| 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 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1050 | 310 | 80 | 56 | 122 | 8 | 42 | 96 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| a0002 | 0/0 | 1050 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| a0003 | 0/0 | 1050 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 3153 | 282 | 68 | 51 | 121 | 5 | 35 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| c0002 | 0/0 | 3153 | 18 | 3 | 5 | 1 | 2 | 7 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| c0003 | 0/0 | 3153 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| c0004 | 0/0 | 3153 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| c0005 | 0/0 | 3153 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| c0006 | 0/0 | 3153 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| c0007 | 0/0 | 3153 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| c0008 | 0/0 | 3153 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| c0009 | 0/0 | 3153 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| c0010 | 0/0 | 3153 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 5332 | 84 | 6 | 15 | 54 | 2 | 7 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| t0002 | 0/0 | 5336 | 69 | 7 | 6 | 45 | 2 | 9 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| t0003 | 0/1 | 5335 | 33 | 12 | 14 | 0 | 1 | 5 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| t0004 | 0/0 | 5336 | 15 | 1 | 5 | 1 | 2 | 6 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| t0005 | 0/0 | 5331 | 7 | 0 | 0 | 5 | 0 | 2 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| t0006 | 0/0 | 5336 | 7 | 7 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| t0007 | 0/0 | 5336 | 6 | 0 | 0 | 6 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| t0008 | 0/0 | 5335 | 5 | 4 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| t0009 | 0/0 | 5335 | 5 | 0 | 4 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| t0010 | 0/0 | 5335 | 5 | 5 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| t0011 | 0/0 | 5335 | 5 | 2 | 0 | 0 | 0 | 3 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| t0012 | 0/0 | 5336 | 4 | 2 | 1 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| t0013 | 0/0 | 5339 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| t0014 | 0/0 | 5336 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| t0015 | 0/0 | 5336 | 3 | 2 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| t0016 | 0/0 | 5335 | 3 | 2 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| t0017 | 0/0 | 5340 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| t0018 | 0/0 | 5336 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| t0019 | 0/0 | 5335 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| t0020 | 0/0 | 5336 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| t0021 | 0/0 | 5337 | 2 | 1 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| t0022 | 0/0 | 5336 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| t0023 | 0/0 | 5336 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| t0024 | 0/0 | 5336 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| t0025 | 0/0 | 5337 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| t0026 | 0/0 | 5336 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| t0027 | 0/0 | 5332 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| t0028 | 0/0 | 5335 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| t0029 | 0/0 | 5336 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| t0030 | 0/0 | 5335 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| t0031 | 0/0 | 5337 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| t0032 | 0/0 | 5336 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| t0033 | 0/0 | 5336 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| t0034 | 0/0 | 5335 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| t0035 | 0/0 | 5336 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| t0036 | 0/0 | 5337 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| t0037 | 0/0 | 5332 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| t0038 | 0/0 | 5336 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| t0039 | 0/0 | 5335 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| t0040 | 0/0 | 5336 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| t0041 | 0/0 | 5333 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| t0042 | 0/0 | 5337 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| t0043 | 0/0 | 5332 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| t0044 | 0/0 | 5335 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| t0045 | 0/0 | 5336 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| t0046 | 0/0 | 5336 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| t0047 | 0/0 | 5340 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| t0048 | 0/0 | 5336 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| t0049 | 0/0 | 5332 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| t0050 | 0/0 | 5332 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| t0051 | 0/0 | 5332 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| t0052 | 0/0 | 5332 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| t0053 | 1/0 | 5336 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| t0054 | 0/0 | 5331 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| t0055 | 0/0 | 5340 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| t0056 | 0/0 | 5335 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| t0057 | 0/0 | 5335 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| t0058 | 0/0 | 5336 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0121 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0295 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 3153 | 282 | 68 | 51 | 121 | 5 | 35 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| a0001c0002 | 0/0 | 3153 | 18 | 3 | 5 | 1 | 2 | 7 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| a0001c0003 | 0/0 | 3153 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| a0001c0004 | 0/0 | 3153 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| a0001c0005 | 0/0 | 3153 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| a0001c0007 | 0/0 | 3153 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| a0001c0009 | 0/0 | 3153 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| a0001c0010 | 0/0 | 3153 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| a0002c0006 | 0/0 | 3153 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| a0003c0008 | 0/0 | 3153 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | 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 | copy fasta | chr7 | 138455259 | 138594996 |
| a0001c0001t0002 | 0/0 | 8488 | 68 | 6 | 6 | 45 | 2 | 9 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| a0001c0001t0003 | 0/1 | 8487 | 32 | 11 | 14 | 0 | 1 | 5 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| a0001c0001t0004 | 0/0 | 8488 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| a0001c0001t0005 | 0/0 | 8483 | 7 | 0 | 0 | 5 | 0 | 2 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| a0001c0001t0006 | 0/0 | 8488 | 6 | 6 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| a0001c0001t0007 | 0/0 | 8488 | 6 | 0 | 0 | 6 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| a0001c0001t0008 | 0/0 | 8487 | 5 | 4 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| a0001c0001t0009 | 0/0 | 8487 | 5 | 0 | 4 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| a0001c0001t0010 | 0/0 | 8487 | 5 | 5 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| a0001c0001t0011 | 0/0 | 8487 | 5 | 2 | 0 | 0 | 0 | 3 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| a0001c0001t0012 | 0/0 | 8488 | 4 | 2 | 1 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| a0001c0001t0016 | 0/0 | 8487 | 3 | 2 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| a0001c0001t0017 | 0/0 | 8492 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| a0001c0001t0018 | 0/0 | 8488 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| a0001c0001t0019 | 0/0 | 8487 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| a0001c0001t0020 | 0/0 | 8488 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| a0001c0001t0021 | 0/0 | 8489 | 2 | 1 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| a0001c0001t0022 | 0/0 | 8488 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| a0001c0001t0023 | 0/0 | 8488 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| a0001c0001t0024 | 0/0 | 8488 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| a0001c0001t0025 | 0/0 | 8489 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| a0001c0001t0026 | 0/0 | 8488 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| a0001c0001t0027 | 0/0 | 8484 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| a0001c0001t0028 | 0/0 | 8487 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| a0001c0001t0029 | 0/0 | 8488 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| a0001c0001t0030 | 0/0 | 8487 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| a0001c0001t0032 | 0/0 | 8488 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| a0001c0001t0033 | 0/0 | 8488 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| a0001c0001t0034 | 0/0 | 8487 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| a0001c0001t0035 | 0/0 | 8488 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| a0001c0001t0037 | 0/0 | 8484 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| a0001c0001t0038 | 0/0 | 8488 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| a0001c0001t0039 | 0/0 | 8487 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| a0001c0001t0040 | 0/0 | 8488 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| a0001c0001t0041 | 0/0 | 8485 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| a0001c0001t0042 | 0/0 | 8489 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| a0001c0001t0043 | 0/0 | 8484 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| a0001c0001t0044 | 0/0 | 8487 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| a0001c0001t0045 | 0/0 | 8488 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| a0001c0001t0046 | 0/0 | 8488 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| a0001c0001t0047 | 0/0 | 8492 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| a0001c0001t0048 | 0/0 | 8488 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| a0001c0001t0049 | 0/0 | 8484 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| a0001c0001t0050 | 0/0 | 8484 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| a0001c0001t0051 | 0/0 | 8484 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| a0001c0001t0052 | 0/0 | 8484 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| a0001c0001t0053 | 1/0 | 8488 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| a0001c0001t0054 | 0/0 | 8483 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| a0001c0001t0055 | 0/0 | 8492 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| a0001c0001t0058 | 0/0 | 8488 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| a0001c0002t0004 | 0/0 | 8488 | 14 | 1 | 4 | 1 | 2 | 6 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| a0001c0002t0015 | 0/0 | 8488 | 3 | 2 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| a0001c0002t0031 | 0/0 | 8489 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| a0001c0003t0014 | 0/0 | 8488 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| a0001c0004t0056 | 0/0 | 8487 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| a0001c0004t0057 | 0/0 | 8487 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| a0001c0005t0013 | 0/0 | 8491 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| a0001c0007t0036 | 0/0 | 8489 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| a0001c0009t0003 | 0/0 | 8487 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| a0001c0010t0013 | 0/0 | 8491 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| a0002c0006t0006 | 0/0 | 8488 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| a0003c0008t0002 | 0/0 | 8488 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | copy fasta | chr7 | 138455259 | 138594996 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 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 | 1 | 0 | 0 | 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 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 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 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 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 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0081 | 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 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0091 | 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 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0001g0226 | 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 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0104 | 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 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0130 | 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 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0155 | 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 |
| 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 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0224 | 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 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0002g0243 | 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 |
| a0001c0001t0003g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0003g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0003g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0003g0276 | 0/0 | 1 | 0 | 1 | 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 |
| a0001c0001t0003g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0003g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0003g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0003g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0003g0300 | 0/0 | 1 | 1 | 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 |
| a0001c0001t0004g0281 | 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 |
| a0001c0001t0006g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0006g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0006g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0006g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0006g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0006g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0007g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0007g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0007g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0007g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0007g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0007g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0008g0272 | 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 |
| a0001c0001t0009g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0009g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0009g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0009g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0009g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0010g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0010g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0010g0188 | 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 |
| a0001c0001t0010g0245 | 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 |
| a0001c0001t0012g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0012g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0012g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0012g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0016g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0016g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0016g0012 | 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 |
| a0001c0001t0019g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0019g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0020g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0020g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0021g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0021g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0022g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0022g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0023g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0023g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0024g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0024g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0025g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0025g0168 | 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 |
| a0001c0001t0027g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0027g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0028g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0029g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0030g0306 | 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 |
| a0001c0001t0033g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0034g0026 | 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 |
| a0001c0001t0037g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0038g0149 | 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 |
| a0001c0001t0040g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0041g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0042g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0043g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0044g0113 | 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 |
| a0001c0001t0047g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0048g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0049g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0050g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0051g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0052g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0053g0121 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0054g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0055g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0001t0058g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0002t0004g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0002t0004g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0002t0004g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0002t0004g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0002t0004g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0002t0004g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0002t0004g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0002t0004g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0002t0004g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0002t0004g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0002t0004g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0002t0004g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0002t0004g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0002t0004g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0002t0015g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0002t0015g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0002t0015g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0002t0031g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0003t0014g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0003t0014g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0003t0014g0098 | 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 |
| a0001c0004t0057g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0005t0013g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0005t0013g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0001c0007t0036g0190 | 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 |
| a0001c0010t0013g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0002c0006t0006g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| a0003c0008t0002g0105 | 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 | g0049 | EUR | GBR | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0296 | EUR | GBR | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG00280 | hp1 | a0001 | c0002 | t0004 | g0196 | EUR | FIN | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0120 | EUR | FIN | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | CHS | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | CHS | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | CHS | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | CHS | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG00438 | hp2 | a0001 | c0001 | t0007 | g0136 | EAS | CHS | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG00609 | hp1 | a0001 | c0001 | t0050 | g0222 | EAS | CHS | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | CHS | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | CHS | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0161 | EAS | CHS | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG00735 | hp1 | a0001 | c0001 | t0020 | g0123 | AMR | PUR | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0276 | 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 | g0246 | AMR | PUR | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG00741 | hp2 | a0001 | c0002 | t0015 | g0204 | AMR | PUR | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01069 | hp1 | a0001 | c0001 | t0043 | g0119 | 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 | g0192 | AMR | PUR | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01070 | hp2 | a0001 | c0001 | t0009 | g0023 | 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 | g0025 | AMR | PUR | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01074 | hp1 | a0001 | c0001 | t0004 | g0281 | 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 | g0048 | AMR | PUR | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01081 | hp2 | a0001 | c0001 | t0020 | g0138 | 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 | g0145 | AMR | PUR | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0060 | 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 | g0075 | AMR | PUR | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0277 | AMR | PUR | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0275 | AMR | PUR | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01167 | hp2 | a0001 | c0002 | t0004 | g0191 | 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 | g0128 | AMR | PUR | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01175 | hp1 | a0001 | c0001 | t0021 | g0167 | 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 | g0148 | AMR | PUR | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0278 | AMR | PUR | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01255 | hp1 | a0001 | c0001 | t0041 | g0054 | AMR | CLM | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0271 | AMR | CLM | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0280 | AMR | CLM | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0085 | 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 | g0027 | AMR | CLM | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0207 | AMR | CLM | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01261 | hp2 | a0001 | c0001 | t0034 | g0026 | 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 | g0203 | AMR | CLM | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0074 | 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 | g0190 | EUR | IBS | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0129 | EUR | IBS | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01884 | hp1 | a0001 | c0001 | t0016 | g0009 | AFR | ACB | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01884 | hp2 | a0001 | c0001 | t0022 | g0189 | AFR | ACB | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01891 | hp1 | a0002 | c0006 | t0006 | g0182 | AFR | ACB | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01891 | hp2 | a0001 | c0001 | t0012 | g0302 | AFR | ACB | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0122 | AMR | PEL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01943 | hp1 | a0001 | c0001 | t0044 | g0113 | AMR | PEL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0013 | 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 | g0220 | AMR | PEL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0118 | AMR | PEL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PEL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0063 | 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 | g0131 | EAS | KHV | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | KHV | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02055 | hp1 | a0003 | c0008 | t0002 | g0105 | AFR | ACB | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02055 | hp2 | a0001 | c0004 | t0057 | g0185 | AFR | ACB | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0043 | 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 | g0159 | EAS | KHV | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | KHV | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0034 | 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 | g0247 | AFR | ACB | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02148 | hp1 | a0001 | c0001 | t0047 | g0157 | AMR | PEL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | CDX | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | CDX | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | CDX | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0214 | 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 | g0050 | AFR | ACB | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0274 | AFR | ACB | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02258 | hp2 | a0001 | c0001 | t0019 | g0305 | AFR | ACB | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02451 | hp1 | a0001 | c0001 | t0016 | g0010 | AFR | ACB | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02451 | hp2 | a0001 | c0002 | t0015 | g0151 | 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 | g0109 | AFR | GWD | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0139 | SAS | PJL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02602 | hp2 | a0001 | c0001 | t0051 | g0030 | 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 | g0079 | AFR | GWD | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02630 | hp1 | a0001 | c0001 | t0033 | g0205 | 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 | g0188 | 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 | g0210 | SAS | PJL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02717 | hp1 | a0001 | c0001 | t0022 | g0201 | AFR | GWD | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02717 | hp2 | a0001 | c0001 | t0029 | g0301 | AFR | GWD | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02723 | hp1 | a0001 | c0001 | t0024 | g0038 | AFR | GWD | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02723 | hp2 | a0001 | c0005 | t0013 | g0110 | 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 | g0137 | SAS | PJL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02738 | hp1 | a0001 | c0002 | t0004 | g0197 | 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 | g0244 | 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 | g0306 | AFR | GWD | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02818 | hp2 | a0001 | c0003 | t0014 | g0096 | AFR | GWD | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0213 | AFR | GWD | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0297 | 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 | g0037 | AFR | GWD | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0032 | 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 | g0003 | AFR | GWD | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0270 | 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 | g0102 | AFR | ESN | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02976 | hp2 | a0001 | c0002 | t0015 | g0152 | AFR | ESN | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG03041 | hp1 | a0001 | c0001 | t0018 | g0002 | 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 | g0033 | 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 | g0279 | AFR | ESN | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG03139 | hp2 | a0001 | c0001 | t0006 | g0178 | AFR | ESN | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0300 | AFR | ESN | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG03195 | hp2 | a0001 | c0001 | t0010 | g0187 | 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 | g0206 | AFR | MSL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG03225 | hp1 | a0001 | c0001 | t0006 | g0177 | AFR | MSL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG03225 | hp2 | a0001 | c0001 | t0010 | g0186 | AFR | MSL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0154 | SAS | PJL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG03453 | hp1 | a0001 | c0003 | t0014 | g0098 | AFR | MSL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0298 | AFR | MSL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG03486 | hp1 | a0001 | c0001 | t0021 | g0171 | AFR | MSL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | MSL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG03490 | hp1 | a0001 | c0002 | t0004 | g0194 | SAS | PJL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0071 | 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 | g0199 | 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 | g0076 | SAS | PJL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0104 | AFR | ESN | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG03516 | hp2 | a0001 | c0001 | t0006 | g0184 | 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 | g0183 | AFR | MSL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG03579 | hp2 | a0001 | c0001 | t0055 | g0209 | AFR | MSL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0208 | SAS | PJL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG03654 | hp2 | a0001 | c0002 | t0004 | g0200 | 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 | g0163 | SAS | PJL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG03688 | hp1 | a0001 | c0001 | t0027 | g0089 | SAS | STU | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0147 | SAS | STU | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0133 | SAS | PJL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG03710 | hp1 | a0001 | c0001 | t0009 | g0011 | SAS | PJL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0282 | SAS | PJL | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0169 | 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 | g0132 | SAS | BEB | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG03927 | hp1 | a0001 | c0001 | t0016 | g0012 | 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 | g0225 | SAS | BEB | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG04115 | hp1 | a0001 | c0001 | t0027 | g0088 | SAS | STU | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0092 | SAS | STU | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | BEB | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0175 | SAS | BEB | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | STU | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0156 | SAS | STU | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18522 | hp1 | a0001 | c0001 | t0019 | g0304 | AFR | YRI | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18522 | hp2 | a0001 | c0010 | t0013 | g0108 | AFR | YRI | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | CHB | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0144 | 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 | g0272 | AFR | YRI | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18939 | hp2 | a0001 | c0001 | t0007 | g0165 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18940 | hp1 | a0001 | c0001 | t0007 | g0162 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0056 | 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 | g0051 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18947 | hp1 | a0001 | c0001 | t0040 | g0164 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0055 | 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 | g0093 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18951 | hp2 | a0001 | c0001 | t0012 | g0112 | 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 | g0135 | 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 | g0116 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0072 | 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 | g0117 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18963 | hp1 | a0001 | c0002 | t0004 | g0198 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18963 | hp2 | a0001 | c0001 | t0007 | g0202 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18967 | hp2 | a0001 | c0001 | t0007 | g0160 | 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 | g0020 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0061 | 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 | g0140 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0044 | 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 | g0014 | 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 | g0172 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19056 | hp2 | a0001 | c0001 | t0054 | g0080 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19058 | hp2 | a0001 | c0001 | t0025 | g0111 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19065 | hp1 | a0001 | c0001 | t0038 | g0149 | 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 | g0039 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19078 | hp1 | a0001 | c0001 | t0042 | g0211 | 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 | g0062 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19081 | hp2 | a0001 | c0001 | t0025 | g0168 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0040 | 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 | g0082 | EAS | JPT | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0212 | AFR | ASW | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA20129 | hp2 | a0001 | c0001 | t0058 | g0181 | AFR | ASW | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0029 | EUR | TSI | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA20805 | hp2 | a0001 | c0002 | t0004 | g0193 | EUR | TSI | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | GIH | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA20905 | hp2 | a0001 | c0002 | t0004 | g0195 | SAS | GIH | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01123 | hp1 | a0001 | c0001 | t0028 | g0303 | AMR | CLM | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG01123 | hp2 | a0001 | c0001 | t0009 | g0024 | 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 | g0273 | AFR | ACB | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02486 | hp1 | a0001 | c0001 | t0010 | g0245 | AFR | ACB | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG02486 | hp2 | a0001 | c0001 | t0012 | g0215 | 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 | g0299 | AFR | ACB | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0103 | 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 | g0046 | AFR | USA | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| HG06807 | hp2 | a0001 | c0001 | t0006 | g0179 | AFR | USA | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA20300 | hp1 | a0001 | c0001 | t0006 | g0180 | AFR | USA | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | USA | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0295 | REF | REF | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0053 | g0121 | REF | REF | TRIM24_chr7_138455259_138594996 | TRIM24 | chr7 | 138455259 | 138594996 |
| 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 |
| 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 | a0001c0005a0001c0010 | 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 | a0001c0002a0001c0007 | 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 |
| 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 | a0001c0001t0017a0001c0001t0018a0001c0001t0058others(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 | a0001c0001t0003a0001c0001t0004a0001c0001t0008others(23): Show | 91 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(88): 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 | a0001c0005t0013a0001c0010t0013 | 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 | a0001c0005t0013a0001c0010t0013 | 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 | a0001c0001t0006a0001c0001t0010a0001c0001t0055others(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 | a0001c0001t0006a0001c0001t0058a0002c0006t0006 | 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 | a0001c0001t0003a0001c0001t0004a0001c0001t0008others(8): Show | 62 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(59): 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 | a0001c0001t0019a0001c0001t0030 | 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 | a0001c0001t0002a0001c0001t0005a0001c0001t0007others(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 | a0001c0004t0056a0001c0004t0057 | 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 | a0001c0001t0017a0001c0001t0025a0001c0001t0029 | 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 | a0001c0001t0010a0001c0004t0056a0001c0004t0057 | 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 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(49): Show | 215 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(212): 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 | a0001c0001t0017a0001c0001t0047a0001c0001t0055 | 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 | a0001c0001t0010a0001c0001t0055a0001c0004t0056others(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 | a0001c0001t0005a0001c0001t0011a0001c0001t0046 | 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 | a0001c0001t0010a0001c0001t0055a0001c0004t0056others(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 | a0001c0001t0010a0001c0001t0055a0001c0004t0056others(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 | a0001c0001t0008a0001c0001t0019a0001c0001t0024others(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 | a0001c0001t0006a0001c0001t0058a0002c0006t0006 | 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 | a0001c0001t0010a0001c0001t0055a0001c0004t0056others(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 | a0001c0001t0026a0001c0001t0035 | 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 | a0001c0001t0005a0001c0001t0010a0001c0001t0011others(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 | a0001c0001t0005a0001c0001t0011a0001c0001t0046others(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 | a0001c0001t0005a0001c0001t0011a0001c0001t0046others(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 | a0001c0001t0026a0001c0001t0035 | 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 | a0001c0005t0013a0001c0010t0013 | 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 | a0001c0001t0004a0001c0001t0021a0001c0001t0041others(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 | a0001c0001t0005a0001c0001t0006a0001c0001t0009others(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 | a0001c0001t0001a0001c0001t0027a0001c0001t0037others(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 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(43): Show | 214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): 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 | a0001c0001t0010a0001c0001t0026a0001c0001t0035 | 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 | a0001c0001t0006a0001c0001t0058a0002c0006t0006 | 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 | a0001c0001t0006a0001c0001t0058a0002c0006t0006 | 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 | a0001c0001t0005a0001c0001t0011a0001c0001t0017others(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 | a0001c0001t0005a0001c0001t0011a0001c0001t0017others(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 | a0001c0001t0001a0001c0001t0010a0001c0001t0026others(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 |
| 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 | 45 | a0001c0001t0003g0001a0001c0001t0003g0269a0001c0001t0003g0270others(42): Show | 46 | HG00140.hp2 HG00735.hp2 HG00738.hp1 others(43): 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 | a0001c0001t0026g0266a0001c0001t0026g0267a0001c0001t0035g0265 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007others(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 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0001t0001g0237others(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 | a0001c0001t0005g0253a0001c0001t0005g0254a0001c0001t0005g0256others(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 | a0001c0001t0002g0228a0001c0001t0002g0229a0001c0001t0002g0230others(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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(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 | a0001c0001t0001g0226a0001c0001t0046g0262a0001c0002t0004g0225 | 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 | a0001c0001t0003g0307a0001c0001t0003g0308a0001c0001t0011g0263others(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 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0022g0189others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | 176 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(173): Show | 177 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(174): 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 | a0001c0001t0002g0106a0001c0001t0002g0107a0001c0001t0002g0240others(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 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033 | 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 | a0001c0001t0002g0102a0001c0001t0002g0103a0001c0001t0002g0104others(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 | a0001c0001t0003g0274 | 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 | a0001c0001t0001g0013a0001c0001t0002g0153a0001c0001t0002g0154others(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 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(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 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0078others(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 | a0001c0001t0001g0097a0001c0001t0001g0099a0001c0001t0001g0100others(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 | a0001c0001t0009g0023a0001c0001t0009g0024a0001c0001t0009g0025 | 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 | a0001c0001t0009g0027a0001c0001t0034g0026 | 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 | 48 | a0001c0001t0002g0228a0001c0001t0003g0001a0001c0001t0003g0269others(45): Show | 49 | HG00140.hp2 HG00280.hp1 HG00738.hp1 others(46): 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 | a0001c0001t0003g0275a0001c0001t0003g0276a0001c0001t0003g0307others(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 | a0001c0007t0036g0190 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0004t0057g0185 | 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 | a0001c0004t0057g0185 | 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 | a0001c0004t0056g0008a0001c0004t0057g0185 | 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 | a0001c0004t0056g0008a0001c0004t0057g0185 | 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 | a0001c0001t0001g0095a0001c0001t0001g0235 | 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 | a0001c0004t0056g0008a0001c0004t0057g0185 | 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 | a0001c0001t0001g0101 | 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 | a0001c0001t0006g0177a0001c0001t0006g0178a0001c0001t0006g0179others(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 | a0001c0001t0003g0296 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0017g0005a0001c0001t0018g0002a0001c0001t0018g0003others(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 | a0001c0001t0010g0244a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0002g0150a0001c0001t0002g0170a0001c0001t0002g0172others(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 | a0001c0001t0001g0014 | 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 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0016others(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 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0032others(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 | a0001c0001t0001g0022a0001c0001t0001g0059a0001c0001t0001g0060others(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 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075others(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 | a0001c0001t0001g0077a0001c0001t0001g0093a0001c0001t0003g0271others(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 | a0001c0001t0003g0001a0001c0001t0003g0274a0001c0001t0003g0275others(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 | a0001c0001t0001g0094a0001c0001t0003g0289a0001c0001t0003g0290others(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 | a0001c0001t0008g0292a0001c0001t0008g0293a0001c0001t0008g0294others(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 | a0001c0001t0005g0261a0001c0002t0004g0194a0001c0002t0004g0247 | 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 |
6 | a0001c0001t0003g0295a0001c0002t0004g0195a0001c0002t0004g0196others(3): Show | 6 | HG00280.hp1 HG02572.hp2 HG02738.hp1 others(3): 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 | a0001c0001t0003g0276a0001c0002t0015g0151a0001c0002t0031g0210 | 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 | a0001c0002t0004g0198a0001c0002t0015g0152 | 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 | a0001c0001t0003g0308a0001c0002t0004g0199 | 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 | a0001c0002t0004g0200a0001c0005t0013g0110 | 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 | a0001c0001t0033g0205a0001c0001t0039g0227 | 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 | a0001c0001t0001g0034a0001c0001t0011g0263a0001c0001t0011g0264others(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 | a0001c0001t0010g0186a0001c0001t0010g0245 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007others(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 | a0001c0001t0001g0100 | 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 | a0001c0001t0003g0283a0001c0001t0003g0284a0001c0001t0003g0310 | 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 | a0001c0004t0056g0008a0001c0004t0057g0185 | 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 | a0001c0001t0038g0149 | 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 | a0001c0001t0002g0114 | 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 | a0001c0001t0001g0029 | 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 | a0001c0001t0003g0273 | 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 | 104 | a0001c0001t0003g0001a0001c0001t0003g0269a0001c0001t0003g0270others(101): Show | 105 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(102): 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 | 233 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(230): Show | 234 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(231): 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 | a0001c0001t0026g0266a0001c0001t0026g0267a0001c0001t0035g0265 | 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 | a0001c0001t0002g0146a0001c0001t0002g0147a0001c0001t0002g0150others(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 | a0001c0002t0004g0191a0001c0002t0004g0193a0001c0002t0004g0194others(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 | a0001c0001t0006g0177a0001c0001t0006g0178a0001c0001t0006g0179others(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 | a0001c0001t0010g0244a0001c0001t0017g0005a0001c0001t0017g0006others(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 | a0001c0001t0003g0275a0001c0001t0005g0253a0001c0001t0005g0254others(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 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0016others(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 |
52 | a0001c0001t0001g0014a0001c0001t0001g0029a0001c0001t0001g0033others(49): Show | 52 | HG00140.hp2 HG00423.hp2 HG00621.hp1 others(49): 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 | a0001c0001t0001g0022a0001c0001t0001g0028a0001c0001t0001g0046others(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 | a0001c0001t0016g0012 | 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 | a0001c0001t0003g0277 | 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 | a0001c0001t0002g0102a0001c0001t0002g0103a0001c0001t0002g0104others(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 | a0001c0001t0001g0071a0001c0001t0001g0076 | 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 | a0001c0001t0001g0021 | 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 | a0001c0010t0013g0108 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | 71 | a0001c0001t0003g0001a0001c0001t0003g0269a0001c0001t0003g0270others(68): Show | 72 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(69): 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 | 217 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(214): Show | 218 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(215): 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 | a0001c0001t0002g0174 | 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 | a0001c0001t0002g0107a0001c0001t0002g0240 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0003g0270a0001c0001t0008g0272 | 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 | a0001c0001t0003g0275 | 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 | a0001c0001t0003g0001a0001c0001t0003g0275a0001c0001t0003g0276others(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 | a0001c0001t0029g0301 | 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 | a0001c0001t0002g0170a0001c0001t0002g0208a0001c0001t0002g0214others(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 | a0001c0001t0009g0011a0001c0001t0009g0023a0001c0001t0009g0024others(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 | a0001c0001t0001g0057a0001c0001t0001g0239a0001c0001t0002g0207others(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 | a0001c0001t0001g0034a0001c0001t0001g0071a0001c0001t0002g0115others(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 | a0001c0001t0055g0209 | 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 | a0001c0001t0006g0177 | 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 | a0001c0001t0011g0252a0001c0001t0011g0255a0001c0001t0011g0258 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0002g0145 | 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 | a0001c0001t0001g0068a0001c0001t0001g0069 | 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 | a0001c0001t0058g0181 | 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 | a0001c0001t0001g0075a0001c0001t0002g0142a0001c0001t0002g0143others(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 | a0001c0001t0002g0207a0001c0001t0018g0002a0001c0001t0018g0003others(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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(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 | 38 | a0001c0001t0001g0034a0001c0001t0001g0071a0001c0001t0001g0083others(35): Show | 39 | HG00140.hp2 HG00735.hp2 HG00738.hp1 others(36): 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 | a0001c0001t0003g0309a0001c0001t0008g0291a0001c0001t0008g0292others(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 | a0001c0001t0002g0153 | 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 | a0001c0001t0009g0027 | 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 | 3 | a0001c0001t0003g0280a0001c0001t0003g0286a0001c0001t0003g0295 | 3 | HG01256.hp1 HG01258.hp1 homoSapiens_chm13v2.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 | a0001c0002t0004g0225 | 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 | a0001c0001t0002g0170a0001c0001t0002g0208a0001c0001t0002g0214others(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 | a0001c0001t0026g0266a0001c0001t0026g0267a0001c0001t0035g0265 | 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 | a0001c0001t0002g0107a0001c0001t0002g0240 | 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 | a0001c0001t0005g0253a0001c0001t0005g0254a0001c0001t0005g0256others(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 | a0001c0001t0033g0205 | 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 | a0001c0001t0002g0153a0001c0001t0005g0253a0001c0001t0005g0254others(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 | a0001c0001t0002g0154a0001c0001t0002g0248 | 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 | a0001c0001t0002g0141 | 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 | a0001c0001t0002g0207 | 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 | a0001c0001t0006g0184 | 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 | a0001c0001t0002g0140 | 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 | a0001c0004t0057g0185 | 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 | a0001c0001t0010g0186 | 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 | a0001c0001t0002g0139 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(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 | a0001c0001t0011g0252a0001c0001t0017g0005a0001c0001t0017g0006others(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 | a0001c0001t0001g0019a0001c0001t0001g0021 | 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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(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 | 217 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(214): Show | 218 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(215): 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 | a0001c0001t0055g0209 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0018g0002a0001c0001t0018g0003a0001c0001t0018g0004 | 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 | a0001c0001t0002g0169 | 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 | a0001c0001t0009g0011a0001c0001t0009g0023a0001c0001t0009g0024others(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 | a0001c0001t0001g0020 | 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 | a0001c0001t0022g0189a0001c0001t0022g0201 | 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 | a0001c0001t0002g0145 | 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 | 200 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(197): Show | 201 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(198): 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 | a0001c0001t0001g0235a0001c0001t0002g0102a0001c0001t0002g0103others(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 | a0001c0004t0056g0008a0001c0004t0057g0185 | 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 | a0001c0001t0001g0022a0001c0001t0001g0028a0001c0001t0001g0029others(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 | a0001c0003t0014g0098 | 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 | a0001c0001t0011g0252a0001c0001t0011g0255a0001c0001t0055g0209 | 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 | a0001c0001t0002g0173a0001c0001t0002g0242 | 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 | a0001c0001t0009g0011 | 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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(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 | a0001c0001t0007g0136 | 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 | a0001c0001t0033g0205a0001c0002t0004g0148a0001c0002t0004g0191others(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 | a0001c0001t0005g0253a0001c0001t0005g0254 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0001g0047a0001c0001t0001g0068a0001c0001t0001g0069others(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 | a0001c0001t0002g0102a0001c0001t0002g0103a0001c0001t0002g0104others(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 | a0001c0001t0002g0140 | 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 | a0001c0001t0009g0011a0001c0001t0009g0023a0001c0001t0009g0024others(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 | a0001c0005t0013g0109a0001c0005t0013g0110a0001c0010t0013g0108 | 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 | a0001c0001t0001g0036a0001c0001t0001g0059a0001c0001t0001g0067others(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 | a0001c0001t0022g0189a0001c0001t0022g0201 | 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 | a0001c0001t0003g0271a0001c0001t0003g0279a0001c0001t0003g0287others(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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(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 | a0001c0001t0001g0044a0001c0001t0010g0186a0001c0001t0010g0187others(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 | a0001c0001t0002g0206 | 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 | a0001c0004t0056g0008a0001c0004t0057g0185 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | 217 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(214): Show | 218 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(215): 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 | a0001c0001t0012g0192 | 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 | a0001c0001t0001g0066a0001c0001t0001g0087 | 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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(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 | a0001c0001t0029g0301 | 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 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0040others(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 | a0001c0001t0002g0155 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(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 | a0001c0001t0012g0192 | 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 | a0001c0001t0006g0177a0001c0001t0006g0178a0001c0001t0006g0179others(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 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0016 | 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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(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 | a0001c0001t0006g0177a0001c0001t0006g0178a0001c0001t0006g0179others(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 | a0001c0001t0002g0114 | 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 | a0001c0001t0009g0011a0001c0001t0009g0023a0001c0001t0009g0024others(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 | a0001c0001t0002g0116a0001c0001t0002g0142 | 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 | a0001c0001t0055g0209 | 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 | a0001c0001t0001g0019 | 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 | a0001c0001t0016g0009 | 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 | a0001c0001t0009g0023a0001c0001t0009g0024a0001c0001t0009g0025others(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 | a0001c0001t0034g0026 | 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 | a0001c0001t0016g0010 | 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 | a0001c0001t0009g0011a0001c0001t0016g0012 | 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 | a0001c0001t0009g0011a0001c0001t0009g0023a0001c0001t0009g0024others(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 | 68 | a0001c0001t0003g0001a0001c0001t0003g0269a0001c0001t0003g0270others(65): Show | 69 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(66): 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 | a0001c0001t0001g0061a0001c0001t0001g0090a0001c0001t0049g0062 | 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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(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 | a0001c0001t0022g0201 | 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 | a0001c0001t0012g0302 | 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 | 65 | a0001c0001t0003g0001a0001c0001t0003g0269a0001c0001t0003g0270others(62): Show | 66 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(63): 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 | a0001c0001t0006g0177a0001c0001t0006g0178a0001c0001t0006g0179others(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 | a0001c0004t0056g0008a0001c0004t0057g0185 | 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 | 215 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(212): Show | 216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): 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 | a0001c0001t0022g0189 | 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 | a0001c0001t0002g0156 | 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 | a0001c0001t0019g0304a0001c0001t0019g0305a0001c0001t0030g0306others(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 | a0001c0001t0001g0071a0001c0001t0001g0076 | 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 | a0001c0001t0001g0017 | 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 | a0001c0001t0001g0061a0001c0001t0001g0090a0001c0001t0049g0062 | 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 | a0001c0001t0037g0050 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0001g0099 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0018g0002a0001c0001t0018g0003a0001c0001t0018g0004 | 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 | a0001c0001t0009g0011a0001c0001t0009g0023a0001c0001t0009g0024others(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 | a0001c0001t0001g0219 | 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 | a0001c0001t0007g0117 | 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 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0009g0011a0001c0001t0009g0023a0001c0001t0009g0024others(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 | a0001c0001t0001g0041 | 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 | a0001c0001t0033g0205a0001c0002t0004g0148a0001c0002t0004g0191others(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 | a0001c0001t0010g0186 | 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 | a0001c0001t0002g0114 | 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 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0001t0001g0220others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0003g0273 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0004t0056g0008a0001c0004t0057g0185 | 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 | 66 | a0001c0001t0003g0001a0001c0001t0003g0269a0001c0001t0003g0270others(63): Show | 67 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(64): 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 | a0001c0004t0056g0008a0001c0004t0057g0185 | 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 | 306 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(303): Show | 307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): 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 | a0001c0005t0013g0109a0001c0005t0013g0110 | 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 | a0001c0001t0055g0209 | 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 | a0001c0004t0056g0008a0001c0004t0057g0185 | 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 | a0001c0001t0012g0192 | 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 | a0001c0001t0001g0057 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0005t0013g0109a0001c0005t0013g0110a0001c0010t0013g0108 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0009g0011a0001c0001t0009g0023a0001c0001t0009g0024others(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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(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 | a0001c0002t0031g0210 | 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 | a0001c0002t0004g0148a0001c0002t0004g0191a0001c0002t0004g0193others(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 | a0001c0001t0001g0043 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0002g0208 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0006g0177a0001c0001t0006g0178a0001c0001t0006g0179others(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 | a0001c0001t0026g0266a0001c0001t0026g0267a0001c0001t0035g0265 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0004t0056g0008a0001c0004t0057g0185 | 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 | a0001c0001t0055g0209 | 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 | a0001c0001t0019g0304a0001c0001t0019g0305a0001c0001t0030g0306others(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 | a0001c0005t0013g0109a0001c0005t0013g0110 | 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 | a0001c0001t0006g0177 | 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 | 81 | a0001c0001t0003g0001a0001c0001t0003g0269a0001c0001t0003g0270others(78): Show | 82 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(79): Show |
intron_variant | MODIFIER | c.365-17756C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138486534 | ||||||
| chr7:138486608
|
T | G | 66 | a0001c0001t0003g0001a0001c0001t0003g0269a0001c0001t0003g0270others(63): Show | 67 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(64): Show |
intron_variant | MODIFIER | c.365-17682T>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138486608 | ||||||
| chr7:138486618
|
G | C | 66 | a0001c0001t0003g0001a0001c0001t0003g0269a0001c0001t0003g0270others(63): Show | 67 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(64): Show |
intron_variant | MODIFIER | c.365-17672G>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138486618 | ||||||
| chr7:138486630
|
G | A | 66 | a0001c0001t0003g0001a0001c0001t0003g0269a0001c0001t0003g0270others(63): Show | 67 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(64): 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | 216 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(213): Show | 217 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(214): 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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(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 | a0001c0001t0002g0208 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0005g0253a0001c0001t0005g0254a0001c0001t0005g0256others(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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0002g0207 | 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 | a0001c0004t0056g0008a0001c0004t0057g0185 | 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 | a0001c0001t0005g0253a0001c0001t0005g0254a0001c0001t0005g0256others(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 | a0001c0001t0001g0087 | 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 | a0001c0001t0033g0205 | 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 | 216 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(213): Show | 217 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(214): 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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(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 | a0001c0001t0044g0113 | 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 | a0001c0001t0047g0157 | 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 | a0001c0001t0003g0309a0001c0001t0012g0302 | 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 | a0001c0001t0006g0177a0001c0001t0006g0178a0001c0001t0006g0179others(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 | a0001c0001t0001g0034a0001c0001t0001g0065a0001c0001t0001g0066others(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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007others(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 | a0001c0001t0037g0050 | 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 | 218 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(215): Show | 219 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(216): 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 | a0001c0001t0002g0133 | 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 | a0001c0002t0015g0151a0001c0002t0015g0152 | 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 | a0001c0001t0003g0274 | 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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(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 | a0001c0001t0028g0303 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | 69 | a0001c0001t0003g0001a0001c0001t0003g0269a0001c0001t0003g0270others(66): Show | 70 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(67): 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 | a0001c0001t0001g0056 | 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 | a0001c0002t0004g0148 | 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 | a0001c0001t0055g0209 | 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 | a0001c0001t0002g0154 | 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 | a0001c0001t0005g0253a0001c0001t0005g0254a0001c0001t0005g0256others(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 | a0001c0001t0033g0205a0001c0002t0004g0148a0001c0002t0004g0191others(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 | 215 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(212): Show | 216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): 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 | a0001c0004t0056g0008a0001c0004t0057g0185 | 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 | a0001c0004t0057g0185 | 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 | a0001c0002t0004g0148a0001c0002t0004g0191a0001c0002t0004g0193others(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 | a0001c0001t0022g0189a0001c0001t0022g0201 | 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 | a0001c0001t0016g0009a0001c0001t0016g0010 | 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 | 216 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(213): Show | 217 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(214): 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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007others(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 | a0001c0004t0056g0008a0001c0004t0057g0185 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | 121 | a0001c0001t0001g0022a0001c0001t0001g0028a0001c0001t0001g0029others(118): Show | 121 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(118): 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 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0043others(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 | a0001c0001t0001g0249a0001c0001t0003g0274a0001c0001t0003g0278others(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 | a0001c0001t0005g0260a0001c0001t0011g0252a0001c0001t0011g0255others(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 | a0001c0004t0057g0185 | 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 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0002g0170others(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 | a0001c0001t0009g0011a0001c0001t0009g0023a0001c0001t0009g0024others(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 | a0001c0001t0001g0091a0001c0001t0010g0186a0001c0001t0010g0187others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0002g0208 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0003g0270a0001c0001t0008g0272 | 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 | a0001c0001t0047g0157 | 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 | a0001c0001t0005g0253a0001c0001t0005g0254a0001c0001t0005g0256others(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 | 216 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(213): Show | 217 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.365-10813A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1/18 | chr7 | 138493477 | ||||||
| chr7:138493544
|
G | A | 92 | a0001c0001t0003g0001a0001c0001t0003g0269a0001c0001t0003g0270others(89): Show | 93 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(90): 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 | a0001c0001t0005g0253a0001c0001t0005g0254a0001c0001t0005g0256others(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 | a0001c0001t0002g0166 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0055g0209 | 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 | a0001c0001t0001g0085a0001c0001t0001g0099 | 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 | 216 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(213): Show | 217 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(214): 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 | a0001c0001t0009g0011a0001c0001t0009g0023a0001c0001t0009g0024others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0022g0189a0001c0001t0022g0201 | 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 | 46 | a0001c0001t0003g0001a0001c0001t0003g0269a0001c0001t0003g0270others(43): Show | 47 | HG00140.hp2 HG00735.hp2 HG00738.hp1 others(44): 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 | a0001c0001t0006g0177a0001c0001t0006g0178a0001c0001t0006g0179others(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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | 67 | a0001c0001t0003g0001a0001c0001t0003g0269a0001c0001t0003g0270others(64): Show | 68 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(65): 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 | a0001c0005t0013g0109a0001c0005t0013g0110a0001c0010t0013g0108 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0021g0171 | 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 | a0001c0001t0002g0173a0001c0001t0002g0242 | 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 | a0001c0001t0020g0123 | 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 | a0001c0001t0005g0253a0001c0001t0005g0254a0001c0001t0005g0256others(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 | a0001c0001t0010g0244 | 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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(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 | a0001c0001t0002g0158 | 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 | a0001c0001t0003g0275a0001c0001t0003g0276a0001c0001t0003g0290others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0004t0056g0008a0001c0004t0057g0185 | 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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(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 | a0001c0001t0002g0206a0001c0001t0002g0212a0001c0001t0002g0213others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0002g0155 | 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 | a0001c0001t0001g0022a0001c0001t0001g0052a0001c0001t0001g0059others(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 | a0001c0001t0001g0017a0001c0001t0001g0085a0001c0001t0002g0127others(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 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(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 | a0001c0003t0014g0079a0001c0003t0014g0096a0001c0003t0014g0098 | 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 | a0001c0001t0010g0186 | 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 | a0001c0005t0013g0109a0001c0005t0013g0110a0001c0010t0013g0108 | 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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(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 | a0001c0001t0055g0209 | 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 | a0001c0001t0050g0222 | 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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0002g0092a0001c0001t0027g0088 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(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 | a0001c0001t0002g0118a0001c0001t0002g0122 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0002g0133a0001c0001t0002g0154 | 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 | a0001c0001t0002g0144 | 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 | a0001c0001t0041g0054 | 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 | a0001c0005t0013g0109a0001c0005t0013g0110 | 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 | a0001c0001t0009g0011a0001c0001t0009g0023a0001c0001t0009g0024others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0054g0080 | 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 | a0002c0006t0006g0182 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0002c0006t0006g0182 | 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 | a0001c0001t0001g0014a0001c0001t0001g0061a0001c0001t0001g0238others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0001g0047a0001c0001t0001g0237a0001c0001t0002g0134others(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 | a0001c0001t0019g0304a0001c0001t0019g0305a0001c0001t0030g0306others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0001g0085a0001c0001t0001g0099 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0002g0114a0001c0001t0002g0174 | 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 | a0001c0001t0006g0177a0001c0001t0006g0178a0001c0001t0006g0179others(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 | 73 | a0001c0001t0003g0001a0001c0001t0003g0269a0001c0001t0003g0270others(70): Show | 74 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(71): 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0033g0205a0001c0002t0004g0148a0001c0002t0004g0191others(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 | a0001c0001t0006g0177a0001c0001t0006g0178a0001c0001t0006g0179others(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 | a0001c0001t0003g0270 | 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 | a0001c0001t0022g0201 | 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 | a0001c0001t0003g0273 | 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 | a0001c0001t0001g0086a0001c0001t0001g0100 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0001g0082a0001c0001t0001g0220a0001c0001t0002g0230others(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 | a0001c0004t0056g0008a0001c0004t0057g0185 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | 6 | a0001c0001t0003g0280a0001c0001t0003g0282a0001c0001t0003g0286others(3): Show | 6 | HG01256.hp1 HG01258.hp1 HG02559.hp2 others(3): 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 | a0001c0001t0016g0012 | 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 | a0001c0004t0056g0008a0001c0004t0057g0185 | 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 | a0001c0002t0004g0198 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0002g0212 | 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 | a0001c0001t0003g0269a0001c0009t0003g0268 | 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 | a0001c0001t0002g0154 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | 216 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(213): Show | 217 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(214): 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 | a0001c0001t0026g0266a0001c0001t0026g0267a0001c0001t0035g0265 | 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 | a0001c0001t0002g0107a0001c0001t0002g0240a0001c0001t0002g0248others(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 | a0001c0001t0009g0011a0001c0001t0009g0023a0001c0001t0009g0024others(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 | 81 | a0001c0001t0003g0001a0001c0001t0003g0269a0001c0001t0003g0270others(78): Show | 82 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(79): 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 | a0001c0001t0001g0061 | 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 | a0001c0002t0004g0148 | 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 | a0001c0001t0002g0127a0001c0001t0002g0129a0001c0001t0002g0130others(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 | a0001c0001t0033g0205a0001c0005t0013g0109a0001c0005t0013g0110others(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 | a0001c0001t0002g0224 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0009g0011a0001c0001t0009g0023a0001c0001t0009g0024others(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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | 46 | a0001c0001t0003g0001a0001c0001t0003g0269a0001c0001t0003g0270others(43): Show | 47 | HG00140.hp2 HG00735.hp2 HG00738.hp1 others(44): 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0001g0020a0001c0001t0001g0028a0001c0001t0001g0055others(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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(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 | a0001c0001t0001g0044a0001c0001t0001g0047a0001c0001t0001g0063others(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 | a0001c0001t0002g0115a0001c0001t0002g0122a0001c0001t0002g0131others(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 | a0001c0001t0002g0243a0001c0001t0003g0285a0001c0001t0006g0178others(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 | a0001c0001t0009g0011a0001c0001t0009g0023a0001c0001t0009g0024others(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 | a0001c0001t0002g0154a0001c0001t0018g0002a0001c0001t0022g0189others(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 | a0001c0001t0001g0028 | 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 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0045others(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 | a0001c0001t0030g0306a0001c0001t0032g0311 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0005g0254others(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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0060others(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 | 68 | a0001c0001t0003g0001a0001c0001t0003g0269a0001c0001t0003g0270others(65): Show | 69 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(66): 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 | a0001c0001t0002g0102a0001c0001t0002g0103a0001c0001t0002g0104others(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 | 68 | a0001c0001t0003g0001a0001c0001t0003g0269a0001c0001t0003g0270others(65): Show | 69 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(66): 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 | a0001c0001t0055g0209 | 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 | a0001c0002t0015g0151a0001c0002t0015g0152 | 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 | a0001c0001t0001g0055a0001c0001t0001g0082a0001c0001t0004g0281others(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 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0018others(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 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0016others(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 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0002t0004g0203 | 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 | a0001c0001t0005g0256a0001c0001t0055g0209a0001c0002t0004g0199 | 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 | a0001c0001t0001g0053 | 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 | a0001c0004t0056g0008a0001c0004t0057g0185 | 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 | 13 | a0001c0001t0002g0124a0001c0001t0002g0125a0001c0001t0002g0126others(10): Show | 13 | HG00609.hp2 HG01256.hp1 HG01258.hp1 others(10): 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 | a0001c0001t0002g0145a0001c0001t0002g0147a0001c0001t0020g0138 | 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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(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 | a0001c0001t0002g0106a0001c0001t0002g0128a0001c0001t0002g0129others(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 | a0001c0001t0007g0165a0001c0001t0016g0010a0001c0001t0022g0189others(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 | a0001c0001t0002g0115a0001c0001t0002g0131 | 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 | a0001c0001t0002g0212 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0009g0011a0001c0001t0009g0023a0001c0001t0009g0024others(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 | a0001c0001t0022g0189a0001c0001t0022g0201 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0011g0263a0001c0001t0011g0264 | 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 | a0001c0001t0024g0037a0001c0001t0024g0038 | 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 | a0001c0001t0007g0162 | 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 | a0001c0001t0005g0253a0001c0001t0005g0254a0001c0001t0005g0256others(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 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(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 | a0001c0001t0009g0011a0001c0001t0009g0023a0001c0001t0009g0024others(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 | a0001c0001t0008g0292a0001c0001t0008g0293a0001c0001t0008g0294 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0022g0189a0001c0001t0022g0201 | 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 | a0001c0001t0009g0011a0001c0001t0009g0023a0001c0001t0009g0024others(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 | 214 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(211): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0003g0298 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0052g0039 | 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 | a0001c0001t0002g0231a0001c0001t0002g0242a0001c0001t0010g0186others(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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0002g0102a0001c0001t0002g0103a0001c0001t0002g0104others(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 | a0001c0001t0002g0120a0001c0001t0043g0119 | 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 | a0001c0001t0009g0011a0001c0001t0009g0023a0001c0001t0009g0024others(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 | a0001c0002t0015g0204 | 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 | a0001c0001t0005g0253a0001c0001t0005g0254a0001c0001t0005g0256others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0001g0033a0001c0001t0002g0207a0001c0001t0002g0216others(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 | a0001c0004t0056g0008a0001c0004t0057g0185 | 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 | a0001c0001t0006g0177a0001c0001t0006g0178a0001c0001t0006g0179others(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 | a0001c0001t0003g0284a0001c0001t0003g0310 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0029g0301 | 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 | a0001c0001t0002g0106a0001c0001t0002g0114a0001c0001t0002g0115others(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 | a0001c0001t0002g0129a0001c0001t0002g0147a0001c0001t0002g0156others(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 | a0001c0001t0002g0135a0001c0001t0002g0142a0001c0001t0022g0201others(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 | a0001c0001t0002g0212a0001c0001t0002g0213a0001c0001t0002g0248others(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 | a0001c0001t0007g0162a0001c0001t0007g0165 | 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 | a0001c0001t0001g0068a0001c0001t0001g0069 | 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 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0045others(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 | a0001c0001t0001g0041a0001c0001t0001g0066 | 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 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0016others(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 | a0001c0001t0001g0067a0001c0001t0001g0073a0001c0001t0001g0091 | 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 | a0001c0001t0001g0014a0001c0001t0001g0034a0001c0001t0001g0035others(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 | a0001c0001t0001g0068a0001c0001t0001g0069 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0244others(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 | a0001c0001t0001g0237a0001c0001t0003g0287a0001c0001t0010g0186others(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 | a0001c0001t0003g0269a0001c0001t0003g0275a0001c0001t0003g0283others(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 | a0001c0001t0003g0270a0001c0001t0003g0273a0001c0001t0003g0274others(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 | a0001c0001t0001g0064 | 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 | a0001c0001t0001g0028a0001c0001t0002g0124a0001c0001t0002g0207others(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 | 26 | a0001c0001t0002g0107a0001c0001t0002g0170a0001c0001t0002g0214others(23): Show | 27 | HG00140.hp2 HG00735.hp2 HG01069.hp2 others(24): 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 | a0001c0001t0006g0179a0001c0001t0006g0183a0001c0001t0006g0184others(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 | a0001c0001t0003g0282a0001c0001t0003g0289a0001c0001t0004g0281others(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 | a0001c0003t0014g0079a0001c0003t0014g0096 | 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 | a0001c0001t0001g0014a0001c0001t0001g0034a0001c0001t0001g0035others(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 | a0001c0001t0001g0043a0001c0001t0011g0255a0001c0001t0011g0258 | 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 | a0001c0001t0001g0071a0001c0001t0005g0254a0001c0001t0005g0256others(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 | a0001c0001t0001g0076 | 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 | a0001c0001t0005g0253a0001c0001t0005g0259 | 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 | a0001c0001t0055g0209 | 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 | a0001c0001t0002g0135 | 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 | a0001c0001t0009g0023a0001c0001t0009g0024a0001c0001t0009g0025others(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 | a0001c0003t0014g0098 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006 | 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 | a0001c0001t0001g0082 | 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 | a0001c0001t0049g0062 | 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 | a0001c0001t0001g0059 | 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 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0019others(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 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(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 | a0001c0001t0001g0044 | 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 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0097others(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 | a0001c0001t0009g0023a0001c0001t0009g0024a0001c0001t0009g0025others(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 | a0001c0001t0001g0063a0001c0001t0001g0094 | 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 | a0001c0001t0001g0066a0001c0001t0001g0226 | 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 | a0001c0004t0057g0185 | 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 | a0001c0001t0002g0104 | 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 | a0001c0002t0004g0191a0001c0002t0004g0193a0001c0002t0004g0246others(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 | a0001c0001t0033g0205a0001c0002t0004g0148a0001c0002t0004g0194others(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 | a0001c0001t0017g0005a0001c0001t0017g0006 | 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 | a0001c0001t0001g0085 | 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 | a0001c0001t0003g0287a0001c0001t0010g0186a0001c0001t0010g0244others(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 | a0001c0001t0002g0206a0001c0001t0002g0212a0001c0001t0002g0213others(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 | a0001c0003t0014g0079a0001c0003t0014g0096 | 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 | a0001c0001t0001g0064a0001c0003t0014g0079a0001c0003t0014g0096 | 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 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0016others(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 |
42 | a0001c0001t0003g0001a0001c0001t0003g0270a0001c0001t0003g0273others(39): Show | 43 | HG00140.hp2 HG00735.hp2 HG00738.hp1 others(40): 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 | a0001c0001t0001g0014a0001c0001t0001g0028a0001c0001t0001g0034others(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 | a0001c0001t0001g0064a0001c0001t0010g0186a0001c0001t0010g0187others(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 | a0001c0001t0043g0119a0001c0004t0057g0185 | 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 | a0001c0001t0001g0032a0001c0001t0001g0073a0001c0001t0001g0100others(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 | a0001c0001t0003g0273a0001c0003t0014g0079a0001c0003t0014g0096 | 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 | a0001c0001t0055g0209 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0001g0032a0001c0001t0001g0040a0001c0001t0001g0051others(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 | a0001c0001t0002g0212a0001c0001t0002g0214a0001c0001t0002g0216others(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 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0078others(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 | a0001c0001t0026g0266a0001c0001t0026g0267a0001c0001t0035g0265 | 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 | a0001c0005t0013g0109a0001c0005t0013g0110a0001c0010t0013g0108 | 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 | a0001c0001t0009g0011a0001c0001t0016g0009a0001c0001t0016g0010 | 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 | a0001c0001t0001g0071a0001c0001t0001g0076 | 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 | a0001c0001t0005g0253a0001c0001t0005g0254a0001c0001t0005g0256others(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 | a0001c0001t0010g0244 | 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 | a0001c0001t0001g0078a0001c0001t0001g0085a0001c0001t0001g0099others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0022g0189a0001c0001t0022g0201 | 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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(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 | a0001c0001t0005g0253a0001c0001t0005g0254a0001c0001t0005g0256others(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 | a0001c0001t0002g0114 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0055g0209 | 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 | a0001c0001t0042g0211 | 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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(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 | a0001c0001t0001g0022a0001c0001t0001g0045a0001c0001t0001g0059others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0021g0167 | 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 | a0001c0002t0004g0191a0001c0002t0004g0193a0001c0002t0004g0199others(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 | 305 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(302): Show | 306 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(303): 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 | a0001c0003t0014g0079a0001c0003t0014g0096a0001c0003t0014g0098 | 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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0001g0223 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0002g0216 | 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 | a0001c0001t0003g0285a0001c0001t0055g0209 | 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 | 46 | a0001c0001t0003g0001a0001c0001t0003g0269a0001c0001t0003g0270others(43): Show | 47 | HG00140.hp2 HG00735.hp2 HG00738.hp1 others(44): 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 | a0001c0004t0056g0008a0001c0004t0057g0185 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0055g0209 | 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 | a0001c0004t0056g0008a0001c0004t0057g0185 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0007g0136a0001c0001t0010g0186a0001c0001t0010g0187others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | 213 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(210): Show | 214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0005g0253others(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 | a0001c0001t0001g0072 | 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 | a0001c0001t0005g0253a0001c0001t0005g0254a0001c0001t0005g0256others(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 | a0001c0001t0005g0253a0001c0001t0005g0254a0001c0001t0005g0256others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0002g0158 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0012g0302 | 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 | a0001c0001t0043g0119 | 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 | a0001c0001t0002g0131 | 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 | a0001c0001t0002g0224 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0007g0160a0001c0001t0007g0202 | 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 | a0001c0001t0016g0012 | 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 | a0001c0004t0056g0008a0001c0004t0057g0185 | 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 | a0001c0001t0009g0011a0001c0001t0009g0023a0001c0001t0009g0024others(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 | a0001c0001t0011g0252a0001c0001t0011g0255 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0002g0115a0001c0001t0002g0131 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0005g0253a0001c0001t0005g0254a0001c0001t0005g0256others(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 | a0002c0006t0006g0182 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0055g0209 | 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 | a0001c0001t0011g0252a0001c0001t0011g0255a0001c0001t0011g0258 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0005g0253a0001c0001t0005g0254a0001c0001t0005g0256others(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 | a0001c0002t0015g0151a0001c0002t0015g0152 | 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 | a0001c0003t0014g0079a0001c0003t0014g0096 | 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 | a0001c0001t0002g0116 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0041g0054 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | 213 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(210): Show | 214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0002t0004g0191a0001c0002t0004g0199 | 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 | a0001c0001t0001g0081a0001c0001t0001g0084a0001c0001t0001g0236 | 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 | 46 | a0001c0001t0003g0001a0001c0001t0003g0269a0001c0001t0003g0270others(43): Show | 47 | HG00140.hp2 HG00735.hp2 HG00738.hp1 others(44): 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0002g0170 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0005t0013g0109a0001c0005t0013g0110 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0244others(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 | a0001c0001t0002g0207a0001c0001t0002g0208a0001c0001t0002g0214others(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 | a0001c0001t0005g0253a0001c0001t0005g0254a0001c0001t0005g0256others(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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007others(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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(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 | a0001c0001t0002g0125 | 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 | a0001c0001t0001g0093a0001c0001t0006g0177a0001c0001t0006g0178others(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 | a0001c0001t0026g0266a0001c0001t0026g0267a0001c0001t0035g0265 | 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 | a0001c0001t0002g0156 | 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 | a0001c0005t0013g0109a0001c0005t0013g0110a0001c0010t0013g0108 | 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 | a0001c0001t0005g0253a0001c0001t0005g0254a0001c0001t0005g0256others(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 | a0001c0001t0006g0177a0001c0001t0006g0178a0001c0001t0006g0179others(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 | a0001c0001t0001g0041a0001c0001t0001g0057a0001c0001t0001g0082others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0001g0035 | 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 | a0001c0001t0010g0245 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0004t0056g0008a0001c0004t0057g0185 | 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 | a0001c0001t0003g0278 | 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 | a0001c0001t0002g0120 | 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 | a0001c0001t0011g0263a0001c0001t0011g0264 | 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 | a0001c0003t0014g0079a0001c0003t0014g0096a0001c0003t0014g0098 | 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 | a0001c0001t0005g0259a0001c0001t0005g0260a0001c0001t0005g0261 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0004t0056g0008a0001c0004t0057g0185 | 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 | a0001c0001t0029g0301 | 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 | a0001c0001t0010g0244 | 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 | a0001c0001t0019g0304a0001c0001t0019g0305a0001c0001t0030g0306others(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 | a0001c0001t0001g0045 | 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 | a0001c0001t0024g0037a0001c0001t0024g0038 | 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 | a0001c0004t0056g0008a0001c0004t0057g0185 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0006g0177a0001c0001t0006g0178a0001c0001t0006g0179others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0002g0241 | 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 | a0001c0001t0023g0137 | 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 | a0001c0001t0023g0137 | 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 | a0001c0001t0002g0142 | 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 | a0001c0002t0004g0200 | 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 | a0001c0001t0026g0266a0001c0001t0026g0267a0001c0001t0035g0265 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0004t0056g0008a0001c0004t0057g0185 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0004t0056g0008a0001c0004t0057g0185 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0003g0279a0001c0001t0003g0297 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | 213 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(210): Show | 214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0005t0013g0109a0001c0005t0013g0110a0001c0010t0013g0108 | 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 | 67 | a0001c0001t0003g0001a0001c0001t0003g0269a0001c0001t0003g0270others(64): Show | 68 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(65): 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 | a0001c0002t0004g0198 | 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 | 213 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(210): Show | 214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.765-2411A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 4/18 | chr7 | 138522830 | ||||||
| chr7:138522853
|
CAAG | C | 67 | a0001c0001t0003g0001a0001c0001t0003g0269a0001c0001t0003g0270others(64): Show | 68 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(65): 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 | a0001c0001t0047g0157 | 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 | a0001c0001t0005g0253a0001c0001t0005g0254a0001c0001t0005g0256others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | 45 | a0001c0001t0003g0001a0001c0001t0003g0269a0001c0001t0003g0270others(42): Show | 46 | HG00140.hp2 HG00735.hp2 HG00738.hp1 others(43): 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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(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 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0045others(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 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(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 | a0001c0001t0001g0059a0001c0001t0001g0067a0001c0001t0001g0084others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0001g0021 | 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 | a0001c0001t0001g0022a0001c0001t0001g0028a0001c0001t0001g0029others(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 | a0001c0001t0016g0012 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | 99 | a0001c0001t0003g0001a0001c0001t0003g0269a0001c0001t0003g0270others(96): Show | 100 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(97): 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 | a0001c0001t0002g0140 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0006g0177a0001c0001t0006g0178a0001c0001t0006g0179others(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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0003t0014g0079a0001c0003t0014g0096a0001c0003t0014g0098 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0005g0253a0001c0001t0005g0254a0001c0001t0005g0256others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0002c0006t0006g0182 | 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 | a0001c0001t0001g0018 | 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 | a0001c0001t0009g0011a0001c0001t0009g0023a0001c0001t0009g0024others(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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(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 | a0001c0001t0011g0263a0001c0001t0011g0264 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0002g0133a0001c0001t0002g0154 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | 214 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(211): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): 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 | a0001c0005t0013g0109a0001c0005t0013g0110a0001c0010t0013g0108 | 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 | a0001c0001t0006g0177a0001c0001t0006g0178a0001c0001t0006g0179others(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 | a0001c0004t0057g0185 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0055g0209 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0004t0056g0008a0001c0004t0057g0185 | 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 | a0001c0001t0002g0106a0001c0001t0002g0128a0001c0001t0002g0129others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0001g0035 | 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 | a0001c0001t0033g0205 | 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 | a0001c0001t0005g0253a0001c0001t0005g0254a0001c0001t0005g0256others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0006g0178a0001c0001t0006g0180 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0002g0135 | 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 | a0001c0004t0056g0008a0001c0004t0057g0185 | 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 | a0001c0001t0006g0177a0001c0001t0006g0178a0001c0001t0006g0179others(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 | a0001c0001t0026g0266a0001c0001t0026g0267a0001c0001t0035g0265 | 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 | a0001c0001t0002g0224 | 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 | a0001c0001t0001g0239a0001c0001t0002g0106a0001c0001t0002g0107others(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 | a0001c0004t0057g0185 | 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 | 145 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(142): Show | 145 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(142): 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 | a0001c0004t0057g0185 | 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 | a0001c0001t0002g0208 | 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 | a0001c0001t0001g0074a0001c0001t0001g0075 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0016others(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 | a0001c0002t0015g0152 | 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 | a0001c0001t0001g0047 | 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 | a0001c0001t0001g0047a0001c0001t0001g0061a0001c0001t0001g0066others(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 | a0001c0004t0056g0008a0001c0004t0057g0185 | 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 | a0001c0001t0001g0064 | 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 | a0001c0003t0014g0079a0001c0003t0014g0096a0001c0003t0014g0098 | 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 | a0001c0001t0002g0114 | 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 | a0001c0001t0002g0116a0001c0001t0002g0135a0001c0001t0002g0142others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0002t0015g0204 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0002t0004g0246 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0010g0187a0001c0001t0010g0188 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0001g0017a0001c0001t0001g0071a0001c0001t0001g0237others(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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0004t0056g0008a0001c0004t0057g0185 | 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 | a0001c0001t0058g0181 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0006g0177a0001c0001t0006g0178a0001c0001t0006g0179others(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 | a0001c0001t0003g0285a0001c0001t0008g0272a0001c0001t0008g0291others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0006g0177a0001c0001t0006g0178a0001c0001t0006g0179others(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 | 74 | a0001c0001t0002g0150a0001c0001t0003g0001a0001c0001t0003g0269others(71): Show | 75 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(72): 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 | a0001c0001t0001g0095a0001c0001t0005g0253a0001c0001t0005g0254others(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 | a0001c0001t0010g0187a0001c0001t0010g0188a0001c0001t0010g0244 | 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 | a0001c0001t0010g0186a0001c0001t0010g0245 | 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 | a0001c0004t0057g0185 | 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 | a0001c0001t0001g0223 | 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 | a0001c0004t0056g0008a0001c0004t0057g0185 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0006g0177a0001c0001t0006g0178a0001c0001t0006g0179others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0003g0270a0001c0001t0003g0309 | 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 | a0001c0001t0006g0177a0001c0001t0006g0178a0001c0001t0006g0179others(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 | a0001c0004t0056g0008a0001c0004t0057g0185 | 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 | a0001c0001t0044g0113 | 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 | a0001c0003t0014g0079a0001c0003t0014g0096a0001c0003t0014g0098 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0003g0270a0001c0001t0003g0309 | 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 | a0001c0001t0005g0253a0001c0001t0005g0254a0001c0001t0005g0256others(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 | 213 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(210): Show | 214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | 213 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(210): Show | 214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0001g0055 | 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 | a0001c0001t0028g0303 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0002t0015g0151a0001c0002t0015g0152 | 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 | a0001c0001t0002g0115a0001c0001t0002g0131a0001c0001t0010g0186others(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 | a0001c0001t0026g0266a0001c0001t0026g0267a0001c0001t0035g0265 | 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 | a0001c0001t0001g0086 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0001g0018a0001c0001t0017g0005a0001c0001t0017g0006others(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 | a0001c0001t0010g0245 | 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 | a0001c0001t0050g0222 | 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 | a0001c0001t0050g0222 | 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 | a0001c0001t0050g0222 | 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 | a0001c0001t0002g0248a0001c0002t0004g0193 | 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 | a0001c0001t0001g0063 | 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 | 17 | a0001c0001t0003g0001a0001c0001t0003g0275a0001c0001t0003g0276others(14): Show | 18 | HG00735.hp2 HG00738.hp1 HG01069.hp2 others(15): 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0003g0270a0001c0001t0003g0273a0001c0001t0003g0309 | 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 | a0001c0001t0005g0253a0001c0001t0005g0254a0001c0001t0005g0256others(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 | a0001c0001t0006g0177a0001c0001t0006g0178a0001c0001t0006g0179others(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 | 80 | a0001c0001t0003g0001a0001c0001t0003g0269a0001c0001t0003g0270others(77): Show | 81 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(78): 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 | a0001c0004t0056g0008a0001c0004t0057g0185 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0010g0244 | 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 | a0001c0001t0005g0253a0001c0001t0005g0254a0001c0001t0005g0256others(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 | a0001c0001t0001g0022a0001c0001t0001g0045 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0006g0178a0001c0001t0006g0180 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007others(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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0023g0163 | 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 | a0001c0003t0014g0079a0001c0003t0014g0096a0001c0003t0014g0098 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0002g0128 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0006g0177a0001c0001t0006g0178a0001c0001t0006g0179others(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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0006g0177a0001c0001t0006g0178a0001c0001t0006g0179others(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 | a0001c0001t0021g0167a0001c0001t0021g0171 | 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 | a0001c0001t0021g0167a0001c0001t0021g0171 | 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 | a0001c0001t0021g0167a0001c0001t0021g0171 | 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 | a0001c0001t0021g0167a0001c0001t0021g0171 | 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 | a0001c0001t0021g0167a0001c0001t0021g0171 | 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 | 208 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(205): Show | 209 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(206): 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0005t0013g0109a0001c0005t0013g0110a0001c0010t0013g0108 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0006g0177a0001c0001t0006g0178a0001c0001t0006g0179others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0002c0006t0006g0182 | 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 | a0001c0001t0001g0048a0001c0001t0001g0060 | 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 | a0001c0001t0048g0132 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0002g0135 | 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 | a0001c0004t0056g0008a0001c0004t0057g0185 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0009g0011a0001c0001t0009g0023a0001c0001t0009g0024others(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 | 233 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(230): Show | 234 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(231): 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 | a0001c0001t0002g0092a0001c0001t0006g0177a0001c0001t0006g0178others(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 | a0001c0001t0001g0075 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007others(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 | a0001c0001t0006g0178a0001c0001t0006g0180 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0005g0253a0001c0001t0005g0254a0001c0001t0005g0256others(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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0017others(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 | 61 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(58): Show | 61 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(58): 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 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0084others(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 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0097others(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 | a0003c0008t0002g0105 | 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 | a0001c0001t0005g0256a0001c0001t0005g0257a0001c0001t0005g0259others(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 | a0001c0001t0001g0052a0001c0001t0002g0208 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0016g0009a0001c0001t0016g0010 | 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 | a0001c0001t0009g0011a0001c0001t0009g0023a0001c0001t0009g0024others(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 | a0001c0001t0002g0147 | 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 | 22 | a0001c0001t0003g0001a0001c0001t0003g0274a0001c0001t0003g0275others(19): Show | 23 | HG00140.hp2 HG00735.hp2 HG00738.hp1 others(20): 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 | a0001c0001t0002g0159a0001c0001t0002g0243a0001c0001t0012g0112others(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 | a0001c0001t0002g0115 | 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 | a0001c0001t0009g0011a0001c0001t0009g0023a0001c0001t0009g0024others(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 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0001t0001g0220others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(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 | a0001c0001t0005g0253a0001c0001t0005g0254a0001c0001t0005g0256others(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 | a0001c0001t0001g0013 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0002t0015g0151 | 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 | a0001c0001t0002g0127a0001c0001t0002g0130 | 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 | a0001c0001t0006g0184 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0002g0217a0001c0001t0017g0005a0001c0001t0017g0006others(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 | a0001c0004t0056g0008a0001c0004t0057g0185 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0016g0009a0001c0001t0016g0010 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0012g0215 | 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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(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 | a0001c0001t0001g0041a0001c0001t0002g0102a0001c0001t0002g0103others(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 | a0001c0004t0056g0008a0001c0004t0057g0185 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0040g0164 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0006g0178 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0003t0014g0079a0001c0003t0014g0096a0001c0003t0014g0098 | 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 | a0001c0002t0004g0194a0001c0002t0004g0195a0001c0002t0004g0196others(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 | a0001c0001t0001g0061a0001c0001t0001g0090a0001c0001t0049g0062 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0004t0056g0008a0001c0004t0057g0185 | 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 | a0001c0001t0002g0241 | 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 | a0001c0001t0002g0124 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0002g0092 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0002g0154 | 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 | a0001c0001t0055g0209 | 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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0055g0209 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0001g0066a0001c0001t0001g0068a0001c0001t0001g0069 | 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 | a0001c0001t0002g0092 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0001g0061a0001c0001t0001g0090a0001c0001t0049g0062 | 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 | a0001c0001t0002g0102a0001c0001t0002g0103a0001c0001t0002g0104others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0055g0209 | 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 | a0001c0001t0006g0177a0001c0001t0006g0178a0001c0001t0006g0179others(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 | a0001c0002t0004g0247 | 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 | a0001c0001t0002g0170a0001c0001t0002g0217a0001c0001t0002g0224others(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 | a0001c0004t0056g0008a0001c0004t0057g0185 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0001g0238a0001c0001t0003g0297a0001c0001t0009g0011others(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 | a0001c0001t0010g0187a0001c0001t0010g0188a0001c0001t0010g0244others(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 | a0001c0001t0002g0170a0001c0001t0002g0207a0001c0001t0002g0208others(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 | a0001c0001t0001g0238a0001c0001t0002g0139a0001c0001t0005g0261others(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 | a0001c0001t0005g0253a0001c0001t0005g0254a0001c0001t0005g0256others(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 | a0001c0001t0001g0022a0001c0001t0001g0045a0001c0001t0001g0097 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0003g0278a0001c0001t0003g0298a0001c0001t0003g0300 | 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 | a0001c0001t0006g0177a0001c0001t0006g0178a0001c0001t0006g0179others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0002g0115a0001c0001t0002g0131 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | 213 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(210): Show | 214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): 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 | a0001c0002t0004g0194a0001c0002t0004g0195a0001c0002t0004g0196others(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 | a0001c0001t0005g0253a0001c0001t0005g0254a0001c0001t0005g0256others(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 | a0001c0001t0001g0220 | 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 | a0001c0001t0055g0209 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0001g0043a0001c0001t0002g0125a0001c0001t0002g0144others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0009g0011a0001c0001t0009g0023a0001c0001t0009g0024others(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 | 213 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(210): Show | 214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): 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 | a0001c0001t0026g0266a0001c0001t0026g0267a0001c0001t0035g0265 | 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 | a0001c0002t0015g0204 | 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 | a0001c0001t0016g0012 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | 215 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(212): Show | 216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): 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 | a0001c0004t0056g0008a0001c0004t0057g0185 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0010g0244 | 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 | a0001c0004t0056g0008a0001c0004t0057g0185 | 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 | a0001c0001t0001g0015 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0002t0015g0151 | 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 | a0001c0001t0001g0239a0001c0001t0009g0011a0001c0001t0009g0023others(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 | 202 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(199): Show | 203 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(200): 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0048g0132 | 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 | a0001c0001t0029g0301 | 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 | a0001c0002t0015g0151a0001c0002t0015g0152 | 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 | a0001c0004t0056g0008a0001c0004t0057g0185 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0004t0057g0185 | 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 | a0001c0001t0002g0216 | 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 | a0001c0001t0022g0189 | 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 | a0001c0001t0003g0271a0001c0001t0003g0287 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0055g0209 | 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 | a0001c0001t0020g0123a0001c0001t0020g0138 | 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 | a0001c0001t0002g0169 | 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 | a0001c0002t0004g0198a0001c0002t0004g0225 | 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 | a0001c0001t0003g0270a0001c0001t0003g0273a0001c0001t0010g0186others(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 | a0001c0001t0021g0167a0001c0001t0021g0171 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | 3 | a0001c0001t0003g0280a0001c0001t0003g0286a0001c0001t0003g0295 | 3 | HG01256.hp1 HG01258.hp1 homoSapiens_chm13v2.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 | a0001c0001t0026g0266a0001c0001t0026g0267a0001c0001t0035g0265 | 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 | 205 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(202): Show | 206 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(203): 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 | a0001c0001t0001g0016 | 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 | a0001c0001t0001g0016 | 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 | a0001c0002t0015g0151a0001c0002t0015g0152 | 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 | a0001c0001t0001g0053 | 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 | a0001c0001t0022g0189a0001c0001t0022g0201 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0001g0074a0001c0001t0002g0147a0001c0001t0006g0177others(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 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0001t0001g0028others(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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0016others(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 | a0001c0001t0005g0253a0001c0001t0005g0259a0001c0001t0005g0260others(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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0002g0173a0001c0001t0002g0242a0001c0002t0031g0210 | 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 | a0001c0001t0055g0209a0001c0005t0013g0109a0001c0005t0013g0110others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0002g0174 | 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 | a0003c0008t0002g0105 | 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 | a0001c0001t0006g0177 | 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 | 232 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(229): Show | 233 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(230): 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 | a0001c0001t0002g0129 | 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 | a0001c0001t0002g0170a0001c0001t0002g0224a0001c0001t0042g0211 | 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 | a0001c0001t0022g0189a0001c0001t0022g0201 | 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 | a0001c0001t0019g0304a0001c0001t0019g0305a0001c0001t0030g0306others(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 | a0001c0001t0002g0146 | 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 | a0001c0001t0001g0053 | 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 | a0001c0005t0013g0109a0001c0005t0013g0110a0001c0010t0013g0108 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0002g0114a0001c0001t0002g0174 | 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 | a0001c0002t0031g0210 | 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 | a0001c0002t0004g0200 | 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 | a0001c0001t0010g0186a0001c0001t0010g0244a0001c0001t0010g0245 | 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 | a0001c0005t0013g0109a0001c0005t0013g0110a0001c0010t0013g0108 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0001g0239a0001c0001t0009g0011a0001c0001t0009g0023others(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 | a0001c0001t0026g0266a0001c0001t0026g0267a0001c0001t0035g0265 | 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 | a0001c0001t0003g0273 | 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 | a0001c0001t0026g0266a0001c0001t0026g0267a0001c0001t0033g0205others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | 67 | a0001c0001t0003g0001a0001c0001t0003g0269a0001c0001t0003g0270others(64): Show | 68 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(65): 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0041g0054 | 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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(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 | a0001c0001t0003g0307a0001c0001t0039g0227 | 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 | a0001c0001t0019g0305 | 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 | a0001c0001t0002g0214a0001c0001t0002g0216 | 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 | a0001c0001t0001g0219a0001c0001t0002g0124a0001c0001t0002g0125others(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 | a0001c0001t0001g0223a0001c0001t0002g0144a0001c0001t0006g0179others(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 | a0001c0001t0009g0011a0001c0001t0009g0024a0001c0001t0009g0025others(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 | a0001c0003t0014g0079a0001c0003t0014g0096a0001c0003t0014g0098 | 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 | 110 | a0001c0001t0003g0001a0001c0001t0003g0269a0001c0001t0003g0270others(107): Show | 111 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(108): 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 | a0001c0001t0028g0303 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0005g0253a0001c0001t0005g0254a0001c0001t0005g0256others(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 | a0001c0001t0003g0271a0001c0001t0003g0287 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0007g0136 | 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 | a0001c0001t0002g0207 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0003g0277 | 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 | a0001c0001t0003g0269a0001c0009t0003g0268 | 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 | a0001c0001t0003g0276 | 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 | a0001c0001t0011g0252a0001c0001t0011g0255a0001c0001t0011g0258 | 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 | a0001c0001t0001g0097 | 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 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(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 | ||||||
| chr7:138556903
|
T | G | 310 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(307): Show | 311 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.1530+1937T>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138556903 | ||||||
| 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0005t0013g0109a0001c0005t0013g0110a0001c0010t0013g0108 | 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 | a0001c0001t0006g0177a0001c0001t0006g0178a0001c0001t0006g0179others(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 | a0001c0001t0026g0266a0001c0001t0026g0267a0001c0001t0035g0265 | 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 | a0001c0001t0003g0283a0001c0001t0003g0284a0001c0001t0003g0289others(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 | 113 | a0001c0001t0001g0239a0001c0001t0003g0001a0001c0001t0003g0269others(110): Show | 114 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(111): 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 | a0001c0005t0013g0109a0001c0005t0013g0110a0001c0010t0013g0108 | 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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(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 | a0001c0004t0056g0008a0001c0004t0057g0185 | 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 | a0001c0001t0006g0177a0001c0001t0006g0178a0001c0001t0006g0179others(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 | a0001c0001t0005g0253a0001c0001t0005g0254a0001c0001t0005g0256others(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 | a0001c0001t0003g0269a0001c0009t0003g0268 | 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 | a0001c0001t0005g0253a0001c0001t0005g0254a0001c0001t0005g0256others(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 | a0001c0001t0003g0282 | 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 | a0001c0001t0043g0119 | 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 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0150 | 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 | a0001c0001t0005g0253a0001c0001t0005g0254a0001c0001t0005g0256others(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 | a0001c0001t0008g0272a0001c0010t0013g0108 | 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 | a0001c0001t0005g0253a0001c0001t0005g0254a0001c0001t0005g0256others(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 | a0001c0001t0026g0266a0001c0001t0026g0267a0001c0001t0035g0265 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0009g0011a0001c0001t0009g0023a0001c0001t0009g0024others(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 | a0001c0001t0046g0262a0001c0005t0013g0109a0001c0005t0013g0110others(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 | a0001c0001t0002g0170a0001c0001t0002g0224a0001c0001t0042g0211 | 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 | 188 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(185): Show | 189 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(186): 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 | a0001c0001t0005g0253a0001c0001t0005g0254a0001c0001t0005g0256others(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 | a0001c0004t0056g0008a0001c0004t0057g0185 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0002g0114 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0005g0253a0001c0001t0005g0254a0001c0001t0005g0256others(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 | a0001c0001t0001g0015 | 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 | a0001c0001t0009g0011a0001c0001t0009g0023a0001c0001t0009g0024others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0001g0075 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0005g0253a0001c0001t0005g0254a0001c0001t0005g0256others(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 | a0001c0001t0002g0214a0001c0001t0002g0216 | 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 | a0001c0001t0012g0215 | 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 | a0001c0001t0002g0174 | 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 | a0001c0001t0001g0220 | 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 | a0001c0003t0014g0079a0001c0003t0014g0096a0001c0003t0014g0098 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0016others(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 | a0001c0001t0038g0149 | 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 | a0001c0001t0002g0140 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0001g0221 | 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 | a0001c0001t0012g0112 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0003g0276 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0001g0058a0001c0001t0001g0072a0001c0001t0001g0077others(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 | a0001c0001t0009g0011a0001c0001t0009g0023a0001c0001t0009g0024others(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 | a0001c0001t0018g0003a0001c0001t0018g0004a0001c0001t0055g0209 | 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 | a0001c0001t0050g0222 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0018g0002a0001c0001t0018g0003a0001c0001t0018g0004 | 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 | a0001c0004t0056g0008a0001c0004t0057g0185 | 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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(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 | a0001c0001t0003g0285a0001c0001t0008g0272a0001c0001t0008g0291others(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 | 206 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(203): Show | 207 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(204): 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0002t0004g0191 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0019g0304 | 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 | a0001c0001t0001g0239a0001c0001t0009g0011a0001c0001t0009g0023others(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 | a0001c0001t0001g0238a0001c0001t0002g0248a0001c0001t0007g0117others(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 | a0001c0001t0006g0183a0001c0001t0006g0184 | 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 | a0001c0001t0001g0239a0001c0001t0009g0011a0001c0001t0009g0023others(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 | a0001c0001t0022g0189a0001c0001t0022g0201 | 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 | a0001c0001t0005g0253a0001c0001t0005g0254a0001c0001t0005g0256others(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 | a0001c0004t0056g0008a0001c0004t0057g0185 | 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 | a0001c0001t0002g0207 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0055g0209 | 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 | a0001c0001t0002g0170a0001c0001t0002g0217a0001c0001t0002g0224others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0002t0004g0195 | 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 | 64 | a0001c0001t0003g0001a0001c0001t0003g0269a0001c0001t0003g0270others(61): Show | 65 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(62): Show |
intron_variant | MODIFIER | c.1531-2240G>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | chr7 | 138565241 | ||||||
| chr7:138565377
|
T | C | 207 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(204): Show | 208 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(205): 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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | 207 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(204): Show | 208 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(205): 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 | a0001c0001t0002g0158 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0003t0014g0079a0001c0003t0014g0096a0001c0003t0014g0098 | 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 | a0001c0001t0001g0059 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0016g0010 | 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 | a0001c0001t0001g0058 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0011g0252a0001c0001t0011g0255 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0002g0174 | 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 | a0001c0001t0055g0209 | 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 | a0001c0001t0055g0209 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0003t0014g0079a0001c0003t0014g0096a0001c0003t0014g0098 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0033g0205 | 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 | a0001c0001t0002g0092 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0004t0056g0008a0001c0004t0057g0185 | 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 | a0001c0001t0003g0288a0001c0001t0003g0296 | 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 | a0001c0002t0004g0148a0001c0002t0004g0191a0001c0002t0004g0193others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0005g0256a0001c0001t0005g0257a0001c0001t0005g0259others(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 | a0001c0004t0056g0008a0001c0004t0057g0185 | 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 | a0001c0001t0001g0081a0001c0001t0001g0084a0001c0001t0001g0236others(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 | a0001c0001t0011g0252a0001c0001t0011g0255 | 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 | a0001c0001t0001g0081a0001c0001t0001g0236a0001c0001t0002g0107others(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 | a0001c0001t0001g0049a0001c0001t0001g0074a0001c0001t0001g0075others(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 | a0001c0001t0001g0035a0001c0001t0001g0042a0001c0001t0001g0044others(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 | a0001c0001t0001g0029a0001c0001t0001g0040a0001c0001t0001g0043others(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 | a0001c0001t0001g0028a0001c0001t0001g0041a0001c0001t0001g0058others(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 | a0001c0001t0001g0047a0001c0001t0001g0063a0001c0001t0001g0095others(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 | a0001c0003t0014g0098 | 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 | a0001c0001t0001g0019a0001c0001t0001g0057a0001c0001t0001g0220 | 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 | a0001c0001t0009g0011a0001c0001t0016g0009 | 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 | a0001c0001t0001g0015a0001c0001t0050g0222 | 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 | a0001c0001t0001g0073a0001c0001t0001g0091 | 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 | a0001c0001t0001g0036a0001c0001t0001g0070 | 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 | a0001c0001t0001g0013a0001c0001t0001g0065a0001c0001t0009g0024others(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 | a0001c0001t0001g0069 | 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 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0066 | 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 | a0001c0001t0001g0087 | 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 | a0001c0001t0001g0021a0001c0001t0001g0059 | 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 | a0001c0001t0055g0209 | 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 | a0001c0001t0009g0027 | 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 | a0001c0001t0001g0020 | 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 | a0001c0001t0002g0106a0001c0001t0002g0144a0001c0001t0002g0206others(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 | a0001c0001t0005g0253a0001c0001t0005g0254a0001c0001t0005g0257others(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 | a0001c0001t0001g0067a0001c0001t0005g0259a0001c0001t0006g0177others(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 | a0001c0001t0001g0045a0001c0001t0003g0270a0001c0001t0003g0309others(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 | 56 | a0001c0001t0001g0071a0001c0001t0001g0076a0001c0001t0003g0001others(53): Show | 57 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(54): 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 | a0001c0001t0001g0018 | 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 | a0001c0001t0016g0012 | 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 | a0001c0001t0001g0055a0001c0001t0001g0082a0001c0001t0054g0080 | 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 | a0001c0001t0001g0071a0001c0001t0001g0076 | 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 | a0001c0001t0007g0160a0001c0001t0007g0202 | 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 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033 | 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 | a0001c0001t0005g0253a0001c0001t0005g0254a0001c0001t0005g0256others(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 | a0001c0001t0005g0253a0001c0001t0005g0254a0001c0001t0005g0256others(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 | a0001c0001t0016g0009a0001c0001t0016g0010 | 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 | a0001c0005t0013g0109a0001c0005t0013g0110a0001c0010t0013g0108 | 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 | a0001c0001t0005g0253a0001c0001t0005g0254a0001c0001t0005g0256others(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 | 196 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(193): Show | 197 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(194): 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 | a0001c0001t0005g0253a0001c0001t0005g0254a0001c0001t0005g0256others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0033g0205 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | 6 | a0001c0001t0003g0280a0001c0001t0003g0282a0001c0001t0003g0286others(3): Show | 6 | HG01256.hp1 HG01258.hp1 HG02559.hp2 others(3): 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0001g0055a0001c0001t0001g0235a0001c0001t0002g0214others(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 | a0001c0001t0001g0072a0001c0001t0001g0226a0001c0001t0003g0280others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0001g0059 | 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 | a0001c0001t0009g0011a0001c0001t0009g0023a0001c0001t0009g0024others(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 | a0001c0001t0009g0011a0001c0001t0009g0023a0001c0001t0009g0024others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(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 | a0001c0001t0001g0035a0001c0001t0001g0052a0001c0001t0001g0059others(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 | a0001c0001t0002g0214a0001c0001t0002g0216 | 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 | a0001c0001t0055g0209 | 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 | a0001c0002t0004g0148a0001c0002t0004g0193a0001c0002t0004g0194others(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 | a0001c0001t0002g0173a0001c0001t0002g0242 | 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 | a0001c0001t0033g0205 | 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 | a0001c0001t0001g0021 | 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 | a0001c0001t0010g0187 | 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 | a0001c0001t0002g0206 | 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 | a0001c0001t0009g0011a0001c0001t0009g0023a0001c0001t0009g0024others(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 | a0001c0001t0020g0123a0001c0001t0020g0138 | 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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(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 | a0001c0004t0056g0008a0001c0004t0057g0185 | 2 | HG02055.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1878+922A>G | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 11/18 | chr7 | 138571925 | ||||||
| chr7:138572164
|
C | T | 1 | a0001c0001t0003g0295 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1878+1161C>T | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 11/18 | chr7 | 138572164 | ||||||
| chr7:138572383
|
A | G | 2 | a0001c0001t0003g0270a0001c0001t0003g0309 | 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 | 63 | a0001c0001t0003g0001a0001c0001t0003g0269a0001c0001t0003g0270others(60): Show | 64 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(61): 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 | 63 | a0001c0001t0003g0001a0001c0001t0003g0269a0001c0001t0003g0270others(60): Show | 64 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(61): 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 | a0001c0005t0013g0109a0001c0005t0013g0110a0001c0010t0013g0108 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0001g0221 | 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 | a0001c0001t0003g0271a0001c0001t0003g0287 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | 206 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(203): Show | 207 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(204): 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 | a0001c0001t0009g0023a0001c0001t0009g0024a0001c0001t0009g0025others(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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(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 | a0001c0001t0026g0266a0001c0001t0026g0267a0001c0001t0035g0265 | 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 | a0001c0001t0026g0266a0001c0001t0026g0267a0001c0001t0035g0265 | 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 | a0001c0001t0009g0011a0001c0001t0009g0023a0001c0001t0009g0024others(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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | 22 | a0001c0001t0003g0001a0001c0001t0003g0274a0001c0001t0003g0275others(19): Show | 23 | HG00140.hp2 HG00735.hp2 HG00738.hp1 others(20): 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0022g0189a0001c0001t0022g0201 | 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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(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 | a0001c0001t0001g0015 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0003g0275 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2014+490T>C | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 12/18 | chr7 | 138574132 | ||||||
| chr7:138574228
|
C | A | 310 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(307): Show | 311 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.2014+586C>A | TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 12/18 | chr7 | 138574228 | ||||||
| chr7:138574414
|
G | A | 1 | a0001c0002t0004g0194 | 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 | a0001c0001t0026g0266a0001c0001t0026g0267a0001c0001t0035g0265 | 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 | a0001c0001t0009g0011a0001c0001t0009g0023a0001c0001t0009g0024others(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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0001g0052a0001c0004t0056g0008a0001c0004t0057g0185 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0001g0018a0001c0001t0001g0084a0001c0001t0001g0099others(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 | a0001c0001t0006g0177a0001c0001t0006g0178a0001c0001t0006g0179others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0007g0160 | 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 | a0001c0001t0007g0160 | 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 | a0001c0001t0007g0160 | 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 | a0001c0001t0007g0160 | 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 | a0001c0001t0007g0160 | 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 | a0001c0001t0007g0160 | 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 | a0001c0001t0007g0160 | 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 | a0001c0001t0007g0160 | 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 | a0001c0001t0007g0160 | 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 | a0001c0001t0007g0160 | 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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(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 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0001t0001g0220others(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 | a0001c0001t0006g0177a0001c0001t0006g0178a0001c0001t0006g0179others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | 44 | a0001c0001t0003g0001a0001c0001t0003g0269a0001c0001t0003g0270others(41): Show | 45 | HG00140.hp2 HG00735.hp2 HG00738.hp1 others(42): 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 | a0001c0001t0040g0164 | 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 | a0001c0001t0001g0015 | 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 | a0001c0001t0011g0263a0001c0001t0011g0264 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | 235 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(232): Show | 236 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(233): 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0002t0015g0151a0001c0002t0015g0152 | 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 | a0001c0001t0002g0173 | 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 | a0001c0004t0056g0008a0001c0004t0057g0185 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0005t0013g0109a0001c0005t0013g0110 | 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 | a0001c0001t0005g0253a0001c0001t0005g0254a0001c0001t0005g0256others(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 | a0001c0001t0040g0164 | 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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(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 | 187 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(184): Show | 188 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(185): 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 | a0001c0005t0013g0109a0001c0005t0013g0110a0001c0010t0013g0108 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0006g0177a0001c0001t0006g0178a0001c0001t0006g0179others(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 | a0001c0001t0003g0274 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0002g0107a0001c0001t0002g0126a0001c0001t0002g0140others(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 | a0001c0001t0003g0269a0001c0001t0003g0290a0001c0001t0003g0298others(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 | 31 | a0001c0001t0003g0001a0001c0001t0003g0270a0001c0001t0003g0271others(28): Show | 32 | HG00140.hp2 HG00735.hp2 HG00738.hp1 others(29): 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 | a0001c0001t0009g0011a0001c0001t0009g0023a0001c0001t0009g0025others(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 | a0001c0001t0001g0071a0001c0001t0001g0076a0001c0001t0009g0024 | 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 | a0001c0007t0036g0190 | 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 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0001t0001g0220others(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 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0001t0001g0220others(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 | a0001c0001t0001g0041a0001c0001t0001g0091a0001c0001t0050g0222 | 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 | a0001c0001t0006g0178a0001c0001t0006g0179a0001c0001t0006g0180others(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 | 72 | a0001c0001t0001g0041a0001c0001t0001g0066a0001c0001t0001g0087others(69): Show | 73 | HG00140.hp2 HG00280.hp1 HG00609.hp1 others(70): 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 | a0001c0001t0005g0253a0001c0001t0005g0254a0001c0001t0005g0259others(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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0017others(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 | a0001c0001t0003g0288a0001c0001t0005g0256a0001c0001t0005g0257others(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 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0031others(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 | a0001c0001t0001g0063 | 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 | a0001c0005t0013g0109a0001c0005t0013g0110a0001c0010t0013g0108 | 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 | a0001c0001t0001g0029a0001c0001t0001g0045a0001c0001t0001g0046others(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 | a0001c0001t0001g0097 | 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 | a0001c0003t0014g0079a0001c0003t0014g0096a0001c0003t0014g0098 | 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 | a0001c0001t0001g0022a0001c0001t0001g0028a0001c0001t0001g0036others(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 | a0001c0001t0017g0007a0001c0001t0026g0266a0001c0001t0026g0267others(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 | a0001c0001t0017g0005a0001c0001t0017g0006 | 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 | a0001c0001t0001g0034 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0004t0056g0008a0001c0004t0057g0185 | 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 | a0001c0002t0004g0197 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0002g0175 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(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 | a0001c0001t0008g0272 | 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 | a0001c0001t0003g0001a0001c0001t0003g0289a0001c0001t0004g0281others(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 | a0001c0001t0006g0177a0001c0001t0006g0178a0001c0001t0006g0179others(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 | a0001c0004t0057g0185 | 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 | a0001c0001t0024g0037a0001c0001t0024g0038 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0026g0266a0001c0001t0026g0267a0001c0001t0033g0205others(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 | 46 | a0001c0001t0003g0001a0001c0001t0003g0269a0001c0001t0003g0270others(43): Show | 47 | HG00140.hp2 HG00735.hp2 HG00738.hp1 others(44): 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 | a0001c0001t0009g0011a0001c0001t0009g0023a0001c0001t0009g0024others(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 | a0001c0010t0013g0108 | 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 | a0001c0001t0003g0279 | 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 | a0001c0001t0002g0228a0001c0001t0002g0251a0001c0001t0045g0233 | 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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(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 | a0001c0004t0056g0008a0001c0004t0057g0185 | 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 | a0001c0001t0003g0299 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0002g0102 | 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 | a0001c0010t0013g0108 | 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 | a0001c0001t0002g0150 | 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 | a0001c0001t0002g0156 | 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 | a0001c0004t0056g0008a0001c0004t0057g0185 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0005g0253a0001c0001t0005g0254a0001c0001t0005g0256others(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 | a0001c0001t0001g0047 | 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 | a0001c0002t0004g0246a0001c0002t0004g0247 | 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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(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 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0051g0030 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0006g0177a0001c0001t0006g0178a0001c0001t0006g0179others(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 | 61 | a0001c0001t0003g0001a0001c0001t0003g0269a0001c0001t0003g0270others(58): Show | 62 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(59): 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 | a0001c0001t0026g0266a0001c0001t0026g0267a0001c0001t0035g0265 | 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0009g0011a0001c0001t0009g0023a0001c0001t0009g0024others(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 | a0001c0001t0001g0033a0001c0001t0001g0078a0001c0001t0001g0090others(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 | a0001c0001t0001g0075a0001c0001t0002g0213a0001c0001t0003g0283others(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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0002g0129 | 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 | a0001c0001t0001g0047a0001c0001t0001g0093 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0009g0011a0001c0001t0009g0023a0001c0001t0009g0024others(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 | a0001c0001t0016g0009a0001c0001t0016g0010 | 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 | a0001c0001t0003g0282 | 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 | a0001c0002t0004g0193 | 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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0001t0010g0188others(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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | 67 | a0001c0001t0003g0001a0001c0001t0003g0269a0001c0001t0003g0270others(64): Show | 68 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(65): 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 | a0001c0001t0017g0005a0001c0001t0017g0006a0001c0001t0017g0007 | 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 | a0001c0001t0008g0272 | 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 | a0001c0001t0006g0177a0001c0001t0006g0178a0001c0001t0006g0179others(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 |