG01261.hp1 HG01358.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.822+13581dupT | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51080536 | ||||||
| chr14:51080650
|
A | G | 1 | a0001c0001t0004g0314 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.822+13468T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51080650 | ||||||
| chr14:51080790
|
C | T | 18 | a0001c0001t0001g0103a0001c0001t0001g0122a0001c0001t0001g0310others(15): Show | 18 | HG01261.hp1 HG01358.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.822+13328G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51080790 | ||||||
| chr14:51080877
|
C | T | 20 | a0001c0001t0001g0132a0001c0001t0002g0141a0001c0001t0002g0147others(17): Show | 21 | HG00738.hp1 HG01074.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.822+13241G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51080877 | ||||||
| chr14:51080999
|
G | T | 1 | a0002c0002t0001g0123 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.822+13119C>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51080999 | ||||||
| chr14:51081168
|
C | A | 13 | a0001c0001t0001g0103a0001c0001t0001g0122a0001c0001t0004g0099others(10): Show | 13 | HG01261.hp1 HG01358.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.822+12950G>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51081168 | ||||||
| chr14:51081180
|
G | C | 1 | a0001c0001t0002g0220 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.822+12938C>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51081180 | ||||||
| chr14:51081308
|
T | C | 3 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0088 | 3 | NA18942.hp1 NA18961.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.822+12810A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51081308 | ||||||
| chr14:51081377
|
T | A | 124 | a0001c0001t0001g0103a0001c0001t0001g0122a0001c0001t0001g0132others(121): Show | 128 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.822+12741A>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51081377 | ||||||
| chr14:51081480
|
C | T | 1 | a0001c0001t0003g0167 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.822+12638G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51081480 | ||||||
| chr14:51081586
|
C | T | 1 | a0002c0012t0005g0161 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.822+12532G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51081586 | ||||||
| chr14:51081700
|
C | G | 8 | a0001c0001t0004g0148a0001c0001t0005g0026a0001c0001t0005g0027others(5): Show | 8 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.822+12418G>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51081700 | ||||||
| chr14:51081730
|
T | G | 1 | a0002c0002t0001g0120 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.822+12388A>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51081730 | ||||||
| chr14:51081731
|
G | A | 110 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0205others(107): Show | 111 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.822+12387C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51081731 | ||||||
| chr14:51081817
|
C | T | 1 | a0002c0002t0001g0030 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.822+12301G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51081817 | ||||||
| chr14:51081822
|
G | A | 246 | a0001c0001t0001g0031a0001c0001t0001g0103a0001c0001t0001g0122others(243): Show | 251 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.822+12296C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51081822 | ||||||
| chr14:51081945
|
A | C | 38 | a0001c0001t0002g0235a0001c0001t0003g0254a0001c0001t0004g0232others(35): Show | 41 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(38): Show |
intron_variant | MODIFIER | c.822+12173T>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51081945 | ||||||
| chr14:51081948
|
T | A | 5 | a0001c0001t0005g0026a0001c0001t0005g0027a0002c0002t0001g0025others(2): Show | 5 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.822+12170A>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51081948 | ||||||
| chr14:51081978
|
G | C | 1 | a0002c0002t0006g0018 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.822+12140C>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51081978 | ||||||
| chr14:51081985
|
G | A | 8 | a0001c0003t0001g0010a0001c0003t0001g0014a0001c0003t0007g0011others(5): Show | 8 | HG01433.hp1 HG02622.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.822+12133C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51081985 | ||||||
| chr14:51082271
|
T | G | 30 | a0001c0001t0001g0287a0001c0001t0001g0324a0001c0001t0002g0283others(27): Show | 30 | HG00639.hp1 HG00642.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.822+11847A>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51082271 | ||||||
| chr14:51082277
|
C | T | 1 | a0002c0002t0001g0303 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.822+11841G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51082277 | ||||||
| chr14:51082322
|
T | C | 1 | a0002c0012t0005g0161 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.822+11796A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51082322 | ||||||
| chr14:51082416
|
T | C | 1 | a0002c0002t0003g0281 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.822+11702A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51082416 | ||||||
| chr14:51082447
|
G | A | 10 | a0001c0001t0009g0096a0001c0003t0001g0010a0001c0003t0001g0014others(7): Show | 10 | HG01433.hp1 HG02572.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.822+11671C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51082447 | ||||||
| chr14:51082733
|
C | T | 22 | a0001c0001t0002g0108a0001c0001t0002g0110a0001c0001t0002g0111others(19): Show | 23 | HG01256.hp1 HG01258.hp1 HG01346.hp1 others(20): Show |
intron_variant | MODIFIER | c.822+11385G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51082733 | ||||||
| chr14:51082877
|
T | C | 7 | a0001c0001t0004g0148a0001c0001t0005g0026a0002c0002t0001g0024others(4): Show | 7 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.822+11241A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51082877 | ||||||
| chr14:51082916
|
G | T | 30 | a0001c0001t0001g0287a0001c0001t0001g0324a0001c0001t0002g0283others(27): Show | 30 | HG00639.hp1 HG00642.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.822+11202C>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51082916 | ||||||
| chr14:51083012
|
T | C | 1 | a0002c0002t0001g0166 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.822+11106A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51083012 | ||||||
| chr14:51083032
|
T | C | 18 | a0001c0001t0001g0103a0001c0001t0001g0122a0001c0001t0001g0310others(15): Show | 18 | HG01261.hp1 HG01358.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.822+11086A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51083032 | ||||||
| chr14:51083088
|
G | C | 1 | a0002c0004t0005g0149 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.822+11030C>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51083088 | ||||||
| chr14:51083120
|
C | T | 76 | a0001c0001t0001g0103a0001c0001t0001g0122a0001c0001t0001g0132others(73): Show | 80 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.822+10998G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51083120 | ||||||
| chr14:51083261
|
T | A | 1 | a0001c0001t0003g0221 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.822+10857A>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51083261 | ||||||
| chr14:51083358
|
T | C | 76 | a0001c0001t0001g0103a0001c0001t0001g0122a0001c0001t0001g0132others(73): Show | 80 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.822+10760A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51083358 | ||||||
| chr14:51083388
|
C | T | 3 | a0001c0001t0002g0283a0001c0001t0002g0284a0001c0001t0002g0285 | 3 | NA18983.hp2 NA19054.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.822+10730G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51083388 | ||||||
| chr14:51083395
|
C | T | 8 | a0001c0001t0004g0148a0001c0001t0005g0026a0001c0001t0005g0027others(5): Show | 8 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.822+10723G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51083395 | ||||||
| chr14:51083406
|
C | T | 76 | a0001c0001t0001g0103a0001c0001t0001g0122a0001c0001t0001g0132others(73): Show | 80 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.822+10712G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51083406 | ||||||
| chr14:51083430
|
A | AT | 34 | a0001c0001t0001g0103a0001c0001t0001g0122a0001c0001t0001g0132others(31): Show | 35 | HG00738.hp1 HG01074.hp2 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.822+10687_822+1068 others(5): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51083430 | ||||||
| chr14:51083431
|
A | AT | 42 | a0001c0001t0001g0310a0001c0001t0002g0235a0001c0001t0003g0254others(39): Show | 45 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(42): Show |
intron_variant | MODIFIER | c.822+10686dupA | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51083431 | ||||||
| chr14:51083431
|
A | T | 34 | a0001c0001t0001g0103a0001c0001t0001g0122a0001c0001t0001g0132others(31): Show | 35 | HG00738.hp1 HG01074.hp2 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.822+10687T>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51083431 | ||||||
| chr14:51083489
|
C | T | 78 | a0001c0001t0001g0103a0001c0001t0001g0122a0001c0001t0001g0132others(75): Show | 83 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.822+10629G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51083489 | ||||||
| chr14:51083529
|
T | C | 76 | a0001c0001t0001g0103a0001c0001t0001g0122a0001c0001t0001g0132others(73): Show | 80 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.822+10589A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51083529 | ||||||
| chr14:51083575
|
C | G | 76 | a0001c0001t0001g0103a0001c0001t0001g0122a0001c0001t0001g0132others(73): Show | 80 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.822+10543G>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51083575 | ||||||
| chr14:51083587
|
G | A | 13 | a0001c0001t0001g0103a0001c0001t0001g0122a0001c0001t0004g0099others(10): Show | 13 | HG01261.hp1 HG01358.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.822+10531C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51083587 | ||||||
| chr14:51083650
|
T | TG | 34 | a0001c0001t0001g0103a0001c0001t0001g0122a0001c0001t0001g0132others(31): Show | 35 | HG00738.hp1 HG01074.hp2 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.822+10467dupC | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51083650 | ||||||
| chr14:51083723
|
T | C | 11 | a0001c0001t0001g0031a0001c0001t0002g0037a0001c0001t0005g0032others(8): Show | 11 | HG02145.hp2 HG02280.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.822+10395A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51083723 | ||||||
| chr14:51083742
|
G | A | 1 | a0002c0002t0001g0022 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.822+10376C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51083742 | ||||||
| chr14:51083812
|
G | A | 76 | a0001c0001t0001g0103a0001c0001t0001g0122a0001c0001t0001g0132others(73): Show | 80 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.822+10306C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51083812 | ||||||
| chr14:51083917
|
G | C | 75 | a0001c0001t0001g0103a0001c0001t0001g0122a0001c0001t0001g0132others(72): Show | 79 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.822+10201C>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51083917 | ||||||
| chr14:51083917
|
G | T | 1 | a0002c0002t0001g0097 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.822+10201C>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51083917 | ||||||
| chr14:51083998
|
T | C | 8 | a0001c0001t0004g0148a0001c0001t0005g0026a0001c0001t0005g0027others(5): Show | 8 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.822+10120A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51083998 | ||||||
| chr14:51084141
|
A | T | 76 | a0001c0001t0001g0103a0001c0001t0001g0122a0001c0001t0001g0132others(73): Show | 80 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.822+9977T>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51084141 | ||||||
| chr14:51084156
|
G | A | 114 | a0001c0001t0001g0103a0001c0001t0001g0122a0001c0001t0001g0132others(111): Show | 118 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.822+9962C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51084156 | ||||||
| chr14:51084173
|
CT | C | 76 | a0001c0001t0001g0103a0001c0001t0001g0122a0001c0001t0001g0132others(73): Show | 80 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.822+9944delA | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51084173 | ||||||
| chr14:51084351
|
C | A | 125 | a0001c0001t0001g0103a0001c0001t0001g0122a0001c0001t0001g0132others(122): Show | 129 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.822+9767G>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51084351 | ||||||
| chr14:51084413
|
G | A | 1 | a0002c0002t0004g0321 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.822+9705C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51084413 | ||||||
| chr14:51084575
|
T | C | 1 | a0001c0001t0003g0222 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.822+9543A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51084575 | ||||||
| chr14:51084868
|
A | C | 34 | a0001c0001t0001g0103a0001c0001t0001g0122a0001c0001t0001g0132others(31): Show | 35 | HG00738.hp1 HG01074.hp2 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.822+9250T>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51084868 | ||||||
| chr14:51084976
|
C | T | 2 | a0001c0001t0004g0148a0002c0004t0005g0149 | 2 | HG02109.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.822+9142G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51084976 | ||||||
| chr14:51084979
|
A | G | 2 | a0001c0001t0009g0096a0002c0002t0003g0029 | 2 | HG02572.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.822+9139T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51084979 | ||||||
| chr14:51085139
|
A | G | 76 | a0001c0001t0001g0103a0001c0001t0001g0122a0001c0001t0001g0132others(73): Show | 80 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.822+8979T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51085139 | ||||||
| chr14:51085144
|
T | G | 76 | a0001c0001t0001g0103a0001c0001t0001g0122a0001c0001t0001g0132others(73): Show | 80 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.822+8974A>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51085144 | ||||||
| chr14:51085280
|
T | C | 1 | a0002c0002t0003g0282 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.822+8838A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51085280 | ||||||
| chr14:51085323
|
G | T | 8 | a0001c0001t0004g0148a0001c0001t0005g0026a0001c0001t0005g0027others(5): Show | 8 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.822+8795C>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51085323 | ||||||
| chr14:51085408
|
G | A | 76 | a0001c0001t0001g0103a0001c0001t0001g0122a0001c0001t0001g0132others(73): Show | 80 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.822+8710C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51085408 | ||||||
| chr14:51085430
|
C | CT | 126 | a0001c0001t0001g0103a0001c0001t0001g0122a0001c0001t0001g0132others(123): Show | 130 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.822+8687dupA | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51085430 | ||||||
| chr14:51085455
|
G | A | 20 | a0001c0001t0001g0132a0001c0001t0002g0141a0001c0001t0002g0147others(17): Show | 21 | HG00738.hp1 HG01074.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.822+8663C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51085455 | ||||||
| chr14:51085488
|
C | T | 4 | a0001c0001t0001g0310a0002c0002t0001g0313a0002c0004t0005g0311others(1): Show | 4 | HG02809.hp2 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.822+8630G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51085488 | ||||||
| chr14:51085598
|
G | A | 5 | a0001c0001t0005g0305a0002c0002t0001g0303a0002c0002t0001g0307others(2): Show | 5 | HG02723.hp1 HG02818.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.822+8520C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51085598 | ||||||
| chr14:51085641
|
G | C | 3 | a0002c0002t0002g0225a0002c0002t0006g0223a0002c0002t0006g0224 | 3 | NA18946.hp1 NA18993.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.822+8477C>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51085641 | ||||||
| chr14:51085699
|
C | T | 1 | a0002c0002t0006g0018 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.822+8419G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51085699 | ||||||
| chr14:51085843
|
T | C | 11 | a0001c0001t0001g0031a0001c0001t0002g0037a0001c0001t0005g0032others(8): Show | 11 | HG02145.hp2 HG02280.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.822+8275A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51085843 | ||||||
| chr14:51085868
|
T | C | 76 | a0001c0001t0001g0103a0001c0001t0001g0122a0001c0001t0001g0132others(73): Show | 80 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.822+8250A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51085868 | ||||||
| chr14:51085911
|
A | C | 114 | a0001c0001t0001g0103a0001c0001t0001g0122a0001c0001t0001g0132others(111): Show | 118 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.822+8207T>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51085911 | ||||||
| chr14:51086012
|
A | C | 76 | a0001c0001t0001g0103a0001c0001t0001g0122a0001c0001t0001g0132others(73): Show | 80 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.822+8106T>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51086012 | ||||||
| chr14:51086076
|
A | G | 76 | a0001c0001t0001g0103a0001c0001t0001g0122a0001c0001t0001g0132others(73): Show | 80 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.822+8042T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51086076 | ||||||
| chr14:51086137
|
A | G | 8 | a0001c0003t0001g0010a0001c0003t0001g0014a0001c0003t0007g0011others(5): Show | 8 | HG01433.hp1 HG02622.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.822+7981T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51086137 | ||||||
| chr14:51086224
|
T | C | 126 | a0001c0001t0001g0103a0001c0001t0001g0122a0001c0001t0001g0132others(123): Show | 130 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.822+7894A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51086224 | ||||||
| chr14:51086273
|
C | T | 76 | a0001c0001t0001g0103a0001c0001t0001g0122a0001c0001t0001g0132others(73): Show | 80 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.822+7845G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51086273 | ||||||
| chr14:51086364
|
CT | C | 76 | a0001c0001t0001g0103a0001c0001t0001g0122a0001c0001t0001g0132others(73): Show | 80 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.822+7753delA | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51086364 | ||||||
| chr14:51086412
|
A | T | 1 | a0002c0002t0006g0018 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.822+7706T>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51086412 | ||||||
| chr14:51086452
|
C | T | 76 | a0001c0001t0001g0103a0001c0001t0001g0122a0001c0001t0001g0132others(73): Show | 80 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.822+7666G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51086452 | ||||||
| chr14:51086590
|
A | G | 1 | a0004c0008t0001g0005 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.822+7528T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51086590 | ||||||
| chr14:51086660
|
G | C | 1 | a0001c0005t0002g0226 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.822+7458C>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51086660 | ||||||
| chr14:51086712
|
C | T | 1 | a0003c0006t0018g0151 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.822+7406G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51086712 | ||||||
| chr14:51086780
|
CCAGATCT others(12): Show |
C | 36 | a0001c0001t0001g0103a0001c0001t0001g0122a0001c0001t0002g0108others(33): Show | 37 | HG01256.hp1 HG01258.hp1 HG01261.hp1 others(34): Show |
intron_variant | MODIFIER | c.822+7319_822+7337d others(21): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51086780 | ||||||
| chr14:51086822
|
C | T | 1 | a0001c0001t0002g0150 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.822+7296G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51086822 | ||||||
| chr14:51086838
|
T | C | 13 | a0001c0001t0001g0103a0001c0001t0001g0122a0001c0001t0004g0099others(10): Show | 13 | HG01261.hp1 HG01358.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.822+7280A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51086838 | ||||||
| chr14:51086916
|
T | G | 20 | a0001c0001t0001g0132a0001c0001t0002g0141a0001c0001t0002g0147others(17): Show | 21 | HG00738.hp1 HG01074.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.822+7202A>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51086916 | ||||||
| chr14:51087195
|
G | T | 77 | a0001c0001t0001g0103a0001c0001t0001g0122a0001c0001t0001g0310others(74): Show | 81 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.822+6923C>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51087195 | ||||||
| chr14:51087277
|
A | C | 78 | a0001c0001t0001g0103a0001c0001t0001g0122a0001c0001t0001g0310others(75): Show | 82 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.822+6841T>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51087277 | ||||||
| chr14:51087338
|
AAG | A | 3 | a0002c0002t0001g0020a0002c0002t0001g0021a0002c0002t0001g0022 | 3 | HG02895.hp2 HG02970.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.822+6778_822+6779d others(4): Show |
TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51087338 | ||||||
| chr14:51087519
|
C | A | 4 | a0001c0001t0003g0094a0002c0002t0001g0089a0002c0002t0001g0090others(1): Show | 4 | NA18941.hp1 NA18983.hp1 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.822+6599G>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51087519 | ||||||
| chr14:51087765
|
G | C | 8 | a0001c0001t0004g0148a0001c0001t0005g0026a0001c0001t0005g0027others(5): Show | 8 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.822+6353C>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51087765 | ||||||
| chr14:51087868
|
A | T | 3 | a0001c0001t0002g0165a0002c0002t0001g0164a0002c0002t0001g0166 | 3 | HG02080.hp1 NA18949.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.822+6250T>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51087868 | ||||||
| chr14:51088084
|
T | G | 1 | a0001c0001t0003g0094 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.822+6034A>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51088084 | ||||||
| chr14:51088597
|
A | T | 1 | a0002c0002t0006g0018 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.822+5521T>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51088597 | ||||||
| chr14:51088670
|
G | A | 5 | a0001c0001t0002g0037a0001c0001t0009g0038a0001c0001t0017g0036others(2): Show | 5 | HG02145.hp2 HG02280.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.822+5448C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51088670 | ||||||
| chr14:51088988
|
GA | G | 76 | a0001c0001t0001g0277a0001c0001t0001g0287a0001c0001t0001g0324others(73): Show | 77 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.822+5129delT | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51088988 | ||||||
| chr14:51089047
|
A | G | 1 | a0002c0002t0001g0107 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.822+5071T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51089047 | ||||||
| chr14:51089057
|
A | G | 1 | a0002c0002t0006g0018 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.822+5061T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51089057 | ||||||
| chr14:51089105
|
G | A | 1 | a0002c0002t0006g0018 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.822+5013C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51089105 | ||||||
| chr14:51089114
|
G | A | 78 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0205others(75): Show | 78 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.822+5004C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51089114 | ||||||
| chr14:51089295
|
T | A | 1 | a0002c0002t0006g0018 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.822+4823A>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51089295 | ||||||
| chr14:51089319
|
G | T | 1 | a0002c0002t0006g0018 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.822+4799C>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51089319 | ||||||
| chr14:51089607
|
C | G | 2 | a0001c0001t0009g0096a0002c0002t0003g0029 | 2 | HG02572.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.822+4511G>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51089607 | ||||||
| chr14:51089782
|
C | T | 145 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0205others(142): Show | 146 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.822+4336G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51089782 | ||||||
| chr14:51089863
|
T | C | 38 | a0001c0001t0002g0235a0001c0001t0003g0254a0001c0001t0004g0232others(35): Show | 41 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(38): Show |
intron_variant | MODIFIER | c.822+4255A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51089863 | ||||||
| chr14:51089877
|
C | T | 1 | a0002c0002t0006g0018 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.822+4241G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51089877 | ||||||
| chr14:51090110
|
A | G | 8 | a0001c0003t0001g0010a0001c0003t0001g0014a0001c0003t0007g0011others(5): Show | 8 | HG01433.hp1 HG02622.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.822+4008T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51090110 | ||||||
| chr14:51090164
|
G | A | 17 | a0001c0001t0002g0108a0001c0001t0002g0110a0001c0001t0002g0111others(14): Show | 18 | HG01256.hp1 HG01258.hp1 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.822+3954C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51090164 | ||||||
| chr14:51090241
|
T | C | 65 | a0001c0001t0001g0277a0001c0001t0001g0287a0001c0001t0001g0310others(62): Show | 66 | HG00438.hp2 HG00544.hp2 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.822+3877A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51090241 | ||||||
| chr14:51090462
|
A | G | 1 | a0001c0001t0003g0043 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.822+3656T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51090462 | ||||||
| chr14:51090467
|
C | A | 1 | a0001c0001t0003g0043 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.822+3651G>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51090467 | ||||||
| chr14:51090468
|
A | C | 1 | a0001c0001t0003g0043 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.822+3650T>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51090468 | ||||||
| chr14:51090509
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.822+3609C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51090509 | ||||||
| chr14:51090551
|
G | T | 8 | a0001c0003t0001g0010a0001c0003t0001g0014a0001c0003t0007g0011others(5): Show | 8 | HG01433.hp1 HG02622.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.822+3567C>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51090551 | ||||||
| chr14:51090565
|
G | A | 1 | a0002c0002t0006g0018 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.822+3553C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51090565 | ||||||
| chr14:51090584
|
G | A | 1 | a0002c0002t0006g0018 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.822+3534C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51090584 | ||||||
| chr14:51090655
|
G | A | 1 | a0002c0002t0001g0095 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.822+3463C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51090655 | ||||||
| chr14:51090829
|
G | T | 1 | a0002c0002t0006g0018 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.822+3289C>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51090829 | ||||||
| chr14:51090848
|
C | T | 4 | a0001c0001t0001g0042a0002c0002t0001g0039a0002c0002t0001g0041others(1): Show | 4 | HG01884.hp1 HG02280.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.822+3270G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51090848 | ||||||
| chr14:51090996
|
T | G | 2 | a0001c0001t0002g0316a0001c0001t0003g0317 | 2 | HG01243.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.822+3122A>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51090996 | ||||||
| chr14:51091317
|
T | C | 3 | a0001c0001t0002g0147a0002c0002t0001g0145a0002c0002t0001g0146 | 3 | HG01981.hp1 HG02738.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.822+2801A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51091317 | ||||||
| chr14:51091467
|
G | A | 1 | a0002c0012t0005g0161 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.822+2651C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51091467 | ||||||
| chr14:51091507
|
G | A | 1 | a0002c0002t0006g0018 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.822+2611C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51091507 | ||||||
| chr14:51091553
|
T | C | 6 | a0001c0001t0004g0148a0001c0001t0005g0026a0001c0001t0005g0027others(3): Show | 6 | HG01884.hp2 HG01891.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.822+2565A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51091553 | ||||||
| chr14:51091604
|
G | A | 8 | a0001c0003t0001g0010a0001c0003t0001g0014a0001c0003t0007g0011others(5): Show | 8 | HG01433.hp1 HG02622.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.822+2514C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51091604 | ||||||
| chr14:51091724
|
T | C | 1 | a0002c0002t0006g0018 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.822+2394A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51091724 | ||||||
| chr14:51091795
|
A | C | 31 | a0001c0001t0001g0103a0001c0001t0001g0122a0001c0001t0002g0108others(28): Show | 32 | HG01256.hp1 HG01258.hp1 HG01261.hp1 others(29): Show |
intron_variant | MODIFIER | c.822+2323T>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51091795 | ||||||
| chr14:51091814
|
A | T | 78 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0205others(75): Show | 78 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.822+2304T>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51091814 | ||||||
| chr14:51091822
|
G | T | 269 | a0001c0001t0001g0031a0001c0001t0001g0103a0001c0001t0001g0122others(266): Show | 275 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.822+2296C>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51091822 | ||||||
| chr14:51091862
|
G | A | 66 | a0001c0001t0001g0277a0001c0001t0001g0287a0001c0001t0001g0310others(63): Show | 67 | HG00438.hp2 HG00544.hp2 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.822+2256C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51091862 | ||||||
| chr14:51091885
|
A | C | 1 | a0002c0012t0005g0161 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.822+2233T>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51091885 | ||||||
| chr14:51092018
|
T | C | 3 | a0001c0001t0005g0026a0001c0001t0005g0027a0002c0002t0001g0025 | 3 | HG01884.hp2 HG01891.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.822+2100A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51092018 | ||||||
| chr14:51092094
|
G | A | 2 | a0001c0001t0002g0316a0001c0001t0003g0317 | 2 | HG01243.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.822+2024C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51092094 | ||||||
| chr14:51092105
|
A | G | 12 | a0001c0001t0002g0150a0001c0001t0002g0152a0001c0001t0002g0153others(9): Show | 12 | HG00280.hp1 HG00735.hp1 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.822+2013T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51092105 | ||||||
| chr14:51092465
|
A | G | 1 | a0001c0001t0001g0028 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.822+1653T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51092465 | ||||||
| chr14:51092482
|
G | C | 1 | a0001c0001t0009g0096 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.822+1636C>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51092482 | ||||||
| chr14:51092484
|
C | A | 1 | a0002c0002t0006g0018 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.822+1634G>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51092484 | ||||||
| chr14:51092551
|
C | T | 1 | a0002c0002t0006g0018 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.822+1567G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51092551 | ||||||
| chr14:51092609
|
T | C | 1 | a0001c0001t0005g0027 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.822+1509A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51092609 | ||||||
| chr14:51092978
|
G | C | 2 | a0001c0001t0003g0318a0002c0002t0001g0319 | 2 | HG00621.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.822+1140C>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51092978 | ||||||
| chr14:51093004
|
A | C | 6 | a0001c0001t0004g0148a0001c0001t0005g0026a0001c0001t0005g0027others(3): Show | 6 | HG01884.hp2 HG01891.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.822+1114T>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51093004 | ||||||
| chr14:51093053
|
G | C | 67 | a0001c0001t0001g0103a0001c0001t0001g0122a0001c0001t0001g0132others(64): Show | 69 | HG00738.hp1 HG01074.hp2 HG01099.hp1 others(66): Show |
intron_variant | MODIFIER | c.822+1065C>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51093053 | ||||||
| chr14:51093213
|
T | C | 2 | a0001c0001t0004g0148a0002c0004t0005g0149 | 2 | HG02109.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.822+905A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51093213 | ||||||
| chr14:51093311
|
G | A | 183 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0205others(180): Show | 187 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.822+807C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51093311 | ||||||
| chr14:51093429
|
C | G | 1 | a0001c0001t0002g0023 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.822+689G>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51093429 | ||||||
| chr14:51093450
|
G | C | 1 | a0002c0002t0004g0321 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.822+668C>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51093450 | ||||||
| chr14:51093517
|
G | C | 2 | a0001c0001t0002g0322a0001c0001t0004g0323 | 2 | HG01361.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.822+601C>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51093517 | ||||||
| chr14:51093604
|
C | G | 1 | a0002c0002t0006g0018 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.822+514G>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51093604 | ||||||
| chr14:51093608
|
C | T | 3 | a0002c0002t0001g0020a0002c0002t0001g0021a0002c0002t0001g0022 | 3 | HG02895.hp2 HG02970.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.822+510G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51093608 | ||||||
| chr14:51093752
|
C | A | 1 | a0001c0001t0001g0324 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.822+366G>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51093752 | ||||||
| chr14:51093782
|
G | A | 1 | a0002c0002t0008g0325 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.822+336C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51093782 | ||||||
| chr14:51093960
|
T | C | 8 | a0001c0003t0001g0010a0001c0003t0001g0014a0001c0003t0007g0011others(5): Show | 8 | HG01433.hp1 HG02622.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.822+158A>G | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51093960 | ||||||
| chr14:51093981
|
C | T | 1 | a0002c0002t0001g0019 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.822+137G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51093981 | ||||||
| chr14:51094036
|
G | T | 1 | a0002c0002t0006g0018 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.822+82C>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51094036 | ||||||
| chr14:51094048
|
G | A | 1 | a0002c0002t0001g0326 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.822+70C>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51094048 | ||||||
| chr14:51094074
|
A | G | 1 | a0001c0014t0002g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.822+44T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51094074 |