Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 51592 |
| ensemblid | ENSG00000197323.12 |
| hgncid | 16290 |
| symbol | TRIM33 |
| name | tripartite motif containing 33 |
| refseq_nuc | NM_015906.4 |
| refseq_prot | NP_056990.3 |
| ensembl_nuc | ENST00000358465.7 |
| ensembl_prot | ENSP00000351250.2 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 114392790 |
| end | 114511203 |
| strand | - |
| ver | v1.2 |
| region | chr1:114392790-114511203 |
| region5000 | chr1:114387790-114516203 |
| regionname0 | TRIM33_chr1_114392790_114511203 |
| regionname5000 | TRIM33_chr1_114387790_114516203 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 1127 | 168 | 61 | 40 | 31 | 6 | 29 | 19 | TRIM33_chr1_114387790_114516203 | TRIM33 | MAENK others(1122): Show |
chr1 | 114387790 | 114516203 |
| a0002 | 1/0 | 1127 | 28 | 1 | 12 | 14 | 0 | 0 | 7 | TRIM33_chr1_114387790_114516203 | TRIM33 | MAENK others(1122): Show |
chr1 | 114387790 | 114516203 |
| a0003 | 0/0 | 1127 | 11 | 9 | 0 | 1 | 0 | 1 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | MAENK others(1122): Show |
chr1 | 114387790 | 114516203 |
| a0004 | 0/0 | 1127 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | MAENK others(1122): Show |
chr1 | 114387790 | 114516203 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 3381 | 93 | 26 | 24 | 25 | 4 | 14 | TRIM33_chr1_114387790_114516203 | TRIM33 | ATGGC others(3376): Show |
chr1 | 114387790 | 114516203 | ||
| a0001c0002 | 0/1 | 3381 | 63 | 25 | 16 | 5 | 2 | 14 | TRIM33_chr1_114387790_114516203 | TRIM33 | ATGGC others(3376): Show |
chr1 | 114387790 | 114516203 | ||
| a0001c0005 | 0/0 | 3381 | 6 | 6 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | ATGGC others(3376): Show |
chr1 | 114387790 | 114516203 | ||
| a0001c0006 | 0/0 | 3381 | 5 | 4 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | ATGGC others(3376): Show |
chr1 | 114387790 | 114516203 | ||
| a0001c0009 | 0/0 | 3381 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | ATGGC others(3376): Show |
chr1 | 114387790 | 114516203 | ||
| a0002c0003 | 1/0 | 3381 | 28 | 1 | 12 | 14 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | ATGGC others(3376): Show |
chr1 | 114387790 | 114516203 | ||
| a0003c0004 | 0/0 | 3381 | 10 | 8 | 0 | 1 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | ATGGC others(3376): Show |
chr1 | 114387790 | 114516203 | ||
| a0003c0008 | 0/0 | 3381 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | ATGGC others(3376): Show |
chr1 | 114387790 | 114516203 | ||
| a0004c0007 | 0/0 | 3381 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | ATGGC others(3376): Show |
chr1 | 114387790 | 114516203 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 8369 | 26 | 6 | 9 | 5 | 1 | 5 | TRIM33_chr1_114387790_114516203 | TRIM33 | GGTTC others(8364): Show |
chr1 | 114387790 | 114516203 |
| a0001c0001t0002 | 0/0 | 8370 | 37 | 10 | 8 | 13 | 0 | 6 | TRIM33_chr1_114387790_114516203 | TRIM33 | GGTTC others(8365): Show |
chr1 | 114387790 | 114516203 |
| a0001c0001t0004 | 0/0 | 8370 | 4 | 3 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | GGTTC others(8365): Show |
chr1 | 114387790 | 114516203 |
| a0001c0001t0011 | 0/0 | 8370 | 3 | 2 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | GGTTC others(8365): Show |
chr1 | 114387790 | 114516203 |
| a0001c0001t0012 | 0/0 | 8371 | 3 | 1 | 0 | 2 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | GGTTC others(8366): Show |
chr1 | 114387790 | 114516203 |
| a0001c0001t0015 | 0/0 | 8369 | 3 | 0 | 1 | 0 | 2 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | GGTTC others(8364): Show |
chr1 | 114387790 | 114516203 |
| a0001c0001t0017 | 0/0 | 8371 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | GGTTC others(8366): Show |
chr1 | 114387790 | 114516203 |
| a0001c0001t0022 | 0/0 | 8369 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM33_chr1_114387790_114516203 | TRIM33 | GGTTC others(8364): Show |
chr1 | 114387790 | 114516203 |
| a0001c0001t0024 | 0/0 | 8368 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | GGTTC others(8363): Show |
chr1 | 114387790 | 114516203 |
| a0001c0001t0026 | 0/0 | 8372 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | GGTTC others(8367): Show |
chr1 | 114387790 | 114516203 |
| a0001c0001t0028 | 0/0 | 8369 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | GGTTC others(8364): Show |
chr1 | 114387790 | 114516203 |
| a0001c0001t0031 | 0/0 | 8371 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | GGTTC others(8366): Show |
chr1 | 114387790 | 114516203 |
| a0001c0001t0036 | 0/0 | 8370 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | GGTTC others(8365): Show |
chr1 | 114387790 | 114516203 |
| a0001c0001t0037 | 0/0 | 8370 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | GGTTC others(8365): Show |
chr1 | 114387790 | 114516203 |
| a0001c0001t0041 | 0/0 | 8369 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | GGTTC others(8364): Show |
chr1 | 114387790 | 114516203 |
| a0001c0001t0042 | 0/0 | 8369 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | GGTTC others(8364): Show |
chr1 | 114387790 | 114516203 |
| a0001c0001t0044 | 0/0 | 8369 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | GGTTC others(8364): Show |
chr1 | 114387790 | 114516203 |
| a0001c0001t0045 | 0/0 | 8369 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | GGTTC others(8364): Show |
chr1 | 114387790 | 114516203 |
| a0001c0001t0047 | 0/0 | 8369 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | GGTTC others(8364): Show |
chr1 | 114387790 | 114516203 |
| a0001c0001t0048 | 0/0 | 8368 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | GGTTC others(8363): Show |
chr1 | 114387790 | 114516203 |
| a0001c0001t0051 | 0/0 | 8370 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | GGTTC others(8365): Show |
chr1 | 114387790 | 114516203 |
| a0001c0002t0003 | 0/0 | 8371 | 18 | 0 | 7 | 4 | 1 | 6 | TRIM33_chr1_114387790_114516203 | TRIM33 | GGTTC others(8366): Show |
chr1 | 114387790 | 114516203 |
| a0001c0002t0004 | 0/0 | 8370 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | GGTTC others(8365): Show |
chr1 | 114387790 | 114516203 |
| a0001c0002t0005 | 0/0 | 8371 | 10 | 4 | 2 | 0 | 0 | 4 | TRIM33_chr1_114387790_114516203 | TRIM33 | GGTTC others(8366): Show |
chr1 | 114387790 | 114516203 |
| a0001c0002t0006 | 0/0 | 8372 | 8 | 6 | 1 | 0 | 1 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | GGTTC others(8367): Show |
chr1 | 114387790 | 114516203 |
| a0001c0002t0009 | 0/0 | 8371 | 4 | 4 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | GGTTC others(8366): Show |
chr1 | 114387790 | 114516203 |
| a0001c0002t0018 | 0/0 | 8372 | 2 | 1 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | GGTTC others(8367): Show |
chr1 | 114387790 | 114516203 |
| a0001c0002t0019 | 0/0 | 8370 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | GGTTC others(8365): Show |
chr1 | 114387790 | 114516203 |
| a0001c0002t0020 | 0/0 | 8370 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | GGTTC others(8365): Show |
chr1 | 114387790 | 114516203 |
| a0001c0002t0021 | 0/0 | 8372 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM33_chr1_114387790_114516203 | TRIM33 | GGTTC others(8367): Show |
chr1 | 114387790 | 114516203 |
| a0001c0002t0023 | 0/0 | 8372 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | GGTTC others(8367): Show |
chr1 | 114387790 | 114516203 |
| a0001c0002t0025 | 0/0 | 8372 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | GGTTC others(8367): Show |
chr1 | 114387790 | 114516203 |
| a0001c0002t0027 | 0/0 | 8374 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | GGTTC others(8369): Show |
chr1 | 114387790 | 114516203 |
| a0001c0002t0029 | 0/0 | 8371 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | GGTTC others(8366): Show |
chr1 | 114387790 | 114516203 |
| a0001c0002t0030 | 0/1 | 8372 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | GGTTC others(8367): Show |
chr1 | 114387790 | 114516203 |
| a0001c0002t0033 | 0/0 | 8371 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | GGTTC others(8366): Show |
chr1 | 114387790 | 114516203 |
| a0001c0002t0034 | 0/0 | 8371 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | GGTTC others(8366): Show |
chr1 | 114387790 | 114516203 |
| a0001c0002t0035 | 0/0 | 8373 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | GGTTC others(8368): Show |
chr1 | 114387790 | 114516203 |
| a0001c0002t0038 | 0/0 | 8371 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | GGTTC others(8366): Show |
chr1 | 114387790 | 114516203 |
| a0001c0002t0043 | 0/0 | 8370 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | GGTTC others(8365): Show |
chr1 | 114387790 | 114516203 |
| a0001c0002t0046 | 0/0 | 8371 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | GGTTC others(8366): Show |
chr1 | 114387790 | 114516203 |
| a0001c0002t0049 | 0/0 | 8371 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | GGTTC others(8366): Show |
chr1 | 114387790 | 114516203 |
| a0001c0005t0007 | 0/0 | 8370 | 6 | 6 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | GGTTC others(8365): Show |
chr1 | 114387790 | 114516203 |
| a0001c0006t0010 | 0/0 | 8370 | 4 | 4 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | GGTTC others(8365): Show |
chr1 | 114387790 | 114516203 |
| a0001c0006t0039 | 0/0 | 8370 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | GGTTC others(8365): Show |
chr1 | 114387790 | 114516203 |
| a0001c0009t0040 | 0/0 | 8370 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | GGTTC others(8365): Show |
chr1 | 114387790 | 114516203 |
| a0002c0003t0001 | 1/0 | 8369 | 17 | 1 | 5 | 10 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | GGTTC others(8364): Show |
chr1 | 114387790 | 114516203 |
| a0002c0003t0004 | 0/0 | 8370 | 2 | 0 | 1 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | GGTTC others(8365): Show |
chr1 | 114387790 | 114516203 |
| a0002c0003t0008 | 0/0 | 8369 | 6 | 0 | 6 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | GGTTC others(8364): Show |
chr1 | 114387790 | 114516203 |
| a0002c0003t0016 | 0/0 | 8368 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | GGTTC others(8363): Show |
chr1 | 114387790 | 114516203 |
| a0003c0004t0001 | 0/0 | 8369 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | GGTTC others(8364): Show |
chr1 | 114387790 | 114516203 |
| a0003c0004t0004 | 0/0 | 8370 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | GGTTC others(8365): Show |
chr1 | 114387790 | 114516203 |
| a0003c0004t0013 | 0/0 | 8371 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | GGTTC others(8366): Show |
chr1 | 114387790 | 114516203 |
| a0003c0004t0014 | 0/0 | 8371 | 3 | 1 | 0 | 1 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | GGTTC others(8366): Show |
chr1 | 114387790 | 114516203 |
| a0003c0004t0032 | 0/0 | 8371 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | GGTTC others(8366): Show |
chr1 | 114387790 | 114516203 |
| a0003c0004t0050 | 0/0 | 8370 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | GGTTC others(8365): Show |
chr1 | 114387790 | 114516203 |
| a0003c0008t0013 | 0/0 | 8371 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | GGTTC others(8366): Show |
chr1 | 114387790 | 114516203 |
| a0004c0007t0001 | 0/0 | 8369 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | GGTTC others(8364): Show |
chr1 | 114387790 | 114516203 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0004g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0004g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0004g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0004g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0011g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0011g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0011g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0012g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0012g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0012g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0015g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0015g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0015g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0017g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0017g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0022g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0022g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0024g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0026g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0028g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0031g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0036g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0037g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0041g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0042g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0044g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0045g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0047g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0048g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0051g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0003g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0003g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0003g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0003g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0003g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0003g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0003g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0003g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0003g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0003g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0003g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0003g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0003g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0003g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0004g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0004g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0004g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0005g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0005g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0005g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0005g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0005g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0005g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0005g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0005g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0005g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0005g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0006g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0006g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0006g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0006g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0006g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0006g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0006g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0006g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0009g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0009g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0009g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0009g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0018g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0018g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0019g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0019g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0020g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0020g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0021g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0021g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0023g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0025g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0027g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0029g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0030g0101 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0033g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0034g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0035g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0038g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0043g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0046g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0049g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0005t0007g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0005t0007g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0005t0007g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0005t0007g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0005t0007g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0005t0007g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0006t0010g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0006t0010g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0006t0010g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0006t0010g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0006t0039g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0009t0040g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0002c0003t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0002c0003t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0002c0003t0001g0018 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0002c0003t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0002c0003t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0002c0003t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0002c0003t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0002c0003t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0002c0003t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0002c0003t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0002c0003t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0002c0003t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0002c0003t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0002c0003t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0002c0003t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0002c0003t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0002c0003t0004g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0002c0003t0004g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0002c0003t0008g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0002c0003t0008g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0002c0003t0008g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0002c0003t0008g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0002c0003t0008g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0002c0003t0008g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0002c0003t0016g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0002c0003t0016g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0002c0003t0016g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0003c0004t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0003c0004t0004g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0003c0004t0004g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0003c0004t0013g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0003c0004t0013g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0003c0004t0014g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0003c0004t0014g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0003c0004t0014g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0003c0004t0032g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0003c0004t0050g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0003c0008t0013g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0004c0007t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0006 | g0088 | EUR | GBR | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG00099 | hp2 | a0001 | c0001 | t0015 | g0051 | EUR | GBR | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG00323 | hp1 | a0001 | c0002 | t0003 | g0138 | EUR | FIN | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG00323 | hp2 | a0001 | c0001 | t0015 | g0065 | EUR | FIN | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0162 | EAS | CHS | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG00438 | hp2 | a0002 | c0003 | t0016 | g0042 | EAS | CHS | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG00558 | hp1 | a0001 | c0001 | t0042 | g0062 | EAS | CHS | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0172 | EAS | CHS | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG00642 | hp1 | a0002 | c0003 | t0008 | g0049 | AMR | PUR | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0192 | AMR | PUR | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG00735 | hp1 | a0001 | c0002 | t0006 | g0087 | AMR | PUR | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG00738 | hp1 | a0001 | c0002 | t0003 | g0127 | AMR | PUR | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG00738 | hp2 | a0002 | c0003 | t0008 | g0047 | AMR | PUR | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG00741 | hp2 | a0001 | c0002 | t0018 | g0146 | AMR | PUR | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01071 | hp1 | a0001 | c0001 | t0045 | g0167 | AMR | PUR | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0064 | AMR | PUR | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0193 | AMR | PUR | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01081 | hp2 | a0001 | c0001 | t0004 | g0059 | AMR | PUR | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01099 | hp1 | a0001 | c0002 | t0003 | g0126 | AMR | PUR | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01099 | hp2 | a0001 | c0001 | t0011 | g0054 | AMR | PUR | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01106 | hp1 | a0001 | c0002 | t0046 | g0091 | AMR | PUR | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01106 | hp2 | a0002 | c0003 | t0008 | g0045 | AMR | PUR | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01167 | hp1 | a0001 | c0002 | t0003 | g0137 | AMR | PUR | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0191 | AMR | PUR | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01168 | hp2 | a0001 | c0002 | t0003 | g0136 | AMR | PUR | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0190 | AMR | PUR | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01169 | hp2 | a0001 | c0002 | t0003 | g0139 | AMR | PUR | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01175 | hp2 | a0001 | c0001 | t0026 | g0196 | AMR | PUR | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01192 | hp1 | a0001 | c0002 | t0005 | g0107 | AMR | PUR | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01192 | hp2 | a0001 | c0001 | t0047 | g0053 | AMR | PUR | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01243 | hp2 | a0001 | c0002 | t0049 | g0129 | AMR | PUR | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01257 | hp1 | a0002 | c0003 | t0004 | g0030 | AMR | CLM | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01257 | hp2 | a0001 | c0002 | t0019 | g0100 | AMR | CLM | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01261 | hp1 | a0002 | c0003 | t0008 | g0048 | AMR | CLM | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01261 | hp2 | a0001 | c0002 | t0019 | g0110 | AMR | CLM | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01346 | hp1 | a0002 | c0003 | t0001 | g0038 | AMR | CLM | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01346 | hp2 | a0001 | c0002 | t0003 | g0130 | AMR | CLM | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01361 | hp1 | a0002 | c0003 | t0008 | g0046 | AMR | CLM | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01361 | hp2 | a0001 | c0002 | t0027 | g0090 | AMR | CLM | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01433 | hp1 | a0002 | c0003 | t0001 | g0001 | AMR | CLM | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01433 | hp2 | a0001 | c0002 | t0005 | g0102 | AMR | CLM | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01496 | hp1 | a0002 | c0003 | t0001 | g0001 | AMR | CLM | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0168 | AMR | CLM | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01884 | hp1 | a0001 | c0005 | t0007 | g0152 | AFR | ACB | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01884 | hp2 | a0001 | c0002 | t0004 | g0115 | AFR | ACB | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0186 | AFR | ACB | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01891 | hp2 | a0001 | c0002 | t0009 | g0202 | AFR | ACB | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01928 | hp1 | a0002 | c0003 | t0001 | g0029 | AMR | PEL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0183 | AMR | PEL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01934 | hp1 | a0001 | c0001 | t0044 | g0016 | AMR | PEL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01934 | hp2 | a0002 | c0003 | t0001 | g0028 | AMR | PEL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PEL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01952 | hp2 | a0001 | c0002 | t0003 | g0125 | AMR | PEL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01993 | hp1 | a0002 | c0003 | t0008 | g0032 | AMR | PEL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0171 | AMR | PEL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PEL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02004 | hp2 | a0001 | c0001 | t0015 | g0066 | AMR | PEL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | KHV | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02015 | hp2 | a0002 | c0003 | t0001 | g0021 | EAS | KHV | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02055 | hp1 | a0001 | c0001 | t0004 | g0050 | AFR | ACB | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02055 | hp2 | a0003 | c0004 | t0014 | g0012 | AFR | ACB | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02056 | hp1 | a0001 | c0001 | t0041 | g0169 | EAS | KHV | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02056 | hp2 | a0002 | c0003 | t0004 | g0031 | EAS | KHV | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02083 | hp1 | a0002 | c0003 | t0016 | g0044 | EAS | KHV | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | KHV | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02129 | hp1 | a0002 | c0003 | t0001 | g0033 | EAS | KHV | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02129 | hp2 | a0001 | c0001 | t0017 | g0176 | EAS | KHV | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | KHV | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02132 | hp2 | a0001 | c0006 | t0039 | g0124 | EAS | KHV | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02145 | hp1 | a0003 | c0008 | t0013 | g0015 | AFR | ACB | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02145 | hp2 | a0001 | c0001 | t0012 | g0197 | AFR | ACB | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02258 | hp1 | a0003 | c0004 | t0013 | g0010 | AFR | ACB | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0198 | AFR | ACB | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02280 | hp1 | a0003 | c0004 | t0004 | g0006 | AFR | ACB | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02280 | hp2 | a0001 | c0002 | t0006 | g0093 | AFR | ACB | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02451 | hp1 | a0004 | c0007 | t0001 | g0014 | AFR | ACB | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02451 | hp2 | a0001 | c0002 | t0034 | g0117 | AFR | ACB | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02523 | hp1 | a0003 | c0004 | t0014 | g0013 | EAS | KHV | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02523 | hp2 | a0002 | c0003 | t0001 | g0035 | EAS | KHV | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0024 | AFR | GWD | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02572 | hp2 | a0001 | c0002 | t0009 | g0203 | AFR | GWD | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02602 | hp2 | a0001 | c0002 | t0003 | g0142 | SAS | PJL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02615 | hp1 | a0001 | c0002 | t0005 | g0108 | AFR | GWD | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02615 | hp2 | a0001 | c0001 | t0024 | g0003 | AFR | GWD | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02622 | hp1 | a0001 | c0002 | t0020 | g0112 | AFR | GWD | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0185 | AFR | GWD | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0194 | AFR | GWD | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02647 | hp2 | a0001 | c0002 | t0038 | g0118 | AFR | GWD | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02698 | hp1 | a0001 | c0009 | t0040 | g0123 | SAS | PJL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02698 | hp2 | a0001 | c0002 | t0003 | g0141 | SAS | PJL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02723 | hp2 | a0001 | c0002 | t0006 | g0094 | AFR | GWD | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02738 | hp1 | a0001 | c0002 | t0043 | g0140 | SAS | PJL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02738 | hp2 | a0001 | c0001 | t0028 | g0063 | SAS | PJL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0155 | AFR | GWD | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02886 | hp1 | a0001 | c0002 | t0033 | g0116 | AFR | GWD | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02886 | hp2 | a0001 | c0001 | t0011 | g0067 | AFR | GWD | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02895 | hp1 | a0001 | c0002 | t0018 | g0145 | AFR | GWD | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02895 | hp2 | a0001 | c0006 | t0010 | g0121 | AFR | GWD | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02897 | hp1 | a0001 | c0006 | t0010 | g0122 | AFR | GWD | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02897 | hp2 | a0001 | c0005 | t0007 | g0150 | AFR | GWD | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02922 | hp1 | a0001 | c0006 | t0010 | g0119 | AFR | ESN | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02922 | hp2 | a0001 | c0002 | t0005 | g0099 | AFR | ESN | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0148 | AFR | ESN | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02965 | hp2 | a0003 | c0004 | t0001 | g0008 | AFR | ESN | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02970 | hp2 | a0001 | c0002 | t0035 | g0085 | AFR | ESN | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02976 | hp1 | a0001 | c0002 | t0006 | g0096 | AFR | ESN | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02976 | hp2 | a0003 | c0004 | t0032 | g0011 | AFR | ESN | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG03017 | hp1 | a0003 | c0004 | t0014 | g0005 | SAS | PJL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0182 | SAS | PJL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG03041 | hp1 | a0003 | c0004 | t0050 | g0206 | AFR | GWD | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG03041 | hp2 | a0001 | c0005 | t0007 | g0151 | AFR | GWD | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG03098 | hp1 | a0001 | c0001 | t0031 | g0157 | AFR | MSL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG03098 | hp2 | a0001 | c0002 | t0005 | g0098 | AFR | MSL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG03130 | hp1 | a0003 | c0004 | t0004 | g0009 | AFR | ESN | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG03130 | hp2 | a0001 | c0005 | t0007 | g0188 | AFR | ESN | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0156 | AFR | ESN | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG03139 | hp2 | a0001 | c0002 | t0005 | g0105 | AFR | ESN | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0153 | AFR | ESN | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG03195 | hp2 | a0001 | c0002 | t0006 | g0097 | AFR | ESN | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG03209 | hp1 | a0001 | c0002 | t0006 | g0095 | AFR | MSL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG03209 | hp2 | a0001 | c0001 | t0048 | g0081 | AFR | MSL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG03225 | hp2 | a0001 | c0002 | t0020 | g0113 | AFR | MSL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG03453 | hp1 | a0001 | c0001 | t0037 | g0154 | AFR | MSL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG03453 | hp2 | a0001 | c0006 | t0010 | g0120 | AFR | MSL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0189 | AFR | MSL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG03486 | hp2 | a0001 | c0002 | t0009 | g0205 | AFR | MSL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG03490 | hp2 | a0001 | c0002 | t0005 | g0109 | SAS | PJL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG03516 | hp1 | a0001 | c0002 | t0006 | g0086 | AFR | ESN | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0023 | AFR | ESN | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG03579 | hp1 | a0001 | c0002 | t0009 | g0204 | AFR | MSL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG03579 | hp2 | a0003 | c0004 | t0013 | g0007 | AFR | MSL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG03654 | hp1 | a0001 | c0002 | t0005 | g0104 | SAS | PJL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG03654 | hp2 | a0001 | c0002 | t0003 | g0144 | SAS | PJL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0170 | SAS | PJL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG03669 | hp2 | a0001 | c0002 | t0005 | g0103 | SAS | PJL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG03704 | hp1 | a0001 | c0001 | t0022 | g0056 | SAS | PJL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG03704 | hp2 | a0001 | c0002 | t0021 | g0089 | SAS | PJL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0163 | SAS | PJL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG03834 | hp1 | a0001 | c0002 | t0003 | g0143 | SAS | BEB | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0179 | SAS | BEB | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | BEB | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG03927 | hp2 | a0001 | c0002 | t0005 | g0106 | SAS | BEB | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG04115 | hp1 | a0001 | c0002 | t0021 | g0092 | SAS | STU | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0184 | SAS | STU | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG04184 | hp1 | a0001 | c0002 | t0025 | g0004 | SAS | BEB | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG04184 | hp2 | a0001 | c0002 | t0003 | g0134 | SAS | BEB | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0069 | SAS | STU | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | STU | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | CHB | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA18612 | hp2 | a0001 | c0002 | t0029 | g0135 | EAS | CHB | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | CHB | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA18747 | hp2 | a0002 | c0003 | t0001 | g0041 | EAS | CHB | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA18906 | hp1 | a0001 | c0005 | t0007 | g0147 | AFR | YRI | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA18906 | hp2 | a0001 | c0001 | t0011 | g0055 | AFR | YRI | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA18942 | hp2 | a0001 | c0002 | t0003 | g0128 | EAS | JPT | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA18954 | hp2 | a0002 | c0003 | t0001 | g0199 | EAS | JPT | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA18957 | hp1 | a0002 | c0003 | t0016 | g0034 | EAS | JPT | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA18957 | hp2 | a0001 | c0002 | t0003 | g0132 | EAS | JPT | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA18960 | hp2 | a0001 | c0002 | t0003 | g0131 | EAS | JPT | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA18973 | hp2 | a0001 | c0001 | t0012 | g0076 | EAS | JPT | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA18983 | hp1 | a0001 | c0001 | t0051 | g0207 | EAS | JPT | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA18984 | hp1 | a0001 | c0001 | t0017 | g0037 | EAS | JPT | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA18984 | hp2 | a0002 | c0003 | t0001 | g0165 | EAS | JPT | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA19009 | hp1 | a0002 | c0003 | t0001 | g0043 | EAS | JPT | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA19009 | hp2 | a0001 | c0001 | t0012 | g0174 | EAS | JPT | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA19056 | hp2 | a0002 | c0003 | t0001 | g0036 | EAS | JPT | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA19060 | hp1 | a0002 | c0003 | t0001 | g0082 | EAS | JPT | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA19240 | hp1 | a0001 | c0002 | t0023 | g0002 | AFR | YRI | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA19240 | hp2 | a0001 | c0005 | t0007 | g0187 | AFR | YRI | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | ASW | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA20129 | hp2 | a0001 | c0002 | t0004 | g0114 | AFR | ASW | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA20752 | hp1 | a0001 | c0001 | t0036 | g0177 | EUR | TSI | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0071 | EUR | TSI | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA20905 | hp1 | a0001 | c0002 | t0003 | g0201 | SAS | GIH | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA20905 | hp2 | a0001 | c0001 | t0022 | g0057 | SAS | GIH | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02109 | hp1 | a0001 | c0002 | t0004 | g0111 | AFR | ACB | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0195 | AFR | ACB | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02486 | hp2 | a0002 | c0003 | t0001 | g0017 | AFR | ACB | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA18955 | hp1 | a0001 | c0002 | t0003 | g0133 | EAS | JPT | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA18955 | hp2 | a0002 | c0003 | t0001 | g0040 | EAS | JPT | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0030 | g0101 | REF | REF | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| homoSapiens | grch38p0 | a0002 | c0003 | t0001 | g0018 | REF | REF | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:114402771 | C | T | 1 | a0004 | 1 | HG02451.hp1 | missense_variant | MODERATE | c.2881G>A | p.Val961Met | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 16/20 | 3008/8369 | 2881/3384 | 961/1127 | chr1 | 114402771 | |||
| chr1:114405659 | A | G | 3 | a0001 a0003 a0004 |
179 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(176): Show |
missense_variant | MODERATE | c.2519T>C | p.Ile840Thr | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 15/20 | 2646/8369 | 2519/3384 | 840/1127 | chr1 | 114405659 | |||
| chr1:114510877 | A | C | 1 | a0003 | 1 | HG02145.hp1 | missense_variant | MODERATE | c.200T>G | p.Val67Gly | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/20 | 327/8369 | 200/3384 | 67/1127 | chr1 | 114510877 | |||
| chr1:114510877 | A | G | 2 | a0003 a0004 |
11 | HG02055.hp2 HG02258.hp1 HG02280.hp1 others(8): Show |
missense_variant | MODERATE | c.200T>C | p.Val67Ala | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/20 | 327/8369 | 200/3384 | 67/1127 | chr1 | 114510877 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:114402772 | G | A | 1 | a0001c0005 | 6 | HG01884.hp1 HG02897.hp2 HG03041.hp2 others(3): Show |
synonymous_variant | LOW | c.2880C>T | p.Pro960Pro | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 16/20 | 3007/8369 | 2880/3384 | 960/1127 | chr1 | 114402772 | |||
| chr1:114405687 | A | G | 2 | a0001c0006 a0001c0009 |
6 | HG02132.hp2 HG02698.hp1 HG02895.hp2 others(3): Show |
synonymous_variant | LOW | c.2491T>C | p.Leu831Leu | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 15/20 | 2618/8369 | 2491/3384 | 831/1127 | chr1 | 114405687 | |||
| chr1:114421583 | G | C | 1 | a0001c0009 | 1 | HG02698.hp1 | synonymous_variant | LOW | c.1914C>G | p.Thr638Thr | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/20 | 2041/8369 | 1914/3384 | 638/1127 | chr1 | 114421583 | |||
| chr1:114430807 | T | C | 6 | a0001c0002 a0001c0006 a0001c0009 others(3): Show |
80 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(77): Show |
synonymous_variant | LOW | c.1146A>G | p.Gln382Gln | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 6/20 | 1273/8369 | 1146/3384 | 382/1127 | chr1 | 114430807 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:114393059 | C | G | 1 | a0001c0006t0039 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4589G>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 4589 | chr1 | 114393059 | ||||||
| chr1:114393457 | T | A | 4 | a0001c0002t0003 a0001c0002t0029 a0001c0002t0043 others(1): Show |
21 | HG00323.hp1 HG00738.hp1 HG01099.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*4191A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 4191 | chr1 | 114393457 | ||||||
| chr1:114393796 | C | T | 1 | a0003c0004t0032 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3852G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 3852 | chr1 | 114393796 | ||||||
| chr1:114394212 | A | G | 2 | a0001c0002t0018 a0001c0002t0038 |
3 | HG00741.hp2 HG02647.hp2 HG02895.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3436T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 3436 | chr1 | 114394212 | ||||||
| chr1:114394693 | G | C | 1 | a0001c0009t0040 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2955C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 2955 | chr1 | 114394693 | ||||||
| chr1:114394900 | T | C | 2 | a0001c0002t0020 a0001c0002t0033 |
3 | HG02622.hp1 HG02886.hp1 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2748A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 2748 | chr1 | 114394900 | ||||||
| chr1:114395014 | G | A | 7 | a0001c0001t0031 a0001c0001t0037 a0001c0002t0034 others(4): Show |
12 | HG02055.hp2 HG02132.hp2 HG02451.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2634C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 2634 | chr1 | 114395014 | ||||||
| chr1:114395074 | A | T | 1 | a0001c0002t0009 | 4 | HG01891.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2574T>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 2574 | chr1 | 114395074 | ||||||
| chr1:114395141 | C | T | 1 | a0001c0001t0022 | 2 | HG03704.hp1 NA20905.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2507G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 2507 | chr1 | 114395141 | ||||||
| chr1:114395250 | C | A | 2 | a0001c0002t0005 a0001c0002t0019 |
12 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2398G>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 2398 | chr1 | 114395250 | ||||||
| chr1:114395468 | A | AT | 12 | a0001c0002t0003 a0001c0002t0006 a0001c0002t0018 others(9): Show |
38 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*2179dupA | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 2179 | chr1 | 114395468 | ||||||
| chr1:114395553 | C | T | 1 | a0001c0001t0015 | 3 | HG00099.hp2 HG00323.hp2 HG02004.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2095G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 2095 | chr1 | 114395553 | ||||||
| chr1:114395635 | G | A | 1 | a0001c0001t0042 | 1 | HG00558.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2013C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 2013 | chr1 | 114395635 | ||||||
| chr1:114395667 | T | G | 3 | a0001c0002t0003 a0001c0002t0043 a0001c0002t0049 |
20 | HG00323.hp1 HG00738.hp1 HG01099.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1981A>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 1981 | chr1 | 114395667 | ||||||
| chr1:114396077 | A | G | 1 | a0001c0005t0007 | 6 | HG01884.hp1 HG02897.hp2 HG03041.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1571T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 1571 | chr1 | 114396077 | ||||||
| chr1:114396216 | G | A | 1 | a0001c0001t0044 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1432C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 1432 | chr1 | 114396216 | ||||||
| chr1:114396268 | G | A | 2 | a0001c0002t0020 a0001c0002t0033 |
3 | HG02622.hp1 HG02886.hp1 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1380C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 1380 | chr1 | 114396268 | ||||||
| chr1:114396276 | G | T | 1 | a0001c0002t0021 | 2 | HG03704.hp2 HG04115.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1372C>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 1372 | chr1 | 114396276 | ||||||
| chr1:114396363 | T | C | 1 | a0001c0002t0034 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1285A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 1285 | chr1 | 114396363 | ||||||
| chr1:114396457 | A | G | 2 | a0001c0002t0005 a0001c0002t0019 |
12 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1191T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 1191 | chr1 | 114396457 | ||||||
| chr1:114396463 | C | T | 1 | a0001c0002t0038 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1185G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 1185 | chr1 | 114396463 | ||||||
| chr1:114396917 | G | A | 1 | a0001c0001t0048 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*731C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 731 | chr1 | 114396917 | ||||||
| chr1:114397011 | G | A | 1 | a0001c0001t0045 | 1 | HG01071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*637C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 637 | chr1 | 114397011 | ||||||
| chr1:114397101 | A | G | 1 | a0001c0002t0049 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*547T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 547 | chr1 | 114397101 | ||||||
| chr1:114397108 | G | GA | 7 | a0001c0002t0006 a0001c0002t0021 a0001c0002t0023 others(4): Show |
15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*539dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 539 | chr1 | 114397108 | ||||||
| chr1:114397117 | T | C | 13 | a0001c0001t0002 a0001c0001t0012 a0001c0001t0017 others(10): Show |
60 | HG00438.hp1 HG00558.hp2 HG00642.hp2 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*531A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 531 | chr1 | 114397117 | ||||||
| chr1:114397322 | A | G | 1 | a0001c0001t0036 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*326T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 326 | chr1 | 114397322 | ||||||
| chr1:114397578 | G | C | 1 | a0001c0001t0047 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*70C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 70 | chr1 | 114397578 | ||||||
| chr1:114397580 | G | GTT | 3 | a0001c0001t0012 a0001c0001t0026 a0001c0001t0031 |
5 | HG01175.hp2 HG02145.hp2 HG03098.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*66_*67dupAA | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 67 | chr1 | 114397580 | ||||||
| chr1:114397587 | G | T | 7 | a0001c0001t0002 a0001c0001t0017 a0001c0001t0036 others(4): Show |
49 | HG00438.hp1 HG00558.hp2 HG00642.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*61C>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 61 | chr1 | 114397587 | ||||||
| chr1:114397589 | G | GT | 21 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0017 others(18): Show |
83 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*58dupA | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 58 | chr1 | 114397589 | ||||||
| chr1:114397589 | G | GTT | 11 | a0001c0002t0005 a0001c0002t0009 a0001c0002t0018 others(8): Show |
27 | HG00741.hp2 HG01192.hp1 HG01361.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*57_*58dupAA | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 58 | chr1 | 114397589 | ||||||
| chr1:114397589 | G | T | 3 | a0001c0001t0012 a0001c0001t0026 a0001c0001t0031 |
5 | HG01175.hp2 HG02145.hp2 HG03098.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*59C>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 59 | chr1 | 114397589 | ||||||
| chr1:114397589 | GT | G | 3 | a0001c0001t0024 a0001c0001t0048 a0002c0003t0016 |
5 | HG00438.hp2 HG02083.hp1 HG02615.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*58delA | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 58 | chr1 | 114397589 | ||||||
| chr1:114397593 | T | TG | 3 | a0001c0002t0003 a0001c0002t0029 a0001c0002t0049 |
20 | HG00323.hp1 HG00738.hp1 HG01099.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*54_*55insC | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 54 | chr1 | 114397593 | ||||||
| chr1:114397605 | T | C | 1 | a0001c0001t0028 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*43A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 43 | chr1 | 114397605 | ||||||
| chr1:114397606 | C | G | 1 | a0001c0001t0028 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*42G>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 42 | chr1 | 114397606 | ||||||
| chr1:114397607 | G | GT | 5 | a0001c0001t0011 a0001c0001t0017 a0001c0001t0026 others(2): Show |
8 | HG01099.hp2 HG01175.hp2 HG01361.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*40dupA | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 40 | chr1 | 114397607 | ||||||
| chr1:114397607 | G | T | 1 | a0001c0001t0028 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*41C>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 41 | chr1 | 114397607 | ||||||
| chr1:114397608 | T | G | 1 | a0002c0003t0008 | 6 | HG00642.hp1 HG00738.hp2 HG01106.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*40A>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 40 | chr1 | 114397608 | ||||||
| chr1:114511107 | C | G | 1 | a0001c0002t0025 | 1 | HG04184.hp1 | 5_prime_UTR_variant | MODIFIER | c.-31G>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/20 | 31 | chr1 | 114511107 | ||||||
| chr1:114511126 | G | C | 1 | a0003c0004t0050 | 1 | HG03041.hp1 | 5_prime_UTR_variant | MODIFIER | c.-50C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/20 | 50 | chr1 | 114511126 | ||||||
| chr1:114511174 | G | T | 1 | a0001c0001t0024 | 1 | HG02615.hp2 | 5_prime_UTR_variant | MODIFIER | c.-98C>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/20 | 98 | chr1 | 114511174 | ||||||
| chr1:114511190 | C | T | 1 | a0001c0002t0023 | 1 | NA19240.hp1 | 5_prime_UTR_variant | MODIFIER | c.-114G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/20 | 114 | chr1 | 114511190 | ||||||
| chr1:114511191 | G | A | 1 | a0001c0001t0051 | 1 | NA18983.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-115C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/20 | chr1 | 114511191 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:114398010 | CA | C | 175 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0022 others(172): Show |
176 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.3121-21delT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 18/19 | chr1 | 114398010 | |||||||
| chr1:114398163 | C | T | 1 | a0001c0002t0005g0108 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3121-173G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 18/19 | chr1 | 114398163 | |||||||
| chr1:114398391 | T | C | 6 | a0001c0002t0004g0111 a0001c0002t0004g0114 a0001c0002t0004g0115 others(3): Show |
6 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.3121-401A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 18/19 | chr1 | 114398391 | |||||||
| chr1:114398547 | T | C | 4 | a0001c0006t0010g0119 a0001c0006t0010g0120 a0001c0006t0010g0121 others(1): Show |
4 | HG02895.hp2 HG02897.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.3121-557A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 18/19 | chr1 | 114398547 | |||||||
| chr1:114398687 | A | G | 1 | a0001c0009t0040g0123 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.3121-697T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 18/19 | chr1 | 114398687 | |||||||
| chr1:114398704 | C | T | 134 | a0001c0001t0002g0039 a0001c0001t0002g0064 a0001c0001t0002g0069 others(131): Show |
134 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.3121-714G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 18/19 | chr1 | 114398704 | |||||||
| chr1:114398853 | T | C | 1 | a0001c0006t0010g0119 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3120+604A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 18/19 | chr1 | 114398853 | |||||||
| chr1:114398898 | C | CA | 16 | a0001c0001t0001g0070 a0001c0001t0001g0084 a0001c0001t0002g0069 others(13): Show |
16 | HG00735.hp2 HG02056.hp1 HG02129.hp1 others(13): Show |
intron_variant | MODIFIER | c.3120+558dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 18/19 | chr1 | 114398898 | |||||||
| chr1:114398898 | C | CAAA | 14 | a0001c0002t0006g0086 a0001c0002t0006g0087 a0001c0002t0006g0088 others(11): Show |
14 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.3120+556_3120+558d others(5): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 18/19 | chr1 | 114398898 | |||||||
| chr1:114398906 | A | C | 3 | a0002c0003t0001g0021 a0002c0003t0016g0034 a0002c0003t0016g0044 |
3 | HG02015.hp2 HG02083.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.3120+551T>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 18/19 | chr1 | 114398906 | |||||||
| chr1:114398911 | A | C | 8 | a0001c0001t0001g0025 a0001c0001t0001g0061 a0001c0001t0004g0024 others(5): Show |
8 | HG00438.hp2 HG02015.hp2 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.3120+546T>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 18/19 | chr1 | 114398911 | |||||||
| chr1:114398912 | A | AC | 2 | a0001c0002t0009g0202 a0001c0002t0009g0203 |
2 | HG01891.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.3120+544_3120+545i others(3): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 18/19 | chr1 | 114398912 | |||||||
| chr1:114398915 | AC | A | 4 | a0001c0001t0002g0156 a0001c0001t0002g0198 a0001c0001t0012g0197 others(1): Show |
4 | HG02145.hp1 HG02145.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.3120+541delG | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 18/19 | chr1 | 114398915 | |||||||
| chr1:114398916 | C | A | 1 | a0001c0001t0002g0148 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3120+541G>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 18/19 | chr1 | 114398916 | |||||||
| chr1:114398918 | A | G | 1 | a0003c0004t0014g0012 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3120+539T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 18/19 | chr1 | 114398918 | |||||||
| chr1:114398926 | C | CA | 4 | a0001c0005t0007g0147 a0001c0005t0007g0150 a0001c0005t0007g0151 others(1): Show |
4 | HG01884.hp1 HG02897.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.3120+530dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 18/19 | chr1 | 114398926 | |||||||
| chr1:114398931 | C | A | 133 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0002g0039 others(130): Show |
133 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.3120+526G>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 18/19 | chr1 | 114398931 | |||||||
| chr1:114398971 | A | C | 1 | a0001c0001t0002g0155 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3120+486T>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 18/19 | chr1 | 114398971 | |||||||
| chr1:114399628 | G | A | 2 | a0001c0002t0018g0145 a0001c0002t0018g0146 |
2 | HG00741.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.2968-19C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 17/19 | chr1 | 114399628 | |||||||
| chr1:114399674 | T | C | 15 | a0001c0002t0006g0086 a0001c0002t0006g0087 a0001c0002t0006g0088 others(12): Show |
15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.2968-65A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 17/19 | chr1 | 114399674 | |||||||
| chr1:114399817 | C | T | 1 | a0001c0001t0002g0173 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2968-208G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 17/19 | chr1 | 114399817 | |||||||
| chr1:114399833 | TTAA | T | 5 | a0003c0004t0001g0008 a0003c0004t0004g0009 a0003c0004t0013g0010 others(2): Show |
5 | HG02145.hp1 HG02258.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.2968-227_2968-225d others(5): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 17/19 | chr1 | 114399833 | |||||||
| chr1:114399882 | T | C | 4 | a0001c0001t0002g0185 a0001c0001t0002g0194 a0001c0005t0007g0187 others(1): Show |
4 | HG02622.hp2 HG02647.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2968-273A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 17/19 | chr1 | 114399882 | |||||||
| chr1:114400036 | G | A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0027 |
2 | HG02809.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2968-427C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 17/19 | chr1 | 114400036 | |||||||
| chr1:114400108 | T | C | 12 | a0001c0002t0009g0202 a0001c0002t0009g0203 a0001c0002t0009g0204 others(9): Show |
12 | HG01891.hp2 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.2968-499A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 17/19 | chr1 | 114400108 | |||||||
| chr1:114400364 | C | T | 15 | a0001c0002t0006g0086 a0001c0002t0006g0087 a0001c0002t0006g0088 others(12): Show |
15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.2968-755G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 17/19 | chr1 | 114400364 | |||||||
| chr1:114400494 | T | C | 6 | a0001c0002t0004g0111 a0001c0002t0004g0114 a0001c0002t0004g0115 others(3): Show |
6 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.2968-885A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 17/19 | chr1 | 114400494 | |||||||
| chr1:114400726 | G | T | 9 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0077 others(6): Show |
9 | HG00099.hp2 HG00323.hp2 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.2967+663C>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 17/19 | chr1 | 114400726 | |||||||
| chr1:114400732 | A | G | 1 | a0001c0001t0001g0025 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2967+657T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 17/19 | chr1 | 114400732 | |||||||
| chr1:114401028 | CT | C | 20 | a0001c0002t0005g0098 a0001c0002t0005g0099 a0001c0002t0005g0102 others(17): Show |
20 | HG00741.hp2 HG01192.hp1 HG01257.hp2 others(17): Show |
intron_variant | MODIFIER | c.2967+360delA | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 17/19 | chr1 | 114401028 | |||||||
| chr1:114401059 | C | T | 2 | a0003c0004t0001g0008 a0003c0004t0004g0009 |
2 | HG02965.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2967+330G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 17/19 | chr1 | 114401059 | |||||||
| chr1:114401098 | G | A | 12 | a0001c0002t0009g0202 a0001c0002t0009g0203 a0001c0002t0009g0204 others(9): Show |
12 | HG01891.hp2 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.2967+291C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 17/19 | chr1 | 114401098 | |||||||
| chr1:114401099 | C | T | 3 | a0001c0002t0018g0145 a0001c0002t0018g0146 a0001c0002t0038g0118 |
3 | HG00741.hp2 HG02647.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.2967+290G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 17/19 | chr1 | 114401099 | |||||||
| chr1:114401161 | G | C | 15 | a0001c0002t0006g0086 a0001c0002t0006g0087 a0001c0002t0006g0088 others(12): Show |
15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.2967+228C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 17/19 | chr1 | 114401161 | |||||||
| chr1:114401260 | G | A | 3 | a0003c0004t0004g0006 a0003c0004t0013g0007 a0003c0004t0050g0206 |
3 | HG02280.hp1 HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2967+129C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 17/19 | chr1 | 114401260 | |||||||
| chr1:114401499 | T | C | 2 | a0001c0002t0009g0202 a0001c0002t0009g0203 |
2 | HG01891.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.2893-36A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 16/19 | chr1 | 114401499 | |||||||
| chr1:114401503 | T | C | 1 | a0001c0002t0046g0091 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2893-40A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 16/19 | chr1 | 114401503 | |||||||
| chr1:114401917 | T | C | 1 | a0001c0001t0002g0172 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2893-454A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 16/19 | chr1 | 114401917 | |||||||
| chr1:114402059 | T | C | 24 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(21): Show |
24 | HG00323.hp1 HG00738.hp1 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.2893-596A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 16/19 | chr1 | 114402059 | |||||||
| chr1:114402063 | C | T | 15 | a0001c0002t0006g0086 a0001c0002t0006g0087 a0001c0002t0006g0088 others(12): Show |
15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.2893-600G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 16/19 | chr1 | 114402063 | |||||||
| chr1:114402326 | CACT | C | 4 | a0001c0002t0009g0202 a0001c0002t0009g0203 a0001c0002t0009g0204 others(1): Show |
4 | HG01891.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2892+431_2892+433d others(5): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 16/19 | chr1 | 114402326 | |||||||
| chr1:114402488 | C | G | 4 | a0001c0002t0009g0202 a0001c0002t0009g0203 a0001c0002t0009g0204 others(1): Show |
4 | HG01891.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2892+272G>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 16/19 | chr1 | 114402488 | |||||||
| chr1:114403012 | G | A | 15 | a0001c0002t0006g0086 a0001c0002t0006g0087 a0001c0002t0006g0088 others(12): Show |
15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.2769-129C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 15/19 | chr1 | 114403012 | |||||||
| chr1:114403317 | C | T | 2 | a0001c0002t0004g0114 a0001c0002t0004g0115 |
2 | HG01884.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2769-434G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 15/19 | chr1 | 114403317 | |||||||
| chr1:114403349 | C | A | 1 | a0001c0002t0003g0137 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2769-466G>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 15/19 | chr1 | 114403349 | |||||||
| chr1:114403425 | C | A | 1 | a0001c0002t0038g0118 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2769-542G>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 15/19 | chr1 | 114403425 | |||||||
| chr1:114403442 | T | C | 1 | a0001c0001t0048g0081 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2769-559A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 15/19 | chr1 | 114403442 | |||||||
| chr1:114403532 | G | A | 12 | a0001c0002t0005g0098 a0001c0002t0005g0099 a0001c0002t0005g0102 others(9): Show |
12 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.2769-649C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 15/19 | chr1 | 114403532 | |||||||
| chr1:114404025 | C | T | 1 | a0001c0002t0003g0133 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2769-1142G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 15/19 | chr1 | 114404025 | |||||||
| chr1:114404634 | T | C | 6 | a0001c0002t0004g0111 a0001c0002t0004g0114 a0001c0002t0004g0115 others(3): Show |
6 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.2768+776A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 15/19 | chr1 | 114404634 | |||||||
| chr1:114404809 | C | CT | 27 | a0001c0001t0001g0083 a0001c0001t0026g0196 a0001c0002t0005g0099 others(24): Show |
27 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.2768+600dupA | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 15/19 | chr1 | 114404809 | |||||||
| chr1:114404809 | C | CTT | 12 | a0001c0001t0004g0050 a0001c0002t0005g0098 a0001c0002t0005g0102 others(9): Show |
12 | HG01192.hp1 HG01261.hp2 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.2768+599_2768+600d others(4): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 15/19 | chr1 | 114404809 | |||||||
| chr1:114404809 | CT | C | 11 | a0001c0001t0001g0200 a0001c0001t0012g0174 a0001c0002t0009g0203 others(8): Show |
11 | HG00741.hp2 HG02280.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.2768+600delA | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 15/19 | chr1 | 114404809 | |||||||
| chr1:114404959 | C | G | 1 | a0001c0001t0041g0169 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2768+451G>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 15/19 | chr1 | 114404959 | |||||||
| chr1:114404982 | G | C | 1 | a0001c0002t0003g0133 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2768+428C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 15/19 | chr1 | 114404982 | |||||||
| chr1:114405078 | G | C | 1 | a0003c0004t0004g0006 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2768+332C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 15/19 | chr1 | 114405078 | |||||||
| chr1:114405772 | G | A | 3 | a0001c0002t0018g0145 a0001c0002t0018g0146 a0001c0002t0038g0118 |
3 | HG00741.hp2 HG02647.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.2419-13C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 14/19 | chr1 | 114405772 | |||||||
| chr1:114405861 | C | T | 4 | a0001c0002t0003g0141 a0001c0002t0003g0142 a0001c0002t0003g0144 others(1): Show |
4 | HG02602.hp2 HG02698.hp2 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.2419-102G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 14/19 | chr1 | 114405861 | |||||||
| chr1:114406016 | T | C | 15 | a0001c0002t0006g0086 a0001c0002t0006g0087 a0001c0002t0006g0088 others(12): Show |
15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.2419-257A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 14/19 | chr1 | 114406016 | |||||||
| chr1:114406147 | T | G | 12 | a0001c0002t0005g0098 a0001c0002t0005g0099 a0001c0002t0005g0102 others(9): Show |
12 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.2419-388A>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 14/19 | chr1 | 114406147 | |||||||
| chr1:114406676 | G | A | 2 | a0001c0006t0039g0124 a0001c0009t0040g0123 |
2 | HG02132.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.2418+265C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 14/19 | chr1 | 114406676 | |||||||
| chr1:114406728 | A | G | 1 | a0001c0002t0021g0089 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2418+213T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 14/19 | chr1 | 114406728 | |||||||
| chr1:114406775 | T | C | 6 | a0001c0006t0010g0119 a0001c0006t0010g0120 a0001c0006t0010g0121 others(3): Show |
6 | HG02132.hp2 HG02698.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.2418+166A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 14/19 | chr1 | 114406775 | |||||||
| chr1:114407198 | T | C | 17 | a0001c0002t0006g0086 a0001c0002t0006g0087 a0001c0002t0006g0088 others(14): Show |
17 | HG00099.hp1 HG00735.hp1 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.2259-98A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 13/19 | chr1 | 114407198 | |||||||
| chr1:114407320 | AT | A | 3 | a0001c0001t0001g0022 a0001c0001t0004g0023 a0001c0001t0024g0003 |
3 | HG02615.hp2 HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2259-221delA | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 13/19 | chr1 | 114407320 | |||||||
| chr1:114407700 | C | T | 4 | a0003c0004t0014g0005 a0003c0004t0014g0012 a0003c0004t0014g0013 others(1): Show |
4 | HG02055.hp2 HG02451.hp1 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.2259-600G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 13/19 | chr1 | 114407700 | |||||||
| chr1:114407751 | T | C | 6 | a0001c0006t0010g0119 a0001c0006t0010g0120 a0001c0006t0010g0121 others(3): Show |
6 | HG02132.hp2 HG02698.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.2259-651A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 13/19 | chr1 | 114407751 | |||||||
| chr1:114407989 | C | T | 6 | a0001c0006t0010g0119 a0001c0006t0010g0120 a0001c0006t0010g0121 others(3): Show |
6 | HG02132.hp2 HG02698.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.2258+688G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 13/19 | chr1 | 114407989 | |||||||
| chr1:114408137 | CAGAA | C | 24 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(21): Show |
24 | HG00323.hp1 HG00738.hp1 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.2258+536_2258+539d others(6): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 13/19 | chr1 | 114408137 | |||||||
| chr1:114408459 | G | GA | 23 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(20): Show |
23 | HG00323.hp1 HG00738.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.2258+217dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 13/19 | chr1 | 114408459 | |||||||
| chr1:114408469 | C | G | 1 | a0002c0003t0001g0041 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2258+208G>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 13/19 | chr1 | 114408469 | |||||||
| chr1:114408519 | T | C | 12 | a0001c0002t0005g0098 a0001c0002t0005g0099 a0001c0002t0005g0102 others(9): Show |
12 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.2258+158A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 13/19 | chr1 | 114408519 | |||||||
| chr1:114408580 | T | A | 1 | a0001c0005t0007g0152 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2258+97A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 13/19 | chr1 | 114408580 | |||||||
| chr1:114408598 | C | T | 71 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(68): Show |
71 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(68): Show |
intron_variant | MODIFIER | c.2258+79G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 13/19 | chr1 | 114408598 | |||||||
| chr1:114408765 | A | G | 1 | a0001c0006t0039g0124 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2195-25T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 12/19 | chr1 | 114408765 | |||||||
| chr1:114408768 | T | A | 26 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(23): Show |
26 | HG00323.hp1 HG00738.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.2195-28A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 12/19 | chr1 | 114408768 | |||||||
| chr1:114408787 | T | C | 2 | a0001c0002t0005g0105 a0001c0002t0005g0108 |
2 | HG02615.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2195-47A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 12/19 | chr1 | 114408787 | |||||||
| chr1:114408878 | C | T | 2 | a0001c0001t0031g0157 a0001c0001t0037g0154 |
2 | HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2195-138G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 12/19 | chr1 | 114408878 | |||||||
| chr1:114408977 | A | T | 1 | a0002c0003t0001g0199 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.2195-237T>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 12/19 | chr1 | 114408977 | |||||||
| chr1:114409241 | A | T | 1 | a0001c0001t0002g0155 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2195-501T>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 12/19 | chr1 | 114409241 | |||||||
| chr1:114409333 | G | A | 1 | a0001c0002t0021g0089 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2195-593C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 12/19 | chr1 | 114409333 | |||||||
| chr1:114409480 | A | C | 4 | a0001c0001t0002g0148 a0001c0001t0002g0156 a0001c0001t0002g0198 others(1): Show |
4 | HG02145.hp2 HG02258.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2194+704T>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 12/19 | chr1 | 114409480 | |||||||
| chr1:114409523 | A | ACT | 12 | a0001c0002t0005g0098 a0001c0002t0005g0099 a0001c0002t0005g0102 others(9): Show |
12 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.2194+659_2194+660d others(4): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 12/19 | chr1 | 114409523 | |||||||
| chr1:114409540 | A | G | 4 | a0001c0001t0002g0158 a0001c0001t0002g0159 a0001c0001t0002g0160 others(1): Show |
4 | NA18942.hp1 NA18970.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.2194+644T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 12/19 | chr1 | 114409540 | |||||||
| chr1:114409541 | T | C | 1 | a0001c0001t0001g0079 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.2194+643A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 12/19 | chr1 | 114409541 | |||||||
| chr1:114409723 | C | T | 6 | a0001c0006t0010g0119 a0001c0006t0010g0120 a0001c0006t0010g0121 others(3): Show |
6 | HG02132.hp2 HG02698.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.2194+461G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 12/19 | chr1 | 114409723 | |||||||
| chr1:114409768 | G | A | 1 | a0002c0003t0001g0017 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2194+416C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 12/19 | chr1 | 114409768 | |||||||
| chr1:114410768 | C | A | 1 | a0001c0002t0006g0088 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2062-452G>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114410768 | |||||||
| chr1:114410778 | CA | C | 80 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(77): Show |
80 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.2062-463delT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114410778 | |||||||
| chr1:114410798 | T | C | 80 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(77): Show |
80 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.2062-482A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114410798 | |||||||
| chr1:114410906 | C | T | 12 | a0001c0002t0005g0098 a0001c0002t0005g0099 a0001c0002t0005g0102 others(9): Show |
12 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.2062-590G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114410906 | |||||||
| chr1:114410990 | T | C | 3 | a0003c0004t0004g0006 a0003c0004t0013g0007 a0003c0004t0050g0206 |
3 | HG02280.hp1 HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2062-674A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114410990 | |||||||
| chr1:114411060 | G | T | 1 | a0001c0002t0018g0146 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2062-744C>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114411060 | |||||||
| chr1:114411198 | G | A | 10 | a0001c0002t0034g0117 a0001c0006t0010g0119 a0001c0006t0010g0120 others(7): Show |
10 | HG02055.hp2 HG02132.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.2062-882C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114411198 | |||||||
| chr1:114411773 | T | C | 2 | a0002c0003t0001g0043 a0002c0003t0001g0082 |
2 | NA19009.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.2062-1457A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114411773 | |||||||
| chr1:114411999 | A | G | 1 | a0001c0001t0026g0196 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2062-1683T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114411999 | |||||||
| chr1:114412063 | CCAAT | C | 24 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(21): Show |
24 | HG00323.hp1 HG00738.hp1 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.2062-1751_2062-174 others(8): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114412063 | |||||||
| chr1:114412094 | T | G | 15 | a0001c0002t0006g0086 a0001c0002t0006g0087 a0001c0002t0006g0088 others(12): Show |
15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.2062-1778A>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114412094 | |||||||
| chr1:114412103 | T | C | 4 | a0001c0006t0010g0119 a0001c0006t0010g0120 a0001c0006t0010g0121 others(1): Show |
4 | HG02895.hp2 HG02897.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2062-1787A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114412103 | |||||||
| chr1:114412385 | A | C | 1 | a0001c0002t0006g0088 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2062-2069T>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114412385 | |||||||
| chr1:114412402 | A | C | 2 | a0001c0002t0009g0202 a0001c0002t0009g0203 |
2 | HG01891.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.2062-2086T>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114412402 | |||||||
| chr1:114412688 | T | C | 6 | a0001c0001t0001g0022 a0001c0001t0001g0025 a0001c0001t0004g0023 others(3): Show |
6 | HG02109.hp2 HG02572.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.2062-2372A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114412688 | |||||||
| chr1:114412732 | C | A | 2 | a0002c0003t0016g0034 a0002c0003t0016g0044 |
2 | HG02083.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.2062-2416G>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114412732 | |||||||
| chr1:114412770 | G | A | 5 | a0001c0002t0003g0128 a0001c0002t0003g0131 a0001c0002t0003g0132 others(2): Show |
5 | NA18612.hp2 NA18942.hp2 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.2062-2454C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114412770 | |||||||
| chr1:114413151 | G | C | 6 | a0001c0002t0004g0111 a0001c0002t0004g0114 a0001c0002t0004g0115 others(3): Show |
6 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.2062-2835C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114413151 | |||||||
| chr1:114413327 | G | A | 1 | a0001c0002t0003g0134 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2062-3011C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114413327 | |||||||
| chr1:114413331 | A | G | 1 | a0001c0002t0003g0128 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2062-3015T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114413331 | |||||||
| chr1:114413431 | G | C | 2 | a0001c0001t0031g0157 a0001c0001t0037g0154 |
2 | HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2062-3115C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114413431 | |||||||
| chr1:114413451 | G | A | 3 | a0001c0002t0018g0145 a0001c0002t0018g0146 a0001c0002t0038g0118 |
3 | HG00741.hp2 HG02647.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.2062-3135C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114413451 | |||||||
| chr1:114413558 | C | CA | 10 | a0001c0001t0001g0058 a0001c0001t0001g0180 a0001c0001t0002g0064 others(7): Show |
10 | HG01071.hp1 HG01071.hp2 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.2062-3243dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114413558 | |||||||
| chr1:114413558 | C | CAA | 18 | a0001c0002t0003g0127 a0001c0002t0003g0128 a0001c0002t0003g0130 others(15): Show |
18 | HG00323.hp1 HG00738.hp1 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.2062-3244_2062-324 others(6): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114413558 | |||||||
| chr1:114413558 | C | CAAA | 10 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0133 others(7): Show |
10 | HG01099.hp1 HG01891.hp2 HG01952.hp2 others(7): Show |
intron_variant | MODIFIER | c.2062-3245_2062-324 others(7): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114413558 | |||||||
| chr1:114413569 | A | G | 1 | a0001c0001t0022g0057 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2062-3253T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114413569 | |||||||
| chr1:114413570 | A | AAG | 15 | a0001c0002t0006g0086 a0001c0002t0006g0087 a0001c0002t0006g0088 others(12): Show |
15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.2062-3255_2062-325 others(6): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114413570 | |||||||
| chr1:114413570 | AAAAGAAA others(2): Show |
A | 10 | a0001c0002t0005g0098 a0001c0002t0005g0099 a0001c0002t0005g0102 others(7): Show |
10 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.2062-3263_2062-325 others(13): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114413570 | |||||||
| chr1:114413574 | G | A | 67 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(64): Show |
67 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.2062-3258C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114413574 | |||||||
| chr1:114413578 | A | AAAGAAAA others(16): Show |
3 | a0001c0002t0018g0145 a0001c0002t0018g0146 a0004c0007t0001g0014 |
3 | HG00741.hp2 HG02451.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.2062-3263_2062-326 others(27): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114413578 | |||||||
| chr1:114413578 | A | AAGAAAAG others(15): Show |
3 | a0001c0002t0034g0117 a0003c0004t0014g0005 a0003c0004t0014g0012 |
3 | HG02055.hp2 HG02451.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.2062-3263_2062-326 others(26): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114413578 | |||||||
| chr1:114413578 | A | AAGAAAAG others(36): Show |
1 | a0003c0004t0014g0013 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2062-3263_2062-326 others(47): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114413578 | |||||||
| chr1:114413578 | A | AGAAAAGA others(14): Show |
1 | a0001c0001t0001g0073 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2062-3283_2062-326 others(25): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114413578 | |||||||
| chr1:114413578 | AGAAAAGA others(13): Show |
A | 2 | a0001c0002t0005g0105 a0001c0002t0005g0108 |
2 | HG02615.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2062-3282_2062-326 others(24): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114413578 | |||||||
| chr1:114413579 | G | A | 9 | a0001c0002t0033g0116 a0003c0004t0001g0008 a0003c0004t0004g0006 others(6): Show |
9 | HG02145.hp1 HG02258.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.2062-3263C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114413579 | |||||||
| chr1:114413580 | AAAAGAAA others(12): Show |
A | 6 | a0001c0002t0033g0116 a0003c0004t0013g0007 a0003c0004t0013g0010 others(3): Show |
6 | HG02145.hp1 HG02258.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.2062-3283_2062-326 others(23): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114413580 | |||||||
| chr1:114413581 | AAAGAAAA others(11): Show |
A | 3 | a0003c0004t0001g0008 a0003c0004t0004g0006 a0003c0004t0004g0009 |
3 | HG02280.hp1 HG02965.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2062-3283_2062-326 others(22): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114413581 | |||||||
| chr1:114413588 | AAGACTTT others(4): Show |
A | 10 | a0001c0002t0005g0098 a0001c0002t0005g0099 a0001c0002t0005g0102 others(7): Show |
10 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.2062-3283_2062-327 others(15): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114413588 | |||||||
| chr1:114413599 | T | A | 2 | a0001c0002t0005g0105 a0001c0002t0005g0108 |
2 | HG02615.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2062-3283A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114413599 | |||||||
| chr1:114413600 | G | C | 15 | a0001c0002t0006g0086 a0001c0002t0006g0087 a0001c0002t0006g0088 others(12): Show |
15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.2062-3284C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114413600 | |||||||
| chr1:114413619 | G | A | 8 | a0003c0004t0001g0008 a0003c0004t0004g0006 a0003c0004t0004g0009 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.2062-3303C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114413619 | |||||||
| chr1:114413628 | T | TA | 42 | a0001c0001t0001g0025 a0001c0001t0001g0070 a0001c0001t0001g0077 others(39): Show |
42 | HG00323.hp1 HG00735.hp2 HG01175.hp1 others(39): Show |
intron_variant | MODIFIER | c.2062-3313dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114413628 | |||||||
| chr1:114413628 | T | TAA | 14 | a0001c0002t0003g0126 a0001c0002t0003g0130 a0001c0002t0003g0137 others(11): Show |
14 | HG01099.hp1 HG01167.hp1 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.2062-3314_2062-331 others(6): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114413628 | |||||||
| chr1:114413833 | C | T | 2 | a0001c0001t0001g0083 a0001c0001t0004g0050 |
2 | HG02055.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.2062-3517G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114413833 | |||||||
| chr1:114413968 | C | T | 1 | a0001c0001t0042g0062 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2062-3652G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114413968 | |||||||
| chr1:114414027 | G | GCA | 23 | a0001c0001t0001g0025 a0001c0001t0001g0071 a0001c0001t0002g0190 others(20): Show |
23 | HG00099.hp2 HG00741.hp2 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.2062-3713_2062-371 others(6): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114414027 | |||||||
| chr1:114414027 | G | GCACA | 24 | a0001c0001t0001g0083 a0001c0001t0002g0192 a0001c0001t0036g0177 others(21): Show |
24 | HG00642.hp2 HG00738.hp1 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.2062-3715_2062-371 others(8): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114414027 | |||||||
| chr1:114414027 | G | GCACACA | 10 | a0001c0001t0002g0064 a0001c0002t0003g0132 a0001c0002t0003g0133 others(7): Show |
10 | HG00099.hp1 HG01071.hp2 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.2062-3717_2062-371 others(10): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114414027 | |||||||
| chr1:114414027 | G | GCACACAC others(1): Show |
12 | a0001c0002t0003g0130 a0001c0002t0003g0138 a0001c0002t0004g0114 others(9): Show |
12 | HG00323.hp1 HG00735.hp1 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.2062-3719_2062-371 others(12): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114414027 | |||||||
| chr1:114414027 | G | GCACACAC others(3): Show |
3 | a0003c0004t0013g0010 a0003c0004t0032g0011 a0004c0007t0001g0014 |
3 | HG02258.hp1 HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2062-3721_2062-371 others(14): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114414027 | |||||||
| chr1:114414027 | G | GCACACAC others(5): Show |
6 | a0001c0002t0003g0128 a0001c0002t0029g0135 a0001c0002t0033g0116 others(3): Show |
6 | HG02523.hp1 HG02886.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.2062-3723_2062-371 others(16): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114414027 | |||||||
| chr1:114414027 | G | GCACACAC others(7): Show |
3 | a0001c0002t0003g0131 a0001c0006t0010g0119 a0003c0004t0014g0005 |
3 | HG02922.hp1 HG03017.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.2062-3725_2062-371 others(18): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114414027 | |||||||
| chr1:114414027 | G | GCACACAC others(11): Show |
1 | a0003c0004t0004g0009 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2062-3729_2062-371 others(22): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114414027 | |||||||
| chr1:114414027 | GCA | G | 56 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0058 others(53): Show |
56 | HG00323.hp2 HG00558.hp1 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.2062-3713_2062-371 others(6): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114414027 | |||||||
| chr1:114414027 | GCACA | G | 4 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0061 others(1): Show |
4 | HG02615.hp2 HG02809.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.2062-3715_2062-371 others(8): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114414027 | |||||||
| chr1:114414027 | GCACACA | G | 1 | a0002c0003t0001g0001 | 2 | HG01433.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.2062-3717_2062-371 others(10): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114414027 | |||||||
| chr1:114414027 | GCACACAC others(1): Show |
G | 5 | a0001c0001t0002g0156 a0001c0002t0009g0202 a0001c0002t0009g0203 others(2): Show |
5 | HG01891.hp2 HG02572.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2062-3719_2062-371 others(12): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114414027 | |||||||
| chr1:114414027 | GCACACAC others(7): Show |
G | 3 | a0003c0004t0004g0006 a0003c0004t0013g0007 a0003c0004t0050g0206 |
3 | HG02280.hp1 HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2062-3725_2062-371 others(18): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114414027 | |||||||
| chr1:114414027 | GCACACAC others(9): Show |
G | 1 | a0001c0001t0002g0153 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2062-3727_2062-371 others(20): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114414027 | |||||||
| chr1:114414379 | T | C | 15 | a0001c0002t0006g0086 a0001c0002t0006g0087 a0001c0002t0006g0088 others(12): Show |
15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.2062-4063A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114414379 | |||||||
| chr1:114414433 | CCTT | C | 24 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(21): Show |
24 | HG00323.hp1 HG00738.hp1 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.2062-4120_2062-411 others(7): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114414433 | |||||||
| chr1:114414456 | G | A | 15 | a0001c0002t0006g0086 a0001c0002t0006g0087 a0001c0002t0006g0088 others(12): Show |
15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.2062-4140C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114414456 | |||||||
| chr1:114414588 | T | C | 1 | a0002c0003t0001g0033 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2062-4272A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114414588 | |||||||
| chr1:114414632 | C | T | 80 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(77): Show |
80 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.2062-4316G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114414632 | |||||||
| chr1:114414671 | G | C | 1 | a0001c0002t0005g0102 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2062-4355C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114414671 | |||||||
| chr1:114414989 | A | AT | 5 | a0001c0001t0001g0020 a0001c0001t0001g0070 a0001c0001t0004g0023 others(2): Show |
5 | HG00735.hp2 HG01243.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.2062-4674dupA | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114414989 | |||||||
| chr1:114414989 | A | ATT | 9 | a0001c0002t0004g0111 a0001c0002t0004g0114 a0001c0002t0004g0115 others(6): Show |
9 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.2062-4675_2062-467 others(6): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114414989 | |||||||
| chr1:114414989 | A | ATTT | 14 | a0001c0002t0005g0098 a0001c0002t0005g0099 a0001c0002t0005g0102 others(11): Show |
14 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.2062-4676_2062-467 others(7): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114414989 | |||||||
| chr1:114414989 | A | ATTTT | 26 | a0001c0002t0005g0105 a0001c0002t0005g0106 a0001c0002t0006g0086 others(23): Show |
26 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.2062-4677_2062-467 others(8): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114414989 | |||||||
| chr1:114414989 | A | ATTTTT | 8 | a0001c0002t0006g0094 a0001c0002t0018g0145 a0001c0002t0018g0146 others(5): Show |
8 | HG00741.hp2 HG02055.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.2062-4678_2062-467 others(9): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114414989 | |||||||
| chr1:114414989 | A | ATTTTTTT | 13 | a0001c0002t0003g0126 a0001c0002t0003g0127 a0001c0002t0003g0131 others(10): Show |
13 | HG00323.hp1 HG00738.hp1 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.2062-4680_2062-467 others(11): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114414989 | |||||||
| chr1:114414989 | A | ATTTTTTT others(1): Show |
6 | a0001c0002t0003g0125 a0001c0002t0003g0128 a0001c0002t0003g0130 others(3): Show |
6 | HG01243.hp2 HG01346.hp2 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.2062-4681_2062-467 others(12): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114414989 | |||||||
| chr1:114415308 | A | T | 1 | a0001c0001t0042g0062 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2062-4992T>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114415308 | |||||||
| chr1:114415364 | C | T | 3 | a0002c0003t0001g0021 a0002c0003t0016g0034 a0002c0003t0016g0044 |
3 | HG02015.hp2 HG02083.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.2062-5048G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114415364 | |||||||
| chr1:114415450 | T | C | 1 | a0001c0001t0002g0194 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2062-5134A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114415450 | |||||||
| chr1:114415532 | A | T | 1 | a0001c0001t0001g0020 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2062-5216T>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114415532 | |||||||
| chr1:114415535 | T | A | 1 | a0001c0001t0001g0020 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2062-5219A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114415535 | |||||||
| chr1:114415553 | C | CT | 11 | a0001c0002t0034g0117 a0001c0006t0010g0119 a0001c0006t0010g0120 others(8): Show |
11 | HG02055.hp2 HG02132.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.2062-5238dupA | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114415553 | |||||||
| chr1:114415580 | T | G | 39 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(36): Show |
39 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.2062-5264A>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114415580 | |||||||
| chr1:114415946 | T | TA | 68 | a0001c0001t0002g0153 a0001c0001t0004g0024 a0001c0001t0012g0197 others(65): Show |
68 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.2061+5489dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114415946 | |||||||
| chr1:114415946 | T | TAA | 6 | a0001c0002t0021g0092 a0001c0002t0034g0117 a0003c0004t0014g0005 others(3): Show |
6 | HG02055.hp2 HG02451.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.2061+5488_2061+548 others(6): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114415946 | |||||||
| chr1:114415946 | T | TAAA | 6 | a0001c0002t0004g0111 a0001c0002t0004g0114 a0001c0002t0004g0115 others(3): Show |
6 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.2061+5487_2061+548 others(7): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114415946 | |||||||
| chr1:114416041 | T | C | 2 | a0001c0006t0010g0121 a0001c0006t0010g0122 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2061+5395A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114416041 | |||||||
| chr1:114416157 | T | C | 80 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(77): Show |
80 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.2061+5279A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114416157 | |||||||
| chr1:114416205 | G | A | 1 | a0002c0003t0001g0001 | 2 | HG01433.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.2061+5231C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114416205 | |||||||
| chr1:114416324 | A | C | 56 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(53): Show |
56 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(53): Show |
intron_variant | MODIFIER | c.2061+5112T>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114416324 | |||||||
| chr1:114416459 | T | C | 1 | a0002c0003t0001g0041 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2061+4977A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114416459 | |||||||
| chr1:114416515 | A | G | 1 | a0002c0003t0001g0199 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.2061+4921T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114416515 | |||||||
| chr1:114416558 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2061+4878G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114416558 | |||||||
| chr1:114416780 | A | G | 2 | a0003c0004t0013g0007 a0003c0004t0050g0206 |
2 | HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2061+4656T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114416780 | |||||||
| chr1:114416918 | G | A | 21 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(18): Show |
21 | HG00323.hp1 HG00738.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.2061+4518C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114416918 | |||||||
| chr1:114417149 | T | C | 1 | a0001c0001t0002g0175 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.2061+4287A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114417149 | |||||||
| chr1:114417266 | A | C | 56 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(53): Show |
56 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(53): Show |
intron_variant | MODIFIER | c.2061+4170T>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114417266 | |||||||
| chr1:114417635 | T | C | 2 | a0001c0002t0005g0105 a0001c0002t0005g0108 |
2 | HG02615.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2061+3801A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114417635 | |||||||
| chr1:114417648 | A | C | 2 | a0001c0001t0001g0026 a0001c0001t0001g0027 |
2 | HG02809.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2061+3788T>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114417648 | |||||||
| chr1:114417819 | C | G | 6 | a0002c0003t0008g0032 a0002c0003t0008g0045 a0002c0003t0008g0046 others(3): Show |
6 | HG00642.hp1 HG00738.hp2 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.2061+3617G>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114417819 | |||||||
| chr1:114418041 | G | A | 15 | a0001c0002t0006g0086 a0001c0002t0006g0087 a0001c0002t0006g0088 others(12): Show |
15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.2061+3395C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114418041 | |||||||
| chr1:114418092 | C | T | 11 | a0001c0002t0034g0117 a0001c0006t0010g0119 a0001c0006t0010g0120 others(8): Show |
11 | HG02055.hp2 HG02132.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.2061+3344G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114418092 | |||||||
| chr1:114418184 | G | C | 3 | a0001c0002t0018g0145 a0001c0002t0018g0146 a0001c0002t0038g0118 |
3 | HG00741.hp2 HG02647.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.2061+3252C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114418184 | |||||||
| chr1:114418244 | G | T | 12 | a0001c0002t0005g0098 a0001c0002t0005g0099 a0001c0002t0005g0102 others(9): Show |
12 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.2061+3192C>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114418244 | |||||||
| chr1:114418728 | T | C | 9 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0060 others(6): Show |
9 | HG00741.hp1 HG01074.hp1 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.2061+2708A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114418728 | |||||||
| chr1:114418931 | C | G | 11 | a0001c0002t0034g0117 a0001c0006t0010g0119 a0001c0006t0010g0120 others(8): Show |
11 | HG02055.hp2 HG02132.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.2061+2505G>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114418931 | |||||||
| chr1:114418946 | G | A | 1 | a0001c0002t0005g0109 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.2061+2490C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114418946 | |||||||
| chr1:114418971 | G | A | 2 | a0001c0001t0001g0025 a0001c0001t0004g0024 |
2 | HG02109.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.2061+2465C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114418971 | |||||||
| chr1:114419157 | C | T | 2 | a0001c0001t0001g0083 a0001c0001t0004g0050 |
2 | HG02055.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.2061+2279G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114419157 | |||||||
| chr1:114419200 | C | CA | 14 | a0001c0001t0001g0025 a0001c0001t0001g0060 a0001c0001t0001g0080 others(11): Show |
14 | HG01106.hp2 HG01891.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.2061+2235dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114419200 | |||||||
| chr1:114419200 | CA | C | 31 | a0001c0001t0002g0148 a0001c0002t0003g0137 a0001c0002t0005g0098 others(28): Show |
31 | HG00735.hp1 HG00741.hp2 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.2061+2235delT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114419200 | |||||||
| chr1:114419218 | A | AG | 4 | a0001c0002t0034g0117 a0003c0004t0014g0005 a0003c0004t0014g0012 others(1): Show |
4 | HG02055.hp2 HG02451.hp2 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.2061+2217_2061+221 others(5): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114419218 | |||||||
| chr1:114419218 | A | G | 5 | a0001c0002t0006g0093 a0001c0002t0006g0094 a0001c0002t0006g0095 others(2): Show |
5 | HG02280.hp2 HG02723.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.2061+2218T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114419218 | |||||||
| chr1:114419277 | CAA | C | 3 | a0003c0004t0013g0010 a0003c0004t0032g0011 a0003c0008t0013g0015 |
3 | HG02145.hp1 HG02258.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2061+2157_2061+215 others(6): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114419277 | |||||||
| chr1:114419318 | C | T | 1 | a0001c0009t0040g0123 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2061+2118G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114419318 | |||||||
| chr1:114419330 | C | T | 1 | a0001c0002t0006g0087 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2061+2106G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114419330 | |||||||
| chr1:114419392 | G | A | 8 | a0003c0004t0001g0008 a0003c0004t0004g0006 a0003c0004t0004g0009 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.2061+2044C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114419392 | |||||||
| chr1:114419634 | TCTC | T | 12 | a0001c0002t0005g0098 a0001c0002t0005g0099 a0001c0002t0005g0102 others(9): Show |
12 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.2061+1799_2061+180 others(7): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114419634 | |||||||
| chr1:114419750 | A | T | 2 | a0001c0002t0003g0141 a0001c0002t0003g0142 |
2 | HG02602.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.2061+1686T>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114419750 | |||||||
| chr1:114419795 | G | A | 2 | a0003c0004t0001g0008 a0003c0004t0004g0009 |
2 | HG02965.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2061+1641C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114419795 | |||||||
| chr1:114419933 | T | C | 15 | a0001c0001t0002g0148 a0001c0001t0002g0155 a0001c0001t0002g0156 others(12): Show |
15 | HG01175.hp2 HG01884.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.2061+1503A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114419933 | |||||||
| chr1:114420295 | A | G | 1 | a0001c0002t0004g0111 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2061+1141T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114420295 | |||||||
| chr1:114420314 | C | A | 12 | a0001c0002t0005g0098 a0001c0002t0005g0099 a0001c0002t0005g0102 others(9): Show |
12 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.2061+1122G>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114420314 | |||||||
| chr1:114420343 | C | A | 2 | a0001c0002t0018g0145 a0001c0002t0018g0146 |
2 | HG00741.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.2061+1093G>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114420343 | |||||||
| chr1:114420454 | G | A | 3 | a0001c0001t0001g0022 a0001c0001t0004g0023 a0001c0001t0024g0003 |
3 | HG02615.hp2 HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2061+982C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114420454 | |||||||
| chr1:114420562 | T | C | 1 | a0001c0001t0002g0155 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2061+874A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114420562 | |||||||
| chr1:114420870 | A | T | 1 | a0001c0002t0005g0103 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2061+566T>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114420870 | |||||||
| chr1:114420952 | G | A | 5 | a0001c0002t0004g0114 a0001c0002t0004g0115 a0001c0002t0020g0112 others(2): Show |
5 | HG01884.hp2 HG02622.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.2061+484C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114420952 | |||||||
| chr1:114421351 | TA | T | 37 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(34): Show |
37 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.2061+84delT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114421351 | |||||||
| chr1:114421941 | G | A | 1 | a0001c0001t0017g0037 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1861-305C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 10/19 | chr1 | 114421941 | |||||||
| chr1:114422183 | A | G | 1 | a0001c0002t0003g0142 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1861-547T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 10/19 | chr1 | 114422183 | |||||||
| chr1:114422421 | G | A | 1 | a0001c0001t0012g0174 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1861-785C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 10/19 | chr1 | 114422421 | |||||||
| chr1:114422495 | G | GA | 68 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(65): Show |
68 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.1861-860dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 10/19 | chr1 | 114422495 | |||||||
| chr1:114422665 | T | C | 1 | a0001c0002t0009g0205 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1861-1029A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 10/19 | chr1 | 114422665 | |||||||
| chr1:114423051 | T | A | 4 | a0001c0002t0009g0202 a0001c0002t0009g0203 a0001c0002t0009g0204 others(1): Show |
4 | HG01891.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1861-1415A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 10/19 | chr1 | 114423051 | |||||||
| chr1:114423190 | T | C | 80 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(77): Show |
80 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.1860+1401A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 10/19 | chr1 | 114423190 | |||||||
| chr1:114423344 | T | C | 13 | a0001c0002t0009g0202 a0001c0002t0009g0203 a0001c0002t0009g0204 others(10): Show |
13 | HG01891.hp2 HG02145.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1860+1247A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 10/19 | chr1 | 114423344 | |||||||
| chr1:114423431 | G | A | 1 | a0003c0004t0032g0011 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1860+1160C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 10/19 | chr1 | 114423431 | |||||||
| chr1:114423478 | C | T | 80 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(77): Show |
80 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.1860+1113G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 10/19 | chr1 | 114423478 | |||||||
| chr1:114423651 | C | T | 1 | a0001c0006t0039g0124 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1860+940G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 10/19 | chr1 | 114423651 | |||||||
| chr1:114423731 | G | C | 3 | a0003c0004t0013g0010 a0003c0004t0032g0011 a0003c0008t0013g0015 |
3 | HG02145.hp1 HG02258.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1860+860C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 10/19 | chr1 | 114423731 | |||||||
| chr1:114423791 | T | G | 1 | a0001c0002t0034g0117 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1860+800A>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 10/19 | chr1 | 114423791 | |||||||
| chr1:114423847 | C | T | 4 | a0001c0002t0034g0117 a0003c0004t0014g0005 a0003c0004t0014g0012 others(1): Show |
4 | HG02055.hp2 HG02451.hp2 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.1860+744G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 10/19 | chr1 | 114423847 | |||||||
| chr1:114423936 | T | A | 1 | a0001c0001t0001g0060 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1860+655A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 10/19 | chr1 | 114423936 | |||||||
| chr1:114424011 | T | C | 1 | a0001c0002t0018g0146 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1860+580A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 10/19 | chr1 | 114424011 | |||||||
| chr1:114424104 | G | A | 1 | a0001c0001t0001g0200 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1860+487C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 10/19 | chr1 | 114424104 | |||||||
| chr1:114424147 | T | TA | 13 | a0001c0002t0005g0098 a0001c0002t0005g0099 a0001c0002t0005g0102 others(10): Show |
13 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.1860+443dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 10/19 | chr1 | 114424147 | |||||||
| chr1:114424154 | A | T | 1 | a0003c0008t0013g0015 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1860+437T>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 10/19 | chr1 | 114424154 | |||||||
| chr1:114424157 | T | A | 1 | a0001c0001t0042g0062 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1860+434A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 10/19 | chr1 | 114424157 | |||||||
| chr1:114424172 | A | G | 1 | a0002c0003t0001g0199 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1860+419T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 10/19 | chr1 | 114424172 | |||||||
| chr1:114424318 | C | T | 1 | a0001c0002t0005g0098 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1860+273G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 10/19 | chr1 | 114424318 | |||||||
| chr1:114424491 | C | T | 1 | a0001c0002t0034g0117 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1860+100G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 10/19 | chr1 | 114424491 | |||||||
| chr1:114424950 | GTCTC | G | 12 | a0001c0002t0005g0098 a0001c0002t0005g0099 a0001c0002t0005g0102 others(9): Show |
12 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.1696-199_1696-196d others(6): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 9/19 | chr1 | 114424950 | |||||||
| chr1:114424969 | A | T | 80 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(77): Show |
80 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.1696-214T>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 9/19 | chr1 | 114424969 | |||||||
| chr1:114425022 | C | T | 1 | a0001c0002t0038g0118 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1696-267G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 9/19 | chr1 | 114425022 | |||||||
| chr1:114425104 | C | T | 1 | a0001c0001t0012g0076 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1695+345G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 9/19 | chr1 | 114425104 | |||||||
| chr1:114425173 | T | G | 6 | a0001c0002t0004g0111 a0001c0002t0004g0114 a0001c0002t0004g0115 others(3): Show |
6 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1695+276A>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 9/19 | chr1 | 114425173 | |||||||
| chr1:114425780 | T | C | 2 | a0001c0002t0005g0105 a0001c0002t0005g0108 |
2 | HG02615.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1421-57A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 8/19 | chr1 | 114425780 | |||||||
| chr1:114425839 | C | T | 12 | a0001c0002t0005g0098 a0001c0002t0005g0099 a0001c0002t0005g0102 others(9): Show |
12 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.1421-116G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 8/19 | chr1 | 114425839 | |||||||
| chr1:114426018 | C | A | 3 | a0001c0002t0005g0106 a0001c0002t0005g0107 a0001c0002t0019g0110 |
3 | HG01192.hp1 HG01261.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1421-295G>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 8/19 | chr1 | 114426018 | |||||||
| chr1:114426142 | C | G | 5 | a0001c0002t0034g0117 a0003c0004t0014g0005 a0003c0004t0014g0012 others(2): Show |
5 | HG02055.hp2 HG02451.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1421-419G>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 8/19 | chr1 | 114426142 | |||||||
| chr1:114426351 | G | A | 12 | a0001c0002t0005g0098 a0001c0002t0005g0099 a0001c0002t0005g0102 others(9): Show |
12 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.1421-628C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 8/19 | chr1 | 114426351 | |||||||
| chr1:114426507 | C | CTT | 6 | a0001c0002t0004g0111 a0001c0002t0004g0114 a0001c0002t0004g0115 others(3): Show |
6 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1420+668_1420+669d others(4): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 8/19 | chr1 | 114426507 | |||||||
| chr1:114426507 | CT | C | 11 | a0001c0001t0001g0052 a0001c0001t0002g0149 a0001c0001t0002g0190 others(8): Show |
11 | HG00323.hp2 HG01169.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1420+669delA | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 8/19 | chr1 | 114426507 | |||||||
| chr1:114426522 | T | A | 2 | a0001c0001t0015g0051 a0002c0003t0004g0031 |
2 | HG00099.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.1420+655A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 8/19 | chr1 | 114426522 | |||||||
| chr1:114426522 | TA | T | 24 | a0001c0002t0003g0128 a0001c0002t0003g0131 a0001c0002t0003g0132 others(21): Show |
24 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.1420+654delT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 8/19 | chr1 | 114426522 | |||||||
| chr1:114426523 | A | T | 53 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0002t0003g0125 others(50): Show |
53 | HG00323.hp1 HG00738.hp1 HG00741.hp2 others(50): Show |
intron_variant | MODIFIER | c.1420+654T>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 8/19 | chr1 | 114426523 | |||||||
| chr1:114426524 | A | T | 22 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(19): Show |
22 | HG00323.hp1 HG00738.hp1 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.1420+653T>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 8/19 | chr1 | 114426524 | |||||||
| chr1:114426533 | G | A | 3 | a0003c0004t0013g0010 a0003c0004t0032g0011 a0003c0008t0013g0015 |
3 | HG02145.hp1 HG02258.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1420+644C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 8/19 | chr1 | 114426533 | |||||||
| chr1:114426581 | T | G | 1 | a0001c0002t0033g0116 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1420+596A>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 8/19 | chr1 | 114426581 | |||||||
| chr1:114426978 | G | T | 80 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(77): Show |
80 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.1420+199C>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 8/19 | chr1 | 114426978 | |||||||
| chr1:114427019 | C | T | 21 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(18): Show |
21 | HG00323.hp1 HG00738.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.1420+158G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 8/19 | chr1 | 114427019 | |||||||
| chr1:114427043 | T | C | 15 | a0001c0002t0006g0086 a0001c0002t0006g0087 a0001c0002t0006g0088 others(12): Show |
15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1420+134A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 8/19 | chr1 | 114427043 | |||||||
| chr1:114427303 | GA | G | 24 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(21): Show |
24 | HG00323.hp1 HG00738.hp1 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.1303-10delT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 7/19 | chr1 | 114427303 | |||||||
| chr1:114427395 | T | C | 1 | a0001c0001t0002g0153 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1303-101A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 7/19 | chr1 | 114427395 | |||||||
| chr1:114427468 | C | T | 12 | a0001c0002t0009g0202 a0001c0002t0009g0203 a0001c0002t0009g0204 others(9): Show |
12 | HG01891.hp2 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1303-174G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 7/19 | chr1 | 114427468 | |||||||
| chr1:114427556 | T | C | 2 | a0001c0006t0010g0121 a0001c0006t0010g0122 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1302+192A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 7/19 | chr1 | 114427556 | |||||||
| chr1:114428038 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1156-144G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 6/19 | chr1 | 114428038 | |||||||
| chr1:114428186 | C | G | 1 | a0003c0004t0004g0006 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1156-292G>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 6/19 | chr1 | 114428186 | |||||||
| chr1:114428268 | A | G | 15 | a0001c0002t0006g0086 a0001c0002t0006g0087 a0001c0002t0006g0088 others(12): Show |
15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1156-374T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 6/19 | chr1 | 114428268 | |||||||
| chr1:114428625 | A | C | 15 | a0001c0002t0006g0086 a0001c0002t0006g0087 a0001c0002t0006g0088 others(12): Show |
15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1156-731T>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 6/19 | chr1 | 114428625 | |||||||
| chr1:114428862 | C | CT | 7 | a0001c0001t0012g0076 a0001c0006t0010g0119 a0001c0006t0010g0120 others(4): Show |
7 | HG02132.hp2 HG02698.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1156-969dupA | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 6/19 | chr1 | 114428862 | |||||||
| chr1:114428890 | T | C | 1 | a0001c0001t0026g0196 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1156-996A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 6/19 | chr1 | 114428890 | |||||||
| chr1:114428893 | C | G | 2 | a0001c0001t0002g0195 a0001c0001t0026g0196 |
2 | HG01175.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.1156-999G>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 6/19 | chr1 | 114428893 | |||||||
| chr1:114429130 | C | T | 1 | a0001c0001t0001g0079 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1156-1236G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 6/19 | chr1 | 114429130 | |||||||
| chr1:114429264 | C | T | 80 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(77): Show |
80 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.1156-1370G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 6/19 | chr1 | 114429264 | |||||||
| chr1:114429344 | C | T | 3 | a0001c0001t0002g0168 a0001c0001t0002g0171 a0001c0001t0002g0183 |
3 | HG01496.hp2 HG01928.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.1156-1450G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 6/19 | chr1 | 114429344 | |||||||
| chr1:114429360 | G | GT | 7 | a0002c0003t0008g0049 a0003c0004t0001g0008 a0003c0004t0004g0009 others(4): Show |
7 | HG00642.hp1 HG02145.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1155+1437dupA | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 6/19 | chr1 | 114429360 | |||||||
| chr1:114429630 | G | GA | 10 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0012g0076 others(7): Show |
10 | HG01081.hp1 HG01884.hp2 HG01952.hp1 others(7): Show |
intron_variant | MODIFIER | c.1155+1167dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 6/19 | chr1 | 114429630 | |||||||
| chr1:114429949 | T | C | 1 | a0001c0002t0038g0118 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1155+849A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 6/19 | chr1 | 114429949 | |||||||
| chr1:114429953 | C | T | 2 | a0002c0003t0016g0034 a0002c0003t0016g0044 |
2 | HG02083.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.1155+845G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 6/19 | chr1 | 114429953 | |||||||
| chr1:114429988 | T | C | 1 | a0001c0002t0003g0133 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1155+810A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 6/19 | chr1 | 114429988 | |||||||
| chr1:114430211 | C | T | 80 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(77): Show |
80 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.1155+587G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 6/19 | chr1 | 114430211 | |||||||
| chr1:114430214 | A | ACATCAC | 11 | a0001c0002t0034g0117 a0001c0006t0010g0119 a0001c0006t0010g0120 others(8): Show |
11 | HG02055.hp2 HG02132.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1155+578_1155+583d others(8): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 6/19 | chr1 | 114430214 | |||||||
| chr1:114430251 | G | T | 80 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(77): Show |
80 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.1155+547C>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 6/19 | chr1 | 114430251 | |||||||
| chr1:114430354 | C | T | 8 | a0002c0003t0001g0043 a0002c0003t0001g0082 a0002c0003t0008g0032 others(5): Show |
8 | HG00642.hp1 HG00738.hp2 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.1155+444G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 6/19 | chr1 | 114430354 | |||||||
| chr1:114430368 | C | T | 9 | a0001c0001t0002g0148 a0001c0001t0002g0155 a0001c0001t0002g0156 others(6): Show |
9 | HG01175.hp2 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1155+430G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 6/19 | chr1 | 114430368 | |||||||
| chr1:114430402 | C | T | 1 | a0003c0004t0014g0012 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1155+396G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 6/19 | chr1 | 114430402 | |||||||
| chr1:114430588 | G | A | 1 | a0001c0002t0021g0092 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1155+210C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 6/19 | chr1 | 114430588 | |||||||
| chr1:114430654 | C | A | 3 | a0003c0004t0013g0010 a0003c0004t0032g0011 a0003c0008t0013g0015 |
3 | HG02145.hp1 HG02258.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1155+144G>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 6/19 | chr1 | 114430654 | |||||||
| chr1:114430738 | T | A | 1 | a0001c0001t0044g0016 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1155+60A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 6/19 | chr1 | 114430738 | |||||||
| chr1:114431068 | T | C | 45 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(42): Show |
45 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.1041-156A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 5/19 | chr1 | 114431068 | |||||||
| chr1:114431739 | A | G | 13 | a0001c0002t0009g0202 a0001c0002t0009g0203 a0001c0002t0009g0204 others(10): Show |
13 | HG01891.hp2 HG02145.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1041-827T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 5/19 | chr1 | 114431739 | |||||||
| chr1:114431802 | T | C | 1 | a0001c0002t0003g0137 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1041-890A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 5/19 | chr1 | 114431802 | |||||||
| chr1:114432034 | T | G | 3 | a0001c0002t0018g0145 a0001c0002t0018g0146 a0001c0002t0038g0118 |
3 | HG00741.hp2 HG02647.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1041-1122A>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 5/19 | chr1 | 114432034 | |||||||
| chr1:114432099 | A | G | 1 | a0001c0001t0002g0163 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1041-1187T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 5/19 | chr1 | 114432099 | |||||||
| chr1:114432194 | T | C | 2 | a0001c0002t0004g0114 a0001c0002t0004g0115 |
2 | HG01884.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1041-1282A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 5/19 | chr1 | 114432194 | |||||||
| chr1:114432679 | G | A | 4 | a0001c0006t0010g0119 a0001c0006t0010g0120 a0001c0006t0010g0121 others(1): Show |
4 | HG02895.hp2 HG02897.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1040+938C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 5/19 | chr1 | 114432679 | |||||||
| chr1:114432803 | C | T | 15 | a0001c0002t0006g0086 a0001c0002t0006g0087 a0001c0002t0006g0088 others(12): Show |
15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1040+814G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 5/19 | chr1 | 114432803 | |||||||
| chr1:114432996 | A | G | 6 | a0001c0002t0004g0111 a0001c0002t0004g0114 a0001c0002t0004g0115 others(3): Show |
6 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1040+621T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 5/19 | chr1 | 114432996 | |||||||
| chr1:114433217 | T | C | 1 | a0001c0009t0040g0123 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1040+400A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 5/19 | chr1 | 114433217 | |||||||
| chr1:114433602 | A | C | 9 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0060 others(6): Show |
9 | HG00741.hp1 HG01074.hp1 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.1040+15T>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 5/19 | chr1 | 114433602 | |||||||
| chr1:114433811 | G | A | 3 | a0001c0001t0001g0060 a0001c0001t0001g0084 a0001c0001t0004g0059 |
3 | HG01081.hp2 HG03710.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.924-78C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114433811 | |||||||
| chr1:114434054 | C | T | 15 | a0001c0002t0006g0086 a0001c0002t0006g0087 a0001c0002t0006g0088 others(12): Show |
15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.924-321G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114434054 | |||||||
| chr1:114434097 | C | T | 1 | a0001c0001t0002g0159 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.924-364G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114434097 | |||||||
| chr1:114434514 | T | G | 1 | a0001c0001t0015g0066 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.924-781A>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114434514 | |||||||
| chr1:114434601 | T | C | 1 | a0002c0003t0001g0021 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.924-868A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114434601 | |||||||
| chr1:114434781 | C | G | 80 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(77): Show |
80 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.924-1048G>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114434781 | |||||||
| chr1:114435237 | C | G | 80 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(77): Show |
80 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.924-1504G>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114435237 | |||||||
| chr1:114435322 | G | A | 2 | a0001c0002t0006g0086 a0001c0002t0035g0085 |
2 | HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.924-1589C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114435322 | |||||||
| chr1:114435396 | C | T | 2 | a0001c0005t0007g0147 a0001c0005t0007g0152 |
2 | HG01884.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.924-1663G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114435396 | |||||||
| chr1:114435401 | C | A | 21 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(18): Show |
21 | HG00323.hp1 HG00738.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.924-1668G>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114435401 | |||||||
| chr1:114435695 | T | C | 4 | a0001c0001t0002g0190 a0001c0001t0002g0191 a0001c0001t0002g0192 others(1): Show |
4 | HG00642.hp2 HG01074.hp2 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.924-1962A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114435695 | |||||||
| chr1:114435771 | A | G | 80 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(77): Show |
80 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.924-2038T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114435771 | |||||||
| chr1:114435877 | C | CT | 41 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0052 others(38): Show |
41 | HG00438.hp1 HG00642.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.924-2145dupA | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114435877 | |||||||
| chr1:114435877 | C | CTT | 19 | a0001c0001t0026g0196 a0001c0002t0003g0125 a0001c0002t0003g0126 others(16): Show |
19 | HG00323.hp1 HG00738.hp1 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.924-2146_924-2145d others(4): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114435877 | |||||||
| chr1:114435877 | C | CTTT | 27 | a0001c0002t0003g0128 a0001c0002t0003g0131 a0001c0002t0003g0132 others(24): Show |
27 | HG01106.hp1 HG01169.hp2 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.924-2147_924-2145d others(5): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114435877 | |||||||
| chr1:114435877 | C | CTTTT | 16 | a0001c0002t0003g0133 a0001c0002t0005g0098 a0001c0002t0005g0104 others(13): Show |
16 | HG00099.hp1 HG00735.hp1 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.924-2148_924-2145d others(6): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114435877 | |||||||
| chr1:114435877 | C | T | 1 | a0001c0001t0002g0039 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.924-2144G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114435877 | |||||||
| chr1:114435877 | CTTTTTTT others(5): Show |
C | 4 | a0001c0002t0020g0112 a0001c0002t0020g0113 a0001c0002t0025g0004 others(1): Show |
4 | HG02622.hp1 HG02886.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.924-2156_924-2145d others(14): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114435877 | |||||||
| chr1:114435985 | G | A | 24 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(21): Show |
24 | HG00323.hp1 HG00738.hp1 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.924-2252C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114435985 | |||||||
| chr1:114436146 | T | C | 1 | a0001c0001t0002g0039 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.924-2413A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114436146 | |||||||
| chr1:114436199 | G | A | 1 | a0001c0002t0003g0141 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.924-2466C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114436199 | |||||||
| chr1:114436261 | G | C | 1 | a0001c0001t0001g0200 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.924-2528C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114436261 | |||||||
| chr1:114436400 | C | CA | 16 | a0001c0001t0001g0077 a0001c0001t0002g0149 a0001c0001t0028g0063 others(13): Show |
16 | HG00323.hp1 HG00738.hp1 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.924-2668dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114436400 | |||||||
| chr1:114436400 | CA | C | 43 | a0001c0001t0002g0153 a0001c0001t0002g0184 a0001c0002t0005g0098 others(40): Show |
43 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(40): Show |
intron_variant | MODIFIER | c.924-2668delT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114436400 | |||||||
| chr1:114436400 | CAA | C | 11 | a0001c0002t0004g0111 a0001c0002t0004g0114 a0001c0002t0004g0115 others(8): Show |
11 | HG01884.hp2 HG02109.hp1 HG02132.hp2 others(8): Show |
intron_variant | MODIFIER | c.924-2669_924-2668d others(4): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114436400 | |||||||
| chr1:114436401 | A | G | 2 | a0001c0001t0002g0195 a0001c0001t0026g0196 |
2 | HG01175.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.924-2668T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114436401 | |||||||
| chr1:114436426 | A | T | 1 | a0003c0004t0004g0006 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.924-2693T>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114436426 | |||||||
| chr1:114436467 | T | C | 68 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(65): Show |
68 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.924-2734A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114436467 | |||||||
| chr1:114436655 | G | T | 1 | a0001c0002t0003g0137 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.924-2922C>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114436655 | |||||||
| chr1:114436703 | G | T | 2 | a0001c0002t0006g0086 a0001c0002t0035g0085 |
2 | HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.924-2970C>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114436703 | |||||||
| chr1:114436813 | T | C | 3 | a0001c0002t0005g0098 a0001c0002t0005g0099 a0001c0002t0005g0102 |
3 | HG01433.hp2 HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.924-3080A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114436813 | |||||||
| chr1:114436820 | G | A | 1 | a0001c0001t0041g0169 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.924-3087C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114436820 | |||||||
| chr1:114436931 | T | C | 138 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0083 others(135): Show |
138 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.924-3198A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114436931 | |||||||
| chr1:114436981 | T | C | 6 | a0001c0006t0010g0119 a0001c0006t0010g0120 a0001c0006t0010g0121 others(3): Show |
6 | HG02132.hp2 HG02698.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.924-3248A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114436981 | |||||||
| chr1:114436982 | T | G | 3 | a0001c0002t0018g0145 a0001c0002t0018g0146 a0001c0002t0038g0118 |
3 | HG00741.hp2 HG02647.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.924-3249A>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114436982 | |||||||
| chr1:114437025 | G | C | 1 | a0001c0002t0034g0117 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.924-3292C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114437025 | |||||||
| chr1:114437141 | A | C | 6 | a0001c0002t0004g0111 a0001c0002t0004g0114 a0001c0002t0004g0115 others(3): Show |
6 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.924-3408T>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114437141 | |||||||
| chr1:114437427 | C | T | 1 | a0002c0003t0008g0045 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.924-3694G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114437427 | |||||||
| chr1:114437483 | C | A | 2 | a0001c0002t0009g0202 a0001c0002t0009g0203 |
2 | HG01891.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.924-3750G>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114437483 | |||||||
| chr1:114437492 | C | T | 12 | a0001c0002t0005g0098 a0001c0002t0005g0099 a0001c0002t0005g0102 others(9): Show |
12 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.924-3759G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114437492 | |||||||
| chr1:114437838 | T | C | 1 | a0001c0006t0039g0124 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.924-4105A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114437838 | |||||||
| chr1:114438239 | A | G | 1 | a0001c0001t0002g0175 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.924-4506T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114438239 | |||||||
| chr1:114438460 | G | C | 1 | a0001c0005t0007g0151 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.924-4727C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114438460 | |||||||
| chr1:114438494 | T | C | 6 | a0003c0004t0001g0008 a0003c0004t0004g0009 a0003c0004t0013g0010 others(3): Show |
6 | HG02145.hp1 HG02258.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.924-4761A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114438494 | |||||||
| chr1:114438681 | ACTT | A | 12 | a0001c0002t0005g0098 a0001c0002t0005g0099 a0001c0002t0005g0102 others(9): Show |
12 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.924-4951_924-4949d others(5): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114438681 | |||||||
| chr1:114438896 | T | C | 1 | a0001c0002t0003g0132 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.924-5163A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114438896 | |||||||
| chr1:114439008 | A | G | 80 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(77): Show |
80 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.924-5275T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114439008 | |||||||
| chr1:114439279 | CTGACCAA others(15): Show |
C | 4 | a0001c0002t0034g0117 a0003c0004t0014g0005 a0003c0004t0014g0012 others(1): Show |
4 | HG02055.hp2 HG02451.hp2 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.924-5568_924-5547d others(24): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114439279 | |||||||
| chr1:114439468 | C | CA | 11 | a0001c0001t0001g0061 a0001c0001t0001g0073 a0001c0001t0001g0075 others(8): Show |
12 | HG00558.hp1 HG01081.hp1 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.924-5736dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114439468 | |||||||
| chr1:114439468 | CA | C | 67 | a0001c0001t0001g0027 a0001c0001t0001g0083 a0001c0001t0001g0166 others(64): Show |
67 | HG00099.hp1 HG00558.hp2 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.924-5736delT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114439468 | |||||||
| chr1:114439468 | CAAA | C | 27 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0128 others(24): Show |
27 | HG00323.hp1 HG00741.hp2 HG01099.hp1 others(24): Show |
intron_variant | MODIFIER | c.924-5738_924-5736d others(5): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114439468 | |||||||
| chr1:114439468 | CAAAA | C | 12 | a0001c0002t0009g0202 a0001c0002t0009g0203 a0001c0002t0009g0204 others(9): Show |
12 | HG01891.hp2 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.924-5739_924-5736d others(6): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114439468 | |||||||
| chr1:114439468 | CAAAAAA | C | 9 | a0001c0002t0005g0098 a0001c0002t0005g0099 a0001c0002t0005g0102 others(6): Show |
9 | HG01192.hp1 HG01261.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.924-5741_924-5736d others(8): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114439468 | |||||||
| chr1:114439512 | TCCTA | T | 10 | a0001c0002t0034g0117 a0001c0006t0010g0119 a0001c0006t0010g0120 others(7): Show |
10 | HG02055.hp2 HG02132.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.924-5783_924-5780d others(6): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114439512 | |||||||
| chr1:114439517 | C | A | 15 | a0001c0002t0006g0086 a0001c0002t0006g0087 a0001c0002t0006g0088 others(12): Show |
15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.924-5784G>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114439517 | |||||||
| chr1:114439537 | C | CA | 42 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(39): Show |
42 | HG00323.hp1 HG00738.hp1 HG01099.hp1 others(39): Show |
intron_variant | MODIFIER | c.924-5805dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114439537 | |||||||
| chr1:114439586 | T | C | 1 | a0001c0002t0025g0004 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.924-5853A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114439586 | |||||||
| chr1:114439642 | G | A | 15 | a0001c0002t0006g0086 a0001c0002t0006g0087 a0001c0002t0006g0088 others(12): Show |
15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.924-5909C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114439642 | |||||||
| chr1:114439765 | C | T | 5 | a0001c0002t0003g0136 a0001c0002t0003g0137 a0001c0002t0003g0138 others(2): Show |
5 | HG00323.hp1 HG01167.hp1 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.924-6032G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114439765 | |||||||
| chr1:114439854 | T | C | 1 | a0004c0007t0001g0014 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.924-6121A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114439854 | |||||||
| chr1:114440722 | G | GA | 3 | a0001c0002t0018g0145 a0001c0002t0018g0146 a0001c0002t0038g0118 |
3 | HG00741.hp2 HG02647.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.924-6990dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114440722 | |||||||
| chr1:114440727 | G | A | 3 | a0003c0004t0004g0006 a0003c0004t0013g0007 a0003c0004t0050g0206 |
3 | HG02280.hp1 HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.924-6994C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114440727 | |||||||
| chr1:114440766 | G | A | 1 | a0001c0002t0006g0095 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.924-7033C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114440766 | |||||||
| chr1:114441087 | C | T | 8 | a0003c0004t0001g0008 a0003c0004t0004g0006 a0003c0004t0004g0009 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.924-7354G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114441087 | |||||||
| chr1:114441249 | C | T | 80 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(77): Show |
80 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.924-7516G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114441249 | |||||||
| chr1:114441456 | T | A | 1 | a0001c0001t0002g0184 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.924-7723A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114441456 | |||||||
| chr1:114441546 | C | T | 1 | a0001c0001t0015g0051 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.924-7813G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114441546 | |||||||
| chr1:114441547 | G | A | 12 | a0001c0002t0009g0202 a0001c0002t0009g0203 a0001c0002t0009g0204 others(9): Show |
12 | HG01891.hp2 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.924-7814C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114441547 | |||||||
| chr1:114441738 | G | A | 3 | a0003c0004t0004g0006 a0003c0004t0013g0007 a0003c0004t0050g0206 |
3 | HG02280.hp1 HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.924-8005C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114441738 | |||||||
| chr1:114441757 | A | G | 1 | a0001c0001t0001g0077 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.924-8024T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114441757 | |||||||
| chr1:114441762 | C | T | 2 | a0001c0001t0022g0056 a0001c0001t0022g0057 |
2 | HG03704.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.924-8029G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114441762 | |||||||
| chr1:114442029 | C | T | 12 | a0001c0002t0005g0098 a0001c0002t0005g0099 a0001c0002t0005g0102 others(9): Show |
12 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.924-8296G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114442029 | |||||||
| chr1:114442045 | G | A | 80 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(77): Show |
80 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.924-8312C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114442045 | |||||||
| chr1:114442200 | G | A | 1 | a0001c0001t0001g0052 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.924-8467C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114442200 | |||||||
| chr1:114442315 | G | A | 1 | a0003c0008t0013g0015 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.924-8582C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114442315 | |||||||
| chr1:114442327 | G | A | 1 | a0002c0003t0004g0031 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.924-8594C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114442327 | |||||||
| chr1:114442687 | C | CA | 18 | a0001c0001t0001g0052 a0001c0001t0002g0182 a0001c0001t0002g0184 others(15): Show |
18 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.924-8955dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114442687 | |||||||
| chr1:114442687 | CA | C | 65 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(62): Show |
65 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.924-8955delT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114442687 | |||||||
| chr1:114442694 | AAAAAAAA others(4): Show |
A | 3 | a0003c0004t0004g0006 a0003c0004t0013g0007 a0003c0004t0050g0206 |
3 | HG02280.hp1 HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.924-8972_924-8962d others(13): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114442694 | |||||||
| chr1:114442705 | G | A | 1 | a0001c0001t0028g0063 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.924-8972C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114442705 | |||||||
| chr1:114442742 | C | T | 1 | a0001c0009t0040g0123 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.924-9009G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114442742 | |||||||
| chr1:114442836 | T | C | 3 | a0003c0004t0004g0006 a0003c0004t0013g0007 a0003c0004t0050g0206 |
3 | HG02280.hp1 HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.924-9103A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114442836 | |||||||
| chr1:114442871 | T | A | 1 | a0001c0002t0038g0118 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.924-9138A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114442871 | |||||||
| chr1:114442916 | A | G | 1 | a0002c0003t0001g0021 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.924-9183T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114442916 | |||||||
| chr1:114442918 | A | AT | 10 | a0001c0002t0005g0098 a0001c0002t0005g0099 a0001c0002t0005g0102 others(7): Show |
10 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.924-9186dupA | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114442918 | |||||||
| chr1:114442928 | A | G | 1 | a0003c0004t0014g0005 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.924-9195T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114442928 | |||||||
| chr1:114443039 | C | T | 1 | a0001c0002t0038g0118 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.924-9306G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114443039 | |||||||
| chr1:114443110 | G | A | 5 | a0001c0002t0034g0117 a0003c0004t0014g0005 a0003c0004t0014g0012 others(2): Show |
5 | HG02055.hp2 HG02451.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.924-9377C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114443110 | |||||||
| chr1:114443121 | C | T | 2 | a0001c0002t0009g0204 a0001c0002t0009g0205 |
2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.924-9388G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114443121 | |||||||
| chr1:114443197 | C | T | 3 | a0001c0001t0015g0051 a0001c0001t0015g0065 a0001c0001t0015g0066 |
3 | HG00099.hp2 HG00323.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.924-9464G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114443197 | |||||||
| chr1:114443214 | A | G | 80 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(77): Show |
80 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.924-9481T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114443214 | |||||||
| chr1:114443227 | C | CA | 5 | a0001c0002t0034g0117 a0003c0004t0014g0005 a0003c0004t0014g0012 others(2): Show |
5 | HG02055.hp2 HG02451.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.924-9495dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114443227 | |||||||
| chr1:114443245 | G | A | 1 | a0001c0001t0015g0051 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.924-9512C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114443245 | |||||||
| chr1:114443305 | A | G | 2 | a0003c0004t0001g0008 a0003c0004t0004g0009 |
2 | HG02965.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.924-9572T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114443305 | |||||||
| chr1:114443341 | G | A | 1 | a0001c0001t0002g0189 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.924-9608C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114443341 | |||||||
| chr1:114443369 | G | A | 3 | a0001c0002t0018g0145 a0001c0002t0018g0146 a0001c0002t0038g0118 |
3 | HG00741.hp2 HG02647.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.924-9636C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114443369 | |||||||
| chr1:114443385 | A | AAATG | 29 | a0001c0001t0002g0195 a0001c0001t0011g0054 a0001c0001t0011g0055 others(26): Show |
29 | HG00558.hp1 HG00741.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.924-9656_924-9653d others(6): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114443385 | |||||||
| chr1:114443385 | A | AAATGAAT others(1): Show |
26 | a0001c0002t0004g0111 a0001c0002t0004g0114 a0001c0002t0004g0115 others(23): Show |
26 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.924-9660_924-9653d others(10): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114443385 | |||||||
| chr1:114443385 | A | AAATGAAT others(5): Show |
4 | a0001c0002t0020g0112 a0001c0002t0020g0113 a0001c0002t0023g0002 others(1): Show |
4 | HG02622.hp1 HG02886.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.924-9664_924-9653d others(14): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114443385 | |||||||
| chr1:114443385 | A | AAATGAAT others(9): Show |
1 | a0003c0004t0013g0010 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.924-9668_924-9653d others(18): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114443385 | |||||||
| chr1:114443385 | A | AAATGAAT others(13): Show |
2 | a0001c0002t0009g0204 a0001c0002t0009g0205 |
2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.924-9672_924-9653d others(22): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114443385 | |||||||
| chr1:114443385 | AAATG | A | 6 | a0001c0006t0010g0119 a0001c0006t0010g0120 a0001c0006t0010g0121 others(3): Show |
6 | HG02132.hp2 HG02698.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.924-9656_924-9653d others(6): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114443385 | |||||||
| chr1:114443528 | C | T | 5 | a0003c0004t0001g0008 a0003c0004t0004g0009 a0003c0004t0013g0010 others(2): Show |
5 | HG02145.hp1 HG02258.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.924-9795G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114443528 | |||||||
| chr1:114443622 | T | C | 8 | a0003c0004t0001g0008 a0003c0004t0004g0006 a0003c0004t0004g0009 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.924-9889A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114443622 | |||||||
| chr1:114443714 | C | T | 1 | a0001c0001t0002g0170 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.924-9981G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114443714 | |||||||
| chr1:114444157 | A | G | 1 | a0001c0001t0041g0169 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.924-10424T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114444157 | |||||||
| chr1:114444222 | G | C | 1 | a0004c0007t0001g0014 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.924-10489C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114444222 | |||||||
| chr1:114444319 | T | C | 3 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0143 |
3 | HG01099.hp1 HG01952.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.924-10586A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114444319 | |||||||
| chr1:114444969 | C | T | 12 | a0001c0002t0005g0098 a0001c0002t0005g0099 a0001c0002t0005g0102 others(9): Show |
12 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.924-11236G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114444969 | |||||||
| chr1:114445096 | C | G | 80 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(77): Show |
80 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.924-11363G>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114445096 | |||||||
| chr1:114445244 | T | A | 3 | a0003c0004t0014g0005 a0003c0004t0014g0012 a0003c0004t0014g0013 |
3 | HG02055.hp2 HG02523.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.924-11511A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114445244 | |||||||
| chr1:114445303 | T | C | 1 | a0001c0002t0004g0111 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.924-11570A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114445303 | |||||||
| chr1:114445341 | G | A | 2 | a0001c0001t0031g0157 a0003c0004t0014g0013 |
2 | HG02523.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.924-11608C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114445341 | |||||||
| chr1:114445553 | T | C | 12 | a0001c0002t0005g0098 a0001c0002t0005g0099 a0001c0002t0005g0102 others(9): Show |
12 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.924-11820A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114445553 | |||||||
| chr1:114446008 | T | C | 80 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(77): Show |
80 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.924-12275A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114446008 | |||||||
| chr1:114446175 | T | G | 2 | a0003c0004t0013g0007 a0003c0004t0050g0206 |
2 | HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.924-12442A>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114446175 | |||||||
| chr1:114446221 | G | C | 10 | a0001c0002t0034g0117 a0001c0006t0010g0119 a0001c0006t0010g0120 others(7): Show |
10 | HG02055.hp2 HG02132.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.924-12488C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114446221 | |||||||
| chr1:114446360 | T | C | 1 | a0001c0001t0002g0175 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.924-12627A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114446360 | |||||||
| chr1:114446400 | A | G | 1 | a0001c0001t0001g0068 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.924-12667T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114446400 | |||||||
| chr1:114446474 | T | G | 4 | a0001c0002t0009g0202 a0001c0002t0009g0203 a0001c0002t0009g0204 others(1): Show |
4 | HG01891.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.924-12741A>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114446474 | |||||||
| chr1:114446567 | G | C | 1 | a0001c0002t0033g0116 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.924-12834C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114446567 | |||||||
| chr1:114446589 | T | G | 68 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(65): Show |
68 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.924-12856A>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114446589 | |||||||
| chr1:114446914 | G | C | 1 | a0001c0001t0002g0149 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.924-13181C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114446914 | |||||||
| chr1:114446958 | T | C | 12 | a0001c0002t0005g0098 a0001c0002t0005g0099 a0001c0002t0005g0102 others(9): Show |
12 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.924-13225A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114446958 | |||||||
| chr1:114447158 | T | G | 1 | a0001c0001t0041g0169 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.924-13425A>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114447158 | |||||||
| chr1:114447265 | T | C | 2 | a0001c0002t0009g0204 a0001c0002t0009g0205 |
2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.924-13532A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114447265 | |||||||
| chr1:114447378 | T | C | 1 | a0001c0001t0048g0081 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.924-13645A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114447378 | |||||||
| chr1:114447533 | T | C | 6 | a0001c0002t0004g0111 a0001c0002t0004g0114 a0001c0002t0004g0115 others(3): Show |
6 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.924-13800A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114447533 | |||||||
| chr1:114447634 | C | T | 80 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(77): Show |
80 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.924-13901G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114447634 | |||||||
| chr1:114447880 | T | C | 1 | a0001c0002t0034g0117 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.924-14147A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114447880 | |||||||
| chr1:114447941 | G | A | 1 | a0001c0001t0041g0169 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.924-14208C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114447941 | |||||||
| chr1:114448206 | G | C | 9 | a0003c0004t0001g0008 a0003c0004t0004g0006 a0003c0004t0004g0009 others(6): Show |
9 | HG02145.hp1 HG02258.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.924-14473C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114448206 | |||||||
| chr1:114448439 | C | T | 1 | a0001c0001t0004g0059 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.923+14665G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114448439 | |||||||
| chr1:114448453 | T | C | 4 | a0001c0006t0010g0119 a0001c0006t0010g0120 a0001c0006t0010g0121 others(1): Show |
4 | HG02895.hp2 HG02897.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.923+14651A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114448453 | |||||||
| chr1:114448807 | A | G | 15 | a0001c0002t0006g0086 a0001c0002t0006g0087 a0001c0002t0006g0088 others(12): Show |
15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.923+14297T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114448807 | |||||||
| chr1:114448822 | G | C | 1 | a0001c0002t0006g0096 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.923+14282C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114448822 | |||||||
| chr1:114448824 | G | A | 2 | a0001c0005t0007g0147 a0001c0005t0007g0152 |
2 | HG01884.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.923+14280C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114448824 | |||||||
| chr1:114448959 | T | C | 1 | a0002c0003t0001g0001 | 2 | HG01433.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.923+14145A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114448959 | |||||||
| chr1:114449163 | T | TA | 21 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(18): Show |
21 | HG00323.hp1 HG00738.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.923+13940dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114449163 | |||||||
| chr1:114449420 | G | A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0027 |
2 | HG02809.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.923+13684C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114449420 | |||||||
| chr1:114449546 | T | C | 4 | a0001c0001t0002g0148 a0001c0001t0002g0156 a0001c0001t0002g0198 others(1): Show |
4 | HG02145.hp2 HG02258.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.923+13558A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114449546 | |||||||
| chr1:114449666 | TA | T | 12 | a0001c0002t0005g0098 a0001c0002t0005g0099 a0001c0002t0005g0102 others(9): Show |
12 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.923+13437delT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114449666 | |||||||
| chr1:114449788 | A | C | 1 | a0001c0002t0003g0143 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.923+13316T>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114449788 | |||||||
| chr1:114449849 | T | G | 4 | a0001c0002t0009g0202 a0001c0002t0009g0203 a0001c0002t0009g0204 others(1): Show |
4 | HG01891.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.923+13255A>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114449849 | |||||||
| chr1:114449927 | T | A | 1 | a0001c0002t0033g0116 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.923+13177A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114449927 | |||||||
| chr1:114450138 | C | T | 80 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(77): Show |
80 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.923+12966G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114450138 | |||||||
| chr1:114450232 | C | G | 1 | a0003c0004t0013g0010 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.923+12872G>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114450232 | |||||||
| chr1:114450273 | A | T | 12 | a0001c0002t0005g0098 a0001c0002t0005g0099 a0001c0002t0005g0102 others(9): Show |
12 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.923+12831T>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114450273 | |||||||
| chr1:114450307 | CTTTCT | C | 4 | a0001c0002t0009g0202 a0001c0002t0009g0203 a0001c0002t0009g0204 others(1): Show |
4 | HG01891.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.923+12792_923+1279 others(9): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114450307 | |||||||
| chr1:114450325 | GTTGTT | G | 6 | a0001c0006t0010g0119 a0001c0006t0010g0120 a0001c0006t0010g0121 others(3): Show |
6 | HG02132.hp2 HG02698.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.923+12774_923+1277 others(9): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114450325 | |||||||
| chr1:114450340 | T | C | 35 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0052 others(32): Show |
35 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.923+12764A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114450340 | |||||||
| chr1:114450484 | A | C | 6 | a0001c0006t0010g0119 a0001c0006t0010g0120 a0001c0006t0010g0121 others(3): Show |
6 | HG02132.hp2 HG02698.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.923+12620T>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114450484 | |||||||
| chr1:114450663 | G | C | 1 | a0002c0003t0001g0082 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.923+12441C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114450663 | |||||||
| chr1:114450892 | T | C | 1 | a0001c0002t0003g0127 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.923+12212A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114450892 | |||||||
| chr1:114451374 | T | TA | 45 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0128 others(42): Show |
45 | HG00099.hp1 HG00323.hp1 HG01099.hp1 others(42): Show |
intron_variant | MODIFIER | c.923+11729dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114451374 | |||||||
| chr1:114451374 | T | TAA | 32 | a0001c0002t0003g0127 a0001c0002t0005g0098 a0001c0002t0005g0099 others(29): Show |
32 | HG00735.hp1 HG00738.hp1 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.923+11728_923+1172 others(6): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114451374 | |||||||
| chr1:114451687 | T | TA | 12 | a0001c0002t0005g0098 a0001c0002t0005g0099 a0001c0002t0005g0102 others(9): Show |
12 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.923+11416dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114451687 | |||||||
| chr1:114451840 | C | G | 1 | a0001c0001t0002g0149 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.923+11264G>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114451840 | |||||||
| chr1:114451877 | C | T | 6 | a0001c0002t0004g0111 a0001c0002t0004g0114 a0001c0002t0004g0115 others(3): Show |
6 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.923+11227G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114451877 | |||||||
| chr1:114451887 | C | A | 1 | a0002c0003t0001g0028 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.923+11217G>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114451887 | |||||||
| chr1:114452079 | A | AAGAAT | 46 | a0001c0002t0004g0111 a0001c0002t0004g0114 a0001c0002t0004g0115 others(43): Show |
46 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(43): Show |
intron_variant | MODIFIER | c.923+11020_923+1102 others(9): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114452079 | |||||||
| chr1:114452122 | A | G | 1 | a0001c0002t0005g0109 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.923+10982T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114452122 | |||||||
| chr1:114452237 | G | A | 2 | a0001c0001t0001g0166 a0001c0001t0001g0200 |
2 | NA18747.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.923+10867C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114452237 | |||||||
| chr1:114452438 | AAC | A | 3 | a0001c0002t0018g0145 a0001c0002t0018g0146 a0001c0002t0038g0118 |
3 | HG00741.hp2 HG02647.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.923+10664_923+1066 others(6): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114452438 | |||||||
| chr1:114452452 | C | G | 12 | a0001c0002t0005g0098 a0001c0002t0005g0099 a0001c0002t0005g0102 others(9): Show |
12 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.923+10652G>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114452452 | |||||||
| chr1:114452522 | T | C | 1 | a0001c0002t0038g0118 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.923+10582A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114452522 | |||||||
| chr1:114452602 | A | G | 3 | a0003c0004t0013g0010 a0003c0004t0032g0011 a0003c0008t0013g0015 |
3 | HG02145.hp1 HG02258.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.923+10502T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114452602 | |||||||
| chr1:114452727 | TA | T | 46 | a0001c0001t0001g0058 a0001c0001t0001g0166 a0001c0001t0001g0180 others(43): Show |
46 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.923+10376delT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114452727 | |||||||
| chr1:114452727 | TAA | T | 11 | a0001c0002t0005g0098 a0001c0002t0005g0099 a0001c0002t0005g0102 others(8): Show |
11 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.923+10375_923+1037 others(6): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114452727 | |||||||
| chr1:114452727 | TAAA | T | 32 | a0001c0002t0004g0111 a0001c0002t0004g0114 a0001c0002t0004g0115 others(29): Show |
32 | HG00741.hp2 HG01106.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.923+10374_923+1037 others(7): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114452727 | |||||||
| chr1:114452727 | TAAAA | T | 37 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(34): Show |
37 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.923+10373_923+1037 others(8): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114452727 | |||||||
| chr1:114452771 | A | G | 1 | a0001c0002t0023g0002 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.923+10333T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114452771 | |||||||
| chr1:114453203 | A | C | 5 | a0001c0002t0034g0117 a0003c0004t0014g0005 a0003c0004t0014g0012 others(2): Show |
5 | HG02055.hp2 HG02451.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.923+9901T>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114453203 | |||||||
| chr1:114453364 | G | GA | 20 | a0001c0002t0006g0086 a0001c0002t0006g0087 a0001c0002t0006g0088 others(17): Show |
20 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.923+9739dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114453364 | |||||||
| chr1:114453490 | A | G | 80 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(77): Show |
80 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.923+9614T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114453490 | |||||||
| chr1:114453546 | G | A | 1 | a0001c0002t0004g0111 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.923+9558C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114453546 | |||||||
| chr1:114453702 | T | C | 21 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(18): Show |
21 | HG00323.hp1 HG00738.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.923+9402A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114453702 | |||||||
| chr1:114453736 | A | G | 6 | a0001c0002t0004g0111 a0001c0002t0004g0114 a0001c0002t0004g0115 others(3): Show |
6 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.923+9368T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114453736 | |||||||
| chr1:114453886 | G | A | 1 | a0002c0003t0004g0030 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.923+9218C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114453886 | |||||||
| chr1:114454122 | C | G | 1 | a0001c0002t0021g0092 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.923+8982G>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114454122 | |||||||
| chr1:114454204 | C | T | 2 | a0001c0001t0001g0083 a0001c0001t0004g0050 |
2 | HG02055.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.923+8900G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114454204 | |||||||
| chr1:114454524 | A | AAAAAAT | 10 | a0001c0002t0005g0098 a0001c0002t0005g0099 a0001c0002t0005g0102 others(7): Show |
10 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.923+8574_923+8579d others(8): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114454524 | |||||||
| chr1:114454673 | T | TA | 62 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(59): Show |
62 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.923+8430dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114454673 | |||||||
| chr1:114454673 | T | TAA | 17 | a0001c0002t0004g0114 a0001c0002t0004g0115 a0001c0002t0005g0098 others(14): Show |
17 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.923+8429_923+8430d others(4): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114454673 | |||||||
| chr1:114454774 | T | C | 1 | a0001c0001t0004g0024 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.923+8330A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114454774 | |||||||
| chr1:114455108 | T | G | 12 | a0001c0002t0005g0098 a0001c0002t0005g0099 a0001c0002t0005g0102 others(9): Show |
12 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.923+7996A>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114455108 | |||||||
| chr1:114455223 | C | T | 4 | a0001c0002t0009g0202 a0001c0002t0009g0203 a0001c0002t0009g0204 others(1): Show |
4 | HG01891.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.923+7881G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114455223 | |||||||
| chr1:114455239 | T | C | 6 | a0001c0002t0004g0111 a0001c0002t0004g0114 a0001c0002t0004g0115 others(3): Show |
6 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.923+7865A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114455239 | |||||||
| chr1:114455325 | T | C | 1 | a0002c0003t0001g0033 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.923+7779A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114455325 | |||||||
| chr1:114455599 | G | C | 30 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(27): Show |
30 | HG00323.hp1 HG00738.hp1 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.923+7505C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114455599 | |||||||
| chr1:114455807 | G | C | 1 | a0002c0003t0016g0042 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.923+7297C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114455807 | |||||||
| chr1:114456205 | A | C | 21 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(18): Show |
21 | HG00323.hp1 HG00738.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.923+6899T>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114456205 | |||||||
| chr1:114456337 | A | G | 1 | a0002c0003t0004g0030 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.923+6767T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114456337 | |||||||
| chr1:114456389 | C | A | 8 | a0003c0004t0001g0008 a0003c0004t0004g0006 a0003c0004t0004g0009 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.923+6715G>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114456389 | |||||||
| chr1:114456476 | G | A | 1 | a0001c0001t0001g0084 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.923+6628C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114456476 | |||||||
| chr1:114456634 | G | A | 12 | a0001c0002t0005g0098 a0001c0002t0005g0099 a0001c0002t0005g0102 others(9): Show |
12 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.923+6470C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114456634 | |||||||
| chr1:114456655 | G | A | 80 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(77): Show |
80 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.923+6449C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114456655 | |||||||
| chr1:114456843 | G | A | 15 | a0001c0002t0006g0086 a0001c0002t0006g0087 a0001c0002t0006g0088 others(12): Show |
15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.923+6261C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114456843 | |||||||
| chr1:114456954 | A | G | 6 | a0001c0002t0004g0111 a0001c0002t0004g0114 a0001c0002t0004g0115 others(3): Show |
6 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.923+6150T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114456954 | |||||||
| chr1:114456971 | T | G | 11 | a0001c0002t0034g0117 a0001c0006t0010g0119 a0001c0006t0010g0120 others(8): Show |
11 | HG02055.hp2 HG02132.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.923+6133A>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114456971 | |||||||
| chr1:114457127 | G | C | 1 | a0001c0001t0001g0084 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.923+5977C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114457127 | |||||||
| chr1:114457356 | T | G | 1 | a0002c0003t0001g0017 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.923+5748A>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114457356 | |||||||
| chr1:114457438 | G | A | 68 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(65): Show |
68 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.923+5666C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114457438 | |||||||
| chr1:114457477 | A | G | 1 | a0001c0001t0002g0148 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.923+5627T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114457477 | |||||||
| chr1:114457840 | C | G | 1 | a0001c0002t0003g0130 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.923+5264G>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114457840 | |||||||
| chr1:114457859 | G | A | 68 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(65): Show |
68 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.923+5245C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114457859 | |||||||
| chr1:114457908 | C | T | 1 | a0001c0002t0033g0116 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.923+5196G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114457908 | |||||||
| chr1:114458020 | C | A | 5 | a0001c0002t0034g0117 a0003c0004t0014g0005 a0003c0004t0014g0012 others(2): Show |
5 | HG02055.hp2 HG02451.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.923+5084G>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114458020 | |||||||
| chr1:114458499 | C | T | 3 | a0003c0004t0004g0006 a0003c0004t0013g0007 a0003c0004t0050g0206 |
3 | HG02280.hp1 HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.923+4605G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114458499 | |||||||
| chr1:114458520 | A | T | 1 | a0003c0004t0001g0008 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.923+4584T>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114458520 | |||||||
| chr1:114458560 | C | A | 1 | a0001c0002t0006g0095 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.923+4544G>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114458560 | |||||||
| chr1:114458916 | T | C | 15 | a0001c0002t0006g0086 a0001c0002t0006g0087 a0001c0002t0006g0088 others(12): Show |
15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.923+4188A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114458916 | |||||||
| chr1:114459301 | T | G | 1 | a0001c0002t0034g0117 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.923+3803A>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114459301 | |||||||
| chr1:114459370 | C | T | 6 | a0001c0002t0004g0111 a0001c0002t0004g0114 a0001c0002t0004g0115 others(3): Show |
6 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.923+3734G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114459370 | |||||||
| chr1:114459400 | T | C | 2 | a0001c0002t0005g0105 a0001c0002t0005g0108 |
2 | HG02615.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.923+3704A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114459400 | |||||||
| chr1:114459509 | C | A | 1 | a0001c0001t0002g0161 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.923+3595G>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114459509 | |||||||
| chr1:114459512 | G | A | 5 | a0001c0001t0001g0166 a0001c0001t0002g0149 a0001c0001t0002g0162 others(2): Show |
5 | HG00438.hp1 HG00558.hp2 HG02015.hp1 others(2): Show |
intron_variant | MODIFIER | c.923+3592C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114459512 | |||||||
| chr1:114459659 | T | C | 6 | a0001c0002t0004g0111 a0001c0002t0004g0114 a0001c0002t0004g0115 others(3): Show |
6 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.923+3445A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114459659 | |||||||
| chr1:114459719 | CAG | C | 68 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(65): Show |
68 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.923+3383_923+3384d others(4): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114459719 | |||||||
| chr1:114459916 | G | A | 3 | a0001c0002t0005g0098 a0001c0002t0005g0099 a0001c0002t0005g0102 |
3 | HG01433.hp2 HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.923+3188C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114459916 | |||||||
| chr1:114460108 | C | T | 1 | a0001c0002t0005g0109 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.923+2996G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114460108 | |||||||
| chr1:114460146 | C | T | 1 | a0001c0001t0002g0195 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.923+2958G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114460146 | |||||||
| chr1:114460184 | A | G | 1 | a0001c0001t0001g0084 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.923+2920T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114460184 | |||||||
| chr1:114460195 | C | G | 2 | a0001c0002t0009g0204 a0001c0002t0009g0205 |
2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.923+2909G>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114460195 | |||||||
| chr1:114460283 | T | G | 8 | a0002c0003t0001g0043 a0002c0003t0001g0082 a0002c0003t0008g0032 others(5): Show |
8 | HG00642.hp1 HG00738.hp2 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.923+2821A>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114460283 | |||||||
| chr1:114460384 | C | T | 4 | a0001c0002t0006g0093 a0001c0002t0006g0094 a0001c0002t0006g0095 others(1): Show |
4 | HG02280.hp2 HG02723.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.923+2720G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114460384 | |||||||
| chr1:114460503 | T | C | 1 | a0001c0001t0026g0196 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.923+2601A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114460503 | |||||||
| chr1:114460573 | CT | C | 156 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0022 others(153): Show |
157 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.923+2530delA | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114460573 | |||||||
| chr1:114460573 | CTT | C | 19 | a0001c0001t0001g0025 a0001c0001t0001g0083 a0001c0001t0001g0180 others(16): Show |
19 | HG01884.hp1 HG01884.hp2 HG01993.hp1 others(16): Show |
intron_variant | MODIFIER | c.923+2529_923+2530d others(4): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114460573 | |||||||
| chr1:114460687 | C | T | 1 | a0001c0002t0003g0131 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.923+2417G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114460687 | |||||||
| chr1:114460781 | T | C | 33 | a0001c0002t0005g0098 a0001c0002t0005g0099 a0001c0002t0005g0102 others(30): Show |
33 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.923+2323A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114460781 | |||||||
| chr1:114461003 | G | A | 1 | a0002c0003t0001g0035 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.923+2101C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114461003 | |||||||
| chr1:114461066 | C | T | 12 | a0001c0002t0005g0098 a0001c0002t0005g0099 a0001c0002t0005g0102 others(9): Show |
12 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.923+2038G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114461066 | |||||||
| chr1:114461154 | T | A | 20 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0052 others(17): Show |
20 | HG00558.hp1 HG00741.hp1 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.923+1950A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114461154 | |||||||
| chr1:114461211 | T | TA | 17 | a0001c0002t0004g0111 a0001c0002t0004g0114 a0001c0002t0004g0115 others(14): Show |
17 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.923+1892dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114461211 | |||||||
| chr1:114461211 | T | TAA | 20 | a0001c0002t0006g0086 a0001c0002t0006g0087 a0001c0002t0006g0088 others(17): Show |
20 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.923+1891_923+1892d others(4): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114461211 | |||||||
| chr1:114461215 | A | AAT | 11 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0060 others(8): Show |
11 | HG00741.hp1 HG01081.hp2 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.923+1887_923+1888d others(4): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114461215 | |||||||
| chr1:114461215 | AAT | A | 57 | a0001c0001t0001g0022 a0001c0001t0001g0025 a0001c0001t0001g0026 others(54): Show |
57 | HG00438.hp1 HG00558.hp2 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.923+1887_923+1888d others(4): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114461215 | |||||||
| chr1:114461216 | AT | A | 41 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(38): Show |
41 | HG00323.hp1 HG00738.hp1 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.923+1887delA | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114461216 | |||||||
| chr1:114461217 | T | A | 36 | a0001c0001t0011g0067 a0001c0001t0022g0056 a0001c0002t0006g0086 others(33): Show |
36 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(33): Show |
intron_variant | MODIFIER | c.923+1887A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114461217 | |||||||
| chr1:114461219 | T | A | 57 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(54): Show |
57 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(54): Show |
intron_variant | MODIFIER | c.923+1885A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114461219 | |||||||
| chr1:114461221 | T | A | 37 | a0001c0002t0003g0128 a0001c0002t0003g0130 a0001c0002t0003g0131 others(34): Show |
37 | HG00099.hp1 HG00735.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.923+1883A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114461221 | |||||||
| chr1:114461223 | T | A | 2 | a0001c0002t0046g0091 a0003c0004t0050g0206 |
2 | HG01106.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.923+1881A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114461223 | |||||||
| chr1:114461235 | T | C | 2 | a0001c0001t0002g0173 a0001c0002t0004g0111 |
2 | HG02109.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.923+1869A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114461235 | |||||||
| chr1:114461290 | A | ATTTATAT | 21 | a0001c0002t0006g0086 a0001c0002t0006g0087 a0001c0002t0006g0088 others(18): Show |
21 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.923+1807_923+1813d others(9): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114461290 | |||||||
| chr1:114461291 | T | TTTATATA | 5 | a0001c0002t0034g0117 a0003c0004t0014g0005 a0003c0004t0014g0012 others(2): Show |
5 | HG02055.hp2 HG02451.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.923+1806_923+1812d others(9): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114461291 | |||||||
| chr1:114461298 | A | ATTATATT | 39 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(36): Show |
39 | HG00323.hp1 HG00738.hp1 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.923+1799_923+1805d others(9): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114461298 | |||||||
| chr1:114461298 | A | T | 21 | a0001c0002t0006g0086 a0001c0002t0006g0087 a0001c0002t0006g0088 others(18): Show |
21 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.923+1806T>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114461298 | |||||||
| chr1:114461306 | T | C | 1 | a0003c0008t0013g0015 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.923+1798A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114461306 | |||||||
| chr1:114461313 | T | A | 5 | a0003c0004t0001g0008 a0003c0004t0004g0009 a0003c0004t0013g0010 others(2): Show |
5 | HG02145.hp1 HG02258.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.923+1791A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114461313 | |||||||
| chr1:114461319 | A | G | 3 | a0001c0002t0003g0131 a0001c0002t0003g0132 a0001c0002t0029g0135 |
3 | NA18612.hp2 NA18957.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.923+1785T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114461319 | |||||||
| chr1:114461432 | C | T | 24 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(21): Show |
24 | HG00323.hp1 HG00738.hp1 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.923+1672G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114461432 | |||||||
| chr1:114461569 | T | A | 15 | a0001c0002t0006g0086 a0001c0002t0006g0087 a0001c0002t0006g0088 others(12): Show |
15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.923+1535A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114461569 | |||||||
| chr1:114461946 | T | A | 3 | a0003c0004t0014g0005 a0003c0004t0014g0012 a0003c0004t0014g0013 |
3 | HG02055.hp2 HG02523.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.923+1158A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114461946 | |||||||
| chr1:114461959 | A | G | 6 | a0001c0006t0010g0119 a0001c0006t0010g0120 a0001c0006t0010g0121 others(3): Show |
6 | HG02132.hp2 HG02698.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.923+1145T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114461959 | |||||||
| chr1:114462020 | AT | A | 2 | a0001c0002t0018g0145 a0001c0002t0018g0146 |
2 | HG00741.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.923+1083delA | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114462020 | |||||||
| chr1:114462159 | C | T | 6 | a0001c0006t0010g0119 a0001c0006t0010g0120 a0001c0006t0010g0121 others(3): Show |
6 | HG02132.hp2 HG02698.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.923+945G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114462159 | |||||||
| chr1:114462216 | C | T | 23 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(20): Show |
23 | HG00323.hp1 HG00738.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.923+888G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114462216 | |||||||
| chr1:114462408 | T | G | 2 | a0002c0003t0001g0036 a0002c0003t0001g0040 |
2 | NA18955.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.923+696A>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114462408 | |||||||
| chr1:114462534 | T | C | 1 | a0001c0001t0001g0075 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.923+570A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114462534 | |||||||
| chr1:114462795 | T | C | 21 | a0001c0002t0006g0086 a0001c0002t0006g0087 a0001c0002t0006g0088 others(18): Show |
21 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.923+309A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114462795 | |||||||
| chr1:114463005 | T | C | 2 | a0001c0002t0005g0105 a0001c0002t0005g0108 |
2 | HG02615.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.923+99A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114463005 | |||||||
| chr1:114463347 | T | C | 1 | a0001c0002t0023g0002 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.790+65A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 3/19 | chr1 | 114463347 | |||||||
| chr1:114463586 | T | A | 1 | a0001c0001t0002g0184 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.646-30A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 2/19 | chr1 | 114463586 | |||||||
| chr1:114463608 | TA | T | 68 | a0001c0001t0002g0148 a0001c0002t0003g0125 a0001c0002t0003g0126 others(65): Show |
68 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.646-53delT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 2/19 | chr1 | 114463608 | |||||||
| chr1:114463752 | T | C | 2 | a0001c0002t0018g0145 a0001c0002t0018g0146 |
2 | HG00741.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.646-196A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 2/19 | chr1 | 114463752 | |||||||
| chr1:114463767 | C | CT | 81 | a0001c0001t0001g0073 a0001c0001t0002g0186 a0001c0001t0004g0059 others(78): Show |
81 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.646-212dupA | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 2/19 | chr1 | 114463767 | |||||||
| chr1:114463767 | C | CTT | 5 | a0001c0002t0034g0117 a0003c0004t0014g0005 a0003c0004t0014g0013 others(2): Show |
5 | HG02145.hp1 HG02451.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.646-213_646-212dup others(2): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 2/19 | chr1 | 114463767 | |||||||
| chr1:114463805 | G | A | 3 | a0003c0004t0014g0005 a0003c0004t0014g0012 a0003c0004t0014g0013 |
3 | HG02055.hp2 HG02523.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.646-249C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 2/19 | chr1 | 114463805 | |||||||
| chr1:114463989 | G | A | 1 | a0001c0002t0005g0106 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.645+281C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 2/19 | chr1 | 114463989 | |||||||
| chr1:114464038 | C | T | 12 | a0001c0002t0005g0098 a0001c0002t0005g0099 a0001c0002t0005g0102 others(9): Show |
12 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.645+232G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 2/19 | chr1 | 114464038 | |||||||
| chr1:114464058 | C | G | 1 | a0001c0002t0006g0097 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.645+212G>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 2/19 | chr1 | 114464058 | |||||||
| chr1:114464086 | G | A | 6 | a0001c0006t0010g0119 a0001c0006t0010g0120 a0001c0006t0010g0121 others(3): Show |
6 | HG02132.hp2 HG02698.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.645+184C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 2/19 | chr1 | 114464086 | |||||||
| chr1:114464602 | T | C | 1 | a0001c0002t0038g0118 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.527-214A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114464602 | |||||||
| chr1:114464747 | G | A | 1 | a0003c0004t0001g0008 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.527-359C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114464747 | |||||||
| chr1:114464757 | C | T | 1 | a0002c0003t0001g0038 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.527-369G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114464757 | |||||||
| chr1:114464903 | C | T | 15 | a0001c0002t0006g0086 a0001c0002t0006g0087 a0001c0002t0006g0088 others(12): Show |
15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.527-515G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114464903 | |||||||
| chr1:114465013 | TG | T | 4 | a0001c0002t0009g0202 a0001c0002t0009g0203 a0001c0002t0009g0204 others(1): Show |
4 | HG01891.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.527-626delC | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114465013 | |||||||
| chr1:114465016 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.527-628G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114465016 | |||||||
| chr1:114465343 | C | A | 3 | a0003c0004t0014g0005 a0003c0004t0014g0012 a0003c0004t0014g0013 |
3 | HG02055.hp2 HG02523.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.527-955G>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114465343 | |||||||
| chr1:114465585 | G | A | 1 | a0001c0001t0051g0207 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.527-1197C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114465585 | |||||||
| chr1:114465613 | C | CA | 4 | a0001c0001t0002g0158 a0001c0001t0002g0159 a0001c0001t0002g0160 others(1): Show |
4 | NA18942.hp1 NA18970.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.527-1226dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114465613 | |||||||
| chr1:114465767 | C | T | 2 | a0001c0002t0005g0105 a0001c0002t0005g0108 |
2 | HG02615.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.527-1379G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114465767 | |||||||
| chr1:114465780 | G | A | 6 | a0001c0002t0004g0111 a0001c0002t0004g0114 a0001c0002t0004g0115 others(3): Show |
6 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.527-1392C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114465780 | |||||||
| chr1:114465806 | C | A | 2 | a0001c0001t0017g0037 a0002c0003t0001g0165 |
2 | NA18984.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.527-1418G>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114465806 | |||||||
| chr1:114465806 | C | T | 3 | a0001c0002t0006g0086 a0001c0002t0023g0002 a0001c0002t0035g0085 |
3 | HG02970.hp2 HG03516.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.527-1418G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114465806 | |||||||
| chr1:114465837 | G | C | 80 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(77): Show |
80 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.527-1449C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114465837 | |||||||
| chr1:114465949 | AG | A | 3 | a0001c0002t0005g0106 a0001c0002t0005g0107 a0001c0002t0019g0110 |
3 | HG01192.hp1 HG01261.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.527-1562delC | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114465949 | |||||||
| chr1:114466040 | CA | C | 12 | a0001c0002t0005g0098 a0001c0002t0005g0099 a0001c0002t0005g0102 others(9): Show |
12 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.527-1653delT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114466040 | |||||||
| chr1:114466048 | A | T | 2 | a0001c0001t0001g0058 a0002c0003t0016g0042 |
2 | HG00438.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.527-1660T>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114466048 | |||||||
| chr1:114466179 | T | A | 12 | a0001c0002t0005g0098 a0001c0002t0005g0099 a0001c0002t0005g0102 others(9): Show |
12 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.527-1791A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114466179 | |||||||
| chr1:114466419 | G | A | 2 | a0001c0002t0018g0145 a0001c0002t0018g0146 |
2 | HG00741.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.527-2031C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114466419 | |||||||
| chr1:114466446 | C | T | 5 | a0001c0002t0034g0117 a0003c0004t0014g0005 a0003c0004t0014g0012 others(2): Show |
5 | HG02055.hp2 HG02451.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.527-2058G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114466446 | |||||||
| chr1:114466472 | C | T | 1 | a0001c0001t0002g0184 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.527-2084G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114466472 | |||||||
| chr1:114467001 | A | C | 23 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(20): Show |
23 | HG00323.hp1 HG00738.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.527-2613T>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114467001 | |||||||
| chr1:114467011 | C | T | 1 | a0001c0001t0002g0069 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.527-2623G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114467011 | |||||||
| chr1:114467178 | G | A | 8 | a0003c0004t0001g0008 a0003c0004t0004g0006 a0003c0004t0004g0009 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.527-2790C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114467178 | |||||||
| chr1:114467373 | G | A | 2 | a0001c0002t0018g0145 a0001c0002t0018g0146 |
2 | HG00741.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.527-2985C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114467373 | |||||||
| chr1:114467527 | C | T | 1 | a0002c0003t0001g0082 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.527-3139G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114467527 | |||||||
| chr1:114467533 | T | A | 1 | a0003c0008t0013g0015 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.527-3145A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114467533 | |||||||
| chr1:114467765 | C | T | 1 | a0001c0002t0005g0106 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.527-3377G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114467765 | |||||||
| chr1:114468065 | G | T | 1 | a0001c0002t0005g0105 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.527-3677C>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114468065 | |||||||
| chr1:114468223 | G | A | 11 | a0001c0002t0034g0117 a0001c0006t0010g0119 a0001c0006t0010g0120 others(8): Show |
11 | HG02055.hp2 HG02132.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.527-3835C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114468223 | |||||||
| chr1:114468247 | G | A | 3 | a0001c0001t0011g0054 a0001c0001t0011g0055 a0001c0001t0011g0067 |
3 | HG01099.hp2 HG02886.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.527-3859C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114468247 | |||||||
| chr1:114468660 | G | A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0027 |
2 | HG02809.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.527-4272C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114468660 | |||||||
| chr1:114468837 | G | A | 1 | a0003c0004t0001g0008 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.527-4449C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114468837 | |||||||
| chr1:114468862 | T | C | 80 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(77): Show |
80 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.527-4474A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114468862 | |||||||
| chr1:114468865 | C | T | 40 | a0001c0001t0001g0166 a0001c0001t0001g0180 a0001c0001t0002g0149 others(37): Show |
40 | HG00438.hp1 HG00558.hp2 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.527-4477G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114468865 | |||||||
| chr1:114468879 | C | T | 2 | a0001c0001t0001g0083 a0001c0001t0004g0050 |
2 | HG02055.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.527-4491G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114468879 | |||||||
| chr1:114468919 | C | G | 1 | a0001c0002t0005g0102 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.527-4531G>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114468919 | |||||||
| chr1:114469051 | G | A | 2 | a0001c0002t0018g0145 a0001c0002t0018g0146 |
2 | HG00741.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.527-4663C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114469051 | |||||||
| chr1:114469440 | C | T | 1 | a0001c0002t0046g0091 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.527-5052G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114469440 | |||||||
| chr1:114469560 | A | T | 6 | a0001c0002t0004g0111 a0001c0002t0004g0114 a0001c0002t0004g0115 others(3): Show |
6 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.527-5172T>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114469560 | |||||||
| chr1:114469567 | A | C | 27 | a0001c0002t0005g0098 a0001c0002t0005g0099 a0001c0002t0005g0102 others(24): Show |
27 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.527-5179T>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114469567 | |||||||
| chr1:114469721 | G | C | 2 | a0001c0002t0025g0004 a0001c0002t0027g0090 |
2 | HG01361.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.527-5333C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114469721 | |||||||
| chr1:114470012 | T | C | 1 | a0001c0001t0017g0176 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.527-5624A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114470012 | |||||||
| chr1:114470529 | C | T | 1 | a0001c0002t0038g0118 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.527-6141G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114470529 | |||||||
| chr1:114470629 | C | G | 2 | a0001c0002t0018g0145 a0001c0002t0018g0146 |
2 | HG00741.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.527-6241G>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114470629 | |||||||
| chr1:114470638 | T | TAAC | 2 | a0001c0001t0048g0081 a0002c0003t0008g0047 |
2 | HG00738.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.527-6253_527-6251d others(5): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114470638 | |||||||
| chr1:114470638 | TAAC | T | 80 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(77): Show |
80 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.527-6253_527-6251d others(5): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114470638 | |||||||
| chr1:114470764 | C | T | 204 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0022 others(201): Show |
205 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.527-6376G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114470764 | |||||||
| chr1:114470857 | A | G | 2 | a0001c0002t0018g0145 a0001c0002t0018g0146 |
2 | HG00741.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.527-6469T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114470857 | |||||||
| chr1:114470930 | T | G | 13 | a0001c0002t0009g0202 a0001c0002t0009g0203 a0001c0002t0009g0204 others(10): Show |
13 | HG01891.hp2 HG02145.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.527-6542A>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114470930 | |||||||
| chr1:114471094 | T | C | 1 | a0003c0004t0032g0011 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.527-6706A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114471094 | |||||||
| chr1:114471407 | C | T | 9 | a0001c0002t0005g0098 a0001c0002t0005g0099 a0001c0002t0005g0102 others(6): Show |
9 | HG01257.hp2 HG01433.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.527-7019G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114471407 | |||||||
| chr1:114471443 | C | CA | 23 | a0001c0001t0002g0069 a0001c0002t0003g0125 a0001c0002t0003g0126 others(20): Show |
23 | HG00323.hp1 HG00738.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.527-7056dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114471443 | |||||||
| chr1:114471593 | A | G | 2 | a0001c0002t0005g0105 a0001c0002t0005g0108 |
2 | HG02615.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.527-7205T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114471593 | |||||||
| chr1:114471594 | A | G | 2 | a0001c0002t0005g0105 a0001c0002t0005g0108 |
2 | HG02615.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.527-7206T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114471594 | |||||||
| chr1:114471741 | C | G | 5 | a0003c0004t0001g0008 a0003c0004t0004g0009 a0003c0004t0013g0010 others(2): Show |
5 | HG02145.hp1 HG02258.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.527-7353G>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114471741 | |||||||
| chr1:114471853 | T | C | 1 | a0001c0001t0011g0054 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.527-7465A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114471853 | |||||||
| chr1:114472106 | C | T | 40 | a0001c0001t0001g0166 a0001c0001t0001g0180 a0001c0001t0002g0149 others(37): Show |
40 | HG00438.hp1 HG00558.hp2 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.527-7718G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114472106 | |||||||
| chr1:114472529 | T | C | 1 | a0001c0005t0007g0147 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.527-8141A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114472529 | |||||||
| chr1:114472711 | T | C | 1 | a0001c0002t0003g0128 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.527-8323A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114472711 | |||||||
| chr1:114472721 | GAAAACA | G | 6 | a0001c0002t0004g0111 a0001c0002t0004g0114 a0001c0002t0004g0115 others(3): Show |
6 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.527-8339_527-8334d others(8): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114472721 | |||||||
| chr1:114472897 | G | A | 2 | a0001c0001t0001g0072 a0001c0001t0028g0063 |
2 | HG02004.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.527-8509C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114472897 | |||||||
| chr1:114472976 | G | A | 2 | a0001c0001t0031g0157 a0001c0001t0037g0154 |
2 | HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.527-8588C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114472976 | |||||||
| chr1:114473046 | A | G | 204 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0022 others(201): Show |
205 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.527-8658T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114473046 | |||||||
| chr1:114473181 | C | T | 3 | a0003c0004t0013g0010 a0003c0004t0032g0011 a0003c0008t0013g0015 |
3 | HG02145.hp1 HG02258.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.527-8793G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114473181 | |||||||
| chr1:114473225 | C | T | 1 | a0002c0003t0001g0033 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.527-8837G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114473225 | |||||||
| chr1:114473243 | C | T | 2 | a0001c0001t0001g0025 a0001c0001t0004g0024 |
2 | HG02109.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.527-8855G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114473243 | |||||||
| chr1:114473244 | G | A | 1 | a0001c0009t0040g0123 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.527-8856C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114473244 | |||||||
| chr1:114473256 | C | CA | 40 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(37): Show |
40 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.527-8869dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114473256 | |||||||
| chr1:114473273 | A | T | 1 | a0001c0001t0047g0053 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.527-8885T>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114473273 | |||||||
| chr1:114473394 | A | G | 1 | a0001c0001t0036g0177 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.527-9006T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114473394 | |||||||
| chr1:114473401 | C | CT | 2 | a0001c0002t0034g0117 a0004c0007t0001g0014 |
2 | HG02451.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.527-9014dupA | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114473401 | |||||||
| chr1:114473659 | T | A | 1 | a0001c0001t0048g0081 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.527-9271A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114473659 | |||||||
| chr1:114473782 | C | G | 15 | a0001c0002t0006g0086 a0001c0002t0006g0087 a0001c0002t0006g0088 others(12): Show |
15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.527-9394G>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114473782 | |||||||
| chr1:114473793 | G | A | 80 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(77): Show |
80 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.527-9405C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114473793 | |||||||
| chr1:114473801 | C | T | 6 | a0001c0002t0004g0111 a0001c0002t0004g0114 a0001c0002t0004g0115 others(3): Show |
6 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.527-9413G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114473801 | |||||||
| chr1:114474045 | T | C | 4 | a0001c0002t0009g0202 a0001c0002t0009g0203 a0001c0002t0009g0204 others(1): Show |
4 | HG01891.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.527-9657A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114474045 | |||||||
| chr1:114474083 | TAG | T | 12 | a0001c0002t0009g0202 a0001c0002t0009g0203 a0001c0002t0009g0204 others(9): Show |
12 | HG01891.hp2 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.527-9697_527-9696d others(4): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114474083 | |||||||
| chr1:114474165 | T | C | 1 | a0002c0003t0001g0082 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.527-9777A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114474165 | |||||||
| chr1:114474393 | C | T | 4 | a0001c0001t0002g0148 a0001c0001t0002g0156 a0001c0001t0002g0198 others(1): Show |
4 | HG02145.hp2 HG02258.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.527-10005G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114474393 | |||||||
| chr1:114474409 | T | TA | 34 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(31): Show |
34 | HG00323.hp1 HG00738.hp1 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.527-10022dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114474409 | |||||||
| chr1:114474434 | T | C | 1 | a0001c0001t0002g0156 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.527-10046A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114474434 | |||||||
| chr1:114474451 | G | A | 1 | a0002c0003t0001g0082 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.527-10063C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114474451 | |||||||
| chr1:114474578 | T | TA | 45 | a0001c0001t0001g0061 a0001c0001t0001g0070 a0001c0001t0002g0186 others(42): Show |
45 | HG00323.hp1 HG00735.hp2 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.527-10191dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114474578 | |||||||
| chr1:114474578 | T | TAA | 36 | a0001c0002t0003g0134 a0001c0002t0005g0104 a0001c0002t0005g0107 others(33): Show |
36 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(33): Show |
intron_variant | MODIFIER | c.527-10192_527-1019 others(6): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114474578 | |||||||
| chr1:114474700 | T | C | 1 | a0001c0001t0002g0195 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.527-10312A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114474700 | |||||||
| chr1:114474761 | G | A | 1 | a0001c0001t0044g0016 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.527-10373C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114474761 | |||||||
| chr1:114474840 | C | T | 1 | a0002c0003t0016g0042 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.527-10452G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114474840 | |||||||
| chr1:114474893 | C | CA | 10 | a0001c0001t0001g0025 a0001c0001t0004g0024 a0001c0002t0019g0100 others(7): Show |
10 | HG01257.hp2 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.527-10506dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114474893 | |||||||
| chr1:114475215 | A | C | 1 | a0001c0001t0002g0179 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.527-10827T>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114475215 | |||||||
| chr1:114475477 | C | T | 4 | a0001c0002t0009g0202 a0001c0002t0009g0203 a0001c0002t0009g0204 others(1): Show |
4 | HG01891.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.527-11089G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114475477 | |||||||
| chr1:114475513 | G | C | 2 | a0001c0001t0011g0054 a0001c0001t0011g0055 |
2 | HG01099.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.527-11125C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114475513 | |||||||
| chr1:114475633 | G | T | 8 | a0003c0004t0001g0008 a0003c0004t0004g0006 a0003c0004t0004g0009 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.527-11245C>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114475633 | |||||||
| chr1:114475638 | C | T | 12 | a0001c0002t0009g0202 a0001c0002t0009g0203 a0001c0002t0009g0204 others(9): Show |
12 | HG01891.hp2 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.527-11250G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114475638 | |||||||
| chr1:114475647 | A | C | 1 | a0001c0001t0002g0189 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.527-11259T>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114475647 | |||||||
| chr1:114475689 | A | AAAT | 80 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(77): Show |
80 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.527-11304_527-1130 others(7): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114475689 | |||||||
| chr1:114476220 | GAA | G | 6 | a0001c0006t0010g0119 a0001c0006t0010g0120 a0001c0006t0010g0121 others(3): Show |
6 | HG02132.hp2 HG02698.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.527-11834_527-1183 others(6): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114476220 | |||||||
| chr1:114476225 | A | C | 9 | a0001c0001t0002g0148 a0001c0001t0002g0155 a0001c0001t0002g0156 others(6): Show |
9 | HG01175.hp2 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.527-11837T>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114476225 | |||||||
| chr1:114476502 | AC | A | 2 | a0001c0002t0009g0202 a0001c0002t0009g0203 |
2 | HG01891.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.527-12115delG | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114476502 | |||||||
| chr1:114476617 | A | T | 24 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(21): Show |
24 | HG00323.hp1 HG00738.hp1 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.527-12229T>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114476617 | |||||||
| chr1:114476845 | T | A | 12 | a0001c0002t0005g0098 a0001c0002t0005g0099 a0001c0002t0005g0102 others(9): Show |
12 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.527-12457A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114476845 | |||||||
| chr1:114477088 | C | T | 33 | a0001c0001t0001g0166 a0001c0001t0001g0180 a0001c0001t0002g0149 others(30): Show |
33 | HG00438.hp1 HG00558.hp2 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.527-12700G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114477088 | |||||||
| chr1:114477585 | A | G | 5 | a0001c0002t0034g0117 a0003c0004t0014g0005 a0003c0004t0014g0012 others(2): Show |
5 | HG02055.hp2 HG02451.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.527-13197T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114477585 | |||||||
| chr1:114477661 | T | A | 4 | a0001c0002t0009g0202 a0001c0002t0009g0203 a0001c0002t0009g0204 others(1): Show |
4 | HG01891.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.527-13273A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114477661 | |||||||
| chr1:114477872 | T | C | 1 | a0001c0001t0002g0153 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.527-13484A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114477872 | |||||||
| chr1:114477874 | G | C | 6 | a0001c0002t0004g0111 a0001c0002t0004g0114 a0001c0002t0004g0115 others(3): Show |
6 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.527-13486C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114477874 | |||||||
| chr1:114477926 | A | T | 11 | a0001c0002t0034g0117 a0001c0006t0010g0119 a0001c0006t0010g0120 others(8): Show |
11 | HG02055.hp2 HG02132.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.527-13538T>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114477926 | |||||||
| chr1:114478043 | A | C | 1 | a0001c0001t0004g0059 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.527-13655T>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114478043 | |||||||
| chr1:114478057 | A | C | 12 | a0001c0002t0005g0098 a0001c0002t0005g0099 a0001c0002t0005g0102 others(9): Show |
12 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.527-13669T>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114478057 | |||||||
| chr1:114478179 | T | C | 5 | a0001c0001t0002g0155 a0001c0001t0002g0195 a0001c0001t0026g0196 others(2): Show |
5 | HG01175.hp2 HG02486.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.527-13791A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114478179 | |||||||
| chr1:114478215 | TAA | T | 3 | a0001c0001t0001g0071 a0001c0001t0002g0064 a0002c0003t0001g0001 |
4 | HG01071.hp2 HG01433.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.527-13829_527-1382 others(6): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114478215 | |||||||
| chr1:114478278 | T | C | 2 | a0001c0002t0003g0136 a0001c0002t0003g0139 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.527-13890A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114478278 | |||||||
| chr1:114478314 | G | C | 2 | a0003c0004t0001g0008 a0003c0004t0004g0009 |
2 | HG02965.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.527-13926C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114478314 | |||||||
| chr1:114478627 | T | C | 45 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(42): Show |
45 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.527-14239A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114478627 | |||||||
| chr1:114478734 | A | G | 2 | a0001c0002t0018g0145 a0001c0002t0018g0146 |
2 | HG00741.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.527-14346T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114478734 | |||||||
| chr1:114478854 | C | G | 1 | a0001c0001t0001g0070 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.527-14466G>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114478854 | |||||||
| chr1:114478961 | T | C | 2 | a0001c0002t0018g0145 a0001c0002t0018g0146 |
2 | HG00741.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.527-14573A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114478961 | |||||||
| chr1:114479151 | A | G | 1 | a0003c0004t0004g0006 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.527-14763T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114479151 | |||||||
| chr1:114479270 | T | C | 2 | a0001c0001t0001g0079 a0001c0001t0001g0080 |
2 | NA18970.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.527-14882A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114479270 | |||||||
| chr1:114479593 | A | T | 12 | a0001c0002t0005g0098 a0001c0002t0005g0099 a0001c0002t0005g0102 others(9): Show |
12 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.527-15205T>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114479593 | |||||||
| chr1:114479638 | G | A | 1 | a0001c0002t0038g0118 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.527-15250C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114479638 | |||||||
| chr1:114479640 | A | T | 1 | a0001c0002t0038g0118 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.527-15252T>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114479640 | |||||||
| chr1:114479652 | A | G | 1 | a0001c0001t0004g0059 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.527-15264T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114479652 | |||||||
| chr1:114479808 | C | CAGGGAGG others(39): Show |
80 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(77): Show |
80 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.527-15421_527-1542 others(50): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114479808 | |||||||
| chr1:114479896 | G | A | 23 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(20): Show |
23 | HG00323.hp1 HG00738.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.527-15508C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114479896 | |||||||
| chr1:114479935 | A | T | 4 | a0001c0001t0002g0190 a0001c0001t0002g0191 a0001c0001t0002g0192 others(1): Show |
4 | HG00642.hp2 HG01074.hp2 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.527-15547T>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114479935 | |||||||
| chr1:114479973 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.527-15585C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114479973 | |||||||
| chr1:114479987 | C | A | 12 | a0001c0002t0005g0098 a0001c0002t0005g0099 a0001c0002t0005g0102 others(9): Show |
12 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.527-15599G>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114479987 | |||||||
| chr1:114480076 | T | C | 6 | a0001c0002t0004g0111 a0001c0002t0004g0114 a0001c0002t0004g0115 others(3): Show |
6 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.527-15688A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114480076 | |||||||
| chr1:114480117 | A | G | 1 | a0001c0001t0001g0073 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.527-15729T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114480117 | |||||||
| chr1:114480164 | G | T | 2 | a0001c0001t0022g0056 a0001c0001t0022g0057 |
2 | HG03704.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.527-15776C>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114480164 | |||||||
| chr1:114480383 | T | C | 12 | a0001c0002t0005g0098 a0001c0002t0005g0099 a0001c0002t0005g0102 others(9): Show |
12 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.527-15995A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114480383 | |||||||
| chr1:114480410 | C | T | 6 | a0001c0002t0004g0111 a0001c0002t0004g0114 a0001c0002t0004g0115 others(3): Show |
6 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.527-16022G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114480410 | |||||||
| chr1:114480424 | CTA | C | 2 | a0001c0002t0005g0105 a0001c0002t0005g0108 |
2 | HG02615.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.527-16038_527-1603 others(6): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114480424 | |||||||
| chr1:114480475 | TTA | T | 5 | a0001c0006t0010g0119 a0001c0006t0010g0120 a0001c0006t0010g0121 others(2): Show |
5 | HG02132.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.527-16089_527-1608 others(6): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114480475 | |||||||
| chr1:114480476 | T | TA | 6 | a0001c0001t0002g0185 a0001c0001t0002g0186 a0001c0001t0002g0189 others(3): Show |
6 | HG01891.hp1 HG02622.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.527-16089dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114480476 | |||||||
| chr1:114480476 | TA | T | 11 | a0001c0001t0002g0039 a0001c0001t0002g0149 a0001c0001t0002g0160 others(8): Show |
11 | HG00323.hp2 HG01167.hp2 HG02897.hp2 others(8): Show |
intron_variant | MODIFIER | c.527-16089delT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114480476 | |||||||
| chr1:114480476 | TAA | T | 48 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(45): Show |
48 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.527-16090_527-1608 others(6): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114480476 | |||||||
| chr1:114480476 | TAAA | T | 25 | a0001c0002t0003g0137 a0001c0002t0003g0144 a0001c0002t0005g0098 others(22): Show |
25 | HG01167.hp1 HG01192.hp1 HG01261.hp2 others(22): Show |
intron_variant | MODIFIER | c.527-16091_527-1608 others(7): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114480476 | |||||||
| chr1:114480491 | A | G | 2 | a0001c0002t0005g0105 a0001c0002t0005g0108 |
2 | HG02615.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.527-16103T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114480491 | |||||||
| chr1:114480493 | A | G | 23 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0002t0003g0125 others(20): Show |
23 | HG00323.hp1 HG00738.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.527-16105T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114480493 | |||||||
| chr1:114480521 | TA | T | 143 | a0001c0001t0001g0022 a0001c0001t0001g0025 a0001c0001t0001g0026 others(140): Show |
143 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.527-16134delT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114480521 | |||||||
| chr1:114480535 | A | G | 8 | a0003c0004t0001g0008 a0003c0004t0004g0006 a0003c0004t0004g0009 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.527-16147T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114480535 | |||||||
| chr1:114480541 | G | T | 1 | a0001c0001t0001g0200 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.527-16153C>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114480541 | |||||||
| chr1:114480563 | A | C | 80 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(77): Show |
80 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.527-16175T>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114480563 | |||||||
| chr1:114480610 | T | C | 1 | a0001c0001t0048g0081 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.527-16222A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114480610 | |||||||
| chr1:114480685 | T | C | 1 | a0001c0005t0007g0187 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.527-16297A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114480685 | |||||||
| chr1:114480688 | C | T | 2 | a0002c0003t0001g0028 a0002c0003t0001g0029 |
2 | HG01928.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.527-16300G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114480688 | |||||||
| chr1:114480847 | A | C | 2 | a0001c0002t0005g0105 a0001c0002t0005g0108 |
2 | HG02615.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.527-16459T>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114480847 | |||||||
| chr1:114480953 | C | G | 6 | a0001c0002t0004g0111 a0001c0002t0004g0114 a0001c0002t0004g0115 others(3): Show |
6 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.527-16565G>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114480953 | |||||||
| chr1:114481101 | A | T | 11 | a0001c0002t0034g0117 a0001c0006t0010g0119 a0001c0006t0010g0120 others(8): Show |
11 | HG02055.hp2 HG02132.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.527-16713T>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114481101 | |||||||
| chr1:114481129 | C | T | 8 | a0002c0003t0001g0043 a0002c0003t0001g0082 a0002c0003t0008g0032 others(5): Show |
8 | HG00642.hp1 HG00738.hp2 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.527-16741G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114481129 | |||||||
| chr1:114481310 | T | C | 1 | a0001c0002t0038g0118 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.527-16922A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114481310 | |||||||
| chr1:114481336 | G | A | 3 | a0001c0001t0011g0054 a0001c0001t0011g0055 a0001c0001t0011g0067 |
3 | HG01099.hp2 HG02886.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.527-16948C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114481336 | |||||||
| chr1:114481359 | C | G | 6 | a0001c0002t0004g0111 a0001c0002t0004g0114 a0001c0002t0004g0115 others(3): Show |
6 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.527-16971G>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114481359 | |||||||
| chr1:114481360 | A | G | 80 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(77): Show |
80 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.527-16972T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114481360 | |||||||
| chr1:114481368 | G | A | 1 | a0001c0002t0038g0118 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.527-16980C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114481368 | |||||||
| chr1:114481527 | G | A | 1 | a0001c0001t0011g0055 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.527-17139C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114481527 | |||||||
| chr1:114481577 | T | A | 2 | a0001c0006t0010g0121 a0001c0006t0010g0122 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.527-17189A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114481577 | |||||||
| chr1:114481629 | C | CTA | 2 | a0001c0002t0009g0202 a0001c0002t0009g0203 |
2 | HG01891.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.527-17243_527-1724 others(6): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114481629 | |||||||
| chr1:114481629 | C | CTATA | 4 | a0003c0004t0001g0008 a0003c0004t0013g0010 a0003c0004t0032g0011 others(1): Show |
4 | HG02145.hp1 HG02258.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.527-17245_527-1724 others(8): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114481629 | |||||||
| chr1:114481639 | A | ATATG | 2 | a0001c0002t0009g0204 a0001c0002t0009g0205 |
2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.527-17252_527-1725 others(8): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114481639 | |||||||
| chr1:114481639 | A | ATG | 3 | a0001c0001t0001g0068 a0001c0001t0017g0176 a0002c0003t0004g0031 |
3 | HG02056.hp2 HG02129.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.527-17253_527-1725 others(6): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114481639 | |||||||
| chr1:114481639 | ATG | A | 3 | a0001c0002t0018g0145 a0001c0002t0018g0146 a0003c0004t0004g0009 |
3 | HG00741.hp2 HG02895.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.527-17253_527-1725 others(6): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114481639 | |||||||
| chr1:114481641 | G | A | 54 | a0001c0001t0001g0083 a0001c0001t0004g0050 a0001c0002t0003g0125 others(51): Show |
54 | HG00323.hp1 HG00738.hp1 HG01099.hp1 others(51): Show |
intron_variant | MODIFIER | c.527-17253C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114481641 | |||||||
| chr1:114481643 | G | A | 22 | a0001c0002t0005g0098 a0001c0002t0005g0099 a0001c0002t0005g0102 others(19): Show |
22 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.527-17255C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114481643 | |||||||
| chr1:114481645 | G | A | 1 | a0003c0004t0004g0009 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.527-17257C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114481645 | |||||||
| chr1:114481661 | GTATATAT others(13): Show |
G | 1 | a0001c0001t0002g0069 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.527-17293_527-1727 others(24): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114481661 | |||||||
| chr1:114481663 | A | G | 39 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(36): Show |
39 | HG00323.hp1 HG00738.hp1 HG01099.hp1 others(36): Show |
intron_variant | MODIFIER | c.527-17275T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114481663 | |||||||
| chr1:114481665 | A | G | 1 | a0001c0002t0003g0144 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.527-17277T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114481665 | |||||||
| chr1:114481667 | ATATG | A | 15 | a0001c0002t0006g0086 a0001c0002t0006g0087 a0001c0002t0006g0088 others(12): Show |
15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.527-17283_527-1728 others(8): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114481667 | |||||||
| chr1:114481671 | G | A | 39 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(36): Show |
39 | HG00323.hp1 HG00738.hp1 HG01099.hp1 others(36): Show |
intron_variant | MODIFIER | c.527-17283C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114481671 | |||||||
| chr1:114481675 | GTA | G | 13 | a0001c0002t0018g0145 a0001c0002t0018g0146 a0001c0002t0034g0117 others(10): Show |
13 | HG00741.hp2 HG01257.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.527-17289_527-1728 others(6): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114481675 | |||||||
| chr1:114481675 | GTATA | G | 2 | a0001c0002t0009g0204 a0001c0002t0009g0205 |
2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.527-17291_527-1728 others(8): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114481675 | |||||||
| chr1:114481677 | A | G | 57 | a0001c0001t0015g0051 a0001c0002t0003g0125 a0001c0002t0003g0126 others(54): Show |
57 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.527-17289T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114481677 | |||||||
| chr1:114481679 | A | G | 1 | a0001c0002t0038g0118 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.527-17291T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114481679 | |||||||
| chr1:114481689 | A | G | 5 | a0001c0002t0034g0117 a0003c0004t0014g0005 a0003c0004t0014g0012 others(2): Show |
5 | HG02055.hp2 HG02451.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.527-17301T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114481689 | |||||||
| chr1:114481746 | G | T | 3 | a0003c0004t0004g0006 a0003c0004t0013g0007 a0003c0004t0050g0206 |
3 | HG02280.hp1 HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.527-17358C>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114481746 | |||||||
| chr1:114481876 | C | T | 1 | a0003c0004t0004g0006 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.527-17488G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114481876 | |||||||
| chr1:114481917 | C | T | 1 | a0003c0004t0004g0009 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.527-17529G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114481917 | |||||||
| chr1:114481933 | G | A | 1 | a0001c0001t0002g0189 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.527-17545C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114481933 | |||||||
| chr1:114482047 | T | G | 6 | a0001c0002t0004g0111 a0001c0002t0004g0114 a0001c0002t0004g0115 others(3): Show |
6 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.527-17659A>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114482047 | |||||||
| chr1:114482276 | G | GA | 4 | a0001c0002t0009g0202 a0001c0002t0009g0203 a0001c0002t0009g0204 others(1): Show |
4 | HG01891.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.527-17889dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114482276 | |||||||
| chr1:114482400 | G | C | 1 | a0001c0001t0002g0161 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.527-18012C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114482400 | |||||||
| chr1:114482448 | C | T | 4 | a0001c0002t0009g0202 a0001c0002t0009g0203 a0001c0002t0009g0204 others(1): Show |
4 | HG01891.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.527-18060G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114482448 | |||||||
| chr1:114482780 | T | A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0027 |
2 | HG02809.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.527-18392A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114482780 | |||||||
| chr1:114482801 | G | A | 3 | a0001c0001t0001g0022 a0001c0001t0004g0023 a0001c0001t0024g0003 |
3 | HG02615.hp2 HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.527-18413C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114482801 | |||||||
| chr1:114483078 | G | C | 21 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(18): Show |
21 | HG00323.hp1 HG00738.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.527-18690C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114483078 | |||||||
| chr1:114483085 | A | G | 15 | a0001c0002t0006g0086 a0001c0002t0006g0087 a0001c0002t0006g0088 others(12): Show |
15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.527-18697T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114483085 | |||||||
| chr1:114483103 | G | A | 7 | a0001c0002t0005g0103 a0001c0002t0005g0104 a0001c0002t0005g0106 others(4): Show |
7 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.527-18715C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114483103 | |||||||
| chr1:114483258 | G | A | 1 | a0001c0002t0006g0087 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.527-18870C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114483258 | |||||||
| chr1:114483288 | C | T | 1 | a0002c0003t0001g0029 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.527-18900G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114483288 | |||||||
| chr1:114483318 | T | A | 7 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0141 others(4): Show |
7 | HG01099.hp1 HG01952.hp2 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.527-18930A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114483318 | |||||||
| chr1:114483416 | G | GT | 12 | a0001c0001t0002g0158 a0001c0002t0034g0117 a0001c0006t0010g0119 others(9): Show |
12 | HG02055.hp2 HG02132.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.527-19029dupA | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114483416 | |||||||
| chr1:114483468 | G | A | 6 | a0001c0002t0004g0111 a0001c0002t0004g0114 a0001c0002t0004g0115 others(3): Show |
6 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.527-19080C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114483468 | |||||||
| chr1:114483536 | C | A | 15 | a0001c0002t0006g0086 a0001c0002t0006g0087 a0001c0002t0006g0088 others(12): Show |
15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.527-19148G>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114483536 | |||||||
| chr1:114483587 | A | G | 1 | a0001c0005t0007g0188 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.527-19199T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114483587 | |||||||
| chr1:114483601 | C | T | 21 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(18): Show |
21 | HG00323.hp1 HG00738.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.527-19213G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114483601 | |||||||
| chr1:114483659 | C | T | 1 | a0003c0004t0004g0009 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.527-19271G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114483659 | |||||||
| chr1:114483766 | C | A | 2 | a0001c0002t0018g0145 a0001c0002t0018g0146 |
2 | HG00741.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.527-19378G>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114483766 | |||||||
| chr1:114483954 | T | C | 21 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(18): Show |
21 | HG00323.hp1 HG00738.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.527-19566A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114483954 | |||||||
| chr1:114483972 | T | C | 4 | a0001c0001t0002g0190 a0001c0001t0002g0191 a0001c0001t0002g0192 others(1): Show |
4 | HG00642.hp2 HG01074.hp2 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.527-19584A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114483972 | |||||||
| chr1:114483986 | T | C | 8 | a0003c0004t0001g0008 a0003c0004t0004g0006 a0003c0004t0004g0009 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.527-19598A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114483986 | |||||||
| chr1:114484150 | AAGG | A | 2 | a0001c0001t0001g0025 a0001c0001t0004g0024 |
2 | HG02109.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.527-19765_527-1976 others(7): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114484150 | |||||||
| chr1:114484341 | T | TA | 8 | a0003c0004t0001g0008 a0003c0004t0004g0006 a0003c0004t0004g0009 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.527-19954dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114484341 | |||||||
| chr1:114484409 | C | T | 80 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(77): Show |
80 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.527-20021G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114484409 | |||||||
| chr1:114484498 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.527-20110C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114484498 | |||||||
| chr1:114484745 | G | A | 15 | a0001c0002t0006g0086 a0001c0002t0006g0087 a0001c0002t0006g0088 others(12): Show |
15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.527-20357C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114484745 | |||||||
| chr1:114484778 | T | C | 1 | a0002c0003t0008g0048 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.527-20390A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114484778 | |||||||
| chr1:114484816 | C | G | 80 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(77): Show |
80 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.527-20428G>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114484816 | |||||||
| chr1:114484819 | C | T | 1 | a0001c0002t0034g0117 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.527-20431G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114484819 | |||||||
| chr1:114484934 | C | A | 21 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(18): Show |
21 | HG00323.hp1 HG00738.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.527-20546G>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114484934 | |||||||
| chr1:114484942 | C | T | 2 | a0001c0006t0010g0121 a0001c0006t0010g0122 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.527-20554G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114484942 | |||||||
| chr1:114484991 | G | C | 5 | a0001c0002t0003g0128 a0001c0002t0003g0131 a0001c0002t0003g0132 others(2): Show |
5 | NA18612.hp2 NA18942.hp2 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.527-20603C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114484991 | |||||||
| chr1:114485053 | T | TA | 33 | a0001c0001t0001g0083 a0001c0001t0001g0200 a0001c0001t0004g0050 others(30): Show |
33 | HG00323.hp1 HG00738.hp1 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.527-20666dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114485053 | |||||||
| chr1:114485071 | G | A | 1 | a0004c0007t0001g0014 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.527-20683C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114485071 | |||||||
| chr1:114485278 | A | AT | 7 | a0001c0001t0001g0060 a0001c0001t0001g0084 a0001c0001t0002g0156 others(4): Show |
7 | HG01081.hp2 HG02738.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.527-20891dupA | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114485278 | |||||||
| chr1:114485289 | A | T | 1 | a0001c0001t0002g0163 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.527-20901T>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114485289 | |||||||
| chr1:114485304 | G | GA | 27 | a0001c0002t0005g0098 a0001c0002t0005g0099 a0001c0002t0005g0102 others(24): Show |
27 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.527-20917dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114485304 | |||||||
| chr1:114485426 | C | T | 8 | a0003c0004t0001g0008 a0003c0004t0004g0006 a0003c0004t0004g0009 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.527-21038G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114485426 | |||||||
| chr1:114485496 | G | C | 1 | a0001c0001t0001g0058 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.527-21108C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114485496 | |||||||
| chr1:114485590 | G | C | 1 | a0001c0002t0019g0100 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.527-21202C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114485590 | |||||||
| chr1:114485655 | C | A | 1 | a0001c0001t0002g0175 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.527-21267G>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114485655 | |||||||
| chr1:114485704 | G | A | 1 | a0001c0002t0005g0099 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.527-21316C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114485704 | |||||||
| chr1:114485854 | T | C | 6 | a0001c0006t0010g0119 a0001c0006t0010g0120 a0001c0006t0010g0121 others(3): Show |
6 | HG02132.hp2 HG02698.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.527-21466A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114485854 | |||||||
| chr1:114486004 | G | C | 21 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(18): Show |
21 | HG00323.hp1 HG00738.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.527-21616C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114486004 | |||||||
| chr1:114486100 | C | T | 1 | a0001c0002t0038g0118 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.527-21712G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114486100 | |||||||
| chr1:114486112 | C | A | 1 | a0002c0003t0008g0048 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.527-21724G>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114486112 | |||||||
| chr1:114486113 | T | C | 18 | a0001c0002t0004g0111 a0001c0002t0004g0114 a0001c0002t0004g0115 others(15): Show |
18 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.527-21725A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114486113 | |||||||
| chr1:114486487 | C | T | 3 | a0001c0002t0006g0086 a0001c0002t0023g0002 a0001c0002t0035g0085 |
3 | HG02970.hp2 HG03516.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.527-22099G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114486487 | |||||||
| chr1:114486546 | C | CA | 81 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0077 others(78): Show |
81 | HG00438.hp1 HG00558.hp2 HG00642.hp1 others(78): Show |
intron_variant | MODIFIER | c.527-22159dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114486546 | |||||||
| chr1:114486546 | C | CAA | 15 | a0001c0001t0002g0148 a0001c0001t0002g0153 a0001c0001t0002g0156 others(12): Show |
15 | HG00099.hp1 HG01106.hp1 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.527-22160_527-2215 others(6): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114486546 | |||||||
| chr1:114486546 | CA | C | 5 | a0001c0002t0018g0145 a0001c0002t0034g0117 a0003c0004t0014g0005 others(2): Show |
5 | HG02055.hp2 HG02451.hp2 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.527-22159delT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114486546 | |||||||
| chr1:114486643 | C | G | 1 | a0001c0001t0042g0062 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.527-22255G>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114486643 | |||||||
| chr1:114486956 | G | A | 8 | a0003c0004t0001g0008 a0003c0004t0004g0006 a0003c0004t0004g0009 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.527-22568C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114486956 | |||||||
| chr1:114486996 | C | T | 1 | a0001c0001t0002g0153 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.527-22608G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114486996 | |||||||
| chr1:114487044 | G | A | 1 | a0001c0001t0017g0176 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.527-22656C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114487044 | |||||||
| chr1:114487086 | C | CA | 39 | a0001c0001t0001g0070 a0001c0001t0001g0180 a0001c0001t0002g0039 others(36): Show |
39 | HG00438.hp1 HG00558.hp2 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.527-22699dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114487086 | |||||||
| chr1:114487235 | T | C | 1 | a0003c0004t0004g0009 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.527-22847A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114487235 | |||||||
| chr1:114487339 | C | CA | 27 | a0001c0001t0001g0027 a0001c0001t0001g0071 a0001c0001t0001g0077 others(24): Show |
27 | HG00642.hp1 HG00642.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.527-22952dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114487339 | |||||||
| chr1:114487504 | A | G | 1 | a0001c0001t0001g0026 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.526+23047T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114487504 | |||||||
| chr1:114487619 | C | T | 4 | a0001c0002t0009g0202 a0001c0002t0009g0203 a0001c0002t0009g0204 others(1): Show |
4 | HG01891.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.526+22932G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114487619 | |||||||
| chr1:114487635 | C | T | 1 | a0001c0002t0038g0118 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.526+22916G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114487635 | |||||||
| chr1:114487681 | A | C | 4 | a0001c0005t0007g0147 a0001c0005t0007g0150 a0001c0005t0007g0151 others(1): Show |
4 | HG01884.hp1 HG02897.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.526+22870T>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114487681 | |||||||
| chr1:114487697 | A | C | 1 | a0001c0001t0004g0059 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.526+22854T>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114487697 | |||||||
| chr1:114487724 | C | T | 1 | a0002c0003t0001g0017 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.526+22827G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114487724 | |||||||
| chr1:114487766 | G | A | 4 | a0001c0001t0002g0158 a0001c0001t0002g0159 a0001c0001t0002g0160 others(1): Show |
4 | NA18942.hp1 NA18970.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.526+22785C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114487766 | |||||||
| chr1:114487770 | G | A | 1 | a0002c0003t0001g0041 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.526+22781C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114487770 | |||||||
| chr1:114487790 | G | A | 6 | a0001c0006t0010g0119 a0001c0006t0010g0120 a0001c0006t0010g0121 others(3): Show |
6 | HG02132.hp2 HG02698.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.526+22761C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114487790 | |||||||
| chr1:114487839 | A | G | 80 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(77): Show |
80 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.526+22712T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114487839 | |||||||
| chr1:114487903 | C | CA | 45 | a0001c0001t0001g0022 a0001c0001t0001g0025 a0001c0001t0001g0027 others(42): Show |
45 | HG00438.hp2 HG01175.hp1 HG01175.hp2 others(42): Show |
intron_variant | MODIFIER | c.526+22647dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114487903 | |||||||
| chr1:114487903 | C | CAA | 13 | a0001c0001t0024g0003 a0001c0002t0005g0098 a0001c0002t0005g0103 others(10): Show |
13 | HG00099.hp1 HG01192.hp1 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.526+22646_526+2264 others(6): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114487903 | |||||||
| chr1:114487903 | C | CAAA | 8 | a0001c0002t0006g0087 a0001c0002t0021g0092 a0001c0002t0025g0004 others(5): Show |
8 | HG00735.hp1 HG01106.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.526+22645_526+2264 others(7): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114487903 | |||||||
| chr1:114487903 | CA | C | 15 | a0001c0001t0001g0020 a0001c0001t0001g0060 a0001c0001t0001g0061 others(12): Show |
15 | HG00642.hp2 HG01074.hp2 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.526+22647delT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114487903 | |||||||
| chr1:114487903 | CAAAAAAA others(3): Show |
C | 1 | a0001c0002t0003g0127 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.526+22638_526+2264 others(14): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114487903 | |||||||
| chr1:114487919 | AAAAAAAA others(5): Show |
A | 1 | a0003c0004t0004g0009 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.526+22620_526+2263 others(16): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114487919 | |||||||
| chr1:114487931 | T | A | 6 | a0003c0004t0001g0008 a0003c0004t0004g0006 a0003c0004t0013g0007 others(3): Show |
6 | HG02258.hp1 HG02280.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.526+22620A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114487931 | |||||||
| chr1:114487932 | G | T | 15 | a0001c0002t0006g0086 a0001c0002t0006g0087 a0001c0002t0006g0088 others(12): Show |
15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.526+22619C>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114487932 | |||||||
| chr1:114488777 | C | A | 3 | a0001c0001t0001g0180 a0001c0001t0002g0163 a0001c0001t0002g0179 |
3 | HG03710.hp1 HG03834.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.526+21774G>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114488777 | |||||||
| chr1:114488923 | C | T | 1 | a0001c0001t0002g0163 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.526+21628G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114488923 | |||||||
| chr1:114488950 | T | A | 1 | a0001c0002t0038g0118 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.526+21601A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114488950 | |||||||
| chr1:114489072 | T | C | 2 | a0003c0004t0001g0008 a0003c0004t0004g0009 |
2 | HG02965.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.526+21479A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114489072 | |||||||
| chr1:114489098 | A | C | 3 | a0001c0002t0005g0098 a0001c0002t0005g0099 a0001c0002t0005g0102 |
3 | HG01433.hp2 HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.526+21453T>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114489098 | |||||||
| chr1:114489212 | C | T | 1 | a0001c0001t0002g0162 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.526+21339G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114489212 | |||||||
| chr1:114489236 | A | G | 1 | a0001c0001t0001g0058 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.526+21315T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114489236 | |||||||
| chr1:114489523 | C | T | 15 | a0001c0002t0006g0086 a0001c0002t0006g0087 a0001c0002t0006g0088 others(12): Show |
15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.526+21028G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114489523 | |||||||
| chr1:114489524 | G | A | 1 | a0001c0002t0038g0118 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.526+21027C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114489524 | |||||||
| chr1:114489569 | T | G | 1 | a0001c0002t0003g0144 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.526+20982A>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114489569 | |||||||
| chr1:114489650 | T | A | 15 | a0001c0002t0006g0086 a0001c0002t0006g0087 a0001c0002t0006g0088 others(12): Show |
15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.526+20901A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114489650 | |||||||
| chr1:114489767 | A | T | 47 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(44): Show |
47 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.526+20784T>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114489767 | |||||||
| chr1:114489934 | A | G | 1 | a0003c0004t0032g0011 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.526+20617T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114489934 | |||||||
| chr1:114489973 | G | C | 1 | a0003c0004t0032g0011 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.526+20578C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114489973 | |||||||
| chr1:114490019 | G | T | 2 | a0001c0001t0022g0056 a0001c0001t0022g0057 |
2 | HG03704.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.526+20532C>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114490019 | |||||||
| chr1:114490029 | T | C | 68 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(65): Show |
68 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.526+20522A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114490029 | |||||||
| chr1:114490030 | T | C | 60 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(57): Show |
60 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.526+20521A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114490030 | |||||||
| chr1:114490084 | C | CA | 24 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0141 others(21): Show |
24 | HG00642.hp1 HG00738.hp2 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.526+20466dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114490084 | |||||||
| chr1:114490084 | C | CAA | 5 | a0001c0001t0048g0081 a0001c0002t0019g0100 a0001c0002t0038g0118 others(2): Show |
5 | HG01257.hp2 HG02132.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.526+20465_526+2046 others(6): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114490084 | |||||||
| chr1:114490084 | C | CAAAAAAA others(3): Show |
1 | a0001c0002t0005g0104 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.526+20457_526+2046 others(14): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114490084 | |||||||
| chr1:114490084 | C | CAAAAAAA others(9): Show |
1 | a0001c0002t0005g0105 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.526+20451_526+2046 others(20): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114490084 | |||||||
| chr1:114490084 | C | CAAAAAAA others(10): Show |
3 | a0001c0002t0005g0099 a0001c0002t0005g0106 a0001c0002t0005g0107 |
3 | HG01192.hp1 HG02922.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.526+20450_526+2046 others(21): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114490084 | |||||||
| chr1:114490084 | C | CAAAAAAA others(11): Show |
4 | a0001c0002t0005g0098 a0001c0002t0005g0108 a0001c0002t0005g0109 others(1): Show |
4 | HG01261.hp2 HG02615.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.526+20449_526+2046 others(22): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114490084 | |||||||
| chr1:114490084 | CA | C | 6 | a0001c0001t0001g0200 a0001c0001t0002g0190 a0001c0001t0011g0054 others(3): Show |
6 | HG01099.hp2 HG01169.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.526+20466delT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114490084 | |||||||
| chr1:114490101 | A | G | 2 | a0001c0002t0006g0086 a0001c0002t0035g0085 |
2 | HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.526+20450T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114490101 | |||||||
| chr1:114490103 | AAG | A | 8 | a0001c0002t0004g0111 a0001c0002t0004g0114 a0001c0002t0004g0115 others(5): Show |
8 | HG01433.hp2 HG01884.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.526+20446_526+2044 others(6): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114490103 | |||||||
| chr1:114490105 | G | A | 63 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(60): Show |
63 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.526+20446C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114490105 | |||||||
| chr1:114490106 | AAAAGG | A | 3 | a0003c0004t0004g0006 a0003c0004t0013g0007 a0003c0004t0050g0206 |
3 | HG02280.hp1 HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.526+20440_526+2044 others(9): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114490106 | |||||||
| chr1:114490111 | G | A | 77 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(74): Show |
77 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(74): Show |
intron_variant | MODIFIER | c.526+20440C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114490111 | |||||||
| chr1:114490136 | GA | G | 4 | a0001c0001t0002g0158 a0001c0001t0002g0159 a0001c0001t0002g0160 others(1): Show |
4 | NA18942.hp1 NA18970.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.526+20414delT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114490136 | |||||||
| chr1:114490137 | A | G | 12 | a0001c0002t0005g0098 a0001c0002t0005g0099 a0001c0002t0005g0102 others(9): Show |
12 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.526+20414T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114490137 | |||||||
| chr1:114490212 | C | T | 1 | a0001c0002t0033g0116 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.526+20339G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114490212 | |||||||
| chr1:114490270 | G | A | 2 | a0001c0002t0018g0145 a0001c0002t0018g0146 |
2 | HG00741.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.526+20281C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114490270 | |||||||
| chr1:114490517 | C | T | 1 | a0001c0001t0024g0003 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.526+20034G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114490517 | |||||||
| chr1:114490890 | C | T | 80 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(77): Show |
80 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.526+19661G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114490890 | |||||||
| chr1:114491057 | T | C | 1 | a0001c0001t0001g0072 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.526+19494A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114491057 | |||||||
| chr1:114491211 | T | C | 1 | a0001c0001t0002g0189 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.526+19340A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114491211 | |||||||
| chr1:114491217 | T | C | 2 | a0001c0001t0001g0026 a0001c0001t0001g0027 |
2 | HG02809.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.526+19334A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114491217 | |||||||
| chr1:114491318 | C | A | 1 | a0001c0001t0001g0073 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.526+19233G>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114491318 | |||||||
| chr1:114491427 | A | G | 2 | a0001c0001t0001g0083 a0001c0001t0004g0050 |
2 | HG02055.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.526+19124T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114491427 | |||||||
| chr1:114491549 | C | G | 6 | a0001c0002t0004g0111 a0001c0002t0004g0114 a0001c0002t0004g0115 others(3): Show |
6 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.526+19002G>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114491549 | |||||||
| chr1:114491636 | T | A | 5 | a0003c0004t0001g0008 a0003c0004t0004g0009 a0003c0004t0013g0010 others(2): Show |
5 | HG02145.hp1 HG02258.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.526+18915A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114491636 | |||||||
| chr1:114491647 | G | A | 80 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(77): Show |
80 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.526+18904C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114491647 | |||||||
| chr1:114491741 | T | C | 1 | a0001c0001t0002g0181 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.526+18810A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114491741 | |||||||
| chr1:114491918 | C | T | 1 | a0001c0001t0048g0081 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.526+18633G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114491918 | |||||||
| chr1:114491933 | T | C | 2 | a0001c0002t0018g0145 a0001c0002t0018g0146 |
2 | HG00741.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.526+18618A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114491933 | |||||||
| chr1:114491962 | G | C | 6 | a0001c0006t0010g0119 a0001c0006t0010g0120 a0001c0006t0010g0121 others(3): Show |
6 | HG02132.hp2 HG02698.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.526+18589C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114491962 | |||||||
| chr1:114492087 | C | G | 80 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(77): Show |
80 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.526+18464G>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114492087 | |||||||
| chr1:114492091 | T | A | 15 | a0001c0002t0006g0086 a0001c0002t0006g0087 a0001c0002t0006g0088 others(12): Show |
15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.526+18460A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114492091 | |||||||
| chr1:114492391 | A | G | 1 | a0001c0001t0002g0195 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.526+18160T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114492391 | |||||||
| chr1:114492469 | A | G | 6 | a0001c0002t0004g0111 a0001c0002t0004g0114 a0001c0002t0004g0115 others(3): Show |
6 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.526+18082T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114492469 | |||||||
| chr1:114492501 | T | C | 1 | a0001c0001t0002g0153 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.526+18050A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114492501 | |||||||
| chr1:114492699 | A | C | 2 | a0001c0002t0018g0145 a0001c0002t0018g0146 |
2 | HG00741.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.526+17852T>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114492699 | |||||||
| chr1:114492842 | G | A | 1 | a0001c0001t0002g0182 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.526+17709C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114492842 | |||||||
| chr1:114492897 | T | A | 3 | a0003c0004t0004g0006 a0003c0004t0013g0007 a0003c0004t0050g0206 |
3 | HG02280.hp1 HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.526+17654A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114492897 | |||||||
| chr1:114492923 | T | C | 1 | a0001c0001t0002g0183 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.526+17628A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114492923 | |||||||
| chr1:114493206 | G | C | 21 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(18): Show |
21 | HG00323.hp1 HG00738.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.526+17345C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114493206 | |||||||
| chr1:114493491 | C | A | 1 | a0001c0001t0002g0184 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.526+17060G>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114493491 | |||||||
| chr1:114493634 | T | C | 80 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(77): Show |
80 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.526+16917A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114493634 | |||||||
| chr1:114493759 | C | T | 13 | a0001c0001t0002g0148 a0001c0001t0002g0155 a0001c0001t0002g0156 others(10): Show |
13 | HG01175.hp2 HG01884.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.526+16792G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114493759 | |||||||
| chr1:114493768 | G | C | 1 | a0001c0009t0040g0123 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.526+16783C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114493768 | |||||||
| chr1:114493912 | C | T | 2 | a0002c0003t0001g0028 a0002c0003t0001g0029 |
2 | HG01928.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.526+16639G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114493912 | |||||||
| chr1:114493957 | C | T | 2 | a0003c0004t0001g0008 a0003c0004t0004g0009 |
2 | HG02965.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.526+16594G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114493957 | |||||||
| chr1:114494045 | G | A | 1 | a0001c0002t0038g0118 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.526+16506C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114494045 | |||||||
| chr1:114494098 | T | C | 1 | a0001c0002t0038g0118 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.526+16453A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114494098 | |||||||
| chr1:114494118 | C | T | 4 | a0001c0002t0009g0202 a0001c0002t0009g0203 a0001c0002t0009g0204 others(1): Show |
4 | HG01891.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.526+16433G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114494118 | |||||||
| chr1:114494123 | AT | A | 67 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(64): Show |
67 | HG00323.hp1 HG00738.hp1 HG00741.hp2 others(64): Show |
intron_variant | MODIFIER | c.526+16427delA | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114494123 | |||||||
| chr1:114494497 | T | C | 12 | a0001c0002t0005g0098 a0001c0002t0005g0099 a0001c0002t0005g0102 others(9): Show |
12 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.526+16054A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114494497 | |||||||
| chr1:114494569 | G | A | 1 | a0001c0002t0034g0117 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.526+15982C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114494569 | |||||||
| chr1:114494598 | G | C | 4 | a0001c0001t0001g0052 a0001c0001t0001g0074 a0001c0001t0001g0075 others(1): Show |
4 | HG01081.hp1 HG01952.hp1 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.526+15953C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114494598 | |||||||
| chr1:114494791 | A | C | 1 | a0001c0002t0006g0087 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.526+15760T>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114494791 | |||||||
| chr1:114494872 | T | C | 3 | a0003c0004t0013g0010 a0003c0004t0032g0011 a0003c0008t0013g0015 |
3 | HG02145.hp1 HG02258.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.526+15679A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114494872 | |||||||
| chr1:114494910 | A | AGTTGTT | 8 | a0003c0004t0001g0008 a0003c0004t0004g0006 a0003c0004t0004g0009 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.526+15635_526+1564 others(10): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114494910 | |||||||
| chr1:114495024 | G | A | 5 | a0001c0002t0006g0093 a0001c0002t0006g0094 a0001c0002t0006g0095 others(2): Show |
5 | HG02280.hp2 HG02723.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.526+15527C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114495024 | |||||||
| chr1:114495038 | C | T | 2 | a0001c0002t0018g0145 a0001c0002t0018g0146 |
2 | HG00741.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.526+15513G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114495038 | |||||||
| chr1:114495077 | C | T | 3 | a0001c0001t0001g0022 a0001c0001t0004g0023 a0001c0001t0024g0003 |
3 | HG02615.hp2 HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.526+15474G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114495077 | |||||||
| chr1:114495455 | C | T | 1 | a0001c0001t0002g0153 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.526+15096G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114495455 | |||||||
| chr1:114495533 | G | C | 19 | a0001c0002t0004g0111 a0001c0002t0004g0114 a0001c0002t0004g0115 others(16): Show |
19 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.526+15018C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114495533 | |||||||
| chr1:114495659 | G | C | 1 | a0001c0001t0001g0077 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.526+14892C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114495659 | |||||||
| chr1:114495994 | T | C | 1 | a0003c0004t0004g0009 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.526+14557A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114495994 | |||||||
| chr1:114496156 | G | A | 5 | a0003c0004t0001g0008 a0003c0004t0004g0009 a0003c0004t0013g0010 others(2): Show |
5 | HG02145.hp1 HG02258.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.526+14395C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114496156 | |||||||
| chr1:114496277 | T | C | 12 | a0001c0002t0005g0098 a0001c0002t0005g0099 a0001c0002t0005g0102 others(9): Show |
12 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.526+14274A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114496277 | |||||||
| chr1:114496497 | T | C | 80 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(77): Show |
80 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.526+14054A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114496497 | |||||||
| chr1:114496521 | A | G | 80 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(77): Show |
80 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.526+14030T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114496521 | |||||||
| chr1:114496527 | T | C | 6 | a0001c0001t0002g0185 a0001c0001t0002g0186 a0001c0001t0002g0189 others(3): Show |
6 | HG01891.hp1 HG02622.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.526+14024A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114496527 | |||||||
| chr1:114496551 | G | A | 1 | a0001c0002t0038g0118 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.526+14000C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114496551 | |||||||
| chr1:114496581 | T | G | 6 | a0001c0006t0010g0119 a0001c0006t0010g0120 a0001c0006t0010g0121 others(3): Show |
6 | HG02132.hp2 HG02698.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.526+13970A>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114496581 | |||||||
| chr1:114496627 | A | T | 3 | a0001c0002t0005g0098 a0001c0002t0005g0099 a0001c0002t0005g0102 |
3 | HG01433.hp2 HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.526+13924T>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114496627 | |||||||
| chr1:114496646 | A | T | 54 | a0001c0001t0001g0166 a0001c0001t0001g0180 a0001c0001t0002g0148 others(51): Show |
54 | HG00438.hp1 HG00558.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.526+13905T>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114496646 | |||||||
| chr1:114496690 | T | C | 6 | a0001c0002t0004g0111 a0001c0002t0004g0114 a0001c0002t0004g0115 others(3): Show |
6 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.526+13861A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114496690 | |||||||
| chr1:114496951 | T | C | 2 | a0001c0005t0007g0147 a0001c0005t0007g0152 |
2 | HG01884.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.526+13600A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114496951 | |||||||
| chr1:114497059 | T | C | 4 | a0001c0002t0009g0202 a0001c0002t0009g0203 a0001c0002t0009g0204 others(1): Show |
4 | HG01891.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.526+13492A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114497059 | |||||||
| chr1:114497087 | T | A | 1 | a0001c0002t0006g0097 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.526+13464A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114497087 | |||||||
| chr1:114497296 | A | G | 54 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(51): Show |
54 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.526+13255T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114497296 | |||||||
| chr1:114497357 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.526+13194G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114497357 | |||||||
| chr1:114497358 | G | A | 2 | a0001c0002t0006g0086 a0001c0002t0035g0085 |
2 | HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.526+13193C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114497358 | |||||||
| chr1:114497662 | C | A | 1 | a0001c0002t0004g0111 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.526+12889G>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114497662 | |||||||
| chr1:114497869 | A | G | 4 | a0001c0002t0009g0202 a0001c0002t0009g0203 a0001c0002t0009g0204 others(1): Show |
4 | HG01891.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.526+12682T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114497869 | |||||||
| chr1:114497879 | G | GA | 10 | a0001c0002t0005g0102 a0001c0002t0005g0103 a0001c0002t0005g0104 others(7): Show |
10 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.526+12671dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114497879 | |||||||
| chr1:114497967 | T | C | 1 | a0001c0001t0044g0016 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.526+12584A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114497967 | |||||||
| chr1:114498050 | T | A | 1 | a0001c0001t0001g0078 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.526+12501A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114498050 | |||||||
| chr1:114498126 | C | CA | 17 | a0001c0001t0001g0020 a0001c0001t0002g0190 a0001c0001t0002g0191 others(14): Show |
17 | HG00642.hp2 HG01074.hp2 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.526+12424dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114498126 | |||||||
| chr1:114498126 | C | CAA | 58 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(55): Show |
58 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(55): Show |
intron_variant | MODIFIER | c.526+12423_526+1242 others(6): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114498126 | |||||||
| chr1:114498203 | A | G | 3 | a0003c0004t0004g0006 a0003c0004t0013g0007 a0003c0004t0050g0206 |
3 | HG02280.hp1 HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.526+12348T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114498203 | |||||||
| chr1:114498310 | C | T | 144 | a0001c0001t0001g0022 a0001c0001t0001g0025 a0001c0001t0001g0026 others(141): Show |
144 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.526+12241G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114498310 | |||||||
| chr1:114498493 | A | C | 2 | a0001c0002t0006g0086 a0001c0002t0035g0085 |
2 | HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.526+12058T>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114498493 | |||||||
| chr1:114498713 | C | A | 1 | a0001c0002t0034g0117 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.526+11838G>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114498713 | |||||||
| chr1:114498715 | G | C | 1 | a0001c0002t0034g0117 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.526+11836C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114498715 | |||||||
| chr1:114498758 | G | A | 21 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(18): Show |
21 | HG00323.hp1 HG00738.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.526+11793C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114498758 | |||||||
| chr1:114499458 | G | A | 2 | a0001c0001t0001g0083 a0001c0001t0004g0050 |
2 | HG02055.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.526+11093C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114499458 | |||||||
| chr1:114499459 | G | C | 8 | a0003c0004t0001g0008 a0003c0004t0004g0006 a0003c0004t0004g0009 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.526+11092C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114499459 | |||||||
| chr1:114499473 | G | T | 204 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0022 others(201): Show |
205 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.526+11078C>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114499473 | |||||||
| chr1:114499793 | C | T | 65 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(62): Show |
65 | HG00323.hp1 HG00738.hp1 HG00741.hp2 others(62): Show |
intron_variant | MODIFIER | c.526+10758G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114499793 | |||||||
| chr1:114499860 | C | T | 80 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(77): Show |
80 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.526+10691G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114499860 | |||||||
| chr1:114499889 | A | G | 80 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(77): Show |
80 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.526+10662T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114499889 | |||||||
| chr1:114499923 | G | C | 12 | a0001c0002t0005g0098 a0001c0002t0005g0099 a0001c0002t0005g0102 others(9): Show |
12 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.526+10628C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114499923 | |||||||
| chr1:114499941 | A | G | 2 | a0001c0006t0010g0121 a0001c0006t0010g0122 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.526+10610T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114499941 | |||||||
| chr1:114500111 | G | A | 1 | a0001c0002t0029g0135 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.526+10440C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114500111 | |||||||
| chr1:114500160 | C | G | 1 | a0001c0001t0001g0052 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.526+10391G>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114500160 | |||||||
| chr1:114500362 | G | T | 2 | a0001c0002t0009g0204 a0001c0002t0009g0205 |
2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.526+10189C>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114500362 | |||||||
| chr1:114500568 | G | GA | 12 | a0001c0002t0005g0098 a0001c0002t0005g0099 a0001c0002t0005g0102 others(9): Show |
12 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.526+9982dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114500568 | |||||||
| chr1:114500608 | TA | T | 11 | a0001c0001t0015g0051 a0001c0005t0007g0147 a0001c0005t0007g0150 others(8): Show |
11 | HG00099.hp2 HG01884.hp1 HG02132.hp2 others(8): Show |
intron_variant | MODIFIER | c.526+9942delT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114500608 | |||||||
| chr1:114500898 | CAAGAATT others(305): Show |
C | 80 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(77): Show |
80 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.526+9341_526+9652d others(2): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114500898 | |||||||
| chr1:114501010 | A | G | 124 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0022 others(121): Show |
125 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.526+9541T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114501010 | |||||||
| chr1:114501047 | G | C | 2 | a0001c0001t0001g0026 a0001c0001t0001g0027 |
2 | HG02809.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.526+9504C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114501047 | |||||||
| chr1:114501189 | C | A | 1 | a0001c0001t0012g0174 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.526+9362G>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114501189 | |||||||
| chr1:114501189 | C | CA | 11 | a0001c0001t0001g0075 a0001c0001t0002g0164 a0001c0001t0004g0050 others(8): Show |
11 | HG01081.hp1 HG01081.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.526+9361dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114501189 | |||||||
| chr1:114501223 | G | C | 8 | a0003c0004t0001g0008 a0003c0004t0004g0006 a0003c0004t0004g0009 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.526+9328C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114501223 | |||||||
| chr1:114501363 | G | GT | 43 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(40): Show |
43 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.526+9187dupA | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114501363 | |||||||
| chr1:114501408 | G | A | 15 | a0001c0002t0006g0086 a0001c0002t0006g0087 a0001c0002t0006g0088 others(12): Show |
15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.526+9143C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114501408 | |||||||
| chr1:114501627 | AAGGGGCC others(5): Show |
A | 1 | a0001c0002t0038g0118 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.526+8912_526+8923d others(14): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114501627 | |||||||
| chr1:114501665 | T | A | 4 | a0001c0002t0009g0202 a0001c0002t0009g0203 a0001c0002t0009g0204 others(1): Show |
4 | HG01891.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.526+8886A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114501665 | |||||||
| chr1:114501821 | T | TATA | 204 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0022 others(201): Show |
205 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.526+8727_526+8729d others(5): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114501821 | |||||||
| chr1:114502245 | C | T | 1 | a0002c0003t0001g0021 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.526+8306G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114502245 | |||||||
| chr1:114502259 | A | C | 1 | a0001c0002t0004g0111 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.526+8292T>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114502259 | |||||||
| chr1:114502710 | T | C | 1 | a0001c0001t0002g0195 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.526+7841A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114502710 | |||||||
| chr1:114502714 | C | T | 2 | a0001c0006t0010g0119 a0001c0006t0010g0120 |
2 | HG02922.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.526+7837G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114502714 | |||||||
| chr1:114502718 | G | C | 1 | a0004c0007t0001g0014 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.526+7833C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114502718 | |||||||
| chr1:114502834 | A | C | 1 | a0001c0009t0040g0123 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.526+7717T>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114502834 | |||||||
| chr1:114502926 | T | C | 2 | a0001c0002t0018g0145 a0001c0002t0018g0146 |
2 | HG00741.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.526+7625A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114502926 | |||||||
| chr1:114503043 | T | C | 35 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0052 others(32): Show |
35 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.526+7508A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114503043 | |||||||
| chr1:114503043 | T | TTA | 6 | a0001c0002t0004g0111 a0001c0002t0004g0114 a0001c0002t0004g0115 others(3): Show |
6 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.526+7507_526+7508i others(4): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114503043 | |||||||
| chr1:114503434 | C | T | 2 | a0001c0001t0001g0019 a0001c0001t0001g0020 |
2 | HG00741.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.526+7117G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114503434 | |||||||
| chr1:114503758 | C | T | 2 | a0001c0002t0018g0145 a0001c0002t0018g0146 |
2 | HG00741.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.526+6793G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114503758 | |||||||
| chr1:114503951 | T | G | 204 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0022 others(201): Show |
205 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.526+6600A>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114503951 | |||||||
| chr1:114503955 | G | A | 15 | a0001c0002t0006g0086 a0001c0002t0006g0087 a0001c0002t0006g0088 others(12): Show |
15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.526+6596C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114503955 | |||||||
| chr1:114504104 | T | A | 1 | a0001c0002t0034g0117 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.526+6447A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114504104 | |||||||
| chr1:114504165 | A | AT | 4 | a0001c0006t0010g0119 a0001c0006t0010g0120 a0001c0006t0010g0121 others(1): Show |
4 | HG02895.hp2 HG02897.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.526+6385dupA | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114504165 | |||||||
| chr1:114504301 | G | A | 1 | a0001c0002t0034g0117 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.526+6250C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114504301 | |||||||
| chr1:114504462 | G | A | 1 | a0001c0002t0034g0117 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.526+6089C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114504462 | |||||||
| chr1:114504485 | T | C | 2 | a0001c0001t0001g0079 a0001c0001t0001g0080 |
2 | NA18970.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.526+6066A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114504485 | |||||||
| chr1:114504510 | G | A | 1 | a0001c0001t0048g0081 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.526+6041C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114504510 | |||||||
| chr1:114504862 | A | C | 23 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(20): Show |
23 | HG00323.hp1 HG00738.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.526+5689T>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114504862 | |||||||
| chr1:114504927 | G | A | 80 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(77): Show |
80 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.526+5624C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114504927 | |||||||
| chr1:114504956 | G | C | 15 | a0001c0002t0006g0086 a0001c0002t0006g0087 a0001c0002t0006g0088 others(12): Show |
15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.526+5595C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114504956 | |||||||
| chr1:114505155 | G | A | 1 | a0001c0002t0033g0116 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.526+5396C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114505155 | |||||||
| chr1:114505215 | T | A | 12 | a0001c0002t0005g0098 a0001c0002t0005g0099 a0001c0002t0005g0102 others(9): Show |
12 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.526+5336A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114505215 | |||||||
| chr1:114505408 | G | A | 6 | a0001c0002t0004g0111 a0001c0002t0004g0114 a0001c0002t0004g0115 others(3): Show |
6 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.526+5143C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114505408 | |||||||
| chr1:114505491 | A | C | 2 | a0001c0002t0009g0202 a0001c0002t0009g0203 |
2 | HG01891.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.526+5060T>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114505491 | |||||||
| chr1:114505523 | CAT | C | 39 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(36): Show |
39 | HG00323.hp1 HG00738.hp1 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.526+5026_526+5027d others(4): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114505523 | |||||||
| chr1:114505524 | A | C | 1 | a0001c0002t0021g0089 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.526+5027T>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114505524 | |||||||
| chr1:114505628 | C | T | 8 | a0003c0004t0001g0008 a0003c0004t0004g0006 a0003c0004t0004g0009 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.526+4923G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114505628 | |||||||
| chr1:114505684 | C | T | 1 | a0002c0003t0001g0001 | 2 | HG01433.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.526+4867G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114505684 | |||||||
| chr1:114505724 | C | G | 6 | a0001c0002t0004g0111 a0001c0002t0004g0114 a0001c0002t0004g0115 others(3): Show |
6 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.526+4827G>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114505724 | |||||||
| chr1:114505815 | G | A | 6 | a0001c0002t0003g0136 a0001c0002t0003g0137 a0001c0002t0003g0138 others(3): Show |
6 | HG00323.hp1 HG01167.hp1 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.526+4736C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114505815 | |||||||
| chr1:114505819 | C | T | 1 | a0001c0001t0012g0197 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.526+4732G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114505819 | |||||||
| chr1:114506113 | G | A | 1 | a0001c0002t0034g0117 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.526+4438C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114506113 | |||||||
| chr1:114506207 | C | T | 1 | a0001c0001t0044g0016 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.526+4344G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114506207 | |||||||
| chr1:114506383 | C | CA | 38 | a0001c0001t0026g0196 a0001c0002t0003g0125 a0001c0002t0003g0126 others(35): Show |
38 | HG00099.hp1 HG00735.hp1 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.526+4167dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114506383 | |||||||
| chr1:114506383 | C | CAAA | 11 | a0001c0002t0005g0099 a0001c0002t0005g0102 a0001c0002t0005g0103 others(8): Show |
11 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.526+4165_526+4167d others(5): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114506383 | |||||||
| chr1:114506383 | CA | C | 12 | a0001c0001t0001g0083 a0001c0001t0002g0148 a0001c0001t0002g0149 others(9): Show |
12 | HG00738.hp1 HG02145.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.526+4167delT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114506383 | |||||||
| chr1:114506519 | AAT | A | 6 | a0001c0006t0010g0119 a0001c0006t0010g0120 a0001c0006t0010g0121 others(3): Show |
6 | HG02132.hp2 HG02698.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.526+4030_526+4031d others(4): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114506519 | |||||||
| chr1:114506657 | A | C | 1 | a0003c0004t0014g0005 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.526+3894T>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114506657 | |||||||
| chr1:114507062 | A | G | 15 | a0001c0002t0006g0086 a0001c0002t0006g0087 a0001c0002t0006g0088 others(12): Show |
15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.526+3489T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114507062 | |||||||
| chr1:114507073 | A | G | 6 | a0001c0002t0004g0111 a0001c0002t0004g0114 a0001c0002t0004g0115 others(3): Show |
6 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.526+3478T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114507073 | |||||||
| chr1:114507574 | C | CT | 2 | a0001c0002t0003g0125 a0001c0002t0003g0126 |
2 | HG01099.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.526+2976_526+2977i others(3): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114507574 | |||||||
| chr1:114507596 | T | C | 2 | a0001c0001t0002g0198 a0001c0001t0012g0197 |
2 | HG02145.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.526+2955A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114507596 | |||||||
| chr1:114507613 | T | C | 1 | a0002c0003t0001g0199 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.526+2938A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114507613 | |||||||
| chr1:114507891 | C | T | 4 | a0001c0002t0009g0202 a0001c0002t0009g0203 a0001c0002t0009g0204 others(1): Show |
4 | HG01891.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.526+2660G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114507891 | |||||||
| chr1:114507983 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.526+2568C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114507983 | |||||||
| chr1:114508111 | T | C | 5 | a0001c0002t0004g0114 a0001c0002t0004g0115 a0001c0002t0020g0112 others(2): Show |
5 | HG01884.hp2 HG02622.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.526+2440A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114508111 | |||||||
| chr1:114508228 | A | G | 6 | a0001c0002t0004g0111 a0001c0002t0004g0114 a0001c0002t0004g0115 others(3): Show |
6 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.526+2323T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114508228 | |||||||
| chr1:114508270 | G | A | 21 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(18): Show |
21 | HG00323.hp1 HG00738.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.526+2281C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114508270 | |||||||
| chr1:114508753 | G | A | 15 | a0001c0002t0006g0086 a0001c0002t0006g0087 a0001c0002t0006g0088 others(12): Show |
15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.526+1798C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114508753 | |||||||
| chr1:114508830 | T | G | 1 | a0001c0001t0001g0084 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.526+1721A>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114508830 | |||||||
| chr1:114508842 | C | T | 12 | a0001c0002t0005g0098 a0001c0002t0005g0099 a0001c0002t0005g0102 others(9): Show |
12 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.526+1709G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114508842 | |||||||
| chr1:114509224 | T | C | 2 | a0001c0002t0009g0204 a0001c0002t0009g0205 |
2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.526+1327A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114509224 | |||||||
| chr1:114509488 | A | C | 15 | a0001c0002t0006g0086 a0001c0002t0006g0087 a0001c0002t0006g0088 others(12): Show |
15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.526+1063T>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114509488 | |||||||
| chr1:114509730 | T | C | 2 | a0001c0002t0018g0145 a0001c0002t0018g0146 |
2 | HG00741.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.526+821A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114509730 | |||||||
| chr1:114509886 | T | C | 12 | a0003c0004t0001g0008 a0003c0004t0004g0006 a0003c0004t0004g0009 others(9): Show |
12 | HG02055.hp2 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.526+665A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114509886 | |||||||
| chr1:114509935 | C | G | 1 | a0001c0005t0007g0147 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.526+616G>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114509935 | |||||||
| chr1:114510044 | T | A | 80 | a0001c0002t0003g0125 a0001c0002t0003g0126 a0001c0002t0003g0127 others(77): Show |
80 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.526+507A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114510044 | |||||||
| chr1:114510087 | C | A | 54 | a0001c0001t0001g0166 a0001c0001t0001g0180 a0001c0001t0002g0148 others(51): Show |
54 | HG00438.hp1 HG00558.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.526+464G>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114510087 | |||||||
| chr1:114510191 | G | A | 1 | a0001c0002t0003g0201 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.526+360C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114510191 | |||||||
| chr1:114510191 | G | C | 1 | a0001c0001t0001g0200 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.526+360C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114510191 | |||||||
| chr1:114510283 | G | A | 4 | a0001c0002t0009g0202 a0001c0002t0009g0203 a0001c0002t0009g0204 others(1): Show |
4 | HG01891.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.526+268C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114510283 |