Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 51592 |
|---|---|
| ensemblid | ENSG00000197323.12 |
| hgncid | 16290 |
| symbol | TRIM33 |
| name | tripartite motif containing 33 |
| refseq_nuc | NM_015906.4 |
| refseq_prot | NP_056990.3 |
| ensembl_nuc | ENST00000358465.7 |
| ensembl_prot | ENSP00000351250.2 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 114392790 |
| end | 114511203 |
| strand | - |
| ver | v1.2 |
| region | chr1:114392790-114511203 |
| region5000 | chr1:114387790-114516203 |
| regionname0 | TRIM33_chr1_114392790_114511203 |
| regionname5000 | TRIM33_chr1_114387790_114516203 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 1127 | 168 | 61 | 40 | 31 | 6 | 29 | 19 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| a0002 | 1/0 | 1127 | 28 | 1 | 12 | 14 | 0 | 0 | 7 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| a0003 | 0/0 | 1127 | 10 | 8 | 0 | 1 | 0 | 1 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| a0004 | 0/0 | 1127 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| a0005 | 0/0 | 1127 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 3384 | 93 | 26 | 24 | 25 | 4 | 14 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| c0002 | 0/1 | 3384 | 63 | 25 | 16 | 5 | 2 | 14 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| c0003 | 1/0 | 3384 | 28 | 1 | 12 | 14 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| c0004 | 0/0 | 3384 | 10 | 8 | 0 | 1 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| c0005 | 0/0 | 3384 | 6 | 6 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| c0006 | 0/0 | 3384 | 5 | 4 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| c0007 | 0/0 | 3384 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| c0008 | 0/0 | 3384 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| c0009 | 0/0 | 3384 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 4986 | 45 | 9 | 14 | 15 | 1 | 5 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| t0002 | 0/0 | 4987 | 37 | 10 | 8 | 13 | 0 | 6 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| t0003 | 0/0 | 4988 | 18 | 0 | 7 | 4 | 1 | 6 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| t0004 | 0/0 | 4987 | 11 | 8 | 2 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| t0005 | 0/0 | 4988 | 10 | 4 | 2 | 0 | 0 | 4 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| t0006 | 0/0 | 4989 | 8 | 6 | 1 | 0 | 1 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| t0007 | 0/0 | 4987 | 6 | 6 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| t0008 | 0/0 | 4986 | 6 | 0 | 6 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| t0009 | 0/0 | 4988 | 4 | 4 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| t0010 | 0/0 | 4987 | 4 | 4 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| t0011 | 0/0 | 4987 | 3 | 2 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| t0012 | 0/0 | 4988 | 3 | 1 | 0 | 2 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| t0013 | 0/0 | 4988 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| t0014 | 0/0 | 4988 | 3 | 1 | 0 | 1 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| t0015 | 0/0 | 4986 | 3 | 0 | 1 | 0 | 2 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| t0016 | 0/0 | 4985 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| t0017 | 0/0 | 4988 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| t0018 | 0/0 | 4989 | 2 | 1 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| t0019 | 0/0 | 4987 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| t0020 | 0/0 | 4987 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| t0021 | 0/0 | 4989 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| t0022 | 0/0 | 4986 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| t0023 | 0/0 | 4989 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| t0024 | 0/0 | 4985 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| t0025 | 0/0 | 4989 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| t0026 | 0/0 | 4989 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| t0027 | 0/0 | 4991 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| t0028 | 0/0 | 4986 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| t0029 | 0/0 | 4988 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| t0030 | 0/0 | 4988 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| t0031 | 0/0 | 4988 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| t0032 | 0/0 | 4988 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| t0033 | 0/0 | 4988 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| t0034 | 0/0 | 4990 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| t0035 | 0/0 | 4987 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| t0036 | 0/0 | 4987 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| t0037 | 0/0 | 4988 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| t0038 | 0/0 | 4987 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| t0039 | 0/0 | 4987 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| t0040 | 0/0 | 4986 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| t0041 | 0/1 | 4986 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| t0042 | 0/0 | 4986 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| t0043 | 0/0 | 4987 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| t0044 | 0/0 | 4986 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| t0045 | 0/0 | 4986 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| t0046 | 0/0 | 4988 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| t0047 | 0/0 | 4986 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| t0048 | 0/0 | 4985 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| t0049 | 0/0 | 4988 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| t0050 | 0/0 | 4987 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| t0051 | 0/0 | 4987 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0018 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0110 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 3384 | 93 | 26 | 24 | 25 | 4 | 14 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| a0001c0002 | 0/1 | 3384 | 63 | 25 | 16 | 5 | 2 | 14 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| a0001c0005 | 0/0 | 3384 | 6 | 6 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| a0001c0006 | 0/0 | 3384 | 5 | 4 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| a0001c0009 | 0/0 | 3384 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| a0002c0003 | 1/0 | 3384 | 28 | 1 | 12 | 14 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| a0003c0004 | 0/0 | 3384 | 10 | 8 | 0 | 1 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| a0004c0007 | 0/0 | 3384 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| a0005c0008 | 0/0 | 3384 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 8369 | 26 | 6 | 9 | 5 | 1 | 5 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| a0001c0001t0002 | 0/0 | 8370 | 37 | 10 | 8 | 13 | 0 | 6 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| a0001c0001t0004 | 0/0 | 8370 | 4 | 3 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| a0001c0001t0011 | 0/0 | 8370 | 3 | 2 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| a0001c0001t0012 | 0/0 | 8371 | 3 | 1 | 0 | 2 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| a0001c0001t0015 | 0/0 | 8369 | 3 | 0 | 1 | 0 | 2 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| a0001c0001t0017 | 0/0 | 8371 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| a0001c0001t0022 | 0/0 | 8369 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| a0001c0001t0024 | 0/0 | 8368 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| a0001c0001t0026 | 0/0 | 8372 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| a0001c0001t0028 | 0/0 | 8369 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| a0001c0001t0030 | 0/0 | 8371 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| a0001c0001t0035 | 0/0 | 8370 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| a0001c0001t0036 | 0/0 | 8370 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| a0001c0001t0040 | 0/0 | 8369 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| a0001c0001t0042 | 0/0 | 8369 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| a0001c0001t0044 | 0/0 | 8369 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| a0001c0001t0045 | 0/0 | 8369 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| a0001c0001t0047 | 0/0 | 8369 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| a0001c0001t0048 | 0/0 | 8368 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| a0001c0001t0051 | 0/0 | 8370 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| a0001c0002t0003 | 0/0 | 8371 | 18 | 0 | 7 | 4 | 1 | 6 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| a0001c0002t0004 | 0/0 | 8370 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| a0001c0002t0005 | 0/0 | 8371 | 10 | 4 | 2 | 0 | 0 | 4 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| a0001c0002t0006 | 0/0 | 8372 | 8 | 6 | 1 | 0 | 1 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| a0001c0002t0009 | 0/0 | 8371 | 4 | 4 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| a0001c0002t0018 | 0/0 | 8372 | 2 | 1 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| a0001c0002t0019 | 0/0 | 8370 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| a0001c0002t0020 | 0/0 | 8370 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| a0001c0002t0021 | 0/0 | 8372 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| a0001c0002t0023 | 0/0 | 8372 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| a0001c0002t0025 | 0/0 | 8372 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| a0001c0002t0027 | 0/0 | 8374 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| a0001c0002t0029 | 0/0 | 8371 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| a0001c0002t0032 | 0/0 | 8371 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| a0001c0002t0033 | 0/0 | 8371 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| a0001c0002t0034 | 0/0 | 8373 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| a0001c0002t0037 | 0/0 | 8371 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| a0001c0002t0041 | 0/1 | 8369 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| a0001c0002t0043 | 0/0 | 8370 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| a0001c0002t0046 | 0/0 | 8371 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| a0001c0002t0049 | 0/0 | 8371 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| a0001c0005t0007 | 0/0 | 8370 | 6 | 6 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| a0001c0006t0010 | 0/0 | 8370 | 4 | 4 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| a0001c0006t0038 | 0/0 | 8370 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| a0001c0009t0039 | 0/0 | 8370 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| a0002c0003t0001 | 1/0 | 8369 | 17 | 1 | 5 | 10 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| a0002c0003t0004 | 0/0 | 8370 | 2 | 0 | 1 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| a0002c0003t0008 | 0/0 | 8369 | 6 | 0 | 6 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| a0002c0003t0016 | 0/0 | 8368 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| a0003c0004t0001 | 0/0 | 8369 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| a0003c0004t0004 | 0/0 | 8370 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| a0003c0004t0013 | 0/0 | 8371 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| a0003c0004t0014 | 0/0 | 8371 | 3 | 1 | 0 | 1 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| a0003c0004t0031 | 0/0 | 8371 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| a0003c0004t0050 | 0/0 | 8370 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| a0004c0007t0001 | 0/0 | 8369 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| a0005c0008t0013 | 0/0 | 8371 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | copy fasta | chr1 | 114387790 | 114516203 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0004g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0004g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0004g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0004g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0011g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0011g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0011g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0012g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0012g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0012g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0015g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0015g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0015g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0017g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0017g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0022g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0022g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0024g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0026g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0028g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0030g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0035g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0036g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0040g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0042g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0044g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0045g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0047g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0048g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0001t0051g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0003g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0003g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0003g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0003g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0003g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0003g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0003g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0003g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0003g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0003g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0003g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0003g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0003g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0003g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0004g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0004g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0004g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0005g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0005g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0005g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0005g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0005g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0005g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0005g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0005g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0005g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0005g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0006g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0006g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0006g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0006g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0006g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0006g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0006g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0006g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0009g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0009g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0009g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0009g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0018g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0018g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0019g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0019g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0020g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0020g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0021g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0021g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0023g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0025g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0027g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0029g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0032g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0033g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0034g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0037g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0041g0110 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0043g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0046g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0002t0049g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0005t0007g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0005t0007g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0005t0007g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0005t0007g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0005t0007g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0005t0007g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0006t0010g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0006t0010g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0006t0010g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0006t0010g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0006t0038g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0001c0009t0039g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0002c0003t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0002c0003t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0002c0003t0001g0018 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0002c0003t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0002c0003t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0002c0003t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0002c0003t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0002c0003t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0002c0003t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0002c0003t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0002c0003t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0002c0003t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0002c0003t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0002c0003t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0002c0003t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0002c0003t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0002c0003t0004g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0002c0003t0004g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0002c0003t0008g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0002c0003t0008g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0002c0003t0008g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0002c0003t0008g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0002c0003t0008g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0002c0003t0008g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0002c0003t0016g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0002c0003t0016g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0002c0003t0016g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0003c0004t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0003c0004t0004g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0003c0004t0004g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0003c0004t0013g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0003c0004t0013g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0003c0004t0014g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0003c0004t0014g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0003c0004t0014g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0003c0004t0031g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0003c0004t0050g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0004c0007t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| a0005c0008t0013g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0006 | g0089 | EUR | GBR | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG00099 | hp2 | a0001 | c0001 | t0015 | g0051 | EUR | GBR | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG00323 | hp1 | a0001 | c0002 | t0003 | g0138 | EUR | FIN | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG00323 | hp2 | a0001 | c0001 | t0015 | g0063 | EUR | FIN | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0161 | EAS | CHS | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG00438 | hp2 | a0002 | c0003 | t0016 | g0038 | EAS | CHS | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG00558 | hp1 | a0001 | c0001 | t0042 | g0061 | EAS | CHS | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | CHS | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG00642 | hp1 | a0002 | c0003 | t0008 | g0044 | AMR | PUR | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0188 | AMR | PUR | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG00735 | hp1 | a0001 | c0002 | t0006 | g0088 | AMR | PUR | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG00738 | hp1 | a0001 | c0002 | t0003 | g0127 | AMR | PUR | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG00738 | hp2 | a0002 | c0003 | t0008 | g0043 | AMR | PUR | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG00741 | hp2 | a0001 | c0002 | t0018 | g0145 | AMR | PUR | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01071 | hp1 | a0001 | c0001 | t0045 | g0165 | AMR | PUR | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0064 | AMR | PUR | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0189 | AMR | PUR | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01081 | hp2 | a0001 | c0001 | t0004 | g0077 | AMR | PUR | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01099 | hp1 | a0001 | c0002 | t0003 | g0126 | AMR | PUR | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01099 | hp2 | a0001 | c0001 | t0011 | g0054 | AMR | PUR | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01106 | hp1 | a0001 | c0002 | t0046 | g0091 | AMR | PUR | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01106 | hp2 | a0002 | c0003 | t0008 | g0041 | AMR | PUR | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01167 | hp1 | a0001 | c0002 | t0003 | g0137 | AMR | PUR | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0187 | AMR | PUR | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01168 | hp2 | a0001 | c0002 | t0003 | g0136 | AMR | PUR | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0186 | AMR | PUR | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01169 | hp2 | a0001 | c0002 | t0003 | g0139 | AMR | PUR | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01175 | hp2 | a0001 | c0001 | t0026 | g0196 | AMR | PUR | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01192 | hp1 | a0001 | c0002 | t0005 | g0106 | AMR | PUR | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01192 | hp2 | a0001 | c0001 | t0047 | g0053 | AMR | PUR | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01243 | hp2 | a0001 | c0002 | t0049 | g0129 | AMR | PUR | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01257 | hp1 | a0002 | c0003 | t0004 | g0027 | AMR | CLM | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01257 | hp2 | a0001 | c0002 | t0019 | g0100 | AMR | CLM | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01261 | hp1 | a0002 | c0003 | t0008 | g0049 | AMR | CLM | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01261 | hp2 | a0001 | c0002 | t0019 | g0109 | AMR | CLM | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01346 | hp1 | a0002 | c0003 | t0001 | g0034 | AMR | CLM | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01346 | hp2 | a0001 | c0002 | t0003 | g0130 | AMR | CLM | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01361 | hp1 | a0002 | c0003 | t0008 | g0042 | AMR | CLM | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01361 | hp2 | a0001 | c0002 | t0027 | g0090 | AMR | CLM | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01433 | hp1 | a0002 | c0003 | t0001 | g0001 | AMR | CLM | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01433 | hp2 | a0001 | c0002 | t0005 | g0101 | AMR | CLM | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01496 | hp1 | a0002 | c0003 | t0001 | g0001 | AMR | CLM | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0166 | AMR | CLM | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01884 | hp1 | a0001 | c0005 | t0007 | g0192 | AFR | ACB | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01884 | hp2 | a0001 | c0002 | t0004 | g0115 | AFR | ACB | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0182 | AFR | ACB | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01891 | hp2 | a0001 | c0002 | t0009 | g0202 | AFR | ACB | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01928 | hp1 | a0002 | c0003 | t0001 | g0026 | AMR | PEL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0179 | AMR | PEL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01934 | hp1 | a0001 | c0001 | t0044 | g0016 | AMR | PEL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01934 | hp2 | a0002 | c0003 | t0001 | g0047 | AMR | PEL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01952 | hp2 | a0001 | c0002 | t0003 | g0125 | AMR | PEL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01993 | hp1 | a0002 | c0003 | t0008 | g0028 | AMR | PEL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0168 | AMR | PEL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PEL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02004 | hp2 | a0001 | c0001 | t0015 | g0065 | AMR | PEL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | KHV | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02015 | hp2 | a0002 | c0003 | t0001 | g0021 | EAS | KHV | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02055 | hp1 | a0001 | c0001 | t0004 | g0050 | AFR | ACB | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02055 | hp2 | a0003 | c0004 | t0014 | g0012 | AFR | ACB | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02056 | hp1 | a0001 | c0001 | t0040 | g0194 | EAS | KHV | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02056 | hp2 | a0002 | c0003 | t0004 | g0048 | EAS | KHV | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02083 | hp1 | a0002 | c0003 | t0016 | g0040 | EAS | KHV | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | KHV | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02129 | hp1 | a0002 | c0003 | t0001 | g0029 | EAS | KHV | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02129 | hp2 | a0001 | c0001 | t0017 | g0172 | EAS | KHV | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | KHV | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02132 | hp2 | a0001 | c0006 | t0038 | g0124 | EAS | KHV | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02145 | hp1 | a0005 | c0008 | t0013 | g0015 | AFR | ACB | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02145 | hp2 | a0001 | c0001 | t0012 | g0197 | AFR | ACB | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02258 | hp1 | a0003 | c0004 | t0013 | g0010 | AFR | ACB | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0198 | AFR | ACB | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02280 | hp1 | a0003 | c0004 | t0004 | g0006 | AFR | ACB | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02280 | hp2 | a0001 | c0002 | t0006 | g0093 | AFR | ACB | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02451 | hp1 | a0004 | c0007 | t0001 | g0014 | AFR | ACB | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02451 | hp2 | a0001 | c0002 | t0033 | g0117 | AFR | ACB | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02523 | hp1 | a0003 | c0004 | t0014 | g0013 | EAS | KHV | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02523 | hp2 | a0002 | c0003 | t0001 | g0031 | EAS | KHV | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0024 | AFR | GWD | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02572 | hp2 | a0001 | c0002 | t0009 | g0203 | AFR | GWD | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02602 | hp2 | a0001 | c0002 | t0003 | g0142 | SAS | PJL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02615 | hp1 | a0001 | c0002 | t0005 | g0107 | AFR | GWD | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02615 | hp2 | a0001 | c0001 | t0024 | g0003 | AFR | GWD | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02622 | hp1 | a0001 | c0002 | t0020 | g0112 | AFR | GWD | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0181 | AFR | GWD | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0190 | AFR | GWD | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02647 | hp2 | a0001 | c0002 | t0037 | g0118 | AFR | GWD | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02698 | hp1 | a0001 | c0009 | t0039 | g0123 | SAS | PJL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02698 | hp2 | a0001 | c0002 | t0003 | g0141 | SAS | PJL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02723 | hp2 | a0001 | c0002 | t0006 | g0094 | AFR | GWD | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02738 | hp1 | a0001 | c0002 | t0043 | g0140 | SAS | PJL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02738 | hp2 | a0001 | c0001 | t0028 | g0062 | SAS | PJL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0154 | AFR | GWD | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02886 | hp1 | a0001 | c0002 | t0032 | g0116 | AFR | GWD | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02886 | hp2 | a0001 | c0001 | t0011 | g0066 | AFR | GWD | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02895 | hp1 | a0001 | c0002 | t0018 | g0146 | AFR | GWD | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02895 | hp2 | a0001 | c0006 | t0010 | g0121 | AFR | GWD | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02897 | hp1 | a0001 | c0006 | t0010 | g0122 | AFR | GWD | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02897 | hp2 | a0001 | c0005 | t0007 | g0150 | AFR | GWD | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02922 | hp1 | a0001 | c0006 | t0010 | g0119 | AFR | ESN | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02922 | hp2 | a0001 | c0002 | t0005 | g0099 | AFR | ESN | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0148 | AFR | ESN | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02965 | hp2 | a0003 | c0004 | t0001 | g0008 | AFR | ESN | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | ESN | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02970 | hp2 | a0001 | c0002 | t0034 | g0086 | AFR | ESN | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02976 | hp1 | a0001 | c0002 | t0006 | g0096 | AFR | ESN | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02976 | hp2 | a0003 | c0004 | t0031 | g0011 | AFR | ESN | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG03017 | hp1 | a0003 | c0004 | t0014 | g0005 | SAS | PJL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0178 | SAS | PJL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG03041 | hp1 | a0003 | c0004 | t0050 | g0206 | AFR | GWD | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG03041 | hp2 | a0001 | c0005 | t0007 | g0151 | AFR | GWD | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG03098 | hp1 | a0001 | c0001 | t0030 | g0156 | AFR | MSL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG03098 | hp2 | a0001 | c0002 | t0005 | g0098 | AFR | MSL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG03130 | hp1 | a0003 | c0004 | t0004 | g0009 | AFR | ESN | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG03130 | hp2 | a0001 | c0005 | t0007 | g0184 | AFR | ESN | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0155 | AFR | ESN | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG03139 | hp2 | a0001 | c0002 | t0005 | g0104 | AFR | ESN | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0152 | AFR | ESN | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG03195 | hp2 | a0001 | c0002 | t0006 | g0097 | AFR | ESN | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG03209 | hp1 | a0001 | c0002 | t0006 | g0095 | AFR | MSL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG03209 | hp2 | a0001 | c0001 | t0048 | g0081 | AFR | MSL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG03225 | hp2 | a0001 | c0002 | t0020 | g0113 | AFR | MSL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG03453 | hp1 | a0001 | c0001 | t0036 | g0153 | AFR | MSL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG03453 | hp2 | a0001 | c0006 | t0010 | g0120 | AFR | MSL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0185 | AFR | MSL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG03486 | hp2 | a0001 | c0002 | t0009 | g0205 | AFR | MSL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG03490 | hp2 | a0001 | c0002 | t0005 | g0108 | SAS | PJL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG03516 | hp1 | a0001 | c0002 | t0006 | g0087 | AFR | ESN | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0023 | AFR | ESN | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG03579 | hp1 | a0001 | c0002 | t0009 | g0204 | AFR | MSL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG03579 | hp2 | a0003 | c0004 | t0013 | g0007 | AFR | MSL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG03654 | hp1 | a0001 | c0002 | t0005 | g0103 | SAS | PJL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG03654 | hp2 | a0001 | c0002 | t0003 | g0144 | SAS | PJL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0167 | SAS | PJL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG03669 | hp2 | a0001 | c0002 | t0005 | g0102 | SAS | PJL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG03704 | hp1 | a0001 | c0001 | t0022 | g0057 | SAS | PJL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG03704 | hp2 | a0001 | c0002 | t0021 | g0085 | SAS | PJL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0162 | SAS | PJL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG03834 | hp1 | a0001 | c0002 | t0003 | g0143 | SAS | BEB | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0175 | SAS | BEB | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | BEB | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG03927 | hp2 | a0001 | c0002 | t0005 | g0105 | SAS | BEB | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG04115 | hp1 | a0001 | c0002 | t0021 | g0092 | SAS | STU | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0180 | SAS | STU | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG04184 | hp1 | a0001 | c0002 | t0025 | g0004 | SAS | BEB | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG04184 | hp2 | a0001 | c0002 | t0003 | g0134 | SAS | BEB | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0068 | SAS | STU | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | STU | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | CHB | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA18612 | hp2 | a0001 | c0002 | t0029 | g0135 | EAS | CHB | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | CHB | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA18747 | hp2 | a0002 | c0003 | t0001 | g0037 | EAS | CHB | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA18906 | hp1 | a0001 | c0005 | t0007 | g0147 | AFR | YRI | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA18906 | hp2 | a0001 | c0001 | t0011 | g0055 | AFR | YRI | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA18942 | hp2 | a0001 | c0002 | t0003 | g0128 | EAS | JPT | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA18954 | hp2 | a0002 | c0003 | t0001 | g0199 | EAS | JPT | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA18957 | hp1 | a0002 | c0003 | t0016 | g0030 | EAS | JPT | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA18957 | hp2 | a0001 | c0002 | t0003 | g0132 | EAS | JPT | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA18960 | hp2 | a0001 | c0002 | t0003 | g0131 | EAS | JPT | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA18973 | hp2 | a0001 | c0001 | t0012 | g0074 | EAS | JPT | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA18983 | hp1 | a0001 | c0001 | t0051 | g0207 | EAS | JPT | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA18984 | hp1 | a0001 | c0001 | t0017 | g0033 | EAS | JPT | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA18984 | hp2 | a0002 | c0003 | t0001 | g0163 | EAS | JPT | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA19009 | hp1 | a0002 | c0003 | t0001 | g0039 | EAS | JPT | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA19009 | hp2 | a0001 | c0001 | t0012 | g0191 | EAS | JPT | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA19056 | hp2 | a0002 | c0003 | t0001 | g0032 | EAS | JPT | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA19060 | hp1 | a0002 | c0003 | t0001 | g0082 | EAS | JPT | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA19240 | hp1 | a0001 | c0002 | t0023 | g0002 | AFR | YRI | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA19240 | hp2 | a0001 | c0005 | t0007 | g0183 | AFR | YRI | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | ASW | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA20129 | hp2 | a0001 | c0002 | t0004 | g0114 | AFR | ASW | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA20752 | hp1 | a0001 | c0001 | t0035 | g0173 | EUR | TSI | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0070 | EUR | TSI | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA20905 | hp1 | a0001 | c0002 | t0003 | g0201 | SAS | GIH | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA20905 | hp2 | a0001 | c0001 | t0022 | g0056 | SAS | GIH | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02109 | hp1 | a0001 | c0002 | t0004 | g0111 | AFR | ACB | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0195 | AFR | ACB | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| HG02486 | hp2 | a0002 | c0003 | t0001 | g0017 | AFR | ACB | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA18955 | hp1 | a0001 | c0002 | t0003 | g0133 | EAS | JPT | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| NA18955 | hp2 | a0002 | c0003 | t0001 | g0036 | EAS | JPT | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0041 | g0110 | REF | REF | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| homoSapiens_grch38 | hp1 | a0002 | c0003 | t0001 | g0018 | REF | REF | TRIM33_chr1_114387790_114516203 | TRIM33 | chr1 | 114387790 | 114516203 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:114402771
|
C | T | 1 | a0004 | 1 | HG02451.hp1 | missense_variant | MODERATE | c.2881G>A | p.Val961Met | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 16/20 | 3008/8369 | 2881/3384 | 961/1127 | chr1 | 114402771 | ||
| chr1:114405659
|
A | G | 4 | a0001a0003a0004others(1): Show | 180 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(177): Show |
missense_variant | MODERATE | c.2519T>C | p.Ile840Thr | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 15/20 | 2646/8369 | 2519/3384 | 840/1127 | chr1 | 114405659 | ||
| chr1:114510877
|
A | C | 1 | a0005 | 1 | HG02145.hp1 | missense_variant | MODERATE | c.200T>G | p.Val67Gly | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/20 | 327/8369 | 200/3384 | 67/1127 | chr1 | 114510877 | ||
| chr1:114510877
|
A | G | 2 | a0003a0004 | 11 | HG02055.hp2 HG02258.hp1 HG02280.hp1 others(8): Show |
missense_variant | MODERATE | c.200T>C | p.Val67Ala | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/20 | 327/8369 | 200/3384 | 67/1127 | chr1 | 114510877 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:114402772
|
G | A | 1 | a0001c0005 | 6 | HG01884.hp1 HG02897.hp2 HG03041.hp2 others(3): Show |
synonymous_variant | LOW | c.2880C>T | p.Pro960Pro | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 16/20 | 3007/8369 | 2880/3384 | 960/1127 | chr1 | 114402772 | ||
| chr1:114405687
|
A | G | 2 | a0001c0006a0001c0009 | 6 | HG02132.hp2 HG02698.hp1 HG02895.hp2 others(3): Show |
synonymous_variant | LOW | c.2491T>C | p.Leu831Leu | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 15/20 | 2618/8369 | 2491/3384 | 831/1127 | chr1 | 114405687 | ||
| chr1:114421583
|
G | C | 1 | a0001c0009 | 1 | HG02698.hp1 | synonymous_variant | LOW | c.1914C>G | p.Thr638Thr | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/20 | 2041/8369 | 1914/3384 | 638/1127 | chr1 | 114421583 | ||
| chr1:114430807
|
T | C | 6 | a0001c0002a0001c0006a0001c0009others(3): Show | 81 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(78): Show |
synonymous_variant | LOW | c.1146A>G | p.Gln382Gln | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 6/20 | 1273/8369 | 1146/3384 | 382/1127 | chr1 | 114430807 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:114393059
|
C | G | 1 | a0001c0006t0038 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4589G>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 4589 | chr1 | 114393059 | |||||
| chr1:114393457
|
T | A | 4 | a0001c0002t0003a0001c0002t0029a0001c0002t0043others(1): Show | 21 | HG00323.hp1 HG00738.hp1 HG01099.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*4191A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 4191 | chr1 | 114393457 | |||||
| chr1:114393796
|
C | T | 1 | a0003c0004t0031 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3852G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 3852 | chr1 | 114393796 | |||||
| chr1:114394212
|
A | G | 2 | a0001c0002t0018a0001c0002t0037 | 3 | HG00741.hp2 HG02647.hp2 HG02895.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3436T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 3436 | chr1 | 114394212 | |||||
| chr1:114394693
|
G | C | 1 | a0001c0009t0039 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2955C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 2955 | chr1 | 114394693 | |||||
| chr1:114394900
|
T | C | 2 | a0001c0002t0020a0001c0002t0032 | 3 | HG02622.hp1 HG02886.hp1 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2748A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 2748 | chr1 | 114394900 | |||||
| chr1:114395014
|
G | A | 7 | a0001c0001t0030a0001c0001t0036a0001c0002t0033others(4): Show | 12 | HG02055.hp2 HG02132.hp2 HG02451.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2634C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 2634 | chr1 | 114395014 | |||||
| chr1:114395074
|
A | T | 1 | a0001c0002t0009 | 4 | HG01891.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2574T>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 2574 | chr1 | 114395074 | |||||
| chr1:114395141
|
C | T | 1 | a0001c0001t0022 | 2 | HG03704.hp1 NA20905.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2507G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 2507 | chr1 | 114395141 | |||||
| chr1:114395250
|
C | A | 3 | a0001c0002t0005a0001c0002t0019a0001c0002t0041 | 13 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2398G>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 2398 | chr1 | 114395250 | |||||
| chr1:114395468
|
A | AT | 12 | a0001c0002t0003a0001c0002t0006a0001c0002t0018others(9): Show | 38 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*2179dupA | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 2179 | chr1 | 114395468 | |||||
| chr1:114395553
|
C | T | 1 | a0001c0001t0015 | 3 | HG00099.hp2 HG00323.hp2 HG02004.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2095G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 2095 | chr1 | 114395553 | |||||
| chr1:114395635
|
G | A | 1 | a0001c0001t0042 | 1 | HG00558.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2013C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 2013 | chr1 | 114395635 | |||||
| chr1:114395667
|
T | G | 3 | a0001c0002t0003a0001c0002t0043a0001c0002t0049 | 20 | HG00323.hp1 HG00738.hp1 HG01099.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1981A>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 1981 | chr1 | 114395667 | |||||
| chr1:114396077
|
A | G | 1 | a0001c0005t0007 | 6 | HG01884.hp1 HG02897.hp2 HG03041.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1571T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 1571 | chr1 | 114396077 | |||||
| chr1:114396216
|
G | A | 1 | a0001c0001t0044 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1432C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 1432 | chr1 | 114396216 | |||||
| chr1:114396268
|
G | A | 2 | a0001c0002t0020a0001c0002t0032 | 3 | HG02622.hp1 HG02886.hp1 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1380C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 1380 | chr1 | 114396268 | |||||
| chr1:114396276
|
G | T | 1 | a0001c0002t0021 | 2 | HG03704.hp2 HG04115.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1372C>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 1372 | chr1 | 114396276 | |||||
| chr1:114396363
|
T | C | 1 | a0001c0002t0033 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1285A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 1285 | chr1 | 114396363 | |||||
| chr1:114396457
|
A | G | 3 | a0001c0002t0005a0001c0002t0019a0001c0002t0041 | 13 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1191T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 1191 | chr1 | 114396457 | |||||
| chr1:114396463
|
C | T | 1 | a0001c0002t0037 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1185G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 1185 | chr1 | 114396463 | |||||
| chr1:114396917
|
G | A | 1 | a0001c0001t0048 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*731C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 731 | chr1 | 114396917 | |||||
| chr1:114397011
|
G | A | 1 | a0001c0001t0045 | 1 | HG01071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*637C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 637 | chr1 | 114397011 | |||||
| chr1:114397101
|
A | G | 1 | a0001c0002t0049 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*547T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 547 | chr1 | 114397101 | |||||
| chr1:114397108
|
G | GA | 7 | a0001c0002t0006a0001c0002t0021a0001c0002t0023others(4): Show | 15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*539dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 539 | chr1 | 114397108 | |||||
| chr1:114397117
|
T | C | 13 | a0001c0001t0002a0001c0001t0012a0001c0001t0017others(10): Show | 60 | HG00438.hp1 HG00558.hp2 HG00642.hp2 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*531A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 531 | chr1 | 114397117 | |||||
| chr1:114397322
|
A | G | 1 | a0001c0001t0035 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*326T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 326 | chr1 | 114397322 | |||||
| chr1:114397578
|
G | C | 1 | a0001c0001t0047 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*70C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 70 | chr1 | 114397578 | |||||
| chr1:114397580
|
G | GTT | 3 | a0001c0001t0012a0001c0001t0026a0001c0001t0030 | 5 | HG01175.hp2 HG02145.hp2 HG03098.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*66_*67dupAA | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 67 | chr1 | 114397580 | |||||
| chr1:114397587
|
G | T | 7 | a0001c0001t0002a0001c0001t0017a0001c0001t0035others(4): Show | 49 | HG00438.hp1 HG00558.hp2 HG00642.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*61C>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 61 | chr1 | 114397587 | |||||
| chr1:114397589
|
G | GT | 21 | a0001c0001t0002a0001c0001t0004a0001c0001t0017others(18): Show | 83 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*58dupA | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 58 | chr1 | 114397589 | |||||
| chr1:114397589
|
G | GTT | 11 | a0001c0002t0005a0001c0002t0009a0001c0002t0018others(8): Show | 27 | HG00741.hp2 HG01192.hp1 HG01361.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*57_*58dupAA | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 58 | chr1 | 114397589 | |||||
| chr1:114397589
|
G | T | 3 | a0001c0001t0012a0001c0001t0026a0001c0001t0030 | 5 | HG01175.hp2 HG02145.hp2 HG03098.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*59C>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 59 | chr1 | 114397589 | |||||
| chr1:114397589
|
GT | G | 3 | a0001c0001t0024a0001c0001t0048a0002c0003t0016 | 5 | HG00438.hp2 HG02083.hp1 HG02615.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*58delA | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 58 | chr1 | 114397589 | |||||
| chr1:114397593
|
T | TG | 3 | a0001c0002t0003a0001c0002t0029a0001c0002t0049 | 20 | HG00323.hp1 HG00738.hp1 HG01099.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*54_*55insC | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 54 | chr1 | 114397593 | |||||
| chr1:114397605
|
T | C | 1 | a0001c0001t0028 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*43A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 43 | chr1 | 114397605 | |||||
| chr1:114397606
|
C | G | 1 | a0001c0001t0028 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*42G>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 42 | chr1 | 114397606 | |||||
| chr1:114397607
|
G | GT | 5 | a0001c0001t0011a0001c0001t0017a0001c0001t0026others(2): Show | 8 | HG01099.hp2 HG01175.hp2 HG01361.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*40dupA | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 40 | chr1 | 114397607 | |||||
| chr1:114397607
|
G | T | 1 | a0001c0001t0028 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*41C>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 41 | chr1 | 114397607 | |||||
| chr1:114397608
|
T | G | 1 | a0002c0003t0008 | 6 | HG00642.hp1 HG00738.hp2 HG01106.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*40A>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 20/20 | 40 | chr1 | 114397608 | |||||
| chr1:114511107
|
C | G | 1 | a0001c0002t0025 | 1 | HG04184.hp1 | 5_prime_UTR_variant | MODIFIER | c.-31G>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/20 | 31 | chr1 | 114511107 | |||||
| chr1:114511126
|
G | C | 1 | a0003c0004t0050 | 1 | HG03041.hp1 | 5_prime_UTR_variant | MODIFIER | c.-50C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/20 | 50 | chr1 | 114511126 | |||||
| chr1:114511174
|
G | T | 1 | a0001c0001t0024 | 1 | HG02615.hp2 | 5_prime_UTR_variant | MODIFIER | c.-98C>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/20 | 98 | chr1 | 114511174 | |||||
| chr1:114511190
|
C | T | 1 | a0001c0002t0023 | 1 | NA19240.hp1 | 5_prime_UTR_variant | MODIFIER | c.-114G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/20 | 114 | chr1 | 114511190 | |||||
| chr1:114511191
|
G | A | 1 | a0001c0001t0051 | 1 | NA18983.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-115C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/20 | chr1 | 114511191 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:114398010
|
CA | C | 176 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0022others(173): Show | 177 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.3121-21delT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 18/19 | chr1 | 114398010 | ||||||
| chr1:114398163
|
C | T | 1 | a0001c0002t0005g0107 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3121-173G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 18/19 | chr1 | 114398163 | ||||||
| chr1:114398391
|
T | C | 6 | a0001c0002t0004g0111a0001c0002t0004g0114a0001c0002t0004g0115others(3): Show | 6 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.3121-401A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 18/19 | chr1 | 114398391 | ||||||
| chr1:114398483
|
C | A | 1 | a0001c0002t0041g0110 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.3121-493G>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 18/19 | chr1 | 114398483 | ||||||
| chr1:114398547
|
T | C | 4 | a0001c0006t0010g0119a0001c0006t0010g0120a0001c0006t0010g0121others(1): Show | 4 | HG02895.hp2 HG02897.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.3121-557A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 18/19 | chr1 | 114398547 | ||||||
| chr1:114398687
|
A | G | 1 | a0001c0009t0039g0123 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.3121-697T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 18/19 | chr1 | 114398687 | ||||||
| chr1:114398704
|
C | T | 135 | a0001c0001t0002g0035a0001c0001t0002g0064a0001c0001t0002g0068others(132): Show | 135 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(132): Show |
intron_variant | MODIFIER | c.3121-714G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 18/19 | chr1 | 114398704 | ||||||
| chr1:114398853
|
T | C | 1 | a0001c0006t0010g0119 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3120+604A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 18/19 | chr1 | 114398853 | ||||||
| chr1:114398898
|
C | CA | 16 | a0001c0001t0001g0069a0001c0001t0001g0084a0001c0001t0002g0068others(13): Show | 16 | HG00735.hp2 HG02056.hp1 HG02129.hp1 others(13): Show |
intron_variant | MODIFIER | c.3120+558dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 18/19 | chr1 | 114398898 | ||||||
| chr1:114398898
|
C | CAAA | 14 | a0001c0002t0006g0087a0001c0002t0006g0088a0001c0002t0006g0089others(11): Show | 14 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.3120+556_3120+558d others(5): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 18/19 | chr1 | 114398898 | ||||||
| chr1:114398906
|
A | C | 3 | a0002c0003t0001g0021a0002c0003t0016g0030a0002c0003t0016g0040 | 3 | HG02015.hp2 HG02083.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.3120+551T>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 18/19 | chr1 | 114398906 | ||||||
| chr1:114398911
|
A | C | 8 | a0001c0001t0001g0025a0001c0001t0001g0060a0001c0001t0004g0024others(5): Show | 8 | HG00438.hp2 HG02015.hp2 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.3120+546T>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 18/19 | chr1 | 114398911 | ||||||
| chr1:114398912
|
A | AC | 2 | a0001c0002t0009g0202a0001c0002t0009g0203 | 2 | HG01891.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.3120+544_3120+545i others(3): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 18/19 | chr1 | 114398912 | ||||||
| chr1:114398915
|
AC | A | 4 | a0001c0001t0002g0155a0001c0001t0002g0198a0001c0001t0012g0197others(1): Show | 4 | HG02145.hp1 HG02145.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.3120+541delG | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 18/19 | chr1 | 114398915 | ||||||
| chr1:114398916
|
C | A | 1 | a0001c0001t0002g0148 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3120+541G>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 18/19 | chr1 | 114398916 | ||||||
| chr1:114398918
|
A | G | 1 | a0003c0004t0014g0012 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3120+539T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 18/19 | chr1 | 114398918 | ||||||
| chr1:114398926
|
C | CA | 4 | a0001c0005t0007g0147a0001c0005t0007g0150a0001c0005t0007g0151others(1): Show | 4 | HG01884.hp1 HG02897.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.3120+530dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 18/19 | chr1 | 114398926 | ||||||
| chr1:114398931
|
C | A | 134 | a0001c0001t0001g0073a0001c0001t0001g0078a0001c0001t0002g0035others(131): Show | 134 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.3120+526G>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 18/19 | chr1 | 114398931 | ||||||
| chr1:114398971
|
A | C | 1 | a0001c0001t0002g0154 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3120+486T>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 18/19 | chr1 | 114398971 | ||||||
| chr1:114399628
|
G | A | 2 | a0001c0002t0018g0145a0001c0002t0018g0146 | 2 | HG00741.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.2968-19C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 17/19 | chr1 | 114399628 | ||||||
| chr1:114399674
|
T | C | 15 | a0001c0002t0006g0087a0001c0002t0006g0088a0001c0002t0006g0089others(12): Show | 15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.2968-65A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 17/19 | chr1 | 114399674 | ||||||
| chr1:114399817
|
C | T | 1 | a0001c0001t0002g0170 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2968-208G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 17/19 | chr1 | 114399817 | ||||||
| chr1:114399833
|
TTAA | T | 5 | a0003c0004t0001g0008a0003c0004t0004g0009a0003c0004t0013g0010others(2): Show | 5 | HG02145.hp1 HG02258.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.2968-227_2968-225d others(5): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 17/19 | chr1 | 114399833 | ||||||
| chr1:114399882
|
T | C | 4 | a0001c0001t0002g0181a0001c0001t0002g0190a0001c0005t0007g0183others(1): Show | 4 | HG02622.hp2 HG02647.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2968-273A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 17/19 | chr1 | 114399882 | ||||||
| chr1:114400036
|
G | A | 2 | a0001c0001t0001g0045a0001c0001t0001g0046 | 2 | HG02809.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2968-427C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 17/19 | chr1 | 114400036 | ||||||
| chr1:114400108
|
T | C | 12 | a0001c0002t0009g0202a0001c0002t0009g0203a0001c0002t0009g0204others(9): Show | 12 | HG01891.hp2 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.2968-499A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 17/19 | chr1 | 114400108 | ||||||
| chr1:114400364
|
C | T | 15 | a0001c0002t0006g0087a0001c0002t0006g0088a0001c0002t0006g0089others(12): Show | 15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.2968-755G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 17/19 | chr1 | 114400364 | ||||||
| chr1:114400494
|
T | C | 6 | a0001c0002t0004g0111a0001c0002t0004g0114a0001c0002t0004g0115others(3): Show | 6 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.2968-885A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 17/19 | chr1 | 114400494 | ||||||
| chr1:114400726
|
G | T | 9 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0075others(6): Show | 9 | HG00099.hp2 HG00323.hp2 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.2967+663C>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 17/19 | chr1 | 114400726 | ||||||
| chr1:114400732
|
A | G | 1 | a0001c0001t0001g0025 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2967+657T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 17/19 | chr1 | 114400732 | ||||||
| chr1:114401028
|
CT | C | 21 | a0001c0002t0005g0098a0001c0002t0005g0099a0001c0002t0005g0101others(18): Show | 21 | HG00741.hp2 HG01192.hp1 HG01257.hp2 others(18): Show |
intron_variant | MODIFIER | c.2967+360delA | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 17/19 | chr1 | 114401028 | ||||||
| chr1:114401059
|
C | T | 2 | a0003c0004t0001g0008a0003c0004t0004g0009 | 2 | HG02965.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2967+330G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 17/19 | chr1 | 114401059 | ||||||
| chr1:114401098
|
G | A | 12 | a0001c0002t0009g0202a0001c0002t0009g0203a0001c0002t0009g0204others(9): Show | 12 | HG01891.hp2 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.2967+291C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 17/19 | chr1 | 114401098 | ||||||
| chr1:114401099
|
C | T | 3 | a0001c0002t0018g0145a0001c0002t0018g0146a0001c0002t0037g0118 | 3 | HG00741.hp2 HG02647.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.2967+290G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 17/19 | chr1 | 114401099 | ||||||
| chr1:114401161
|
G | C | 15 | a0001c0002t0006g0087a0001c0002t0006g0088a0001c0002t0006g0089others(12): Show | 15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.2967+228C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 17/19 | chr1 | 114401161 | ||||||
| chr1:114401260
|
G | A | 3 | a0003c0004t0004g0006a0003c0004t0013g0007a0003c0004t0050g0206 | 3 | HG02280.hp1 HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2967+129C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 17/19 | chr1 | 114401260 | ||||||
| chr1:114401499
|
T | C | 2 | a0001c0002t0009g0202a0001c0002t0009g0203 | 2 | HG01891.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.2893-36A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 16/19 | chr1 | 114401499 | ||||||
| chr1:114401503
|
T | C | 1 | a0001c0002t0046g0091 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2893-40A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 16/19 | chr1 | 114401503 | ||||||
| chr1:114401917
|
T | C | 1 | a0001c0001t0002g0169 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2893-454A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 16/19 | chr1 | 114401917 | ||||||
| chr1:114402059
|
T | C | 24 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(21): Show | 24 | HG00323.hp1 HG00738.hp1 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.2893-596A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 16/19 | chr1 | 114402059 | ||||||
| chr1:114402063
|
C | T | 15 | a0001c0002t0006g0087a0001c0002t0006g0088a0001c0002t0006g0089others(12): Show | 15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.2893-600G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 16/19 | chr1 | 114402063 | ||||||
| chr1:114402326
|
CACT | C | 4 | a0001c0002t0009g0202a0001c0002t0009g0203a0001c0002t0009g0204others(1): Show | 4 | HG01891.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2892+431_2892+433d others(5): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 16/19 | chr1 | 114402326 | ||||||
| chr1:114402488
|
C | G | 4 | a0001c0002t0009g0202a0001c0002t0009g0203a0001c0002t0009g0204others(1): Show | 4 | HG01891.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2892+272G>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 16/19 | chr1 | 114402488 | ||||||
| chr1:114403012
|
G | A | 15 | a0001c0002t0006g0087a0001c0002t0006g0088a0001c0002t0006g0089others(12): Show | 15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.2769-129C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 15/19 | chr1 | 114403012 | ||||||
| chr1:114403317
|
C | T | 2 | a0001c0002t0004g0114a0001c0002t0004g0115 | 2 | HG01884.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2769-434G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 15/19 | chr1 | 114403317 | ||||||
| chr1:114403349
|
C | A | 1 | a0001c0002t0003g0137 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2769-466G>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 15/19 | chr1 | 114403349 | ||||||
| chr1:114403425
|
C | A | 1 | a0001c0002t0037g0118 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2769-542G>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 15/19 | chr1 | 114403425 | ||||||
| chr1:114403442
|
T | C | 1 | a0001c0001t0048g0081 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2769-559A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 15/19 | chr1 | 114403442 | ||||||
| chr1:114403532
|
G | A | 13 | a0001c0002t0005g0098a0001c0002t0005g0099a0001c0002t0005g0101others(10): Show | 13 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.2769-649C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 15/19 | chr1 | 114403532 | ||||||
| chr1:114404025
|
C | T | 1 | a0001c0002t0003g0133 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2769-1142G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 15/19 | chr1 | 114404025 | ||||||
| chr1:114404634
|
T | C | 6 | a0001c0002t0004g0111a0001c0002t0004g0114a0001c0002t0004g0115others(3): Show | 6 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.2768+776A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 15/19 | chr1 | 114404634 | ||||||
| chr1:114404809
|
C | CT | 27 | a0001c0001t0001g0083a0001c0001t0026g0196a0001c0002t0005g0099others(24): Show | 27 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.2768+600dupA | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 15/19 | chr1 | 114404809 | ||||||
| chr1:114404809
|
C | CTT | 13 | a0001c0001t0004g0050a0001c0002t0005g0098a0001c0002t0005g0101others(10): Show | 13 | HG01192.hp1 HG01261.hp2 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.2768+599_2768+600d others(4): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 15/19 | chr1 | 114404809 | ||||||
| chr1:114404809
|
CT | C | 11 | a0001c0001t0001g0200a0001c0001t0012g0191a0001c0002t0009g0203others(8): Show | 11 | HG00741.hp2 HG02280.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.2768+600delA | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 15/19 | chr1 | 114404809 | ||||||
| chr1:114404959
|
C | G | 1 | a0001c0001t0040g0194 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2768+451G>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 15/19 | chr1 | 114404959 | ||||||
| chr1:114404982
|
G | C | 1 | a0001c0002t0003g0133 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2768+428C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 15/19 | chr1 | 114404982 | ||||||
| chr1:114405078
|
G | C | 1 | a0003c0004t0004g0006 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2768+332C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 15/19 | chr1 | 114405078 | ||||||
| chr1:114405772
|
G | A | 3 | a0001c0002t0018g0145a0001c0002t0018g0146a0001c0002t0037g0118 | 3 | HG00741.hp2 HG02647.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.2419-13C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 14/19 | chr1 | 114405772 | ||||||
| chr1:114405861
|
C | T | 4 | a0001c0002t0003g0141a0001c0002t0003g0142a0001c0002t0003g0144others(1): Show | 4 | HG02602.hp2 HG02698.hp2 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.2419-102G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 14/19 | chr1 | 114405861 | ||||||
| chr1:114406016
|
T | C | 15 | a0001c0002t0006g0087a0001c0002t0006g0088a0001c0002t0006g0089others(12): Show | 15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.2419-257A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 14/19 | chr1 | 114406016 | ||||||
| chr1:114406147
|
T | G | 13 | a0001c0002t0005g0098a0001c0002t0005g0099a0001c0002t0005g0101others(10): Show | 13 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.2419-388A>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 14/19 | chr1 | 114406147 | ||||||
| chr1:114406676
|
G | A | 2 | a0001c0006t0038g0124a0001c0009t0039g0123 | 2 | HG02132.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.2418+265C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 14/19 | chr1 | 114406676 | ||||||
| chr1:114406728
|
A | G | 1 | a0001c0002t0021g0085 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2418+213T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 14/19 | chr1 | 114406728 | ||||||
| chr1:114406775
|
T | C | 6 | a0001c0006t0010g0119a0001c0006t0010g0120a0001c0006t0010g0121others(3): Show | 6 | HG02132.hp2 HG02698.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.2418+166A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 14/19 | chr1 | 114406775 | ||||||
| chr1:114407198
|
T | C | 17 | a0001c0002t0006g0087a0001c0002t0006g0088a0001c0002t0006g0089others(14): Show | 17 | HG00099.hp1 HG00735.hp1 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.2259-98A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 13/19 | chr1 | 114407198 | ||||||
| chr1:114407320
|
AT | A | 3 | a0001c0001t0001g0022a0001c0001t0004g0023a0001c0001t0024g0003 | 3 | HG02615.hp2 HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2259-221delA | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 13/19 | chr1 | 114407320 | ||||||
| chr1:114407700
|
C | T | 4 | a0003c0004t0014g0005a0003c0004t0014g0012a0003c0004t0014g0013others(1): Show | 4 | HG02055.hp2 HG02451.hp1 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.2259-600G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 13/19 | chr1 | 114407700 | ||||||
| chr1:114407751
|
T | C | 6 | a0001c0006t0010g0119a0001c0006t0010g0120a0001c0006t0010g0121others(3): Show | 6 | HG02132.hp2 HG02698.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.2259-651A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 13/19 | chr1 | 114407751 | ||||||
| chr1:114407989
|
C | T | 6 | a0001c0006t0010g0119a0001c0006t0010g0120a0001c0006t0010g0121others(3): Show | 6 | HG02132.hp2 HG02698.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.2258+688G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 13/19 | chr1 | 114407989 | ||||||
| chr1:114408137
|
CAGAA | C | 24 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(21): Show | 24 | HG00323.hp1 HG00738.hp1 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.2258+536_2258+539d others(6): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 13/19 | chr1 | 114408137 | ||||||
| chr1:114408459
|
G | GA | 23 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(20): Show | 23 | HG00323.hp1 HG00738.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.2258+217dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 13/19 | chr1 | 114408459 | ||||||
| chr1:114408469
|
C | G | 1 | a0002c0003t0001g0037 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2258+208G>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 13/19 | chr1 | 114408469 | ||||||
| chr1:114408519
|
T | C | 13 | a0001c0002t0005g0098a0001c0002t0005g0099a0001c0002t0005g0101others(10): Show | 13 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.2258+158A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 13/19 | chr1 | 114408519 | ||||||
| chr1:114408580
|
T | A | 1 | a0001c0005t0007g0192 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2258+97A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 13/19 | chr1 | 114408580 | ||||||
| chr1:114408598
|
C | T | 72 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(69): Show | 72 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.2258+79G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 13/19 | chr1 | 114408598 | ||||||
| chr1:114408765
|
A | G | 1 | a0001c0006t0038g0124 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2195-25T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 12/19 | chr1 | 114408765 | ||||||
| chr1:114408768
|
T | A | 26 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(23): Show | 26 | HG00323.hp1 HG00738.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.2195-28A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 12/19 | chr1 | 114408768 | ||||||
| chr1:114408787
|
T | C | 2 | a0001c0002t0005g0104a0001c0002t0005g0107 | 2 | HG02615.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2195-47A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 12/19 | chr1 | 114408787 | ||||||
| chr1:114408878
|
C | T | 2 | a0001c0001t0030g0156a0001c0001t0036g0153 | 2 | HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2195-138G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 12/19 | chr1 | 114408878 | ||||||
| chr1:114408977
|
A | T | 1 | a0002c0003t0001g0199 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.2195-237T>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 12/19 | chr1 | 114408977 | ||||||
| chr1:114409241
|
A | T | 1 | a0001c0001t0002g0154 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2195-501T>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 12/19 | chr1 | 114409241 | ||||||
| chr1:114409333
|
G | A | 1 | a0001c0002t0021g0085 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2195-593C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 12/19 | chr1 | 114409333 | ||||||
| chr1:114409480
|
A | C | 4 | a0001c0001t0002g0148a0001c0001t0002g0155a0001c0001t0002g0198others(1): Show | 4 | HG02145.hp2 HG02258.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2194+704T>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 12/19 | chr1 | 114409480 | ||||||
| chr1:114409523
|
A | ACT | 13 | a0001c0002t0005g0098a0001c0002t0005g0099a0001c0002t0005g0101others(10): Show | 13 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.2194+659_2194+660d others(4): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 12/19 | chr1 | 114409523 | ||||||
| chr1:114409540
|
A | G | 4 | a0001c0001t0002g0157a0001c0001t0002g0158a0001c0001t0002g0159others(1): Show | 4 | NA18942.hp1 NA18970.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.2194+644T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 12/19 | chr1 | 114409540 | ||||||
| chr1:114409541
|
T | C | 1 | a0001c0001t0001g0079 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.2194+643A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 12/19 | chr1 | 114409541 | ||||||
| chr1:114409690
|
T | C | 1 | a0001c0002t0041g0110 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2194+494A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 12/19 | chr1 | 114409690 | ||||||
| chr1:114409723
|
C | T | 6 | a0001c0006t0010g0119a0001c0006t0010g0120a0001c0006t0010g0121others(3): Show | 6 | HG02132.hp2 HG02698.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.2194+461G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 12/19 | chr1 | 114409723 | ||||||
| chr1:114409768
|
G | A | 1 | a0002c0003t0001g0017 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2194+416C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 12/19 | chr1 | 114409768 | ||||||
| chr1:114410768
|
C | A | 1 | a0001c0002t0006g0089 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2062-452G>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114410768 | ||||||
| chr1:114410778
|
CA | C | 81 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(78): Show | 81 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.2062-463delT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114410778 | ||||||
| chr1:114410798
|
T | C | 81 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(78): Show | 81 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.2062-482A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114410798 | ||||||
| chr1:114410906
|
C | T | 13 | a0001c0002t0005g0098a0001c0002t0005g0099a0001c0002t0005g0101others(10): Show | 13 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.2062-590G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114410906 | ||||||
| chr1:114410990
|
T | C | 3 | a0003c0004t0004g0006a0003c0004t0013g0007a0003c0004t0050g0206 | 3 | HG02280.hp1 HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2062-674A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114410990 | ||||||
| chr1:114411060
|
G | T | 1 | a0001c0002t0018g0145 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2062-744C>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114411060 | ||||||
| chr1:114411198
|
G | A | 10 | a0001c0002t0033g0117a0001c0006t0010g0119a0001c0006t0010g0120others(7): Show | 10 | HG02055.hp2 HG02132.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.2062-882C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114411198 | ||||||
| chr1:114411773
|
T | C | 2 | a0002c0003t0001g0039a0002c0003t0001g0082 | 2 | NA19009.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.2062-1457A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114411773 | ||||||
| chr1:114411999
|
A | G | 1 | a0001c0001t0026g0196 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2062-1683T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114411999 | ||||||
| chr1:114412063
|
CCAAT | C | 24 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(21): Show | 24 | HG00323.hp1 HG00738.hp1 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.2062-1751_2062-174 others(8): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114412063 | ||||||
| chr1:114412094
|
T | G | 15 | a0001c0002t0006g0087a0001c0002t0006g0088a0001c0002t0006g0089others(12): Show | 15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.2062-1778A>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114412094 | ||||||
| chr1:114412103
|
T | C | 4 | a0001c0006t0010g0119a0001c0006t0010g0120a0001c0006t0010g0121others(1): Show | 4 | HG02895.hp2 HG02897.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2062-1787A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114412103 | ||||||
| chr1:114412385
|
A | C | 1 | a0001c0002t0006g0089 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2062-2069T>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114412385 | ||||||
| chr1:114412402
|
A | C | 2 | a0001c0002t0009g0202a0001c0002t0009g0203 | 2 | HG01891.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.2062-2086T>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114412402 | ||||||
| chr1:114412688
|
T | C | 6 | a0001c0001t0001g0022a0001c0001t0001g0025a0001c0001t0004g0023others(3): Show | 6 | HG02109.hp2 HG02572.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.2062-2372A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114412688 | ||||||
| chr1:114412732
|
C | A | 2 | a0002c0003t0016g0030a0002c0003t0016g0040 | 2 | HG02083.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.2062-2416G>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114412732 | ||||||
| chr1:114412770
|
G | A | 5 | a0001c0002t0003g0128a0001c0002t0003g0131a0001c0002t0003g0132others(2): Show | 5 | NA18612.hp2 NA18942.hp2 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.2062-2454C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114412770 | ||||||
| chr1:114413151
|
G | C | 6 | a0001c0002t0004g0111a0001c0002t0004g0114a0001c0002t0004g0115others(3): Show | 6 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.2062-2835C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114413151 | ||||||
| chr1:114413327
|
G | A | 1 | a0001c0002t0003g0134 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2062-3011C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114413327 | ||||||
| chr1:114413331
|
A | G | 1 | a0001c0002t0003g0128 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2062-3015T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114413331 | ||||||
| chr1:114413431
|
G | C | 2 | a0001c0001t0030g0156a0001c0001t0036g0153 | 2 | HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2062-3115C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114413431 | ||||||
| chr1:114413451
|
G | A | 3 | a0001c0002t0018g0145a0001c0002t0018g0146a0001c0002t0037g0118 | 3 | HG00741.hp2 HG02647.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.2062-3135C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114413451 | ||||||
| chr1:114413558
|
C | CA | 10 | a0001c0001t0001g0058a0001c0001t0001g0176a0001c0001t0002g0064others(7): Show | 10 | HG01071.hp1 HG01071.hp2 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.2062-3243dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114413558 | ||||||
| chr1:114413558
|
C | CAA | 18 | a0001c0002t0003g0127a0001c0002t0003g0128a0001c0002t0003g0130others(15): Show | 18 | HG00323.hp1 HG00738.hp1 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.2062-3244_2062-324 others(6): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114413558 | ||||||
| chr1:114413558
|
C | CAAA | 10 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0133others(7): Show | 10 | HG01099.hp1 HG01891.hp2 HG01952.hp2 others(7): Show |
intron_variant | MODIFIER | c.2062-3245_2062-324 others(7): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114413558 | ||||||
| chr1:114413569
|
A | G | 1 | a0001c0001t0022g0056 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2062-3253T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114413569 | ||||||
| chr1:114413570
|
A | AAG | 15 | a0001c0002t0006g0087a0001c0002t0006g0088a0001c0002t0006g0089others(12): Show | 15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.2062-3255_2062-325 others(6): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114413570 | ||||||
| chr1:114413570
|
AAAAGAAA others(2): Show |
A | 11 | a0001c0002t0005g0098a0001c0002t0005g0099a0001c0002t0005g0101others(8): Show | 11 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.2062-3263_2062-325 others(13): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114413570 | ||||||
| chr1:114413574
|
G | A | 67 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(64): Show | 67 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.2062-3258C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114413574 | ||||||
| chr1:114413578
|
A | AAAGAAAA others(16): Show |
3 | a0001c0002t0018g0145a0001c0002t0018g0146a0004c0007t0001g0014 | 3 | HG00741.hp2 HG02451.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.2062-3263_2062-326 others(27): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114413578 | ||||||
| chr1:114413578
|
A | AAGAAAAG others(15): Show |
3 | a0001c0002t0033g0117a0003c0004t0014g0005a0003c0004t0014g0012 | 3 | HG02055.hp2 HG02451.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.2062-3263_2062-326 others(26): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114413578 | ||||||
| chr1:114413578
|
A | AAGAAAAG others(36): Show |
1 | a0003c0004t0014g0013 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2062-3263_2062-326 others(47): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114413578 | ||||||
| chr1:114413578
|
A | AGAAAAGA others(14): Show |
1 | a0001c0001t0001g0072 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2062-3283_2062-326 others(25): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114413578 | ||||||
| chr1:114413578
|
AGAAAAGA others(13): Show |
A | 2 | a0001c0002t0005g0104a0001c0002t0005g0107 | 2 | HG02615.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2062-3282_2062-326 others(24): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114413578 | ||||||
| chr1:114413579
|
G | A | 9 | a0001c0002t0032g0116a0003c0004t0001g0008a0003c0004t0004g0006others(6): Show | 9 | HG02145.hp1 HG02258.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.2062-3263C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114413579 | ||||||
| chr1:114413580
|
AAAAGAAA others(12): Show |
A | 6 | a0001c0002t0032g0116a0003c0004t0013g0007a0003c0004t0013g0010others(3): Show | 6 | HG02145.hp1 HG02258.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.2062-3283_2062-326 others(23): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114413580 | ||||||
| chr1:114413581
|
AAAGAAAA others(11): Show |
A | 3 | a0003c0004t0001g0008a0003c0004t0004g0006a0003c0004t0004g0009 | 3 | HG02280.hp1 HG02965.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2062-3283_2062-326 others(22): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114413581 | ||||||
| chr1:114413588
|
AAGACTTT others(4): Show |
A | 11 | a0001c0002t0005g0098a0001c0002t0005g0099a0001c0002t0005g0101others(8): Show | 11 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.2062-3283_2062-327 others(15): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114413588 | ||||||
| chr1:114413599
|
T | A | 2 | a0001c0002t0005g0104a0001c0002t0005g0107 | 2 | HG02615.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2062-3283A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114413599 | ||||||
| chr1:114413600
|
G | C | 15 | a0001c0002t0006g0087a0001c0002t0006g0088a0001c0002t0006g0089others(12): Show | 15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.2062-3284C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114413600 | ||||||
| chr1:114413619
|
G | A | 8 | a0003c0004t0001g0008a0003c0004t0004g0006a0003c0004t0004g0009others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.2062-3303C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114413619 | ||||||
| chr1:114413628
|
T | TA | 42 | a0001c0001t0001g0025a0001c0001t0001g0069a0001c0001t0001g0075others(39): Show | 42 | HG00323.hp1 HG00735.hp2 HG01175.hp1 others(39): Show |
intron_variant | MODIFIER | c.2062-3313dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114413628 | ||||||
| chr1:114413628
|
T | TAA | 14 | a0001c0002t0003g0126a0001c0002t0003g0130a0001c0002t0003g0137others(11): Show | 14 | HG01099.hp1 HG01167.hp1 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.2062-3314_2062-331 others(6): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114413628 | ||||||
| chr1:114413833
|
C | T | 2 | a0001c0001t0001g0083a0001c0001t0004g0050 | 2 | HG02055.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.2062-3517G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114413833 | ||||||
| chr1:114413968
|
C | T | 1 | a0001c0001t0042g0061 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2062-3652G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114413968 | ||||||
| chr1:114414027
|
G | GCA | 23 | a0001c0001t0001g0025a0001c0001t0001g0070a0001c0001t0002g0186others(20): Show | 23 | HG00099.hp2 HG00741.hp2 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.2062-3713_2062-371 others(6): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114414027 | ||||||
| chr1:114414027
|
G | GCACA | 24 | a0001c0001t0001g0083a0001c0001t0002g0188a0001c0001t0035g0173others(21): Show | 24 | HG00642.hp2 HG00738.hp1 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.2062-3715_2062-371 others(8): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114414027 | ||||||
| chr1:114414027
|
G | GCACACA | 10 | a0001c0001t0002g0064a0001c0002t0003g0132a0001c0002t0003g0133others(7): Show | 10 | HG00099.hp1 HG01071.hp2 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.2062-3717_2062-371 others(10): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114414027 | ||||||
| chr1:114414027
|
G | GCACACAC others(1): Show |
12 | a0001c0002t0003g0130a0001c0002t0003g0138a0001c0002t0004g0114others(9): Show | 12 | HG00323.hp1 HG00735.hp1 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.2062-3719_2062-371 others(12): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114414027 | ||||||
| chr1:114414027
|
G | GCACACAC others(3): Show |
3 | a0003c0004t0013g0010a0003c0004t0031g0011a0004c0007t0001g0014 | 3 | HG02258.hp1 HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2062-3721_2062-371 others(14): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114414027 | ||||||
| chr1:114414027
|
G | GCACACAC others(5): Show |
6 | a0001c0002t0003g0128a0001c0002t0029g0135a0001c0002t0032g0116others(3): Show | 6 | HG02523.hp1 HG02886.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.2062-3723_2062-371 others(16): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114414027 | ||||||
| chr1:114414027
|
G | GCACACAC others(7): Show |
3 | a0001c0002t0003g0131a0001c0006t0010g0119a0003c0004t0014g0005 | 3 | HG02922.hp1 HG03017.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.2062-3725_2062-371 others(18): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114414027 | ||||||
| chr1:114414027
|
G | GCACACAC others(11): Show |
1 | a0003c0004t0004g0009 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2062-3729_2062-371 others(22): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114414027 | ||||||
| chr1:114414027
|
GCA | G | 56 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0058others(53): Show | 56 | HG00323.hp2 HG00558.hp1 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.2062-3713_2062-371 others(6): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114414027 | ||||||
| chr1:114414027
|
GCACA | G | 4 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0060others(1): Show | 4 | HG02615.hp2 HG02809.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.2062-3715_2062-371 others(8): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114414027 | ||||||
| chr1:114414027
|
GCACACA | G | 1 | a0002c0003t0001g0001 | 2 | HG01433.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.2062-3717_2062-371 others(10): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114414027 | ||||||
| chr1:114414027
|
GCACACAC others(1): Show |
G | 5 | a0001c0001t0002g0155a0001c0002t0009g0202a0001c0002t0009g0203others(2): Show | 5 | HG01891.hp2 HG02572.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2062-3719_2062-371 others(12): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114414027 | ||||||
| chr1:114414027
|
GCACACAC others(7): Show |
G | 3 | a0003c0004t0004g0006a0003c0004t0013g0007a0003c0004t0050g0206 | 3 | HG02280.hp1 HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2062-3725_2062-371 others(18): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114414027 | ||||||
| chr1:114414027
|
GCACACAC others(9): Show |
G | 1 | a0001c0001t0002g0152 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2062-3727_2062-371 others(20): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114414027 | ||||||
| chr1:114414379
|
T | C | 15 | a0001c0002t0006g0087a0001c0002t0006g0088a0001c0002t0006g0089others(12): Show | 15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.2062-4063A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114414379 | ||||||
| chr1:114414433
|
CCTT | C | 24 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(21): Show | 24 | HG00323.hp1 HG00738.hp1 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.2062-4120_2062-411 others(7): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114414433 | ||||||
| chr1:114414456
|
G | A | 15 | a0001c0002t0006g0087a0001c0002t0006g0088a0001c0002t0006g0089others(12): Show | 15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.2062-4140C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114414456 | ||||||
| chr1:114414588
|
T | C | 1 | a0002c0003t0001g0029 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2062-4272A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114414588 | ||||||
| chr1:114414632
|
C | T | 81 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(78): Show | 81 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.2062-4316G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114414632 | ||||||
| chr1:114414671
|
G | C | 1 | a0001c0002t0005g0101 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2062-4355C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114414671 | ||||||
| chr1:114414989
|
A | AT | 5 | a0001c0001t0001g0020a0001c0001t0001g0069a0001c0001t0004g0023others(2): Show | 5 | HG00735.hp2 HG01243.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.2062-4674dupA | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114414989 | ||||||
| chr1:114414989
|
A | ATT | 9 | a0001c0002t0004g0111a0001c0002t0004g0114a0001c0002t0004g0115others(6): Show | 9 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.2062-4675_2062-467 others(6): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114414989 | ||||||
| chr1:114414989
|
A | ATTT | 14 | a0001c0002t0005g0098a0001c0002t0005g0099a0001c0002t0005g0101others(11): Show | 14 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.2062-4676_2062-467 others(7): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114414989 | ||||||
| chr1:114414989
|
A | ATTTT | 27 | a0001c0002t0005g0104a0001c0002t0005g0105a0001c0002t0006g0087others(24): Show | 27 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.2062-4677_2062-467 others(8): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114414989 | ||||||
| chr1:114414989
|
A | ATTTTT | 8 | a0001c0002t0006g0094a0001c0002t0018g0145a0001c0002t0018g0146others(5): Show | 8 | HG00741.hp2 HG02055.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.2062-4678_2062-467 others(9): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114414989 | ||||||
| chr1:114414989
|
A | ATTTTTTT | 13 | a0001c0002t0003g0126a0001c0002t0003g0127a0001c0002t0003g0131others(10): Show | 13 | HG00323.hp1 HG00738.hp1 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.2062-4680_2062-467 others(11): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114414989 | ||||||
| chr1:114414989
|
A | ATTTTTTT others(1): Show |
6 | a0001c0002t0003g0125a0001c0002t0003g0128a0001c0002t0003g0130others(3): Show | 6 | HG01243.hp2 HG01346.hp2 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.2062-4681_2062-467 others(12): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114414989 | ||||||
| chr1:114415308
|
A | T | 1 | a0001c0001t0042g0061 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2062-4992T>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114415308 | ||||||
| chr1:114415364
|
C | T | 3 | a0002c0003t0001g0021a0002c0003t0016g0030a0002c0003t0016g0040 | 3 | HG02015.hp2 HG02083.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.2062-5048G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114415364 | ||||||
| chr1:114415450
|
T | C | 1 | a0001c0001t0002g0190 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2062-5134A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114415450 | ||||||
| chr1:114415532
|
A | T | 1 | a0001c0001t0001g0020 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2062-5216T>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114415532 | ||||||
| chr1:114415535
|
T | A | 1 | a0001c0001t0001g0020 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2062-5219A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114415535 | ||||||
| chr1:114415553
|
C | CT | 11 | a0001c0002t0033g0117a0001c0006t0010g0119a0001c0006t0010g0120others(8): Show | 11 | HG02055.hp2 HG02132.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.2062-5238dupA | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114415553 | ||||||
| chr1:114415580
|
T | G | 39 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(36): Show | 39 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.2062-5264A>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114415580 | ||||||
| chr1:114415946
|
T | TA | 69 | a0001c0001t0002g0152a0001c0001t0004g0024a0001c0001t0012g0197others(66): Show | 69 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(66): Show |
intron_variant | MODIFIER | c.2061+5489dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114415946 | ||||||
| chr1:114415946
|
T | TAA | 6 | a0001c0002t0021g0092a0001c0002t0033g0117a0003c0004t0014g0005others(3): Show | 6 | HG02055.hp2 HG02451.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.2061+5488_2061+548 others(6): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114415946 | ||||||
| chr1:114415946
|
T | TAAA | 6 | a0001c0002t0004g0111a0001c0002t0004g0114a0001c0002t0004g0115others(3): Show | 6 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.2061+5487_2061+548 others(7): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114415946 | ||||||
| chr1:114416041
|
T | C | 2 | a0001c0006t0010g0121a0001c0006t0010g0122 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2061+5395A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114416041 | ||||||
| chr1:114416157
|
T | C | 81 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(78): Show | 81 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.2061+5279A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114416157 | ||||||
| chr1:114416205
|
G | A | 1 | a0002c0003t0001g0001 | 2 | HG01433.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.2061+5231C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114416205 | ||||||
| chr1:114416324
|
A | C | 56 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(53): Show | 56 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(53): Show |
intron_variant | MODIFIER | c.2061+5112T>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114416324 | ||||||
| chr1:114416459
|
T | C | 1 | a0002c0003t0001g0037 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2061+4977A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114416459 | ||||||
| chr1:114416515
|
A | G | 1 | a0002c0003t0001g0199 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.2061+4921T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114416515 | ||||||
| chr1:114416558
|
C | T | 1 | a0001c0001t0001g0067 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2061+4878G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114416558 | ||||||
| chr1:114416780
|
A | G | 2 | a0003c0004t0013g0007a0003c0004t0050g0206 | 2 | HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2061+4656T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114416780 | ||||||
| chr1:114416918
|
G | A | 21 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(18): Show | 21 | HG00323.hp1 HG00738.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.2061+4518C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114416918 | ||||||
| chr1:114417149
|
T | C | 1 | a0001c0001t0002g0171 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.2061+4287A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114417149 | ||||||
| chr1:114417266
|
A | C | 56 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(53): Show | 56 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(53): Show |
intron_variant | MODIFIER | c.2061+4170T>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114417266 | ||||||
| chr1:114417635
|
T | C | 2 | a0001c0002t0005g0104a0001c0002t0005g0107 | 2 | HG02615.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2061+3801A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114417635 | ||||||
| chr1:114417648
|
A | C | 2 | a0001c0001t0001g0045a0001c0001t0001g0046 | 2 | HG02809.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2061+3788T>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114417648 | ||||||
| chr1:114417819
|
C | G | 6 | a0002c0003t0008g0028a0002c0003t0008g0041a0002c0003t0008g0042others(3): Show | 6 | HG00642.hp1 HG00738.hp2 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.2061+3617G>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114417819 | ||||||
| chr1:114418041
|
G | A | 15 | a0001c0002t0006g0087a0001c0002t0006g0088a0001c0002t0006g0089others(12): Show | 15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.2061+3395C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114418041 | ||||||
| chr1:114418092
|
C | T | 11 | a0001c0002t0033g0117a0001c0006t0010g0119a0001c0006t0010g0120others(8): Show | 11 | HG02055.hp2 HG02132.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.2061+3344G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114418092 | ||||||
| chr1:114418184
|
G | C | 3 | a0001c0002t0018g0145a0001c0002t0018g0146a0001c0002t0037g0118 | 3 | HG00741.hp2 HG02647.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.2061+3252C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114418184 | ||||||
| chr1:114418244
|
G | T | 13 | a0001c0002t0005g0098a0001c0002t0005g0099a0001c0002t0005g0101others(10): Show | 13 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.2061+3192C>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114418244 | ||||||
| chr1:114418728
|
T | C | 9 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0059others(6): Show | 9 | HG00741.hp1 HG01074.hp1 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.2061+2708A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114418728 | ||||||
| chr1:114418931
|
C | G | 11 | a0001c0002t0033g0117a0001c0006t0010g0119a0001c0006t0010g0120others(8): Show | 11 | HG02055.hp2 HG02132.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.2061+2505G>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114418931 | ||||||
| chr1:114418946
|
G | A | 1 | a0001c0002t0005g0108 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.2061+2490C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114418946 | ||||||
| chr1:114418971
|
G | A | 2 | a0001c0001t0001g0025a0001c0001t0004g0024 | 2 | HG02109.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.2061+2465C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114418971 | ||||||
| chr1:114419157
|
C | T | 2 | a0001c0001t0001g0083a0001c0001t0004g0050 | 2 | HG02055.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.2061+2279G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114419157 | ||||||
| chr1:114419200
|
C | CA | 14 | a0001c0001t0001g0025a0001c0001t0001g0059a0001c0001t0001g0080others(11): Show | 14 | HG01106.hp2 HG01891.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.2061+2235dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114419200 | ||||||
| chr1:114419200
|
CA | C | 32 | a0001c0001t0002g0148a0001c0002t0003g0137a0001c0002t0005g0098others(29): Show | 32 | HG00735.hp1 HG00741.hp2 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.2061+2235delT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114419200 | ||||||
| chr1:114419218
|
A | AG | 4 | a0001c0002t0033g0117a0003c0004t0014g0005a0003c0004t0014g0012others(1): Show | 4 | HG02055.hp2 HG02451.hp2 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.2061+2217_2061+221 others(5): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114419218 | ||||||
| chr1:114419218
|
A | G | 5 | a0001c0002t0006g0093a0001c0002t0006g0094a0001c0002t0006g0095others(2): Show | 5 | HG02280.hp2 HG02723.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.2061+2218T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114419218 | ||||||
| chr1:114419277
|
CAA | C | 3 | a0003c0004t0013g0010a0003c0004t0031g0011a0005c0008t0013g0015 | 3 | HG02145.hp1 HG02258.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2061+2157_2061+215 others(6): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114419277 | ||||||
| chr1:114419318
|
C | T | 1 | a0001c0009t0039g0123 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2061+2118G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114419318 | ||||||
| chr1:114419330
|
C | T | 1 | a0001c0002t0006g0088 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2061+2106G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114419330 | ||||||
| chr1:114419392
|
G | A | 8 | a0003c0004t0001g0008a0003c0004t0004g0006a0003c0004t0004g0009others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.2061+2044C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114419392 | ||||||
| chr1:114419634
|
TCTC | T | 13 | a0001c0002t0005g0098a0001c0002t0005g0099a0001c0002t0005g0101others(10): Show | 13 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.2061+1799_2061+180 others(7): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114419634 | ||||||
| chr1:114419750
|
A | T | 2 | a0001c0002t0003g0141a0001c0002t0003g0142 | 2 | HG02602.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.2061+1686T>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114419750 | ||||||
| chr1:114419795
|
G | A | 2 | a0003c0004t0001g0008a0003c0004t0004g0009 | 2 | HG02965.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2061+1641C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114419795 | ||||||
| chr1:114419933
|
T | C | 15 | a0001c0001t0002g0148a0001c0001t0002g0154a0001c0001t0002g0155others(12): Show | 15 | HG01175.hp2 HG01884.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.2061+1503A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114419933 | ||||||
| chr1:114420295
|
A | G | 1 | a0001c0002t0004g0111 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2061+1141T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114420295 | ||||||
| chr1:114420314
|
C | A | 13 | a0001c0002t0005g0098a0001c0002t0005g0099a0001c0002t0005g0101others(10): Show | 13 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.2061+1122G>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114420314 | ||||||
| chr1:114420343
|
C | A | 2 | a0001c0002t0018g0145a0001c0002t0018g0146 | 2 | HG00741.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.2061+1093G>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114420343 | ||||||
| chr1:114420454
|
G | A | 3 | a0001c0001t0001g0022a0001c0001t0004g0023a0001c0001t0024g0003 | 3 | HG02615.hp2 HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2061+982C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114420454 | ||||||
| chr1:114420562
|
T | C | 1 | a0001c0001t0002g0154 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2061+874A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114420562 | ||||||
| chr1:114420870
|
A | T | 1 | a0001c0002t0005g0102 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2061+566T>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114420870 | ||||||
| chr1:114420952
|
G | A | 5 | a0001c0002t0004g0114a0001c0002t0004g0115a0001c0002t0020g0112others(2): Show | 5 | HG01884.hp2 HG02622.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.2061+484C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114420952 | ||||||
| chr1:114421351
|
TA | T | 37 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(34): Show | 37 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.2061+84delT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 11/19 | chr1 | 114421351 | ||||||
| chr1:114421941
|
G | A | 1 | a0001c0001t0017g0033 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1861-305C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 10/19 | chr1 | 114421941 | ||||||
| chr1:114422183
|
A | G | 1 | a0001c0002t0003g0142 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1861-547T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 10/19 | chr1 | 114422183 | ||||||
| chr1:114422421
|
G | A | 1 | a0001c0001t0012g0191 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1861-785C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 10/19 | chr1 | 114422421 | ||||||
| chr1:114422495
|
G | GA | 68 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(65): Show | 68 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.1861-860dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 10/19 | chr1 | 114422495 | ||||||
| chr1:114422665
|
T | C | 1 | a0001c0002t0009g0205 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1861-1029A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 10/19 | chr1 | 114422665 | ||||||
| chr1:114423051
|
T | A | 4 | a0001c0002t0009g0202a0001c0002t0009g0203a0001c0002t0009g0204others(1): Show | 4 | HG01891.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1861-1415A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 10/19 | chr1 | 114423051 | ||||||
| chr1:114423190
|
T | C | 81 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(78): Show | 81 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.1860+1401A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 10/19 | chr1 | 114423190 | ||||||
| chr1:114423344
|
T | C | 13 | a0001c0002t0009g0202a0001c0002t0009g0203a0001c0002t0009g0204others(10): Show | 13 | HG01891.hp2 HG02145.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1860+1247A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 10/19 | chr1 | 114423344 | ||||||
| chr1:114423431
|
G | A | 1 | a0003c0004t0031g0011 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1860+1160C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 10/19 | chr1 | 114423431 | ||||||
| chr1:114423478
|
C | T | 81 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(78): Show | 81 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.1860+1113G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 10/19 | chr1 | 114423478 | ||||||
| chr1:114423651
|
C | T | 1 | a0001c0006t0038g0124 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1860+940G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 10/19 | chr1 | 114423651 | ||||||
| chr1:114423731
|
G | C | 3 | a0003c0004t0013g0010a0003c0004t0031g0011a0005c0008t0013g0015 | 3 | HG02145.hp1 HG02258.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1860+860C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 10/19 | chr1 | 114423731 | ||||||
| chr1:114423791
|
T | G | 1 | a0001c0002t0033g0117 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1860+800A>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 10/19 | chr1 | 114423791 | ||||||
| chr1:114423847
|
C | T | 4 | a0001c0002t0033g0117a0003c0004t0014g0005a0003c0004t0014g0012others(1): Show | 4 | HG02055.hp2 HG02451.hp2 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.1860+744G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 10/19 | chr1 | 114423847 | ||||||
| chr1:114423936
|
T | A | 1 | a0001c0001t0001g0059 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1860+655A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 10/19 | chr1 | 114423936 | ||||||
| chr1:114424011
|
T | C | 1 | a0001c0002t0018g0145 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1860+580A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 10/19 | chr1 | 114424011 | ||||||
| chr1:114424104
|
G | A | 1 | a0001c0001t0001g0200 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1860+487C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 10/19 | chr1 | 114424104 | ||||||
| chr1:114424147
|
T | TA | 14 | a0001c0002t0005g0098a0001c0002t0005g0099a0001c0002t0005g0101others(11): Show | 14 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.1860+443dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 10/19 | chr1 | 114424147 | ||||||
| chr1:114424154
|
A | T | 1 | a0005c0008t0013g0015 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1860+437T>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 10/19 | chr1 | 114424154 | ||||||
| chr1:114424157
|
T | A | 1 | a0001c0001t0042g0061 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1860+434A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 10/19 | chr1 | 114424157 | ||||||
| chr1:114424172
|
A | G | 1 | a0002c0003t0001g0199 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1860+419T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 10/19 | chr1 | 114424172 | ||||||
| chr1:114424318
|
C | T | 1 | a0001c0002t0005g0098 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1860+273G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 10/19 | chr1 | 114424318 | ||||||
| chr1:114424491
|
C | T | 1 | a0001c0002t0033g0117 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1860+100G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 10/19 | chr1 | 114424491 | ||||||
| chr1:114424950
|
GTCTC | G | 13 | a0001c0002t0005g0098a0001c0002t0005g0099a0001c0002t0005g0101others(10): Show | 13 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.1696-199_1696-196d others(6): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 9/19 | chr1 | 114424950 | ||||||
| chr1:114424969
|
A | T | 81 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(78): Show | 81 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.1696-214T>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 9/19 | chr1 | 114424969 | ||||||
| chr1:114425022
|
C | T | 1 | a0001c0002t0037g0118 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1696-267G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 9/19 | chr1 | 114425022 | ||||||
| chr1:114425104
|
C | T | 1 | a0001c0001t0012g0074 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1695+345G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 9/19 | chr1 | 114425104 | ||||||
| chr1:114425173
|
T | G | 6 | a0001c0002t0004g0111a0001c0002t0004g0114a0001c0002t0004g0115others(3): Show | 6 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1695+276A>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 9/19 | chr1 | 114425173 | ||||||
| chr1:114425780
|
T | C | 2 | a0001c0002t0005g0104a0001c0002t0005g0107 | 2 | HG02615.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1421-57A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 8/19 | chr1 | 114425780 | ||||||
| chr1:114425839
|
C | T | 13 | a0001c0002t0005g0098a0001c0002t0005g0099a0001c0002t0005g0101others(10): Show | 13 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.1421-116G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 8/19 | chr1 | 114425839 | ||||||
| chr1:114426018
|
C | A | 3 | a0001c0002t0005g0105a0001c0002t0005g0106a0001c0002t0019g0109 | 3 | HG01192.hp1 HG01261.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1421-295G>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 8/19 | chr1 | 114426018 | ||||||
| chr1:114426142
|
C | G | 5 | a0001c0002t0033g0117a0003c0004t0014g0005a0003c0004t0014g0012others(2): Show | 5 | HG02055.hp2 HG02451.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1421-419G>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 8/19 | chr1 | 114426142 | ||||||
| chr1:114426351
|
G | A | 13 | a0001c0002t0005g0098a0001c0002t0005g0099a0001c0002t0005g0101others(10): Show | 13 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.1421-628C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 8/19 | chr1 | 114426351 | ||||||
| chr1:114426507
|
C | CTT | 6 | a0001c0002t0004g0111a0001c0002t0004g0114a0001c0002t0004g0115others(3): Show | 6 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1420+668_1420+669d others(4): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 8/19 | chr1 | 114426507 | ||||||
| chr1:114426507
|
CT | C | 11 | a0001c0001t0001g0052a0001c0001t0002g0149a0001c0001t0002g0186others(8): Show | 11 | HG00323.hp2 HG01169.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1420+669delA | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 8/19 | chr1 | 114426507 | ||||||
| chr1:114426522
|
T | A | 2 | a0001c0001t0015g0051a0002c0003t0004g0048 | 2 | HG00099.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.1420+655A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 8/19 | chr1 | 114426522 | ||||||
| chr1:114426522
|
TA | T | 24 | a0001c0002t0003g0128a0001c0002t0003g0131a0001c0002t0003g0132others(21): Show | 24 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.1420+654delT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 8/19 | chr1 | 114426522 | ||||||
| chr1:114426523
|
A | T | 54 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0002t0003g0125others(51): Show | 54 | HG00323.hp1 HG00738.hp1 HG00741.hp2 others(51): Show |
intron_variant | MODIFIER | c.1420+654T>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 8/19 | chr1 | 114426523 | ||||||
| chr1:114426524
|
A | T | 22 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(19): Show | 22 | HG00323.hp1 HG00738.hp1 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.1420+653T>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 8/19 | chr1 | 114426524 | ||||||
| chr1:114426533
|
G | A | 3 | a0003c0004t0013g0010a0003c0004t0031g0011a0005c0008t0013g0015 | 3 | HG02145.hp1 HG02258.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1420+644C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 8/19 | chr1 | 114426533 | ||||||
| chr1:114426581
|
T | G | 1 | a0001c0002t0032g0116 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1420+596A>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 8/19 | chr1 | 114426581 | ||||||
| chr1:114426776
|
A | T | 1 | a0001c0002t0041g0110 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1420+401T>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 8/19 | chr1 | 114426776 | ||||||
| chr1:114426978
|
G | T | 81 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(78): Show | 81 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.1420+199C>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 8/19 | chr1 | 114426978 | ||||||
| chr1:114427019
|
C | T | 21 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(18): Show | 21 | HG00323.hp1 HG00738.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.1420+158G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 8/19 | chr1 | 114427019 | ||||||
| chr1:114427043
|
T | C | 15 | a0001c0002t0006g0087a0001c0002t0006g0088a0001c0002t0006g0089others(12): Show | 15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1420+134A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 8/19 | chr1 | 114427043 | ||||||
| chr1:114427303
|
GA | G | 24 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(21): Show | 24 | HG00323.hp1 HG00738.hp1 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.1303-10delT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 7/19 | chr1 | 114427303 | ||||||
| chr1:114427395
|
T | C | 1 | a0001c0001t0002g0152 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1303-101A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 7/19 | chr1 | 114427395 | ||||||
| chr1:114427468
|
C | T | 12 | a0001c0002t0009g0202a0001c0002t0009g0203a0001c0002t0009g0204others(9): Show | 12 | HG01891.hp2 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1303-174G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 7/19 | chr1 | 114427468 | ||||||
| chr1:114427556
|
T | C | 2 | a0001c0006t0010g0121a0001c0006t0010g0122 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1302+192A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 7/19 | chr1 | 114427556 | ||||||
| chr1:114428038
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1156-144G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 6/19 | chr1 | 114428038 | ||||||
| chr1:114428186
|
C | G | 1 | a0003c0004t0004g0006 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1156-292G>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 6/19 | chr1 | 114428186 | ||||||
| chr1:114428268
|
A | G | 15 | a0001c0002t0006g0087a0001c0002t0006g0088a0001c0002t0006g0089others(12): Show | 15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1156-374T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 6/19 | chr1 | 114428268 | ||||||
| chr1:114428625
|
A | C | 15 | a0001c0002t0006g0087a0001c0002t0006g0088a0001c0002t0006g0089others(12): Show | 15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1156-731T>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 6/19 | chr1 | 114428625 | ||||||
| chr1:114428862
|
C | CT | 7 | a0001c0001t0012g0074a0001c0006t0010g0119a0001c0006t0010g0120others(4): Show | 7 | HG02132.hp2 HG02698.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1156-969dupA | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 6/19 | chr1 | 114428862 | ||||||
| chr1:114428890
|
T | C | 1 | a0001c0001t0026g0196 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1156-996A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 6/19 | chr1 | 114428890 | ||||||
| chr1:114428893
|
C | G | 2 | a0001c0001t0002g0195a0001c0001t0026g0196 | 2 | HG01175.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.1156-999G>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 6/19 | chr1 | 114428893 | ||||||
| chr1:114429130
|
C | T | 1 | a0001c0001t0001g0079 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1156-1236G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 6/19 | chr1 | 114429130 | ||||||
| chr1:114429264
|
C | T | 81 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(78): Show | 81 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.1156-1370G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 6/19 | chr1 | 114429264 | ||||||
| chr1:114429344
|
C | T | 3 | a0001c0001t0002g0166a0001c0001t0002g0168a0001c0001t0002g0179 | 3 | HG01496.hp2 HG01928.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.1156-1450G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 6/19 | chr1 | 114429344 | ||||||
| chr1:114429360
|
G | GT | 7 | a0002c0003t0008g0044a0003c0004t0001g0008a0003c0004t0004g0009others(4): Show | 7 | HG00642.hp1 HG02145.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1155+1437dupA | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 6/19 | chr1 | 114429360 | ||||||
| chr1:114429630
|
G | GA | 10 | a0001c0001t0001g0073a0001c0001t0001g0078a0001c0001t0012g0074others(7): Show | 10 | HG01081.hp1 HG01884.hp2 HG01952.hp1 others(7): Show |
intron_variant | MODIFIER | c.1155+1167dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 6/19 | chr1 | 114429630 | ||||||
| chr1:114429897
|
C | T | 1 | a0001c0002t0041g0110 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1155+901G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 6/19 | chr1 | 114429897 | ||||||
| chr1:114429949
|
T | C | 1 | a0001c0002t0037g0118 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1155+849A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 6/19 | chr1 | 114429949 | ||||||
| chr1:114429953
|
C | T | 2 | a0002c0003t0016g0030a0002c0003t0016g0040 | 2 | HG02083.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.1155+845G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 6/19 | chr1 | 114429953 | ||||||
| chr1:114429988
|
T | C | 1 | a0001c0002t0003g0133 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1155+810A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 6/19 | chr1 | 114429988 | ||||||
| chr1:114430211
|
C | T | 81 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(78): Show | 81 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.1155+587G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 6/19 | chr1 | 114430211 | ||||||
| chr1:114430214
|
A | ACATCAC | 11 | a0001c0002t0033g0117a0001c0006t0010g0119a0001c0006t0010g0120others(8): Show | 11 | HG02055.hp2 HG02132.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1155+578_1155+583d others(8): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 6/19 | chr1 | 114430214 | ||||||
| chr1:114430251
|
G | T | 81 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(78): Show | 81 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.1155+547C>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 6/19 | chr1 | 114430251 | ||||||
| chr1:114430354
|
C | T | 8 | a0002c0003t0001g0039a0002c0003t0001g0082a0002c0003t0008g0028others(5): Show | 8 | HG00642.hp1 HG00738.hp2 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.1155+444G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 6/19 | chr1 | 114430354 | ||||||
| chr1:114430368
|
C | T | 9 | a0001c0001t0002g0148a0001c0001t0002g0154a0001c0001t0002g0155others(6): Show | 9 | HG01175.hp2 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1155+430G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 6/19 | chr1 | 114430368 | ||||||
| chr1:114430402
|
C | T | 1 | a0003c0004t0014g0012 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1155+396G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 6/19 | chr1 | 114430402 | ||||||
| chr1:114430588
|
G | A | 1 | a0001c0002t0021g0092 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1155+210C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 6/19 | chr1 | 114430588 | ||||||
| chr1:114430654
|
C | A | 3 | a0003c0004t0013g0010a0003c0004t0031g0011a0005c0008t0013g0015 | 3 | HG02145.hp1 HG02258.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1155+144G>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 6/19 | chr1 | 114430654 | ||||||
| chr1:114430738
|
T | A | 1 | a0001c0001t0044g0016 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1155+60A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 6/19 | chr1 | 114430738 | ||||||
| chr1:114431068
|
T | C | 45 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(42): Show | 45 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.1041-156A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 5/19 | chr1 | 114431068 | ||||||
| chr1:114431739
|
A | G | 13 | a0001c0002t0009g0202a0001c0002t0009g0203a0001c0002t0009g0204others(10): Show | 13 | HG01891.hp2 HG02145.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1041-827T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 5/19 | chr1 | 114431739 | ||||||
| chr1:114431802
|
T | C | 1 | a0001c0002t0003g0137 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1041-890A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 5/19 | chr1 | 114431802 | ||||||
| chr1:114432034
|
T | G | 3 | a0001c0002t0018g0145a0001c0002t0018g0146a0001c0002t0037g0118 | 3 | HG00741.hp2 HG02647.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1041-1122A>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 5/19 | chr1 | 114432034 | ||||||
| chr1:114432099
|
A | G | 1 | a0001c0001t0002g0162 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1041-1187T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 5/19 | chr1 | 114432099 | ||||||
| chr1:114432194
|
T | C | 2 | a0001c0002t0004g0114a0001c0002t0004g0115 | 2 | HG01884.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1041-1282A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 5/19 | chr1 | 114432194 | ||||||
| chr1:114432679
|
G | A | 4 | a0001c0006t0010g0119a0001c0006t0010g0120a0001c0006t0010g0121others(1): Show | 4 | HG02895.hp2 HG02897.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1040+938C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 5/19 | chr1 | 114432679 | ||||||
| chr1:114432803
|
C | T | 15 | a0001c0002t0006g0087a0001c0002t0006g0088a0001c0002t0006g0089others(12): Show | 15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1040+814G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 5/19 | chr1 | 114432803 | ||||||
| chr1:114432996
|
A | G | 6 | a0001c0002t0004g0111a0001c0002t0004g0114a0001c0002t0004g0115others(3): Show | 6 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1040+621T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 5/19 | chr1 | 114432996 | ||||||
| chr1:114433217
|
T | C | 1 | a0001c0009t0039g0123 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1040+400A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 5/19 | chr1 | 114433217 | ||||||
| chr1:114433602
|
A | C | 9 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0059others(6): Show | 9 | HG00741.hp1 HG01074.hp1 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.1040+15T>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 5/19 | chr1 | 114433602 | ||||||
| chr1:114433811
|
G | A | 3 | a0001c0001t0001g0059a0001c0001t0001g0084a0001c0001t0004g0077 | 3 | HG01081.hp2 HG03710.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.924-78C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114433811 | ||||||
| chr1:114434054
|
C | T | 15 | a0001c0002t0006g0087a0001c0002t0006g0088a0001c0002t0006g0089others(12): Show | 15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.924-321G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114434054 | ||||||
| chr1:114434097
|
C | T | 1 | a0001c0001t0002g0159 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.924-364G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114434097 | ||||||
| chr1:114434514
|
T | G | 1 | a0001c0001t0015g0065 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.924-781A>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114434514 | ||||||
| chr1:114434601
|
T | C | 1 | a0002c0003t0001g0021 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.924-868A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114434601 | ||||||
| chr1:114434781
|
C | G | 81 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(78): Show | 81 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.924-1048G>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114434781 | ||||||
| chr1:114435237
|
C | G | 81 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(78): Show | 81 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.924-1504G>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114435237 | ||||||
| chr1:114435322
|
G | A | 2 | a0001c0002t0006g0087a0001c0002t0034g0086 | 2 | HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.924-1589C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114435322 | ||||||
| chr1:114435396
|
C | T | 2 | a0001c0005t0007g0147a0001c0005t0007g0192 | 2 | HG01884.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.924-1663G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114435396 | ||||||
| chr1:114435401
|
C | A | 21 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(18): Show | 21 | HG00323.hp1 HG00738.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.924-1668G>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114435401 | ||||||
| chr1:114435695
|
T | C | 4 | a0001c0001t0002g0186a0001c0001t0002g0187a0001c0001t0002g0188others(1): Show | 4 | HG00642.hp2 HG01074.hp2 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.924-1962A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114435695 | ||||||
| chr1:114435771
|
A | G | 81 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(78): Show | 81 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.924-2038T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114435771 | ||||||
| chr1:114435877
|
C | CT | 41 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0052others(38): Show | 41 | HG00438.hp1 HG00642.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.924-2145dupA | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114435877 | ||||||
| chr1:114435877
|
C | CTT | 19 | a0001c0001t0026g0196a0001c0002t0003g0125a0001c0002t0003g0126others(16): Show | 19 | HG00323.hp1 HG00738.hp1 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.924-2146_924-2145d others(4): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114435877 | ||||||
| chr1:114435877
|
C | CTTT | 28 | a0001c0002t0003g0128a0001c0002t0003g0131a0001c0002t0003g0132others(25): Show | 28 | HG01106.hp1 HG01169.hp2 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.924-2147_924-2145d others(5): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114435877 | ||||||
| chr1:114435877
|
C | CTTTT | 16 | a0001c0002t0003g0133a0001c0002t0005g0098a0001c0002t0005g0103others(13): Show | 16 | HG00099.hp1 HG00735.hp1 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.924-2148_924-2145d others(6): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114435877 | ||||||
| chr1:114435877
|
C | T | 1 | a0001c0001t0002g0035 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.924-2144G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114435877 | ||||||
| chr1:114435877
|
CTTTTTTT others(5): Show |
C | 4 | a0001c0002t0020g0112a0001c0002t0020g0113a0001c0002t0025g0004others(1): Show | 4 | HG02622.hp1 HG02886.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.924-2156_924-2145d others(14): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114435877 | ||||||
| chr1:114435985
|
G | A | 24 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(21): Show | 24 | HG00323.hp1 HG00738.hp1 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.924-2252C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114435985 | ||||||
| chr1:114436146
|
T | C | 1 | a0001c0001t0002g0035 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.924-2413A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114436146 | ||||||
| chr1:114436199
|
G | A | 1 | a0001c0002t0003g0141 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.924-2466C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114436199 | ||||||
| chr1:114436261
|
G | C | 1 | a0001c0001t0001g0200 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.924-2528C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114436261 | ||||||
| chr1:114436400
|
C | CA | 16 | a0001c0001t0001g0075a0001c0001t0002g0149a0001c0001t0028g0062others(13): Show | 16 | HG00323.hp1 HG00738.hp1 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.924-2668dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114436400 | ||||||
| chr1:114436400
|
CA | C | 44 | a0001c0001t0002g0152a0001c0001t0002g0180a0001c0002t0005g0098others(41): Show | 44 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(41): Show |
intron_variant | MODIFIER | c.924-2668delT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114436400 | ||||||
| chr1:114436400
|
CAA | C | 11 | a0001c0002t0004g0111a0001c0002t0004g0114a0001c0002t0004g0115others(8): Show | 11 | HG01884.hp2 HG02109.hp1 HG02132.hp2 others(8): Show |
intron_variant | MODIFIER | c.924-2669_924-2668d others(4): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114436400 | ||||||
| chr1:114436401
|
A | G | 2 | a0001c0001t0002g0195a0001c0001t0026g0196 | 2 | HG01175.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.924-2668T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114436401 | ||||||
| chr1:114436426
|
A | T | 1 | a0003c0004t0004g0006 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.924-2693T>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114436426 | ||||||
| chr1:114436467
|
T | C | 68 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(65): Show | 68 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.924-2734A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114436467 | ||||||
| chr1:114436655
|
G | T | 1 | a0001c0002t0003g0137 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.924-2922C>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114436655 | ||||||
| chr1:114436703
|
G | T | 2 | a0001c0002t0006g0087a0001c0002t0034g0086 | 2 | HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.924-2970C>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114436703 | ||||||
| chr1:114436813
|
T | C | 3 | a0001c0002t0005g0098a0001c0002t0005g0099a0001c0002t0005g0101 | 3 | HG01433.hp2 HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.924-3080A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114436813 | ||||||
| chr1:114436820
|
G | A | 1 | a0001c0001t0040g0194 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.924-3087C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114436820 | ||||||
| chr1:114436931
|
T | C | 139 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0083others(136): Show | 139 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.924-3198A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114436931 | ||||||
| chr1:114436981
|
T | C | 6 | a0001c0006t0010g0119a0001c0006t0010g0120a0001c0006t0010g0121others(3): Show | 6 | HG02132.hp2 HG02698.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.924-3248A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114436981 | ||||||
| chr1:114436982
|
T | G | 3 | a0001c0002t0018g0145a0001c0002t0018g0146a0001c0002t0037g0118 | 3 | HG00741.hp2 HG02647.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.924-3249A>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114436982 | ||||||
| chr1:114437025
|
G | C | 1 | a0001c0002t0033g0117 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.924-3292C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114437025 | ||||||
| chr1:114437141
|
A | C | 6 | a0001c0002t0004g0111a0001c0002t0004g0114a0001c0002t0004g0115others(3): Show | 6 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.924-3408T>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114437141 | ||||||
| chr1:114437427
|
C | T | 1 | a0002c0003t0008g0041 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.924-3694G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114437427 | ||||||
| chr1:114437483
|
C | A | 2 | a0001c0002t0009g0202a0001c0002t0009g0203 | 2 | HG01891.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.924-3750G>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114437483 | ||||||
| chr1:114437492
|
C | T | 13 | a0001c0002t0005g0098a0001c0002t0005g0099a0001c0002t0005g0101others(10): Show | 13 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.924-3759G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114437492 | ||||||
| chr1:114437838
|
T | C | 1 | a0001c0006t0038g0124 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.924-4105A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114437838 | ||||||
| chr1:114438239
|
A | G | 1 | a0001c0001t0002g0171 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.924-4506T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114438239 | ||||||
| chr1:114438460
|
G | C | 1 | a0001c0005t0007g0151 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.924-4727C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114438460 | ||||||
| chr1:114438494
|
T | C | 6 | a0003c0004t0001g0008a0003c0004t0004g0009a0003c0004t0013g0010others(3): Show | 6 | HG02145.hp1 HG02258.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.924-4761A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114438494 | ||||||
| chr1:114438681
|
ACTT | A | 13 | a0001c0002t0005g0098a0001c0002t0005g0099a0001c0002t0005g0101others(10): Show | 13 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.924-4951_924-4949d others(5): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114438681 | ||||||
| chr1:114438896
|
T | C | 1 | a0001c0002t0003g0132 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.924-5163A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114438896 | ||||||
| chr1:114439008
|
A | G | 81 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(78): Show | 81 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.924-5275T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114439008 | ||||||
| chr1:114439279
|
CTGACCAA others(15): Show |
C | 4 | a0001c0002t0033g0117a0003c0004t0014g0005a0003c0004t0014g0012others(1): Show | 4 | HG02055.hp2 HG02451.hp2 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.924-5568_924-5547d others(24): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114439279 | ||||||
| chr1:114439468
|
C | CA | 11 | a0001c0001t0001g0060a0001c0001t0001g0072a0001c0001t0001g0075others(8): Show | 12 | HG00558.hp1 HG01081.hp1 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.924-5736dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114439468 | ||||||
| chr1:114439468
|
CA | C | 67 | a0001c0001t0001g0046a0001c0001t0001g0083a0001c0001t0001g0164others(64): Show | 67 | HG00099.hp1 HG00558.hp2 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.924-5736delT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114439468 | ||||||
| chr1:114439468
|
CAAA | C | 27 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0128others(24): Show | 27 | HG00323.hp1 HG00741.hp2 HG01099.hp1 others(24): Show |
intron_variant | MODIFIER | c.924-5738_924-5736d others(5): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114439468 | ||||||
| chr1:114439468
|
CAAAA | C | 12 | a0001c0002t0009g0202a0001c0002t0009g0203a0001c0002t0009g0204others(9): Show | 12 | HG01891.hp2 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.924-5739_924-5736d others(6): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114439468 | ||||||
| chr1:114439468
|
CAAAAAA | C | 10 | a0001c0002t0005g0098a0001c0002t0005g0099a0001c0002t0005g0101others(7): Show | 10 | HG01192.hp1 HG01261.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.924-5741_924-5736d others(8): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114439468 | ||||||
| chr1:114439512
|
TCCTA | T | 10 | a0001c0002t0033g0117a0001c0006t0010g0119a0001c0006t0010g0120others(7): Show | 10 | HG02055.hp2 HG02132.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.924-5783_924-5780d others(6): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114439512 | ||||||
| chr1:114439517
|
C | A | 15 | a0001c0002t0006g0087a0001c0002t0006g0088a0001c0002t0006g0089others(12): Show | 15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.924-5784G>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114439517 | ||||||
| chr1:114439537
|
C | CA | 43 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(40): Show | 43 | HG00323.hp1 HG00738.hp1 HG01099.hp1 others(40): Show |
intron_variant | MODIFIER | c.924-5805dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114439537 | ||||||
| chr1:114439586
|
T | C | 1 | a0001c0002t0025g0004 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.924-5853A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114439586 | ||||||
| chr1:114439642
|
G | A | 15 | a0001c0002t0006g0087a0001c0002t0006g0088a0001c0002t0006g0089others(12): Show | 15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.924-5909C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114439642 | ||||||
| chr1:114439765
|
C | T | 5 | a0001c0002t0003g0136a0001c0002t0003g0137a0001c0002t0003g0138others(2): Show | 5 | HG00323.hp1 HG01167.hp1 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.924-6032G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114439765 | ||||||
| chr1:114439854
|
T | C | 1 | a0004c0007t0001g0014 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.924-6121A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114439854 | ||||||
| chr1:114440722
|
G | GA | 3 | a0001c0002t0018g0145a0001c0002t0018g0146a0001c0002t0037g0118 | 3 | HG00741.hp2 HG02647.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.924-6990dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114440722 | ||||||
| chr1:114440727
|
G | A | 3 | a0003c0004t0004g0006a0003c0004t0013g0007a0003c0004t0050g0206 | 3 | HG02280.hp1 HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.924-6994C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114440727 | ||||||
| chr1:114440766
|
G | A | 1 | a0001c0002t0006g0095 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.924-7033C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114440766 | ||||||
| chr1:114441087
|
C | T | 8 | a0003c0004t0001g0008a0003c0004t0004g0006a0003c0004t0004g0009others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.924-7354G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114441087 | ||||||
| chr1:114441249
|
C | T | 81 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(78): Show | 81 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.924-7516G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114441249 | ||||||
| chr1:114441456
|
T | A | 1 | a0001c0001t0002g0180 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.924-7723A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114441456 | ||||||
| chr1:114441546
|
C | T | 1 | a0001c0001t0015g0051 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.924-7813G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114441546 | ||||||
| chr1:114441547
|
G | A | 12 | a0001c0002t0009g0202a0001c0002t0009g0203a0001c0002t0009g0204others(9): Show | 12 | HG01891.hp2 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.924-7814C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114441547 | ||||||
| chr1:114441738
|
G | A | 3 | a0003c0004t0004g0006a0003c0004t0013g0007a0003c0004t0050g0206 | 3 | HG02280.hp1 HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.924-8005C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114441738 | ||||||
| chr1:114441757
|
A | G | 1 | a0001c0001t0001g0075 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.924-8024T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114441757 | ||||||
| chr1:114441762
|
C | T | 2 | a0001c0001t0022g0056a0001c0001t0022g0057 | 2 | HG03704.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.924-8029G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114441762 | ||||||
| chr1:114442029
|
C | T | 13 | a0001c0002t0005g0098a0001c0002t0005g0099a0001c0002t0005g0101others(10): Show | 13 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.924-8296G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114442029 | ||||||
| chr1:114442045
|
G | A | 81 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(78): Show | 81 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.924-8312C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114442045 | ||||||
| chr1:114442200
|
G | A | 1 | a0001c0001t0001g0052 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.924-8467C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114442200 | ||||||
| chr1:114442315
|
G | A | 1 | a0005c0008t0013g0015 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.924-8582C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114442315 | ||||||
| chr1:114442327
|
G | A | 1 | a0002c0003t0004g0048 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.924-8594C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114442327 | ||||||
| chr1:114442687
|
C | CA | 19 | a0001c0001t0001g0052a0001c0001t0002g0178a0001c0001t0002g0180others(16): Show | 19 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.924-8955dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114442687 | ||||||
| chr1:114442687
|
CA | C | 65 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(62): Show | 65 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.924-8955delT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114442687 | ||||||
| chr1:114442694
|
AAAAAAAA others(4): Show |
A | 3 | a0003c0004t0004g0006a0003c0004t0013g0007a0003c0004t0050g0206 | 3 | HG02280.hp1 HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.924-8972_924-8962d others(13): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114442694 | ||||||
| chr1:114442705
|
G | A | 1 | a0001c0001t0028g0062 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.924-8972C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114442705 | ||||||
| chr1:114442742
|
C | T | 1 | a0001c0009t0039g0123 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.924-9009G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114442742 | ||||||
| chr1:114442836
|
T | C | 3 | a0003c0004t0004g0006a0003c0004t0013g0007a0003c0004t0050g0206 | 3 | HG02280.hp1 HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.924-9103A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114442836 | ||||||
| chr1:114442871
|
T | A | 1 | a0001c0002t0037g0118 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.924-9138A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114442871 | ||||||
| chr1:114442916
|
A | G | 1 | a0002c0003t0001g0021 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.924-9183T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114442916 | ||||||
| chr1:114442918
|
A | AT | 11 | a0001c0002t0005g0098a0001c0002t0005g0099a0001c0002t0005g0101others(8): Show | 11 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.924-9186dupA | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114442918 | ||||||
| chr1:114442928
|
A | G | 1 | a0003c0004t0014g0005 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.924-9195T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114442928 | ||||||
| chr1:114443039
|
C | T | 1 | a0001c0002t0037g0118 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.924-9306G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114443039 | ||||||
| chr1:114443110
|
G | A | 5 | a0001c0002t0033g0117a0003c0004t0014g0005a0003c0004t0014g0012others(2): Show | 5 | HG02055.hp2 HG02451.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.924-9377C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114443110 | ||||||
| chr1:114443121
|
C | T | 2 | a0001c0002t0009g0204a0001c0002t0009g0205 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.924-9388G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114443121 | ||||||
| chr1:114443197
|
C | T | 3 | a0001c0001t0015g0051a0001c0001t0015g0063a0001c0001t0015g0065 | 3 | HG00099.hp2 HG00323.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.924-9464G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114443197 | ||||||
| chr1:114443214
|
A | G | 81 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(78): Show | 81 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.924-9481T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114443214 | ||||||
| chr1:114443227
|
C | CA | 5 | a0001c0002t0033g0117a0003c0004t0014g0005a0003c0004t0014g0012others(2): Show | 5 | HG02055.hp2 HG02451.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.924-9495dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114443227 | ||||||
| chr1:114443245
|
G | A | 1 | a0001c0001t0015g0051 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.924-9512C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114443245 | ||||||
| chr1:114443305
|
A | G | 2 | a0003c0004t0001g0008a0003c0004t0004g0009 | 2 | HG02965.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.924-9572T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114443305 | ||||||
| chr1:114443341
|
G | A | 1 | a0001c0001t0002g0185 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.924-9608C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114443341 | ||||||
| chr1:114443369
|
G | A | 3 | a0001c0002t0018g0145a0001c0002t0018g0146a0001c0002t0037g0118 | 3 | HG00741.hp2 HG02647.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.924-9636C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114443369 | ||||||
| chr1:114443385
|
A | AAATG | 30 | a0001c0001t0002g0195a0001c0001t0011g0054a0001c0001t0011g0055others(27): Show | 30 | HG00558.hp1 HG00741.hp2 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.924-9656_924-9653d others(6): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114443385 | ||||||
| chr1:114443385
|
A | AAATGAAT others(1): Show |
26 | a0001c0002t0004g0111a0001c0002t0004g0114a0001c0002t0004g0115others(23): Show | 26 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.924-9660_924-9653d others(10): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114443385 | ||||||
| chr1:114443385
|
A | AAATGAAT others(5): Show |
4 | a0001c0002t0020g0112a0001c0002t0020g0113a0001c0002t0023g0002others(1): Show | 4 | HG02622.hp1 HG02886.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.924-9664_924-9653d others(14): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114443385 | ||||||
| chr1:114443385
|
A | AAATGAAT others(9): Show |
1 | a0003c0004t0013g0010 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.924-9668_924-9653d others(18): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114443385 | ||||||
| chr1:114443385
|
A | AAATGAAT others(13): Show |
2 | a0001c0002t0009g0204a0001c0002t0009g0205 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.924-9672_924-9653d others(22): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114443385 | ||||||
| chr1:114443385
|
AAATG | A | 6 | a0001c0006t0010g0119a0001c0006t0010g0120a0001c0006t0010g0121others(3): Show | 6 | HG02132.hp2 HG02698.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.924-9656_924-9653d others(6): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114443385 | ||||||
| chr1:114443528
|
C | T | 5 | a0003c0004t0001g0008a0003c0004t0004g0009a0003c0004t0013g0010others(2): Show | 5 | HG02145.hp1 HG02258.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.924-9795G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114443528 | ||||||
| chr1:114443622
|
T | C | 8 | a0003c0004t0001g0008a0003c0004t0004g0006a0003c0004t0004g0009others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.924-9889A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114443622 | ||||||
| chr1:114443714
|
C | T | 1 | a0001c0001t0002g0167 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.924-9981G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114443714 | ||||||
| chr1:114444157
|
A | G | 1 | a0001c0001t0040g0194 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.924-10424T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114444157 | ||||||
| chr1:114444222
|
G | C | 1 | a0004c0007t0001g0014 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.924-10489C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114444222 | ||||||
| chr1:114444319
|
T | C | 3 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0143 | 3 | HG01099.hp1 HG01952.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.924-10586A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114444319 | ||||||
| chr1:114444969
|
C | T | 13 | a0001c0002t0005g0098a0001c0002t0005g0099a0001c0002t0005g0101others(10): Show | 13 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.924-11236G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114444969 | ||||||
| chr1:114445096
|
C | G | 81 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(78): Show | 81 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.924-11363G>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114445096 | ||||||
| chr1:114445244
|
T | A | 3 | a0003c0004t0014g0005a0003c0004t0014g0012a0003c0004t0014g0013 | 3 | HG02055.hp2 HG02523.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.924-11511A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114445244 | ||||||
| chr1:114445303
|
T | C | 1 | a0001c0002t0004g0111 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.924-11570A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114445303 | ||||||
| chr1:114445341
|
G | A | 2 | a0001c0001t0030g0156a0003c0004t0014g0013 | 2 | HG02523.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.924-11608C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114445341 | ||||||
| chr1:114445553
|
T | C | 13 | a0001c0002t0005g0098a0001c0002t0005g0099a0001c0002t0005g0101others(10): Show | 13 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.924-11820A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114445553 | ||||||
| chr1:114446008
|
T | C | 81 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(78): Show | 81 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.924-12275A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114446008 | ||||||
| chr1:114446175
|
T | G | 2 | a0003c0004t0013g0007a0003c0004t0050g0206 | 2 | HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.924-12442A>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114446175 | ||||||
| chr1:114446221
|
G | C | 10 | a0001c0002t0033g0117a0001c0006t0010g0119a0001c0006t0010g0120others(7): Show | 10 | HG02055.hp2 HG02132.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.924-12488C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114446221 | ||||||
| chr1:114446360
|
T | C | 1 | a0001c0001t0002g0171 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.924-12627A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114446360 | ||||||
| chr1:114446400
|
A | G | 1 | a0001c0001t0001g0067 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.924-12667T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114446400 | ||||||
| chr1:114446474
|
T | G | 4 | a0001c0002t0009g0202a0001c0002t0009g0203a0001c0002t0009g0204others(1): Show | 4 | HG01891.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.924-12741A>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114446474 | ||||||
| chr1:114446567
|
G | C | 1 | a0001c0002t0032g0116 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.924-12834C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114446567 | ||||||
| chr1:114446589
|
T | G | 68 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(65): Show | 68 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.924-12856A>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114446589 | ||||||
| chr1:114446914
|
G | C | 1 | a0001c0001t0002g0149 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.924-13181C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114446914 | ||||||
| chr1:114446958
|
T | C | 13 | a0001c0002t0005g0098a0001c0002t0005g0099a0001c0002t0005g0101others(10): Show | 13 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.924-13225A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114446958 | ||||||
| chr1:114447158
|
T | G | 1 | a0001c0001t0040g0194 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.924-13425A>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114447158 | ||||||
| chr1:114447265
|
T | C | 2 | a0001c0002t0009g0204a0001c0002t0009g0205 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.924-13532A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114447265 | ||||||
| chr1:114447378
|
T | C | 1 | a0001c0001t0048g0081 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.924-13645A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114447378 | ||||||
| chr1:114447533
|
T | C | 6 | a0001c0002t0004g0111a0001c0002t0004g0114a0001c0002t0004g0115others(3): Show | 6 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.924-13800A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114447533 | ||||||
| chr1:114447634
|
C | T | 81 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(78): Show | 81 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.924-13901G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114447634 | ||||||
| chr1:114447880
|
T | C | 1 | a0001c0002t0033g0117 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.924-14147A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114447880 | ||||||
| chr1:114447941
|
G | A | 1 | a0001c0001t0040g0194 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.924-14208C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114447941 | ||||||
| chr1:114448206
|
G | C | 9 | a0003c0004t0001g0008a0003c0004t0004g0006a0003c0004t0004g0009others(6): Show | 9 | HG02145.hp1 HG02258.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.924-14473C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114448206 | ||||||
| chr1:114448439
|
C | T | 1 | a0001c0001t0004g0077 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.923+14665G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114448439 | ||||||
| chr1:114448453
|
T | C | 4 | a0001c0006t0010g0119a0001c0006t0010g0120a0001c0006t0010g0121others(1): Show | 4 | HG02895.hp2 HG02897.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.923+14651A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114448453 | ||||||
| chr1:114448807
|
A | G | 15 | a0001c0002t0006g0087a0001c0002t0006g0088a0001c0002t0006g0089others(12): Show | 15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.923+14297T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114448807 | ||||||
| chr1:114448822
|
G | C | 1 | a0001c0002t0006g0096 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.923+14282C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114448822 | ||||||
| chr1:114448824
|
G | A | 2 | a0001c0005t0007g0147a0001c0005t0007g0192 | 2 | HG01884.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.923+14280C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114448824 | ||||||
| chr1:114448959
|
T | C | 1 | a0002c0003t0001g0001 | 2 | HG01433.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.923+14145A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114448959 | ||||||
| chr1:114449163
|
T | TA | 21 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(18): Show | 21 | HG00323.hp1 HG00738.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.923+13940dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114449163 | ||||||
| chr1:114449420
|
G | A | 2 | a0001c0001t0001g0045a0001c0001t0001g0046 | 2 | HG02809.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.923+13684C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114449420 | ||||||
| chr1:114449546
|
T | C | 4 | a0001c0001t0002g0148a0001c0001t0002g0155a0001c0001t0002g0198others(1): Show | 4 | HG02145.hp2 HG02258.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.923+13558A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114449546 | ||||||
| chr1:114449666
|
TA | T | 13 | a0001c0002t0005g0098a0001c0002t0005g0099a0001c0002t0005g0101others(10): Show | 13 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.923+13437delT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114449666 | ||||||
| chr1:114449788
|
A | C | 1 | a0001c0002t0003g0143 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.923+13316T>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114449788 | ||||||
| chr1:114449849
|
T | G | 4 | a0001c0002t0009g0202a0001c0002t0009g0203a0001c0002t0009g0204others(1): Show | 4 | HG01891.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.923+13255A>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114449849 | ||||||
| chr1:114449927
|
T | A | 1 | a0001c0002t0032g0116 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.923+13177A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114449927 | ||||||
| chr1:114450138
|
C | T | 81 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(78): Show | 81 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.923+12966G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114450138 | ||||||
| chr1:114450232
|
C | G | 1 | a0003c0004t0013g0010 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.923+12872G>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114450232 | ||||||
| chr1:114450273
|
A | T | 13 | a0001c0002t0005g0098a0001c0002t0005g0099a0001c0002t0005g0101others(10): Show | 13 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.923+12831T>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114450273 | ||||||
| chr1:114450307
|
CTTTCT | C | 4 | a0001c0002t0009g0202a0001c0002t0009g0203a0001c0002t0009g0204others(1): Show | 4 | HG01891.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.923+12792_923+1279 others(9): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114450307 | ||||||
| chr1:114450325
|
GTTGTT | G | 6 | a0001c0006t0010g0119a0001c0006t0010g0120a0001c0006t0010g0121others(3): Show | 6 | HG02132.hp2 HG02698.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.923+12774_923+1277 others(9): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114450325 | ||||||
| chr1:114450340
|
T | C | 35 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0052others(32): Show | 35 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.923+12764A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114450340 | ||||||
| chr1:114450484
|
A | C | 6 | a0001c0006t0010g0119a0001c0006t0010g0120a0001c0006t0010g0121others(3): Show | 6 | HG02132.hp2 HG02698.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.923+12620T>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114450484 | ||||||
| chr1:114450663
|
G | C | 1 | a0002c0003t0001g0082 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.923+12441C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114450663 | ||||||
| chr1:114450892
|
T | C | 1 | a0001c0002t0003g0127 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.923+12212A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114450892 | ||||||
| chr1:114451374
|
T | TA | 45 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0128others(42): Show | 45 | HG00099.hp1 HG00323.hp1 HG01099.hp1 others(42): Show |
intron_variant | MODIFIER | c.923+11729dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114451374 | ||||||
| chr1:114451374
|
T | TAA | 33 | a0001c0002t0003g0127a0001c0002t0005g0098a0001c0002t0005g0099others(30): Show | 33 | HG00735.hp1 HG00738.hp1 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.923+11728_923+1172 others(6): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114451374 | ||||||
| chr1:114451687
|
T | TA | 13 | a0001c0002t0005g0098a0001c0002t0005g0099a0001c0002t0005g0101others(10): Show | 13 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.923+11416dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114451687 | ||||||
| chr1:114451840
|
C | G | 1 | a0001c0001t0002g0149 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.923+11264G>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114451840 | ||||||
| chr1:114451877
|
C | T | 6 | a0001c0002t0004g0111a0001c0002t0004g0114a0001c0002t0004g0115others(3): Show | 6 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.923+11227G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114451877 | ||||||
| chr1:114451887
|
C | A | 1 | a0002c0003t0001g0047 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.923+11217G>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114451887 | ||||||
| chr1:114452079
|
A | AAGAAT | 47 | a0001c0002t0004g0111a0001c0002t0004g0114a0001c0002t0004g0115others(44): Show | 47 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(44): Show |
intron_variant | MODIFIER | c.923+11020_923+1102 others(9): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114452079 | ||||||
| chr1:114452122
|
A | G | 1 | a0001c0002t0005g0108 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.923+10982T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114452122 | ||||||
| chr1:114452237
|
G | A | 2 | a0001c0001t0001g0164a0001c0001t0001g0200 | 2 | NA18747.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.923+10867C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114452237 | ||||||
| chr1:114452438
|
AAC | A | 3 | a0001c0002t0018g0145a0001c0002t0018g0146a0001c0002t0037g0118 | 3 | HG00741.hp2 HG02647.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.923+10664_923+1066 others(6): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114452438 | ||||||
| chr1:114452452
|
C | G | 13 | a0001c0002t0005g0098a0001c0002t0005g0099a0001c0002t0005g0101others(10): Show | 13 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.923+10652G>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114452452 | ||||||
| chr1:114452522
|
T | C | 1 | a0001c0002t0037g0118 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.923+10582A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114452522 | ||||||
| chr1:114452602
|
A | G | 3 | a0003c0004t0013g0010a0003c0004t0031g0011a0005c0008t0013g0015 | 3 | HG02145.hp1 HG02258.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.923+10502T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114452602 | ||||||
| chr1:114452727
|
TA | T | 46 | a0001c0001t0001g0058a0001c0001t0001g0164a0001c0001t0001g0176others(43): Show | 46 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.923+10376delT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114452727 | ||||||
| chr1:114452727
|
TAA | T | 12 | a0001c0002t0005g0098a0001c0002t0005g0099a0001c0002t0005g0101others(9): Show | 12 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.923+10375_923+1037 others(6): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114452727 | ||||||
| chr1:114452727
|
TAAA | T | 32 | a0001c0002t0004g0111a0001c0002t0004g0114a0001c0002t0004g0115others(29): Show | 32 | HG00741.hp2 HG01106.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.923+10374_923+1037 others(7): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114452727 | ||||||
| chr1:114452727
|
TAAAA | T | 37 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(34): Show | 37 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.923+10373_923+1037 others(8): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114452727 | ||||||
| chr1:114452771
|
A | G | 1 | a0001c0002t0023g0002 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.923+10333T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114452771 | ||||||
| chr1:114453203
|
A | C | 5 | a0001c0002t0033g0117a0003c0004t0014g0005a0003c0004t0014g0012others(2): Show | 5 | HG02055.hp2 HG02451.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.923+9901T>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114453203 | ||||||
| chr1:114453364
|
G | GA | 20 | a0001c0002t0006g0087a0001c0002t0006g0088a0001c0002t0006g0089others(17): Show | 20 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.923+9739dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114453364 | ||||||
| chr1:114453490
|
A | G | 81 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(78): Show | 81 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.923+9614T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114453490 | ||||||
| chr1:114453546
|
G | A | 1 | a0001c0002t0004g0111 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.923+9558C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114453546 | ||||||
| chr1:114453702
|
T | C | 21 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(18): Show | 21 | HG00323.hp1 HG00738.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.923+9402A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114453702 | ||||||
| chr1:114453736
|
A | G | 6 | a0001c0002t0004g0111a0001c0002t0004g0114a0001c0002t0004g0115others(3): Show | 6 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.923+9368T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114453736 | ||||||
| chr1:114453886
|
G | A | 1 | a0002c0003t0004g0027 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.923+9218C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114453886 | ||||||
| chr1:114454122
|
C | G | 1 | a0001c0002t0021g0092 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.923+8982G>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114454122 | ||||||
| chr1:114454204
|
C | T | 2 | a0001c0001t0001g0083a0001c0001t0004g0050 | 2 | HG02055.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.923+8900G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114454204 | ||||||
| chr1:114454524
|
A | AAAAAAT | 11 | a0001c0002t0005g0098a0001c0002t0005g0099a0001c0002t0005g0101others(8): Show | 11 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.923+8574_923+8579d others(8): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114454524 | ||||||
| chr1:114454673
|
T | TA | 62 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(59): Show | 62 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.923+8430dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114454673 | ||||||
| chr1:114454673
|
T | TAA | 18 | a0001c0002t0004g0114a0001c0002t0004g0115a0001c0002t0005g0098others(15): Show | 18 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.923+8429_923+8430d others(4): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114454673 | ||||||
| chr1:114454774
|
T | C | 1 | a0001c0001t0004g0024 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.923+8330A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114454774 | ||||||
| chr1:114455108
|
T | G | 13 | a0001c0002t0005g0098a0001c0002t0005g0099a0001c0002t0005g0101others(10): Show | 13 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.923+7996A>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114455108 | ||||||
| chr1:114455223
|
C | T | 4 | a0001c0002t0009g0202a0001c0002t0009g0203a0001c0002t0009g0204others(1): Show | 4 | HG01891.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.923+7881G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114455223 | ||||||
| chr1:114455239
|
T | C | 6 | a0001c0002t0004g0111a0001c0002t0004g0114a0001c0002t0004g0115others(3): Show | 6 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.923+7865A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114455239 | ||||||
| chr1:114455325
|
T | C | 1 | a0002c0003t0001g0029 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.923+7779A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114455325 | ||||||
| chr1:114455599
|
G | C | 30 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(27): Show | 30 | HG00323.hp1 HG00738.hp1 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.923+7505C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114455599 | ||||||
| chr1:114455807
|
G | C | 1 | a0002c0003t0016g0038 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.923+7297C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114455807 | ||||||
| chr1:114456205
|
A | C | 21 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(18): Show | 21 | HG00323.hp1 HG00738.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.923+6899T>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114456205 | ||||||
| chr1:114456337
|
A | G | 1 | a0002c0003t0004g0027 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.923+6767T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114456337 | ||||||
| chr1:114456389
|
C | A | 8 | a0003c0004t0001g0008a0003c0004t0004g0006a0003c0004t0004g0009others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.923+6715G>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114456389 | ||||||
| chr1:114456476
|
G | A | 1 | a0001c0001t0001g0084 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.923+6628C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114456476 | ||||||
| chr1:114456634
|
G | A | 13 | a0001c0002t0005g0098a0001c0002t0005g0099a0001c0002t0005g0101others(10): Show | 13 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.923+6470C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114456634 | ||||||
| chr1:114456655
|
G | A | 81 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(78): Show | 81 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.923+6449C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114456655 | ||||||
| chr1:114456843
|
G | A | 15 | a0001c0002t0006g0087a0001c0002t0006g0088a0001c0002t0006g0089others(12): Show | 15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.923+6261C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114456843 | ||||||
| chr1:114456954
|
A | G | 6 | a0001c0002t0004g0111a0001c0002t0004g0114a0001c0002t0004g0115others(3): Show | 6 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.923+6150T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114456954 | ||||||
| chr1:114456971
|
T | G | 11 | a0001c0002t0033g0117a0001c0006t0010g0119a0001c0006t0010g0120others(8): Show | 11 | HG02055.hp2 HG02132.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.923+6133A>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114456971 | ||||||
| chr1:114457127
|
G | C | 1 | a0001c0001t0001g0084 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.923+5977C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114457127 | ||||||
| chr1:114457356
|
T | G | 1 | a0002c0003t0001g0017 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.923+5748A>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114457356 | ||||||
| chr1:114457438
|
G | A | 68 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(65): Show | 68 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.923+5666C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114457438 | ||||||
| chr1:114457477
|
A | G | 1 | a0001c0001t0002g0148 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.923+5627T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114457477 | ||||||
| chr1:114457840
|
C | G | 1 | a0001c0002t0003g0130 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.923+5264G>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114457840 | ||||||
| chr1:114457859
|
G | A | 68 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(65): Show | 68 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.923+5245C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114457859 | ||||||
| chr1:114457908
|
C | T | 1 | a0001c0002t0032g0116 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.923+5196G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114457908 | ||||||
| chr1:114458020
|
C | A | 5 | a0001c0002t0033g0117a0003c0004t0014g0005a0003c0004t0014g0012others(2): Show | 5 | HG02055.hp2 HG02451.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.923+5084G>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114458020 | ||||||
| chr1:114458499
|
C | T | 3 | a0003c0004t0004g0006a0003c0004t0013g0007a0003c0004t0050g0206 | 3 | HG02280.hp1 HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.923+4605G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114458499 | ||||||
| chr1:114458520
|
A | T | 1 | a0003c0004t0001g0008 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.923+4584T>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114458520 | ||||||
| chr1:114458560
|
C | A | 1 | a0001c0002t0006g0095 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.923+4544G>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114458560 | ||||||
| chr1:114458916
|
T | C | 15 | a0001c0002t0006g0087a0001c0002t0006g0088a0001c0002t0006g0089others(12): Show | 15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.923+4188A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114458916 | ||||||
| chr1:114459301
|
T | G | 1 | a0001c0002t0033g0117 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.923+3803A>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114459301 | ||||||
| chr1:114459370
|
C | T | 6 | a0001c0002t0004g0111a0001c0002t0004g0114a0001c0002t0004g0115others(3): Show | 6 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.923+3734G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114459370 | ||||||
| chr1:114459400
|
T | C | 2 | a0001c0002t0005g0104a0001c0002t0005g0107 | 2 | HG02615.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.923+3704A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114459400 | ||||||
| chr1:114459509
|
C | A | 1 | a0001c0001t0002g0160 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.923+3595G>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114459509 | ||||||
| chr1:114459512
|
G | A | 5 | a0001c0001t0001g0164a0001c0001t0002g0149a0001c0001t0002g0161others(2): Show | 5 | HG00438.hp1 HG00558.hp2 HG02015.hp1 others(2): Show |
intron_variant | MODIFIER | c.923+3592C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114459512 | ||||||
| chr1:114459659
|
T | C | 6 | a0001c0002t0004g0111a0001c0002t0004g0114a0001c0002t0004g0115others(3): Show | 6 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.923+3445A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114459659 | ||||||
| chr1:114459719
|
CAG | C | 68 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(65): Show | 68 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.923+3383_923+3384d others(4): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114459719 | ||||||
| chr1:114459916
|
G | A | 3 | a0001c0002t0005g0098a0001c0002t0005g0099a0001c0002t0005g0101 | 3 | HG01433.hp2 HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.923+3188C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114459916 | ||||||
| chr1:114460108
|
C | T | 1 | a0001c0002t0005g0108 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.923+2996G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114460108 | ||||||
| chr1:114460146
|
C | T | 1 | a0001c0001t0002g0195 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.923+2958G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114460146 | ||||||
| chr1:114460184
|
A | G | 1 | a0001c0001t0001g0084 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.923+2920T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114460184 | ||||||
| chr1:114460195
|
C | G | 2 | a0001c0002t0009g0204a0001c0002t0009g0205 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.923+2909G>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114460195 | ||||||
| chr1:114460283
|
T | G | 8 | a0002c0003t0001g0039a0002c0003t0001g0082a0002c0003t0008g0028others(5): Show | 8 | HG00642.hp1 HG00738.hp2 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.923+2821A>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114460283 | ||||||
| chr1:114460384
|
C | T | 4 | a0001c0002t0006g0093a0001c0002t0006g0094a0001c0002t0006g0095others(1): Show | 4 | HG02280.hp2 HG02723.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.923+2720G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114460384 | ||||||
| chr1:114460503
|
T | C | 1 | a0001c0001t0026g0196 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.923+2601A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114460503 | ||||||
| chr1:114460573
|
CT | C | 156 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0022others(153): Show | 157 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.923+2530delA | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114460573 | ||||||
| chr1:114460573
|
CTT | C | 19 | a0001c0001t0001g0025a0001c0001t0001g0083a0001c0001t0001g0176others(16): Show | 19 | HG01884.hp1 HG01884.hp2 HG01993.hp1 others(16): Show |
intron_variant | MODIFIER | c.923+2529_923+2530d others(4): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114460573 | ||||||
| chr1:114460687
|
C | T | 1 | a0001c0002t0003g0131 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.923+2417G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114460687 | ||||||
| chr1:114460781
|
T | C | 34 | a0001c0002t0005g0098a0001c0002t0005g0099a0001c0002t0005g0101others(31): Show | 34 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.923+2323A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114460781 | ||||||
| chr1:114461003
|
G | A | 1 | a0002c0003t0001g0031 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.923+2101C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114461003 | ||||||
| chr1:114461066
|
C | T | 13 | a0001c0002t0005g0098a0001c0002t0005g0099a0001c0002t0005g0101others(10): Show | 13 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.923+2038G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114461066 | ||||||
| chr1:114461154
|
T | A | 20 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0052others(17): Show | 20 | HG00558.hp1 HG00741.hp1 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.923+1950A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114461154 | ||||||
| chr1:114461211
|
T | TA | 17 | a0001c0002t0004g0111a0001c0002t0004g0114a0001c0002t0004g0115others(14): Show | 17 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.923+1892dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114461211 | ||||||
| chr1:114461211
|
T | TAA | 20 | a0001c0002t0006g0087a0001c0002t0006g0088a0001c0002t0006g0089others(17): Show | 20 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.923+1891_923+1892d others(4): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114461211 | ||||||
| chr1:114461215
|
A | AAT | 11 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0059others(8): Show | 11 | HG00741.hp1 HG01081.hp2 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.923+1887_923+1888d others(4): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114461215 | ||||||
| chr1:114461215
|
AAT | A | 57 | a0001c0001t0001g0022a0001c0001t0001g0025a0001c0001t0001g0045others(54): Show | 57 | HG00438.hp1 HG00558.hp2 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.923+1887_923+1888d others(4): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114461215 | ||||||
| chr1:114461216
|
AT | A | 42 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(39): Show | 42 | HG00323.hp1 HG00738.hp1 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.923+1887delA | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114461216 | ||||||
| chr1:114461217
|
T | A | 36 | a0001c0001t0011g0066a0001c0001t0022g0057a0001c0002t0006g0087others(33): Show | 36 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(33): Show |
intron_variant | MODIFIER | c.923+1887A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114461217 | ||||||
| chr1:114461219
|
T | A | 57 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(54): Show | 57 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(54): Show |
intron_variant | MODIFIER | c.923+1885A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114461219 | ||||||
| chr1:114461221
|
T | A | 37 | a0001c0002t0003g0128a0001c0002t0003g0130a0001c0002t0003g0131others(34): Show | 37 | HG00099.hp1 HG00735.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.923+1883A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114461221 | ||||||
| chr1:114461223
|
T | A | 2 | a0001c0002t0046g0091a0003c0004t0050g0206 | 2 | HG01106.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.923+1881A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114461223 | ||||||
| chr1:114461235
|
T | C | 2 | a0001c0001t0002g0170a0001c0002t0004g0111 | 2 | HG02109.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.923+1869A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114461235 | ||||||
| chr1:114461290
|
A | ATTTATAT | 21 | a0001c0002t0006g0087a0001c0002t0006g0088a0001c0002t0006g0089others(18): Show | 21 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.923+1807_923+1813d others(9): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114461290 | ||||||
| chr1:114461291
|
T | TTTATATA | 5 | a0001c0002t0033g0117a0003c0004t0014g0005a0003c0004t0014g0012others(2): Show | 5 | HG02055.hp2 HG02451.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.923+1806_923+1812d others(9): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114461291 | ||||||
| chr1:114461298
|
A | ATTATATT | 40 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(37): Show | 40 | HG00323.hp1 HG00738.hp1 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.923+1799_923+1805d others(9): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114461298 | ||||||
| chr1:114461298
|
A | T | 21 | a0001c0002t0006g0087a0001c0002t0006g0088a0001c0002t0006g0089others(18): Show | 21 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.923+1806T>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114461298 | ||||||
| chr1:114461306
|
T | C | 1 | a0005c0008t0013g0015 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.923+1798A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114461306 | ||||||
| chr1:114461313
|
T | A | 5 | a0003c0004t0001g0008a0003c0004t0004g0009a0003c0004t0013g0010others(2): Show | 5 | HG02145.hp1 HG02258.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.923+1791A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114461313 | ||||||
| chr1:114461319
|
A | G | 3 | a0001c0002t0003g0131a0001c0002t0003g0132a0001c0002t0029g0135 | 3 | NA18612.hp2 NA18957.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.923+1785T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114461319 | ||||||
| chr1:114461432
|
C | T | 24 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(21): Show | 24 | HG00323.hp1 HG00738.hp1 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.923+1672G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114461432 | ||||||
| chr1:114461569
|
T | A | 15 | a0001c0002t0006g0087a0001c0002t0006g0088a0001c0002t0006g0089others(12): Show | 15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.923+1535A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114461569 | ||||||
| chr1:114461946
|
T | A | 3 | a0003c0004t0014g0005a0003c0004t0014g0012a0003c0004t0014g0013 | 3 | HG02055.hp2 HG02523.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.923+1158A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114461946 | ||||||
| chr1:114461959
|
A | G | 6 | a0001c0006t0010g0119a0001c0006t0010g0120a0001c0006t0010g0121others(3): Show | 6 | HG02132.hp2 HG02698.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.923+1145T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114461959 | ||||||
| chr1:114462020
|
AT | A | 2 | a0001c0002t0018g0145a0001c0002t0018g0146 | 2 | HG00741.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.923+1083delA | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114462020 | ||||||
| chr1:114462159
|
C | T | 6 | a0001c0006t0010g0119a0001c0006t0010g0120a0001c0006t0010g0121others(3): Show | 6 | HG02132.hp2 HG02698.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.923+945G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114462159 | ||||||
| chr1:114462216
|
C | T | 23 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(20): Show | 23 | HG00323.hp1 HG00738.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.923+888G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114462216 | ||||||
| chr1:114462408
|
T | G | 2 | a0002c0003t0001g0032a0002c0003t0001g0036 | 2 | NA18955.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.923+696A>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114462408 | ||||||
| chr1:114462534
|
T | C | 1 | a0001c0001t0001g0078 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.923+570A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114462534 | ||||||
| chr1:114462795
|
T | C | 21 | a0001c0002t0006g0087a0001c0002t0006g0088a0001c0002t0006g0089others(18): Show | 21 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.923+309A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114462795 | ||||||
| chr1:114463005
|
T | C | 2 | a0001c0002t0005g0104a0001c0002t0005g0107 | 2 | HG02615.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.923+99A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 4/19 | chr1 | 114463005 | ||||||
| chr1:114463347
|
T | C | 1 | a0001c0002t0023g0002 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.790+65A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 3/19 | chr1 | 114463347 | ||||||
| chr1:114463586
|
T | A | 1 | a0001c0001t0002g0180 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.646-30A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 2/19 | chr1 | 114463586 | ||||||
| chr1:114463608
|
TA | T | 68 | a0001c0001t0002g0148a0001c0002t0003g0125a0001c0002t0003g0126others(65): Show | 68 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.646-53delT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 2/19 | chr1 | 114463608 | ||||||
| chr1:114463752
|
T | C | 2 | a0001c0002t0018g0145a0001c0002t0018g0146 | 2 | HG00741.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.646-196A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 2/19 | chr1 | 114463752 | ||||||
| chr1:114463767
|
C | CT | 82 | a0001c0001t0001g0072a0001c0001t0002g0182a0001c0001t0004g0077others(79): Show | 82 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.646-212dupA | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 2/19 | chr1 | 114463767 | ||||||
| chr1:114463767
|
C | CTT | 5 | a0001c0002t0033g0117a0003c0004t0014g0005a0003c0004t0014g0013others(2): Show | 5 | HG02145.hp1 HG02451.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.646-213_646-212dup others(2): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 2/19 | chr1 | 114463767 | ||||||
| chr1:114463805
|
G | A | 3 | a0003c0004t0014g0005a0003c0004t0014g0012a0003c0004t0014g0013 | 3 | HG02055.hp2 HG02523.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.646-249C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 2/19 | chr1 | 114463805 | ||||||
| chr1:114463989
|
G | A | 1 | a0001c0002t0005g0105 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.645+281C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 2/19 | chr1 | 114463989 | ||||||
| chr1:114464038
|
C | T | 13 | a0001c0002t0005g0098a0001c0002t0005g0099a0001c0002t0005g0101others(10): Show | 13 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.645+232G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 2/19 | chr1 | 114464038 | ||||||
| chr1:114464058
|
C | G | 1 | a0001c0002t0006g0097 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.645+212G>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 2/19 | chr1 | 114464058 | ||||||
| chr1:114464086
|
G | A | 6 | a0001c0006t0010g0119a0001c0006t0010g0120a0001c0006t0010g0121others(3): Show | 6 | HG02132.hp2 HG02698.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.645+184C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 2/19 | chr1 | 114464086 | ||||||
| chr1:114464602
|
T | C | 1 | a0001c0002t0037g0118 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.527-214A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114464602 | ||||||
| chr1:114464747
|
G | A | 1 | a0003c0004t0001g0008 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.527-359C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114464747 | ||||||
| chr1:114464757
|
C | T | 1 | a0002c0003t0001g0034 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.527-369G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114464757 | ||||||
| chr1:114464903
|
C | T | 15 | a0001c0002t0006g0087a0001c0002t0006g0088a0001c0002t0006g0089others(12): Show | 15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.527-515G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114464903 | ||||||
| chr1:114465013
|
TG | T | 4 | a0001c0002t0009g0202a0001c0002t0009g0203a0001c0002t0009g0204others(1): Show | 4 | HG01891.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.527-626delC | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114465013 | ||||||
| chr1:114465016
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.527-628G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114465016 | ||||||
| chr1:114465343
|
C | A | 3 | a0003c0004t0014g0005a0003c0004t0014g0012a0003c0004t0014g0013 | 3 | HG02055.hp2 HG02523.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.527-955G>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114465343 | ||||||
| chr1:114465585
|
G | A | 1 | a0001c0001t0051g0207 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.527-1197C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114465585 | ||||||
| chr1:114465613
|
C | CA | 4 | a0001c0001t0002g0157a0001c0001t0002g0158a0001c0001t0002g0159others(1): Show | 4 | NA18942.hp1 NA18970.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.527-1226dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114465613 | ||||||
| chr1:114465767
|
C | T | 2 | a0001c0002t0005g0104a0001c0002t0005g0107 | 2 | HG02615.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.527-1379G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114465767 | ||||||
| chr1:114465780
|
G | A | 6 | a0001c0002t0004g0111a0001c0002t0004g0114a0001c0002t0004g0115others(3): Show | 6 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.527-1392C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114465780 | ||||||
| chr1:114465806
|
C | A | 2 | a0001c0001t0017g0033a0002c0003t0001g0163 | 2 | NA18984.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.527-1418G>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114465806 | ||||||
| chr1:114465806
|
C | T | 3 | a0001c0002t0006g0087a0001c0002t0023g0002a0001c0002t0034g0086 | 3 | HG02970.hp2 HG03516.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.527-1418G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114465806 | ||||||
| chr1:114465837
|
G | C | 81 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(78): Show | 81 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.527-1449C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114465837 | ||||||
| chr1:114465949
|
AG | A | 3 | a0001c0002t0005g0105a0001c0002t0005g0106a0001c0002t0019g0109 | 3 | HG01192.hp1 HG01261.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.527-1562delC | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114465949 | ||||||
| chr1:114466040
|
CA | C | 13 | a0001c0002t0005g0098a0001c0002t0005g0099a0001c0002t0005g0101others(10): Show | 13 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.527-1653delT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114466040 | ||||||
| chr1:114466048
|
A | T | 2 | a0001c0001t0001g0058a0002c0003t0016g0038 | 2 | HG00438.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.527-1660T>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114466048 | ||||||
| chr1:114466179
|
T | A | 13 | a0001c0002t0005g0098a0001c0002t0005g0099a0001c0002t0005g0101others(10): Show | 13 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.527-1791A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114466179 | ||||||
| chr1:114466370
|
T | C | 206 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0022others(203): Show | 207 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.527-1982A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114466370 | ||||||
| chr1:114466419
|
G | A | 2 | a0001c0002t0018g0145a0001c0002t0018g0146 | 2 | HG00741.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.527-2031C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114466419 | ||||||
| chr1:114466446
|
C | T | 5 | a0001c0002t0033g0117a0003c0004t0014g0005a0003c0004t0014g0012others(2): Show | 5 | HG02055.hp2 HG02451.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.527-2058G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114466446 | ||||||
| chr1:114466472
|
C | T | 1 | a0001c0001t0002g0180 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.527-2084G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114466472 | ||||||
| chr1:114467001
|
A | C | 23 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(20): Show | 23 | HG00323.hp1 HG00738.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.527-2613T>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114467001 | ||||||
| chr1:114467011
|
C | T | 1 | a0001c0001t0002g0068 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.527-2623G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114467011 | ||||||
| chr1:114467178
|
G | A | 8 | a0003c0004t0001g0008a0003c0004t0004g0006a0003c0004t0004g0009others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.527-2790C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114467178 | ||||||
| chr1:114467373
|
G | A | 2 | a0001c0002t0018g0145a0001c0002t0018g0146 | 2 | HG00741.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.527-2985C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114467373 | ||||||
| chr1:114467527
|
C | T | 1 | a0002c0003t0001g0082 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.527-3139G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114467527 | ||||||
| chr1:114467533
|
T | A | 1 | a0005c0008t0013g0015 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.527-3145A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114467533 | ||||||
| chr1:114467765
|
C | T | 1 | a0001c0002t0005g0105 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.527-3377G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114467765 | ||||||
| chr1:114468065
|
G | T | 1 | a0001c0002t0005g0104 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.527-3677C>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114468065 | ||||||
| chr1:114468223
|
G | A | 11 | a0001c0002t0033g0117a0001c0006t0010g0119a0001c0006t0010g0120others(8): Show | 11 | HG02055.hp2 HG02132.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.527-3835C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114468223 | ||||||
| chr1:114468247
|
G | A | 3 | a0001c0001t0011g0054a0001c0001t0011g0055a0001c0001t0011g0066 | 3 | HG01099.hp2 HG02886.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.527-3859C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114468247 | ||||||
| chr1:114468660
|
G | A | 2 | a0001c0001t0001g0045a0001c0001t0001g0046 | 2 | HG02809.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.527-4272C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114468660 | ||||||
| chr1:114468837
|
G | A | 1 | a0003c0004t0001g0008 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.527-4449C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114468837 | ||||||
| chr1:114468862
|
T | C | 81 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(78): Show | 81 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.527-4474A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114468862 | ||||||
| chr1:114468865
|
C | T | 40 | a0001c0001t0001g0164a0001c0001t0001g0176a0001c0001t0002g0149others(37): Show | 40 | HG00438.hp1 HG00558.hp2 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.527-4477G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114468865 | ||||||
| chr1:114468879
|
C | T | 2 | a0001c0001t0001g0083a0001c0001t0004g0050 | 2 | HG02055.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.527-4491G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114468879 | ||||||
| chr1:114468919
|
C | G | 1 | a0001c0002t0005g0101 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.527-4531G>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114468919 | ||||||
| chr1:114469051
|
G | A | 2 | a0001c0002t0018g0145a0001c0002t0018g0146 | 2 | HG00741.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.527-4663C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114469051 | ||||||
| chr1:114469440
|
C | T | 1 | a0001c0002t0046g0091 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.527-5052G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114469440 | ||||||
| chr1:114469560
|
A | T | 6 | a0001c0002t0004g0111a0001c0002t0004g0114a0001c0002t0004g0115others(3): Show | 6 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.527-5172T>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114469560 | ||||||
| chr1:114469567
|
A | C | 28 | a0001c0002t0005g0098a0001c0002t0005g0099a0001c0002t0005g0101others(25): Show | 28 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.527-5179T>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114469567 | ||||||
| chr1:114469721
|
G | C | 2 | a0001c0002t0025g0004a0001c0002t0027g0090 | 2 | HG01361.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.527-5333C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114469721 | ||||||
| chr1:114470012
|
T | C | 1 | a0001c0001t0017g0172 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.527-5624A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114470012 | ||||||
| chr1:114470529
|
C | T | 1 | a0001c0002t0037g0118 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.527-6141G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114470529 | ||||||
| chr1:114470629
|
C | G | 2 | a0001c0002t0018g0145a0001c0002t0018g0146 | 2 | HG00741.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.527-6241G>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114470629 | ||||||
| chr1:114470638
|
T | TAAC | 2 | a0001c0001t0048g0081a0002c0003t0008g0043 | 2 | HG00738.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.527-6253_527-6251d others(5): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114470638 | ||||||
| chr1:114470638
|
TAAC | T | 81 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(78): Show | 81 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.527-6253_527-6251d others(5): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114470638 | ||||||
| chr1:114470764
|
C | T | 205 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0022others(202): Show | 206 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.527-6376G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114470764 | ||||||
| chr1:114470857
|
A | G | 2 | a0001c0002t0018g0145a0001c0002t0018g0146 | 2 | HG00741.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.527-6469T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114470857 | ||||||
| chr1:114470930
|
T | G | 13 | a0001c0002t0009g0202a0001c0002t0009g0203a0001c0002t0009g0204others(10): Show | 13 | HG01891.hp2 HG02145.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.527-6542A>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114470930 | ||||||
| chr1:114471094
|
T | C | 1 | a0003c0004t0031g0011 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.527-6706A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114471094 | ||||||
| chr1:114471407
|
C | T | 10 | a0001c0002t0005g0098a0001c0002t0005g0099a0001c0002t0005g0101others(7): Show | 10 | HG01257.hp2 HG01433.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.527-7019G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114471407 | ||||||
| chr1:114471443
|
C | CA | 23 | a0001c0001t0002g0068a0001c0002t0003g0125a0001c0002t0003g0126others(20): Show | 23 | HG00323.hp1 HG00738.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.527-7056dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114471443 | ||||||
| chr1:114471593
|
A | G | 2 | a0001c0002t0005g0104a0001c0002t0005g0107 | 2 | HG02615.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.527-7205T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114471593 | ||||||
| chr1:114471594
|
A | G | 2 | a0001c0002t0005g0104a0001c0002t0005g0107 | 2 | HG02615.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.527-7206T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114471594 | ||||||
| chr1:114471741
|
C | G | 5 | a0003c0004t0001g0008a0003c0004t0004g0009a0003c0004t0013g0010others(2): Show | 5 | HG02145.hp1 HG02258.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.527-7353G>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114471741 | ||||||
| chr1:114471853
|
T | C | 1 | a0001c0001t0011g0054 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.527-7465A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114471853 | ||||||
| chr1:114472106
|
C | T | 40 | a0001c0001t0001g0164a0001c0001t0001g0176a0001c0001t0002g0149others(37): Show | 40 | HG00438.hp1 HG00558.hp2 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.527-7718G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114472106 | ||||||
| chr1:114472529
|
T | C | 1 | a0001c0005t0007g0147 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.527-8141A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114472529 | ||||||
| chr1:114472711
|
T | C | 1 | a0001c0002t0003g0128 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.527-8323A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114472711 | ||||||
| chr1:114472721
|
GAAAACA | G | 6 | a0001c0002t0004g0111a0001c0002t0004g0114a0001c0002t0004g0115others(3): Show | 6 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.527-8339_527-8334d others(8): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114472721 | ||||||
| chr1:114472897
|
G | A | 2 | a0001c0001t0001g0071a0001c0001t0028g0062 | 2 | HG02004.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.527-8509C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114472897 | ||||||
| chr1:114472976
|
G | A | 2 | a0001c0001t0030g0156a0001c0001t0036g0153 | 2 | HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.527-8588C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114472976 | ||||||
| chr1:114473046
|
A | G | 205 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0022others(202): Show | 206 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.527-8658T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114473046 | ||||||
| chr1:114473181
|
C | T | 3 | a0003c0004t0013g0010a0003c0004t0031g0011a0005c0008t0013g0015 | 3 | HG02145.hp1 HG02258.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.527-8793G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114473181 | ||||||
| chr1:114473225
|
C | T | 1 | a0002c0003t0001g0029 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.527-8837G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114473225 | ||||||
| chr1:114473243
|
C | T | 2 | a0001c0001t0001g0025a0001c0001t0004g0024 | 2 | HG02109.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.527-8855G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114473243 | ||||||
| chr1:114473244
|
G | A | 1 | a0001c0009t0039g0123 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.527-8856C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114473244 | ||||||
| chr1:114473256
|
C | CA | 40 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(37): Show | 40 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.527-8869dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114473256 | ||||||
| chr1:114473273
|
A | T | 1 | a0001c0001t0047g0053 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.527-8885T>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114473273 | ||||||
| chr1:114473394
|
A | G | 1 | a0001c0001t0035g0173 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.527-9006T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114473394 | ||||||
| chr1:114473401
|
C | CT | 2 | a0001c0002t0033g0117a0004c0007t0001g0014 | 2 | HG02451.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.527-9014dupA | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114473401 | ||||||
| chr1:114473659
|
T | A | 1 | a0001c0001t0048g0081 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.527-9271A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114473659 | ||||||
| chr1:114473782
|
C | G | 15 | a0001c0002t0006g0087a0001c0002t0006g0088a0001c0002t0006g0089others(12): Show | 15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.527-9394G>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114473782 | ||||||
| chr1:114473793
|
G | A | 81 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(78): Show | 81 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.527-9405C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114473793 | ||||||
| chr1:114473801
|
C | T | 6 | a0001c0002t0004g0111a0001c0002t0004g0114a0001c0002t0004g0115others(3): Show | 6 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.527-9413G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114473801 | ||||||
| chr1:114474045
|
T | C | 4 | a0001c0002t0009g0202a0001c0002t0009g0203a0001c0002t0009g0204others(1): Show | 4 | HG01891.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.527-9657A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114474045 | ||||||
| chr1:114474083
|
TAG | T | 12 | a0001c0002t0009g0202a0001c0002t0009g0203a0001c0002t0009g0204others(9): Show | 12 | HG01891.hp2 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.527-9697_527-9696d others(4): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114474083 | ||||||
| chr1:114474165
|
T | C | 1 | a0002c0003t0001g0082 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.527-9777A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114474165 | ||||||
| chr1:114474393
|
C | T | 4 | a0001c0001t0002g0148a0001c0001t0002g0155a0001c0001t0002g0198others(1): Show | 4 | HG02145.hp2 HG02258.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.527-10005G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114474393 | ||||||
| chr1:114474409
|
T | TA | 35 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(32): Show | 35 | HG00323.hp1 HG00738.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.527-10022dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114474409 | ||||||
| chr1:114474434
|
T | C | 1 | a0001c0001t0002g0155 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.527-10046A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114474434 | ||||||
| chr1:114474451
|
G | A | 1 | a0002c0003t0001g0082 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.527-10063C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114474451 | ||||||
| chr1:114474578
|
T | TA | 46 | a0001c0001t0001g0060a0001c0001t0001g0069a0001c0001t0002g0182others(43): Show | 46 | HG00323.hp1 HG00735.hp2 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.527-10191dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114474578 | ||||||
| chr1:114474578
|
T | TAA | 36 | a0001c0002t0003g0134a0001c0002t0005g0103a0001c0002t0005g0106others(33): Show | 36 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(33): Show |
intron_variant | MODIFIER | c.527-10192_527-1019 others(6): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114474578 | ||||||
| chr1:114474700
|
T | C | 1 | a0001c0001t0002g0195 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.527-10312A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114474700 | ||||||
| chr1:114474761
|
G | A | 1 | a0001c0001t0044g0016 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.527-10373C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114474761 | ||||||
| chr1:114474840
|
C | T | 1 | a0002c0003t0016g0038 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.527-10452G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114474840 | ||||||
| chr1:114474893
|
C | CA | 10 | a0001c0001t0001g0025a0001c0001t0004g0024a0001c0002t0019g0100others(7): Show | 10 | HG01257.hp2 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.527-10506dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114474893 | ||||||
| chr1:114475215
|
A | C | 1 | a0001c0001t0002g0175 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.527-10827T>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114475215 | ||||||
| chr1:114475477
|
C | T | 4 | a0001c0002t0009g0202a0001c0002t0009g0203a0001c0002t0009g0204others(1): Show | 4 | HG01891.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.527-11089G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114475477 | ||||||
| chr1:114475513
|
G | C | 2 | a0001c0001t0011g0054a0001c0001t0011g0055 | 2 | HG01099.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.527-11125C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114475513 | ||||||
| chr1:114475633
|
G | T | 8 | a0003c0004t0001g0008a0003c0004t0004g0006a0003c0004t0004g0009others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.527-11245C>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114475633 | ||||||
| chr1:114475638
|
C | T | 12 | a0001c0002t0009g0202a0001c0002t0009g0203a0001c0002t0009g0204others(9): Show | 12 | HG01891.hp2 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.527-11250G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114475638 | ||||||
| chr1:114475647
|
A | C | 1 | a0001c0001t0002g0185 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.527-11259T>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114475647 | ||||||
| chr1:114475689
|
A | AAAT | 81 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(78): Show | 81 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.527-11304_527-1130 others(7): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114475689 | ||||||
| chr1:114476220
|
GAA | G | 6 | a0001c0006t0010g0119a0001c0006t0010g0120a0001c0006t0010g0121others(3): Show | 6 | HG02132.hp2 HG02698.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.527-11834_527-1183 others(6): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114476220 | ||||||
| chr1:114476225
|
A | C | 9 | a0001c0001t0002g0148a0001c0001t0002g0154a0001c0001t0002g0155others(6): Show | 9 | HG01175.hp2 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.527-11837T>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114476225 | ||||||
| chr1:114476502
|
AC | A | 2 | a0001c0002t0009g0202a0001c0002t0009g0203 | 2 | HG01891.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.527-12115delG | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114476502 | ||||||
| chr1:114476617
|
A | T | 24 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(21): Show | 24 | HG00323.hp1 HG00738.hp1 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.527-12229T>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114476617 | ||||||
| chr1:114476845
|
T | A | 13 | a0001c0002t0005g0098a0001c0002t0005g0099a0001c0002t0005g0101others(10): Show | 13 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.527-12457A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114476845 | ||||||
| chr1:114477088
|
C | T | 33 | a0001c0001t0001g0164a0001c0001t0001g0176a0001c0001t0002g0149others(30): Show | 33 | HG00438.hp1 HG00558.hp2 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.527-12700G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114477088 | ||||||
| chr1:114477585
|
A | G | 5 | a0001c0002t0033g0117a0003c0004t0014g0005a0003c0004t0014g0012others(2): Show | 5 | HG02055.hp2 HG02451.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.527-13197T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114477585 | ||||||
| chr1:114477661
|
T | A | 4 | a0001c0002t0009g0202a0001c0002t0009g0203a0001c0002t0009g0204others(1): Show | 4 | HG01891.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.527-13273A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114477661 | ||||||
| chr1:114477872
|
T | C | 1 | a0001c0001t0002g0152 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.527-13484A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114477872 | ||||||
| chr1:114477874
|
G | C | 6 | a0001c0002t0004g0111a0001c0002t0004g0114a0001c0002t0004g0115others(3): Show | 6 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.527-13486C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114477874 | ||||||
| chr1:114477926
|
A | T | 11 | a0001c0002t0033g0117a0001c0006t0010g0119a0001c0006t0010g0120others(8): Show | 11 | HG02055.hp2 HG02132.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.527-13538T>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114477926 | ||||||
| chr1:114478043
|
A | C | 1 | a0001c0001t0004g0077 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.527-13655T>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114478043 | ||||||
| chr1:114478057
|
A | C | 13 | a0001c0002t0005g0098a0001c0002t0005g0099a0001c0002t0005g0101others(10): Show | 13 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.527-13669T>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114478057 | ||||||
| chr1:114478179
|
T | C | 5 | a0001c0001t0002g0154a0001c0001t0002g0195a0001c0001t0026g0196others(2): Show | 5 | HG01175.hp2 HG02486.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.527-13791A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114478179 | ||||||
| chr1:114478215
|
TAA | T | 3 | a0001c0001t0001g0070a0001c0001t0002g0064a0002c0003t0001g0001 | 4 | HG01071.hp2 HG01433.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.527-13829_527-1382 others(6): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114478215 | ||||||
| chr1:114478278
|
T | C | 2 | a0001c0002t0003g0136a0001c0002t0003g0139 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.527-13890A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114478278 | ||||||
| chr1:114478314
|
G | C | 2 | a0003c0004t0001g0008a0003c0004t0004g0009 | 2 | HG02965.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.527-13926C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114478314 | ||||||
| chr1:114478627
|
T | C | 45 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(42): Show | 45 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.527-14239A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114478627 | ||||||
| chr1:114478734
|
A | G | 2 | a0001c0002t0018g0145a0001c0002t0018g0146 | 2 | HG00741.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.527-14346T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114478734 | ||||||
| chr1:114478854
|
C | G | 1 | a0001c0001t0001g0069 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.527-14466G>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114478854 | ||||||
| chr1:114478961
|
T | C | 2 | a0001c0002t0018g0145a0001c0002t0018g0146 | 2 | HG00741.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.527-14573A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114478961 | ||||||
| chr1:114479151
|
A | G | 1 | a0003c0004t0004g0006 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.527-14763T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114479151 | ||||||
| chr1:114479270
|
T | C | 2 | a0001c0001t0001g0079a0001c0001t0001g0080 | 2 | NA18970.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.527-14882A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114479270 | ||||||
| chr1:114479593
|
A | T | 13 | a0001c0002t0005g0098a0001c0002t0005g0099a0001c0002t0005g0101others(10): Show | 13 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.527-15205T>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114479593 | ||||||
| chr1:114479638
|
G | A | 1 | a0001c0002t0037g0118 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.527-15250C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114479638 | ||||||
| chr1:114479640
|
A | T | 1 | a0001c0002t0037g0118 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.527-15252T>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114479640 | ||||||
| chr1:114479652
|
A | G | 1 | a0001c0001t0004g0077 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.527-15264T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114479652 | ||||||
| chr1:114479808
|
C | CAGGGAGG others(39): Show |
81 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(78): Show | 81 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.527-15421_527-1542 others(50): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114479808 | ||||||
| chr1:114479896
|
G | A | 23 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(20): Show | 23 | HG00323.hp1 HG00738.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.527-15508C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114479896 | ||||||
| chr1:114479935
|
A | T | 4 | a0001c0001t0002g0186a0001c0001t0002g0187a0001c0001t0002g0188others(1): Show | 4 | HG00642.hp2 HG01074.hp2 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.527-15547T>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114479935 | ||||||
| chr1:114479973
|
G | A | 1 | a0001c0001t0001g0072 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.527-15585C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114479973 | ||||||
| chr1:114479987
|
C | A | 13 | a0001c0002t0005g0098a0001c0002t0005g0099a0001c0002t0005g0101others(10): Show | 13 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.527-15599G>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114479987 | ||||||
| chr1:114480076
|
T | C | 6 | a0001c0002t0004g0111a0001c0002t0004g0114a0001c0002t0004g0115others(3): Show | 6 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.527-15688A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114480076 | ||||||
| chr1:114480117
|
A | G | 1 | a0001c0001t0001g0072 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.527-15729T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114480117 | ||||||
| chr1:114480164
|
G | T | 2 | a0001c0001t0022g0056a0001c0001t0022g0057 | 2 | HG03704.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.527-15776C>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114480164 | ||||||
| chr1:114480383
|
T | C | 13 | a0001c0002t0005g0098a0001c0002t0005g0099a0001c0002t0005g0101others(10): Show | 13 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.527-15995A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114480383 | ||||||
| chr1:114480410
|
C | T | 6 | a0001c0002t0004g0111a0001c0002t0004g0114a0001c0002t0004g0115others(3): Show | 6 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.527-16022G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114480410 | ||||||
| chr1:114480424
|
CTA | C | 2 | a0001c0002t0005g0104a0001c0002t0005g0107 | 2 | HG02615.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.527-16038_527-1603 others(6): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114480424 | ||||||
| chr1:114480475
|
TTA | T | 5 | a0001c0006t0010g0119a0001c0006t0010g0120a0001c0006t0010g0121others(2): Show | 5 | HG02132.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.527-16089_527-1608 others(6): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114480475 | ||||||
| chr1:114480476
|
T | TA | 6 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0185others(3): Show | 6 | HG01891.hp1 HG02622.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.527-16089dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114480476 | ||||||
| chr1:114480476
|
TA | T | 11 | a0001c0001t0002g0035a0001c0001t0002g0149a0001c0001t0002g0158others(8): Show | 11 | HG00323.hp2 HG01167.hp2 HG02897.hp2 others(8): Show |
intron_variant | MODIFIER | c.527-16089delT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114480476 | ||||||
| chr1:114480476
|
TAA | T | 48 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(45): Show | 48 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.527-16090_527-1608 others(6): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114480476 | ||||||
| chr1:114480476
|
TAAA | T | 26 | a0001c0002t0003g0137a0001c0002t0003g0144a0001c0002t0005g0098others(23): Show | 26 | HG01167.hp1 HG01192.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.527-16091_527-1608 others(7): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114480476 | ||||||
| chr1:114480491
|
A | G | 2 | a0001c0002t0005g0104a0001c0002t0005g0107 | 2 | HG02615.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.527-16103T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114480491 | ||||||
| chr1:114480493
|
A | G | 23 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0002t0003g0125others(20): Show | 23 | HG00323.hp1 HG00738.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.527-16105T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114480493 | ||||||
| chr1:114480521
|
TA | T | 144 | a0001c0001t0001g0022a0001c0001t0001g0025a0001c0001t0001g0045others(141): Show | 144 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.527-16134delT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114480521 | ||||||
| chr1:114480535
|
A | G | 8 | a0003c0004t0001g0008a0003c0004t0004g0006a0003c0004t0004g0009others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.527-16147T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114480535 | ||||||
| chr1:114480541
|
G | T | 1 | a0001c0001t0001g0200 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.527-16153C>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114480541 | ||||||
| chr1:114480563
|
A | C | 81 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(78): Show | 81 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.527-16175T>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114480563 | ||||||
| chr1:114480610
|
T | C | 1 | a0001c0001t0048g0081 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.527-16222A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114480610 | ||||||
| chr1:114480685
|
T | C | 1 | a0001c0005t0007g0183 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.527-16297A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114480685 | ||||||
| chr1:114480688
|
C | T | 2 | a0002c0003t0001g0026a0002c0003t0001g0047 | 2 | HG01928.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.527-16300G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114480688 | ||||||
| chr1:114480847
|
A | C | 2 | a0001c0002t0005g0104a0001c0002t0005g0107 | 2 | HG02615.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.527-16459T>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114480847 | ||||||
| chr1:114480953
|
C | G | 6 | a0001c0002t0004g0111a0001c0002t0004g0114a0001c0002t0004g0115others(3): Show | 6 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.527-16565G>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114480953 | ||||||
| chr1:114481101
|
A | T | 11 | a0001c0002t0033g0117a0001c0006t0010g0119a0001c0006t0010g0120others(8): Show | 11 | HG02055.hp2 HG02132.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.527-16713T>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114481101 | ||||||
| chr1:114481129
|
C | T | 8 | a0002c0003t0001g0039a0002c0003t0001g0082a0002c0003t0008g0028others(5): Show | 8 | HG00642.hp1 HG00738.hp2 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.527-16741G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114481129 | ||||||
| chr1:114481310
|
T | C | 1 | a0001c0002t0037g0118 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.527-16922A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114481310 | ||||||
| chr1:114481336
|
G | A | 3 | a0001c0001t0011g0054a0001c0001t0011g0055a0001c0001t0011g0066 | 3 | HG01099.hp2 HG02886.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.527-16948C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114481336 | ||||||
| chr1:114481359
|
C | G | 6 | a0001c0002t0004g0111a0001c0002t0004g0114a0001c0002t0004g0115others(3): Show | 6 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.527-16971G>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114481359 | ||||||
| chr1:114481360
|
A | G | 81 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(78): Show | 81 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.527-16972T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114481360 | ||||||
| chr1:114481368
|
G | A | 1 | a0001c0002t0037g0118 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.527-16980C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114481368 | ||||||
| chr1:114481527
|
G | A | 1 | a0001c0001t0011g0055 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.527-17139C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114481527 | ||||||
| chr1:114481577
|
T | A | 2 | a0001c0006t0010g0121a0001c0006t0010g0122 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.527-17189A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114481577 | ||||||
| chr1:114481629
|
C | CTA | 2 | a0001c0002t0009g0202a0001c0002t0009g0203 | 2 | HG01891.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.527-17243_527-1724 others(6): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114481629 | ||||||
| chr1:114481629
|
C | CTATA | 4 | a0003c0004t0001g0008a0003c0004t0013g0010a0003c0004t0031g0011others(1): Show | 4 | HG02145.hp1 HG02258.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.527-17245_527-1724 others(8): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114481629 | ||||||
| chr1:114481639
|
A | ATATG | 2 | a0001c0002t0009g0204a0001c0002t0009g0205 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.527-17252_527-1725 others(8): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114481639 | ||||||
| chr1:114481639
|
A | ATG | 3 | a0001c0001t0001g0067a0001c0001t0017g0172a0002c0003t0004g0048 | 3 | HG02056.hp2 HG02129.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.527-17253_527-1725 others(6): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114481639 | ||||||
| chr1:114481639
|
ATG | A | 3 | a0001c0002t0018g0145a0001c0002t0018g0146a0003c0004t0004g0009 | 3 | HG00741.hp2 HG02895.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.527-17253_527-1725 others(6): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114481639 | ||||||
| chr1:114481641
|
G | A | 55 | a0001c0001t0001g0083a0001c0001t0004g0050a0001c0002t0003g0125others(52): Show | 55 | HG00323.hp1 HG00738.hp1 HG01099.hp1 others(52): Show |
intron_variant | MODIFIER | c.527-17253C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114481641 | ||||||
| chr1:114481643
|
G | A | 23 | a0001c0002t0005g0098a0001c0002t0005g0099a0001c0002t0005g0101others(20): Show | 23 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(20): Show |
intron_variant | MODIFIER | c.527-17255C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114481643 | ||||||
| chr1:114481645
|
G | A | 1 | a0003c0004t0004g0009 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.527-17257C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114481645 | ||||||
| chr1:114481661
|
GTATATAT others(13): Show |
G | 1 | a0001c0001t0002g0068 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.527-17293_527-1727 others(24): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114481661 | ||||||
| chr1:114481663
|
A | G | 39 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(36): Show | 39 | HG00323.hp1 HG00738.hp1 HG01099.hp1 others(36): Show |
intron_variant | MODIFIER | c.527-17275T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114481663 | ||||||
| chr1:114481665
|
A | G | 1 | a0001c0002t0003g0144 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.527-17277T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114481665 | ||||||
| chr1:114481667
|
ATATG | A | 15 | a0001c0002t0006g0087a0001c0002t0006g0088a0001c0002t0006g0089others(12): Show | 15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.527-17283_527-1728 others(8): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114481667 | ||||||
| chr1:114481671
|
G | A | 39 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(36): Show | 39 | HG00323.hp1 HG00738.hp1 HG01099.hp1 others(36): Show |
intron_variant | MODIFIER | c.527-17283C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114481671 | ||||||
| chr1:114481675
|
GTA | G | 13 | a0001c0002t0018g0145a0001c0002t0018g0146a0001c0002t0033g0117others(10): Show | 13 | HG00741.hp2 HG01257.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.527-17289_527-1728 others(6): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114481675 | ||||||
| chr1:114481675
|
GTATA | G | 2 | a0001c0002t0009g0204a0001c0002t0009g0205 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.527-17291_527-1728 others(8): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114481675 | ||||||
| chr1:114481677
|
A | G | 57 | a0001c0001t0015g0051a0001c0002t0003g0125a0001c0002t0003g0126others(54): Show | 57 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.527-17289T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114481677 | ||||||
| chr1:114481679
|
A | G | 1 | a0001c0002t0037g0118 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.527-17291T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114481679 | ||||||
| chr1:114481689
|
A | G | 5 | a0001c0002t0033g0117a0003c0004t0014g0005a0003c0004t0014g0012others(2): Show | 5 | HG02055.hp2 HG02451.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.527-17301T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114481689 | ||||||
| chr1:114481746
|
G | T | 3 | a0003c0004t0004g0006a0003c0004t0013g0007a0003c0004t0050g0206 | 3 | HG02280.hp1 HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.527-17358C>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114481746 | ||||||
| chr1:114481876
|
C | T | 1 | a0003c0004t0004g0006 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.527-17488G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114481876 | ||||||
| chr1:114481917
|
C | T | 1 | a0003c0004t0004g0009 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.527-17529G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114481917 | ||||||
| chr1:114481933
|
G | A | 1 | a0001c0001t0002g0185 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.527-17545C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114481933 | ||||||
| chr1:114482047
|
T | G | 6 | a0001c0002t0004g0111a0001c0002t0004g0114a0001c0002t0004g0115others(3): Show | 6 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.527-17659A>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114482047 | ||||||
| chr1:114482276
|
G | GA | 4 | a0001c0002t0009g0202a0001c0002t0009g0203a0001c0002t0009g0204others(1): Show | 4 | HG01891.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.527-17889dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114482276 | ||||||
| chr1:114482400
|
G | C | 1 | a0001c0001t0002g0160 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.527-18012C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114482400 | ||||||
| chr1:114482448
|
C | T | 4 | a0001c0002t0009g0202a0001c0002t0009g0203a0001c0002t0009g0204others(1): Show | 4 | HG01891.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.527-18060G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114482448 | ||||||
| chr1:114482780
|
T | A | 2 | a0001c0001t0001g0045a0001c0001t0001g0046 | 2 | HG02809.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.527-18392A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114482780 | ||||||
| chr1:114482801
|
G | A | 3 | a0001c0001t0001g0022a0001c0001t0004g0023a0001c0001t0024g0003 | 3 | HG02615.hp2 HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.527-18413C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114482801 | ||||||
| chr1:114483078
|
G | C | 21 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(18): Show | 21 | HG00323.hp1 HG00738.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.527-18690C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114483078 | ||||||
| chr1:114483085
|
A | G | 15 | a0001c0002t0006g0087a0001c0002t0006g0088a0001c0002t0006g0089others(12): Show | 15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.527-18697T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114483085 | ||||||
| chr1:114483103
|
G | A | 8 | a0001c0002t0005g0102a0001c0002t0005g0103a0001c0002t0005g0105others(5): Show | 8 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.527-18715C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114483103 | ||||||
| chr1:114483258
|
G | A | 1 | a0001c0002t0006g0088 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.527-18870C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114483258 | ||||||
| chr1:114483288
|
C | T | 1 | a0002c0003t0001g0026 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.527-18900G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114483288 | ||||||
| chr1:114483318
|
T | A | 7 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0141others(4): Show | 7 | HG01099.hp1 HG01952.hp2 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.527-18930A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114483318 | ||||||
| chr1:114483416
|
G | GT | 12 | a0001c0001t0002g0157a0001c0002t0033g0117a0001c0006t0010g0119others(9): Show | 12 | HG02055.hp2 HG02132.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.527-19029dupA | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114483416 | ||||||
| chr1:114483468
|
G | A | 6 | a0001c0002t0004g0111a0001c0002t0004g0114a0001c0002t0004g0115others(3): Show | 6 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.527-19080C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114483468 | ||||||
| chr1:114483536
|
C | A | 15 | a0001c0002t0006g0087a0001c0002t0006g0088a0001c0002t0006g0089others(12): Show | 15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.527-19148G>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114483536 | ||||||
| chr1:114483587
|
A | G | 1 | a0001c0005t0007g0184 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.527-19199T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114483587 | ||||||
| chr1:114483601
|
C | T | 21 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(18): Show | 21 | HG00323.hp1 HG00738.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.527-19213G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114483601 | ||||||
| chr1:114483659
|
C | T | 1 | a0003c0004t0004g0009 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.527-19271G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114483659 | ||||||
| chr1:114483766
|
C | A | 2 | a0001c0002t0018g0145a0001c0002t0018g0146 | 2 | HG00741.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.527-19378G>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114483766 | ||||||
| chr1:114483954
|
T | C | 21 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(18): Show | 21 | HG00323.hp1 HG00738.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.527-19566A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114483954 | ||||||
| chr1:114483972
|
T | C | 4 | a0001c0001t0002g0186a0001c0001t0002g0187a0001c0001t0002g0188others(1): Show | 4 | HG00642.hp2 HG01074.hp2 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.527-19584A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114483972 | ||||||
| chr1:114483986
|
T | C | 8 | a0003c0004t0001g0008a0003c0004t0004g0006a0003c0004t0004g0009others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.527-19598A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114483986 | ||||||
| chr1:114484150
|
AAGG | A | 2 | a0001c0001t0001g0025a0001c0001t0004g0024 | 2 | HG02109.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.527-19765_527-1976 others(7): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114484150 | ||||||
| chr1:114484341
|
T | TA | 8 | a0003c0004t0001g0008a0003c0004t0004g0006a0003c0004t0004g0009others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.527-19954dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114484341 | ||||||
| chr1:114484409
|
C | T | 81 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(78): Show | 81 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.527-20021G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114484409 | ||||||
| chr1:114484498
|
G | A | 1 | a0001c0001t0001g0067 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.527-20110C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114484498 | ||||||
| chr1:114484745
|
G | A | 15 | a0001c0002t0006g0087a0001c0002t0006g0088a0001c0002t0006g0089others(12): Show | 15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.527-20357C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114484745 | ||||||
| chr1:114484778
|
T | C | 1 | a0002c0003t0008g0049 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.527-20390A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114484778 | ||||||
| chr1:114484816
|
C | G | 81 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(78): Show | 81 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.527-20428G>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114484816 | ||||||
| chr1:114484819
|
C | T | 1 | a0001c0002t0033g0117 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.527-20431G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114484819 | ||||||
| chr1:114484934
|
C | A | 21 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(18): Show | 21 | HG00323.hp1 HG00738.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.527-20546G>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114484934 | ||||||
| chr1:114484942
|
C | T | 2 | a0001c0006t0010g0121a0001c0006t0010g0122 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.527-20554G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114484942 | ||||||
| chr1:114484991
|
G | C | 5 | a0001c0002t0003g0128a0001c0002t0003g0131a0001c0002t0003g0132others(2): Show | 5 | NA18612.hp2 NA18942.hp2 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.527-20603C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114484991 | ||||||
| chr1:114485053
|
T | TA | 33 | a0001c0001t0001g0083a0001c0001t0001g0200a0001c0001t0004g0050others(30): Show | 33 | HG00323.hp1 HG00738.hp1 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.527-20666dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114485053 | ||||||
| chr1:114485071
|
G | A | 1 | a0004c0007t0001g0014 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.527-20683C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114485071 | ||||||
| chr1:114485278
|
A | AT | 7 | a0001c0001t0001g0059a0001c0001t0001g0084a0001c0001t0002g0155others(4): Show | 7 | HG01081.hp2 HG02738.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.527-20891dupA | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114485278 | ||||||
| chr1:114485289
|
A | T | 1 | a0001c0001t0002g0162 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.527-20901T>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114485289 | ||||||
| chr1:114485304
|
G | GA | 28 | a0001c0002t0005g0098a0001c0002t0005g0099a0001c0002t0005g0101others(25): Show | 28 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.527-20917dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114485304 | ||||||
| chr1:114485426
|
C | T | 8 | a0003c0004t0001g0008a0003c0004t0004g0006a0003c0004t0004g0009others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.527-21038G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114485426 | ||||||
| chr1:114485496
|
G | C | 1 | a0001c0001t0001g0058 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.527-21108C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114485496 | ||||||
| chr1:114485590
|
G | C | 2 | a0001c0002t0019g0100a0001c0002t0041g0110 | 2 | HG01257.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.527-21202C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114485590 | ||||||
| chr1:114485655
|
C | A | 1 | a0001c0001t0002g0171 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.527-21267G>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114485655 | ||||||
| chr1:114485704
|
G | A | 1 | a0001c0002t0005g0099 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.527-21316C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114485704 | ||||||
| chr1:114485854
|
T | C | 6 | a0001c0006t0010g0119a0001c0006t0010g0120a0001c0006t0010g0121others(3): Show | 6 | HG02132.hp2 HG02698.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.527-21466A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114485854 | ||||||
| chr1:114486004
|
G | C | 21 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(18): Show | 21 | HG00323.hp1 HG00738.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.527-21616C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114486004 | ||||||
| chr1:114486100
|
C | T | 1 | a0001c0002t0037g0118 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.527-21712G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114486100 | ||||||
| chr1:114486112
|
C | A | 1 | a0002c0003t0008g0049 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.527-21724G>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114486112 | ||||||
| chr1:114486113
|
T | C | 18 | a0001c0002t0004g0111a0001c0002t0004g0114a0001c0002t0004g0115others(15): Show | 18 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.527-21725A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114486113 | ||||||
| chr1:114486487
|
C | T | 3 | a0001c0002t0006g0087a0001c0002t0023g0002a0001c0002t0034g0086 | 3 | HG02970.hp2 HG03516.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.527-22099G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114486487 | ||||||
| chr1:114486546
|
C | CA | 82 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0075others(79): Show | 82 | HG00438.hp1 HG00558.hp2 HG00642.hp1 others(79): Show |
intron_variant | MODIFIER | c.527-22159dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114486546 | ||||||
| chr1:114486546
|
C | CAA | 15 | a0001c0001t0002g0148a0001c0001t0002g0152a0001c0001t0002g0155others(12): Show | 15 | HG00099.hp1 HG01106.hp1 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.527-22160_527-2215 others(6): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114486546 | ||||||
| chr1:114486546
|
CA | C | 5 | a0001c0002t0018g0146a0001c0002t0033g0117a0003c0004t0014g0005others(2): Show | 5 | HG02055.hp2 HG02451.hp2 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.527-22159delT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114486546 | ||||||
| chr1:114486643
|
C | G | 1 | a0001c0001t0042g0061 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.527-22255G>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114486643 | ||||||
| chr1:114486956
|
G | A | 8 | a0003c0004t0001g0008a0003c0004t0004g0006a0003c0004t0004g0009others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.527-22568C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114486956 | ||||||
| chr1:114486996
|
C | T | 1 | a0001c0001t0002g0152 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.527-22608G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114486996 | ||||||
| chr1:114487044
|
G | A | 1 | a0001c0001t0017g0172 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.527-22656C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114487044 | ||||||
| chr1:114487086
|
C | CA | 39 | a0001c0001t0001g0069a0001c0001t0001g0176a0001c0001t0002g0035others(36): Show | 39 | HG00438.hp1 HG00558.hp2 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.527-22699dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114487086 | ||||||
| chr1:114487235
|
T | C | 1 | a0003c0004t0004g0009 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.527-22847A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114487235 | ||||||
| chr1:114487339
|
C | CA | 27 | a0001c0001t0001g0046a0001c0001t0001g0070a0001c0001t0001g0075others(24): Show | 27 | HG00642.hp1 HG00642.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.527-22952dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114487339 | ||||||
| chr1:114487504
|
A | G | 1 | a0001c0001t0001g0045 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.526+23047T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114487504 | ||||||
| chr1:114487511
|
T | C | 1 | a0001c0002t0041g0110 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.526+23040A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114487511 | ||||||
| chr1:114487619
|
C | T | 4 | a0001c0002t0009g0202a0001c0002t0009g0203a0001c0002t0009g0204others(1): Show | 4 | HG01891.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.526+22932G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114487619 | ||||||
| chr1:114487635
|
C | T | 1 | a0001c0002t0037g0118 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.526+22916G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114487635 | ||||||
| chr1:114487681
|
A | C | 4 | a0001c0005t0007g0147a0001c0005t0007g0150a0001c0005t0007g0151others(1): Show | 4 | HG01884.hp1 HG02897.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.526+22870T>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114487681 | ||||||
| chr1:114487697
|
A | C | 1 | a0001c0001t0004g0077 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.526+22854T>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114487697 | ||||||
| chr1:114487724
|
C | T | 1 | a0002c0003t0001g0017 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.526+22827G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114487724 | ||||||
| chr1:114487766
|
G | A | 4 | a0001c0001t0002g0157a0001c0001t0002g0158a0001c0001t0002g0159others(1): Show | 4 | NA18942.hp1 NA18970.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.526+22785C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114487766 | ||||||
| chr1:114487770
|
G | A | 1 | a0002c0003t0001g0037 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.526+22781C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114487770 | ||||||
| chr1:114487790
|
G | A | 6 | a0001c0006t0010g0119a0001c0006t0010g0120a0001c0006t0010g0121others(3): Show | 6 | HG02132.hp2 HG02698.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.526+22761C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114487790 | ||||||
| chr1:114487839
|
A | G | 81 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(78): Show | 81 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.526+22712T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114487839 | ||||||
| chr1:114487903
|
C | CA | 46 | a0001c0001t0001g0022a0001c0001t0001g0025a0001c0001t0001g0046others(43): Show | 46 | HG00438.hp2 HG01175.hp1 HG01175.hp2 others(43): Show |
intron_variant | MODIFIER | c.526+22647dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114487903 | ||||||
| chr1:114487903
|
C | CAA | 13 | a0001c0001t0024g0003a0001c0002t0005g0098a0001c0002t0005g0102others(10): Show | 13 | HG00099.hp1 HG01192.hp1 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.526+22646_526+2264 others(6): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114487903 | ||||||
| chr1:114487903
|
C | CAAA | 8 | a0001c0002t0006g0088a0001c0002t0021g0092a0001c0002t0025g0004others(5): Show | 8 | HG00735.hp1 HG01106.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.526+22645_526+2264 others(7): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114487903 | ||||||
| chr1:114487903
|
CA | C | 15 | a0001c0001t0001g0020a0001c0001t0001g0059a0001c0001t0001g0060others(12): Show | 15 | HG00642.hp2 HG01074.hp2 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.526+22647delT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114487903 | ||||||
| chr1:114487903
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0002t0003g0127 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.526+22638_526+2264 others(14): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114487903 | ||||||
| chr1:114487919
|
AAAAAAAA others(5): Show |
A | 1 | a0003c0004t0004g0009 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.526+22620_526+2263 others(16): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114487919 | ||||||
| chr1:114487931
|
T | A | 6 | a0003c0004t0001g0008a0003c0004t0004g0006a0003c0004t0013g0007others(3): Show | 6 | HG02258.hp1 HG02280.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.526+22620A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114487931 | ||||||
| chr1:114487932
|
G | T | 15 | a0001c0002t0006g0087a0001c0002t0006g0088a0001c0002t0006g0089others(12): Show | 15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.526+22619C>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114487932 | ||||||
| chr1:114488777
|
C | A | 3 | a0001c0001t0001g0176a0001c0001t0002g0162a0001c0001t0002g0175 | 3 | HG03710.hp1 HG03834.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.526+21774G>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114488777 | ||||||
| chr1:114488923
|
C | T | 1 | a0001c0001t0002g0162 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.526+21628G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114488923 | ||||||
| chr1:114488950
|
T | A | 1 | a0001c0002t0037g0118 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.526+21601A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114488950 | ||||||
| chr1:114489072
|
T | C | 2 | a0003c0004t0001g0008a0003c0004t0004g0009 | 2 | HG02965.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.526+21479A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114489072 | ||||||
| chr1:114489098
|
A | C | 3 | a0001c0002t0005g0098a0001c0002t0005g0099a0001c0002t0005g0101 | 3 | HG01433.hp2 HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.526+21453T>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114489098 | ||||||
| chr1:114489212
|
C | T | 1 | a0001c0001t0002g0161 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.526+21339G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114489212 | ||||||
| chr1:114489236
|
A | G | 1 | a0001c0001t0001g0058 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.526+21315T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114489236 | ||||||
| chr1:114489523
|
C | T | 15 | a0001c0002t0006g0087a0001c0002t0006g0088a0001c0002t0006g0089others(12): Show | 15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.526+21028G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114489523 | ||||||
| chr1:114489524
|
G | A | 1 | a0001c0002t0037g0118 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.526+21027C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114489524 | ||||||
| chr1:114489569
|
T | G | 1 | a0001c0002t0003g0144 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.526+20982A>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114489569 | ||||||
| chr1:114489650
|
T | A | 15 | a0001c0002t0006g0087a0001c0002t0006g0088a0001c0002t0006g0089others(12): Show | 15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.526+20901A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114489650 | ||||||
| chr1:114489767
|
A | T | 47 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(44): Show | 47 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.526+20784T>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114489767 | ||||||
| chr1:114489934
|
A | G | 1 | a0003c0004t0031g0011 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.526+20617T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114489934 | ||||||
| chr1:114489973
|
G | C | 1 | a0003c0004t0031g0011 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.526+20578C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114489973 | ||||||
| chr1:114490019
|
G | T | 2 | a0001c0001t0022g0056a0001c0001t0022g0057 | 2 | HG03704.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.526+20532C>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114490019 | ||||||
| chr1:114490029
|
T | C | 68 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(65): Show | 68 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.526+20522A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114490029 | ||||||
| chr1:114490030
|
T | C | 60 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(57): Show | 60 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.526+20521A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114490030 | ||||||
| chr1:114490084
|
C | CA | 24 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0141others(21): Show | 24 | HG00642.hp1 HG00738.hp2 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.526+20466dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114490084 | ||||||
| chr1:114490084
|
C | CAA | 5 | a0001c0001t0048g0081a0001c0002t0019g0100a0001c0002t0037g0118others(2): Show | 5 | HG01257.hp2 HG02132.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.526+20465_526+2046 others(6): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114490084 | ||||||
| chr1:114490084
|
C | CAAAAAAA others(3): Show |
1 | a0001c0002t0005g0103 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.526+20457_526+2046 others(14): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114490084 | ||||||
| chr1:114490084
|
C | CAAAAAAA others(9): Show |
1 | a0001c0002t0005g0104 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.526+20451_526+2046 others(20): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114490084 | ||||||
| chr1:114490084
|
C | CAAAAAAA others(10): Show |
3 | a0001c0002t0005g0099a0001c0002t0005g0105a0001c0002t0005g0106 | 3 | HG01192.hp1 HG02922.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.526+20450_526+2046 others(21): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114490084 | ||||||
| chr1:114490084
|
C | CAAAAAAA others(11): Show |
5 | a0001c0002t0005g0098a0001c0002t0005g0107a0001c0002t0005g0108others(2): Show | 5 | HG01261.hp2 HG02615.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.526+20449_526+2046 others(22): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114490084 | ||||||
| chr1:114490084
|
CA | C | 6 | a0001c0001t0001g0200a0001c0001t0002g0186a0001c0001t0011g0054others(3): Show | 6 | HG01099.hp2 HG01169.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.526+20466delT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114490084 | ||||||
| chr1:114490101
|
A | G | 2 | a0001c0002t0006g0087a0001c0002t0034g0086 | 2 | HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.526+20450T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114490101 | ||||||
| chr1:114490103
|
AAG | A | 8 | a0001c0002t0004g0111a0001c0002t0004g0114a0001c0002t0004g0115others(5): Show | 8 | HG01433.hp2 HG01884.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.526+20446_526+2044 others(6): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114490103 | ||||||
| chr1:114490105
|
G | A | 64 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(61): Show | 64 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.526+20446C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114490105 | ||||||
| chr1:114490106
|
AAAAGG | A | 3 | a0003c0004t0004g0006a0003c0004t0013g0007a0003c0004t0050g0206 | 3 | HG02280.hp1 HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.526+20440_526+2044 others(9): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114490106 | ||||||
| chr1:114490111
|
G | A | 78 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(75): Show | 78 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(75): Show |
intron_variant | MODIFIER | c.526+20440C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114490111 | ||||||
| chr1:114490136
|
GA | G | 4 | a0001c0001t0002g0157a0001c0001t0002g0158a0001c0001t0002g0159others(1): Show | 4 | NA18942.hp1 NA18970.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.526+20414delT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114490136 | ||||||
| chr1:114490137
|
A | G | 13 | a0001c0002t0005g0098a0001c0002t0005g0099a0001c0002t0005g0101others(10): Show | 13 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.526+20414T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114490137 | ||||||
| chr1:114490212
|
C | T | 1 | a0001c0002t0032g0116 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.526+20339G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114490212 | ||||||
| chr1:114490270
|
G | A | 2 | a0001c0002t0018g0145a0001c0002t0018g0146 | 2 | HG00741.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.526+20281C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114490270 | ||||||
| chr1:114490517
|
C | T | 1 | a0001c0001t0024g0003 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.526+20034G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114490517 | ||||||
| chr1:114490890
|
C | T | 81 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(78): Show | 81 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.526+19661G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114490890 | ||||||
| chr1:114491057
|
T | C | 1 | a0001c0001t0001g0071 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.526+19494A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114491057 | ||||||
| chr1:114491211
|
T | C | 1 | a0001c0001t0002g0185 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.526+19340A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114491211 | ||||||
| chr1:114491217
|
T | C | 2 | a0001c0001t0001g0045a0001c0001t0001g0046 | 2 | HG02809.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.526+19334A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114491217 | ||||||
| chr1:114491318
|
C | A | 1 | a0001c0001t0001g0072 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.526+19233G>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114491318 | ||||||
| chr1:114491427
|
A | G | 2 | a0001c0001t0001g0083a0001c0001t0004g0050 | 2 | HG02055.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.526+19124T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114491427 | ||||||
| chr1:114491434
|
C | T | 206 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0022others(203): Show | 207 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.526+19117G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114491434 | ||||||
| chr1:114491549
|
C | G | 6 | a0001c0002t0004g0111a0001c0002t0004g0114a0001c0002t0004g0115others(3): Show | 6 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.526+19002G>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114491549 | ||||||
| chr1:114491636
|
T | A | 5 | a0003c0004t0001g0008a0003c0004t0004g0009a0003c0004t0013g0010others(2): Show | 5 | HG02145.hp1 HG02258.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.526+18915A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114491636 | ||||||
| chr1:114491647
|
G | A | 81 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(78): Show | 81 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.526+18904C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114491647 | ||||||
| chr1:114491741
|
T | C | 1 | a0001c0001t0002g0177 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.526+18810A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114491741 | ||||||
| chr1:114491918
|
C | T | 1 | a0001c0001t0048g0081 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.526+18633G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114491918 | ||||||
| chr1:114491933
|
T | C | 2 | a0001c0002t0018g0145a0001c0002t0018g0146 | 2 | HG00741.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.526+18618A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114491933 | ||||||
| chr1:114491962
|
G | C | 6 | a0001c0006t0010g0119a0001c0006t0010g0120a0001c0006t0010g0121others(3): Show | 6 | HG02132.hp2 HG02698.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.526+18589C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114491962 | ||||||
| chr1:114492087
|
C | G | 81 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(78): Show | 81 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.526+18464G>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114492087 | ||||||
| chr1:114492091
|
T | A | 15 | a0001c0002t0006g0087a0001c0002t0006g0088a0001c0002t0006g0089others(12): Show | 15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.526+18460A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114492091 | ||||||
| chr1:114492391
|
A | G | 1 | a0001c0001t0002g0195 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.526+18160T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114492391 | ||||||
| chr1:114492469
|
A | G | 6 | a0001c0002t0004g0111a0001c0002t0004g0114a0001c0002t0004g0115others(3): Show | 6 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.526+18082T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114492469 | ||||||
| chr1:114492501
|
T | C | 1 | a0001c0001t0002g0152 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.526+18050A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114492501 | ||||||
| chr1:114492699
|
A | C | 2 | a0001c0002t0018g0145a0001c0002t0018g0146 | 2 | HG00741.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.526+17852T>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114492699 | ||||||
| chr1:114492842
|
G | A | 1 | a0001c0001t0002g0178 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.526+17709C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114492842 | ||||||
| chr1:114492897
|
T | A | 3 | a0003c0004t0004g0006a0003c0004t0013g0007a0003c0004t0050g0206 | 3 | HG02280.hp1 HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.526+17654A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114492897 | ||||||
| chr1:114492923
|
T | C | 1 | a0001c0001t0002g0179 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.526+17628A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114492923 | ||||||
| chr1:114493206
|
G | C | 21 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(18): Show | 21 | HG00323.hp1 HG00738.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.526+17345C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114493206 | ||||||
| chr1:114493491
|
C | A | 1 | a0001c0001t0002g0180 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.526+17060G>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114493491 | ||||||
| chr1:114493634
|
T | C | 81 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(78): Show | 81 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.526+16917A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114493634 | ||||||
| chr1:114493759
|
C | T | 13 | a0001c0001t0002g0148a0001c0001t0002g0154a0001c0001t0002g0155others(10): Show | 13 | HG01175.hp2 HG01884.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.526+16792G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114493759 | ||||||
| chr1:114493768
|
G | C | 1 | a0001c0009t0039g0123 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.526+16783C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114493768 | ||||||
| chr1:114493912
|
C | T | 2 | a0002c0003t0001g0026a0002c0003t0001g0047 | 2 | HG01928.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.526+16639G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114493912 | ||||||
| chr1:114493957
|
C | T | 2 | a0003c0004t0001g0008a0003c0004t0004g0009 | 2 | HG02965.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.526+16594G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114493957 | ||||||
| chr1:114494045
|
G | A | 1 | a0001c0002t0037g0118 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.526+16506C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114494045 | ||||||
| chr1:114494098
|
T | C | 1 | a0001c0002t0037g0118 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.526+16453A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114494098 | ||||||
| chr1:114494118
|
C | T | 4 | a0001c0002t0009g0202a0001c0002t0009g0203a0001c0002t0009g0204others(1): Show | 4 | HG01891.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.526+16433G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114494118 | ||||||
| chr1:114494123
|
AT | A | 68 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(65): Show | 68 | HG00323.hp1 HG00738.hp1 HG00741.hp2 others(65): Show |
intron_variant | MODIFIER | c.526+16427delA | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114494123 | ||||||
| chr1:114494497
|
T | C | 13 | a0001c0002t0005g0098a0001c0002t0005g0099a0001c0002t0005g0101others(10): Show | 13 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.526+16054A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114494497 | ||||||
| chr1:114494569
|
G | A | 1 | a0001c0002t0033g0117 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.526+15982C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114494569 | ||||||
| chr1:114494598
|
G | C | 4 | a0001c0001t0001g0052a0001c0001t0001g0073a0001c0001t0001g0078others(1): Show | 4 | HG01081.hp1 HG01952.hp1 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.526+15953C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114494598 | ||||||
| chr1:114494791
|
A | C | 1 | a0001c0002t0006g0088 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.526+15760T>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114494791 | ||||||
| chr1:114494872
|
T | C | 3 | a0003c0004t0013g0010a0003c0004t0031g0011a0005c0008t0013g0015 | 3 | HG02145.hp1 HG02258.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.526+15679A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114494872 | ||||||
| chr1:114494910
|
A | AGTTGTT | 8 | a0003c0004t0001g0008a0003c0004t0004g0006a0003c0004t0004g0009others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.526+15635_526+1564 others(10): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114494910 | ||||||
| chr1:114495024
|
G | A | 5 | a0001c0002t0006g0093a0001c0002t0006g0094a0001c0002t0006g0095others(2): Show | 5 | HG02280.hp2 HG02723.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.526+15527C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114495024 | ||||||
| chr1:114495038
|
C | T | 2 | a0001c0002t0018g0145a0001c0002t0018g0146 | 2 | HG00741.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.526+15513G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114495038 | ||||||
| chr1:114495077
|
C | T | 3 | a0001c0001t0001g0022a0001c0001t0004g0023a0001c0001t0024g0003 | 3 | HG02615.hp2 HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.526+15474G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114495077 | ||||||
| chr1:114495455
|
C | T | 1 | a0001c0001t0002g0152 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.526+15096G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114495455 | ||||||
| chr1:114495533
|
G | C | 19 | a0001c0002t0004g0111a0001c0002t0004g0114a0001c0002t0004g0115others(16): Show | 19 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.526+15018C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114495533 | ||||||
| chr1:114495659
|
G | C | 1 | a0001c0001t0001g0075 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.526+14892C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114495659 | ||||||
| chr1:114495994
|
T | C | 1 | a0003c0004t0004g0009 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.526+14557A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114495994 | ||||||
| chr1:114496156
|
G | A | 5 | a0003c0004t0001g0008a0003c0004t0004g0009a0003c0004t0013g0010others(2): Show | 5 | HG02145.hp1 HG02258.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.526+14395C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114496156 | ||||||
| chr1:114496277
|
T | C | 13 | a0001c0002t0005g0098a0001c0002t0005g0099a0001c0002t0005g0101others(10): Show | 13 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.526+14274A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114496277 | ||||||
| chr1:114496497
|
T | C | 81 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(78): Show | 81 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.526+14054A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114496497 | ||||||
| chr1:114496521
|
A | G | 81 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(78): Show | 81 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.526+14030T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114496521 | ||||||
| chr1:114496527
|
T | C | 6 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0185others(3): Show | 6 | HG01891.hp1 HG02622.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.526+14024A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114496527 | ||||||
| chr1:114496551
|
G | A | 1 | a0001c0002t0037g0118 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.526+14000C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114496551 | ||||||
| chr1:114496581
|
T | G | 6 | a0001c0006t0010g0119a0001c0006t0010g0120a0001c0006t0010g0121others(3): Show | 6 | HG02132.hp2 HG02698.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.526+13970A>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114496581 | ||||||
| chr1:114496627
|
A | T | 3 | a0001c0002t0005g0098a0001c0002t0005g0099a0001c0002t0005g0101 | 3 | HG01433.hp2 HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.526+13924T>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114496627 | ||||||
| chr1:114496646
|
A | T | 54 | a0001c0001t0001g0164a0001c0001t0001g0176a0001c0001t0002g0148others(51): Show | 54 | HG00438.hp1 HG00558.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.526+13905T>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114496646 | ||||||
| chr1:114496690
|
T | C | 6 | a0001c0002t0004g0111a0001c0002t0004g0114a0001c0002t0004g0115others(3): Show | 6 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.526+13861A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114496690 | ||||||
| chr1:114496951
|
T | C | 2 | a0001c0005t0007g0147a0001c0005t0007g0192 | 2 | HG01884.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.526+13600A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114496951 | ||||||
| chr1:114497059
|
T | C | 4 | a0001c0002t0009g0202a0001c0002t0009g0203a0001c0002t0009g0204others(1): Show | 4 | HG01891.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.526+13492A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114497059 | ||||||
| chr1:114497087
|
T | A | 1 | a0001c0002t0006g0097 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.526+13464A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114497087 | ||||||
| chr1:114497296
|
A | G | 54 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(51): Show | 54 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.526+13255T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114497296 | ||||||
| chr1:114497357
|
C | T | 1 | a0001c0001t0001g0076 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.526+13194G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114497357 | ||||||
| chr1:114497358
|
G | A | 2 | a0001c0002t0006g0087a0001c0002t0034g0086 | 2 | HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.526+13193C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114497358 | ||||||
| chr1:114497591
|
C | G | 206 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0022others(203): Show | 207 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.526+12960G>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114497591 | ||||||
| chr1:114497662
|
C | A | 1 | a0001c0002t0004g0111 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.526+12889G>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114497662 | ||||||
| chr1:114497869
|
A | G | 4 | a0001c0002t0009g0202a0001c0002t0009g0203a0001c0002t0009g0204others(1): Show | 4 | HG01891.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.526+12682T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114497869 | ||||||
| chr1:114497879
|
G | GA | 11 | a0001c0002t0005g0101a0001c0002t0005g0102a0001c0002t0005g0103others(8): Show | 11 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.526+12671dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114497879 | ||||||
| chr1:114497967
|
T | C | 1 | a0001c0001t0044g0016 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.526+12584A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114497967 | ||||||
| chr1:114498050
|
T | A | 1 | a0001c0001t0001g0076 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.526+12501A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114498050 | ||||||
| chr1:114498126
|
C | CA | 17 | a0001c0001t0001g0020a0001c0001t0002g0186a0001c0001t0002g0187others(14): Show | 17 | HG00642.hp2 HG01074.hp2 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.526+12424dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114498126 | ||||||
| chr1:114498126
|
C | CAA | 59 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(56): Show | 59 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.526+12423_526+1242 others(6): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114498126 | ||||||
| chr1:114498203
|
A | G | 3 | a0003c0004t0004g0006a0003c0004t0013g0007a0003c0004t0050g0206 | 3 | HG02280.hp1 HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.526+12348T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114498203 | ||||||
| chr1:114498310
|
C | T | 145 | a0001c0001t0001g0022a0001c0001t0001g0025a0001c0001t0001g0045others(142): Show | 145 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.526+12241G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114498310 | ||||||
| chr1:114498493
|
A | C | 2 | a0001c0002t0006g0087a0001c0002t0034g0086 | 2 | HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.526+12058T>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114498493 | ||||||
| chr1:114498713
|
C | A | 1 | a0001c0002t0033g0117 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.526+11838G>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114498713 | ||||||
| chr1:114498715
|
G | C | 1 | a0001c0002t0033g0117 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.526+11836C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114498715 | ||||||
| chr1:114498758
|
G | A | 21 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(18): Show | 21 | HG00323.hp1 HG00738.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.526+11793C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114498758 | ||||||
| chr1:114499458
|
G | A | 2 | a0001c0001t0001g0083a0001c0001t0004g0050 | 2 | HG02055.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.526+11093C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114499458 | ||||||
| chr1:114499459
|
G | C | 8 | a0003c0004t0001g0008a0003c0004t0004g0006a0003c0004t0004g0009others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.526+11092C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114499459 | ||||||
| chr1:114499473
|
G | T | 205 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0022others(202): Show | 206 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.526+11078C>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114499473 | ||||||
| chr1:114499793
|
C | T | 66 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(63): Show | 66 | HG00323.hp1 HG00738.hp1 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.526+10758G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114499793 | ||||||
| chr1:114499860
|
C | T | 81 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(78): Show | 81 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.526+10691G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114499860 | ||||||
| chr1:114499889
|
A | G | 81 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(78): Show | 81 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.526+10662T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114499889 | ||||||
| chr1:114499923
|
G | C | 13 | a0001c0002t0005g0098a0001c0002t0005g0099a0001c0002t0005g0101others(10): Show | 13 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.526+10628C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114499923 | ||||||
| chr1:114499941
|
A | G | 2 | a0001c0006t0010g0121a0001c0006t0010g0122 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.526+10610T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114499941 | ||||||
| chr1:114500111
|
G | A | 1 | a0001c0002t0029g0135 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.526+10440C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114500111 | ||||||
| chr1:114500160
|
C | G | 1 | a0001c0001t0001g0052 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.526+10391G>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114500160 | ||||||
| chr1:114500362
|
G | T | 2 | a0001c0002t0009g0204a0001c0002t0009g0205 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.526+10189C>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114500362 | ||||||
| chr1:114500568
|
G | GA | 13 | a0001c0002t0005g0098a0001c0002t0005g0099a0001c0002t0005g0101others(10): Show | 13 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.526+9982dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114500568 | ||||||
| chr1:114500608
|
TA | T | 11 | a0001c0001t0015g0051a0001c0005t0007g0147a0001c0005t0007g0150others(8): Show | 11 | HG00099.hp2 HG01884.hp1 HG02132.hp2 others(8): Show |
intron_variant | MODIFIER | c.526+9942delT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114500608 | ||||||
| chr1:114500898
|
CAAGAATT others(305): Show |
C | 81 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(78): Show | 81 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.526+9341_526+9652d others(2): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114500898 | ||||||
| chr1:114501010
|
A | G | 124 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0022others(121): Show | 125 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.526+9541T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114501010 | ||||||
| chr1:114501047
|
G | C | 2 | a0001c0001t0001g0045a0001c0001t0001g0046 | 2 | HG02809.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.526+9504C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114501047 | ||||||
| chr1:114501189
|
C | A | 1 | a0001c0001t0012g0191 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.526+9362G>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114501189 | ||||||
| chr1:114501189
|
C | CA | 11 | a0001c0001t0001g0078a0001c0001t0002g0193a0001c0001t0004g0050others(8): Show | 11 | HG01081.hp1 HG01081.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.526+9361dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114501189 | ||||||
| chr1:114501223
|
G | C | 8 | a0003c0004t0001g0008a0003c0004t0004g0006a0003c0004t0004g0009others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.526+9328C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114501223 | ||||||
| chr1:114501363
|
G | GT | 43 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(40): Show | 43 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.526+9187dupA | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114501363 | ||||||
| chr1:114501408
|
G | A | 15 | a0001c0002t0006g0087a0001c0002t0006g0088a0001c0002t0006g0089others(12): Show | 15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.526+9143C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114501408 | ||||||
| chr1:114501627
|
AAGGGGCC others(5): Show |
A | 1 | a0001c0002t0037g0118 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.526+8912_526+8923d others(14): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114501627 | ||||||
| chr1:114501665
|
T | A | 4 | a0001c0002t0009g0202a0001c0002t0009g0203a0001c0002t0009g0204others(1): Show | 4 | HG01891.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.526+8886A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114501665 | ||||||
| chr1:114501821
|
T | TATA | 205 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0022others(202): Show | 206 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.526+8727_526+8729d others(5): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114501821 | ||||||
| chr1:114502245
|
C | T | 1 | a0002c0003t0001g0021 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.526+8306G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114502245 | ||||||
| chr1:114502259
|
A | C | 1 | a0001c0002t0004g0111 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.526+8292T>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114502259 | ||||||
| chr1:114502710
|
T | C | 1 | a0001c0001t0002g0195 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.526+7841A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114502710 | ||||||
| chr1:114502714
|
C | T | 2 | a0001c0006t0010g0119a0001c0006t0010g0120 | 2 | HG02922.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.526+7837G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114502714 | ||||||
| chr1:114502718
|
G | C | 1 | a0004c0007t0001g0014 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.526+7833C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114502718 | ||||||
| chr1:114502834
|
A | C | 1 | a0001c0009t0039g0123 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.526+7717T>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114502834 | ||||||
| chr1:114502926
|
T | C | 2 | a0001c0002t0018g0145a0001c0002t0018g0146 | 2 | HG00741.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.526+7625A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114502926 | ||||||
| chr1:114503043
|
T | C | 35 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0052others(32): Show | 35 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.526+7508A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114503043 | ||||||
| chr1:114503043
|
T | TTA | 6 | a0001c0002t0004g0111a0001c0002t0004g0114a0001c0002t0004g0115others(3): Show | 6 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.526+7507_526+7508i others(4): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114503043 | ||||||
| chr1:114503434
|
C | T | 2 | a0001c0001t0001g0019a0001c0001t0001g0020 | 2 | HG00741.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.526+7117G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114503434 | ||||||
| chr1:114503758
|
C | T | 2 | a0001c0002t0018g0145a0001c0002t0018g0146 | 2 | HG00741.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.526+6793G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114503758 | ||||||
| chr1:114503951
|
T | G | 205 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0022others(202): Show | 206 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.526+6600A>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114503951 | ||||||
| chr1:114503955
|
G | A | 15 | a0001c0002t0006g0087a0001c0002t0006g0088a0001c0002t0006g0089others(12): Show | 15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.526+6596C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114503955 | ||||||
| chr1:114504104
|
T | A | 1 | a0001c0002t0033g0117 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.526+6447A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114504104 | ||||||
| chr1:114504165
|
A | AT | 4 | a0001c0006t0010g0119a0001c0006t0010g0120a0001c0006t0010g0121others(1): Show | 4 | HG02895.hp2 HG02897.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.526+6385dupA | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114504165 | ||||||
| chr1:114504301
|
G | A | 1 | a0001c0002t0033g0117 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.526+6250C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114504301 | ||||||
| chr1:114504462
|
G | A | 1 | a0001c0002t0033g0117 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.526+6089C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114504462 | ||||||
| chr1:114504485
|
T | C | 2 | a0001c0001t0001g0079a0001c0001t0001g0080 | 2 | NA18970.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.526+6066A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114504485 | ||||||
| chr1:114504510
|
G | A | 1 | a0001c0001t0048g0081 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.526+6041C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114504510 | ||||||
| chr1:114504862
|
A | C | 23 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(20): Show | 23 | HG00323.hp1 HG00738.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.526+5689T>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114504862 | ||||||
| chr1:114504927
|
G | A | 81 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(78): Show | 81 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.526+5624C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114504927 | ||||||
| chr1:114504956
|
G | C | 15 | a0001c0002t0006g0087a0001c0002t0006g0088a0001c0002t0006g0089others(12): Show | 15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.526+5595C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114504956 | ||||||
| chr1:114505155
|
G | A | 1 | a0001c0002t0032g0116 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.526+5396C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114505155 | ||||||
| chr1:114505215
|
T | A | 13 | a0001c0002t0005g0098a0001c0002t0005g0099a0001c0002t0005g0101others(10): Show | 13 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.526+5336A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114505215 | ||||||
| chr1:114505408
|
G | A | 6 | a0001c0002t0004g0111a0001c0002t0004g0114a0001c0002t0004g0115others(3): Show | 6 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.526+5143C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114505408 | ||||||
| chr1:114505491
|
A | C | 2 | a0001c0002t0009g0202a0001c0002t0009g0203 | 2 | HG01891.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.526+5060T>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114505491 | ||||||
| chr1:114505523
|
CAT | C | 39 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(36): Show | 39 | HG00323.hp1 HG00738.hp1 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.526+5026_526+5027d others(4): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114505523 | ||||||
| chr1:114505524
|
A | C | 1 | a0001c0002t0021g0085 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.526+5027T>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114505524 | ||||||
| chr1:114505628
|
C | T | 8 | a0003c0004t0001g0008a0003c0004t0004g0006a0003c0004t0004g0009others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.526+4923G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114505628 | ||||||
| chr1:114505684
|
C | T | 1 | a0002c0003t0001g0001 | 2 | HG01433.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.526+4867G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114505684 | ||||||
| chr1:114505724
|
C | G | 6 | a0001c0002t0004g0111a0001c0002t0004g0114a0001c0002t0004g0115others(3): Show | 6 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.526+4827G>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114505724 | ||||||
| chr1:114505815
|
G | A | 6 | a0001c0002t0003g0136a0001c0002t0003g0137a0001c0002t0003g0138others(3): Show | 6 | HG00323.hp1 HG01167.hp1 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.526+4736C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114505815 | ||||||
| chr1:114505819
|
C | T | 1 | a0001c0001t0012g0197 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.526+4732G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114505819 | ||||||
| chr1:114506113
|
G | A | 1 | a0001c0002t0033g0117 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.526+4438C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114506113 | ||||||
| chr1:114506207
|
C | T | 1 | a0001c0001t0044g0016 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.526+4344G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114506207 | ||||||
| chr1:114506383
|
C | CA | 38 | a0001c0001t0026g0196a0001c0002t0003g0125a0001c0002t0003g0126others(35): Show | 38 | HG00099.hp1 HG00735.hp1 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.526+4167dupT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114506383 | ||||||
| chr1:114506383
|
C | CAAA | 12 | a0001c0002t0005g0099a0001c0002t0005g0101a0001c0002t0005g0102others(9): Show | 12 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.526+4165_526+4167d others(5): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114506383 | ||||||
| chr1:114506383
|
CA | C | 12 | a0001c0001t0001g0083a0001c0001t0002g0148a0001c0001t0002g0149others(9): Show | 12 | HG00738.hp1 HG02145.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.526+4167delT | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114506383 | ||||||
| chr1:114506519
|
AAT | A | 6 | a0001c0006t0010g0119a0001c0006t0010g0120a0001c0006t0010g0121others(3): Show | 6 | HG02132.hp2 HG02698.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.526+4030_526+4031d others(4): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114506519 | ||||||
| chr1:114506657
|
A | C | 1 | a0003c0004t0014g0005 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.526+3894T>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114506657 | ||||||
| chr1:114507062
|
A | G | 15 | a0001c0002t0006g0087a0001c0002t0006g0088a0001c0002t0006g0089others(12): Show | 15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.526+3489T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114507062 | ||||||
| chr1:114507073
|
A | G | 6 | a0001c0002t0004g0111a0001c0002t0004g0114a0001c0002t0004g0115others(3): Show | 6 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.526+3478T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114507073 | ||||||
| chr1:114507574
|
C | CT | 2 | a0001c0002t0003g0125a0001c0002t0003g0126 | 2 | HG01099.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.526+2976_526+2977i others(3): Show |
TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114507574 | ||||||
| chr1:114507596
|
T | C | 2 | a0001c0001t0002g0198a0001c0001t0012g0197 | 2 | HG02145.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.526+2955A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114507596 | ||||||
| chr1:114507613
|
T | C | 1 | a0002c0003t0001g0199 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.526+2938A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114507613 | ||||||
| chr1:114507891
|
C | T | 4 | a0001c0002t0009g0202a0001c0002t0009g0203a0001c0002t0009g0204others(1): Show | 4 | HG01891.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.526+2660G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114507891 | ||||||
| chr1:114507983
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.526+2568C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114507983 | ||||||
| chr1:114508111
|
T | C | 5 | a0001c0002t0004g0114a0001c0002t0004g0115a0001c0002t0020g0112others(2): Show | 5 | HG01884.hp2 HG02622.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.526+2440A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114508111 | ||||||
| chr1:114508228
|
A | G | 6 | a0001c0002t0004g0111a0001c0002t0004g0114a0001c0002t0004g0115others(3): Show | 6 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.526+2323T>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114508228 | ||||||
| chr1:114508270
|
G | A | 21 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(18): Show | 21 | HG00323.hp1 HG00738.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.526+2281C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114508270 | ||||||
| chr1:114508753
|
G | A | 15 | a0001c0002t0006g0087a0001c0002t0006g0088a0001c0002t0006g0089others(12): Show | 15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.526+1798C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114508753 | ||||||
| chr1:114508830
|
T | G | 1 | a0001c0001t0001g0084 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.526+1721A>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114508830 | ||||||
| chr1:114508842
|
C | T | 13 | a0001c0002t0005g0098a0001c0002t0005g0099a0001c0002t0005g0101others(10): Show | 13 | HG01192.hp1 HG01257.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.526+1709G>A | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114508842 | ||||||
| chr1:114509224
|
T | C | 2 | a0001c0002t0009g0204a0001c0002t0009g0205 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.526+1327A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114509224 | ||||||
| chr1:114509488
|
A | C | 15 | a0001c0002t0006g0087a0001c0002t0006g0088a0001c0002t0006g0089others(12): Show | 15 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.526+1063T>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114509488 | ||||||
| chr1:114509730
|
T | C | 2 | a0001c0002t0018g0145a0001c0002t0018g0146 | 2 | HG00741.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.526+821A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114509730 | ||||||
| chr1:114509886
|
T | C | 12 | a0003c0004t0001g0008a0003c0004t0004g0006a0003c0004t0004g0009others(9): Show | 12 | HG02055.hp2 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.526+665A>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114509886 | ||||||
| chr1:114509935
|
C | G | 1 | a0001c0005t0007g0147 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.526+616G>C | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114509935 | ||||||
| chr1:114510044
|
T | A | 81 | a0001c0002t0003g0125a0001c0002t0003g0126a0001c0002t0003g0127others(78): Show | 81 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.526+507A>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114510044 | ||||||
| chr1:114510087
|
C | A | 54 | a0001c0001t0001g0164a0001c0001t0001g0176a0001c0001t0002g0148others(51): Show | 54 | HG00438.hp1 HG00558.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.526+464G>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114510087 | ||||||
| chr1:114510191
|
G | A | 1 | a0001c0002t0003g0201 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.526+360C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114510191 | ||||||
| chr1:114510191
|
G | C | 1 | a0001c0001t0001g0200 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.526+360C>G | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114510191 | ||||||
| chr1:114510283
|
G | A | 4 | a0001c0002t0009g0202a0001c0002t0009g0203a0001c0002t0009g0204others(1): Show | 4 | HG01891.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.526+268C>T | TRIM33 | ENSG00000197323.12 | transcript | ENST00000358465.7 | protein_coding | 1/19 | chr1 | 114510283 |