Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | 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 | MEEME others(790): Show |
chr14 | 50970266 | 51100105 |
| a0002 | 1/1 | 795 | 150 | 52 | 25 | 50 | 5 | 16 | 39 | TRIM9_chr14_50970266_51100105 | TRIM9 | MEEME others(790): Show |
chr14 | 50970266 | 51100105 |
| a0003 | 0/0 | 795 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | MEEME others(790): Show |
chr14 | 50970266 | 51100105 |
| a0004 | 0/0 | 795 | 2 | 0 | 0 | 0 | 2 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | MEEME others(790): Show |
chr14 | 50970266 | 51100105 |
| a0005 | 0/0 | 795 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | MEEME others(790): Show |
chr14 | 50970266 | 51100105 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2385 | 175 | 31 | 40 | 79 | 7 | 18 | TRIM9_chr14_50970266_51100105 | TRIM9 | ATGGA others(2380): Show |
chr14 | 50970266 | 51100105 | ||
| a0001c0003 | 0/0 | 2385 | 5 | 4 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | ATGGA others(2380): Show |
chr14 | 50970266 | 51100105 | ||
| a0001c0005 | 0/0 | 2385 | 4 | 0 | 0 | 4 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | ATGGA others(2380): Show |
chr14 | 50970266 | 51100105 | ||
| a0001c0009 | 0/0 | 2385 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | ATGGA others(2380): Show |
chr14 | 50970266 | 51100105 | ||
| a0001c0014 | 0/0 | 2385 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | ATGGA others(2380): Show |
chr14 | 50970266 | 51100105 | ||
| a0002c0002 | 1/1 | 2385 | 140 | 44 | 24 | 49 | 5 | 16 | TRIM9_chr14_50970266_51100105 | TRIM9 | ATGGA others(2380): Show |
chr14 | 50970266 | 51100105 | ||
| a0002c0004 | 0/0 | 2385 | 5 | 5 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | ATGGA others(2380): Show |
chr14 | 50970266 | 51100105 | ||
| a0002c0007 | 0/0 | 2385 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | ATGGA others(2380): Show |
chr14 | 50970266 | 51100105 | ||
| a0002c0010 | 0/0 | 2385 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | ATGGA others(2380): Show |
chr14 | 50970266 | 51100105 | ||
| a0002c0012 | 0/0 | 2385 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | ATGGA others(2380): Show |
chr14 | 50970266 | 51100105 | ||
| a0002c0013 | 0/0 | 2385 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | ATGGA others(2380): Show |
chr14 | 50970266 | 51100105 | ||
| a0003c0006 | 0/0 | 2385 | 3 | 0 | 3 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | ATGGA others(2380): Show |
chr14 | 50970266 | 51100105 | ||
| a0004c0008 | 0/0 | 2385 | 2 | 0 | 0 | 0 | 2 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | ATGGA others(2380): Show |
chr14 | 50970266 | 51100105 | ||
| a0005c0011 | 0/0 | 2385 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | ATGGA others(2380): Show |
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 | ACAGA others(4574): Show |
chr14 | 50970266 | 51100105 |
| a0001c0001t0002 | 0/0 | 4579 | 72 | 2 | 19 | 34 | 4 | 13 | TRIM9_chr14_50970266_51100105 | TRIM9 | ACAGA others(4574): Show |
chr14 | 50970266 | 51100105 |
| a0001c0001t0003 | 0/0 | 4579 | 57 | 2 | 12 | 36 | 2 | 5 | TRIM9_chr14_50970266_51100105 | TRIM9 | ACAGA others(4574): Show |
chr14 | 50970266 | 51100105 |
| a0001c0001t0004 | 0/0 | 4579 | 15 | 6 | 5 | 3 | 1 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | ACAGA others(4574): Show |
chr14 | 50970266 | 51100105 |
| a0001c0001t0005 | 0/0 | 4579 | 5 | 5 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | ACAGA others(4574): Show |
chr14 | 50970266 | 51100105 |
| a0001c0001t0009 | 0/0 | 4579 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | ACAGA others(4574): Show |
chr14 | 50970266 | 51100105 |
| a0001c0001t0010 | 0/0 | 4579 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | ACAGA others(4574): Show |
chr14 | 50970266 | 51100105 |
| a0001c0001t0012 | 0/0 | 4579 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | ACAGA others(4574): Show |
chr14 | 50970266 | 51100105 |
| a0001c0001t0015 | 0/0 | 4579 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | ACAGA others(4574): Show |
chr14 | 50970266 | 51100105 |
| a0001c0001t0017 | 0/0 | 4579 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | ACAGA others(4574): Show |
chr14 | 50970266 | 51100105 |
| a0001c0001t0019 | 0/0 | 4579 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | ACAGA others(4574): Show |
chr14 | 50970266 | 51100105 |
| a0001c0003t0001 | 0/0 | 4579 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | ACAGA others(4574): Show |
chr14 | 50970266 | 51100105 |
| a0001c0003t0007 | 0/0 | 4579 | 3 | 2 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | ACAGA others(4574): Show |
chr14 | 50970266 | 51100105 |
| a0001c0005t0002 | 0/0 | 4579 | 4 | 0 | 0 | 4 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | ACAGA others(4574): Show |
chr14 | 50970266 | 51100105 |
| a0001c0009t0002 | 0/0 | 4579 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | ACAGA others(4574): Show |
chr14 | 50970266 | 51100105 |
| a0001c0014t0002 | 0/0 | 4579 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | ACAGA others(4574): Show |
chr14 | 50970266 | 51100105 |
| a0002c0002t0001 | 1/1 | 4579 | 91 | 24 | 18 | 31 | 3 | 13 | TRIM9_chr14_50970266_51100105 | TRIM9 | ACAGA others(4574): Show |
chr14 | 50970266 | 51100105 |
| a0002c0002t0002 | 0/0 | 4579 | 2 | 0 | 1 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | ACAGA others(4574): Show |
chr14 | 50970266 | 51100105 |
| a0002c0002t0003 | 0/0 | 4579 | 19 | 7 | 3 | 7 | 2 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | ACAGA others(4574): Show |
chr14 | 50970266 | 51100105 |
| a0002c0002t0004 | 0/0 | 4579 | 4 | 4 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | ACAGA others(4574): Show |
chr14 | 50970266 | 51100105 |
| a0002c0002t0005 | 0/0 | 4579 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | ACAGA others(4574): Show |
chr14 | 50970266 | 51100105 |
| a0002c0002t0006 | 0/0 | 4579 | 12 | 0 | 0 | 9 | 0 | 3 | TRIM9_chr14_50970266_51100105 | TRIM9 | ACAGA others(4574): Show |
chr14 | 50970266 | 51100105 |
| a0002c0002t0008 | 0/0 | 4579 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | ACAGA others(4574): Show |
chr14 | 50970266 | 51100105 |
| a0002c0002t0010 | 0/0 | 4579 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | ACAGA others(4574): Show |
chr14 | 50970266 | 51100105 |
| a0002c0002t0011 | 0/0 | 4579 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | ACAGA others(4574): Show |
chr14 | 50970266 | 51100105 |
| a0002c0002t0013 | 0/0 | 4579 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | ACAGA others(4574): Show |
chr14 | 50970266 | 51100105 |
| a0002c0002t0014 | 0/0 | 4579 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | ACAGA others(4574): Show |
chr14 | 50970266 | 51100105 |
| a0002c0002t0016 | 0/0 | 4579 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | ACAGA others(4574): Show |
chr14 | 50970266 | 51100105 |
| a0002c0004t0005 | 0/0 | 4579 | 5 | 5 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | ACAGA others(4574): Show |
chr14 | 50970266 | 51100105 |
| a0002c0007t0001 | 0/0 | 4579 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | ACAGA others(4574): Show |
chr14 | 50970266 | 51100105 |
| a0002c0007t0011 | 0/0 | 4579 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | ACAGA others(4574): Show |
chr14 | 50970266 | 51100105 |
| a0002c0010t0005 | 0/0 | 4579 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | ACAGA others(4574): Show |
chr14 | 50970266 | 51100105 |
| a0002c0012t0005 | 0/0 | 4579 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | ACAGA others(4574): Show |
chr14 | 50970266 | 51100105 |
| a0002c0013t0001 | 0/0 | 4579 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | ACAGA others(4574): Show |
chr14 | 50970266 | 51100105 |
| a0003c0006t0001 | 0/0 | 4579 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | ACAGA others(4574): Show |
chr14 | 50970266 | 51100105 |
| a0003c0006t0018 | 0/0 | 4579 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | ACAGA others(4574): Show |
chr14 | 50970266 | 51100105 |
| a0004c0008t0001 | 0/0 | 4579 | 2 | 0 | 0 | 0 | 2 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | ACAGA others(4574): Show |
chr14 | 50970266 | 51100105 |
| a0005c0011t0001 | 0/0 | 4579 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | ACAGA others(4574): Show |
chr14 | 50970266 | 51100105 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0001g0064 | 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 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0054 | 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 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0072 | 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 |
| a0001c0001t0002g0077 | 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 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0090 | 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 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0116 | 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 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0194 | 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 | 0 | 0 | 0 | 1 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 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 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0266 | 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 |
| a0001c0001t0002g0271 | 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 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0282 | 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 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0002g0320 | 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 |
| a0001c0001t0003g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0003g0076 | 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 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0003g0096 | 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 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0003g0196 | 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 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0003g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0003g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0003g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0003g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0003g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0003g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0003g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0003g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0003g0316 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0004g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0004g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0004g0101 | 0/0 | 1 | 0 | 1 | 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 |
| a0001c0001t0004g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0004g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0004g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0004g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0004g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0004g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0005g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0005g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0005g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0005g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0005g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0009g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0009g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0009g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0010g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0012g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0012g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0015g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0017g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0001t0019g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0003t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0003t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0003t0007g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0003t0007g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0003t0007g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0005t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0005t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0005t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0005t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0009t0002g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0001c0014t0002g0326 | 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 |
| a0002c0002t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 |
| a0002c0002t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0032 | 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 |
| a0002c0002t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0053 | 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 |
| a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0087 | 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 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0099 | 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 |
| a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| 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 |
| a0002c0002t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 |
| a0002c0002t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0244 | 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 |
| a0002c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0002c0002t0001g0277 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0003g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0003g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0003g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0003g0100 | 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 |
| a0002c0002t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0003g0111 | 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 |
| a0002c0002t0003g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0003g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0003g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0003g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0004g0048 | 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 |
| a0002c0002t0004g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0004g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0005g0300 | 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 |
| a0002c0002t0006g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0002c0002t0006g0080 | 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 |
| a0002c0002t0006g0083 | 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 |
| a0002c0002t0006g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0006g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0002c0002t0006g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0008g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0008g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0008g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0010g0328 | 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 |
| a0002c0002t0011g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0013g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0013g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0014g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0002t0016g0078 | 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 |
| a0002c0004t0005g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0004t0005g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0004t0005g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0004t0005g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0007t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0007t0011g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0002c0010t0005g0018 | 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 |
| a0002c0013t0001g0325 | 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 |
| a0004c0008t0001g0006 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| a0005c0011t0001g0313 | 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 | g0237 | EUR | GBR | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0051 | 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 | g0233 | EUR | FIN | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG00408 | hp1 | a0001 | c0014 | t0002 | g0326 | 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 | g0097 | 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 | g0271 | EAS | CHS | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG00544 | hp1 | a0001 | c0005 | t0002 | g0224 | EAS | CHS | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG00544 | hp2 | a0002 | c0002 | t0001 | g0261 | 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 | g0025 | 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 | g0316 | EAS | CHS | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0297 | 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 | g0229 | AMR | PUR | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0298 | AMR | PUR | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0061 | AMR | PUR | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG00733 | hp2 | a0002 | c0002 | t0003 | g0279 | AMR | PUR | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG00735 | hp1 | a0001 | c0009 | t0002 | g0011 | 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 | g0307 | 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 | g0069 | AMR | PUR | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01069 | hp2 | a0002 | c0002 | t0001 | g0232 | AMR | PUR | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01070 | hp2 | a0001 | c0001 | t0015 | g0238 | AMR | PUR | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01071 | hp2 | a0002 | c0002 | t0003 | g0068 | AMR | PUR | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0255 | 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 | g0306 | AMR | PUR | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01081 | hp2 | a0002 | c0002 | t0001 | g0009 | 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 | g0225 | 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 | g0239 | 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 | g0009 | AMR | PUR | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01175 | hp1 | a0002 | c0002 | t0001 | g0235 | 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 | g0314 | 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 | g0230 | 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 | g0116 | 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 | g0010 | AMR | CLM | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0115 | AMR | CLM | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01258 | hp2 | a0002 | c0002 | t0014 | g0010 | AMR | CLM | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01261 | hp1 | a0001 | c0001 | t0004 | g0101 | 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 | g0066 | 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 | g0320 | AMR | CLM | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01361 | hp2 | a0001 | c0001 | t0004 | g0321 | AMR | CLM | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01433 | hp1 | a0001 | c0003 | t0007 | g0013 | 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 | g0228 | AMR | CLM | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0021 | EUR | IBS | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0060 | EUR | IBS | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01516 | hp1 | a0004 | c0008 | t0001 | g0006 | EUR | IBS | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0269 | EUR | IBS | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0062 | EUR | IBS | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01517 | hp2 | a0004 | c0008 | t0001 | g0006 | EUR | IBS | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01884 | hp1 | a0002 | c0002 | t0001 | g0041 | AFR | ACB | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01884 | hp2 | a0002 | c0002 | t0001 | g0027 | AFR | ACB | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01891 | hp1 | a0001 | c0001 | t0005 | g0029 | AFR | ACB | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01891 | hp2 | a0002 | c0002 | t0001 | g0095 | 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 | g0220 | 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 | g0234 | AMR | PEL | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0193 | 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 | g0057 | 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 | g0064 | 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 | g0085 | EAS | KHV | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02055 | hp1 | a0002 | c0002 | t0004 | g0048 | AFR | ACB | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02055 | hp2 | a0002 | c0002 | t0003 | g0046 | 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 | g0065 | 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 | g0312 | EAS | KHV | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0196 | EAS | KHV | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02135 | hp1 | a0002 | c0002 | t0001 | g0291 | EAS | KHV | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0294 | EAS | KHV | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02145 | hp1 | a0002 | c0002 | t0001 | g0324 | AFR | ACB | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02145 | hp2 | a0002 | c0002 | t0004 | g0319 | AFR | ACB | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0071 | EAS | CDX | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02155 | hp2 | a0002 | c0002 | t0006 | g0080 | 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 | g0078 | EAS | CDX | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02257 | hp1 | a0001 | c0001 | t0019 | g0329 | AFR | ACB | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02257 | hp2 | a0001 | c0001 | t0009 | g0299 | 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 | g0037 | AFR | ACB | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02280 | hp2 | a0002 | c0002 | t0001 | g0043 | AFR | ACB | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0063 | 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 | g0052 | EAS | KHV | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0267 | EAS | KHV | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02572 | hp1 | a0002 | c0002 | t0003 | g0031 | AFR | GWD | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02572 | hp2 | a0001 | c0001 | t0004 | g0102 | AFR | GWD | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0218 | 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 | g0028 | 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 | g0019 | 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 | g0327 | AFR | GWD | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02630 | hp2 | a0002 | c0002 | t0001 | g0226 | 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 | g0012 | 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 | g0313 | AFR | GWD | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02717 | hp2 | a0002 | c0002 | t0008 | g0042 | AFR | GWD | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02723 | hp1 | a0001 | c0001 | t0005 | g0303 | AFR | GWD | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02723 | hp2 | a0001 | c0003 | t0001 | g0016 | 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 | g0070 | 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 | g0330 | AFR | GWD | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0308 | AFR | GWD | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02818 | hp1 | a0002 | c0002 | t0001 | g0305 | AFR | GWD | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02818 | hp2 | a0002 | c0002 | t0001 | g0293 | AFR | GWD | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02886 | hp1 | a0002 | c0002 | t0013 | g0248 | AFR | GWD | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02886 | hp2 | a0002 | c0002 | t0001 | g0286 | AFR | GWD | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02895 | hp1 | a0001 | c0001 | t0005 | g0035 | AFR | GWD | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02895 | hp2 | a0002 | c0002 | t0001 | g0024 | AFR | GWD | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02897 | hp1 | a0001 | c0001 | t0005 | g0034 | AFR | GWD | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0044 | 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 | g0036 | AFR | ESN | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02970 | hp1 | a0002 | c0002 | t0001 | g0244 | AFR | ESN | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02970 | hp2 | a0002 | c0002 | t0001 | g0023 | AFR | ESN | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02976 | hp1 | a0002 | c0002 | t0001 | g0247 | 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 | g0304 | AFR | GWD | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG03041 | hp2 | a0002 | c0004 | t0005 | g0309 | AFR | GWD | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG03098 | hp1 | a0001 | c0001 | t0009 | g0040 | AFR | MSL | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG03098 | hp2 | a0002 | c0002 | t0001 | g0311 | 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 | g0322 | AFR | ESN | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG03139 | hp1 | a0002 | c0002 | t0001 | g0246 | AFR | ESN | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG03139 | hp2 | a0002 | c0002 | t0008 | g0323 | 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 | g0254 | AFR | ESN | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG03209 | hp1 | a0002 | c0002 | t0001 | g0094 | AFR | MSL | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG03209 | hp2 | a0002 | c0002 | t0001 | g0301 | AFR | MSL | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG03225 | hp1 | a0002 | c0002 | t0003 | g0100 | AFR | MSL | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG03225 | hp2 | a0001 | c0001 | t0017 | g0038 | AFR | MSL | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG03453 | hp1 | a0002 | c0002 | t0010 | g0328 | AFR | MSL | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG03453 | hp2 | a0002 | c0007 | t0011 | g0015 | AFR | MSL | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG03486 | hp1 | a0001 | c0001 | t0009 | g0098 | AFR | MSL | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0005 | 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 | g0007 | SAS | PJL | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0007 | 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 | g0302 | AFR | ESN | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG03516 | hp2 | a0002 | c0002 | t0003 | g0245 | 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 | g0017 | 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 | g0191 | SAS | PJL | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG03704 | hp1 | a0002 | c0002 | t0001 | g0049 | 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 | g0058 | SAS | PJL | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG03710 | hp2 | a0002 | c0002 | t0006 | g0020 | SAS | PJL | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG03834 | hp1 | a0002 | c0002 | t0001 | g0241 | 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 | g0192 | 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 | g0047 | 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 | g0026 | 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 | g0194 | 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 | g0032 | AFR | YRI | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18612 | hp1 | a0002 | c0002 | t0001 | g0074 | EAS | CHB | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | CHB | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18906 | hp1 | a0002 | c0010 | t0005 | g0018 | AFR | YRI | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18906 | hp2 | a0002 | c0002 | t0005 | g0300 | AFR | YRI | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18939 | hp2 | a0002 | c0002 | t0001 | g0262 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18941 | hp1 | a0002 | c0002 | t0001 | g0091 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18942 | hp2 | a0001 | c0001 | t0003 | g0195 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0318 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18943 | hp2 | a0002 | c0002 | t0006 | g0290 | 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 | g0112 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18946 | hp1 | a0002 | c0002 | t0006 | g0223 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0054 | 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 | g0274 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18951 | hp2 | a0001 | c0001 | t0003 | g0258 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18954 | hp1 | a0001 | c0005 | t0002 | g0249 | 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 | g0260 | 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 | g0325 | 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 | g0264 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0089 | 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 | g0076 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0272 | 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 | g0055 | 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 | g0266 | 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 | g0250 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18974 | hp1 | a0001 | c0001 | t0003 | g0045 | 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 | g0086 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18980 | hp1 | a0001 | c0001 | t0003 | g0050 | 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 | g0257 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18981 | hp2 | a0001 | c0001 | t0003 | g0082 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18983 | hp1 | a0002 | c0002 | t0001 | g0093 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18984 | hp1 | a0001 | c0005 | t0002 | g0253 | 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 | g0270 | 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 | g0087 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18992 | hp2 | a0001 | c0001 | t0003 | g0219 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18993 | hp1 | a0001 | c0001 | t0003 | g0096 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18993 | hp2 | a0002 | c0002 | t0006 | g0221 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18998 | hp1 | a0002 | c0002 | t0001 | g0263 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18998 | hp2 | a0002 | c0002 | t0003 | g0240 | 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 | g0053 | 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 | g0276 | 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 | g0265 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA19004 | hp1 | a0002 | c0002 | t0003 | g0110 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA19004 | hp2 | a0001 | c0001 | t0003 | g0059 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA19005 | hp1 | a0002 | c0002 | t0001 | g0113 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0088 | 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 | g0278 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA19010 | hp1 | a0002 | c0002 | t0003 | g0111 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0295 | 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 | g0092 | 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 | g0056 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA19030 | hp1 | a0002 | c0002 | t0001 | g0243 | AFR | LWK | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0030 | 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 | g0281 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA19056 | hp2 | a0002 | c0002 | t0002 | g0222 | 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 | g0288 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA19058 | hp1 | a0002 | c0002 | t0006 | g0079 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA19058 | hp2 | a0001 | c0001 | t0004 | g0251 | 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 | g0259 | 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 | g0252 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA19066 | hp2 | a0002 | c0002 | t0006 | g0083 | 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 | g0114 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA19078 | hp1 | a0001 | c0001 | t0003 | g0256 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA19078 | hp2 | a0002 | c0002 | t0006 | g0081 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA19079 | hp1 | a0001 | c0001 | t0012 | g0289 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA19079 | hp2 | a0002 | c0002 | t0001 | g0317 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA19081 | hp1 | a0001 | c0001 | t0003 | g0084 | 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 | g0273 | 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 | g0283 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA19087 | hp2 | a0001 | c0001 | t0003 | g0073 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0033 | 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 | g0005 | 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 | g0236 | EUR | TSI | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA20752 | hp2 | a0002 | c0002 | t0003 | g0280 | 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 | g0242 | EUR | TSI | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0227 | SAS | GIH | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0284 | 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 | g0039 | AFR | ACB | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0285 | 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 | g0315 | AFR | MSL | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG06807 | hp1 | a0001 | c0003 | t0007 | g0014 | AFR | USA | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| HG06807 | hp2 | a0002 | c0002 | t0001 | g0099 | AFR | USA | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0287 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA20300 | hp1 | a0002 | c0004 | t0005 | g0310 | 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 | g0022 | AFR | LWK | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| NA21309 | hp2 | a0002 | c0004 | t0005 | g0296 | AFR | LWK | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0277 | REF | REF | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0067 | REF | REF | TRIM9_chr14_50970266_51100105 | TRIM9 | chr14 | 50970266 | 51100105 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:50979498 | T | G | 2 | a0001 a0003 |
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 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | a0002c0004 a0002c0010 a0002c0012 |
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 | a0001c0003 a0002c0007 a0002c0010 |
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 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | a0001c0001t0004 a0001c0001t0009 a0002c0002t0004 others(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 | a0001c0001t0003 a0001c0001t0012 a0002c0002t0003 others(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 | a0002c0002t0011 a0002c0007t0011 |
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 | a0001c0001t0002 a0001c0001t0012 a0001c0005t0002 others(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 | a0001c0001t0004 a0002c0002t0004 a0002c0002t0006 others(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 | a0002c0002t0011 a0002c0007t0011 |
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 | a0001c0001t0019 a0001c0003t0007 a0002c0002t0006 |
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 | a0001c0001t0005 a0002c0002t0005 a0002c0004t0005 others(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 | a0001c0001t0010 a0001c0001t0019 a0002c0002t0010 |
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 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:50977395 | C | T | 1 | a0001c0001t0001g0285 | 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 | a0002c0002t0001g0244 | 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 | a0002c0002t0003g0172 a0002c0002t0003g0177 a0002c0002t0003g0245 |
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 | a0002c0002t0001g0226 | 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 | a0001c0001t0002g0283 | 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 | a0002c0002t0013g0037 a0002c0002t0013g0248 |
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 | 27 | a0001c0001t0004g0005 a0001c0001t0004g0101 a0001c0001t0004g0102 others(24): 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 | 27 | a0001c0001t0004g0005 a0001c0001t0004g0101 a0001c0001t0004g0102 others(24): 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 | a0001c0001t0009g0040 a0001c0001t0009g0098 a0001c0001t0009g0299 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0044 others(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 | 145 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0044 others(142): 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 | a0002c0002t0011g0036 a0002c0007t0011g0015 |
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 | a0001c0001t0009g0098 a0001c0001t0009g0299 |
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 | a0002c0002t0013g0037 a0002c0002t0013g0248 |
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 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0044 others(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 | a0001c0001t0001g0206 a0001c0001t0001g0285 a0001c0001t0001g0308 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0044 a0001c0001t0001g0064 others(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 | 219 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0044 others(216): 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 | 3 | a0001c0001t0002g0008 a0001c0001t0002g0063 a0001c0001t0002g0141 |
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 | a0001c0001t0001g0285 a0001c0001t0001g0308 a0001c0003t0001g0012 |
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 | a0002c0002t0011g0036 a0002c0007t0011g0015 |
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 | a0001c0001t0004g0264 | 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 | a0001c0001t0019g0329 a0001c0003t0007g0013 a0001c0003t0007g0014 others(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 | a0002c0002t0011g0036 a0002c0007t0011g0015 |
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 | a0001c0001t0002g0025 a0001c0001t0002g0047 a0001c0001t0002g0055 others(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 | a0002c0002t0004g0212 a0002c0002t0004g0302 a0002c0002t0004g0319 |
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 | a0001c0001t0004g0264 | 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 | a0001c0001t0001g0179 a0001c0001t0003g0001 a0001c0001t0003g0007 others(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 | 77 | a0001c0001t0001g0179 a0001c0001t0003g0001 a0001c0001t0003g0007 others(74): 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 | a0001c0001t0009g0299 | 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 | a0001c0001t0001g0179 a0001c0001t0003g0001 a0001c0001t0003g0007 others(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 | a0001c0001t0002g0271 | 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 | a0001c0001t0001g0030 a0001c0001t0001g0044 a0001c0001t0001g0064 others(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 | a0001c0001t0005g0028 a0001c0001t0005g0029 a0001c0001t0005g0034 others(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 | a0001c0001t0001g0285 a0001c0001t0001g0308 a0001c0001t0002g0058 others(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 | a0002c0002t0002g0222 a0002c0002t0006g0004 a0002c0002t0006g0020 others(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 | a0001c0001t0002g0047 a0001c0001t0002g0108 a0001c0001t0002g0115 others(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 | a0001c0001t0009g0098 a0002c0002t0004g0212 a0002c0002t0004g0302 others(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 | a0002c0004t0005g0149 a0002c0004t0005g0254 a0002c0004t0005g0296 others(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 | a0001c0001t0004g0239 | 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 | a0001c0001t0001g0285 a0001c0001t0001g0308 a0001c0001t0002g0058 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0044 a0001c0001t0001g0064 others(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 | a0002c0002t0013g0037 | 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 | a0001c0001t0001g0205 a0001c0001t0003g0129 a0001c0001t0003g0130 others(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 | a0001c0001t0002g0058 a0001c0001t0003g0001 a0001c0001t0003g0057 others(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 | a0001c0001t0001g0033 a0001c0001t0002g0061 a0001c0001t0002g0062 others(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 | a0001c0001t0005g0029 a0001c0001t0005g0303 a0002c0002t0003g0172 others(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 | a0001c0001t0002g0089 | 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 | a0001c0001t0009g0040 | 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 | a0001c0001t0005g0303 | 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 | a0002c0002t0002g0222 a0002c0002t0006g0004 a0002c0002t0006g0020 others(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 | 93 | a0001c0001t0001g0206 a0001c0001t0001g0275 a0001c0001t0002g0008 others(90): 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 | a0002c0004t0005g0309 | 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 | 135 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0275 others(132): 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 | a0001c0001t0003g0208 a0001c0001t0003g0210 |
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 | 165 | a0001c0001t0001g0030 a0001c0001t0001g0044 a0001c0001t0001g0064 others(162): 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 | a0002c0002t0001g0305 | 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 | a0002c0002t0001g0305 | 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 | a0002c0002t0001g0243 | 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 | a0002c0002t0002g0222 a0002c0002t0006g0004 a0002c0002t0006g0020 others(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 | a0001c0001t0002g0058 | 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 | a0001c0001t0003g0050 a0001c0001t0003g0059 a0001c0001t0003g0096 others(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 | a0002c0002t0004g0319 | 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 | a0001c0001t0002g0270 | 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 | 169 | a0001c0001t0001g0030 a0001c0001t0001g0044 a0001c0001t0001g0064 others(166): 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 | 268 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0044 others(265): 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 | a0001c0001t0001g0322 a0001c0001t0005g0028 a0001c0001t0005g0029 others(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 | a0001c0001t0001g0122 a0001c0001t0001g0132 a0001c0001t0001g0178 others(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 | 11 | a0001c0001t0004g0005 a0001c0001t0004g0101 a0001c0001t0004g0102 others(8): 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 | a0001c0001t0004g0312 | 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 | a0002c0002t0011g0036 | 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 | a0002c0002t0002g0222 a0002c0002t0006g0004 a0002c0002t0006g0020 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0044 a0001c0001t0001g0064 others(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 | a0002c0002t0001g0091 a0002c0002t0001g0092 a0002c0002t0001g0093 |
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 | 169 | a0001c0001t0001g0033 a0001c0001t0001g0206 a0001c0001t0001g0275 others(166): 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 | 182 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0044 others(179): 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 | 179 | a0001c0001t0001g0030 a0001c0001t0001g0044 a0001c0001t0001g0064 others(176): 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 | a0002c0002t0001g0097 a0002c0002t0001g0174 |
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 | 86 | a0001c0001t0001g0206 a0001c0001t0001g0275 a0001c0001t0002g0008 others(83): 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 | a0002c0002t0001g0113 | 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 | 5 | a0001c0001t0004g0005 a0001c0001t0004g0101 a0001c0001t0004g0102 others(2): 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 | a0001c0001t0001g0030 a0001c0001t0001g0044 a0001c0001t0001g0064 others(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 | a0001c0001t0001g0322 a0001c0001t0005g0028 a0001c0001t0005g0029 others(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 | a0001c0001t0002g0199 a0001c0001t0002g0281 a0001c0001t0002g0282 others(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 | a0001c0001t0002g0054 | 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 | a0001c0001t0003g0007 | 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 | a0002c0002t0003g0046 | 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 | a0001c0001t0001g0030 a0001c0001t0001g0044 a0001c0001t0001g0064 others(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 | a0001c0001t0001g0322 a0001c0001t0005g0028 a0001c0001t0005g0029 others(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 | a0002c0002t0001g0043 a0002c0002t0001g0311 a0002c0002t0003g0106 |
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 | a0002c0002t0003g0046 a0002c0002t0003g0100 |
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 | a0002c0002t0002g0222 a0002c0002t0006g0004 a0002c0002t0006g0020 others(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 | |||||||
| chr14:50987380 | T | C | 11 | a0002c0002t0002g0222 a0002c0002t0006g0004 a0002c0002t0006g0020 others(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 | 59 | a0001c0001t0001g0179 a0001c0001t0002g0171 a0001c0001t0002g0173 others(56): Show |
64 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(61): 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 | a0001c0001t0001g0285 a0001c0001t0001g0308 a0001c0001t0002g0058 others(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 | a0002c0002t0002g0222 a0002c0002t0006g0004 a0002c0002t0006g0020 others(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 | a0001c0001t0001g0285 a0001c0001t0001g0308 a0001c0001t0002g0058 others(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 | 77 | a0001c0001t0001g0206 a0001c0001t0001g0275 a0001c0001t0002g0008 others(74): 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 | a0001c0001t0001g0030 a0001c0001t0001g0044 a0001c0001t0001g0064 others(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 | a0001c0001t0001g0285 a0001c0001t0001g0308 a0001c0001t0002g0058 others(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 | a0002c0002t0006g0144 a0002c0002t0006g0192 |
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 | a0001c0001t0001g0033 a0001c0001t0001g0285 a0001c0001t0001g0308 others(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 | 268 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0044 others(265): 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 | a0001c0001t0001g0033 a0001c0001t0001g0285 a0001c0001t0001g0308 others(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 | 52 | a0001c0001t0001g0322 a0001c0001t0002g0116 a0001c0001t0002g0127 others(49): 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 | a0001c0001t0001g0030 a0001c0001t0001g0044 a0001c0001t0001g0064 others(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 | a0001c0001t0001g0285 a0001c0001t0001g0308 a0001c0001t0002g0058 others(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 | a0001c0001t0001g0033 a0001c0001t0002g0060 a0001c0001t0002g0061 others(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 | a0002c0002t0001g0043 a0002c0002t0001g0311 a0002c0002t0003g0106 others(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 | a0001c0001t0001g0285 a0001c0001t0001g0308 a0001c0001t0002g0058 others(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 | a0001c0001t0001g0275 a0001c0001t0002g0025 a0001c0001t0002g0047 others(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 | a0002c0002t0001g0293 | 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 | a0002c0002t0001g0053 a0002c0002t0001g0091 a0002c0002t0001g0092 others(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 | 75 | a0001c0001t0001g0206 a0001c0001t0001g0275 a0001c0001t0002g0008 others(72): 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 | a0001c0001t0001g0285 a0001c0001t0001g0308 a0001c0001t0002g0058 others(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 | a0001c0001t0009g0098 a0002c0002t0004g0212 a0002c0002t0004g0302 others(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 | a0002c0002t0002g0222 a0002c0002t0006g0004 a0002c0002t0006g0020 others(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 | a0001c0001t0001g0285 a0001c0001t0001g0308 a0001c0001t0002g0058 others(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 | a0002c0002t0001g0131 a0002c0002t0001g0133 a0002c0002t0001g0207 others(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 | a0001c0001t0017g0038 | 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 | a0001c0014t0002g0326 | 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 | a0001c0001t0001g0205 a0001c0001t0003g0129 a0001c0001t0003g0130 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0044 others(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 | a0001c0001t0017g0038 | 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 | a0001c0001t0002g0056 | 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 | a0002c0002t0004g0212 a0002c0002t0004g0302 a0002c0002t0004g0319 |
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 | a0002c0002t0004g0212 a0002c0002t0004g0302 a0002c0002t0004g0319 |
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 | a0002c0002t0004g0212 a0002c0002t0004g0302 a0002c0002t0004g0319 |
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 | a0001c0001t0001g0205 a0002c0002t0001g0026 |
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 | a0001c0001t0017g0038 | 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 | a0001c0001t0001g0033 a0001c0001t0001g0285 a0001c0001t0001g0308 others(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 | 258 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0044 others(255): 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 | a0001c0001t0001g0205 a0001c0001t0003g0129 a0001c0001t0003g0130 others(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 | a0001c0001t0001g0033 a0001c0001t0002g0060 a0001c0001t0002g0061 others(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 | a0001c0001t0004g0233 | 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 | a0001c0001t0001g0030 a0001c0001t0001g0044 a0001c0001t0001g0064 others(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 | 5 | a0001c0001t0004g0005 a0001c0001t0004g0101 a0001c0001t0004g0102 others(2): 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 | a0001c0001t0001g0285 a0001c0001t0001g0308 a0001c0001t0002g0058 others(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 | a0001c0001t0001g0285 a0001c0001t0001g0308 a0001c0001t0002g0058 others(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 | a0001c0001t0001g0285 a0001c0001t0001g0308 a0001c0001t0002g0058 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0044 others(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 | a0001c0001t0002g0306 | 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 | a0002c0004t0005g0254 a0002c0004t0005g0310 a0002c0010t0005g0018 |
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 | a0001c0001t0002g0039 a0001c0001t0002g0147 a0001c0001t0002g0155 others(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 | a0002c0002t0001g0027 | 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 | a0001c0001t0001g0033 a0001c0001t0001g0285 a0001c0001t0001g0308 others(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 | 76 | a0001c0001t0001g0206 a0001c0001t0001g0275 a0001c0001t0002g0008 others(73): 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 | a0001c0001t0001g0033 a0001c0001t0001g0285 a0001c0001t0001g0308 others(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 | a0001c0001t0001g0033 a0001c0001t0002g0060 a0001c0001t0002g0061 others(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 | a0002c0002t0001g0305 | 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 | a0002c0002t0003g0100 | 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 | a0001c0001t0001g0030 a0001c0001t0001g0044 a0001c0001t0001g0064 others(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 | a0002c0002t0003g0046 a0002c0002t0003g0100 |
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 | 11 | a0001c0001t0004g0005 a0001c0001t0004g0101 a0001c0001t0004g0102 others(8): 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 | a0002c0002t0001g0002 a0002c0002t0001g0121 a0002c0002t0001g0137 others(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 | a0001c0001t0001g0322 a0001c0001t0005g0028 a0001c0001t0005g0029 others(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 | a0001c0001t0009g0098 a0002c0002t0004g0212 a0002c0002t0004g0302 others(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 | 89 | a0001c0001t0001g0033 a0001c0001t0001g0206 a0001c0001t0001g0275 others(86): 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 | a0001c0001t0001g0033 a0001c0001t0002g0060 a0001c0001t0002g0061 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0044 a0001c0001t0001g0064 others(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 | a0002c0002t0001g0324 | 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 | a0002c0002t0001g0027 | 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 | a0002c0002t0013g0037 | 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 | a0002c0002t0001g0043 a0002c0002t0001g0311 a0002c0002t0003g0106 |
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 | a0001c0001t0001g0033 a0001c0001t0002g0060 a0001c0001t0002g0061 others(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 | a0002c0002t0003g0046 a0002c0002t0003g0100 |
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 | 268 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0044 others(265): 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 | a0001c0001t0001g0033 a0001c0001t0002g0060 a0001c0001t0002g0061 others(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 | 121 | a0001c0001t0001g0030 a0001c0001t0001g0044 a0001c0001t0001g0064 others(118): 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 | a0001c0001t0004g0101 | 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 | a0001c0001t0001g0322 a0001c0001t0005g0028 a0001c0001t0005g0029 others(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 | a0001c0001t0017g0038 | 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 | a0001c0001t0001g0033 a0001c0001t0002g0060 a0001c0001t0002g0061 others(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 | a0001c0001t0003g0082 a0001c0001t0009g0040 a0002c0002t0010g0328 others(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 | a0002c0002t0001g0043 a0002c0002t0001g0311 a0002c0002t0003g0106 |
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 | a0002c0004t0005g0149 a0002c0004t0005g0296 a0002c0012t0005g0161 |
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 | a0002c0004t0005g0149 a0002c0004t0005g0296 a0002c0012t0005g0161 |
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 | a0002c0004t0005g0254 a0002c0004t0005g0309 a0002c0004t0005g0310 others(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 | a0001c0001t0001g0285 a0001c0001t0001g0308 a0001c0001t0002g0058 others(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 | a0001c0001t0002g0089 | 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 | a0002c0002t0001g0009 a0002c0002t0001g0225 a0002c0002t0001g0228 others(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 | a0003c0006t0001g0140 a0003c0006t0001g0142 a0003c0006t0018g0151 |
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 | 124 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0044 others(121): 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 | a0002c0004t0005g0149 a0002c0004t0005g0296 |
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 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0044 others(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 | a0002c0002t0001g0228 a0002c0002t0001g0230 |
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 | a0001c0001t0001g0030 a0001c0001t0001g0044 a0001c0001t0001g0103 others(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 | a0001c0001t0001g0064 a0001c0001t0002g0173 a0001c0001t0003g0208 others(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 | a0002c0002t0001g0262 | 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 | a0002c0002t0001g0247 | 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 | a0001c0001t0002g0055 | 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 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0122 others(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 | 95 | a0001c0001t0001g0206 a0001c0001t0001g0275 a0001c0001t0002g0008 others(92): 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 | a0001c0001t0001g0285 a0001c0001t0001g0308 a0001c0001t0002g0058 others(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 | a0001c0001t0017g0038 a0002c0002t0001g0305 |
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 | 109 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0122 others(106): 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 | a0001c0001t0017g0038 | 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 | a0001c0001t0001g0044 a0001c0001t0001g0103 a0001c0001t0001g0216 others(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 | a0001c0001t0002g0060 a0001c0001t0002g0061 a0001c0001t0002g0062 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0122 others(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 | a0002c0002t0002g0222 a0002c0002t0006g0004 a0002c0002t0006g0020 others(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 | a0001c0001t0001g0132 a0001c0001t0001g0285 a0001c0001t0001g0308 others(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 | a0001c0001t0004g0102 | 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 | a0001c0001t0002g0294 | 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 | 255 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0044 others(252): 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 | a0001c0001t0017g0038 | 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 | a0001c0001t0002g0060 a0001c0001t0002g0061 a0001c0001t0002g0062 others(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 | a0002c0002t0002g0222 a0002c0002t0006g0004 a0002c0002t0006g0020 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0122 a0001c0001t0001g0178 others(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 | a0001c0001t0003g0269 a0001c0001t0003g0315 a0001c0001t0009g0098 others(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 | a0002c0002t0013g0037 | 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 | 98 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0122 others(95): 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 | 258 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0044 others(255): 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 | a0001c0001t0002g0152 a0001c0001t0002g0314 |
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 | 17 | a0001c0001t0001g0044 a0001c0001t0001g0103 a0001c0001t0004g0005 others(14): 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 | a0001c0001t0003g0269 a0001c0001t0003g0315 a0001c0001t0015g0238 others(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 | a0001c0001t0002g0058 a0001c0001t0002g0075 a0002c0002t0001g0049 others(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 | a0002c0002t0006g0223 | 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 | a0005c0011t0001g0313 | 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 | a0001c0001t0003g0076 | 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 | a0002c0004t0005g0296 a0002c0004t0005g0309 a0002c0012t0005g0161 |
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 | a0002c0002t0011g0036 | 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 | a0002c0004t0005g0296 a0002c0004t0005g0309 a0002c0012t0005g0161 |
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 | a0001c0001t0001g0216 a0002c0002t0003g0046 a0002c0002t0003g0100 others(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 | a0001c0001t0003g0007 a0001c0001t0003g0168 a0001c0001t0003g0252 others(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 | 156 | a0001c0001t0001g0030 a0001c0001t0001g0044 a0001c0001t0001g0103 others(153): 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 | a0001c0001t0001g0033 a0001c0001t0001g0122 a0001c0001t0001g0178 others(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 | a0002c0002t0002g0222 a0002c0002t0006g0004 a0002c0002t0006g0020 others(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 | a0002c0002t0001g0074 a0002c0002t0001g0261 a0002c0002t0001g0317 |
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 | a0001c0001t0003g0168 a0001c0001t0003g0169 |
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 | a0002c0002t0001g0262 | 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 | 104 | a0001c0001t0001g0206 a0001c0001t0001g0275 a0001c0001t0002g0008 others(101): 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 | a0002c0002t0001g0032 | 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 | 23 | a0001c0001t0001g0044 a0001c0001t0001g0103 a0001c0001t0001g0216 others(20): 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 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0122 others(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 | 162 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0044 others(159): 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 | a0002c0002t0002g0222 a0002c0002t0006g0004 a0002c0002t0006g0020 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0122 others(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 | a0002c0002t0006g0081 | 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 | a0001c0001t0009g0040 a0002c0002t0006g0081 a0002c0002t0010g0328 |
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 | a0001c0001t0001g0030 a0005c0011t0001g0313 |
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 | 102 | a0001c0001t0001g0206 a0001c0001t0001g0275 a0001c0001t0002g0008 others(99): 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 | a0001c0001t0005g0029 a0001c0001t0005g0034 a0001c0001t0005g0035 others(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 | 142 | a0001c0001t0001g0206 a0001c0001t0001g0275 a0001c0001t0001g0285 others(139): 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 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0122 others(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 | 90 | a0001c0001t0001g0206 a0001c0001t0001g0275 a0001c0001t0002g0008 others(87): 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 | a0001c0001t0003g0269 a0001c0001t0003g0315 a0001c0001t0015g0238 others(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 | a0002c0002t0011g0036 | 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 | a0001c0001t0001g0205 a0001c0001t0003g0129 a0001c0001t0003g0130 others(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 | a0001c0001t0002g0060 a0001c0001t0002g0061 a0001c0001t0002g0062 others(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 | a0001c0001t0005g0029 a0001c0001t0005g0034 a0001c0001t0005g0035 others(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 | a0002c0002t0008g0323 | 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 | a0002c0002t0011g0036 | 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 | a0002c0002t0002g0222 a0002c0002t0006g0020 a0002c0002t0006g0144 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0122 others(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 | a0001c0001t0001g0285 a0001c0001t0001g0308 a0001c0001t0002g0058 others(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 | a0001c0001t0001g0285 a0001c0001t0001g0308 a0001c0001t0002g0058 others(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 | a0001c0001t0001g0044 a0001c0001t0001g0103 a0001c0001t0001g0216 others(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 | 97 | a0001c0001t0001g0206 a0001c0001t0001g0275 a0001c0001t0002g0008 others(94): 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 | a0001c0001t0002g0060 a0001c0001t0002g0061 a0001c0001t0002g0062 others(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 | 252 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0044 others(249): 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 | a0001c0001t0001g0285 a0001c0001t0001g0308 a0001c0001t0002g0058 others(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 | a0001c0001t0001g0285 a0001c0001t0001g0308 a0001c0001t0002g0058 others(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 | a0001c0001t0002g0025 | 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 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0122 others(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 | 92 | a0001c0001t0001g0206 a0001c0001t0001g0275 a0001c0001t0002g0008 others(89): 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 | a0001c0001t0001g0322 a0001c0001t0005g0029 a0001c0001t0005g0034 others(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 | a0001c0001t0002g0090 a0001c0001t0003g0252 a0001c0001t0003g0287 others(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 | 72 | a0001c0001t0001g0044 a0001c0001t0001g0103 a0001c0001t0001g0132 others(69): 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 | a0001c0001t0002g0153 a0001c0001t0002g0154 |
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 | 149 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0122 others(146): 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 | a0001c0001t0002g0047 a0001c0001t0002g0108 a0001c0001t0002g0115 others(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 | a0001c0001t0009g0098 a0002c0002t0001g0246 a0002c0002t0008g0304 others(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 | a0001c0001t0003g0269 a0001c0001t0003g0315 a0001c0001t0015g0238 others(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 | a0001c0001t0004g0251 | 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 | a0001c0001t0009g0098 a0002c0002t0001g0246 a0002c0002t0008g0304 others(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 | a0001c0001t0003g0045 | 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 | a0002c0002t0002g0222 a0002c0002t0006g0004 a0002c0002t0006g0020 others(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 | a0001c0001t0003g0219 | 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 | 118 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0044 others(115): 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 | a0001c0001t0001g0132 a0001c0001t0001g0205 a0001c0001t0003g0129 others(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 | a0001c0001t0004g0126 a0001c0001t0004g0233 a0001c0001t0004g0239 others(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 | a0002c0002t0011g0036 | 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 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0044 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0044 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0044 others(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 | a0002c0002t0011g0036 | 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 | a0001c0001t0001g0285 a0001c0001t0001g0308 a0001c0001t0002g0058 others(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 | a0001c0001t0003g0269 a0001c0001t0015g0238 a0002c0002t0001g0002 others(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 | a0002c0002t0001g0043 a0002c0002t0001g0311 a0002c0002t0003g0106 |
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 | a0002c0002t0004g0212 a0002c0002t0004g0302 a0002c0002t0004g0319 |
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 | a0001c0001t0001g0211 a0003c0006t0001g0140 a0003c0006t0001g0142 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0122 others(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 | a0002c0002t0002g0222 a0002c0002t0006g0004 a0002c0002t0006g0020 others(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 | a0001c0001t0003g0269 a0001c0001t0003g0315 a0001c0001t0015g0238 others(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 | 143 | a0001c0001t0001g0044 a0001c0001t0001g0064 a0001c0001t0001g0103 others(140): 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 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0122 others(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 | a0002c0002t0001g0131 a0002c0002t0001g0133 |
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 | a0001c0001t0003g0269 a0001c0001t0003g0315 a0001c0001t0015g0238 others(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 | a0001c0001t0003g0269 a0001c0001t0003g0315 a0001c0001t0015g0238 others(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 | a0002c0002t0001g0043 a0002c0002t0001g0311 a0002c0002t0003g0106 |
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 | a0001c0001t0001g0132 a0001c0001t0019g0329 a0002c0002t0001g0131 others(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 | a0001c0001t0002g0060 a0001c0001t0002g0061 a0001c0001t0002g0062 others(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 | a0002c0002t0001g0244 | 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 | 256 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0044 others(253): 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 | a0002c0002t0002g0222 a0002c0002t0006g0004 a0002c0002t0006g0020 others(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 | a0001c0001t0002g0025 a0001c0001t0002g0259 |
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 | a0002c0002t0016g0078 | 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 | a0002c0002t0013g0037 | 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 | 218 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0064 others(215): 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 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0122 others(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 | a0001c0001t0002g0268 | 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 | a0001c0001t0003g0267 | 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 | a0002c0002t0013g0037 | 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 | 17 | a0001c0001t0002g0060 a0001c0001t0002g0061 a0001c0001t0002g0062 others(14): 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 | 81 | a0001c0001t0001g0206 a0001c0001t0001g0275 a0001c0001t0002g0008 others(78): 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 | a0001c0001t0001g0132 a0001c0001t0019g0329 a0002c0002t0001g0131 others(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 | a0001c0001t0001g0216 a0002c0002t0003g0046 a0002c0002t0003g0100 |
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 | 244 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0044 others(241): 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 | a0001c0001t0009g0098 a0002c0002t0001g0246 a0002c0002t0008g0304 others(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 | a0002c0002t0002g0222 a0002c0002t0006g0004 a0002c0002t0006g0020 others(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 | a0001c0001t0001g0322 a0001c0001t0005g0029 a0001c0001t0005g0034 others(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 | a0001c0001t0009g0098 a0002c0002t0001g0246 a0002c0002t0008g0304 others(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 | a0002c0002t0003g0100 | 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 | a0002c0002t0003g0100 | 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 | a0001c0001t0017g0038 | 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 | a0001c0001t0002g0294 | 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 | a0002c0004t0005g0254 | 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 | a0001c0001t0002g0060 a0001c0001t0002g0061 a0001c0001t0002g0062 others(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 | a0002c0002t0002g0222 a0002c0002t0006g0004 a0002c0002t0006g0020 others(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 | 254 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0044 others(251): 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 | a0002c0002t0004g0212 a0002c0002t0004g0302 a0002c0002t0004g0319 |
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 | 26 | a0001c0001t0002g0060 a0001c0001t0002g0061 a0001c0001t0002g0062 others(23): 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 | a0002c0002t0001g0120 a0002c0013t0001g0325 |
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 | 254 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0044 others(251): 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 | 254 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0044 others(251): 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 | a0002c0002t0003g0280 | 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 | 6 | a0001c0001t0004g0005 a0001c0001t0004g0101 a0001c0001t0004g0102 others(3): 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 | a0001c0001t0001g0064 a0001c0001t0001g0285 a0001c0001t0001g0308 others(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 | a0002c0002t0006g0221 | 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 | 254 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0044 others(251): 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 | a0002c0002t0001g0305 | 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 | 106 | a0001c0001t0001g0206 a0001c0001t0001g0275 a0001c0001t0002g0008 others(103): 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 | a0002c0002t0011g0036 | 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 | a0001c0001t0001g0033 | 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 | a0001c0001t0001g0044 a0001c0001t0001g0064 a0001c0001t0001g0103 others(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 | 5 | a0001c0001t0004g0005 a0001c0001t0004g0101 a0001c0001t0004g0102 others(2): 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 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0122 others(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 | 256 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0044 others(253): 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 | a0002c0002t0001g0305 | 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 | 106 | a0001c0001t0001g0206 a0001c0001t0001g0275 a0001c0001t0002g0008 others(103): 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 | a0001c0001t0004g0264 | 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 | 106 | a0001c0001t0001g0206 a0001c0001t0001g0275 a0001c0001t0002g0008 others(103): 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 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0122 others(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 | a0001c0001t0001g0103 a0001c0001t0009g0098 a0001c0003t0001g0016 others(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 | 146 | a0001c0001t0001g0044 a0001c0001t0001g0064 a0001c0001t0001g0206 others(143): 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 | a0001c0001t0009g0098 a0002c0002t0001g0246 a0002c0002t0008g0304 others(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 | 106 | a0001c0001t0001g0206 a0001c0001t0001g0275 a0001c0001t0002g0008 others(103): 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 | a0001c0001t0001g0132 a0001c0001t0019g0329 a0002c0002t0001g0131 others(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 | a0001c0001t0001g0322 a0001c0001t0005g0029 a0001c0001t0005g0034 others(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 | a0001c0001t0009g0098 a0002c0002t0001g0246 a0002c0002t0008g0304 others(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 | a0002c0002t0004g0212 a0002c0002t0004g0302 a0002c0002t0004g0319 |
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 | a0002c0002t0003g0280 | 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 | a0001c0001t0001g0044 a0001c0001t0001g0103 a0001c0001t0001g0216 others(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 | a0002c0002t0003g0068 a0002c0002t0003g0069 |
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 | a0001c0001t0001g0030 a0001c0001t0001g0122 a0001c0001t0001g0132 others(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 | a0001c0001t0001g0285 a0001c0001t0001g0308 a0001c0001t0002g0060 others(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 | a0001c0001t0001g0030 a0001c0001t0004g0126 a0001c0001t0004g0233 others(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 | a0001c0001t0003g0269 a0001c0001t0003g0315 a0001c0001t0010g0327 others(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 | a0001c0001t0001g0044 a0001c0001t0001g0103 a0001c0001t0001g0216 others(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 | a0001c0001t0009g0098 a0002c0002t0001g0246 a0002c0002t0008g0304 others(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 | a0001c0001t0001g0216 a0002c0002t0003g0046 a0002c0002t0003g0100 others(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 | a0002c0002t0006g0221 | 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 | a0001c0001t0001g0030 a0001c0001t0001g0122 a0001c0001t0001g0132 others(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 | 138 | a0001c0001t0001g0064 a0001c0001t0001g0206 a0001c0001t0001g0285 others(135): 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 | 158 | a0001c0001t0001g0033 a0001c0001t0001g0044 a0001c0001t0001g0064 others(155): 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 | a0001c0003t0007g0013 a0001c0003t0007g0014 a0001c0003t0007g0017 |
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 | a0001c0001t0001g0033 a0001c0001t0005g0034 a0001c0001t0005g0035 others(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 | a0001c0001t0002g0060 a0001c0001t0002g0061 a0001c0001t0002g0062 others(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 | a0002c0002t0011g0036 | 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 | 139 | a0001c0001t0001g0064 a0001c0001t0001g0206 a0001c0001t0001g0285 others(136): 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 | a0001c0001t0001g0044 a0001c0001t0001g0103 a0001c0001t0001g0216 others(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 | a0001c0001t0001g0064 a0001c0001t0002g0039 a0001c0001t0002g0058 others(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 | a0001c0001t0001g0322 a0001c0001t0003g0045 a0001c0001t0003g0050 others(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 | a0001c0001t0001g0122 a0001c0001t0001g0178 a0001c0001t0001g0211 others(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 | a0001c0001t0001g0033 | 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 | a0001c0001t0001g0044 a0001c0001t0001g0103 a0001c0003t0001g0016 others(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 | a0002c0007t0001g0019 a0002c0007t0011g0015 |
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 | a0001c0001t0001g0216 a0002c0002t0003g0046 |
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 | a0002c0002t0003g0100 | 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 | a0001c0001t0005g0034 a0001c0001t0005g0035 a0002c0002t0008g0304 |
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 | a0002c0002t0008g0323 | 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 | a0002c0002t0001g0246 | 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 | a0001c0001t0009g0098 | 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 | a0001c0001t0001g0132 a0001c0001t0001g0205 a0001c0001t0002g0075 others(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 | 37 | a0001c0001t0001g0064 a0001c0001t0002g0039 a0001c0001t0002g0054 others(34): 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 | 76 | a0001c0001t0001g0206 a0001c0001t0001g0285 a0001c0001t0002g0008 others(73): 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 | a0001c0001t0002g0072 a0001c0001t0002g0077 a0001c0001t0002g0215 others(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 | a0001c0001t0002g0060 a0001c0001t0002g0061 a0001c0001t0002g0062 others(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 | a0002c0002t0001g0286 | 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 | a0001c0001t0001g0033 | 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 | 102 | a0001c0001t0001g0206 a0001c0001t0001g0285 a0001c0001t0002g0008 others(99): 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 | a0001c0001t0001g0308 a0001c0001t0003g0269 a0001c0001t0009g0299 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0122 a0001c0001t0001g0178 others(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 | 144 | a0001c0001t0001g0064 a0001c0001t0001g0206 a0001c0001t0001g0285 others(141): 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 | a0002c0002t0001g0026 | 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 | a0002c0002t0001g0074 | 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 | a0002c0002t0001g0087 | 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 | a0001c0001t0001g0030 a0001c0001t0001g0122 a0001c0001t0001g0132 others(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 | a0002c0002t0011g0036 | 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 | a0001c0001t0004g0233 a0002c0002t0013g0037 |
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 | a0001c0001t0002g0054 a0001c0001t0002g0268 |
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 | 256 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0044 others(253): 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 | a0001c0001t0003g0307 | 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 | 140 | a0001c0001t0001g0064 a0001c0001t0001g0206 a0001c0001t0001g0285 others(137): 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 | a0002c0002t0006g0004 a0002c0002t0006g0020 a0002c0002t0006g0079 others(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 | a0001c0001t0001g0103 a0002c0002t0001g0301 a0002c0007t0011g0015 |
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 | a0001c0001t0003g0045 a0001c0001t0003g0057 a0001c0001t0003g0193 others(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 | a0001c0001t0003g0045 a0001c0001t0003g0057 a0001c0001t0003g0193 others(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 | a0001c0001t0001g0033 | 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 | a0002c0002t0001g0227 | 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 | a0001c0001t0001g0030 a0001c0001t0001g0122 a0001c0001t0001g0132 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0122 a0001c0001t0001g0132 others(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 | a0001c0001t0017g0038 a0002c0002t0001g0305 |
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 | a0002c0002t0001g0305 | 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 | a0001c0001t0004g0126 a0001c0001t0004g0233 a0001c0001t0004g0239 others(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 | a0001c0001t0001g0308 a0001c0001t0003g0269 a0001c0001t0009g0299 others(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 | a0001c0001t0001g0132 a0001c0001t0001g0205 a0001c0001t0001g0322 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0122 a0001c0001t0001g0178 others(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 | a0001c0001t0001g0308 a0001c0001t0003g0269 a0001c0001t0009g0299 others(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 | 144 | a0001c0001t0001g0064 a0001c0001t0001g0206 a0001c0001t0001g0285 others(141): 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 | a0001c0001t0002g0039 a0002c0004t0005g0254 a0002c0004t0005g0310 others(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 | a0001c0001t0017g0038 | 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 | 144 | a0001c0001t0001g0064 a0001c0001t0001g0206 a0001c0001t0001g0285 others(141): 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 | 144 | a0001c0001t0001g0064 a0001c0001t0001g0206 a0001c0001t0001g0285 others(141): 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 | 258 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0044 others(255): 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 | a0001c0001t0004g0251 | 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 | 144 | a0001c0001t0001g0064 a0001c0001t0001g0206 a0001c0001t0001g0285 others(141): 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 | a0001c0001t0009g0040 a0002c0002t0010g0328 |
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 | a0001c0001t0005g0034 a0001c0001t0005g0035 a0001c0001t0009g0098 others(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 | a0001c0001t0002g0236 | 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 | 246 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0064 others(243): 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 | 136 | a0001c0001t0001g0064 a0001c0001t0001g0206 a0001c0001t0001g0285 others(133): 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 | a0001c0001t0001g0033 | 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 | a0001c0001t0003g0084 | 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 | 41 | a0001c0001t0001g0064 a0001c0001t0002g0039 a0001c0001t0002g0058 others(38): 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 | a0001c0001t0001g0064 a0001c0001t0002g0039 a0001c0001t0002g0058 others(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 | 41 | a0001c0001t0001g0064 a0001c0001t0002g0039 a0001c0001t0002g0058 others(38): 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 | a0002c0002t0001g0041 | 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 | 5 | a0001c0001t0004g0005 a0001c0001t0004g0101 a0001c0001t0004g0102 others(2): 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 | a0001c0001t0002g0025 | 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 | a0001c0001t0004g0126 a0001c0001t0004g0233 a0001c0001t0004g0239 others(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 | a0002c0002t0003g0117 a0002c0002t0003g0118 |
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 | a0002c0002t0001g0026 | 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 | a0002c0002t0016g0078 | 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 | 41 | a0001c0001t0001g0064 a0001c0001t0002g0039 a0001c0001t0002g0058 others(38): 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 | 41 | a0001c0001t0001g0064 a0001c0001t0002g0039 a0001c0001t0002g0058 others(38): 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 | a0001c0001t0001g0132 a0001c0001t0001g0205 a0001c0001t0001g0322 others(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 | a0002c0002t0001g0241 | 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 | 41 | a0001c0001t0001g0064 a0001c0001t0002g0039 a0001c0001t0002g0058 others(38): 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 | a0002c0002t0016g0078 | 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 | a0001c0001t0001g0030 a0005c0011t0001g0313 |
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 | 45 | a0001c0001t0001g0064 a0001c0001t0002g0039 a0001c0001t0002g0058 others(42): 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 | a0001c0001t0005g0034 a0001c0001t0005g0035 a0001c0001t0009g0098 others(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 | a0001c0001t0005g0034 a0001c0001t0005g0035 a0001c0001t0009g0098 others(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 | a0001c0001t0001g0064 a0001c0001t0002g0039 a0001c0001t0002g0058 others(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 | a0002c0002t0011g0036 | 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 | a0001c0001t0002g0025 | 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 | a0001c0001t0001g0030 a0001c0001t0001g0122 a0001c0001t0001g0178 others(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 | a0002c0002t0003g0172 a0002c0002t0003g0177 a0002c0002t0003g0245 |
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 | a0001c0001t0001g0064 a0001c0001t0002g0039 a0001c0001t0002g0058 others(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 | a0001c0001t0003g0051 a0001c0001t0003g0070 |
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 | a0001c0001t0001g0033 | 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 | a0001c0001t0001g0178 a0001c0001t0001g0205 a0001c0001t0001g0322 others(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 | a0001c0001t0001g0178 a0001c0001t0001g0205 a0001c0001t0001g0322 others(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 | a0001c0001t0001g0216 a0002c0002t0003g0046 |
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 | a0001c0001t0001g0064 a0001c0001t0001g0122 a0001c0001t0001g0132 others(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 | a0001c0001t0009g0098 a0002c0002t0001g0305 |
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 | 142 | a0001c0001t0001g0064 a0001c0001t0001g0132 a0001c0001t0001g0206 others(139): 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 |
252 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0044 others(249): 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 | a0002c0002t0008g0323 | 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 | a0002c0002t0003g0100 | 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 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0044 others(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 | a0001c0001t0001g0033 | 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 | a0001c0001t0001g0044 a0001c0001t0001g0064 a0001c0001t0001g0103 others(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 | a0002c0002t0004g0212 a0002c0002t0004g0302 a0002c0002t0004g0319 |
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 | a0002c0002t0001g0023 | 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 | 245 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0044 others(242): 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 | a0001c0001t0001g0122 a0001c0001t0001g0178 a0001c0001t0001g0285 others(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 | a0002c0004t0005g0296 a0002c0004t0005g0309 |
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 | 253 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0044 others(250): 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 | a0001c0001t0004g0312 | 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 | a0001c0001t0002g0089 | 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 | a0002c0002t0010g0328 | 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 | 246 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0044 others(243): 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 | a0002c0002t0006g0020 | 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 | a0002c0002t0003g0172 a0002c0002t0003g0177 a0002c0002t0003g0245 |
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 | 239 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0064 others(236): 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 | a0001c0001t0002g0270 | 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 | 16 | a0001c0001t0001g0103 a0001c0001t0001g0205 a0001c0001t0002g0187 others(13): 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 | 13 | a0001c0001t0001g0103 a0001c0001t0001g0205 a0001c0001t0002g0187 others(10): 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 | a0001c0001t0001g0033 | 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 | a0001c0001t0002g0199 a0001c0001t0002g0281 a0001c0001t0002g0282 others(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 | a0001c0001t0001g0044 a0001c0001t0001g0216 a0001c0001t0001g0285 others(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 | 9 | a0001c0001t0002g0159 a0001c0001t0003g0255 a0001c0001t0003g0269 others(6): Show |
11 | HG00140.hp1 HG00733.hp2 HG01074.hp1 others(8): 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 | a0001c0001t0001g0132 a0001c0001t0004g0126 a0001c0001t0004g0239 others(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 | a0001c0001t0005g0029 | 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 | 149 | a0001c0001t0001g0103 a0001c0001t0001g0205 a0001c0001t0001g0206 others(146): Show |
156 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.823-1584A>T | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51026944 | |||||||
| chr14:51027106 | C | T | 82 | a0001c0001t0001g0033 a0001c0001t0001g0044 a0001c0001t0001g0103 others(79): 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 | a0001c0001t0001g0211 a0001c0001t0002g0056 a0001c0001t0002g0153 others(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 | a0001c0001t0002g0141 a0001c0001t0002g0154 a0001c0001t0002g0187 others(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 | 74 | a0001c0001t0001g0064 a0001c0001t0001g0179 a0001c0001t0001g0206 others(71): 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 | a0001c0001t0001g0030 a0001c0001t0001g0178 a0001c0001t0002g0054 others(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 | a0001c0001t0001g0132 a0001c0001t0002g0055 a0001c0001t0002g0058 others(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 | 113 | a0001c0001t0001g0033 a0001c0001t0001g0044 a0001c0001t0001g0103 others(110): 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 | a0001c0001t0001g0216 a0001c0001t0003g0315 a0001c0001t0005g0035 others(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 | a0001c0001t0003g0295 | 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 | a0002c0002t0003g0100 | 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 | 216 | a0001c0001t0001g0033 a0001c0001t0001g0044 a0001c0001t0001g0064 others(213): Show |
224 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(221): Show |
intron_variant | MODIFIER | c.823-1883T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51027243 | |||||||
| chr14:51027261 | A | C | 217 | a0001c0001t0001g0033 a0001c0001t0001g0044 a0001c0001t0001g0064 others(214): Show |
225 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(222): 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 | a0002c0002t0003g0031 | 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 | a0001c0001t0005g0028 a0002c0002t0001g0311 a0002c0002t0003g0106 others(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 | a0001c0001t0002g0025 a0001c0001t0002g0072 a0001c0001t0002g0077 others(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 | |||||||
| chr14:51027682 | T | C | 1 | a0001c0003t0007g0014 | 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 | a0002c0002t0001g0293 | 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 | a0001c0001t0002g0314 a0002c0002t0001g0305 |
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 | 132 | a0001c0001t0001g0030 a0001c0001t0001g0044 a0001c0001t0001g0103 others(129): 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 | 128 | a0001c0001t0001g0030 a0001c0001t0001g0044 a0001c0001t0001g0103 others(125): 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 | a0002c0010t0005g0018 | 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 | 69 | a0001c0001t0001g0103 a0001c0001t0001g0205 a0001c0001t0001g0216 others(66): 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 | 132 | a0001c0001t0001g0030 a0001c0001t0001g0044 a0001c0001t0001g0103 others(129): 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 | a0001c0001t0001g0275 | 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 | 143 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0044 others(140): 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 | a0002c0002t0001g0123 a0002c0002t0001g0124 a0002c0002t0001g0188 |
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 | 33 | a0001c0001t0001g0030 a0001c0001t0001g0103 a0001c0001t0001g0178 others(30): 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 | 128 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0103 others(125): 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 | 128 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0103 others(125): 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 | 238 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0044 others(235): Show |
246 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(243): 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 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0044 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0122 a0001c0001t0001g0178 others(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 | a0001c0001t0001g0033 a0001c0001t0002g0141 a0001c0001t0003g0007 others(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 | a0001c0001t0001g0033 a0001c0001t0002g0141 a0001c0001t0003g0007 others(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 | a0001c0001t0001g0044 a0001c0001t0001g0122 a0001c0001t0002g0039 others(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 | 250 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0044 others(247): Show |
259 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.823-3620G>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51028980 | |||||||
| chr14:51029082 | T | C | 239 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0044 others(236): Show |
247 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(244): 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 | a0001c0001t0003g0307 | 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 | a0002c0002t0001g0053 | 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 | a0001c0001t0001g0216 a0001c0001t0002g0314 a0002c0002t0001g0305 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0044 others(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 | 115 | a0001c0001t0001g0030 a0001c0001t0001g0178 a0001c0001t0001g0179 others(112): Show |
118 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(115): 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 | a0001c0001t0001g0033 a0001c0001t0001g0122 a0001c0001t0002g0047 others(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 | a0001c0001t0001g0216 a0001c0001t0002g0314 a0001c0001t0009g0098 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0178 others(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 | a0001c0001t0004g0148 a0001c0001t0009g0098 a0002c0002t0001g0286 others(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 | a0001c0001t0002g0257 a0001c0001t0002g0271 a0002c0002t0001g0128 |
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 | a0001c0001t0001g0216 a0001c0001t0002g0314 a0002c0002t0001g0305 others(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 | a0001c0001t0003g0086 | 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 | 81 | a0001c0001t0001g0179 a0001c0001t0001g0206 a0001c0001t0001g0275 others(78): Show |
84 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.823-4417delA | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51029776 | |||||||
| chr14:51029803 | C | T | 44 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0178 others(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 | a0001c0001t0001g0044 a0001c0001t0002g0039 a0001c0001t0009g0040 others(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 | a0001c0001t0004g0233 a0002c0002t0001g0232 |
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 | 6 | a0001c0001t0001g0103 a0001c0001t0004g0005 a0001c0001t0004g0101 others(3): 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 | a0002c0002t0001g0123 a0002c0002t0001g0124 a0002c0002t0001g0188 |
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 | a0002c0002t0003g0279 | 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 | a0001c0001t0001g0033 a0001c0001t0002g0141 a0001c0001t0003g0007 others(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 | a0001c0001t0001g0033 a0001c0001t0002g0141 a0001c0001t0003g0007 others(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 | a0001c0001t0001g0033 a0001c0001t0002g0141 a0001c0001t0003g0007 others(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 | a0002c0002t0001g0261 | 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 | a0002c0002t0001g0293 | 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 | 175 | a0001c0001t0001g0044 a0001c0001t0001g0064 a0001c0001t0001g0103 others(172): 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 | 90 | a0001c0001t0001g0179 a0001c0001t0001g0206 a0001c0001t0001g0275 others(87): Show |
94 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(91): 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 | a0001c0001t0002g0072 a0001c0001t0002g0077 a0001c0001t0003g0007 others(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 | a0001c0001t0001g0122 a0002c0002t0001g0023 a0002c0002t0001g0024 others(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 | 9 | a0001c0001t0001g0103 a0001c0001t0001g0308 a0001c0001t0004g0005 others(6): 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 | 244 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0044 others(241): Show |
253 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(250): 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 | a0001c0001t0001g0322 a0001c0001t0002g0281 a0001c0001t0002g0282 others(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 | a0001c0001t0001g0122 a0001c0001t0002g0047 a0001c0001t0002g0108 others(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 | a0001c0001t0002g0072 a0001c0001t0002g0077 a0001c0001t0002g0089 others(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 | a0001c0001t0002g0072 a0001c0001t0002g0077 a0001c0001t0002g0089 others(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 | a0001c0001t0002g0072 a0001c0001t0002g0077 a0001c0001t0002g0089 others(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 | a0001c0001t0009g0098 a0002c0002t0003g0031 |
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 | a0002c0002t0006g0020 | 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 | a0001c0001t0002g0156 a0001c0001t0002g0157 |
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 | a0002c0002t0001g0027 | 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 | a0001c0001t0002g0072 a0001c0001t0002g0077 a0001c0001t0002g0089 others(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 | a0001c0001t0005g0034 a0001c0001t0005g0035 a0002c0002t0008g0323 others(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 | a0001c0001t0005g0028 a0002c0002t0003g0100 |
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 | a0001c0001t0002g0176 a0001c0001t0002g0186 |
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 | a0001c0001t0002g0165 a0002c0002t0001g0241 |
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 | a0001c0001t0009g0098 a0002c0002t0003g0031 |
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 | 238 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0044 others(235): Show |
246 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(243): 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 | a0001c0001t0001g0122 a0001c0001t0002g0108 a0001c0001t0002g0115 others(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 | a0002c0002t0003g0100 | 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 | a0001c0001t0001g0322 a0001c0001t0002g0281 a0001c0001t0002g0282 others(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 | a0002c0002t0006g0020 | 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 | a0002c0002t0001g0112 | 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 | a0001c0001t0001g0122 a0001c0001t0002g0108 a0001c0001t0002g0115 others(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 | a0001c0001t0002g0108 a0001c0001t0002g0115 a0001c0001t0002g0116 others(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 | a0001c0001t0009g0098 a0002c0002t0001g0166 a0002c0002t0003g0031 |
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 | a0001c0001t0009g0040 | 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 | a0002c0002t0006g0083 | 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 | a0001c0001t0002g0039 a0001c0001t0002g0257 a0001c0001t0002g0314 others(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 | a0001c0001t0002g0072 a0001c0001t0002g0077 a0001c0001t0002g0089 others(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 | 103 | a0001c0001t0001g0179 a0001c0001t0001g0206 a0001c0001t0001g0216 others(100): Show |
107 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(104): 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 | a0002c0002t0006g0020 | 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 | a0002c0002t0001g0324 a0002c0002t0002g0234 |
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 | 187 | a0001c0001t0001g0122 a0001c0001t0001g0179 a0001c0001t0001g0206 others(184): Show |
195 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(192): 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 | a0001c0001t0005g0034 a0001c0001t0005g0035 a0002c0002t0008g0323 others(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 | a0001c0001t0002g0194 | 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 | a0001c0001t0002g0141 a0001c0001t0003g0007 a0001c0001t0003g0057 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0205 a0001c0001t0001g0285 others(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 | a0001c0001t0002g0141 a0001c0001t0003g0007 a0001c0001t0003g0057 others(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 | a0001c0001t0002g0306 a0001c0001t0003g0307 |
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 | a0001c0001t0001g0030 a0001c0001t0001g0178 a0001c0001t0002g0165 others(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 | 237 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0044 others(234): Show |
245 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.823-10573T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51035933 | |||||||
| chr14:51036266 | T | G | 3 | a0001c0001t0009g0098 a0002c0002t0003g0031 a0002c0002t0006g0020 |
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 | a0001c0001t0001g0322 a0001c0001t0002g0281 a0001c0001t0002g0282 others(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 | a0001c0001t0004g0148 a0002c0004t0005g0149 |
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 | a0001c0001t0001g0322 a0001c0001t0002g0281 a0001c0001t0002g0282 others(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 | a0001c0001t0002g0141 a0001c0001t0003g0007 a0001c0001t0003g0057 others(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 | 29 | a0001c0001t0001g0275 a0001c0001t0002g0025 a0001c0001t0002g0159 others(26): Show |
31 | HG00140.hp1 HG00597.hp2 HG00733.hp2 others(28): 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 | a0002c0002t0006g0020 | 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 | a0002c0002t0003g0240 | 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 | 84 | a0001c0001t0001g0179 a0001c0001t0001g0206 a0001c0001t0001g0216 others(81): Show |
87 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(84): 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 | a0002c0002t0001g0311 a0002c0002t0003g0106 a0002c0004t0005g0309 others(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 | a0001c0001t0001g0322 a0001c0001t0002g0281 a0001c0001t0002g0282 others(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 | a0001c0001t0002g0306 | 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 | a0001c0001t0002g0072 a0001c0001t0002g0077 a0001c0001t0002g0089 others(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 | 1 | a0001c0001t0002g0008 | 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 | a0001c0001t0009g0098 a0002c0002t0003g0031 |
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 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 |
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 | a0001c0001t0004g0148 a0002c0002t0001g0311 a0002c0002t0003g0106 others(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 | a0001c0001t0001g0064 a0001c0001t0002g0075 a0002c0002t0006g0004 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0178 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0205 a0001c0001t0001g0285 others(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 | a0001c0001t0009g0098 a0002c0002t0003g0031 a0002c0002t0006g0020 |
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 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0178 others(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 | a0001c0001t0002g0072 a0001c0001t0002g0077 a0001c0001t0002g0089 others(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 | a0001c0001t0002g0039 a0001c0001t0009g0040 a0001c0001t0017g0038 others(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 | a0001c0001t0002g0025 | 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 | a0001c0001t0009g0098 a0002c0002t0003g0031 |
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 | a0001c0001t0001g0322 a0001c0001t0002g0281 a0001c0001t0002g0282 others(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 | a0001c0001t0001g0179 a0001c0001t0003g0065 a0001c0001t0003g0180 others(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 | a0002c0002t0001g0021 | 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 | a0001c0001t0002g0072 a0001c0001t0002g0077 a0001c0001t0002g0089 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0178 a0001c0001t0002g0298 others(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 | a0002c0002t0010g0330 | 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 | a0001c0001t0002g0072 a0001c0001t0002g0077 a0001c0001t0002g0089 others(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 | a0001c0001t0001g0122 a0001c0001t0001g0322 a0001c0001t0002g0039 others(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 | a0002c0002t0004g0048 | 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 | a0001c0001t0001g0122 a0001c0001t0001g0322 a0001c0001t0002g0108 others(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 | a0002c0002t0003g0240 | 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 | a0002c0002t0006g0020 | 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 | a0001c0001t0002g0141 a0001c0001t0003g0007 a0001c0001t0003g0057 others(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 | a0001c0001t0002g0025 | 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 | 99 | a0001c0001t0001g0179 a0001c0001t0001g0206 a0001c0001t0001g0211 others(96): Show |
102 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(99): 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 | a0001c0001t0003g0220 | 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 | a0001c0001t0002g0072 a0001c0001t0002g0077 a0001c0001t0002g0089 others(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 | a0001c0001t0002g0039 a0001c0001t0009g0040 a0001c0001t0017g0038 others(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 | a0001c0001t0001g0122 a0001c0001t0002g0108 a0001c0001t0002g0115 others(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 | a0001c0001t0001g0322 a0001c0001t0002g0281 a0001c0001t0002g0282 others(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 | a0001c0001t0001g0030 | 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 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0122 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0205 a0001c0001t0001g0285 others(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 | a0001c0001t0002g0141 a0001c0001t0003g0007 a0001c0001t0003g0057 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0178 a0001c0001t0002g0298 others(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 | a0001c0001t0002g0072 a0001c0001t0002g0077 a0001c0001t0002g0089 others(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 | 250 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0122 others(247): Show |
258 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(255): 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 | a0002c0002t0006g0020 | 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 | a0001c0001t0002g0072 a0001c0001t0002g0077 a0001c0001t0002g0089 others(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 | a0001c0001t0009g0098 a0002c0002t0003g0031 a0002c0002t0006g0020 |
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 | a0001c0001t0002g0025 a0001c0001t0002g0259 a0001c0001t0002g0268 |
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 | a0001c0001t0002g0314 | 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 | a0001c0001t0002g0265 | 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 | a0001c0001t0005g0034 a0001c0001t0005g0035 a0002c0002t0008g0323 others(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 | a0001c0001t0001g0122 a0001c0001t0001g0322 a0001c0001t0002g0108 others(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 | a0001c0001t0005g0028 a0001c0001t0005g0029 |
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 | a0002c0002t0006g0020 | 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 | a0001c0001t0002g0072 a0001c0001t0002g0077 a0001c0001t0002g0089 others(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 | a0001c0001t0002g0072 a0001c0001t0002g0077 a0001c0001t0002g0089 others(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 | a0005c0011t0001g0313 | 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 | a0001c0001t0002g0072 a0001c0001t0002g0077 a0001c0001t0002g0089 others(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 | a0001c0001t0002g0072 a0001c0001t0002g0077 a0001c0001t0002g0089 others(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 | a0001c0001t0002g0072 a0001c0001t0002g0077 a0001c0001t0002g0089 others(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 | a0002c0002t0001g0305 | 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 | a0001c0001t0005g0028 a0001c0001t0005g0029 |
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 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0122 others(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 | a0002c0002t0003g0110 | 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 | 99 | a0001c0001t0001g0179 a0001c0001t0001g0206 a0001c0001t0001g0211 others(96): Show |
102 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(99): 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 | a0002c0002t0001g0260 | 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 | a0002c0002t0002g0234 | 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 | a0002c0002t0006g0020 | 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 | a0001c0001t0009g0098 a0002c0002t0003g0031 |
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 | a0001c0001t0005g0028 | 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 | a0001c0001t0002g0072 a0001c0001t0002g0077 a0001c0001t0002g0089 others(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 | a0001c0001t0001g0122 a0001c0001t0002g0047 a0001c0001t0002g0115 others(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 | 99 | a0001c0001t0001g0179 a0001c0001t0001g0206 a0001c0001t0001g0211 others(96): Show |
102 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.823-19698delT | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51045057 | |||||||
| chr14:51045115 | G | T | 135 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0122 others(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 | a0002c0002t0001g0311 a0002c0002t0003g0106 a0002c0004t0005g0309 others(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 | a0002c0002t0003g0031 | 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 | a0001c0001t0002g0058 | 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 | a0001c0001t0002g0072 a0001c0001t0002g0077 a0001c0001t0002g0089 others(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 | a0001c0001t0002g0072 a0001c0001t0002g0077 a0001c0001t0002g0089 others(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 | a0001c0001t0002g0072 a0001c0001t0002g0077 a0001c0001t0002g0089 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0205 a0001c0001t0001g0285 others(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 | a0001c0001t0002g0072 a0001c0001t0002g0077 a0001c0001t0002g0089 others(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 | a0002c0002t0006g0020 | 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 | a0001c0001t0002g0072 a0001c0001t0002g0077 a0001c0001t0002g0089 others(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 | a0001c0001t0003g0256 a0001c0001t0003g0258 |
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 | a0001c0001t0002g0176 a0001c0001t0002g0186 a0002c0002t0003g0237 |
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 | a0001c0001t0003g0045 | 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 | a0001c0001t0002g0072 a0001c0001t0002g0077 a0001c0001t0002g0089 others(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 | a0002c0004t0005g0310 | 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 | a0001c0001t0009g0098 a0002c0002t0003g0031 |
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 | a0002c0002t0013g0037 | 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 | a0001c0001t0004g0148 a0002c0004t0005g0149 |
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 | a0001c0001t0003g0073 | 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 | a0001c0001t0001g0044 a0002c0002t0001g0041 a0002c0002t0001g0043 others(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 | a0001c0001t0002g0072 a0001c0001t0002g0077 a0001c0001t0002g0089 others(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 | a0001c0001t0005g0034 a0001c0001t0005g0035 a0002c0002t0008g0323 others(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 | 99 | a0001c0001t0001g0179 a0001c0001t0001g0206 a0001c0001t0001g0211 others(96): Show |
102 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(99): 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 | a0001c0001t0002g0141 a0001c0001t0003g0007 a0001c0001t0003g0057 others(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 | a0001c0001t0002g0072 a0001c0001t0002g0077 a0001c0001t0002g0089 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0178 a0001c0001t0002g0298 others(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 | a0001c0001t0003g0183 a0002c0002t0001g0003 a0002c0002t0001g0112 others(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 | a0001c0001t0003g0267 | 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 | a0001c0001t0002g0259 | 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 | a0001c0001t0002g0056 a0001c0001t0002g0058 a0001c0001t0004g0239 others(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 | 188 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0103 others(185): Show |
192 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.823-22600delT | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51047959 | |||||||
| chr14:51047959 | CAA | C | 30 | a0001c0001t0002g0072 a0001c0001t0002g0077 a0001c0001t0002g0089 others(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 | a0001c0001t0010g0327 | 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 | a0001c0014t0002g0326 | 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 | 327 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0044 others(324): Show |
339 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.823-22741T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51048101 | |||||||
| chr14:51048220 | C | T | 99 | a0001c0001t0001g0179 a0001c0001t0001g0206 a0001c0001t0001g0211 others(96): Show |
102 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(99): 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 | a0001c0001t0002g0072 a0001c0001t0002g0077 a0001c0001t0002g0089 others(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 | a0001c0001t0002g0072 a0001c0001t0002g0077 a0001c0001t0002g0089 others(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 | a0001c0001t0002g0058 | 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 | a0001c0001t0005g0034 a0001c0001t0005g0035 a0002c0002t0008g0323 others(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 | a0001c0001t0002g0039 a0001c0001t0009g0040 |
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 | a0001c0001t0001g0030 a0001c0001t0001g0178 a0001c0001t0002g0298 others(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 | a0001c0001t0002g0072 a0001c0001t0002g0077 a0001c0001t0002g0089 others(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 |
228 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0122 others(225): Show |
235 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(232): 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 | a0001c0001t0002g0039 a0001c0001t0009g0040 |
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 | a0001c0001t0002g0088 | 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 | a0001c0001t0001g0030 a0001c0001t0001g0178 a0001c0001t0002g0298 others(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 | a0001c0001t0002g0088 a0001c0001t0003g0050 a0002c0002t0001g0166 |
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 | 131 | a0001c0001t0001g0179 a0001c0001t0001g0206 a0001c0001t0001g0211 others(128): Show |
137 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(134): 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 | a0001c0001t0002g0156 a0001c0001t0002g0157 |
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 | a0001c0001t0002g0072 a0001c0001t0002g0077 a0001c0001t0002g0089 others(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 | a0001c0001t0004g0148 a0002c0002t0001g0311 a0002c0002t0003g0106 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0178 a0001c0001t0002g0298 others(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 | a0001c0001t0002g0072 a0001c0001t0002g0077 a0001c0001t0002g0089 others(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 | 29 | a0001c0001t0001g0275 a0001c0001t0002g0025 a0001c0001t0002g0159 others(26): Show |
31 | HG00140.hp1 HG00597.hp2 HG00733.hp2 others(28): 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 | a0001c0001t0002g0141 a0001c0001t0003g0057 a0003c0006t0001g0140 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0178 a0001c0001t0002g0298 others(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 | a0002c0002t0001g0311 a0002c0002t0003g0106 a0002c0004t0005g0309 others(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 | a0001c0001t0002g0108 a0001c0001t0003g0084 |
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 | a0001c0001t0009g0098 a0002c0002t0003g0031 |
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 | a0001c0001t0002g0072 a0001c0001t0002g0077 a0001c0001t0002g0089 others(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 | 6 | a0001c0001t0001g0103 a0001c0001t0004g0005 a0001c0001t0004g0101 others(3): 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 | a0001c0001t0002g0058 a0001c0001t0003g0082 |
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 | a0001c0001t0002g0058 | 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 | a0001c0001t0002g0072 a0001c0001t0002g0077 a0001c0001t0002g0089 others(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 | a0002c0002t0001g0311 a0002c0002t0003g0106 a0002c0004t0005g0309 others(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 | a0001c0001t0002g0259 | 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 | a0001c0001t0002g0047 a0001c0001t0003g0082 a0001c0001t0003g0256 others(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 | a0001c0001t0005g0034 a0001c0001t0005g0035 a0002c0002t0006g0020 others(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 | |||||||
| chr14:51049950 | A | G | 37 | a0001c0001t0001g0322 a0001c0001t0002g0072 a0001c0001t0002g0077 others(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 | a0001c0001t0002g0039 | 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 | 96 | a0001c0001t0001g0179 a0001c0001t0001g0206 a0001c0001t0001g0211 others(93): Show |
99 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(96): 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 | a0001c0001t0002g0141 a0001c0001t0003g0007 a0001c0001t0003g0057 others(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 | a0001c0001t0003g0315 | 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 | a0001c0001t0002g0058 | 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 | a0001c0001t0002g0058 | 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 | a0002c0002t0006g0020 a0002c0002t0006g0221 |
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 | a0001c0001t0002g0089 a0001c0001t0002g0314 a0001c0001t0003g0073 others(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 | a0001c0001t0001g0132 a0001c0001t0001g0205 a0001c0001t0001g0206 others(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 | a0001c0001t0001g0030 | 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 | a0001c0001t0003g0220 | 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 | a0001c0001t0002g0108 a0001c0001t0002g0115 a0001c0001t0002g0116 others(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 | a0002c0002t0006g0020 | 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 | a0001c0001t0001g0206 a0001c0001t0001g0322 a0001c0001t0002g0281 others(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 | a0001c0001t0005g0034 a0001c0001t0005g0035 a0002c0002t0008g0323 others(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 | a0001c0001t0005g0034 a0001c0001t0005g0035 a0002c0002t0008g0323 others(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 | 327 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0044 others(324): Show |
339 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(336): 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 | a0001c0001t0005g0034 a0001c0001t0005g0035 a0002c0002t0008g0323 others(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 | a0001c0001t0002g0281 a0001c0001t0002g0282 |
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 | a0001c0001t0001g0044 a0002c0002t0001g0041 a0002c0002t0001g0043 others(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 | a0001c0001t0002g0218 | 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 | a0001c0001t0002g0281 a0001c0001t0002g0282 a0001c0001t0002g0283 others(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 | a0001c0001t0005g0034 a0001c0001t0005g0035 a0002c0002t0008g0323 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0122 a0001c0001t0001g0308 others(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 | a0001c0001t0003g0284 | 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 | a0001c0001t0005g0034 a0001c0001t0005g0035 a0002c0002t0008g0323 others(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 | a0001c0001t0001g0132 a0001c0001t0001g0205 a0001c0001t0001g0285 others(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 | a0001c0001t0005g0034 a0001c0001t0005g0035 a0002c0002t0008g0323 others(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 | a0001c0001t0005g0034 a0001c0001t0005g0035 a0002c0002t0008g0323 others(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 | a0001c0001t0001g0033 | 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 | a0001c0001t0005g0034 a0001c0001t0005g0035 a0002c0002t0008g0323 others(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 | a0001c0001t0005g0034 a0001c0001t0005g0035 a0002c0002t0008g0323 others(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 | a0001c0001t0001g0308 a0001c0001t0002g0039 a0001c0001t0009g0040 others(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 | a0001c0001t0004g0148 a0001c0001t0005g0028 a0001c0001t0005g0029 others(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 | a0001c0001t0005g0034 a0001c0001t0005g0035 a0002c0002t0008g0323 others(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 | a0001c0001t0003g0129 a0001c0001t0003g0130 |
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 | a0001c0001t0004g0148 a0001c0001t0005g0028 a0001c0001t0005g0029 others(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 | a0002c0002t0006g0083 | 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 | 141 | a0001c0001t0001g0122 a0001c0001t0001g0178 a0001c0001t0001g0179 others(138): Show |
145 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.823-27800dupT | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51053159 | |||||||
| chr14:51053159 | CA | C | 39 | a0001c0001t0002g0236 a0001c0001t0002g0298 a0001c0001t0003g0252 others(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 | a0001c0001t0001g0132 a0001c0001t0002g0141 a0001c0001t0002g0147 others(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 | a0001c0001t0002g0176 a0001c0001t0002g0186 |
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 | a0001c0001t0005g0034 a0001c0001t0005g0035 a0002c0002t0008g0323 others(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 | a0001c0001t0005g0034 a0001c0001t0005g0035 a0002c0002t0008g0323 others(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 | a0001c0001t0001g0033 a0001c0001t0002g0090 a0001c0001t0004g0138 others(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 | a0001c0001t0001g0103 a0001c0001t0003g0143 a0001c0001t0004g0005 others(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 | a0001c0001t0001g0205 a0001c0001t0001g0285 a0001c0001t0001g0308 others(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 | 102 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0206 others(99): Show |
104 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(101): 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 | a0001c0001t0001g0122 a0001c0001t0001g0322 a0001c0001t0002g0108 others(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 | a0001c0001t0001g0132 a0001c0001t0002g0141 a0001c0001t0002g0147 others(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 | a0001c0001t0001g0122 a0001c0001t0002g0108 a0001c0001t0002g0115 others(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 | a0002c0002t0003g0245 | 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 | a0001c0001t0002g0314 a0001c0001t0003g0183 a0001c0001t0003g0315 others(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 | a0001c0001t0002g0108 a0001c0001t0002g0115 a0001c0001t0002g0116 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0132 a0001c0001t0001g0308 others(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 | 19 | a0001c0001t0002g0141 a0001c0001t0002g0147 a0001c0001t0003g0129 others(16): Show |
20 | HG00733.hp2 HG00738.hp1 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.823-28221dupA | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51053580 | |||||||
| chr14:51053580 | CT | C | 25 | a0001c0001t0001g0030 a0001c0001t0001g0103 a0001c0001t0001g0179 others(22): 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 | a0001c0001t0002g0298 a0002c0002t0001g0232 a0002c0002t0001g0241 others(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 | a0001c0001t0002g0236 a0001c0001t0003g0252 a0001c0001t0004g0233 others(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 | a0001c0001t0001g0322 a0001c0001t0002g0141 a0001c0001t0002g0147 others(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 | a0001c0001t0001g0322 a0001c0001t0002g0159 a0001c0001t0002g0281 others(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 | a0001c0001t0002g0056 a0001c0001t0002g0060 a0001c0001t0002g0062 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0122 a0001c0001t0001g0132 others(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 | a0001c0001t0001g0322 a0001c0001t0002g0281 a0001c0001t0002g0282 others(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 | a0002c0002t0001g0305 | 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 | a0001c0001t0001g0132 a0001c0001t0002g0141 a0001c0001t0002g0147 others(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 | a0002c0002t0006g0223 | 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 | a0002c0002t0001g0305 | 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 | a0001c0001t0002g0090 | 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 | a0001c0001t0001g0122 a0001c0001t0002g0108 a0001c0001t0002g0115 others(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 | a0002c0002t0001g0286 a0002c0004t0005g0296 |
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 | a0001c0001t0005g0034 a0001c0001t0005g0035 a0002c0002t0008g0323 others(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 | a0001c0001t0001g0179 a0001c0001t0002g0171 a0001c0001t0003g0180 others(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 | a0001c0001t0001g0122 a0001c0001t0002g0108 a0001c0001t0002g0115 others(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 | a0002c0002t0003g0237 | 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 | a0001c0001t0005g0034 a0001c0001t0005g0035 a0002c0002t0008g0323 others(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 | a0001c0001t0005g0034 a0001c0001t0005g0035 a0002c0002t0008g0323 others(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 |
188 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0205 others(185): Show |
193 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(190): 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 | a0001c0001t0001g0132 a0001c0001t0002g0141 a0001c0001t0002g0147 others(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 | a0002c0002t0001g0094 a0002c0002t0001g0095 |
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 | 252 | a0001c0001t0001g0122 a0001c0001t0001g0132 a0001c0001t0001g0178 others(249): Show |
260 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(257): 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 | 121 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0206 others(118): Show |
123 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(120): 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 | a0001c0001t0001g0308 a0002c0002t0001g0032 a0002c0002t0001g0243 others(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 | a0002c0002t0001g0263 | 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 | a0001c0001t0004g0148 a0001c0001t0005g0028 a0001c0001t0005g0029 others(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 | 114 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0206 others(111): Show |
116 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(113): 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 | 113 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0206 others(110): Show |
115 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(112): 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 | a0001c0001t0003g0082 | 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 | a0001c0001t0004g0264 | 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 | a0001c0001t0001g0122 a0001c0001t0001g0132 a0001c0001t0001g0322 others(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 | a0001c0001t0001g0122 a0001c0001t0001g0132 a0001c0001t0001g0322 others(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 | a0001c0001t0001g0122 a0001c0001t0001g0132 a0001c0001t0001g0322 others(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 | a0001c0001t0004g0148 a0001c0001t0005g0028 a0001c0001t0005g0029 others(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 | a0001c0001t0001g0122 a0001c0001t0001g0132 a0001c0001t0001g0205 others(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 | a0001c0001t0005g0028 | 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 | a0001c0001t0001g0122 a0001c0001t0001g0132 a0001c0001t0001g0205 others(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 | a0001c0001t0001g0122 a0001c0001t0001g0132 a0001c0001t0001g0205 others(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 | a0001c0001t0001g0322 a0001c0001t0002g0281 a0001c0001t0002g0282 others(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 | a0001c0001t0001g0122 a0001c0001t0001g0132 a0001c0001t0001g0205 others(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 | a0001c0001t0001g0033 | 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 | a0001c0001t0001g0122 a0001c0001t0001g0132 a0001c0001t0001g0205 others(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 | a0002c0002t0001g0226 a0002c0002t0013g0248 |
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 | a0001c0001t0001g0122 a0001c0001t0001g0132 a0001c0001t0001g0205 others(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 | 114 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0206 others(111): Show |
116 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(113): 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 | a0001c0001t0005g0034 a0001c0001t0005g0035 a0002c0002t0008g0323 others(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 | a0002c0002t0003g0046 | 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 | a0001c0001t0001g0122 a0001c0001t0001g0132 a0001c0001t0001g0205 others(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 | a0001c0001t0001g0122 a0001c0001t0001g0132 a0001c0001t0001g0205 others(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 | a0001c0001t0001g0122 a0001c0001t0001g0132 a0001c0001t0001g0205 others(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 | 252 | a0001c0001t0001g0122 a0001c0001t0001g0132 a0001c0001t0001g0178 others(249): Show |
260 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(257): 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 | a0002c0002t0004g0048 | 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 | a0001c0001t0001g0122 a0001c0001t0001g0132 a0001c0001t0001g0205 others(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 | a0001c0001t0012g0289 | 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 | a0001c0001t0001g0122 a0001c0001t0001g0132 a0001c0001t0001g0205 others(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 | a0001c0001t0001g0122 a0001c0001t0001g0132 a0001c0001t0001g0205 others(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 | a0001c0001t0001g0122 a0001c0001t0001g0322 a0001c0001t0002g0108 others(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 | a0001c0001t0001g0122 a0002c0002t0001g0022 a0002c0002t0001g0023 others(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 | a0001c0001t0002g0236 a0001c0001t0003g0252 a0001c0001t0004g0233 others(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 | a0001c0001t0005g0034 a0001c0001t0005g0035 a0002c0002t0008g0323 others(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 | a0001c0001t0001g0122 a0001c0001t0001g0132 a0001c0001t0001g0205 others(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 | a0001c0001t0009g0098 | 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 | a0001c0001t0001g0122 a0001c0001t0001g0132 a0001c0001t0001g0205 others(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 | a0002c0002t0014g0010 | 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 | a0001c0001t0001g0122 a0001c0001t0001g0132 a0001c0001t0001g0205 others(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 | a0001c0001t0002g0314 | 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 | a0001c0001t0001g0122 a0001c0001t0001g0132 a0001c0001t0001g0205 others(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 | a0001c0001t0001g0322 a0001c0001t0002g0281 a0001c0001t0002g0282 others(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 | a0001c0001t0001g0132 a0001c0001t0001g0205 a0001c0001t0001g0285 others(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 | 1 | a0001c0001t0002g0008 | 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 | a0001c0001t0001g0285 | 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 | 129 | a0001c0001t0001g0132 a0001c0001t0001g0178 a0001c0001t0001g0179 others(126): Show |
132 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(129): Show |
intron_variant | MODIFIER | c.822+34320dupT | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51059797 | |||||||
| chr14:51059797 | C | CAA | 7 | a0001c0001t0002g0147 a0001c0001t0002g0152 a0001c0001t0002g0199 others(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 | a0001c0001t0002g0236 a0001c0001t0003g0252 a0001c0001t0004g0233 others(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 | a0001c0001t0001g0122 a0001c0001t0002g0108 a0001c0001t0002g0115 others(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 | a0002c0002t0013g0037 | 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 | a0001c0001t0002g0314 a0001c0001t0003g0315 |
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 | a0001c0005t0002g0253 | 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 | 116 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0206 others(113): Show |
118 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(115): 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 | a0001c0001t0001g0322 a0001c0001t0002g0281 a0001c0001t0002g0282 others(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 | 145 | a0001c0001t0001g0132 a0001c0001t0001g0178 a0001c0001t0001g0179 others(142): Show |
148 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(145): 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 | a0001c0001t0002g0060 a0001c0001t0002g0061 a0001c0001t0002g0062 |
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 | a0002c0010t0005g0018 | 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 | 114 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0206 others(111): Show |
116 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(113): 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 | a0001c0001t0015g0238 a0002c0002t0003g0237 |
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 | 114 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0206 others(111): Show |
116 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.822+33565T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51060553 | |||||||
| chr14:51060626 | C | T | 114 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0206 others(111): Show |
116 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(113): 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 | a0001c0001t0002g0153 a0001c0001t0002g0154 a0001c0001t0002g0155 others(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 | a0001c0001t0001g0205 a0001c0001t0001g0285 a0001c0003t0001g0016 others(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 | a0001c0001t0002g0236 a0001c0001t0003g0252 a0001c0001t0004g0233 others(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 | a0001c0001t0002g0236 a0001c0001t0003g0252 a0001c0001t0004g0233 others(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 | a0001c0001t0002g0314 a0001c0001t0003g0315 |
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 | a0001c0001t0002g0236 a0001c0001t0003g0252 a0001c0001t0004g0233 others(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 | a0001c0001t0002g0176 a0001c0001t0002g0186 |
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 | a0001c0001t0004g0148 a0001c0001t0005g0028 a0001c0001t0005g0029 others(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 | a0001c0001t0001g0122 a0001c0001t0001g0132 a0001c0001t0001g0205 others(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 | a0001c0001t0003g0252 a0001c0001t0004g0251 a0001c0005t0002g0249 others(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 | a0001c0001t0002g0236 a0001c0001t0004g0233 a0001c0001t0010g0327 others(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 | a0001c0001t0002g0314 a0001c0001t0003g0315 |
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 | a0001c0001t0002g0281 a0001c0001t0002g0282 a0001c0001t0002g0283 others(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 | a0002c0002t0006g0020 | 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 | a0002c0002t0001g0032 | 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 | a0001c0001t0002g0236 a0001c0001t0003g0252 a0001c0001t0004g0233 others(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 | a0001c0001t0001g0132 a0001c0001t0001g0205 a0001c0001t0001g0285 others(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 | a0002c0002t0001g0286 | 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 | a0001c0001t0001g0033 | 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 | a0001c0001t0002g0236 a0001c0001t0003g0252 a0001c0001t0004g0233 others(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 | a0001c0001t0001g0322 a0001c0001t0002g0281 a0001c0001t0002g0282 others(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 | a0001c0001t0004g0148 a0001c0001t0005g0028 a0001c0001t0005g0029 others(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 | a0001c0001t0002g0058 | 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 | a0001c0001t0001g0132 a0001c0001t0001g0205 a0001c0001t0001g0285 others(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 | a0001c0001t0001g0122 a0001c0001t0001g0132 a0001c0001t0001g0205 others(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 | a0002c0002t0003g0117 a0002c0002t0003g0118 |
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 | a0001c0001t0003g0065 | 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 | a0001c0001t0002g0236 a0001c0001t0003g0252 a0001c0001t0004g0233 others(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 | a0002c0002t0006g0221 | 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 | a0001c0001t0001g0132 a0001c0001t0001g0205 a0001c0001t0001g0285 others(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 | a0001c0001t0004g0148 a0001c0001t0005g0028 a0001c0001t0005g0029 others(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 | a0001c0001t0001g0216 a0002c0002t0001g0175 a0002c0002t0004g0212 |
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 | a0001c0001t0004g0148 a0001c0001t0005g0028 a0001c0001t0005g0029 others(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 | a0001c0001t0004g0148 a0001c0001t0005g0028 a0001c0001t0005g0029 others(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 | a0001c0001t0004g0148 a0001c0001t0005g0028 a0001c0001t0005g0029 others(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 | a0001c0001t0001g0122 a0001c0001t0001g0132 a0001c0001t0001g0205 others(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 | a0001c0001t0004g0148 a0001c0001t0005g0028 a0001c0001t0005g0029 others(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 | a0001c0001t0002g0320 | 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 | a0001c0001t0001g0132 a0001c0001t0001g0205 a0001c0001t0001g0285 others(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 | a0001c0001t0004g0148 a0001c0001t0005g0028 a0001c0001t0005g0029 others(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 | a0001c0001t0004g0148 a0001c0001t0005g0028 a0001c0001t0005g0029 others(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 | a0001c0001t0002g0236 a0001c0001t0003g0252 a0001c0001t0004g0233 others(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 | a0002c0002t0003g0279 | 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 | a0001c0001t0001g0122 a0001c0001t0001g0132 a0001c0001t0001g0205 others(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 | a0001c0001t0004g0148 a0001c0001t0005g0028 a0001c0001t0005g0029 others(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 | a0001c0001t0003g0129 a0001c0001t0003g0130 |
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 | a0001c0001t0001g0122 a0001c0001t0001g0132 a0001c0001t0001g0205 others(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 | a0001c0001t0002g0314 | 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 | a0001c0001t0004g0148 a0001c0001t0005g0028 a0001c0001t0005g0029 others(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 | a0001c0001t0004g0148 a0001c0001t0005g0028 a0001c0001t0005g0029 others(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 | a0002c0002t0001g0026 | 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 | a0001c0001t0001g0122 a0001c0001t0001g0132 a0001c0001t0001g0205 others(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 | a0001c0001t0004g0066 | 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 | a0001c0001t0001g0122 a0001c0001t0001g0308 a0001c0001t0002g0108 others(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 | a0001c0001t0001g0132 a0001c0001t0001g0205 a0001c0001t0001g0285 others(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 | a0001c0001t0004g0148 a0001c0001t0005g0028 a0001c0001t0005g0029 others(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 | a0001c0001t0001g0122 a0001c0001t0002g0108 a0001c0001t0002g0115 others(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 | a0001c0001t0004g0148 a0001c0001t0005g0028 a0001c0001t0005g0029 others(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 | a0001c0001t0004g0148 a0001c0001t0005g0028 a0001c0001t0005g0029 others(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 | a0001c0001t0004g0148 a0001c0001t0005g0028 a0001c0001t0005g0029 others(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 | a0002c0002t0004g0048 | 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 | a0001c0001t0004g0148 a0001c0001t0005g0028 a0001c0001t0005g0029 others(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 | a0001c0001t0001g0122 a0001c0001t0001g0132 a0001c0001t0001g0205 others(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 | a0001c0001t0005g0034 a0001c0001t0005g0035 a0002c0002t0008g0323 others(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 | a0001c0001t0002g0236 a0001c0001t0003g0252 a0001c0001t0004g0233 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0064 a0001c0001t0002g0089 others(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 | 117 | a0001c0001t0001g0122 a0001c0001t0001g0178 a0001c0001t0001g0179 others(114): Show |
119 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(116): 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 | a0001c0001t0001g0122 a0001c0001t0001g0132 a0001c0001t0001g0205 others(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 | a0001c0001t0005g0028 a0002c0002t0001g0027 a0002c0002t0001g0094 others(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 | a0001c0001t0005g0029 | 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 | a0001c0001t0001g0122 a0001c0001t0001g0132 a0001c0001t0001g0205 others(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 | a0001c0001t0003g0129 a0001c0001t0003g0130 |
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 | a0001c0001t0004g0321 | 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 | 253 | a0001c0001t0001g0033 a0001c0001t0001g0122 a0001c0001t0001g0132 others(250): Show |
261 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(258): 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 | a0001c0001t0004g0148 a0001c0001t0005g0028 a0001c0001t0005g0029 others(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 | a0001c0001t0004g0148 a0001c0001t0005g0028 a0001c0001t0005g0029 others(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 | a0001c0001t0001g0064 a0001c0001t0002g0056 a0001c0001t0002g0072 others(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 | a0002c0002t0001g0027 | 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 | a0001c0001t0004g0148 a0001c0001t0005g0028 a0001c0001t0005g0029 others(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 | a0001c0001t0001g0322 a0001c0001t0002g0281 a0001c0001t0002g0282 others(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 | a0001c0001t0001g0132 a0001c0001t0002g0141 a0001c0001t0002g0147 others(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 | a0001c0001t0001g0122 a0001c0001t0002g0108 a0001c0001t0002g0115 others(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 | a0001c0001t0004g0066 a0001c0001t0004g0148 a0001c0001t0005g0028 others(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 | a0001c0001t0004g0148 a0001c0001t0005g0028 a0001c0001t0005g0029 others(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 | a0001c0001t0002g0270 | 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 | 111 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0206 others(108): Show |
114 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(111): 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 | a0001c0001t0002g0236 a0001c0001t0003g0252 a0001c0001t0004g0233 others(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 | a0001c0001t0002g0236 a0001c0001t0003g0252 a0001c0001t0004g0233 others(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 | a0001c0001t0003g0315 | 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 | a0001c0001t0002g0236 a0001c0001t0003g0252 a0001c0001t0004g0233 others(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 | a0001c0001t0004g0148 a0001c0001t0005g0028 a0001c0001t0005g0029 others(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 | a0001c0001t0002g0236 a0001c0001t0003g0252 a0001c0001t0004g0233 others(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 | a0001c0001t0002g0236 a0001c0001t0003g0252 a0001c0001t0004g0233 others(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 | a0002c0002t0006g0020 | 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 | a0002c0002t0006g0020 | 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 | a0001c0001t0002g0236 a0001c0001t0003g0252 a0001c0001t0004g0233 others(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 | a0001c0001t0002g0236 a0001c0001t0003g0252 a0001c0001t0004g0233 others(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 | a0001c0001t0002g0236 a0001c0001t0003g0252 a0001c0001t0004g0233 others(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 | a0001c0001t0002g0055 a0001c0001t0003g0045 |
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 | a0001c0001t0010g0327 a0001c0001t0019g0329 a0002c0002t0010g0328 |
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 | a0002c0002t0001g0227 | 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 | a0001c0001t0002g0320 a0001c0001t0004g0239 a0001c0001t0004g0321 others(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 | 238 | a0001c0001t0001g0103 a0001c0001t0001g0122 a0001c0001t0001g0132 others(235): Show |
246 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(243): 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 | a0001c0001t0002g0314 a0001c0001t0003g0315 |
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 | a0001c0001t0005g0034 a0001c0001t0005g0035 a0002c0002t0008g0323 others(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 | a0001c0001t0002g0270 | 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 | a0001c0001t0005g0034 a0001c0001t0005g0035 a0002c0002t0008g0323 others(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 | 121 | a0001c0001t0001g0103 a0001c0001t0001g0122 a0001c0001t0001g0132 others(118): 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 | a0001c0001t0002g0236 a0001c0001t0003g0252 a0001c0001t0004g0233 others(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 | a0002c0002t0006g0020 | 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 | a0002c0004t0005g0296 | 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 | a0001c0001t0001g0205 a0001c0001t0002g0141 a0001c0001t0002g0147 others(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 | a0002c0002t0006g0020 | 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 | a0001c0001t0001g0132 a0001c0001t0001g0308 a0001c0001t0001g0322 others(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 | 21 | a0001c0001t0001g0103 a0001c0001t0001g0122 a0001c0001t0001g0285 others(18): 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 | a0001c0001t0001g0285 a0001c0001t0001g0322 a0001c0001t0002g0281 others(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 | a0001c0001t0003g0051 | 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 | a0001c0001t0005g0028 | 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 | a0001c0001t0005g0028 | 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 | a0001c0001t0001g0132 a0001c0001t0001g0285 a0001c0001t0001g0308 others(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 | a0001c0001t0001g0132 a0001c0001t0001g0275 a0001c0001t0001g0285 others(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 | a0002c0002t0001g0324 | 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 | a0001c0001t0001g0308 a0001c0001t0002g0039 a0001c0001t0009g0040 others(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 | a0001c0001t0001g0285 a0001c0001t0001g0322 a0001c0001t0002g0281 others(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 | a0001c0001t0001g0132 a0001c0001t0001g0285 a0001c0001t0001g0308 others(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 | a0002c0002t0001g0009 a0002c0002t0001g0225 |
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 | a0001c0001t0002g0281 a0001c0001t0002g0282 a0001c0001t0002g0283 others(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 | a0001c0001t0003g0007 | 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 | a0001c0001t0001g0030 a0001c0001t0002g0266 a0001c0003t0001g0012 others(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 | a0001c0001t0001g0308 a0001c0001t0002g0075 a0001c0001t0002g0236 others(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 | a0001c0001t0001g0132 a0001c0001t0001g0205 a0001c0001t0001g0285 others(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 | a0001c0001t0003g0219 | 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 | a0001c0001t0001g0285 a0001c0001t0001g0322 a0001c0001t0002g0281 others(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 | a0002c0002t0001g0032 | 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 | a0001c0001t0002g0025 a0001c0001t0002g0259 a0001c0001t0002g0268 others(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 | a0001c0001t0001g0205 a0001c0001t0002g0236 a0001c0001t0003g0252 others(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 | a0001c0001t0001g0205 a0001c0001t0002g0236 a0001c0001t0003g0252 others(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 | a0001c0001t0001g0285 a0001c0001t0001g0308 a0001c0001t0001g0322 others(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 | a0002c0002t0006g0020 | 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 | 73 | a0001c0001t0001g0103 a0001c0001t0001g0122 a0001c0001t0001g0132 others(70): 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 | a0002c0002t0006g0020 | 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 | 76 | a0001c0001t0001g0103 a0001c0001t0001g0122 a0001c0001t0001g0132 others(73): 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 | a0001c0001t0001g0205 a0001c0001t0002g0236 a0001c0001t0003g0252 others(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 | a0001c0001t0001g0132 a0001c0001t0002g0141 a0001c0001t0002g0147 others(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 | a0001c0001t0002g0108 a0001c0001t0002g0115 a0001c0001t0002g0116 others(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 | 239 | a0001c0001t0001g0103 a0001c0001t0001g0122 a0001c0001t0001g0132 others(236): Show |
247 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(244): 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 | a0001c0001t0001g0205 a0001c0001t0002g0236 a0001c0001t0003g0252 others(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 | a0002c0002t0001g0226 a0002c0002t0001g0243 a0002c0002t0001g0244 others(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 | a0004c0008t0001g0006 | 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 | a0001c0001t0001g0132 a0001c0001t0001g0308 a0001c0001t0002g0039 others(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 | a0001c0001t0003g0252 a0001c0001t0004g0251 a0001c0005t0002g0249 others(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 | a0001c0001t0001g0285 a0001c0001t0001g0322 a0001c0001t0002g0281 others(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 | 8 | a0001c0001t0001g0103 a0001c0001t0004g0005 a0001c0001t0004g0101 others(5): 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 | a0001c0001t0010g0327 a0001c0001t0019g0329 a0002c0002t0010g0328 others(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 | a0002c0002t0001g0094 a0002c0002t0001g0095 |
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 | a0001c0001t0001g0064 a0001c0001t0002g0056 a0001c0001t0002g0063 others(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 | a0001c0001t0001g0285 a0001c0001t0001g0322 a0001c0001t0002g0281 others(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 | a0001c0001t0001g0205 a0001c0001t0002g0236 a0001c0001t0003g0252 others(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 | 106 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0206 others(103): Show |
109 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.822+19282G>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51074836 | |||||||
| chr14:51074890 | A | G | 178 | a0001c0001t0001g0103 a0001c0001t0001g0122 a0001c0001t0001g0178 others(175): Show |
185 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(182): 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 | a0002c0002t0006g0020 | 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 | a0001c0001t0009g0299 a0002c0002t0005g0300 |
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 | a0001c0014t0002g0326 | 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 | a0001c0003t0001g0016 a0001c0003t0007g0013 a0001c0003t0007g0014 others(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 | a0001c0001t0002g0039 a0001c0001t0009g0040 a0001c0001t0017g0038 others(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 | a0001c0001t0002g0320 a0001c0001t0004g0321 |
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 | a0001c0001t0015g0238 | 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 | 71 | a0001c0001t0001g0103 a0001c0001t0001g0122 a0001c0001t0001g0205 others(68): 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 | a0002c0002t0006g0020 | 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 | a0001c0001t0001g0275 a0001c0001t0003g0256 a0001c0001t0003g0258 others(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 | a0002c0002t0001g0286 a0002c0004t0005g0296 |
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 | a0001c0001t0002g0039 a0001c0001t0005g0034 a0001c0001t0005g0035 others(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 | a0001c0001t0001g0132 a0001c0001t0002g0141 a0001c0001t0002g0147 others(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 | 241 | a0001c0001t0001g0103 a0001c0001t0001g0122 a0001c0001t0001g0132 others(238): Show |
248 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(245): 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 | a0001c0001t0003g0168 a0001c0001t0003g0169 |
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 | a0001c0001t0001g0308 a0001c0001t0002g0236 a0001c0001t0003g0252 others(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 | a0001c0003t0001g0012 a0002c0007t0001g0019 a0002c0007t0011g0015 |
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 | a0001c0003t0001g0012 a0002c0007t0001g0019 a0002c0007t0011g0015 |
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 | a0002c0002t0003g0100 | 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 | a0002c0002t0006g0083 | 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 | a0002c0004t0005g0309 | 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 | a0001c0001t0002g0047 a0001c0001t0002g0054 a0001c0001t0002g0055 others(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 | a0001c0003t0001g0012 a0001c0003t0001g0016 a0001c0003t0007g0013 others(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 | 53 | a0001c0001t0001g0030 a0001c0001t0001g0122 a0001c0001t0001g0132 others(50): 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 | 67 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0216 others(64): 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 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0211 others(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 | 6 | a0001c0001t0003g0208 a0001c0001t0003g0256 a0001c0001t0003g0316 others(3): Show |
6 | HG00621.hp2 HG00741.hp2 HG03195.hp1 others(3): 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 | a0001c0001t0002g0072 a0001c0001t0002g0108 a0001c0001t0002g0115 others(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 | a0001c0001t0004g0148 a0001c0001t0005g0028 a0001c0003t0001g0012 others(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 | a0001c0001t0002g0236 a0001c0001t0003g0252 a0001c0001t0004g0233 others(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 | a0001c0001t0009g0098 a0002c0002t0003g0031 |
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 | 133 | a0001c0001t0001g0103 a0001c0001t0001g0122 a0001c0001t0001g0132 others(130): 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 | a0001c0001t0001g0308 a0002c0002t0001g0311 a0002c0004t0005g0309 others(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 | a0004c0008t0001g0006 | 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 | a0001c0001t0001g0308 a0001c0001t0002g0236 a0001c0001t0003g0252 others(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 | 33 | a0001c0001t0001g0103 a0001c0001t0001g0122 a0001c0001t0001g0132 others(30): 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 | a0001c0001t0004g0126 a0002c0002t0001g0021 a0002c0002t0001g0125 |
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 | a0001c0001t0004g0148 a0001c0001t0005g0028 a0001c0001t0005g0029 others(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 | a0001c0001t0004g0148 a0001c0001t0005g0028 a0001c0001t0005g0029 others(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 | a0001c0001t0001g0132 a0001c0001t0002g0141 a0001c0001t0002g0147 others(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 | a0002c0002t0001g0311 | 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 | a0002c0002t0006g0020 | 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 | a0002c0002t0001g0027 | 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 | a0001c0001t0004g0148 a0001c0001t0005g0028 a0001c0001t0005g0029 others(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 | a0001c0001t0004g0148 a0001c0001t0005g0028 a0001c0001t0005g0029 others(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 | a0001c0001t0003g0084 a0001c0001t0003g0086 |
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 | a0002c0002t0006g0020 | 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 | a0002c0007t0001g0019 | 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 | a0001c0001t0002g0265 a0001c0001t0002g0266 a0001c0001t0003g0316 others(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 | 243 | a0001c0001t0001g0033 a0001c0001t0001g0103 a0001c0001t0001g0122 others(240): Show |
250 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.822+14607delA | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51079510 | |||||||
| chr14:51079751 | T | G | 20 | a0001c0001t0001g0132 a0001c0001t0002g0141 a0001c0001t0002g0147 others(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 | a0001c0001t0002g0320 | 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 | a0002c0002t0001g0026 | 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 | a0001c0001t0001g0285 a0001c0001t0001g0322 a0001c0001t0002g0281 others(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 | a0001c0001t0004g0148 a0001c0001t0005g0028 a0001c0001t0005g0029 others(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 | a0001c0001t0001g0285 a0001c0001t0001g0322 a0001c0001t0002g0281 others(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 | a0001c0001t0009g0098 a0002c0002t0003g0031 |
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 | a0001c0001t0004g0148 a0001c0001t0005g0028 a0001c0001t0005g0029 others(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 | a0001c0001t0003g0050 a0001c0001t0003g0051 a0002c0002t0001g0041 others(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 | a0001c0001t0001g0044 a0001c0001t0002g0075 a0001c0001t0002g0108 others(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 | a0001c0001t0001g0132 a0001c0001t0001g0285 a0001c0001t0002g0077 others(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 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0205 others(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 | 45 | a0001c0001t0001g0033 a0001c0001t0001g0211 a0001c0001t0001g0216 others(42): Show |
45 | HG00738.hp2 HG00741.hp2 HG01099.hp1 others(42): 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 | 30 | a0001c0001t0002g0008 a0001c0001t0002g0165 a0001c0001t0002g0236 others(27): 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 | a0001c0001t0001g0308 a0001c0001t0003g0252 a0001c0001t0004g0251 others(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 | a0002c0002t0001g0311 a0002c0004t0005g0309 a0002c0004t0005g0310 |
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 | 12 | a0001c0001t0001g0103 a0001c0001t0001g0122 a0001c0001t0004g0005 others(9): 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 | 17 | a0001c0001t0001g0103 a0001c0001t0001g0122 a0001c0001t0001g0308 others(14): 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 | a0001c0001t0004g0312 | 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 | 17 | a0001c0001t0001g0103 a0001c0001t0001g0122 a0001c0001t0001g0308 others(14): 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 | a0001c0001t0001g0132 a0001c0001t0002g0141 a0001c0001t0002g0147 others(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 | 12 | a0001c0001t0001g0103 a0001c0001t0001g0122 a0001c0001t0004g0005 others(9): 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 | a0001c0001t0002g0218 | 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 | a0001c0001t0002g0088 a0001c0001t0002g0089 a0001c0001t0002g0090 |
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 | 123 | a0001c0001t0001g0103 a0001c0001t0001g0122 a0001c0001t0001g0132 others(120): 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 | a0001c0001t0004g0148 a0001c0001t0005g0028 a0001c0001t0005g0029 others(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 | 108 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0205 others(105): Show |
110 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(107): 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 | a0002c0002t0001g0032 | 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 | 243 | a0001c0001t0001g0033 a0001c0001t0001g0103 a0001c0001t0001g0122 others(240): Show |
250 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(247): 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 | a0001c0001t0002g0236 a0001c0001t0003g0252 a0001c0001t0004g0233 others(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 | a0001c0001t0005g0028 a0001c0001t0005g0029 a0002c0002t0001g0027 others(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 | a0002c0002t0006g0020 | 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 | a0001c0003t0001g0012 a0001c0003t0001g0016 a0001c0003t0007g0013 others(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 | a0001c0001t0001g0285 a0001c0001t0001g0322 a0001c0001t0002g0281 others(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 | a0002c0002t0001g0301 | 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 | a0002c0002t0003g0279 | 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 | a0001c0001t0009g0098 a0001c0003t0001g0012 a0001c0003t0001g0016 others(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 | a0001c0001t0002g0108 a0001c0001t0002g0115 a0001c0001t0002g0116 others(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 | a0001c0001t0004g0148 a0001c0001t0005g0028 a0002c0002t0001g0026 others(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 | a0001c0001t0001g0285 a0001c0001t0001g0322 a0001c0001t0002g0281 others(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 | 17 | a0001c0001t0001g0103 a0001c0001t0001g0122 a0001c0001t0001g0308 others(14): 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 | 75 | a0001c0001t0001g0103 a0001c0001t0001g0122 a0001c0001t0001g0132 others(72): 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 | a0001c0001t0003g0219 | 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 | 75 | a0001c0001t0001g0103 a0001c0001t0001g0122 a0001c0001t0001g0132 others(72): 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 | a0001c0001t0002g0281 a0001c0001t0002g0282 a0001c0001t0002g0283 |
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 | a0001c0001t0004g0148 a0001c0001t0005g0028 a0001c0001t0005g0029 others(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 | 75 | a0001c0001t0001g0103 a0001c0001t0001g0122 a0001c0001t0001g0132 others(72): 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 | 33 | a0001c0001t0001g0103 a0001c0001t0001g0122 a0001c0001t0001g0132 others(30): 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 | a0001c0001t0001g0308 a0001c0001t0002g0236 a0001c0001t0003g0252 others(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 | 33 | a0001c0001t0001g0103 a0001c0001t0001g0122 a0001c0001t0001g0132 others(30): 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 | 77 | a0001c0001t0001g0103 a0001c0001t0001g0122 a0001c0001t0001g0132 others(74): 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 | 75 | a0001c0001t0001g0103 a0001c0001t0001g0122 a0001c0001t0001g0132 others(72): 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 | 75 | a0001c0001t0001g0103 a0001c0001t0001g0122 a0001c0001t0001g0132 others(72): 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 | 12 | a0001c0001t0001g0103 a0001c0001t0001g0122 a0001c0001t0004g0005 others(9): 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 | 33 | a0001c0001t0001g0103 a0001c0001t0001g0122 a0001c0001t0001g0132 others(30): 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 | a0001c0001t0001g0033 a0001c0001t0002g0039 a0001c0001t0005g0034 others(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 | a0002c0002t0001g0024 | 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 | 75 | a0001c0001t0001g0103 a0001c0001t0001g0122 a0001c0001t0001g0132 others(72): 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 | 74 | a0001c0001t0001g0103 a0001c0001t0001g0122 a0001c0001t0001g0132 others(71): 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 | a0002c0002t0001g0099 | 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 | a0001c0001t0004g0148 a0001c0001t0005g0028 a0001c0001t0005g0029 others(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 | 75 | a0001c0001t0001g0103 a0001c0001t0001g0122 a0001c0001t0001g0132 others(72): 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 | 113 | a0001c0001t0001g0103 a0001c0001t0001g0122 a0001c0001t0001g0132 others(110): 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 | 75 | a0001c0001t0001g0103 a0001c0001t0001g0122 a0001c0001t0001g0132 others(72): 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 | 124 | a0001c0001t0001g0103 a0001c0001t0001g0122 a0001c0001t0001g0132 others(121): 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 | a0002c0002t0004g0319 | 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 | a0001c0001t0003g0220 | 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 | 33 | a0001c0001t0001g0103 a0001c0001t0001g0122 a0001c0001t0001g0132 others(30): 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 | a0001c0001t0004g0148 a0002c0004t0005g0149 |
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 | a0001c0001t0009g0098 a0002c0002t0003g0031 |
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 | 75 | a0001c0001t0001g0103 a0001c0001t0001g0122 a0001c0001t0001g0132 others(72): 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 | 75 | a0001c0001t0001g0103 a0001c0001t0001g0122 a0001c0001t0001g0132 others(72): 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 | a0002c0002t0003g0280 | 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 | a0001c0001t0004g0148 a0001c0001t0005g0028 a0001c0001t0005g0029 others(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 | 75 | a0001c0001t0001g0103 a0001c0001t0001g0122 a0001c0001t0001g0132 others(72): 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 | 125 | a0001c0001t0001g0103 a0001c0001t0001g0122 a0001c0001t0001g0132 others(122): 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 | a0001c0001t0001g0132 a0001c0001t0002g0141 a0001c0001t0002g0147 others(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 | a0001c0001t0001g0308 a0002c0002t0001g0311 a0002c0004t0005g0309 others(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 | a0001c0001t0005g0303 a0002c0002t0001g0301 a0002c0002t0001g0305 others(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 | a0002c0002t0002g0222 a0002c0002t0006g0221 a0002c0002t0006g0223 |
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 | a0002c0002t0006g0020 | 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 | a0001c0001t0001g0033 a0001c0001t0002g0039 a0001c0001t0005g0034 others(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 | 75 | a0001c0001t0001g0103 a0001c0001t0001g0122 a0001c0001t0001g0132 others(72): 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 | 113 | a0001c0001t0001g0103 a0001c0001t0001g0122 a0001c0001t0001g0132 others(110): 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 | 75 | a0001c0001t0001g0103 a0001c0001t0001g0122 a0001c0001t0001g0132 others(72): 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 | 75 | a0001c0001t0001g0103 a0001c0001t0001g0122 a0001c0001t0001g0132 others(72): 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 | a0001c0003t0001g0012 a0001c0003t0001g0016 a0001c0003t0007g0013 others(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 | 125 | a0001c0001t0001g0103 a0001c0001t0001g0122 a0001c0001t0001g0132 others(122): 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 | 75 | a0001c0001t0001g0103 a0001c0001t0001g0122 a0001c0001t0001g0132 others(72): 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 | 75 | a0001c0001t0001g0103 a0001c0001t0001g0122 a0001c0001t0001g0132 others(72): 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 | a0002c0002t0006g0020 | 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 | 75 | a0001c0001t0001g0103 a0001c0001t0001g0122 a0001c0001t0001g0132 others(72): 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 | a0004c0008t0001g0006 | 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 | a0001c0005t0002g0224 | 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 | 35 | a0001c0001t0001g0103 a0001c0001t0001g0122 a0001c0001t0002g0108 others(32): 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 | 12 | a0001c0001t0001g0103 a0001c0001t0001g0122 a0001c0001t0004g0005 others(9): 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 | a0001c0001t0001g0132 a0001c0001t0002g0141 a0001c0001t0002g0147 others(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 | 76 | a0001c0001t0001g0103 a0001c0001t0001g0122 a0001c0001t0001g0308 others(73): 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 | 77 | a0001c0001t0001g0103 a0001c0001t0001g0122 a0001c0001t0001g0308 others(74): 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 | a0002c0002t0001g0022 a0002c0002t0001g0023 a0002c0002t0001g0024 |
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 | a0001c0001t0003g0096 a0002c0002t0001g0091 a0002c0002t0001g0092 others(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 | a0001c0001t0004g0148 a0001c0001t0005g0028 a0001c0001t0005g0029 others(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 | a0001c0001t0002g0165 a0002c0002t0001g0164 a0002c0002t0001g0166 |
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 | a0001c0001t0003g0096 | 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 | a0002c0002t0006g0020 | 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 | a0001c0001t0002g0039 a0001c0001t0009g0040 a0001c0001t0017g0038 others(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 | 75 | a0001c0001t0001g0275 a0001c0001t0001g0285 a0001c0001t0001g0322 others(72): Show |
76 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(73): 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 | a0002c0002t0006g0020 | 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 | a0002c0002t0006g0020 | 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 | 77 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0205 others(74): 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 | a0002c0002t0006g0020 | 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 | a0002c0002t0006g0020 | 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 | a0001c0001t0009g0098 a0002c0002t0003g0031 |
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 | 143 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0205 others(140): Show |
145 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(142): 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 | a0001c0001t0002g0236 a0001c0001t0003g0252 a0001c0001t0004g0233 others(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 | a0002c0002t0006g0020 | 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 | a0001c0003t0001g0012 a0001c0003t0001g0016 a0001c0003t0007g0013 others(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 | a0001c0001t0002g0108 a0001c0001t0002g0115 a0001c0001t0002g0116 others(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 | 64 | a0001c0001t0001g0275 a0001c0001t0001g0285 a0001c0001t0001g0308 others(61): Show |
65 | HG00438.hp2 HG00544.hp2 HG00597.hp2 others(62): 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 | a0001c0001t0003g0045 | 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 | a0001c0001t0003g0045 | 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 | a0001c0001t0003g0045 | 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 | a0001c0003t0001g0012 a0001c0003t0001g0016 a0001c0003t0007g0013 others(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 | a0002c0002t0006g0020 | 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 | a0002c0002t0006g0020 | 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 | a0002c0002t0001g0097 | 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 | a0002c0002t0006g0020 | 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 | a0001c0001t0001g0044 a0002c0002t0001g0041 a0002c0002t0001g0043 others(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 | a0001c0001t0002g0314 a0001c0001t0003g0315 |
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 | a0001c0001t0002g0147 a0002c0002t0001g0145 a0002c0002t0001g0146 |
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 | a0002c0002t0006g0020 | 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 | a0001c0001t0004g0148 a0001c0001t0005g0028 a0001c0001t0005g0029 others(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 | a0001c0003t0001g0012 a0001c0003t0001g0016 a0001c0003t0007g0013 others(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 | a0002c0002t0006g0020 | 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 | 30 | a0001c0001t0001g0103 a0001c0001t0001g0122 a0001c0001t0002g0108 others(27): 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 | 77 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0205 others(74): 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 | 266 | a0001c0001t0001g0033 a0001c0001t0001g0103 a0001c0001t0001g0122 others(263): Show |
274 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(271): Show |
intron_variant | MODIFIER | c.822+2296C>A | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51091822 | |||||||
| chr14:51091862 | G | A | 65 | a0001c0001t0001g0275 a0001c0001t0001g0285 a0001c0001t0001g0308 others(62): Show |
66 | HG00438.hp2 HG00544.hp2 HG00597.hp2 others(63): 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 | a0001c0001t0005g0028 a0001c0001t0005g0029 a0002c0002t0001g0027 |
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 | a0001c0001t0002g0314 a0001c0001t0003g0315 |
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 | a0001c0001t0002g0150 a0001c0001t0002g0152 a0001c0001t0002g0153 others(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 | a0001c0001t0001g0030 | 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 | a0001c0001t0009g0098 | 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 | a0002c0002t0006g0020 | 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 | a0002c0002t0006g0020 | 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 | a0001c0001t0005g0029 | 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 | a0001c0001t0003g0316 a0002c0002t0001g0317 |
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 | a0001c0001t0004g0148 a0001c0001t0005g0028 a0001c0001t0005g0029 others(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 | 66 | a0001c0001t0001g0103 a0001c0001t0001g0122 a0001c0001t0001g0132 others(63): 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 | a0001c0001t0004g0148 a0002c0004t0005g0149 |
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 | 181 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0205 others(178): Show |
186 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(183): 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 | a0001c0001t0002g0025 | 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 | a0002c0002t0004g0319 | 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 | a0001c0001t0002g0320 a0001c0001t0004g0321 |
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 | a0002c0002t0006g0020 | 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 | a0002c0002t0001g0022 a0002c0002t0001g0023 a0002c0002t0001g0024 |
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 | a0001c0001t0001g0322 | 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 | a0002c0002t0008g0323 | 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 | a0001c0003t0001g0012 a0001c0003t0001g0016 a0001c0003t0007g0013 others(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 | a0002c0002t0001g0021 | 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 | a0002c0002t0006g0020 | 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 | a0002c0002t0001g0324 | 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 | a0001c0014t0002g0326 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.822+44T>C | TRIM9 | ENSG00000100505.14 | transcript | ENST00000684578.1 | protein_coding | 1/12 | chr14 | 51094074 |