Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 4591 |
| ensemblid | ENSG00000108395.14 |
| hgncid | 7523 |
| symbol | TRIM37 |
| name | tripartite motif containing 37 |
| refseq_nuc | NM_015294.6 |
| refseq_prot | NP_056109.1 |
| ensembl_nuc | ENST00000262294.12 |
| ensembl_prot | ENSP00000262294.7 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 58998202 |
| end | 59106880 |
| strand | - |
| ver | v1.2 |
| region | chr17:58998202-59106880 |
| region5000 | chr17:58993202-59111880 |
| regionname0 | TRIM37_chr17_58998202_59106880 |
| regionname5000 | TRIM37_chr17_58993202_59111880 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 964 | 333 | 85 | 64 | 139 | 12 | 31 | 110 | TRIM37_chr17_58993202_59111880 | TRIM37 | MDEQS others(959): Show |
chr17 | 58993202 | 59111880 |
| a0002 | 0/0 | 964 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | MDEQS others(959): Show |
chr17 | 58993202 | 59111880 |
| a0003 | 0/0 | 964 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | MDEQS others(959): Show |
chr17 | 58993202 | 59111880 |
| a0004 | 0/0 | 964 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | MDEQS others(959): Show |
chr17 | 58993202 | 59111880 |
| a0005 | 0/0 | 964 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | MDEQS others(959): Show |
chr17 | 58993202 | 59111880 |
| a0006 | 0/0 | 964 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | MDEQS others(959): Show |
chr17 | 58993202 | 59111880 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2892 | 327 | 84 | 63 | 138 | 10 | 30 | TRIM37_chr17_58993202_59111880 | TRIM37 | ATGGA others(2887): Show |
chr17 | 58993202 | 59111880 | ||
| a0001c0003 | 0/0 | 2892 | 4 | 0 | 1 | 0 | 2 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | ATGGA others(2887): Show |
chr17 | 58993202 | 59111880 | ||
| a0001c0006 | 0/0 | 2892 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | ATGGA others(2887): Show |
chr17 | 58993202 | 59111880 | ||
| a0001c0008 | 0/0 | 2892 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | ATGGA others(2887): Show |
chr17 | 58993202 | 59111880 | ||
| a0002c0002 | 0/0 | 2892 | 5 | 4 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | ATGGA others(2887): Show |
chr17 | 58993202 | 59111880 | ||
| a0003c0007 | 0/0 | 2892 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | ATGGA others(2887): Show |
chr17 | 58993202 | 59111880 | ||
| a0004c0009 | 0/0 | 2892 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | ATGGA others(2887): Show |
chr17 | 58993202 | 59111880 | ||
| a0005c0005 | 0/0 | 2892 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | ATGGA others(2887): Show |
chr17 | 58993202 | 59111880 | ||
| a0006c0004 | 0/0 | 2892 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | ATGGA others(2887): Show |
chr17 | 58993202 | 59111880 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 4489 | 117 | 16 | 30 | 58 | 2 | 9 | TRIM37_chr17_58993202_59111880 | TRIM37 | GCAGC others(4484): Show |
chr17 | 58993202 | 59111880 |
| a0001c0001t0002 | 0/0 | 4489 | 93 | 19 | 17 | 40 | 5 | 12 | TRIM37_chr17_58993202_59111880 | TRIM37 | GCAGC others(4484): Show |
chr17 | 58993202 | 59111880 |
| a0001c0001t0003 | 0/0 | 4489 | 89 | 37 | 14 | 30 | 2 | 6 | TRIM37_chr17_58993202_59111880 | TRIM37 | GCAGC others(4484): Show |
chr17 | 58993202 | 59111880 |
| a0001c0001t0004 | 0/0 | 4488 | 4 | 4 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | GCAGC others(4483): Show |
chr17 | 58993202 | 59111880 |
| a0001c0001t0005 | 0/0 | 4489 | 4 | 0 | 0 | 4 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | GCAGC others(4484): Show |
chr17 | 58993202 | 59111880 |
| a0001c0001t0007 | 0/0 | 4489 | 4 | 3 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | GCAGC others(4484): Show |
chr17 | 58993202 | 59111880 |
| a0001c0001t0008 | 0/0 | 4489 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | GCAGC others(4484): Show |
chr17 | 58993202 | 59111880 |
| a0001c0001t0009 | 0/0 | 4489 | 3 | 2 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | GCAGC others(4484): Show |
chr17 | 58993202 | 59111880 |
| a0001c0001t0010 | 0/0 | 4489 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | GCAGC others(4484): Show |
chr17 | 58993202 | 59111880 |
| a0001c0001t0011 | 0/0 | 4489 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | GCAGC others(4484): Show |
chr17 | 58993202 | 59111880 |
| a0001c0001t0012 | 0/0 | 4489 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | GCAGC others(4484): Show |
chr17 | 58993202 | 59111880 |
| a0001c0001t0013 | 0/0 | 4514 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | GCAGC others(4509): Show |
chr17 | 58993202 | 59111880 |
| a0001c0001t0014 | 0/0 | 4489 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | GCAGC others(4484): Show |
chr17 | 58993202 | 59111880 |
| a0001c0001t0015 | 0/0 | 4489 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | GCAGC others(4484): Show |
chr17 | 58993202 | 59111880 |
| a0001c0001t0016 | 0/0 | 4489 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | GCAGC others(4484): Show |
chr17 | 58993202 | 59111880 |
| a0001c0001t0017 | 0/0 | 4489 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | GCAGC others(4484): Show |
chr17 | 58993202 | 59111880 |
| a0001c0001t0018 | 0/0 | 4489 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | GCAGC others(4484): Show |
chr17 | 58993202 | 59111880 |
| a0001c0003t0006 | 0/0 | 4489 | 4 | 0 | 1 | 0 | 2 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | GCAGC others(4484): Show |
chr17 | 58993202 | 59111880 |
| a0001c0006t0003 | 0/0 | 4489 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | GCAGC others(4484): Show |
chr17 | 58993202 | 59111880 |
| a0001c0008t0003 | 0/0 | 4489 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | GCAGC others(4484): Show |
chr17 | 58993202 | 59111880 |
| a0002c0002t0002 | 0/0 | 4489 | 5 | 4 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | GCAGC others(4484): Show |
chr17 | 58993202 | 59111880 |
| a0003c0007t0002 | 0/0 | 4489 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | GCAGC others(4484): Show |
chr17 | 58993202 | 59111880 |
| a0004c0009t0001 | 0/0 | 4489 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | GCAGC others(4484): Show |
chr17 | 58993202 | 59111880 |
| a0005c0005t0003 | 0/0 | 4489 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | GCAGC others(4484): Show |
chr17 | 58993202 | 59111880 |
| a0006c0004t0002 | 0/0 | 4489 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | GCAGC others(4484): Show |
chr17 | 58993202 | 59111880 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0259 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0299 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0004g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0004g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0004g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0004g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0005g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0005g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0005g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0005g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0007g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0007g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0007g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0007g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0008g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0008g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0008g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0009g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0009g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0009g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0010g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0010g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0011g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0012g0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0013g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0014g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0015g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0016g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0017g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0018g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0003t0006g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0003t0006g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0003t0006g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0003t0006g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0006t0003g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0008t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0002c0002t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0002c0002t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0002c0002t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0002c0002t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0002c0002t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0003c0007t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0004c0009t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0005c0005t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0006c0004t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0211 | EUR | GBR | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0013 | EUR | GBR | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0251 | EUR | FIN | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0014 | EUR | FIN | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0164 | EUR | FIN | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0305 | EUR | FIN | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | CHS | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | CHS | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | CHS | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | CHS | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | CHS | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | CHS | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG00597 | hp1 | a0003 | c0007 | t0002 | g0179 | EAS | CHS | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | CHS | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0329 | EAS | CHS | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | CHS | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG00642 | hp1 | a0004 | c0009 | t0001 | g0295 | AMR | PUR | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG00642 | hp2 | a0001 | c0003 | t0006 | g0219 | AMR | PUR | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | CHS | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | CHS | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | PUR | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0039 | AMR | PUR | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0291 | AMR | PUR | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0166 | AMR | PUR | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0025 | AMR | PUR | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0162 | AMR | PUR | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0174 | AMR | PUR | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0285 | AMR | PUR | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0298 | AMR | PUR | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0173 | AMR | PUR | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0304 | AMR | PUR | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0160 | AMR | PUR | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0159 | AMR | PUR | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0274 | AMR | PUR | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0123 | AMR | PUR | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0132 | AMR | PUR | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | PUR | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0099 | AMR | PUR | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0100 | AMR | PUR | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0289 | AMR | PUR | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0199 | AMR | PUR | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0338 | AMR | PUR | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0046 | AMR | PUR | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0059 | AMR | PUR | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01243 | hp2 | a0001 | c0001 | t0007 | g0216 | AMR | PUR | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0185 | AMR | CLM | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0294 | AMR | CLM | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | CLM | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0121 | AMR | CLM | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0120 | AMR | CLM | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0293 | AMR | CLM | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0156 | AMR | CLM | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01261 | hp2 | a0001 | c0001 | t0003 | g0029 | AMR | CLM | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | CLM | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0037 | AMR | CLM | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0158 | AMR | CLM | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0302 | AMR | CLM | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0277 | AMR | CLM | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0171 | AMR | CLM | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0169 | AMR | CLM | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0314 | AMR | CLM | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0307 | AMR | CLM | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0130 | AMR | CLM | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0161 | EUR | IBS | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01515 | hp2 | a0001 | c0001 | t0012 | g0002 | EUR | IBS | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0112 | AFR | ACB | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0101 | AFR | ACB | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | PEL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0271 | AMR | PEL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0272 | AMR | PEL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01952 | hp2 | a0002 | c0002 | t0002 | g0207 | AMR | PEL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | PEL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | PEL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0010 | AMR | PEL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0023 | AMR | PEL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | PEL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02027 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | KHV | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | KHV | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | KHV | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0034 | EAS | KHV | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0066 | AFR | ACB | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0337 | AFR | ACB | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0147 | EAS | KHV | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | KHV | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | KHV | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | KHV | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | KHV | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | KHV | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0313 | AFR | ACB | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0114 | AFR | ACB | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0170 | AMR | PEL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0275 | AMR | PEL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | CDX | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | CDX | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0209 | AFR | ACB | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0106 | AFR | ACB | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0320 | AFR | ACB | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0210 | AFR | ACB | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0163 | AFR | ACB | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | ACB | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02293 | hp1 | a0001 | c0001 | t0009 | g0168 | AMR | PEL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0287 | AMR | PEL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0309 | AMR | PEL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0290 | AMR | PEL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0079 | AFR | ACB | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0109 | AFR | ACB | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | KHV | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | KHV | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02572 | hp1 | a0001 | c0001 | t0009 | g0165 | AFR | GWD | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0064 | AFR | GWD | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0321 | SAS | PJL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0154 | SAS | PJL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0086 | AFR | GWD | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02615 | hp2 | a0002 | c0002 | t0002 | g0208 | AFR | GWD | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0069 | AFR | GWD | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0117 | AFR | GWD | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | GWD | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0075 | AFR | GWD | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0095 | AFR | GWD | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | GWD | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02723 | hp1 | a0001 | c0001 | t0018 | g0342 | AFR | GWD | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02723 | hp2 | a0001 | c0001 | t0009 | g0183 | AFR | GWD | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02735 | hp1 | a0001 | c0001 | t0017 | g0341 | SAS | PJL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0181 | SAS | PJL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0089 | AFR | GWD | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0062 | AFR | GWD | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | GWD | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0061 | AFR | GWD | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0084 | AFR | GWD | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0115 | AFR | GWD | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0306 | AFR | GWD | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0087 | AFR | GWD | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0118 | AFR | GWD | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | GWD | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0088 | AFR | GWD | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | GWD | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02922 | hp1 | a0002 | c0002 | t0002 | g0206 | AFR | ESN | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0067 | AFR | ESN | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0155 | AFR | ESN | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02965 | hp2 | a0001 | c0006 | t0003 | g0105 | AFR | ESN | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0113 | AFR | ESN | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0110 | AFR | ESN | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03017 | hp1 | a0001 | c0001 | t0013 | g0024 | SAS | PJL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0267 | SAS | PJL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | GWD | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0153 | AFR | GWD | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | MSL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0081 | AFR | MSL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0092 | AFR | ESN | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0083 | AFR | ESN | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0063 | AFR | ESN | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0028 | AFR | ESN | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0065 | AFR | ESN | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03195 | hp2 | a0002 | c0002 | t0002 | g0125 | AFR | ESN | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0094 | AFR | MSL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03209 | hp2 | a0005 | c0005 | t0003 | g0085 | AFR | MSL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0107 | AFR | MSL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0070 | AFR | MSL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0077 | AFR | MSL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | MSL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0204 | SAS | PJL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0252 | SAS | PJL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0253 | SAS | PJL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0303 | SAS | PJL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03516 | hp1 | a0001 | c0001 | t0010 | g0090 | AFR | ESN | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0102 | AFR | ESN | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03540 | hp1 | a0001 | c0001 | t0007 | g0215 | AFR | GWD | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0093 | AFR | GWD | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0098 | AFR | MSL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0073 | AFR | MSL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03654 | hp1 | a0001 | c0001 | t0011 | g0001 | SAS | PJL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0036 | SAS | PJL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0226 | SAS | STU | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0050 | SAS | STU | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0182 | SAS | PJL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03704 | hp2 | a0001 | c0003 | t0006 | g0212 | SAS | PJL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0004 | SAS | BEB | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0148 | SAS | BEB | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0150 | SAS | BEB | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0151 | SAS | BEB | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0330 | SAS | BEB | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03927 | hp2 | a0006 | c0004 | t0002 | g0144 | SAS | BEB | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0146 | SAS | BEB | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0152 | SAS | BEB | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0186 | SAS | STU | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0008 | SAS | STU | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0328 | SAS | STU | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0129 | SAS | STU | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0047 | SAS | STU | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | STU | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0096 | AFR | YRI | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18522 | hp2 | a0001 | c0001 | t0007 | g0214 | AFR | YRI | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0332 | EAS | CHB | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18612 | hp2 | a0001 | c0001 | t0003 | g0057 | EAS | CHB | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | CHB | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0149 | EAS | CHB | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0076 | AFR | YRI | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0103 | AFR | YRI | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0056 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0051 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0339 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18945 | hp1 | a0001 | c0001 | t0005 | g0042 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18949 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18949 | hp2 | a0001 | c0001 | t0015 | g0331 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18950 | hp1 | a0001 | c0001 | t0003 | g0058 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18952 | hp1 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18953 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18963 | hp2 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18965 | hp2 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18978 | hp2 | a0001 | c0001 | t0003 | g0060 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18991 | hp1 | a0001 | c0001 | t0003 | g0035 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18992 | hp2 | a0001 | c0001 | t0003 | g0122 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18993 | hp1 | a0001 | c0001 | t0003 | g0055 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0033 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19001 | hp2 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19006 | hp2 | a0001 | c0001 | t0005 | g0040 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19007 | hp1 | a0001 | c0001 | t0005 | g0041 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19030 | hp1 | a0002 | c0002 | t0002 | g0205 | AFR | LWK | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | LWK | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19055 | hp2 | a0001 | c0001 | t0005 | g0044 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19056 | hp2 | a0001 | c0001 | t0008 | g0027 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19057 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19062 | hp1 | a0001 | c0001 | t0003 | g0032 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19062 | hp2 | a0001 | c0001 | t0016 | g0244 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19063 | hp1 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19064 | hp1 | a0001 | c0008 | t0003 | g0038 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19066 | hp1 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19068 | hp2 | a0001 | c0001 | t0008 | g0017 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19078 | hp1 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19083 | hp2 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19084 | hp1 | a0001 | c0001 | t0008 | g0026 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0053 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0072 | AFR | YRI | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19240 | hp2 | a0001 | c0001 | t0004 | g0104 | AFR | YRI | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0119 | AFR | ASW | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0172 | AFR | ASW | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA20752 | hp1 | a0001 | c0003 | t0006 | g0218 | EUR | TSI | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0157 | EUR | TSI | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA20805 | hp1 | a0001 | c0003 | t0006 | g0217 | EUR | TSI | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0167 | EUR | TSI | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0007 | SAS | GIH | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0184 | SAS | GIH | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02109 | hp1 | a0001 | c0001 | t0010 | g0078 | AFR | ACB | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0080 | AFR | ACB | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0111 | AFR | ACB | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0074 | AFR | ACB | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0082 | AFR | ACB | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | ACB | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03471 | hp1 | a0001 | c0001 | t0007 | g0213 | AFR | MSL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0068 | AFR | MSL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0108 | AFR | USA | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG06807 | hp2 | a0001 | c0001 | t0004 | g0091 | AFR | USA | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18955 | hp1 | a0001 | c0001 | t0014 | g0262 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18955 | hp2 | a0001 | c0001 | t0003 | g0054 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0071 | AFR | USA | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | USA | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0116 | AFR | LWK | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0097 | AFR | LWK | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0259 | REF | REF | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0299 | REF | REF | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:59015674 | C | T | 1 | a0002 | 5 | HG01952.hp2 HG02615.hp2 HG02922.hp1 others(2): Show |
missense_variant | MODERATE | c.2512G>A | p.Val838Ile | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 21/24 | 2931/4489 | 2512/2895 | 838/964 | chr17 | 59015674 | |||
| chr17:59041818 | G | T | 1 | a0005 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.1748C>A | p.Pro583His | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/24 | 2167/4489 | 1748/2895 | 583/964 | chr17 | 59041818 | |||
| chr17:59041827 | G | A | 1 | a0003 | 1 | HG00597.hp1 | missense_variant | MODERATE | c.1739C>T | p.Ala580Val | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/24 | 2158/4489 | 1739/2895 | 580/964 | chr17 | 59041827 | |||
| chr17:59041842 | A | G | 1 | a0006 | 1 | HG03927.hp2 | missense_variant | MODERATE | c.1724T>C | p.Met575Thr | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/24 | 2143/4489 | 1724/2895 | 575/964 | chr17 | 59041842 | |||
| chr17:59079795 | C | A | 1 | a0004 | 1 | HG00642.hp1 | missense_variant | MODERATE | c.575G>T | p.Arg192Leu | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 7/24 | 994/4489 | 575/2895 | 192/964 | chr17 | 59079795 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:59028623 | G | A | 1 | a0001c0006 | 1 | HG02965.hp2 | synonymous_variant | LOW | c.2049C>T | p.Ala683Ala | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/24 | 2468/4489 | 2049/2895 | 683/964 | chr17 | 59028623 | |||
| chr17:59049378 | G | A | 1 | a0001c0008 | 1 | NA19064.hp1 | synonymous_variant | LOW | c.1330C>T | p.Leu444Leu | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 15/24 | 1749/4489 | 1330/2895 | 444/964 | chr17 | 59049378 | |||
| chr17:59051264 | A | G | 1 | a0001c0003 | 4 | HG00642.hp2 HG03704.hp2 NA20752.hp1 others(1): Show |
synonymous_variant | LOW | c.1264T>C | p.Leu422Leu | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 14/24 | 1683/4489 | 1264/2895 | 422/964 | chr17 | 59051264 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:58998347 | A | G | 1 | a0001c0001t0014 | 1 | NA18955.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1030T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 24/24 | 1030 | chr17 | 58998347 | ||||||
| chr17:58998399 | TG | T | 1 | a0001c0001t0004 | 4 | HG03516.hp2 HG06807.hp2 NA18906.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*977delC | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 24/24 | 977 | chr17 | 58998399 | ||||||
| chr17:58998416 | T | C | 1 | a0001c0001t0008 | 3 | NA19056.hp2 NA19068.hp2 NA19084.hp1 |
3_prime_UTR_variant | MODIFIER | c.*961A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 24/24 | 961 | chr17 | 58998416 | ||||||
| chr17:58998541 | T | C | 1 | a0001c0001t0005 | 4 | NA18945.hp1 NA19006.hp2 NA19007.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*836A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 24/24 | 836 | chr17 | 58998541 | ||||||
| chr17:58998618 | A | G | 1 | a0001c0001t0009 | 3 | HG02293.hp1 HG02572.hp1 HG02723.hp2 |
3_prime_UTR_variant | MODIFIER | c.*759T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 24/24 | 759 | chr17 | 58998618 | ||||||
| chr17:58998628 | C | CACTACAG others(18): Show |
1 | a0001c0001t0013 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*724_*748dupCTGCCT others(19): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 24/24 | 748 | chr17 | 58998628 | ||||||
| chr17:58998743 | T | A | 7 | a0001c0001t0002 a0001c0001t0009 a0001c0001t0011 others(4): Show |
105 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*634A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 24/24 | 634 | chr17 | 58998743 | ||||||
| chr17:58998954 | C | A | 1 | a0001c0001t0016 | 1 | NA19062.hp2 | 3_prime_UTR_variant | MODIFIER | c.*423G>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 24/24 | 423 | chr17 | 58998954 | ||||||
| chr17:58999004 | T | C | 1 | a0001c0001t0007 | 4 | HG01243.hp2 HG03471.hp1 HG03540.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*373A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 24/24 | 373 | chr17 | 58999004 | ||||||
| chr17:58999100 | C | T | 1 | a0001c0001t0010 | 2 | HG02109.hp1 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*277G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 24/24 | 277 | chr17 | 58999100 | ||||||
| chr17:59106596 | C | G | 1 | a0001c0001t0012 | 1 | HG01515.hp2 | 5_prime_UTR_variant | MODIFIER | c.-135G>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 1/24 | 135 | chr17 | 59106596 | ||||||
| chr17:59106685 | T | C | 2 | a0001c0001t0007 a0001c0003t0006 |
8 | HG00642.hp2 HG01243.hp2 HG03471.hp1 others(5): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-224A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 1/24 | chr17 | 59106685 | |||||||
| chr17:59106697 | T | C | 1 | a0001c0001t0017 | 1 | HG02735.hp1 | 5_prime_UTR_variant | MODIFIER | c.-236A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 1/24 | 236 | chr17 | 59106697 | ||||||
| chr17:59106706 | C | T | 1 | a0001c0001t0011 | 1 | HG03654.hp1 | 5_prime_UTR_variant | MODIFIER | c.-245G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 1/24 | 245 | chr17 | 59106706 | ||||||
| chr17:59106801 | A | C | 18 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(15): Show |
219 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(216): Show |
5_prime_UTR_variant | MODIFIER | c.-340T>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 1/24 | 340 | chr17 | 59106801 | ||||||
| chr17:59106871 | G | A | 1 | a0001c0001t0018 | 1 | HG02723.hp1 | 5_prime_UTR_variant | MODIFIER | c.-410C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 1/24 | 410 | chr17 | 59106871 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:58999491 | A | G | 1 | a0001c0001t0001g0306 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2813-32T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 23/23 | chr17 | 58999491 | |||||||
| chr17:58999532 | T | A | 111 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(108): Show |
111 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.2813-73A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 23/23 | chr17 | 58999532 | |||||||
| chr17:58999640 | C | T | 1 | a0001c0001t0001g0309 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2813-181G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 23/23 | chr17 | 58999640 | |||||||
| chr17:59000389 | C | A | 1 | a0001c0001t0001g0310 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2813-930G>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 23/23 | chr17 | 59000389 | |||||||
| chr17:59000391 | G | A | 1 | a0001c0001t0003g0077 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2813-932C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 23/23 | chr17 | 59000391 | |||||||
| chr17:59000453 | TAGCTGGA others(9): Show |
T | 1 | a0001c0001t0003g0060 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.2813-1010_2813-995 others(19): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 23/23 | chr17 | 59000453 | |||||||
| chr17:59000547 | G | A | 4 | a0001c0001t0003g0073 a0001c0001t0003g0074 a0001c0001t0003g0075 others(1): Show |
4 | HG02486.hp2 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2812+1051C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 23/23 | chr17 | 59000547 | |||||||
| chr17:59000799 | G | GA | 21 | a0001c0001t0001g0223 a0001c0001t0001g0255 a0001c0001t0001g0284 others(18): Show |
21 | HG00438.hp1 HG00438.hp2 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.2812+798dupT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 23/23 | chr17 | 59000799 | |||||||
| chr17:59001092 | G | C | 1 | a0001c0006t0003g0105 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2812+506C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 23/23 | chr17 | 59001092 | |||||||
| chr17:59001156 | C | T | 2 | a0001c0001t0003g0087 a0001c0001t0003g0088 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2812+442G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 23/23 | chr17 | 59001156 | |||||||
| chr17:59001199 | C | CAA | 9 | a0001c0001t0003g0106 a0001c0001t0007g0213 a0001c0001t0007g0214 others(6): Show |
9 | HG00642.hp2 HG01243.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.2812+397_2812+398d others(4): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 23/23 | chr17 | 59001199 | |||||||
| chr17:59001207 | A | G | 1 | a0001c0001t0003g0070 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2812+391T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 23/23 | chr17 | 59001207 | |||||||
| chr17:59001366 | G | A | 1 | a0001c0001t0001g0234 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.2812+232C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 23/23 | chr17 | 59001366 | |||||||
| chr17:59001454 | TA | T | 9 | a0001c0001t0001g0222 a0001c0001t0001g0228 a0001c0001t0001g0237 others(6): Show |
9 | HG01168.hp1 HG01256.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.2812+143delT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 23/23 | chr17 | 59001454 | |||||||
| chr17:59001502 | G | A | 2 | a0001c0001t0001g0278 a0001c0001t0001g0286 |
2 | HG00558.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.2812+96C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 23/23 | chr17 | 59001502 | |||||||
| chr17:59001530 | A | C | 2 | a0001c0001t0001g0298 a0001c0006t0003g0105 |
2 | HG01071.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.2812+68T>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 23/23 | chr17 | 59001530 | |||||||
| chr17:59002221 | C | T | 4 | a0001c0001t0003g0053 a0001c0001t0003g0055 a0001c0001t0003g0056 others(1): Show |
4 | NA18612.hp2 NA18939.hp1 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.2696-507G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59002221 | |||||||
| chr17:59002381 | C | T | 88 | a0001c0001t0002g0110 a0001c0001t0002g0124 a0001c0001t0002g0126 others(85): Show |
88 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.2696-667G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59002381 | |||||||
| chr17:59002489 | C | A | 1 | a0001c0001t0003g0060 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.2696-775G>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59002489 | |||||||
| chr17:59002913 | G | T | 1 | a0001c0001t0001g0226 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2696-1199C>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59002913 | |||||||
| chr17:59002952 | T | C | 3 | a0001c0001t0004g0102 a0001c0001t0004g0103 a0001c0001t0004g0104 |
3 | HG03516.hp2 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2696-1238A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59002952 | |||||||
| chr17:59003052 | T | C | 1 | a0001c0006t0003g0105 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2696-1338A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59003052 | |||||||
| chr17:59003110 | G | A | 96 | a0001c0001t0001g0339 a0001c0001t0002g0089 a0001c0001t0002g0098 others(93): Show |
96 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.2696-1396C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59003110 | |||||||
| chr17:59003436 | G | A | 4 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0007 others(1): Show |
4 | HG01978.hp2 HG03831.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.2696-1722C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59003436 | |||||||
| chr17:59003645 | T | TA | 92 | a0001c0001t0001g0249 a0001c0001t0001g0334 a0001c0001t0001g0339 others(89): Show |
92 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.2696-1932dupT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59003645 | |||||||
| chr17:59003645 | T | TAA | 12 | a0001c0001t0003g0011 a0001c0001t0003g0048 a0001c0001t0003g0051 others(9): Show |
12 | HG02055.hp1 HG02559.hp1 NA18612.hp2 others(9): Show |
intron_variant | MODIFIER | c.2696-1933_2696-193 others(6): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59003645 | |||||||
| chr17:59003663 | C | A | 10 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(7): Show |
10 | NA18939.hp2 NA18954.hp2 NA18964.hp1 others(7): Show |
intron_variant | MODIFIER | c.2696-1949G>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59003663 | |||||||
| chr17:59003727 | C | T | 1 | a0001c0001t0011g0001 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2696-2013G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59003727 | |||||||
| chr17:59003919 | C | A | 4 | a0001c0001t0007g0213 a0001c0001t0007g0214 a0001c0001t0007g0215 others(1): Show |
4 | HG01243.hp2 HG03471.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.2696-2205G>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59003919 | |||||||
| chr17:59003922 | T | TA | 123 | a0001c0001t0001g0223 a0001c0001t0001g0225 a0001c0001t0001g0227 others(120): Show |
123 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.2696-2209dupT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59003922 | |||||||
| chr17:59003922 | T | TAA | 11 | a0001c0001t0002g0152 a0001c0001t0002g0154 a0001c0001t0002g0163 others(8): Show |
11 | HG02155.hp2 HG02280.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.2696-2210_2696-220 others(6): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59003922 | |||||||
| chr17:59003922 | TA | T | 23 | a0001c0001t0001g0221 a0001c0001t0001g0237 a0001c0001t0001g0241 others(20): Show |
23 | HG00639.hp2 HG01070.hp2 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.2696-2209delT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59003922 | |||||||
| chr17:59004057 | T | C | 1 | a0001c0001t0004g0091 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2696-2343A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59004057 | |||||||
| chr17:59004090 | C | A | 1 | a0001c0001t0001g0264 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2696-2376G>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59004090 | |||||||
| chr17:59004340 | A | G | 1 | a0001c0001t0002g0130 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2696-2626T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59004340 | |||||||
| chr17:59004343 | T | TTAAG | 337 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(334): Show |
337 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(334): Show |
intron_variant | MODIFIER | c.2696-2630_2696-262 others(8): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59004343 | |||||||
| chr17:59004524 | G | A | 2 | a0001c0001t0002g0151 a0001c0001t0002g0152 |
2 | HG03834.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.2696-2810C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59004524 | |||||||
| chr17:59004552 | T | A | 1 | a0001c0001t0003g0106 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2696-2838A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59004552 | |||||||
| chr17:59004652 | C | A | 214 | a0001c0001t0001g0339 a0001c0001t0002g0080 a0001c0001t0002g0089 others(211): Show |
214 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.2696-2938G>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59004652 | |||||||
| chr17:59004741 | T | A | 6 | a0001c0001t0003g0009 a0001c0001t0003g0043 a0001c0001t0005g0040 others(3): Show |
6 | HG00438.hp1 NA18945.hp1 NA19006.hp2 others(3): Show |
intron_variant | MODIFIER | c.2696-3027A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59004741 | |||||||
| chr17:59004761 | T | G | 1 | a0001c0001t0001g0302 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2696-3047A>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59004761 | |||||||
| chr17:59004811 | G | A | 2 | a0001c0001t0003g0050 a0001c0001t0013g0024 |
2 | HG03017.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.2696-3097C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59004811 | |||||||
| chr17:59004864 | G | A | 2 | a0001c0001t0002g0151 a0001c0001t0002g0152 |
2 | HG03834.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.2696-3150C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59004864 | |||||||
| chr17:59004885 | C | T | 1 | a0001c0001t0002g0116 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2696-3171G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59004885 | |||||||
| chr17:59004936 | A | T | 23 | a0001c0001t0002g0089 a0001c0001t0002g0098 a0001c0001t0003g0079 others(20): Show |
23 | HG01168.hp2 HG01169.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.2696-3222T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59004936 | |||||||
| chr17:59005241 | T | TA | 7 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0001c0001t0001g0287 others(4): Show |
7 | HG02071.hp2 HG02293.hp2 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.2696-3528dupT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59005241 | |||||||
| chr17:59005261 | T | C | 1 | a0001c0001t0003g0086 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2696-3547A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59005261 | |||||||
| chr17:59005282 | C | T | 4 | a0001c0001t0001g0236 a0001c0001t0001g0237 a0001c0001t0001g0238 others(1): Show |
4 | HG01168.hp1 HG02647.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.2696-3568G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59005282 | |||||||
| chr17:59005309 | C | T | 8 | a0001c0001t0007g0213 a0001c0001t0007g0214 a0001c0001t0007g0215 others(5): Show |
8 | HG00642.hp2 HG01243.hp2 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.2696-3595G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59005309 | |||||||
| chr17:59005529 | C | T | 3 | a0001c0003t0006g0217 a0001c0003t0006g0218 a0001c0003t0006g0219 |
3 | HG00642.hp2 NA20752.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.2696-3815G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59005529 | |||||||
| chr17:59005567 | G | A | 1 | a0001c0001t0002g0185 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2696-3853C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59005567 | |||||||
| chr17:59006093 | C | G | 1 | a0001c0001t0001g0250 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2696-4379G>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59006093 | |||||||
| chr17:59006244 | G | A | 1 | a0001c0001t0003g0077 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2696-4530C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59006244 | |||||||
| chr17:59006295 | T | C | 1 | a0001c0001t0001g0325 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2696-4581A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59006295 | |||||||
| chr17:59006395 | A | T | 2 | a0001c0001t0002g0173 a0001c0001t0002g0174 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.2696-4681T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59006395 | |||||||
| chr17:59006396 | T | A | 1 | a0001c0001t0002g0191 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2696-4682A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59006396 | |||||||
| chr17:59006745 | C | T | 1 | a0001c0001t0001g0234 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.2696-5031G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59006745 | |||||||
| chr17:59006804 | G | A | 2 | a0001c0001t0001g0313 a0001c0001t0001g0314 |
2 | HG01433.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.2696-5090C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59006804 | |||||||
| chr17:59006842 | T | C | 1 | a0001c0001t0012g0002 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2696-5128A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59006842 | |||||||
| chr17:59007086 | G | A | 1 | a0001c0001t0002g0177 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2695+5242C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007086 | |||||||
| chr17:59007158 | A | AAC | 53 | a0001c0001t0001g0224 a0001c0001t0001g0226 a0001c0001t0001g0236 others(50): Show |
53 | HG00544.hp2 HG00735.hp1 HG00735.hp2 others(50): Show |
intron_variant | MODIFIER | c.2695+5168_2695+516 others(6): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007158 | |||||||
| chr17:59007158 | A | AACAC | 62 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(59): Show |
62 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.2695+5166_2695+516 others(8): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007158 | |||||||
| chr17:59007158 | A | AACACAC | 20 | a0001c0001t0001g0227 a0001c0001t0001g0228 a0001c0001t0001g0232 others(17): Show |
20 | HG01070.hp2 HG01175.hp1 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.2695+5164_2695+516 others(10): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007158 | |||||||
| chr17:59007158 | A | AACACACA others(1): Show |
14 | a0001c0001t0001g0230 a0001c0001t0001g0243 a0001c0001t0001g0264 others(11): Show |
14 | HG00621.hp2 HG01243.hp2 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.2695+5162_2695+516 others(12): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007158 | |||||||
| chr17:59007158 | A | AACACACA others(5): Show |
4 | a0001c0001t0001g0248 a0001c0001t0001g0280 a0001c0001t0001g0296 others(1): Show |
4 | NA18952.hp2 NA18979.hp1 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.2695+5158_2695+516 others(16): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007158 | |||||||
| chr17:59007158 | A | AACACACA others(7): Show |
3 | a0001c0001t0001g0239 a0001c0001t0001g0247 a0001c0001t0003g0077 |
3 | HG03486.hp1 NA18964.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.2695+5156_2695+516 others(18): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007158 | |||||||
| chr17:59007158 | A | AACACACA others(9): Show |
1 | a0001c0001t0001g0327 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2695+5154_2695+516 others(20): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007158 | |||||||
| chr17:59007158 | AAC | A | 44 | a0001c0001t0001g0254 a0001c0001t0001g0281 a0001c0001t0001g0313 others(41): Show |
44 | HG00099.hp2 HG00280.hp2 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.2695+5168_2695+516 others(6): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007158 | |||||||
| chr17:59007158 | AACAC | A | 11 | a0001c0001t0002g0107 a0001c0001t0002g0111 a0001c0001t0002g0134 others(8): Show |
11 | HG00673.hp1 HG00741.hp1 HG02004.hp1 others(8): Show |
intron_variant | MODIFIER | c.2695+5166_2695+516 others(8): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007158 | |||||||
| chr17:59007158 | AACACAC | A | 9 | a0001c0001t0001g0303 a0001c0001t0002g0117 a0001c0001t0003g0058 others(6): Show |
9 | HG00642.hp2 HG02622.hp2 HG03492.hp2 others(6): Show |
intron_variant | MODIFIER | c.2695+5164_2695+516 others(10): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007158 | |||||||
| chr17:59007158 | AACACACA others(3): Show |
A | 4 | a0001c0001t0002g0116 a0001c0001t0002g0120 a0001c0001t0002g0121 others(1): Show |
4 | HG01257.hp2 HG01258.hp1 NA19085.hp2 others(1): Show |
intron_variant | MODIFIER | c.2695+5160_2695+516 others(14): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007158 | |||||||
| chr17:59007158 | AACACACA others(5): Show |
A | 7 | a0001c0001t0002g0080 a0001c0001t0002g0112 a0001c0001t0002g0113 others(4): Show |
7 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.2695+5158_2695+516 others(16): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007158 | |||||||
| chr17:59007158 | AACACACA others(7): Show |
A | 1 | a0001c0006t0003g0105 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2695+5156_2695+516 others(18): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007158 | |||||||
| chr17:59007158 | AACACACA others(9): Show |
A | 6 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0006 others(3): Show |
6 | HG01106.hp2 HG01978.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.2695+5154_2695+516 others(20): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007158 | |||||||
| chr17:59007158 | AACACACA others(11): Show |
A | 1 | a0001c0001t0001g0255 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2695+5152_2695+516 others(22): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007158 | |||||||
| chr17:59007185 | A | T | 1 | a0001c0003t0006g0212 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2695+5143T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007185 | |||||||
| chr17:59007186 | C | A | 1 | a0001c0003t0006g0212 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2695+5142G>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007186 | |||||||
| chr17:59007189 | A | C | 1 | a0001c0003t0006g0212 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2695+5139T>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007189 | |||||||
| chr17:59007195 | A | C | 1 | a0001c0003t0006g0212 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2695+5133T>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007195 | |||||||
| chr17:59007199 | A | C | 1 | a0001c0003t0006g0212 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2695+5129T>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007199 | |||||||
| chr17:59007201 | A | ACACTAAA others(17): Show |
3 | a0001c0001t0008g0017 a0001c0001t0008g0026 a0001c0001t0008g0027 |
3 | NA19056.hp2 NA19068.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.2695+5126_2695+512 others(28): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007201 | |||||||
| chr17:59007203 | A | C | 1 | a0001c0003t0006g0212 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2695+5125T>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007203 | |||||||
| chr17:59007207 | T | C | 1 | a0001c0003t0006g0212 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2695+5121A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007207 | |||||||
| chr17:59007208 | A | C | 1 | a0001c0003t0006g0212 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2695+5120T>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007208 | |||||||
| chr17:59007210 | A | C | 1 | a0001c0003t0006g0212 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2695+5118T>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007210 | |||||||
| chr17:59007215 | C | A | 1 | a0001c0003t0006g0212 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2695+5113G>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007215 | |||||||
| chr17:59007217 | C | A | 1 | a0001c0003t0006g0212 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2695+5111G>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007217 | |||||||
| chr17:59007221 | C | A | 8 | a0001c0001t0007g0213 a0001c0001t0007g0214 a0001c0001t0007g0215 others(5): Show |
8 | HG00642.hp2 HG01243.hp2 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.2695+5107G>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007221 | |||||||
| chr17:59007221 | C | CCCCA | 96 | a0001c0001t0002g0080 a0001c0001t0002g0107 a0001c0001t0002g0110 others(93): Show |
96 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.2695+5103_2695+510 others(8): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007221 | |||||||
| chr17:59007223 | C | A | 1 | a0001c0003t0006g0212 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2695+5105G>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007223 | |||||||
| chr17:59007227 | C | A | 1 | a0001c0003t0006g0212 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2695+5101G>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007227 | |||||||
| chr17:59007231 | C | A | 2 | a0001c0001t0001g0310 a0001c0003t0006g0212 |
2 | HG00597.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.2695+5097G>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007231 | |||||||
| chr17:59007231 | C | CCACACAC others(13): Show |
4 | a0001c0001t0007g0213 a0001c0001t0007g0214 a0001c0001t0007g0215 others(1): Show |
4 | HG01243.hp2 HG03471.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.2695+5096_2695+509 others(24): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007231 | |||||||
| chr17:59007231 | C | CCACACAC others(15): Show |
2 | a0001c0003t0006g0217 a0001c0003t0006g0218 |
2 | NA20752.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.2695+5096_2695+509 others(26): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007231 | |||||||
| chr17:59007231 | C | CCACACAC others(17): Show |
1 | a0001c0003t0006g0219 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2695+5096_2695+509 others(28): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007231 | |||||||
| chr17:59007231 | C | CCACCCA | 6 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0006 others(3): Show |
6 | HG01106.hp2 HG01978.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.2695+5096_2695+509 others(10): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007231 | |||||||
| chr17:59007231 | C | CCACCCAC others(1): Show |
194 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(191): Show |
194 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.2695+5096_2695+509 others(12): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007231 | |||||||
| chr17:59007231 | C | CCACCCAC others(3): Show |
18 | a0001c0001t0001g0250 a0001c0001t0001g0265 a0001c0001t0001g0280 others(15): Show |
18 | HG02055.hp1 HG02523.hp2 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.2695+5096_2695+509 others(14): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007231 | |||||||
| chr17:59007231 | C | CCACCCAC others(5): Show |
1 | a0001c0001t0001g0296 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.2695+5096_2695+509 others(16): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007231 | |||||||
| chr17:59007231 | C | CCACCCAC others(7): Show |
2 | a0001c0001t0001g0313 a0001c0001t0001g0314 |
2 | HG01433.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.2695+5096_2695+509 others(18): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007231 | |||||||
| chr17:59007372 | A | G | 1 | a0001c0001t0001g0338 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2695+4956T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007372 | |||||||
| chr17:59007432 | A | G | 1 | a0001c0001t0002g0204 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2695+4896T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007432 | |||||||
| chr17:59007652 | AAAT | A | 84 | a0001c0001t0001g0281 a0001c0001t0001g0339 a0001c0001t0002g0089 others(81): Show |
84 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.2695+4673_2695+467 others(7): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007652 | |||||||
| chr17:59007916 | G | A | 4 | a0001c0001t0003g0073 a0001c0001t0003g0074 a0001c0001t0003g0075 others(1): Show |
4 | HG02486.hp2 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2695+4412C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007916 | |||||||
| chr17:59008190 | T | G | 6 | a0001c0001t0001g0225 a0001c0001t0001g0242 a0001c0001t0001g0246 others(3): Show |
6 | HG01070.hp2 HG01081.hp2 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.2695+4138A>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59008190 | |||||||
| chr17:59008374 | C | T | 2 | a0001c0001t0002g0120 a0001c0001t0002g0121 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.2695+3954G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59008374 | |||||||
| chr17:59008416 | A | C | 1 | a0001c0006t0003g0105 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2695+3912T>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59008416 | |||||||
| chr17:59008664 | T | C | 1 | a0001c0001t0001g0243 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2695+3664A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59008664 | |||||||
| chr17:59009106 | G | A | 1 | a0001c0001t0003g0035 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.2695+3222C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59009106 | |||||||
| chr17:59009112 | C | T | 118 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(115): Show |
118 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(115): Show |
intron_variant | MODIFIER | c.2695+3216G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59009112 | |||||||
| chr17:59009298 | T | C | 11 | a0001c0001t0002g0080 a0001c0001t0002g0112 a0001c0001t0002g0113 others(8): Show |
11 | HG01257.hp2 HG01258.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.2695+3030A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59009298 | |||||||
| chr17:59009443 | C | CT | 12 | a0001c0001t0002g0098 a0001c0001t0002g0107 a0001c0001t0002g0128 others(9): Show |
12 | HG00642.hp2 HG03453.hp1 HG03516.hp2 others(9): Show |
intron_variant | MODIFIER | c.2695+2884dupA | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59009443 | |||||||
| chr17:59009443 | CT | C | 6 | a0001c0001t0002g0089 a0001c0001t0002g0118 a0001c0001t0002g0163 others(3): Show |
6 | HG01070.hp1 HG02280.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.2695+2884delA | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59009443 | |||||||
| chr17:59009448 | T | TC | 117 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(114): Show |
117 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(114): Show |
intron_variant | MODIFIER | c.2695+2879_2695+288 others(5): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59009448 | |||||||
| chr17:59009449 | T | C | 2 | a0001c0001t0001g0230 a0001c0001t0001g0318 |
2 | HG02897.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.2695+2879A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59009449 | |||||||
| chr17:59009531 | C | T | 1 | a0001c0001t0002g0119 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2695+2797G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59009531 | |||||||
| chr17:59009607 | A | G | 226 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(223): Show |
226 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.2695+2721T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59009607 | |||||||
| chr17:59009761 | C | G | 1 | a0001c0001t0001g0309 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2695+2567G>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59009761 | |||||||
| chr17:59009885 | A | T | 8 | a0001c0001t0007g0213 a0001c0001t0007g0214 a0001c0001t0007g0215 others(5): Show |
8 | HG00642.hp2 HG01243.hp2 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.2695+2443T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59009885 | |||||||
| chr17:59009931 | G | T | 1 | a0001c0001t0003g0097 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2695+2397C>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59009931 | |||||||
| chr17:59009976 | C | T | 1 | a0001c0001t0001g0250 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2695+2352G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59009976 | |||||||
| chr17:59009977 | G | A | 1 | a0001c0001t0002g0192 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2695+2351C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59009977 | |||||||
| chr17:59010016 | T | G | 1 | a0001c0001t0002g0194 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.2695+2312A>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59010016 | |||||||
| chr17:59010069 | A | G | 7 | a0001c0001t0003g0086 a0001c0001t0003g0092 a0001c0001t0003g0093 others(4): Show |
7 | HG02109.hp1 HG02615.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.2695+2259T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59010069 | |||||||
| chr17:59010448 | C | T | 1 | a0001c0001t0001g0325 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2695+1880G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59010448 | |||||||
| chr17:59010463 | A | G | 5 | a0001c0001t0001g0232 a0001c0001t0001g0236 a0001c0001t0001g0237 others(2): Show |
5 | HG01168.hp1 HG02559.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.2695+1865T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59010463 | |||||||
| chr17:59010784 | C | T | 4 | a0001c0003t0006g0212 a0001c0003t0006g0217 a0001c0003t0006g0218 others(1): Show |
4 | HG00642.hp2 HG03704.hp2 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.2695+1544G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59010784 | |||||||
| chr17:59010953 | G | A | 2 | a0001c0001t0001g0315 a0001c0001t0001g0316 |
2 | NA18963.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.2695+1375C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59010953 | |||||||
| chr17:59011164 | G | A | 23 | a0001c0001t0002g0089 a0001c0001t0002g0098 a0001c0001t0003g0079 others(20): Show |
23 | HG01168.hp2 HG01169.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.2695+1164C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59011164 | |||||||
| chr17:59011172 | G | GA | 7 | a0001c0001t0001g0236 a0001c0001t0001g0247 a0001c0001t0001g0313 others(4): Show |
7 | HG02145.hp1 HG02486.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.2695+1155dupT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59011172 | |||||||
| chr17:59011185 | C | A | 1 | a0001c0006t0003g0105 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2695+1143G>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59011185 | |||||||
| chr17:59011429 | G | A | 1 | a0001c0001t0012g0002 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2695+899C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59011429 | |||||||
| chr17:59011516 | G | A | 1 | a0001c0001t0003g0005 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.2695+812C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59011516 | |||||||
| chr17:59011651 | G | A | 2 | a0001c0001t0003g0079 a0001c0001t0003g0101 |
2 | HG01884.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.2695+677C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59011651 | |||||||
| chr17:59011674 | G | A | 1 | a0001c0001t0003g0079 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2695+654C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59011674 | |||||||
| chr17:59011727 | G | A | 1 | a0001c0001t0001g0340 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.2695+601C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59011727 | |||||||
| chr17:59012132 | T | C | 4 | a0001c0001t0003g0073 a0001c0001t0003g0074 a0001c0001t0003g0075 others(1): Show |
4 | HG02486.hp2 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2695+196A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59012132 | |||||||
| chr17:59012153 | C | T | 1 | a0001c0001t0001g0339 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2695+175G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59012153 | |||||||
| chr17:59012215 | C | CCAGCAGC others(8): Show |
2 | a0001c0001t0002g0126 a0001c0001t0002g0143 |
2 | NA18995.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.2695+112_2695+113i others(17): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59012215 | |||||||
| chr17:59012215 | C | CCAGCAGC others(11): Show |
2 | a0001c0001t0001g0310 a0001c0001t0003g0094 |
2 | HG00597.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2695+112_2695+113i others(20): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59012215 | |||||||
| chr17:59012215 | C | CCAGCAGC others(14): Show |
3 | a0001c0001t0001g0263 a0001c0001t0002g0107 a0001c0001t0002g0111 |
3 | HG01978.hp1 HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2695+112_2695+113i others(23): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59012215 | |||||||
| chr17:59012227 | G | GCAGCAGC others(11): Show |
4 | a0001c0001t0001g0228 a0001c0001t0001g0230 a0001c0001t0003g0047 others(1): Show |
4 | HG00642.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.2695+100_2695+101i others(20): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59012227 | |||||||
| chr17:59012227 | G | GCAGCAGC others(11): Show |
188 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(185): Show |
188 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.2695+100_2695+101i others(20): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59012227 | |||||||
| chr17:59012227 | G | GCAGCAGC others(14): Show |
6 | a0001c0001t0002g0117 a0001c0001t0003g0086 a0001c0001t0004g0091 others(3): Show |
6 | HG02615.hp1 HG02622.hp2 HG03704.hp2 others(3): Show |
intron_variant | MODIFIER | c.2695+100_2695+101i others(23): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59012227 | |||||||
| chr17:59012227 | G | GCAGCAGC others(14): Show |
24 | a0001c0001t0001g0256 a0001c0001t0002g0112 a0001c0001t0002g0115 others(21): Show |
24 | HG01243.hp2 HG01884.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.2695+100_2695+101i others(23): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59012227 | |||||||
| chr17:59012227 | G | GCAGCAGC others(17): Show |
3 | a0001c0001t0004g0102 a0001c0001t0004g0103 a0001c0001t0004g0104 |
3 | HG03516.hp2 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2695+100_2695+101i others(26): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59012227 | |||||||
| chr17:59012227 | G | GCAGCAGC others(17): Show |
6 | a0001c0001t0003g0030 a0001c0001t0003g0031 a0001c0001t0003g0077 others(3): Show |
6 | HG03486.hp1 NA18952.hp1 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.2695+100_2695+101i others(26): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59012227 | |||||||
| chr17:59012227 | G | GCAGCAGC others(20): Show |
6 | a0001c0001t0001g0270 a0001c0001t0002g0080 a0001c0001t0002g0113 others(3): Show |
6 | HG01257.hp2 HG01258.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.2695+100_2695+101i others(29): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59012227 | |||||||
| chr17:59012227 | G | GCAGCAGC others(23): Show |
3 | a0001c0001t0003g0073 a0001c0001t0003g0075 a0001c0001t0003g0076 |
3 | HG02630.hp2 HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2695+100_2695+101i others(32): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59012227 | |||||||
| chr17:59012227 | G | GCAGCAGC others(26): Show |
1 | a0001c0006t0003g0105 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2695+100_2695+101i others(35): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59012227 | |||||||
| chr17:59012250 | ACCACCAC | A | 6 | a0001c0001t0001g0256 a0001c0001t0003g0073 a0001c0001t0003g0074 others(3): Show |
6 | HG02280.hp2 HG02486.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2695+71_2695+77del others(7): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59012250 | |||||||
| chr17:59012767 | C | T | 1 | a0001c0001t0003g0068 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2577-321G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 21/23 | chr17 | 59012767 | |||||||
| chr17:59012854 | C | T | 1 | a0001c0001t0003g0077 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2577-408G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 21/23 | chr17 | 59012854 | |||||||
| chr17:59012875 | C | CA | 102 | a0001c0001t0001g0281 a0001c0001t0001g0323 a0001c0001t0001g0339 others(99): Show |
102 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.2577-430dupT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 21/23 | chr17 | 59012875 | |||||||
| chr17:59012889 | A | T | 5 | a0001c0001t0001g0245 a0001c0003t0006g0212 a0001c0003t0006g0217 others(2): Show |
5 | HG00642.hp2 HG03704.hp2 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.2577-443T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 21/23 | chr17 | 59012889 | |||||||
| chr17:59012890 | T | A | 2 | a0001c0001t0003g0032 a0001c0001t0003g0122 |
2 | NA18992.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.2577-444A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 21/23 | chr17 | 59012890 | |||||||
| chr17:59012894 | T | A | 3 | a0001c0001t0003g0019 a0001c0001t0003g0032 a0001c0001t0003g0122 |
3 | NA18992.hp2 NA19001.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.2577-448A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 21/23 | chr17 | 59012894 | |||||||
| chr17:59012962 | G | A | 1 | a0001c0001t0003g0023 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2577-516C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 21/23 | chr17 | 59012962 | |||||||
| chr17:59013058 | T | C | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2577-612A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 21/23 | chr17 | 59013058 | |||||||
| chr17:59013330 | T | C | 2 | a0001c0001t0001g0260 a0001c0001t0001g0290 |
2 | HG01257.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.2577-884A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 21/23 | chr17 | 59013330 | |||||||
| chr17:59013367 | G | A | 5 | a0001c0001t0003g0079 a0001c0001t0003g0097 a0001c0001t0003g0099 others(2): Show |
5 | HG01168.hp2 HG01169.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.2577-921C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 21/23 | chr17 | 59013367 | |||||||
| chr17:59013506 | G | C | 2 | a0001c0001t0001g0273 a0001c0001t0001g0320 |
2 | HG00639.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.2577-1060C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 21/23 | chr17 | 59013506 | |||||||
| chr17:59013636 | A | G | 7 | a0001c0001t0002g0140 a0001c0001t0002g0141 a0001c0001t0002g0142 others(4): Show |
7 | HG00558.hp2 HG02155.hp2 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.2577-1190T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 21/23 | chr17 | 59013636 | |||||||
| chr17:59013731 | T | C | 4 | a0001c0003t0006g0212 a0001c0003t0006g0217 a0001c0003t0006g0218 others(1): Show |
4 | HG00642.hp2 HG03704.hp2 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.2577-1285A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 21/23 | chr17 | 59013731 | |||||||
| chr17:59013734 | C | A | 1 | a0001c0001t0001g0227 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2577-1288G>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 21/23 | chr17 | 59013734 | |||||||
| chr17:59014260 | T | C | 6 | a0001c0001t0003g0081 a0001c0001t0003g0082 a0001c0001t0003g0083 others(3): Show |
6 | HG02559.hp1 HG02647.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.2576+1350A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 21/23 | chr17 | 59014260 | |||||||
| chr17:59014307 | G | A | 3 | a0001c0001t0004g0102 a0001c0001t0004g0103 a0001c0001t0004g0104 |
3 | HG03516.hp2 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2576+1303C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 21/23 | chr17 | 59014307 | |||||||
| chr17:59014371 | T | A | 1 | a0001c0001t0001g0232 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2576+1239A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 21/23 | chr17 | 59014371 | |||||||
| chr17:59014473 | G | A | 1 | a0001c0001t0012g0002 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2576+1137C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 21/23 | chr17 | 59014473 | |||||||
| chr17:59014515 | C | T | 3 | a0001c0001t0004g0102 a0001c0001t0004g0103 a0001c0001t0004g0104 |
3 | HG03516.hp2 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2576+1095G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 21/23 | chr17 | 59014515 | |||||||
| chr17:59014546 | A | G | 1 | a0001c0001t0001g0303 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.2576+1064T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 21/23 | chr17 | 59014546 | |||||||
| chr17:59014631 | T | C | 2 | a0001c0001t0002g0107 a0001c0001t0002g0111 |
2 | HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2576+979A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 21/23 | chr17 | 59014631 | |||||||
| chr17:59014714 | G | GA | 11 | a0001c0001t0001g0224 a0001c0001t0001g0256 a0001c0001t0002g0132 others(8): Show |
11 | HG01106.hp1 HG01978.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.2576+895dupT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 21/23 | chr17 | 59014714 | |||||||
| chr17:59014742 | C | G | 1 | a0001c0001t0003g0172 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2576+868G>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 21/23 | chr17 | 59014742 | |||||||
| chr17:59014742 | C | T | 3 | a0001c0001t0004g0102 a0001c0001t0004g0103 a0001c0001t0004g0104 |
3 | HG03516.hp2 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2576+868G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 21/23 | chr17 | 59014742 | |||||||
| chr17:59014881 | A | C | 1 | a0001c0001t0002g0177 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2576+729T>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 21/23 | chr17 | 59014881 | |||||||
| chr17:59014911 | C | CA | 10 | a0001c0001t0001g0281 a0001c0001t0001g0322 a0001c0001t0002g0180 others(7): Show |
10 | HG02135.hp1 HG02486.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.2576+698dupT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 21/23 | chr17 | 59014911 | |||||||
| chr17:59015107 | TA | T | 247 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(244): Show |
247 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.2576+502delT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 21/23 | chr17 | 59015107 | |||||||
| chr17:59015269 | G | A | 1 | a0001c0001t0001g0269 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2576+341C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 21/23 | chr17 | 59015269 | |||||||
| chr17:59015364 | G | C | 247 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(244): Show |
247 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.2576+246C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 21/23 | chr17 | 59015364 | |||||||
| chr17:59015365 | G | A | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2576+245C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 21/23 | chr17 | 59015365 | |||||||
| chr17:59015426 | C | A | 1 | a0001c0001t0002g0184 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2576+184G>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 21/23 | chr17 | 59015426 | |||||||
| chr17:59015427 | G | A | 96 | a0001c0001t0001g0339 a0001c0001t0002g0089 a0001c0001t0002g0098 others(93): Show |
96 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.2576+183C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 21/23 | chr17 | 59015427 | |||||||
| chr17:59015457 | A | T | 1 | a0001c0001t0002g0169 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2576+153T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 21/23 | chr17 | 59015457 | |||||||
| chr17:59015464 | T | C | 1 | a0001c0001t0003g0172 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2576+146A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 21/23 | chr17 | 59015464 | |||||||
| chr17:59015533 | A | G | 2 | a0001c0001t0002g0151 a0001c0001t0002g0152 |
2 | HG03834.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.2576+77T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 21/23 | chr17 | 59015533 | |||||||
| chr17:59015848 | G | A | 1 | a0001c0001t0002g0171 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2387-49C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 20/23 | chr17 | 59015848 | |||||||
| chr17:59015851 | C | T | 1 | a0001c0001t0004g0102 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2387-52G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 20/23 | chr17 | 59015851 | |||||||
| chr17:59016076 | A | G | 1 | a0001c0001t0003g0072 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2387-277T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 20/23 | chr17 | 59016076 | |||||||
| chr17:59016254 | C | G | 4 | a0001c0001t0002g0124 a0001c0001t0002g0131 a0001c0001t0002g0201 others(1): Show |
4 | HG02132.hp1 NA18947.hp1 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.2387-455G>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 20/23 | chr17 | 59016254 | |||||||
| chr17:59016275 | T | C | 2 | a0001c0001t0003g0019 a0001c0001t0003g0032 |
2 | NA19001.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.2387-476A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 20/23 | chr17 | 59016275 | |||||||
| chr17:59016329 | G | A | 1 | a0001c0001t0003g0025 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2387-530C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 20/23 | chr17 | 59016329 | |||||||
| chr17:59016396 | C | CA | 29 | a0001c0001t0001g0224 a0001c0001t0001g0237 a0001c0001t0001g0264 others(26): Show |
29 | HG00544.hp2 HG00642.hp1 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.2387-598dupT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 20/23 | chr17 | 59016396 | |||||||
| chr17:59016396 | CA | C | 19 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(16): Show |
19 | HG01346.hp1 HG02155.hp1 HG02300.hp1 others(16): Show |
intron_variant | MODIFIER | c.2387-598delT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 20/23 | chr17 | 59016396 | |||||||
| chr17:59016464 | C | T | 247 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(244): Show |
247 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.2387-665G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 20/23 | chr17 | 59016464 | |||||||
| chr17:59016557 | G | A | 1 | a0001c0001t0002g0107 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2386+739C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 20/23 | chr17 | 59016557 | |||||||
| chr17:59016568 | G | A | 1 | a0001c0001t0002g0209 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2386+728C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 20/23 | chr17 | 59016568 | |||||||
| chr17:59016599 | C | CA | 37 | a0001c0001t0002g0110 a0001c0001t0002g0111 a0001c0001t0002g0124 others(34): Show |
37 | HG00438.hp2 HG00544.hp2 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.2386+696dupT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 20/23 | chr17 | 59016599 | |||||||
| chr17:59016599 | C | CAA | 11 | a0001c0001t0002g0171 a0001c0001t0002g0185 a0001c0001t0002g0188 others(8): Show |
11 | HG01175.hp2 HG01256.hp1 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.2386+695_2386+696d others(4): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 20/23 | chr17 | 59016599 | |||||||
| chr17:59016599 | CA | C | 71 | a0001c0001t0001g0223 a0001c0001t0001g0226 a0001c0001t0001g0227 others(68): Show |
71 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.2386+696delT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 20/23 | chr17 | 59016599 | |||||||
| chr17:59016599 | CAA | C | 119 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(116): Show |
119 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.2386+695_2386+696d others(4): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 20/23 | chr17 | 59016599 | |||||||
| chr17:59016599 | CAAA | C | 42 | a0001c0001t0001g0232 a0001c0001t0001g0237 a0001c0001t0001g0258 others(39): Show |
42 | HG00099.hp2 HG01099.hp1 HG01168.hp1 others(39): Show |
intron_variant | MODIFIER | c.2386+694_2386+696d others(5): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 20/23 | chr17 | 59016599 | |||||||
| chr17:59016599 | CAAAAAAA others(9): Show |
C | 2 | a0001c0001t0002g0120 a0001c0001t0002g0121 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.2386+681_2386+696d others(18): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 20/23 | chr17 | 59016599 | |||||||
| chr17:59016720 | C | T | 5 | a0001c0001t0003g0073 a0001c0001t0003g0074 a0001c0001t0003g0075 others(2): Show |
5 | HG02486.hp2 HG02630.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.2386+576G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 20/23 | chr17 | 59016720 | |||||||
| chr17:59016835 | T | C | 1 | a0001c0001t0001g0272 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2386+461A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 20/23 | chr17 | 59016835 | |||||||
| chr17:59016999 | T | C | 2 | a0001c0001t0001g0304 a0001c0001t0001g0305 |
2 | HG00323.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.2386+297A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 20/23 | chr17 | 59016999 | |||||||
| chr17:59017088 | C | T | 2 | a0001c0001t0002g0133 a0001c0001t0002g0145 |
2 | HG00621.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.2386+208G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 20/23 | chr17 | 59017088 | |||||||
| chr17:59017256 | T | C | 251 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(248): Show |
251 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.2386+40A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 20/23 | chr17 | 59017256 | |||||||
| chr17:59017486 | T | C | 11 | a0001c0001t0001g0225 a0001c0001t0001g0231 a0001c0001t0001g0234 others(8): Show |
11 | HG01070.hp2 HG01081.hp2 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.2258-62A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59017486 | |||||||
| chr17:59017583 | T | C | 1 | a0001c0001t0001g0285 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.2258-159A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59017583 | |||||||
| chr17:59017630 | T | C | 1 | a0001c0001t0001g0254 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2258-206A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59017630 | |||||||
| chr17:59017851 | C | T | 120 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(117): Show |
120 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.2258-427G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59017851 | |||||||
| chr17:59017889 | A | G | 226 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(223): Show |
226 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.2258-465T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59017889 | |||||||
| chr17:59018722 | G | GT | 10 | a0001c0001t0001g0220 a0001c0001t0001g0226 a0001c0001t0001g0277 others(7): Show |
10 | HG01361.hp1 HG03688.hp1 HG03831.hp2 others(7): Show |
intron_variant | MODIFIER | c.2258-1299dupA | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59018722 | |||||||
| chr17:59019014 | G | A | 2 | a0001c0001t0003g0108 a0001c0001t0003g0109 |
2 | HG02451.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2258-1590C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59019014 | |||||||
| chr17:59019129 | G | T | 1 | a0001c0001t0002g0134 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2258-1705C>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59019129 | |||||||
| chr17:59019444 | T | C | 8 | a0001c0001t0007g0213 a0001c0001t0007g0214 a0001c0001t0007g0215 others(5): Show |
8 | HG00642.hp2 HG01243.hp2 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.2258-2020A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59019444 | |||||||
| chr17:59019445 | C | T | 2 | a0001c0001t0003g0108 a0001c0001t0003g0109 |
2 | HG02451.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2258-2021G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59019445 | |||||||
| chr17:59019481 | G | A | 5 | a0001c0001t0003g0073 a0001c0001t0003g0074 a0001c0001t0003g0075 others(2): Show |
5 | HG02486.hp2 HG02630.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.2258-2057C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59019481 | |||||||
| chr17:59019537 | G | A | 2 | a0001c0001t0002g0107 a0001c0001t0002g0111 |
2 | HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2258-2113C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59019537 | |||||||
| chr17:59019615 | G | A | 7 | a0001c0001t0002g0209 a0001c0001t0002g0210 a0002c0002t0002g0125 others(4): Show |
7 | HG01952.hp2 HG02257.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.2258-2191C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59019615 | |||||||
| chr17:59019620 | A | G | 8 | a0001c0001t0007g0213 a0001c0001t0007g0214 a0001c0001t0007g0215 others(5): Show |
8 | HG00642.hp2 HG01243.hp2 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.2258-2196T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59019620 | |||||||
| chr17:59019686 | T | C | 245 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(242): Show |
245 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.2258-2262A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59019686 | |||||||
| chr17:59019703 | G | A | 73 | a0001c0001t0001g0339 a0001c0001t0003g0003 a0001c0001t0003g0004 others(70): Show |
73 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.2258-2279C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59019703 | |||||||
| chr17:59019750 | A | T | 2 | a0001c0001t0003g0087 a0001c0001t0003g0088 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2258-2326T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59019750 | |||||||
| chr17:59020029 | G | A | 121 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(118): Show |
121 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.2258-2605C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59020029 | |||||||
| chr17:59020065 | T | C | 1 | a0001c0001t0002g0115 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2258-2641A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59020065 | |||||||
| chr17:59020094 | G | C | 1 | a0001c0001t0003g0106 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2258-2670C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59020094 | |||||||
| chr17:59020230 | C | CA | 9 | a0001c0001t0002g0121 a0001c0001t0002g0130 a0001c0001t0002g0132 others(6): Show |
9 | HG00735.hp2 HG00741.hp2 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.2258-2807dupT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59020230 | |||||||
| chr17:59020230 | CA | C | 58 | a0001c0001t0001g0240 a0001c0001t0001g0269 a0001c0001t0001g0300 others(55): Show |
58 | HG00099.hp1 HG00544.hp2 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.2258-2807delT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59020230 | |||||||
| chr17:59020230 | CAA | C | 33 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0242 others(30): Show |
33 | HG00639.hp2 HG00642.hp1 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.2258-2808_2258-280 others(6): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59020230 | |||||||
| chr17:59020230 | CAAA | C | 76 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0231 others(73): Show |
76 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.2258-2809_2258-280 others(7): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59020230 | |||||||
| chr17:59020230 | CAAAA | C | 56 | a0001c0001t0001g0223 a0001c0001t0001g0228 a0001c0001t0001g0229 others(53): Show |
56 | HG00280.hp1 HG00639.hp1 HG00741.hp1 others(53): Show |
intron_variant | MODIFIER | c.2258-2810_2258-280 others(8): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59020230 | |||||||
| chr17:59020230 | CAAAAA | C | 66 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0245 others(63): Show |
66 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.2258-2811_2258-280 others(9): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59020230 | |||||||
| chr17:59020230 | CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0003g0106 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2258-2818_2258-280 others(16): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59020230 | |||||||
| chr17:59020391 | A | G | 7 | a0001c0001t0002g0098 a0001c0001t0003g0079 a0001c0001t0003g0096 others(4): Show |
7 | HG01168.hp2 HG01169.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.2258-2967T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59020391 | |||||||
| chr17:59020417 | A | G | 1 | a0001c0001t0001g0243 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2258-2993T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59020417 | |||||||
| chr17:59020691 | G | A | 1 | a0001c0001t0001g0334 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.2258-3267C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59020691 | |||||||
| chr17:59020950 | T | C | 22 | a0001c0001t0001g0339 a0001c0001t0003g0005 a0001c0001t0003g0010 others(19): Show |
22 | HG01261.hp2 HG01943.hp1 HG01981.hp2 others(19): Show |
intron_variant | MODIFIER | c.2258-3526A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59020950 | |||||||
| chr17:59020955 | T | C | 7 | a0001c0001t0003g0086 a0001c0001t0003g0092 a0001c0001t0003g0093 others(4): Show |
7 | HG02109.hp1 HG02615.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.2258-3531A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59020955 | |||||||
| chr17:59021014 | G | C | 1 | a0001c0001t0002g0161 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.2258-3590C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59021014 | |||||||
| chr17:59021803 | G | C | 1 | a0001c0001t0002g0129 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2258-4379C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59021803 | |||||||
| chr17:59021854 | G | A | 3 | a0001c0001t0002g0126 a0001c0001t0002g0143 a0001c0001t0002g0147 |
3 | HG02071.hp1 NA18995.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.2258-4430C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59021854 | |||||||
| chr17:59022051 | T | G | 5 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0006 others(2): Show |
5 | HG01106.hp2 HG01978.hp2 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.2258-4627A>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59022051 | |||||||
| chr17:59022087 | G | C | 10 | a0001c0001t0003g0062 a0001c0001t0003g0063 a0001c0001t0003g0064 others(7): Show |
10 | HG02055.hp1 HG02572.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.2258-4663C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59022087 | |||||||
| chr17:59022475 | G | A | 1 | a0001c0001t0003g0077 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2258-5051C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59022475 | |||||||
| chr17:59022828 | GAAATGGT others(10): Show |
G | 3 | a0001c0001t0001g0234 a0001c0001t0001g0240 a0001c0001t0001g0241 |
3 | HG02004.hp2 NA18951.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.2258-5421_2258-540 others(21): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59022828 | |||||||
| chr17:59022910 | A | G | 1 | a0001c0001t0001g0282 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.2258-5486T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59022910 | |||||||
| chr17:59022916 | T | C | 1 | a0001c0001t0003g0034 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2258-5492A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59022916 | |||||||
| chr17:59022922 | T | C | 2 | a0001c0001t0003g0013 a0001c0001t0003g0014 |
2 | HG00099.hp2 HG00280.hp2 |
intron_variant | MODIFIER | c.2257+5493A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59022922 | |||||||
| chr17:59023185 | A | C | 247 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(244): Show |
247 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.2257+5230T>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59023185 | |||||||
| chr17:59023238 | G | A | 4 | a0001c0001t0003g0073 a0001c0001t0003g0074 a0001c0001t0003g0075 others(1): Show |
4 | HG02486.hp2 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2257+5177C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59023238 | |||||||
| chr17:59023828 | T | C | 1 | a0001c0001t0002g0156 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2257+4587A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59023828 | |||||||
| chr17:59023872 | A | G | 4 | a0001c0001t0001g0269 a0001c0001t0001g0273 a0001c0001t0001g0298 others(1): Show |
4 | HG00639.hp2 HG01071.hp1 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.2257+4543T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59023872 | |||||||
| chr17:59024009 | T | C | 2 | a0001c0001t0002g0141 a0001c0001t0002g0178 |
2 | HG00438.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.2257+4406A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59024009 | |||||||
| chr17:59024082 | C | A | 1 | a0001c0006t0003g0105 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2257+4333G>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59024082 | |||||||
| chr17:59024144 | G | A | 1 | a0001c0001t0008g0017 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.2257+4271C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59024144 | |||||||
| chr17:59024145 | G | C | 1 | a0006c0004t0002g0144 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2257+4270C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59024145 | |||||||
| chr17:59024177 | G | A | 96 | a0001c0001t0001g0339 a0001c0001t0002g0089 a0001c0001t0002g0098 others(93): Show |
96 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.2257+4238C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59024177 | |||||||
| chr17:59024210 | G | A | 1 | a0001c0003t0006g0219 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2257+4205C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59024210 | |||||||
| chr17:59024214 | C | CA | 12 | a0001c0001t0002g0080 a0001c0001t0002g0110 a0001c0001t0002g0114 others(9): Show |
12 | HG00673.hp1 HG00741.hp2 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.2257+4200dupT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59024214 | |||||||
| chr17:59024214 | CA | C | 106 | a0001c0001t0001g0225 a0001c0001t0001g0228 a0001c0001t0001g0229 others(103): Show |
106 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.2257+4200delT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59024214 | |||||||
| chr17:59024214 | CAA | C | 106 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0223 others(103): Show |
106 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.2257+4199_2257+420 others(6): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59024214 | |||||||
| chr17:59024214 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0009g0183 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2257+4191_2257+420 others(14): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59024214 | |||||||
| chr17:59024239 | AT | A | 3 | a0001c0001t0003g0077 a0001c0001t0004g0103 a0001c0001t0004g0104 |
3 | HG03486.hp1 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2257+4175delA | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59024239 | |||||||
| chr17:59024240 | T | A | 1 | a0001c0001t0004g0102 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2257+4175A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59024240 | |||||||
| chr17:59024279 | A | G | 4 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0230 others(1): Show |
4 | HG00639.hp1 HG02630.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.2257+4136T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59024279 | |||||||
| chr17:59024369 | T | C | 1 | a0001c0006t0003g0105 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2257+4046A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59024369 | |||||||
| chr17:59024474 | G | C | 1 | a0001c0001t0001g0226 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2257+3941C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59024474 | |||||||
| chr17:59024725 | T | A | 1 | a0001c0001t0015g0331 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.2257+3690A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59024725 | |||||||
| chr17:59024772 | T | C | 225 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(222): Show |
225 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.2257+3643A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59024772 | |||||||
| chr17:59025159 | C | A | 1 | a0001c0001t0001g0251 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2257+3256G>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59025159 | |||||||
| chr17:59025160 | A | C | 1 | a0001c0001t0003g0021 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2257+3255T>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59025160 | |||||||
| chr17:59025198 | C | T | 1 | a0001c0001t0001g0336 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.2257+3217G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59025198 | |||||||
| chr17:59025381 | T | G | 97 | a0001c0001t0001g0339 a0001c0001t0002g0089 a0001c0001t0002g0098 others(94): Show |
97 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.2257+3034A>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59025381 | |||||||
| chr17:59025659 | T | C | 1 | a0001c0001t0001g0232 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2257+2756A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59025659 | |||||||
| chr17:59025712 | G | A | 7 | a0001c0001t0001g0265 a0001c0001t0001g0280 a0001c0001t0001g0281 others(4): Show |
7 | HG02523.hp2 NA18952.hp2 NA18979.hp1 others(4): Show |
intron_variant | MODIFIER | c.2257+2703C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59025712 | |||||||
| chr17:59025747 | G | A | 5 | a0001c0001t0003g0073 a0001c0001t0003g0074 a0001c0001t0003g0075 others(2): Show |
5 | HG02486.hp2 HG02630.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.2257+2668C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59025747 | |||||||
| chr17:59025779 | T | C | 62 | a0001c0001t0001g0339 a0001c0001t0003g0003 a0001c0001t0003g0004 others(59): Show |
62 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.2257+2636A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59025779 | |||||||
| chr17:59026051 | C | G | 1 | a0001c0006t0003g0105 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2257+2364G>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59026051 | |||||||
| chr17:59026439 | A | C | 1 | a0001c0001t0001g0336 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.2257+1976T>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59026439 | |||||||
| chr17:59026487 | G | T | 4 | a0001c0001t0001g0326 a0001c0001t0001g0329 a0001c0001t0001g0332 others(1): Show |
4 | HG00621.hp1 NA18612.hp1 NA18949.hp2 others(1): Show |
intron_variant | MODIFIER | c.2257+1928C>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59026487 | |||||||
| chr17:59026509 | T | C | 1 | a0001c0001t0003g0009 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2257+1906A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59026509 | |||||||
| chr17:59026581 | C | A | 1 | a0001c0003t0006g0218 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2257+1834G>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59026581 | |||||||
| chr17:59026743 | C | T | 1 | a0001c0001t0001g0322 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2257+1672G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59026743 | |||||||
| chr17:59027025 | T | A | 8 | a0001c0001t0007g0213 a0001c0001t0007g0214 a0001c0001t0007g0215 others(5): Show |
8 | HG00642.hp2 HG01243.hp2 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.2257+1390A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59027025 | |||||||
| chr17:59027153 | G | T | 8 | a0001c0001t0003g0051 a0001c0001t0003g0052 a0001c0001t0003g0053 others(5): Show |
8 | NA18612.hp2 NA18939.hp1 NA18943.hp1 others(5): Show |
intron_variant | MODIFIER | c.2257+1262C>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59027153 | |||||||
| chr17:59027274 | T | A | 2 | a0001c0001t0002g0107 a0001c0001t0002g0111 |
2 | HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2257+1141A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59027274 | |||||||
| chr17:59027362 | T | C | 1 | a0001c0001t0001g0303 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.2257+1053A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59027362 | |||||||
| chr17:59027635 | T | C | 1 | a0001c0001t0001g0275 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2257+780A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59027635 | |||||||
| chr17:59027862 | C | T | 247 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(244): Show |
247 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.2257+553G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59027862 | |||||||
| chr17:59027884 | G | A | 1 | a0001c0001t0001g0251 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2257+531C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59027884 | |||||||
| chr17:59027954 | T | A | 1 | a0001c0001t0002g0184 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2257+461A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59027954 | |||||||
| chr17:59027996 | C | G | 1 | a0001c0001t0002g0163 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2257+419G>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59027996 | |||||||
| chr17:59028193 | T | C | 1 | a0001c0001t0002g0116 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2257+222A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59028193 | |||||||
| chr17:59028257 | T | C | 2 | a0001c0001t0003g0087 a0001c0001t0003g0088 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2257+158A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59028257 | |||||||
| chr17:59028345 | T | C | 8 | a0001c0001t0007g0213 a0001c0001t0007g0214 a0001c0001t0007g0215 others(5): Show |
8 | HG00642.hp2 HG01243.hp2 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.2257+70A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59028345 | |||||||
| chr17:59028824 | G | A | 5 | a0001c0001t0001g0263 a0001c0001t0001g0271 a0001c0001t0001g0272 others(2): Show |
5 | HG01192.hp1 HG01943.hp2 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.1949-101C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 18/23 | chr17 | 59028824 | |||||||
| chr17:59028932 | T | C | 1 | a0001c0001t0002g0161 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1949-209A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 18/23 | chr17 | 59028932 | |||||||
| chr17:59028945 | C | T | 4 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0230 others(1): Show |
4 | HG00639.hp1 HG02630.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1949-222G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 18/23 | chr17 | 59028945 | |||||||
| chr17:59029105 | A | C | 1 | a0001c0006t0003g0105 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1949-382T>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 18/23 | chr17 | 59029105 | |||||||
| chr17:59029208 | G | A | 3 | a0001c0001t0001g0225 a0001c0001t0001g0242 a0001c0001t0001g0246 |
3 | NA18966.hp2 NA19005.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.1949-485C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 18/23 | chr17 | 59029208 | |||||||
| chr17:59029269 | A | G | 129 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(126): Show |
129 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(126): Show |
intron_variant | MODIFIER | c.1949-546T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 18/23 | chr17 | 59029269 | |||||||
| chr17:59029274 | T | A | 7 | a0001c0001t0002g0080 a0001c0001t0002g0112 a0001c0001t0002g0113 others(4): Show |
7 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.1949-551A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 18/23 | chr17 | 59029274 | |||||||
| chr17:59029300 | A | G | 1 | a0001c0001t0001g0231 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1949-577T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 18/23 | chr17 | 59029300 | |||||||
| chr17:59029544 | A | C | 1 | a0001c0006t0003g0105 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1949-821T>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 18/23 | chr17 | 59029544 | |||||||
| chr17:59029615 | G | C | 2 | a0001c0001t0001g0278 a0001c0001t0001g0286 |
2 | HG00558.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.1949-892C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 18/23 | chr17 | 59029615 | |||||||
| chr17:59029668 | G | A | 2 | a0001c0001t0002g0107 a0001c0001t0002g0111 |
2 | HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1949-945C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 18/23 | chr17 | 59029668 | |||||||
| chr17:59029798 | A | T | 1 | a0001c0001t0003g0123 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1949-1075T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 18/23 | chr17 | 59029798 | |||||||
| chr17:59029987 | TATTCATC others(3): Show |
T | 96 | a0001c0001t0001g0339 a0001c0001t0002g0089 a0001c0001t0002g0098 others(93): Show |
96 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.1949-1274_1949-126 others(14): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 18/23 | chr17 | 59029987 | |||||||
| chr17:59030056 | C | T | 7 | a0001c0001t0002g0098 a0001c0001t0003g0079 a0001c0001t0003g0096 others(4): Show |
7 | HG01168.hp2 HG01169.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.1949-1333G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 18/23 | chr17 | 59030056 | |||||||
| chr17:59030058 | C | T | 1 | a0001c0001t0003g0054 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1949-1335G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 18/23 | chr17 | 59030058 | |||||||
| chr17:59030202 | T | G | 1 | a0001c0001t0002g0200 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1949-1479A>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 18/23 | chr17 | 59030202 | |||||||
| chr17:59030256 | C | A | 4 | a0001c0001t0007g0213 a0001c0001t0007g0214 a0001c0001t0007g0215 others(1): Show |
4 | HG01243.hp2 HG03471.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1949-1533G>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 18/23 | chr17 | 59030256 | |||||||
| chr17:59030275 | T | G | 1 | a0001c0001t0001g0255 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1949-1552A>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 18/23 | chr17 | 59030275 | |||||||
| chr17:59030367 | C | T | 96 | a0001c0001t0001g0339 a0001c0001t0002g0089 a0001c0001t0002g0098 others(93): Show |
96 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.1948+1529G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 18/23 | chr17 | 59030367 | |||||||
| chr17:59030580 | A | T | 1 | a0001c0001t0001g0266 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1948+1316T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 18/23 | chr17 | 59030580 | |||||||
| chr17:59030610 | C | T | 10 | a0001c0001t0003g0062 a0001c0001t0003g0063 a0001c0001t0003g0064 others(7): Show |
10 | HG02055.hp1 HG02572.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1948+1286G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 18/23 | chr17 | 59030610 | |||||||
| chr17:59030697 | T | C | 1 | a0001c0001t0003g0067 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1948+1199A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 18/23 | chr17 | 59030697 | |||||||
| chr17:59031076 | G | C | 74 | a0001c0001t0001g0339 a0001c0001t0003g0003 a0001c0001t0003g0004 others(71): Show |
74 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.1948+820C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 18/23 | chr17 | 59031076 | |||||||
| chr17:59031182 | A | G | 247 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(244): Show |
247 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.1948+714T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 18/23 | chr17 | 59031182 | |||||||
| chr17:59031315 | T | C | 1 | a0001c0001t0001g0335 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1948+581A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 18/23 | chr17 | 59031315 | |||||||
| chr17:59031539 | G | A | 1 | a0001c0001t0014g0262 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1948+357C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 18/23 | chr17 | 59031539 | |||||||
| chr17:59031618 | T | C | 1 | a0001c0001t0003g0051 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1948+278A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 18/23 | chr17 | 59031618 | |||||||
| chr17:59032251 | C | T | 2 | a0001c0001t0002g0130 a0001c0001t0002g0162 |
2 | HG00741.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.1754-161G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59032251 | |||||||
| chr17:59032254 | G | A | 1 | a0001c0001t0003g0009 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1754-164C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59032254 | |||||||
| chr17:59032292 | G | A | 1 | a0001c0001t0001g0254 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1754-202C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59032292 | |||||||
| chr17:59032322 | GAGACCAT others(8514): Show |
G | 5 | a0001c0001t0001g0266 a0001c0001t0001g0318 a0001c0001t0001g0319 others(2): Show |
5 | NA18943.hp2 NA18955.hp1 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.1753+970_1754-233d others(2): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59032322 | |||||||
| chr17:59032387 | C | A | 3 | a0001c0001t0004g0102 a0001c0001t0004g0103 a0001c0001t0004g0104 |
3 | HG03516.hp2 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1754-297G>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59032387 | |||||||
| chr17:59032398 | G | T | 1 | a0001c0001t0002g0134 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1754-308C>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59032398 | |||||||
| chr17:59032531 | C | CA | 122 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0223 others(119): Show |
122 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.1754-442dupT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59032531 | |||||||
| chr17:59032531 | C | CAA | 11 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0001g0236 others(8): Show |
11 | HG01168.hp1 HG01952.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1754-443_1754-442d others(4): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59032531 | |||||||
| chr17:59032531 | CA | C | 89 | a0001c0001t0001g0339 a0001c0001t0002g0089 a0001c0001t0002g0098 others(86): Show |
89 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.1754-442delT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59032531 | |||||||
| chr17:59032550 | A | G | 8 | a0001c0001t0007g0213 a0001c0001t0007g0214 a0001c0001t0007g0215 others(5): Show |
8 | HG00642.hp2 HG01243.hp2 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.1754-460T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59032550 | |||||||
| chr17:59032554 | G | C | 4 | a0001c0001t0007g0213 a0001c0001t0007g0214 a0001c0001t0007g0215 others(1): Show |
4 | HG01243.hp2 HG03471.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1754-464C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59032554 | |||||||
| chr17:59032694 | G | A | 8 | a0001c0001t0002g0134 a0001c0001t0002g0140 a0001c0001t0002g0141 others(5): Show |
8 | HG00558.hp2 HG00673.hp1 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.1754-604C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59032694 | |||||||
| chr17:59032966 | T | C | 115 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(112): Show |
115 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.1754-876A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59032966 | |||||||
| chr17:59033558 | G | A | 1 | a0001c0001t0001g0249 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1754-1468C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59033558 | |||||||
| chr17:59033712 | C | A | 1 | a0001c0001t0002g0127 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1754-1622G>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59033712 | |||||||
| chr17:59033740 | T | C | 115 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(112): Show |
115 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.1754-1650A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59033740 | |||||||
| chr17:59033827 | G | A | 1 | a0001c0001t0002g0134 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1754-1737C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59033827 | |||||||
| chr17:59033889 | G | A | 115 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(112): Show |
115 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.1754-1799C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59033889 | |||||||
| chr17:59033908 | A | C | 71 | a0001c0001t0001g0224 a0001c0001t0001g0226 a0001c0001t0001g0227 others(68): Show |
71 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.1754-1818T>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59033908 | |||||||
| chr17:59033917 | A | C | 1 | a0001c0001t0001g0250 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1754-1827T>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59033917 | |||||||
| chr17:59033953 | A | G | 1 | a0001c0001t0001g0250 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1754-1863T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59033953 | |||||||
| chr17:59033972 | T | A | 1 | a0001c0001t0002g0186 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1754-1882A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59033972 | |||||||
| chr17:59034050 | T | G | 1 | a0001c0001t0001g0256 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1754-1960A>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59034050 | |||||||
| chr17:59034178 | T | G | 1 | a0001c0001t0001g0227 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1754-2088A>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59034178 | |||||||
| chr17:59034245 | G | C | 2 | a0001c0001t0002g0173 a0001c0001t0002g0174 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1754-2155C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59034245 | |||||||
| chr17:59034293 | G | A | 335 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(332): Show |
335 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.1754-2203C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59034293 | |||||||
| chr17:59034509 | A | G | 247 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(244): Show |
247 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.1754-2419T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59034509 | |||||||
| chr17:59034658 | C | G | 1 | a0001c0001t0003g0045 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1754-2568G>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59034658 | |||||||
| chr17:59034824 | T | C | 2 | a0001c0001t0003g0087 a0001c0001t0003g0088 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1754-2734A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59034824 | |||||||
| chr17:59034939 | G | T | 1 | a0001c0006t0003g0105 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1754-2849C>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59034939 | |||||||
| chr17:59035007 | G | A | 3 | a0001c0001t0004g0102 a0001c0001t0004g0103 a0001c0001t0004g0104 |
3 | HG03516.hp2 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1754-2917C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59035007 | |||||||
| chr17:59035093 | T | C | 1 | a0001c0001t0001g0339 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1754-3003A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59035093 | |||||||
| chr17:59035132 | TCACCGCA others(12): Show |
T | 1 | a0001c0001t0001g0246 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1754-3061_1754-304 others(23): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59035132 | |||||||
| chr17:59035251 | AG | A | 4 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0230 others(1): Show |
4 | HG00639.hp1 HG02630.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1754-3162delC | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59035251 | |||||||
| chr17:59035413 | T | G | 2 | a0001c0001t0002g0107 a0001c0001t0002g0111 |
2 | HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1754-3323A>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59035413 | |||||||
| chr17:59035755 | ACAAAAAA others(1): Show |
A | 7 | a0001c0001t0001g0232 a0001c0001t0001g0236 a0001c0001t0001g0237 others(4): Show |
7 | HG01099.hp2 HG01168.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1754-3673_1754-366 others(12): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59035755 | |||||||
| chr17:59035763 | C | A | 108 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(105): Show |
108 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.1754-3673G>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59035763 | |||||||
| chr17:59035958 | GC | G | 3 | a0001c0001t0004g0102 a0001c0001t0004g0103 a0001c0001t0004g0104 |
3 | HG03516.hp2 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1754-3869delG | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59035958 | |||||||
| chr17:59036191 | T | C | 3 | a0001c0001t0004g0102 a0001c0001t0004g0103 a0001c0001t0004g0104 |
3 | HG03516.hp2 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1754-4101A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59036191 | |||||||
| chr17:59036330 | A | C | 1 | a0001c0001t0002g0145 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1754-4240T>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59036330 | |||||||
| chr17:59036347 | A | C | 4 | a0001c0001t0007g0213 a0001c0001t0007g0214 a0001c0001t0007g0215 others(1): Show |
4 | HG01243.hp2 HG03471.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1754-4257T>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59036347 | |||||||
| chr17:59036443 | TGG | T | 4 | a0001c0001t0003g0073 a0001c0001t0003g0074 a0001c0001t0003g0076 others(1): Show |
4 | HG02486.hp2 HG03486.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1754-4355_1754-435 others(6): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59036443 | |||||||
| chr17:59036447 | G | GGGGTGT | 7 | a0001c0001t0002g0080 a0001c0001t0002g0112 a0001c0001t0002g0114 others(4): Show |
7 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.1754-4358_1754-435 others(10): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59036447 | |||||||
| chr17:59036447 | G | GGT | 120 | a0001c0001t0001g0225 a0001c0001t0001g0231 a0001c0001t0001g0232 others(117): Show |
120 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.1754-4359_1754-435 others(6): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59036447 | |||||||
| chr17:59036447 | G | GGTGT | 24 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(21): Show |
24 | HG00280.hp1 HG00733.hp2 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.1754-4361_1754-435 others(8): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59036447 | |||||||
| chr17:59036447 | G | GGTGTGT | 12 | a0001c0001t0001g0236 a0001c0001t0001g0237 a0001c0001t0001g0238 others(9): Show |
12 | HG01168.hp1 HG01261.hp1 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.1754-4363_1754-435 others(10): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59036447 | |||||||
| chr17:59036447 | G | GTGT | 3 | a0001c0001t0001g0261 a0001c0001t0001g0276 a0001c0001t0001g0330 |
3 | HG00544.hp1 HG03927.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.1754-4358_1754-435 others(7): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59036447 | |||||||
| chr17:59036447 | G | T | 7 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0230 others(4): Show |
7 | HG00639.hp1 HG02630.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1754-4357C>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59036447 | |||||||
| chr17:59036447 | GGT | G | 11 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0002g0175 others(8): Show |
11 | HG01175.hp1 HG02559.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1754-4359_1754-435 others(6): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59036447 | |||||||
| chr17:59036447 | GGTGT | G | 6 | a0001c0001t0002g0187 a0001c0001t0007g0213 a0001c0001t0007g0214 others(3): Show |
6 | HG00597.hp1 HG01243.hp2 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.1754-4361_1754-435 others(8): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59036447 | |||||||
| chr17:59036447 | GGTGTGTG others(1): Show |
G | 18 | a0001c0001t0001g0254 a0001c0001t0001g0339 a0001c0001t0003g0005 others(15): Show |
18 | HG00642.hp2 HG01099.hp2 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.1754-4365_1754-435 others(12): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59036447 | |||||||
| chr17:59036447 | GGTGTGTG others(5): Show |
G | 1 | a0001c0006t0003g0105 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1754-4369_1754-435 others(16): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59036447 | |||||||
| chr17:59036449 | T | G | 15 | a0001c0001t0002g0089 a0001c0001t0002g0098 a0001c0001t0002g0107 others(12): Show |
15 | HG01168.hp2 HG01169.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.1754-4359A>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59036449 | |||||||
| chr17:59036451 | T | G | 1 | a0001c0001t0002g0107 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1754-4361A>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59036451 | |||||||
| chr17:59036483 | T | C | 9 | a0001c0001t0002g0080 a0001c0001t0002g0112 a0001c0001t0002g0113 others(6): Show |
9 | HG01257.hp2 HG01258.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.1754-4393A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59036483 | |||||||
| chr17:59036593 | C | T | 1 | a0001c0001t0001g0235 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1754-4503G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59036593 | |||||||
| chr17:59036755 | A | C | 2 | a0001c0001t0001g0326 a0001c0001t0001g0332 |
2 | NA18612.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.1754-4665T>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59036755 | |||||||
| chr17:59036787 | C | G | 242 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(239): Show |
242 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.1754-4697G>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59036787 | |||||||
| chr17:59037136 | C | G | 97 | a0001c0001t0001g0339 a0001c0001t0002g0089 a0001c0001t0002g0098 others(94): Show |
97 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.1753+4677G>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59037136 | |||||||
| chr17:59037234 | C | T | 1 | a0001c0001t0002g0110 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1753+4579G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59037234 | |||||||
| chr17:59037292 | A | T | 1 | a0001c0001t0003g0005 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1753+4521T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59037292 | |||||||
| chr17:59037354 | C | T | 1 | a0001c0003t0006g0217 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1753+4459G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59037354 | |||||||
| chr17:59037402 | C | G | 4 | a0001c0001t0003g0073 a0001c0001t0003g0074 a0001c0001t0003g0075 others(1): Show |
4 | HG02486.hp2 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1753+4411G>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59037402 | |||||||
| chr17:59037427 | G | A | 61 | a0001c0001t0001g0339 a0001c0001t0003g0003 a0001c0001t0003g0004 others(58): Show |
61 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.1753+4386C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59037427 | |||||||
| chr17:59037442 | C | T | 1 | a0001c0001t0002g0119 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1753+4371G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59037442 | |||||||
| chr17:59037490 | G | A | 5 | a0001c0001t0003g0073 a0001c0001t0003g0074 a0001c0001t0003g0075 others(2): Show |
5 | HG02486.hp2 HG02630.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1753+4323C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59037490 | |||||||
| chr17:59037535 | G | T | 2 | a0001c0001t0003g0108 a0001c0001t0003g0109 |
2 | HG02451.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1753+4278C>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59037535 | |||||||
| chr17:59037557 | C | CA | 31 | a0001c0001t0002g0080 a0001c0001t0002g0112 a0001c0001t0002g0113 others(28): Show |
31 | HG00673.hp1 HG00735.hp2 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.1753+4255dupT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59037557 | |||||||
| chr17:59037557 | C | CAA | 14 | a0001c0001t0002g0117 a0001c0001t0002g0120 a0001c0001t0002g0121 others(11): Show |
14 | HG00558.hp2 HG01257.hp2 HG01258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1753+4254_1753+425 others(6): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59037557 | |||||||
| chr17:59037557 | C | CAAAAAAA others(10): Show |
1 | a0001c0003t0006g0212 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1753+4239_1753+425 others(21): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59037557 | |||||||
| chr17:59037557 | C | CAAAAAAA others(13): Show |
2 | a0001c0001t0007g0215 a0001c0001t0007g0216 |
2 | HG01243.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1753+4236_1753+425 others(24): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59037557 | |||||||
| chr17:59037557 | C | CAAAAAAA others(15): Show |
2 | a0001c0001t0007g0213 a0001c0001t0007g0214 |
2 | HG03471.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1753+4234_1753+425 others(26): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59037557 | |||||||
| chr17:59037557 | CA | C | 6 | a0001c0001t0001g0243 a0001c0001t0001g0246 a0001c0001t0001g0256 others(3): Show |
6 | HG00099.hp1 HG01358.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.1753+4255delT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59037557 | |||||||
| chr17:59037557 | CAA | C | 42 | a0001c0001t0001g0220 a0001c0001t0001g0223 a0001c0001t0001g0224 others(39): Show |
42 | HG00558.hp1 HG00597.hp2 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.1753+4254_1753+425 others(6): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59037557 | |||||||
| chr17:59037557 | CAAA | C | 68 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0225 others(65): Show |
68 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.1753+4253_1753+425 others(7): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59037557 | |||||||
| chr17:59037557 | CAAAAAAA others(4): Show |
C | 3 | a0001c0001t0003g0100 a0001c0001t0003g0101 a0001c0006t0003g0105 |
3 | HG01169.hp1 HG01884.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1753+4245_1753+425 others(15): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59037557 | |||||||
| chr17:59037557 | CAAAAAAA others(5): Show |
C | 22 | a0001c0001t0002g0089 a0001c0001t0002g0098 a0001c0001t0002g0119 others(19): Show |
22 | HG01168.hp2 HG02109.hp1 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.1753+4244_1753+425 others(16): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59037557 | |||||||
| chr17:59037557 | CAAAAAAA others(9): Show |
C | 1 | a0001c0001t0002g0177 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1753+4240_1753+425 others(20): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59037557 | |||||||
| chr17:59037557 | CAAAAAAA others(13): Show |
C | 74 | a0001c0001t0001g0339 a0001c0001t0003g0003 a0001c0001t0003g0004 others(71): Show |
74 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.1753+4236_1753+425 others(24): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59037557 | |||||||
| chr17:59037584 | A | T | 1 | a0001c0001t0001g0308 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1753+4229T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59037584 | |||||||
| chr17:59037591 | G | C | 115 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(112): Show |
115 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.1753+4222C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59037591 | |||||||
| chr17:59037653 | A | T | 1 | a0001c0001t0001g0261 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1753+4160T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59037653 | |||||||
| chr17:59038078 | C | G | 1 | a0001c0001t0001g0254 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1753+3735G>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59038078 | |||||||
| chr17:59038090 | C | T | 1 | a0001c0001t0001g0303 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1753+3723G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59038090 | |||||||
| chr17:59038155 | T | C | 3 | a0001c0001t0004g0102 a0001c0001t0004g0103 a0001c0001t0004g0104 |
3 | HG03516.hp2 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1753+3658A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59038155 | |||||||
| chr17:59038305 | T | C | 1 | a0001c0001t0002g0161 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1753+3508A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59038305 | |||||||
| chr17:59038338 | T | A | 1 | a0001c0001t0001g0227 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1753+3475A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59038338 | |||||||
| chr17:59038486 | T | C | 1 | a0001c0001t0002g0195 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1753+3327A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59038486 | |||||||
| chr17:59038753 | T | C | 8 | a0001c0001t0007g0213 a0001c0001t0007g0214 a0001c0001t0007g0215 others(5): Show |
8 | HG00642.hp2 HG01243.hp2 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.1753+3060A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59038753 | |||||||
| chr17:59038761 | C | G | 1 | a0001c0001t0001g0325 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1753+3052G>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59038761 | |||||||
| chr17:59038810 | T | G | 1 | a0001c0001t0001g0246 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1753+3003A>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59038810 | |||||||
| chr17:59039071 | C | T | 3 | a0001c0001t0003g0086 a0001c0001t0003g0094 a0001c0001t0004g0091 |
3 | HG02615.hp1 HG03209.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1753+2742G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59039071 | |||||||
| chr17:59039151 | A | T | 1 | a0001c0001t0001g0246 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1753+2662T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59039151 | |||||||
| chr17:59039323 | A | C | 1 | a0001c0003t0006g0217 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1753+2490T>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59039323 | |||||||
| chr17:59039350 | CT | C | 62 | a0001c0001t0001g0246 a0001c0001t0001g0339 a0001c0001t0003g0003 others(59): Show |
62 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.1753+2462delA | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59039350 | |||||||
| chr17:59039448 | G | A | 96 | a0001c0001t0001g0339 a0001c0001t0002g0089 a0001c0001t0002g0098 others(93): Show |
96 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.1753+2365C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59039448 | |||||||
| chr17:59039491 | C | G | 4 | a0001c0001t0002g0150 a0001c0001t0002g0154 a0001c0001t0002g0211 others(1): Show |
4 | HG00099.hp1 HG02602.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.1753+2322G>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59039491 | |||||||
| chr17:59039510 | C | T | 1 | a0001c0006t0003g0105 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1753+2303G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59039510 | |||||||
| chr17:59039883 | A | G | 11 | a0001c0001t0002g0080 a0001c0001t0002g0112 a0001c0001t0002g0113 others(8): Show |
11 | HG01257.hp2 HG01258.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1753+1930T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59039883 | |||||||
| chr17:59039974 | T | C | 10 | a0001c0001t0003g0062 a0001c0001t0003g0063 a0001c0001t0003g0064 others(7): Show |
10 | HG02055.hp1 HG02572.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1753+1839A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59039974 | |||||||
| chr17:59040144 | G | A | 1 | a0001c0001t0001g0325 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1753+1669C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59040144 | |||||||
| chr17:59040356 | G | A | 5 | a0001c0001t0003g0073 a0001c0001t0003g0074 a0001c0001t0003g0075 others(2): Show |
5 | HG02486.hp2 HG02630.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1753+1457C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59040356 | |||||||
| chr17:59040461 | C | T | 4 | a0001c0003t0006g0212 a0001c0003t0006g0217 a0001c0003t0006g0218 others(1): Show |
4 | HG00642.hp2 HG03704.hp2 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.1753+1352G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59040461 | |||||||
| chr17:59040640 | G | T | 1 | a0001c0001t0001g0246 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1753+1173C>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59040640 | |||||||
| chr17:59040760 | T | C | 98 | a0001c0001t0001g0339 a0001c0001t0002g0089 a0001c0001t0002g0098 others(95): Show |
98 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.1753+1053A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59040760 | |||||||
| chr17:59040784 | C | T | 3 | a0001c0001t0004g0102 a0001c0001t0004g0103 a0001c0001t0004g0104 |
3 | HG03516.hp2 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1753+1029G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59040784 | |||||||
| chr17:59040785 | G | A | 11 | a0001c0001t0002g0080 a0001c0001t0002g0112 a0001c0001t0002g0113 others(8): Show |
11 | HG01257.hp2 HG01258.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1753+1028C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59040785 | |||||||
| chr17:59040843 | A | C | 1 | a0001c0001t0003g0077 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1753+970T>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59040843 | |||||||
| chr17:59040843 | A | G | 221 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(218): Show |
221 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.1753+970T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59040843 | |||||||
| chr17:59040873 | C | T | 2 | a0001c0001t0002g0120 a0001c0001t0002g0121 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1753+940G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59040873 | |||||||
| chr17:59040903 | G | A | 1 | a0002c0002t0002g0205 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1753+910C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59040903 | |||||||
| chr17:59040907 | G | A | 1 | a0001c0001t0001g0309 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1753+906C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59040907 | |||||||
| chr17:59040918 | C | T | 3 | a0001c0001t0002g0132 a0001c0001t0002g0157 a0001c0001t0002g0158 |
3 | HG01106.hp1 HG01358.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1753+895G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59040918 | |||||||
| chr17:59041022 | C | G | 3 | a0001c0001t0002g0119 a0001c0001t0002g0120 a0001c0001t0002g0121 |
3 | HG01257.hp2 HG01258.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1753+791G>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59041022 | |||||||
| chr17:59041036 | G | A | 1 | a0001c0001t0003g0051 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1753+777C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59041036 | |||||||
| chr17:59041126 | CTTTTAAT others(6): Show |
C | 1 | a0001c0001t0001g0247 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1753+674_1753+686d others(15): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59041126 | |||||||
| chr17:59041285 | G | A | 1 | a0001c0001t0001g0307 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1753+528C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59041285 | |||||||
| chr17:59041310 | T | C | 1 | a0001c0001t0003g0097 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1753+503A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59041310 | |||||||
| chr17:59041331 | T | A | 1 | a0001c0001t0001g0261 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1753+482A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59041331 | |||||||
| chr17:59041752 | C | T | 8 | a0001c0001t0007g0213 a0001c0001t0007g0214 a0001c0001t0007g0215 others(5): Show |
8 | HG00642.hp2 HG01243.hp2 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.1753+61G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59041752 | |||||||
| chr17:59042057 | C | T | 1 | a0001c0001t0009g0165 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1668-159G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042057 | |||||||
| chr17:59042098 | C | T | 2 | a0001c0001t0002g0107 a0001c0001t0002g0111 |
2 | HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1668-200G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042098 | |||||||
| chr17:59042105 | G | A | 6 | a0001c0001t0003g0081 a0001c0001t0003g0082 a0001c0001t0003g0083 others(3): Show |
6 | HG02559.hp1 HG02647.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1668-207C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042105 | |||||||
| chr17:59042142 | T | A | 1 | a0001c0001t0001g0301 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1668-244A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042142 | |||||||
| chr17:59042153 | G | A | 1 | a0001c0001t0001g0246 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1668-255C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042153 | |||||||
| chr17:59042251 | C | T | 6 | a0001c0001t0001g0232 a0001c0001t0001g0236 a0001c0001t0001g0237 others(3): Show |
6 | HG01168.hp1 HG02559.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1668-353G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042251 | |||||||
| chr17:59042270 | G | A | 1 | a0001c0001t0002g0210 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1668-372C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042270 | |||||||
| chr17:59042293 | G | A | 7 | a0001c0001t0002g0080 a0001c0001t0002g0112 a0001c0001t0002g0113 others(4): Show |
7 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.1668-395C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042293 | |||||||
| chr17:59042304 | A | G | 2 | a0001c0001t0002g0140 a0001c0001t0002g0142 |
2 | HG00558.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.1668-406T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042304 | |||||||
| chr17:59042374 | C | CA | 11 | a0001c0001t0001g0243 a0001c0001t0001g0315 a0001c0001t0001g0316 others(8): Show |
11 | HG02257.hp2 HG02486.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.1668-477dupT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042374 | |||||||
| chr17:59042430 | TTAA | T | 3 | a0001c0001t0003g0033 a0001c0001t0008g0026 a0001c0001t0008g0027 |
3 | NA18998.hp1 NA19056.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1668-535_1668-533d others(5): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042430 | |||||||
| chr17:59042430 | TTAAAAAA | T | 5 | a0001c0001t0003g0005 a0001c0001t0003g0036 a0001c0001t0003g0046 others(2): Show |
5 | HG01099.hp1 HG01192.hp2 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.1668-539_1668-533d others(9): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042430 | |||||||
| chr17:59042430 | TTAAAAAA others(1): Show |
T | 7 | a0001c0001t0003g0009 a0001c0001t0003g0039 a0001c0001t0003g0043 others(4): Show |
7 | HG00438.hp1 HG00733.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.1668-540_1668-533d others(10): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042430 | |||||||
| chr17:59042430 | TTAAAAAA others(4): Show |
T | 1 | a0001c0001t0012g0002 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1668-543_1668-533d others(13): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042430 | |||||||
| chr17:59042430 | TTAAAAAA others(7): Show |
T | 9 | a0001c0001t0001g0282 a0001c0001t0007g0213 a0001c0001t0007g0214 others(6): Show |
9 | HG00642.hp2 HG01243.hp2 HG03471.hp1 others(6): Show |
intron_variant | MODIFIER | c.1668-546_1668-533d others(16): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042430 | |||||||
| chr17:59042431 | T | A | 198 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(195): Show |
198 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.1668-533A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042431 | |||||||
| chr17:59042431 | TA | T | 29 | a0001c0001t0002g0080 a0001c0001t0002g0112 a0001c0001t0002g0113 others(26): Show |
29 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(26): Show |
intron_variant | MODIFIER | c.1668-534delT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042431 | |||||||
| chr17:59042437 | A | AATATATA others(3): Show |
1 | a0001c0001t0003g0101 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1668-540_1668-539i others(12): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042437 | |||||||
| chr17:59042437 | A | AATATATA others(11): Show |
2 | a0001c0001t0003g0099 a0001c0001t0003g0100 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1668-540_1668-539i others(20): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042437 | |||||||
| chr17:59042437 | A | ATATATAT others(28): Show |
1 | a0001c0001t0003g0025 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1668-540_1668-539i others(37): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042437 | |||||||
| chr17:59042437 | AAAAAAAA others(9): Show |
A | 5 | a0001c0001t0001g0232 a0001c0001t0001g0236 a0001c0001t0001g0237 others(2): Show |
5 | HG01168.hp1 HG02559.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1668-555_1668-540d others(18): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042437 | |||||||
| chr17:59042438 | AAAAAAAA others(8): Show |
A | 17 | a0001c0001t0001g0227 a0001c0001t0001g0228 a0001c0001t0001g0229 others(14): Show |
17 | HG00639.hp1 HG00639.hp2 HG00673.hp2 others(14): Show |
intron_variant | MODIFIER | c.1668-555_1668-541d others(17): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042438 | |||||||
| chr17:59042439 | A | AATATATA others(11): Show |
2 | a0001c0001t0010g0078 a0001c0001t0010g0090 |
2 | HG02109.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1668-542_1668-541i others(20): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042439 | |||||||
| chr17:59042439 | A | AATATATA others(13): Show |
1 | a0001c0001t0003g0079 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1668-542_1668-541i others(22): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042439 | |||||||
| chr17:59042439 | A | ATATATAT others(14): Show |
1 | a0001c0001t0008g0017 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1668-542_1668-541i others(23): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042439 | |||||||
| chr17:59042439 | A | T | 4 | a0001c0001t0003g0025 a0001c0001t0003g0099 a0001c0001t0003g0100 others(1): Show |
4 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.1668-541T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042439 | |||||||
| chr17:59042439 | AAAAAAAA others(7): Show |
A | 3 | a0001c0001t0003g0086 a0001c0001t0003g0094 a0001c0001t0004g0091 |
3 | HG02615.hp1 HG03209.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1668-555_1668-542d others(16): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042439 | |||||||
| chr17:59042439 | AAAAAAAA others(9): Show |
A | 3 | a0001c0001t0001g0238 a0001c0001t0001g0252 a0001c0001t0001g0253 |
3 | HG03098.hp1 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1668-557_1668-542d others(18): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042439 | |||||||
| chr17:59042440 | AAAAAAAA others(6): Show |
A | 1 | a0001c0001t0001g0297 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1668-555_1668-543d others(15): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042440 | |||||||
| chr17:59042440 | AAAAAAAA others(8): Show |
A | 70 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(67): Show |
70 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.1668-557_1668-543d others(17): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042440 | |||||||
| chr17:59042441 | A | AATATATA others(3): Show |
1 | a0001c0001t0003g0012 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1668-544_1668-543i others(12): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042441 | |||||||
| chr17:59042441 | A | AATATATA others(11): Show |
1 | a0001c0001t0003g0092 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1668-544_1668-543i others(20): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042441 | |||||||
| chr17:59042441 | A | AATATATA others(13): Show |
2 | a0001c0001t0003g0087 a0001c0001t0003g0088 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1668-544_1668-543i others(22): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042441 | |||||||
| chr17:59042441 | A | AATATATA others(15): Show |
1 | a0001c0001t0003g0021 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1668-544_1668-543i others(24): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042441 | |||||||
| chr17:59042441 | A | AATATATA others(17): Show |
1 | a0001c0001t0003g0020 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1668-544_1668-543i others(26): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042441 | |||||||
| chr17:59042441 | A | ATATATAT others(2): Show |
3 | a0001c0001t0003g0081 a0001c0001t0003g0095 a0001c0001t0013g0024 |
3 | HG02647.hp1 HG03017.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1668-544_1668-543i others(11): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042441 | |||||||
| chr17:59042441 | A | ATATATAT others(8): Show |
1 | a0001c0001t0003g0053 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1668-544_1668-543i others(17): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042441 | |||||||
| chr17:59042441 | A | ATATATAT others(34): Show |
1 | a0001c0001t0003g0047 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1668-544_1668-543i others(43): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042441 | |||||||
| chr17:59042441 | A | T | 14 | a0001c0001t0002g0089 a0001c0001t0002g0098 a0001c0001t0003g0025 others(11): Show |
14 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.1668-543T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042441 | |||||||
| chr17:59042441 | AAAAAAAA others(5): Show |
A | 2 | a0001c0001t0001g0318 a0001c0001t0001g0319 |
2 | NA18943.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.1668-555_1668-544d others(14): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042441 | |||||||
| chr17:59042441 | AAAAAAAA others(7): Show |
A | 1 | a0001c0001t0001g0241 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1668-557_1668-544d others(16): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042441 | |||||||
| chr17:59042441 | AAAAAAAA others(9): Show |
A | 1 | a0001c0001t0001g0224 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1668-559_1668-544d others(18): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042441 | |||||||
| chr17:59042442 | AAAAAAAA others(8): Show |
A | 14 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0231 others(11): Show |
14 | HG01169.hp2 HG02004.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.1668-559_1668-545d others(17): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042442 | |||||||
| chr17:59042443 | A | AATATATA others(3): Show |
1 | a0001c0001t0003g0069 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1668-546_1668-545i others(12): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042443 | |||||||
| chr17:59042443 | A | AATATATA others(5): Show |
1 | a0001c0001t0003g0061 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1668-546_1668-545i others(14): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042443 | |||||||
| chr17:59042443 | A | AATATATA others(13): Show |
2 | a0001c0001t0003g0018 a0001c0001t0003g0019 |
2 | NA19001.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.1668-546_1668-545i others(22): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042443 | |||||||
| chr17:59042443 | A | ATATATAT others(4): Show |
1 | a0001c0001t0003g0083 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1668-546_1668-545i others(13): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042443 | |||||||
| chr17:59042443 | A | ATATATAT others(8): Show |
1 | a0001c0001t0003g0057 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1668-546_1668-545i others(17): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042443 | |||||||
| chr17:59042443 | A | ATATATAT others(12): Show |
1 | a0001c0001t0003g0056 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1668-546_1668-545i others(21): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042443 | |||||||
| chr17:59042443 | A | ATATATAT others(14): Show |
3 | a0001c0001t0001g0339 a0001c0001t0003g0011 a0001c0001t0003g0122 |
3 | NA18944.hp1 NA18949.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.1668-546_1668-545i others(23): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042443 | |||||||
| chr17:59042443 | A | ATATATAT others(16): Show |
1 | a0001c0001t0003g0015 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1668-546_1668-545i others(25): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042443 | |||||||
| chr17:59042443 | A | ATATATAT others(28): Show |
1 | a0001c0001t0003g0037 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1668-546_1668-545i others(37): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042443 | |||||||
| chr17:59042443 | A | T | 27 | a0001c0001t0002g0089 a0001c0001t0002g0098 a0001c0001t0003g0012 others(24): Show |
27 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(24): Show |
intron_variant | MODIFIER | c.1668-545T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042443 | |||||||
| chr17:59042443 | AAAAAAAA others(7): Show |
A | 1 | a0001c0001t0001g0321 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1668-559_1668-546d others(16): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042443 | |||||||
| chr17:59042444 | AAAAAAAT others(8): Show |
A | 3 | a0001c0001t0001g0234 a0001c0001t0001g0307 a0001c0001t0001g0330 |
3 | HG01496.hp1 HG03927.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.1668-561_1668-547d others(17): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042444 | |||||||
| chr17:59042445 | A | AATATATA others(5): Show |
1 | a0001c0001t0003g0054 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1668-548_1668-547i others(14): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042445 | |||||||
| chr17:59042445 | A | AATATATA others(13): Show |
1 | a0001c0001t0003g0032 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1668-548_1668-547i others(22): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042445 | |||||||
| chr17:59042445 | A | AATATATA others(17): Show |
1 | a0001c0001t0003g0014 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1668-548_1668-547i others(26): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042445 | |||||||
| chr17:59042445 | A | AATATATA others(19): Show |
1 | a0001c0006t0003g0105 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1668-548_1668-547i others(28): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042445 | |||||||
| chr17:59042445 | A | AATATATA others(23): Show |
1 | a0001c0001t0003g0028 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1668-548_1668-547i others(32): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042445 | |||||||
| chr17:59042445 | A | AATATATA others(31): Show |
1 | a0001c0001t0003g0055 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1668-548_1668-547i others(40): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042445 | |||||||
| chr17:59042445 | A | ATATATAT others(4): Show |
4 | a0001c0001t0003g0008 a0001c0001t0003g0016 a0001c0001t0003g0062 others(1): Show |
4 | HG02027.hp1 HG02809.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1668-548_1668-547i others(13): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042445 | |||||||
| chr17:59042445 | A | ATATATAT others(6): Show |
1 | a0001c0001t0003g0084 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1668-548_1668-547i others(15): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042445 | |||||||
| chr17:59042445 | A | ATATATAT others(10): Show |
1 | a0001c0001t0003g0058 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1668-548_1668-547i others(19): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042445 | |||||||
| chr17:59042445 | A | ATATATAT others(14): Show |
1 | a0001c0001t0003g0045 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1668-548_1668-547i others(23): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042445 | |||||||
| chr17:59042445 | A | ATATATAT others(18): Show |
1 | a0001c0001t0003g0010 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1668-548_1668-547i others(27): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042445 | |||||||
| chr17:59042445 | A | ATATATAT others(20): Show |
2 | a0001c0001t0003g0013 a0001c0001t0003g0022 |
2 | HG00099.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1668-548_1668-547i others(29): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042445 | |||||||
| chr17:59042445 | A | ATATATAT others(24): Show |
1 | a0001c0001t0003g0048 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1668-548_1668-547i others(33): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042445 | |||||||
| chr17:59042445 | A | ATATATAT others(26): Show |
2 | a0001c0001t0003g0007 a0001c0001t0003g0029 |
2 | HG01261.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1668-548_1668-547i others(35): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042445 | |||||||
| chr17:59042445 | A | ATATATAT others(34): Show |
1 | a0001c0001t0003g0034 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1668-548_1668-547i others(43): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042445 | |||||||
| chr17:59042445 | A | T | 47 | a0001c0001t0001g0339 a0001c0001t0002g0089 a0001c0001t0002g0098 others(44): Show |
47 | HG00741.hp1 HG01106.hp2 HG01168.hp2 others(44): Show |
intron_variant | MODIFIER | c.1668-547T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042445 | |||||||
| chr17:59042445 | AAAAAATA others(7): Show |
A | 1 | a0001c0001t0001g0246 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1668-561_1668-548d others(16): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042445 | |||||||
| chr17:59042447 | A | AT | 4 | a0001c0001t0002g0111 a0001c0001t0002g0129 a0001c0001t0002g0137 others(1): Show |
4 | HG02486.hp1 HG04204.hp2 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.1668-550_1668-549i others(3): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042447 | |||||||
| chr17:59042447 | A | ATATATAT others(14): Show |
2 | a0001c0001t0003g0030 a0001c0001t0003g0031 |
2 | NA18952.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.1668-550_1668-549i others(23): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042447 | |||||||
| chr17:59042447 | A | ATATATAT others(18): Show |
1 | a0001c0001t0003g0023 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1668-550_1668-549i others(27): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042447 | |||||||
| chr17:59042447 | A | ATATATAT others(22): Show |
4 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0052 others(1): Show |
4 | HG01978.hp2 HG03831.hp1 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.1668-550_1668-549i others(31): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042447 | |||||||
| chr17:59042447 | A | T | 92 | a0001c0001t0001g0339 a0001c0001t0002g0080 a0001c0001t0002g0089 others(89): Show |
92 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.1668-549T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042447 | |||||||
| chr17:59042449 | A | AAT | 9 | a0001c0001t0002g0128 a0001c0001t0002g0164 a0001c0001t0002g0188 others(6): Show |
9 | HG00323.hp1 NA18944.hp2 NA18994.hp1 others(6): Show |
intron_variant | MODIFIER | c.1668-553_1668-552d others(4): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042449 | |||||||
| chr17:59042449 | A | AATATATA others(5): Show |
1 | a0001c0001t0003g0064 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1668-563_1668-552d others(14): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042449 | |||||||
| chr17:59042449 | A | AT | 3 | a0001c0001t0002g0126 a0001c0001t0002g0143 a0001c0001t0002g0147 |
3 | HG02071.hp1 NA18995.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1668-552_1668-551i others(3): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042449 | |||||||
| chr17:59042449 | A | ATATATAT others(22): Show |
1 | a0001c0001t0003g0071 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1668-552_1668-551i others(31): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042449 | |||||||
| chr17:59042449 | A | ATATATAT others(38): Show |
1 | a0001c0001t0003g0051 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1668-552_1668-551i others(47): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042449 | |||||||
| chr17:59042449 | A | T | 138 | a0001c0001t0001g0339 a0001c0001t0002g0080 a0001c0001t0002g0089 others(135): Show |
138 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.1668-551T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042449 | |||||||
| chr17:59042450 | AT | A | 4 | a0001c0001t0002g0210 a0001c0001t0003g0108 a0001c0001t0009g0165 others(1): Show |
4 | HG02258.hp2 HG02293.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1668-553delA | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042450 | |||||||
| chr17:59042450 | ATAT | A | 5 | a0001c0001t0003g0073 a0001c0001t0003g0074 a0001c0001t0003g0075 others(2): Show |
5 | HG02486.hp2 HG02630.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.1668-555_1668-553d others(5): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042450 | |||||||
| chr17:59042451 | T | A | 12 | a0001c0001t0001g0282 a0001c0001t0003g0005 a0001c0001t0003g0009 others(9): Show |
12 | HG00438.hp1 HG01515.hp2 HG01943.hp1 others(9): Show |
intron_variant | MODIFIER | c.1668-553A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042451 | |||||||
| chr17:59042453 | T | A | 2 | a0001c0001t0003g0108 a0001c0001t0003g0109 |
2 | HG02451.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1668-555A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042453 | |||||||
| chr17:59042472 | A | C | 6 | a0001c0001t0003g0009 a0001c0001t0003g0043 a0001c0001t0005g0040 others(3): Show |
6 | HG00438.hp1 NA18945.hp1 NA19006.hp2 others(3): Show |
intron_variant | MODIFIER | c.1668-574T>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042472 | |||||||
| chr17:59042624 | G | C | 1 | a0001c0001t0003g0106 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1668-726C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042624 | |||||||
| chr17:59042730 | T | A | 1 | a0001c0001t0001g0246 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1668-832A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042730 | |||||||
| chr17:59042742 | G | A | 12 | a0001c0001t0003g0061 a0001c0001t0003g0062 a0001c0001t0003g0063 others(9): Show |
12 | HG02055.hp1 HG02572.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1668-844C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042742 | |||||||
| chr17:59042894 | C | G | 1 | a0001c0001t0001g0339 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1668-996G>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042894 | |||||||
| chr17:59043063 | T | C | 12 | a0001c0001t0003g0061 a0001c0001t0003g0062 a0001c0001t0003g0063 others(9): Show |
12 | HG02055.hp1 HG02572.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1668-1165A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59043063 | |||||||
| chr17:59043165 | T | G | 1 | a0001c0006t0003g0105 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1668-1267A>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59043165 | |||||||
| chr17:59043419 | A | G | 2 | a0001c0001t0001g0315 a0001c0001t0001g0316 |
2 | NA18963.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1668-1521T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59043419 | |||||||
| chr17:59043631 | G | A | 2 | a0001c0001t0001g0234 a0001c0001t0001g0241 |
2 | NA18951.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1668-1733C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59043631 | |||||||
| chr17:59043635 | C | A | 8 | a0001c0001t0007g0213 a0001c0001t0007g0214 a0001c0001t0007g0215 others(5): Show |
8 | HG00642.hp2 HG01243.hp2 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.1668-1737G>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59043635 | |||||||
| chr17:59043787 | T | C | 1 | a0001c0001t0001g0227 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1668-1889A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59043787 | |||||||
| chr17:59043952 | C | T | 128 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(125): Show |
128 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(125): Show |
intron_variant | MODIFIER | c.1668-2054G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59043952 | |||||||
| chr17:59043961 | T | C | 3 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0001c0001t0001g0312 |
3 | NA18993.hp2 NA19086.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1668-2063A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59043961 | |||||||
| chr17:59044393 | T | G | 1 | a0001c0001t0001g0328 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1668-2495A>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59044393 | |||||||
| chr17:59044398 | T | A | 1 | a0001c0006t0003g0105 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1668-2500A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59044398 | |||||||
| chr17:59044421 | G | A | 1 | a0001c0006t0003g0105 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1668-2523C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59044421 | |||||||
| chr17:59044875 | A | G | 3 | a0001c0001t0004g0102 a0001c0001t0004g0103 a0001c0001t0004g0104 |
3 | HG03516.hp2 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1667+2808T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59044875 | |||||||
| chr17:59044932 | C | T | 1 | a0001c0001t0003g0106 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1667+2751G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59044932 | |||||||
| chr17:59045453 | C | T | 1 | a0001c0001t0003g0106 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1667+2230G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59045453 | |||||||
| chr17:59045466 | C | T | 1 | a0001c0001t0001g0302 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1667+2217G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59045466 | |||||||
| chr17:59045470 | T | C | 120 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(117): Show |
120 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.1667+2213A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59045470 | |||||||
| chr17:59045545 | A | C | 5 | a0001c0001t0003g0079 a0001c0001t0003g0097 a0001c0001t0003g0099 others(2): Show |
5 | HG01168.hp2 HG01169.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.1667+2138T>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59045545 | |||||||
| chr17:59045564 | G | A | 1 | a0001c0001t0001g0338 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1667+2119C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59045564 | |||||||
| chr17:59045915 | C | T | 4 | a0001c0001t0001g0326 a0001c0001t0001g0329 a0001c0001t0001g0332 others(1): Show |
4 | HG00621.hp1 NA18612.hp1 NA18949.hp2 others(1): Show |
intron_variant | MODIFIER | c.1667+1768G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59045915 | |||||||
| chr17:59045970 | C | T | 11 | a0001c0001t0002g0080 a0001c0001t0002g0112 a0001c0001t0002g0113 others(8): Show |
11 | HG01257.hp2 HG01258.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1667+1713G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59045970 | |||||||
| chr17:59046015 | CA | C | 7 | a0001c0001t0002g0209 a0001c0001t0002g0210 a0002c0002t0002g0125 others(4): Show |
7 | HG01952.hp2 HG02257.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1667+1667delT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59046015 | |||||||
| chr17:59046164 | T | C | 1 | a0001c0001t0003g0058 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1667+1519A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59046164 | |||||||
| chr17:59046212 | T | C | 5 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0006 others(2): Show |
5 | HG01106.hp2 HG01978.hp2 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.1667+1471A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59046212 | |||||||
| chr17:59046314 | C | T | 1 | a0001c0001t0002g0127 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1667+1369G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59046314 | |||||||
| chr17:59046540 | G | GT | 13 | a0001c0001t0001g0225 a0001c0001t0001g0235 a0001c0001t0001g0238 others(10): Show |
13 | HG01978.hp1 HG02145.hp2 HG03098.hp1 others(10): Show |
intron_variant | MODIFIER | c.1667+1142dupA | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59046540 | |||||||
| chr17:59046550 | T | C | 1 | a0001c0001t0003g0032 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1667+1133A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59046550 | |||||||
| chr17:59046570 | A | ACT | 247 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(244): Show |
247 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.1667+1111_1667+111 others(6): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59046570 | |||||||
| chr17:59046741 | C | T | 1 | a0001c0001t0003g0066 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1667+942G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59046741 | |||||||
| chr17:59046921 | G | A | 7 | a0001c0001t0002g0080 a0001c0001t0002g0112 a0001c0001t0002g0113 others(4): Show |
7 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.1667+762C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59046921 | |||||||
| chr17:59047011 | G | A | 1 | a0001c0001t0001g0233 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1667+672C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59047011 | |||||||
| chr17:59047075 | T | C | 1 | a0001c0001t0001g0268 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1667+608A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59047075 | |||||||
| chr17:59047077 | C | T | 1 | a0001c0001t0001g0336 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1667+606G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59047077 | |||||||
| chr17:59047147 | C | T | 2 | a0001c0001t0002g0191 a0001c0001t0002g0192 |
2 | NA18970.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.1667+536G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59047147 | |||||||
| chr17:59047662 | G | A | 3 | a0001c0001t0004g0102 a0001c0001t0004g0103 a0001c0001t0004g0104 |
3 | HG03516.hp2 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1667+21C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59047662 | |||||||
| chr17:59048007 | A | G | 1 | a0001c0001t0002g0110 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1531-188T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 15/23 | chr17 | 59048007 | |||||||
| chr17:59048019 | G | A | 1 | a0001c0001t0001g0336 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1531-200C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 15/23 | chr17 | 59048019 | |||||||
| chr17:59048068 | C | G | 1 | a0001c0001t0003g0006 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1531-249G>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 15/23 | chr17 | 59048068 | |||||||
| chr17:59048300 | A | C | 1 | a0001c0001t0002g0194 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1531-481T>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 15/23 | chr17 | 59048300 | |||||||
| chr17:59048343 | C | G | 8 | a0001c0001t0001g0260 a0001c0001t0001g0289 a0001c0001t0001g0290 others(5): Show |
8 | HG00642.hp1 HG00733.hp1 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.1531-524G>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 15/23 | chr17 | 59048343 | |||||||
| chr17:59048347 | C | T | 2 | a0001c0001t0003g0028 a0001c0001t0012g0002 |
2 | HG01515.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1531-528G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 15/23 | chr17 | 59048347 | |||||||
| chr17:59048462 | T | G | 1 | a0001c0001t0001g0309 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1531-643A>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 15/23 | chr17 | 59048462 | |||||||
| chr17:59048564 | T | G | 1 | a0001c0001t0001g0264 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1530+614A>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 15/23 | chr17 | 59048564 | |||||||
| chr17:59048890 | C | T | 11 | a0001c0001t0003g0061 a0001c0001t0003g0062 a0001c0001t0003g0063 others(8): Show |
11 | HG02055.hp1 HG02572.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.1530+288G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 15/23 | chr17 | 59048890 | |||||||
| chr17:59049481 | G | A | 73 | a0001c0001t0001g0339 a0001c0001t0003g0003 a0001c0001t0003g0004 others(70): Show |
73 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.1315-88C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 14/23 | chr17 | 59049481 | |||||||
| chr17:59049486 | T | A | 4 | a0001c0001t0003g0073 a0001c0001t0003g0074 a0001c0001t0003g0075 others(1): Show |
4 | HG02486.hp2 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1315-93A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 14/23 | chr17 | 59049486 | |||||||
| chr17:59050008 | A | G | 1 | a0001c0001t0002g0209 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1315-615T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 14/23 | chr17 | 59050008 | |||||||
| chr17:59050170 | G | A | 1 | a0001c0001t0003g0047 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1315-777C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 14/23 | chr17 | 59050170 | |||||||
| chr17:59050318 | G | A | 2 | a0001c0001t0001g0234 a0001c0001t0001g0241 |
2 | NA18951.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1314+896C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 14/23 | chr17 | 59050318 | |||||||
| chr17:59050319 | C | T | 2 | a0001c0001t0001g0234 a0001c0001t0001g0241 |
2 | NA18951.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1314+895G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 14/23 | chr17 | 59050319 | |||||||
| chr17:59050363 | C | G | 5 | a0001c0001t0003g0073 a0001c0001t0003g0074 a0001c0001t0003g0075 others(2): Show |
5 | HG02486.hp2 HG02630.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1314+851G>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 14/23 | chr17 | 59050363 | |||||||
| chr17:59050556 | C | T | 2 | a0001c0001t0002g0151 a0001c0001t0002g0152 |
2 | HG03834.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1314+658G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 14/23 | chr17 | 59050556 | |||||||
| chr17:59050838 | G | A | 1 | a0001c0001t0001g0246 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1314+376C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 14/23 | chr17 | 59050838 | |||||||
| chr17:59050973 | CCTT | C | 13 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(10): Show |
13 | HG00558.hp2 HG00673.hp1 HG02155.hp2 others(10): Show |
intron_variant | MODIFIER | c.1314+238_1314+240d others(5): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 14/23 | chr17 | 59050973 | |||||||
| chr17:59051025 | A | G | 1 | a0001c0001t0002g0107 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1314+189T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 14/23 | chr17 | 59051025 | |||||||
| chr17:59051449 | G | T | 1 | a0001c0001t0003g0061 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1200-121C>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59051449 | |||||||
| chr17:59051754 | G | A | 4 | a0001c0001t0003g0073 a0001c0001t0003g0074 a0001c0001t0003g0075 others(1): Show |
4 | HG02486.hp2 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1200-426C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59051754 | |||||||
| chr17:59051769 | C | T | 1 | a0001c0001t0003g0077 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1200-441G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59051769 | |||||||
| chr17:59051863 | T | G | 130 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(127): Show |
130 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.1200-535A>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59051863 | |||||||
| chr17:59052008 | C | T | 3 | a0001c0001t0004g0102 a0001c0001t0004g0103 a0001c0001t0004g0104 |
3 | HG03516.hp2 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1200-680G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59052008 | |||||||
| chr17:59052213 | TA | T | 246 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(243): Show |
246 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.1200-886delT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59052213 | |||||||
| chr17:59052280 | C | T | 3 | a0001c0001t0004g0102 a0001c0001t0004g0103 a0001c0001t0004g0104 |
3 | HG03516.hp2 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1200-952G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59052280 | |||||||
| chr17:59052489 | T | A | 1 | a0001c0006t0003g0105 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1200-1161A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59052489 | |||||||
| chr17:59052521 | C | A | 92 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(89): Show |
92 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.1200-1193G>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59052521 | |||||||
| chr17:59052531 | C | T | 5 | a0001c0001t0003g0073 a0001c0001t0003g0074 a0001c0001t0003g0075 others(2): Show |
5 | HG02486.hp2 HG02630.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1200-1203G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59052531 | |||||||
| chr17:59052551 | T | C | 1 | a0001c0001t0002g0169 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1200-1223A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59052551 | |||||||
| chr17:59052661 | AAGAG | A | 7 | a0001c0001t0002g0080 a0001c0001t0002g0112 a0001c0001t0002g0113 others(4): Show |
7 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.1200-1337_1200-133 others(8): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59052661 | |||||||
| chr17:59052753 | G | C | 1 | a0001c0001t0002g0140 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1200-1425C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59052753 | |||||||
| chr17:59052800 | C | T | 11 | a0001c0001t0002g0080 a0001c0001t0002g0112 a0001c0001t0002g0113 others(8): Show |
11 | HG01257.hp2 HG01258.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1200-1472G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59052800 | |||||||
| chr17:59052824 | G | A | 1 | a0001c0001t0002g0140 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1200-1496C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59052824 | |||||||
| chr17:59052942 | G | A | 4 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(1): Show |
4 | NA18939.hp2 NA18954.hp2 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.1200-1614C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59052942 | |||||||
| chr17:59052956 | AAAAATC | A | 11 | a0001c0001t0002g0080 a0001c0001t0002g0112 a0001c0001t0002g0113 others(8): Show |
11 | HG01257.hp2 HG01258.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1200-1634_1200-162 others(10): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59052956 | |||||||
| chr17:59052957 | A | AAAATC | 50 | a0001c0001t0001g0224 a0001c0001t0001g0232 a0001c0001t0001g0236 others(47): Show |
50 | HG00621.hp1 HG00642.hp1 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.1200-1634_1200-163 others(9): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59052957 | |||||||
| chr17:59052957 | A | AAAATCAA others(3): Show |
73 | a0001c0001t0001g0258 a0001c0001t0001g0278 a0001c0001t0001g0286 others(70): Show |
73 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.1200-1639_1200-163 others(14): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59052957 | |||||||
| chr17:59052957 | A | AAAATCAA others(8): Show |
8 | a0001c0001t0003g0011 a0001c0001t0003g0018 a0001c0001t0003g0028 others(5): Show |
8 | HG00642.hp2 HG03139.hp2 HG03704.hp2 others(5): Show |
intron_variant | MODIFIER | c.1200-1644_1200-163 others(19): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59052957 | |||||||
| chr17:59052957 | AAAATCAA others(8): Show |
A | 1 | a0001c0001t0001g0338 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1200-1644_1200-163 others(19): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59052957 | |||||||
| chr17:59053066 | G | A | 23 | a0001c0001t0002g0089 a0001c0001t0002g0098 a0001c0001t0003g0079 others(20): Show |
23 | HG01168.hp2 HG01169.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.1200-1738C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59053066 | |||||||
| chr17:59053186 | C | T | 7 | a0001c0001t0002g0098 a0001c0001t0003g0079 a0001c0001t0003g0096 others(4): Show |
7 | HG01168.hp2 HG01169.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.1200-1858G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59053186 | |||||||
| chr17:59053227 | T | G | 1 | a0001c0001t0002g0163 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1200-1899A>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59053227 | |||||||
| chr17:59053308 | T | C | 1 | a0001c0001t0001g0250 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1200-1980A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59053308 | |||||||
| chr17:59053321 | T | C | 1 | a0001c0001t0003g0047 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1200-1993A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59053321 | |||||||
| chr17:59053351 | G | A | 2 | a0001c0001t0003g0030 a0001c0001t0003g0031 |
2 | NA18952.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.1200-2023C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59053351 | |||||||
| chr17:59053424 | C | T | 123 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(120): Show |
123 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.1200-2096G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59053424 | |||||||
| chr17:59053578 | T | G | 1 | a0001c0001t0001g0250 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1200-2250A>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59053578 | |||||||
| chr17:59053666 | T | C | 1 | a0001c0001t0002g0131 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1200-2338A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59053666 | |||||||
| chr17:59053726 | A | G | 2 | a0001c0001t0002g0120 a0001c0001t0002g0121 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1200-2398T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59053726 | |||||||
| chr17:59053828 | G | A | 1 | a0001c0001t0003g0106 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1200-2500C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59053828 | |||||||
| chr17:59053933 | T | TAAACA | 226 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(223): Show |
226 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.1200-2610_1200-260 others(9): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59053933 | |||||||
| chr17:59053990 | C | A | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1200-2662G>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59053990 | |||||||
| chr17:59054220 | T | A | 120 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(117): Show |
120 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.1199+2655A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59054220 | |||||||
| chr17:59054311 | G | A | 3 | a0001c0001t0004g0102 a0001c0001t0004g0103 a0001c0001t0004g0104 |
3 | HG03516.hp2 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1199+2564C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59054311 | |||||||
| chr17:59054360 | G | C | 3 | a0001c0001t0003g0039 a0001c0001t0003g0046 a0001c0001t0003g0123 |
3 | HG00733.hp2 HG01099.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1199+2515C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59054360 | |||||||
| chr17:59054389 | C | G | 3 | a0001c0001t0004g0102 a0001c0001t0004g0103 a0001c0001t0004g0104 |
3 | HG03516.hp2 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1199+2486G>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59054389 | |||||||
| chr17:59054404 | C | T | 1 | a0001c0001t0003g0007 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1199+2471G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59054404 | |||||||
| chr17:59054591 | G | A | 1 | a0001c0001t0002g0210 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1199+2284C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59054591 | |||||||
| chr17:59054753 | C | G | 1 | a0001c0001t0001g0264 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1199+2122G>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59054753 | |||||||
| chr17:59054809 | C | T | 1 | a0001c0001t0001g0255 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1199+2066G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59054809 | |||||||
| chr17:59054991 | A | G | 5 | a0001c0001t0003g0073 a0001c0001t0003g0074 a0001c0001t0003g0075 others(2): Show |
5 | HG02486.hp2 HG02630.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1199+1884T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59054991 | |||||||
| chr17:59055158 | G | A | 8 | a0001c0001t0007g0213 a0001c0001t0007g0214 a0001c0001t0007g0215 others(5): Show |
8 | HG00642.hp2 HG01243.hp2 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.1199+1717C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59055158 | |||||||
| chr17:59055207 | G | A | 228 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(225): Show |
228 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.1199+1668C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59055207 | |||||||
| chr17:59055332 | C | CA | 16 | a0001c0001t0002g0080 a0001c0001t0002g0112 a0001c0001t0002g0113 others(13): Show |
16 | HG00099.hp1 HG00438.hp2 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.1199+1542dupT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59055332 | |||||||
| chr17:59055332 | C | CAA | 7 | a0001c0001t0002g0114 a0001c0001t0002g0120 a0001c0001t0002g0121 others(4): Show |
7 | HG01257.hp2 HG01258.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.1199+1541_1199+154 others(6): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59055332 | |||||||
| chr17:59055332 | C | CAAA | 6 | a0001c0001t0002g0117 a0001c0001t0002g0119 a0001c0001t0003g0073 others(3): Show |
6 | HG02486.hp2 HG02622.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1199+1540_1199+154 others(7): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59055332 | |||||||
| chr17:59055332 | CA | C | 40 | a0001c0001t0001g0223 a0001c0001t0001g0236 a0001c0001t0001g0261 others(37): Show |
40 | HG00544.hp1 HG00639.hp2 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.1199+1542delT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59055332 | |||||||
| chr17:59055332 | CAA | C | 177 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(174): Show |
177 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.1199+1541_1199+154 others(6): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59055332 | |||||||
| chr17:59055524 | C | A | 6 | a0001c0001t0001g0232 a0001c0001t0001g0236 a0001c0001t0001g0237 others(3): Show |
6 | HG01168.hp1 HG02559.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1199+1351G>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59055524 | |||||||
| chr17:59055647 | G | A | 1 | a0001c0001t0001g0283 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1199+1228C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59055647 | |||||||
| chr17:59055649 | T | G | 248 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(245): Show |
248 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.1199+1226A>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59055649 | |||||||
| chr17:59055685 | C | CA | 44 | a0001c0001t0001g0223 a0001c0001t0001g0227 a0001c0001t0001g0233 others(41): Show |
44 | HG00438.hp2 HG00597.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.1199+1189dupT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59055685 | |||||||
| chr17:59055685 | CA | C | 19 | a0001c0001t0001g0241 a0001c0001t0001g0257 a0001c0001t0001g0338 others(16): Show |
19 | HG00438.hp1 HG01099.hp1 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.1199+1189delT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59055685 | |||||||
| chr17:59055768 | T | C | 1 | a0001c0001t0002g0185 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1199+1107A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59055768 | |||||||
| chr17:59055775 | G | C | 1 | a0001c0001t0003g0036 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1199+1100C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59055775 | |||||||
| chr17:59055816 | T | C | 2 | a0001c0001t0003g0108 a0001c0001t0003g0109 |
2 | HG02451.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1199+1059A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59055816 | |||||||
| chr17:59056068 | T | G | 20 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(17): Show |
20 | HG01346.hp1 HG02071.hp1 HG02155.hp1 others(17): Show |
intron_variant | MODIFIER | c.1199+807A>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056068 | |||||||
| chr17:59056179 | T | A | 1 | a0001c0001t0001g0298 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1199+696A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056179 | |||||||
| chr17:59056267 | C | T | 2 | a0001c0001t0002g0133 a0001c0001t0002g0145 |
2 | HG00621.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.1199+608G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056267 | |||||||
| chr17:59056298 | C | T | 1 | a0001c0001t0003g0081 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1199+577G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056298 | |||||||
| chr17:59056323 | C | T | 1 | a0001c0001t0002g0117 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1199+552G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056323 | |||||||
| chr17:59056446 | G | A | 1 | a0001c0001t0001g0302 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1199+429C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056446 | |||||||
| chr17:59056458 | G | A | 3 | a0001c0001t0004g0102 a0001c0001t0004g0103 a0001c0001t0004g0104 |
3 | HG03516.hp2 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1199+417C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056458 | |||||||
| chr17:59056495 | C | A | 1 | a0001c0001t0003g0037 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1199+380G>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056495 | |||||||
| chr17:59056586 | C | T | 4 | a0001c0001t0007g0213 a0001c0001t0007g0214 a0001c0001t0007g0215 others(1): Show |
4 | HG01243.hp2 HG03471.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1199+289G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056586 | |||||||
| chr17:59056587 | A | G | 250 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(247): Show |
250 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.1199+288T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056587 | |||||||
| chr17:59056593 | G | A | 4 | a0001c0001t0005g0040 a0001c0001t0005g0041 a0001c0001t0005g0042 others(1): Show |
4 | NA18945.hp1 NA19006.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.1199+282C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056593 | |||||||
| chr17:59056598 | C | T | 3 | a0001c0001t0004g0102 a0001c0001t0004g0103 a0001c0001t0004g0104 |
3 | HG03516.hp2 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1199+277G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056598 | |||||||
| chr17:59056649 | G | C | 3 | a0001c0001t0003g0019 a0001c0001t0003g0032 a0001c0001t0003g0122 |
3 | NA18992.hp2 NA19001.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.1199+226C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056649 | |||||||
| chr17:59056654 | C | T | 1 | a0001c0001t0001g0297 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1199+221G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056654 | |||||||
| chr17:59056661 | C | T | 1 | a0001c0001t0003g0033 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1199+214G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056661 | |||||||
| chr17:59056667 | T | C | 5 | a0001c0001t0003g0073 a0001c0001t0003g0074 a0001c0001t0003g0075 others(2): Show |
5 | HG02486.hp2 HG02630.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1199+208A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056667 | |||||||
| chr17:59056698 | A | G | 253 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(250): Show |
253 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(250): Show |
intron_variant | MODIFIER | c.1199+177T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056698 | |||||||
| chr17:59056716 | C | CA | 14 | a0001c0001t0001g0238 a0001c0001t0001g0258 a0001c0001t0002g0129 others(11): Show |
14 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.1199+158dupT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056716 | |||||||
| chr17:59056716 | C | CAA | 13 | a0001c0001t0001g0340 a0001c0001t0002g0132 a0001c0001t0002g0148 others(10): Show |
13 | HG01106.hp1 HG01358.hp1 HG02148.hp1 others(10): Show |
intron_variant | MODIFIER | c.1199+157_1199+158d others(4): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056716 | |||||||
| chr17:59056716 | C | CAAA | 13 | a0001c0001t0001g0308 a0001c0001t0001g0309 a0001c0001t0002g0107 others(10): Show |
13 | HG00099.hp1 HG01261.hp1 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.1199+156_1199+158d others(5): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056716 | |||||||
| chr17:59056716 | C | CAAAA | 30 | a0001c0001t0001g0237 a0001c0001t0001g0239 a0001c0001t0001g0243 others(27): Show |
30 | HG00597.hp1 HG00673.hp1 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.1199+155_1199+158d others(6): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056716 | |||||||
| chr17:59056716 | C | CAAAAA | 41 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(38): Show |
41 | HG00438.hp2 HG00544.hp1 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.1199+154_1199+158d others(7): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056716 | |||||||
| chr17:59056716 | C | CAAAAAA | 39 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0226 others(36): Show |
39 | HG00280.hp1 HG00558.hp2 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.1199+153_1199+158d others(8): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056716 | |||||||
| chr17:59056716 | C | CAAAAAAA | 26 | a0001c0001t0001g0225 a0001c0001t0001g0234 a0001c0001t0001g0254 others(23): Show |
26 | HG00544.hp2 HG00597.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.1199+152_1199+158d others(9): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056716 | |||||||
| chr17:59056716 | C | CAAAAAAA others(1): Show |
24 | a0001c0001t0001g0233 a0001c0001t0001g0250 a0001c0001t0001g0255 others(21): Show |
24 | HG00558.hp1 HG00621.hp1 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.1199+151_1199+158d others(10): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056716 | |||||||
| chr17:59056716 | C | CAAAAAAA others(2): Show |
22 | a0001c0001t0001g0231 a0001c0001t0001g0235 a0001c0001t0001g0241 others(19): Show |
22 | HG01243.hp2 HG02135.hp1 HG02280.hp2 others(19): Show |
intron_variant | MODIFIER | c.1199+150_1199+158d others(11): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056716 | |||||||
| chr17:59056716 | C | CAAAAAAA others(3): Show |
15 | a0001c0001t0001g0302 a0001c0001t0001g0305 a0001c0001t0001g0337 others(12): Show |
15 | HG00323.hp2 HG00741.hp1 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.1199+149_1199+158d others(12): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056716 | |||||||
| chr17:59056716 | C | CAAAAAAA others(4): Show |
4 | a0001c0001t0003g0004 a0001c0001t0003g0009 a0001c0001t0008g0017 others(1): Show |
4 | HG00438.hp1 HG03831.hp1 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.1199+148_1199+158d others(13): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056716 | |||||||
| chr17:59056716 | C | CAAAAAAA others(5): Show |
7 | a0001c0001t0003g0011 a0001c0001t0003g0013 a0001c0001t0003g0060 others(4): Show |
7 | HG00099.hp2 HG01515.hp2 NA18949.hp1 others(4): Show |
intron_variant | MODIFIER | c.1199+147_1199+158d others(14): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056716 | |||||||
| chr17:59056716 | C | CAAAAAAA others(6): Show |
3 | a0001c0001t0001g0311 a0001c0001t0003g0047 a0001c0001t0005g0042 |
3 | HG02523.hp2 HG04228.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.1199+146_1199+158d others(15): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056716 | |||||||
| chr17:59056716 | C | CAAAAAAA others(7): Show |
3 | a0001c0001t0001g0257 a0001c0001t0003g0070 a0001c0001t0005g0040 |
3 | HG02155.hp1 HG03453.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.1199+145_1199+158d others(16): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056716 | |||||||
| chr17:59056716 | C | CAAAAAAA others(8): Show |
4 | a0001c0001t0001g0339 a0001c0001t0003g0007 a0001c0001t0003g0033 others(1): Show |
4 | HG01346.hp2 NA18944.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.1199+144_1199+158d others(17): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056716 | |||||||
| chr17:59056716 | C | CAAAAAAA others(9): Show |
2 | a0001c0001t0003g0008 a0001c0001t0003g0036 |
2 | HG03654.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1199+143_1199+158d others(18): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056716 | |||||||
| chr17:59056716 | C | CAAAAAAA others(12): Show |
2 | a0001c0001t0003g0034 a0001c0001t0003g0050 |
2 | HG02040.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.1199+140_1199+158d others(21): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056716 | |||||||
| chr17:59056716 | C | CAAAAAAA others(15): Show |
2 | a0001c0001t0003g0014 a0001c0001t0003g0019 |
2 | HG00280.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.1199+137_1199+158d others(24): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056716 | |||||||
| chr17:59056716 | C | CAAAAAAA others(16): Show |
1 | a0001c0001t0001g0303 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1199+136_1199+158d others(25): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056716 | |||||||
| chr17:59056716 | C | CAAAAAAA others(18): Show |
1 | a0001c0001t0003g0032 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1199+134_1199+158d others(27): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056716 | |||||||
| chr17:59056716 | C | CAAAAAAA others(19): Show |
1 | a0001c0001t0003g0046 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1199+133_1199+158d others(28): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056716 | |||||||
| chr17:59056716 | C | CAAAAAAA others(20): Show |
1 | a0001c0001t0003g0028 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1199+132_1199+158d others(29): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056716 | |||||||
| chr17:59056716 | C | CAAAAAAA others(25): Show |
1 | a0001c0001t0003g0039 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1199+158_1199+159i others(34): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056716 | |||||||
| chr17:59056716 | C | CAAAAAAA others(26): Show |
1 | a0001c0001t0003g0006 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1199+158_1199+159i others(35): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056716 | |||||||
| chr17:59056716 | CA | C | 6 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0002g0119 others(3): Show |
6 | HG00639.hp1 HG00642.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1199+158delT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056716 | |||||||
| chr17:59056716 | CAA | C | 9 | a0001c0001t0001g0230 a0001c0001t0002g0080 a0001c0001t0002g0111 others(6): Show |
9 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1199+157_1199+158d others(4): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056716 | |||||||
| chr17:59056716 | CAAA | C | 6 | a0001c0001t0002g0112 a0001c0001t0002g0113 a0001c0001t0002g0118 others(3): Show |
6 | HG01884.hp1 HG02451.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1199+156_1199+158d others(5): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056716 | |||||||
| chr17:59056716 | CAAAAAA | C | 8 | a0001c0001t0002g0089 a0001c0001t0003g0079 a0001c0001t0003g0095 others(5): Show |
8 | HG01168.hp2 HG01169.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.1199+153_1199+158d others(8): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056716 | |||||||
| chr17:59056716 | CAAAAAAA | C | 15 | a0001c0001t0002g0098 a0001c0001t0003g0081 a0001c0001t0003g0082 others(12): Show |
15 | HG02109.hp1 HG02559.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.1199+152_1199+158d others(9): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056716 | |||||||
| chr17:59056716 | CAAAAAAA others(3): Show |
C | 1 | a0001c0008t0003g0038 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1199+149_1199+158d others(12): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056716 | |||||||
| chr17:59056716 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0003g0045 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1199+148_1199+158d others(13): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056716 | |||||||
| chr17:59056716 | CAAAAAAA others(5): Show |
C | 3 | a0001c0001t0004g0102 a0001c0001t0004g0103 a0001c0001t0004g0104 |
3 | HG03516.hp2 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1199+147_1199+158d others(14): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056716 | |||||||
| chr17:59056716 | CAAAAAAA others(8): Show |
C | 1 | a0001c0001t0003g0003 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1199+144_1199+158d others(17): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056716 | |||||||
| chr17:59056763 | G | T | 74 | a0001c0001t0001g0339 a0001c0001t0003g0003 a0001c0001t0003g0004 others(71): Show |
74 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.1199+112C>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056763 | |||||||
| chr17:59056836 | C | T | 1 | a0001c0001t0001g0243 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1199+39G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056836 | |||||||
| chr17:59057488 | G | C | 23 | a0001c0001t0002g0089 a0001c0001t0002g0098 a0001c0001t0003g0079 others(20): Show |
23 | HG01168.hp2 HG01169.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.1020-434C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 12/23 | chr17 | 59057488 | |||||||
| chr17:59057522 | A | G | 1 | a0001c0001t0002g0155 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1020-468T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 12/23 | chr17 | 59057522 | |||||||
| chr17:59057588 | G | T | 3 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0230 |
3 | HG00639.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1020-534C>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 12/23 | chr17 | 59057588 | |||||||
| chr17:59057600 | T | G | 3 | a0001c0001t0004g0102 a0001c0001t0004g0103 a0001c0001t0004g0104 |
3 | HG03516.hp2 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1020-546A>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 12/23 | chr17 | 59057600 | |||||||
| chr17:59057752 | G | C | 4 | a0001c0001t0005g0040 a0001c0001t0005g0041 a0001c0001t0005g0042 others(1): Show |
4 | NA18945.hp1 NA19006.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.1020-698C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 12/23 | chr17 | 59057752 | |||||||
| chr17:59057816 | G | A | 8 | a0001c0001t0007g0213 a0001c0001t0007g0214 a0001c0001t0007g0215 others(5): Show |
8 | HG00642.hp2 HG01243.hp2 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.1020-762C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 12/23 | chr17 | 59057816 | |||||||
| chr17:59058342 | G | C | 1 | a0001c0001t0011g0001 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1020-1288C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 12/23 | chr17 | 59058342 | |||||||
| chr17:59058516 | G | A | 2 | a0001c0001t0002g0107 a0001c0001t0002g0111 |
2 | HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1020-1462C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 12/23 | chr17 | 59058516 | |||||||
| chr17:59058690 | T | A | 1 | a0001c0001t0001g0302 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1020-1636A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 12/23 | chr17 | 59058690 | |||||||
| chr17:59058700 | C | T | 5 | a0001c0001t0003g0073 a0001c0001t0003g0074 a0001c0001t0003g0075 others(2): Show |
5 | HG02486.hp2 HG02630.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1020-1646G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 12/23 | chr17 | 59058700 | |||||||
| chr17:59058843 | G | A | 2 | a0001c0001t0001g0293 a0001c0001t0001g0294 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1020-1789C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 12/23 | chr17 | 59058843 | |||||||
| chr17:59058850 | C | T | 4 | a0001c0001t0003g0073 a0001c0001t0003g0074 a0001c0001t0003g0075 others(1): Show |
4 | HG02486.hp2 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1020-1796G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 12/23 | chr17 | 59058850 | |||||||
| chr17:59059132 | G | A | 1 | a0001c0001t0001g0330 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1019+1900C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 12/23 | chr17 | 59059132 | |||||||
| chr17:59059245 | G | A | 1 | a0001c0001t0002g0117 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1019+1787C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 12/23 | chr17 | 59059245 | |||||||
| chr17:59059460 | C | T | 23 | a0001c0001t0002g0089 a0001c0001t0002g0098 a0001c0001t0003g0079 others(20): Show |
23 | HG01168.hp2 HG01169.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.1019+1572G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 12/23 | chr17 | 59059460 | |||||||
| chr17:59059513 | C | T | 1 | a0002c0002t0002g0208 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1019+1519G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 12/23 | chr17 | 59059513 | |||||||
| chr17:59059517 | T | C | 2 | a0001c0001t0002g0107 a0001c0001t0002g0111 |
2 | HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1019+1515A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 12/23 | chr17 | 59059517 | |||||||
| chr17:59059577 | T | C | 245 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(242): Show |
245 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.1019+1455A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 12/23 | chr17 | 59059577 | |||||||
| chr17:59059768 | G | A | 132 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(129): Show |
132 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(129): Show |
intron_variant | MODIFIER | c.1019+1264C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 12/23 | chr17 | 59059768 | |||||||
| chr17:59059823 | C | T | 1 | a0001c0001t0001g0270 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1019+1209G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 12/23 | chr17 | 59059823 | |||||||
| chr17:59059891 | G | A | 1 | a0001c0001t0002g0150 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1019+1141C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 12/23 | chr17 | 59059891 | |||||||
| chr17:59060052 | G | A | 2 | a0001c0001t0002g0173 a0001c0001t0002g0174 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1019+980C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 12/23 | chr17 | 59060052 | |||||||
| chr17:59060073 | T | C | 1 | a0001c0001t0001g0322 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1019+959A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 12/23 | chr17 | 59060073 | |||||||
| chr17:59060516 | G | A | 4 | a0001c0001t0005g0040 a0001c0001t0005g0041 a0001c0001t0005g0042 others(1): Show |
4 | NA18945.hp1 NA19006.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.1019+516C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 12/23 | chr17 | 59060516 | |||||||
| chr17:59060622 | G | A | 1 | a0001c0001t0001g0264 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1019+410C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 12/23 | chr17 | 59060622 | |||||||
| chr17:59060673 | T | C | 1 | a0001c0001t0002g0127 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1019+359A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 12/23 | chr17 | 59060673 | |||||||
| chr17:59060760 | A | T | 1 | a0001c0001t0001g0254 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1019+272T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 12/23 | chr17 | 59060760 | |||||||
| chr17:59061243 | T | C | 5 | a0001c0001t0002g0080 a0001c0001t0002g0112 a0001c0001t0002g0113 others(2): Show |
5 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.943-135A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 11/23 | chr17 | 59061243 | |||||||
| chr17:59061501 | C | T | 1 | a0001c0001t0001g0269 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.943-393G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 11/23 | chr17 | 59061501 | |||||||
| chr17:59061561 | G | T | 6 | a0001c0001t0003g0081 a0001c0001t0003g0082 a0001c0001t0003g0083 others(3): Show |
6 | HG02559.hp1 HG02647.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.943-453C>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 11/23 | chr17 | 59061561 | |||||||
| chr17:59061773 | G | A | 97 | a0001c0001t0001g0339 a0001c0001t0002g0089 a0001c0001t0002g0098 others(94): Show |
97 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.943-665C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 11/23 | chr17 | 59061773 | |||||||
| chr17:59061932 | G | A | 225 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(222): Show |
225 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.942+635C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 11/23 | chr17 | 59061932 | |||||||
| chr17:59061958 | T | A | 4 | a0001c0003t0006g0212 a0001c0003t0006g0217 a0001c0003t0006g0218 others(1): Show |
4 | HG00642.hp2 HG03704.hp2 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.942+609A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 11/23 | chr17 | 59061958 | |||||||
| chr17:59062098 | G | A | 1 | a0001c0001t0002g0149 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.942+469C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 11/23 | chr17 | 59062098 | |||||||
| chr17:59062229 | T | C | 1 | a0001c0001t0001g0339 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.942+338A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 11/23 | chr17 | 59062229 | |||||||
| chr17:59062453 | A | G | 4 | a0001c0001t0003g0082 a0001c0001t0003g0083 a0001c0001t0003g0084 others(1): Show |
4 | HG02559.hp1 HG02886.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.942+114T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 11/23 | chr17 | 59062453 | |||||||
| chr17:59062461 | C | T | 2 | a0001c0001t0002g0150 a0001c0001t0002g0211 |
2 | HG00099.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.942+106G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 11/23 | chr17 | 59062461 | |||||||
| chr17:59062654 | G | A | 4 | a0001c0003t0006g0212 a0001c0003t0006g0217 a0001c0003t0006g0218 others(1): Show |
4 | HG00642.hp2 HG03704.hp2 NA20752.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.861-6C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 10/23 | chr17 | 59062654 | |||||||
| chr17:59062810 | T | C | 1 | a0001c0001t0003g0029 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.861-162A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 10/23 | chr17 | 59062810 | |||||||
| chr17:59062940 | A | G | 97 | a0001c0001t0001g0339 a0001c0001t0002g0089 a0001c0001t0002g0098 others(94): Show |
97 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.861-292T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 10/23 | chr17 | 59062940 | |||||||
| chr17:59062943 | A | T | 247 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(244): Show |
247 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.861-295T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 10/23 | chr17 | 59062943 | |||||||
| chr17:59063233 | G | A | 96 | a0001c0001t0001g0339 a0001c0001t0002g0089 a0001c0001t0002g0098 others(93): Show |
96 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.861-585C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 10/23 | chr17 | 59063233 | |||||||
| chr17:59063242 | C | T | 1 | a0001c0001t0001g0301 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.861-594G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 10/23 | chr17 | 59063242 | |||||||
| chr17:59063243 | G | T | 1 | a0001c0001t0001g0257 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.861-595C>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 10/23 | chr17 | 59063243 | |||||||
| chr17:59063386 | C | T | 3 | a0001c0003t0006g0217 a0001c0003t0006g0218 a0001c0003t0006g0219 |
3 | HG00642.hp2 NA20752.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.861-738G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 10/23 | chr17 | 59063386 | |||||||
| chr17:59063412 | C | T | 3 | a0001c0001t0004g0102 a0001c0001t0004g0103 a0001c0001t0004g0104 |
3 | HG03516.hp2 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.861-764G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 10/23 | chr17 | 59063412 | |||||||
| chr17:59063415 | T | A | 12 | a0001c0001t0003g0061 a0001c0001t0003g0062 a0001c0001t0003g0063 others(9): Show |
12 | HG02055.hp1 HG02572.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.861-767A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 10/23 | chr17 | 59063415 | |||||||
| chr17:59063424 | C | T | 1 | a0001c0001t0002g0210 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.861-776G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 10/23 | chr17 | 59063424 | |||||||
| chr17:59063427 | C | G | 1 | a0001c0001t0002g0127 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.861-779G>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 10/23 | chr17 | 59063427 | |||||||
| chr17:59063684 | T | C | 1 | a0001c0001t0001g0310 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.860+671A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 10/23 | chr17 | 59063684 | |||||||
| chr17:59064162 | G | C | 1 | a0001c0001t0001g0280 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.860+193C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 10/23 | chr17 | 59064162 | |||||||
| chr17:59064407 | T | TA | 8 | a0001c0001t0007g0213 a0001c0001t0007g0214 a0001c0001t0007g0215 others(5): Show |
8 | HG00642.hp2 HG01243.hp2 HG03471.hp1 others(5): Show |
splice_region_variant&intron_variant | LOW | c.810-3dupT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 9/23 | chr17 | 59064407 | |||||||
| chr17:59064552 | T | G | 1 | a0001c0006t0003g0105 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.810-147A>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 9/23 | chr17 | 59064552 | |||||||
| chr17:59064785 | C | A | 1 | a0001c0006t0003g0105 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.810-380G>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 9/23 | chr17 | 59064785 | |||||||
| chr17:59064930 | A | C | 97 | a0001c0001t0001g0339 a0001c0001t0002g0089 a0001c0001t0002g0098 others(94): Show |
97 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.810-525T>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 9/23 | chr17 | 59064930 | |||||||
| chr17:59064943 | T | C | 8 | a0001c0001t0007g0213 a0001c0001t0007g0214 a0001c0001t0007g0215 others(5): Show |
8 | HG00642.hp2 HG01243.hp2 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.810-538A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 9/23 | chr17 | 59064943 | |||||||
| chr17:59065023 | C | T | 1 | a0001c0006t0003g0105 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.810-618G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 9/23 | chr17 | 59065023 | |||||||
| chr17:59065296 | C | T | 324 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(321): Show |
324 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.810-891G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 9/23 | chr17 | 59065296 | |||||||
| chr17:59065541 | T | C | 1 | a0001c0001t0003g0172 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.810-1136A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 9/23 | chr17 | 59065541 | |||||||
| chr17:59065596 | T | C | 1 | a0001c0001t0001g0254 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.810-1191A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 9/23 | chr17 | 59065596 | |||||||
| chr17:59065996 | T | C | 4 | a0001c0003t0006g0212 a0001c0003t0006g0217 a0001c0003t0006g0218 others(1): Show |
4 | HG00642.hp2 HG03704.hp2 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.810-1591A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 9/23 | chr17 | 59065996 | |||||||
| chr17:59066043 | T | G | 90 | a0001c0001t0002g0110 a0001c0001t0002g0124 a0001c0001t0002g0126 others(87): Show |
90 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.810-1638A>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 9/23 | chr17 | 59066043 | |||||||
| chr17:59066431 | G | A | 6 | a0001c0001t0001g0232 a0001c0001t0001g0236 a0001c0001t0001g0237 others(3): Show |
6 | HG01168.hp1 HG02559.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.810-2026C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 9/23 | chr17 | 59066431 | |||||||
| chr17:59066502 | A | G | 3 | a0001c0001t0001g0225 a0001c0001t0001g0242 a0001c0001t0001g0246 |
3 | NA18966.hp2 NA19005.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.810-2097T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 9/23 | chr17 | 59066502 | |||||||
| chr17:59066810 | T | C | 1 | a0001c0001t0001g0300 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.810-2405A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 9/23 | chr17 | 59066810 | |||||||
| chr17:59066838 | T | C | 1 | a0001c0001t0001g0296 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.810-2433A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 9/23 | chr17 | 59066838 | |||||||
| chr17:59066994 | C | T | 114 | a0001c0001t0002g0080 a0001c0001t0002g0107 a0001c0001t0002g0110 others(111): Show |
114 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.810-2589G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 9/23 | chr17 | 59066994 | |||||||
| chr17:59067006 | C | T | 220 | a0001c0001t0001g0339 a0001c0001t0002g0080 a0001c0001t0002g0089 others(217): Show |
220 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.810-2601G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 9/23 | chr17 | 59067006 | |||||||
| chr17:59067026 | T | TTTTA | 3 | a0001c0001t0004g0102 a0001c0001t0004g0103 a0001c0001t0004g0104 |
3 | HG03516.hp2 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.810-2625_810-2622d others(6): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 9/23 | chr17 | 59067026 | |||||||
| chr17:59067026 | TTTTA | T | 8 | a0001c0001t0002g0148 a0001c0001t0003g0009 a0001c0001t0003g0012 others(5): Show |
8 | HG00438.hp1 HG03831.hp2 NA18945.hp1 others(5): Show |
intron_variant | MODIFIER | c.810-2625_810-2622d others(6): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 9/23 | chr17 | 59067026 | |||||||
| chr17:59067092 | T | G | 2 | a0001c0001t0003g0108 a0001c0001t0003g0109 |
2 | HG02451.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.810-2687A>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 9/23 | chr17 | 59067092 | |||||||
| chr17:59067175 | C | G | 1 | a0001c0001t0002g0147 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.810-2770G>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 9/23 | chr17 | 59067175 | |||||||
| chr17:59067176 | C | T | 1 | a0001c0001t0003g0106 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.810-2771G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 9/23 | chr17 | 59067176 | |||||||
| chr17:59067307 | T | C | 2 | a0001c0001t0002g0191 a0001c0001t0002g0192 |
2 | NA18970.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.810-2902A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 9/23 | chr17 | 59067307 | |||||||
| chr17:59067737 | TGTTGGTC others(107): Show |
T | 3 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0255 |
3 | HG01346.hp1 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.809+2972_809+3085d others(2): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 9/23 | chr17 | 59067737 | |||||||
| chr17:59067882 | A | G | 1 | a0001c0001t0012g0002 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.809+2941T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 9/23 | chr17 | 59067882 | |||||||
| chr17:59067897 | G | A | 1 | a0001c0006t0003g0105 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.809+2926C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 9/23 | chr17 | 59067897 | |||||||
| chr17:59068135 | C | G | 1 | a0001c0001t0002g0184 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.809+2688G>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 9/23 | chr17 | 59068135 | |||||||
| chr17:59068269 | G | C | 1 | a0001c0001t0003g0052 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.809+2554C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 9/23 | chr17 | 59068269 | |||||||
| chr17:59068352 | T | C | 1 | a0001c0001t0001g0307 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.809+2471A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 9/23 | chr17 | 59068352 | |||||||
| chr17:59068976 | C | T | 2 | a0001c0001t0002g0107 a0001c0001t0002g0111 |
2 | HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.809+1847G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 9/23 | chr17 | 59068976 | |||||||
| chr17:59069058 | T | C | 1 | a0001c0001t0001g0305 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.809+1765A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 9/23 | chr17 | 59069058 | |||||||
| chr17:59069412 | G | C | 2 | a0001c0001t0002g0107 a0001c0001t0002g0111 |
2 | HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.809+1411C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 9/23 | chr17 | 59069412 | |||||||
| chr17:59070020 | T | C | 1 | a0001c0001t0001g0255 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.809+803A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 9/23 | chr17 | 59070020 | |||||||
| chr17:59070143 | T | C | 4 | a0001c0003t0006g0212 a0001c0003t0006g0217 a0001c0003t0006g0218 others(1): Show |
4 | HG00642.hp2 HG03704.hp2 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.809+680A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 9/23 | chr17 | 59070143 | |||||||
| chr17:59070259 | A | G | 5 | a0001c0001t0003g0073 a0001c0001t0003g0074 a0001c0001t0003g0075 others(2): Show |
5 | HG02486.hp2 HG02630.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.809+564T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 9/23 | chr17 | 59070259 | |||||||
| chr17:59070339 | T | G | 1 | a0001c0001t0002g0167 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.809+484A>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 9/23 | chr17 | 59070339 | |||||||
| chr17:59070342 | T | C | 6 | a0001c0001t0003g0081 a0001c0001t0003g0082 a0001c0001t0003g0083 others(3): Show |
6 | HG02559.hp1 HG02647.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.809+481A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 9/23 | chr17 | 59070342 | |||||||
| chr17:59070666 | C | T | 60 | a0001c0001t0001g0339 a0001c0001t0003g0003 a0001c0001t0003g0004 others(57): Show |
60 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.809+157G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 9/23 | chr17 | 59070666 | |||||||
| chr17:59070738 | T | TA | 11 | a0001c0001t0002g0128 a0001c0001t0002g0149 a0001c0001t0002g0188 others(8): Show |
11 | HG02257.hp2 NA18747.hp2 NA18944.hp2 others(8): Show |
intron_variant | MODIFIER | c.809+84dupT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 9/23 | chr17 | 59070738 | |||||||
| chr17:59070999 | C | T | 1 | a0001c0001t0003g0097 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.685-52G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 8/23 | chr17 | 59070999 | |||||||
| chr17:59071283 | C | CT | 15 | a0001c0001t0001g0224 a0001c0001t0001g0234 a0001c0001t0001g0238 others(12): Show |
15 | HG01169.hp2 HG01978.hp1 HG02027.hp2 others(12): Show |
intron_variant | MODIFIER | c.685-337dupA | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 8/23 | chr17 | 59071283 | |||||||
| chr17:59071397 | T | C | 8 | a0001c0001t0007g0213 a0001c0001t0007g0214 a0001c0001t0007g0215 others(5): Show |
8 | HG00642.hp2 HG01243.hp2 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.685-450A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 8/23 | chr17 | 59071397 | |||||||
| chr17:59071478 | G | C | 3 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0230 |
3 | HG00639.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.685-531C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 8/23 | chr17 | 59071478 | |||||||
| chr17:59071630 | G | A | 219 | a0001c0001t0001g0339 a0001c0001t0002g0080 a0001c0001t0002g0089 others(216): Show |
219 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.685-683C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 8/23 | chr17 | 59071630 | |||||||
| chr17:59071659 | C | T | 1 | a0001c0001t0003g0081 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.685-712G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 8/23 | chr17 | 59071659 | |||||||
| chr17:59071784 | T | C | 5 | a0002c0002t0002g0125 a0002c0002t0002g0205 a0002c0002t0002g0206 others(2): Show |
5 | HG01952.hp2 HG02615.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.685-837A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 8/23 | chr17 | 59071784 | |||||||
| chr17:59072334 | G | A | 219 | a0001c0001t0001g0339 a0001c0001t0002g0080 a0001c0001t0002g0089 others(216): Show |
219 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.685-1387C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 8/23 | chr17 | 59072334 | |||||||
| chr17:59072543 | C | T | 95 | a0001c0001t0002g0107 a0001c0001t0002g0110 a0001c0001t0002g0111 others(92): Show |
95 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.685-1596G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 8/23 | chr17 | 59072543 | |||||||
| chr17:59072747 | C | CA | 101 | a0001c0001t0001g0232 a0001c0001t0001g0236 a0001c0001t0001g0237 others(98): Show |
101 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.685-1801dupT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 8/23 | chr17 | 59072747 | |||||||
| chr17:59073325 | G | A | 1 | a0001c0001t0002g0142 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.684+2322C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 8/23 | chr17 | 59073325 | |||||||
| chr17:59073371 | G | A | 1 | a0001c0001t0002g0137 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.684+2276C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 8/23 | chr17 | 59073371 | |||||||
| chr17:59073491 | A | G | 1 | a0001c0001t0001g0267 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.684+2156T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 8/23 | chr17 | 59073491 | |||||||
| chr17:59073543 | G | A | 2 | a0001c0001t0002g0107 a0001c0001t0002g0111 |
2 | HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.684+2104C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 8/23 | chr17 | 59073543 | |||||||
| chr17:59073641 | C | T | 1 | a0001c0001t0001g0232 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.684+2006G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 8/23 | chr17 | 59073641 | |||||||
| chr17:59073998 | C | T | 1 | a0001c0001t0002g0155 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.684+1649G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 8/23 | chr17 | 59073998 | |||||||
| chr17:59074144 | C | T | 1 | a0001c0001t0003g0050 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.684+1503G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 8/23 | chr17 | 59074144 | |||||||
| chr17:59074145 | T | G | 4 | a0001c0001t0007g0213 a0001c0001t0007g0214 a0001c0001t0007g0215 others(1): Show |
4 | HG01243.hp2 HG03471.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.684+1502A>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 8/23 | chr17 | 59074145 | |||||||
| chr17:59074218 | T | C | 95 | a0001c0001t0002g0107 a0001c0001t0002g0110 a0001c0001t0002g0111 others(92): Show |
95 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.684+1429A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 8/23 | chr17 | 59074218 | |||||||
| chr17:59074289 | G | A | 4 | a0001c0001t0002g0150 a0001c0001t0002g0154 a0001c0001t0002g0211 others(1): Show |
4 | HG00099.hp1 HG02602.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.684+1358C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 8/23 | chr17 | 59074289 | |||||||
| chr17:59074403 | G | A | 7 | a0001c0001t0002g0098 a0001c0001t0003g0079 a0001c0001t0003g0096 others(4): Show |
7 | HG01168.hp2 HG01169.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.684+1244C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 8/23 | chr17 | 59074403 | |||||||
| chr17:59074578 | T | C | 1 | a0001c0001t0003g0058 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.684+1069A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 8/23 | chr17 | 59074578 | |||||||
| chr17:59074599 | G | A | 1 | a0001c0001t0002g0204 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.684+1048C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 8/23 | chr17 | 59074599 | |||||||
| chr17:59075021 | A | G | 1 | a0001c0001t0001g0235 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.684+626T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 8/23 | chr17 | 59075021 | |||||||
| chr17:59075073 | T | C | 1 | a0001c0001t0001g0310 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.684+574A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 8/23 | chr17 | 59075073 | |||||||
| chr17:59075103 | T | C | 3 | a0001c0001t0004g0102 a0001c0001t0004g0103 a0001c0001t0004g0104 |
3 | HG03516.hp2 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.684+544A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 8/23 | chr17 | 59075103 | |||||||
| chr17:59075251 | C | CA | 10 | a0001c0001t0001g0250 a0001c0001t0001g0265 a0001c0001t0001g0330 others(7): Show |
10 | HG00597.hp1 HG01175.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.684+395dupT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 8/23 | chr17 | 59075251 | |||||||
| chr17:59075399 | T | C | 7 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 others(4): Show |
7 | HG02293.hp2 NA18946.hp2 NA18980.hp1 others(4): Show |
intron_variant | MODIFIER | c.684+248A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 8/23 | chr17 | 59075399 | |||||||
| chr17:59075559 | A | G | 220 | a0001c0001t0001g0339 a0001c0001t0002g0080 a0001c0001t0002g0089 others(217): Show |
220 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.684+88T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 8/23 | chr17 | 59075559 | |||||||
| chr17:59075563 | C | CA | 29 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0248 others(26): Show |
29 | HG00438.hp2 HG01070.hp2 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.684+83dupT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 8/23 | chr17 | 59075563 | |||||||
| chr17:59075563 | CA | C | 90 | a0001c0001t0001g0257 a0001c0001t0001g0339 a0001c0001t0002g0080 others(87): Show |
90 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.684+83delT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 8/23 | chr17 | 59075563 | |||||||
| chr17:59075583 | A | C | 1 | a0001c0001t0003g0019 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.684+64T>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 8/23 | chr17 | 59075583 | |||||||
| chr17:59075590 | A | G | 1 | a0001c0001t0003g0018 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.684+57T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 8/23 | chr17 | 59075590 | |||||||
| chr17:59075827 | T | C | 3 | a0001c0001t0001g0235 a0001c0001t0001g0256 a0001c0001t0001g0337 |
3 | HG02055.hp2 HG02280.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.617-113A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 7/23 | chr17 | 59075827 | |||||||
| chr17:59075914 | A | T | 1 | a0001c0001t0001g0234 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.617-200T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 7/23 | chr17 | 59075914 | |||||||
| chr17:59076112 | G | A | 1 | a0001c0003t0006g0219 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.617-398C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 7/23 | chr17 | 59076112 | |||||||
| chr17:59076135 | T | C | 1 | a0001c0001t0001g0241 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.617-421A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 7/23 | chr17 | 59076135 | |||||||
| chr17:59076176 | AG | A | 3 | a0001c0001t0004g0102 a0001c0001t0004g0103 a0001c0001t0004g0104 |
3 | HG03516.hp2 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.617-463delC | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 7/23 | chr17 | 59076176 | |||||||
| chr17:59076326 | A | G | 1 | a0001c0001t0001g0266 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.617-612T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 7/23 | chr17 | 59076326 | |||||||
| chr17:59076351 | G | C | 7 | a0001c0001t0002g0080 a0001c0001t0002g0112 a0001c0001t0002g0113 others(4): Show |
7 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.617-637C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 7/23 | chr17 | 59076351 | |||||||
| chr17:59076506 | T | C | 5 | a0001c0001t0003g0073 a0001c0001t0003g0074 a0001c0001t0003g0075 others(2): Show |
5 | HG02486.hp2 HG02630.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.617-792A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 7/23 | chr17 | 59076506 | |||||||
| chr17:59076827 | T | A | 1 | a0001c0001t0003g0061 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.617-1113A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 7/23 | chr17 | 59076827 | |||||||
| chr17:59076865 | C | T | 3 | a0001c0001t0001g0261 a0001c0001t0001g0315 a0001c0001t0001g0316 |
3 | HG00544.hp1 NA18963.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.617-1151G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 7/23 | chr17 | 59076865 | |||||||
| chr17:59077267 | C | CT | 6 | a0001c0001t0001g0265 a0001c0001t0002g0114 a0001c0001t0002g0157 others(3): Show |
6 | HG01175.hp2 HG01358.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.617-1554dupA | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 7/23 | chr17 | 59077267 | |||||||
| chr17:59077308 | T | C | 1 | a0001c0001t0001g0339 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.617-1594A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 7/23 | chr17 | 59077308 | |||||||
| chr17:59077412 | T | C | 1 | a0001c0001t0001g0323 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.617-1698A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 7/23 | chr17 | 59077412 | |||||||
| chr17:59077617 | C | T | 2 | a0001c0001t0003g0011 a0001c0001t0003g0018 |
2 | NA18949.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.617-1903G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 7/23 | chr17 | 59077617 | |||||||
| chr17:59077809 | C | CA | 116 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0001g0287 others(113): Show |
116 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.616+1944dupT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 7/23 | chr17 | 59077809 | |||||||
| chr17:59077809 | C | CAA | 85 | a0001c0001t0002g0107 a0001c0001t0002g0110 a0001c0001t0002g0111 others(82): Show |
85 | HG00099.hp1 HG00544.hp2 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.616+1943_616+1944d others(4): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 7/23 | chr17 | 59077809 | |||||||
| chr17:59077809 | C | CAAA | 10 | a0001c0001t0002g0137 a0001c0001t0002g0145 a0001c0001t0002g0146 others(7): Show |
10 | HG00438.hp2 HG01361.hp2 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.616+1942_616+1944d others(5): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 7/23 | chr17 | 59077809 | |||||||
| chr17:59077881 | C | T | 1 | a0001c0006t0003g0105 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.616+1873G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 7/23 | chr17 | 59077881 | |||||||
| chr17:59077888 | C | T | 1 | a0001c0001t0001g0220 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.616+1866G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 7/23 | chr17 | 59077888 | |||||||
| chr17:59078881 | A | G | 4 | a0001c0001t0007g0213 a0001c0001t0007g0214 a0001c0001t0007g0215 others(1): Show |
4 | HG01243.hp2 HG03471.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.616+873T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 7/23 | chr17 | 59078881 | |||||||
| chr17:59079050 | C | CA | 13 | a0001c0001t0001g0232 a0001c0001t0001g0236 a0001c0001t0001g0237 others(10): Show |
13 | HG01168.hp1 HG01192.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.616+703dupT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 7/23 | chr17 | 59079050 | |||||||
| chr17:59079474 | A | G | 1 | a0002c0002t0002g0206 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.616+280T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 7/23 | chr17 | 59079474 | |||||||
| chr17:59079724 | G | A | 1 | a0001c0001t0001g0313 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.616+30C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 7/23 | chr17 | 59079724 | |||||||
| chr17:59080015 | T | G | 2 | a0001c0001t0002g0120 a0001c0001t0002g0121 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.493-138A>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 6/23 | chr17 | 59080015 | |||||||
| chr17:59080085 | C | T | 1 | a0001c0001t0003g0122 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.493-208G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 6/23 | chr17 | 59080085 | |||||||
| chr17:59080215 | T | C | 1 | a0001c0001t0002g0210 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.493-338A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 6/23 | chr17 | 59080215 | |||||||
| chr17:59080372 | G | A | 1 | a0001c0006t0003g0105 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.493-495C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 6/23 | chr17 | 59080372 | |||||||
| chr17:59080659 | T | C | 1 | a0001c0001t0001g0338 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.492+438A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 6/23 | chr17 | 59080659 | |||||||
| chr17:59080984 | T | C | 93 | a0001c0001t0002g0110 a0001c0001t0002g0124 a0001c0001t0002g0126 others(90): Show |
93 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.492+113A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 6/23 | chr17 | 59080984 | |||||||
| chr17:59080993 | T | C | 1 | a0001c0001t0001g0288 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.492+104A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 6/23 | chr17 | 59080993 | |||||||
| chr17:59081027 | T | C | 8 | a0001c0001t0007g0213 a0001c0001t0007g0214 a0001c0001t0007g0215 others(5): Show |
8 | HG00642.hp2 HG01243.hp2 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.492+70A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 6/23 | chr17 | 59081027 | |||||||
| chr17:59081072 | A | G | 1 | a0001c0001t0001g0233 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.492+25T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 6/23 | chr17 | 59081072 | |||||||
| chr17:59081403 | C | T | 8 | a0001c0001t0001g0260 a0001c0001t0001g0289 a0001c0001t0001g0290 others(5): Show |
8 | HG00642.hp1 HG00733.hp1 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.370-184G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59081403 | |||||||
| chr17:59081479 | G | A | 212 | a0001c0001t0001g0339 a0001c0001t0002g0080 a0001c0001t0002g0089 others(209): Show |
212 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.370-260C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59081479 | |||||||
| chr17:59081558 | C | A | 2 | a0001c0001t0002g0107 a0001c0001t0002g0111 |
2 | HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.370-339G>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59081558 | |||||||
| chr17:59081579 | A | G | 11 | a0001c0001t0002g0080 a0001c0001t0002g0112 a0001c0001t0002g0113 others(8): Show |
11 | HG01257.hp2 HG01258.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.370-360T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59081579 | |||||||
| chr17:59081645 | T | C | 9 | a0001c0001t0001g0260 a0001c0001t0001g0289 a0001c0001t0001g0290 others(6): Show |
9 | HG00642.hp1 HG00733.hp1 HG00735.hp1 others(6): Show |
intron_variant | MODIFIER | c.370-426A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59081645 | |||||||
| chr17:59081737 | G | A | 3 | a0001c0001t0002g0126 a0001c0001t0002g0143 a0001c0001t0002g0147 |
3 | HG02071.hp1 NA18995.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.370-518C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59081737 | |||||||
| chr17:59081821 | T | C | 2 | a0001c0001t0002g0120 a0001c0001t0002g0121 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.370-602A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59081821 | |||||||
| chr17:59081906 | C | T | 3 | a0001c0001t0004g0102 a0001c0001t0004g0103 a0001c0001t0004g0104 |
3 | HG03516.hp2 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.370-687G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59081906 | |||||||
| chr17:59081907 | A | C | 114 | a0001c0001t0002g0080 a0001c0001t0002g0107 a0001c0001t0002g0110 others(111): Show |
114 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.370-688T>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59081907 | |||||||
| chr17:59081941 | AAAAAAAA others(5): Show |
A | 2 | a0001c0001t0010g0078 a0001c0001t0010g0090 |
2 | HG02109.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.370-734_370-723del others(12): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59081941 | |||||||
| chr17:59081944 | A | T | 7 | a0001c0001t0001g0232 a0001c0001t0001g0236 a0001c0001t0001g0237 others(4): Show |
7 | HG01168.hp1 HG02559.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.370-725T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59081944 | |||||||
| chr17:59081947 | A | T | 1 | a0001c0001t0001g0229 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.370-728T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59081947 | |||||||
| chr17:59081949 | AAAAT | A | 27 | a0001c0001t0002g0130 a0001c0001t0002g0132 a0001c0001t0002g0150 others(24): Show |
27 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.370-734_370-731del others(4): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59081949 | |||||||
| chr17:59081950 | A | T | 2 | a0001c0001t0007g0213 a0001c0001t0007g0214 |
2 | HG03471.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.370-731T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59081950 | |||||||
| chr17:59081950 | AAAT | A | 55 | a0001c0001t0002g0110 a0001c0001t0002g0124 a0001c0001t0002g0126 others(52): Show |
55 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.370-734_370-732del others(3): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59081950 | |||||||
| chr17:59081951 | AAT | A | 54 | a0001c0001t0001g0339 a0001c0001t0002g0098 a0001c0001t0002g0186 others(51): Show |
54 | HG01261.hp2 HG01346.hp2 HG01943.hp1 others(51): Show |
intron_variant | MODIFIER | c.370-734_370-733del others(2): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59081951 | |||||||
| chr17:59081952 | AT | A | 32 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0013 others(29): Show |
32 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(29): Show |
intron_variant | MODIFIER | c.370-734delA | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59081952 | |||||||
| chr17:59081953 | T | A | 26 | a0001c0001t0002g0080 a0001c0001t0002g0107 a0001c0001t0002g0111 others(23): Show |
26 | HG01106.hp2 HG01257.hp2 HG01258.hp1 others(23): Show |
intron_variant | MODIFIER | c.370-734A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59081953 | |||||||
| chr17:59081953 | TAAAAAAA others(4): Show |
T | 2 | a0001c0001t0001g0296 a0001c0001t0001g0300 |
2 | NA18979.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.370-745_370-735del others(11): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59081953 | |||||||
| chr17:59081954 | A | T | 1 | a0001c0001t0001g0257 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.370-735T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59081954 | |||||||
| chr17:59081955 | A | ATAATAAT | 3 | a0001c0001t0007g0214 a0001c0001t0007g0215 a0001c0001t0007g0216 |
3 | HG01243.hp2 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.370-737_370-736ins others(7): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59081955 | |||||||
| chr17:59081955 | A | ATAATAAT others(3): Show |
1 | a0001c0001t0007g0213 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.370-737_370-736ins others(10): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59081955 | |||||||
| chr17:59081955 | A | T | 3 | a0001c0001t0002g0155 a0001c0001t0003g0006 a0001c0001t0003g0054 |
3 | HG01106.hp2 HG02965.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.370-736T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59081955 | |||||||
| chr17:59081958 | A | T | 24 | a0001c0001t0002g0089 a0001c0001t0002g0117 a0001c0001t0002g0137 others(21): Show |
24 | HG01106.hp2 HG01243.hp2 HG01261.hp1 others(21): Show |
intron_variant | MODIFIER | c.370-739T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59081958 | |||||||
| chr17:59081959 | A | T | 1 | a0001c0001t0001g0338 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.370-740T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59081959 | |||||||
| chr17:59081961 | A | AAATAATA others(5): Show |
1 | a0001c0001t0002g0118 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.370-743_370-742ins others(12): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59081961 | |||||||
| chr17:59081961 | A | AATAATAA others(4): Show |
1 | a0001c0001t0002g0116 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.370-743_370-742ins others(11): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59081961 | |||||||
| chr17:59081961 | A | ATAATAAT others(6): Show |
1 | a0001c0001t0002g0115 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.370-743_370-742ins others(13): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59081961 | |||||||
| chr17:59081961 | A | T | 116 | a0001c0001t0001g0234 a0001c0001t0001g0240 a0001c0001t0001g0241 others(113): Show |
116 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(113): Show |
intron_variant | MODIFIER | c.370-742T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59081961 | |||||||
| chr17:59081964 | A | AAAAAAAA others(7): Show |
1 | a0001c0001t0002g0080 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.370-746_370-745ins others(14): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59081964 | |||||||
| chr17:59081964 | A | AAAAAAAT others(6): Show |
1 | a0001c0001t0002g0113 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.370-746_370-745ins others(13): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59081964 | |||||||
| chr17:59081964 | A | AAAAATAA others(7): Show |
1 | a0001c0001t0002g0114 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.370-746_370-745ins others(14): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59081964 | |||||||
| chr17:59081964 | A | AAATAATA others(5): Show |
1 | a0001c0001t0002g0112 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.370-757_370-746dup others(12): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59081964 | |||||||
| chr17:59081964 | A | T | 291 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0223 others(288): Show |
291 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(288): Show |
intron_variant | MODIFIER | c.370-745T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59081964 | |||||||
| chr17:59081967 | T | A | 2 | a0001c0001t0001g0301 a0001c0001t0001g0302 |
2 | HG01358.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.370-748A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59081967 | |||||||
| chr17:59081970 | T | A | 1 | a0001c0001t0001g0302 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.370-751A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59081970 | |||||||
| chr17:59082132 | G | A | 1 | a0001c0001t0001g0303 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.370-913C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59082132 | |||||||
| chr17:59082137 | G | A | 2 | a0001c0001t0002g0153 a0001c0001t0002g0155 |
2 | HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.370-918C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59082137 | |||||||
| chr17:59082196 | G | A | 4 | a0001c0001t0003g0073 a0001c0001t0003g0074 a0001c0001t0003g0075 others(1): Show |
4 | HG02486.hp2 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.370-977C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59082196 | |||||||
| chr17:59082248 | G | A | 1 | a0001c0001t0003g0035 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.370-1029C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59082248 | |||||||
| chr17:59082274 | A | G | 1 | a0001c0001t0003g0072 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.370-1055T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59082274 | |||||||
| chr17:59082513 | A | C | 1 | a0001c0001t0002g0141 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.370-1294T>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59082513 | |||||||
| chr17:59082629 | A | T | 95 | a0001c0001t0002g0107 a0001c0001t0002g0110 a0001c0001t0002g0111 others(92): Show |
95 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.369+1373T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59082629 | |||||||
| chr17:59082753 | T | C | 1 | a0001c0006t0003g0105 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.369+1249A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59082753 | |||||||
| chr17:59082856 | T | C | 1 | a0001c0001t0012g0002 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.369+1146A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59082856 | |||||||
| chr17:59083152 | G | C | 97 | a0001c0001t0001g0339 a0001c0001t0002g0089 a0001c0001t0002g0098 others(94): Show |
97 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.369+850C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59083152 | |||||||
| chr17:59083274 | A | G | 1 | a0001c0001t0001g0239 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.369+728T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59083274 | |||||||
| chr17:59083302 | G | A | 1 | a0001c0001t0001g0330 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.369+700C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59083302 | |||||||
| chr17:59083434 | C | CA | 8 | a0001c0001t0002g0186 a0001c0001t0002g0204 a0001c0001t0003g0036 others(5): Show |
8 | HG00733.hp2 HG01099.hp1 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.369+567dupT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59083434 | |||||||
| chr17:59083497 | C | G | 2 | a0001c0001t0002g0151 a0001c0001t0002g0152 |
2 | HG03834.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.369+505G>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59083497 | |||||||
| chr17:59083620 | G | A | 1 | a0001c0006t0003g0105 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.369+382C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59083620 | |||||||
| chr17:59083752 | T | C | 2 | a0001c0001t0002g0120 a0001c0001t0002g0121 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.369+250A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59083752 | |||||||
| chr17:59083773 | T | C | 2 | a0001c0001t0001g0252 a0001c0001t0001g0253 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.369+229A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59083773 | |||||||
| chr17:59083862 | C | A | 1 | a0001c0008t0003g0038 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.369+140G>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59083862 | |||||||
| chr17:59084408 | G | C | 12 | a0001c0001t0003g0061 a0001c0001t0003g0062 a0001c0001t0003g0063 others(9): Show |
12 | HG02055.hp1 HG02572.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.282-319C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 4/23 | chr17 | 59084408 | |||||||
| chr17:59084517 | T | G | 1 | a0001c0001t0003g0077 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.282-428A>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 4/23 | chr17 | 59084517 | |||||||
| chr17:59084774 | A | G | 5 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0006 others(2): Show |
5 | HG01106.hp2 HG01978.hp2 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.282-685T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 4/23 | chr17 | 59084774 | |||||||
| chr17:59084806 | T | C | 2 | a0001c0001t0003g0039 a0001c0001t0003g0046 |
2 | HG00733.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.282-717A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 4/23 | chr17 | 59084806 | |||||||
| chr17:59084835 | G | A | 8 | a0001c0001t0007g0213 a0001c0001t0007g0214 a0001c0001t0007g0215 others(5): Show |
8 | HG00642.hp2 HG01243.hp2 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.282-746C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 4/23 | chr17 | 59084835 | |||||||
| chr17:59084848 | A | G | 96 | a0001c0001t0001g0311 a0001c0001t0002g0124 a0001c0001t0002g0126 others(93): Show |
96 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.282-759T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 4/23 | chr17 | 59084848 | |||||||
| chr17:59085103 | A | T | 224 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0230 others(221): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(221): Show |
intron_variant | MODIFIER | c.282-1014T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 4/23 | chr17 | 59085103 | |||||||
| chr17:59085292 | A | C | 1 | a0001c0001t0001g0231 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.282-1203T>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 4/23 | chr17 | 59085292 | |||||||
| chr17:59085515 | G | C | 1 | a0001c0001t0003g0049 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.282-1426C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 4/23 | chr17 | 59085515 | |||||||
| chr17:59085667 | C | T | 1 | a0001c0001t0001g0264 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.282-1578G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 4/23 | chr17 | 59085667 | |||||||
| chr17:59085787 | G | A | 3 | a0001c0001t0002g0119 a0001c0001t0002g0120 a0001c0001t0002g0121 |
3 | HG01257.hp2 HG01258.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.282-1698C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 4/23 | chr17 | 59085787 | |||||||
| chr17:59086012 | T | C | 1 | a0001c0001t0003g0077 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.282-1923A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 4/23 | chr17 | 59086012 | |||||||
| chr17:59086140 | C | T | 97 | a0001c0001t0001g0339 a0001c0001t0002g0089 a0001c0001t0002g0098 others(94): Show |
97 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.282-2051G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 4/23 | chr17 | 59086140 | |||||||
| chr17:59086161 | G | C | 1 | a0001c0001t0003g0047 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.282-2072C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 4/23 | chr17 | 59086161 | |||||||
| chr17:59086238 | A | AT | 6 | a0001c0001t0002g0198 a0001c0001t0002g0201 a0001c0001t0003g0010 others(3): Show |
6 | HG01981.hp2 HG03098.hp2 NA18978.hp1 others(3): Show |
intron_variant | MODIFIER | c.281+2052dupA | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 4/23 | chr17 | 59086238 | |||||||
| chr17:59086395 | C | T | 11 | a0001c0001t0002g0080 a0001c0001t0002g0112 a0001c0001t0002g0113 others(8): Show |
11 | HG01257.hp2 HG01258.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.281+1896G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 4/23 | chr17 | 59086395 | |||||||
| chr17:59086430 | G | A | 93 | a0001c0001t0002g0110 a0001c0001t0002g0124 a0001c0001t0002g0126 others(90): Show |
93 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.281+1861C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 4/23 | chr17 | 59086430 | |||||||
| chr17:59086511 | T | A | 95 | a0001c0001t0002g0107 a0001c0001t0002g0110 a0001c0001t0002g0111 others(92): Show |
95 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.281+1780A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 4/23 | chr17 | 59086511 | |||||||
| chr17:59086632 | A | G | 2 | a0001c0001t0003g0051 a0001c0001t0003g0052 |
2 | NA18943.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.281+1659T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 4/23 | chr17 | 59086632 | |||||||
| chr17:59086834 | T | A | 74 | a0001c0001t0001g0339 a0001c0001t0003g0003 a0001c0001t0003g0004 others(71): Show |
74 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.281+1457A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 4/23 | chr17 | 59086834 | |||||||
| chr17:59087028 | C | A | 1 | a0001c0001t0002g0198 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.281+1263G>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 4/23 | chr17 | 59087028 | |||||||
| chr17:59087250 | G | A | 6 | a0001c0001t0001g0232 a0001c0001t0001g0236 a0001c0001t0001g0237 others(3): Show |
6 | HG01168.hp1 HG02559.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.281+1041C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 4/23 | chr17 | 59087250 | |||||||
| chr17:59087458 | C | CT | 93 | a0001c0001t0001g0339 a0001c0001t0002g0098 a0001c0001t0003g0003 others(90): Show |
93 | HG00099.hp2 HG00438.hp1 HG00733.hp2 others(90): Show |
intron_variant | MODIFIER | c.281+832dupA | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 4/23 | chr17 | 59087458 | |||||||
| chr17:59087458 | CT | C | 15 | a0001c0001t0001g0230 a0001c0001t0001g0254 a0001c0001t0001g0305 others(12): Show |
15 | HG00323.hp2 HG00642.hp2 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.281+832delA | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 4/23 | chr17 | 59087458 | |||||||
| chr17:59087662 | G | A | 1 | a0001c0001t0009g0168 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.281+629C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 4/23 | chr17 | 59087662 | |||||||
| chr17:59087735 | AG | A | 7 | a0001c0001t0002g0080 a0001c0001t0002g0112 a0001c0001t0002g0113 others(4): Show |
7 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.281+555delC | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 4/23 | chr17 | 59087735 | |||||||
| chr17:59087736 | G | A | 213 | a0001c0001t0001g0339 a0001c0001t0002g0089 a0001c0001t0002g0098 others(210): Show |
213 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.281+555C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 4/23 | chr17 | 59087736 | |||||||
| chr17:59087737 | G | A | 7 | a0001c0001t0002g0080 a0001c0001t0002g0112 a0001c0001t0002g0113 others(4): Show |
7 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.281+554C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 4/23 | chr17 | 59087737 | |||||||
| chr17:59087851 | TCTTTC | T | 7 | a0001c0001t0002g0080 a0001c0001t0002g0112 a0001c0001t0002g0113 others(4): Show |
7 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.281+435_281+439del others(5): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 4/23 | chr17 | 59087851 | |||||||
| chr17:59087856 | C | T | 23 | a0001c0001t0002g0089 a0001c0001t0002g0098 a0001c0001t0003g0079 others(20): Show |
23 | HG01168.hp2 HG01169.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.281+435G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 4/23 | chr17 | 59087856 | |||||||
| chr17:59087920 | A | G | 1 | a0001c0001t0002g0155 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.281+371T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 4/23 | chr17 | 59087920 | |||||||
| chr17:59087942 | G | T | 1 | a0001c0001t0002g0089 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.281+349C>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 4/23 | chr17 | 59087942 | |||||||
| chr17:59087958 | A | T | 1 | a0001c0001t0001g0232 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.281+333T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 4/23 | chr17 | 59087958 | |||||||
| chr17:59088535 | A | G | 1 | a0001c0001t0009g0183 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.165-128T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 3/23 | chr17 | 59088535 | |||||||
| chr17:59088571 | G | A | 2 | a0001c0001t0001g0304 a0001c0001t0001g0305 |
2 | HG00323.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.165-164C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 3/23 | chr17 | 59088571 | |||||||
| chr17:59088847 | A | G | 6 | a0001c0001t0003g0081 a0001c0001t0003g0082 a0001c0001t0003g0083 others(3): Show |
6 | HG02559.hp1 HG02647.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.165-440T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 3/23 | chr17 | 59088847 | |||||||
| chr17:59088871 | T | G | 4 | a0001c0003t0006g0212 a0001c0003t0006g0217 a0001c0003t0006g0218 others(1): Show |
4 | HG00642.hp2 HG03704.hp2 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.165-464A>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 3/23 | chr17 | 59088871 | |||||||
| chr17:59089132 | C | T | 4 | a0001c0001t0007g0213 a0001c0001t0007g0214 a0001c0001t0007g0215 others(1): Show |
4 | HG01243.hp2 HG03471.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.165-725G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 3/23 | chr17 | 59089132 | |||||||
| chr17:59089228 | T | C | 2 | a0001c0001t0001g0306 a0001c0001t0001g0307 |
2 | HG01496.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.165-821A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 3/23 | chr17 | 59089228 | |||||||
| chr17:59089414 | G | A | 11 | a0001c0001t0002g0080 a0001c0001t0002g0112 a0001c0001t0002g0113 others(8): Show |
11 | HG01257.hp2 HG01258.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.165-1007C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 3/23 | chr17 | 59089414 | |||||||
| chr17:59089421 | T | A | 1 | a0001c0001t0002g0147 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.165-1014A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 3/23 | chr17 | 59089421 | |||||||
| chr17:59089458 | T | C | 2 | a0001c0001t0001g0308 a0001c0001t0001g0309 |
2 | HG02300.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.165-1051A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 3/23 | chr17 | 59089458 | |||||||
| chr17:59089498 | G | A | 1 | a0001c0001t0003g0061 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.165-1091C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 3/23 | chr17 | 59089498 | |||||||
| chr17:59089616 | G | T | 1 | a0001c0001t0002g0140 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.165-1209C>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 3/23 | chr17 | 59089616 | |||||||
| chr17:59089625 | G | C | 1 | a0001c0001t0002g0153 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.165-1218C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 3/23 | chr17 | 59089625 | |||||||
| chr17:59089822 | G | A | 1 | a0001c0001t0002g0169 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.165-1415C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 3/23 | chr17 | 59089822 | |||||||
| chr17:59090164 | T | C | 4 | a0001c0001t0001g0236 a0001c0001t0001g0237 a0001c0001t0001g0238 others(1): Show |
4 | HG01168.hp1 HG02647.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.164+1136A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 3/23 | chr17 | 59090164 | |||||||
| chr17:59090242 | T | A | 8 | a0001c0001t0007g0213 a0001c0001t0007g0214 a0001c0001t0007g0215 others(5): Show |
8 | HG00642.hp2 HG01243.hp2 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.164+1058A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 3/23 | chr17 | 59090242 | |||||||
| chr17:59090632 | G | A | 1 | a0001c0001t0001g0255 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.164+668C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 3/23 | chr17 | 59090632 | |||||||
| chr17:59090652 | G | A | 1 | a0001c0001t0002g0134 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.164+648C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 3/23 | chr17 | 59090652 | |||||||
| chr17:59090683 | C | A | 2 | a0001c0001t0003g0108 a0001c0001t0003g0109 |
2 | HG02451.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.164+617G>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 3/23 | chr17 | 59090683 | |||||||
| chr17:59090688 | C | T | 4 | a0001c0001t0003g0073 a0001c0001t0003g0074 a0001c0001t0003g0075 others(1): Show |
4 | HG02486.hp2 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.164+612G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 3/23 | chr17 | 59090688 | |||||||
| chr17:59090933 | C | T | 2 | a0001c0001t0003g0013 a0001c0001t0003g0014 |
2 | HG00099.hp2 HG00280.hp2 |
intron_variant | MODIFIER | c.164+367G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 3/23 | chr17 | 59090933 | |||||||
| chr17:59091098 | G | A | 1 | a0001c0001t0003g0008 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.164+202C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 3/23 | chr17 | 59091098 | |||||||
| chr17:59091134 | T | G | 2 | a0001c0001t0003g0108 a0001c0001t0003g0109 |
2 | HG02451.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.164+166A>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 3/23 | chr17 | 59091134 | |||||||
| chr17:59091217 | G | A | 1 | a0003c0007t0002g0179 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.164+83C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 3/23 | chr17 | 59091217 | |||||||
| chr17:59091415 | T | A | 1 | a0001c0001t0002g0136 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.124-75A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59091415 | |||||||
| chr17:59091471 | CATAATAT | C | 7 | a0001c0001t0001g0311 a0001c0001t0003g0009 a0001c0001t0003g0043 others(4): Show |
7 | HG00438.hp1 HG02523.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.124-138_124-132del others(7): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59091471 | |||||||
| chr17:59091483 | TATATA | T | 8 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0001c0001t0001g0287 others(5): Show |
8 | HG02293.hp2 HG02886.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.124-148_124-144del others(5): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59091483 | |||||||
| chr17:59091509 | T | TTA | 4 | a0001c0003t0006g0212 a0001c0003t0006g0217 a0001c0003t0006g0218 others(1): Show |
4 | HG00642.hp2 HG03704.hp2 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.124-170_124-169ins others(2): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59091509 | |||||||
| chr17:59091509 | TCA | T | 127 | a0001c0001t0002g0080 a0001c0001t0002g0107 a0001c0001t0002g0110 others(124): Show |
127 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.124-171_124-170del others(2): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59091509 | |||||||
| chr17:59091510 | C | T | 103 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0230 others(100): Show |
103 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.124-170G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59091510 | |||||||
| chr17:59091531 | GTATAATA others(35): Show |
G | 16 | a0001c0001t0002g0126 a0001c0001t0002g0134 a0001c0001t0002g0135 others(13): Show |
16 | HG00558.hp2 HG00673.hp1 HG02071.hp1 others(13): Show |
intron_variant | MODIFIER | c.124-233_124-192del others(42): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59091531 | |||||||
| chr17:59091535 | AATAATGT others(32): Show |
A | 202 | a0001c0001t0001g0339 a0001c0001t0002g0080 a0001c0001t0002g0089 others(199): Show |
202 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.124-234_124-196del others(39): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59091535 | |||||||
| chr17:59091541 | GTATAA | G | 5 | a0001c0001t0001g0263 a0001c0001t0001g0271 a0001c0001t0001g0272 others(2): Show |
5 | HG01192.hp1 HG01943.hp2 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.124-206_124-202del others(5): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59091541 | |||||||
| chr17:59091558 | TTATATAT others(34): Show |
T | 2 | a0001c0001t0002g0117 a0001c0001t0002g0128 |
2 | HG02622.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.124-259_124-219del others(41): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59091558 | |||||||
| chr17:59091567 | T | A | 4 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0001c0001t0001g0288 others(1): Show |
4 | NA18946.hp2 NA18993.hp2 NA19086.hp2 others(1): Show |
intron_variant | MODIFIER | c.124-227A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59091567 | |||||||
| chr17:59091568 | A | AAT | 94 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(91): Show |
94 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.124-230_124-229dup others(2): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59091568 | |||||||
| chr17:59091568 | A | AATATATA others(36): Show |
1 | a0001c0001t0001g0330 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.124-229_124-228ins others(43): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59091568 | |||||||
| chr17:59091568 | A | ATT | 12 | a0001c0001t0001g0225 a0001c0001t0001g0234 a0001c0001t0001g0240 others(9): Show |
12 | HG01070.hp2 HG01081.hp2 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.124-229_124-228ins others(2): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59091568 | |||||||
| chr17:59091568 | A | T | 4 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0001c0001t0001g0288 others(1): Show |
4 | NA18946.hp2 NA18993.hp2 NA19086.hp2 others(1): Show |
intron_variant | MODIFIER | c.124-228T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59091568 | |||||||
| chr17:59091595 | C | T | 5 | a0001c0001t0003g0073 a0001c0001t0003g0074 a0001c0001t0003g0075 others(2): Show |
5 | HG02486.hp2 HG02630.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.124-255G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59091595 | |||||||
| chr17:59091622 | TATA | T | 3 | a0001c0003t0006g0217 a0001c0003t0006g0218 a0001c0003t0006g0219 |
3 | HG00642.hp2 NA20752.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.124-285_124-283del others(3): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59091622 | |||||||
| chr17:59091640 | A | G | 1 | a0001c0001t0003g0096 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.124-300T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59091640 | |||||||
| chr17:59091828 | A | C | 1 | a0001c0006t0003g0105 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.124-488T>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59091828 | |||||||
| chr17:59091897 | A | C | 1 | a0001c0001t0002g0131 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.124-557T>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59091897 | |||||||
| chr17:59092055 | G | GA | 8 | a0001c0001t0007g0213 a0001c0001t0007g0214 a0001c0001t0007g0215 others(5): Show |
8 | HG00642.hp2 HG01243.hp2 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.124-716dupT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59092055 | |||||||
| chr17:59092120 | C | T | 11 | a0001c0001t0002g0080 a0001c0001t0002g0112 a0001c0001t0002g0113 others(8): Show |
11 | HG01257.hp2 HG01258.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.124-780G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59092120 | |||||||
| chr17:59092232 | A | G | 6 | a0001c0001t0001g0232 a0001c0001t0001g0236 a0001c0001t0001g0237 others(3): Show |
6 | HG01168.hp1 HG02559.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.124-892T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59092232 | |||||||
| chr17:59092247 | G | T | 1 | a0001c0003t0006g0212 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.124-907C>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59092247 | |||||||
| chr17:59092348 | G | A | 1 | a0002c0002t0002g0208 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.124-1008C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59092348 | |||||||
| chr17:59092398 | C | CA | 11 | a0001c0001t0001g0256 a0001c0001t0001g0310 a0001c0001t0001g0311 others(8): Show |
11 | HG00597.hp2 HG01361.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.124-1059dupT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59092398 | |||||||
| chr17:59092412 | C | A | 2 | a0001c0001t0002g0115 a0001c0001t0003g0060 |
2 | HG02886.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.124-1072G>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59092412 | |||||||
| chr17:59092412 | C | CA | 8 | a0001c0001t0001g0312 a0001c0001t0001g0314 a0001c0001t0001g0323 others(5): Show |
8 | HG01192.hp2 HG01433.hp2 NA18906.hp1 others(5): Show |
intron_variant | MODIFIER | c.124-1073dupT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59092412 | |||||||
| chr17:59092710 | TATTTGTT others(90): Show |
T | 1 | a0001c0001t0015g0331 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.124-1467_124-1371d others(99): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59092710 | |||||||
| chr17:59092808 | G | C | 1 | a0001c0001t0015g0331 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.124-1468C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59092808 | |||||||
| chr17:59093026 | T | C | 4 | a0001c0001t0003g0073 a0001c0001t0003g0074 a0001c0001t0003g0075 others(1): Show |
4 | HG02486.hp2 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.124-1686A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59093026 | |||||||
| chr17:59093156 | TAAAATA | T | 4 | a0001c0001t0002g0135 a0001c0001t0002g0137 a0001c0001t0002g0138 others(1): Show |
4 | NA18946.hp1 NA18964.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.124-1822_124-1817d others(8): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59093156 | |||||||
| chr17:59093306 | G | A | 6 | a0001c0001t0002g0080 a0001c0001t0002g0112 a0001c0001t0002g0113 others(3): Show |
6 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.124-1966C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59093306 | |||||||
| chr17:59093504 | G | C | 1 | a0001c0001t0003g0047 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.124-2164C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59093504 | |||||||
| chr17:59093508 | C | T | 1 | a0001c0001t0001g0332 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.124-2168G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59093508 | |||||||
| chr17:59093737 | T | C | 2 | a0001c0001t0001g0313 a0001c0001t0001g0314 |
2 | HG01433.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.124-2397A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59093737 | |||||||
| chr17:59093762 | C | T | 1 | a0001c0001t0001g0263 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.124-2422G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59093762 | |||||||
| chr17:59093778 | G | A | 1 | a0001c0001t0011g0001 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.124-2438C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59093778 | |||||||
| chr17:59093778 | G | T | 2 | a0001c0001t0002g0107 a0001c0001t0002g0111 |
2 | HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.124-2438C>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59093778 | |||||||
| chr17:59093973 | C | T | 1 | a0001c0001t0001g0235 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.124-2633G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59093973 | |||||||
| chr17:59094058 | A | C | 3 | a0001c0001t0004g0102 a0001c0001t0004g0103 a0001c0001t0004g0104 |
3 | HG03516.hp2 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.124-2718T>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59094058 | |||||||
| chr17:59094556 | C | T | 98 | a0001c0001t0001g0339 a0001c0001t0002g0089 a0001c0001t0002g0098 others(95): Show |
98 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.124-3216G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59094556 | |||||||
| chr17:59094692 | G | A | 5 | a0001c0001t0002g0124 a0001c0001t0002g0131 a0001c0001t0002g0187 others(2): Show |
5 | HG02132.hp1 HG02135.hp2 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.124-3352C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59094692 | |||||||
| chr17:59095088 | G | A | 1 | a0001c0001t0001g0257 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.124-3748C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59095088 | |||||||
| chr17:59095395 | T | C | 2 | a0001c0001t0003g0099 a0001c0001t0003g0100 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.124-4055A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59095395 | |||||||
| chr17:59095869 | C | T | 3 | a0001c0001t0001g0318 a0001c0001t0001g0319 a0001c0001t0014g0262 |
3 | NA18943.hp2 NA18955.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.124-4529G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59095869 | |||||||
| chr17:59096083 | A | T | 1 | a0001c0006t0003g0105 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.124-4743T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59096083 | |||||||
| chr17:59096479 | G | A | 62 | a0001c0001t0001g0339 a0001c0001t0003g0003 a0001c0001t0003g0004 others(59): Show |
62 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.124-5139C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59096479 | |||||||
| chr17:59096484 | A | G | 220 | a0001c0001t0001g0339 a0001c0001t0002g0080 a0001c0001t0002g0089 others(217): Show |
220 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.124-5144T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59096484 | |||||||
| chr17:59096548 | TCAAAAAA others(7): Show |
T | 4 | a0001c0003t0006g0212 a0001c0003t0006g0217 a0001c0003t0006g0218 others(1): Show |
4 | HG00642.hp2 HG03704.hp2 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.124-5222_124-5209d others(16): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59096548 | |||||||
| chr17:59096549 | C | CA | 109 | a0001c0001t0001g0223 a0001c0001t0001g0227 a0001c0001t0001g0275 others(106): Show |
109 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.124-5210dupT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59096549 | |||||||
| chr17:59096549 | C | CAA | 6 | a0001c0001t0002g0152 a0001c0001t0002g0173 a0001c0001t0002g0194 others(3): Show |
6 | HG01071.hp2 HG03516.hp2 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.124-5211_124-5210d others(4): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59096549 | |||||||
| chr17:59096559 | A | C | 2 | a0001c0001t0001g0315 a0001c0001t0001g0316 |
2 | NA18963.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.124-5219T>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59096559 | |||||||
| chr17:59096563 | C | A | 7 | a0001c0001t0002g0148 a0001c0001t0002g0173 a0001c0001t0002g0174 others(4): Show |
7 | HG01070.hp1 HG01071.hp2 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.124-5223G>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59096563 | |||||||
| chr17:59096563 | CA | C | 72 | a0001c0001t0001g0234 a0001c0001t0001g0339 a0001c0001t0003g0003 others(69): Show |
72 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.124-5224delT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59096563 | |||||||
| chr17:59096564 | A | C | 1 | a0001c0001t0003g0010 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.124-5224T>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59096564 | |||||||
| chr17:59096626 | A | C | 1 | a0001c0001t0001g0261 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.124-5286T>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59096626 | |||||||
| chr17:59096704 | T | C | 23 | a0001c0001t0002g0089 a0001c0001t0002g0098 a0001c0001t0003g0079 others(20): Show |
23 | HG01168.hp2 HG01169.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.124-5364A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59096704 | |||||||
| chr17:59096896 | C | T | 8 | a0001c0001t0007g0213 a0001c0001t0007g0214 a0001c0001t0007g0215 others(5): Show |
8 | HG00642.hp2 HG01243.hp2 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.124-5556G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59096896 | |||||||
| chr17:59096965 | T | C | 2 | a0001c0001t0001g0315 a0001c0001t0001g0316 |
2 | NA18963.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.124-5625A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59096965 | |||||||
| chr17:59097254 | T | C | 2 | a0001c0001t0004g0103 a0001c0001t0004g0104 |
2 | NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.124-5914A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59097254 | |||||||
| chr17:59097325 | C | T | 23 | a0001c0001t0002g0089 a0001c0001t0002g0098 a0001c0001t0003g0079 others(20): Show |
23 | HG01168.hp2 HG01169.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.124-5985G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59097325 | |||||||
| chr17:59097668 | A | T | 2 | a0001c0001t0003g0087 a0001c0001t0003g0088 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.124-6328T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59097668 | |||||||
| chr17:59097752 | G | C | 1 | a0001c0001t0012g0002 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.124-6412C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59097752 | |||||||
| chr17:59097837 | G | C | 1 | a0001c0001t0002g0130 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.123+6456C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59097837 | |||||||
| chr17:59097869 | A | G | 1 | a0001c0001t0002g0181 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.123+6424T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59097869 | |||||||
| chr17:59098266 | C | T | 23 | a0001c0001t0002g0089 a0001c0001t0002g0098 a0001c0001t0003g0079 others(20): Show |
23 | HG01168.hp2 HG01169.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.123+6027G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59098266 | |||||||
| chr17:59098341 | C | T | 1 | a0001c0001t0002g0209 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.123+5952G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59098341 | |||||||
| chr17:59098608 | T | C | 43 | a0001c0001t0002g0124 a0001c0001t0002g0126 a0001c0001t0002g0127 others(40): Show |
43 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(40): Show |
intron_variant | MODIFIER | c.123+5685A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59098608 | |||||||
| chr17:59098668 | T | TA | 97 | a0001c0001t0001g0223 a0001c0001t0002g0110 a0001c0001t0002g0124 others(94): Show |
97 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.123+5624dupT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59098668 | |||||||
| chr17:59098668 | TA | T | 11 | a0001c0001t0001g0228 a0001c0001t0001g0260 a0001c0001t0002g0080 others(8): Show |
11 | HG01257.hp1 HG01884.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.123+5624delT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59098668 | |||||||
| chr17:59098700 | A | G | 1 | a0001c0006t0003g0105 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.123+5593T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59098700 | |||||||
| chr17:59098745 | A | T | 114 | a0001c0001t0002g0080 a0001c0001t0002g0107 a0001c0001t0002g0110 others(111): Show |
114 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.123+5548T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59098745 | |||||||
| chr17:59098942 | T | C | 1 | a0001c0001t0001g0317 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.123+5351A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59098942 | |||||||
| chr17:59098977 | G | C | 4 | a0001c0003t0006g0212 a0001c0003t0006g0217 a0001c0003t0006g0218 others(1): Show |
4 | HG00642.hp2 HG03704.hp2 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.123+5316C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59098977 | |||||||
| chr17:59099058 | C | G | 1 | a0001c0001t0002g0203 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.123+5235G>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59099058 | |||||||
| chr17:59099163 | C | T | 1 | a0001c0006t0003g0105 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.123+5130G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59099163 | |||||||
| chr17:59099167 | G | A | 2 | a0001c0001t0002g0120 a0001c0001t0002g0121 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.123+5126C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59099167 | |||||||
| chr17:59099169 | G | A | 5 | a0001c0001t0003g0073 a0001c0001t0003g0074 a0001c0001t0003g0075 others(2): Show |
5 | HG02486.hp2 HG02630.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+5124C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59099169 | |||||||
| chr17:59099741 | T | C | 12 | a0001c0001t0003g0061 a0001c0001t0003g0062 a0001c0001t0003g0063 others(9): Show |
12 | HG02055.hp1 HG02572.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.123+4552A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59099741 | |||||||
| chr17:59099873 | G | C | 2 | a0001c0001t0002g0181 a0001c0001t0002g0182 |
2 | HG02735.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.123+4420C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59099873 | |||||||
| chr17:59099996 | T | A | 1 | a0001c0001t0001g0258 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.123+4297A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59099996 | |||||||
| chr17:59100188 | G | A | 99 | a0001c0001t0001g0318 a0001c0001t0001g0319 a0001c0001t0001g0339 others(96): Show |
99 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.123+4105C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59100188 | |||||||
| chr17:59100246 | C | T | 1 | a0001c0006t0003g0105 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.123+4047G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59100246 | |||||||
| chr17:59100317 | C | T | 11 | a0001c0001t0002g0080 a0001c0001t0002g0112 a0001c0001t0002g0113 others(8): Show |
11 | HG01257.hp2 HG01258.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.123+3976G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59100317 | |||||||
| chr17:59100361 | G | A | 3 | a0001c0001t0004g0102 a0001c0001t0004g0103 a0001c0001t0004g0104 |
3 | HG03516.hp2 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.123+3932C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59100361 | |||||||
| chr17:59100409 | T | C | 93 | a0001c0001t0002g0110 a0001c0001t0002g0124 a0001c0001t0002g0126 others(90): Show |
93 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.123+3884A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59100409 | |||||||
| chr17:59100669 | G | A | 2 | a0001c0001t0002g0120 a0001c0001t0002g0121 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.123+3624C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59100669 | |||||||
| chr17:59100792 | G | A | 1 | a0001c0001t0001g0320 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.123+3501C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59100792 | |||||||
| chr17:59100908 | G | A | 1 | a0001c0001t0001g0231 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.123+3385C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59100908 | |||||||
| chr17:59100917 | G | C | 1 | a0001c0001t0003g0123 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.123+3376C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59100917 | |||||||
| chr17:59100936 | C | T | 1 | a0001c0001t0003g0086 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.123+3357G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59100936 | |||||||
| chr17:59100970 | G | A | 1 | a0001c0001t0002g0210 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.123+3323C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59100970 | |||||||
| chr17:59101022 | C | CA | 106 | a0001c0001t0002g0080 a0001c0001t0002g0107 a0001c0001t0002g0110 others(103): Show |
106 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.123+3270dupT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59101022 | |||||||
| chr17:59101209 | A | C | 1 | a0001c0001t0002g0134 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.123+3084T>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59101209 | |||||||
| chr17:59101274 | A | G | 6 | a0001c0001t0003g0081 a0001c0001t0003g0082 a0001c0001t0003g0083 others(3): Show |
6 | HG02559.hp1 HG02647.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.123+3019T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59101274 | |||||||
| chr17:59101477 | A | G | 97 | a0001c0001t0001g0339 a0001c0001t0002g0089 a0001c0001t0002g0098 others(94): Show |
97 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.123+2816T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59101477 | |||||||
| chr17:59101531 | G | T | 4 | a0001c0001t0003g0073 a0001c0001t0003g0074 a0001c0001t0003g0075 others(1): Show |
4 | HG02486.hp2 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.123+2762C>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59101531 | |||||||
| chr17:59101655 | C | CA | 16 | a0001c0001t0001g0233 a0001c0001t0001g0321 a0001c0001t0001g0322 others(13): Show |
16 | HG01256.hp1 HG02135.hp1 HG02135.hp2 others(13): Show |
intron_variant | MODIFIER | c.123+2637dupT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59101655 | |||||||
| chr17:59101655 | C | CAA | 23 | a0001c0001t0002g0111 a0001c0001t0002g0124 a0001c0001t0002g0131 others(20): Show |
23 | HG00099.hp1 HG00544.hp2 HG00621.hp2 others(20): Show |
intron_variant | MODIFIER | c.123+2636_123+2637d others(4): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59101655 | |||||||
| chr17:59101655 | CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.123+2625_123+2637d others(15): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59101655 | |||||||
| chr17:59101664 | AAAAAAAA others(8): Show |
A | 11 | a0001c0001t0003g0050 a0001c0001t0003g0061 a0001c0001t0003g0062 others(8): Show |
11 | HG02055.hp1 HG02572.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.123+2614_123+2628d others(17): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59101664 | |||||||
| chr17:59101665 | AAAAAAAA others(7): Show |
A | 1 | a0001c0001t0012g0002 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.123+2614_123+2627d others(16): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59101665 | |||||||
| chr17:59101666 | AAAAAAAA others(6): Show |
A | 2 | a0001c0001t0003g0059 a0001c0001t0003g0095 |
2 | HG01243.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.123+2614_123+2626d others(15): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59101666 | |||||||
| chr17:59101666 | AAAAAAAA others(8): Show |
A | 73 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0005 others(70): Show |
73 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.123+2612_123+2626d others(17): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59101666 | |||||||
| chr17:59101667 | AAAAAAAA others(5): Show |
A | 5 | a0001c0001t0003g0079 a0001c0001t0003g0097 a0001c0001t0003g0099 others(2): Show |
5 | HG01168.hp2 HG01169.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.123+2614_123+2625d others(14): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59101667 | |||||||
| chr17:59101668 | AAAAAAAA others(8): Show |
A | 2 | a0001c0001t0001g0339 a0001c0001t0002g0089 |
2 | HG02809.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.123+2610_123+2624d others(17): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59101668 | |||||||
| chr17:59101669 | AAAAAAAA others(5): Show |
A | 2 | a0001c0001t0002g0098 a0001c0001t0003g0096 |
2 | HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.123+2612_123+2623d others(14): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59101669 | |||||||
| chr17:59101670 | AAAAAAAA others(6): Show |
A | 1 | a0001c0006t0003g0105 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.123+2610_123+2622d others(15): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59101670 | |||||||
| chr17:59101677 | A | AAT | 6 | a0001c0001t0001g0234 a0001c0001t0001g0236 a0001c0001t0001g0238 others(3): Show |
6 | HG02647.hp2 HG02818.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.123+2614_123+2615d others(4): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59101677 | |||||||
| chr17:59101677 | A | AT | 12 | a0001c0001t0001g0237 a0001c0001t0001g0263 a0001c0001t0001g0271 others(9): Show |
12 | HG01070.hp2 HG01168.hp1 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.123+2615_123+2616i others(3): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59101677 | |||||||
| chr17:59101677 | A | T | 20 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(17): Show |
20 | HG01346.hp1 HG01361.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.123+2616T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59101677 | |||||||
| chr17:59101678 | AT | A | 11 | a0001c0001t0001g0229 a0001c0001t0001g0230 a0001c0001t0001g0264 others(8): Show |
11 | HG00639.hp1 HG01070.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.123+2614delA | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59101678 | |||||||
| chr17:59101679 | T | A | 92 | a0001c0001t0001g0228 a0001c0001t0001g0233 a0001c0001t0002g0080 others(89): Show |
92 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.123+2614A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59101679 | |||||||
| chr17:59101681 | T | A | 58 | a0001c0001t0002g0117 a0001c0001t0002g0128 a0001c0001t0002g0129 others(55): Show |
58 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.123+2612A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59101681 | |||||||
| chr17:59101683 | T | A | 1 | a0001c0001t0002g0132 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.123+2610A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59101683 | |||||||
| chr17:59101685 | T | A | 1 | a0001c0001t0002g0132 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.123+2608A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59101685 | |||||||
| chr17:59101693 | T | C | 2 | a0001c0001t0002g0120 a0001c0001t0002g0121 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.123+2600A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59101693 | |||||||
| chr17:59101695 | T | C | 11 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0334 others(8): Show |
11 | HG01257.hp2 HG01258.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.123+2598A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59101695 | |||||||
| chr17:59101695 | T | TAC | 8 | a0001c0001t0001g0324 a0001c0001t0001g0325 a0001c0001t0001g0326 others(5): Show |
8 | HG00621.hp1 HG02040.hp1 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.123+2596_123+2597d others(4): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59101695 | |||||||
| chr17:59101697 | C | T | 134 | a0001c0001t0001g0225 a0001c0001t0001g0228 a0001c0001t0001g0229 others(131): Show |
134 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.123+2596G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59101697 | |||||||
| chr17:59101699 | C | T | 2 | a0001c0001t0001g0233 a0001c0001t0002g0132 |
2 | HG01106.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.123+2594G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59101699 | |||||||
| chr17:59101723 | T | C | 1 | a0001c0001t0002g0141 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.123+2570A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59101723 | |||||||
| chr17:59101727 | T | C | 1 | a0001c0001t0002g0203 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.123+2566A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59101727 | |||||||
| chr17:59101777 | T | C | 1 | a0001c0001t0003g0072 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.123+2516A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59101777 | |||||||
| chr17:59101796 | G | A | 1 | a0001c0001t0002g0204 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.123+2497C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59101796 | |||||||
| chr17:59101877 | C | T | 220 | a0001c0001t0001g0339 a0001c0001t0002g0080 a0001c0001t0002g0089 others(217): Show |
220 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.123+2416G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59101877 | |||||||
| chr17:59101938 | C | CA | 12 | a0001c0001t0003g0061 a0001c0001t0003g0062 a0001c0001t0003g0063 others(9): Show |
12 | HG02055.hp1 HG02572.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.123+2354dupT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59101938 | |||||||
| chr17:59102215 | C | T | 3 | a0001c0001t0004g0102 a0001c0001t0004g0103 a0001c0001t0004g0104 |
3 | HG03516.hp2 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.123+2078G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59102215 | |||||||
| chr17:59102263 | T | C | 2 | a0001c0001t0003g0007 a0001c0001t0003g0008 |
2 | HG04115.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.123+2030A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59102263 | |||||||
| chr17:59102287 | A | T | 1 | a0001c0001t0002g0131 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.123+2006T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59102287 | |||||||
| chr17:59102811 | G | C | 1 | a0001c0001t0002g0204 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.123+1482C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59102811 | |||||||
| chr17:59102873 | A | C | 98 | a0001c0001t0001g0232 a0001c0001t0001g0339 a0001c0001t0002g0089 others(95): Show |
98 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.123+1420T>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59102873 | |||||||
| chr17:59102896 | C | T | 1 | a0001c0001t0002g0130 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.123+1397G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59102896 | |||||||
| chr17:59102936 | CATCTCTG others(47): Show |
C | 1 | a0001c0001t0001g0231 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.123+1303_123+1356d others(56): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59102936 | |||||||
| chr17:59103169 | G | A | 1 | a0001c0001t0001g0335 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.123+1124C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59103169 | |||||||
| chr17:59103189 | T | C | 11 | a0001c0001t0002g0080 a0001c0001t0002g0112 a0001c0001t0002g0113 others(8): Show |
11 | HG01257.hp2 HG01258.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.123+1104A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59103189 | |||||||
| chr17:59103373 | G | T | 1 | a0001c0003t0006g0212 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.123+920C>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59103373 | |||||||
| chr17:59103631 | C | T | 3 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0230 |
3 | HG00639.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.123+662G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59103631 | |||||||
| chr17:59103635 | C | G | 5 | a0001c0001t0003g0073 a0001c0001t0003g0074 a0001c0001t0003g0075 others(2): Show |
5 | HG02486.hp2 HG02630.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+658G>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59103635 | |||||||
| chr17:59103650 | G | GT | 14 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(11): Show |
14 | HG00438.hp1 HG01175.hp1 HG01981.hp2 others(11): Show |
intron_variant | MODIFIER | c.123+642dupA | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59103650 | |||||||
| chr17:59103729 | C | T | 5 | a0001c0001t0003g0073 a0001c0001t0003g0074 a0001c0001t0003g0075 others(2): Show |
5 | HG02486.hp2 HG02630.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+564G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59103729 | |||||||
| chr17:59104141 | T | C | 1 | a0001c0001t0001g0336 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.123+152A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59104141 | |||||||
| chr17:59104144 | G | A | 7 | a0001c0001t0002g0209 a0001c0001t0002g0210 a0002c0002t0002g0125 others(4): Show |
7 | HG01952.hp2 HG02257.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.123+149C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59104144 | |||||||
| chr17:59104163 | C | T | 74 | a0001c0001t0001g0339 a0001c0001t0003g0003 a0001c0001t0003g0004 others(71): Show |
74 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.123+130G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59104163 | |||||||
| chr17:59104921 | G | A | 1 | a0001c0001t0003g0122 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.22-527C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 1/23 | chr17 | 59104921 | |||||||
| chr17:59104947 | C | G | 1 | a0001c0001t0001g0224 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.22-553G>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 1/23 | chr17 | 59104947 | |||||||
| chr17:59105091 | C | CA | 214 | a0001c0001t0001g0337 a0001c0001t0001g0338 a0001c0001t0001g0339 others(211): Show |
214 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.22-698dupT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 1/23 | chr17 | 59105091 | |||||||
| chr17:59105278 | AATCCAGA others(31): Show |
A | 1 | a0001c0001t0003g0123 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.22-922_22-885delCT others(36): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 1/23 | chr17 | 59105278 | |||||||
| chr17:59105432 | G | C | 220 | a0001c0001t0001g0339 a0001c0001t0002g0080 a0001c0001t0002g0089 others(217): Show |
220 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.21+1009C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 1/23 | chr17 | 59105432 | |||||||
| chr17:59105483 | C | T | 4 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(1): Show |
4 | NA18939.hp2 NA18954.hp2 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.21+958G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 1/23 | chr17 | 59105483 | |||||||
| chr17:59105669 | T | C | 1 | a0001c0001t0001g0340 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.21+772A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 1/23 | chr17 | 59105669 | |||||||
| chr17:59105905 | CATAT | C | 89 | a0001c0001t0002g0124 a0001c0001t0002g0126 a0001c0001t0002g0127 others(86): Show |
89 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.21+532_21+535delAT others(2): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 1/23 | chr17 | 59105905 | |||||||
| chr17:59106082 | T | C | 1 | a0001c0001t0002g0211 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.21+359A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 1/23 | chr17 | 59106082 |