Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 8805 |
| ensemblid | ENSG00000122779.18 |
| hgncid | 11812 |
| symbol | TRIM24 |
| name | tripartite motif containing 24 |
| refseq_nuc | NM_015905.3 |
| refseq_prot | NP_056989.2 |
| ensembl_nuc | ENST00000343526.9 |
| ensembl_prot | ENSP00000340507.4 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 138460259 |
| end | 138589996 |
| strand | + |
| ver | v1.2 |
| region | chr7:138460259-138589996 |
| region5000 | chr7:138455259-138594996 |
| regionname0 | TRIM24_chr7_138460259_138589996 |
| regionname5000 | TRIM24_chr7_138455259_138594996 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1050 | 310 | 80 | 56 | 122 | 8 | 42 | 96 | TRIM24_chr7_138455259_138594996 | TRIM24 | MEVAV others(1045): Show |
chr7 | 138455259 | 138594996 |
| a0002 | 0/0 | 1050 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | MEVAV others(1045): Show |
chr7 | 138455259 | 138594996 |
| a0003 | 0/0 | 1050 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | MEVAV others(1045): Show |
chr7 | 138455259 | 138594996 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 3150 | 282 | 68 | 51 | 121 | 5 | 35 | TRIM24_chr7_138455259_138594996 | TRIM24 | ATGGA others(3145): Show |
chr7 | 138455259 | 138594996 | ||
| a0001c0002 | 0/0 | 3150 | 18 | 3 | 5 | 1 | 2 | 7 | TRIM24_chr7_138455259_138594996 | TRIM24 | ATGGA others(3145): Show |
chr7 | 138455259 | 138594996 | ||
| a0001c0003 | 0/0 | 3150 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | ATGGA others(3145): Show |
chr7 | 138455259 | 138594996 | ||
| a0001c0004 | 0/0 | 3150 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | ATGGA others(3145): Show |
chr7 | 138455259 | 138594996 | ||
| a0001c0005 | 0/0 | 3150 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | ATGGA others(3145): Show |
chr7 | 138455259 | 138594996 | ||
| a0001c0007 | 0/0 | 3150 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | ATGGA others(3145): Show |
chr7 | 138455259 | 138594996 | ||
| a0001c0009 | 0/0 | 3150 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | ATGGA others(3145): Show |
chr7 | 138455259 | 138594996 | ||
| a0001c0010 | 0/0 | 3150 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | ATGGA others(3145): Show |
chr7 | 138455259 | 138594996 | ||
| a0002c0006 | 0/0 | 3150 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | ATGGA others(3145): Show |
chr7 | 138455259 | 138594996 | ||
| a0003c0008 | 0/0 | 3150 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | ATGGA others(3145): Show |
chr7 | 138455259 | 138594996 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 8484 | 84 | 6 | 15 | 54 | 2 | 7 | TRIM24_chr7_138455259_138594996 | TRIM24 | GTATT others(8479): Show |
chr7 | 138455259 | 138594996 |
| a0001c0001t0002 | 0/0 | 8488 | 68 | 6 | 6 | 45 | 2 | 9 | TRIM24_chr7_138455259_138594996 | TRIM24 | GTATT others(8483): Show |
chr7 | 138455259 | 138594996 |
| a0001c0001t0003 | 0/1 | 8487 | 32 | 11 | 14 | 0 | 1 | 5 | TRIM24_chr7_138455259_138594996 | TRIM24 | GTATT others(8482): Show |
chr7 | 138455259 | 138594996 |
| a0001c0001t0004 | 0/0 | 8488 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | GTATT others(8483): Show |
chr7 | 138455259 | 138594996 |
| a0001c0001t0005 | 0/0 | 8483 | 7 | 0 | 0 | 5 | 0 | 2 | TRIM24_chr7_138455259_138594996 | TRIM24 | GTATT others(8478): Show |
chr7 | 138455259 | 138594996 |
| a0001c0001t0006 | 0/0 | 8488 | 6 | 6 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | GTATT others(8483): Show |
chr7 | 138455259 | 138594996 |
| a0001c0001t0007 | 0/0 | 8488 | 6 | 0 | 0 | 6 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | GTATT others(8483): Show |
chr7 | 138455259 | 138594996 |
| a0001c0001t0008 | 0/0 | 8487 | 5 | 4 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | GTATT others(8482): Show |
chr7 | 138455259 | 138594996 |
| a0001c0001t0009 | 0/0 | 8487 | 5 | 0 | 4 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | GTATT others(8482): Show |
chr7 | 138455259 | 138594996 |
| a0001c0001t0010 | 0/0 | 8487 | 5 | 5 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | GTATT others(8482): Show |
chr7 | 138455259 | 138594996 |
| a0001c0001t0011 | 0/0 | 8487 | 5 | 2 | 0 | 0 | 0 | 3 | TRIM24_chr7_138455259_138594996 | TRIM24 | GTATT others(8482): Show |
chr7 | 138455259 | 138594996 |
| a0001c0001t0012 | 0/0 | 8488 | 4 | 2 | 1 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | GTATT others(8483): Show |
chr7 | 138455259 | 138594996 |
| a0001c0001t0016 | 0/0 | 8487 | 3 | 2 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | GTATT others(8482): Show |
chr7 | 138455259 | 138594996 |
| a0001c0001t0017 | 0/0 | 8492 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | GTATT others(8487): Show |
chr7 | 138455259 | 138594996 |
| a0001c0001t0018 | 0/0 | 8488 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | GTATT others(8483): Show |
chr7 | 138455259 | 138594996 |
| a0001c0001t0019 | 0/0 | 8487 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | GTATT others(8482): Show |
chr7 | 138455259 | 138594996 |
| a0001c0001t0020 | 0/0 | 8488 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | GTATT others(8483): Show |
chr7 | 138455259 | 138594996 |
| a0001c0001t0021 | 0/0 | 8489 | 2 | 1 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | GTATT others(8484): Show |
chr7 | 138455259 | 138594996 |
| a0001c0001t0022 | 0/0 | 8488 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | GTATT others(8483): Show |
chr7 | 138455259 | 138594996 |
| a0001c0001t0023 | 0/0 | 8488 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM24_chr7_138455259_138594996 | TRIM24 | GTATT others(8483): Show |
chr7 | 138455259 | 138594996 |
| a0001c0001t0024 | 0/0 | 8488 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | GTATT others(8483): Show |
chr7 | 138455259 | 138594996 |
| a0001c0001t0025 | 0/0 | 8489 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | GTATT others(8484): Show |
chr7 | 138455259 | 138594996 |
| a0001c0001t0026 | 0/0 | 8488 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | GTATT others(8483): Show |
chr7 | 138455259 | 138594996 |
| a0001c0001t0027 | 0/0 | 8484 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM24_chr7_138455259_138594996 | TRIM24 | GTATT others(8479): Show |
chr7 | 138455259 | 138594996 |
| a0001c0001t0028 | 0/0 | 8487 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | GTATT others(8482): Show |
chr7 | 138455259 | 138594996 |
| a0001c0001t0029 | 0/0 | 8488 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | GTATT others(8483): Show |
chr7 | 138455259 | 138594996 |
| a0001c0001t0030 | 0/0 | 8487 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | GTATT others(8482): Show |
chr7 | 138455259 | 138594996 |
| a0001c0001t0032 | 0/0 | 8488 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | GTATT others(8483): Show |
chr7 | 138455259 | 138594996 |
| a0001c0001t0033 | 0/0 | 8488 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | GTATT others(8483): Show |
chr7 | 138455259 | 138594996 |
| a0001c0001t0034 | 0/0 | 8487 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | GTATT others(8482): Show |
chr7 | 138455259 | 138594996 |
| a0001c0001t0035 | 0/0 | 8488 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | GTATT others(8483): Show |
chr7 | 138455259 | 138594996 |
| a0001c0001t0037 | 0/0 | 8484 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | GTATT others(8479): Show |
chr7 | 138455259 | 138594996 |
| a0001c0001t0038 | 0/0 | 8488 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | GTATT others(8483): Show |
chr7 | 138455259 | 138594996 |
| a0001c0001t0039 | 0/0 | 8487 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | GTATT others(8482): Show |
chr7 | 138455259 | 138594996 |
| a0001c0001t0040 | 0/0 | 8488 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | GTATT others(8483): Show |
chr7 | 138455259 | 138594996 |
| a0001c0001t0041 | 0/0 | 8485 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | GTATT others(8480): Show |
chr7 | 138455259 | 138594996 |
| a0001c0001t0042 | 0/0 | 8489 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | GTATT others(8484): Show |
chr7 | 138455259 | 138594996 |
| a0001c0001t0043 | 0/0 | 8484 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | GTATT others(8479): Show |
chr7 | 138455259 | 138594996 |
| a0001c0001t0044 | 0/0 | 8487 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | GTATT others(8482): Show |
chr7 | 138455259 | 138594996 |
| a0001c0001t0045 | 0/0 | 8488 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | GTATT others(8483): Show |
chr7 | 138455259 | 138594996 |
| a0001c0001t0046 | 0/0 | 8488 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | GTATT others(8483): Show |
chr7 | 138455259 | 138594996 |
| a0001c0001t0047 | 0/0 | 8492 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | GTATT others(8487): Show |
chr7 | 138455259 | 138594996 |
| a0001c0001t0048 | 0/0 | 8488 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | GTATT others(8483): Show |
chr7 | 138455259 | 138594996 |
| a0001c0001t0049 | 0/0 | 8484 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | GTATT others(8479): Show |
chr7 | 138455259 | 138594996 |
| a0001c0001t0050 | 0/0 | 8484 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | GTATT others(8479): Show |
chr7 | 138455259 | 138594996 |
| a0001c0001t0051 | 0/0 | 8484 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | GTATT others(8479): Show |
chr7 | 138455259 | 138594996 |
| a0001c0001t0052 | 0/0 | 8484 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | GTATT others(8479): Show |
chr7 | 138455259 | 138594996 |
| a0001c0001t0053 | 1/0 | 8488 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | GTATT others(8483): Show |
chr7 | 138455259 | 138594996 |
| a0001c0001t0054 | 0/0 | 8483 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | GTATT others(8478): Show |
chr7 | 138455259 | 138594996 |
| a0001c0001t0055 | 0/0 | 8492 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | GTATT others(8487): Show |
chr7 | 138455259 | 138594996 |
| a0001c0001t0058 | 0/0 | 8488 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | GTATT others(8483): Show |
chr7 | 138455259 | 138594996 |
| a0001c0002t0004 | 0/0 | 8488 | 14 | 1 | 4 | 1 | 2 | 6 | TRIM24_chr7_138455259_138594996 | TRIM24 | GTATT others(8483): Show |
chr7 | 138455259 | 138594996 |
| a0001c0002t0015 | 0/0 | 8488 | 3 | 2 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | GTATT others(8483): Show |
chr7 | 138455259 | 138594996 |
| a0001c0002t0031 | 0/0 | 8489 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | GTATT others(8484): Show |
chr7 | 138455259 | 138594996 |
| a0001c0003t0014 | 0/0 | 8488 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | GTATT others(8483): Show |
chr7 | 138455259 | 138594996 |
| a0001c0004t0056 | 0/0 | 8487 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | GTATT others(8482): Show |
chr7 | 138455259 | 138594996 |
| a0001c0004t0057 | 0/0 | 8487 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | GTATT others(8482): Show |
chr7 | 138455259 | 138594996 |
| a0001c0005t0013 | 0/0 | 8491 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | GTATT others(8486): Show |
chr7 | 138455259 | 138594996 |
| a0001c0007t0036 | 0/0 | 8489 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | GTATT others(8484): Show |
chr7 | 138455259 | 138594996 |
| a0001c0009t0003 | 0/0 | 8487 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | GTATT others(8482): Show |
chr7 | 138455259 | 138594996 |
| a0001c0010t0013 | 0/0 | 8491 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | GTATT others(8486): Show |
chr7 | 138455259 | 138594996 |
| a0002c0006t0006 | 0/0 | 8488 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | GTATT others(8483): Show |
chr7 | 138455259 | 138594996 |
| a0003c0008t0002 | 0/0 | 8488 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | GTATT others(8483): Show |
chr7 | 138455259 | 138594996 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0003g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0003g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0003g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0003g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0003g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0003g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0003g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0003g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0003g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0003g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0003g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0003g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0003g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0003g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0003g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0003g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0003g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0003g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0003g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0003g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0003g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0003g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0003g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0003g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0003g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0003g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0003g0306 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0003g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0003g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0003g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0003g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0004g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0005g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0005g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0005g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0005g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0005g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0005g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0005g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0006g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0006g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0006g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0006g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0006g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0006g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0007g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0007g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0007g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0007g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0007g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0007g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0008g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0008g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0008g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0008g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0008g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0009g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0009g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0009g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0009g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0009g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0010g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0010g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0010g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0010g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0010g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0011g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0011g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0011g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0011g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0011g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0012g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0012g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0012g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0012g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0016g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0016g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0016g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0017g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0017g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0017g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0018g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0018g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0018g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0019g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0019g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0020g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0020g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0021g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0021g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0022g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0022g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0023g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0023g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0024g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0024g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0025g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0025g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0026g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0026g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0027g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0027g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0028g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0029g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0030g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0032g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0033g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0034g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0035g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0037g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0038g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0039g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0040g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0041g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0042g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0043g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0044g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0045g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0046g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0047g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0048g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0049g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0050g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0051g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0052g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0053g0137 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0054g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0055g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0058g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0002t0004g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0002t0004g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0002t0004g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0002t0004g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0002t0004g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0002t0004g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0002t0004g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0002t0004g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0002t0004g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0002t0004g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0002t0004g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0002t0004g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0002t0004g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0002t0004g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0002t0015g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0002t0015g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0002t0015g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0002t0031g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0003t0014g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0003t0014g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0003t0014g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0004t0056g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0004t0057g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0005t0013g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0005t0013g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0007t0036g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0009t0003g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0010t0013g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0002c0006t0006g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0003c0008t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0040 | EUR | GBR | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0295 | EUR | GBR | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG00280 | hp1 | a0001 | c0002 | t0004 | g0123 | EUR | FIN | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0135 | EUR | FIN | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | CHS | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | CHS | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | CHS | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | CHS | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | CHS | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG00438 | hp2 | a0001 | c0001 | t0007 | g0153 | EAS | CHS | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG00609 | hp1 | a0001 | c0001 | t0050 | g0213 | EAS | CHS | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | CHS | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | CHS | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | CHS | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG00735 | hp1 | a0001 | c0001 | t0020 | g0139 | AMR | PUR | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0272 | AMR | PUR | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0283 | AMR | PUR | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG00738 | hp2 | a0001 | c0002 | t0004 | g0242 | AMR | PUR | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG00741 | hp2 | a0001 | c0002 | t0015 | g0169 | AMR | PUR | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01069 | hp1 | a0001 | c0001 | t0043 | g0136 | AMR | PUR | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01069 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01070 | hp1 | a0001 | c0001 | t0012 | g0119 | AMR | PUR | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01070 | hp2 | a0001 | c0001 | t0009 | g0094 | AMR | PUR | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01071 | hp2 | a0001 | c0001 | t0009 | g0096 | AMR | PUR | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01074 | hp1 | a0001 | c0001 | t0004 | g0279 | AMR | PUR | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0106 | AMR | PUR | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01081 | hp2 | a0001 | c0001 | t0020 | g0155 | AMR | PUR | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01099 | hp1 | a0001 | c0001 | t0008 | g0291 | AMR | PUR | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0162 | AMR | PUR | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0310 | AMR | PUR | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0273 | AMR | PUR | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0271 | AMR | PUR | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01167 | hp2 | a0001 | c0002 | t0004 | g0116 | AMR | PUR | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0284 | AMR | PUR | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0144 | AMR | PUR | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01175 | hp1 | a0001 | c0001 | t0021 | g0189 | AMR | PUR | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01243 | hp1 | a0001 | c0002 | t0004 | g0165 | AMR | PUR | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0274 | AMR | PUR | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01255 | hp1 | a0001 | c0001 | t0041 | g0045 | AMR | CLM | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0278 | AMR | CLM | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0277 | AMR | CLM | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0286 | AMR | CLM | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01258 | hp2 | a0001 | c0001 | t0009 | g0098 | AMR | CLM | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0174 | AMR | CLM | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01261 | hp2 | a0001 | c0001 | t0034 | g0097 | AMR | CLM | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | CLM | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01346 | hp2 | a0001 | c0002 | t0004 | g0168 | AMR | CLM | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | CLM | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0289 | AMR | CLM | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01515 | hp1 | a0001 | c0007 | t0036 | g0108 | EUR | IBS | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0145 | EUR | IBS | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01884 | hp1 | a0001 | c0001 | t0016 | g0012 | AFR | ACB | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01884 | hp2 | a0001 | c0001 | t0022 | g0226 | AFR | ACB | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01891 | hp1 | a0002 | c0006 | t0006 | g0221 | AFR | ACB | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01891 | hp2 | a0001 | c0001 | t0012 | g0301 | AFR | ACB | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0138 | AMR | PEL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01943 | hp1 | a0001 | c0001 | t0044 | g0128 | AMR | PEL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0290 | AMR | PEL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PEL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0134 | AMR | PEL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PEL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | KHV | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0107 | EAS | KHV | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0147 | EAS | KHV | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | KHV | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02055 | hp1 | a0003 | c0008 | t0002 | g0102 | AFR | ACB | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02055 | hp2 | a0001 | c0004 | t0057 | g0109 | AFR | ACB | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | KHV | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | KHV | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | KHV | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02145 | hp1 | a0001 | c0001 | t0032 | g0311 | AFR | ACB | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02145 | hp2 | a0001 | c0002 | t0004 | g0243 | AFR | ACB | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02148 | hp1 | a0001 | c0001 | t0047 | g0179 | AMR | PEL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PEL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | CDX | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | CDX | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | CDX | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | CDX | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02257 | hp1 | a0001 | c0009 | t0003 | g0268 | AFR | ACB | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02257 | hp2 | a0001 | c0001 | t0037 | g0041 | AFR | ACB | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0270 | AFR | ACB | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02258 | hp2 | a0001 | c0001 | t0019 | g0304 | AFR | ACB | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02451 | hp1 | a0001 | c0001 | t0016 | g0013 | AFR | ACB | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02451 | hp2 | a0001 | c0002 | t0015 | g0170 | AFR | ACB | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02572 | hp1 | a0001 | c0001 | t0008 | g0292 | AFR | GWD | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02572 | hp2 | a0001 | c0005 | t0013 | g0114 | AFR | GWD | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0156 | SAS | PJL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02602 | hp2 | a0001 | c0001 | t0051 | g0105 | SAS | PJL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02622 | hp1 | a0001 | c0004 | t0056 | g0008 | AFR | GWD | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02622 | hp2 | a0001 | c0003 | t0014 | g0071 | AFR | GWD | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02630 | hp1 | a0001 | c0001 | t0033 | g0172 | AFR | GWD | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02630 | hp2 | a0001 | c0001 | t0026 | g0267 | AFR | GWD | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02647 | hp1 | a0001 | c0001 | t0011 | g0263 | AFR | GWD | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02647 | hp2 | a0001 | c0001 | t0010 | g0111 | AFR | GWD | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02683 | hp1 | a0001 | c0001 | t0005 | g0254 | SAS | PJL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02683 | hp2 | a0001 | c0002 | t0031 | g0200 | SAS | PJL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02717 | hp1 | a0001 | c0001 | t0022 | g0130 | AFR | GWD | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02717 | hp2 | a0001 | c0001 | t0029 | g0300 | AFR | GWD | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02723 | hp1 | a0001 | c0001 | t0024 | g0025 | AFR | GWD | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02723 | hp2 | a0001 | c0005 | t0013 | g0115 | AFR | GWD | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02735 | hp1 | a0001 | c0001 | t0005 | g0253 | SAS | PJL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02735 | hp2 | a0001 | c0001 | t0023 | g0154 | SAS | PJL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02738 | hp1 | a0001 | c0002 | t0004 | g0124 | SAS | PJL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02738 | hp2 | a0001 | c0001 | t0039 | g0227 | SAS | PJL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02809 | hp1 | a0001 | c0001 | t0010 | g0241 | AFR | GWD | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02809 | hp2 | a0001 | c0001 | t0008 | g0294 | AFR | GWD | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02818 | hp1 | a0001 | c0001 | t0030 | g0305 | AFR | GWD | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02818 | hp2 | a0001 | c0003 | t0014 | g0088 | AFR | GWD | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0204 | AFR | GWD | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0296 | AFR | GWD | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02895 | hp1 | a0001 | c0001 | t0018 | g0004 | AFR | GWD | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02895 | hp2 | a0001 | c0001 | t0024 | g0024 | AFR | GWD | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02896 | hp2 | a0001 | c0001 | t0017 | g0006 | AFR | GWD | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02897 | hp1 | a0001 | c0001 | t0017 | g0005 | AFR | GWD | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02897 | hp2 | a0001 | c0001 | t0018 | g0002 | AFR | GWD | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0276 | AFR | ESN | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0269 | AFR | ESN | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0099 | AFR | ESN | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02976 | hp2 | a0001 | c0002 | t0015 | g0171 | AFR | ESN | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG03041 | hp1 | a0001 | c0001 | t0018 | g0003 | AFR | GWD | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG03041 | hp2 | a0001 | c0001 | t0046 | g0262 | AFR | GWD | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG03098 | hp2 | a0001 | c0001 | t0011 | g0264 | AFR | MSL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0275 | AFR | ESN | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG03139 | hp2 | a0001 | c0001 | t0006 | g0216 | AFR | ESN | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0299 | AFR | ESN | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG03195 | hp2 | a0001 | c0001 | t0010 | g0112 | AFR | ESN | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG03209 | hp1 | a0001 | c0001 | t0017 | g0007 | AFR | MSL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0173 | AFR | MSL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG03225 | hp1 | a0001 | c0001 | t0006 | g0215 | AFR | MSL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG03225 | hp2 | a0001 | c0001 | t0010 | g0110 | AFR | MSL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0176 | SAS | PJL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG03453 | hp1 | a0001 | c0003 | t0014 | g0090 | AFR | MSL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0297 | AFR | MSL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG03486 | hp1 | a0001 | c0001 | t0021 | g0194 | AFR | MSL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG03490 | hp1 | a0001 | c0002 | t0004 | g0121 | SAS | PJL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG03491 | hp1 | a0001 | c0001 | t0011 | g0252 | SAS | PJL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG03491 | hp2 | a0001 | c0002 | t0004 | g0126 | SAS | PJL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG03492 | hp1 | a0001 | c0001 | t0011 | g0255 | SAS | PJL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0101 | AFR | ESN | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG03516 | hp2 | a0001 | c0001 | t0006 | g0223 | AFR | ESN | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0285 | AFR | GWD | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG03540 | hp2 | a0001 | c0001 | t0026 | g0266 | AFR | GWD | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG03579 | hp1 | a0001 | c0001 | t0006 | g0222 | AFR | MSL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG03579 | hp2 | a0001 | c0001 | t0055 | g0199 | AFR | MSL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0192 | SAS | PJL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG03654 | hp2 | a0001 | c0002 | t0004 | g0127 | SAS | PJL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0287 | SAS | PJL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG03669 | hp2 | a0001 | c0001 | t0023 | g0185 | SAS | PJL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG03688 | hp1 | a0001 | c0001 | t0027 | g0081 | SAS | STU | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0164 | SAS | STU | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0150 | SAS | PJL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG03710 | hp1 | a0001 | c0001 | t0009 | g0014 | SAS | PJL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0280 | SAS | PJL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0191 | SAS | BEB | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0288 | SAS | BEB | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG03834 | hp1 | a0001 | c0001 | t0011 | g0258 | SAS | BEB | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG03834 | hp2 | a0001 | c0001 | t0048 | g0148 | SAS | BEB | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG03927 | hp1 | a0001 | c0001 | t0016 | g0015 | SAS | BEB | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0307 | SAS | BEB | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0308 | SAS | BEB | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG03942 | hp2 | a0001 | c0002 | t0004 | g0224 | SAS | BEB | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG04115 | hp1 | a0001 | c0001 | t0027 | g0080 | SAS | STU | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0084 | SAS | STU | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | BEB | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0198 | SAS | BEB | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | STU | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0178 | SAS | STU | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18522 | hp1 | a0001 | c0001 | t0019 | g0303 | AFR | YRI | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18522 | hp2 | a0001 | c0010 | t0013 | g0113 | AFR | YRI | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | CHB | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0161 | EAS | CHB | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0309 | AFR | YRI | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18906 | hp2 | a0001 | c0001 | t0008 | g0281 | AFR | YRI | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18939 | hp2 | a0001 | c0001 | t0007 | g0187 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18940 | hp1 | a0001 | c0001 | t0007 | g0184 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18944 | hp2 | a0001 | c0001 | t0005 | g0257 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18947 | hp1 | a0001 | c0001 | t0040 | g0186 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18951 | hp2 | a0001 | c0001 | t0012 | g0118 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18954 | hp1 | a0001 | c0001 | t0005 | g0259 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18962 | hp1 | a0001 | c0001 | t0005 | g0256 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18962 | hp2 | a0001 | c0001 | t0007 | g0133 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18963 | hp1 | a0001 | c0002 | t0004 | g0125 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18963 | hp2 | a0001 | c0001 | t0007 | g0149 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18967 | hp2 | a0001 | c0001 | t0007 | g0182 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18969 | hp1 | a0001 | c0001 | t0005 | g0261 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19056 | hp2 | a0001 | c0001 | t0054 | g0072 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19058 | hp2 | a0001 | c0001 | t0025 | g0117 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19065 | hp1 | a0001 | c0001 | t0038 | g0166 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19065 | hp2 | a0001 | c0001 | t0005 | g0260 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19066 | hp1 | a0001 | c0001 | t0045 | g0233 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19066 | hp2 | a0001 | c0001 | t0052 | g0027 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19078 | hp1 | a0001 | c0001 | t0042 | g0201 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19081 | hp1 | a0001 | c0001 | t0049 | g0053 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19081 | hp2 | a0001 | c0001 | t0025 | g0190 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0202 | AFR | ASW | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA20129 | hp2 | a0001 | c0001 | t0058 | g0220 | AFR | ASW | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0104 | EUR | TSI | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA20805 | hp2 | a0001 | c0002 | t0004 | g0120 | EUR | TSI | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | GIH | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA20905 | hp2 | a0001 | c0002 | t0004 | g0122 | SAS | GIH | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01123 | hp1 | a0001 | c0001 | t0028 | g0302 | AMR | CLM | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01123 | hp2 | a0001 | c0001 | t0009 | g0095 | AMR | CLM | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02109 | hp1 | a0001 | c0001 | t0035 | g0265 | AFR | ACB | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0282 | AFR | ACB | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02486 | hp1 | a0001 | c0001 | t0010 | g0244 | AFR | ACB | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02486 | hp2 | a0001 | c0001 | t0012 | g0205 | AFR | ACB | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | ACB | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0298 | AFR | ACB | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0100 | AFR | MSL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG03471 | hp2 | a0001 | c0001 | t0008 | g0293 | AFR | MSL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | USA | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG06807 | hp2 | a0001 | c0001 | t0006 | g0217 | AFR | USA | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA20300 | hp1 | a0001 | c0001 | t0006 | g0218 | AFR | USA | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | USA | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0306 | REF | REF | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0053 | g0137 | REF | REF | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:138579334 | A | G | 1 | a0003 | 1 | HG02055.hp1 | missense_variant | MODERATE | c.2387A>G | p.Asn796Ser | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 15/19 | 2677/8488 | 2387/3153 | 796/1050 | chr7 | 138579334 | |||
| chr7:138579354 | G | C | 1 | a0002 | 1 | HG01891.hp1 | missense_variant | MODERATE | c.2407G>C | p.Glu803Gln | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 15/19 | 2697/8488 | 2407/3153 | 803/1050 | chr7 | 138579354 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:138519283 | A | G | 2 | a0001c0005 a0001c0010 |
3 | HG02572.hp2 HG02723.hp2 NA18522.hp2 |
synonymous_variant | LOW | c.726A>G | p.Thr242Thr | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 4/19 | 1016/8488 | 726/3153 | 242/1050 | chr7 | 138519283 | |||
| chr7:138538722 | A | G | 1 | a0001c0009 | 1 | HG02257.hp1 | synonymous_variant | LOW | c.1062A>G | p.Lys354Lys | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/19 | 1352/8488 | 1062/3153 | 354/1050 | chr7 | 138538722 | |||
| chr7:138554903 | A | C | 1 | a0001c0005 | 2 | HG02572.hp2 HG02723.hp2 |
synonymous_variant | LOW | c.1467A>C | p.Ala489Ala | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/19 | 1757/8488 | 1467/3153 | 489/1050 | chr7 | 138554903 | |||
| chr7:138570940 | T | C | 1 | a0001c0004 | 2 | HG02055.hp2 HG02622.hp1 |
synonymous_variant | LOW | c.1815T>C | p.Gly605Gly | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 11/19 | 2105/8488 | 1815/3153 | 605/1050 | chr7 | 138570940 | |||
| chr7:138570956 | T | C | 1 | a0001c0010 | 1 | NA18522.hp2 | synonymous_variant | LOW | c.1831T>C | p.Leu611Leu | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 11/19 | 2121/8488 | 1831/3153 | 611/1050 | chr7 | 138570956 | |||
| chr7:138579488 | A | T | 1 | a0001c0003 | 3 | HG02622.hp2 HG02818.hp2 HG03453.hp1 |
synonymous_variant | LOW | c.2541A>T | p.Val847Val | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 15/19 | 2831/8488 | 2541/3153 | 847/1050 | chr7 | 138579488 | |||
| chr7:138580565 | A | G | 2 | a0001c0002 a0001c0007 |
19 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(16): Show |
synonymous_variant | LOW | c.2589A>G | p.Gly863Gly | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 16/19 | 2879/8488 | 2589/3153 | 863/1050 | chr7 | 138580565 | |||
| chr7:138583981 | C | T | 1 | a0001c0007 | 1 | HG01515.hp1 | synonymous_variant | LOW | c.2925C>T | p.Asn975Asn | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 18/19 | 3215/8488 | 2925/3153 | 975/1050 | chr7 | 138583981 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:138460329 | C | T | 5 | a0001c0001t0017 a0001c0001t0018 a0001c0001t0058 others(2): Show |
9 | HG02055.hp2 HG02622.hp1 HG02895.hp1 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-220C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/19 | 220 | chr7 | 138460329 | ||||||
| chr7:138460408 | T | C | 26 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0008 others(23): Show |
90 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(87): Show |
5_prime_UTR_variant | MODIFIER | c.-141T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/19 | 141 | chr7 | 138460408 | ||||||
| chr7:138585015 | G | A | 1 | a0001c0001t0038 | 1 | NA19065.hp1 | 3_prime_UTR_variant | MODIFIER | c.*64G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 19/19 | 64 | chr7 | 138585015 | ||||||
| chr7:138585021 | T | TAAC | 2 | a0001c0005t0013 a0001c0010t0013 |
3 | HG02572.hp2 HG02723.hp2 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*72_*74dupACA | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 19/19 | 75 | INFO_REALIGN_3_PRIME | chr7 | 138585021 | |||||
| chr7:138585056 | C | G | 2 | a0001c0005t0013 a0001c0010t0013 |
3 | HG02572.hp2 HG02723.hp2 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*105C>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 19/19 | 105 | chr7 | 138585056 | ||||||
| chr7:138585156 | A | G | 7 | a0001c0001t0006 a0001c0001t0010 a0001c0001t0055 others(4): Show |
16 | HG01891.hp1 HG02055.hp2 HG02486.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*205A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 19/19 | 205 | chr7 | 138585156 | ||||||
| chr7:138585451 | A | G | 3 | a0001c0001t0006 a0001c0001t0058 a0002c0006t0006 |
8 | HG01891.hp1 HG03139.hp2 HG03225.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*500A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 19/19 | 500 | chr7 | 138585451 | ||||||
| chr7:138585590 | G | A | 1 | a0001c0003t0014 | 3 | HG02622.hp2 HG02818.hp2 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*639G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 19/19 | 639 | chr7 | 138585590 | ||||||
| chr7:138585595 | AT | A | 11 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0008 others(8): Show |
61 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*649delT | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 19/19 | 649 | INFO_REALIGN_3_PRIME | chr7 | 138585595 | |||||
| chr7:138585638 | A | G | 2 | a0001c0001t0019 a0001c0001t0030 |
3 | HG02258.hp2 HG02818.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*687A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 19/19 | 687 | chr7 | 138585638 | ||||||
| chr7:138585645 | G | A | 1 | a0001c0001t0017 | 3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*694G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 19/19 | 694 | chr7 | 138585645 | ||||||
| chr7:138585912 | G | A | 27 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0007 others(24): Show |
124 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(121): Show |
3_prime_UTR_variant | MODIFIER | c.*961G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 19/19 | 961 | chr7 | 138585912 | ||||||
| chr7:138585986 | G | A | 2 | a0001c0004t0056 a0001c0004t0057 |
2 | HG02055.hp2 HG02622.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1035G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 19/19 | 1035 | chr7 | 138585986 | ||||||
| chr7:138585999 | A | AT | 3 | a0001c0001t0017 a0001c0001t0025 a0001c0001t0029 |
6 | HG02717.hp2 HG02896.hp2 HG02897.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1060dupT | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 19/19 | 1061 | INFO_REALIGN_3_PRIME | chr7 | 138585999 | |||||
| chr7:138586018 | G | C | 1 | a0001c0001t0055 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1067G>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 19/19 | 1067 | chr7 | 138586018 | ||||||
| chr7:138586059 | A | G | 3 | a0001c0001t0010 a0001c0004t0056 a0001c0004t0057 |
7 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1108A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 19/19 | 1108 | chr7 | 138586059 | ||||||
| chr7:138586093 | T | C | 52 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(49): Show |
214 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(211): Show |
3_prime_UTR_variant | MODIFIER | c.*1142T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 19/19 | 1142 | chr7 | 138586093 | ||||||
| chr7:138586178 | T | TATAG | 3 | a0001c0001t0017 a0001c0001t0047 a0001c0001t0055 |
5 | HG02148.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1245_*1248dupTAGA | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 19/19 | 1249 | INFO_REALIGN_3_PRIME | chr7 | 138586178 | |||||
| chr7:138586178 | TATAG | T | 1 | a0001c0001t0005 | 7 | HG02683.hp1 HG02735.hp1 NA18944.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1245_*1248delTAGA | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 19/19 | 1245 | INFO_REALIGN_3_PRIME | chr7 | 138586178 | |||||
| chr7:138586343 | A | G | 4 | a0001c0001t0010 a0001c0001t0055 a0001c0004t0056 others(1): Show |
8 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1392A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 19/19 | 1392 | chr7 | 138586343 | ||||||
| chr7:138586450 | T | C | 1 | a0001c0001t0055 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1499T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 19/19 | 1499 | chr7 | 138586450 | ||||||
| chr7:138586552 | A | C | 3 | a0001c0001t0005 a0001c0001t0011 a0001c0001t0046 |
13 | HG02647.hp1 HG02683.hp1 HG02735.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1601A>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 19/19 | 1601 | chr7 | 138586552 | ||||||
| chr7:138586577 | C | A | 4 | a0001c0001t0010 a0001c0001t0055 a0001c0004t0056 others(1): Show |
8 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1626C>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 19/19 | 1626 | chr7 | 138586577 | ||||||
| chr7:138586580 | A | G | 4 | a0001c0001t0010 a0001c0001t0055 a0001c0004t0056 others(1): Show |
8 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1629A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 19/19 | 1629 | chr7 | 138586580 | ||||||
| chr7:138586829 | A | G | 5 | a0001c0001t0008 a0001c0001t0019 a0001c0001t0024 others(2): Show |
11 | HG01099.hp1 HG02145.hp1 HG02258.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1878A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 19/19 | 1878 | chr7 | 138586829 | ||||||
| chr7:138586975 | T | C | 1 | a0001c0001t0055 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2024T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 19/19 | 2024 | chr7 | 138586975 | ||||||
| chr7:138587014 | G | A | 1 | a0001c0001t0020 | 2 | HG00735.hp1 HG01081.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2063G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 19/19 | 2063 | chr7 | 138587014 | ||||||
| chr7:138587103 | C | T | 1 | a0001c0001t0027 | 2 | HG03688.hp1 HG04115.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2152C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 19/19 | 2152 | chr7 | 138587103 | ||||||
| chr7:138587304 | G | C | 1 | a0001c0001t0049 | 1 | NA19081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2353G>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 19/19 | 2353 | chr7 | 138587304 | ||||||
| chr7:138587446 | T | C | 1 | a0001c0001t0007 | 6 | HG00438.hp2 NA18939.hp2 NA18940.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2495T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 19/19 | 2495 | chr7 | 138587446 | ||||||
| chr7:138587633 | A | T | 3 | a0001c0001t0006 a0001c0001t0058 a0002c0006t0006 |
8 | HG01891.hp1 HG03139.hp2 HG03225.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2682A>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 19/19 | 2682 | chr7 | 138587633 | ||||||
| chr7:138587734 | C | G | 1 | a0001c0001t0030 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2783C>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 19/19 | 2783 | chr7 | 138587734 | ||||||
| chr7:138587810 | C | T | 1 | a0001c0001t0045 | 1 | NA19066.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2859C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 19/19 | 2859 | chr7 | 138587810 | ||||||
| chr7:138587861 | G | A | 4 | a0001c0001t0010 a0001c0001t0055 a0001c0004t0056 others(1): Show |
8 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2910G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 19/19 | 2910 | chr7 | 138587861 | ||||||
| chr7:138587890 | A | T | 1 | a0001c0001t0023 | 2 | HG02735.hp2 HG03669.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2939A>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 19/19 | 2939 | chr7 | 138587890 | ||||||
| chr7:138588074 | A | C | 2 | a0001c0001t0026 a0001c0001t0035 |
3 | HG02109.hp1 HG02630.hp2 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3123A>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 19/19 | 3123 | chr7 | 138588074 | ||||||
| chr7:138588169 | C | A | 7 | a0001c0001t0005 a0001c0001t0010 a0001c0001t0011 others(4): Show |
21 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*3218C>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 19/19 | 3218 | chr7 | 138588169 | ||||||
| chr7:138588358 | G | A | 1 | a0001c0001t0017 | 3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3407G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 19/19 | 3407 | chr7 | 138588358 | ||||||
| chr7:138588410 | T | C | 5 | a0001c0001t0005 a0001c0001t0011 a0001c0001t0046 others(2): Show |
15 | HG02055.hp2 HG02622.hp1 HG02647.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*3459T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 19/19 | 3459 | chr7 | 138588410 | ||||||
| chr7:138588423 | G | A | 5 | a0001c0001t0005 a0001c0001t0011 a0001c0001t0046 others(2): Show |
15 | HG02055.hp2 HG02622.hp1 HG02647.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*3472G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 19/19 | 3472 | chr7 | 138588423 | ||||||
| chr7:138588430 | G | C | 1 | a0001c0001t0050 | 1 | HG00609.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3479G>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 19/19 | 3479 | chr7 | 138588430 | ||||||
| chr7:138588466 | C | T | 1 | a0001c0001t0028 | 1 | HG01123.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3515C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 19/19 | 3515 | chr7 | 138588466 | ||||||
| chr7:138588683 | A | G | 2 | a0001c0001t0026 a0001c0001t0035 |
3 | HG02109.hp1 HG02630.hp2 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3732A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 19/19 | 3732 | chr7 | 138588683 | ||||||
| chr7:138588712 | T | A | 1 | a0001c0001t0040 | 1 | NA18947.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3761T>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 19/19 | 3761 | chr7 | 138588712 | ||||||
| chr7:138588876 | G | A | 1 | a0001c0001t0046 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3925G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 19/19 | 3925 | chr7 | 138588876 | ||||||
| chr7:138588898 | T | A | 1 | a0001c0001t0051 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3947T>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 19/19 | 3947 | chr7 | 138588898 | ||||||
| chr7:138588937 | G | A | 1 | a0001c0001t0052 | 1 | NA19066.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3986G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 19/19 | 3986 | chr7 | 138588937 | ||||||
| chr7:138588957 | G | A | 2 | a0001c0005t0013 a0001c0010t0013 |
3 | HG02572.hp2 HG02723.hp2 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4006G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 19/19 | 4006 | chr7 | 138588957 | ||||||
| chr7:138589008 | C | CA | 8 | a0001c0001t0004 a0001c0001t0021 a0001c0001t0041 others(5): Show |
24 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*4072dupA | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 19/19 | 4073 | INFO_REALIGN_3_PRIME | chr7 | 138589008 | |||||
| chr7:138589008 | CA | C | 14 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0009 others(11): Show |
41 | HG01070.hp2 HG01071.hp2 HG01123.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*4072delA | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 19/19 | 4072 | INFO_REALIGN_3_PRIME | chr7 | 138589008 | |||||
| chr7:138589024 | T | C | 1 | a0001c0001t0022 | 2 | HG01884.hp2 HG02717.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4073T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 19/19 | 4073 | chr7 | 138589024 | ||||||
| chr7:138589087 | A | G | 1 | a0001c0003t0014 | 3 | HG02622.hp2 HG02818.hp2 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4136A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 19/19 | 4136 | chr7 | 138589087 | ||||||
| chr7:138589124 | AAATT | A | 10 | a0001c0001t0001 a0001c0001t0027 a0001c0001t0037 others(7): Show |
94 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(91): Show |
3_prime_UTR_variant | MODIFIER | c.*4177_*4180delTAAT | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 19/19 | 4177 | INFO_REALIGN_3_PRIME | chr7 | 138589124 | |||||
| chr7:138589308 | G | A | 1 | a0001c0001t0017 | 3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4357G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 19/19 | 4357 | chr7 | 138589308 | ||||||
| chr7:138589442 | T | A | 46 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(43): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
3_prime_UTR_variant | MODIFIER | c.*4491T>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 19/19 | 4491 | chr7 | 138589442 | ||||||
| chr7:138589506 | G | A | 3 | a0001c0001t0010 a0001c0001t0026 a0001c0001t0035 |
8 | HG02109.hp1 HG02486.hp1 HG02630.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4555G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 19/19 | 4555 | chr7 | 138589506 | ||||||
| chr7:138589588 | A | AT | 3 | a0001c0001t0006 a0001c0001t0058 a0002c0006t0006 |
8 | HG01891.hp1 HG03139.hp2 HG03225.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4640dupT | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 19/19 | 4641 | INFO_REALIGN_3_PRIME | chr7 | 138589588 | |||||
| chr7:138589618 | C | T | 1 | a0001c0001t0034 | 1 | HG01261.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4667C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 19/19 | 4667 | chr7 | 138589618 | ||||||
| chr7:138589738 | C | G | 3 | a0001c0001t0006 a0001c0001t0058 a0002c0006t0006 |
8 | HG01891.hp1 HG03139.hp2 HG03225.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4787C>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 19/19 | 4787 | chr7 | 138589738 | ||||||
| chr7:138589777 | T | C | 1 | a0001c0004t0056 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4826T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 19/19 | 4826 | chr7 | 138589777 | ||||||
| chr7:138589793 | G | A | 7 | a0001c0001t0005 a0001c0001t0011 a0001c0001t0017 others(4): Show |
21 | HG02055.hp2 HG02622.hp1 HG02622.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*4842G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 19/19 | 4842 | chr7 | 138589793 | ||||||
| chr7:138589814 | T | G | 7 | a0001c0001t0005 a0001c0001t0011 a0001c0001t0017 others(4): Show |
21 | HG02055.hp2 HG02622.hp1 HG02622.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*4863T>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 19/19 | 4863 | chr7 | 138589814 | ||||||
| chr7:138589989 | C | T | 13 | a0001c0001t0001 a0001c0001t0010 a0001c0001t0026 others(10): Show |
102 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*5038C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 19/19 | 5038 | chr7 | 138589989 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:138461033 | C | T | 44 | a0001c0001t0003g0001 a0001c0001t0003g0269 a0001c0001t0003g0270 others(41): Show |
45 | HG00140.hp2 HG00735.hp2 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.364+121C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138461033 | |||||||
| chr7:138461189 | C | G | 3 | a0001c0001t0026g0266 a0001c0001t0026g0267 a0001c0001t0035g0265 |
3 | HG02109.hp1 HG02630.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.364+277C>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138461189 | |||||||
| chr7:138462191 | G | A | 6 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 others(3): Show |
6 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.364+1279G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138462191 | |||||||
| chr7:138462338 | C | CT | 26 | a0001c0001t0001g0235 a0001c0001t0001g0236 a0001c0001t0001g0237 others(23): Show |
26 | HG00738.hp2 HG01106.hp2 HG01175.hp2 others(23): Show |
intron_variant | MODIFIER | c.364+1446dupT | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138462338 | ||||||
| chr7:138462338 | C | CTT | 13 | a0001c0001t0005g0253 a0001c0001t0005g0254 a0001c0001t0005g0256 others(10): Show |
13 | HG02647.hp1 HG02683.hp1 HG02735.hp1 others(10): Show |
intron_variant | MODIFIER | c.364+1445_364+1446d others(4): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138462338 | ||||||
| chr7:138462372 | G | A | 1 | a0001c0004t0056g0008 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.364+1460G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138462372 | |||||||
| chr7:138462586 | C | T | 1 | a0001c0001t0001g0234 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.364+1674C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138462586 | |||||||
| chr7:138462659 | T | G | 1 | a0001c0001t0001g0235 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.364+1747T>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138462659 | |||||||
| chr7:138462731 | A | G | 7 | a0001c0001t0002g0228 a0001c0001t0002g0229 a0001c0001t0002g0230 others(4): Show |
7 | NA18945.hp1 NA18950.hp1 NA18953.hp2 others(4): Show |
intron_variant | MODIFIER | c.364+1819A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138462731 | |||||||
| chr7:138462778 | C | A | 106 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(103): Show |
106 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.364+1866C>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138462778 | |||||||
| chr7:138462872 | A | AT | 3 | a0001c0001t0001g0225 a0001c0001t0046g0262 a0001c0002t0004g0224 |
3 | HG01993.hp2 HG03041.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.364+1963dupT | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138462872 | ||||||
| chr7:138462872 | A | T | 5 | a0001c0001t0003g0307 a0001c0001t0003g0308 a0001c0001t0011g0263 others(2): Show |
5 | HG02647.hp1 HG02738.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.364+1960A>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138462872 | |||||||
| chr7:138462875 | TA | T | 4 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0022g0226 others(1): Show |
4 | HG01884.hp2 HG02602.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.364+1964delA | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138462875 | |||||||
| chr7:138462876 | A | G | 13 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(10): Show |
13 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.364+1964A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138462876 | |||||||
| chr7:138462876 | A | T | 175 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(172): Show |
176 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.364+1964A>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138462876 | |||||||
| chr7:138462880 | T | A | 5 | a0001c0001t0002g0106 a0001c0001t0002g0107 a0001c0001t0002g0240 others(2): Show |
5 | HG01074.hp2 HG02027.hp2 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.364+1968T>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138462880 | |||||||
| chr7:138462891 | CG | C | 3 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 |
3 | HG02896.hp1 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.364+1981delG | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138462891 | ||||||
| chr7:138462946 | C | T | 4 | a0001c0001t0002g0099 a0001c0001t0002g0100 a0001c0001t0002g0101 others(1): Show |
4 | HG02055.hp1 HG02976.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.364+2034C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138462946 | |||||||
| chr7:138463040 | T | G | 1 | a0001c0001t0003g0270 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.364+2128T>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138463040 | |||||||
| chr7:138463043 | G | GT | 44 | a0001c0001t0001g0016 a0001c0001t0002g0173 a0001c0001t0002g0174 others(41): Show |
44 | HG00621.hp2 HG01175.hp1 HG01261.hp1 others(41): Show |
intron_variant | MODIFIER | c.364+2157dupT | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138463043 | ||||||
| chr7:138463043 | G | GTT | 87 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0017 others(84): Show |
87 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.364+2156_364+2157d others(4): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138463043 | ||||||
| chr7:138463043 | G | GTTT | 30 | a0001c0001t0001g0011 a0001c0001t0001g0070 a0001c0001t0001g0073 others(27): Show |
30 | HG01175.hp2 HG01256.hp2 HG01346.hp1 others(27): Show |
intron_variant | MODIFIER | c.364+2155_364+2157d others(5): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138463043 | ||||||
| chr7:138463043 | G | GTTTT | 8 | a0001c0001t0001g0089 a0001c0001t0001g0091 a0001c0001t0001g0092 others(5): Show |
8 | HG00621.hp1 HG02148.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.364+2154_364+2157d others(6): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138463043 | ||||||
| chr7:138463043 | G | GTTTTTTT others(4): Show |
3 | a0001c0001t0009g0094 a0001c0001t0009g0095 a0001c0001t0009g0096 |
3 | HG01070.hp2 HG01071.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.364+2147_364+2157d others(13): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138463043 | ||||||
| chr7:138463043 | G | GTTTTTTT others(5): Show |
2 | a0001c0001t0009g0098 a0001c0001t0034g0097 |
2 | HG01258.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.364+2146_364+2157d others(14): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138463043 | ||||||
| chr7:138463043 | GT | G | 47 | a0001c0001t0002g0228 a0001c0001t0003g0001 a0001c0001t0003g0269 others(44): Show |
48 | HG00140.hp2 HG00280.hp1 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.364+2157delT | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138463043 | ||||||
| chr7:138463043 | GTT | G | 6 | a0001c0001t0003g0271 a0001c0001t0003g0272 a0001c0001t0003g0307 others(3): Show |
6 | HG00735.hp2 HG01167.hp1 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.364+2156_364+2157d others(4): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138463043 | ||||||
| chr7:138463046 | T | G | 1 | a0001c0007t0036g0108 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.364+2134T>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138463046 | |||||||
| chr7:138463050 | T | TTTG | 7 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(4): Show |
7 | HG02572.hp2 HG02647.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.364+2140_364+2141i others(5): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138463050 | ||||||
| chr7:138463051 | T | G | 1 | a0001c0004t0057g0109 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.364+2139T>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138463051 | |||||||
| chr7:138463053 | T | G | 1 | a0001c0004t0057g0109 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.364+2141T>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138463053 | |||||||
| chr7:138463055 | T | G | 2 | a0001c0004t0056g0008 a0001c0004t0057g0109 |
2 | HG02055.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.364+2143T>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138463055 | |||||||
| chr7:138463057 | T | G | 2 | a0001c0004t0056g0008 a0001c0004t0057g0109 |
2 | HG02055.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.364+2145T>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138463057 | |||||||
| chr7:138463070 | G | T | 2 | a0001c0001t0001g0087 a0001c0001t0001g0235 |
2 | NA18978.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.364+2158G>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138463070 | |||||||
| chr7:138463100 | G | T | 2 | a0001c0004t0056g0008 a0001c0004t0057g0109 |
2 | HG02055.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.364+2188G>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138463100 | |||||||
| chr7:138463179 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.364+2267C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138463179 | |||||||
| chr7:138463187 | G | T | 8 | a0001c0001t0006g0215 a0001c0001t0006g0216 a0001c0001t0006g0217 others(5): Show |
8 | HG01891.hp1 HG03139.hp2 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.364+2275G>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138463187 | |||||||
| chr7:138463189 | C | T | 1 | a0001c0001t0003g0295 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.364+2277C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138463189 | |||||||
| chr7:138463771 | C | A | 13 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(10): Show |
13 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.364+2859C>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138463771 | |||||||
| chr7:138463843 | A | C | 13 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(10): Show |
13 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.364+2931A>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138463843 | |||||||
| chr7:138463989 | C | CATTTTTT | 4 | a0001c0001t0017g0005 a0001c0001t0018g0002 a0001c0001t0018g0003 others(1): Show |
4 | HG02895.hp1 HG02897.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.364+3077_364+3078i others(9): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138463989 | |||||||
| chr7:138463989 | C | CATTTTTT others(1): Show |
3 | a0001c0001t0010g0241 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02809.hp1 HG02896.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.364+3077_364+3078i others(10): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138463989 | |||||||
| chr7:138463989 | C | CT | 20 | a0001c0001t0002g0167 a0001c0001t0002g0192 a0001c0001t0002g0193 others(17): Show |
20 | HG02165.hp2 HG02257.hp1 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.364+3100dupT | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138463989 | ||||||
| chr7:138463989 | C | CTTTTTTT others(3): Show |
1 | a0001c0001t0001g0019 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.364+3091_364+3100d others(12): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138463989 | ||||||
| chr7:138463989 | C | CTTTTTTT others(4): Show |
1 | a0001c0001t0026g0266 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.364+3090_364+3100d others(13): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138463989 | ||||||
| chr7:138463989 | C | CTTTTTTT others(5): Show |
29 | a0001c0001t0001g0016 a0001c0001t0001g0020 a0001c0001t0001g0021 others(26): Show |
29 | HG00408.hp2 HG01928.hp2 HG01934.hp2 others(26): Show |
intron_variant | MODIFIER | c.364+3089_364+3100d others(14): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138463989 | ||||||
| chr7:138463989 | C | CTTTTTTT others(6): Show |
41 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0038 others(38): Show |
41 | HG00140.hp1 HG00423.hp2 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.364+3088_364+3100d others(15): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138463989 | ||||||
| chr7:138463989 | C | CTTTTTTT others(7): Show |
27 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(24): Show |
27 | HG00438.hp1 HG00609.hp1 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.364+3087_364+3100d others(16): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138463989 | ||||||
| chr7:138463989 | C | CTTTTTTT others(8): Show |
11 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(8): Show |
11 | HG01109.hp1 HG01496.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.364+3086_364+3100d others(17): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138463989 | ||||||
| chr7:138463989 | C | CTTTTTTT others(9): Show |
19 | a0001c0001t0001g0069 a0001c0001t0001g0085 a0001c0001t0003g0277 others(16): Show |
19 | HG00140.hp2 HG01074.hp1 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.364+3085_364+3100d others(18): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138463989 | ||||||
| chr7:138463989 | C | CTTTTTTT others(10): Show |
13 | a0001c0001t0003g0001 a0001c0001t0003g0270 a0001c0001t0003g0271 others(10): Show |
14 | HG00738.hp1 HG01069.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.364+3084_364+3100d others(19): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138463989 | ||||||
| chr7:138463989 | C | CTTTTTTT others(11): Show |
11 | a0001c0001t0001g0086 a0001c0001t0003g0289 a0001c0001t0003g0290 others(8): Show |
11 | HG01099.hp1 HG01106.hp2 HG01346.hp2 others(8): Show |
intron_variant | MODIFIER | c.364+3083_364+3100d others(20): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138463989 | ||||||
| chr7:138463989 | C | CTTTTTTT others(12): Show |
8 | a0001c0001t0008g0292 a0001c0001t0008g0293 a0001c0001t0008g0294 others(5): Show |
8 | HG00738.hp2 HG00741.hp2 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.364+3082_364+3100d others(21): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138463989 | ||||||
| chr7:138463989 | C | CTTTTTTT others(13): Show |
3 | a0001c0001t0005g0261 a0001c0002t0004g0121 a0001c0002t0004g0243 |
3 | HG02145.hp2 HG03490.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.364+3081_364+3100d others(22): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138463989 | ||||||
| chr7:138463989 | C | CTTTTTTT others(14): Show |
5 | a0001c0002t0004g0122 a0001c0002t0004g0123 a0001c0002t0004g0124 others(2): Show |
5 | HG00280.hp1 HG02572.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.364+3080_364+3100d others(23): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138463989 | ||||||
| chr7:138463989 | C | CTTTTTTT others(15): Show |
3 | a0001c0001t0003g0272 a0001c0002t0015g0170 a0001c0002t0031g0200 |
3 | HG00735.hp2 HG02451.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.364+3079_364+3100d others(24): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138463989 | ||||||
| chr7:138463989 | C | CTTTTTTT others(16): Show |
2 | a0001c0002t0004g0125 a0001c0002t0015g0171 |
2 | HG02976.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.364+3078_364+3100d others(25): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138463989 | ||||||
| chr7:138463989 | C | CTTTTTTT others(17): Show |
2 | a0001c0001t0003g0308 a0001c0002t0004g0126 |
2 | HG03491.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.364+3100_364+3101i others(26): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138463989 | ||||||
| chr7:138463989 | C | CTTTTTTT others(18): Show |
1 | a0001c0001t0005g0257 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.364+3100_364+3101i others(27): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138463989 | ||||||
| chr7:138463989 | C | CTTTTTTT others(20): Show |
2 | a0001c0002t0004g0127 a0001c0005t0013g0115 |
2 | HG02723.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.364+3100_364+3101i others(29): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138463989 | ||||||
| chr7:138463989 | C | CTTTTTTT others(21): Show |
2 | a0001c0001t0033g0172 a0001c0001t0039g0227 |
2 | HG02630.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.364+3100_364+3101i others(30): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138463989 | ||||||
| chr7:138463989 | CT | C | 6 | a0001c0001t0001g0017 a0001c0001t0011g0263 a0001c0001t0011g0264 others(3): Show |
6 | HG01943.hp1 HG02132.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.364+3100delT | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138463989 | ||||||
| chr7:138463999 | T | A | 2 | a0001c0001t0010g0110 a0001c0001t0010g0244 |
2 | HG02486.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.364+3087T>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138463999 | |||||||
| chr7:138464107 | G | T | 6 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 others(3): Show |
6 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.364+3195G>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138464107 | |||||||
| chr7:138464151 | C | T | 1 | a0001c0001t0002g0248 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.364+3239C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138464151 | |||||||
| chr7:138464357 | C | G | 1 | a0001c0001t0001g0092 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.364+3445C>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138464357 | |||||||
| chr7:138464607 | G | A | 3 | a0001c0001t0003g0283 a0001c0001t0003g0284 a0001c0001t0003g0310 |
3 | HG00738.hp1 HG01106.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.364+3695G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138464607 | |||||||
| chr7:138464656 | A | G | 2 | a0001c0004t0056g0008 a0001c0004t0057g0109 |
2 | HG02055.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.364+3744A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138464656 | |||||||
| chr7:138464677 | A | G | 1 | a0001c0001t0001g0239 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.364+3765A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138464677 | |||||||
| chr7:138464704 | C | T | 1 | a0001c0001t0038g0166 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.364+3792C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138464704 | |||||||
| chr7:138464778 | A | C | 1 | a0001c0001t0001g0235 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.364+3866A>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138464778 | |||||||
| chr7:138464815 | A | T | 1 | a0001c0001t0011g0264 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.364+3903A>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138464815 | |||||||
| chr7:138464853 | T | C | 1 | a0001c0001t0002g0129 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.364+3941T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138464853 | |||||||
| chr7:138464945 | T | C | 1 | a0001c0001t0001g0104 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.364+4033T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138464945 | |||||||
| chr7:138465455 | A | G | 1 | a0001c0001t0003g0282 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.364+4543A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138465455 | |||||||
| chr7:138465946 | A | T | 103 | a0001c0001t0003g0001 a0001c0001t0003g0269 a0001c0001t0003g0270 others(100): Show |
104 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(101): Show |
intron_variant | MODIFIER | c.364+5034A>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138465946 | |||||||
| chr7:138465967 | A | C | 1 | a0001c0001t0035g0265 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.364+5055A>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138465967 | |||||||
| chr7:138466072 | T | C | 232 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(229): Show |
233 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.364+5160T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138466072 | |||||||
| chr7:138466123 | C | G | 3 | a0001c0001t0026g0266 a0001c0001t0026g0267 a0001c0001t0035g0265 |
3 | HG02109.hp1 HG02630.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.364+5211C>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138466123 | |||||||
| chr7:138466463 | C | CT | 13 | a0001c0001t0002g0163 a0001c0001t0002g0164 a0001c0001t0002g0167 others(10): Show |
13 | HG00609.hp2 HG02083.hp2 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.364+5569dupT | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138466463 | ||||||
| chr7:138466463 | C | CTT | 17 | a0001c0002t0004g0116 a0001c0002t0004g0120 a0001c0002t0004g0121 others(14): Show |
17 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.364+5568_364+5569d others(4): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138466463 | ||||||
| chr7:138466463 | C | CTTTTTT | 11 | a0001c0001t0006g0215 a0001c0001t0006g0216 a0001c0001t0006g0217 others(8): Show |
11 | HG02486.hp1 HG02647.hp2 HG03139.hp2 others(8): Show |
intron_variant | MODIFIER | c.364+5564_364+5569d others(8): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138466463 | ||||||
| chr7:138466463 | C | CTTTTTTT | 6 | a0001c0001t0010g0241 a0001c0001t0017g0005 a0001c0001t0017g0006 others(3): Show |
6 | HG01891.hp1 HG02809.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.364+5563_364+5569d others(9): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138466463 | ||||||
| chr7:138466463 | C | CTTTTTTT others(1): Show |
16 | a0001c0001t0003g0271 a0001c0001t0005g0253 a0001c0001t0005g0254 others(13): Show |
16 | HG00609.hp1 HG01167.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.364+5562_364+5569d others(10): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138466463 | ||||||
| chr7:138466463 | C | CTTTTTTT others(2): Show |
97 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0016 others(94): Show |
98 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.364+5561_364+5569d others(11): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138466463 | ||||||
| chr7:138466463 | C | CTTTTTTT others(3): Show |
51 | a0001c0001t0001g0011 a0001c0001t0001g0019 a0001c0001t0001g0033 others(48): Show |
51 | HG00140.hp2 HG00423.hp2 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.364+5560_364+5569d others(12): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138466463 | ||||||
| chr7:138466463 | C | CTTTTTTT others(4): Show |
11 | a0001c0001t0001g0037 a0001c0001t0001g0049 a0001c0001t0001g0063 others(8): Show |
11 | HG01071.hp2 HG01175.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.364+5559_364+5569d others(13): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138466463 | ||||||
| chr7:138466463 | C | CTTTTTTT others(5): Show |
1 | a0001c0001t0016g0015 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.364+5558_364+5569d others(14): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138466463 | ||||||
| chr7:138466526 | G | A | 1 | a0001c0001t0003g0273 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.364+5614G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138466526 | |||||||
| chr7:138466606 | G | A | 4 | a0001c0001t0002g0099 a0001c0001t0002g0100 a0001c0001t0002g0101 others(1): Show |
4 | HG02055.hp1 HG02976.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.364+5694G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138466606 | |||||||
| chr7:138466610 | C | T | 2 | a0001c0001t0001g0062 a0001c0001t0001g0068 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.364+5698C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138466610 | |||||||
| chr7:138466693 | A | G | 1 | a0001c0001t0001g0032 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.364+5781A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138466693 | |||||||
| chr7:138467048 | T | G | 1 | a0001c0010t0013g0113 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.364+6136T>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138467048 | |||||||
| chr7:138467327 | G | GTGTTTTG others(3): Show |
3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.364+6437_364+6446d others(12): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138467327 | ||||||
| chr7:138467348 | T | TGTTTA | 70 | a0001c0001t0003g0001 a0001c0001t0003g0269 a0001c0001t0003g0270 others(67): Show |
71 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(68): Show |
intron_variant | MODIFIER | c.364+6440_364+6441i others(7): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138467348 | ||||||
| chr7:138467393 | G | A | 1 | a0001c0001t0003g0288 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.364+6481G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138467393 | |||||||
| chr7:138467686 | G | T | 216 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(213): Show |
217 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.364+6774G>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138467686 | |||||||
| chr7:138467817 | T | C | 1 | a0001c0001t0002g0197 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.364+6905T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138467817 | |||||||
| chr7:138468047 | C | T | 1 | a0001c0001t0003g0308 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.364+7135C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138468047 | |||||||
| chr7:138468283 | A | C | 2 | a0001c0001t0002g0107 a0001c0001t0002g0240 |
2 | HG02027.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.364+7371A>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138468283 | |||||||
| chr7:138468306 | A | T | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.364+7394A>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138468306 | |||||||
| chr7:138468465 | TG | T | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.364+7554delG | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138468465 | |||||||
| chr7:138468521 | C | T | 2 | a0001c0001t0003g0276 a0001c0001t0008g0281 |
2 | HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.364+7609C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138468521 | |||||||
| chr7:138468668 | T | G | 1 | a0001c0001t0003g0271 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.364+7756T>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138468668 | |||||||
| chr7:138468746 | C | G | 5 | a0001c0001t0003g0001 a0001c0001t0003g0271 a0001c0001t0003g0272 others(2): Show |
6 | HG00735.hp2 HG01069.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.364+7834C>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138468746 | |||||||
| chr7:138468856 | A | G | 1 | a0001c0001t0029g0300 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.364+7944A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138468856 | |||||||
| chr7:138468891 | C | G | 8 | a0001c0001t0002g0192 a0001c0001t0002g0193 a0001c0001t0002g0206 others(5): Show |
8 | HG02165.hp2 HG02486.hp2 HG03654.hp1 others(5): Show |
intron_variant | MODIFIER | c.364+7979C>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138468891 | |||||||
| chr7:138469263 | TA | T | 9 | a0001c0001t0009g0014 a0001c0001t0009g0094 a0001c0001t0009g0095 others(6): Show |
9 | HG01070.hp2 HG01071.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.364+8354delA | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138469263 | ||||||
| chr7:138469331 | A | AT | 10 | a0001c0001t0001g0048 a0001c0001t0001g0239 a0001c0001t0002g0174 others(7): Show |
10 | HG00423.hp2 HG01175.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.364+8436dupT | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138469331 | ||||||
| chr7:138469331 | AT | A | 9 | a0001c0001t0001g0017 a0001c0001t0001g0062 a0001c0001t0002g0131 others(6): Show |
9 | HG01070.hp2 HG01256.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.364+8436delT | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138469331 | ||||||
| chr7:138469367 | G | C | 1 | a0001c0001t0055g0199 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.364+8455G>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138469367 | |||||||
| chr7:138469562 | A | G | 1 | a0001c0001t0006g0215 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.364+8650A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138469562 | |||||||
| chr7:138469631 | A | T | 3 | a0001c0001t0011g0252 a0001c0001t0011g0255 a0001c0001t0011g0258 |
3 | HG03491.hp1 HG03492.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.364+8719A>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138469631 | |||||||
| chr7:138469945 | G | C | 5 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(2): Show |
5 | HG02486.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.364+9033G>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138469945 | |||||||
| chr7:138470012 | A | G | 1 | a0001c0001t0002g0162 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.364+9100A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138470012 | |||||||
| chr7:138470026 | A | G | 1 | a0001c0001t0046g0262 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.364+9114A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138470026 | |||||||
| chr7:138470087 | A | G | 2 | a0001c0001t0001g0059 a0001c0001t0001g0060 |
2 | HG00438.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.364+9175A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138470087 | |||||||
| chr7:138470121 | T | C | 1 | a0001c0001t0058g0220 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.364+9209T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138470121 | |||||||
| chr7:138470123 | A | AT | 22 | a0001c0001t0001g0067 a0001c0001t0002g0159 a0001c0001t0002g0160 others(19): Show |
22 | HG00423.hp1 HG00741.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.364+9237dupT | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138470123 | ||||||
| chr7:138470123 | A | ATT | 6 | a0001c0001t0002g0174 a0001c0001t0018g0002 a0001c0001t0018g0003 others(3): Show |
6 | HG01261.hp1 HG02055.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.364+9236_364+9237d others(4): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138470123 | ||||||
| chr7:138470123 | AT | A | 120 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(117): Show |
120 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.364+9237delT | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138470123 | ||||||
| chr7:138470123 | ATT | A | 37 | a0001c0001t0001g0017 a0001c0001t0001g0062 a0001c0001t0001g0075 others(34): Show |
38 | HG00140.hp2 HG00735.hp2 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.364+9236_364+9237d others(4): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138470123 | ||||||
| chr7:138470123 | ATTTTTTT others(2): Show |
A | 8 | a0001c0001t0003g0309 a0001c0001t0008g0291 a0001c0001t0008g0292 others(5): Show |
8 | HG01099.hp1 HG01891.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.364+9229_364+9237d others(11): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138470123 | ||||||
| chr7:138470123 | ATTTTTTT others(4): Show |
A | 1 | a0001c0001t0002g0175 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.364+9227_364+9237d others(13): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138470123 | ||||||
| chr7:138470275 | C | T | 1 | a0001c0001t0009g0098 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.364+9363C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138470275 | |||||||
| chr7:138470412 | C | T | 2 | a0001c0001t0003g0277 a0001c0001t0003g0286 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.364+9500C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138470412 | |||||||
| chr7:138470525 | T | A | 1 | a0001c0002t0004g0224 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.364+9613T>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138470525 | |||||||
| chr7:138470669 | G | A | 8 | a0001c0001t0002g0192 a0001c0001t0002g0193 a0001c0001t0002g0206 others(5): Show |
8 | HG02165.hp2 HG02486.hp2 HG03654.hp1 others(5): Show |
intron_variant | MODIFIER | c.364+9757G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138470669 | |||||||
| chr7:138470674 | C | A | 3 | a0001c0001t0026g0266 a0001c0001t0026g0267 a0001c0001t0035g0265 |
3 | HG02109.hp1 HG02630.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.364+9762C>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138470674 | |||||||
| chr7:138470674 | C | T | 2 | a0001c0001t0002g0107 a0001c0001t0002g0240 |
2 | HG02027.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.364+9762C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138470674 | |||||||
| chr7:138470997 | T | G | 21 | a0001c0001t0005g0253 a0001c0001t0005g0254 a0001c0001t0005g0256 others(18): Show |
21 | HG01891.hp1 HG02647.hp1 HG02683.hp1 others(18): Show |
intron_variant | MODIFIER | c.364+10085T>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138470997 | |||||||
| chr7:138471148 | A | G | 1 | a0001c0001t0033g0172 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.364+10236A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138471148 | |||||||
| chr7:138471262 | C | T | 14 | a0001c0001t0002g0175 a0001c0001t0005g0253 a0001c0001t0005g0254 others(11): Show |
14 | HG02647.hp1 HG02683.hp1 HG02735.hp1 others(11): Show |
intron_variant | MODIFIER | c.364+10350C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138471262 | |||||||
| chr7:138471263 | G | A | 2 | a0001c0001t0002g0176 a0001c0001t0002g0248 |
2 | HG03239.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.364+10351G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138471263 | |||||||
| chr7:138471410 | C | T | 1 | a0001c0001t0002g0158 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.364+10498C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138471410 | |||||||
| chr7:138471422 | C | A | 1 | a0001c0001t0002g0174 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.364+10510C>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138471422 | |||||||
| chr7:138471489 | A | G | 1 | a0001c0001t0011g0263 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.364+10577A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138471489 | |||||||
| chr7:138471671 | G | C | 1 | a0001c0001t0006g0223 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.364+10759G>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138471671 | |||||||
| chr7:138471689 | C | T | 1 | a0001c0001t0002g0157 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.364+10777C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138471689 | |||||||
| chr7:138471748 | C | T | 1 | a0001c0004t0057g0109 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.364+10836C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138471748 | |||||||
| chr7:138471794 | G | T | 1 | a0001c0001t0010g0110 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.364+10882G>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138471794 | |||||||
| chr7:138471950 | C | T | 1 | a0001c0001t0002g0156 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.364+11038C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138471950 | |||||||
| chr7:138472022 | G | GA | 5 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(2): Show |
5 | HG02486.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.364+11118dupA | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138472022 | ||||||
| chr7:138472214 | A | G | 100 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(97): Show |
100 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.364+11302A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138472214 | |||||||
| chr7:138472290 | TA | T | 7 | a0001c0001t0011g0252 a0001c0001t0017g0005 a0001c0001t0017g0006 others(4): Show |
7 | HG01081.hp2 HG02735.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.364+11391delA | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138472290 | ||||||
| chr7:138472332 | A | G | 2 | a0001c0001t0001g0030 a0001c0001t0001g0032 |
2 | HG00408.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.364+11420A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138472332 | |||||||
| chr7:138472334 | G | A | 100 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(97): Show |
100 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.364+11422G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138472334 | |||||||
| chr7:138472645 | A | G | 216 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(213): Show |
217 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.364+11733A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138472645 | |||||||
| chr7:138472875 | A | T | 1 | a0001c0001t0055g0199 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.364+11963A>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138472875 | |||||||
| chr7:138472975 | G | A | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.364+12063G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138472975 | |||||||
| chr7:138473086 | T | C | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.364+12174T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138473086 | |||||||
| chr7:138473141 | G | A | 3 | a0001c0001t0018g0002 a0001c0001t0018g0003 a0001c0001t0018g0004 |
3 | HG02895.hp1 HG02897.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.364+12229G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138473141 | |||||||
| chr7:138473384 | G | A | 1 | a0001c0001t0002g0191 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.364+12472G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138473384 | |||||||
| chr7:138473401 | A | G | 12 | a0001c0001t0009g0014 a0001c0001t0009g0094 a0001c0001t0009g0095 others(9): Show |
12 | HG01070.hp2 HG01071.hp2 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.364+12489A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138473401 | |||||||
| chr7:138473633 | C | G | 1 | a0001c0001t0001g0031 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.364+12721C>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138473633 | |||||||
| chr7:138473651 | G | A | 2 | a0001c0001t0022g0130 a0001c0001t0022g0226 |
2 | HG01884.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.364+12739G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138473651 | |||||||
| chr7:138473714 | C | T | 1 | a0001c0001t0011g0258 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.364+12802C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138473714 | |||||||
| chr7:138474074 | C | T | 1 | a0001c0001t0002g0162 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.364+13162C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138474074 | |||||||
| chr7:138474128 | C | CT | 199 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(196): Show |
200 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.364+13231dupT | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138474128 | ||||||
| chr7:138474128 | C | CTT | 14 | a0001c0001t0001g0235 a0001c0001t0002g0099 a0001c0001t0002g0100 others(11): Show |
14 | HG02055.hp1 HG02055.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.364+13230_364+1323 others(6): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138474128 | ||||||
| chr7:138474181 | A | G | 1 | a0001c0001t0003g0001 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.364+13269A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138474181 | |||||||
| chr7:138474280 | T | C | 2 | a0001c0004t0056g0008 a0001c0004t0057g0109 |
2 | HG02055.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.364+13368T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138474280 | |||||||
| chr7:138474337 | G | T | 13 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0062 others(10): Show |
13 | HG01175.hp2 HG02602.hp2 HG03490.hp2 others(10): Show |
intron_variant | MODIFIER | c.364+13425G>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138474337 | |||||||
| chr7:138474371 | C | T | 1 | a0001c0003t0014g0090 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.364+13459C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138474371 | |||||||
| chr7:138474690 | G | A | 3 | a0001c0001t0011g0252 a0001c0001t0011g0255 a0001c0001t0055g0199 |
3 | HG03491.hp1 HG03492.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.364+13778G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138474690 | |||||||
| chr7:138474973 | C | T | 2 | a0001c0001t0002g0196 a0001c0001t0002g0246 |
2 | NA18973.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.364+14061C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138474973 | |||||||
| chr7:138475112 | A | G | 1 | a0001c0001t0009g0014 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.364+14200A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138475112 | |||||||
| chr7:138475246 | C | T | 114 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(111): Show |
114 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.364+14334C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138475246 | |||||||
| chr7:138475273 | A | C | 1 | a0001c0001t0007g0153 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.364+14361A>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138475273 | |||||||
| chr7:138475528 | C | T | 20 | a0001c0001t0033g0172 a0001c0002t0004g0116 a0001c0002t0004g0120 others(17): Show |
20 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.364+14616C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138475528 | |||||||
| chr7:138475572 | A | G | 2 | a0001c0001t0005g0253 a0001c0001t0005g0254 |
2 | HG02683.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.364+14660A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138475572 | |||||||
| chr7:138475790 | G | A | 5 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(2): Show |
5 | HG02486.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.364+14878G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138475790 | |||||||
| chr7:138475819 | C | G | 11 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(8): Show |
11 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.364+14907C>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138475819 | |||||||
| chr7:138475854 | ACT | A | 5 | a0001c0001t0001g0038 a0001c0001t0001g0059 a0001c0001t0001g0060 others(2): Show |
5 | HG00438.hp1 NA18950.hp2 NA19058.hp1 others(2): Show |
intron_variant | MODIFIER | c.364+14944_364+1494 others(6): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138475854 | ||||||
| chr7:138475997 | G | A | 4 | a0001c0001t0002g0099 a0001c0001t0002g0100 a0001c0001t0002g0101 others(1): Show |
4 | HG02055.hp1 HG02976.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.364+15085G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138475997 | |||||||
| chr7:138476232 | A | G | 1 | a0001c0001t0002g0157 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.364+15320A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138476232 | |||||||
| chr7:138476249 | C | T | 12 | a0001c0001t0009g0014 a0001c0001t0009g0094 a0001c0001t0009g0095 others(9): Show |
12 | HG01070.hp2 HG01071.hp2 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.364+15337C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138476249 | |||||||
| chr7:138476333 | G | A | 3 | a0001c0005t0013g0114 a0001c0005t0013g0115 a0001c0010t0013g0113 |
3 | HG02572.hp2 HG02723.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.364+15421G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138476333 | |||||||
| chr7:138476368 | G | A | 4 | a0001c0001t0001g0020 a0001c0001t0001g0050 a0001c0001t0001g0058 others(1): Show |
4 | NA18612.hp1 NA18939.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.364+15456G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138476368 | |||||||
| chr7:138476435 | A | G | 2 | a0001c0001t0022g0130 a0001c0001t0022g0226 |
2 | HG01884.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.364+15523A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138476435 | |||||||
| chr7:138476549 | T | C | 1 | a0001c0001t0005g0256 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.364+15637T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138476549 | |||||||
| chr7:138476550 | G | A | 1 | a0001c0001t0005g0256 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.364+15638G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138476550 | |||||||
| chr7:138476592 | C | CA | 6 | a0001c0001t0003g0275 a0001c0001t0003g0278 a0001c0001t0003g0287 others(3): Show |
6 | HG01255.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.364+15697dupA | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138476592 | ||||||
| chr7:138476592 | CA | C | 137 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(134): Show |
137 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.364+15697delA | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138476592 | ||||||
| chr7:138476592 | CAA | C | 12 | a0001c0001t0001g0035 a0001c0001t0010g0110 a0001c0001t0010g0111 others(9): Show |
12 | HG01255.hp1 HG02055.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.364+15696_364+1569 others(6): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138476592 | ||||||
| chr7:138476627 | G | A | 1 | a0001c0001t0002g0173 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.364+15715G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138476627 | |||||||
| chr7:138476776 | C | T | 2 | a0001c0004t0056g0008 a0001c0004t0057g0109 |
2 | HG02055.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.364+15864C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138476776 | |||||||
| chr7:138476839 | C | T | 1 | a0001c0001t0005g0260 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.364+15927C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138476839 | |||||||
| chr7:138476942 | G | C | 5 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(2): Show |
5 | HG02486.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.364+16030G>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138476942 | |||||||
| chr7:138477059 | CTG | C | 216 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(213): Show |
217 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.364+16161_364+1616 others(6): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138477059 | ||||||
| chr7:138477246 | G | A | 1 | a0001c0001t0012g0119 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.364+16334G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138477246 | |||||||
| chr7:138477267 | C | T | 2 | a0001c0001t0001g0057 a0001c0001t0001g0079 |
2 | NA18943.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.364+16355C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138477267 | |||||||
| chr7:138477316 | C | T | 134 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(131): Show |
134 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.364+16404C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138477316 | |||||||
| chr7:138477332 | A | C | 1 | a0001c0001t0029g0300 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.364+16420A>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138477332 | |||||||
| chr7:138477934 | C | T | 55 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0028 others(52): Show |
55 | HG00423.hp2 HG00438.hp1 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.364+17022C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138477934 | |||||||
| chr7:138477935 | G | A | 1 | a0001c0001t0002g0177 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.364+17023G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138477935 | |||||||
| chr7:138478257 | T | C | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.364+17345T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138478257 | |||||||
| chr7:138478398 | CTG | C | 100 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(97): Show |
100 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.364+17487_364+1748 others(6): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138478398 | |||||||
| chr7:138478572 | G | A | 1 | a0001c0001t0012g0119 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.364+17660G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138478572 | |||||||
| chr7:138478596 | C | T | 8 | a0001c0001t0006g0215 a0001c0001t0006g0216 a0001c0001t0006g0217 others(5): Show |
8 | HG01891.hp1 HG03139.hp2 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.364+17684C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138478596 | |||||||
| chr7:138478599 | CTT | C | 3 | a0001c0001t0001g0016 a0001c0001t0001g0021 a0001c0001t0001g0022 |
3 | HG01928.hp2 HG01934.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.364+17688_364+1768 others(6): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138478599 | |||||||
| chr7:138478679 | G | A | 103 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(100): Show |
103 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.364+17767G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138478679 | |||||||
| chr7:138478741 | G | C | 9 | a0001c0001t0006g0215 a0001c0001t0006g0216 a0001c0001t0006g0217 others(6): Show |
9 | HG01891.hp1 HG03139.hp2 HG03225.hp1 others(6): Show |
intron_variant | MODIFIER | c.364+17829G>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138478741 | |||||||
| chr7:138478747 | G | T | 1 | a0001c0001t0001g0238 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.364+17835G>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138478747 | |||||||
| chr7:138478852 | G | C | 1 | a0001c0001t0001g0238 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.364+17940G>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138478852 | |||||||
| chr7:138478869 | G | A | 1 | a0001c0001t0002g0129 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.364+17957G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138478869 | |||||||
| chr7:138479043 | A | G | 12 | a0001c0001t0009g0014 a0001c0001t0009g0094 a0001c0001t0009g0095 others(9): Show |
12 | HG01070.hp2 HG01071.hp2 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.364+18131A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138479043 | |||||||
| chr7:138479179 | T | C | 2 | a0001c0001t0002g0132 a0001c0001t0002g0159 |
2 | HG00423.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.364+18267T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138479179 | |||||||
| chr7:138479303 | C | T | 1 | a0001c0001t0003g0288 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.364+18391C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138479303 | |||||||
| chr7:138479342 | A | T | 1 | a0001c0001t0055g0199 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.364+18430A>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138479342 | |||||||
| chr7:138479562 | G | T | 1 | a0001c0001t0001g0030 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.364+18650G>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138479562 | |||||||
| chr7:138479670 | G | GCTAATTT others(315): Show |
1 | a0001c0001t0016g0012 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.364+18775_364+1877 others(326): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138479670 | ||||||
| chr7:138479670 | G | GCTAATTT others(318): Show |
4 | a0001c0001t0009g0094 a0001c0001t0009g0095 a0001c0001t0009g0096 others(1): Show |
4 | HG01070.hp2 HG01071.hp2 HG01123.hp2 others(1): Show |
intron_variant | MODIFIER | c.364+18775_364+1877 others(329): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138479670 | ||||||
| chr7:138479670 | G | GCTAATTT others(319): Show |
1 | a0001c0001t0034g0097 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.364+18775_364+1877 others(330): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138479670 | ||||||
| chr7:138479670 | G | GCTAATTT others(331): Show |
1 | a0001c0001t0016g0013 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.364+18775_364+1877 others(342): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138479670 | ||||||
| chr7:138479670 | G | GCTAATTT others(335): Show |
2 | a0001c0001t0009g0014 a0001c0001t0016g0015 |
2 | HG03710.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.364+18775_364+1877 others(346): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138479670 | ||||||
| chr7:138479712 | T | A | 9 | a0001c0001t0009g0014 a0001c0001t0009g0094 a0001c0001t0009g0095 others(6): Show |
9 | HG01070.hp2 HG01071.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.364+18800T>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138479712 | |||||||
| chr7:138479727 | C | T | 67 | a0001c0001t0003g0001 a0001c0001t0003g0269 a0001c0001t0003g0270 others(64): Show |
68 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(65): Show |
intron_variant | MODIFIER | c.364+18815C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138479727 | |||||||
| chr7:138479736 | G | A | 3 | a0001c0001t0001g0052 a0001c0001t0001g0082 a0001c0001t0049g0053 |
3 | NA18975.hp2 NA18994.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.364+18824G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138479736 | |||||||
| chr7:138479787 | C | T | 103 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(100): Show |
103 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.364+18875C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138479787 | |||||||
| chr7:138479861 | C | T | 1 | a0001c0001t0022g0130 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.364+18949C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138479861 | |||||||
| chr7:138479873 | G | A | 1 | a0001c0001t0012g0301 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.364+18961G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138479873 | |||||||
| chr7:138479967 | C | T | 64 | a0001c0001t0003g0001 a0001c0001t0003g0269 a0001c0001t0003g0270 others(61): Show |
65 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(62): Show |
intron_variant | MODIFIER | c.364+19055C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138479967 | |||||||
| chr7:138479968 | G | A | 8 | a0001c0001t0006g0215 a0001c0001t0006g0216 a0001c0001t0006g0217 others(5): Show |
8 | HG01891.hp1 HG03139.hp2 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.364+19056G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138479968 | |||||||
| chr7:138479979 | C | T | 2 | a0001c0004t0056g0008 a0001c0004t0057g0109 |
2 | HG02055.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.364+19067C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138479979 | |||||||
| chr7:138480124 | AT | A | 214 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(211): Show |
215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.364+19214delT | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138480124 | ||||||
| chr7:138480154 | C | T | 1 | a0001c0001t0001g0239 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.364+19242C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138480154 | |||||||
| chr7:138480298 | C | T | 1 | a0001c0001t0022g0226 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.364+19386C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138480298 | |||||||
| chr7:138480569 | G | A | 1 | a0001c0001t0002g0178 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.364+19657G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138480569 | |||||||
| chr7:138480589 | G | A | 4 | a0001c0001t0019g0303 a0001c0001t0019g0304 a0001c0001t0030g0305 others(1): Show |
4 | HG02145.hp1 HG02258.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.364+19677G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138480589 | |||||||
| chr7:138480591 | A | G | 2 | a0001c0001t0001g0062 a0001c0001t0001g0068 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.364+19679A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138480591 | |||||||
| chr7:138480746 | G | A | 1 | a0001c0001t0001g0023 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.364+19834G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138480746 | |||||||
| chr7:138480746 | GTTGGCTC others(14): Show |
G | 3 | a0001c0001t0001g0052 a0001c0001t0001g0082 a0001c0001t0049g0053 |
3 | NA18975.hp2 NA18994.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.364+19835_364+1985 others(25): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138480746 | |||||||
| chr7:138480812 | G | A | 1 | a0001c0001t0037g0041 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.364+19900G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138480812 | |||||||
| chr7:138480870 | G | A | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.364+19958G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138480870 | |||||||
| chr7:138480971 | T | G | 1 | a0001c0001t0001g0091 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.364+20059T>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138480971 | |||||||
| chr7:138481018 | G | A | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.364+20106G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138481018 | |||||||
| chr7:138481067 | G | GC | 3 | a0001c0001t0018g0002 a0001c0001t0018g0003 a0001c0001t0018g0004 |
3 | HG02895.hp1 HG02897.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.364+20156dupC | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138481067 | ||||||
| chr7:138481087 | G | T | 9 | a0001c0001t0009g0014 a0001c0001t0009g0094 a0001c0001t0009g0095 others(6): Show |
9 | HG01070.hp2 HG01071.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.364+20175G>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138481087 | |||||||
| chr7:138481141 | C | T | 1 | a0001c0001t0001g0210 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.364+20229C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138481141 | |||||||
| chr7:138481150 | G | A | 1 | a0001c0001t0007g0133 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.364+20238G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138481150 | |||||||
| chr7:138481163 | T | C | 3 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 |
3 | HG02896.hp1 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.364+20251T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138481163 | |||||||
| chr7:138481281 | T | C | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.364+20369T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138481281 | |||||||
| chr7:138481541 | C | T | 9 | a0001c0001t0009g0014 a0001c0001t0009g0094 a0001c0001t0009g0095 others(6): Show |
9 | HG01070.hp2 HG01071.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.364+20629C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138481541 | |||||||
| chr7:138481662 | C | T | 1 | a0001c0001t0001g0029 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.364+20750C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138481662 | |||||||
| chr7:138481805 | C | T | 20 | a0001c0001t0033g0172 a0001c0002t0004g0116 a0001c0002t0004g0120 others(17): Show |
20 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.364+20893C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138481805 | |||||||
| chr7:138481980 | C | T | 1 | a0001c0001t0010g0110 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.364+21068C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138481980 | |||||||
| chr7:138482003 | C | T | 1 | a0001c0001t0002g0129 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.364+21091C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138482003 | |||||||
| chr7:138482156 | C | G | 1 | a0001c0001t0046g0262 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.364+21244C>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138482156 | |||||||
| chr7:138482164 | TC | T | 7 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(4): Show |
7 | HG01346.hp1 HG01978.hp2 HG01993.hp2 others(4): Show |
intron_variant | MODIFIER | c.364+21253delC | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138482164 | |||||||
| chr7:138482450 | A | AT | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.364+21540dupT | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138482450 | ||||||
| chr7:138482639 | A | T | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.365-21651A>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138482639 | |||||||
| chr7:138482890 | G | T | 1 | a0001c0001t0003g0282 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.365-21400G>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138482890 | |||||||
| chr7:138482898 | C | G | 1 | a0001c0001t0046g0262 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.365-21392C>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138482898 | |||||||
| chr7:138483042 | C | T | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.365-21248C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138483042 | |||||||
| chr7:138483175 | C | A | 2 | a0001c0004t0056g0008 a0001c0004t0057g0109 |
2 | HG02055.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.365-21115C>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138483175 | |||||||
| chr7:138483210 | C | T | 65 | a0001c0001t0003g0001 a0001c0001t0003g0269 a0001c0001t0003g0270 others(62): Show |
66 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(63): Show |
intron_variant | MODIFIER | c.365-21080C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138483210 | |||||||
| chr7:138483213 | G | C | 1 | a0001c0001t0003g0310 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.365-21077G>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138483213 | |||||||
| chr7:138483446 | G | A | 2 | a0001c0004t0056g0008 a0001c0004t0057g0109 |
2 | HG02055.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.365-20844G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138483446 | |||||||
| chr7:138483449 | A | T | 305 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(302): Show |
306 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.365-20841A>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138483449 | |||||||
| chr7:138483542 | G | A | 2 | a0001c0005t0013g0114 a0001c0005t0013g0115 |
2 | HG02572.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.365-20748G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138483542 | |||||||
| chr7:138483601 | C | T | 1 | a0001c0001t0055g0199 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.365-20689C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138483601 | |||||||
| chr7:138483709 | G | T | 1 | a0001c0001t0003g0288 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.365-20581G>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138483709 | |||||||
| chr7:138483775 | A | G | 2 | a0001c0004t0056g0008 a0001c0004t0057g0109 |
2 | HG02055.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.365-20515A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138483775 | |||||||
| chr7:138484017 | T | C | 1 | a0001c0001t0012g0119 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.365-20273T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138484017 | |||||||
| chr7:138484084 | G | T | 1 | a0001c0001t0001g0048 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.365-20206G>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138484084 | |||||||
| chr7:138484112 | A | AT | 7 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(4): Show |
7 | HG02486.hp1 HG02647.hp2 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.365-20164dupT | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138484112 | ||||||
| chr7:138484196 | G | A | 3 | a0001c0005t0013g0114 a0001c0005t0013g0115 a0001c0010t0013g0113 |
3 | HG02572.hp2 HG02723.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.365-20094G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138484196 | |||||||
| chr7:138484207 | T | C | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.365-20083T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138484207 | |||||||
| chr7:138484212 | T | A | 9 | a0001c0001t0009g0014 a0001c0001t0009g0094 a0001c0001t0009g0095 others(6): Show |
9 | HG01070.hp2 HG01071.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.365-20078T>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138484212 | |||||||
| chr7:138484413 | A | AT | 131 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(128): Show |
131 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.365-19864dupT | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138484413 | ||||||
| chr7:138484465 | G | T | 148 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(145): Show |
148 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.365-19825G>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138484465 | |||||||
| chr7:138485018 | G | A | 1 | a0001c0002t0031g0200 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.365-19272G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138485018 | |||||||
| chr7:138485069 | T | C | 17 | a0001c0002t0004g0116 a0001c0002t0004g0120 a0001c0002t0004g0121 others(14): Show |
17 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.365-19221T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138485069 | |||||||
| chr7:138485086 | A | G | 1 | a0001c0001t0001g0034 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.365-19204A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138485086 | |||||||
| chr7:138485090 | T | C | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.365-19200T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138485090 | |||||||
| chr7:138485134 | G | A | 1 | a0001c0001t0002g0192 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.365-19156G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138485134 | |||||||
| chr7:138485262 | A | T | 5 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(2): Show |
5 | HG02486.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.365-19028A>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138485262 | |||||||
| chr7:138485352 | CT | C | 9 | a0001c0001t0006g0215 a0001c0001t0006g0216 a0001c0001t0006g0217 others(6): Show |
9 | HG01891.hp1 HG03139.hp2 HG03225.hp1 others(6): Show |
intron_variant | MODIFIER | c.365-18925delT | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138485352 | ||||||
| chr7:138485373 | C | CT | 3 | a0001c0001t0026g0266 a0001c0001t0026g0267 a0001c0001t0035g0265 |
3 | HG02109.hp1 HG02630.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.365-18914dupT | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138485373 | ||||||
| chr7:138485527 | T | C | 9 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(6): Show |
9 | HG02486.hp1 HG02622.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.365-18763T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138485527 | |||||||
| chr7:138485557 | A | G | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.365-18733A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138485557 | |||||||
| chr7:138485714 | G | A | 1 | a0001c0001t0001g0237 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.365-18576G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138485714 | |||||||
| chr7:138485888 | A | C | 2 | a0001c0004t0056g0008 a0001c0004t0057g0109 |
2 | HG02055.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.365-18402A>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138485888 | |||||||
| chr7:138485946 | A | G | 1 | a0001c0001t0055g0199 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.365-18344A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138485946 | |||||||
| chr7:138486039 | G | T | 4 | a0001c0001t0019g0303 a0001c0001t0019g0304 a0001c0001t0030g0305 others(1): Show |
4 | HG02145.hp1 HG02258.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.365-18251G>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138486039 | |||||||
| chr7:138486041 | G | A | 2 | a0001c0005t0013g0114 a0001c0005t0013g0115 |
2 | HG02572.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.365-18249G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138486041 | |||||||
| chr7:138486110 | T | C | 1 | a0001c0001t0003g0287 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.365-18180T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138486110 | |||||||
| chr7:138486482 | A | G | 1 | a0001c0001t0006g0215 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.365-17808A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138486482 | |||||||
| chr7:138486502 | T | G | 1 | a0001c0001t0001g0237 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.365-17788T>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138486502 | |||||||
| chr7:138486534 | C | T | 80 | a0001c0001t0003g0001 a0001c0001t0003g0269 a0001c0001t0003g0270 others(77): Show |
81 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.365-17756C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138486534 | |||||||
| chr7:138486608 | T | G | 65 | a0001c0001t0003g0001 a0001c0001t0003g0269 a0001c0001t0003g0270 others(62): Show |
66 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(63): Show |
intron_variant | MODIFIER | c.365-17682T>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138486608 | |||||||
| chr7:138486618 | G | C | 65 | a0001c0001t0003g0001 a0001c0001t0003g0269 a0001c0001t0003g0270 others(62): Show |
66 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(63): Show |
intron_variant | MODIFIER | c.365-17672G>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138486618 | |||||||
| chr7:138486630 | G | A | 65 | a0001c0001t0003g0001 a0001c0001t0003g0269 a0001c0001t0003g0270 others(62): Show |
66 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(63): Show |
intron_variant | MODIFIER | c.365-17660G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138486630 | |||||||
| chr7:138486727 | T | G | 5 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(2): Show |
5 | HG02486.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.365-17563T>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138486727 | |||||||
| chr7:138486818 | G | A | 5 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(2): Show |
5 | HG02486.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.365-17472G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138486818 | |||||||
| chr7:138486918 | C | T | 215 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(212): Show |
216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.365-17372C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138486918 | |||||||
| chr7:138487045 | G | T | 100 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(97): Show |
100 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.365-17245G>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138487045 | |||||||
| chr7:138487096 | A | C | 1 | a0001c0001t0002g0192 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.365-17194A>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138487096 | |||||||
| chr7:138487276 | A | G | 5 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(2): Show |
5 | HG02486.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.365-17014A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138487276 | |||||||
| chr7:138487407 | G | T | 7 | a0001c0001t0005g0253 a0001c0001t0005g0254 a0001c0001t0005g0256 others(4): Show |
7 | HG02683.hp1 HG02735.hp1 NA18944.hp2 others(4): Show |
intron_variant | MODIFIER | c.365-16883G>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138487407 | |||||||
| chr7:138487513 | C | T | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.365-16777C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138487513 | |||||||
| chr7:138487523 | A | G | 1 | a0001c0001t0002g0174 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.365-16767A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138487523 | |||||||
| chr7:138487557 | G | A | 2 | a0001c0004t0056g0008 a0001c0004t0057g0109 |
2 | HG02055.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.365-16733G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138487557 | |||||||
| chr7:138487645 | G | A | 12 | a0001c0001t0005g0253 a0001c0001t0005g0254 a0001c0001t0005g0256 others(9): Show |
12 | HG02647.hp1 HG02683.hp1 HG02735.hp1 others(9): Show |
intron_variant | MODIFIER | c.365-16645G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138487645 | |||||||
| chr7:138487702 | A | G | 1 | a0001c0001t0001g0079 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.365-16588A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138487702 | |||||||
| chr7:138487705 | T | A | 1 | a0001c0001t0033g0172 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.365-16585T>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138487705 | |||||||
| chr7:138487726 | A | G | 215 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(212): Show |
216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.365-16564A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138487726 | |||||||
| chr7:138487780 | C | T | 100 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(97): Show |
100 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.365-16510C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138487780 | |||||||
| chr7:138487978 | T | A | 1 | a0001c0001t0044g0128 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.365-16312T>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138487978 | |||||||
| chr7:138488031 | G | C | 1 | a0001c0001t0047g0179 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.365-16259G>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138488031 | |||||||
| chr7:138488059 | G | A | 2 | a0001c0001t0003g0309 a0001c0001t0012g0301 |
2 | HG01891.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.365-16231G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138488059 | |||||||
| chr7:138488230 | C | T | 7 | a0001c0001t0006g0215 a0001c0001t0006g0216 a0001c0001t0006g0217 others(4): Show |
7 | HG03139.hp2 HG03225.hp1 HG03516.hp2 others(4): Show |
intron_variant | MODIFIER | c.365-16060C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138488230 | |||||||
| chr7:138488326 | G | T | 6 | a0001c0001t0001g0017 a0001c0001t0001g0056 a0001c0001t0001g0057 others(3): Show |
6 | HG01934.hp1 HG02132.hp2 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.365-15964G>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138488326 | |||||||
| chr7:138488350 | AGTTCTGC others(65): Show |
A | 1 | a0001c0001t0008g0294 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.365-15939_365-1586 others(76): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138488350 | |||||||
| chr7:138488387 | T | C | 5 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 others(2): Show |
5 | HG02055.hp2 HG02622.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.365-15903T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138488387 | |||||||
| chr7:138488413 | A | T | 1 | a0001c0001t0037g0041 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.365-15877A>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138488413 | |||||||
| chr7:138488449 | G | A | 217 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(214): Show |
218 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.365-15841G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138488449 | |||||||
| chr7:138488739 | A | G | 1 | a0001c0001t0002g0150 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.365-15551A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138488739 | |||||||
| chr7:138489230 | C | T | 2 | a0001c0002t0015g0170 a0001c0002t0015g0171 |
2 | HG02451.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.365-15060C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138489230 | |||||||
| chr7:138489596 | C | G | 1 | a0001c0001t0003g0270 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.365-14694C>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138489596 | |||||||
| chr7:138489613 | G | A | 100 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(97): Show |
100 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.365-14677G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138489613 | |||||||
| chr7:138489648 | C | A | 1 | a0001c0001t0028g0302 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.365-14642C>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138489648 | |||||||
| chr7:138489684 | T | G | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.365-14606T>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138489684 | |||||||
| chr7:138489748 | A | G | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.365-14542A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138489748 | |||||||
| chr7:138489956 | G | C | 68 | a0001c0001t0003g0001 a0001c0001t0003g0269 a0001c0001t0003g0270 others(65): Show |
69 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.365-14334G>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138489956 | |||||||
| chr7:138490056 | A | C | 1 | a0001c0001t0001g0047 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.365-14234A>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138490056 | |||||||
| chr7:138490109 | A | C | 1 | a0001c0001t0001g0234 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.365-14181A>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138490109 | |||||||
| chr7:138490248 | C | T | 1 | a0001c0002t0004g0165 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.365-14042C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138490248 | |||||||
| chr7:138490432 | C | T | 1 | a0001c0001t0055g0199 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.365-13858C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138490432 | |||||||
| chr7:138490755 | G | A | 1 | a0001c0001t0002g0176 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.365-13535G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138490755 | |||||||
| chr7:138490767 | C | T | 1 | a0001c0001t0026g0267 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.365-13523C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138490767 | |||||||
| chr7:138490836 | G | T | 12 | a0001c0001t0005g0253 a0001c0001t0005g0254 a0001c0001t0005g0256 others(9): Show |
12 | HG02647.hp1 HG02683.hp1 HG02735.hp1 others(9): Show |
intron_variant | MODIFIER | c.365-13454G>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138490836 | |||||||
| chr7:138490866 | A | G | 20 | a0001c0001t0033g0172 a0001c0002t0004g0116 a0001c0002t0004g0120 others(17): Show |
20 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.365-13424A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138490866 | |||||||
| chr7:138491010 | A | G | 1 | a0001c0001t0003g0285 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.365-13280A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138491010 | |||||||
| chr7:138491018 | G | C | 214 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(211): Show |
215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.365-13272G>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138491018 | |||||||
| chr7:138491247 | T | A | 2 | a0001c0004t0056g0008 a0001c0004t0057g0109 |
2 | HG02055.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.365-13043T>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138491247 | |||||||
| chr7:138491557 | T | G | 1 | a0001c0004t0057g0109 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.365-12733T>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138491557 | |||||||
| chr7:138491562 | CATTTT | C | 19 | a0001c0002t0004g0116 a0001c0002t0004g0120 a0001c0002t0004g0121 others(16): Show |
19 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.365-12723_365-1271 others(9): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138491562 | ||||||
| chr7:138491575 | C | T | 2 | a0001c0001t0022g0130 a0001c0001t0022g0226 |
2 | HG01884.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.365-12715C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138491575 | |||||||
| chr7:138491622 | C | T | 2 | a0001c0001t0016g0012 a0001c0001t0016g0013 |
2 | HG01884.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.365-12668C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138491622 | |||||||
| chr7:138491793 | C | T | 215 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(212): Show |
216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.365-12497C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138491793 | |||||||
| chr7:138491951 | G | GT | 89 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(86): Show |
89 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.365-12329dupT | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138491951 | ||||||
| chr7:138491951 | GT | G | 7 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 others(4): Show |
7 | HG02622.hp2 HG02683.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.365-12329delT | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138491951 | ||||||
| chr7:138492037 | G | A | 2 | a0001c0004t0056g0008 a0001c0004t0057g0109 |
2 | HG02055.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.365-12253G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138492037 | |||||||
| chr7:138492211 | G | T | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.365-12079G>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138492211 | |||||||
| chr7:138492273 | C | CA | 120 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0018 others(117): Show |
120 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.365-11992dupA | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138492273 | ||||||
| chr7:138492273 | C | CAA | 37 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0034 others(34): Show |
38 | HG00140.hp2 HG00423.hp2 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.365-11993_365-1199 others(6): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138492273 | ||||||
| chr7:138492273 | C | CAAA | 13 | a0001c0001t0001g0249 a0001c0001t0003g0270 a0001c0001t0003g0274 others(10): Show |
13 | HG01243.hp2 HG01978.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.365-11994_365-1199 others(7): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138492273 | ||||||
| chr7:138492273 | C | CAAAA | 8 | a0001c0001t0005g0260 a0001c0001t0011g0252 a0001c0001t0011g0255 others(5): Show |
8 | HG02647.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.365-11995_365-1199 others(8): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138492273 | ||||||
| chr7:138492273 | C | CAAAAAAA others(6): Show |
1 | a0001c0004t0057g0109 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.365-12004_365-1199 others(17): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138492273 | ||||||
| chr7:138492273 | C | CAAAAAAA others(7): Show |
1 | a0001c0004t0056g0008 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.365-12005_365-1199 others(18): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138492273 | ||||||
| chr7:138492273 | CA | C | 9 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0002g0193 others(6): Show |
9 | NA18945.hp1 NA18950.hp1 NA18953.hp2 others(6): Show |
intron_variant | MODIFIER | c.365-11992delA | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138492273 | ||||||
| chr7:138492273 | CAAAAAAA others(4): Show |
C | 12 | a0001c0001t0009g0014 a0001c0001t0009g0094 a0001c0001t0009g0095 others(9): Show |
12 | HG01070.hp2 HG01071.hp2 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.365-12002_365-1199 others(15): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138492273 | ||||||
| chr7:138492299 | G | A | 6 | a0001c0001t0001g0083 a0001c0001t0010g0110 a0001c0001t0010g0111 others(3): Show |
6 | HG02486.hp1 HG02647.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.365-11991G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138492299 | |||||||
| chr7:138492494 | C | T | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.365-11796C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138492494 | |||||||
| chr7:138492704 | C | T | 1 | a0001c0001t0003g0001 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.365-11586C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138492704 | |||||||
| chr7:138492711 | G | A | 1 | a0001c0001t0003g0307 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.365-11579G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138492711 | |||||||
| chr7:138492885 | A | G | 1 | a0001c0001t0002g0192 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.365-11405A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138492885 | |||||||
| chr7:138493088 | A | G | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.365-11202A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138493088 | |||||||
| chr7:138493182 | G | GACAGTTG others(27): Show |
2 | a0001c0001t0003g0276 a0001c0001t0008g0281 |
2 | HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.365-11108_365-1110 others(38): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138493182 | |||||||
| chr7:138493452 | G | A | 1 | a0001c0001t0047g0179 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.365-10838G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138493452 | |||||||
| chr7:138493454 | G | A | 12 | a0001c0001t0005g0253 a0001c0001t0005g0254 a0001c0001t0005g0256 others(9): Show |
12 | HG02647.hp1 HG02683.hp1 HG02735.hp1 others(9): Show |
intron_variant | MODIFIER | c.365-10836G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138493454 | |||||||
| chr7:138493477 | A | G | 215 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(212): Show |
216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.365-10813A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138493477 | |||||||
| chr7:138493544 | G | A | 91 | a0001c0001t0003g0001 a0001c0001t0003g0269 a0001c0001t0003g0270 others(88): Show |
92 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(89): Show |
intron_variant | MODIFIER | c.365-10746G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138493544 | |||||||
| chr7:138493564 | G | A | 12 | a0001c0001t0005g0253 a0001c0001t0005g0254 a0001c0001t0005g0256 others(9): Show |
12 | HG02647.hp1 HG02683.hp1 HG02735.hp1 others(9): Show |
intron_variant | MODIFIER | c.365-10726G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138493564 | |||||||
| chr7:138493883 | A | G | 1 | a0001c0001t0002g0188 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.365-10407A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138493883 | |||||||
| chr7:138493960 | ATTG | A | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.365-10312_365-1031 others(7): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138493960 | ||||||
| chr7:138494107 | A | G | 1 | a0001c0001t0005g0260 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.365-10183A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138494107 | |||||||
| chr7:138494396 | G | T | 1 | a0001c0001t0055g0199 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.365-9894G>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138494396 | |||||||
| chr7:138494780 | A | G | 2 | a0001c0001t0001g0077 a0001c0001t0001g0091 |
2 | HG01256.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.365-9510A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138494780 | |||||||
| chr7:138494959 | A | G | 215 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(212): Show |
216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.365-9331A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138494959 | |||||||
| chr7:138495000 | G | A | 12 | a0001c0001t0009g0014 a0001c0001t0009g0094 a0001c0001t0009g0095 others(9): Show |
12 | HG01070.hp2 HG01071.hp2 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.365-9290G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138495000 | |||||||
| chr7:138495094 | A | G | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.365-9196A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138495094 | |||||||
| chr7:138495120 | A | G | 2 | a0001c0001t0022g0130 a0001c0001t0022g0226 |
2 | HG01884.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.365-9170A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138495120 | |||||||
| chr7:138495241 | A | T | 45 | a0001c0001t0003g0001 a0001c0001t0003g0269 a0001c0001t0003g0270 others(42): Show |
46 | HG00140.hp2 HG00735.hp2 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.365-9049A>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138495241 | |||||||
| chr7:138495295 | A | G | 1 | a0001c0001t0005g0254 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.365-8995A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138495295 | |||||||
| chr7:138495313 | A | G | 8 | a0001c0001t0006g0215 a0001c0001t0006g0216 a0001c0001t0006g0217 others(5): Show |
8 | HG01891.hp1 HG03139.hp2 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.365-8977A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138495313 | |||||||
| chr7:138495505 | T | C | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.365-8785T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138495505 | |||||||
| chr7:138495506 | A | T | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.365-8784A>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138495506 | |||||||
| chr7:138495507 | A | G | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.365-8783A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138495507 | |||||||
| chr7:138495508 | C | T | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.365-8782C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138495508 | |||||||
| chr7:138495509 | A | T | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.365-8781A>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138495509 | |||||||
| chr7:138495510 | G | A | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.365-8780G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138495510 | |||||||
| chr7:138495530 | C | T | 66 | a0001c0001t0003g0001 a0001c0001t0003g0269 a0001c0001t0003g0270 others(63): Show |
67 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(64): Show |
intron_variant | MODIFIER | c.365-8760C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138495530 | |||||||
| chr7:138495570 | C | A | 3 | a0001c0005t0013g0114 a0001c0005t0013g0115 a0001c0010t0013g0113 |
3 | HG02572.hp2 HG02723.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.365-8720C>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138495570 | |||||||
| chr7:138495604 | T | C | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.365-8686T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138495604 | |||||||
| chr7:138495739 | T | C | 1 | a0001c0001t0021g0194 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.365-8551T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138495739 | |||||||
| chr7:138495838 | A | C | 2 | a0001c0001t0002g0196 a0001c0001t0002g0246 |
2 | NA18973.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.365-8452A>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138495838 | |||||||
| chr7:138495927 | G | A | 1 | a0001c0001t0046g0262 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.365-8363G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138495927 | |||||||
| chr7:138496164 | T | C | 1 | a0001c0001t0020g0139 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.365-8126T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138496164 | |||||||
| chr7:138496280 | A | G | 13 | a0001c0001t0005g0253 a0001c0001t0005g0254 a0001c0001t0005g0256 others(10): Show |
13 | HG02647.hp1 HG02683.hp1 HG02735.hp1 others(10): Show |
intron_variant | MODIFIER | c.365-8010A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138496280 | |||||||
| chr7:138496325 | A | G | 1 | a0001c0001t0010g0241 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.365-7965A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138496325 | |||||||
| chr7:138496378 | C | G | 100 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(97): Show |
100 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.365-7912C>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138496378 | |||||||
| chr7:138496483 | G | A | 1 | a0001c0001t0002g0180 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.365-7807G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138496483 | |||||||
| chr7:138496764 | G | A | 4 | a0001c0001t0003g0271 a0001c0001t0003g0272 a0001c0001t0003g0290 others(1): Show |
4 | HG00735.hp2 HG01123.hp1 HG01167.hp1 others(1): Show |
intron_variant | MODIFIER | c.365-7526G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138496764 | |||||||
| chr7:138497275 | C | T | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.365-7015C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138497275 | |||||||
| chr7:138497323 | C | T | 2 | a0001c0004t0056g0008 a0001c0004t0057g0109 |
2 | HG02055.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.365-6967C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138497323 | |||||||
| chr7:138497326 | C | T | 103 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(100): Show |
103 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.365-6964C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138497326 | |||||||
| chr7:138497339 | A | T | 6 | a0001c0001t0002g0173 a0001c0001t0002g0202 a0001c0001t0002g0204 others(3): Show |
6 | HG02886.hp1 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.365-6951A>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138497339 | |||||||
| chr7:138497355 | A | G | 5 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(2): Show |
5 | HG02486.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.365-6935A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138497355 | |||||||
| chr7:138497357 | C | T | 1 | a0001c0001t0002g0177 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.365-6933C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138497357 | |||||||
| chr7:138497393 | C | CT | 34 | a0001c0001t0001g0043 a0001c0001t0001g0050 a0001c0001t0001g0052 others(31): Show |
34 | HG00438.hp1 HG00621.hp1 HG01099.hp2 others(31): Show |
intron_variant | MODIFIER | c.365-6872dupT | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138497393 | ||||||
| chr7:138497393 | CT | C | 28 | a0001c0001t0001g0023 a0001c0001t0001g0077 a0001c0001t0002g0143 others(25): Show |
28 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.365-6872delT | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138497393 | ||||||
| chr7:138497393 | CTTTTTTT | C | 9 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(6): Show |
9 | HG00140.hp1 HG01081.hp1 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.365-6878_365-6872d others(9): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138497393 | ||||||
| chr7:138497393 | CTTTTTTT others(5): Show |
C | 3 | a0001c0003t0014g0071 a0001c0003t0014g0088 a0001c0003t0014g0090 |
3 | HG02622.hp2 HG02818.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.365-6883_365-6872d others(14): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138497393 | ||||||
| chr7:138497554 | A | G | 1 | a0001c0001t0010g0110 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.365-6736A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138497554 | |||||||
| chr7:138497695 | T | C | 3 | a0001c0005t0013g0114 a0001c0005t0013g0115 a0001c0010t0013g0113 |
3 | HG02572.hp2 HG02723.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.365-6595T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138497695 | |||||||
| chr7:138497746 | A | G | 103 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(100): Show |
103 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.365-6544A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138497746 | |||||||
| chr7:138497885 | G | A | 1 | a0001c0001t0055g0199 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.365-6405G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138497885 | |||||||
| chr7:138497991 | C | T | 1 | a0001c0001t0050g0213 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.365-6299C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138497991 | |||||||
| chr7:138498001 | T | C | 103 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(100): Show |
103 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.365-6289T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138498001 | |||||||
| chr7:138498019 | T | A | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.365-6271T>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138498019 | |||||||
| chr7:138498208 | A | C | 2 | a0001c0001t0002g0084 a0001c0001t0027g0080 |
2 | HG04115.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.365-6082A>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138498208 | |||||||
| chr7:138498242 | C | T | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.365-6048C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138498242 | |||||||
| chr7:138498328 | C | G | 122 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(119): Show |
122 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.365-5962C>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138498328 | |||||||
| chr7:138498411 | G | A | 2 | a0001c0001t0002g0134 a0001c0001t0002g0138 |
2 | HG01928.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.365-5879G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138498411 | |||||||
| chr7:138498813 | T | A | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.365-5477T>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138498813 | |||||||
| chr7:138498910 | A | G | 2 | a0001c0001t0002g0150 a0001c0001t0002g0176 |
2 | HG03239.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.365-5380A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138498910 | |||||||
| chr7:138499026 | C | G | 1 | a0001c0001t0002g0161 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.365-5264C>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138499026 | |||||||
| chr7:138499089 | T | A | 1 | a0001c0001t0041g0045 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.365-5201T>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138499089 | |||||||
| chr7:138499804 | C | G | 2 | a0001c0005t0013g0114 a0001c0005t0013g0115 |
2 | HG02572.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.365-4486C>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138499804 | |||||||
| chr7:138499818 | T | C | 12 | a0001c0001t0009g0014 a0001c0001t0009g0094 a0001c0001t0009g0095 others(9): Show |
12 | HG01070.hp2 HG01071.hp2 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.365-4472T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138499818 | |||||||
| chr7:138499949 | G | A | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.365-4341G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138499949 | |||||||
| chr7:138500195 | C | T | 1 | a0001c0001t0054g0072 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.365-4095C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138500195 | |||||||
| chr7:138500202 | A | T | 1 | a0002c0006t0006g0221 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.365-4088A>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138500202 | |||||||
| chr7:138500417 | G | A | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.365-3873G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138500417 | |||||||
| chr7:138500492 | G | A | 1 | a0002c0006t0006g0221 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.365-3798G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138500492 | |||||||
| chr7:138500563 | C | CA | 20 | a0001c0001t0001g0019 a0001c0001t0001g0052 a0001c0001t0001g0238 others(17): Show |
20 | HG00621.hp2 HG01891.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.365-3706dupA | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138500563 | ||||||
| chr7:138500563 | C | CAA | 6 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(3): Show |
6 | HG02486.hp1 HG02622.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.365-3707_365-3706d others(4): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138500563 | ||||||
| chr7:138500563 | CA | C | 19 | a0001c0001t0001g0038 a0001c0001t0001g0237 a0001c0001t0002g0151 others(16): Show |
19 | HG01070.hp2 HG01071.hp2 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.365-3706delA | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138500563 | ||||||
| chr7:138500614 | C | G | 4 | a0001c0001t0019g0303 a0001c0001t0019g0304 a0001c0001t0030g0305 others(1): Show |
4 | HG02145.hp1 HG02258.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.365-3676C>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138500614 | |||||||
| chr7:138500691 | C | T | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.365-3599C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138500691 | |||||||
| chr7:138500702 | A | G | 2 | a0001c0001t0001g0077 a0001c0001t0001g0091 |
2 | HG01256.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.365-3588A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138500702 | |||||||
| chr7:138500713 | T | TA | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.365-3565dupA | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138500713 | ||||||
| chr7:138500734 | G | T | 5 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(2): Show |
5 | HG02486.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.365-3556G>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138500734 | |||||||
| chr7:138500761 | G | A | 2 | a0001c0001t0002g0129 a0001c0001t0002g0197 |
2 | HG00408.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.365-3529G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138500761 | |||||||
| chr7:138500798 | A | G | 8 | a0001c0001t0006g0215 a0001c0001t0006g0216 a0001c0001t0006g0217 others(5): Show |
8 | HG01891.hp1 HG03139.hp2 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.365-3492A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138500798 | |||||||
| chr7:138500967 | TA | T | 72 | a0001c0001t0003g0001 a0001c0001t0003g0269 a0001c0001t0003g0270 others(69): Show |
73 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(70): Show |
intron_variant | MODIFIER | c.365-3312delA | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138500967 | ||||||
| chr7:138501037 | A | G | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.365-3253A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138501037 | |||||||
| chr7:138501045 | A | G | 20 | a0001c0001t0033g0172 a0001c0002t0004g0116 a0001c0002t0004g0120 others(17): Show |
20 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.365-3245A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138501045 | |||||||
| chr7:138501251 | T | G | 8 | a0001c0001t0006g0215 a0001c0001t0006g0216 a0001c0001t0006g0217 others(5): Show |
8 | HG01891.hp1 HG03139.hp2 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.365-3039T>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138501251 | |||||||
| chr7:138501396 | A | G | 1 | a0001c0001t0046g0262 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.365-2894A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138501396 | |||||||
| chr7:138501513 | G | C | 1 | a0001c0001t0003g0276 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.365-2777G>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138501513 | |||||||
| chr7:138501625 | C | T | 1 | a0001c0001t0022g0130 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.365-2665C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138501625 | |||||||
| chr7:138501744 | G | A | 1 | a0001c0001t0003g0282 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.365-2546G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138501744 | |||||||
| chr7:138501757 | C | T | 2 | a0001c0001t0001g0078 a0001c0001t0001g0092 |
2 | NA19010.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.365-2533C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138501757 | |||||||
| chr7:138501817 | G | A | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.365-2473G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138501817 | |||||||
| chr7:138501887 | C | CA | 11 | a0001c0001t0001g0074 a0001c0001t0001g0211 a0001c0001t0002g0230 others(8): Show |
11 | HG00738.hp2 HG01167.hp2 HG01346.hp2 others(8): Show |
intron_variant | MODIFIER | c.365-2392dupA | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138501887 | ||||||
| chr7:138501893 | A | AAAAAAAA others(13): Show |
2 | a0001c0004t0056g0008 a0001c0004t0057g0109 |
2 | HG02055.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.365-2392_365-2391i others(22): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138501893 | ||||||
| chr7:138501893 | A | AAAAAAAA others(9): Show |
3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.365-2392_365-2391i others(18): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138501893 | ||||||
| chr7:138501899 | C | A | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.365-2391C>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138501899 | |||||||
| chr7:138501936 | A | G | 5 | a0001c0001t0003g0277 a0001c0001t0003g0280 a0001c0001t0003g0286 others(2): Show |
5 | HG01256.hp1 HG01258.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.365-2354A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138501936 | |||||||
| chr7:138502125 | T | C | 1 | a0001c0001t0016g0015 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.365-2165T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138502125 | |||||||
| chr7:138502126 | C | T | 2 | a0001c0004t0056g0008 a0001c0004t0057g0109 |
2 | HG02055.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.365-2164C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138502126 | |||||||
| chr7:138502249 | A | C | 1 | a0001c0002t0004g0125 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.365-2041A>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138502249 | |||||||
| chr7:138502298 | T | C | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.365-1992T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138502298 | |||||||
| chr7:138502307 | A | G | 1 | a0001c0001t0026g0267 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.365-1983A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138502307 | |||||||
| chr7:138502447 | A | G | 1 | a0001c0001t0002g0202 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.365-1843A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138502447 | |||||||
| chr7:138502655 | G | A | 2 | a0001c0001t0003g0269 a0001c0009t0003g0268 |
2 | HG02257.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.365-1635G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138502655 | |||||||
| chr7:138502761 | C | A | 1 | a0001c0001t0002g0176 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.365-1529C>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138502761 | |||||||
| chr7:138503010 | T | TA | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.365-1280_365-1279i others(3): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138503010 | |||||||
| chr7:138503160 | A | AT | 215 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(212): Show |
216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.365-1130_365-1129i others(3): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138503160 | |||||||
| chr7:138503185 | C | G | 3 | a0001c0001t0026g0266 a0001c0001t0026g0267 a0001c0001t0035g0265 |
3 | HG02109.hp1 HG02630.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.365-1105C>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138503185 | |||||||
| chr7:138503214 | C | T | 9 | a0001c0001t0002g0107 a0001c0001t0002g0240 a0001c0001t0002g0248 others(6): Show |
9 | HG00438.hp2 HG02027.hp2 HG02083.hp2 others(6): Show |
intron_variant | MODIFIER | c.365-1076C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138503214 | |||||||
| chr7:138503381 | A | C | 10 | a0001c0001t0009g0014 a0001c0001t0009g0094 a0001c0001t0009g0095 others(7): Show |
10 | HG01070.hp2 HG01071.hp2 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.365-909A>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138503381 | |||||||
| chr7:138503445 | G | A | 80 | a0001c0001t0003g0001 a0001c0001t0003g0269 a0001c0001t0003g0270 others(77): Show |
81 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.365-845G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138503445 | |||||||
| chr7:138503455 | T | C | 1 | a0001c0001t0001g0052 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.365-835T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138503455 | |||||||
| chr7:138503486 | T | G | 1 | a0001c0002t0004g0165 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.365-804T>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138503486 | |||||||
| chr7:138503625 | GT | G | 27 | a0001c0001t0002g0143 a0001c0001t0002g0145 a0001c0001t0002g0146 others(24): Show |
27 | HG01515.hp2 HG02109.hp1 HG02132.hp1 others(24): Show |
intron_variant | MODIFIER | c.365-650delT | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138503625 | ||||||
| chr7:138503673 | C | T | 4 | a0001c0001t0033g0172 a0001c0005t0013g0114 a0001c0005t0013g0115 others(1): Show |
4 | HG02572.hp2 HG02630.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.365-617C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138503673 | |||||||
| chr7:138503703 | G | T | 1 | a0001c0001t0002g0219 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.365-587G>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138503703 | |||||||
| chr7:138504091 | T | G | 5 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(2): Show |
5 | HG02486.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.365-199T>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138504091 | |||||||
| chr7:138504100 | A | G | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.365-190A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138504100 | |||||||
| chr7:138504133 | T | C | 10 | a0001c0001t0009g0014 a0001c0001t0009g0094 a0001c0001t0009g0095 others(7): Show |
10 | HG01070.hp2 HG01071.hp2 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.365-157T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138504133 | |||||||
| chr7:138504183 | T | TAAAAAGA others(10): Show |
3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.365-99_365-98insCG others(15): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 138504183 | ||||||
| chr7:138504187 | A | G | 45 | a0001c0001t0003g0001 a0001c0001t0003g0269 a0001c0001t0003g0270 others(42): Show |
46 | HG00140.hp2 HG00735.hp2 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.365-103A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138504187 | |||||||
| chr7:138504192 | T | C | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.365-98T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138504192 | |||||||
| chr7:138504444 | GCTCT | G | 22 | a0001c0001t0001g0031 a0001c0001t0001g0046 a0001c0001t0001g0049 others(19): Show |
22 | HG00609.hp1 HG00741.hp1 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.483+37_483+40delCT others(2): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138504444 | |||||||
| chr7:138504444 | GCTCTT | G | 76 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(73): Show |
76 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.483+37_483+41delCT others(3): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138504444 | |||||||
| chr7:138504444 | GCTCTTT | G | 4 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0054 others(1): Show |
4 | HG02027.hp1 HG02895.hp2 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.483+37_483+42delCT others(4): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138504444 | |||||||
| chr7:138504447 | C | CT | 38 | a0001c0001t0002g0131 a0001c0001t0002g0138 a0001c0001t0002g0147 others(35): Show |
38 | HG00609.hp2 HG00735.hp1 HG01168.hp1 others(35): Show |
intron_variant | MODIFIER | c.483+65dupT | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138504447 | ||||||
| chr7:138504447 | C | CTT | 7 | a0001c0001t0002g0247 a0001c0001t0003g0285 a0001c0001t0006g0216 others(4): Show |
7 | HG02109.hp1 HG03139.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.483+64_483+65dupTT | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138504447 | ||||||
| chr7:138504447 | C | CTTT | 7 | a0001c0001t0009g0014 a0001c0001t0009g0094 a0001c0001t0009g0095 others(4): Show |
7 | HG01070.hp2 HG01071.hp2 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.483+63_483+65dupTT others(1): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138504447 | ||||||
| chr7:138504447 | CT | C | 6 | a0001c0001t0002g0176 a0001c0001t0018g0003 a0001c0001t0022g0130 others(3): Show |
6 | HG01884.hp2 HG01943.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.483+65delT | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138504447 | ||||||
| chr7:138504455 | T | G | 1 | a0001c0001t0001g0103 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.483+47T>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138504455 | |||||||
| chr7:138504456 | T | G | 12 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0062 others(9): Show |
12 | HG01175.hp2 HG02602.hp2 HG03490.hp2 others(9): Show |
intron_variant | MODIFIER | c.483+48T>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138504456 | |||||||
| chr7:138504480 | G | A | 2 | a0001c0001t0030g0305 a0001c0001t0032g0311 |
2 | HG02145.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.483+72G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138504480 | |||||||
| chr7:138504533 | G | A | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.483+125G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138504533 | |||||||
| chr7:138504687 | C | T | 5 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(2): Show |
5 | HG02486.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.483+279C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138504687 | |||||||
| chr7:138504761 | C | CT | 22 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0005g0254 others(19): Show |
22 | HG01109.hp1 HG01496.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.483+366dupT | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138504761 | ||||||
| chr7:138504859 | T | C | 146 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(143): Show |
146 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.483+451T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138504859 | |||||||
| chr7:138504860 | G | A | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.483+452G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138504860 | |||||||
| chr7:138504933 | G | T | 7 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0051 others(4): Show |
7 | HG00140.hp1 HG01081.hp1 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.483+525G>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138504933 | |||||||
| chr7:138504973 | C | G | 67 | a0001c0001t0003g0001 a0001c0001t0003g0269 a0001c0001t0003g0270 others(64): Show |
68 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(65): Show |
intron_variant | MODIFIER | c.483+565C>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138504973 | |||||||
| chr7:138505026 | G | T | 4 | a0001c0001t0002g0099 a0001c0001t0002g0100 a0001c0001t0002g0101 others(1): Show |
4 | HG02055.hp1 HG02976.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.483+618G>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138505026 | |||||||
| chr7:138505236 | C | G | 67 | a0001c0001t0003g0001 a0001c0001t0003g0269 a0001c0001t0003g0270 others(64): Show |
68 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(65): Show |
intron_variant | MODIFIER | c.483+828C>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138505236 | |||||||
| chr7:138505277 | A | G | 1 | a0001c0001t0055g0199 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.483+869A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138505277 | |||||||
| chr7:138505299 | T | C | 2 | a0001c0002t0015g0170 a0001c0002t0015g0171 |
2 | HG02451.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.483+891T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138505299 | |||||||
| chr7:138505502 | GGGT | G | 9 | a0001c0001t0001g0046 a0001c0001t0001g0074 a0001c0001t0004g0279 others(6): Show |
9 | HG00609.hp1 HG01074.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.483+1101_483+1103d others(5): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138505502 | ||||||
| chr7:138505506 | G | GGTT | 109 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(106): Show |
110 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.483+1100_483+1101i others(5): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138505506 | ||||||
| chr7:138505506 | G | GGTTGTT | 26 | a0001c0001t0001g0016 a0001c0001t0001g0021 a0001c0001t0001g0022 others(23): Show |
26 | HG00140.hp1 HG00280.hp1 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.483+1100_483+1101i others(8): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138505506 | ||||||
| chr7:138505506 | G | GGTTGTTG others(2): Show |
3 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0002t0004g0168 |
3 | HG01346.hp2 HG04184.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.483+1100_483+1101i others(11): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138505506 | ||||||
| chr7:138505506 | GGTGGTT | G | 3 | a0001c0001t0005g0256 a0001c0001t0055g0199 a0001c0002t0004g0126 |
3 | HG03491.hp2 HG03579.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.483+1101_483+1106d others(8): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138505506 | ||||||
| chr7:138505506 | GGTGGTTG others(5): Show |
G | 1 | a0001c0001t0001g0044 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.483+1101_483+1112d others(14): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138505506 | ||||||
| chr7:138505506 | GGTGGTTG others(17): Show |
G | 2 | a0001c0004t0056g0008 a0001c0004t0057g0109 |
2 | HG02055.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.483+1101_483+1124d others(26): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138505506 | ||||||
| chr7:138505509 | G | GGTT | 12 | a0001c0001t0002g0140 a0001c0001t0002g0141 a0001c0001t0002g0142 others(9): Show |
12 | HG00609.hp2 HG01256.hp1 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.483+1145_483+1147d others(5): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138505509 | ||||||
| chr7:138505509 | G | GGTTGTT | 3 | a0001c0001t0002g0162 a0001c0001t0002g0164 a0001c0001t0020g0155 |
3 | HG01081.hp2 HG01099.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.483+1142_483+1147d others(8): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138505509 | ||||||
| chr7:138505509 | G | T | 184 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(181): Show |
185 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.483+1101G>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138505509 | |||||||
| chr7:138505509 | GGTT | G | 14 | a0001c0001t0002g0106 a0001c0001t0002g0144 a0001c0001t0002g0145 others(11): Show |
14 | HG01070.hp2 HG01071.hp2 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.483+1145_483+1147d others(5): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138505509 | ||||||
| chr7:138505509 | GGTTGTT | G | 4 | a0001c0001t0007g0187 a0001c0001t0016g0013 a0001c0001t0022g0130 others(1): Show |
4 | HG01884.hp2 HG02451.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.483+1142_483+1147d others(8): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138505509 | ||||||
| chr7:138505509 | GGTTGTTG others(5): Show |
G | 2 | a0001c0001t0002g0131 a0001c0001t0002g0147 |
2 | HG02040.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.483+1136_483+1147d others(14): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138505509 | ||||||
| chr7:138505512 | T | G | 1 | a0001c0001t0002g0202 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.483+1104T>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138505512 | |||||||
| chr7:138505524 | TGTTG | T | 5 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(2): Show |
5 | HG02486.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.483+1117_483+1120d others(6): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138505524 | |||||||
| chr7:138505537 | G | C | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.483+1129G>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138505537 | |||||||
| chr7:138505582 | T | C | 10 | a0001c0001t0009g0014 a0001c0001t0009g0094 a0001c0001t0009g0095 others(7): Show |
10 | HG01070.hp2 HG01071.hp2 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.483+1174T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138505582 | |||||||
| chr7:138505920 | T | A | 2 | a0001c0001t0022g0130 a0001c0001t0022g0226 |
2 | HG01884.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.483+1512T>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138505920 | |||||||
| chr7:138506072 | T | C | 5 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(2): Show |
5 | HG02486.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.483+1664T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138506072 | |||||||
| chr7:138506174 | T | C | 2 | a0001c0001t0011g0263 a0001c0001t0011g0264 |
2 | HG02647.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.483+1766T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138506174 | |||||||
| chr7:138506206 | G | C | 2 | a0001c0001t0024g0024 a0001c0001t0024g0025 |
2 | HG02723.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.483+1798G>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138506206 | |||||||
| chr7:138506264 | T | G | 1 | a0001c0001t0007g0184 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.483+1856T>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138506264 | |||||||
| chr7:138506294 | G | A | 13 | a0001c0001t0005g0253 a0001c0001t0005g0254 a0001c0001t0005g0256 others(10): Show |
13 | HG02647.hp1 HG02683.hp1 HG02735.hp1 others(10): Show |
intron_variant | MODIFIER | c.483+1886G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138506294 | |||||||
| chr7:138506470 | A | G | 7 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(4): Show |
7 | HG00621.hp1 HG02083.hp1 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.483+2062A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138506470 | |||||||
| chr7:138506492 | G | A | 9 | a0001c0001t0009g0014 a0001c0001t0009g0094 a0001c0001t0009g0095 others(6): Show |
9 | HG01070.hp2 HG01071.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.483+2084G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138506492 | |||||||
| chr7:138506512 | A | G | 3 | a0001c0001t0008g0292 a0001c0001t0008g0293 a0001c0001t0008g0294 |
3 | HG02572.hp1 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.483+2104A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138506512 | |||||||
| chr7:138506641 | G | A | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.483+2233G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138506641 | |||||||
| chr7:138506779 | A | G | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.483+2371A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138506779 | |||||||
| chr7:138506884 | G | C | 2 | a0001c0001t0022g0130 a0001c0001t0022g0226 |
2 | HG01884.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.483+2476G>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138506884 | |||||||
| chr7:138506890 | G | C | 10 | a0001c0001t0009g0014 a0001c0001t0009g0094 a0001c0001t0009g0095 others(7): Show |
10 | HG01070.hp2 HG01071.hp2 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.483+2482G>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138506890 | |||||||
| chr7:138506911 | G | A | 213 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(210): Show |
214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.483+2503G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138506911 | |||||||
| chr7:138507018 | C | G | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.483+2610C>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138507018 | |||||||
| chr7:138507234 | C | T | 1 | a0001c0001t0003g0297 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.483+2826C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138507234 | |||||||
| chr7:138507250 | G | A | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.483+2842G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138507250 | |||||||
| chr7:138507329 | T | A | 1 | a0001c0001t0052g0027 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.483+2921T>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138507329 | |||||||
| chr7:138507359 | A | AT | 10 | a0001c0001t0002g0231 a0001c0001t0002g0246 a0001c0001t0010g0110 others(7): Show |
10 | HG01891.hp1 HG02055.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.483+2969dupT | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138507359 | ||||||
| chr7:138507359 | AT | A | 122 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(119): Show |
122 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.483+2969delT | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138507359 | ||||||
| chr7:138507469 | C | T | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.483+3061C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138507469 | |||||||
| chr7:138507528 | C | T | 4 | a0001c0001t0002g0099 a0001c0001t0002g0100 a0001c0001t0002g0101 others(1): Show |
4 | HG02055.hp1 HG02976.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.483+3120C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138507528 | |||||||
| chr7:138507560 | T | C | 2 | a0001c0001t0002g0135 a0001c0001t0043g0136 |
2 | HG00280.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.483+3152T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138507560 | |||||||
| chr7:138507589 | CTG | C | 10 | a0001c0001t0009g0014 a0001c0001t0009g0094 a0001c0001t0009g0095 others(7): Show |
10 | HG01070.hp2 HG01071.hp2 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.483+3182_483+3183d others(4): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138507589 | |||||||
| chr7:138507603 | A | G | 1 | a0001c0002t0015g0169 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.483+3195A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138507603 | |||||||
| chr7:138507767 | C | A | 13 | a0001c0001t0005g0253 a0001c0001t0005g0254 a0001c0001t0005g0256 others(10): Show |
13 | HG02647.hp1 HG02683.hp1 HG02735.hp1 others(10): Show |
intron_variant | MODIFIER | c.483+3359C>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138507767 | |||||||
| chr7:138507880 | G | A | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.483+3472G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138507880 | |||||||
| chr7:138507915 | CAG | C | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.483+3510_483+3511d others(4): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138507915 | ||||||
| chr7:138507933 | C | CA | 17 | a0001c0001t0001g0011 a0001c0001t0002g0174 a0001c0001t0002g0207 others(14): Show |
17 | HG01070.hp2 HG01071.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.483+3538dupA | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138507933 | ||||||
| chr7:138507944 | A | T | 1 | a0001c0004t0056g0008 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.483+3536A>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138507944 | |||||||
| chr7:138507945 | A | T | 2 | a0001c0004t0056g0008 a0001c0004t0057g0109 |
2 | HG02055.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.483+3537A>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138507945 | |||||||
| chr7:138507946 | A | T | 19 | a0001c0001t0006g0215 a0001c0001t0006g0216 a0001c0001t0006g0217 others(16): Show |
19 | HG01891.hp1 HG02055.hp2 HG02486.hp1 others(16): Show |
intron_variant | MODIFIER | c.483+3538A>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138507946 | |||||||
| chr7:138508181 | C | T | 2 | a0001c0001t0003g0284 a0001c0001t0003g0310 |
2 | HG01106.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.483+3773C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138508181 | |||||||
| chr7:138508338 | A | G | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.483+3930A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138508338 | |||||||
| chr7:138508503 | G | A | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.483+4095G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138508503 | |||||||
| chr7:138508592 | C | G | 1 | a0001c0001t0029g0300 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.483+4184C>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138508592 | |||||||
| chr7:138508662 | A | AGT | 46 | a0001c0001t0002g0106 a0001c0001t0002g0129 a0001c0001t0002g0131 others(43): Show |
46 | HG00280.hp2 HG00408.hp1 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.483+4284_483+4285d others(4): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138508662 | ||||||
| chr7:138508662 | A | AGTGT | 11 | a0001c0001t0002g0145 a0001c0001t0002g0164 a0001c0001t0002g0178 others(8): Show |
11 | HG00735.hp1 HG01515.hp2 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.483+4282_483+4285d others(6): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138508662 | ||||||
| chr7:138508662 | A | AGTGTGT | 4 | a0001c0001t0002g0152 a0001c0001t0002g0159 a0001c0001t0022g0130 others(1): Show |
4 | HG00423.hp1 HG02055.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.483+4280_483+4285d others(8): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138508662 | ||||||
| chr7:138508662 | AGT | A | 5 | a0001c0001t0002g0202 a0001c0001t0002g0204 a0001c0001t0002g0248 others(2): Show |
5 | HG02886.hp1 NA18963.hp2 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.483+4284_483+4285d others(4): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138508662 | ||||||
| chr7:138508666 | TGTGTGTG others(47): Show |
T | 2 | a0001c0001t0007g0184 a0001c0001t0007g0187 |
2 | NA18939.hp2 NA18940.hp1 |
intron_variant | MODIFIER | c.483+4285_483+4338d others(56): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138508666 | ||||||
| chr7:138508668 | T | C | 2 | a0001c0001t0001g0059 a0001c0001t0001g0060 |
2 | HG00438.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.483+4260T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138508668 | |||||||
| chr7:138508668 | TGTGTGTG others(45): Show |
T | 1 | a0001c0001t0001g0238 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.483+4286_483+4337d others(54): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138508668 | ||||||
| chr7:138508676 | T | TGTGTGC | 13 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0064 others(10): Show |
13 | HG02055.hp1 HG02976.hp1 HG03471.hp1 others(10): Show |
intron_variant | MODIFIER | c.483+4273_483+4274i others(8): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138508676 | ||||||
| chr7:138508678 | T | C | 2 | a0001c0001t0001g0029 a0001c0001t0001g0057 |
2 | HG02155.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.483+4270T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138508678 | |||||||
| chr7:138508678 | T | TGTGC | 53 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(50): Show |
53 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.483+4273_483+4274i others(6): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138508678 | ||||||
| chr7:138508678 | T | TGTGTGC | 3 | a0001c0001t0001g0058 a0001c0001t0001g0065 a0001c0001t0001g0083 |
3 | NA18612.hp1 NA18939.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.483+4275_483+4276i others(8): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138508678 | ||||||
| chr7:138508682 | T | C | 24 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(21): Show |
24 | HG00438.hp1 HG00609.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.483+4274T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138508682 | |||||||
| chr7:138508684 | TGTGTGTG others(17): Show |
T | 2 | a0001c0001t0001g0059 a0001c0001t0001g0060 |
2 | HG00438.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.483+4286_483+4309d others(26): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138508684 | ||||||
| chr7:138508686 | T | C | 8 | a0001c0001t0010g0110 a0001c0001t0010g0112 a0001c0001t0010g0241 others(5): Show |
8 | HG02486.hp1 HG02809.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.483+4278T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138508686 | |||||||
| chr7:138508688 | T | C | 10 | a0001c0001t0001g0237 a0001c0001t0003g0287 a0001c0001t0010g0110 others(7): Show |
10 | HG02486.hp1 HG02647.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.483+4280T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138508688 | |||||||
| chr7:138508690 | T | C | 17 | a0001c0001t0003g0269 a0001c0001t0003g0271 a0001c0001t0003g0283 others(14): Show |
17 | HG00280.hp1 HG00738.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.483+4282T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138508690 | |||||||
| chr7:138508690 | T | TGC | 18 | a0001c0001t0003g0270 a0001c0001t0003g0274 a0001c0001t0003g0276 others(15): Show |
18 | HG01106.hp2 HG01168.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.483+4283_483+4284i others(4): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138508690 | ||||||
| chr7:138508690 | TGTGCGCG others(3): Show |
T | 1 | a0001c0001t0001g0055 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.483+4286_483+4295d others(12): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138508690 | ||||||
| chr7:138508691 | G | GTGTGTGC others(12): Show |
1 | a0001c0001t0011g0252 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.483+4285_483+4286i others(21): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138508691 | ||||||
| chr7:138508692 | T | C | 49 | a0001c0001t0001g0103 a0001c0001t0002g0142 a0001c0001t0002g0174 others(46): Show |
49 | HG00280.hp1 HG00738.hp1 HG00741.hp2 others(46): Show |
intron_variant | MODIFIER | c.483+4284T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138508692 | |||||||
| chr7:138508692 | T | TGC | 25 | a0001c0001t0002g0107 a0001c0001t0002g0193 a0001c0001t0002g0206 others(22): Show |
26 | HG00140.hp2 HG00735.hp2 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.483+4292_483+4293d others(4): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138508692 | ||||||
| chr7:138508692 | T | TGCGC | 9 | a0001c0001t0006g0217 a0001c0001t0006g0222 a0001c0001t0006g0223 others(6): Show |
9 | HG01099.hp1 HG02109.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.483+4290_483+4293d others(6): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138508692 | ||||||
| chr7:138508692 | T | TGTGC | 10 | a0001c0001t0003g0280 a0001c0001t0003g0289 a0001c0001t0004g0279 others(7): Show |
10 | HG01074.hp1 HG01346.hp2 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.483+4285_483+4286i others(6): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138508692 | ||||||
| chr7:138508692 | T | TGTGCGCG others(3): Show |
2 | a0001c0003t0014g0071 a0001c0003t0014g0088 |
2 | HG02622.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.483+4285_483+4286i others(12): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138508692 | ||||||
| chr7:138508692 | T | TGTGTGCG others(3): Show |
19 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(16): Show |
19 | HG00609.hp1 HG01261.hp2 HG01346.hp1 others(16): Show |
intron_variant | MODIFIER | c.483+4285_483+4286i others(12): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138508692 | ||||||
| chr7:138508692 | T | TGTGTGCG others(11): Show |
3 | a0001c0001t0001g0034 a0001c0001t0011g0255 a0001c0001t0011g0258 |
3 | HG02083.hp1 HG03492.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.483+4285_483+4286i others(20): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138508692 | ||||||
| chr7:138508692 | T | TGTGTGTG others(9): Show |
4 | a0001c0001t0001g0062 a0001c0001t0005g0254 a0001c0001t0005g0256 others(1): Show |
4 | HG02683.hp1 HG03490.hp2 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.483+4285_483+4286i others(18): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138508692 | ||||||
| chr7:138508692 | T | TGTGTGTG others(11): Show |
1 | a0001c0001t0001g0068 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.483+4285_483+4286i others(20): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138508692 | ||||||
| chr7:138508692 | T | TGTGTGTG others(7): Show |
1 | a0001c0001t0005g0257 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.483+4285_483+4286i others(16): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138508692 | ||||||
| chr7:138508692 | T | TGTGTGTG others(9): Show |
1 | a0001c0004t0056g0008 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.483+4285_483+4286i others(18): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138508692 | ||||||
| chr7:138508692 | T | TGTGTGTG others(11): Show |
2 | a0001c0001t0005g0253 a0001c0001t0005g0259 |
2 | HG02735.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.483+4285_483+4286i others(20): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138508692 | ||||||
| chr7:138508692 | T | TGTGTGTG others(13): Show |
1 | a0001c0001t0005g0260 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.483+4285_483+4286i others(22): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138508692 | ||||||
| chr7:138508692 | T | TGTGTGTG others(7): Show |
1 | a0001c0001t0055g0199 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.483+4285_483+4286i others(16): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138508692 | ||||||
| chr7:138508692 | T | TGTGTGTG others(13): Show |
1 | a0001c0001t0011g0263 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.483+4285_483+4286i others(22): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138508692 | ||||||
| chr7:138508692 | T | TGTGTGTG others(15): Show |
1 | a0001c0001t0011g0264 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.483+4285_483+4286i others(24): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138508692 | ||||||
| chr7:138508694 | C | G | 1 | a0001c0001t0002g0152 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.483+4286C>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138508694 | |||||||
| chr7:138508694 | C | T | 4 | a0001c0001t0009g0094 a0001c0001t0009g0095 a0001c0001t0009g0096 others(1): Show |
4 | HG01070.hp2 HG01071.hp2 HG01123.hp2 others(1): Show |
intron_variant | MODIFIER | c.483+4286C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138508694 | |||||||
| chr7:138508694 | CGCGCGCG others(17): Show |
C | 1 | a0001c0003t0014g0090 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.483+4290_483+4313d others(26): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138508694 | ||||||
| chr7:138508696 | C | T | 1 | a0001c0001t0017g0007 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.483+4288C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138508696 | |||||||
| chr7:138508698 | C | T | 2 | a0001c0001t0017g0005 a0001c0001t0017g0006 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.483+4290C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138508698 | |||||||
| chr7:138508700 | C | CGCAGCGC others(21): Show |
1 | a0001c0001t0001g0074 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.483+4293_483+4294i others(30): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138508700 | ||||||
| chr7:138508700 | C | CGCGCAGC others(20): Show |
1 | a0001c0001t0049g0053 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.483+4293_483+4294i others(29): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138508700 | ||||||
| chr7:138508700 | C | CGCGCGCG others(23): Show |
1 | a0001c0001t0001g0050 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.483+4293_483+4294i others(32): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138508700 | ||||||
| chr7:138508700 | C | CGCGCGCG others(21): Show |
23 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0020 others(20): Show |
23 | HG00408.hp2 HG00423.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.483+4293_483+4294i others(30): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138508700 | ||||||
| chr7:138508700 | C | CGCGCGCG others(19): Show |
33 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0022 others(30): Show |
33 | HG00140.hp1 HG01081.hp1 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.483+4293_483+4294i others(28): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138508700 | ||||||
| chr7:138508700 | C | CGCGCGCG others(33): Show |
1 | a0001c0001t0001g0035 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.483+4293_483+4294i others(42): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138508700 | ||||||
| chr7:138508700 | C | CGCGCGCG others(18): Show |
1 | a0001c0001t0001g0249 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.483+4293_483+4294i others(27): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138508700 | ||||||
| chr7:138508700 | C | CGCGCGCG others(17): Show |
8 | a0001c0001t0001g0064 a0001c0001t0001g0089 a0001c0001t0001g0104 others(5): Show |
8 | HG01175.hp2 HG02055.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.483+4293_483+4294i others(26): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138508700 | ||||||
| chr7:138508700 | C | CGCGCGCG others(7): Show |
4 | a0001c0001t0009g0094 a0001c0001t0009g0095 a0001c0001t0009g0096 others(1): Show |
4 | HG01070.hp2 HG01071.hp2 HG01123.hp2 others(1): Show |
intron_variant | MODIFIER | c.483+4293_483+4294i others(16): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138508700 | ||||||
| chr7:138508700 | C | CGCGCGCG others(15): Show |
2 | a0001c0001t0001g0054 a0001c0001t0001g0086 |
2 | HG02027.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.483+4293_483+4294i others(24): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138508700 | ||||||
| chr7:138508700 | C | CGCGCGCG others(13): Show |
2 | a0001c0001t0001g0057 a0001c0001t0001g0225 |
2 | HG01993.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.483+4293_483+4294i others(22): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138508700 | ||||||
| chr7:138508700 | C | CGCGCGCG others(29): Show |
1 | a0001c0004t0057g0109 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.483+4293_483+4294i others(38): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138508700 | ||||||
| chr7:138508700 | C | CGCGCGCT others(19): Show |
1 | a0001c0001t0002g0101 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.483+4293_483+4294i others(28): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138508700 | ||||||
| chr7:138508700 | C | CGCGCGTG others(11): Show |
4 | a0001c0002t0004g0116 a0001c0002t0004g0120 a0001c0002t0004g0242 others(1): Show |
4 | HG00738.hp2 HG01167.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.483+4293_483+4294i others(20): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138508700 | ||||||
| chr7:138508700 | C | CGCGTGTG others(9): Show |
8 | a0001c0001t0033g0172 a0001c0002t0004g0121 a0001c0002t0004g0122 others(5): Show |
8 | HG00741.hp2 HG01243.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.483+4293_483+4294i others(18): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138508700 | ||||||
| chr7:138508700 | C | CGCGTGTG others(23): Show |
2 | a0001c0001t0017g0005 a0001c0001t0017g0006 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.483+4293_483+4294i others(32): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138508700 | ||||||
| chr7:138508700 | C | CGGCGAGC others(22): Show |
1 | a0001c0001t0001g0077 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.483+4293_483+4294i others(31): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138508700 | ||||||
| chr7:138508700 | C | CGTGTGTG others(21): Show |
1 | a0001c0001t0017g0007 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.483+4307_483+4308i others(30): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138508700 | ||||||
| chr7:138508700 | C | T | 5 | a0001c0001t0003g0287 a0001c0001t0010g0110 a0001c0001t0010g0241 others(2): Show |
5 | HG02486.hp1 HG02622.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.483+4292C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138508700 | |||||||
| chr7:138508702 | T | C | 9 | a0001c0001t0002g0173 a0001c0001t0002g0202 a0001c0001t0002g0204 others(6): Show |
9 | HG01255.hp2 HG02486.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.483+4294T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138508702 | |||||||
| chr7:138508704 | T | C | 2 | a0001c0003t0014g0071 a0001c0003t0014g0088 |
2 | HG02622.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.483+4296T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138508704 | |||||||
| chr7:138508706 | T | C | 3 | a0001c0001t0001g0055 a0001c0003t0014g0071 a0001c0003t0014g0088 |
3 | HG00741.hp1 HG02622.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.483+4298T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138508706 | |||||||
| chr7:138508708 | C | CGT | 89 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0016 others(86): Show |
89 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.483+4310_483+4311d others(4): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138508708 | ||||||
| chr7:138508708 | C | CGTGTGCG others(1): Show |
41 | a0001c0001t0003g0001 a0001c0001t0003g0270 a0001c0001t0003g0271 others(38): Show |
42 | HG00140.hp2 HG00735.hp2 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.483+4305_483+4306i others(10): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138508708 | ||||||
| chr7:138508708 | C | CGTGTGTG others(9): Show |
25 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(22): Show |
25 | HG00280.hp1 HG00609.hp1 HG01346.hp1 others(22): Show |
intron_variant | MODIFIER | c.483+4311_483+4312i others(18): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138508708 | ||||||
| chr7:138508708 | C | T | 6 | a0001c0001t0001g0055 a0001c0001t0010g0110 a0001c0001t0010g0111 others(3): Show |
6 | HG00741.hp1 HG02486.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.483+4300C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138508708 | |||||||
| chr7:138508716 | T | C | 1 | a0001c0004t0056g0008 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.483+4308T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138508716 | |||||||
| chr7:138508718 | T | C | 2 | a0001c0001t0043g0136 a0001c0004t0057g0109 |
2 | HG01069.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.483+4310T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138508718 | |||||||
| chr7:138508718 | T | TGTGC | 4 | a0001c0001t0001g0010 a0001c0001t0001g0065 a0001c0001t0001g0092 others(1): Show |
4 | HG02896.hp1 HG02976.hp2 NA18939.hp1 others(1): Show |
intron_variant | MODIFIER | c.483+4311_483+4312i others(6): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138508718 | ||||||
| chr7:138508720 | C | CGT | 3 | a0001c0001t0003g0282 a0001c0003t0014g0071 a0001c0003t0014g0088 |
3 | HG02109.hp2 HG02622.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.483+4337_483+4338d others(4): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138508720 | ||||||
| chr7:138508720 | C | CGTGTGTG others(9): Show |
1 | a0001c0001t0055g0199 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.483+4325_483+4326i others(18): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138508720 | ||||||
| chr7:138508720 | C | CTGTGTGT others(2): Show |
4 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(1): Show |
4 | HG02486.hp1 HG02647.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.483+4312_483+4313i others(11): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138508720 | |||||||
| chr7:138508720 | C | T | 30 | a0001c0001t0001g0010 a0001c0001t0001g0028 a0001c0001t0001g0042 others(27): Show |
30 | HG01069.hp1 HG01070.hp2 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.483+4312C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138508720 | |||||||
| chr7:138508720 | CGT | C | 4 | a0001c0001t0002g0202 a0001c0001t0002g0206 a0001c0001t0002g0207 others(1): Show |
4 | HG02165.hp2 HG02717.hp1 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.483+4337_483+4338d others(4): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138508720 | ||||||
| chr7:138508722 | T | C | 21 | a0001c0001t0001g0028 a0001c0001t0001g0042 a0001c0001t0001g0070 others(18): Show |
21 | HG01070.hp2 HG01071.hp2 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.483+4314T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138508722 | |||||||
| chr7:138508722 | T | TGC | 3 | a0001c0001t0026g0266 a0001c0001t0026g0267 a0001c0001t0035g0265 |
3 | HG02109.hp1 HG02630.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.483+4315_483+4316i others(4): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138508722 | ||||||
| chr7:138508722 | T | TGTGTGTG others(1): Show |
3 | a0001c0005t0013g0114 a0001c0005t0013g0115 a0001c0010t0013g0113 |
3 | HG02572.hp2 HG02723.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.483+4321_483+4322i others(10): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138508722 | ||||||
| chr7:138508722 | T | TGTGTGTG others(5): Show |
3 | a0001c0001t0009g0014 a0001c0001t0016g0012 a0001c0001t0016g0013 |
3 | HG01884.hp1 HG02451.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.483+4325_483+4326i others(14): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138508722 | ||||||
| chr7:138508724 | T | TGTGTGTG others(3): Show |
2 | a0001c0001t0001g0062 a0001c0001t0001g0068 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.483+4325_483+4326i others(12): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138508724 | ||||||
| chr7:138508724 | T | TGTGTGTG others(7): Show |
13 | a0001c0001t0005g0253 a0001c0001t0005g0254 a0001c0001t0005g0256 others(10): Show |
13 | HG02647.hp1 HG02683.hp1 HG02735.hp1 others(10): Show |
intron_variant | MODIFIER | c.483+4329_483+4330i others(16): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138508724 | ||||||
| chr7:138508726 | T | C | 1 | a0001c0001t0010g0241 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.483+4318T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138508726 | |||||||
| chr7:138508728 | T | C | 4 | a0001c0001t0001g0070 a0001c0001t0001g0077 a0001c0001t0001g0091 others(1): Show |
4 | HG01256.hp2 HG02055.hp2 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.483+4320T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138508728 | |||||||
| chr7:138508728 | T | TGTGTGTG others(11): Show |
1 | a0001c0004t0056g0008 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.483+4327_483+4328i others(20): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138508728 | ||||||
| chr7:138508732 | T | C | 1 | a0001c0001t0001g0238 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.483+4324T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138508732 | |||||||
| chr7:138508981 | C | A | 5 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(2): Show |
5 | HG02486.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.483+4573C>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138508981 | |||||||
| chr7:138509074 | G | A | 2 | a0001c0001t0022g0130 a0001c0001t0022g0226 |
2 | HG01884.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.483+4666G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138509074 | |||||||
| chr7:138509103 | C | T | 101 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(98): Show |
101 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.483+4695C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138509103 | |||||||
| chr7:138509186 | T | A | 21 | a0001c0001t0005g0253 a0001c0001t0005g0254 a0001c0001t0005g0256 others(18): Show |
21 | HG01891.hp1 HG02647.hp1 HG02683.hp1 others(18): Show |
intron_variant | MODIFIER | c.483+4778T>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138509186 | |||||||
| chr7:138509208 | C | T | 1 | a0001c0001t0002g0129 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.483+4800C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138509208 | |||||||
| chr7:138509226 | A | G | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.483+4818A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138509226 | |||||||
| chr7:138509357 | G | A | 1 | a0001c0001t0055g0199 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.483+4949G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138509357 | |||||||
| chr7:138509531 | G | A | 1 | a0001c0001t0042g0201 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.483+5123G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138509531 | |||||||
| chr7:138509701 | C | CA | 154 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(151): Show |
154 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.483+5313dupA | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138509701 | ||||||
| chr7:138509701 | C | CAA | 14 | a0001c0001t0001g0036 a0001c0001t0001g0050 a0001c0001t0001g0064 others(11): Show |
14 | HG01256.hp2 HG02055.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.483+5312_483+5313d others(4): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138509701 | ||||||
| chr7:138509701 | CAAAAA | C | 8 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(5): Show |
8 | HG02486.hp1 HG02647.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.483+5309_483+5313d others(7): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138509701 | ||||||
| chr7:138509748 | T | A | 1 | a0001c0001t0021g0189 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.483+5340T>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138509748 | |||||||
| chr7:138509971 | C | T | 6 | a0001c0002t0004g0116 a0001c0002t0004g0120 a0001c0002t0004g0126 others(3): Show |
6 | HG00738.hp2 HG01167.hp2 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.484-5241C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138509971 | |||||||
| chr7:138510006 | A | G | 304 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(301): Show |
305 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.484-5206A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138510006 | |||||||
| chr7:138510011 | C | T | 3 | a0001c0003t0014g0071 a0001c0003t0014g0088 a0001c0003t0014g0090 |
3 | HG02622.hp2 HG02818.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.484-5201C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138510011 | |||||||
| chr7:138510061 | T | A | 98 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(95): Show |
98 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.484-5151T>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138510061 | |||||||
| chr7:138510137 | G | T | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.484-5075G>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138510137 | |||||||
| chr7:138510157 | C | T | 1 | a0001c0001t0001g0214 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.484-5055C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138510157 | |||||||
| chr7:138510394 | T | A | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.484-4818T>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138510394 | |||||||
| chr7:138510407 | T | G | 1 | a0001c0001t0002g0207 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.484-4805T>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138510407 | |||||||
| chr7:138510411 | G | T | 2 | a0001c0001t0003g0285 a0001c0001t0055g0199 |
2 | HG03540.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.484-4801G>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138510411 | |||||||
| chr7:138510535 | C | T | 45 | a0001c0001t0003g0001 a0001c0001t0003g0269 a0001c0001t0003g0270 others(42): Show |
46 | HG00140.hp2 HG00735.hp2 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.484-4677C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138510535 | |||||||
| chr7:138510761 | C | A | 2 | a0001c0004t0056g0008 a0001c0004t0057g0109 |
2 | HG02055.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.484-4451C>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138510761 | |||||||
| chr7:138510761 | C | G | 8 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(5): Show |
8 | HG02486.hp1 HG02647.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.484-4451C>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138510761 | |||||||
| chr7:138511228 | A | T | 1 | a0001c0001t0055g0199 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.484-3984A>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138511228 | |||||||
| chr7:138511244 | A | G | 1 | a0001c0001t0011g0264 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.484-3968A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138511244 | |||||||
| chr7:138511248 | G | C | 2 | a0001c0004t0056g0008 a0001c0004t0057g0109 |
2 | HG02055.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.484-3964G>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138511248 | |||||||
| chr7:138511288 | A | G | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.484-3924A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138511288 | |||||||
| chr7:138511304 | C | CT | 15 | a0001c0001t0007g0153 a0001c0001t0010g0110 a0001c0001t0010g0111 others(12): Show |
15 | HG00438.hp2 HG01255.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.484-3894dupT | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138511304 | ||||||
| chr7:138511369 | T | C | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.484-3843T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138511369 | |||||||
| chr7:138511429 | C | T | 212 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(209): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.484-3783C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138511429 | |||||||
| chr7:138511478 | C | T | 5 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(2): Show |
5 | HG02486.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.484-3734C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138511478 | |||||||
| chr7:138511482 | A | G | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.484-3730A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138511482 | |||||||
| chr7:138511570 | G | A | 1 | a0001c0001t0005g0257 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.484-3642G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138511570 | |||||||
| chr7:138511581 | C | T | 15 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0005g0253 others(12): Show |
15 | HG02647.hp1 HG02683.hp1 HG02735.hp1 others(12): Show |
intron_variant | MODIFIER | c.484-3631C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138511581 | |||||||
| chr7:138511769 | A | T | 1 | a0001c0001t0001g0063 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.484-3443A>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138511769 | |||||||
| chr7:138511981 | AT | A | 13 | a0001c0001t0005g0253 a0001c0001t0005g0254 a0001c0001t0005g0256 others(10): Show |
13 | HG02647.hp1 HG02683.hp1 HG02735.hp1 others(10): Show |
intron_variant | MODIFIER | c.484-3229delT | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138511981 | ||||||
| chr7:138512163 | G | T | 13 | a0001c0001t0005g0253 a0001c0001t0005g0254 a0001c0001t0005g0256 others(10): Show |
13 | HG02647.hp1 HG02683.hp1 HG02735.hp1 others(10): Show |
intron_variant | MODIFIER | c.484-3049G>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138512163 | |||||||
| chr7:138512322 | T | A | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.484-2890T>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138512322 | |||||||
| chr7:138512332 | C | T | 1 | a0001c0001t0002g0180 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.484-2880C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138512332 | |||||||
| chr7:138512358 | T | G | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.484-2854T>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138512358 | |||||||
| chr7:138512461 | C | T | 1 | a0001c0001t0005g0256 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.484-2751C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138512461 | |||||||
| chr7:138512532 | G | A | 1 | a0001c0001t0012g0301 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.484-2680G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138512532 | |||||||
| chr7:138512629 | TGGCTGGA others(8): Show |
T | 1 | a0001c0001t0043g0136 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.484-2576_484-2562d others(17): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 138512629 | ||||||
| chr7:138512721 | A | G | 1 | a0001c0001t0002g0147 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.484-2491A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138512721 | |||||||
| chr7:138513032 | T | C | 1 | a0001c0001t0002g0219 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.484-2180T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138513032 | |||||||
| chr7:138513117 | G | T | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.484-2095G>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138513117 | |||||||
| chr7:138513133 | A | G | 2 | a0001c0001t0007g0149 a0001c0001t0007g0182 |
2 | NA18963.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.484-2079A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138513133 | |||||||
| chr7:138513362 | C | T | 1 | a0001c0001t0016g0015 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.484-1850C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138513362 | |||||||
| chr7:138513566 | G | A | 1 | a0001c0001t0003g0287 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.484-1646G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138513566 | |||||||
| chr7:138513810 | T | C | 2 | a0001c0004t0056g0008 a0001c0004t0057g0109 |
2 | HG02055.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.484-1402T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138513810 | |||||||
| chr7:138513880 | G | T | 13 | a0001c0001t0009g0014 a0001c0001t0009g0094 a0001c0001t0009g0095 others(10): Show |
13 | HG01070.hp2 HG01071.hp2 HG01123.hp2 others(10): Show |
intron_variant | MODIFIER | c.484-1332G>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138513880 | |||||||
| chr7:138513882 | T | C | 2 | a0001c0001t0011g0252 a0001c0001t0011g0255 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.484-1330T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138513882 | |||||||
| chr7:138513976 | A | G | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.484-1236A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138513976 | |||||||
| chr7:138514092 | T | C | 2 | a0001c0001t0002g0131 a0001c0001t0002g0147 |
2 | HG02040.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.484-1120T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138514092 | |||||||
| chr7:138514211 | T | C | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.484-1001T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138514211 | |||||||
| chr7:138514254 | C | G | 11 | a0001c0001t0005g0253 a0001c0001t0005g0254 a0001c0001t0005g0256 others(8): Show |
11 | HG02683.hp1 HG02735.hp1 HG03041.hp2 others(8): Show |
intron_variant | MODIFIER | c.484-958C>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138514254 | |||||||
| chr7:138514287 | A | C | 1 | a0002c0006t0006g0221 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.484-925A>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138514287 | |||||||
| chr7:138514306 | T | C | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.484-906T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138514306 | |||||||
| chr7:138514337 | A | G | 1 | a0001c0001t0055g0199 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.484-875A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138514337 | |||||||
| chr7:138514398 | C | G | 3 | a0001c0001t0011g0252 a0001c0001t0011g0255 a0001c0001t0011g0258 |
3 | HG03491.hp1 HG03492.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.484-814C>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138514398 | |||||||
| chr7:138514432 | CCT | C | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.484-779_484-778del others(2): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138514432 | |||||||
| chr7:138514575 | A | C | 21 | a0001c0001t0005g0253 a0001c0001t0005g0254 a0001c0001t0005g0256 others(18): Show |
21 | HG01891.hp1 HG02647.hp1 HG02683.hp1 others(18): Show |
intron_variant | MODIFIER | c.484-637A>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138514575 | |||||||
| chr7:138514648 | T | G | 2 | a0001c0002t0015g0170 a0001c0002t0015g0171 |
2 | HG02451.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.484-564T>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138514648 | |||||||
| chr7:138514665 | T | C | 2 | a0001c0003t0014g0071 a0001c0003t0014g0088 |
2 | HG02622.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.484-547T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138514665 | |||||||
| chr7:138514667 | A | C | 1 | a0001c0001t0002g0132 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.484-545A>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138514667 | |||||||
| chr7:138514707 | A | G | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.484-505A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138514707 | |||||||
| chr7:138514748 | G | A | 1 | a0001c0001t0041g0045 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.484-464G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138514748 | |||||||
| chr7:138514910 | G | A | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.484-302G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | chr7 | 138514910 | |||||||
| chr7:138515372 | A | T | 212 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(209): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.631+13A>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 3/18 | chr7 | 138515372 | |||||||
| chr7:138515403 | C | CCT | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.631+44_631+45insCT | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 3/18 | chr7 | 138515403 | |||||||
| chr7:138515404 | G | A | 2 | a0001c0002t0004g0116 a0001c0002t0004g0126 |
2 | HG01167.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.631+45G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 3/18 | chr7 | 138515404 | |||||||
| chr7:138515418 | C | G | 3 | a0001c0001t0001g0073 a0001c0001t0001g0076 a0001c0001t0001g0236 |
3 | NA18947.hp2 NA18953.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.631+59C>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 3/18 | chr7 | 138515418 | |||||||
| chr7:138515465 | T | C | 45 | a0001c0001t0003g0001 a0001c0001t0003g0269 a0001c0001t0003g0270 others(42): Show |
46 | HG00140.hp2 HG00735.hp2 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.631+106T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 3/18 | chr7 | 138515465 | |||||||
| chr7:138515756 | G | A | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.631+397G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 3/18 | chr7 | 138515756 | |||||||
| chr7:138515784 | A | G | 1 | a0001c0001t0003g0308 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.631+425A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 3/18 | chr7 | 138515784 | |||||||
| chr7:138516131 | G | C | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.631+772G>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 3/18 | chr7 | 138516131 | |||||||
| chr7:138516163 | G | A | 1 | a0001c0001t0011g0264 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.631+804G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 3/18 | chr7 | 138516163 | |||||||
| chr7:138516308 | T | A | 1 | a0001c0001t0002g0193 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.631+949T>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 3/18 | chr7 | 138516308 | |||||||
| chr7:138516342 | C | G | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.631+983C>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 3/18 | chr7 | 138516342 | |||||||
| chr7:138516596 | C | A | 2 | a0001c0005t0013g0114 a0001c0005t0013g0115 |
2 | HG02572.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.631+1237C>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 3/18 | chr7 | 138516596 | |||||||
| chr7:138516653 | C | T | 1 | a0001c0001t0001g0234 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.631+1294C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 3/18 | chr7 | 138516653 | |||||||
| chr7:138516698 | C | T | 1 | a0001c0001t0005g0259 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.631+1339C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 3/18 | chr7 | 138516698 | |||||||
| chr7:138516807 | CGTTTT | C | 4 | a0001c0001t0010g0110 a0001c0001t0010g0112 a0001c0001t0010g0241 others(1): Show |
4 | HG02486.hp1 HG02809.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.631+1454_631+1458d others(7): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr7 | 138516807 | ||||||
| chr7:138516813 | G | GT | 30 | a0001c0001t0002g0174 a0001c0001t0002g0192 a0001c0001t0002g0206 others(27): Show |
30 | HG00280.hp1 HG00738.hp2 HG01167.hp2 others(27): Show |
intron_variant | MODIFIER | c.631+1470dupT | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr7 | 138516813 | ||||||
| chr7:138516813 | G | GTT | 10 | a0001c0001t0005g0253 a0001c0001t0005g0254 a0001c0001t0005g0256 others(7): Show |
10 | HG02647.hp1 HG02683.hp1 HG02735.hp1 others(7): Show |
intron_variant | MODIFIER | c.631+1469_631+1470d others(4): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr7 | 138516813 | ||||||
| chr7:138516813 | G | T | 7 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 others(4): Show |
7 | HG02055.hp2 HG02622.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.631+1454G>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 3/18 | chr7 | 138516813 | |||||||
| chr7:138516813 | GT | G | 99 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(96): Show |
99 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.631+1470delT | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr7 | 138516813 | ||||||
| chr7:138516815 | T | A | 1 | a0001c0001t0002g0140 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.631+1456T>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 3/18 | chr7 | 138516815 | |||||||
| chr7:138516815 | T | G | 10 | a0001c0001t0001g0085 a0001c0001t0006g0215 a0001c0001t0006g0216 others(7): Show |
10 | HG01891.hp1 HG03139.hp2 HG03225.hp1 others(7): Show |
intron_variant | MODIFIER | c.631+1456T>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 3/18 | chr7 | 138516815 | |||||||
| chr7:138516818 | T | G | 1 | a0001c0001t0003g0284 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.631+1459T>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 3/18 | chr7 | 138516818 | |||||||
| chr7:138516875 | G | T | 3 | a0001c0001t0026g0266 a0001c0001t0026g0267 a0001c0001t0035g0265 |
3 | HG02109.hp1 HG02630.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.631+1516G>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 3/18 | chr7 | 138516875 | |||||||
| chr7:138516939 | T | C | 1 | a0001c0001t0002g0178 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.631+1580T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 3/18 | chr7 | 138516939 | |||||||
| chr7:138517037 | C | G | 3 | a0001c0005t0013g0114 a0001c0005t0013g0115 a0001c0010t0013g0113 |
3 | HG02572.hp2 HG02723.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.631+1678C>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 3/18 | chr7 | 138517037 | |||||||
| chr7:138517064 | C | T | 13 | a0001c0001t0005g0253 a0001c0001t0005g0254 a0001c0001t0005g0256 others(10): Show |
13 | HG02647.hp1 HG02683.hp1 HG02735.hp1 others(10): Show |
intron_variant | MODIFIER | c.631+1705C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 3/18 | chr7 | 138517064 | |||||||
| chr7:138517083 | C | T | 10 | a0001c0001t0006g0215 a0001c0001t0006g0216 a0001c0001t0006g0217 others(7): Show |
10 | HG01891.hp1 HG02055.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.631+1724C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 3/18 | chr7 | 138517083 | |||||||
| chr7:138517105 | C | CA | 11 | a0001c0001t0001g0029 a0001c0001t0001g0048 a0001c0001t0001g0074 others(8): Show |
11 | HG00423.hp2 HG02055.hp1 HG02155.hp1 others(8): Show |
intron_variant | MODIFIER | c.631+1759dupA | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr7 | 138517105 | ||||||
| chr7:138517105 | CA | C | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.631+1759delA | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr7 | 138517105 | ||||||
| chr7:138517123 | C | T | 1 | a0001c0001t0001g0018 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.631+1764C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 3/18 | chr7 | 138517123 | |||||||
| chr7:138517190 | T | C | 1 | a0001c0001t0010g0244 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.631+1831T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 3/18 | chr7 | 138517190 | |||||||
| chr7:138517352 | G | T | 8 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(5): Show |
8 | HG02486.hp1 HG02647.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.632-1837G>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 3/18 | chr7 | 138517352 | |||||||
| chr7:138517360 | G | GTGTTTTG others(8): Show |
8 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(5): Show |
8 | HG02486.hp1 HG02647.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.632-1817_632-1803d others(17): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr7 | 138517360 | ||||||
| chr7:138517360 | G | GTGTTTTG others(18): Show |
2 | a0001c0004t0056g0008 a0001c0004t0057g0109 |
2 | HG02055.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.632-1827_632-1803d others(27): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr7 | 138517360 | ||||||
| chr7:138517563 | G | A | 1 | a0001c0001t0003g0274 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.632-1626G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 3/18 | chr7 | 138517563 | |||||||
| chr7:138517712 | A | C | 1 | a0001c0001t0046g0262 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.632-1477A>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 3/18 | chr7 | 138517712 | |||||||
| chr7:138517857 | T | C | 1 | a0001c0001t0002g0135 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.632-1332T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 3/18 | chr7 | 138517857 | |||||||
| chr7:138518034 | A | G | 2 | a0001c0001t0011g0263 a0001c0001t0011g0264 |
2 | HG02647.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.632-1155A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 3/18 | chr7 | 138518034 | |||||||
| chr7:138518189 | A | G | 3 | a0001c0003t0014g0071 a0001c0003t0014g0088 a0001c0003t0014g0090 |
3 | HG02622.hp2 HG02818.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.632-1000A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 3/18 | chr7 | 138518189 | |||||||
| chr7:138518251 | T | C | 3 | a0001c0001t0005g0259 a0001c0001t0005g0260 a0001c0001t0005g0261 |
3 | NA18954.hp1 NA18969.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.632-938T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 3/18 | chr7 | 138518251 | |||||||
| chr7:138518360 | C | A | 7 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(4): Show |
7 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.632-829C>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 3/18 | chr7 | 138518360 | |||||||
| chr7:138518551 | G | A | 2 | a0001c0004t0056g0008 a0001c0004t0057g0109 |
2 | HG02055.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.632-638G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 3/18 | chr7 | 138518551 | |||||||
| chr7:138518612 | A | G | 1 | a0001c0001t0029g0300 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.632-577A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 3/18 | chr7 | 138518612 | |||||||
| chr7:138518644 | C | G | 1 | a0001c0001t0010g0241 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.632-545C>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 3/18 | chr7 | 138518644 | |||||||
| chr7:138519141 | A | C | 4 | a0001c0001t0019g0303 a0001c0001t0019g0304 a0001c0001t0030g0305 others(1): Show |
4 | HG02145.hp1 HG02258.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.632-48A>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 3/18 | chr7 | 138519141 | |||||||
| chr7:138519391 | C | T | 1 | a0001c0001t0001g0036 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.764+70C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 4/18 | chr7 | 138519391 | |||||||
| chr7:138519772 | G | A | 2 | a0001c0001t0024g0024 a0001c0001t0024g0025 |
2 | HG02723.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.764+451G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 4/18 | chr7 | 138519772 | |||||||
| chr7:138519794 | C | T | 2 | a0001c0004t0056g0008 a0001c0004t0057g0109 |
2 | HG02055.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.764+473C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 4/18 | chr7 | 138519794 | |||||||
| chr7:138519912 | G | C | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.764+591G>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 4/18 | chr7 | 138519912 | |||||||
| chr7:138520279 | T | C | 8 | a0001c0001t0006g0215 a0001c0001t0006g0216 a0001c0001t0006g0217 others(5): Show |
8 | HG01891.hp1 HG03139.hp2 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.764+958T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 4/18 | chr7 | 138520279 | |||||||
| chr7:138520374 | T | C | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.764+1053T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 4/18 | chr7 | 138520374 | |||||||
| chr7:138520435 | T | C | 1 | a0001c0001t0002g0245 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.764+1114T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 4/18 | chr7 | 138520435 | |||||||
| chr7:138520473 | T | G | 1 | a0001c0001t0005g0259 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.764+1152T>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 4/18 | chr7 | 138520473 | |||||||
| chr7:138520532 | C | A | 1 | a0001c0001t0023g0154 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.764+1211C>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 4/18 | chr7 | 138520532 | |||||||
| chr7:138520534 | C | A | 1 | a0001c0001t0023g0154 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.764+1213C>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 4/18 | chr7 | 138520534 | |||||||
| chr7:138520573 | C | G | 1 | a0001c0001t0002g0159 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.764+1252C>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 4/18 | chr7 | 138520573 | |||||||
| chr7:138520640 | G | A | 1 | a0001c0002t0004g0127 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.764+1319G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 4/18 | chr7 | 138520640 | |||||||
| chr7:138520748 | A | G | 3 | a0001c0001t0026g0266 a0001c0001t0026g0267 a0001c0001t0035g0265 |
3 | HG02109.hp1 HG02630.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.764+1427A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 4/18 | chr7 | 138520748 | |||||||
| chr7:138520874 | A | C | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.764+1553A>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 4/18 | chr7 | 138520874 | |||||||
| chr7:138520898 | G | A | 2 | a0001c0004t0056g0008 a0001c0004t0057g0109 |
2 | HG02055.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.764+1577G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 4/18 | chr7 | 138520898 | |||||||
| chr7:138520954 | G | T | 5 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(2): Show |
5 | HG02486.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.764+1633G>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 4/18 | chr7 | 138520954 | |||||||
| chr7:138520960 | T | C | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.764+1639T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 4/18 | chr7 | 138520960 | |||||||
| chr7:138521005 | C | G | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.764+1684C>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 4/18 | chr7 | 138521005 | |||||||
| chr7:138521157 | T | A | 2 | a0001c0004t0056g0008 a0001c0004t0057g0109 |
2 | HG02055.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.764+1836T>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 4/18 | chr7 | 138521157 | |||||||
| chr7:138521174 | T | C | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.764+1853T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 4/18 | chr7 | 138521174 | |||||||
| chr7:138521191 | T | C | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.764+1870T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 4/18 | chr7 | 138521191 | |||||||
| chr7:138521386 | A | T | 2 | a0001c0001t0003g0275 a0001c0001t0003g0296 |
2 | HG02886.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.764+2065A>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 4/18 | chr7 | 138521386 | |||||||
| chr7:138521494 | G | T | 1 | a0001c0001t0002g0251 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.764+2173G>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 4/18 | chr7 | 138521494 | |||||||
| chr7:138521773 | A | G | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.764+2452A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 4/18 | chr7 | 138521773 | |||||||
| chr7:138521967 | T | C | 212 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(209): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.764+2646T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 4/18 | chr7 | 138521967 | |||||||
| chr7:138522036 | GAGAAATC others(2): Show |
G | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.764+2718_764+2726d others(11): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr7 | 138522036 | ||||||
| chr7:138522122 | G | A | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.764+2801G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 4/18 | chr7 | 138522122 | |||||||
| chr7:138522130 | G | A | 3 | a0001c0005t0013g0114 a0001c0005t0013g0115 a0001c0010t0013g0113 |
3 | HG02572.hp2 HG02723.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.764+2809G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 4/18 | chr7 | 138522130 | |||||||
| chr7:138522232 | A | G | 66 | a0001c0001t0003g0001 a0001c0001t0003g0269 a0001c0001t0003g0270 others(63): Show |
67 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(64): Show |
intron_variant | MODIFIER | c.764+2911A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 4/18 | chr7 | 138522232 | |||||||
| chr7:138522251 | A | C | 1 | a0001c0002t0004g0125 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.764+2930A>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 4/18 | chr7 | 138522251 | |||||||
| chr7:138522830 | A | G | 212 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(209): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.765-2411A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 4/18 | chr7 | 138522830 | |||||||
| chr7:138522853 | CAAG | C | 66 | a0001c0001t0003g0001 a0001c0001t0003g0269 a0001c0001t0003g0270 others(63): Show |
67 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(64): Show |
intron_variant | MODIFIER | c.765-2382_765-2380d others(5): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr7 | 138522853 | ||||||
| chr7:138523483 | A | C | 1 | a0001c0001t0047g0179 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.765-1758A>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 4/18 | chr7 | 138523483 | |||||||
| chr7:138523531 | G | A | 13 | a0001c0001t0005g0253 a0001c0001t0005g0254 a0001c0001t0005g0256 others(10): Show |
13 | HG02647.hp1 HG02683.hp1 HG02735.hp1 others(10): Show |
intron_variant | MODIFIER | c.765-1710G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 4/18 | chr7 | 138523531 | |||||||
| chr7:138523587 | C | G | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.765-1654C>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 4/18 | chr7 | 138523587 | |||||||
| chr7:138523729 | C | T | 44 | a0001c0001t0003g0001 a0001c0001t0003g0269 a0001c0001t0003g0270 others(41): Show |
45 | HG00140.hp2 HG00735.hp2 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.765-1512C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 4/18 | chr7 | 138523729 | |||||||
| chr7:138523737 | C | T | 101 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(98): Show |
101 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.765-1504C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 4/18 | chr7 | 138523737 | |||||||
| chr7:138523750 | C | CA | 29 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0036 others(26): Show |
29 | HG00735.hp2 HG01943.hp2 HG01993.hp2 others(26): Show |
intron_variant | MODIFIER | c.765-1470dupA | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr7 | 138523750 | ||||||
| chr7:138523750 | C | CAA | 88 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(85): Show |
88 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.765-1471_765-1470d others(4): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr7 | 138523750 | ||||||
| chr7:138523750 | C | CAAA | 11 | a0001c0001t0001g0050 a0001c0001t0001g0058 a0001c0001t0001g0076 others(8): Show |
11 | HG01346.hp1 HG02055.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.765-1472_765-1470d others(5): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr7 | 138523750 | ||||||
| chr7:138524271 | A | C | 1 | a0001c0001t0032g0311 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.765-970A>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 4/18 | chr7 | 138524271 | |||||||
| chr7:138524298 | T | C | 5 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(2): Show |
5 | HG02486.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.765-943T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 4/18 | chr7 | 138524298 | |||||||
| chr7:138524314 | C | G | 1 | a0001c0001t0001g0032 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.765-927C>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 4/18 | chr7 | 138524314 | |||||||
| chr7:138524643 | A | C | 13 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0062 others(10): Show |
13 | HG01175.hp2 HG02602.hp2 HG03490.hp2 others(10): Show |
intron_variant | MODIFIER | c.765-598A>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 4/18 | chr7 | 138524643 | |||||||
| chr7:138524774 | G | A | 1 | a0001c0001t0016g0015 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.765-467G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 4/18 | chr7 | 138524774 | |||||||
| chr7:138524814 | A | G | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.765-427A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 4/18 | chr7 | 138524814 | |||||||
| chr7:138524940 | G | A | 98 | a0001c0001t0003g0001 a0001c0001t0003g0269 a0001c0001t0003g0270 others(95): Show |
99 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(96): Show |
intron_variant | MODIFIER | c.765-301G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 4/18 | chr7 | 138524940 | |||||||
| chr7:138525111 | C | T | 1 | a0001c0001t0002g0157 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.765-130C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 4/18 | chr7 | 138525111 | |||||||
| chr7:138525112 | G | T | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.765-129G>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 4/18 | chr7 | 138525112 | |||||||
| chr7:138525478 | C | T | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.881+121C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 5/18 | chr7 | 138525478 | |||||||
| chr7:138525552 | T | C | 8 | a0001c0001t0006g0215 a0001c0001t0006g0216 a0001c0001t0006g0217 others(5): Show |
8 | HG01891.hp1 HG03139.hp2 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.881+195T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 5/18 | chr7 | 138525552 | |||||||
| chr7:138525557 | T | G | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.881+200T>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 5/18 | chr7 | 138525557 | |||||||
| chr7:138525896 | A | C | 3 | a0001c0003t0014g0071 a0001c0003t0014g0088 a0001c0003t0014g0090 |
3 | HG02622.hp2 HG02818.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.881+539A>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 5/18 | chr7 | 138525896 | |||||||
| chr7:138525964 | G | A | 7 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(4): Show |
7 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.881+607G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 5/18 | chr7 | 138525964 | |||||||
| chr7:138526039 | C | T | 1 | a0001c0001t0005g0257 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.881+682C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 5/18 | chr7 | 138526039 | |||||||
| chr7:138526082 | G | A | 5 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(2): Show |
5 | HG02486.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.881+725G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 5/18 | chr7 | 138526082 | |||||||
| chr7:138526141 | G | A | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.881+784G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 5/18 | chr7 | 138526141 | |||||||
| chr7:138526170 | A | G | 1 | a0001c0001t0001g0249 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.881+813A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 5/18 | chr7 | 138526170 | |||||||
| chr7:138526322 | T | C | 7 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(4): Show |
7 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.881+965T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 5/18 | chr7 | 138526322 | |||||||
| chr7:138526327 | A | C | 5 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(2): Show |
5 | HG02486.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.881+970A>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 5/18 | chr7 | 138526327 | |||||||
| chr7:138526432 | GTTTTTGT | G | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.881+1095_881+1101d others(9): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr7 | 138526432 | ||||||
| chr7:138526466 | C | T | 12 | a0001c0001t0005g0253 a0001c0001t0005g0254 a0001c0001t0005g0256 others(9): Show |
12 | HG02647.hp1 HG02683.hp1 HG02735.hp1 others(9): Show |
intron_variant | MODIFIER | c.881+1109C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 5/18 | chr7 | 138526466 | |||||||
| chr7:138526612 | A | G | 7 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(4): Show |
7 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.881+1255A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 5/18 | chr7 | 138526612 | |||||||
| chr7:138526627 | G | T | 1 | a0002c0006t0006g0221 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.881+1270G>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 5/18 | chr7 | 138526627 | |||||||
| chr7:138526669 | C | T | 1 | a0001c0001t0001g0026 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.881+1312C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 5/18 | chr7 | 138526669 | |||||||
| chr7:138526691 | G | A | 28 | a0001c0001t0009g0014 a0001c0001t0009g0094 a0001c0001t0009g0095 others(25): Show |
28 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.881+1334G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 5/18 | chr7 | 138526691 | |||||||
| chr7:138526792 | A | G | 101 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(98): Show |
101 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.881+1435A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 5/18 | chr7 | 138526792 | |||||||
| chr7:138526838 | C | G | 2 | a0001c0001t0011g0263 a0001c0001t0011g0264 |
2 | HG02647.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.881+1481C>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 5/18 | chr7 | 138526838 | |||||||
| chr7:138526845 | A | G | 5 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(2): Show |
5 | HG02486.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.881+1488A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 5/18 | chr7 | 138526845 | |||||||
| chr7:138527018 | G | C | 2 | a0001c0001t0002g0150 a0001c0001t0002g0176 |
2 | HG03239.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.881+1661G>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 5/18 | chr7 | 138527018 | |||||||
| chr7:138527043 | AT | A | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.881+1695delT | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr7 | 138527043 | ||||||
| chr7:138527052 | T | A | 7 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(4): Show |
7 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.881+1695T>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 5/18 | chr7 | 138527052 | |||||||
| chr7:138527056 | T | C | 213 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(210): Show |
214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.881+1699T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 5/18 | chr7 | 138527056 | |||||||
| chr7:138527074 | C | G | 3 | a0001c0005t0013g0114 a0001c0005t0013g0115 a0001c0010t0013g0113 |
3 | HG02572.hp2 HG02723.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.881+1717C>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 5/18 | chr7 | 138527074 | |||||||
| chr7:138527086 | G | C | 8 | a0001c0001t0006g0215 a0001c0001t0006g0216 a0001c0001t0006g0217 others(5): Show |
8 | HG01891.hp1 HG03139.hp2 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.881+1729G>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 5/18 | chr7 | 138527086 | |||||||
| chr7:138527097 | T | C | 1 | a0001c0001t0003g0285 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.881+1740T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 5/18 | chr7 | 138527097 | |||||||
| chr7:138527099 | T | C | 1 | a0001c0004t0057g0109 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.881+1742T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 5/18 | chr7 | 138527099 | |||||||
| chr7:138527323 | T | C | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.882-1793T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 5/18 | chr7 | 138527323 | |||||||
| chr7:138527398 | G | C | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.882-1718G>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 5/18 | chr7 | 138527398 | |||||||
| chr7:138527466 | T | C | 1 | a0001c0001t0055g0199 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.882-1650T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 5/18 | chr7 | 138527466 | |||||||
| chr7:138527581 | A | C | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.882-1535A>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 5/18 | chr7 | 138527581 | |||||||
| chr7:138527599 | T | C | 2 | a0001c0004t0056g0008 a0001c0004t0057g0109 |
2 | HG02055.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.882-1517T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 5/18 | chr7 | 138527599 | |||||||
| chr7:138527823 | G | A | 5 | a0001c0001t0002g0106 a0001c0001t0002g0144 a0001c0001t0002g0145 others(2): Show |
5 | HG01074.hp2 HG01099.hp2 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.882-1293G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 5/18 | chr7 | 138527823 | |||||||
| chr7:138527844 | A | G | 7 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(4): Show |
7 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.882-1272A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 5/18 | chr7 | 138527844 | |||||||
| chr7:138527850 | C | T | 1 | a0001c0001t0005g0261 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.882-1266C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 5/18 | chr7 | 138527850 | |||||||
| chr7:138527885 | ACTGGGCC others(11): Show |
A | 1 | a0001c0001t0001g0018 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.882-1213_882-1196d others(20): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr7 | 138527885 | ||||||
| chr7:138527903 | GCTGGGCC others(11): Show |
G | 1 | a0001c0001t0033g0172 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.882-1208_882-1191d others(20): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr7 | 138527903 | ||||||
| chr7:138528105 | G | T | 13 | a0001c0001t0005g0253 a0001c0001t0005g0254 a0001c0001t0005g0256 others(10): Show |
13 | HG02647.hp1 HG02683.hp1 HG02735.hp1 others(10): Show |
intron_variant | MODIFIER | c.882-1011G>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 5/18 | chr7 | 138528105 | |||||||
| chr7:138528135 | T | C | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.882-981T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 5/18 | chr7 | 138528135 | |||||||
| chr7:138528188 | G | A | 2 | a0001c0001t0006g0216 a0001c0001t0006g0218 |
2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.882-928G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 5/18 | chr7 | 138528188 | |||||||
| chr7:138528263 | A | G | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.882-853A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 5/18 | chr7 | 138528263 | |||||||
| chr7:138528270 | A | G | 1 | a0001c0001t0002g0152 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.882-846A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 5/18 | chr7 | 138528270 | |||||||
| chr7:138528324 | T | A | 2 | a0001c0004t0056g0008 a0001c0004t0057g0109 |
2 | HG02055.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.882-792T>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 5/18 | chr7 | 138528324 | |||||||
| chr7:138528442 | T | C | 9 | a0001c0001t0006g0215 a0001c0001t0006g0216 a0001c0001t0006g0217 others(6): Show |
9 | HG01891.hp1 HG03139.hp2 HG03225.hp1 others(6): Show |
intron_variant | MODIFIER | c.882-674T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 5/18 | chr7 | 138528442 | |||||||
| chr7:138528603 | T | C | 3 | a0001c0001t0026g0266 a0001c0001t0026g0267 a0001c0001t0035g0265 |
3 | HG02109.hp1 HG02630.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.882-513T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 5/18 | chr7 | 138528603 | |||||||
| chr7:138528714 | G | A | 1 | a0001c0001t0002g0219 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.882-402G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 5/18 | chr7 | 138528714 | |||||||
| chr7:138528777 | A | C | 1 | a0001c0004t0056g0008 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.882-339A>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 5/18 | chr7 | 138528777 | |||||||
| chr7:138528783 | A | AC | 72 | a0001c0001t0001g0239 a0001c0001t0002g0106 a0001c0001t0002g0107 others(69): Show |
72 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.882-322dupC | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr7 | 138528783 | ||||||
| chr7:138528783 | A | C | 1 | a0001c0004t0057g0109 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.882-333A>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 5/18 | chr7 | 138528783 | |||||||
| chr7:138528783 | AC | A | 144 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(141): Show |
144 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.882-322delC | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr7 | 138528783 | ||||||
| chr7:138528785 | C | A | 1 | a0001c0004t0057g0109 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.882-331C>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 5/18 | chr7 | 138528785 | |||||||
| chr7:138528787 | C | G | 1 | a0001c0001t0002g0192 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.882-329C>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 5/18 | chr7 | 138528787 | |||||||
| chr7:138528789 | C | A | 1 | a0001c0001t0001g0238 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.882-327C>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 5/18 | chr7 | 138528789 | |||||||
| chr7:138528792 | C | A | 2 | a0001c0001t0001g0066 a0001c0001t0001g0067 |
2 | HG01109.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.882-324C>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 5/18 | chr7 | 138528792 | |||||||
| chr7:138528966 | C | T | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.882-150C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 5/18 | chr7 | 138528966 | |||||||
| chr7:138529000 | C | G | 9 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0022 others(6): Show |
9 | HG00408.hp2 HG01928.hp2 HG01934.hp1 others(6): Show |
intron_variant | MODIFIER | c.882-116C>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 5/18 | chr7 | 138529000 | |||||||
| chr7:138529033 | T | C | 1 | a0001c0002t0015g0171 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.882-83T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 5/18 | chr7 | 138529033 | |||||||
| chr7:138529034 | G | C | 1 | a0001c0001t0001g0038 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.882-82G>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 5/18 | chr7 | 138529034 | |||||||
| chr7:138529273 | A | G | 9 | a0001c0001t0001g0038 a0001c0001t0001g0052 a0001c0001t0001g0057 others(6): Show |
9 | HG00438.hp1 NA18950.hp2 NA18975.hp2 others(6): Show |
intron_variant | MODIFIER | c.996+43A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138529273 | |||||||
| chr7:138529287 | T | C | 2 | a0001c0004t0056g0008 a0001c0004t0057g0109 |
2 | HG02055.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.996+57T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138529287 | |||||||
| chr7:138529331 | T | A | 1 | a0001c0001t0001g0055 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.996+101T>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138529331 | |||||||
| chr7:138529414 | C | T | 3 | a0001c0003t0014g0071 a0001c0003t0014g0088 a0001c0003t0014g0090 |
3 | HG02622.hp2 HG02818.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.996+184C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138529414 | |||||||
| chr7:138529684 | C | T | 1 | a0001c0001t0002g0129 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.996+454C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138529684 | |||||||
| chr7:138529696 | T | C | 5 | a0001c0001t0002g0132 a0001c0001t0002g0152 a0001c0001t0002g0159 others(2): Show |
5 | HG00423.hp1 NA18954.hp2 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.996+466T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138529696 | |||||||
| chr7:138529738 | G | A | 1 | a0001c0001t0002g0248 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.996+508G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138529738 | |||||||
| chr7:138529819 | C | A | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.996+589C>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138529819 | |||||||
| chr7:138529845 | T | C | 1 | a0001c0002t0015g0169 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.996+615T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138529845 | |||||||
| chr7:138529848 | A | C | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.996+618A>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138529848 | |||||||
| chr7:138529977 | A | G | 1 | a0001c0002t0004g0242 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.996+747A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138529977 | |||||||
| chr7:138530180 | C | G | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.996+950C>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138530180 | |||||||
| chr7:138530185 | A | G | 2 | a0001c0001t0010g0111 a0001c0001t0010g0112 |
2 | HG02647.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.996+955A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138530185 | |||||||
| chr7:138530227 | T | TA | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.996+1012dupA | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr7 | 138530227 | ||||||
| chr7:138530227 | TA | T | 11 | a0001c0001t0001g0023 a0001c0001t0001g0062 a0001c0001t0001g0237 others(8): Show |
11 | HG01070.hp1 HG01255.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.996+1012delA | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr7 | 138530227 | ||||||
| chr7:138530243 | T | A | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.996+1013T>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138530243 | |||||||
| chr7:138530476 | T | A | 2 | a0001c0004t0056g0008 a0001c0004t0057g0109 |
2 | HG02055.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.996+1246T>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138530476 | |||||||
| chr7:138530687 | C | T | 1 | a0001c0001t0058g0220 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.996+1457C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138530687 | |||||||
| chr7:138530837 | G | A | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.996+1607G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138530837 | |||||||
| chr7:138530912 | A | AT | 8 | a0001c0001t0006g0215 a0001c0001t0006g0216 a0001c0001t0006g0217 others(5): Show |
8 | HG01891.hp1 HG03139.hp2 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.996+1688dupT | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr7 | 138530912 | ||||||
| chr7:138531019 | C | T | 1 | a0001c0001t0003g0285 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.996+1789C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138531019 | |||||||
| chr7:138531020 | C | G | 11 | a0001c0001t0003g0285 a0001c0001t0008g0281 a0001c0001t0008g0291 others(8): Show |
11 | HG01099.hp1 HG02145.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.996+1790C>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138531020 | |||||||
| chr7:138531067 | G | A | 7 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(4): Show |
7 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.996+1837G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138531067 | |||||||
| chr7:138531123 | T | C | 1 | a0001c0009t0003g0268 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.996+1893T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138531123 | |||||||
| chr7:138531123 | T | TTTA | 101 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(98): Show |
101 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.996+1910_996+1912d others(5): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr7 | 138531123 | ||||||
| chr7:138531123 | TTTA | T | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.996+1910_996+1912d others(5): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr7 | 138531123 | ||||||
| chr7:138531141 | A | C | 1 | a0001c0001t0032g0311 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.996+1911A>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138531141 | |||||||
| chr7:138531163 | T | C | 9 | a0001c0001t0006g0215 a0001c0001t0006g0216 a0001c0001t0006g0217 others(6): Show |
9 | HG01891.hp1 HG03139.hp2 HG03225.hp1 others(6): Show |
intron_variant | MODIFIER | c.996+1933T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138531163 | |||||||
| chr7:138531186 | TATGTATA others(1): Show |
T | 73 | a0001c0001t0002g0167 a0001c0001t0003g0001 a0001c0001t0003g0269 others(70): Show |
74 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(71): Show |
intron_variant | MODIFIER | c.996+1973_996+1980d others(10): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr7 | 138531186 | ||||||
| chr7:138531210 | C | T | 23 | a0001c0001t0001g0087 a0001c0001t0005g0253 a0001c0001t0005g0254 others(20): Show |
23 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(20): Show |
intron_variant | MODIFIER | c.996+1980C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138531210 | |||||||
| chr7:138531246 | A | ATGTTACA others(61): Show |
3 | a0001c0001t0010g0111 a0001c0001t0010g0112 a0001c0001t0010g0241 |
3 | HG02647.hp2 HG02809.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.996+2034_996+2035i others(70): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr7 | 138531246 | ||||||
| chr7:138531246 | A | ATGTTACA others(89): Show |
2 | a0001c0001t0010g0110 a0001c0001t0010g0244 |
2 | HG02486.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.996+2034_996+2035i others(98): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr7 | 138531246 | ||||||
| chr7:138531246 | A | ATGTTACA others(198): Show |
1 | a0001c0004t0056g0008 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.996+2056_996+2057i others(207): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr7 | 138531246 | ||||||
| chr7:138531246 | A | ATGTTACA others(189): Show |
1 | a0001c0004t0057g0109 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.996+2056_996+2057i others(198): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr7 | 138531246 | ||||||
| chr7:138531263 | T | C | 1 | a0001c0001t0001g0214 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.996+2033T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138531263 | |||||||
| chr7:138531293 | G | C | 2 | a0001c0004t0056g0008 a0001c0004t0057g0109 |
2 | HG02055.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.996+2063G>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138531293 | |||||||
| chr7:138531313 | A | G | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.996+2083A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138531313 | |||||||
| chr7:138531328 | A | G | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.996+2098A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138531328 | |||||||
| chr7:138531392 | G | A | 8 | a0001c0001t0006g0215 a0001c0001t0006g0216 a0001c0001t0006g0217 others(5): Show |
8 | HG01891.hp1 HG03139.hp2 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.996+2162G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138531392 | |||||||
| chr7:138531452 | A | G | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.996+2222A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138531452 | |||||||
| chr7:138531464 | G | A | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.996+2234G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138531464 | |||||||
| chr7:138531546 | C | T | 2 | a0001c0001t0003g0276 a0001c0001t0003g0309 |
2 | HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.996+2316C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138531546 | |||||||
| chr7:138531550 | T | G | 8 | a0001c0001t0006g0215 a0001c0001t0006g0216 a0001c0001t0006g0217 others(5): Show |
8 | HG01891.hp1 HG03139.hp2 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.996+2320T>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138531550 | |||||||
| chr7:138531642 | A | C | 2 | a0001c0004t0056g0008 a0001c0004t0057g0109 |
2 | HG02055.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.996+2412A>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138531642 | |||||||
| chr7:138531680 | G | A | 1 | a0001c0001t0044g0128 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.996+2450G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138531680 | |||||||
| chr7:138531741 | A | C | 3 | a0001c0003t0014g0071 a0001c0003t0014g0088 a0001c0003t0014g0090 |
3 | HG02622.hp2 HG02818.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.996+2511A>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138531741 | |||||||
| chr7:138531788 | G | A | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.996+2558G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138531788 | |||||||
| chr7:138531815 | C | G | 1 | a0001c0001t0035g0265 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.996+2585C>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138531815 | |||||||
| chr7:138531818 | G | C | 2 | a0001c0001t0003g0276 a0001c0001t0003g0309 |
2 | HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.996+2588G>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138531818 | |||||||
| chr7:138531903 | G | C | 13 | a0001c0001t0005g0253 a0001c0001t0005g0254 a0001c0001t0005g0256 others(10): Show |
13 | HG02647.hp1 HG02683.hp1 HG02735.hp1 others(10): Show |
intron_variant | MODIFIER | c.996+2673G>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138531903 | |||||||
| chr7:138531924 | C | A | 212 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(209): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.996+2694C>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138531924 | |||||||
| chr7:138531981 | A | T | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.996+2751A>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138531981 | |||||||
| chr7:138532041 | T | C | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.996+2811T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138532041 | |||||||
| chr7:138532144 | C | A | 212 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(209): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.996+2914C>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138532144 | |||||||
| chr7:138532167 | C | T | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.996+2937C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138532167 | |||||||
| chr7:138532201 | T | C | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.996+2971T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138532201 | |||||||
| chr7:138532255 | A | T | 1 | a0001c0001t0001g0046 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.996+3025A>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138532255 | |||||||
| chr7:138532271 | T | G | 1 | a0001c0001t0028g0302 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.996+3041T>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138532271 | |||||||
| chr7:138532274 | A | T | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.996+3044A>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138532274 | |||||||
| chr7:138532275 | C | G | 2 | a0001c0002t0015g0170 a0001c0002t0015g0171 |
2 | HG02451.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.996+3045C>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138532275 | |||||||
| chr7:138532394 | C | A | 15 | a0001c0001t0002g0131 a0001c0001t0002g0147 a0001c0001t0010g0110 others(12): Show |
15 | HG02040.hp1 HG02055.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.996+3164C>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138532394 | |||||||
| chr7:138532396 | G | C | 3 | a0001c0001t0026g0266 a0001c0001t0026g0267 a0001c0001t0035g0265 |
3 | HG02109.hp1 HG02630.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.996+3166G>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138532396 | |||||||
| chr7:138532399 | G | A | 1 | a0001c0001t0001g0078 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.996+3169G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138532399 | |||||||
| chr7:138532491 | G | A | 1 | a0001c0004t0056g0008 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.996+3261G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138532491 | |||||||
| chr7:138532555 | C | G | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.996+3325C>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138532555 | |||||||
| chr7:138532574 | C | T | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.996+3344C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138532574 | |||||||
| chr7:138532769 | C | T | 4 | a0001c0001t0001g0026 a0001c0001t0017g0005 a0001c0001t0017g0006 others(1): Show |
4 | HG02129.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.996+3539C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138532769 | |||||||
| chr7:138532802 | G | A | 1 | a0001c0001t0003g0288 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.996+3572G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138532802 | |||||||
| chr7:138532842 | T | C | 1 | a0001c0001t0010g0244 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.996+3612T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138532842 | |||||||
| chr7:138532912 | A | T | 1 | a0001c0001t0050g0213 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.996+3682A>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138532912 | |||||||
| chr7:138532918 | G | A | 1 | a0001c0001t0050g0213 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.996+3688G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138532918 | |||||||
| chr7:138532920 | G | T | 1 | a0001c0001t0050g0213 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.996+3690G>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138532920 | |||||||
| chr7:138532968 | C | T | 2 | a0001c0001t0002g0248 a0001c0002t0004g0120 |
2 | NA18986.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.996+3738C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138532968 | |||||||
| chr7:138532969 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.996+3739G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138532969 | |||||||
| chr7:138533149 | T | A | 16 | a0001c0001t0003g0001 a0001c0001t0003g0271 a0001c0001t0003g0272 others(13): Show |
17 | HG00735.hp2 HG00738.hp1 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.996+3919T>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138533149 | |||||||
| chr7:138533198 | A | C | 5 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(2): Show |
5 | HG02486.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.996+3968A>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138533198 | |||||||
| chr7:138533255 | ATAG | A | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.996+4029_996+4031d others(5): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr7 | 138533255 | ||||||
| chr7:138533259 | T | C | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.996+4029T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138533259 | |||||||
| chr7:138533375 | T | C | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.996+4145T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138533375 | |||||||
| chr7:138533386 | G | A | 3 | a0001c0001t0003g0276 a0001c0001t0003g0282 a0001c0001t0003g0309 |
3 | HG02109.hp2 HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.996+4156G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138533386 | |||||||
| chr7:138533458 | A | G | 7 | a0001c0001t0005g0253 a0001c0001t0005g0254 a0001c0001t0005g0256 others(4): Show |
7 | HG02683.hp1 HG02735.hp1 NA18944.hp2 others(4): Show |
intron_variant | MODIFIER | c.996+4228A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138533458 | |||||||
| chr7:138533460 | C | T | 9 | a0001c0001t0006g0215 a0001c0001t0006g0216 a0001c0001t0006g0217 others(6): Show |
9 | HG01891.hp1 HG03139.hp2 HG03225.hp1 others(6): Show |
intron_variant | MODIFIER | c.996+4230C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138533460 | |||||||
| chr7:138533476 | G | A | 79 | a0001c0001t0003g0001 a0001c0001t0003g0269 a0001c0001t0003g0270 others(76): Show |
80 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(77): Show |
intron_variant | MODIFIER | c.996+4246G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138533476 | |||||||
| chr7:138533480 | T | G | 2 | a0001c0004t0056g0008 a0001c0004t0057g0109 |
2 | HG02055.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.996+4250T>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138533480 | |||||||
| chr7:138533499 | T | G | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.996+4269T>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138533499 | |||||||
| chr7:138533598 | G | A | 1 | a0001c0001t0010g0241 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.996+4368G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138533598 | |||||||
| chr7:138533609 | C | T | 13 | a0001c0001t0005g0253 a0001c0001t0005g0254 a0001c0001t0005g0256 others(10): Show |
13 | HG02647.hp1 HG02683.hp1 HG02735.hp1 others(10): Show |
intron_variant | MODIFIER | c.996+4379C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138533609 | |||||||
| chr7:138533641 | A | G | 2 | a0001c0001t0001g0036 a0001c0001t0001g0064 |
2 | NA18940.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.996+4411A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138533641 | |||||||
| chr7:138533766 | G | A | 7 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(4): Show |
7 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.996+4536G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138533766 | |||||||
| chr7:138534044 | G | A | 2 | a0001c0001t0006g0216 a0001c0001t0006g0218 |
2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.997-4613G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138534044 | |||||||
| chr7:138534052 | G | A | 4 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 others(1): Show |
4 | HG02896.hp2 HG02897.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.997-4605G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138534052 | |||||||
| chr7:138534084 | C | T | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.997-4573C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138534084 | |||||||
| chr7:138534100 | CTCTGTTT | C | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.997-4553_997-4547d others(9): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr7 | 138534100 | ||||||
| chr7:138534153 | A | G | 1 | a0001c0001t0023g0185 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.997-4504A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138534153 | |||||||
| chr7:138534369 | C | G | 3 | a0001c0003t0014g0071 a0001c0003t0014g0088 a0001c0003t0014g0090 |
3 | HG02622.hp2 HG02818.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.997-4288C>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138534369 | |||||||
| chr7:138534379 | C | T | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.997-4278C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138534379 | |||||||
| chr7:138534401 | C | T | 1 | a0001c0001t0002g0144 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.997-4256C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138534401 | |||||||
| chr7:138534402 | A | T | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.997-4255A>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138534402 | |||||||
| chr7:138534408 | G | A | 1 | a0001c0001t0005g0254 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.997-4249G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138534408 | |||||||
| chr7:138534809 | T | A | 8 | a0001c0001t0006g0215 a0001c0001t0006g0216 a0001c0001t0006g0217 others(5): Show |
8 | HG01891.hp1 HG03139.hp2 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.997-3848T>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138534809 | |||||||
| chr7:138535011 | T | A | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.997-3646T>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138535011 | |||||||
| chr7:138535206 | C | T | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.997-3451C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138535206 | |||||||
| chr7:138535449 | G | A | 8 | a0001c0001t0006g0215 a0001c0001t0006g0216 a0001c0001t0006g0217 others(5): Show |
8 | HG01891.hp1 HG03139.hp2 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.997-3208G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138535449 | |||||||
| chr7:138535527 | G | A | 2 | a0001c0001t0021g0189 a0001c0001t0021g0194 |
2 | HG01175.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.997-3130G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138535527 | |||||||
| chr7:138535528 | C | G | 2 | a0001c0001t0021g0189 a0001c0001t0021g0194 |
2 | HG01175.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.997-3129C>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138535528 | |||||||
| chr7:138535545 | C | T | 2 | a0001c0001t0021g0189 a0001c0001t0021g0194 |
2 | HG01175.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.997-3112C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138535545 | |||||||
| chr7:138535546 | T | C | 2 | a0001c0001t0021g0189 a0001c0001t0021g0194 |
2 | HG01175.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.997-3111T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138535546 | |||||||
| chr7:138535558 | T | G | 2 | a0001c0001t0021g0189 a0001c0001t0021g0194 |
2 | HG01175.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.997-3099T>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138535558 | |||||||
| chr7:138535711 | A | G | 207 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(204): Show |
208 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.997-2946A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138535711 | |||||||
| chr7:138535729 | A | G | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.997-2928A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138535729 | |||||||
| chr7:138535735 | C | T | 146 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(143): Show |
146 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.997-2922C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138535735 | |||||||
| chr7:138535840 | C | T | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.997-2817C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138535840 | |||||||
| chr7:138535953 | C | T | 3 | a0001c0005t0013g0114 a0001c0005t0013g0115 a0001c0010t0013g0113 |
3 | HG02572.hp2 HG02723.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.997-2704C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138535953 | |||||||
| chr7:138535992 | T | C | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.997-2665T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138535992 | |||||||
| chr7:138536028 | T | G | 9 | a0001c0001t0006g0215 a0001c0001t0006g0216 a0001c0001t0006g0217 others(6): Show |
9 | HG01891.hp1 HG03139.hp2 HG03225.hp1 others(6): Show |
intron_variant | MODIFIER | c.997-2629T>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138536028 | |||||||
| chr7:138536050 | A | G | 7 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(4): Show |
7 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.997-2607A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138536050 | |||||||
| chr7:138536092 | C | G | 1 | a0002c0006t0006g0221 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.997-2565C>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138536092 | |||||||
| chr7:138536178 | G | A | 2 | a0001c0001t0001g0039 a0001c0001t0001g0051 |
2 | HG01081.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.997-2479G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138536178 | |||||||
| chr7:138536436 | T | A | 1 | a0001c0001t0048g0148 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.997-2221T>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138536436 | |||||||
| chr7:138536512 | T | C | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.997-2145T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138536512 | |||||||
| chr7:138536699 | A | T | 1 | a0001c0001t0002g0152 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.997-1958A>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138536699 | |||||||
| chr7:138536711 | G | A | 2 | a0001c0004t0056g0008 a0001c0004t0057g0109 |
2 | HG02055.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.997-1946G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138536711 | |||||||
| chr7:138536822 | G | A | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.997-1835G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138536822 | |||||||
| chr7:138536853 | C | T | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.997-1804C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138536853 | |||||||
| chr7:138536942 | C | T | 1 | a0001c0001t0046g0262 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.997-1715C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138536942 | |||||||
| chr7:138536983 | C | T | 13 | a0001c0001t0009g0014 a0001c0001t0009g0094 a0001c0001t0009g0095 others(10): Show |
13 | HG01070.hp2 HG01071.hp2 HG01123.hp2 others(10): Show |
intron_variant | MODIFIER | c.997-1674C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138536983 | |||||||
| chr7:138537150 | G | C | 232 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(229): Show |
233 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.997-1507G>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138537150 | |||||||
| chr7:138537191 | G | A | 9 | a0001c0001t0002g0084 a0001c0001t0006g0215 a0001c0001t0006g0216 others(6): Show |
9 | HG01891.hp1 HG03139.hp2 HG03225.hp1 others(6): Show |
intron_variant | MODIFIER | c.997-1466G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138537191 | |||||||
| chr7:138537192 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.997-1465G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138537192 | |||||||
| chr7:138537237 | G | A | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.997-1420G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138537237 | |||||||
| chr7:138537300 | C | T | 4 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 others(1): Show |
4 | HG02896.hp2 HG02897.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.997-1357C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138537300 | |||||||
| chr7:138537309 | C | T | 2 | a0001c0001t0006g0216 a0001c0001t0006g0218 |
2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.997-1348C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138537309 | |||||||
| chr7:138537342 | C | T | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.997-1315C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138537342 | |||||||
| chr7:138537365 | C | T | 15 | a0001c0001t0005g0253 a0001c0001t0005g0254 a0001c0001t0005g0256 others(12): Show |
15 | HG02055.hp2 HG02622.hp1 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.997-1292C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138537365 | |||||||
| chr7:138537379 | G | GT | 79 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0016 others(76): Show |
79 | HG00408.hp2 HG00621.hp1 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.997-1249dupT | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr7 | 138537379 | ||||||
| chr7:138537379 | G | GTT | 60 | a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0021 others(57): Show |
60 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.997-1250_997-1249d others(4): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr7 | 138537379 | ||||||
| chr7:138537379 | G | GTTT | 18 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0076 others(15): Show |
19 | HG01069.hp2 HG01071.hp1 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.997-1251_997-1249d others(5): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr7 | 138537379 | ||||||
| chr7:138537379 | G | GTTTT | 10 | a0001c0001t0001g0089 a0001c0001t0001g0103 a0001c0001t0001g0104 others(7): Show |
10 | HG01099.hp1 HG02109.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.997-1252_997-1249d others(6): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr7 | 138537379 | ||||||
| chr7:138537379 | G | T | 1 | a0003c0008t0002g0102 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.997-1278G>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138537379 | |||||||
| chr7:138537379 | GT | G | 14 | a0001c0001t0005g0256 a0001c0001t0005g0257 a0001c0001t0005g0259 others(11): Show |
14 | HG01891.hp1 HG02055.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.997-1249delT | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr7 | 138537379 | ||||||
| chr7:138537379 | GTTTTTTT others(4): Show |
G | 2 | a0001c0001t0001g0043 a0001c0001t0002g0192 |
2 | HG02165.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.997-1259_997-1249d others(13): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr7 | 138537379 | ||||||
| chr7:138537379 | GTTTTTTT others(5): Show |
G | 5 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(2): Show |
5 | HG02486.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.997-1260_997-1249d others(14): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr7 | 138537379 | ||||||
| chr7:138537379 | GTTTTTTT others(6): Show |
G | 2 | a0001c0001t0016g0012 a0001c0001t0016g0013 |
2 | HG01884.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.997-1261_997-1249d others(15): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr7 | 138537379 | ||||||
| chr7:138537379 | GTTTTTTT others(7): Show |
G | 11 | a0001c0001t0009g0014 a0001c0001t0009g0094 a0001c0001t0009g0095 others(8): Show |
11 | HG01070.hp2 HG01071.hp2 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.997-1262_997-1249d others(16): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr7 | 138537379 | ||||||
| chr7:138537393 | T | G | 1 | a0001c0001t0002g0164 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.997-1264T>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138537393 | |||||||
| chr7:138537694 | A | T | 21 | a0001c0001t0003g0001 a0001c0001t0003g0270 a0001c0001t0003g0271 others(18): Show |
22 | HG00140.hp2 HG00735.hp2 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.997-963A>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138537694 | |||||||
| chr7:138537706 | C | T | 5 | a0001c0001t0002g0181 a0001c0001t0002g0247 a0001c0001t0012g0118 others(2): Show |
5 | HG01943.hp1 HG02129.hp1 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.997-951C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138537706 | |||||||
| chr7:138537708 | T | C | 1 | a0001c0001t0002g0131 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.997-949T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138537708 | |||||||
| chr7:138537815 | G | C | 13 | a0001c0001t0009g0014 a0001c0001t0009g0094 a0001c0001t0009g0095 others(10): Show |
13 | HG01070.hp2 HG01071.hp2 HG01123.hp2 others(10): Show |
intron_variant | MODIFIER | c.997-842G>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138537815 | |||||||
| chr7:138537890 | G | T | 1 | a0001c0001t0001g0234 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.997-767G>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138537890 | |||||||
| chr7:138538129 | T | C | 7 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(4): Show |
7 | HG01346.hp1 HG01978.hp2 HG01993.hp2 others(4): Show |
intron_variant | MODIFIER | c.997-528T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138538129 | |||||||
| chr7:138538161 | T | C | 7 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(4): Show |
7 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.997-496T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138538161 | |||||||
| chr7:138538242 | A | G | 146 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(143): Show |
146 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.997-415A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138538242 | |||||||
| chr7:138538266 | A | G | 21 | a0001c0001t0005g0253 a0001c0001t0005g0254 a0001c0001t0005g0256 others(18): Show |
21 | HG01891.hp1 HG02647.hp1 HG02683.hp1 others(18): Show |
intron_variant | MODIFIER | c.997-391A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138538266 | |||||||
| chr7:138538274 | G | C | 1 | a0001c0001t0001g0016 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.997-383G>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138538274 | |||||||
| chr7:138538400 | C | G | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.997-257C>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138538400 | |||||||
| chr7:138538552 | G | C | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.997-105G>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138538552 | |||||||
| chr7:138538622 | T | C | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.997-35T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138538622 | |||||||
| chr7:138538641 | A | G | 1 | a0001c0002t0015g0170 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.997-16A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | chr7 | 138538641 | |||||||
| chr7:138538865 | G | T | 2 | a0001c0001t0002g0143 a0001c0001t0002g0146 |
2 | NA19002.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1143+62G>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138538865 | |||||||
| chr7:138538891 | T | C | 1 | a0001c0001t0006g0223 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1143+88T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138538891 | |||||||
| chr7:138539156 | T | C | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1143+353T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138539156 | |||||||
| chr7:138539307 | G | A | 4 | a0001c0001t0002g0208 a0001c0001t0017g0005 a0001c0001t0017g0006 others(1): Show |
4 | HG02896.hp2 HG02897.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1143+504G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138539307 | |||||||
| chr7:138539340 | A | C | 2 | a0001c0004t0056g0008 a0001c0004t0057g0109 |
2 | HG02055.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1143+537A>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138539340 | |||||||
| chr7:138539401 | C | A | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1143+598C>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138539401 | |||||||
| chr7:138539550 | A | G | 2 | a0001c0001t0016g0012 a0001c0001t0016g0013 |
2 | HG01884.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1143+747A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138539550 | |||||||
| chr7:138539649 | C | T | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1143+846C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138539649 | |||||||
| chr7:138539767 | T | A | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1143+964T>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138539767 | |||||||
| chr7:138539798 | A | G | 1 | a0001c0001t0012g0205 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1143+995A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138539798 | |||||||
| chr7:138539801 | C | CT | 145 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(142): Show |
145 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.1143+1015dupT | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr7 | 138539801 | ||||||
| chr7:138539801 | C | CTT | 7 | a0001c0001t0001g0029 a0001c0001t0002g0099 a0001c0001t0002g0100 others(4): Show |
7 | HG02055.hp1 HG02155.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143+1014_1143+101 others(6): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr7 | 138539801 | ||||||
| chr7:138540089 | T | C | 2 | a0001c0004t0056g0008 a0001c0004t0057g0109 |
2 | HG02055.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1143+1286T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138540089 | |||||||
| chr7:138540356 | T | C | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1143+1553T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138540356 | |||||||
| chr7:138540404 | C | A | 1 | a0001c0001t0040g0186 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1143+1601C>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138540404 | |||||||
| chr7:138540463 | A | G | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1143+1660A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138540463 | |||||||
| chr7:138540774 | A | G | 5 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(2): Show |
5 | HG02486.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1143+1971A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138540774 | |||||||
| chr7:138540809 | T | C | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1143+2006T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138540809 | |||||||
| chr7:138540877 | T | C | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1143+2074T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138540877 | |||||||
| chr7:138541139 | G | A | 1 | a0001c0001t0006g0216 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1143+2336G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138541139 | |||||||
| chr7:138541246 | C | T | 5 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(2): Show |
5 | HG02486.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1143+2443C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138541246 | |||||||
| chr7:138541257 | T | C | 5 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(2): Show |
5 | HG02486.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1143+2454T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138541257 | |||||||
| chr7:138541259 | C | T | 3 | a0001c0003t0014g0071 a0001c0003t0014g0088 a0001c0003t0014g0090 |
3 | HG02622.hp2 HG02818.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1143+2456C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138541259 | |||||||
| chr7:138541280 | C | T | 5 | a0001c0002t0004g0121 a0001c0002t0004g0122 a0001c0002t0004g0123 others(2): Show |
5 | HG00280.hp1 HG02738.hp1 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.1143+2477C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138541280 | |||||||
| chr7:138541281 | G | A | 3 | a0001c0001t0001g0052 a0001c0001t0001g0082 a0001c0001t0049g0053 |
3 | NA18975.hp2 NA18994.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1143+2478G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138541281 | |||||||
| chr7:138541329 | G | A | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1143+2526G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138541329 | |||||||
| chr7:138541363 | G | A | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1143+2560G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138541363 | |||||||
| chr7:138541536 | G | A | 2 | a0001c0004t0056g0008 a0001c0004t0057g0109 |
2 | HG02055.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1143+2733G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138541536 | |||||||
| chr7:138541569 | C | T | 1 | a0001c0001t0002g0245 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1143+2766C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138541569 | |||||||
| chr7:138541618 | A | G | 1 | a0001c0001t0002g0142 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1143+2815A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138541618 | |||||||
| chr7:138541633 | A | G | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1143+2830A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138541633 | |||||||
| chr7:138541717 | A | G | 1 | a0001c0001t0002g0084 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1143+2914A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138541717 | |||||||
| chr7:138541768 | T | C | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1143+2965T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138541768 | |||||||
| chr7:138541773 | A | C | 1 | a0001c0001t0002g0176 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1143+2970A>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138541773 | |||||||
| chr7:138541775 | G | A | 1 | a0001c0001t0055g0199 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1143+2972G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138541775 | |||||||
| chr7:138541834 | C | T | 92 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(89): Show |
92 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.1143+3031C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138541834 | |||||||
| chr7:138541990 | A | T | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1143+3187A>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138541990 | |||||||
| chr7:138542048 | A | G | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1143+3245A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138542048 | |||||||
| chr7:138542065 | A | G | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1143+3262A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138542065 | |||||||
| chr7:138542076 | A | G | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1143+3273A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138542076 | |||||||
| chr7:138542150 | G | A | 1 | a0001c0001t0003g0285 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1143+3347G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138542150 | |||||||
| chr7:138542177 | A | G | 1 | a0001c0001t0001g0237 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1143+3374A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138542177 | |||||||
| chr7:138542570 | G | A | 1 | a0001c0001t0055g0199 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1143+3767G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138542570 | |||||||
| chr7:138542618 | A | T | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1143+3815A>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138542618 | |||||||
| chr7:138542638 | C | T | 3 | a0001c0001t0001g0057 a0001c0001t0001g0059 a0001c0001t0001g0060 |
3 | HG00438.hp1 NA19063.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.1143+3835C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138542638 | |||||||
| chr7:138542945 | C | G | 1 | a0001c0001t0002g0084 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1143+4142C>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138542945 | |||||||
| chr7:138543073 | T | C | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1143+4270T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138543073 | |||||||
| chr7:138543093 | G | T | 5 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(2): Show |
5 | HG02486.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1143+4290G>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138543093 | |||||||
| chr7:138543246 | T | C | 3 | a0001c0001t0001g0052 a0001c0001t0001g0082 a0001c0001t0049g0053 |
3 | NA18975.hp2 NA18994.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1143+4443T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138543246 | |||||||
| chr7:138543288 | C | T | 4 | a0001c0001t0002g0099 a0001c0001t0002g0100 a0001c0001t0002g0101 others(1): Show |
4 | HG02055.hp1 HG02976.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1143+4485C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138543288 | |||||||
| chr7:138543379 | T | C | 7 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(4): Show |
7 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143+4576T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138543379 | |||||||
| chr7:138543564 | C | T | 1 | a0001c0001t0055g0199 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1143+4761C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138543564 | |||||||
| chr7:138543614 | A | C | 1 | a0001c0001t0001g0239 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1143+4811A>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138543614 | |||||||
| chr7:138543616 | T | A | 7 | a0001c0001t0006g0215 a0001c0001t0006g0216 a0001c0001t0006g0217 others(4): Show |
7 | HG03139.hp2 HG03225.hp1 HG03516.hp2 others(4): Show |
intron_variant | MODIFIER | c.1143+4813T>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138543616 | |||||||
| chr7:138543629 | T | C | 1 | a0001c0002t0004g0243 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1143+4826T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138543629 | |||||||
| chr7:138543651 | A | G | 4 | a0001c0001t0002g0193 a0001c0001t0002g0208 a0001c0001t0002g0219 others(1): Show |
4 | NA18966.hp1 NA19057.hp2 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.1143+4848A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138543651 | |||||||
| chr7:138543802 | G | T | 2 | a0001c0004t0056g0008 a0001c0004t0057g0109 |
2 | HG02055.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1143+4999G>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138543802 | |||||||
| chr7:138543822 | T | G | 5 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(2): Show |
5 | HG02486.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1143+5019T>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138543822 | |||||||
| chr7:138543831 | G | GT | 18 | a0001c0001t0001g0238 a0001c0001t0003g0296 a0001c0001t0009g0014 others(15): Show |
18 | HG01070.hp2 HG01071.hp2 HG01123.hp2 others(15): Show |
intron_variant | MODIFIER | c.1143+5036dupT | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr7 | 138543831 | ||||||
| chr7:138543831 | G | GTT | 6 | a0001c0001t0010g0111 a0001c0001t0010g0112 a0001c0001t0010g0241 others(3): Show |
6 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1143+5035_1143+503 others(6): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr7 | 138543831 | ||||||
| chr7:138543836 | T | C | 11 | a0001c0001t0002g0174 a0001c0001t0002g0192 a0001c0001t0002g0193 others(8): Show |
11 | HG01261.hp1 HG02165.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1143+5033T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138543836 | |||||||
| chr7:138543999 | A | AT | 6 | a0001c0001t0001g0238 a0001c0001t0002g0156 a0001c0001t0005g0261 others(3): Show |
6 | HG02602.hp1 HG02622.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1143+5207dupT | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr7 | 138543999 | ||||||
| chr7:138544042 | C | A | 21 | a0001c0001t0005g0253 a0001c0001t0005g0254 a0001c0001t0005g0256 others(18): Show |
21 | HG01891.hp1 HG02647.hp1 HG02683.hp1 others(18): Show |
intron_variant | MODIFIER | c.1143+5239C>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138544042 | |||||||
| chr7:138544060 | G | A | 3 | a0001c0001t0001g0036 a0001c0001t0001g0064 a0001c0001t0001g0089 |
3 | NA18940.hp2 NA18966.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.1143+5257G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138544060 | |||||||
| chr7:138544089 | G | A | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1143+5286G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138544089 | |||||||
| chr7:138544241 | A | C | 3 | a0001c0001t0003g0274 a0001c0001t0003g0297 a0001c0001t0003g0299 |
3 | HG01243.hp2 HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1143+5438A>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138544241 | |||||||
| chr7:138544420 | A | G | 7 | a0001c0001t0006g0215 a0001c0001t0006g0216 a0001c0001t0006g0217 others(4): Show |
7 | HG03139.hp2 HG03225.hp1 HG03516.hp2 others(4): Show |
intron_variant | MODIFIER | c.1143+5617A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138544420 | |||||||
| chr7:138544440 | CTA | C | 7 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(4): Show |
7 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143+5639_1143+564 others(6): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr7 | 138544440 | ||||||
| chr7:138544465 | T | A | 2 | a0001c0001t0002g0131 a0001c0001t0002g0147 |
2 | HG02040.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1143+5662T>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138544465 | |||||||
| chr7:138544557 | G | C | 7 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(4): Show |
7 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143+5754G>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138544557 | |||||||
| chr7:138544657 | G | A | 212 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(209): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.1143+5854G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138544657 | |||||||
| chr7:138544677 | C | A | 4 | a0001c0002t0004g0121 a0001c0002t0004g0122 a0001c0002t0004g0123 others(1): Show |
4 | HG00280.hp1 HG02738.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.1143+5874C>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138544677 | |||||||
| chr7:138544681 | C | A | 21 | a0001c0001t0005g0253 a0001c0001t0005g0254 a0001c0001t0005g0256 others(18): Show |
21 | HG01891.hp1 HG02647.hp1 HG02683.hp1 others(18): Show |
intron_variant | MODIFIER | c.1143+5878C>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138544681 | |||||||
| chr7:138544757 | A | G | 1 | a0001c0001t0001g0211 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1143+5954A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138544757 | |||||||
| chr7:138545052 | G | C | 1 | a0001c0001t0055g0199 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1144-6011G>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138545052 | |||||||
| chr7:138545069 | G | A | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1144-5994G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138545069 | |||||||
| chr7:138545163 | C | CGT | 28 | a0001c0001t0001g0034 a0001c0001t0002g0140 a0001c0001t0002g0161 others(25): Show |
28 | HG00140.hp2 HG01891.hp1 HG02083.hp1 others(25): Show |
intron_variant | MODIFIER | c.1144-5879_1144-587 others(6): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr7 | 138545163 | ||||||
| chr7:138545163 | C | CGTGTGT | 5 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(2): Show |
5 | HG02486.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1144-5883_1144-587 others(10): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr7 | 138545163 | ||||||
| chr7:138545163 | CGTGTGTG others(3): Show |
C | 9 | a0001c0001t0009g0014 a0001c0001t0009g0094 a0001c0001t0009g0095 others(6): Show |
9 | HG01070.hp2 HG01071.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.1144-5887_1144-587 others(14): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr7 | 138545163 | ||||||
| chr7:138545245 | G | A | 212 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(209): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.1144-5818G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138545245 | |||||||
| chr7:138545269 | A | C | 3 | a0001c0001t0026g0266 a0001c0001t0026g0267 a0001c0001t0035g0265 |
3 | HG02109.hp1 HG02630.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1144-5794A>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138545269 | |||||||
| chr7:138545355 | G | A | 1 | a0001c0002t0015g0169 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1144-5708G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138545355 | |||||||
| chr7:138545964 | A | G | 1 | a0001c0001t0016g0015 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1144-5099A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138545964 | |||||||
| chr7:138546027 | A | G | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1144-5036A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138546027 | |||||||
| chr7:138546075 | C | T | 214 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(211): Show |
215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1144-4988C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138546075 | |||||||
| chr7:138546170 | C | A | 2 | a0001c0004t0056g0008 a0001c0004t0057g0109 |
2 | HG02055.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1144-4893C>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138546170 | |||||||
| chr7:138546196 | C | T | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1144-4867C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138546196 | |||||||
| chr7:138546242 | A | G | 5 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(2): Show |
5 | HG02486.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1144-4821A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138546242 | |||||||
| chr7:138546465 | G | C | 1 | a0001c0001t0010g0241 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1144-4598G>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138546465 | |||||||
| chr7:138546637 | G | A | 2 | a0001c0004t0056g0008 a0001c0004t0057g0109 |
2 | HG02055.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1144-4426G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138546637 | |||||||
| chr7:138546785 | G | A | 1 | a0001c0001t0001g0021 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1144-4278G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138546785 | |||||||
| chr7:138546856 | C | T | 7 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(4): Show |
7 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1144-4207C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138546856 | |||||||
| chr7:138546869 | C | G | 1 | a0001c0002t0015g0170 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1144-4194C>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138546869 | |||||||
| chr7:138547022 | T | C | 13 | a0001c0001t0001g0239 a0001c0001t0009g0014 a0001c0001t0009g0094 others(10): Show |
13 | HG01070.hp2 HG01071.hp2 HG01123.hp2 others(10): Show |
intron_variant | MODIFIER | c.1144-4041T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138547022 | |||||||
| chr7:138547042 | A | G | 201 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(198): Show |
202 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.1144-4021A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138547042 | |||||||
| chr7:138547155 | T | C | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1144-3908T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138547155 | |||||||
| chr7:138547240 | G | A | 1 | a0001c0001t0048g0148 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1144-3823G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138547240 | |||||||
| chr7:138547324 | C | T | 1 | a0001c0001t0029g0300 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1144-3739C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138547324 | |||||||
| chr7:138547347 | A | C | 2 | a0001c0002t0015g0170 a0001c0002t0015g0171 |
2 | HG02451.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1144-3716A>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138547347 | |||||||
| chr7:138547376 | A | G | 2 | a0001c0004t0056g0008 a0001c0004t0057g0109 |
2 | HG02055.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1144-3687A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138547376 | |||||||
| chr7:138547562 | CA | C | 7 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(4): Show |
7 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1144-3499delA | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr7 | 138547562 | ||||||
| chr7:138547630 | G | A | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1144-3433G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138547630 | |||||||
| chr7:138547648 | A | C | 1 | a0001c0004t0057g0109 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1144-3415A>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138547648 | |||||||
| chr7:138547657 | A | T | 1 | a0001c0001t0002g0207 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1144-3406A>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138547657 | |||||||
| chr7:138547698 | C | T | 1 | a0001c0001t0022g0226 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1144-3365C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138547698 | |||||||
| chr7:138547711 | T | A | 2 | a0001c0001t0003g0278 a0001c0001t0003g0287 |
2 | HG01255.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.1144-3352T>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138547711 | |||||||
| chr7:138547971 | A | G | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1144-3092A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138547971 | |||||||
| chr7:138547982 | C | T | 1 | a0001c0001t0003g0285 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1144-3081C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138547982 | |||||||
| chr7:138548074 | A | G | 7 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(4): Show |
7 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1144-2989A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138548074 | |||||||
| chr7:138548160 | C | T | 1 | a0001c0001t0055g0199 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1144-2903C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138548160 | |||||||
| chr7:138548222 | G | A | 2 | a0001c0001t0020g0139 a0001c0001t0020g0155 |
2 | HG00735.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.1144-2841G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138548222 | |||||||
| chr7:138548379 | G | A | 1 | a0001c0001t0002g0191 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1144-2684G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138548379 | |||||||
| chr7:138548388 | C | T | 2 | a0001c0002t0004g0125 a0001c0002t0004g0224 |
2 | HG03942.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.1144-2675C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138548388 | |||||||
| chr7:138548417 | CA | C | 9 | a0001c0001t0003g0276 a0001c0001t0003g0282 a0001c0001t0010g0110 others(6): Show |
9 | HG02055.hp2 HG02109.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1144-2633delA | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr7 | 138548417 | ||||||
| chr7:138548627 | T | G | 2 | a0001c0001t0021g0189 a0001c0001t0021g0194 |
2 | HG01175.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1144-2436T>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138548627 | |||||||
| chr7:138549122 | T | C | 7 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(4): Show |
7 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1144-1941T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138549122 | |||||||
| chr7:138549275 | T | A | 7 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(4): Show |
7 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1144-1788T>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138549275 | |||||||
| chr7:138549301 | G | C | 2 | a0001c0001t0003g0277 a0001c0001t0003g0286 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1144-1762G>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138549301 | |||||||
| chr7:138549323 | T | A | 3 | a0001c0001t0026g0266 a0001c0001t0026g0267 a0001c0001t0035g0265 |
3 | HG02109.hp1 HG02630.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1144-1740T>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138549323 | |||||||
| chr7:138549584 | G | A | 204 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(201): Show |
205 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.1144-1479G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138549584 | |||||||
| chr7:138549644 | A | C | 1 | a0001c0001t0001g0022 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1144-1419A>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138549644 | |||||||
| chr7:138549645 | C | A | 1 | a0001c0001t0001g0022 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1144-1418C>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138549645 | |||||||
| chr7:138549646 | G | A | 2 | a0001c0002t0015g0170 a0001c0002t0015g0171 |
2 | HG02451.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1144-1417G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138549646 | |||||||
| chr7:138549801 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1144-1262G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138549801 | |||||||
| chr7:138549841 | G | A | 2 | a0001c0001t0022g0130 a0001c0001t0022g0226 |
2 | HG01884.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1144-1222G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138549841 | |||||||
| chr7:138550144 | TCAG | T | 7 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(4): Show |
7 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1144-914_1144-912d others(5): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr7 | 138550144 | ||||||
| chr7:138550318 | G | GGT | 12 | a0001c0001t0001g0066 a0001c0001t0002g0164 a0001c0001t0006g0215 others(9): Show |
12 | HG01496.hp1 HG01891.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.1144-719_1144-718d others(4): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr7 | 138550318 | ||||||
| chr7:138550318 | G | GGTGT | 105 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(102): Show |
105 | HG00140.hp1 HG00423.hp2 HG00621.hp1 others(102): Show |
intron_variant | MODIFIER | c.1144-721_1144-718d others(6): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr7 | 138550318 | ||||||
| chr7:138550318 | G | GGTGTGT | 17 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0022 others(14): Show |
17 | HG00408.hp2 HG00609.hp1 HG01928.hp2 others(14): Show |
intron_variant | MODIFIER | c.1144-723_1144-718d others(8): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr7 | 138550318 | ||||||
| chr7:138550318 | G | GGTGTGTG others(3): Show |
5 | a0001c0001t0005g0253 a0001c0001t0005g0259 a0001c0001t0005g0260 others(2): Show |
5 | HG02735.hp1 HG03041.hp2 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.1144-727_1144-718d others(12): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr7 | 138550318 | ||||||
| chr7:138550318 | G | GGTGTGTG others(13): Show |
3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1144-737_1144-718d others(22): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr7 | 138550318 | ||||||
| chr7:138550318 | GGT | G | 3 | a0001c0001t0002g0196 a0001c0001t0002g0246 a0001c0002t0031g0200 |
3 | HG02683.hp2 NA18973.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.1144-719_1144-718d others(4): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr7 | 138550318 | ||||||
| chr7:138550318 | GGTGT | G | 4 | a0001c0001t0055g0199 a0001c0005t0013g0114 a0001c0005t0013g0115 others(1): Show |
4 | HG02572.hp2 HG02723.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1144-721_1144-718d others(6): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr7 | 138550318 | ||||||
| chr7:138550501 | T | C | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1144-562T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138550501 | |||||||
| chr7:138550578 | T | G | 5 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(2): Show |
5 | HG02486.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1144-485T>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138550578 | |||||||
| chr7:138550765 | A | T | 1 | a0001c0001t0002g0197 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1144-298A>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138550765 | |||||||
| chr7:138550804 | T | C | 1 | a0003c0008t0002g0102 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1144-259T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138550804 | |||||||
| chr7:138550884 | G | A | 1 | a0001c0001t0006g0215 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1144-179G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138550884 | |||||||
| chr7:138550898 | G | C | 231 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(228): Show |
232 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.1144-165G>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138550898 | |||||||
| chr7:138550916 | A | G | 1 | a0001c0001t0002g0145 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1144-147A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138550916 | |||||||
| chr7:138550935 | G | C | 3 | a0001c0001t0002g0193 a0001c0001t0002g0219 a0001c0001t0042g0201 |
3 | NA18966.hp1 NA19057.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.1144-128G>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | chr7 | 138550935 | |||||||
| chr7:138551281 | G | A | 2 | a0001c0001t0022g0130 a0001c0001t0022g0226 |
2 | HG01884.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1261+101G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 8/18 | chr7 | 138551281 | |||||||
| chr7:138551313 | A | T | 4 | a0001c0001t0019g0303 a0001c0001t0019g0304 a0001c0001t0030g0305 others(1): Show |
4 | HG02145.hp1 HG02258.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1261+133A>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 8/18 | chr7 | 138551313 | |||||||
| chr7:138551433 | G | A | 1 | a0001c0001t0002g0163 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1261+253G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 8/18 | chr7 | 138551433 | |||||||
| chr7:138551622 | A | T | 1 | a0001c0001t0001g0044 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1261+442A>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 8/18 | chr7 | 138551622 | |||||||
| chr7:138551973 | A | G | 3 | a0001c0005t0013g0114 a0001c0005t0013g0115 a0001c0010t0013g0113 |
3 | HG02572.hp2 HG02723.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1261+793A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 8/18 | chr7 | 138551973 | |||||||
| chr7:138552028 | A | T | 7 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(4): Show |
7 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1261+848A>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 8/18 | chr7 | 138552028 | |||||||
| chr7:138552322 | T | A | 2 | a0001c0001t0002g0129 a0001c0001t0002g0197 |
2 | HG00408.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1261+1142T>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 8/18 | chr7 | 138552322 | |||||||
| chr7:138552575 | G | A | 1 | a0001c0002t0031g0200 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1261+1395G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 8/18 | chr7 | 138552575 | |||||||
| chr7:138552670 | C | T | 1 | a0001c0002t0004g0127 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1261+1490C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 8/18 | chr7 | 138552670 | |||||||
| chr7:138552727 | C | T | 3 | a0001c0001t0010g0110 a0001c0001t0010g0241 a0001c0001t0010g0244 |
3 | HG02486.hp1 HG02809.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1261+1547C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 8/18 | chr7 | 138552727 | |||||||
| chr7:138552728 | G | A | 3 | a0001c0005t0013g0114 a0001c0005t0013g0115 a0001c0010t0013g0113 |
3 | HG02572.hp2 HG02723.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1261+1548G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 8/18 | chr7 | 138552728 | |||||||
| chr7:138552731 | A | C | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1261+1551A>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 8/18 | chr7 | 138552731 | |||||||
| chr7:138552803 | A | G | 10 | a0001c0001t0001g0239 a0001c0001t0009g0014 a0001c0001t0009g0094 others(7): Show |
10 | HG01070.hp2 HG01071.hp2 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.1261+1623A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 8/18 | chr7 | 138552803 | |||||||
| chr7:138552808 | A | G | 3 | a0001c0001t0026g0266 a0001c0001t0026g0267 a0001c0001t0035g0265 |
3 | HG02109.hp1 HG02630.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1261+1628A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 8/18 | chr7 | 138552808 | |||||||
| chr7:138553010 | C | T | 1 | a0001c0001t0003g0282 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1262-1688C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 8/18 | chr7 | 138553010 | |||||||
| chr7:138553314 | G | C | 1 | a0001c0009t0003g0268 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1262-1384G>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 8/18 | chr7 | 138553314 | |||||||
| chr7:138553819 | A | C | 4 | a0001c0001t0026g0266 a0001c0001t0026g0267 a0001c0001t0033g0172 others(1): Show |
4 | HG02109.hp1 HG02630.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1262-879A>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 8/18 | chr7 | 138553819 | |||||||
| chr7:138554092 | A | G | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1262-606A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 8/18 | chr7 | 138554092 | |||||||
| chr7:138554099 | G | A | 66 | a0001c0001t0003g0001 a0001c0001t0003g0269 a0001c0001t0003g0270 others(63): Show |
67 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(64): Show |
intron_variant | MODIFIER | c.1262-599G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 8/18 | chr7 | 138554099 | |||||||
| chr7:138554153 | A | G | 7 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(4): Show |
7 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1262-545A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 8/18 | chr7 | 138554153 | |||||||
| chr7:138554363 | A | G | 1 | a0001c0001t0041g0045 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1262-335A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 8/18 | chr7 | 138554363 | |||||||
| chr7:138554422 | C | T | 94 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(91): Show |
94 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.1262-276C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 8/18 | chr7 | 138554422 | |||||||
| chr7:138555079 | A | C | 2 | a0001c0001t0003g0307 a0001c0001t0039g0227 |
2 | HG02738.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1530+113A>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138555079 | |||||||
| chr7:138555426 | A | T | 1 | a0001c0001t0019g0304 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1530+460A>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138555426 | |||||||
| chr7:138555462 | C | A | 2 | a0001c0001t0002g0206 a0001c0001t0002g0207 |
2 | HG02165.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.1530+496C>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138555462 | |||||||
| chr7:138555482 | A | AT | 18 | a0001c0001t0001g0210 a0001c0001t0002g0140 a0001c0001t0002g0141 others(15): Show |
18 | HG00609.hp2 HG01943.hp1 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.1530+534dupT | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr7 | 138555482 | ||||||
| chr7:138555482 | AT | A | 7 | a0001c0001t0001g0214 a0001c0001t0002g0161 a0001c0001t0006g0217 others(4): Show |
7 | HG02055.hp1 HG02809.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1530+534delT | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr7 | 138555482 | ||||||
| chr7:138555482 | ATT | A | 15 | a0001c0001t0009g0014 a0001c0001t0009g0095 a0001c0001t0009g0096 others(12): Show |
15 | HG01071.hp2 HG01123.hp2 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1530+533_1530+534d others(4): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr7 | 138555482 | ||||||
| chr7:138555585 | C | T | 3 | a0001c0003t0014g0071 a0001c0003t0014g0088 a0001c0003t0014g0090 |
3 | HG02622.hp2 HG02818.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1530+619C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138555585 | |||||||
| chr7:138555595 | A | G | 109 | a0001c0001t0003g0001 a0001c0001t0003g0269 a0001c0001t0003g0270 others(106): Show |
110 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(107): Show |
intron_variant | MODIFIER | c.1530+629A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138555595 | |||||||
| chr7:138555699 | G | A | 1 | a0001c0001t0028g0302 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1530+733G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138555699 | |||||||
| chr7:138555735 | G | C | 7 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(4): Show |
7 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1530+769G>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138555735 | |||||||
| chr7:138555776 | C | T | 1 | a0001c0001t0001g0234 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1530+810C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138555776 | |||||||
| chr7:138555892 | C | A | 13 | a0001c0001t0005g0253 a0001c0001t0005g0254 a0001c0001t0005g0256 others(10): Show |
13 | HG02647.hp1 HG02683.hp1 HG02735.hp1 others(10): Show |
intron_variant | MODIFIER | c.1530+926C>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138555892 | |||||||
| chr7:138555913 | G | A | 2 | a0001c0001t0003g0278 a0001c0001t0003g0287 |
2 | HG01255.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.1530+947G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138555913 | |||||||
| chr7:138555944 | A | G | 7 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(4): Show |
7 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1530+978A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138555944 | |||||||
| chr7:138555986 | A | G | 1 | a0001c0001t0007g0153 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1530+1020A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138555986 | |||||||
| chr7:138556012 | A | G | 1 | a0001c0001t0002g0174 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1530+1046A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138556012 | |||||||
| chr7:138556280 | C | T | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1530+1314C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138556280 | |||||||
| chr7:138556345 | A | G | 1 | a0001c0001t0003g0273 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1530+1379A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138556345 | |||||||
| chr7:138556525 | T | C | 2 | a0001c0001t0003g0269 a0001c0009t0003g0268 |
2 | HG02257.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1530+1559T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138556525 | |||||||
| chr7:138556526 | T | G | 1 | a0001c0001t0003g0272 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1530+1560T>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138556526 | |||||||
| chr7:138556696 | C | T | 3 | a0001c0001t0011g0252 a0001c0001t0011g0255 a0001c0001t0011g0258 |
3 | HG03491.hp1 HG03492.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1530+1730C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138556696 | |||||||
| chr7:138556736 | G | C | 1 | a0001c0001t0001g0089 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1530+1770G>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138556736 | |||||||
| chr7:138556897 | A | G | 6 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(3): Show |
6 | HG02083.hp1 NA18944.hp1 NA18956.hp1 others(3): Show |
intron_variant | MODIFIER | c.1530+1931A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138556897 | |||||||
| chr7:138557178 | G | T | 1 | a0001c0001t0046g0262 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1530+2212G>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138557178 | |||||||
| chr7:138557252 | C | T | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1530+2286C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138557252 | |||||||
| chr7:138557261 | T | C | 3 | a0001c0005t0013g0114 a0001c0005t0013g0115 a0001c0010t0013g0113 |
3 | HG02572.hp2 HG02723.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1530+2295T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138557261 | |||||||
| chr7:138557283 | G | A | 7 | a0001c0001t0006g0215 a0001c0001t0006g0216 a0001c0001t0006g0217 others(4): Show |
7 | HG03139.hp2 HG03225.hp1 HG03516.hp2 others(4): Show |
intron_variant | MODIFIER | c.1530+2317G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138557283 | |||||||
| chr7:138557330 | A | C | 3 | a0001c0001t0026g0266 a0001c0001t0026g0267 a0001c0001t0035g0265 |
3 | HG02109.hp1 HG02630.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1530+2364A>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138557330 | |||||||
| chr7:138557622 | A | C | 4 | a0001c0001t0003g0283 a0001c0001t0003g0284 a0001c0001t0003g0289 others(1): Show |
4 | HG00738.hp1 HG01106.hp2 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.1530+2656A>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138557622 | |||||||
| chr7:138557882 | A | G | 112 | a0001c0001t0001g0239 a0001c0001t0003g0001 a0001c0001t0003g0269 others(109): Show |
113 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(110): Show |
intron_variant | MODIFIER | c.1530+2916A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138557882 | |||||||
| chr7:138557923 | G | T | 3 | a0001c0005t0013g0114 a0001c0005t0013g0115 a0001c0010t0013g0113 |
3 | HG02572.hp2 HG02723.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1530+2957G>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138557923 | |||||||
| chr7:138557948 | CAG | C | 94 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(91): Show |
94 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.1530+2983_1530+298 others(6): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138557948 | |||||||
| chr7:138557965 | T | C | 2 | a0001c0004t0056g0008 a0001c0004t0057g0109 |
2 | HG02055.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1530+2999T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138557965 | |||||||
| chr7:138558089 | T | C | 9 | a0001c0001t0006g0215 a0001c0001t0006g0216 a0001c0001t0006g0217 others(6): Show |
9 | HG01891.hp1 HG03139.hp2 HG03225.hp1 others(6): Show |
intron_variant | MODIFIER | c.1530+3123T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138558089 | |||||||
| chr7:138558266 | A | C | 13 | a0001c0001t0005g0253 a0001c0001t0005g0254 a0001c0001t0005g0256 others(10): Show |
13 | HG02647.hp1 HG02683.hp1 HG02735.hp1 others(10): Show |
intron_variant | MODIFIER | c.1530+3300A>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138558266 | |||||||
| chr7:138558323 | A | T | 2 | a0001c0001t0003g0269 a0001c0009t0003g0268 |
2 | HG02257.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1530+3357A>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138558323 | |||||||
| chr7:138558350 | C | T | 13 | a0001c0001t0005g0253 a0001c0001t0005g0254 a0001c0001t0005g0256 others(10): Show |
13 | HG02647.hp1 HG02683.hp1 HG02735.hp1 others(10): Show |
intron_variant | MODIFIER | c.1530+3384C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138558350 | |||||||
| chr7:138558448 | T | A | 1 | a0001c0001t0003g0280 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1530+3482T>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138558448 | |||||||
| chr7:138558568 | A | G | 1 | a0001c0001t0043g0136 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1530+3602A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138558568 | |||||||
| chr7:138558599 | C | T | 3 | a0001c0001t0002g0140 a0001c0001t0002g0141 a0001c0001t0002g0167 |
3 | NA18949.hp1 NA18998.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.1530+3633C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138558599 | |||||||
| chr7:138558658 | C | T | 13 | a0001c0001t0005g0253 a0001c0001t0005g0254 a0001c0001t0005g0256 others(10): Show |
13 | HG02647.hp1 HG02683.hp1 HG02735.hp1 others(10): Show |
intron_variant | MODIFIER | c.1530+3692C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138558658 | |||||||
| chr7:138558659 | G | A | 2 | a0001c0001t0008g0281 a0001c0010t0013g0113 |
2 | NA18522.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1530+3693G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138558659 | |||||||
| chr7:138558895 | G | A | 13 | a0001c0001t0005g0253 a0001c0001t0005g0254 a0001c0001t0005g0256 others(10): Show |
13 | HG02647.hp1 HG02683.hp1 HG02735.hp1 others(10): Show |
intron_variant | MODIFIER | c.1530+3929G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138558895 | |||||||
| chr7:138558918 | G | A | 3 | a0001c0001t0026g0266 a0001c0001t0026g0267 a0001c0001t0035g0265 |
3 | HG02109.hp1 HG02630.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1530+3952G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138558918 | |||||||
| chr7:138558933 | A | G | 7 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(4): Show |
7 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1530+3967A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138558933 | |||||||
| chr7:138558990 | C | T | 9 | a0001c0001t0009g0014 a0001c0001t0009g0094 a0001c0001t0009g0095 others(6): Show |
9 | HG01070.hp2 HG01071.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.1530+4024C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138558990 | |||||||
| chr7:138559221 | G | A | 4 | a0001c0001t0046g0262 a0001c0005t0013g0114 a0001c0005t0013g0115 others(1): Show |
4 | HG02572.hp2 HG02723.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1530+4255G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138559221 | |||||||
| chr7:138559240 | T | C | 1 | a0001c0001t0001g0235 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1530+4274T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138559240 | |||||||
| chr7:138559273 | C | T | 3 | a0001c0001t0002g0193 a0001c0001t0002g0219 a0001c0001t0042g0201 |
3 | NA18966.hp1 NA19057.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.1530+4307C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138559273 | |||||||
| chr7:138559300 | C | T | 187 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(184): Show |
188 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.1530+4334C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138559300 | |||||||
| chr7:138559365 | AG | A | 13 | a0001c0001t0005g0253 a0001c0001t0005g0254 a0001c0001t0005g0256 others(10): Show |
13 | HG02647.hp1 HG02683.hp1 HG02735.hp1 others(10): Show |
intron_variant | MODIFIER | c.1530+4400delG | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138559365 | |||||||
| chr7:138559463 | T | G | 2 | a0001c0004t0056g0008 a0001c0004t0057g0109 |
2 | HG02055.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1530+4497T>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138559463 | |||||||
| chr7:138559532 | A | G | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1530+4566A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138559532 | |||||||
| chr7:138559672 | T | C | 1 | a0001c0001t0002g0129 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1530+4706T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138559672 | |||||||
| chr7:138559682 | T | C | 7 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(4): Show |
7 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1530+4716T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138559682 | |||||||
| chr7:138559684 | G | A | 13 | a0001c0001t0005g0253 a0001c0001t0005g0254 a0001c0001t0005g0256 others(10): Show |
13 | HG02647.hp1 HG02683.hp1 HG02735.hp1 others(10): Show |
intron_variant | MODIFIER | c.1530+4718G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138559684 | |||||||
| chr7:138559740 | G | A | 1 | a0001c0001t0001g0021 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1530+4774G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138559740 | |||||||
| chr7:138559934 | C | A | 9 | a0001c0001t0009g0014 a0001c0001t0009g0094 a0001c0001t0009g0095 others(6): Show |
9 | HG01070.hp2 HG01071.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.1530+4968C>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138559934 | |||||||
| chr7:138559953 | CT | C | 7 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(4): Show |
7 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1530+4989delT | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr7 | 138559953 | ||||||
| chr7:138560014 | C | A | 1 | a0001c0001t0001g0067 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1530+5048C>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138560014 | |||||||
| chr7:138560275 | C | CTA | 7 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(4): Show |
7 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1530+5311_1530+531 others(6): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr7 | 138560275 | ||||||
| chr7:138560281 | C | T | 13 | a0001c0001t0005g0253 a0001c0001t0005g0254 a0001c0001t0005g0256 others(10): Show |
13 | HG02647.hp1 HG02683.hp1 HG02735.hp1 others(10): Show |
intron_variant | MODIFIER | c.1530+5315C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138560281 | |||||||
| chr7:138560425 | A | T | 1 | a0001c0001t0046g0262 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1530+5459A>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138560425 | |||||||
| chr7:138560572 | A | G | 2 | a0001c0001t0002g0206 a0001c0001t0002g0207 |
2 | HG02165.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.1530+5606A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138560572 | |||||||
| chr7:138560591 | C | T | 1 | a0001c0001t0012g0205 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1530+5625C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138560591 | |||||||
| chr7:138560594 | G | T | 1 | a0001c0001t0002g0197 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1530+5628G>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138560594 | |||||||
| chr7:138560632 | A | T | 1 | a0001c0001t0001g0211 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1530+5666A>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138560632 | |||||||
| chr7:138560860 | C | T | 3 | a0001c0003t0014g0071 a0001c0003t0014g0088 a0001c0003t0014g0090 |
3 | HG02622.hp2 HG02818.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1530+5894C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138560860 | |||||||
| chr7:138560867 | G | A | 7 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(4): Show |
7 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1530+5901G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138560867 | |||||||
| chr7:138561087 | A | G | 7 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(4): Show |
7 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1530+6121A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138561087 | |||||||
| chr7:138561170 | G | A | 7 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(4): Show |
7 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1530+6204G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138561170 | |||||||
| chr7:138561251 | G | A | 9 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0022 others(6): Show |
9 | HG00408.hp2 HG01928.hp2 HG01934.hp1 others(6): Show |
intron_variant | MODIFIER | c.1531-6230G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138561251 | |||||||
| chr7:138561279 | A | T | 1 | a0001c0001t0038g0166 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1531-6202A>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138561279 | |||||||
| chr7:138561368 | G | A | 1 | a0001c0001t0001g0238 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1531-6113G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138561368 | |||||||
| chr7:138561457 | C | A | 1 | a0001c0001t0002g0157 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1531-6024C>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138561457 | |||||||
| chr7:138561585 | T | C | 7 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(4): Show |
7 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1531-5896T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138561585 | |||||||
| chr7:138562085 | G | C | 1 | a0001c0001t0001g0212 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1531-5396G>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138562085 | |||||||
| chr7:138562277 | C | T | 1 | a0001c0001t0012g0118 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1531-5204C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138562277 | |||||||
| chr7:138562467 | T | C | 7 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(4): Show |
7 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1531-5014T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138562467 | |||||||
| chr7:138562817 | C | T | 1 | a0001c0001t0003g0272 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1531-4664C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138562817 | |||||||
| chr7:138563009 | G | A | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1531-4472G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138563009 | |||||||
| chr7:138563300 | C | T | 4 | a0001c0001t0001g0049 a0001c0001t0001g0063 a0001c0001t0001g0069 others(1): Show |
4 | NA18960.hp2 NA18978.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.1531-4181C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138563300 | |||||||
| chr7:138563388 | G | A | 9 | a0001c0001t0009g0014 a0001c0001t0009g0094 a0001c0001t0009g0095 others(6): Show |
9 | HG01070.hp2 HG01071.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.1531-4093G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138563388 | |||||||
| chr7:138563433 | C | T | 3 | a0001c0001t0018g0002 a0001c0001t0018g0004 a0001c0001t0055g0199 |
3 | HG02895.hp1 HG02897.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1531-4048C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138563433 | |||||||
| chr7:138563462 | C | T | 1 | a0001c0001t0050g0213 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1531-4019C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138563462 | |||||||
| chr7:138563484 | T | C | 7 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(4): Show |
7 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1531-3997T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138563484 | |||||||
| chr7:138563604 | C | G | 7 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(4): Show |
7 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1531-3877C>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138563604 | |||||||
| chr7:138563651 | T | C | 3 | a0001c0001t0018g0002 a0001c0001t0018g0003 a0001c0001t0018g0004 |
3 | HG02895.hp1 HG02897.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1531-3830T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138563651 | |||||||
| chr7:138563665 | C | T | 2 | a0001c0004t0056g0008 a0001c0004t0057g0109 |
2 | HG02055.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1531-3816C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138563665 | |||||||
| chr7:138563796 | C | T | 90 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(87): Show |
90 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.1531-3685C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138563796 | |||||||
| chr7:138563951 | C | T | 11 | a0001c0001t0003g0285 a0001c0001t0008g0281 a0001c0001t0008g0291 others(8): Show |
11 | HG01099.hp1 HG02145.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1531-3530C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138563951 | |||||||
| chr7:138563974 | G | C | 205 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(202): Show |
206 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.1531-3507G>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138563974 | |||||||
| chr7:138564056 | G | A | 1 | a0001c0001t0003g0307 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1531-3425G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138564056 | |||||||
| chr7:138564058 | A | T | 7 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(4): Show |
7 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1531-3423A>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138564058 | |||||||
| chr7:138564193 | C | T | 1 | a0001c0002t0004g0116 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1531-3288C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138564193 | |||||||
| chr7:138564278 | T | C | 7 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(4): Show |
7 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1531-3203T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138564278 | |||||||
| chr7:138564312 | C | G | 1 | a0001c0001t0019g0303 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1531-3169C>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138564312 | |||||||
| chr7:138564316 | G | C | 10 | a0001c0001t0001g0239 a0001c0001t0009g0014 a0001c0001t0009g0094 others(7): Show |
10 | HG01070.hp2 HG01071.hp2 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.1531-3165G>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138564316 | |||||||
| chr7:138564331 | C | T | 8 | a0001c0001t0001g0238 a0001c0001t0002g0248 a0001c0001t0007g0133 others(5): Show |
8 | HG00438.hp2 NA18939.hp2 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.1531-3150C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138564331 | |||||||
| chr7:138564385 | C | T | 2 | a0001c0001t0006g0222 a0001c0001t0006g0223 |
2 | HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1531-3096C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138564385 | |||||||
| chr7:138564512 | G | A | 1 | a0001c0001t0003g0001 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1531-2969G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138564512 | |||||||
| chr7:138564545 | T | C | 10 | a0001c0001t0001g0239 a0001c0001t0009g0014 a0001c0001t0009g0094 others(7): Show |
10 | HG01070.hp2 HG01071.hp2 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.1531-2936T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138564545 | |||||||
| chr7:138564678 | C | T | 2 | a0001c0001t0022g0130 a0001c0001t0022g0226 |
2 | HG01884.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1531-2803C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138564678 | |||||||
| chr7:138564740 | G | C | 13 | a0001c0001t0005g0253 a0001c0001t0005g0254 a0001c0001t0005g0256 others(10): Show |
13 | HG02647.hp1 HG02683.hp1 HG02735.hp1 others(10): Show |
intron_variant | MODIFIER | c.1531-2741G>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138564740 | |||||||
| chr7:138564747 | C | T | 2 | a0001c0004t0056g0008 a0001c0004t0057g0109 |
2 | HG02055.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1531-2734C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138564747 | |||||||
| chr7:138564806 | C | T | 1 | a0001c0001t0002g0174 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1531-2675C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138564806 | |||||||
| chr7:138564898 | A | G | 5 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(2): Show |
5 | HG02486.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1531-2583A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138564898 | |||||||
| chr7:138565058 | T | C | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1531-2423T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138565058 | |||||||
| chr7:138565102 | C | T | 1 | a0001c0001t0055g0199 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1531-2379C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138565102 | |||||||
| chr7:138565137 | C | T | 4 | a0001c0001t0002g0193 a0001c0001t0002g0208 a0001c0001t0002g0219 others(1): Show |
4 | NA18966.hp1 NA19057.hp2 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.1531-2344C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138565137 | |||||||
| chr7:138565140 | A | G | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1531-2341A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138565140 | |||||||
| chr7:138565186 | C | T | 1 | a0001c0002t0004g0122 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1531-2295C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138565186 | |||||||
| chr7:138565241 | G | A | 63 | a0001c0001t0003g0001 a0001c0001t0003g0269 a0001c0001t0003g0270 others(60): Show |
64 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.1531-2240G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138565241 | |||||||
| chr7:138565377 | T | C | 206 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(203): Show |
207 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.1531-2104T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138565377 | |||||||
| chr7:138565426 | TC | T | 94 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(91): Show |
94 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.1531-2053delC | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr7 | 138565426 | ||||||
| chr7:138565526 | T | C | 7 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(4): Show |
7 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1531-1955T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138565526 | |||||||
| chr7:138565554 | C | T | 7 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(4): Show |
7 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1531-1927C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138565554 | |||||||
| chr7:138565646 | G | T | 206 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(203): Show |
207 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.1531-1835G>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138565646 | |||||||
| chr7:138565770 | G | A | 1 | a0001c0001t0002g0180 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1531-1711G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138565770 | |||||||
| chr7:138565774 | T | C | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1531-1707T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138565774 | |||||||
| chr7:138565895 | T | C | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1531-1586T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138565895 | |||||||
| chr7:138565948 | G | A | 3 | a0001c0003t0014g0071 a0001c0003t0014g0088 a0001c0003t0014g0090 |
3 | HG02622.hp2 HG02818.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1531-1533G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138565948 | |||||||
| chr7:138566166 | C | T | 1 | a0001c0001t0001g0050 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1531-1315C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138566166 | |||||||
| chr7:138566269 | A | T | 5 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(2): Show |
5 | HG02486.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1531-1212A>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138566269 | |||||||
| chr7:138566337 | A | T | 1 | a0001c0001t0016g0013 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1531-1144A>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138566337 | |||||||
| chr7:138566380 | G | A | 1 | a0001c0001t0001g0049 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1531-1101G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138566380 | |||||||
| chr7:138566495 | C | G | 7 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(4): Show |
7 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1531-986C>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138566495 | |||||||
| chr7:138566520 | G | T | 7 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(4): Show |
7 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1531-961G>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138566520 | |||||||
| chr7:138566577 | A | G | 7 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(4): Show |
7 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1531-904A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138566577 | |||||||
| chr7:138566868 | C | T | 7 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(4): Show |
7 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1531-613C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138566868 | |||||||
| chr7:138566870 | G | A | 2 | a0001c0001t0011g0252 a0001c0001t0011g0255 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1531-611G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138566870 | |||||||
| chr7:138566901 | A | G | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1531-580A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138566901 | |||||||
| chr7:138566945 | C | T | 1 | a0001c0001t0005g0260 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1531-536C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138566945 | |||||||
| chr7:138566947 | G | A | 1 | a0001c0001t0002g0197 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1531-534G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138566947 | |||||||
| chr7:138567097 | C | G | 1 | a0001c0001t0055g0199 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1531-384C>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138567097 | |||||||
| chr7:138567098 | T | A | 1 | a0001c0001t0055g0199 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1531-383T>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138567098 | |||||||
| chr7:138567191 | T | C | 7 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(4): Show |
7 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1531-290T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138567191 | |||||||
| chr7:138567700 | T | A | 3 | a0001c0003t0014g0071 a0001c0003t0014g0088 a0001c0003t0014g0090 |
3 | HG02622.hp2 HG02818.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1704+46T>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 10/18 | chr7 | 138567700 | |||||||
| chr7:138567724 | C | T | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1704+70C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 10/18 | chr7 | 138567724 | |||||||
| chr7:138567736 | C | T | 1 | a0001c0001t0033g0172 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1704+82C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 10/18 | chr7 | 138567736 | |||||||
| chr7:138567744 | A | G | 1 | a0001c0001t0002g0084 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1704+90A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 10/18 | chr7 | 138567744 | |||||||
| chr7:138567917 | G | A | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1704+263G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 10/18 | chr7 | 138567917 | |||||||
| chr7:138568001 | C | T | 2 | a0001c0004t0056g0008 a0001c0004t0057g0109 |
2 | HG02055.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1704+347C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 10/18 | chr7 | 138568001 | |||||||
| chr7:138568002 | G | A | 2 | a0001c0001t0003g0288 a0001c0001t0003g0295 |
2 | HG00140.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.1704+348G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 10/18 | chr7 | 138568002 | |||||||
| chr7:138568014 | T | C | 19 | a0001c0002t0004g0116 a0001c0002t0004g0120 a0001c0002t0004g0121 others(16): Show |
19 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.1704+360T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 10/18 | chr7 | 138568014 | |||||||
| chr7:138568099 | T | C | 7 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(4): Show |
7 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1704+445T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 10/18 | chr7 | 138568099 | |||||||
| chr7:138568180 | G | A | 5 | a0001c0001t0005g0256 a0001c0001t0005g0257 a0001c0001t0005g0259 others(2): Show |
5 | NA18944.hp2 NA18954.hp1 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.1704+526G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 10/18 | chr7 | 138568180 | |||||||
| chr7:138568268 | C | T | 2 | a0001c0004t0056g0008 a0001c0004t0057g0109 |
2 | HG02055.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1704+614C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 10/18 | chr7 | 138568268 | |||||||
| chr7:138568323 | G | A | 12 | a0001c0001t0001g0073 a0001c0001t0001g0076 a0001c0001t0001g0236 others(9): Show |
12 | HG01070.hp2 HG01071.hp2 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.1704+669G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 10/18 | chr7 | 138568323 | |||||||
| chr7:138568366 | C | T | 2 | a0001c0001t0011g0252 a0001c0001t0011g0255 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1704+712C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 10/18 | chr7 | 138568366 | |||||||
| chr7:138568379 | C | CT | 17 | a0001c0001t0001g0073 a0001c0001t0001g0236 a0001c0001t0002g0107 others(14): Show |
17 | HG00280.hp2 HG00438.hp2 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.1704+755dupT | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 138568379 | ||||||
| chr7:138568379 | C | CTTTTTTT | 9 | a0001c0001t0001g0040 a0001c0001t0001g0066 a0001c0001t0001g0067 others(6): Show |
9 | HG00140.hp1 HG01071.hp2 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1704+749_1704+755d others(9): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 138568379 | ||||||
| chr7:138568379 | C | CTTTTTTT others(1): Show |
12 | a0001c0001t0001g0018 a0001c0001t0001g0033 a0001c0001t0001g0035 others(9): Show |
12 | HG00741.hp1 HG01256.hp2 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.1704+748_1704+755d others(10): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 138568379 | ||||||
| chr7:138568379 | C | CTTTTTTT others(2): Show |
17 | a0001c0001t0001g0028 a0001c0001t0001g0034 a0001c0001t0001g0042 others(14): Show |
17 | HG00438.hp1 HG02083.hp1 HG02148.hp2 others(14): Show |
intron_variant | MODIFIER | c.1704+747_1704+755d others(11): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 138568379 | ||||||
| chr7:138568379 | C | CTTTTTTT others(3): Show |
9 | a0001c0001t0001g0029 a0001c0001t0001g0049 a0001c0001t0001g0069 others(6): Show |
9 | HG00621.hp1 HG02155.hp1 HG04184.hp1 others(6): Show |
intron_variant | MODIFIER | c.1704+746_1704+755d others(12): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 138568379 | ||||||
| chr7:138568379 | C | CTTTTTTT others(4): Show |
9 | a0001c0001t0001g0038 a0001c0001t0001g0054 a0001c0001t0001g0087 others(6): Show |
9 | HG01346.hp1 HG01993.hp2 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.1704+745_1704+755d others(13): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 138568379 | ||||||
| chr7:138568379 | C | CTTTTTTT others(5): Show |
1 | a0001c0003t0014g0090 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1704+744_1704+755d others(14): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 138568379 | ||||||
| chr7:138568379 | C | CTTTTTTT others(6): Show |
3 | a0001c0001t0001g0030 a0001c0001t0001g0048 a0001c0001t0001g0211 |
3 | HG00408.hp2 HG00423.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.1704+743_1704+755d others(15): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 138568379 | ||||||
| chr7:138568379 | C | CTTTTTTT others(8): Show |
2 | a0001c0001t0009g0014 a0001c0001t0016g0012 |
2 | HG01884.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1704+741_1704+755d others(17): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 138568379 | ||||||
| chr7:138568379 | C | CTTTTTTT others(9): Show |
2 | a0001c0001t0001g0021 a0001c0001t0050g0213 |
2 | HG00609.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.1704+740_1704+755d others(18): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 138568379 | ||||||
| chr7:138568379 | C | CTTTTTTT others(10): Show |
2 | a0001c0001t0001g0065 a0001c0001t0001g0083 |
2 | NA18939.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.1704+739_1704+755d others(19): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 138568379 | ||||||
| chr7:138568379 | C | CTTTTTTT others(11): Show |
2 | a0001c0001t0001g0020 a0001c0001t0001g0061 |
2 | NA18998.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.1704+738_1704+755d others(20): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 138568379 | ||||||
| chr7:138568379 | C | CTTTTTTT others(12): Show |
1 | a0001c0001t0001g0239 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1704+737_1704+755d others(21): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 138568379 | ||||||
| chr7:138568379 | C | CTTTTTTT others(13): Show |
4 | a0001c0001t0001g0016 a0001c0001t0001g0056 a0001c0001t0009g0095 others(1): Show |
4 | HG01123.hp2 HG01261.hp2 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.1704+736_1704+755d others(22): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 138568379 | ||||||
| chr7:138568379 | C | CTTTTTTT others(14): Show |
1 | a0001c0001t0001g0060 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1704+735_1704+755d others(23): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 138568379 | ||||||
| chr7:138568379 | C | CTTTTTTT others(15): Show |
3 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0057 |
3 | HG01928.hp2 NA18993.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.1704+734_1704+755d others(24): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 138568379 | ||||||
| chr7:138568379 | C | CTTTTTTT others(17): Show |
1 | a0001c0001t0001g0079 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1704+732_1704+755d others(26): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 138568379 | ||||||
| chr7:138568379 | C | CTTTTTTT others(18): Show |
2 | a0001c0001t0001g0032 a0001c0001t0001g0050 |
2 | NA18979.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.1704+731_1704+755d others(27): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 138568379 | ||||||
| chr7:138568379 | C | CTTTTTTT others(19): Show |
1 | a0001c0001t0055g0199 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1704+730_1704+755d others(28): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 138568379 | ||||||
| chr7:138568379 | C | CTTTTTTT others(25): Show |
1 | a0001c0001t0009g0098 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1704+755_1704+756i others(34): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 138568379 | ||||||
| chr7:138568379 | C | CTTTTTTT others(26): Show |
1 | a0001c0001t0001g0031 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1704+755_1704+756i others(35): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 138568379 | ||||||
| chr7:138568379 | CT | C | 17 | a0001c0001t0002g0106 a0001c0001t0002g0161 a0001c0001t0002g0173 others(14): Show |
17 | HG01074.hp2 HG02258.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.1704+755delT | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 138568379 | ||||||
| chr7:138568379 | CTT | C | 10 | a0001c0001t0005g0253 a0001c0001t0005g0254 a0001c0001t0005g0257 others(7): Show |
10 | HG02647.hp1 HG02683.hp1 HG02735.hp1 others(7): Show |
intron_variant | MODIFIER | c.1704+754_1704+755d others(4): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 138568379 | ||||||
| chr7:138568379 | CTTT | C | 11 | a0001c0001t0001g0058 a0001c0001t0005g0259 a0001c0001t0006g0215 others(8): Show |
11 | HG01891.hp1 HG03041.hp2 HG03139.hp2 others(8): Show |
intron_variant | MODIFIER | c.1704+753_1704+755d others(5): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 138568379 | ||||||
| chr7:138568379 | CTTTTT | C | 10 | a0001c0001t0001g0036 a0001c0001t0003g0276 a0001c0001t0003g0309 others(7): Show |
10 | HG01099.hp1 HG01243.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1704+751_1704+755d others(7): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 138568379 | ||||||
| chr7:138568379 | CTTTTTT | C | 55 | a0001c0001t0001g0062 a0001c0001t0001g0068 a0001c0001t0003g0001 others(52): Show |
56 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.1704+750_1704+755d others(8): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 138568379 | ||||||
| chr7:138568379 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0026 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1704+746_1704+755d others(12): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 138568379 | ||||||
| chr7:138568379 | CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0016g0015 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1704+744_1704+755d others(14): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 138568379 | ||||||
| chr7:138568379 | CTTTTTTT others(7): Show |
C | 3 | a0001c0001t0001g0046 a0001c0001t0001g0074 a0001c0001t0054g0072 |
3 | NA18949.hp2 NA19056.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1704+742_1704+755d others(16): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 138568379 | ||||||
| chr7:138568390 | T | G | 2 | a0001c0001t0001g0062 a0001c0001t0001g0068 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1704+736T>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 10/18 | chr7 | 138568390 | |||||||
| chr7:138568403 | T | C | 2 | a0001c0001t0007g0149 a0001c0001t0007g0182 |
2 | NA18963.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.1704+749T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 10/18 | chr7 | 138568403 | |||||||
| chr7:138568410 | A | T | 3 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 |
3 | HG02896.hp1 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1704+756A>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 10/18 | chr7 | 138568410 | |||||||
| chr7:138568416 | T | A | 13 | a0001c0001t0005g0253 a0001c0001t0005g0254 a0001c0001t0005g0256 others(10): Show |
13 | HG02647.hp1 HG02683.hp1 HG02735.hp1 others(10): Show |
intron_variant | MODIFIER | c.1704+762T>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 10/18 | chr7 | 138568416 | |||||||
| chr7:138568429 | C | T | 13 | a0001c0001t0005g0253 a0001c0001t0005g0254 a0001c0001t0005g0256 others(10): Show |
13 | HG02647.hp1 HG02683.hp1 HG02735.hp1 others(10): Show |
intron_variant | MODIFIER | c.1704+775C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 10/18 | chr7 | 138568429 | |||||||
| chr7:138568479 | C | T | 2 | a0001c0001t0016g0012 a0001c0001t0016g0013 |
2 | HG01884.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1704+825C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 10/18 | chr7 | 138568479 | |||||||
| chr7:138568531 | C | T | 3 | a0001c0005t0013g0114 a0001c0005t0013g0115 a0001c0010t0013g0113 |
3 | HG02572.hp2 HG02723.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1704+877C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 10/18 | chr7 | 138568531 | |||||||
| chr7:138568682 | C | T | 13 | a0001c0001t0005g0253 a0001c0001t0005g0254 a0001c0001t0005g0256 others(10): Show |
13 | HG02647.hp1 HG02683.hp1 HG02735.hp1 others(10): Show |
intron_variant | MODIFIER | c.1704+1028C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 10/18 | chr7 | 138568682 | |||||||
| chr7:138568746 | T | TAAAGTA | 195 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(192): Show |
196 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.1704+1097_1704+109 others(10): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 138568746 | ||||||
| chr7:138568746 | T | TTAAGTA | 13 | a0001c0001t0005g0253 a0001c0001t0005g0254 a0001c0001t0005g0256 others(10): Show |
13 | HG02647.hp1 HG02683.hp1 HG02735.hp1 others(10): Show |
intron_variant | MODIFIER | c.1704+1092_1704+109 others(10): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 10/18 | chr7 | 138568746 | |||||||
| chr7:138568983 | C | T | 5 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(2): Show |
5 | HG02486.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1704+1329C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 10/18 | chr7 | 138568983 | |||||||
| chr7:138569056 | A | T | 1 | a0001c0001t0033g0172 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1704+1402A>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 10/18 | chr7 | 138569056 | |||||||
| chr7:138569369 | CT | C | 7 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(4): Show |
7 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1705-1457delT | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 138569369 | ||||||
| chr7:138569530 | T | C | 5 | a0001c0001t0003g0277 a0001c0001t0003g0280 a0001c0001t0003g0286 others(2): Show |
5 | HG01256.hp1 HG01258.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.1705-1300T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 10/18 | chr7 | 138569530 | |||||||
| chr7:138569844 | T | G | 7 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(4): Show |
7 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1705-986T>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 10/18 | chr7 | 138569844 | |||||||
| chr7:138569946 | C | CT | 24 | a0001c0001t0001g0046 a0001c0001t0001g0235 a0001c0001t0002g0206 others(21): Show |
24 | HG01070.hp2 HG01071.hp2 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.1705-867dupT | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 138569946 | ||||||
| chr7:138569946 | CT | C | 10 | a0001c0001t0001g0063 a0001c0001t0001g0225 a0001c0001t0003g0277 others(7): Show |
10 | HG00738.hp2 HG01256.hp1 HG01993.hp2 others(7): Show |
intron_variant | MODIFIER | c.1705-867delT | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 138569946 | ||||||
| chr7:138569969 | A | G | 7 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(4): Show |
7 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1705-861A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 10/18 | chr7 | 138569969 | |||||||
| chr7:138570088 | C | T | 1 | a0001c0001t0001g0050 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1705-742C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 10/18 | chr7 | 138570088 | |||||||
| chr7:138570193 | C | T | 9 | a0001c0001t0009g0014 a0001c0001t0009g0094 a0001c0001t0009g0095 others(6): Show |
9 | HG01070.hp2 HG01071.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.1705-637C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 10/18 | chr7 | 138570193 | |||||||
| chr7:138570359 | A | G | 9 | a0001c0001t0009g0014 a0001c0001t0009g0094 a0001c0001t0009g0095 others(6): Show |
9 | HG01070.hp2 HG01071.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.1705-471A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 10/18 | chr7 | 138570359 | |||||||
| chr7:138570525 | A | G | 7 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(4): Show |
7 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1705-305A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 10/18 | chr7 | 138570525 | |||||||
| chr7:138570644 | G | GT | 123 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(120): Show |
123 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.1705-171dupT | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 138570644 | ||||||
| chr7:138570644 | G | GTT | 6 | a0001c0001t0001g0018 a0001c0001t0001g0043 a0001c0001t0001g0050 others(3): Show |
6 | HG02027.hp1 HG02055.hp2 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.1705-172_1705-171d others(4): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 138570644 | ||||||
| chr7:138571015 | C | T | 2 | a0001c0001t0002g0206 a0001c0001t0002g0207 |
2 | HG02165.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.1878+12C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 11/18 | chr7 | 138571015 | |||||||
| chr7:138571180 | A | T | 1 | a0001c0001t0055g0199 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1878+177A>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 11/18 | chr7 | 138571180 | |||||||
| chr7:138571203 | C | T | 17 | a0001c0002t0004g0120 a0001c0002t0004g0121 a0001c0002t0004g0122 others(14): Show |
17 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.1878+200C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 11/18 | chr7 | 138571203 | |||||||
| chr7:138571230 | C | T | 2 | a0001c0001t0002g0196 a0001c0001t0002g0246 |
2 | NA18973.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.1878+227C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 11/18 | chr7 | 138571230 | |||||||
| chr7:138571281 | C | T | 1 | a0001c0001t0033g0172 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1878+278C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 11/18 | chr7 | 138571281 | |||||||
| chr7:138571311 | T | A | 1 | a0001c0001t0001g0032 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1878+308T>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 11/18 | chr7 | 138571311 | |||||||
| chr7:138571459 | C | G | 1 | a0001c0001t0010g0112 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1878+456C>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 11/18 | chr7 | 138571459 | |||||||
| chr7:138571536 | A | G | 1 | a0001c0001t0002g0173 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1878+533A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 11/18 | chr7 | 138571536 | |||||||
| chr7:138571707 | C | T | 9 | a0001c0001t0009g0014 a0001c0001t0009g0094 a0001c0001t0009g0095 others(6): Show |
9 | HG01070.hp2 HG01071.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.1878+704C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 11/18 | chr7 | 138571707 | |||||||
| chr7:138571765 | C | T | 2 | a0001c0001t0020g0139 a0001c0001t0020g0155 |
2 | HG00735.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.1878+762C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 11/18 | chr7 | 138571765 | |||||||
| chr7:138571862 | CACCCAGC others(6): Show |
C | 103 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(100): Show |
103 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.1878+860_1878+872d others(15): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 11/18 | chr7 | 138571862 | |||||||
| chr7:138571925 | A | G | 2 | a0001c0004t0056g0008 a0001c0004t0057g0109 |
2 | HG02055.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1878+922A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 11/18 | chr7 | 138571925 | |||||||
| chr7:138572383 | A | G | 2 | a0001c0001t0003g0276 a0001c0001t0003g0309 |
2 | HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1879-1124A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 11/18 | chr7 | 138572383 | |||||||
| chr7:138572439 | G | A | 1 | a0001c0001t0032g0311 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1879-1068G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 11/18 | chr7 | 138572439 | |||||||
| chr7:138572460 | AAAATTCT others(34): Show |
A | 62 | a0001c0001t0003g0001 a0001c0001t0003g0269 a0001c0001t0003g0270 others(59): Show |
63 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(60): Show |
intron_variant | MODIFIER | c.1879-1044_1879-100 others(45): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr7 | 138572460 | ||||||
| chr7:138572503 | A | G | 62 | a0001c0001t0003g0001 a0001c0001t0003g0269 a0001c0001t0003g0270 others(59): Show |
63 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(60): Show |
intron_variant | MODIFIER | c.1879-1004A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 11/18 | chr7 | 138572503 | |||||||
| chr7:138572559 | CTGAAA | C | 3 | a0001c0005t0013g0114 a0001c0005t0013g0115 a0001c0010t0013g0113 |
3 | HG02572.hp2 HG02723.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1879-944_1879-940d others(7): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr7 | 138572559 | ||||||
| chr7:138572984 | C | T | 5 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(2): Show |
5 | HG02486.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1879-523C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 11/18 | chr7 | 138572984 | |||||||
| chr7:138572997 | C | T | 1 | a0001c0001t0001g0212 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1879-510C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 11/18 | chr7 | 138572997 | |||||||
| chr7:138573026 | C | G | 2 | a0001c0001t0003g0278 a0001c0001t0003g0287 |
2 | HG01255.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.1879-481C>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 11/18 | chr7 | 138573026 | |||||||
| chr7:138573127 | T | G | 7 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(4): Show |
7 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1879-380T>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 11/18 | chr7 | 138573127 | |||||||
| chr7:138573148 | C | T | 205 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(202): Show |
206 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.1879-359C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 11/18 | chr7 | 138573148 | |||||||
| chr7:138573182 | C | T | 5 | a0001c0001t0009g0094 a0001c0001t0009g0095 a0001c0001t0009g0096 others(2): Show |
5 | HG01070.hp2 HG01071.hp2 HG01123.hp2 others(2): Show |
intron_variant | MODIFIER | c.1879-325C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 11/18 | chr7 | 138573182 | |||||||
| chr7:138573414 | AATT | A | 137 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(134): Show |
137 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.1879-88_1879-86del others(3): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr7 | 138573414 | ||||||
| chr7:138573417 | T | TA | 3 | a0001c0001t0026g0266 a0001c0001t0026g0267 a0001c0001t0035g0265 |
3 | HG02109.hp1 HG02630.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1879-89dupA | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr7 | 138573417 | ||||||
| chr7:138573419 | T | G | 3 | a0001c0001t0026g0266 a0001c0001t0026g0267 a0001c0001t0035g0265 |
3 | HG02109.hp1 HG02630.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1879-88T>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 11/18 | chr7 | 138573419 | |||||||
| chr7:138573722 | C | CCTT | 16 | a0001c0001t0009g0014 a0001c0001t0009g0094 a0001c0001t0009g0095 others(13): Show |
16 | HG01070.hp2 HG01071.hp2 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.2014+81_2014+83dup others(3): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr7 | 138573722 | ||||||
| chr7:138573766 | T | A | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2014+124T>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 12/18 | chr7 | 138573766 | |||||||
| chr7:138573776 | T | G | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2014+134T>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 12/18 | chr7 | 138573776 | |||||||
| chr7:138573833 | C | T | 21 | a0001c0001t0003g0001 a0001c0001t0003g0270 a0001c0001t0003g0271 others(18): Show |
22 | HG00140.hp2 HG00735.hp2 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.2014+191C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 12/18 | chr7 | 138573833 | |||||||
| chr7:138573834 | G | A | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2014+192G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 12/18 | chr7 | 138573834 | |||||||
| chr7:138573888 | C | A | 2 | a0001c0001t0022g0130 a0001c0001t0022g0226 |
2 | HG01884.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.2014+246C>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 12/18 | chr7 | 138573888 | |||||||
| chr7:138573916 | A | C | 124 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(121): Show |
124 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.2014+274A>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 12/18 | chr7 | 138573916 | |||||||
| chr7:138573917 | G | A | 1 | a0001c0001t0001g0021 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2014+275G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 12/18 | chr7 | 138573917 | |||||||
| chr7:138574028 | C | T | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2014+386C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 12/18 | chr7 | 138574028 | |||||||
| chr7:138574132 | T | C | 1 | a0001c0001t0003g0271 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2014+490T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 12/18 | chr7 | 138574132 | |||||||
| chr7:138574414 | G | A | 1 | a0001c0002t0004g0121 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2014+772G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 12/18 | chr7 | 138574414 | |||||||
| chr7:138574877 | T | C | 3 | a0001c0001t0026g0266 a0001c0001t0026g0267 a0001c0001t0035g0265 |
3 | HG02109.hp1 HG02630.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2014+1235T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 12/18 | chr7 | 138574877 | |||||||
| chr7:138574953 | G | A | 9 | a0001c0001t0009g0014 a0001c0001t0009g0094 a0001c0001t0009g0095 others(6): Show |
9 | HG01070.hp2 HG01071.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.2014+1311G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 12/18 | chr7 | 138574953 | |||||||
| chr7:138575174 | T | C | 104 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(101): Show |
104 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.2015-1199T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 12/18 | chr7 | 138575174 | |||||||
| chr7:138575284 | C | G | 5 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(2): Show |
5 | HG02486.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.2015-1089C>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 12/18 | chr7 | 138575284 | |||||||
| chr7:138575382 | G | A | 3 | a0001c0001t0001g0043 a0001c0004t0056g0008 a0001c0004t0057g0109 |
3 | HG02055.hp2 HG02165.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.2015-991G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 12/18 | chr7 | 138575382 | |||||||
| chr7:138575402 | C | T | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2015-971C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 12/18 | chr7 | 138575402 | |||||||
| chr7:138575459 | A | AT | 29 | a0001c0001t0001g0026 a0001c0001t0001g0076 a0001c0001t0001g0091 others(26): Show |
29 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.2015-895dupT | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr7 | 138575459 | ||||||
| chr7:138575459 | A | ATT | 8 | a0001c0001t0006g0215 a0001c0001t0006g0216 a0001c0001t0006g0217 others(5): Show |
8 | HG01891.hp1 HG03139.hp2 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.2015-896_2015-895d others(4): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr7 | 138575459 | ||||||
| chr7:138575459 | A | ATTTTT | 6 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(3): Show |
6 | HG02055.hp2 HG02486.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.2015-899_2015-895d others(7): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr7 | 138575459 | ||||||
| chr7:138575544 | A | C | 1 | a0001c0001t0007g0182 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2015-829A>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 12/18 | chr7 | 138575544 | |||||||
| chr7:138575545 | C | A | 1 | a0001c0001t0007g0182 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2015-828C>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 12/18 | chr7 | 138575545 | |||||||
| chr7:138575547 | A | T | 1 | a0001c0001t0007g0182 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2015-826A>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 12/18 | chr7 | 138575547 | |||||||
| chr7:138575552 | A | T | 1 | a0001c0001t0007g0182 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2015-821A>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 12/18 | chr7 | 138575552 | |||||||
| chr7:138575553 | A | C | 1 | a0001c0001t0007g0182 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2015-820A>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 12/18 | chr7 | 138575553 | |||||||
| chr7:138575554 | T | G | 1 | a0001c0001t0007g0182 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2015-819T>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 12/18 | chr7 | 138575554 | |||||||
| chr7:138575555 | G | C | 1 | a0001c0001t0007g0182 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2015-818G>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 12/18 | chr7 | 138575555 | |||||||
| chr7:138575556 | A | G | 1 | a0001c0001t0007g0182 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2015-817A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 12/18 | chr7 | 138575556 | |||||||
| chr7:138575558 | A | G | 1 | a0001c0001t0007g0182 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2015-815A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 12/18 | chr7 | 138575558 | |||||||
| chr7:138575559 | A | T | 1 | a0001c0001t0007g0182 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2015-814A>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 12/18 | chr7 | 138575559 | |||||||
| chr7:138575646 | C | A | 95 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(92): Show |
95 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.2015-727C>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 12/18 | chr7 | 138575646 | |||||||
| chr7:138575673 | G | A | 7 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(4): Show |
7 | HG01346.hp1 HG01978.hp2 HG01993.hp2 others(4): Show |
intron_variant | MODIFIER | c.2015-700G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 12/18 | chr7 | 138575673 | |||||||
| chr7:138575973 | G | A | 8 | a0001c0001t0006g0215 a0001c0001t0006g0216 a0001c0001t0006g0217 others(5): Show |
8 | HG01891.hp1 HG03139.hp2 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.2015-400G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 12/18 | chr7 | 138575973 | |||||||
| chr7:138576477 | TA | T | 7 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(4): Show |
7 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.2087+37delA | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr7 | 138576477 | ||||||
| chr7:138576574 | TAAC | T | 43 | a0001c0001t0003g0001 a0001c0001t0003g0269 a0001c0001t0003g0270 others(40): Show |
44 | HG00140.hp2 HG00735.hp2 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.2087+130_2087+132d others(5): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 13/18 | chr7 | 138576574 | |||||||
| chr7:138576601 | T | G | 1 | a0001c0001t0040g0186 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.2087+156T>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 13/18 | chr7 | 138576601 | |||||||
| chr7:138576623 | A | G | 1 | a0001c0001t0001g0021 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2087+178A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 13/18 | chr7 | 138576623 | |||||||
| chr7:138576625 | T | A | 2 | a0001c0001t0011g0263 a0001c0001t0011g0264 |
2 | HG02647.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2087+180T>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 13/18 | chr7 | 138576625 | |||||||
| chr7:138576721 | C | T | 10 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.2087+276C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 13/18 | chr7 | 138576721 | |||||||
| chr7:138576825 | A | G | 234 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(231): Show |
235 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.2087+380A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 13/18 | chr7 | 138576825 | |||||||
| chr7:138576836 | G | A | 5 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(2): Show |
5 | HG02486.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.2087+391G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 13/18 | chr7 | 138576836 | |||||||
| chr7:138577004 | G | A | 2 | a0001c0002t0015g0170 a0001c0002t0015g0171 |
2 | HG02451.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.2088-416G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 13/18 | chr7 | 138577004 | |||||||
| chr7:138577165 | A | T | 1 | a0001c0001t0002g0196 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.2088-255A>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 13/18 | chr7 | 138577165 | |||||||
| chr7:138577239 | C | CATTTTTA others(6): Show |
2 | a0001c0004t0056g0008 a0001c0004t0057g0109 |
2 | HG02055.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.2088-178_2088-166d others(15): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr7 | 138577239 | ||||||
| chr7:138577344 | A | G | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2088-76A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 13/18 | chr7 | 138577344 | |||||||
| chr7:138577889 | G | A | 7 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(4): Show |
7 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.2256+301G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 14/18 | chr7 | 138577889 | |||||||
| chr7:138577921 | A | G | 2 | a0001c0005t0013g0114 a0001c0005t0013g0115 |
2 | HG02572.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.2256+333A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 14/18 | chr7 | 138577921 | |||||||
| chr7:138577946 | T | C | 21 | a0001c0001t0005g0253 a0001c0001t0005g0254 a0001c0001t0005g0256 others(18): Show |
21 | HG01891.hp1 HG02647.hp1 HG02683.hp1 others(18): Show |
intron_variant | MODIFIER | c.2256+358T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 14/18 | chr7 | 138577946 | |||||||
| chr7:138578024 | A | G | 1 | a0001c0001t0040g0186 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.2256+436A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 14/18 | chr7 | 138578024 | |||||||
| chr7:138578036 | A | G | 99 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(96): Show |
99 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.2256+448A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 14/18 | chr7 | 138578036 | |||||||
| chr7:138578145 | A | G | 186 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(183): Show |
187 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.2256+557A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 14/18 | chr7 | 138578145 | |||||||
| chr7:138578274 | AAAT | A | 3 | a0001c0005t0013g0114 a0001c0005t0013g0115 a0001c0010t0013g0113 |
3 | HG02572.hp2 HG02723.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2256+699_2256+701d others(5): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr7 | 138578274 | ||||||
| chr7:138578287 | A | AATG | 7 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(4): Show |
7 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.2256+703_2256+705d others(5): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr7 | 138578287 | ||||||
| chr7:138578299 | A | G | 8 | a0001c0001t0006g0215 a0001c0001t0006g0216 a0001c0001t0006g0217 others(5): Show |
8 | HG01891.hp1 HG03139.hp2 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.2256+711A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 14/18 | chr7 | 138578299 | |||||||
| chr7:138578436 | G | A | 1 | a0001c0001t0003g0270 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2257-768G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 14/18 | chr7 | 138578436 | |||||||
| chr7:138578532 | T | G | 5 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(2): Show |
5 | HG02486.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.2257-672T>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 14/18 | chr7 | 138578532 | |||||||
| chr7:138578532 | T | TTG | 16 | a0001c0001t0002g0107 a0001c0001t0002g0141 a0001c0001t0002g0157 others(13): Show |
16 | HG01891.hp2 HG02027.hp2 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.2257-641_2257-640d others(4): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr7 | 138578532 | ||||||
| chr7:138578532 | TTG | T | 27 | a0001c0001t0003g0269 a0001c0001t0003g0290 a0001c0001t0003g0297 others(24): Show |
27 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.2257-641_2257-640d others(4): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr7 | 138578532 | ||||||
| chr7:138578532 | TTGTG | T | 30 | a0001c0001t0003g0001 a0001c0001t0003g0270 a0001c0001t0003g0271 others(27): Show |
31 | HG00140.hp2 HG00735.hp2 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.2257-643_2257-640d others(6): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr7 | 138578532 | ||||||
| chr7:138578553 | TGTGTGTG others(7): Show |
T | 8 | a0001c0001t0009g0014 a0001c0001t0009g0094 a0001c0001t0009g0096 others(5): Show |
8 | HG01070.hp2 HG01071.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.2257-649_2257-636d others(16): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr7 | 138578553 | ||||||
| chr7:138578555 | TGTGTGTG others(5): Show |
T | 3 | a0001c0001t0001g0062 a0001c0001t0001g0068 a0001c0001t0009g0095 |
3 | HG01123.hp2 HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.2257-647_2257-636d others(14): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr7 | 138578555 | ||||||
| chr7:138578559 | T | C | 1 | a0001c0007t0036g0108 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.2257-645T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 14/18 | chr7 | 138578559 | |||||||
| chr7:138578559 | T | TGC | 7 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(4): Show |
7 | HG01346.hp1 HG01978.hp2 HG01993.hp2 others(4): Show |
intron_variant | MODIFIER | c.2257-644_2257-643i others(4): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr7 | 138578559 | ||||||
| chr7:138578561 | T | C | 17 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(14): Show |
17 | HG01099.hp1 HG01346.hp1 HG01978.hp2 others(14): Show |
intron_variant | MODIFIER | c.2257-643T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 14/18 | chr7 | 138578561 | |||||||
| chr7:138578561 | T | TGCGC | 3 | a0001c0001t0001g0029 a0001c0001t0001g0083 a0001c0001t0050g0213 |
3 | HG00609.hp1 HG02155.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.2257-642_2257-641i others(6): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr7 | 138578561 | ||||||
| chr7:138578561 | TGTGC | T | 7 | a0001c0001t0006g0216 a0001c0001t0006g0217 a0001c0001t0006g0218 others(4): Show |
7 | HG01891.hp1 HG03139.hp2 HG03516.hp2 others(4): Show |
intron_variant | MODIFIER | c.2257-641_2257-638d others(6): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr7 | 138578561 | ||||||
| chr7:138578563 | T | C | 71 | a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 others(68): Show |
72 | HG00140.hp2 HG00280.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.2257-641T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 14/18 | chr7 | 138578563 | |||||||
| chr7:138578563 | T | TGC | 11 | a0001c0001t0005g0253 a0001c0001t0005g0254 a0001c0001t0005g0259 others(8): Show |
11 | HG01175.hp1 HG02647.hp1 HG02683.hp1 others(8): Show |
intron_variant | MODIFIER | c.2257-636_2257-635d others(4): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr7 | 138578563 | ||||||
| chr7:138578563 | T | TGCGCGC | 33 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0019 others(30): Show |
33 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(30): Show |
intron_variant | MODIFIER | c.2257-640_2257-635d others(8): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr7 | 138578563 | ||||||
| chr7:138578563 | T | TGTGC | 5 | a0001c0001t0003g0288 a0001c0001t0005g0256 a0001c0001t0005g0257 others(2): Show |
5 | HG03831.hp2 HG03834.hp1 NA18944.hp2 others(2): Show |
intron_variant | MODIFIER | c.2257-640_2257-639i others(6): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr7 | 138578563 | ||||||
| chr7:138578563 | T | TGTGCGCG others(1): Show |
21 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(18): Show |
21 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.2257-640_2257-639i others(10): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr7 | 138578563 | ||||||
| chr7:138578563 | T | TGTGCGCG others(3): Show |
1 | a0001c0001t0001g0054 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2257-640_2257-639i others(12): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr7 | 138578563 | ||||||
| chr7:138578563 | T | TGTGTGC | 3 | a0001c0005t0013g0114 a0001c0005t0013g0115 a0001c0010t0013g0113 |
3 | HG02572.hp2 HG02723.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2257-640_2257-639i others(8): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr7 | 138578563 | ||||||
| chr7:138578563 | T | TGTGTGCG others(3): Show |
10 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0043 others(7): Show |
10 | HG00621.hp1 HG02165.hp1 HG03688.hp1 others(7): Show |
intron_variant | MODIFIER | c.2257-640_2257-639i others(12): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr7 | 138578563 | ||||||
| chr7:138578563 | T | TGTGTGCG others(5): Show |
1 | a0001c0001t0001g0089 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2257-640_2257-639i others(14): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr7 | 138578563 | ||||||
| chr7:138578563 | T | TGTGTGTG others(3): Show |
3 | a0001c0003t0014g0071 a0001c0003t0014g0088 a0001c0003t0014g0090 |
3 | HG02622.hp2 HG02818.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2257-640_2257-639i others(12): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr7 | 138578563 | ||||||
| chr7:138578563 | T | TGTGTGTG others(5): Show |
12 | a0001c0001t0001g0020 a0001c0001t0001g0049 a0001c0001t0001g0050 others(9): Show |
12 | HG01175.hp2 HG02602.hp2 HG04115.hp1 others(9): Show |
intron_variant | MODIFIER | c.2257-640_2257-639i others(14): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr7 | 138578563 | ||||||
| chr7:138578563 | T | TGTGTGTG others(5): Show |
4 | a0001c0001t0017g0007 a0001c0001t0026g0266 a0001c0001t0026g0267 others(1): Show |
4 | HG02109.hp1 HG02630.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.2257-640_2257-639i others(14): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr7 | 138578563 | ||||||
| chr7:138578563 | T | TGTGTGTG others(5): Show |
2 | a0001c0001t0017g0005 a0001c0001t0017g0006 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2257-640_2257-639i others(14): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr7 | 138578563 | ||||||
| chr7:138578563 | T | TGTGTGTG others(9): Show |
1 | a0001c0001t0001g0017 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2257-640_2257-639i others(18): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr7 | 138578563 | ||||||
| chr7:138578565 | C | T | 6 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(3): Show |
6 | HG02486.hp1 HG02647.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2257-639C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 14/18 | chr7 | 138578565 | |||||||
| chr7:138578566 | GCGCA | G | 5 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(2): Show |
5 | HG02486.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.2257-631_2257-628d others(6): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr7 | 138578566 | ||||||
| chr7:138578570 | A | G | 2 | a0001c0004t0056g0008 a0001c0004t0057g0109 |
2 | HG02055.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.2257-634A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 14/18 | chr7 | 138578570 | |||||||
| chr7:138578571 | C | T | 1 | a0001c0002t0004g0124 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2257-633C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 14/18 | chr7 | 138578571 | |||||||
| chr7:138578617 | C | T | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2257-587C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 14/18 | chr7 | 138578617 | |||||||
| chr7:138578704 | C | A | 1 | a0001c0001t0002g0198 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2257-500C>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 14/18 | chr7 | 138578704 | |||||||
| chr7:138578707 | A | G | 7 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(4): Show |
7 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.2257-497A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 14/18 | chr7 | 138578707 | |||||||
| chr7:138578757 | ACT | A | 95 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(92): Show |
95 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.2257-446_2257-445d others(4): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 14/18 | chr7 | 138578757 | |||||||
| chr7:138578760 | A | G | 1 | a0001c0001t0008g0281 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2257-444A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 14/18 | chr7 | 138578760 | |||||||
| chr7:138578920 | G | GTA | 7 | a0001c0001t0003g0001 a0001c0001t0003g0289 a0001c0001t0004g0279 others(4): Show |
8 | HG01069.hp2 HG01071.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.2257-267_2257-266d others(4): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr7 | 138578920 | ||||||
| chr7:138578920 | G | GTATA | 8 | a0001c0001t0006g0215 a0001c0001t0006g0216 a0001c0001t0006g0217 others(5): Show |
8 | HG01891.hp1 HG03139.hp2 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.2257-269_2257-266d others(6): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr7 | 138578920 | ||||||
| chr7:138578920 | G | GTATATAT others(7): Show |
1 | a0001c0004t0056g0008 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2257-279_2257-266d others(16): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr7 | 138578920 | ||||||
| chr7:138578920 | G | GTATATAT others(9): Show |
1 | a0001c0004t0057g0109 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2257-281_2257-266d others(18): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr7 | 138578920 | ||||||
| chr7:138578933 | T | C | 2 | a0001c0001t0024g0024 a0001c0001t0024g0025 |
2 | HG02723.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.2257-271T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 14/18 | chr7 | 138578933 | |||||||
| chr7:138578936 | A | ATATATG | 5 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(2): Show |
5 | HG02486.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.2257-266_2257-265i others(8): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr7 | 138578936 | ||||||
| chr7:138578939 | G | T | 7 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(4): Show |
7 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.2257-265G>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 14/18 | chr7 | 138578939 | |||||||
| chr7:138579006 | A | AT | 4 | a0001c0001t0026g0266 a0001c0001t0026g0267 a0001c0001t0033g0172 others(1): Show |
4 | HG02109.hp1 HG02630.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.2257-192dupT | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr7 | 138579006 | ||||||
| chr7:138579021 | A | AT | 45 | a0001c0001t0003g0001 a0001c0001t0003g0269 a0001c0001t0003g0270 others(42): Show |
46 | HG00140.hp2 HG00735.hp2 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.2257-179dupT | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr7 | 138579021 | ||||||
| chr7:138579595 | A | G | 9 | a0001c0001t0009g0014 a0001c0001t0009g0094 a0001c0001t0009g0095 others(6): Show |
9 | HG01070.hp2 HG01071.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.2585+63A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 15/18 | chr7 | 138579595 | |||||||
| chr7:138579687 | C | T | 1 | a0001c0010t0013g0113 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2585+155C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 15/18 | chr7 | 138579687 | |||||||
| chr7:138579721 | C | T | 1 | a0001c0001t0003g0275 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2585+189C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 15/18 | chr7 | 138579721 | |||||||
| chr7:138579780 | G | A | 3 | a0001c0001t0002g0228 a0001c0001t0002g0251 a0001c0001t0045g0233 |
3 | NA18953.hp2 NA18993.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.2585+248G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 15/18 | chr7 | 138579780 | |||||||
| chr7:138579807 | C | G | 92 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(89): Show |
92 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.2585+275C>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 15/18 | chr7 | 138579807 | |||||||
| chr7:138579862 | G | A | 2 | a0001c0004t0056g0008 a0001c0004t0057g0109 |
2 | HG02055.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.2585+330G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 15/18 | chr7 | 138579862 | |||||||
| chr7:138579996 | C | T | 1 | a0001c0001t0003g0298 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2585+464C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 15/18 | chr7 | 138579996 | |||||||
| chr7:138580055 | C | T | 5 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(2): Show |
5 | HG02486.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.2586-507C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 15/18 | chr7 | 138580055 | |||||||
| chr7:138580148 | C | T | 1 | a0001c0001t0002g0099 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2586-414C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 15/18 | chr7 | 138580148 | |||||||
| chr7:138580176 | A | G | 1 | a0001c0010t0013g0113 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2586-386A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 15/18 | chr7 | 138580176 | |||||||
| chr7:138580471 | A | G | 1 | a0001c0001t0002g0167 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.2586-91A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 15/18 | chr7 | 138580471 | |||||||
| chr7:138580486 | G | A | 1 | a0001c0001t0002g0178 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2586-76G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 15/18 | chr7 | 138580486 | |||||||
| chr7:138580807 | G | A | 2 | a0001c0004t0056g0008 a0001c0004t0057g0109 |
2 | HG02055.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.2718+113G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 16/18 | chr7 | 138580807 | |||||||
| chr7:138581054 | A | G | 5 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(2): Show |
5 | HG02486.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.2718+360A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 16/18 | chr7 | 138581054 | |||||||
| chr7:138581075 | T | C | 28 | a0001c0001t0005g0253 a0001c0001t0005g0254 a0001c0001t0005g0256 others(25): Show |
28 | HG01891.hp1 HG02055.hp2 HG02486.hp1 others(25): Show |
intron_variant | MODIFIER | c.2718+381T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 16/18 | chr7 | 138581075 | |||||||
| chr7:138581156 | T | C | 1 | a0001c0001t0001g0038 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2718+462T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 16/18 | chr7 | 138581156 | |||||||
| chr7:138581193 | G | A | 2 | a0001c0002t0004g0242 a0001c0002t0004g0243 |
2 | HG00738.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.2718+499G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 16/18 | chr7 | 138581193 | |||||||
| chr7:138581264 | C | A | 95 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(92): Show |
95 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.2719-433C>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 16/18 | chr7 | 138581264 | |||||||
| chr7:138581519 | C | A | 3 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0051g0105 |
3 | HG02602.hp2 HG04184.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.2719-178C>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 16/18 | chr7 | 138581519 | |||||||
| chr7:138582020 | A | G | 7 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(4): Show |
7 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.2793+249A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 17/18 | chr7 | 138582020 | |||||||
| chr7:138582174 | G | A | 9 | a0001c0001t0006g0215 a0001c0001t0006g0216 a0001c0001t0006g0217 others(6): Show |
9 | HG01891.hp1 HG03139.hp2 HG03225.hp1 others(6): Show |
intron_variant | MODIFIER | c.2793+403G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 17/18 | chr7 | 138582174 | |||||||
| chr7:138582435 | G | A | 60 | a0001c0001t0003g0001 a0001c0001t0003g0269 a0001c0001t0003g0270 others(57): Show |
61 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(58): Show |
intron_variant | MODIFIER | c.2793+664G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 17/18 | chr7 | 138582435 | |||||||
| chr7:138582466 | T | C | 3 | a0001c0001t0026g0266 a0001c0001t0026g0267 a0001c0001t0035g0265 |
3 | HG02109.hp1 HG02630.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2793+695T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 17/18 | chr7 | 138582466 | |||||||
| chr7:138582504 | T | A | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2793+733T>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 17/18 | chr7 | 138582504 | |||||||
| chr7:138582537 | G | A | 9 | a0001c0001t0009g0014 a0001c0001t0009g0094 a0001c0001t0009g0095 others(6): Show |
9 | HG01070.hp2 HG01071.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.2793+766G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 17/18 | chr7 | 138582537 | |||||||
| chr7:138582541 | C | CA | 29 | a0001c0001t0001g0011 a0001c0001t0001g0070 a0001c0001t0001g0082 others(26): Show |
29 | HG01070.hp2 HG01071.hp2 HG01123.hp2 others(26): Show |
intron_variant | MODIFIER | c.2793+788dupA | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr7 | 138582541 | ||||||
| chr7:138582541 | CA | C | 11 | a0001c0001t0001g0067 a0001c0001t0002g0204 a0001c0001t0003g0283 others(8): Show |
11 | HG00738.hp1 HG01070.hp1 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.2793+788delA | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr7 | 138582541 | ||||||
| chr7:138582673 | T | C | 150 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(147): Show |
150 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(147): Show |
intron_variant | MODIFIER | c.2793+902T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 17/18 | chr7 | 138582673 | |||||||
| chr7:138582818 | C | T | 7 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(4): Show |
7 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.2794-1032C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 17/18 | chr7 | 138582818 | |||||||
| chr7:138582877 | T | C | 1 | a0001c0001t0002g0145 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2794-973T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 17/18 | chr7 | 138582877 | |||||||
| chr7:138582912 | G | A | 2 | a0001c0001t0001g0038 a0001c0001t0001g0085 |
2 | NA18950.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.2794-938G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 17/18 | chr7 | 138582912 | |||||||
| chr7:138582932 | A | G | 5 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(2): Show |
5 | HG02486.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.2794-918A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 17/18 | chr7 | 138582932 | |||||||
| chr7:138583171 | T | G | 9 | a0001c0001t0009g0014 a0001c0001t0009g0094 a0001c0001t0009g0095 others(6): Show |
9 | HG01070.hp2 HG01071.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.2794-679T>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 17/18 | chr7 | 138583171 | |||||||
| chr7:138583372 | C | T | 2 | a0001c0001t0016g0012 a0001c0001t0016g0013 |
2 | HG01884.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.2794-478C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 17/18 | chr7 | 138583372 | |||||||
| chr7:138583427 | C | T | 1 | a0001c0001t0003g0280 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2794-423C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 17/18 | chr7 | 138583427 | |||||||
| chr7:138583463 | T | A | 1 | a0001c0002t0004g0120 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2794-387T>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 17/18 | chr7 | 138583463 | |||||||
| chr7:138583513 | G | A | 5 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(2): Show |
5 | HG02486.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.2794-337G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 17/18 | chr7 | 138583513 | |||||||
| chr7:138583569 | G | A | 7 | a0001c0001t0010g0110 a0001c0001t0010g0111 a0001c0001t0010g0112 others(4): Show |
7 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.2794-281G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 17/18 | chr7 | 138583569 | |||||||
| chr7:138583671 | G | A | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2794-179G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 17/18 | chr7 | 138583671 | |||||||
| chr7:138583818 | A | G | 66 | a0001c0001t0003g0001 a0001c0001t0003g0269 a0001c0001t0003g0270 others(63): Show |
67 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(64): Show |
intron_variant | MODIFIER | c.2794-32A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 17/18 | chr7 | 138583818 | |||||||
| chr7:138584188 | G | A | 3 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2943+189G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 18/18 | chr7 | 138584188 | |||||||
| chr7:138584706 | G | T | 1 | a0001c0001t0008g0281 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2944-36G>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 18/18 | chr7 | 138584706 | |||||||
| chr7:138584709 | C | CT | 16 | a0001c0001t0006g0215 a0001c0001t0006g0216 a0001c0001t0006g0217 others(13): Show |
16 | HG01891.hp1 HG02055.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.2944-26dupT | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr7 | 138584709 |