Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 23321 |
| ensemblid | ENSG00000109654.16 |
| hgncid | 15974 |
| symbol | TRIM2 |
| name | tripartite motif containing 2 |
| refseq_nuc | NM_015271.5 |
| refseq_prot | NP_056086.2 |
| ensembl_nuc | ENST00000338700.10 |
| ensembl_prot | ENSP00000339659.5 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 153204443 |
| end | 153339317 |
| strand | + |
| ver | v1.2 |
| region | chr4:153204443-153339317 |
| region5000 | chr4:153199443-153344317 |
| regionname0 | TRIM2_chr4_153204443_153339317 |
| regionname5000 | TRIM2_chr4_153199443_153344317 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 771 | 266 | 84 | 50 | 84 | 12 | 34 | 68 | TRIM2_chr4_153199443_153344317 | TRIM2 | MHRSG others(766): Show |
chr4 | 153199443 | 153344317 |
| a0002 | 0/0 | 771 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | MHRSG others(766): Show |
chr4 | 153199443 | 153344317 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 2313 | 133 | 31 | 28 | 53 | 6 | 14 | TRIM2_chr4_153199443_153344317 | TRIM2 | ATGCA others(2308): Show |
chr4 | 153199443 | 153344317 | ||
| a0001c0002 | 0/1 | 2313 | 79 | 30 | 9 | 21 | 2 | 16 | TRIM2_chr4_153199443_153344317 | TRIM2 | ATGCA others(2308): Show |
chr4 | 153199443 | 153344317 | ||
| a0001c0003 | 0/0 | 2313 | 44 | 20 | 12 | 6 | 3 | 3 | TRIM2_chr4_153199443_153344317 | TRIM2 | ATGCA others(2308): Show |
chr4 | 153199443 | 153344317 | ||
| a0001c0004 | 0/0 | 2313 | 3 | 1 | 0 | 2 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | ATGCA others(2308): Show |
chr4 | 153199443 | 153344317 | ||
| a0001c0005 | 0/0 | 2313 | 3 | 0 | 1 | 1 | 1 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | ATGCA others(2308): Show |
chr4 | 153199443 | 153344317 | ||
| a0001c0007 | 0/0 | 2313 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | ATGCA others(2308): Show |
chr4 | 153199443 | 153344317 | ||
| a0001c0008 | 0/0 | 2313 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | ATGCA others(2308): Show |
chr4 | 153199443 | 153344317 | ||
| a0001c0009 | 0/0 | 2313 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | ATGCA others(2308): Show |
chr4 | 153199443 | 153344317 | ||
| a0001c0010 | 0/0 | 2313 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM2_chr4_153199443_153344317 | TRIM2 | ATGCA others(2308): Show |
chr4 | 153199443 | 153344317 | ||
| a0002c0006 | 0/0 | 2313 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | ATGCA others(2308): Show |
chr4 | 153199443 | 153344317 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 6755 | 67 | 8 | 20 | 27 | 2 | 9 | TRIM2_chr4_153199443_153344317 | TRIM2 | GGCAG others(6750): Show |
chr4 | 153199443 | 153344317 |
| a0001c0001t0002 | 0/0 | 6756 | 12 | 4 | 1 | 4 | 2 | 1 | TRIM2_chr4_153199443_153344317 | TRIM2 | GGCAG others(6751): Show |
chr4 | 153199443 | 153344317 |
| a0001c0001t0003 | 0/0 | 6757 | 8 | 1 | 3 | 3 | 0 | 1 | TRIM2_chr4_153199443_153344317 | TRIM2 | GGCAG others(6752): Show |
chr4 | 153199443 | 153344317 |
| a0001c0001t0004 | 0/0 | 6756 | 5 | 4 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | GGCAG others(6751): Show |
chr4 | 153199443 | 153344317 |
| a0001c0001t0005 | 0/0 | 6756 | 9 | 0 | 0 | 7 | 0 | 2 | TRIM2_chr4_153199443_153344317 | TRIM2 | GGCAG others(6751): Show |
chr4 | 153199443 | 153344317 |
| a0001c0001t0006 | 0/0 | 6759 | 9 | 8 | 1 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | GGCAG others(6754): Show |
chr4 | 153199443 | 153344317 |
| a0001c0001t0007 | 0/0 | 6758 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | GGCAG others(6753): Show |
chr4 | 153199443 | 153344317 |
| a0001c0001t0008 | 0/0 | 6757 | 7 | 0 | 0 | 7 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | GGCAG others(6752): Show |
chr4 | 153199443 | 153344317 |
| a0001c0001t0009 | 0/0 | 6758 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | GGCAG others(6753): Show |
chr4 | 153199443 | 153344317 |
| a0001c0001t0010 | 0/0 | 6758 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | GGCAG others(6753): Show |
chr4 | 153199443 | 153344317 |
| a0001c0001t0015 | 0/0 | 6754 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | GGCAG others(6749): Show |
chr4 | 153199443 | 153344317 |
| a0001c0001t0016 | 0/0 | 6756 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | GGCAG others(6751): Show |
chr4 | 153199443 | 153344317 |
| a0001c0001t0020 | 0/0 | 6755 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | GGCAG others(6750): Show |
chr4 | 153199443 | 153344317 |
| a0001c0001t0021 | 0/0 | 6756 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | GGCAG others(6751): Show |
chr4 | 153199443 | 153344317 |
| a0001c0001t0025 | 0/0 | 6757 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | GGCAG others(6752): Show |
chr4 | 153199443 | 153344317 |
| a0001c0001t0027 | 0/0 | 6760 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | GGCAG others(6755): Show |
chr4 | 153199443 | 153344317 |
| a0001c0001t0030 | 0/0 | 6755 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | GGCAG others(6750): Show |
chr4 | 153199443 | 153344317 |
| a0001c0001t0031 | 0/0 | 6755 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | GGCAG others(6750): Show |
chr4 | 153199443 | 153344317 |
| a0001c0001t0032 | 0/0 | 6755 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM2_chr4_153199443_153344317 | TRIM2 | GGCAG others(6750): Show |
chr4 | 153199443 | 153344317 |
| a0001c0002t0001 | 0/1 | 6755 | 13 | 0 | 3 | 3 | 2 | 4 | TRIM2_chr4_153199443_153344317 | TRIM2 | GGCAG others(6750): Show |
chr4 | 153199443 | 153344317 |
| a0001c0002t0002 | 0/0 | 6756 | 32 | 8 | 5 | 12 | 0 | 7 | TRIM2_chr4_153199443_153344317 | TRIM2 | GGCAG others(6751): Show |
chr4 | 153199443 | 153344317 |
| a0001c0002t0003 | 0/0 | 6757 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | GGCAG others(6752): Show |
chr4 | 153199443 | 153344317 |
| a0001c0002t0004 | 0/0 | 6756 | 8 | 5 | 1 | 0 | 0 | 2 | TRIM2_chr4_153199443_153344317 | TRIM2 | GGCAG others(6751): Show |
chr4 | 153199443 | 153344317 |
| a0001c0002t0005 | 0/0 | 6756 | 2 | 0 | 0 | 1 | 0 | 1 | TRIM2_chr4_153199443_153344317 | TRIM2 | GGCAG others(6751): Show |
chr4 | 153199443 | 153344317 |
| a0001c0002t0007 | 0/0 | 6758 | 2 | 1 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | GGCAG others(6753): Show |
chr4 | 153199443 | 153344317 |
| a0001c0002t0010 | 0/0 | 6758 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | GGCAG others(6753): Show |
chr4 | 153199443 | 153344317 |
| a0001c0002t0011 | 0/0 | 6759 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | GGCAG others(6754): Show |
chr4 | 153199443 | 153344317 |
| a0001c0002t0012 | 0/0 | 6755 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | GGCAG others(6750): Show |
chr4 | 153199443 | 153344317 |
| a0001c0002t0013 | 0/0 | 6759 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | GGCAG others(6754): Show |
chr4 | 153199443 | 153344317 |
| a0001c0002t0017 | 0/0 | 6758 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM2_chr4_153199443_153344317 | TRIM2 | GGCAG others(6753): Show |
chr4 | 153199443 | 153344317 |
| a0001c0002t0018 | 0/0 | 6757 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | GGCAG others(6752): Show |
chr4 | 153199443 | 153344317 |
| a0001c0002t0019 | 0/0 | 6755 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | GGCAG others(6750): Show |
chr4 | 153199443 | 153344317 |
| a0001c0002t0022 | 0/0 | 6755 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | GGCAG others(6750): Show |
chr4 | 153199443 | 153344317 |
| a0001c0002t0023 | 0/0 | 6756 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | GGCAG others(6751): Show |
chr4 | 153199443 | 153344317 |
| a0001c0002t0024 | 0/0 | 6759 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | GGCAG others(6754): Show |
chr4 | 153199443 | 153344317 |
| a0001c0002t0028 | 0/0 | 6757 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | GGCAG others(6752): Show |
chr4 | 153199443 | 153344317 |
| a0001c0002t0029 | 0/0 | 6761 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | GGCAG others(6756): Show |
chr4 | 153199443 | 153344317 |
| a0001c0002t0033 | 0/0 | 6757 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | GGCAG others(6752): Show |
chr4 | 153199443 | 153344317 |
| a0001c0003t0001 | 0/0 | 6755 | 5 | 4 | 1 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | GGCAG others(6750): Show |
chr4 | 153199443 | 153344317 |
| a0001c0003t0002 | 0/0 | 6756 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | GGCAG others(6751): Show |
chr4 | 153199443 | 153344317 |
| a0001c0003t0003 | 0/0 | 6757 | 27 | 9 | 8 | 6 | 2 | 2 | TRIM2_chr4_153199443_153344317 | TRIM2 | GGCAG others(6752): Show |
chr4 | 153199443 | 153344317 |
| a0001c0003t0004 | 0/0 | 6756 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | GGCAG others(6751): Show |
chr4 | 153199443 | 153344317 |
| a0001c0003t0007 | 0/0 | 6758 | 4 | 0 | 3 | 0 | 1 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | GGCAG others(6753): Show |
chr4 | 153199443 | 153344317 |
| a0001c0003t0010 | 0/0 | 6758 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | GGCAG others(6753): Show |
chr4 | 153199443 | 153344317 |
| a0001c0003t0013 | 0/0 | 6759 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | GGCAG others(6754): Show |
chr4 | 153199443 | 153344317 |
| a0001c0003t0014 | 0/0 | 6761 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | GGCAG others(6756): Show |
chr4 | 153199443 | 153344317 |
| a0001c0003t0026 | 0/0 | 6758 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM2_chr4_153199443_153344317 | TRIM2 | GGCAG others(6753): Show |
chr4 | 153199443 | 153344317 |
| a0001c0004t0001 | 0/0 | 6755 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | GGCAG others(6750): Show |
chr4 | 153199443 | 153344317 |
| a0001c0004t0003 | 0/0 | 6757 | 2 | 1 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | GGCAG others(6752): Show |
chr4 | 153199443 | 153344317 |
| a0001c0005t0003 | 0/0 | 6757 | 3 | 0 | 1 | 1 | 1 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | GGCAG others(6752): Show |
chr4 | 153199443 | 153344317 |
| a0001c0007t0003 | 0/0 | 6757 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | GGCAG others(6752): Show |
chr4 | 153199443 | 153344317 |
| a0001c0008t0002 | 0/0 | 6756 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | GGCAG others(6751): Show |
chr4 | 153199443 | 153344317 |
| a0001c0009t0003 | 0/0 | 6757 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | GGCAG others(6752): Show |
chr4 | 153199443 | 153344317 |
| a0001c0010t0004 | 0/0 | 6756 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM2_chr4_153199443_153344317 | TRIM2 | GGCAG others(6751): Show |
chr4 | 153199443 | 153344317 |
| a0002c0006t0003 | 0/0 | 6757 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | GGCAG others(6752): Show |
chr4 | 153199443 | 153344317 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0001g0238 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0002g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0002g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0003g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0003g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0004g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0004g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0004g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0004g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0004g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0005g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0005g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0005g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0005g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0005g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0005g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0005g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0005g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0005g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0006g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0006g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0006g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0006g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0006g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0006g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0006g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0006g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0006g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0007g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0008g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0008g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0008g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0008g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0008g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0008g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0008g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0009g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0009g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0009g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0010g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0015g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0015g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0016g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0016g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0020g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0021g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0025g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0027g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0030g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0031g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0001t0032g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0002t0001g0236 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0002t0002g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0002t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0002t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0002t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0002t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0002t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0002t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0002t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0002t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0002t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0002t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0002t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0002t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0002t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0002t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0002t0002g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0002t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0002t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0002t0003g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0002t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0002t0003g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0002t0004g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0002t0004g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0002t0004g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0002t0004g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0002t0004g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0002t0004g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0002t0004g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0002t0004g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0002t0005g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0002t0005g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0002t0007g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0002t0007g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0002t0010g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0002t0011g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0002t0011g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0002t0011g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0002t0012g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0002t0012g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0002t0012g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0002t0013g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0002t0017g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0002t0017g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0002t0018g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0002t0018g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0002t0019g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0002t0022g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0002t0023g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0002t0024g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0002t0028g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0002t0029g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0002t0033g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0003t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0003t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0003t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0003t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0003t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0003t0002g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0003t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0003t0003g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0003t0003g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0003t0003g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0003t0003g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0003t0003g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0003t0003g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0003t0003g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0003t0003g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0003t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0003t0003g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0003t0003g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0003t0003g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0003t0003g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0003t0003g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0003t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0003t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0003t0003g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0003t0003g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0003t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0003t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0003t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0003t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0003t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0003t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0003t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0003t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0003t0003g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0003t0004g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0003t0007g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0003t0007g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0003t0007g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0003t0007g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0003t0010g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0003t0013g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0003t0014g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0003t0014g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0003t0026g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0004t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0004t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0004t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0005t0003g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0005t0003g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0005t0003g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0007t0003g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0008t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0009t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0001c0010t0004g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0002c0006t0003g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| a0002c0006t0003g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0097 | EUR | GBR | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG00140 | hp2 | a0001 | c0002 | t0001 | g0167 | EUR | GBR | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG00280 | hp1 | a0001 | c0001 | t0031 | g0191 | EUR | FIN | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0241 | EUR | FIN | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG00323 | hp1 | a0001 | c0003 | t0003 | g0029 | EUR | FIN | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG00323 | hp2 | a0001 | c0002 | t0001 | g0116 | EUR | FIN | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG00438 | hp1 | a0001 | c0003 | t0003 | g0207 | EAS | CHS | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | CHS | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0173 | EAS | CHS | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | CHS | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | CHS | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG00558 | hp2 | a0001 | c0002 | t0002 | g0254 | EAS | CHS | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0175 | AMR | PUR | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG00735 | hp2 | a0001 | c0002 | t0002 | g0089 | AMR | PUR | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG00741 | hp1 | a0001 | c0003 | t0003 | g0057 | AMR | PUR | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG01069 | hp1 | a0001 | c0003 | t0003 | g0051 | AMR | PUR | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG01070 | hp1 | a0001 | c0002 | t0004 | g0069 | AMR | PUR | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG01074 | hp1 | a0001 | c0003 | t0003 | g0043 | AMR | PUR | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG01074 | hp2 | a0001 | c0003 | t0007 | g0223 | AMR | PUR | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG01081 | hp1 | a0001 | c0001 | t0015 | g0117 | AMR | PUR | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG01081 | hp2 | a0001 | c0002 | t0002 | g0215 | AMR | PUR | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG01106 | hp2 | a0001 | c0003 | t0007 | g0225 | AMR | PUR | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0066 | AMR | PUR | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG01109 | hp2 | a0001 | c0002 | t0002 | g0194 | AMR | PUR | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG01168 | hp1 | a0001 | c0002 | t0002 | g0171 | AMR | PUR | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0265 | AMR | PUR | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG01243 | hp2 | a0001 | c0001 | t0006 | g0146 | AMR | PUR | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0210 | AMR | CLM | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0221 | AMR | CLM | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG01261 | hp1 | a0001 | c0001 | t0015 | g0192 | AMR | CLM | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG01346 | hp1 | a0001 | c0003 | t0003 | g0026 | AMR | CLM | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG01346 | hp2 | a0001 | c0001 | t0020 | g0228 | AMR | CLM | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG01433 | hp1 | a0001 | c0003 | t0003 | g0028 | AMR | CLM | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG01433 | hp2 | a0001 | c0005 | t0003 | g0198 | AMR | CLM | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0232 | AMR | CLM | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | CLM | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0240 | EUR | IBS | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG01516 | hp2 | a0001 | c0005 | t0003 | g0169 | EUR | IBS | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG01517 | hp1 | a0001 | c0003 | t0003 | g0031 | EUR | IBS | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0235 | EUR | IBS | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG01884 | hp1 | a0001 | c0002 | t0004 | g0048 | AFR | ACB | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG01884 | hp2 | a0001 | c0003 | t0001 | g0003 | AFR | ACB | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG01891 | hp1 | a0001 | c0003 | t0013 | g0262 | AFR | ACB | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG01891 | hp2 | a0001 | c0001 | t0010 | g0078 | AFR | ACB | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PEL | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG01934 | hp2 | a0001 | c0003 | t0003 | g0071 | AMR | PEL | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG01975 | hp1 | a0001 | c0003 | t0003 | g0015 | AMR | PEL | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PEL | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PEL | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG01981 | hp2 | a0001 | c0003 | t0003 | g0025 | AMR | PEL | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PEL | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG01993 | hp2 | a0001 | c0003 | t0007 | g0106 | AMR | PEL | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG02004 | hp1 | a0001 | c0003 | t0001 | g0027 | AMR | PEL | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG02027 | hp1 | a0001 | c0002 | t0007 | g0155 | EAS | KHV | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG02027 | hp2 | a0001 | c0004 | t0001 | g0184 | EAS | KHV | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG02055 | hp1 | a0001 | c0003 | t0003 | g0074 | AFR | ACB | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0088 | AFR | ACB | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | KHV | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG02080 | hp2 | a0001 | c0002 | t0002 | g0246 | EAS | KHV | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG02129 | hp1 | a0001 | c0001 | t0016 | g0197 | EAS | KHV | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG02129 | hp2 | a0001 | c0009 | t0003 | g0159 | EAS | KHV | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG02145 | hp1 | a0001 | c0002 | t0022 | g0140 | AFR | ACB | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG02145 | hp2 | a0001 | c0003 | t0003 | g0073 | AFR | ACB | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG02257 | hp1 | a0001 | c0001 | t0025 | g0007 | AFR | ACB | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | ACB | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG02258 | hp1 | a0001 | c0002 | t0010 | g0134 | AFR | ACB | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG02258 | hp2 | a0001 | c0003 | t0003 | g0054 | AFR | ACB | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG02280 | hp1 | a0001 | c0002 | t0028 | g0080 | AFR | ACB | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG02280 | hp2 | a0001 | c0001 | t0009 | g0264 | AFR | ACB | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG02523 | hp1 | a0001 | c0002 | t0002 | g0181 | EAS | KHV | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | KHV | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG02572 | hp1 | a0001 | c0007 | t0003 | g0233 | AFR | GWD | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG02572 | hp2 | a0001 | c0001 | t0006 | g0123 | AFR | GWD | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0229 | SAS | PJL | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG02615 | hp1 | a0001 | c0001 | t0004 | g0129 | AFR | GWD | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG02615 | hp2 | a0001 | c0003 | t0010 | g0079 | AFR | GWD | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG02622 | hp1 | a0001 | c0002 | t0002 | g0137 | AFR | GWD | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG02683 | hp2 | a0001 | c0003 | t0026 | g0107 | SAS | PJL | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG02717 | hp1 | a0001 | c0002 | t0018 | g0135 | AFR | GWD | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0008 | AFR | GWD | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG02735 | hp2 | a0001 | c0010 | t0004 | g0085 | SAS | PJL | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0257 | SAS | PJL | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG02738 | hp2 | a0001 | c0002 | t0002 | g0050 | SAS | PJL | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG02809 | hp1 | a0001 | c0002 | t0013 | g0133 | AFR | GWD | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG02809 | hp2 | a0001 | c0003 | t0003 | g0075 | AFR | GWD | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG02818 | hp1 | a0001 | c0003 | t0014 | g0076 | AFR | GWD | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG02818 | hp2 | a0001 | c0002 | t0002 | g0138 | AFR | GWD | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG02886 | hp1 | a0001 | c0002 | t0002 | g0141 | AFR | GWD | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG02895 | hp1 | a0001 | c0001 | t0006 | g0160 | AFR | GWD | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | GWD | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG02896 | hp1 | a0001 | c0003 | t0002 | g0052 | AFR | GWD | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG02896 | hp2 | a0001 | c0002 | t0011 | g0005 | AFR | GWD | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | GWD | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG02897 | hp2 | a0001 | c0002 | t0011 | g0006 | AFR | GWD | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG02922 | hp1 | a0001 | c0002 | t0003 | g0148 | AFR | ESN | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG02922 | hp2 | a0001 | c0002 | t0029 | g0261 | AFR | ESN | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG02965 | hp1 | a0002 | c0006 | t0003 | g0013 | AFR | ESN | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG02965 | hp2 | a0001 | c0004 | t0003 | g0058 | AFR | ESN | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG02976 | hp1 | a0001 | c0003 | t0003 | g0064 | AFR | ESN | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG02976 | hp2 | a0001 | c0002 | t0004 | g0047 | AFR | ESN | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG03017 | hp1 | a0001 | c0002 | t0002 | g0176 | SAS | PJL | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG03017 | hp2 | a0001 | c0001 | t0005 | g0103 | SAS | PJL | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG03041 | hp1 | a0001 | c0003 | t0004 | g0142 | AFR | GWD | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG03041 | hp2 | a0001 | c0001 | t0009 | g0060 | AFR | GWD | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG03098 | hp1 | a0001 | c0003 | t0001 | g0041 | AFR | MSL | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG03098 | hp2 | a0001 | c0002 | t0033 | g0234 | AFR | MSL | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG03130 | hp1 | a0001 | c0001 | t0006 | g0061 | AFR | ESN | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG03130 | hp2 | a0001 | c0001 | t0006 | g0086 | AFR | ESN | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG03139 | hp1 | a0001 | c0001 | t0006 | g0019 | AFR | ESN | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG03139 | hp2 | a0001 | c0003 | t0003 | g0053 | AFR | ESN | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG03209 | hp1 | a0001 | c0001 | t0009 | g0263 | AFR | MSL | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG03209 | hp2 | a0001 | c0001 | t0006 | g0143 | AFR | MSL | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG03225 | hp1 | a0001 | c0001 | t0007 | g0122 | AFR | MSL | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG03225 | hp2 | a0001 | c0002 | t0003 | g0144 | AFR | MSL | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG03239 | hp1 | a0001 | c0002 | t0002 | g0212 | SAS | PJL | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0249 | SAS | PJL | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG03453 | hp1 | a0001 | c0002 | t0002 | g0139 | AFR | MSL | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG03453 | hp2 | a0001 | c0001 | t0006 | g0147 | AFR | MSL | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0016 | AFR | MSL | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG03486 | hp2 | a0001 | c0003 | t0001 | g0132 | AFR | MSL | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG03491 | hp1 | a0001 | c0002 | t0002 | g0090 | SAS | PJL | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG03491 | hp2 | a0001 | c0002 | t0017 | g0095 | SAS | PJL | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG03492 | hp1 | a0001 | c0002 | t0002 | g0024 | SAS | PJL | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG03492 | hp2 | a0001 | c0002 | t0017 | g0096 | SAS | PJL | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG03516 | hp1 | a0001 | c0002 | t0003 | g0239 | AFR | ESN | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0087 | AFR | ESN | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG03540 | hp1 | a0001 | c0001 | t0006 | g0149 | AFR | GWD | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG03540 | hp2 | a0001 | c0003 | t0002 | g0004 | AFR | GWD | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG03654 | hp1 | a0001 | c0002 | t0005 | g0251 | SAS | PJL | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG03654 | hp2 | a0001 | c0002 | t0001 | g0220 | SAS | PJL | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG03688 | hp1 | a0001 | c0003 | t0003 | g0030 | SAS | STU | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0153 | SAS | STU | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG03704 | hp1 | a0001 | c0003 | t0003 | g0230 | SAS | PJL | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0253 | SAS | PJL | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG03831 | hp1 | a0001 | c0002 | t0002 | g0145 | SAS | BEB | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0036 | SAS | BEB | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG03834 | hp1 | a0001 | c0001 | t0032 | g0243 | SAS | BEB | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG03834 | hp2 | a0001 | c0002 | t0004 | g0010 | SAS | BEB | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0255 | SAS | BEB | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0126 | SAS | BEB | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG04115 | hp1 | a0001 | c0002 | t0002 | g0152 | SAS | STU | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0187 | SAS | STU | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG04228 | hp1 | a0001 | c0002 | t0004 | g0172 | SAS | STU | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | STU | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA18522 | hp1 | a0001 | c0002 | t0011 | g0070 | AFR | YRI | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA18522 | hp2 | a0001 | c0002 | t0002 | g0268 | AFR | YRI | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | CHB | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0105 | EAS | CHB | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA18906 | hp1 | a0001 | c0008 | t0002 | g0059 | AFR | YRI | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA18906 | hp2 | a0001 | c0002 | t0004 | g0083 | AFR | YRI | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA18939 | hp1 | a0001 | c0002 | t0002 | g0124 | EAS | JPT | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA18942 | hp1 | a0001 | c0001 | t0005 | g0110 | EAS | JPT | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA18942 | hp2 | a0001 | c0002 | t0002 | g0248 | EAS | JPT | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA18943 | hp2 | a0001 | c0001 | t0030 | g0217 | EAS | JPT | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA18944 | hp1 | a0001 | c0001 | t0008 | g0168 | EAS | JPT | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA18944 | hp2 | a0001 | c0005 | t0003 | g0021 | EAS | JPT | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA18948 | hp2 | a0001 | c0002 | t0012 | g0178 | EAS | JPT | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0150 | EAS | JPT | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA18951 | hp2 | a0001 | c0002 | t0002 | g0114 | EAS | JPT | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA18954 | hp1 | a0001 | c0002 | t0002 | g0109 | EAS | JPT | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA18954 | hp2 | a0001 | c0001 | t0004 | g0104 | EAS | JPT | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA18959 | hp1 | a0001 | c0002 | t0002 | g0250 | EAS | JPT | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA18966 | hp1 | a0001 | c0002 | t0002 | g0108 | EAS | JPT | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA18966 | hp2 | a0001 | c0004 | t0003 | g0119 | EAS | JPT | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA18968 | hp1 | a0001 | c0001 | t0005 | g0161 | EAS | JPT | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA18970 | hp1 | a0001 | c0002 | t0005 | g0154 | EAS | JPT | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA18970 | hp2 | a0001 | c0003 | t0003 | g0208 | EAS | JPT | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA18971 | hp1 | a0001 | c0001 | t0005 | g0252 | EAS | JPT | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA18979 | hp2 | a0001 | c0001 | t0008 | g0034 | EAS | JPT | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA18985 | hp1 | a0001 | c0001 | t0008 | g0049 | EAS | JPT | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA18985 | hp2 | a0001 | c0002 | t0019 | g0180 | EAS | JPT | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA18988 | hp1 | a0001 | c0003 | t0003 | g0165 | EAS | JPT | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA18988 | hp2 | a0001 | c0001 | t0008 | g0038 | EAS | JPT | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA18998 | hp1 | a0001 | c0002 | t0001 | g0127 | EAS | JPT | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA18998 | hp2 | a0001 | c0003 | t0003 | g0216 | EAS | JPT | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA19002 | hp1 | a0001 | c0003 | t0003 | g0185 | EAS | JPT | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA19006 | hp1 | a0001 | c0001 | t0005 | g0214 | EAS | JPT | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA19007 | hp2 | a0001 | c0001 | t0005 | g0037 | EAS | JPT | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA19011 | hp1 | a0001 | c0002 | t0012 | g0177 | EAS | JPT | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA19030 | hp1 | a0002 | c0006 | t0003 | g0012 | AFR | LWK | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA19030 | hp2 | a0001 | c0003 | t0014 | g0077 | AFR | LWK | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA19043 | hp1 | a0001 | c0002 | t0004 | g0045 | AFR | LWK | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | LWK | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA19063 | hp2 | a0001 | c0002 | t0012 | g0163 | EAS | JPT | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA19065 | hp1 | a0001 | c0001 | t0003 | g0035 | EAS | JPT | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA19065 | hp2 | a0001 | c0001 | t0005 | g0244 | EAS | JPT | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA19068 | hp1 | a0001 | c0001 | t0008 | g0020 | EAS | JPT | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA19070 | hp1 | a0001 | c0002 | t0002 | g0259 | EAS | JPT | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA19078 | hp2 | a0001 | c0001 | t0016 | g0231 | EAS | JPT | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA19082 | hp1 | a0001 | c0002 | t0002 | g0256 | EAS | JPT | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA19082 | hp2 | a0001 | c0003 | t0003 | g0067 | EAS | JPT | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA19084 | hp1 | a0001 | c0001 | t0005 | g0094 | EAS | JPT | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA19084 | hp2 | a0001 | c0001 | t0003 | g0209 | EAS | JPT | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA19085 | hp1 | a0001 | c0002 | t0002 | g0166 | EAS | JPT | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA19085 | hp2 | a0001 | c0001 | t0008 | g0044 | EAS | JPT | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA19088 | hp1 | a0001 | c0001 | t0008 | g0032 | EAS | JPT | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA19090 | hp1 | a0001 | c0001 | t0021 | g0111 | EAS | JPT | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA19240 | hp1 | a0001 | c0003 | t0003 | g0042 | AFR | YRI | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA19240 | hp2 | a0001 | c0002 | t0002 | g0136 | AFR | YRI | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA20129 | hp1 | a0001 | c0003 | t0003 | g0082 | AFR | ASW | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | ASW | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA20752 | hp1 | a0001 | c0001 | t0027 | g0068 | EUR | TSI | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA20752 | hp2 | a0001 | c0003 | t0007 | g0224 | EUR | TSI | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA20905 | hp1 | a0001 | c0001 | t0005 | g0242 | SAS | GIH | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0226 | SAS | GIH | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG01123 | hp1 | a0001 | c0002 | t0002 | g0260 | AMR | CLM | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0115 | AMR | CLM | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG02109 | hp1 | a0001 | c0002 | t0002 | g0267 | AFR | ACB | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG02109 | hp2 | a0001 | c0003 | t0003 | g0011 | AFR | ACB | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG02486 | hp1 | a0001 | c0002 | t0002 | g0130 | AFR | ACB | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG02486 | hp2 | a0001 | c0003 | t0001 | g0131 | AFR | ACB | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG02559 | hp1 | a0001 | c0002 | t0024 | g0128 | AFR | ACB | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | ACB | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | MSL | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG03471 | hp2 | a0001 | c0002 | t0004 | g0046 | AFR | MSL | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | USA | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| HG06807 | hp2 | a0001 | c0002 | t0023 | g0014 | AFR | USA | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | USA | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA20300 | hp2 | a0001 | c0002 | t0018 | g0009 | AFR | USA | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA21309 | hp1 | a0001 | c0002 | t0007 | g0266 | AFR | LWK | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | LWK | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0236 | REF | REF | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0238 | REF | REF | TRIM2_chr4_153199443_153344317 | TRIM2 | chr4 | 153199443 | 153344317 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:153334865 | C | T | 1 | a0002 | 2 | HG02965.hp1 NA19030.hp1 |
missense_variant | MODERATE | c.2215C>T | p.Pro739Ser | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 12/12 | 2303/6755 | 2215/2316 | 739/771 | chr4 | 153334865 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:153275968 | C | T | 1 | a0001c0010 | 1 | HG02735.hp2 | synonymous_variant | LOW | c.291C>T | p.Pro97Pro | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/12 | 379/6755 | 291/2316 | 97/771 | chr4 | 153275968 | |||
| chr4:153276082 | T | G | 4 | a0001c0003 a0001c0004 a0001c0007 others(1): Show |
50 | HG00323.hp1 HG00438.hp1 HG00741.hp1 others(47): Show |
synonymous_variant | LOW | c.405T>G | p.Thr135Thr | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/12 | 493/6755 | 405/2316 | 135/771 | chr4 | 153276082 | |||
| chr4:153295396 | C | T | 1 | a0001c0005 | 3 | HG01433.hp2 HG01516.hp2 NA18944.hp2 |
synonymous_variant | LOW | c.870C>T | p.Asn290Asn | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/12 | 958/6755 | 870/2316 | 290/771 | chr4 | 153295396 | |||
| chr4:153295543 | C | T | 1 | a0001c0009 | 1 | HG02129.hp2 | synonymous_variant | LOW | c.1017C>T | p.Ile339Ile | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/12 | 1105/6755 | 1017/2316 | 339/771 | chr4 | 153295543 | |||
| chr4:153295558 | G | A | 6 | a0001c0002 a0001c0003 a0001c0007 others(3): Show |
127 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(124): Show |
synonymous_variant | LOW | c.1032G>A | p.Thr344Thr | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/12 | 1120/6755 | 1032/2316 | 344/771 | chr4 | 153295558 | |||
| chr4:153295603 | C | T | 1 | a0001c0008 | 1 | NA18906.hp1 | synonymous_variant | LOW | c.1077C>T | p.Gly359Gly | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/12 | 1165/6755 | 1077/2316 | 359/771 | chr4 | 153295603 | |||
| chr4:153334882 | A | G | 1 | a0001c0007 | 1 | HG02572.hp1 | synonymous_variant | LOW | c.2232A>G | p.Gln744Gln | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 12/12 | 2320/6755 | 2232/2316 | 744/771 | chr4 | 153334882 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:153204497 | T | A | 1 | a0001c0002t0019 | 1 | NA18985.hp2 | 5_prime_UTR_variant | MODIFIER | c.-34T>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/12 | 34 | chr4 | 153204497 | ||||||
| chr4:153335099 | T | C | 1 | a0001c0001t0020 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*133T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 12/12 | 133 | chr4 | 153335099 | ||||||
| chr4:153335187 | A | G | 2 | a0001c0002t0018 a0001c0002t0033 |
3 | HG02717.hp1 HG03098.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*221A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 12/12 | 221 | chr4 | 153335187 | ||||||
| chr4:153335271 | T | TA | 38 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(35): Show |
153 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(150): Show |
3_prime_UTR_variant | MODIFIER | c.*311dupA | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 12/12 | 312 | INFO_REALIGN_3_PRIME | chr4 | 153335271 | |||||
| chr4:153335342 | C | T | 6 | a0001c0001t0010 a0001c0002t0010 a0001c0002t0011 others(3): Show |
9 | HG01891.hp2 HG02258.hp1 HG02615.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*376C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 12/12 | 376 | chr4 | 153335342 | ||||||
| chr4:153335743 | C | T | 15 | a0001c0001t0003 a0001c0001t0008 a0001c0001t0009 others(12): Show |
63 | HG00323.hp1 HG00438.hp1 HG00642.hp1 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*777C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 12/12 | 777 | chr4 | 153335743 | ||||||
| chr4:153335799 | G | A | 1 | a0001c0001t0030 | 1 | NA18943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*833G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 12/12 | 833 | chr4 | 153335799 | ||||||
| chr4:153336116 | T | TTA | 23 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0006 others(20): Show |
88 | HG00323.hp1 HG00438.hp1 HG00642.hp1 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*1167_*1168dupTA | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 12/12 | 1169 | INFO_REALIGN_3_PRIME | chr4 | 153336116 | |||||
| chr4:153336116 | T | TTATA | 9 | a0001c0001t0010 a0001c0001t0027 a0001c0002t0010 others(6): Show |
12 | HG01891.hp1 HG01891.hp2 HG02258.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1165_*1168dupTATA | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 12/12 | 1169 | INFO_REALIGN_3_PRIME | chr4 | 153336116 | |||||
| chr4:153336116 | T | TTATATA | 1 | a0001c0003t0014 | 2 | HG02818.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1163_*1168dupTATA others(2): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 12/12 | 1169 | INFO_REALIGN_3_PRIME | chr4 | 153336116 | |||||
| chr4:153336133 | T | C | 1 | a0001c0001t0031 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1167T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 12/12 | 1167 | chr4 | 153336133 | ||||||
| chr4:153336133 | T | TAC | 1 | a0001c0001t0008 | 7 | NA18944.hp1 NA18979.hp2 NA18985.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1177_*1178dupCA | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 12/12 | 1179 | INFO_REALIGN_3_PRIME | chr4 | 153336133 | |||||
| chr4:153336135 | C | T | 1 | a0001c0002t0012 | 3 | NA18948.hp2 NA19011.hp1 NA19063.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1169C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 12/12 | 1169 | chr4 | 153336135 | ||||||
| chr4:153336347 | CA | C | 37 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(34): Show |
152 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(149): Show |
3_prime_UTR_variant | MODIFIER | c.*1392delA | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 12/12 | 1392 | INFO_REALIGN_3_PRIME | chr4 | 153336347 | |||||
| chr4:153336358 | A | C | 6 | a0001c0001t0004 a0001c0002t0004 a0001c0002t0017 others(3): Show |
18 | HG01070.hp1 HG01884.hp1 HG02055.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1392A>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 12/12 | 1392 | chr4 | 153336358 | ||||||
| chr4:153336359 | C | A | 6 | a0001c0001t0004 a0001c0002t0004 a0001c0002t0017 others(3): Show |
18 | HG01070.hp1 HG01884.hp1 HG02055.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1393C>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 12/12 | 1393 | chr4 | 153336359 | ||||||
| chr4:153336369 | A | C | 2 | a0001c0002t0013 a0001c0003t0013 |
2 | HG01891.hp1 HG02809.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1403A>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 12/12 | 1403 | chr4 | 153336369 | ||||||
| chr4:153336784 | A | C | 1 | a0001c0002t0033 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1818A>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 12/12 | 1818 | chr4 | 153336784 | ||||||
| chr4:153336972 | A | G | 2 | a0001c0001t0005 a0001c0002t0005 |
11 | HG03017.hp2 HG03654.hp1 NA18942.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2006A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 12/12 | 2006 | chr4 | 153336972 | ||||||
| chr4:153336978 | A | T | 1 | a0001c0002t0023 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2012A>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 12/12 | 2012 | chr4 | 153336978 | ||||||
| chr4:153337102 | G | A | 2 | a0001c0002t0018 a0001c0002t0033 |
3 | HG02717.hp1 HG03098.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2136G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 12/12 | 2136 | chr4 | 153337102 | ||||||
| chr4:153337483 | A | C | 1 | a0001c0003t0026 | 1 | HG02683.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2517A>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 12/12 | 2517 | chr4 | 153337483 | ||||||
| chr4:153337493 | C | G | 18 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 others(15): Show |
82 | HG00558.hp2 HG00735.hp2 HG01074.hp2 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*2527C>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 12/12 | 2527 | chr4 | 153337493 | ||||||
| chr4:153337571 | T | C | 1 | a0001c0001t0027 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2605T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 12/12 | 2605 | chr4 | 153337571 | ||||||
| chr4:153337878 | C | T | 1 | a0001c0001t0032 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2912C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 12/12 | 2912 | chr4 | 153337878 | ||||||
| chr4:153337891 | A | G | 1 | a0001c0002t0028 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2925A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 12/12 | 2925 | chr4 | 153337891 | ||||||
| chr4:153337944 | G | C | 2 | a0001c0001t0005 a0001c0002t0005 |
11 | HG03017.hp2 HG03654.hp1 NA18942.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2978G>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 12/12 | 2978 | chr4 | 153337944 | ||||||
| chr4:153337985 | T | C | 5 | a0001c0001t0004 a0001c0002t0004 a0001c0002t0017 others(2): Show |
17 | HG01070.hp1 HG01884.hp1 HG02055.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*3019T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 12/12 | 3019 | chr4 | 153337985 | ||||||
| chr4:153338051 | C | T | 4 | a0001c0001t0006 a0001c0001t0025 a0001c0002t0023 others(1): Show |
12 | HG01243.hp2 HG02257.hp1 HG02572.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3085C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 12/12 | 3085 | chr4 | 153338051 | ||||||
| chr4:153338224 | G | A | 1 | a0001c0001t0021 | 1 | NA19090.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3258G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 12/12 | 3258 | chr4 | 153338224 | ||||||
| chr4:153338337 | A | C | 5 | a0001c0001t0010 a0001c0002t0010 a0001c0002t0011 others(2): Show |
8 | HG01891.hp2 HG02258.hp1 HG02615.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3371A>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 12/12 | 3371 | chr4 | 153338337 | ||||||
| chr4:153338426 | T | C | 1 | a0001c0002t0023 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3460T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 12/12 | 3460 | chr4 | 153338426 | ||||||
| chr4:153338952 | G | GTT | 2 | a0001c0001t0006 a0001c0002t0029 |
10 | HG01243.hp2 HG02572.hp2 HG02895.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3986_*3987insTT | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 12/12 | 3987 | chr4 | 153338952 | ||||||
| chr4:153338953 | G | GT | 16 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0007 others(13): Show |
75 | HG00558.hp2 HG00735.hp2 HG01074.hp2 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*3999dupT | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 12/12 | 4000 | INFO_REALIGN_3_PRIME | chr4 | 153338953 | |||||
| chr4:153338953 | G | T | 3 | a0001c0001t0006 a0001c0001t0025 a0001c0002t0029 |
11 | HG01243.hp2 HG02257.hp1 HG02572.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3987G>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 12/12 | 3987 | chr4 | 153338953 | ||||||
| chr4:153338953 | GT | G | 9 | a0001c0001t0004 a0001c0001t0010 a0001c0001t0015 others(6): Show |
22 | HG01070.hp1 HG01081.hp1 HG01261.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*3999delT | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 12/12 | 3999 | INFO_REALIGN_3_PRIME | chr4 | 153338953 | |||||
| chr4:153339175 | C | T | 4 | a0001c0001t0010 a0001c0002t0010 a0001c0002t0011 others(1): Show |
6 | HG01891.hp2 HG02258.hp1 HG02615.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4209C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 12/12 | 4209 | chr4 | 153339175 | ||||||
| chr4:153339239 | A | T | 4 | a0001c0001t0010 a0001c0002t0010 a0001c0002t0011 others(1): Show |
6 | HG01891.hp2 HG02258.hp1 HG02615.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4273A>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 12/12 | 4273 | chr4 | 153339239 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:153204745 | A | G | 3 | a0001c0002t0002g0267 a0001c0002t0002g0268 a0001c0002t0007g0266 |
3 | HG02109.hp1 NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.30+185A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153204745 | |||||||
| chr4:153204781 | A | T | 1 | a0001c0001t0003g0265 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.30+221A>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153204781 | |||||||
| chr4:153204846 | T | C | 66 | a0001c0001t0001g0017 a0001c0001t0001g0023 a0001c0001t0001g0033 others(63): Show |
66 | HG00323.hp1 HG00438.hp2 HG00741.hp1 others(63): Show |
intron_variant | MODIFIER | c.30+286T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153204846 | |||||||
| chr4:153204907 | G | A | 1 | a0001c0001t0002g0001 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.30+347G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153204907 | |||||||
| chr4:153205408 | C | G | 3 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0006g0061 |
3 | HG03130.hp1 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.30+848C>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153205408 | |||||||
| chr4:153205534 | C | T | 4 | a0001c0001t0009g0263 a0001c0001t0009g0264 a0001c0002t0029g0261 others(1): Show |
4 | HG01891.hp1 HG02280.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.30+974C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153205534 | |||||||
| chr4:153205642 | T | C | 64 | a0001c0001t0001g0072 a0001c0001t0001g0081 a0001c0001t0001g0084 others(61): Show |
64 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.30+1082T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153205642 | |||||||
| chr4:153205783 | G | A | 1 | a0001c0002t0001g0127 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.30+1223G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153205783 | |||||||
| chr4:153205910 | T | A | 22 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0004g0129 others(19): Show |
22 | HG01884.hp2 HG02145.hp1 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.30+1350T>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153205910 | |||||||
| chr4:153205921 | A | G | 22 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0004g0129 others(19): Show |
22 | HG01884.hp2 HG02145.hp1 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.30+1361A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153205921 | |||||||
| chr4:153205995 | T | G | 22 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0004g0129 others(19): Show |
22 | HG01884.hp2 HG02145.hp1 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.30+1435T>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153205995 | |||||||
| chr4:153206007 | C | T | 10 | a0001c0001t0001g0253 a0001c0001t0001g0255 a0001c0001t0001g0257 others(7): Show |
10 | HG00558.hp2 HG01123.hp1 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.30+1447C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153206007 | |||||||
| chr4:153206012 | G | A | 55 | a0001c0001t0001g0017 a0001c0001t0001g0023 a0001c0001t0001g0033 others(52): Show |
55 | HG00323.hp1 HG00438.hp2 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.30+1452G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153206012 | |||||||
| chr4:153206190 | A | G | 1 | a0001c0003t0003g0057 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.30+1630A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153206190 | |||||||
| chr4:153206405 | G | A | 1 | a0001c0002t0003g0144 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.30+1845G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153206405 | |||||||
| chr4:153206503 | G | A | 1 | a0001c0002t0002g0145 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.30+1943G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153206503 | |||||||
| chr4:153206702 | G | T | 1 | a0001c0002t0002g0250 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.30+2142G>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153206702 | |||||||
| chr4:153206787 | C | T | 1 | a0001c0002t0001g0126 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.30+2227C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153206787 | |||||||
| chr4:153206917 | G | A | 99 | a0001c0001t0001g0151 a0001c0001t0001g0156 a0001c0001t0001g0157 others(96): Show |
99 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.30+2357G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153206917 | |||||||
| chr4:153206941 | C | T | 93 | a0001c0001t0001g0125 a0001c0001t0001g0151 a0001c0001t0001g0156 others(90): Show |
93 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.30+2381C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153206941 | |||||||
| chr4:153207119 | T | C | 31 | a0001c0001t0001g0151 a0001c0001t0001g0156 a0001c0001t0001g0157 others(28): Show |
31 | HG00544.hp2 HG00558.hp2 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.30+2559T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153207119 | |||||||
| chr4:153207208 | T | C | 2 | a0001c0001t0002g0002 a0001c0002t0024g0128 |
2 | HG02559.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.30+2648T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153207208 | |||||||
| chr4:153207272 | G | A | 8 | a0001c0001t0009g0060 a0001c0001t0009g0263 a0001c0001t0009g0264 others(5): Show |
8 | HG01891.hp1 HG02280.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.30+2712G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153207272 | |||||||
| chr4:153207276 | A | C | 1 | a0001c0002t0002g0259 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.30+2716A>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153207276 | |||||||
| chr4:153207305 | C | T | 1 | a0001c0002t0004g0069 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.30+2745C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153207305 | |||||||
| chr4:153207335 | G | A | 58 | a0001c0001t0001g0017 a0001c0001t0001g0023 a0001c0001t0001g0033 others(55): Show |
58 | HG00323.hp1 HG00438.hp2 HG00741.hp1 others(55): Show |
intron_variant | MODIFIER | c.30+2775G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153207335 | |||||||
| chr4:153207487 | T | C | 61 | a0001c0001t0001g0017 a0001c0001t0001g0023 a0001c0001t0001g0033 others(58): Show |
61 | HG00323.hp1 HG00438.hp2 HG00741.hp1 others(58): Show |
intron_variant | MODIFIER | c.30+2927T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153207487 | |||||||
| chr4:153207613 | G | A | 3 | a0001c0002t0011g0005 a0001c0002t0011g0006 a0001c0002t0011g0070 |
3 | HG02896.hp2 HG02897.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.30+3053G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153207613 | |||||||
| chr4:153207796 | G | T | 88 | a0001c0001t0001g0125 a0001c0001t0001g0162 a0001c0001t0001g0164 others(85): Show |
88 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.30+3236G>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153207796 | |||||||
| chr4:153208117 | T | G | 153 | a0001c0001t0001g0055 a0001c0001t0001g0062 a0001c0001t0001g0063 others(150): Show |
153 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.30+3557T>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153208117 | |||||||
| chr4:153208203 | C | T | 19 | a0001c0001t0001g0055 a0001c0001t0001g0062 a0001c0001t0001g0063 others(16): Show |
19 | HG01169.hp1 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.30+3643C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153208203 | |||||||
| chr4:153208546 | A | C | 6 | a0001c0001t0006g0146 a0001c0001t0006g0147 a0001c0001t0006g0149 others(3): Show |
6 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.30+3986A>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153208546 | |||||||
| chr4:153208635 | T | G | 5 | a0001c0002t0002g0267 a0001c0002t0002g0268 a0001c0002t0007g0266 others(2): Show |
5 | HG02109.hp1 HG02896.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.30+4075T>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153208635 | |||||||
| chr4:153208787 | T | C | 152 | a0001c0001t0001g0055 a0001c0001t0001g0062 a0001c0001t0001g0063 others(149): Show |
152 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.30+4227T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153208787 | |||||||
| chr4:153208922 | G | A | 29 | a0001c0001t0001g0151 a0001c0001t0001g0156 a0001c0001t0001g0157 others(26): Show |
29 | HG00544.hp2 HG00558.hp2 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.30+4362G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153208922 | |||||||
| chr4:153208966 | C | T | 1 | a0001c0002t0024g0128 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.30+4406C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153208966 | |||||||
| chr4:153209054 | C | A | 1 | a0001c0001t0002g0002 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.30+4494C>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153209054 | |||||||
| chr4:153209116 | C | G | 1 | a0001c0003t0007g0223 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.30+4556C>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153209116 | |||||||
| chr4:153209133 | G | T | 2 | a0001c0001t0002g0001 a0001c0003t0002g0004 |
2 | HG03540.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.30+4573G>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153209133 | |||||||
| chr4:153209287 | A | G | 61 | a0001c0001t0001g0017 a0001c0001t0001g0023 a0001c0001t0001g0033 others(58): Show |
61 | HG00323.hp1 HG00438.hp2 HG00741.hp1 others(58): Show |
intron_variant | MODIFIER | c.30+4727A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153209287 | |||||||
| chr4:153209302 | C | A | 1 | a0001c0002t0024g0128 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.30+4742C>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153209302 | |||||||
| chr4:153209394 | G | A | 4 | a0001c0002t0002g0267 a0001c0002t0002g0268 a0001c0002t0007g0266 others(1): Show |
4 | HG02109.hp1 HG03098.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.30+4834G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153209394 | |||||||
| chr4:153209690 | T | G | 1 | a0001c0002t0033g0234 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.30+5130T>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153209690 | |||||||
| chr4:153209702 | C | T | 88 | a0001c0001t0001g0125 a0001c0001t0001g0162 a0001c0001t0001g0164 others(85): Show |
88 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.30+5142C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153209702 | |||||||
| chr4:153209773 | C | A | 1 | a0001c0002t0004g0083 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.30+5213C>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153209773 | |||||||
| chr4:153209798 | G | A | 2 | a0001c0001t0002g0001 a0001c0003t0002g0004 |
2 | HG03540.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.30+5238G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153209798 | |||||||
| chr4:153209908 | G | A | 2 | a0001c0001t0001g0017 a0001c0001t0003g0016 |
2 | HG02622.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.30+5348G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153209908 | |||||||
| chr4:153209979 | C | G | 8 | a0001c0001t0002g0002 a0001c0001t0006g0146 a0001c0001t0006g0147 others(5): Show |
8 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.30+5419C>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153209979 | |||||||
| chr4:153210058 | A | AT | 13 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0222 others(10): Show |
13 | HG00741.hp1 HG00741.hp2 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.30+5522dupT | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153210058 | ||||||
| chr4:153210058 | AT | A | 40 | a0001c0001t0001g0017 a0001c0001t0001g0062 a0001c0001t0001g0081 others(37): Show |
40 | HG01070.hp2 HG01169.hp1 HG01346.hp2 others(37): Show |
intron_variant | MODIFIER | c.30+5522delT | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153210058 | ||||||
| chr4:153210058 | ATTT | A | 6 | a0001c0001t0006g0146 a0001c0001t0006g0147 a0001c0001t0006g0149 others(3): Show |
6 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.30+5520_30+5522del others(3): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153210058 | ||||||
| chr4:153210280 | G | A | 19 | a0001c0001t0001g0055 a0001c0001t0001g0062 a0001c0001t0001g0063 others(16): Show |
19 | HG01169.hp1 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.30+5720G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153210280 | |||||||
| chr4:153210340 | C | T | 6 | a0001c0002t0002g0130 a0001c0002t0002g0136 a0001c0002t0002g0137 others(3): Show |
6 | HG02145.hp1 HG02486.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.30+5780C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153210340 | |||||||
| chr4:153210363 | G | C | 220 | a0001c0001t0001g0017 a0001c0001t0001g0023 a0001c0001t0001g0033 others(217): Show |
220 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.30+5803G>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153210363 | |||||||
| chr4:153210425 | G | A | 1 | a0001c0002t0002g0136 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.30+5865G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153210425 | |||||||
| chr4:153210516 | A | G | 1 | a0001c0004t0003g0119 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.30+5956A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153210516 | |||||||
| chr4:153210562 | G | A | 91 | a0001c0001t0001g0125 a0001c0001t0001g0162 a0001c0001t0001g0164 others(88): Show |
91 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.30+6002G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153210562 | |||||||
| chr4:153210565 | A | C | 1 | a0001c0001t0002g0002 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.30+6005A>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153210565 | |||||||
| chr4:153210585 | G | A | 4 | a0001c0002t0002g0267 a0001c0002t0002g0268 a0001c0002t0007g0266 others(1): Show |
4 | HG02109.hp1 HG03098.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.30+6025G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153210585 | |||||||
| chr4:153210706 | C | T | 23 | a0001c0001t0001g0151 a0001c0001t0001g0156 a0001c0001t0001g0157 others(20): Show |
23 | HG00544.hp2 HG00558.hp2 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.30+6146C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153210706 | |||||||
| chr4:153210867 | G | A | 1 | a0001c0001t0008g0020 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.30+6307G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153210867 | |||||||
| chr4:153210889 | G | A | 8 | a0001c0001t0002g0002 a0001c0001t0006g0146 a0001c0001t0006g0147 others(5): Show |
8 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.30+6329G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153210889 | |||||||
| chr4:153210920 | T | C | 2 | a0001c0001t0002g0002 a0001c0002t0024g0128 |
2 | HG02559.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.30+6360T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153210920 | |||||||
| chr4:153211044 | C | T | 2 | a0001c0001t0002g0002 a0001c0002t0024g0128 |
2 | HG02559.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.30+6484C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153211044 | |||||||
| chr4:153211096 | T | C | 91 | a0001c0001t0001g0125 a0001c0001t0001g0162 a0001c0001t0001g0164 others(88): Show |
91 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.30+6536T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153211096 | |||||||
| chr4:153211141 | C | T | 27 | a0001c0001t0001g0055 a0001c0001t0001g0062 a0001c0001t0001g0063 others(24): Show |
27 | HG01169.hp1 HG01891.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.30+6581C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153211141 | |||||||
| chr4:153211145 | G | A | 6 | a0001c0001t0006g0146 a0001c0001t0006g0147 a0001c0001t0006g0149 others(3): Show |
6 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.30+6585G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153211145 | |||||||
| chr4:153211175 | G | A | 1 | a0001c0001t0032g0243 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.30+6615G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153211175 | |||||||
| chr4:153211365 | G | A | 19 | a0001c0001t0001g0055 a0001c0001t0001g0062 a0001c0001t0001g0063 others(16): Show |
19 | HG01169.hp1 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.30+6805G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153211365 | |||||||
| chr4:153211488 | C | CT | 86 | a0001c0001t0001g0017 a0001c0001t0001g0023 a0001c0001t0001g0033 others(83): Show |
86 | HG00323.hp1 HG00438.hp2 HG00741.hp1 others(83): Show |
intron_variant | MODIFIER | c.30+6945dupT | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153211488 | ||||||
| chr4:153211488 | C | CTT | 5 | a0001c0001t0006g0143 a0001c0001t0008g0049 a0001c0002t0002g0050 others(2): Show |
5 | HG01069.hp1 HG02145.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.30+6944_30+6945dup others(2): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153211488 | ||||||
| chr4:153211488 | CTTT | C | 6 | a0001c0001t0006g0146 a0001c0001t0006g0147 a0001c0001t0006g0149 others(3): Show |
6 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.30+6943_30+6945del others(3): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153211488 | ||||||
| chr4:153211494 | T | C | 91 | a0001c0001t0001g0125 a0001c0001t0001g0162 a0001c0001t0001g0164 others(88): Show |
91 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.30+6934T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153211494 | |||||||
| chr4:153211546 | G | C | 54 | a0001c0001t0001g0017 a0001c0001t0001g0023 a0001c0001t0001g0033 others(51): Show |
54 | HG00323.hp1 HG00438.hp2 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.30+6986G>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153211546 | |||||||
| chr4:153211582 | G | C | 1 | a0001c0005t0003g0021 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.30+7022G>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153211582 | |||||||
| chr4:153211757 | G | A | 8 | a0001c0001t0009g0060 a0001c0001t0009g0263 a0001c0001t0009g0264 others(5): Show |
8 | HG01891.hp1 HG02280.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.30+7197G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153211757 | |||||||
| chr4:153211782 | C | T | 91 | a0001c0001t0001g0125 a0001c0001t0001g0162 a0001c0001t0001g0164 others(88): Show |
91 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.30+7222C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153211782 | |||||||
| chr4:153211845 | G | C | 1 | a0001c0005t0003g0021 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.30+7285G>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153211845 | |||||||
| chr4:153211908 | A | T | 31 | a0001c0001t0001g0055 a0001c0001t0001g0062 a0001c0001t0001g0063 others(28): Show |
31 | HG01169.hp1 HG01496.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.30+7348A>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153211908 | |||||||
| chr4:153212464 | A | G | 5 | a0001c0002t0002g0267 a0001c0002t0002g0268 a0001c0002t0007g0266 others(2): Show |
5 | HG02109.hp1 HG02896.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.30+7904A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153212464 | |||||||
| chr4:153212542 | C | G | 6 | a0001c0001t0006g0146 a0001c0001t0006g0147 a0001c0001t0006g0149 others(3): Show |
6 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.30+7982C>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153212542 | |||||||
| chr4:153212706 | A | C | 5 | a0001c0002t0002g0267 a0001c0002t0002g0268 a0001c0002t0007g0266 others(2): Show |
5 | HG02109.hp1 HG02896.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.30+8146A>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153212706 | |||||||
| chr4:153212889 | G | A | 3 | a0001c0002t0011g0005 a0001c0002t0011g0006 a0001c0002t0011g0070 |
3 | HG02896.hp2 HG02897.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.30+8329G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153212889 | |||||||
| chr4:153213118 | A | C | 1 | a0001c0001t0002g0221 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.30+8558A>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153213118 | |||||||
| chr4:153213193 | G | C | 1 | a0001c0001t0002g0221 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.30+8633G>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153213193 | |||||||
| chr4:153213307 | T | C | 2 | a0001c0001t0002g0002 a0001c0002t0024g0128 |
2 | HG02559.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.30+8747T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153213307 | |||||||
| chr4:153213360 | T | G | 5 | a0001c0002t0002g0267 a0001c0002t0002g0268 a0001c0002t0007g0266 others(2): Show |
5 | HG02109.hp1 HG02896.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.30+8800T>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153213360 | |||||||
| chr4:153213442 | C | T | 5 | a0001c0002t0002g0267 a0001c0002t0002g0268 a0001c0002t0007g0266 others(2): Show |
5 | HG02109.hp1 HG02896.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.30+8882C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153213442 | |||||||
| chr4:153213451 | A | T | 222 | a0001c0001t0001g0017 a0001c0001t0001g0023 a0001c0001t0001g0033 others(219): Show |
222 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.30+8891A>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153213451 | |||||||
| chr4:153213642 | C | T | 1 | a0001c0009t0003g0159 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.30+9082C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153213642 | |||||||
| chr4:153213716 | C | T | 48 | a0001c0001t0001g0017 a0001c0001t0001g0023 a0001c0001t0001g0033 others(45): Show |
48 | HG00323.hp1 HG00438.hp2 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.30+9156C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153213716 | |||||||
| chr4:153213773 | G | A | 1 | a0001c0001t0001g0162 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.30+9213G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153213773 | |||||||
| chr4:153213997 | G | GA | 11 | a0001c0001t0006g0146 a0001c0001t0006g0147 a0001c0001t0006g0149 others(8): Show |
11 | HG01243.hp2 HG01884.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.30+9448dupA | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153213997 | ||||||
| chr4:153213997 | GA | G | 97 | a0001c0001t0001g0125 a0001c0001t0001g0158 a0001c0001t0001g0162 others(94): Show |
97 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.30+9448delA | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153213997 | ||||||
| chr4:153214013 | A | G | 1 | a0001c0002t0002g0268 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.30+9453A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153214013 | |||||||
| chr4:153214090 | T | C | 2 | a0001c0001t0002g0002 a0001c0002t0024g0128 |
2 | HG02559.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.30+9530T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153214090 | |||||||
| chr4:153214132 | T | C | 1 | a0001c0003t0003g0053 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.30+9572T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153214132 | |||||||
| chr4:153214305 | A | G | 28 | a0001c0001t0001g0151 a0001c0001t0001g0156 a0001c0001t0001g0157 others(25): Show |
28 | HG00544.hp2 HG00558.hp2 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.30+9745A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153214305 | |||||||
| chr4:153214352 | G | A | 1 | a0001c0002t0007g0266 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.30+9792G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153214352 | |||||||
| chr4:153214396 | T | C | 6 | a0001c0001t0006g0146 a0001c0001t0006g0147 a0001c0001t0006g0149 others(3): Show |
6 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.30+9836T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153214396 | |||||||
| chr4:153214436 | T | C | 155 | a0001c0001t0001g0017 a0001c0001t0001g0023 a0001c0001t0001g0033 others(152): Show |
155 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.30+9876T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153214436 | |||||||
| chr4:153214540 | C | T | 3 | a0001c0001t0015g0117 a0001c0002t0001g0115 a0001c0002t0001g0116 |
3 | HG00323.hp2 HG01081.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.30+9980C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153214540 | |||||||
| chr4:153214657 | G | A | 102 | a0001c0001t0001g0125 a0001c0001t0001g0158 a0001c0001t0001g0162 others(99): Show |
102 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.30+10097G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153214657 | |||||||
| chr4:153214882 | G | T | 6 | a0001c0001t0006g0146 a0001c0001t0006g0147 a0001c0001t0006g0149 others(3): Show |
6 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.30+10322G>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153214882 | |||||||
| chr4:153215234 | C | G | 1 | a0001c0003t0007g0225 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.30+10674C>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153215234 | |||||||
| chr4:153215424 | T | G | 94 | a0001c0001t0001g0125 a0001c0001t0001g0158 a0001c0001t0001g0162 others(91): Show |
94 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.30+10864T>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153215424 | |||||||
| chr4:153215471 | CTCTT | C | 6 | a0001c0001t0006g0146 a0001c0001t0006g0147 a0001c0001t0006g0149 others(3): Show |
6 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.30+10912_30+10915d others(6): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153215471 | |||||||
| chr4:153215498 | T | TA | 10 | a0001c0001t0002g0002 a0001c0001t0006g0146 a0001c0001t0006g0147 others(7): Show |
10 | HG01243.hp2 HG01884.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.30+10948dupA | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153215498 | ||||||
| chr4:153215499 | A | T | 1 | a0001c0002t0018g0135 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.30+10939A>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153215499 | |||||||
| chr4:153215576 | G | A | 2 | a0001c0001t0006g0123 a0001c0001t0007g0122 |
2 | HG02572.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.30+11016G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153215576 | |||||||
| chr4:153215594 | T | C | 226 | a0001c0001t0001g0017 a0001c0001t0001g0023 a0001c0001t0001g0033 others(223): Show |
226 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.30+11034T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153215594 | |||||||
| chr4:153215703 | G | A | 1 | a0001c0003t0002g0052 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.30+11143G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153215703 | |||||||
| chr4:153215727 | T | A | 39 | a0001c0001t0001g0055 a0001c0001t0001g0062 a0001c0001t0001g0063 others(36): Show |
39 | HG01169.hp1 HG01496.hp1 HG01891.hp1 others(36): Show |
intron_variant | MODIFIER | c.30+11167T>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153215727 | |||||||
| chr4:153215739 | C | A | 48 | a0001c0001t0001g0017 a0001c0001t0001g0023 a0001c0001t0001g0033 others(45): Show |
48 | HG00323.hp1 HG00438.hp2 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.30+11179C>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153215739 | |||||||
| chr4:153216032 | A | C | 8 | a0001c0001t0002g0002 a0001c0001t0006g0146 a0001c0001t0006g0147 others(5): Show |
8 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.30+11472A>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153216032 | |||||||
| chr4:153216160 | G | A | 1 | a0001c0002t0002g0267 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.30+11600G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153216160 | |||||||
| chr4:153216843 | G | A | 96 | a0001c0001t0001g0125 a0001c0001t0001g0158 a0001c0001t0001g0162 others(93): Show |
96 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.30+12283G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153216843 | |||||||
| chr4:153216934 | A | G | 226 | a0001c0001t0001g0017 a0001c0001t0001g0023 a0001c0001t0001g0033 others(223): Show |
226 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.30+12374A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153216934 | |||||||
| chr4:153216962 | G | A | 94 | a0001c0001t0001g0125 a0001c0001t0001g0158 a0001c0001t0001g0162 others(91): Show |
94 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.30+12402G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153216962 | |||||||
| chr4:153216966 | T | A | 1 | a0001c0001t0008g0020 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.30+12406T>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153216966 | |||||||
| chr4:153216987 | ATTTAGAT others(8): Show |
A | 1 | a0001c0002t0001g0220 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.30+12442_30+12456d others(17): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153216987 | ||||||
| chr4:153217214 | C | A | 4 | a0001c0001t0009g0060 a0001c0001t0009g0263 a0001c0001t0009g0264 others(1): Show |
4 | HG01891.hp1 HG02280.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.30+12654C>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153217214 | |||||||
| chr4:153217317 | T | C | 1 | a0001c0001t0003g0150 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.30+12757T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153217317 | |||||||
| chr4:153217359 | T | C | 1 | a0001c0003t0003g0071 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.30+12799T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153217359 | |||||||
| chr4:153217368 | G | A | 1 | a0001c0002t0033g0234 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.30+12808G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153217368 | |||||||
| chr4:153217385 | T | C | 3 | a0001c0001t0002g0001 a0001c0003t0002g0004 a0001c0003t0003g0064 |
3 | HG02976.hp1 HG03540.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.30+12825T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153217385 | |||||||
| chr4:153217606 | T | C | 94 | a0001c0001t0001g0125 a0001c0001t0001g0158 a0001c0001t0001g0162 others(91): Show |
94 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.30+13046T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153217606 | |||||||
| chr4:153217689 | TGGCTATG others(6): Show |
T | 28 | a0001c0001t0001g0151 a0001c0001t0001g0156 a0001c0001t0001g0157 others(25): Show |
28 | HG00544.hp2 HG00558.hp2 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.30+13139_30+13151d others(15): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153217689 | ||||||
| chr4:153217733 | A | T | 94 | a0001c0001t0001g0125 a0001c0001t0001g0158 a0001c0001t0001g0162 others(91): Show |
94 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.30+13173A>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153217733 | |||||||
| chr4:153218154 | T | C | 183 | a0001c0001t0001g0017 a0001c0001t0001g0023 a0001c0001t0001g0033 others(180): Show |
183 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.30+13594T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153218154 | |||||||
| chr4:153218157 | A | G | 1 | a0001c0001t0002g0001 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.30+13597A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153218157 | |||||||
| chr4:153218298 | C | G | 1 | a0002c0006t0003g0013 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.30+13738C>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153218298 | |||||||
| chr4:153218355 | G | C | 184 | a0001c0001t0001g0017 a0001c0001t0001g0023 a0001c0001t0001g0033 others(181): Show |
184 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.30+13795G>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153218355 | |||||||
| chr4:153218428 | T | G | 1 | a0001c0002t0012g0163 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.30+13868T>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153218428 | |||||||
| chr4:153218431 | C | A | 211 | a0001c0001t0001g0017 a0001c0001t0001g0023 a0001c0001t0001g0033 others(208): Show |
211 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.30+13871C>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153218431 | |||||||
| chr4:153218491 | G | A | 6 | a0001c0001t0006g0146 a0001c0001t0006g0147 a0001c0001t0006g0149 others(3): Show |
6 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.30+13931G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153218491 | |||||||
| chr4:153218660 | G | A | 2 | a0001c0001t0002g0002 a0001c0002t0024g0128 |
2 | HG02559.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.30+14100G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153218660 | |||||||
| chr4:153218811 | A | G | 1 | a0001c0001t0001g0157 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.30+14251A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153218811 | |||||||
| chr4:153218994 | AC | A | 222 | a0001c0001t0001g0017 a0001c0001t0001g0023 a0001c0001t0001g0033 others(219): Show |
222 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.30+14442delC | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153218994 | ||||||
| chr4:153219022 | T | A | 1 | a0001c0002t0002g0141 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.30+14462T>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153219022 | |||||||
| chr4:153219034 | A | G | 1 | a0001c0001t0001g0219 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.30+14474A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153219034 | |||||||
| chr4:153219041 | C | G | 4 | a0001c0002t0004g0045 a0001c0002t0004g0046 a0001c0002t0004g0047 others(1): Show |
4 | HG01884.hp1 HG02976.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.30+14481C>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153219041 | |||||||
| chr4:153219258 | T | G | 48 | a0001c0001t0001g0017 a0001c0001t0001g0023 a0001c0001t0001g0033 others(45): Show |
48 | HG00323.hp1 HG00438.hp2 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.30+14698T>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153219258 | |||||||
| chr4:153219289 | C | T | 1 | a0001c0001t0001g0218 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.30+14729C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153219289 | |||||||
| chr4:153219337 | C | G | 209 | a0001c0001t0001g0017 a0001c0001t0001g0023 a0001c0001t0001g0033 others(206): Show |
209 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.30+14777C>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153219337 | |||||||
| chr4:153219340 | T | C | 209 | a0001c0001t0001g0017 a0001c0001t0001g0023 a0001c0001t0001g0033 others(206): Show |
209 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.30+14780T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153219340 | |||||||
| chr4:153219817 | G | A | 1 | a0001c0001t0001g0164 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.30+15257G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153219817 | |||||||
| chr4:153219854 | T | C | 178 | a0001c0001t0001g0017 a0001c0001t0001g0023 a0001c0001t0001g0033 others(175): Show |
178 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.30+15294T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153219854 | |||||||
| chr4:153220106 | T | G | 178 | a0001c0001t0001g0017 a0001c0001t0001g0023 a0001c0001t0001g0033 others(175): Show |
178 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.30+15546T>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153220106 | |||||||
| chr4:153220217 | T | C | 4 | a0001c0002t0002g0267 a0001c0002t0002g0268 a0001c0002t0007g0266 others(1): Show |
4 | HG02109.hp1 HG03098.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.30+15657T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153220217 | |||||||
| chr4:153220282 | G | GA | 178 | a0001c0001t0001g0017 a0001c0001t0001g0023 a0001c0001t0001g0033 others(175): Show |
178 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.30+15732dupA | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153220282 | ||||||
| chr4:153220546 | A | T | 1 | a0001c0003t0003g0015 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.30+15986A>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153220546 | |||||||
| chr4:153220614 | T | C | 4 | a0001c0002t0002g0267 a0001c0002t0002g0268 a0001c0002t0007g0266 others(1): Show |
4 | HG02109.hp1 HG03098.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.30+16054T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153220614 | |||||||
| chr4:153220651 | C | T | 8 | a0001c0001t0009g0060 a0001c0001t0009g0263 a0001c0001t0009g0264 others(5): Show |
8 | HG01891.hp1 HG02280.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.30+16091C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153220651 | |||||||
| chr4:153220712 | AT | A | 31 | a0001c0001t0001g0055 a0001c0001t0001g0062 a0001c0001t0001g0063 others(28): Show |
31 | HG01169.hp1 HG01496.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.30+16159delT | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153220712 | ||||||
| chr4:153220825 | G | T | 1 | a0001c0001t0008g0044 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.30+16265G>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153220825 | |||||||
| chr4:153220839 | A | G | 1 | a0001c0002t0023g0014 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.30+16279A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153220839 | |||||||
| chr4:153220974 | T | C | 181 | a0001c0001t0001g0017 a0001c0001t0001g0023 a0001c0001t0001g0033 others(178): Show |
181 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.30+16414T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153220974 | |||||||
| chr4:153221021 | A | C | 181 | a0001c0001t0001g0017 a0001c0001t0001g0023 a0001c0001t0001g0033 others(178): Show |
181 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.30+16461A>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153221021 | |||||||
| chr4:153221107 | A | G | 181 | a0001c0001t0001g0017 a0001c0001t0001g0023 a0001c0001t0001g0033 others(178): Show |
181 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.30+16547A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153221107 | |||||||
| chr4:153221436 | CAAACAA | C | 3 | a0001c0002t0002g0267 a0001c0002t0002g0268 a0001c0002t0007g0266 |
3 | HG02109.hp1 NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.30+16880_30+16885d others(8): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153221436 | ||||||
| chr4:153221505 | T | C | 6 | a0001c0001t0006g0146 a0001c0001t0006g0147 a0001c0001t0006g0149 others(3): Show |
6 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.30+16945T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153221505 | |||||||
| chr4:153221724 | G | A | 5 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 others(2): Show |
5 | NA18964.hp2 NA19007.hp1 NA19009.hp2 others(2): Show |
intron_variant | MODIFIER | c.30+17164G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153221724 | |||||||
| chr4:153221739 | T | C | 222 | a0001c0001t0001g0017 a0001c0001t0001g0023 a0001c0001t0001g0033 others(219): Show |
222 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.30+17179T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153221739 | |||||||
| chr4:153221763 | T | TAAGGAAG others(12): Show |
41 | a0001c0001t0001g0055 a0001c0001t0001g0062 a0001c0001t0001g0063 others(38): Show |
41 | HG01169.hp1 HG01496.hp1 HG01891.hp1 others(38): Show |
intron_variant | MODIFIER | c.30+17219_30+17220i others(21): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153221763 | ||||||
| chr4:153221763 | TAAGGAAG others(58): Show |
T | 2 | a0001c0002t0002g0267 a0001c0002t0002g0268 |
2 | HG02109.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.30+17220_30+17284d others(67): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153221763 | ||||||
| chr4:153221778 | A | AGCGCAAG others(4): Show |
54 | a0001c0001t0001g0017 a0001c0001t0001g0023 a0001c0001t0001g0033 others(51): Show |
54 | HG00323.hp1 HG00438.hp2 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.30+17219_30+17220i others(13): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153221778 | ||||||
| chr4:153221783 | A | G | 54 | a0001c0001t0001g0017 a0001c0001t0001g0023 a0001c0001t0001g0033 others(51): Show |
54 | HG00323.hp1 HG00438.hp2 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.30+17223A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153221783 | |||||||
| chr4:153221784 | A | AGGGAGAG others(80): Show |
1 | a0001c0002t0007g0266 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.30+17224_30+17225i others(89): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153221784 | |||||||
| chr4:153221784 | AAAGG | A | 6 | a0001c0001t0006g0146 a0001c0001t0006g0147 a0001c0001t0006g0149 others(3): Show |
6 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.30+17231_30+17234d others(6): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153221784 | ||||||
| chr4:153221787 | G | GAAGA | 54 | a0001c0001t0001g0017 a0001c0001t0001g0023 a0001c0001t0001g0033 others(51): Show |
54 | HG00323.hp1 HG00438.hp2 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.30+17227_30+17228i others(6): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153221787 | |||||||
| chr4:153221788 | G | A | 54 | a0001c0001t0001g0017 a0001c0001t0001g0023 a0001c0001t0001g0033 others(51): Show |
54 | HG00323.hp1 HG00438.hp2 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.30+17228G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153221788 | |||||||
| chr4:153221799 | C | G | 1 | a0001c0002t0007g0266 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.30+17239C>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153221799 | |||||||
| chr4:153221808 | A | AAGGG | 214 | a0001c0001t0001g0017 a0001c0001t0001g0023 a0001c0001t0001g0033 others(211): Show |
214 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.30+17260_30+17263d others(6): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153221808 | ||||||
| chr4:153221812 | G | A | 1 | a0001c0002t0007g0266 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.30+17252G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153221812 | |||||||
| chr4:153221819 | G | A | 1 | a0001c0002t0007g0266 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.30+17259G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153221819 | |||||||
| chr4:153221827 | T | G | 1 | a0001c0002t0007g0266 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.30+17267T>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153221827 | |||||||
| chr4:153221831 | G | A | 1 | a0001c0002t0007g0266 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.30+17271G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153221831 | |||||||
| chr4:153221845 | C | A | 1 | a0001c0002t0007g0266 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.30+17285C>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153221845 | |||||||
| chr4:153221845 | C | T | 1 | a0001c0001t0030g0217 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.30+17285C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153221845 | |||||||
| chr4:153221848 | G | A | 31 | a0001c0001t0001g0151 a0001c0001t0001g0157 a0001c0001t0001g0227 others(28): Show |
31 | HG00140.hp2 HG00544.hp2 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.30+17288G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153221848 | |||||||
| chr4:153221851 | G | GAAGGAAG others(87): Show |
1 | a0001c0002t0007g0266 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.30+17293_30+17294i others(96): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153221851 | ||||||
| chr4:153221854 | A | G | 1 | a0001c0002t0007g0266 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.30+17294A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153221854 | |||||||
| chr4:153221859 | A | G | 218 | a0001c0001t0001g0017 a0001c0001t0001g0023 a0001c0001t0001g0033 others(215): Show |
218 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.30+17299A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153221859 | |||||||
| chr4:153221863 | A | G | 1 | a0001c0002t0007g0266 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.30+17303A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153221863 | |||||||
| chr4:153221880 | GAGGA | G | 51 | a0001c0001t0001g0017 a0001c0001t0001g0023 a0001c0001t0001g0033 others(48): Show |
51 | HG00323.hp1 HG00438.hp2 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.30+17333_30+17336d others(6): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153221880 | ||||||
| chr4:153221893 | A | G | 1 | a0001c0002t0007g0266 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.30+17333A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153221893 | |||||||
| chr4:153221903 | A | G | 1 | a0001c0002t0007g0266 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.30+17343A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153221903 | |||||||
| chr4:153221907 | AAGGG | A | 119 | a0001c0001t0001g0125 a0001c0001t0001g0151 a0001c0001t0001g0156 others(116): Show |
119 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.30+17358_30+17361d others(6): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153221907 | ||||||
| chr4:153221915 | G | A | 1 | a0001c0002t0007g0266 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.30+17355G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153221915 | |||||||
| chr4:153221919 | G | A | 1 | a0001c0002t0007g0266 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.30+17359G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153221919 | |||||||
| chr4:153221923 | G | A | 1 | a0001c0003t0003g0165 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.30+17363G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153221923 | |||||||
| chr4:153221928 | A | G | 1 | a0001c0002t0007g0266 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.30+17368A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153221928 | |||||||
| chr4:153221929 | A | G | 1 | a0001c0002t0007g0266 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.30+17369A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153221929 | |||||||
| chr4:153221936 | C | G | 1 | a0001c0002t0007g0266 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.30+17376C>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153221936 | |||||||
| chr4:153221940 | A | G | 1 | a0001c0002t0007g0266 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.30+17380A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153221940 | |||||||
| chr4:153221943 | G | A | 1 | a0001c0002t0007g0266 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.30+17383G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153221943 | |||||||
| chr4:153221944 | T | A | 1 | a0001c0002t0007g0266 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.30+17384T>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153221944 | |||||||
| chr4:153221958 | A | G | 1 | a0001c0002t0007g0266 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.30+17398A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153221958 | |||||||
| chr4:153221959 | A | G | 1 | a0001c0002t0007g0266 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.30+17399A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153221959 | |||||||
| chr4:153221960 | GAGGGAGG others(1): Show |
G | 216 | a0001c0001t0001g0017 a0001c0001t0001g0023 a0001c0001t0001g0033 others(213): Show |
216 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.30+17412_30+17419d others(10): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153221960 | ||||||
| chr4:153221967 | G | GGAGGGAG others(38): Show |
1 | a0001c0002t0024g0128 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.30+17407_30+17408i others(47): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153221967 | |||||||
| chr4:153221968 | A | AAGGAAGG others(150): Show |
1 | a0001c0001t0001g0218 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.30+17411_30+17412i others(159): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153221968 | ||||||
| chr4:153221968 | A | G | 2 | a0001c0002t0007g0266 a0001c0002t0024g0128 |
2 | HG02559.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.30+17408A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153221968 | |||||||
| chr4:153221971 | G | T | 1 | a0001c0001t0002g0002 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.30+17411G>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153221971 | |||||||
| chr4:153221984 | A | AAAGAGGA others(3): Show |
1 | a0001c0002t0007g0266 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.30+17425_30+17426i others(12): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153221984 | ||||||
| chr4:153221986 | G | A | 1 | a0001c0002t0007g0266 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.30+17426G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153221986 | |||||||
| chr4:153221987 | G | GAAA | 3 | a0001c0002t0023g0014 a0001c0003t0007g0224 a0001c0003t0007g0225 |
3 | HG01106.hp2 HG06807.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.30+17427_30+17428i others(5): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153221987 | |||||||
| chr4:153221991 | A | C | 3 | a0001c0002t0023g0014 a0001c0003t0007g0224 a0001c0003t0007g0225 |
3 | HG01106.hp2 HG06807.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.30+17431A>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153221991 | |||||||
| chr4:153221991 | A | G | 1 | a0001c0002t0007g0266 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.30+17431A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153221991 | |||||||
| chr4:153221994 | GGAAGGAA others(5): Show |
G | 1 | a0001c0001t0001g0158 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.30+17449_30+17460d others(14): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153221994 | ||||||
| chr4:153221996 | A | G | 1 | a0001c0002t0007g0266 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.30+17436A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153221996 | |||||||
| chr4:153222000 | A | G | 4 | a0001c0002t0007g0266 a0001c0002t0023g0014 a0001c0003t0007g0224 others(1): Show |
4 | HG01106.hp2 HG06807.hp2 NA20752.hp2 others(1): Show |
intron_variant | MODIFIER | c.30+17440A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153222000 | |||||||
| chr4:153222004 | A | G | 4 | a0001c0002t0007g0266 a0001c0002t0023g0014 a0001c0003t0007g0224 others(1): Show |
4 | HG01106.hp2 HG06807.hp2 NA20752.hp2 others(1): Show |
intron_variant | MODIFIER | c.30+17444A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153222004 | |||||||
| chr4:153222006 | A | G | 4 | a0001c0002t0007g0266 a0001c0002t0023g0014 a0001c0003t0007g0224 others(1): Show |
4 | HG01106.hp2 HG06807.hp2 NA20752.hp2 others(1): Show |
intron_variant | MODIFIER | c.30+17446A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153222006 | |||||||
| chr4:153222018 | A | G | 3 | a0001c0002t0023g0014 a0001c0003t0007g0224 a0001c0003t0007g0225 |
3 | HG01106.hp2 HG06807.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.30+17458A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153222018 | |||||||
| chr4:153222022 | C | G | 4 | a0001c0002t0007g0266 a0001c0002t0023g0014 a0001c0003t0007g0224 others(1): Show |
4 | HG01106.hp2 HG06807.hp2 NA20752.hp2 others(1): Show |
intron_variant | MODIFIER | c.30+17462C>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153222022 | |||||||
| chr4:153222032 | A | G | 1 | a0001c0002t0007g0266 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.30+17472A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153222032 | |||||||
| chr4:153222033 | G | A | 3 | a0001c0002t0023g0014 a0001c0003t0007g0224 a0001c0003t0007g0225 |
3 | HG01106.hp2 HG06807.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.30+17473G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153222033 | |||||||
| chr4:153222035 | A | AAAGCAAG others(76): Show |
1 | a0001c0002t0023g0014 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.30+17478_30+17479i others(85): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153222035 | ||||||
| chr4:153222035 | A | AGGGAGGG others(658): Show |
1 | a0001c0002t0007g0266 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.30+17475_30+17476i others(667): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153222035 | |||||||
| chr4:153222037 | A | AGCAAGGA others(80): Show |
2 | a0001c0003t0007g0224 a0001c0003t0007g0225 |
2 | HG01106.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.30+17478_30+17479i others(89): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153222037 | ||||||
| chr4:153222041 | C | G | 2 | a0001c0003t0007g0224 a0001c0003t0007g0225 |
2 | HG01106.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.30+17481C>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153222041 | |||||||
| chr4:153222046 | A | AAGGGAGG others(385): Show |
1 | a0001c0001t0001g0218 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.30+17493_30+17494i others(394): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153222046 | ||||||
| chr4:153222046 | A | AGGAGGGA others(690): Show |
1 | a0001c0003t0003g0165 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.30+17486_30+17487i others(699): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153222046 | |||||||
| chr4:153222046 | A | G | 4 | a0001c0002t0007g0266 a0001c0002t0023g0014 a0001c0003t0007g0224 others(1): Show |
4 | HG01106.hp2 HG06807.hp2 NA20752.hp2 others(1): Show |
intron_variant | MODIFIER | c.30+17486A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153222046 | |||||||
| chr4:153222058 | A | AAGGAAGG others(718): Show |
1 | a0001c0001t0025g0007 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.30+17507_30+17508i others(727): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153222058 | ||||||
| chr4:153222058 | A | AAGGAAGG others(422): Show |
5 | a0001c0001t0006g0146 a0001c0001t0006g0147 a0001c0001t0006g0149 others(2): Show |
5 | HG01243.hp2 HG01884.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.30+17507_30+17508i others(431): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153222058 | ||||||
| chr4:153222058 | A | AAGGAAGG others(388): Show |
1 | a0001c0001t0001g0158 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.30+17506_30+17507i others(397): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153222058 | ||||||
| chr4:153222058 | A | AAGGAAGG others(388): Show |
1 | a0001c0001t0001g0170 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.30+17506_30+17507i others(397): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153222058 | ||||||
| chr4:153222058 | A | AAGGAAGG others(387): Show |
1 | a0001c0001t0001g0151 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.30+17506_30+17507i others(396): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153222058 | ||||||
| chr4:153222058 | A | AAGGAAGG others(403): Show |
22 | a0001c0001t0001g0157 a0001c0001t0001g0227 a0001c0001t0001g0253 others(19): Show |
22 | HG00544.hp2 HG00558.hp2 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.30+17506_30+17507i others(412): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153222058 | ||||||
| chr4:153222058 | A | AAGGAAGG others(385): Show |
1 | a0001c0002t0002g0171 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.30+17506_30+17507i others(394): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153222058 | ||||||
| chr4:153222058 | A | AAGGAAGG others(389): Show |
1 | a0001c0002t0004g0172 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.30+17506_30+17507i others(398): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153222058 | ||||||
| chr4:153222058 | A | AAGGAAGG others(423): Show |
1 | a0001c0002t0001g0173 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.30+17506_30+17507i others(432): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153222058 | ||||||
| chr4:153222058 | A | AAGGAAGG others(355): Show |
1 | a0001c0001t0001g0174 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.30+17506_30+17507i others(364): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153222058 | ||||||
| chr4:153222058 | A | AAGGAAGG others(544): Show |
1 | a0001c0001t0003g0175 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.30+17506_30+17507i others(553): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153222058 | ||||||
| chr4:153222058 | A | AAGGAAGG others(389): Show |
1 | a0001c0001t0001g0156 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.30+17506_30+17507i others(398): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153222058 | ||||||
| chr4:153222058 | A | AAGGAAGG others(404): Show |
1 | a0001c0001t0030g0217 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.30+17506_30+17507i others(413): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153222058 | ||||||
| chr4:153222058 | A | AAGGAAGG others(389): Show |
69 | a0001c0001t0001g0125 a0001c0001t0001g0162 a0001c0001t0001g0179 others(66): Show |
69 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.30+17506_30+17507i others(398): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153222058 | ||||||
| chr4:153222058 | A | AAGGAAGG others(374): Show |
2 | a0001c0001t0001g0164 a0001c0001t0001g0211 |
2 | HG01069.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.30+17506_30+17507i others(383): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153222058 | ||||||
| chr4:153222058 | A | AAGGAAGG others(423): Show |
4 | a0001c0001t0001g0249 a0001c0001t0006g0123 a0001c0001t0007g0122 others(1): Show |
4 | HG02572.hp2 HG03225.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+17506_30+17507i others(432): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153222058 | ||||||
| chr4:153222058 | A | AAGGAAGG others(555): Show |
1 | a0001c0001t0008g0168 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.30+17506_30+17507i others(564): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153222058 | ||||||
| chr4:153222058 | A | AAGGAAGG others(522): Show |
1 | a0001c0005t0003g0169 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.30+17506_30+17507i others(531): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153222058 | ||||||
| chr4:153222058 | A | AAGGAAGG others(393): Show |
1 | a0001c0001t0001g0213 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.30+17506_30+17507i others(402): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153222058 | ||||||
| chr4:153222058 | A | AAGGAAGG others(514): Show |
2 | a0001c0002t0002g0267 a0001c0002t0002g0268 |
2 | HG02109.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.30+17506_30+17507i others(523): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153222058 | ||||||
| chr4:153222058 | A | AAGGAAGG others(465): Show |
1 | a0001c0009t0003g0159 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.30+17506_30+17507i others(474): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153222058 | ||||||
| chr4:153222058 | A | AAGGAAGG others(405): Show |
1 | a0001c0001t0005g0214 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.30+17506_30+17507i others(414): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153222058 | ||||||
| chr4:153222058 | A | AAGGAAGG others(389): Show |
1 | a0001c0002t0002g0215 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.30+17506_30+17507i others(398): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153222058 | ||||||
| chr4:153222058 | A | AAGGAAGG others(317): Show |
1 | a0001c0003t0003g0216 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.30+17506_30+17507i others(326): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153222058 | ||||||
| chr4:153222058 | A | AAGGAAGG others(400): Show |
1 | a0001c0002t0007g0155 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.30+17506_30+17507i others(409): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153222058 | ||||||
| chr4:153222058 | A | AAGGAAGG others(410): Show |
1 | a0001c0003t0002g0052 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.30+17506_30+17507i others(419): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153222058 | ||||||
| chr4:153222058 | A | AAGGAAGG others(406): Show |
1 | a0001c0003t0003g0071 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.30+17506_30+17507i others(415): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153222058 | ||||||
| chr4:153222058 | A | AAGGAAGG others(410): Show |
48 | a0001c0001t0001g0017 a0001c0001t0001g0023 a0001c0001t0001g0033 others(45): Show |
48 | HG00323.hp1 HG00438.hp2 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.30+17506_30+17507i others(419): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153222058 | ||||||
| chr4:153222058 | A | AAGGAAGG others(402): Show |
1 | a0001c0001t0002g0002 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.30+17506_30+17507i others(411): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153222058 | ||||||
| chr4:153222058 | A | G | 6 | a0001c0001t0001g0218 a0001c0002t0007g0266 a0001c0002t0023g0014 others(3): Show |
6 | HG01106.hp2 HG02602.hp1 HG06807.hp2 others(3): Show |
intron_variant | MODIFIER | c.30+17498A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153222058 | |||||||
| chr4:153222062 | A | AAGGAGAG others(385): Show |
1 | a0001c0001t0027g0068 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.30+17506_30+17507i others(394): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153222062 | ||||||
| chr4:153222072 | A | G | 1 | a0001c0001t0027g0068 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.30+17512A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153222072 | |||||||
| chr4:153222079 | G | A | 1 | a0001c0001t0027g0068 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.30+17519G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153222079 | |||||||
| chr4:153222218 | AT | A | 6 | a0001c0001t0006g0146 a0001c0001t0006g0147 a0001c0001t0006g0149 others(3): Show |
6 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.30+17666delT | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153222218 | ||||||
| chr4:153222601 | C | T | 3 | a0001c0001t0001g0113 a0001c0001t0001g0118 a0001c0002t0002g0114 |
3 | NA18951.hp2 NA19002.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.30+18041C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153222601 | |||||||
| chr4:153222855 | G | T | 4 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0120 others(1): Show |
4 | NA18964.hp2 NA19007.hp1 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.30+18295G>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153222855 | |||||||
| chr4:153222876 | A | C | 48 | a0001c0001t0001g0017 a0001c0001t0001g0033 a0001c0001t0001g0039 others(45): Show |
48 | HG00323.hp1 HG00438.hp2 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.30+18316A>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153222876 | |||||||
| chr4:153222936 | A | G | 1 | a0001c0010t0004g0085 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.30+18376A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153222936 | |||||||
| chr4:153222954 | C | G | 99 | a0001c0001t0001g0023 a0001c0001t0001g0056 a0001c0001t0001g0091 others(96): Show |
99 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.30+18394C>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153222954 | |||||||
| chr4:153223070 | ACCCT | A | 3 | a0001c0003t0003g0011 a0002c0006t0003g0012 a0002c0006t0003g0013 |
3 | HG02109.hp2 HG02965.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.30+18514_30+18517d others(6): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153223070 | ||||||
| chr4:153223075 | C | A | 120 | a0001c0001t0001g0023 a0001c0001t0001g0056 a0001c0001t0001g0072 others(117): Show |
120 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.30+18515C>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153223075 | |||||||
| chr4:153223151 | G | A | 1 | a0001c0001t0007g0122 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.30+18591G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153223151 | |||||||
| chr4:153223162 | G | T | 1 | a0001c0001t0006g0149 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.30+18602G>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153223162 | |||||||
| chr4:153223478 | T | C | 103 | a0001c0001t0001g0017 a0001c0001t0001g0033 a0001c0001t0001g0039 others(100): Show |
103 | HG00323.hp1 HG00438.hp2 HG00741.hp1 others(100): Show |
intron_variant | MODIFIER | c.30+18918T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153223478 | |||||||
| chr4:153223481 | T | C | 103 | a0001c0001t0001g0017 a0001c0001t0001g0033 a0001c0001t0001g0039 others(100): Show |
103 | HG00323.hp1 HG00438.hp2 HG00741.hp1 others(100): Show |
intron_variant | MODIFIER | c.30+18921T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153223481 | |||||||
| chr4:153223760 | T | C | 2 | a0001c0003t0007g0224 a0001c0003t0007g0225 |
2 | HG01106.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.30+19200T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153223760 | |||||||
| chr4:153224065 | C | T | 2 | a0001c0001t0002g0002 a0001c0002t0024g0128 |
2 | HG02559.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.30+19505C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153224065 | |||||||
| chr4:153224319 | C | T | 2 | a0001c0001t0004g0087 a0001c0001t0004g0088 |
2 | HG02055.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.30+19759C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153224319 | |||||||
| chr4:153224379 | T | C | 1 | a0001c0002t0007g0266 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.30+19819T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153224379 | |||||||
| chr4:153224388 | G | C | 3 | a0001c0001t0001g0072 a0001c0001t0001g0164 a0001c0001t0001g0211 |
3 | HG01069.hp2 HG01975.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.30+19828G>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153224388 | |||||||
| chr4:153224439 | C | A | 7 | a0001c0002t0002g0130 a0001c0002t0002g0136 a0001c0002t0002g0137 others(4): Show |
7 | HG02145.hp1 HG02486.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.30+19879C>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153224439 | |||||||
| chr4:153224518 | G | A | 100 | a0001c0001t0001g0017 a0001c0001t0001g0033 a0001c0001t0001g0039 others(97): Show |
100 | HG00323.hp1 HG00438.hp2 HG00741.hp1 others(97): Show |
intron_variant | MODIFIER | c.30+19958G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153224518 | |||||||
| chr4:153224754 | A | G | 1 | a0001c0001t0001g0151 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.30+20194A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153224754 | |||||||
| chr4:153225086 | C | T | 33 | a0001c0001t0001g0055 a0001c0001t0001g0062 a0001c0001t0001g0063 others(30): Show |
33 | HG01169.hp1 HG01496.hp1 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.30+20526C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153225086 | |||||||
| chr4:153225330 | G | T | 2 | a0001c0003t0007g0224 a0001c0003t0007g0225 |
2 | HG01106.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.30+20770G>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153225330 | |||||||
| chr4:153225354 | A | G | 3 | a0001c0003t0003g0011 a0002c0006t0003g0012 a0002c0006t0003g0013 |
3 | HG02109.hp2 HG02965.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.30+20794A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153225354 | |||||||
| chr4:153225372 | T | C | 1 | a0001c0001t0001g0151 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.30+20812T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153225372 | |||||||
| chr4:153225405 | G | A | 33 | a0001c0001t0001g0055 a0001c0001t0001g0062 a0001c0001t0001g0063 others(30): Show |
33 | HG01169.hp1 HG01496.hp1 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.30+20845G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153225405 | |||||||
| chr4:153225432 | G | A | 1 | a0001c0001t0003g0150 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.30+20872G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153225432 | |||||||
| chr4:153225528 | C | G | 1 | a0001c0002t0002g0124 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.30+20968C>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153225528 | |||||||
| chr4:153225600 | G | A | 2 | a0001c0001t0002g0002 a0001c0002t0024g0128 |
2 | HG02559.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.30+21040G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153225600 | |||||||
| chr4:153225740 | T | C | 1 | a0001c0001t0001g0151 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.30+21180T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153225740 | |||||||
| chr4:153225741 | G | A | 1 | a0001c0001t0001g0151 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.30+21181G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153225741 | |||||||
| chr4:153225774 | CAG | C | 3 | a0001c0002t0011g0005 a0001c0002t0011g0006 a0001c0002t0011g0070 |
3 | HG02896.hp2 HG02897.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.30+21216_30+21217d others(4): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153225774 | ||||||
| chr4:153225835 | C | T | 2 | a0001c0001t0002g0002 a0001c0002t0024g0128 |
2 | HG02559.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.30+21275C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153225835 | |||||||
| chr4:153225918 | T | G | 101 | a0001c0001t0001g0017 a0001c0001t0001g0033 a0001c0001t0001g0039 others(98): Show |
101 | HG00323.hp1 HG00438.hp2 HG00741.hp1 others(98): Show |
intron_variant | MODIFIER | c.30+21358T>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153225918 | |||||||
| chr4:153225934 | A | G | 1 | a0001c0002t0023g0014 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.30+21374A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153225934 | |||||||
| chr4:153226129 | C | T | 1 | a0001c0002t0029g0261 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.30+21569C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153226129 | |||||||
| chr4:153226283 | A | G | 4 | a0001c0002t0003g0144 a0001c0002t0011g0005 a0001c0002t0011g0006 others(1): Show |
4 | HG02896.hp2 HG02897.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.30+21723A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153226283 | |||||||
| chr4:153226366 | A | G | 1 | a0001c0003t0003g0043 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.30+21806A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153226366 | |||||||
| chr4:153226528 | T | G | 3 | a0001c0003t0003g0185 a0001c0003t0003g0216 a0001c0004t0001g0184 |
3 | HG02027.hp2 NA18998.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.30+21968T>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153226528 | |||||||
| chr4:153226636 | A | C | 2 | a0001c0001t0001g0017 a0001c0001t0003g0016 |
2 | HG02622.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.30+22076A>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153226636 | |||||||
| chr4:153226688 | G | A | 34 | a0001c0001t0001g0055 a0001c0001t0001g0062 a0001c0001t0001g0063 others(31): Show |
34 | HG01169.hp1 HG01496.hp1 HG01891.hp2 others(31): Show |
intron_variant | MODIFIER | c.30+22128G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153226688 | |||||||
| chr4:153226696 | G | A | 3 | a0001c0002t0002g0050 a0001c0002t0004g0069 a0001c0003t0007g0223 |
3 | HG01070.hp1 HG01074.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.30+22136G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153226696 | |||||||
| chr4:153226805 | A | T | 2 | a0001c0002t0001g0126 a0001c0002t0001g0210 |
2 | HG01255.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.30+22245A>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153226805 | |||||||
| chr4:153226939 | C | T | 34 | a0001c0001t0001g0055 a0001c0001t0001g0062 a0001c0001t0001g0063 others(31): Show |
34 | HG01169.hp1 HG01496.hp1 HG01891.hp2 others(31): Show |
intron_variant | MODIFIER | c.30+22379C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153226939 | |||||||
| chr4:153227105 | T | C | 56 | a0001c0001t0001g0017 a0001c0001t0001g0033 a0001c0001t0001g0039 others(53): Show |
56 | HG00323.hp1 HG00438.hp2 HG00741.hp1 others(53): Show |
intron_variant | MODIFIER | c.30+22545T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153227105 | |||||||
| chr4:153227304 | C | T | 1 | a0001c0001t0002g0221 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.30+22744C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153227304 | |||||||
| chr4:153227314 | C | T | 3 | a0001c0001t0005g0110 a0001c0001t0005g0161 a0001c0001t0021g0111 |
3 | NA18942.hp1 NA18968.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.30+22754C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153227314 | |||||||
| chr4:153227342 | C | T | 4 | a0001c0001t0009g0060 a0001c0001t0009g0263 a0001c0001t0009g0264 others(1): Show |
4 | HG01891.hp1 HG02280.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.30+22782C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153227342 | |||||||
| chr4:153227414 | A | G | 2 | a0001c0001t0004g0087 a0001c0001t0004g0088 |
2 | HG02055.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.30+22854A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153227414 | |||||||
| chr4:153227645 | G | C | 3 | a0001c0002t0002g0050 a0001c0002t0004g0069 a0001c0003t0007g0223 |
3 | HG01070.hp1 HG01074.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.30+23085G>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153227645 | |||||||
| chr4:153227659 | A | G | 1 | a0001c0002t0023g0014 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.30+23099A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153227659 | |||||||
| chr4:153227754 | G | A | 1 | a0001c0002t0003g0144 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.30+23194G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153227754 | |||||||
| chr4:153227766 | G | A | 1 | a0001c0003t0003g0011 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.30+23206G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153227766 | |||||||
| chr4:153227857 | T | C | 3 | a0001c0001t0002g0018 a0001c0001t0002g0022 a0001c0001t0003g0265 |
3 | HG01169.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.30+23297T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153227857 | |||||||
| chr4:153228243 | G | T | 1 | a0001c0002t0003g0148 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.30+23683G>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153228243 | |||||||
| chr4:153228688 | C | T | 18 | a0001c0001t0001g0247 a0001c0001t0001g0249 a0001c0001t0002g0245 others(15): Show |
18 | HG00438.hp1 HG00544.hp1 HG02027.hp2 others(15): Show |
intron_variant | MODIFIER | c.30+24128C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153228688 | |||||||
| chr4:153228742 | C | T | 59 | a0001c0001t0001g0023 a0001c0001t0001g0092 a0001c0001t0001g0093 others(56): Show |
59 | HG00438.hp1 HG00544.hp1 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.30+24182C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153228742 | |||||||
| chr4:153228744 | C | T | 5 | a0001c0001t0009g0060 a0001c0001t0009g0263 a0001c0001t0009g0264 others(2): Show |
5 | HG01891.hp1 HG02280.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.30+24184C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153228744 | |||||||
| chr4:153228759 | T | C | 2 | a0001c0002t0017g0095 a0001c0002t0017g0096 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.30+24199T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153228759 | |||||||
| chr4:153229059 | G | C | 1 | a0001c0001t0002g0002 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.30+24499G>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153229059 | |||||||
| chr4:153229509 | C | T | 2 | a0001c0004t0003g0058 a0001c0008t0002g0059 |
2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.30+24949C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153229509 | |||||||
| chr4:153230116 | C | T | 1 | a0001c0002t0033g0234 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.30+25556C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153230116 | |||||||
| chr4:153230422 | T | G | 59 | a0001c0001t0001g0017 a0001c0001t0001g0033 a0001c0001t0001g0039 others(56): Show |
59 | HG00323.hp1 HG00438.hp2 HG00741.hp1 others(56): Show |
intron_variant | MODIFIER | c.30+25862T>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153230422 | |||||||
| chr4:153230484 | A | G | 22 | a0001c0001t0001g0017 a0001c0001t0001g0062 a0001c0001t0001g0063 others(19): Show |
22 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.30+25924A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153230484 | |||||||
| chr4:153230489 | C | T | 1 | a0001c0002t0033g0234 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.30+25929C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153230489 | |||||||
| chr4:153230555 | G | A | 13 | a0001c0002t0001g0229 a0001c0003t0001g0027 a0001c0003t0003g0015 others(10): Show |
13 | HG00323.hp1 HG00741.hp1 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.30+25995G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153230555 | |||||||
| chr4:153230639 | C | A | 1 | a0001c0003t0007g0106 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.30+26079C>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153230639 | |||||||
| chr4:153230836 | A | G | 92 | a0001c0001t0001g0017 a0001c0001t0001g0033 a0001c0001t0001g0039 others(89): Show |
92 | HG00323.hp1 HG00438.hp2 HG00741.hp1 others(89): Show |
intron_variant | MODIFIER | c.30+26276A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153230836 | |||||||
| chr4:153231083 | G | A | 1 | a0001c0002t0002g0267 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.30+26523G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153231083 | |||||||
| chr4:153231216 | T | C | 2 | a0001c0002t0001g0126 a0001c0002t0001g0210 |
2 | HG01255.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.30+26656T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153231216 | |||||||
| chr4:153231236 | A | G | 1 | a0001c0001t0001g0213 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.30+26676A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153231236 | |||||||
| chr4:153231304 | T | C | 1 | a0001c0001t0001g0162 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.30+26744T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153231304 | |||||||
| chr4:153231409 | C | T | 5 | a0001c0001t0001g0247 a0001c0001t0003g0209 a0001c0002t0001g0173 others(2): Show |
5 | HG00544.hp1 HG02080.hp2 NA18942.hp2 others(2): Show |
intron_variant | MODIFIER | c.30+26849C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153231409 | |||||||
| chr4:153231497 | A | C | 1 | a0001c0002t0002g0136 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.30+26937A>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153231497 | |||||||
| chr4:153231694 | C | T | 1 | a0001c0002t0023g0014 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.30+27134C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153231694 | |||||||
| chr4:153231722 | G | T | 1 | a0001c0002t0023g0014 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.30+27162G>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153231722 | |||||||
| chr4:153232053 | T | A | 1 | a0001c0002t0002g0137 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.30+27493T>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153232053 | |||||||
| chr4:153232054 | G | T | 1 | a0001c0002t0002g0137 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.30+27494G>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153232054 | |||||||
| chr4:153232464 | G | A | 1 | a0001c0002t0002g0267 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.30+27904G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153232464 | |||||||
| chr4:153232546 | G | A | 1 | a0001c0001t0002g0002 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.30+27986G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153232546 | |||||||
| chr4:153232620 | A | G | 102 | a0001c0001t0001g0017 a0001c0001t0001g0033 a0001c0001t0001g0039 others(99): Show |
102 | HG00323.hp1 HG00438.hp2 HG00741.hp1 others(99): Show |
intron_variant | MODIFIER | c.30+28060A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153232620 | |||||||
| chr4:153232637 | G | C | 102 | a0001c0001t0001g0017 a0001c0001t0001g0033 a0001c0001t0001g0039 others(99): Show |
102 | HG00323.hp1 HG00438.hp2 HG00741.hp1 others(99): Show |
intron_variant | MODIFIER | c.30+28077G>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153232637 | |||||||
| chr4:153232655 | G | A | 2 | a0001c0003t0007g0224 a0001c0003t0007g0225 |
2 | HG01106.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.30+28095G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153232655 | |||||||
| chr4:153232848 | A | G | 27 | a0001c0001t0001g0084 a0001c0001t0001g0097 a0001c0001t0001g0098 others(24): Show |
27 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.30+28288A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153232848 | |||||||
| chr4:153232948 | C | A | 3 | a0001c0001t0004g0087 a0001c0001t0004g0088 a0001c0002t0003g0144 |
3 | HG02055.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.30+28388C>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153232948 | |||||||
| chr4:153233041 | T | C | 1 | a0001c0001t0001g0174 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.30+28481T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153233041 | |||||||
| chr4:153233062 | G | A | 1 | a0001c0002t0001g0226 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.30+28502G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153233062 | |||||||
| chr4:153233364 | G | A | 2 | a0001c0003t0007g0224 a0001c0003t0007g0225 |
2 | HG01106.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.30+28804G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153233364 | |||||||
| chr4:153233663 | G | A | 1 | a0001c0002t0001g0126 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.30+29103G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153233663 | |||||||
| chr4:153233861 | A | G | 250 | a0001c0001t0001g0017 a0001c0001t0001g0023 a0001c0001t0001g0033 others(247): Show |
250 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.30+29301A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153233861 | |||||||
| chr4:153233895 | C | G | 1 | a0001c0001t0002g0002 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.30+29335C>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153233895 | |||||||
| chr4:153233899 | C | T | 1 | a0001c0002t0005g0154 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.30+29339C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153233899 | |||||||
| chr4:153234228 | C | T | 4 | a0001c0001t0009g0060 a0001c0001t0009g0263 a0001c0001t0009g0264 others(1): Show |
4 | HG01891.hp1 HG02280.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.30+29668C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153234228 | |||||||
| chr4:153234265 | T | C | 95 | a0001c0001t0001g0017 a0001c0001t0001g0033 a0001c0001t0001g0039 others(92): Show |
95 | HG00323.hp1 HG00438.hp2 HG00741.hp1 others(92): Show |
intron_variant | MODIFIER | c.30+29705T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153234265 | |||||||
| chr4:153234314 | G | C | 1 | a0001c0001t0001g0151 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.30+29754G>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153234314 | |||||||
| chr4:153234643 | C | T | 1 | a0001c0001t0002g0002 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.30+30083C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153234643 | |||||||
| chr4:153234934 | C | A | 2 | a0001c0003t0007g0224 a0001c0003t0007g0225 |
2 | HG01106.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.30+30374C>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153234934 | |||||||
| chr4:153234980 | C | G | 2 | a0001c0003t0014g0076 a0001c0003t0014g0077 |
2 | HG02818.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.30+30420C>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153234980 | |||||||
| chr4:153235058 | G | C | 2 | a0001c0003t0007g0224 a0001c0003t0007g0225 |
2 | HG01106.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.30+30498G>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153235058 | |||||||
| chr4:153235244 | C | G | 1 | a0001c0003t0003g0054 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.30+30684C>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153235244 | |||||||
| chr4:153235288 | A | AT | 48 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0001g0206 others(45): Show |
48 | HG01106.hp2 HG01169.hp1 HG01496.hp1 others(45): Show |
intron_variant | MODIFIER | c.30+30742dupT | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153235288 | ||||||
| chr4:153235325 | C | A | 1 | a0001c0001t0003g0175 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.30+30765C>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153235325 | |||||||
| chr4:153235353 | C | T | 26 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0002g0018 others(23): Show |
26 | HG01169.hp1 HG01496.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.30+30793C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153235353 | |||||||
| chr4:153235730 | G | T | 1 | a0001c0002t0023g0014 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.30+31170G>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153235730 | |||||||
| chr4:153235777 | G | T | 1 | a0001c0003t0001g0132 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.30+31217G>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153235777 | |||||||
| chr4:153235975 | G | A | 16 | a0001c0002t0001g0229 a0001c0002t0002g0152 a0001c0003t0001g0027 others(13): Show |
16 | HG00323.hp1 HG00741.hp1 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.30+31415G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153235975 | |||||||
| chr4:153235988 | G | A | 1 | a0001c0002t0023g0014 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.30+31428G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153235988 | |||||||
| chr4:153236348 | T | C | 1 | a0001c0003t0001g0131 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.30+31788T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153236348 | |||||||
| chr4:153236392 | T | C | 45 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0151 others(42): Show |
45 | HG00323.hp1 HG00735.hp2 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.30+31832T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153236392 | |||||||
| chr4:153236505 | T | C | 1 | a0001c0001t0005g0214 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.30+31945T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153236505 | |||||||
| chr4:153236573 | T | C | 11 | a0001c0001t0001g0033 a0001c0001t0003g0035 a0001c0001t0003g0036 others(8): Show |
11 | HG03831.hp2 NA18944.hp2 NA18979.hp2 others(8): Show |
intron_variant | MODIFIER | c.30+32013T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153236573 | |||||||
| chr4:153236658 | T | TTTTTC | 30 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0001g0151 others(27): Show |
30 | HG01169.hp1 HG01496.hp1 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.30+32123_30+32127d others(7): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153236658 | ||||||
| chr4:153236658 | T | TTTTTCTT others(3): Show |
32 | a0001c0001t0001g0017 a0001c0001t0001g0033 a0001c0001t0003g0016 others(29): Show |
32 | HG00323.hp1 HG01074.hp1 HG01517.hp1 others(29): Show |
intron_variant | MODIFIER | c.30+32118_30+32127d others(12): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153236658 | ||||||
| chr4:153236658 | T | TTTTTCTT others(8): Show |
16 | a0001c0002t0003g0144 a0001c0003t0001g0027 a0001c0003t0002g0004 others(13): Show |
16 | HG00741.hp1 HG01069.hp1 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.30+32113_30+32127d others(17): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153236658 | ||||||
| chr4:153236658 | T | TTTTTCTT others(13): Show |
6 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0003t0003g0053 others(3): Show |
6 | HG02818.hp1 HG03139.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.30+32108_30+32127d others(22): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153236658 | ||||||
| chr4:153236658 | TTTTTC | T | 3 | a0001c0001t0002g0001 a0001c0001t0006g0143 a0001c0003t0003g0064 |
3 | HG02976.hp1 HG03209.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.30+32123_30+32127d others(7): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153236658 | ||||||
| chr4:153236658 | TTTTTCTT others(3): Show |
T | 4 | a0001c0001t0009g0060 a0001c0001t0009g0263 a0001c0001t0009g0264 others(1): Show |
4 | HG01891.hp1 HG02280.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.30+32118_30+32127d others(12): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153236658 | ||||||
| chr4:153236713 | C | T | 8 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0092 others(5): Show |
8 | HG00438.hp2 HG00544.hp2 HG02080.hp1 others(5): Show |
intron_variant | MODIFIER | c.30+32153C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153236713 | |||||||
| chr4:153236883 | G | A | 16 | a0001c0001t0001g0033 a0001c0001t0003g0035 a0001c0001t0003g0036 others(13): Show |
16 | HG02896.hp2 HG02897.hp2 HG03831.hp2 others(13): Show |
intron_variant | MODIFIER | c.30+32323G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153236883 | |||||||
| chr4:153237087 | A | G | 12 | a0001c0001t0001g0033 a0001c0001t0003g0035 a0001c0001t0003g0036 others(9): Show |
12 | HG03831.hp2 NA18944.hp2 NA18979.hp2 others(9): Show |
intron_variant | MODIFIER | c.30+32527A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153237087 | |||||||
| chr4:153237108 | G | C | 1 | a0001c0002t0033g0234 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.30+32548G>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153237108 | |||||||
| chr4:153237182 | A | C | 1 | a0001c0001t0002g0002 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.30+32622A>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153237182 | |||||||
| chr4:153237360 | G | A | 4 | a0001c0001t0009g0060 a0001c0001t0009g0263 a0001c0001t0009g0264 others(1): Show |
4 | HG01891.hp1 HG02280.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.30+32800G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153237360 | |||||||
| chr4:153237384 | T | TAA | 166 | a0001c0001t0001g0017 a0001c0001t0001g0033 a0001c0001t0001g0055 others(163): Show |
166 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.30+32828_30+32829d others(4): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153237384 | ||||||
| chr4:153237455 | C | T | 2 | a0001c0002t0002g0089 a0001c0002t0002g0090 |
2 | HG00735.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.31-32880C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153237455 | |||||||
| chr4:153237537 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.31-32798G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153237537 | |||||||
| chr4:153237541 | G | A | 1 | a0001c0001t0006g0143 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.31-32794G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153237541 | |||||||
| chr4:153237756 | A | G | 50 | a0001c0001t0001g0017 a0001c0001t0001g0062 a0001c0001t0001g0063 others(47): Show |
50 | HG00323.hp1 HG00735.hp2 HG00741.hp1 others(47): Show |
intron_variant | MODIFIER | c.31-32579A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153237756 | |||||||
| chr4:153237811 | GTTATACA others(4): Show |
G | 24 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0002g0018 others(21): Show |
24 | HG01169.hp1 HG01496.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.31-32509_31-32499d others(13): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153237811 | ||||||
| chr4:153237859 | C | CAAAAAAA others(5): Show |
1 | a0001c0002t0004g0172 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.31-32475_31-32464d others(14): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153237859 | ||||||
| chr4:153237979 | G | A | 1 | a0001c0001t0002g0002 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.31-32356G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153237979 | |||||||
| chr4:153237986 | A | C | 95 | a0001c0001t0001g0017 a0001c0001t0001g0033 a0001c0001t0001g0055 others(92): Show |
95 | HG00323.hp1 HG00735.hp2 HG00741.hp1 others(92): Show |
intron_variant | MODIFIER | c.31-32349A>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153237986 | |||||||
| chr4:153238265 | G | T | 5 | a0001c0001t0001g0151 a0001c0001t0005g0103 a0001c0001t0005g0242 others(2): Show |
5 | HG00735.hp2 HG03017.hp2 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.31-32070G>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153238265 | |||||||
| chr4:153238272 | C | T | 1 | a0001c0001t0002g0002 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.31-32063C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153238272 | |||||||
| chr4:153238377 | TA | T | 99 | a0001c0001t0001g0017 a0001c0001t0001g0033 a0001c0001t0001g0055 others(96): Show |
99 | HG00323.hp1 HG00735.hp2 HG00741.hp1 others(96): Show |
intron_variant | MODIFIER | c.31-31955delA | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153238377 | ||||||
| chr4:153238395 | G | A | 99 | a0001c0001t0001g0017 a0001c0001t0001g0033 a0001c0001t0001g0055 others(96): Show |
99 | HG00323.hp1 HG00735.hp2 HG00741.hp1 others(96): Show |
intron_variant | MODIFIER | c.31-31940G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153238395 | |||||||
| chr4:153238420 | T | C | 24 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0002g0018 others(21): Show |
24 | HG01169.hp1 HG01496.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.31-31915T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153238420 | |||||||
| chr4:153238620 | T | C | 1 | a0001c0001t0006g0143 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.31-31715T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153238620 | |||||||
| chr4:153238655 | A | G | 4 | a0001c0001t0005g0103 a0001c0001t0005g0242 a0001c0002t0002g0089 others(1): Show |
4 | HG00735.hp2 HG03017.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-31680A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153238655 | |||||||
| chr4:153238664 | T | C | 1 | a0001c0002t0023g0014 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.31-31671T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153238664 | |||||||
| chr4:153238716 | T | C | 15 | a0001c0001t0001g0033 a0001c0001t0003g0035 a0001c0001t0003g0036 others(12): Show |
15 | HG02896.hp2 HG02897.hp2 HG03831.hp2 others(12): Show |
intron_variant | MODIFIER | c.31-31619T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153238716 | |||||||
| chr4:153238733 | G | C | 49 | a0001c0001t0001g0017 a0001c0001t0001g0062 a0001c0001t0001g0063 others(46): Show |
49 | HG00323.hp1 HG00735.hp2 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.31-31602G>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153238733 | |||||||
| chr4:153238803 | C | A | 1 | a0001c0002t0003g0239 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.31-31532C>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153238803 | |||||||
| chr4:153238813 | C | T | 40 | a0001c0001t0001g0017 a0001c0001t0001g0062 a0001c0001t0001g0063 others(37): Show |
40 | HG00323.hp1 HG00741.hp1 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.31-31522C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153238813 | |||||||
| chr4:153238852 | G | A | 2 | a0001c0001t0010g0078 a0001c0002t0018g0135 |
2 | HG01891.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.31-31483G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153238852 | |||||||
| chr4:153238965 | C | T | 98 | a0001c0001t0001g0017 a0001c0001t0001g0033 a0001c0001t0001g0055 others(95): Show |
98 | HG00323.hp1 HG00735.hp2 HG00741.hp1 others(95): Show |
intron_variant | MODIFIER | c.31-31370C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153238965 | |||||||
| chr4:153239152 | A | T | 7 | a0001c0002t0001g0126 a0001c0002t0001g0210 a0001c0003t0002g0052 others(4): Show |
7 | HG01255.hp1 HG01993.hp2 HG02683.hp2 others(4): Show |
intron_variant | MODIFIER | c.31-31183A>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153239152 | |||||||
| chr4:153239215 | C | G | 98 | a0001c0001t0001g0017 a0001c0001t0001g0033 a0001c0001t0001g0055 others(95): Show |
98 | HG00323.hp1 HG00735.hp2 HG00741.hp1 others(95): Show |
intron_variant | MODIFIER | c.31-31120C>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153239215 | |||||||
| chr4:153239220 | C | T | 98 | a0001c0001t0001g0017 a0001c0001t0001g0033 a0001c0001t0001g0055 others(95): Show |
98 | HG00323.hp1 HG00735.hp2 HG00741.hp1 others(95): Show |
intron_variant | MODIFIER | c.31-31115C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153239220 | |||||||
| chr4:153239301 | G | A | 1 | a0001c0002t0002g0145 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.31-31034G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153239301 | |||||||
| chr4:153239351 | CA | C | 7 | a0001c0001t0001g0204 a0001c0001t0002g0002 a0001c0001t0008g0032 others(4): Show |
7 | HG02523.hp1 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.31-30968delA | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153239351 | ||||||
| chr4:153239351 | CAA | C | 89 | a0001c0001t0001g0017 a0001c0001t0001g0033 a0001c0001t0001g0055 others(86): Show |
89 | HG00323.hp1 HG00735.hp2 HG00741.hp1 others(86): Show |
intron_variant | MODIFIER | c.31-30969_31-30968d others(4): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153239351 | ||||||
| chr4:153239371 | C | T | 15 | a0001c0001t0001g0033 a0001c0001t0003g0035 a0001c0001t0003g0036 others(12): Show |
15 | HG02896.hp2 HG02897.hp2 HG03831.hp2 others(12): Show |
intron_variant | MODIFIER | c.31-30964C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153239371 | |||||||
| chr4:153239418 | GCT | G | 20 | a0001c0001t0001g0033 a0001c0001t0001g0179 a0001c0001t0002g0245 others(17): Show |
20 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(17): Show |
intron_variant | MODIFIER | c.31-30894_31-30893d others(4): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153239418 | ||||||
| chr4:153239418 | GCTCT | G | 18 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0006g0019 others(15): Show |
18 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.31-30896_31-30893d others(6): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153239418 | ||||||
| chr4:153239418 | GCTCTCT | G | 4 | a0001c0002t0033g0234 a0001c0003t0007g0223 a0001c0003t0007g0224 others(1): Show |
4 | HG01074.hp2 HG01106.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.31-30898_31-30893d others(8): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153239418 | ||||||
| chr4:153239489 | G | T | 39 | a0001c0001t0001g0033 a0001c0001t0001g0055 a0001c0001t0001g0081 others(36): Show |
39 | HG01169.hp1 HG01496.hp1 HG01891.hp2 others(36): Show |
intron_variant | MODIFIER | c.31-30846G>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153239489 | |||||||
| chr4:153239547 | C | T | 1 | a0001c0001t0002g0002 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.31-30788C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153239547 | |||||||
| chr4:153239832 | C | CT | 5 | a0001c0001t0009g0060 a0001c0001t0009g0263 a0001c0001t0009g0264 others(2): Show |
5 | HG01891.hp1 HG02280.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-30502dupT | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153239832 | ||||||
| chr4:153239832 | C | CTT | 79 | a0001c0001t0001g0017 a0001c0001t0001g0033 a0001c0001t0001g0055 others(76): Show |
79 | HG00323.hp1 HG01069.hp1 HG01074.hp1 others(76): Show |
intron_variant | MODIFIER | c.31-30502_31-30501i others(4): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153239832 | ||||||
| chr4:153239832 | C | CTTT | 3 | a0001c0001t0006g0143 a0001c0003t0007g0223 a0001c0003t0007g0224 |
3 | HG01074.hp2 HG03209.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.31-30502_31-30501i others(5): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153239832 | ||||||
| chr4:153239832 | C | CTTTT | 7 | a0001c0001t0001g0151 a0001c0001t0004g0088 a0001c0001t0005g0103 others(4): Show |
7 | HG00735.hp2 HG02055.hp2 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.31-30502_31-30501i others(6): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153239832 | ||||||
| chr4:153239834 | C | CT | 25 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(22): Show |
25 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(22): Show |
intron_variant | MODIFIER | c.31-30483dupT | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153239834 | ||||||
| chr4:153239834 | C | T | 57 | a0001c0001t0001g0033 a0001c0001t0001g0055 a0001c0001t0001g0081 others(54): Show |
57 | HG00735.hp2 HG00741.hp1 HG01074.hp2 others(54): Show |
intron_variant | MODIFIER | c.31-30501C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153239834 | |||||||
| chr4:153239867 | C | T | 3 | a0001c0001t0004g0087 a0001c0001t0004g0088 a0001c0002t0003g0144 |
3 | HG02055.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.31-30468C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153239867 | |||||||
| chr4:153239981 | C | A | 1 | a0001c0002t0002g0260 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.31-30354C>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153239981 | |||||||
| chr4:153239982 | G | A | 5 | a0001c0001t0009g0060 a0001c0001t0009g0263 a0001c0001t0009g0264 others(2): Show |
5 | HG01891.hp1 HG02280.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-30353G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153239982 | |||||||
| chr4:153239990 | C | T | 39 | a0001c0001t0001g0033 a0001c0001t0001g0055 a0001c0001t0001g0081 others(36): Show |
39 | HG01169.hp1 HG01496.hp1 HG01891.hp2 others(36): Show |
intron_variant | MODIFIER | c.31-30345C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153239990 | |||||||
| chr4:153240023 | A | G | 162 | a0001c0001t0001g0017 a0001c0001t0001g0033 a0001c0001t0001g0055 others(159): Show |
162 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.31-30312A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153240023 | |||||||
| chr4:153240085 | C | T | 1 | a0001c0002t0002g0114 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.31-30250C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153240085 | |||||||
| chr4:153240133 | C | A | 2 | a0001c0001t0001g0156 a0001c0009t0003g0159 |
2 | HG02129.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.31-30202C>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153240133 | |||||||
| chr4:153240243 | A | G | 26 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(23): Show |
26 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(23): Show |
intron_variant | MODIFIER | c.31-30092A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153240243 | |||||||
| chr4:153240334 | C | T | 7 | a0001c0002t0002g0130 a0001c0002t0002g0136 a0001c0002t0002g0137 others(4): Show |
7 | HG02145.hp1 HG02486.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.31-30001C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153240334 | |||||||
| chr4:153240436 | C | G | 2 | a0001c0002t0017g0095 a0001c0002t0017g0096 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.31-29899C>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153240436 | |||||||
| chr4:153240450 | C | T | 1 | a0001c0001t0002g0002 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.31-29885C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153240450 | |||||||
| chr4:153240533 | G | T | 2 | a0001c0001t0001g0189 a0001c0001t0001g0190 |
2 | HG01175.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.31-29802G>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153240533 | |||||||
| chr4:153240582 | C | T | 1 | a0001c0001t0002g0002 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.31-29753C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153240582 | |||||||
| chr4:153240613 | C | T | 3 | a0001c0001t0004g0087 a0001c0001t0004g0088 a0001c0002t0003g0144 |
3 | HG02055.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.31-29722C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153240613 | |||||||
| chr4:153240645 | T | G | 98 | a0001c0001t0001g0017 a0001c0001t0001g0033 a0001c0001t0001g0055 others(95): Show |
98 | HG00323.hp1 HG00735.hp2 HG00741.hp1 others(95): Show |
intron_variant | MODIFIER | c.31-29690T>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153240645 | |||||||
| chr4:153240853 | C | T | 2 | a0001c0001t0002g0001 a0001c0003t0003g0064 |
2 | HG02976.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.31-29482C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153240853 | |||||||
| chr4:153240970 | C | T | 4 | a0001c0001t0001g0113 a0001c0001t0001g0158 a0001c0001t0001g0219 others(1): Show |
4 | NA18998.hp1 NA19002.hp2 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-29365C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153240970 | |||||||
| chr4:153241143 | G | T | 25 | a0001c0001t0001g0227 a0001c0001t0001g0253 a0001c0001t0001g0255 others(22): Show |
25 | HG00140.hp2 HG00558.hp2 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.31-29192G>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153241143 | |||||||
| chr4:153241232 | C | T | 59 | a0001c0001t0001g0017 a0001c0001t0001g0062 a0001c0001t0001g0063 others(56): Show |
59 | HG00323.hp1 HG00735.hp2 HG00741.hp1 others(56): Show |
intron_variant | MODIFIER | c.31-29103C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153241232 | |||||||
| chr4:153241301 | G | A | 2 | a0001c0001t0001g0162 a0001c0001t0006g0143 |
2 | HG03209.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.31-29034G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153241301 | |||||||
| chr4:153241368 | A | C | 1 | a0001c0001t0002g0002 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.31-28967A>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153241368 | |||||||
| chr4:153241398 | C | G | 1 | a0001c0002t0033g0234 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.31-28937C>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153241398 | |||||||
| chr4:153241554 | G | A | 17 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0006g0019 others(14): Show |
17 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.31-28781G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153241554 | |||||||
| chr4:153241554 | G | T | 1 | a0001c0002t0001g0116 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.31-28781G>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153241554 | |||||||
| chr4:153241705 | T | A | 2 | a0001c0001t0001g0099 a0001c0001t0001g0100 |
2 | HG01261.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.31-28630T>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153241705 | |||||||
| chr4:153241726 | C | T | 52 | a0001c0001t0001g0017 a0001c0001t0001g0033 a0001c0001t0001g0062 others(49): Show |
52 | HG00323.hp1 HG00741.hp1 HG01069.hp1 others(49): Show |
intron_variant | MODIFIER | c.31-28609C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153241726 | |||||||
| chr4:153241740 | G | T | 3 | a0001c0002t0011g0005 a0001c0002t0011g0006 a0001c0002t0011g0070 |
3 | HG02896.hp2 HG02897.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.31-28595G>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153241740 | |||||||
| chr4:153241780 | A | G | 44 | a0001c0001t0001g0017 a0001c0001t0001g0062 a0001c0001t0001g0063 others(41): Show |
44 | HG00323.hp1 HG00741.hp1 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.31-28555A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153241780 | |||||||
| chr4:153241802 | A | G | 1 | a0001c0001t0006g0143 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.31-28533A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153241802 | |||||||
| chr4:153241815 | C | T | 1 | a0001c0002t0033g0234 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.31-28520C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153241815 | |||||||
| chr4:153241861 | C | G | 1 | a0001c0002t0023g0014 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.31-28474C>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153241861 | |||||||
| chr4:153241870 | C | T | 1 | a0001c0001t0001g0162 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.31-28465C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153241870 | |||||||
| chr4:153242018 | G | A | 12 | a0001c0001t0001g0033 a0001c0001t0003g0035 a0001c0001t0003g0036 others(9): Show |
12 | HG03831.hp2 NA18944.hp2 NA18979.hp2 others(9): Show |
intron_variant | MODIFIER | c.31-28317G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153242018 | |||||||
| chr4:153242132 | C | T | 72 | a0001c0001t0001g0017 a0001c0001t0001g0055 a0001c0001t0001g0062 others(69): Show |
72 | HG00323.hp1 HG00735.hp2 HG00741.hp1 others(69): Show |
intron_variant | MODIFIER | c.31-28203C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153242132 | |||||||
| chr4:153242153 | C | G | 25 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0003g0232 others(22): Show |
25 | HG01168.hp1 HG01496.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.31-28182C>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153242153 | |||||||
| chr4:153242242 | T | C | 94 | a0001c0001t0001g0017 a0001c0001t0001g0033 a0001c0001t0001g0055 others(91): Show |
94 | HG00323.hp1 HG00735.hp2 HG00741.hp1 others(91): Show |
intron_variant | MODIFIER | c.31-28093T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153242242 | |||||||
| chr4:153242318 | C | CT | 5 | a0001c0001t0006g0143 a0001c0002t0033g0234 a0001c0003t0007g0223 others(2): Show |
5 | HG01074.hp2 HG01106.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-28005dupT | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153242318 | ||||||
| chr4:153242318 | CT | C | 47 | a0001c0001t0001g0017 a0001c0001t0001g0062 a0001c0001t0001g0063 others(44): Show |
47 | HG00323.hp1 HG00741.hp1 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.31-28005delT | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153242318 | ||||||
| chr4:153242318 | CTT | C | 25 | a0001c0001t0001g0033 a0001c0001t0001g0151 a0001c0001t0002g0002 others(22): Show |
25 | HG00735.hp2 HG01169.hp1 HG02895.hp2 others(22): Show |
intron_variant | MODIFIER | c.31-28006_31-28005d others(4): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153242318 | ||||||
| chr4:153242946 | G | A | 1 | a0001c0001t0003g0232 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.31-27389G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153242946 | |||||||
| chr4:153243092 | T | C | 15 | a0001c0001t0001g0033 a0001c0001t0002g0018 a0001c0001t0002g0022 others(12): Show |
15 | HG01169.hp1 HG02895.hp2 HG02897.hp1 others(12): Show |
intron_variant | MODIFIER | c.31-27243T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153243092 | |||||||
| chr4:153243098 | A | G | 1 | a0001c0002t0024g0128 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.31-27237A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153243098 | |||||||
| chr4:153243211 | C | G | 1 | a0001c0002t0003g0144 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.31-27124C>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153243211 | |||||||
| chr4:153243355 | G | A | 1 | a0001c0001t0006g0086 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.31-26980G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153243355 | |||||||
| chr4:153243418 | G | A | 24 | a0001c0001t0001g0033 a0001c0001t0002g0002 a0001c0001t0002g0018 others(21): Show |
24 | HG01169.hp1 HG01891.hp1 HG02280.hp2 others(21): Show |
intron_variant | MODIFIER | c.31-26917G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153243418 | |||||||
| chr4:153243529 | C | T | 1 | a0001c0001t0020g0228 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.31-26806C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153243529 | |||||||
| chr4:153243562 | A | G | 1 | a0001c0001t0002g0002 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.31-26773A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153243562 | |||||||
| chr4:153243615 | T | C | 1 | a0001c0002t0033g0234 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.31-26720T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153243615 | |||||||
| chr4:153243677 | A | G | 24 | a0001c0001t0001g0033 a0001c0001t0002g0002 a0001c0001t0002g0018 others(21): Show |
24 | HG01169.hp1 HG01891.hp1 HG02280.hp2 others(21): Show |
intron_variant | MODIFIER | c.31-26658A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153243677 | |||||||
| chr4:153243792 | T | C | 3 | a0001c0003t0007g0223 a0001c0003t0007g0224 a0001c0003t0007g0225 |
3 | HG01074.hp2 HG01106.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.31-26543T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153243792 | |||||||
| chr4:153243807 | C | CT | 20 | a0001c0001t0001g0081 a0001c0001t0001g0120 a0001c0001t0001g0182 others(17): Show |
20 | HG00735.hp1 HG00741.hp2 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.31-26517dupT | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153243807 | ||||||
| chr4:153243807 | CT | C | 23 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0112 others(20): Show |
23 | HG00140.hp1 HG00323.hp2 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.31-26517delT | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153243807 | ||||||
| chr4:153243817 | T | C | 1 | a0001c0003t0014g0076 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.31-26518T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153243817 | |||||||
| chr4:153243818 | T | C | 16 | a0001c0001t0005g0110 a0001c0001t0005g0161 a0001c0001t0005g0252 others(13): Show |
16 | HG00323.hp2 HG01255.hp1 HG02080.hp2 others(13): Show |
intron_variant | MODIFIER | c.31-26517T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153243818 | |||||||
| chr4:153243818 | T | TC | 15 | a0001c0001t0001g0158 a0001c0001t0001g0196 a0001c0001t0001g0253 others(12): Show |
15 | HG01109.hp1 HG01255.hp2 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.31-26507dupC | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153243818 | ||||||
| chr4:153243818 | TC | T | 66 | a0001c0001t0001g0017 a0001c0001t0001g0033 a0001c0001t0001g0062 others(63): Show |
66 | HG00323.hp1 HG00741.hp1 HG01069.hp1 others(63): Show |
intron_variant | MODIFIER | c.31-26507delC | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153243818 | ||||||
| chr4:153243819 | C | T | 36 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0001g0099 others(33): Show |
36 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.31-26516C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153243819 | |||||||
| chr4:153243820 | C | T | 61 | a0001c0001t0001g0033 a0001c0001t0001g0055 a0001c0001t0001g0081 others(58): Show |
61 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(58): Show |
intron_variant | MODIFIER | c.31-26515C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153243820 | |||||||
| chr4:153243821 | C | T | 24 | a0001c0001t0001g0033 a0001c0001t0002g0002 a0001c0001t0002g0018 others(21): Show |
24 | HG01169.hp1 HG01891.hp1 HG02280.hp2 others(21): Show |
intron_variant | MODIFIER | c.31-26514C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153243821 | |||||||
| chr4:153243822 | C | T | 19 | a0001c0001t0001g0033 a0001c0001t0002g0018 a0001c0001t0002g0022 others(16): Show |
19 | HG01169.hp1 HG01891.hp1 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.31-26513C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153243822 | |||||||
| chr4:153243826 | C | G | 40 | a0001c0001t0001g0017 a0001c0001t0001g0062 a0001c0001t0001g0063 others(37): Show |
40 | HG00323.hp1 HG00741.hp1 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.31-26509C>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153243826 | |||||||
| chr4:153243827 | C | G | 2 | a0001c0001t0001g0156 a0001c0009t0003g0159 |
2 | HG02129.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.31-26508C>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153243827 | |||||||
| chr4:153243827 | C | T | 13 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(10): Show |
13 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.31-26508C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153243827 | |||||||
| chr4:153244012 | G | T | 1 | a0001c0002t0023g0014 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.31-26323G>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244012 | |||||||
| chr4:153244116 | C | G | 1 | a0001c0002t0033g0234 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.31-26219C>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244116 | |||||||
| chr4:153244121 | A | G | 1 | a0001c0002t0033g0234 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.31-26214A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244121 | |||||||
| chr4:153244122 | T | C | 1 | a0001c0002t0033g0234 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.31-26213T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244122 | |||||||
| chr4:153244134 | TCTTCTTC others(44): Show |
T | 23 | a0001c0001t0001g0033 a0001c0001t0002g0002 a0001c0001t0002g0018 others(20): Show |
23 | HG01169.hp1 HG01891.hp1 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.31-26191_31-26141d others(53): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244134 | ||||||
| chr4:153244135 | CTTCTTCT others(2): Show |
C | 3 | a0001c0001t0001g0091 a0001c0002t0002g0246 a0001c0002t0002g0248 |
3 | HG02080.hp2 NA18942.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.31-26182_31-26174d others(11): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244135 | ||||||
| chr4:153244140 | TCTTGTTC others(38): Show |
T | 1 | a0001c0002t0003g0144 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.31-26191_31-26147d others(47): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244140 | ||||||
| chr4:153244144 | G | C | 3 | a0001c0002t0002g0181 a0001c0002t0019g0180 a0001c0002t0033g0234 |
3 | HG02523.hp1 HG03098.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.31-26191G>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244144 | |||||||
| chr4:153244144 | G | GTTC | 2 | a0001c0001t0001g0101 a0001c0002t0002g0145 |
2 | HG02559.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.31-26185_31-26183d others(5): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244144 | ||||||
| chr4:153244144 | G | GTTCTTCT others(2): Show |
5 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0241 others(2): Show |
5 | HG00280.hp2 HG01261.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.31-26183_31-26182i others(11): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244144 | ||||||
| chr4:153244144 | G | GTTCTTCT others(11): Show |
1 | a0001c0001t0001g0102 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.31-26183_31-26182i others(20): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244144 | ||||||
| chr4:153244150 | CTTG | C | 24 | a0001c0001t0001g0227 a0001c0001t0001g0258 a0001c0001t0002g0153 others(21): Show |
24 | HG00140.hp2 HG00544.hp1 HG00558.hp2 others(21): Show |
intron_variant | MODIFIER | c.31-26182_31-26180d others(5): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244150 | ||||||
| chr4:153244153 | G | C | 15 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(12): Show |
15 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.31-26182G>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244153 | |||||||
| chr4:153244153 | G | GTTC | 8 | a0001c0001t0001g0200 a0001c0002t0001g0126 a0001c0002t0001g0210 others(5): Show |
8 | HG01255.hp1 HG01993.hp2 HG02683.hp2 others(5): Show |
intron_variant | MODIFIER | c.31-26156_31-26154d others(5): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244153 | ||||||
| chr4:153244153 | GTTC | G | 3 | a0001c0001t0001g0174 a0001c0001t0001g0203 a0001c0003t0001g0132 |
3 | HG00558.hp1 HG03486.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.31-26156_31-26154d others(5): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244153 | ||||||
| chr4:153244159 | C | G | 1 | a0001c0001t0001g0186 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.31-26176C>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244159 | |||||||
| chr4:153244162 | C | G | 2 | a0001c0002t0002g0267 a0001c0002t0002g0268 |
2 | HG02109.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.31-26173C>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244162 | |||||||
| chr4:153244173 | T | G | 1 | a0001c0002t0033g0234 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.31-26162T>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244173 | |||||||
| chr4:153244178 | T | C | 1 | a0001c0002t0019g0180 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.31-26157T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244178 | |||||||
| chr4:153244179 | T | C | 41 | a0001c0001t0001g0017 a0001c0001t0001g0062 a0001c0001t0001g0063 others(38): Show |
41 | HG00323.hp1 HG00741.hp1 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.31-26156T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244179 | |||||||
| chr4:153244179 | T | G | 1 | a0001c0002t0033g0234 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.31-26156T>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244179 | |||||||
| chr4:153244182 | C | T | 2 | a0001c0001t0005g0214 a0001c0002t0033g0234 |
2 | HG03098.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.31-26153C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244182 | |||||||
| chr4:153244185 | C | G | 1 | a0001c0002t0033g0234 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.31-26150C>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244185 | |||||||
| chr4:153244190 | T | C | 2 | a0001c0002t0002g0181 a0001c0002t0019g0180 |
2 | HG02523.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.31-26145T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244190 | |||||||
| chr4:153244193 | TTCTCCTC others(119): Show |
T | 1 | a0001c0002t0033g0234 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.31-26138_31-26013d others(2): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244193 | ||||||
| chr4:153244197 | C | T | 24 | a0001c0001t0001g0033 a0001c0001t0002g0002 a0001c0001t0002g0018 others(21): Show |
24 | HG01169.hp1 HG01891.hp1 HG02280.hp2 others(21): Show |
intron_variant | MODIFIER | c.31-26138C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244197 | |||||||
| chr4:153244222 | C | CTT | 5 | a0001c0002t0002g0181 a0001c0002t0012g0163 a0001c0002t0012g0177 others(2): Show |
5 | HG02523.hp1 NA18948.hp2 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-26112_31-26111i others(4): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244222 | ||||||
| chr4:153244230 | T | C | 5 | a0001c0002t0002g0181 a0001c0002t0012g0163 a0001c0002t0012g0177 others(2): Show |
5 | HG02523.hp1 NA18948.hp2 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-26105T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244230 | |||||||
| chr4:153244233 | T | C | 5 | a0001c0002t0002g0181 a0001c0002t0012g0163 a0001c0002t0012g0177 others(2): Show |
5 | HG02523.hp1 NA18948.hp2 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-26102T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244233 | |||||||
| chr4:153244236 | CTT | C | 3 | a0001c0002t0012g0163 a0001c0002t0012g0177 a0001c0002t0012g0178 |
3 | NA18948.hp2 NA19011.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.31-26098_31-26097d others(4): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244236 | |||||||
| chr4:153244236 | CTTCTCCT others(134): Show |
C | 24 | a0001c0001t0001g0033 a0001c0001t0002g0002 a0001c0001t0002g0018 others(21): Show |
24 | HG01169.hp1 HG01891.hp1 HG02280.hp2 others(21): Show |
intron_variant | MODIFIER | c.31-26098_31-25958d others(2): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244236 | |||||||
| chr4:153244237 | T | C | 2 | a0001c0002t0002g0181 a0001c0002t0019g0180 |
2 | HG02523.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.31-26098T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244237 | |||||||
| chr4:153244238 | T | C | 1 | a0001c0001t0005g0214 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.31-26097T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244238 | |||||||
| chr4:153244240 | T | C | 2 | a0001c0002t0002g0181 a0001c0002t0019g0180 |
2 | HG02523.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.31-26095T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244240 | |||||||
| chr4:153244241 | C | T | 2 | a0001c0002t0002g0181 a0001c0002t0019g0180 |
2 | HG02523.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.31-26094C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244241 | |||||||
| chr4:153244242 | CT | C | 3 | a0001c0002t0012g0163 a0001c0002t0012g0177 a0001c0002t0012g0178 |
3 | NA18948.hp2 NA19011.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.31-26091delT | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244242 | ||||||
| chr4:153244243 | T | C | 2 | a0001c0002t0002g0181 a0001c0002t0019g0180 |
2 | HG02523.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.31-26092T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244243 | |||||||
| chr4:153244249 | T | C | 5 | a0001c0002t0002g0181 a0001c0002t0012g0163 a0001c0002t0012g0177 others(2): Show |
5 | HG02523.hp1 NA18948.hp2 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-26086T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244249 | |||||||
| chr4:153244251 | CT | C | 3 | a0001c0002t0012g0163 a0001c0002t0012g0177 a0001c0002t0012g0178 |
3 | NA18948.hp2 NA19011.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.31-26081delT | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244251 | ||||||
| chr4:153244252 | T | C | 3 | a0001c0002t0002g0181 a0001c0002t0002g0248 a0001c0002t0019g0180 |
3 | HG02523.hp1 NA18942.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.31-26083T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244252 | |||||||
| chr4:153244253 | T | C | 4 | a0001c0002t0002g0248 a0001c0002t0012g0163 a0001c0002t0012g0177 others(1): Show |
4 | NA18942.hp2 NA18948.hp2 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-26082T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244253 | |||||||
| chr4:153244253 | T | TTCC | 4 | a0001c0001t0001g0092 a0001c0001t0001g0193 a0001c0002t0001g0127 others(1): Show |
4 | HG01169.hp2 HG01516.hp2 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.31-26016_31-26014d others(5): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244253 | ||||||
| chr4:153244253 | T | TTCCTCC | 7 | a0001c0001t0001g0039 a0001c0001t0002g0065 a0001c0001t0004g0104 others(4): Show |
7 | HG02027.hp2 HG02080.hp1 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.31-26019_31-26014d others(8): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244253 | ||||||
| chr4:153244253 | T | TTCCTCCT others(2): Show |
7 | a0001c0001t0001g0179 a0001c0001t0001g0199 a0001c0001t0001g0219 others(4): Show |
7 | HG01993.hp1 HG02965.hp2 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.31-26022_31-26014d others(11): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244253 | ||||||
| chr4:153244253 | T | TTCCTCCT others(5): Show |
7 | a0001c0001t0001g0023 a0001c0001t0001g0040 a0001c0001t0001g0121 others(4): Show |
7 | HG00438.hp2 HG01346.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.31-26025_31-26014d others(14): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244253 | ||||||
| chr4:153244253 | T | TTCCTCCT others(23): Show |
1 | a0001c0001t0002g0001 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.31-26067_31-26066i others(32): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244253 | ||||||
| chr4:153244253 | T | TTCCTCCT others(29): Show |
1 | a0001c0003t0003g0064 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.31-26067_31-26066i others(38): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244253 | ||||||
| chr4:153244253 | T | TTCCTCCT others(14): Show |
2 | a0001c0002t0002g0050 a0001c0003t0002g0052 |
2 | HG02738.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.31-26034_31-26014d others(23): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244253 | ||||||
| chr4:153244253 | T | TTCCTCCT others(17): Show |
1 | a0001c0002t0005g0251 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.31-26037_31-26014d others(26): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244253 | ||||||
| chr4:153244253 | T | TTCCTCCT others(35): Show |
1 | a0001c0002t0004g0083 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.31-26055_31-26014d others(44): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244253 | ||||||
| chr4:153244253 | T | TTCCTCCT others(38): Show |
1 | a0001c0002t0002g0254 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.31-26058_31-26014d others(47): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244253 | ||||||
| chr4:153244253 | TTCCTCCT others(11): Show |
T | 1 | a0001c0001t0001g0101 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.31-26031_31-26014d others(20): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244253 | ||||||
| chr4:153244253 | TTCCTCCT others(14): Show |
T | 1 | a0001c0001t0001g0241 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.31-26034_31-26014d others(23): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244253 | ||||||
| chr4:153244253 | TTCCTCCT others(17): Show |
T | 1 | a0001c0001t0001g0091 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.31-26037_31-26014d others(26): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244253 | ||||||
| chr4:153244256 | C | CTCCTCCT others(52): Show |
1 | a0001c0002t0001g0126 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.31-26021_31-26020i others(61): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244256 | ||||||
| chr4:153244259 | C | T | 29 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0001g0099 others(26): Show |
29 | HG00642.hp2 HG00735.hp2 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.31-26076C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244259 | |||||||
| chr4:153244262 | C | T | 3 | a0001c0002t0002g0171 a0001c0002t0022g0140 a0001c0002t0028g0080 |
3 | HG01168.hp1 HG02145.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.31-26073C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244262 | |||||||
| chr4:153244264 | C | CCTCCTCC others(31): Show |
1 | a0001c0002t0002g0259 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.31-26056_31-26055i others(40): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244264 | ||||||
| chr4:153244265 | C | T | 29 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0001g0099 others(26): Show |
29 | HG00642.hp2 HG00735.hp2 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.31-26070C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244265 | |||||||
| chr4:153244268 | C | T | 2 | a0001c0001t0001g0151 a0001c0002t0002g0171 |
2 | HG01168.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.31-26067C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244268 | |||||||
| chr4:153244271 | C | T | 17 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0010g0078 others(14): Show |
17 | HG01891.hp2 HG02258.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.31-26064C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244271 | |||||||
| chr4:153244272 | T | C | 1 | a0001c0002t0001g0173 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.31-26063T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244272 | |||||||
| chr4:153244274 | C | T | 1 | a0001c0001t0001g0151 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.31-26061C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244274 | |||||||
| chr4:153244277 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.31-26058C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244277 | |||||||
| chr4:153244278 | T | C | 1 | a0001c0002t0001g0173 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.31-26057T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244278 | |||||||
| chr4:153244280 | C | T | 1 | a0001c0001t0001g0241 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.31-26055C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244280 | |||||||
| chr4:153244280 | CTCCTCCT others(62): Show |
C | 1 | a0001c0003t0003g0011 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.31-26052_31-25984d others(71): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244280 | ||||||
| chr4:153244283 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.31-26052C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244283 | |||||||
| chr4:153244283 | CTCCTCCT others(59): Show |
C | 1 | a0001c0003t0003g0042 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.31-26049_31-25984d others(68): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244283 | ||||||
| chr4:153244283 | CTCCTCCT others(62): Show |
C | 4 | a0001c0001t0006g0019 a0001c0002t0004g0045 a0001c0003t0001g0041 others(1): Show |
4 | HG02486.hp2 HG03098.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-26046_31-25978d others(71): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244283 | ||||||
| chr4:153244283 | CTCCTCCT others(71): Show |
C | 1 | a0001c0003t0003g0075 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.31-26049_31-25972d others(80): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244283 | ||||||
| chr4:153244286 | C | T | 1 | a0001c0001t0001g0241 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.31-26049C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244286 | |||||||
| chr4:153244286 | CTCCTCCT others(56): Show |
C | 5 | a0001c0003t0001g0132 a0001c0003t0002g0004 a0001c0003t0003g0026 others(2): Show |
5 | HG01069.hp1 HG01346.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-26046_31-25984d others(65): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244286 | ||||||
| chr4:153244286 | CTCCTCCT others(65): Show |
C | 10 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0002t0004g0046 others(7): Show |
10 | HG02055.hp1 HG02145.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.31-26046_31-25975d others(74): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244286 | ||||||
| chr4:153244286 | CTCCTCCT others(68): Show |
C | 4 | a0001c0001t0003g0016 a0001c0003t0014g0076 a0002c0006t0003g0012 others(1): Show |
4 | HG02818.hp1 HG02965.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-26046_31-25972d others(77): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244286 | ||||||
| chr4:153244286 | CTCCTCCT others(71): Show |
C | 1 | a0001c0001t0001g0017 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.31-26046_31-25969d others(80): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244286 | ||||||
| chr4:153244286 | CTCCTCCT others(74): Show |
C | 1 | a0001c0002t0004g0048 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.31-26046_31-25966d others(83): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244286 | ||||||
| chr4:153244287 | T | TCCTCCTC others(15): Show |
1 | a0001c0001t0005g0214 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.31-26046_31-26025d others(24): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244287 | ||||||
| chr4:153244289 | CTCCTCCT others(53): Show |
C | 11 | a0001c0002t0001g0229 a0001c0003t0001g0027 a0001c0003t0003g0015 others(8): Show |
11 | HG00323.hp1 HG00741.hp1 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.31-26043_31-25984d others(62): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244289 | ||||||
| chr4:153244295 | CTCCTCCT others(20): Show |
C | 1 | a0001c0003t0003g0028 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.31-26037_31-26011d others(29): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244295 | ||||||
| chr4:153244298 | CTCCTCCT others(32): Show |
C | 2 | a0001c0001t0002g0235 a0001c0001t0002g0240 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.31-26034_31-25996d others(41): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244298 | ||||||
| chr4:153244299 | T | C | 1 | a0001c0002t0023g0014 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.31-26036T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244299 | |||||||
| chr4:153244301 | C | T | 2 | a0001c0001t0001g0100 a0001c0002t0012g0178 |
2 | HG01261.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.31-26034C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244301 | |||||||
| chr4:153244304 | C | T | 5 | a0001c0001t0001g0100 a0001c0002t0012g0163 a0001c0002t0012g0177 others(2): Show |
5 | HG01261.hp2 NA18948.hp2 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-26031C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244304 | |||||||
| chr4:153244305 | T | C | 1 | a0001c0002t0023g0014 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.31-26030T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244305 | |||||||
| chr4:153244307 | C | T | 5 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0002t0012g0163 others(2): Show |
5 | HG01261.hp2 HG02300.hp2 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-26028C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244307 | |||||||
| chr4:153244307 | CTCCTCCT others(35): Show |
C | 1 | a0001c0003t0007g0225 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.31-26025_31-25984d others(44): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244307 | ||||||
| chr4:153244310 | C | T | 7 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0002t0002g0090 others(4): Show |
7 | HG01261.hp2 HG02300.hp2 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.31-26025C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244310 | |||||||
| chr4:153244310 | CTCCTCCT others(17): Show |
C | 1 | a0001c0003t0007g0224 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.31-26022_31-25999d others(26): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244310 | ||||||
| chr4:153244310 | CTCCTCCT others(26): Show |
C | 1 | a0001c0003t0007g0223 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.31-26022_31-25990d others(35): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244310 | ||||||
| chr4:153244311 | T | C | 1 | a0001c0002t0023g0014 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.31-26024T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244311 | |||||||
| chr4:153244313 | C | T | 6 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0002t0002g0090 others(3): Show |
6 | HG01261.hp2 HG02300.hp2 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.31-26022C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244313 | |||||||
| chr4:153244313 | CTCCTCCT others(14): Show |
C | 1 | a0001c0001t0006g0147 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.31-26019_31-25999d others(23): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244313 | ||||||
| chr4:153244313 | CTCCTCCT others(17): Show |
C | 1 | a0001c0001t0001g0213 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.31-26019_31-25996d others(26): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244313 | ||||||
| chr4:153244314 | T | C | 1 | a0001c0002t0005g0154 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.31-26021T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244314 | |||||||
| chr4:153244316 | C | T | 8 | a0001c0001t0001g0091 a0001c0001t0001g0099 a0001c0001t0001g0100 others(5): Show |
8 | HG01261.hp2 HG02300.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.31-26019C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244316 | |||||||
| chr4:153244316 | CTCCTCT | C | 3 | a0001c0001t0010g0078 a0001c0002t0002g0130 a0001c0002t0002g0141 |
3 | HG01891.hp2 HG02486.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.31-26016_31-26011d others(8): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244316 | ||||||
| chr4:153244316 | CTCCTCTT others(8): Show |
C | 3 | a0001c0001t0001g0203 a0001c0001t0005g0103 a0001c0002t0002g0137 |
3 | HG02622.hp1 HG03017.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.31-26016_31-26002d others(17): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244316 | ||||||
| chr4:153244317 | T | C | 1 | a0001c0002t0023g0014 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.31-26018T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244317 | |||||||
| chr4:153244318 | C | CCTCCTCC others(75): Show |
1 | a0001c0001t0003g0209 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.31-26014_31-26013i others(84): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244318 | ||||||
| chr4:153244319 | C | CTCCTCCT others(65): Show |
1 | a0001c0002t0002g0212 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.31-26014_31-26013i others(74): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244319 | ||||||
| chr4:153244319 | C | CTCCTCCT others(83): Show |
1 | a0001c0002t0002g0114 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.31-26014_31-26013i others(92): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244319 | ||||||
| chr4:153244319 | C | CTCCTCCT others(59): Show |
1 | a0001c0002t0002g0248 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.31-26014_31-26013i others(68): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244319 | ||||||
| chr4:153244319 | C | CTCCTCCT others(77): Show |
1 | a0001c0002t0002g0166 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.31-26014_31-26013i others(86): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244319 | ||||||
| chr4:153244319 | C | CTCCTCCT others(50): Show |
1 | a0001c0002t0001g0226 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.31-26014_31-26013i others(59): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244319 | ||||||
| chr4:153244319 | C | CTCCTCCT others(56): Show |
1 | a0001c0002t0001g0173 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.31-26014_31-26013i others(65): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244319 | ||||||
| chr4:153244319 | C | CTCCTCCT others(71): Show |
1 | a0001c0001t0002g0153 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.31-26014_31-26013i others(80): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244319 | ||||||
| chr4:153244319 | C | CTCCTCCT others(56): Show |
1 | a0001c0002t0002g0256 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.31-26014_31-26013i others(65): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244319 | ||||||
| chr4:153244319 | C | CTCCTCCT others(83): Show |
1 | a0001c0001t0001g0112 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.31-26014_31-26013i others(92): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244319 | ||||||
| chr4:153244319 | C | CTCCTCCT others(50): Show |
1 | a0001c0003t0026g0107 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.31-26014_31-26013i others(59): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244319 | ||||||
| chr4:153244319 | C | CTCCTCCT others(56): Show |
2 | a0001c0001t0001g0097 a0001c0002t0004g0172 |
2 | HG00140.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.31-26014_31-26013i others(65): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244319 | ||||||
| chr4:153244319 | C | CTCCTCCT others(74): Show |
1 | a0001c0002t0002g0215 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.31-26014_31-26013i others(83): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244319 | ||||||
| chr4:153244319 | C | CTCCTCCT others(47): Show |
1 | a0001c0002t0003g0239 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.31-26014_31-26013i others(56): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244319 | ||||||
| chr4:153244319 | C | CTCCTCCT others(68): Show |
1 | a0001c0001t0001g0098 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.31-26014_31-26013i others(77): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244319 | ||||||
| chr4:153244319 | C | CTCCTCCT others(74): Show |
1 | a0001c0002t0002g0124 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.31-26014_31-26013i others(83): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244319 | ||||||
| chr4:153244319 | C | CTCCTCCT others(38): Show |
1 | a0001c0002t0002g0260 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.31-26014_31-26013i others(47): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244319 | ||||||
| chr4:153244319 | C | CTCCTCCT others(47): Show |
1 | a0001c0001t0001g0258 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.31-26014_31-26013i others(56): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244319 | ||||||
| chr4:153244319 | C | CTCCTCCT others(59): Show |
1 | a0001c0002t0005g0154 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.31-26014_31-26013i others(68): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244319 | ||||||
| chr4:153244319 | C | CTCCTCCT others(68): Show |
1 | a0001c0002t0001g0167 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.31-26014_31-26013i others(77): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244319 | ||||||
| chr4:153244319 | C | CTCCTCCT others(38): Show |
1 | a0001c0001t0006g0143 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.31-26014_31-26013i others(47): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244319 | ||||||
| chr4:153244319 | C | CTCCTCCT others(47): Show |
1 | a0001c0002t0002g0176 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.31-26014_31-26013i others(56): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244319 | ||||||
| chr4:153244319 | C | CTCCTCCT others(53): Show |
1 | a0001c0002t0017g0096 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.31-26014_31-26013i others(62): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244319 | ||||||
| chr4:153244319 | C | CTCCTCCT others(74): Show |
1 | a0001c0002t0001g0210 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.31-26014_31-26013i others(83): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244319 | ||||||
| chr4:153244319 | C | CTCCTCCT others(48): Show |
1 | a0001c0002t0017g0095 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.31-26014_31-26013i others(57): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244319 | ||||||
| chr4:153244319 | C | CTCCTCCT others(35): Show |
1 | a0001c0002t0002g0250 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.31-26014_31-26013i others(44): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244319 | ||||||
| chr4:153244319 | C | CTCCTCCT others(59): Show |
1 | a0001c0002t0002g0246 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.31-26014_31-26013i others(68): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244319 | ||||||
| chr4:153244319 | C | CTCCTCCT others(39): Show |
1 | a0001c0003t0007g0106 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.31-26014_31-26013i others(48): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244319 | ||||||
| chr4:153244319 | C | CTCCTCCT others(29): Show |
1 | a0001c0008t0002g0059 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.31-26014_31-26013i others(38): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244319 | ||||||
| chr4:153244319 | C | CTCCTCCT others(59): Show |
1 | a0001c0001t0001g0187 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.31-26014_31-26013i others(68): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244319 | ||||||
| chr4:153244319 | C | CTCCTCCT others(27): Show |
1 | a0001c0002t0002g0145 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.31-26014_31-26013i others(36): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244319 | ||||||
| chr4:153244319 | C | CTCCTCCT others(53): Show |
1 | a0001c0002t0007g0155 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.31-26014_31-26013i others(62): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244319 | ||||||
| chr4:153244319 | C | CTCCTCCT others(26): Show |
1 | a0001c0001t0005g0110 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.31-26014_31-26013i others(35): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244319 | ||||||
| chr4:153244319 | C | CTCCTCCT others(47): Show |
1 | a0001c0001t0001g0222 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.31-26014_31-26013i others(56): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244319 | ||||||
| chr4:153244319 | C | CTCCTCCT others(65): Show |
1 | a0001c0001t0031g0191 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.31-26014_31-26013i others(74): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244319 | ||||||
| chr4:153244319 | C | CTCCTCCT others(21): Show |
1 | a0001c0001t0001g0093 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.31-26014_31-26013i others(30): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244319 | ||||||
| chr4:153244319 | C | CTCCTCCT others(17): Show |
1 | a0001c0001t0001g0072 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.31-26014_31-26013i others(26): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244319 | ||||||
| chr4:153244319 | C | CTCCTCCT others(146): Show |
1 | a0001c0002t0007g0266 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.31-26014_31-26013i others(155): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244319 | ||||||
| chr4:153244319 | C | CTCCTCCT others(152): Show |
1 | a0001c0001t0002g0221 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.31-26014_31-26013i others(161): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244319 | ||||||
| chr4:153244319 | C | CTCCTCCT others(14): Show |
2 | a0001c0001t0001g0249 a0001c0002t0001g0220 |
2 | HG03239.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.31-26014_31-26013i others(23): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244319 | ||||||
| chr4:153244319 | C | CTCCTCCT others(11): Show |
1 | a0001c0001t0001g0188 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.31-26014_31-26013i others(20): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244319 | ||||||
| chr4:153244319 | C | CTCCTCCT others(14): Show |
1 | a0001c0004t0003g0119 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.31-26014_31-26013i others(23): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244319 | ||||||
| chr4:153244319 | C | CTCCTCCT others(17): Show |
1 | a0001c0003t0003g0207 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.31-26014_31-26013i others(26): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244319 | ||||||
| chr4:153244319 | C | CTCCTCCT others(20): Show |
1 | a0001c0001t0001g0164 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.31-26014_31-26013i others(29): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244319 | ||||||
| chr4:153244319 | C | CTCCTCCT others(23): Show |
1 | a0001c0001t0001g0211 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.31-26014_31-26013i others(32): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244319 | ||||||
| chr4:153244319 | C | CTCCTCCT others(38): Show |
1 | a0001c0010t0004g0085 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.31-26014_31-26013i others(47): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244319 | ||||||
| chr4:153244319 | C | CTCCTCCT others(5): Show |
2 | a0001c0001t0001g0120 a0001c0002t0001g0066 |
2 | HG01109.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.31-26014_31-26013i others(14): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244319 | ||||||
| chr4:153244319 | C | CTCCTCCT others(8): Show |
2 | a0001c0001t0001g0186 a0001c0002t0004g0010 |
2 | HG03834.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.31-26014_31-26013i others(17): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244319 | ||||||
| chr4:153244319 | C | CTCCTCCT others(128): Show |
1 | a0001c0001t0006g0086 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.31-26014_31-26013i others(137): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244319 | ||||||
| chr4:153244319 | C | CTCCTCCT others(2): Show |
5 | a0001c0001t0001g0156 a0001c0001t0002g0201 a0001c0001t0005g0252 others(2): Show |
5 | HG02523.hp2 NA18968.hp2 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-26014_31-26013i others(11): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244319 | ||||||
| chr4:153244319 | C | CTCCTCCT others(5): Show |
2 | a0001c0001t0001g0056 a0001c0001t0007g0122 |
2 | HG02683.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.31-26014_31-26013i others(14): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244319 | ||||||
| chr4:153244319 | C | CTCCTCCT others(8): Show |
1 | a0001c0001t0001g0218 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.31-26014_31-26013i others(17): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244319 | ||||||
| chr4:153244319 | C | CTCCTCCT others(14): Show |
1 | a0001c0001t0001g0257 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.31-26014_31-26013i others(23): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244319 | ||||||
| chr4:153244319 | C | CTCCTCCT others(26): Show |
1 | a0001c0001t0001g0200 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.31-26014_31-26013i others(35): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244319 | ||||||
| chr4:153244319 | C | CTCCTCCT others(32): Show |
1 | a0001c0001t0001g0227 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.31-26014_31-26013i others(41): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244319 | ||||||
| chr4:153244319 | C | CTCCTCTC others(27): Show |
1 | a0001c0001t0001g0113 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.31-26014_31-26013i others(36): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244319 | ||||||
| chr4:153244319 | C | CTCCTCTT others(92): Show |
1 | a0001c0001t0001g0084 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.31-26014_31-26013i others(101): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244319 | ||||||
| chr4:153244319 | C | CTCTTCCT others(147): Show |
1 | a0001c0002t0019g0180 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.31-26011_31-26010i others(156): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244319 | ||||||
| chr4:153244319 | C | T | 18 | a0001c0001t0001g0091 a0001c0001t0001g0099 a0001c0001t0001g0100 others(15): Show |
18 | HG00642.hp2 HG00735.hp2 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.31-26016C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244319 | |||||||
| chr4:153244319 | CTCTTCTT others(5): Show |
C | 1 | a0001c0002t0023g0014 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.31-25992_31-25981d others(14): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244319 | ||||||
| chr4:153244319 | CTCTTCTT others(8): Show |
C | 2 | a0001c0001t0004g0008 a0001c0001t0004g0129 |
2 | HG02615.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.31-25995_31-25981d others(17): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244319 | ||||||
| chr4:153244319 | CTCTTCTT others(11): Show |
C | 1 | a0001c0002t0018g0009 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.31-25998_31-25981d others(20): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244319 | ||||||
| chr4:153244319 | CTCTTCTT others(56): Show |
C | 2 | a0001c0001t0004g0087 a0001c0001t0004g0088 |
2 | HG02055.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.31-25980_31-25918d others(65): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244319 | ||||||
| chr4:153244321 | C | CCTCCTCC others(10): Show |
1 | a0001c0002t0002g0152 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.31-26014_31-26013i others(19): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244321 | |||||||
| chr4:153244322 | T | C | 60 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0055 others(57): Show |
60 | HG00323.hp2 HG00438.hp2 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.31-26013T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244322 | |||||||
| chr4:153244324 | CTTCTTCT others(12): Show |
C | 1 | a0001c0003t0001g0003 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.31-26009_31-25991d others(21): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244324 | ||||||
| chr4:153244325 | T | C | 30 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0001g0179 others(27): Show |
30 | HG00323.hp2 HG00558.hp2 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.31-26010T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244325 | |||||||
| chr4:153244327 | CTTCTTCT others(3): Show |
C | 1 | a0001c0001t0006g0061 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.31-26006_31-25997d others(12): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244327 | ||||||
| chr4:153244328 | T | C | 19 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0001g0182 others(16): Show |
19 | HG00323.hp2 HG00558.hp2 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.31-26007T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244328 | |||||||
| chr4:153244329 | T | TCTTCTTC others(32): Show |
1 | a0001c0002t0002g0181 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.31-25981_31-25980i others(41): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244329 | ||||||
| chr4:153244330 | CTTCTTCT others(9): Show |
C | 1 | a0001c0001t0025g0007 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.31-26003_31-25988d others(18): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244330 | ||||||
| chr4:153244331 | T | C | 11 | a0001c0001t0001g0081 a0001c0001t0001g0253 a0001c0002t0001g0105 others(8): Show |
11 | HG00323.hp2 HG01070.hp1 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.31-26004T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244331 | |||||||
| chr4:153244334 | T | C | 10 | a0001c0001t0001g0081 a0001c0001t0001g0253 a0001c0001t0006g0160 others(7): Show |
10 | HG00323.hp2 HG01070.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.31-26001T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244334 | |||||||
| chr4:153244334 | TTCTTCTT others(14): Show |
T | 2 | a0001c0003t0004g0142 a0001c0003t0010g0079 |
2 | HG02615.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.31-25980_31-25960d others(23): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244334 | ||||||
| chr4:153244335 | T | C | 1 | a0001c0002t0023g0014 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.31-26000T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244335 | |||||||
| chr4:153244337 | T | C | 8 | a0001c0001t0001g0253 a0001c0001t0004g0008 a0001c0001t0004g0129 others(5): Show |
8 | HG01123.hp2 HG02615.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.31-25998T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244337 | |||||||
| chr4:153244338 | T | C | 1 | a0001c0002t0033g0234 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.31-25997T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244338 | |||||||
| chr4:153244340 | T | C | 9 | a0001c0001t0001g0113 a0001c0001t0004g0008 a0001c0001t0004g0129 others(6): Show |
9 | HG00323.hp2 HG01070.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.31-25995T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244340 | |||||||
| chr4:153244340 | TTCTTCTT others(8): Show |
T | 1 | a0001c0001t0005g0242 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.31-25980_31-25966d others(17): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244340 | ||||||
| chr4:153244341 | T | C | 1 | a0001c0002t0023g0014 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.31-25994T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244341 | |||||||
| chr4:153244342 | C | T | 1 | a0001c0002t0033g0234 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.31-25993C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244342 | |||||||
| chr4:153244343 | T | C | 7 | a0001c0001t0004g0008 a0001c0001t0004g0129 a0001c0001t0005g0110 others(4): Show |
7 | HG01123.hp2 HG02615.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.31-25992T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244343 | |||||||
| chr4:153244343 | TTCTTCTT others(5): Show |
T | 6 | a0001c0001t0001g0202 a0001c0001t0001g0253 a0001c0002t0002g0194 others(3): Show |
6 | HG01109.hp2 HG01934.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.31-25980_31-25969d others(14): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244343 | ||||||
| chr4:153244344 | T | C | 1 | a0001c0002t0033g0234 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.31-25991T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244344 | |||||||
| chr4:153244346 | T | C | 8 | a0001c0001t0004g0008 a0001c0001t0004g0129 a0001c0001t0006g0160 others(5): Show |
8 | HG00323.hp2 HG01070.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.31-25989T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244346 | |||||||
| chr4:153244346 | T | TTCTTCTT others(8): Show |
1 | a0001c0003t0003g0067 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.31-25981_31-25980i others(17): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244346 | ||||||
| chr4:153244346 | TTCTTCTT others(2): Show |
T | 3 | a0001c0001t0001g0055 a0001c0001t0001g0157 a0001c0002t0010g0134 |
3 | HG00544.hp2 HG02258.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.31-25980_31-25972d others(11): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244346 | ||||||
| chr4:153244347 | T | C | 1 | a0001c0002t0023g0014 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.31-25988T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244347 | |||||||
| chr4:153244349 | T | C | 12 | a0001c0001t0001g0164 a0001c0001t0001g0200 a0001c0001t0001g0211 others(9): Show |
12 | HG00438.hp1 HG01069.hp2 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.31-25986T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244349 | |||||||
| chr4:153244349 | T | TCTTCCTC others(10): Show |
1 | a0001c0001t0005g0214 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.31-25986_31-25985i others(19): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244349 | |||||||
| chr4:153244349 | T | TTCCTCTT others(8): Show |
1 | a0001c0001t0021g0111 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.31-25984_31-25983i others(17): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244349 | ||||||
| chr4:153244349 | T | TTCCTCTT others(20): Show |
1 | a0001c0001t0005g0094 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.31-25984_31-25983i others(29): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244349 | ||||||
| chr4:153244349 | TTCTTCC | T | 4 | a0001c0001t0001g0118 a0001c0001t0001g0195 a0001c0001t0001g0205 others(1): Show |
4 | HG01981.hp1 HG02004.hp2 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.31-25980_31-25975d others(8): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244349 | ||||||
| chr4:153244350 | T | C | 1 | a0001c0002t0033g0234 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.31-25985T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244350 | |||||||
| chr4:153244352 | T | C | 5 | a0001c0001t0004g0129 a0001c0002t0001g0105 a0001c0002t0001g0116 others(2): Show |
5 | HG00323.hp2 HG01070.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.31-25983T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244352 | |||||||
| chr4:153244352 | TTCC | T | 8 | a0001c0001t0001g0081 a0001c0001t0001g0158 a0001c0001t0001g0182 others(5): Show |
8 | HG00642.hp1 HG02809.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.31-25980_31-25978d others(5): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244352 | ||||||
| chr4:153244353 | T | C | 1 | a0001c0002t0023g0014 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.31-25982T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244353 | |||||||
| chr4:153244353 | T | TCTTCTTC others(128): Show |
1 | a0001c0002t0012g0178 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.31-25981_31-25980i others(137): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244353 | ||||||
| chr4:153244353 | T | TCTTCTTC others(131): Show |
1 | a0001c0002t0012g0177 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.31-25981_31-25980i others(140): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244353 | ||||||
| chr4:153244355 | C | CTCT | 3 | a0001c0001t0001g0249 a0001c0001t0007g0122 a0001c0008t0002g0059 |
3 | HG03225.hp1 HG03239.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.31-25900_31-25898d others(5): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244355 | ||||||
| chr4:153244355 | C | T | 147 | a0001c0001t0001g0023 a0001c0001t0001g0039 a0001c0001t0001g0040 others(144): Show |
147 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.31-25980C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244355 | |||||||
| chr4:153244356 | T | TCCTCCTC others(15): Show |
1 | a0001c0002t0001g0105 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.31-25978_31-25977i others(24): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244356 | ||||||
| chr4:153244358 | T | C | 16 | a0001c0001t0001g0056 a0001c0001t0001g0072 a0001c0001t0001g0120 others(13): Show |
16 | HG00323.hp2 HG01070.hp1 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.31-25977T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244358 | |||||||
| chr4:153244358 | T | TTCC | 4 | a0001c0001t0005g0094 a0001c0001t0005g0110 a0001c0001t0015g0192 others(1): Show |
4 | HG01261.hp1 NA18942.hp1 NA19084.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-25975_31-25974i others(5): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244358 | ||||||
| chr4:153244358 | T | TTCCTCTT others(8): Show |
1 | a0001c0001t0005g0161 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.31-25975_31-25974i others(17): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244358 | ||||||
| chr4:153244359 | T | C | 2 | a0001c0002t0001g0105 a0001c0002t0023g0014 |
2 | HG06807.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.31-25976T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244359 | |||||||
| chr4:153244361 | T | C | 21 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0186 others(18): Show |
21 | HG01109.hp1 HG01123.hp2 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.31-25974T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244361 | |||||||
| chr4:153244362 | T | C | 2 | a0001c0002t0001g0105 a0001c0002t0033g0234 |
2 | HG03098.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.31-25973T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244362 | |||||||
| chr4:153244362 | T | TCTTCTTC others(122): Show |
1 | a0001c0002t0012g0163 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.31-25953_31-25952i others(131): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244362 | ||||||
| chr4:153244364 | T | C | 30 | a0001c0001t0001g0023 a0001c0001t0001g0039 a0001c0001t0001g0040 others(27): Show |
30 | HG00323.hp2 HG00438.hp2 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.31-25971T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244364 | |||||||
| chr4:153244365 | T | C | 2 | a0001c0002t0001g0105 a0001c0002t0033g0234 |
2 | HG03098.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.31-25970T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244365 | |||||||
| chr4:153244367 | T | C | 19 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0179 others(16): Show |
19 | HG00544.hp2 HG02572.hp2 HG02615.hp1 others(16): Show |
intron_variant | MODIFIER | c.31-25968T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244367 | |||||||
| chr4:153244368 | T | C | 1 | a0001c0002t0001g0105 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.31-25967T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244368 | |||||||
| chr4:153244369 | C | G | 1 | a0001c0002t0002g0024 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.31-25966C>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244369 | |||||||
| chr4:153244370 | T | C | 12 | a0001c0001t0001g0017 a0001c0001t0001g0118 a0001c0001t0001g0121 others(9): Show |
12 | HG00558.hp1 HG00642.hp1 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.31-25965T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244370 | |||||||
| chr4:153244373 | T | C | 9 | a0001c0001t0001g0182 a0001c0001t0001g0195 a0001c0001t0001g0203 others(6): Show |
9 | HG01884.hp1 HG02004.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.31-25962T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244373 | |||||||
| chr4:153244374 | T | C | 1 | a0001c0002t0033g0234 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.31-25961T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244374 | |||||||
| chr4:153244376 | T | C | 1 | a0001c0001t0001g0121 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.31-25959T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244376 | |||||||
| chr4:153244379 | T | C | 1 | a0001c0001t0001g0213 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.31-25956T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244379 | |||||||
| chr4:153244379 | TTCTTCTT others(28): Show |
T | 1 | a0001c0002t0003g0148 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.31-25954_31-25920d others(37): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244379 | ||||||
| chr4:153244383 | T | C | 1 | a0001c0002t0033g0234 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.31-25952T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244383 | |||||||
| chr4:153244385 | T | C | 2 | a0001c0001t0004g0087 a0001c0001t0004g0088 |
2 | HG02055.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.31-25950T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244385 | |||||||
| chr4:153244385 | TTCTTCTT others(22): Show |
T | 1 | a0001c0001t0006g0146 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.31-25948_31-25920d others(31): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244385 | ||||||
| chr4:153244386 | T | C | 24 | a0001c0001t0001g0033 a0001c0001t0002g0002 a0001c0001t0002g0018 others(21): Show |
24 | HG01169.hp1 HG01891.hp1 HG02280.hp2 others(21): Show |
intron_variant | MODIFIER | c.31-25949T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244386 | |||||||
| chr4:153244388 | T | C | 1 | a0001c0002t0033g0234 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.31-25947T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244388 | |||||||
| chr4:153244391 | T | C | 26 | a0001c0001t0001g0033 a0001c0001t0002g0002 a0001c0001t0002g0018 others(23): Show |
26 | HG01169.hp1 HG01891.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.31-25944T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244391 | |||||||
| chr4:153244394 | TTCTTCTT others(13): Show |
T | 1 | a0001c0001t0006g0149 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.31-25939_31-25920d others(22): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244394 | ||||||
| chr4:153244399 | CTT | C | 24 | a0001c0001t0001g0033 a0001c0001t0002g0002 a0001c0001t0002g0018 others(21): Show |
24 | HG01169.hp1 HG01891.hp1 HG02280.hp2 others(21): Show |
intron_variant | MODIFIER | c.31-25935_31-25934d others(4): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244399 | |||||||
| chr4:153244406 | T | C | 1 | a0001c0002t0002g0145 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.31-25929T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244406 | |||||||
| chr4:153244409 | T | C | 3 | a0001c0003t0007g0223 a0001c0003t0007g0224 a0001c0003t0007g0225 |
3 | HG01074.hp2 HG01106.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.31-25926T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244409 | |||||||
| chr4:153244409 | TTC | T | 25 | a0001c0001t0001g0033 a0001c0001t0002g0002 a0001c0001t0002g0018 others(22): Show |
25 | HG01169.hp1 HG01891.hp1 HG02280.hp2 others(22): Show |
intron_variant | MODIFIER | c.31-25924_31-25923d others(4): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244409 | ||||||
| chr4:153244412 | TTC | T | 4 | a0001c0001t0006g0061 a0001c0001t0006g0147 a0001c0001t0025g0007 others(1): Show |
4 | HG01884.hp2 HG02257.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-25921_31-25920d others(4): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244412 | ||||||
| chr4:153244413 | T | G | 3 | a0001c0002t0012g0163 a0001c0002t0012g0177 a0001c0002t0012g0178 |
3 | NA18948.hp2 NA19011.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.31-25922T>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244413 | |||||||
| chr4:153244413 | TCTTC | T | 8 | a0001c0002t0001g0229 a0001c0003t0003g0029 a0001c0003t0003g0030 others(5): Show |
8 | HG00323.hp1 HG01074.hp1 HG01517.hp1 others(5): Show |
intron_variant | MODIFIER | c.31-25921_31-25918d others(6): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244413 | |||||||
| chr4:153244415 | T | C | 4 | a0001c0001t0001g0101 a0001c0001t0001g0241 a0001c0001t0002g0235 others(1): Show |
4 | HG00280.hp2 HG01516.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.31-25920T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244415 | |||||||
| chr4:153244416 | TC | T | 20 | a0001c0001t0001g0017 a0001c0001t0001g0063 a0001c0001t0003g0016 others(17): Show |
20 | HG01433.hp1 HG01884.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.31-25918delC | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244416 | |||||||
| chr4:153244419 | TC | T | 5 | a0001c0003t0001g0027 a0001c0003t0003g0011 a0001c0003t0003g0015 others(2): Show |
5 | HG01069.hp1 HG01346.hp1 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.31-25915delC | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244419 | |||||||
| chr4:153244421 | T | C | 25 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0001g0099 others(22): Show |
25 | HG00280.hp2 HG01109.hp2 HG01516.hp1 others(22): Show |
intron_variant | MODIFIER | c.31-25914T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244421 | |||||||
| chr4:153244421 | T | TTCC | 3 | a0001c0002t0002g0136 a0001c0002t0002g0171 a0001c0002t0022g0140 |
3 | HG01168.hp1 HG02145.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.31-25912_31-25911i others(5): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244421 | ||||||
| chr4:153244421 | T | TTCTTCC | 2 | a0001c0002t0002g0139 a0001c0002t0028g0080 |
2 | HG02280.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.31-25909_31-25908i others(8): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244421 | ||||||
| chr4:153244421 | T | TTCTTCTT others(8): Show |
2 | a0001c0001t0001g0100 a0001c0002t0002g0089 |
2 | HG00735.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.31-25900_31-25899i others(17): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244421 | ||||||
| chr4:153244421 | T | TTCTTCTT others(17): Show |
1 | a0001c0001t0001g0102 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.31-25898_31-25897i others(26): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244421 | ||||||
| chr4:153244422 | TC | T | 3 | a0001c0003t0003g0025 a0001c0003t0003g0057 a0001c0003t0003g0071 |
3 | HG00741.hp1 HG01934.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.31-25912delC | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244422 | |||||||
| chr4:153244423 | C | CT | 3 | a0001c0002t0001g0116 a0001c0002t0002g0259 a0001c0002t0004g0069 |
3 | HG00323.hp2 HG01070.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.31-25910dupT | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244423 | ||||||
| chr4:153244425 | T | G | 3 | a0001c0002t0012g0163 a0001c0002t0012g0177 a0001c0002t0012g0178 |
3 | NA18948.hp2 NA19011.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.31-25910T>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244425 | |||||||
| chr4:153244426 | C | A | 2 | a0001c0001t0004g0087 a0001c0001t0004g0088 |
2 | HG02055.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.31-25909C>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244426 | |||||||
| chr4:153244426 | CTTCTTCT others(4): Show |
C | 1 | a0001c0001t0001g0196 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.31-25906_31-25896d others(13): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244426 | ||||||
| chr4:153244429 | C | A | 2 | a0001c0001t0004g0087 a0001c0001t0004g0088 |
2 | HG02055.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.31-25906C>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244429 | |||||||
| chr4:153244432 | C | A | 2 | a0001c0001t0004g0087 a0001c0001t0004g0088 |
2 | HG02055.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.31-25903C>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244432 | |||||||
| chr4:153244435 | C | A | 2 | a0001c0001t0004g0087 a0001c0001t0004g0088 |
2 | HG02055.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.31-25900C>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244435 | |||||||
| chr4:153244435 | C | T | 25 | a0001c0001t0001g0033 a0001c0001t0002g0002 a0001c0001t0002g0018 others(22): Show |
25 | HG01169.hp1 HG01891.hp1 HG02280.hp2 others(22): Show |
intron_variant | MODIFIER | c.31-25900C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244435 | |||||||
| chr4:153244435 | CTT | C | 6 | a0001c0003t0001g0027 a0001c0003t0001g0132 a0001c0003t0003g0011 others(3): Show |
6 | HG01069.hp1 HG01346.hp1 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.31-25897_31-25896d others(4): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244435 | ||||||
| chr4:153244435 | CTTTTA | C | 31 | a0001c0001t0001g0017 a0001c0001t0001g0062 a0001c0001t0001g0063 others(28): Show |
31 | HG00323.hp1 HG01074.hp1 HG01433.hp1 others(28): Show |
intron_variant | MODIFIER | c.31-25899_31-25895d others(7): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244435 | |||||||
| chr4:153244437 | T | TC | 3 | a0001c0003t0003g0025 a0001c0003t0003g0057 a0001c0003t0003g0071 |
3 | HG00741.hp1 HG01934.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.31-25898_31-25897i others(3): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244437 | |||||||
| chr4:153244438 | T | A | 2 | a0001c0001t0004g0087 a0001c0001t0004g0088 |
2 | HG02055.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.31-25897T>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244438 | |||||||
| chr4:153244438 | T | C | 2 | a0001c0001t0002g0221 a0001c0002t0002g0250 |
2 | HG01255.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.31-25897T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244438 | |||||||
| chr4:153244440 | A | C | 9 | a0001c0003t0001g0027 a0001c0003t0001g0132 a0001c0003t0003g0011 others(6): Show |
9 | HG00741.hp1 HG01069.hp1 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.31-25895A>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244440 | |||||||
| chr4:153244440 | A | T | 2 | a0001c0001t0004g0087 a0001c0001t0004g0088 |
2 | HG02055.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.31-25895A>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244440 | |||||||
| chr4:153244445 | G | C | 2 | a0001c0001t0001g0097 a0001c0001t0001g0098 |
2 | HG00140.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.31-25890G>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244445 | |||||||
| chr4:153244462 | T | C | 1 | a0001c0001t0002g0001 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.31-25873T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244462 | |||||||
| chr4:153244469 | C | T | 1 | a0001c0001t0001g0113 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.31-25866C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244469 | |||||||
| chr4:153244488 | T | C | 1 | a0001c0002t0028g0080 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.31-25847T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244488 | |||||||
| chr4:153244509 | C | A | 2 | a0001c0001t0004g0087 a0001c0001t0004g0088 |
2 | HG02055.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.31-25826C>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244509 | |||||||
| chr4:153244527 | C | CTGAGATT | 18 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0112 others(15): Show |
18 | HG00140.hp1 HG00323.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.31-25807_31-25801d others(9): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244527 | ||||||
| chr4:153244566 | T | A | 40 | a0001c0001t0001g0017 a0001c0001t0001g0062 a0001c0001t0001g0063 others(37): Show |
40 | HG00323.hp1 HG00741.hp1 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.31-25769T>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244566 | |||||||
| chr4:153244584 | C | CAAGA | 25 | a0001c0001t0001g0033 a0001c0001t0002g0002 a0001c0001t0002g0018 others(22): Show |
25 | HG01169.hp1 HG01891.hp1 HG02280.hp2 others(22): Show |
intron_variant | MODIFIER | c.31-25749_31-25748i others(6): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153244584 | ||||||
| chr4:153244603 | A | G | 12 | a0001c0001t0001g0033 a0001c0001t0003g0035 a0001c0001t0003g0036 others(9): Show |
12 | HG03831.hp2 NA18944.hp2 NA18979.hp2 others(9): Show |
intron_variant | MODIFIER | c.31-25732A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244603 | |||||||
| chr4:153244636 | G | A | 3 | a0001c0003t0007g0223 a0001c0003t0007g0224 a0001c0003t0007g0225 |
3 | HG01074.hp2 HG01106.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.31-25699G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244636 | |||||||
| chr4:153244727 | A | G | 24 | a0001c0001t0001g0033 a0001c0001t0002g0002 a0001c0001t0002g0018 others(21): Show |
24 | HG01169.hp1 HG01891.hp1 HG02280.hp2 others(21): Show |
intron_variant | MODIFIER | c.31-25608A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244727 | |||||||
| chr4:153244775 | G | T | 24 | a0001c0001t0001g0033 a0001c0001t0002g0002 a0001c0001t0002g0018 others(21): Show |
24 | HG01169.hp1 HG01891.hp1 HG02280.hp2 others(21): Show |
intron_variant | MODIFIER | c.31-25560G>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244775 | |||||||
| chr4:153244902 | A | T | 24 | a0001c0001t0001g0033 a0001c0001t0002g0002 a0001c0001t0002g0018 others(21): Show |
24 | HG01169.hp1 HG01891.hp1 HG02280.hp2 others(21): Show |
intron_variant | MODIFIER | c.31-25433A>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244902 | |||||||
| chr4:153244944 | G | T | 1 | a0001c0002t0007g0155 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.31-25391G>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153244944 | |||||||
| chr4:153245020 | T | C | 4 | a0001c0001t0009g0060 a0001c0001t0009g0263 a0001c0001t0009g0264 others(1): Show |
4 | HG01891.hp1 HG02280.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.31-25315T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153245020 | |||||||
| chr4:153245065 | C | T | 1 | a0001c0001t0016g0197 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.31-25270C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153245065 | |||||||
| chr4:153245287 | G | A | 2 | a0001c0001t0004g0087 a0001c0001t0004g0088 |
2 | HG02055.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.31-25048G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153245287 | |||||||
| chr4:153245301 | C | A | 1 | a0001c0001t0001g0023 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.31-25034C>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153245301 | |||||||
| chr4:153245415 | T | G | 27 | a0001c0001t0001g0033 a0001c0001t0002g0002 a0001c0001t0002g0018 others(24): Show |
27 | HG01169.hp1 HG01891.hp1 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.31-24920T>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153245415 | |||||||
| chr4:153245422 | G | A | 24 | a0001c0001t0001g0033 a0001c0001t0002g0002 a0001c0001t0002g0018 others(21): Show |
24 | HG01169.hp1 HG01891.hp1 HG02280.hp2 others(21): Show |
intron_variant | MODIFIER | c.31-24913G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153245422 | |||||||
| chr4:153245534 | T | G | 1 | a0001c0008t0002g0059 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.31-24801T>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153245534 | |||||||
| chr4:153245592 | T | G | 1 | a0001c0002t0023g0014 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.31-24743T>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153245592 | |||||||
| chr4:153245779 | C | T | 1 | a0001c0002t0033g0234 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.31-24556C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153245779 | |||||||
| chr4:153245876 | GC | G | 3 | a0001c0003t0007g0223 a0001c0003t0007g0224 a0001c0003t0007g0225 |
3 | HG01074.hp2 HG01106.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.31-24457delC | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153245876 | ||||||
| chr4:153246008 | C | G | 1 | a0001c0002t0033g0234 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.31-24327C>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153246008 | |||||||
| chr4:153246059 | C | T | 28 | a0001c0001t0001g0227 a0001c0001t0001g0253 a0001c0001t0001g0258 others(25): Show |
28 | HG00140.hp2 HG00544.hp1 HG00558.hp2 others(25): Show |
intron_variant | MODIFIER | c.31-24276C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153246059 | |||||||
| chr4:153246341 | C | A | 1 | a0001c0003t0003g0011 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.31-23994C>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153246341 | |||||||
| chr4:153246571 | A | T | 29 | a0001c0001t0001g0227 a0001c0001t0001g0253 a0001c0001t0001g0258 others(26): Show |
29 | HG00140.hp2 HG00544.hp1 HG00558.hp2 others(26): Show |
intron_variant | MODIFIER | c.31-23764A>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153246571 | |||||||
| chr4:153246673 | G | C | 2 | a0001c0001t0002g0002 a0001c0002t0023g0014 |
2 | HG06807.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.31-23662G>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153246673 | |||||||
| chr4:153246723 | C | G | 27 | a0001c0001t0001g0125 a0001c0001t0001g0188 a0001c0001t0001g0227 others(24): Show |
27 | HG00140.hp2 HG00544.hp1 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.31-23612C>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153246723 | |||||||
| chr4:153246864 | C | T | 2 | a0001c0004t0003g0058 a0001c0008t0002g0059 |
2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.31-23471C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153246864 | |||||||
| chr4:153246989 | G | A | 3 | a0001c0001t0002g0018 a0001c0001t0002g0022 a0001c0001t0003g0265 |
3 | HG01169.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.31-23346G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153246989 | |||||||
| chr4:153247081 | C | A | 1 | a0001c0003t0003g0075 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.31-23254C>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153247081 | |||||||
| chr4:153247315 | A | G | 32 | a0001c0001t0001g0227 a0001c0001t0001g0253 a0001c0001t0002g0153 others(29): Show |
32 | HG00140.hp2 HG00544.hp1 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.31-23020A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153247315 | |||||||
| chr4:153247677 | C | CA | 29 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0091 others(26): Show |
29 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(26): Show |
intron_variant | MODIFIER | c.31-22634dupA | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153247677 | ||||||
| chr4:153247677 | C | CAA | 17 | a0001c0001t0001g0182 a0001c0001t0002g0018 a0001c0001t0002g0022 others(14): Show |
17 | HG01169.hp1 HG01891.hp2 HG02717.hp1 others(14): Show |
intron_variant | MODIFIER | c.31-22635_31-22634d others(4): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153247677 | ||||||
| chr4:153247677 | C | CAAA | 11 | a0001c0001t0001g0033 a0001c0001t0001g0258 a0001c0001t0002g0001 others(8): Show |
11 | HG02055.hp2 HG02280.hp1 HG02602.hp2 others(8): Show |
intron_variant | MODIFIER | c.31-22636_31-22634d others(5): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153247677 | ||||||
| chr4:153247677 | C | CAAAA | 26 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(23): Show |
26 | HG00140.hp2 HG00280.hp2 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.31-22637_31-22634d others(6): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153247677 | ||||||
| chr4:153247677 | C | CAAAAA | 19 | a0001c0001t0002g0002 a0001c0001t0002g0235 a0001c0001t0005g0094 others(16): Show |
19 | HG00544.hp1 HG00558.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.31-22638_31-22634d others(7): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153247677 | ||||||
| chr4:153247677 | CAA | C | 25 | a0001c0002t0001g0105 a0001c0002t0001g0115 a0001c0002t0001g0116 others(22): Show |
25 | HG00323.hp2 HG01070.hp1 HG01123.hp2 others(22): Show |
intron_variant | MODIFIER | c.31-22635_31-22634d others(4): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153247677 | ||||||
| chr4:153247677 | CAAA | C | 60 | a0001c0001t0001g0017 a0001c0001t0001g0055 a0001c0001t0001g0062 others(57): Show |
60 | HG00323.hp1 HG00741.hp1 HG01069.hp1 others(57): Show |
intron_variant | MODIFIER | c.31-22636_31-22634d others(5): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153247677 | ||||||
| chr4:153247677 | CAAAAAAA others(7): Show |
C | 3 | a0001c0001t0009g0060 a0001c0001t0009g0263 a0001c0001t0009g0264 |
3 | HG02280.hp2 HG03041.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.31-22647_31-22634d others(16): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153247677 | ||||||
| chr4:153247953 | T | A | 12 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(9): Show |
12 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.31-22382T>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153247953 | |||||||
| chr4:153247995 | G | GT | 74 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0056 others(71): Show |
74 | HG00323.hp1 HG00438.hp2 HG00741.hp1 others(71): Show |
intron_variant | MODIFIER | c.31-22322dupT | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153247995 | ||||||
| chr4:153247995 | G | GTT | 13 | a0001c0001t0001g0017 a0001c0001t0006g0160 a0001c0002t0002g0138 others(10): Show |
13 | HG01168.hp1 HG01981.hp2 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.31-22323_31-22322d others(4): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153247995 | ||||||
| chr4:153247995 | GT | G | 5 | a0001c0001t0021g0111 a0001c0002t0002g0050 a0001c0002t0002g0254 others(2): Show |
5 | HG00558.hp2 HG02027.hp1 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-22322delT | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153247995 | ||||||
| chr4:153247995 | GTT | G | 50 | a0001c0001t0001g0092 a0001c0001t0001g0099 a0001c0001t0001g0100 others(47): Show |
50 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.31-22323_31-22322d others(4): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153247995 | ||||||
| chr4:153248002 | T | G | 2 | a0001c0001t0001g0125 a0001c0001t0001g0188 |
2 | HG02735.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.31-22333T>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153248002 | |||||||
| chr4:153248077 | C | T | 3 | a0001c0001t0008g0168 a0001c0005t0003g0169 a0001c0005t0003g0198 |
3 | HG01433.hp2 HG01516.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.31-22258C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153248077 | |||||||
| chr4:153248098 | C | T | 4 | a0001c0002t0004g0045 a0001c0002t0004g0046 a0001c0002t0004g0047 others(1): Show |
4 | HG01884.hp1 HG02976.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.31-22237C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153248098 | |||||||
| chr4:153248129 | G | T | 1 | a0001c0001t0001g0247 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.31-22206G>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153248129 | |||||||
| chr4:153248200 | T | A | 1 | a0001c0003t0003g0067 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.31-22135T>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153248200 | |||||||
| chr4:153248318 | C | T | 1 | a0001c0002t0023g0014 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.31-22017C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153248318 | |||||||
| chr4:153248327 | C | A | 2 | a0001c0001t0001g0055 a0001c0001t0001g0081 |
2 | HG02886.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.31-22008C>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153248327 | |||||||
| chr4:153248347 | C | T | 2 | a0001c0001t0004g0087 a0001c0001t0004g0088 |
2 | HG02055.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.31-21988C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153248347 | |||||||
| chr4:153248397 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.31-21938G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153248397 | |||||||
| chr4:153248402 | A | G | 1 | a0001c0002t0004g0045 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.31-21933A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153248402 | |||||||
| chr4:153248643 | C | G | 2 | a0001c0001t0005g0103 a0001c0001t0005g0242 |
2 | HG03017.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.31-21692C>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153248643 | |||||||
| chr4:153248983 | G | C | 170 | a0001c0001t0001g0017 a0001c0001t0001g0033 a0001c0001t0001g0055 others(167): Show |
170 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.31-21352G>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153248983 | |||||||
| chr4:153249258 | C | T | 1 | a0001c0002t0005g0154 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.31-21077C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153249258 | |||||||
| chr4:153249273 | C | T | 1 | a0001c0001t0002g0002 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.31-21062C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153249273 | |||||||
| chr4:153249331 | C | T | 1 | a0001c0001t0008g0044 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.31-21004C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153249331 | |||||||
| chr4:153249445 | G | T | 2 | a0001c0001t0002g0002 a0001c0002t0023g0014 |
2 | HG06807.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.31-20890G>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153249445 | |||||||
| chr4:153249448 | G | A | 8 | a0001c0001t0001g0092 a0001c0001t0001g0121 a0001c0001t0005g0094 others(5): Show |
8 | NA18942.hp1 NA18943.hp1 NA18964.hp2 others(5): Show |
intron_variant | MODIFIER | c.31-20887G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153249448 | |||||||
| chr4:153249470 | G | A | 1 | a0001c0001t0002g0065 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.31-20865G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153249470 | |||||||
| chr4:153249578 | T | TCCGCCTC others(16): Show |
1 | a0001c0002t0001g0126 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.31-20728_31-20706d others(25): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153249578 | ||||||
| chr4:153249578 | TCCGCCTC others(16): Show |
T | 3 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0002g0002 |
3 | HG02886.hp2 HG06807.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.31-20728_31-20706d others(25): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153249578 | ||||||
| chr4:153249603 | C | T | 1 | a0001c0001t0006g0143 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.31-20732C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153249603 | |||||||
| chr4:153249708 | G | C | 49 | a0001c0001t0001g0092 a0001c0001t0001g0099 a0001c0001t0001g0100 others(46): Show |
49 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.31-20627G>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153249708 | |||||||
| chr4:153249913 | C | T | 74 | a0001c0001t0001g0017 a0001c0001t0001g0062 a0001c0001t0001g0063 others(71): Show |
74 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.31-20422C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153249913 | |||||||
| chr4:153249931 | A | G | 3 | a0001c0002t0011g0005 a0001c0002t0011g0006 a0001c0002t0011g0070 |
3 | HG02896.hp2 HG02897.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.31-20404A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153249931 | |||||||
| chr4:153250108 | C | CT | 19 | a0001c0001t0001g0017 a0001c0001t0001g0062 a0001c0001t0001g0063 others(16): Show |
19 | HG01891.hp1 HG02055.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.31-20216dupT | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153250108 | ||||||
| chr4:153250190 | G | A | 75 | a0001c0001t0001g0017 a0001c0001t0001g0062 a0001c0001t0001g0063 others(72): Show |
75 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.31-20145G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153250190 | |||||||
| chr4:153250227 | C | T | 3 | a0001c0001t0009g0060 a0001c0001t0009g0263 a0001c0001t0009g0264 |
3 | HG02280.hp2 HG03041.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.31-20108C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153250227 | |||||||
| chr4:153250229 | C | T | 4 | a0001c0001t0009g0060 a0001c0001t0009g0263 a0001c0001t0009g0264 others(1): Show |
4 | HG02280.hp2 HG03041.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-20106C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153250229 | |||||||
| chr4:153250309 | G | T | 1 | a0001c0002t0029g0261 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.31-20026G>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153250309 | |||||||
| chr4:153250604 | A | G | 20 | a0001c0001t0001g0092 a0001c0001t0001g0099 a0001c0001t0001g0100 others(17): Show |
20 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.31-19731A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153250604 | |||||||
| chr4:153250765 | G | T | 1 | a0001c0002t0002g0171 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.31-19570G>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153250765 | |||||||
| chr4:153251003 | C | G | 152 | a0001c0001t0001g0017 a0001c0001t0001g0055 a0001c0001t0001g0062 others(149): Show |
152 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.31-19332C>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153251003 | |||||||
| chr4:153251332 | C | T | 42 | a0001c0001t0001g0227 a0001c0001t0003g0232 a0001c0002t0001g0066 others(39): Show |
42 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(39): Show |
intron_variant | MODIFIER | c.31-19003C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153251332 | |||||||
| chr4:153251394 | A | G | 46 | a0001c0001t0001g0227 a0001c0001t0003g0232 a0001c0002t0001g0066 others(43): Show |
46 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.31-18941A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153251394 | |||||||
| chr4:153251804 | C | A | 1 | a0001c0002t0003g0144 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.31-18531C>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153251804 | |||||||
| chr4:153251933 | GCACTCC | G | 100 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0001g0092 others(97): Show |
100 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.31-18395_31-18390d others(8): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153251933 | ||||||
| chr4:153251955 | A | G | 147 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0001g0092 others(144): Show |
147 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.31-18380A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153251955 | |||||||
| chr4:153252077 | G | A | 1 | a0001c0001t0025g0007 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.31-18258G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153252077 | |||||||
| chr4:153252225 | A | G | 1 | a0001c0002t0003g0144 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.31-18110A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153252225 | |||||||
| chr4:153252268 | T | C | 13 | a0001c0002t0002g0130 a0001c0002t0002g0136 a0001c0002t0002g0137 others(10): Show |
13 | HG01168.hp1 HG02145.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.31-18067T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153252268 | |||||||
| chr4:153252722 | C | A | 1 | a0001c0002t0003g0144 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.31-17613C>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153252722 | |||||||
| chr4:153252888 | G | C | 1 | a0001c0003t0003g0064 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.31-17447G>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153252888 | |||||||
| chr4:153252934 | A | G | 13 | a0001c0002t0002g0130 a0001c0002t0002g0136 a0001c0002t0002g0137 others(10): Show |
13 | HG01168.hp1 HG02145.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.31-17401A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153252934 | |||||||
| chr4:153253008 | A | G | 74 | a0001c0001t0001g0092 a0001c0001t0001g0099 a0001c0001t0001g0100 others(71): Show |
74 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.31-17327A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153253008 | |||||||
| chr4:153253174 | G | A | 54 | a0001c0001t0002g0002 a0001c0001t0006g0160 a0001c0001t0009g0060 others(51): Show |
54 | HG00323.hp1 HG00438.hp1 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.31-17161G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153253174 | |||||||
| chr4:153253195 | G | A | 74 | a0001c0001t0001g0092 a0001c0001t0001g0099 a0001c0001t0001g0100 others(71): Show |
74 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.31-17140G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153253195 | |||||||
| chr4:153253254 | T | C | 2 | a0001c0001t0001g0255 a0001c0001t0001g0257 |
2 | HG02738.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.31-17081T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153253254 | |||||||
| chr4:153253423 | C | T | 1 | a0001c0004t0003g0058 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.31-16912C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153253423 | |||||||
| chr4:153253459 | G | A | 1 | a0001c0002t0023g0014 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.31-16876G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153253459 | |||||||
| chr4:153253673 | G | C | 3 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0004t0003g0058 |
3 | HG02886.hp2 HG02965.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.31-16662G>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153253673 | |||||||
| chr4:153253688 | C | T | 1 | a0001c0002t0004g0010 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.31-16647C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153253688 | |||||||
| chr4:153253690 | G | A | 1 | a0001c0009t0003g0159 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.31-16645G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153253690 | |||||||
| chr4:153253813 | T | C | 1 | a0001c0003t0010g0079 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.31-16522T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153253813 | |||||||
| chr4:153253882 | A | T | 33 | a0001c0002t0001g0126 a0001c0002t0001g0210 a0001c0003t0001g0003 others(30): Show |
33 | HG00323.hp1 HG00438.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.31-16453A>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153253882 | |||||||
| chr4:153253975 | C | T | 77 | a0001c0001t0001g0092 a0001c0001t0001g0099 a0001c0001t0001g0100 others(74): Show |
77 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.31-16360C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153253975 | |||||||
| chr4:153254008 | G | T | 1 | a0001c0001t0010g0078 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.31-16327G>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153254008 | |||||||
| chr4:153254039 | G | A | 54 | a0001c0001t0002g0002 a0001c0001t0006g0160 a0001c0001t0009g0060 others(51): Show |
54 | HG00323.hp1 HG00438.hp1 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.31-16296G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153254039 | |||||||
| chr4:153254077 | G | C | 20 | a0001c0001t0001g0092 a0001c0001t0001g0099 a0001c0001t0001g0100 others(17): Show |
20 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.31-16258G>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153254077 | |||||||
| chr4:153254265 | G | A | 1 | a0001c0007t0003g0233 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.31-16070G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153254265 | |||||||
| chr4:153254302 | C | T | 6 | a0001c0002t0002g0267 a0001c0002t0002g0268 a0001c0002t0003g0239 others(3): Show |
6 | HG02109.hp1 HG02717.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.31-16033C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153254302 | |||||||
| chr4:153254330 | T | C | 77 | a0001c0001t0001g0092 a0001c0001t0001g0099 a0001c0001t0001g0100 others(74): Show |
77 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.31-16005T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153254330 | |||||||
| chr4:153254527 | G | A | 2 | a0001c0001t0004g0087 a0001c0001t0004g0088 |
2 | HG02055.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.31-15808G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153254527 | |||||||
| chr4:153254631 | C | T | 1 | a0001c0008t0002g0059 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.31-15704C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153254631 | |||||||
| chr4:153254744 | G | T | 20 | a0001c0001t0001g0092 a0001c0001t0001g0099 a0001c0001t0001g0100 others(17): Show |
20 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.31-15591G>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153254744 | |||||||
| chr4:153254817 | G | A | 12 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(9): Show |
12 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.31-15518G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153254817 | |||||||
| chr4:153254907 | G | A | 5 | a0001c0001t0002g0002 a0001c0001t0009g0060 a0001c0001t0009g0263 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-15428G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153254907 | |||||||
| chr4:153254923 | T | C | 116 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0001g0092 others(113): Show |
116 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.31-15412T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153254923 | |||||||
| chr4:153254957 | G | T | 100 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0001g0092 others(97): Show |
100 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.31-15378G>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153254957 | |||||||
| chr4:153255017 | C | G | 8 | a0001c0001t0004g0087 a0001c0001t0004g0088 a0001c0002t0002g0267 others(5): Show |
8 | HG02055.hp2 HG02109.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.31-15318C>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153255017 | |||||||
| chr4:153255227 | T | C | 163 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0001g0092 others(160): Show |
163 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.31-15108T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153255227 | |||||||
| chr4:153255260 | T | C | 53 | a0001c0002t0001g0126 a0001c0002t0001g0210 a0001c0002t0003g0144 others(50): Show |
53 | HG00323.hp1 HG00438.hp1 HG00741.hp1 others(50): Show |
intron_variant | MODIFIER | c.31-15075T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153255260 | |||||||
| chr4:153255432 | C | T | 41 | a0001c0002t0001g0066 a0001c0002t0001g0105 a0001c0002t0001g0115 others(38): Show |
41 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.31-14903C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153255432 | |||||||
| chr4:153255590 | G | T | 1 | a0001c0001t0002g0002 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.31-14745G>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153255590 | |||||||
| chr4:153255677 | T | C | 3 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0004t0003g0058 |
3 | HG02886.hp2 HG02965.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.31-14658T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153255677 | |||||||
| chr4:153256045 | G | A | 2 | a0001c0001t0004g0087 a0001c0001t0004g0088 |
2 | HG02055.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.31-14290G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153256045 | |||||||
| chr4:153256051 | C | A | 1 | a0001c0001t0002g0002 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.31-14284C>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153256051 | |||||||
| chr4:153256228 | G | GT | 21 | a0001c0001t0001g0092 a0001c0001t0001g0099 a0001c0001t0001g0100 others(18): Show |
21 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.31-14106dupT | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153256228 | ||||||
| chr4:153256278 | C | G | 43 | a0001c0002t0001g0066 a0001c0002t0001g0105 a0001c0002t0001g0115 others(40): Show |
43 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.31-14057C>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153256278 | |||||||
| chr4:153256795 | A | G | 32 | a0001c0001t0001g0092 a0001c0001t0001g0099 a0001c0001t0001g0100 others(29): Show |
32 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.31-13540A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153256795 | |||||||
| chr4:153256808 | T | C | 3 | a0001c0002t0010g0134 a0001c0002t0013g0133 a0001c0002t0029g0261 |
3 | HG02258.hp1 HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.31-13527T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153256808 | |||||||
| chr4:153256838 | G | A | 32 | a0001c0001t0001g0092 a0001c0001t0001g0099 a0001c0001t0001g0100 others(29): Show |
32 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.31-13497G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153256838 | |||||||
| chr4:153256907 | C | CTGTTTGT others(1): Show |
6 | a0001c0002t0002g0267 a0001c0002t0002g0268 a0001c0002t0003g0239 others(3): Show |
6 | HG02109.hp1 HG02717.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.31-13414_31-13407d others(10): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153256907 | ||||||
| chr4:153256907 | C | CTGTTTGT others(5): Show |
23 | a0001c0001t0001g0092 a0001c0001t0001g0099 a0001c0001t0001g0100 others(20): Show |
23 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.31-13418_31-13407d others(14): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153256907 | ||||||
| chr4:153256907 | C | CTGTTTGT others(9): Show |
2 | a0001c0001t0005g0094 a0001c0002t0028g0080 |
2 | HG02280.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.31-13422_31-13407d others(18): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153256907 | ||||||
| chr4:153256992 | G | A | 3 | a0001c0001t0002g0001 a0001c0001t0004g0008 a0001c0001t0004g0129 |
3 | HG02615.hp1 HG02717.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.31-13343G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153256992 | |||||||
| chr4:153257097 | A | G | 2 | a0001c0001t0015g0117 a0001c0001t0015g0192 |
2 | HG01081.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.31-13238A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153257097 | |||||||
| chr4:153257397 | G | A | 28 | a0001c0001t0001g0092 a0001c0001t0001g0099 a0001c0001t0001g0100 others(25): Show |
28 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.31-12938G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153257397 | |||||||
| chr4:153257545 | A | G | 76 | a0001c0001t0001g0092 a0001c0001t0001g0099 a0001c0001t0001g0100 others(73): Show |
76 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.31-12790A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153257545 | |||||||
| chr4:153257648 | A | G | 12 | a0001c0002t0002g0130 a0001c0002t0002g0136 a0001c0002t0002g0137 others(9): Show |
12 | HG01168.hp1 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.31-12687A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153257648 | |||||||
| chr4:153257864 | T | C | 75 | a0001c0001t0001g0092 a0001c0001t0001g0099 a0001c0001t0001g0100 others(72): Show |
75 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.31-12471T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153257864 | |||||||
| chr4:153258216 | C | T | 1 | a0001c0001t0006g0146 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.31-12119C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153258216 | |||||||
| chr4:153258761 | T | A | 160 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0001g0092 others(157): Show |
160 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.31-11574T>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153258761 | |||||||
| chr4:153258908 | A | G | 6 | a0001c0002t0002g0267 a0001c0002t0002g0268 a0001c0002t0003g0239 others(3): Show |
6 | HG02109.hp1 HG02717.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.31-11427A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153258908 | |||||||
| chr4:153259002 | C | T | 6 | a0001c0002t0002g0267 a0001c0002t0002g0268 a0001c0002t0003g0239 others(3): Show |
6 | HG02109.hp1 HG02717.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.31-11333C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153259002 | |||||||
| chr4:153259126 | G | A | 1 | a0001c0002t0028g0080 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.31-11209G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153259126 | |||||||
| chr4:153259204 | T | A | 3 | a0001c0002t0011g0005 a0001c0002t0011g0006 a0001c0002t0011g0070 |
3 | HG02896.hp2 HG02897.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.31-11131T>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153259204 | |||||||
| chr4:153259225 | T | C | 1 | a0001c0002t0004g0083 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.31-11110T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153259225 | |||||||
| chr4:153259267 | A | C | 3 | a0001c0001t0001g0182 a0001c0001t0002g0065 a0001c0001t0002g0245 |
3 | NA18957.hp1 NA18979.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.31-11068A>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153259267 | |||||||
| chr4:153259320 | A | C | 8 | a0001c0001t0001g0258 a0001c0001t0005g0037 a0001c0001t0008g0032 others(5): Show |
8 | NA18944.hp2 NA18979.hp2 NA18985.hp1 others(5): Show |
intron_variant | MODIFIER | c.31-11015A>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153259320 | |||||||
| chr4:153259358 | G | A | 6 | a0001c0002t0002g0267 a0001c0002t0002g0268 a0001c0002t0003g0239 others(3): Show |
6 | HG02109.hp1 HG02717.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.31-10977G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153259358 | |||||||
| chr4:153259485 | T | C | 4 | a0001c0002t0004g0045 a0001c0002t0004g0046 a0001c0002t0004g0047 others(1): Show |
4 | HG01884.hp1 HG02976.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.31-10850T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153259485 | |||||||
| chr4:153259638 | T | C | 1 | a0001c0002t0002g0194 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.31-10697T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153259638 | |||||||
| chr4:153259642 | T | A | 1 | a0001c0001t0015g0117 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.31-10693T>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153259642 | |||||||
| chr4:153259649 | G | A | 9 | a0001c0001t0001g0092 a0001c0001t0001g0121 a0001c0001t0005g0094 others(6): Show |
9 | NA18942.hp1 NA18943.hp1 NA18964.hp2 others(6): Show |
intron_variant | MODIFIER | c.31-10686G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153259649 | |||||||
| chr4:153259996 | T | C | 1 | a0001c0002t0028g0080 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.31-10339T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153259996 | |||||||
| chr4:153260178 | C | A | 8 | a0001c0001t0006g0061 a0001c0001t0006g0143 a0001c0001t0006g0146 others(5): Show |
8 | HG01243.hp2 HG02257.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.31-10157C>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153260178 | |||||||
| chr4:153260243 | T | G | 1 | a0001c0001t0001g0195 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.31-10092T>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153260243 | |||||||
| chr4:153260671 | C | G | 1 | a0001c0007t0003g0233 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.31-9664C>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153260671 | |||||||
| chr4:153260686 | A | C | 1 | a0001c0002t0004g0047 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.31-9649A>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153260686 | |||||||
| chr4:153260690 | A | AC | 28 | a0001c0001t0001g0023 a0001c0001t0001g0033 a0001c0001t0001g0056 others(25): Show |
28 | HG00323.hp2 HG00544.hp2 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.31-9634dupC | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153260690 | ||||||
| chr4:153260690 | A | C | 5 | a0001c0002t0004g0045 a0001c0002t0004g0046 a0001c0002t0004g0047 others(2): Show |
5 | HG01884.hp1 HG02976.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-9645A>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153260690 | |||||||
| chr4:153260690 | ACCCCCC | A | 12 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(9): Show |
12 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.31-9639_31-9634del others(6): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153260690 | ||||||
| chr4:153260694 | C | CCTCACAC others(3): Show |
8 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0002g0002 others(5): Show |
8 | HG01891.hp2 HG02258.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.31-9640_31-9639ins others(10): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153260694 | ||||||
| chr4:153260694 | C | CCTCACAC others(7): Show |
5 | a0001c0001t0006g0061 a0001c0001t0006g0143 a0001c0001t0009g0060 others(2): Show |
5 | HG02280.hp2 HG03041.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.31-9640_31-9639ins others(14): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153260694 | ||||||
| chr4:153260694 | C | CCTCACAC others(9): Show |
5 | a0001c0001t0006g0146 a0001c0001t0006g0149 a0001c0001t0006g0160 others(2): Show |
5 | HG01243.hp2 HG02257.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.31-9640_31-9639ins others(16): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153260694 | ||||||
| chr4:153260694 | C | CCTCACAC others(11): Show |
1 | a0001c0001t0006g0147 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.31-9640_31-9639ins others(18): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153260694 | ||||||
| chr4:153260694 | CCCCCCCC others(3): Show |
C | 9 | a0001c0001t0001g0092 a0001c0001t0001g0121 a0001c0001t0005g0094 others(6): Show |
9 | NA18942.hp1 NA18943.hp1 NA18964.hp2 others(6): Show |
intron_variant | MODIFIER | c.31-9639_31-9630del others(10): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153260694 | ||||||
| chr4:153260696 | C | A | 37 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0002g0002 others(34): Show |
37 | HG01168.hp1 HG01243.hp2 HG01891.hp2 others(34): Show |
intron_variant | MODIFIER | c.31-9639C>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153260696 | |||||||
| chr4:153260696 | C | T | 47 | a0001c0003t0001g0003 a0001c0003t0001g0027 a0001c0003t0001g0041 others(44): Show |
47 | HG00323.hp1 HG00438.hp1 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.31-9639C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153260696 | |||||||
| chr4:153260698 | C | A | 85 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0002g0002 others(82): Show |
85 | HG00323.hp1 HG00438.hp1 HG00741.hp1 others(82): Show |
intron_variant | MODIFIER | c.31-9637C>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153260698 | |||||||
| chr4:153260700 | C | A | 92 | a0001c0001t0001g0055 a0001c0001t0001g0072 a0001c0001t0001g0081 others(89): Show |
92 | HG00323.hp1 HG00438.hp1 HG00735.hp1 others(89): Show |
intron_variant | MODIFIER | c.31-9635C>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153260700 | |||||||
| chr4:153260701 | CA | C | 4 | a0001c0001t0001g0017 a0001c0001t0001g0062 a0001c0001t0001g0162 others(1): Show |
4 | HG02280.hp1 HG02622.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.31-9633delA | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153260701 | |||||||
| chr4:153260702 | A | C | 49 | a0001c0001t0001g0023 a0001c0001t0001g0040 a0001c0001t0001g0063 others(46): Show |
49 | HG00323.hp2 HG00438.hp2 HG01070.hp1 others(46): Show |
intron_variant | MODIFIER | c.31-9633A>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153260702 | |||||||
| chr4:153260702 | A | T | 12 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(9): Show |
12 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.31-9633A>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153260702 | |||||||
| chr4:153260704 | A | ACCCCCCC others(3): Show |
1 | a0001c0002t0012g0163 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.31-9630_31-9629ins others(10): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153260704 | ||||||
| chr4:153260704 | A | C | 21 | a0001c0001t0001g0120 a0001c0001t0001g0151 a0001c0001t0008g0044 others(18): Show |
21 | HG00323.hp2 HG01070.hp1 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.31-9631A>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153260704 | |||||||
| chr4:153260706 | A | C | 15 | a0001c0002t0001g0066 a0001c0002t0001g0105 a0001c0002t0001g0115 others(12): Show |
15 | HG00323.hp2 HG01070.hp1 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.31-9629A>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153260706 | |||||||
| chr4:153260706 | A | T | 9 | a0001c0001t0001g0092 a0001c0001t0001g0121 a0001c0001t0005g0094 others(6): Show |
9 | NA18942.hp1 NA18943.hp1 NA18964.hp2 others(6): Show |
intron_variant | MODIFIER | c.31-9629A>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153260706 | |||||||
| chr4:153260708 | A | C | 7 | a0001c0002t0001g0066 a0001c0002t0001g0105 a0001c0002t0001g0115 others(4): Show |
7 | HG00323.hp2 HG01070.hp1 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.31-9627A>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153260708 | |||||||
| chr4:153260710 | A | C | 3 | a0001c0002t0001g0066 a0001c0002t0001g0115 a0001c0002t0004g0069 |
3 | HG01070.hp1 HG01109.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.31-9625A>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153260710 | |||||||
| chr4:153260722 | AC | A | 12 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(9): Show |
12 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.31-9612delC | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153260722 | |||||||
| chr4:153260724 | A | T | 12 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(9): Show |
12 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.31-9611A>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153260724 | |||||||
| chr4:153260724 | ACAT | A | 20 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0002t0002g0130 others(17): Show |
20 | HG01168.hp1 HG02109.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.31-9592_31-9590del others(3): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153260724 | ||||||
| chr4:153260726 | A | AC | 40 | a0001c0003t0001g0003 a0001c0003t0001g0027 a0001c0003t0001g0041 others(37): Show |
40 | HG00323.hp1 HG00438.hp1 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.31-9609_31-9608ins others(1): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153260726 | |||||||
| chr4:153260727 | T | A | 40 | a0001c0003t0001g0003 a0001c0003t0001g0027 a0001c0003t0001g0041 others(37): Show |
40 | HG00323.hp1 HG00438.hp1 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.31-9608T>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153260727 | |||||||
| chr4:153260728 | CATCATCA others(11): Show |
C | 4 | a0001c0001t0004g0008 a0001c0001t0004g0087 a0001c0001t0004g0088 others(1): Show |
4 | HG02055.hp2 HG02615.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.31-9589_31-9572del others(18): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153260728 | ||||||
| chr4:153260737 | C | G | 1 | a0001c0001t0001g0249 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.31-9598C>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153260737 | |||||||
| chr4:153260740 | C | G | 1 | a0001c0002t0001g0220 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.31-9595C>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153260740 | |||||||
| chr4:153260743 | C | G | 12 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(9): Show |
12 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.31-9592C>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153260743 | |||||||
| chr4:153260746 | G | C | 15 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(12): Show |
15 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.31-9589G>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153260746 | |||||||
| chr4:153260777 | G | A | 21 | a0001c0001t0001g0092 a0001c0001t0001g0099 a0001c0001t0001g0100 others(18): Show |
21 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.31-9558G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153260777 | |||||||
| chr4:153260965 | T | A | 1 | a0001c0002t0003g0144 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.31-9370T>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153260965 | |||||||
| chr4:153261138 | T | C | 17 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0002g0002 others(14): Show |
17 | HG01243.hp2 HG01891.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.31-9197T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153261138 | |||||||
| chr4:153261282 | T | G | 21 | a0001c0001t0001g0092 a0001c0001t0001g0099 a0001c0001t0001g0100 others(18): Show |
21 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.31-9053T>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153261282 | |||||||
| chr4:153261492 | G | A | 2 | a0001c0001t0001g0039 a0001c0001t0001g0040 |
2 | HG00438.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.31-8843G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153261492 | |||||||
| chr4:153261768 | G | T | 6 | a0001c0002t0002g0267 a0001c0002t0002g0268 a0001c0002t0003g0239 others(3): Show |
6 | HG02109.hp1 HG02717.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.31-8567G>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153261768 | |||||||
| chr4:153262164 | C | T | 11 | a0001c0001t0002g0018 a0001c0001t0002g0022 a0001c0001t0003g0265 others(8): Show |
11 | HG01169.hp1 HG01243.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.31-8171C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153262164 | |||||||
| chr4:153262243 | A | G | 1 | a0001c0001t0005g0110 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.31-8092A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153262243 | |||||||
| chr4:153262561 | C | G | 21 | a0001c0001t0001g0092 a0001c0001t0001g0099 a0001c0001t0001g0100 others(18): Show |
21 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.31-7774C>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153262561 | |||||||
| chr4:153262624 | C | T | 12 | a0001c0002t0002g0130 a0001c0002t0002g0136 a0001c0002t0002g0137 others(9): Show |
12 | HG01168.hp1 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.31-7711C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153262624 | |||||||
| chr4:153262846 | G | A | 3 | a0001c0002t0001g0167 a0001c0002t0002g0215 a0001c0002t0002g0260 |
3 | HG00140.hp2 HG01081.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.31-7489G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153262846 | |||||||
| chr4:153262926 | C | T | 3 | a0001c0001t0002g0018 a0001c0001t0002g0022 a0001c0001t0003g0265 |
3 | HG01169.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.31-7409C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153262926 | |||||||
| chr4:153263036 | C | G | 4 | a0001c0002t0004g0045 a0001c0002t0004g0046 a0001c0002t0004g0047 others(1): Show |
4 | HG01884.hp1 HG02976.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.31-7299C>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153263036 | |||||||
| chr4:153263040 | C | T | 6 | a0001c0002t0002g0267 a0001c0002t0002g0268 a0001c0002t0003g0239 others(3): Show |
6 | HG02109.hp1 HG02717.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.31-7295C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153263040 | |||||||
| chr4:153263129 | G | A | 4 | a0001c0001t0005g0037 a0001c0001t0008g0032 a0001c0001t0008g0038 others(1): Show |
4 | HG03834.hp2 NA18988.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.31-7206G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153263129 | |||||||
| chr4:153263189 | T | C | 21 | a0001c0001t0001g0092 a0001c0001t0001g0099 a0001c0001t0001g0100 others(18): Show |
21 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.31-7146T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153263189 | |||||||
| chr4:153263252 | C | G | 3 | a0001c0001t0002g0018 a0001c0001t0002g0022 a0001c0001t0003g0265 |
3 | HG01169.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.31-7083C>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153263252 | |||||||
| chr4:153263255 | G | A | 1 | a0001c0002t0002g0166 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.31-7080G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153263255 | |||||||
| chr4:153263303 | C | A | 1 | a0001c0001t0008g0020 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.31-7032C>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153263303 | |||||||
| chr4:153263315 | G | A | 21 | a0001c0001t0001g0092 a0001c0001t0001g0099 a0001c0001t0001g0100 others(18): Show |
21 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.31-7020G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153263315 | |||||||
| chr4:153263369 | A | G | 6 | a0001c0002t0002g0267 a0001c0002t0002g0268 a0001c0002t0003g0239 others(3): Show |
6 | HG02109.hp1 HG02717.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.31-6966A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153263369 | |||||||
| chr4:153263480 | T | A | 17 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0002g0002 others(14): Show |
17 | HG01243.hp2 HG01891.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.31-6855T>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153263480 | |||||||
| chr4:153263624 | C | A | 1 | a0001c0001t0001g0157 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.31-6711C>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153263624 | |||||||
| chr4:153263660 | A | G | 6 | a0001c0002t0002g0267 a0001c0002t0002g0268 a0001c0002t0003g0239 others(3): Show |
6 | HG02109.hp1 HG02717.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.31-6675A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153263660 | |||||||
| chr4:153263680 | A | G | 4 | a0001c0002t0004g0045 a0001c0002t0004g0046 a0001c0002t0004g0047 others(1): Show |
4 | HG01884.hp1 HG02976.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.31-6655A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153263680 | |||||||
| chr4:153263696 | G | A | 21 | a0001c0001t0001g0092 a0001c0001t0001g0099 a0001c0001t0001g0100 others(18): Show |
21 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.31-6639G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153263696 | |||||||
| chr4:153263769 | C | T | 1 | a0001c0002t0002g0090 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.31-6566C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153263769 | |||||||
| chr4:153263917 | C | T | 12 | a0001c0002t0002g0130 a0001c0002t0002g0136 a0001c0002t0002g0137 others(9): Show |
12 | HG01168.hp1 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.31-6418C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153263917 | |||||||
| chr4:153263935 | G | A | 21 | a0001c0001t0001g0092 a0001c0001t0001g0099 a0001c0001t0001g0100 others(18): Show |
21 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.31-6400G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153263935 | |||||||
| chr4:153264146 | G | C | 21 | a0001c0001t0001g0092 a0001c0001t0001g0099 a0001c0001t0001g0100 others(18): Show |
21 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.31-6189G>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153264146 | |||||||
| chr4:153264287 | C | G | 12 | a0001c0002t0002g0130 a0001c0002t0002g0136 a0001c0002t0002g0137 others(9): Show |
12 | HG01168.hp1 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.31-6048C>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153264287 | |||||||
| chr4:153264384 | G | A | 93 | a0001c0001t0001g0092 a0001c0001t0001g0099 a0001c0001t0001g0100 others(90): Show |
93 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.31-5951G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153264384 | |||||||
| chr4:153264514 | G | A | 1 | a0001c0003t0002g0052 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.31-5821G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153264514 | |||||||
| chr4:153264525 | GTC | G | 21 | a0001c0001t0001g0092 a0001c0001t0001g0099 a0001c0001t0001g0100 others(18): Show |
21 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.31-5806_31-5805del others(2): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153264525 | ||||||
| chr4:153264770 | C | G | 21 | a0001c0001t0001g0092 a0001c0001t0001g0099 a0001c0001t0001g0100 others(18): Show |
21 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.31-5565C>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153264770 | |||||||
| chr4:153264817 | G | T | 137 | a0001c0001t0001g0092 a0001c0001t0001g0099 a0001c0001t0001g0100 others(134): Show |
137 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.31-5518G>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153264817 | |||||||
| chr4:153264818 | C | A | 17 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0002g0002 others(14): Show |
17 | HG01243.hp2 HG01891.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.31-5517C>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153264818 | |||||||
| chr4:153264857 | C | T | 1 | a0001c0002t0004g0083 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.31-5478C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153264857 | |||||||
| chr4:153265077 | T | C | 1 | a0001c0001t0001g0033 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.31-5258T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153265077 | |||||||
| chr4:153265103 | C | T | 4 | a0001c0003t0003g0030 a0001c0003t0003g0031 a0001c0003t0003g0043 others(1): Show |
4 | HG01074.hp1 HG01517.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-5232C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153265103 | |||||||
| chr4:153265338 | GT | G | 50 | a0001c0003t0001g0003 a0001c0003t0001g0027 a0001c0003t0001g0041 others(47): Show |
50 | HG00323.hp1 HG00438.hp1 HG00741.hp1 others(47): Show |
intron_variant | MODIFIER | c.31-4988delT | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153265338 | ||||||
| chr4:153265339 | T | G | 65 | a0001c0002t0001g0066 a0001c0002t0001g0105 a0001c0002t0001g0115 others(62): Show |
65 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.31-4996T>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153265339 | |||||||
| chr4:153265351 | A | AT | 10 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0003t0003g0067 others(7): Show |
10 | HG00438.hp1 HG02027.hp2 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.31-4973dupT | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153265351 | ||||||
| chr4:153265370 | A | G | 1 | a0001c0001t0001g0179 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.31-4965A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153265370 | |||||||
| chr4:153265467 | C | T | 8 | a0001c0001t0006g0061 a0001c0001t0006g0143 a0001c0001t0006g0146 others(5): Show |
8 | HG01243.hp2 HG02257.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.31-4868C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153265467 | |||||||
| chr4:153265489 | G | A | 1 | a0001c0003t0003g0165 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.31-4846G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153265489 | |||||||
| chr4:153265491 | C | T | 4 | a0001c0001t0006g0019 a0001c0001t0006g0086 a0001c0001t0006g0123 others(1): Show |
4 | HG02572.hp2 HG03130.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-4844C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153265491 | |||||||
| chr4:153265634 | C | A | 3 | a0001c0002t0002g0108 a0001c0002t0002g0109 a0001c0002t0002g0124 |
3 | NA18939.hp1 NA18954.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.31-4701C>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153265634 | |||||||
| chr4:153265635 | G | T | 12 | a0001c0003t0001g0041 a0001c0003t0003g0053 a0001c0003t0003g0054 others(9): Show |
12 | HG01891.hp1 HG02055.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.31-4700G>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153265635 | |||||||
| chr4:153265773 | T | TAC | 160 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0001g0092 others(157): Show |
160 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.31-4551_31-4550dup others(2): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153265773 | ||||||
| chr4:153266238 | C | T | 1 | a0001c0002t0002g0260 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.31-4097C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153266238 | |||||||
| chr4:153266254 | T | C | 1 | a0001c0002t0028g0080 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.31-4081T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153266254 | |||||||
| chr4:153266321 | C | T | 1 | a0001c0001t0001g0164 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.31-4014C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153266321 | |||||||
| chr4:153266343 | G | GT | 5 | a0001c0002t0002g0267 a0001c0002t0002g0268 a0001c0002t0003g0239 others(2): Show |
5 | HG02109.hp1 HG02717.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.31-3992_31-3991ins others(1): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153266343 | |||||||
| chr4:153266344 | G | GT | 87 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0001g0091 others(84): Show |
87 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.31-3974dupT | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153266344 | ||||||
| chr4:153266344 | G | GTT | 16 | a0001c0001t0006g0143 a0001c0002t0001g0066 a0001c0002t0002g0108 others(13): Show |
16 | HG01109.hp1 HG02055.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.31-3975_31-3974dup others(2): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153266344 | ||||||
| chr4:153266344 | G | GTTT | 30 | a0001c0003t0001g0003 a0001c0003t0001g0041 a0001c0003t0001g0131 others(27): Show |
30 | HG00323.hp1 HG00438.hp1 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.31-3976_31-3974dup others(3): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153266344 | ||||||
| chr4:153266344 | G | GTTTT | 8 | a0001c0003t0001g0027 a0001c0003t0003g0015 a0001c0003t0003g0025 others(5): Show |
8 | HG01069.hp1 HG01346.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.31-3977_31-3974dup others(4): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153266344 | ||||||
| chr4:153266344 | G | T | 6 | a0001c0002t0002g0267 a0001c0002t0002g0268 a0001c0002t0003g0239 others(3): Show |
6 | HG02109.hp1 HG02717.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.31-3991G>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153266344 | |||||||
| chr4:153266404 | G | A | 50 | a0001c0003t0001g0003 a0001c0003t0001g0027 a0001c0003t0001g0041 others(47): Show |
50 | HG00323.hp1 HG00438.hp1 HG00741.hp1 others(47): Show |
intron_variant | MODIFIER | c.31-3931G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153266404 | |||||||
| chr4:153266458 | A | T | 163 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0001g0092 others(160): Show |
163 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.31-3877A>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153266458 | |||||||
| chr4:153266631 | G | C | 4 | a0001c0002t0004g0045 a0001c0002t0004g0046 a0001c0002t0004g0047 others(1): Show |
4 | HG01884.hp1 HG02976.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.31-3704G>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153266631 | |||||||
| chr4:153266640 | C | CT | 81 | a0001c0001t0001g0055 a0001c0001t0001g0118 a0001c0001t0002g0002 others(78): Show |
81 | HG00323.hp1 HG00438.hp1 HG00741.hp1 others(78): Show |
intron_variant | MODIFIER | c.31-3679dupT | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153266640 | ||||||
| chr4:153266640 | C | CTT | 11 | a0001c0001t0001g0072 a0001c0001t0001g0081 a0001c0002t0002g0171 others(8): Show |
11 | HG01168.hp1 HG01884.hp2 HG01975.hp2 others(8): Show |
intron_variant | MODIFIER | c.31-3680_31-3679dup others(2): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153266640 | ||||||
| chr4:153266640 | CT | C | 5 | a0001c0001t0001g0056 a0001c0001t0002g0018 a0001c0001t0002g0022 others(2): Show |
5 | HG00323.hp2 HG01169.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.31-3679delT | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153266640 | ||||||
| chr4:153266650 | T | C | 1 | a0001c0001t0002g0237 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.31-3685T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153266650 | |||||||
| chr4:153266877 | C | T | 1 | a0001c0002t0003g0144 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.31-3458C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153266877 | |||||||
| chr4:153266893 | G | GT | 14 | a0001c0001t0001g0040 a0001c0001t0001g0170 a0001c0001t0001g0188 others(11): Show |
14 | HG00280.hp1 HG00438.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.31-3423dupT | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153266893 | ||||||
| chr4:153266893 | GT | G | 91 | a0001c0001t0001g0193 a0001c0001t0002g0018 a0001c0002t0001g0066 others(88): Show |
91 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.31-3423delT | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153266893 | ||||||
| chr4:153266893 | GTT | G | 20 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0002g0002 others(17): Show |
20 | HG01243.hp2 HG01891.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.31-3424_31-3423del others(2): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153266893 | ||||||
| chr4:153267068 | T | G | 21 | a0001c0001t0001g0092 a0001c0001t0001g0099 a0001c0001t0001g0100 others(18): Show |
21 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.31-3267T>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153267068 | |||||||
| chr4:153267095 | G | GGAAAAGA others(322): Show |
1 | a0001c0001t0001g0121 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.31-3222_31-3221ins others(329): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153267095 | ||||||
| chr4:153267095 | G | GGAAAAGA others(332): Show |
1 | a0001c0001t0005g0214 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.31-3222_31-3221ins others(339): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153267095 | ||||||
| chr4:153267095 | G | GGAAAAGA others(334): Show |
1 | a0001c0001t0005g0252 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.31-3222_31-3221ins others(341): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153267095 | ||||||
| chr4:153267095 | G | GGAAAAGA others(335): Show |
1 | a0001c0001t0005g0110 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.31-3222_31-3221ins others(342): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153267095 | ||||||
| chr4:153267095 | G | GGAAAAGA others(336): Show |
2 | a0001c0001t0005g0094 a0001c0001t0021g0111 |
2 | NA19084.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.31-3222_31-3221ins others(343): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153267095 | ||||||
| chr4:153267095 | G | GGAAAAGA others(343): Show |
2 | a0001c0001t0001g0092 a0001c0001t0005g0161 |
2 | NA18964.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.31-3222_31-3221ins others(350): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153267095 | ||||||
| chr4:153267095 | G | GGAAAAGA others(347): Show |
1 | a0001c0001t0005g0244 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.31-3222_31-3221ins others(354): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153267095 | ||||||
| chr4:153267095 | G | GGAAAAGA others(319): Show |
1 | a0001c0001t0005g0242 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.31-3226_31-3225ins others(326): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153267095 | ||||||
| chr4:153267095 | G | GGAAAAGA others(320): Show |
1 | a0001c0001t0005g0103 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.31-3226_31-3225ins others(327): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153267095 | ||||||
| chr4:153267095 | G | GGAAAAGA others(329): Show |
1 | a0001c0002t0002g0090 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.31-3226_31-3225ins others(336): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153267095 | ||||||
| chr4:153267095 | G | GGAAAAGA others(331): Show |
1 | a0001c0002t0002g0194 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.31-3226_31-3225ins others(338): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153267095 | ||||||
| chr4:153267095 | G | GGAAAAGA others(332): Show |
4 | a0001c0001t0001g0099 a0001c0001t0001g0102 a0001c0001t0002g0235 others(1): Show |
4 | HG00642.hp2 HG00735.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.31-3226_31-3225ins others(339): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153267095 | ||||||
| chr4:153267095 | G | GGAAAAGA others(333): Show |
2 | a0001c0001t0001g0100 a0001c0001t0002g0240 |
2 | HG01261.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.31-3226_31-3225ins others(340): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153267095 | ||||||
| chr4:153267095 | G | GGAAAAGA others(337): Show |
2 | a0001c0001t0001g0101 a0001c0001t0001g0241 |
2 | HG00280.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.31-3226_31-3225ins others(344): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153267095 | ||||||
| chr4:153267423 | C | T | 6 | a0001c0002t0002g0267 a0001c0002t0002g0268 a0001c0002t0003g0239 others(3): Show |
6 | HG02109.hp1 HG02717.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.31-2912C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153267423 | |||||||
| chr4:153267434 | C | T | 133 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0002g0002 others(130): Show |
133 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.31-2901C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153267434 | |||||||
| chr4:153267468 | T | C | 133 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0002g0002 others(130): Show |
133 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.31-2867T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153267468 | |||||||
| chr4:153267480 | A | G | 139 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0002g0002 others(136): Show |
139 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.31-2855A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153267480 | |||||||
| chr4:153267488 | T | TAA | 133 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0002g0002 others(130): Show |
133 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.31-2843_31-2842dup others(2): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153267488 | ||||||
| chr4:153267757 | CTCTT | C | 21 | a0001c0001t0001g0092 a0001c0001t0001g0099 a0001c0001t0001g0100 others(18): Show |
21 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.31-2572_31-2569del others(4): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153267757 | ||||||
| chr4:153267760 | TTTC | T | 3 | a0001c0002t0002g0108 a0001c0002t0002g0109 a0001c0002t0002g0124 |
3 | NA18939.hp1 NA18954.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.31-2572_31-2570del others(3): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 153267760 | ||||||
| chr4:153267836 | C | G | 1 | a0001c0003t0007g0223 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.31-2499C>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153267836 | |||||||
| chr4:153267858 | T | C | 3 | a0001c0003t0001g0003 a0001c0003t0001g0131 a0001c0003t0001g0132 |
3 | HG01884.hp2 HG02486.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.31-2477T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153267858 | |||||||
| chr4:153267882 | G | A | 1 | a0001c0001t0001g0200 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.31-2453G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153267882 | |||||||
| chr4:153267900 | T | A | 133 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0002g0002 others(130): Show |
133 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.31-2435T>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153267900 | |||||||
| chr4:153267967 | A | G | 2 | a0001c0002t0002g0139 a0001c0002t0022g0140 |
2 | HG02145.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.31-2368A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153267967 | |||||||
| chr4:153268214 | G | A | 1 | a0001c0001t0002g0002 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.31-2121G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153268214 | |||||||
| chr4:153268236 | T | A | 133 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0002g0002 others(130): Show |
133 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.31-2099T>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153268236 | |||||||
| chr4:153268237 | C | A | 133 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0002g0002 others(130): Show |
133 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.31-2098C>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153268237 | |||||||
| chr4:153268249 | G | A | 133 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0002g0002 others(130): Show |
133 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.31-2086G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153268249 | |||||||
| chr4:153268323 | G | T | 6 | a0001c0002t0002g0267 a0001c0002t0002g0268 a0001c0002t0003g0239 others(3): Show |
6 | HG02109.hp1 HG02717.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.31-2012G>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153268323 | |||||||
| chr4:153268372 | T | TG | 133 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0002g0002 others(130): Show |
133 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.31-1963_31-1962ins others(1): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153268372 | |||||||
| chr4:153268429 | G | A | 49 | a0001c0001t0001g0100 a0001c0002t0001g0066 a0001c0002t0001g0105 others(46): Show |
49 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.31-1906G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153268429 | |||||||
| chr4:153268643 | T | G | 3 | a0001c0001t0009g0060 a0001c0001t0009g0263 a0001c0001t0009g0264 |
3 | HG02280.hp2 HG03041.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.31-1692T>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153268643 | |||||||
| chr4:153268792 | C | T | 2 | a0001c0001t0001g0183 a0001c0001t0001g0189 |
2 | HG01175.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.31-1543C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153268792 | |||||||
| chr4:153268972 | T | G | 1 | a0001c0002t0003g0144 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.31-1363T>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153268972 | |||||||
| chr4:153269139 | G | A | 84 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0002g0002 others(81): Show |
84 | HG00323.hp1 HG00438.hp1 HG00741.hp1 others(81): Show |
intron_variant | MODIFIER | c.31-1196G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153269139 | |||||||
| chr4:153269212 | T | G | 12 | a0001c0002t0002g0130 a0001c0002t0002g0136 a0001c0002t0002g0137 others(9): Show |
12 | HG01168.hp1 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.31-1123T>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153269212 | |||||||
| chr4:153269253 | G | A | 1 | a0001c0002t0001g0210 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.31-1082G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153269253 | |||||||
| chr4:153269290 | T | C | 1 | a0001c0002t0002g0254 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.31-1045T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153269290 | |||||||
| chr4:153269387 | A | G | 1 | a0001c0001t0001g0182 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.31-948A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153269387 | |||||||
| chr4:153269388 | G | A | 50 | a0001c0003t0001g0003 a0001c0003t0001g0027 a0001c0003t0001g0041 others(47): Show |
50 | HG00323.hp1 HG00438.hp1 HG00741.hp1 others(47): Show |
intron_variant | MODIFIER | c.31-947G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153269388 | |||||||
| chr4:153269569 | T | A | 4 | a0001c0002t0004g0045 a0001c0002t0004g0046 a0001c0002t0004g0047 others(1): Show |
4 | HG01884.hp1 HG02976.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.31-766T>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153269569 | |||||||
| chr4:153269737 | C | T | 76 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0002g0001 others(73): Show |
76 | HG00323.hp1 HG00438.hp1 HG00741.hp1 others(73): Show |
intron_variant | MODIFIER | c.31-598C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153269737 | |||||||
| chr4:153269756 | A | C | 1 | a0001c0001t0001g0039 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.31-579A>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153269756 | |||||||
| chr4:153269813 | A | G | 19 | a0001c0002t0001g0066 a0001c0002t0001g0105 a0001c0002t0001g0115 others(16): Show |
19 | HG00323.hp2 HG01070.hp1 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.31-522A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153269813 | |||||||
| chr4:153269991 | C | T | 1 | a0001c0001t0001g0179 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.31-344C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153269991 | |||||||
| chr4:153269998 | A | G | 94 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0002g0001 others(91): Show |
94 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.31-337A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153269998 | |||||||
| chr4:153270074 | G | A | 19 | a0001c0002t0001g0066 a0001c0002t0001g0105 a0001c0002t0001g0115 others(16): Show |
19 | HG00323.hp2 HG01070.hp1 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.31-261G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153270074 | |||||||
| chr4:153270118 | C | T | 12 | a0001c0002t0002g0130 a0001c0002t0002g0136 a0001c0002t0002g0137 others(9): Show |
12 | HG01168.hp1 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.31-217C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153270118 | |||||||
| chr4:153270129 | T | C | 49 | a0001c0002t0001g0066 a0001c0002t0001g0105 a0001c0002t0001g0115 others(46): Show |
49 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.31-206T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 1/11 | chr4 | 153270129 | |||||||
| chr4:153270558 | G | A | 46 | a0001c0002t0001g0066 a0001c0002t0001g0105 a0001c0002t0001g0115 others(43): Show |
46 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.215+39G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 2/11 | chr4 | 153270558 | |||||||
| chr4:153270736 | G | A | 12 | a0001c0002t0002g0130 a0001c0002t0002g0136 a0001c0002t0002g0137 others(9): Show |
12 | HG01168.hp1 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.215+217G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 2/11 | chr4 | 153270736 | |||||||
| chr4:153270974 | C | G | 6 | a0001c0002t0002g0267 a0001c0002t0002g0268 a0001c0002t0003g0239 others(3): Show |
6 | HG02109.hp1 HG02717.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.215+455C>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 2/11 | chr4 | 153270974 | |||||||
| chr4:153271099 | T | C | 1 | a0001c0001t0001g0118 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.215+580T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 2/11 | chr4 | 153271099 | |||||||
| chr4:153271230 | AAAGTT | A | 6 | a0001c0002t0002g0267 a0001c0002t0002g0268 a0001c0002t0003g0239 others(3): Show |
6 | HG02109.hp1 HG02717.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.215+713_215+717del others(5): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 153271230 | ||||||
| chr4:153271352 | G | A | 95 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0002g0001 others(92): Show |
95 | HG00323.hp1 HG00438.hp1 HG00741.hp1 others(92): Show |
intron_variant | MODIFIER | c.215+833G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 2/11 | chr4 | 153271352 | |||||||
| chr4:153271602 | T | A | 50 | a0001c0003t0001g0003 a0001c0003t0001g0027 a0001c0003t0001g0041 others(47): Show |
50 | HG00323.hp1 HG00438.hp1 HG00741.hp1 others(47): Show |
intron_variant | MODIFIER | c.215+1083T>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 2/11 | chr4 | 153271602 | |||||||
| chr4:153271761 | A | C | 116 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0001g0092 others(113): Show |
116 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.215+1242A>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 2/11 | chr4 | 153271761 | |||||||
| chr4:153271772 | C | T | 2 | a0001c0001t0001g0183 a0001c0001t0001g0189 |
2 | HG01175.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.215+1253C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 2/11 | chr4 | 153271772 | |||||||
| chr4:153271795 | G | A | 6 | a0001c0003t0002g0004 a0001c0003t0003g0011 a0001c0003t0003g0042 others(3): Show |
6 | HG02109.hp2 HG02965.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.215+1276G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 2/11 | chr4 | 153271795 | |||||||
| chr4:153271826 | G | A | 2 | a0001c0001t0001g0097 a0001c0001t0001g0098 |
2 | HG00140.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.215+1307G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 2/11 | chr4 | 153271826 | |||||||
| chr4:153271922 | G | C | 1 | a0001c0003t0010g0079 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.215+1403G>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 2/11 | chr4 | 153271922 | |||||||
| chr4:153272145 | T | TTTTA | 95 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0002g0001 others(92): Show |
95 | HG00323.hp1 HG00438.hp1 HG00741.hp1 others(92): Show |
intron_variant | MODIFIER | c.215+1629_215+1630i others(6): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 153272145 | ||||||
| chr4:153272178 | G | A | 2 | a0001c0001t0005g0103 a0001c0001t0005g0242 |
2 | HG03017.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.215+1659G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 2/11 | chr4 | 153272178 | |||||||
| chr4:153272209 | C | T | 1 | a0001c0001t0010g0078 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.215+1690C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 2/11 | chr4 | 153272209 | |||||||
| chr4:153272242 | G | A | 1 | a0001c0002t0028g0080 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.215+1723G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 2/11 | chr4 | 153272242 | |||||||
| chr4:153272250 | G | A | 1 | a0001c0002t0028g0080 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.215+1731G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 2/11 | chr4 | 153272250 | |||||||
| chr4:153272477 | A | ATTAT | 12 | a0001c0002t0002g0130 a0001c0002t0002g0136 a0001c0002t0002g0137 others(9): Show |
12 | HG01168.hp1 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.215+1961_215+1962i others(6): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 153272477 | ||||||
| chr4:153272481 | A | T | 91 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0002g0001 others(88): Show |
91 | HG00323.hp1 HG00438.hp1 HG00741.hp1 others(88): Show |
intron_variant | MODIFIER | c.215+1962A>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 2/11 | chr4 | 153272481 | |||||||
| chr4:153272491 | A | T | 67 | a0001c0002t0002g0130 a0001c0002t0002g0136 a0001c0002t0002g0137 others(64): Show |
67 | HG00323.hp1 HG00438.hp1 HG00741.hp1 others(64): Show |
intron_variant | MODIFIER | c.215+1972A>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 2/11 | chr4 | 153272491 | |||||||
| chr4:153272509 | C | T | 1 | a0001c0001t0001g0033 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.215+1990C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 2/11 | chr4 | 153272509 | |||||||
| chr4:153272751 | G | T | 1 | a0001c0001t0016g0231 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.215+2232G>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 2/11 | chr4 | 153272751 | |||||||
| chr4:153272771 | GAGA | G | 20 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0002g0001 others(17): Show |
20 | HG01243.hp2 HG01891.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.215+2256_215+2258d others(5): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 153272771 | ||||||
| chr4:153272826 | G | T | 2 | a0001c0002t0002g0050 a0001c0002t0002g0145 |
2 | HG02738.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.215+2307G>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 2/11 | chr4 | 153272826 | |||||||
| chr4:153272829 | TTTTG | T | 95 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0002g0001 others(92): Show |
95 | HG00323.hp1 HG00438.hp1 HG00741.hp1 others(92): Show |
intron_variant | MODIFIER | c.215+2334_215+2337d others(6): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 153272829 | ||||||
| chr4:153273088 | C | T | 2 | a0001c0001t0001g0195 a0001c0001t0001g0222 |
2 | HG00741.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.215+2569C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 2/11 | chr4 | 153273088 | |||||||
| chr4:153273090 | G | A | 7 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(4): Show |
7 | HG00280.hp2 HG00642.hp2 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.215+2571G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 2/11 | chr4 | 153273090 | |||||||
| chr4:153273128 | C | T | 1 | a0001c0001t0004g0104 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.215+2609C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 2/11 | chr4 | 153273128 | |||||||
| chr4:153273270 | C | CATTTTTT others(11): Show |
1 | a0001c0001t0004g0008 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.216-2623_216-2622i others(20): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 2/11 | chr4 | 153273270 | |||||||
| chr4:153273270 | C | CATTTTTT others(12): Show |
3 | a0001c0001t0004g0087 a0001c0001t0004g0088 a0001c0001t0004g0129 |
3 | HG02055.hp2 HG02615.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.216-2623_216-2622i others(21): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 2/11 | chr4 | 153273270 | |||||||
| chr4:153273270 | C | CTTTTTTT others(3): Show |
1 | a0001c0008t0002g0059 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.216-2609_216-2600d others(12): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 153273270 | ||||||
| chr4:153273270 | C | CTTTTTTT others(4): Show |
2 | a0001c0002t0002g0109 a0001c0002t0002g0124 |
2 | NA18939.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.216-2610_216-2600d others(13): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 153273270 | ||||||
| chr4:153273270 | C | CTTTTTTT others(5): Show |
1 | a0001c0002t0002g0108 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.216-2611_216-2600d others(14): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 153273270 | ||||||
| chr4:153273270 | C | CTTTTTTT others(8): Show |
15 | a0001c0001t0002g0001 a0001c0002t0001g0116 a0001c0002t0001g0167 others(12): Show |
15 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(12): Show |
intron_variant | MODIFIER | c.216-2614_216-2600d others(17): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 153273270 | ||||||
| chr4:153273270 | C | CTTTTTTT others(9): Show |
14 | a0001c0002t0001g0115 a0001c0002t0001g0220 a0001c0002t0002g0050 others(11): Show |
14 | HG00558.hp2 HG01081.hp2 HG01123.hp2 others(11): Show |
intron_variant | MODIFIER | c.216-2615_216-2600d others(18): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 153273270 | ||||||
| chr4:153273270 | C | CTTTTTTT others(10): Show |
11 | a0001c0002t0002g0250 a0001c0002t0004g0010 a0001c0002t0004g0045 others(8): Show |
11 | HG01884.hp1 HG02896.hp2 HG02897.hp2 others(8): Show |
intron_variant | MODIFIER | c.216-2616_216-2600d others(19): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 153273270 | ||||||
| chr4:153273270 | C | CTTTTTTT others(11): Show |
4 | a0001c0002t0001g0105 a0001c0002t0001g0127 a0001c0002t0018g0009 others(1): Show |
4 | HG03098.hp2 NA18747.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.216-2617_216-2600d others(20): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 153273270 | ||||||
| chr4:153273270 | C | CTTTTTTT others(12): Show |
2 | a0001c0002t0001g0066 a0001c0002t0003g0239 |
2 | HG01109.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.216-2618_216-2600d others(21): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 153273270 | ||||||
| chr4:153273270 | C | CTTTTTTT others(14): Show |
1 | a0001c0002t0002g0268 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.216-2620_216-2600d others(23): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 153273270 | ||||||
| chr4:153273270 | C | CTTTTTTT others(15): Show |
1 | a0001c0002t0002g0260 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.216-2621_216-2600d others(24): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 153273270 | ||||||
| chr4:153273270 | C | CTTTTTTT others(16): Show |
1 | a0001c0002t0004g0047 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.216-2622_216-2600d others(25): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 153273270 | ||||||
| chr4:153273270 | C | CTTTTTTT others(17): Show |
2 | a0001c0002t0004g0046 a0001c0002t0004g0069 |
2 | HG01070.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.216-2600_216-2599i others(26): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 153273270 | ||||||
| chr4:153273270 | C | CTTTTTTT others(22): Show |
1 | a0001c0001t0010g0078 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.216-2600_216-2599i others(31): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 153273270 | ||||||
| chr4:153273270 | C | CTTTTTTT others(23): Show |
1 | a0001c0002t0018g0135 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.216-2600_216-2599i others(32): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 153273270 | ||||||
| chr4:153273270 | C | CTTTTTTT others(24): Show |
1 | a0001c0001t0009g0060 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.216-2600_216-2599i others(33): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 153273270 | ||||||
| chr4:153273270 | C | CTTTTTTT others(25): Show |
2 | a0001c0001t0009g0263 a0001c0001t0009g0264 |
2 | HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.216-2600_216-2599i others(34): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 153273270 | ||||||
| chr4:153273270 | CT | C | 89 | a0001c0001t0001g0017 a0001c0001t0001g0023 a0001c0001t0001g0033 others(86): Show |
89 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.216-2600delT | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 153273270 | ||||||
| chr4:153273270 | CTTT | C | 7 | a0001c0001t0006g0061 a0001c0001t0006g0143 a0001c0001t0006g0146 others(4): Show |
7 | HG01243.hp2 HG02257.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.216-2602_216-2600d others(5): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 153273270 | ||||||
| chr4:153273270 | CTTTTTT | C | 22 | a0001c0001t0001g0092 a0001c0001t0001g0099 a0001c0001t0001g0100 others(19): Show |
22 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.216-2605_216-2600d others(8): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 153273270 | ||||||
| chr4:153273271 | T | C | 2 | a0001c0001t0002g0018 a0001c0001t0002g0022 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.216-2622T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 2/11 | chr4 | 153273271 | |||||||
| chr4:153273302 | G | C | 4 | a0001c0002t0004g0045 a0001c0002t0004g0046 a0001c0002t0004g0047 others(1): Show |
4 | HG01884.hp1 HG02976.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.216-2591G>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 2/11 | chr4 | 153273302 | |||||||
| chr4:153273315 | G | A | 27 | a0001c0002t0001g0167 a0001c0002t0001g0173 a0001c0002t0001g0229 others(24): Show |
27 | HG00140.hp2 HG00544.hp1 HG00558.hp2 others(24): Show |
intron_variant | MODIFIER | c.216-2578G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 2/11 | chr4 | 153273315 | |||||||
| chr4:153273331 | C | T | 1 | a0001c0002t0004g0010 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.216-2562C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 2/11 | chr4 | 153273331 | |||||||
| chr4:153273368 | C | T | 24 | a0001c0003t0001g0041 a0001c0003t0002g0004 a0001c0003t0002g0052 others(21): Show |
24 | HG01074.hp2 HG01106.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.216-2525C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 2/11 | chr4 | 153273368 | |||||||
| chr4:153273442 | A | AT | 75 | a0001c0001t0001g0023 a0001c0001t0001g0040 a0001c0001t0001g0091 others(72): Show |
75 | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.216-2427dupT | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 153273442 | ||||||
| chr4:153273442 | A | ATT | 21 | a0001c0001t0001g0162 a0001c0001t0001g0199 a0001c0002t0002g0137 others(18): Show |
21 | HG01517.hp1 HG01993.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.216-2428_216-2427d others(4): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 153273442 | ||||||
| chr4:153273442 | A | ATTTTT | 14 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0002g0001 others(11): Show |
14 | HG01243.hp2 HG01891.hp2 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.216-2431_216-2427d others(7): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 153273442 | ||||||
| chr4:153273504 | A | G | 4 | a0001c0002t0004g0045 a0001c0002t0004g0046 a0001c0002t0004g0047 others(1): Show |
4 | HG01884.hp1 HG02976.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.216-2389A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 2/11 | chr4 | 153273504 | |||||||
| chr4:153273654 | A | C | 1 | a0001c0002t0028g0080 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.216-2239A>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 2/11 | chr4 | 153273654 | |||||||
| chr4:153273813 | T | C | 116 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0001g0092 others(113): Show |
116 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.216-2080T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 2/11 | chr4 | 153273813 | |||||||
| chr4:153274029 | G | A | 1 | a0001c0002t0028g0080 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.216-1864G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 2/11 | chr4 | 153274029 | |||||||
| chr4:153274040 | G | A | 6 | a0001c0002t0004g0045 a0001c0002t0004g0046 a0001c0002t0004g0047 others(3): Show |
6 | HG01884.hp1 HG02258.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.216-1853G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 2/11 | chr4 | 153274040 | |||||||
| chr4:153274182 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.216-1711C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 2/11 | chr4 | 153274182 | |||||||
| chr4:153274377 | C | T | 1 | a0001c0001t0001g0186 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.216-1516C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 2/11 | chr4 | 153274377 | |||||||
| chr4:153274461 | G | C | 4 | a0001c0002t0004g0045 a0001c0002t0004g0046 a0001c0002t0004g0047 others(1): Show |
4 | HG01884.hp1 HG02976.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.216-1432G>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 2/11 | chr4 | 153274461 | |||||||
| chr4:153274531 | T | A | 2 | a0001c0001t0002g0235 a0001c0001t0002g0240 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.216-1362T>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 2/11 | chr4 | 153274531 | |||||||
| chr4:153274549 | A | G | 1 | a0001c0002t0002g0130 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.216-1344A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 2/11 | chr4 | 153274549 | |||||||
| chr4:153274594 | C | A | 4 | a0001c0002t0004g0045 a0001c0002t0004g0046 a0001c0002t0004g0047 others(1): Show |
4 | HG01884.hp1 HG02976.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.216-1299C>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 2/11 | chr4 | 153274594 | |||||||
| chr4:153274848 | C | T | 1 | a0001c0003t0003g0075 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.216-1045C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 2/11 | chr4 | 153274848 | |||||||
| chr4:153274903 | G | C | 1 | a0001c0001t0001g0190 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.216-990G>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 2/11 | chr4 | 153274903 | |||||||
| chr4:153274908 | C | G | 1 | a0001c0001t0001g0179 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.216-985C>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 2/11 | chr4 | 153274908 | |||||||
| chr4:153274930 | G | A | 89 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0002g0001 others(86): Show |
89 | HG00323.hp1 HG00438.hp1 HG00741.hp1 others(86): Show |
intron_variant | MODIFIER | c.216-963G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 2/11 | chr4 | 153274930 | |||||||
| chr4:153275053 | A | G | 6 | a0001c0002t0002g0267 a0001c0002t0002g0268 a0001c0002t0003g0239 others(3): Show |
6 | HG02109.hp1 HG02717.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.216-840A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 2/11 | chr4 | 153275053 | |||||||
| chr4:153275142 | G | A | 89 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0002g0001 others(86): Show |
89 | HG00323.hp1 HG00438.hp1 HG00741.hp1 others(86): Show |
intron_variant | MODIFIER | c.216-751G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 2/11 | chr4 | 153275142 | |||||||
| chr4:153275408 | G | A | 3 | a0001c0001t0001g0113 a0001c0001t0001g0219 a0001c0001t0002g0201 |
3 | NA18968.hp2 NA19002.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.216-485G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 2/11 | chr4 | 153275408 | |||||||
| chr4:153275446 | G | T | 1 | a0001c0001t0008g0038 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.216-447G>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 2/11 | chr4 | 153275446 | |||||||
| chr4:153275656 | A | G | 2 | a0001c0001t0002g0002 a0001c0001t0010g0078 |
2 | HG01891.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.216-237A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 2/11 | chr4 | 153275656 | |||||||
| chr4:153276421 | AT | A | 85 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0002g0001 others(82): Show |
85 | HG00323.hp1 HG00438.hp1 HG00741.hp1 others(82): Show |
intron_variant | MODIFIER | c.453+294delT | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 153276421 | ||||||
| chr4:153276433 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.453+303G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153276433 | |||||||
| chr4:153276736 | G | A | 6 | a0001c0002t0002g0267 a0001c0002t0002g0268 a0001c0002t0003g0239 others(3): Show |
6 | HG02109.hp1 HG02717.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.453+606G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153276736 | |||||||
| chr4:153277224 | C | T | 1 | a0001c0001t0020g0228 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.453+1094C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153277224 | |||||||
| chr4:153277365 | T | A | 10 | a0001c0002t0002g0130 a0001c0002t0002g0136 a0001c0002t0002g0137 others(7): Show |
10 | HG01168.hp1 HG02145.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.453+1235T>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153277365 | |||||||
| chr4:153277527 | A | G | 2 | a0001c0002t0002g0166 a0001c0002t0002g0181 |
2 | HG02523.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.453+1397A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153277527 | |||||||
| chr4:153277598 | A | G | 1 | a0001c0002t0028g0080 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.453+1468A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153277598 | |||||||
| chr4:153277856 | T | C | 21 | a0001c0001t0001g0092 a0001c0001t0001g0099 a0001c0001t0001g0100 others(18): Show |
21 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.453+1726T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153277856 | |||||||
| chr4:153277875 | C | G | 2 | a0001c0002t0003g0144 a0001c0008t0002g0059 |
2 | HG03225.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.453+1745C>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153277875 | |||||||
| chr4:153278101 | T | C | 2 | a0001c0002t0010g0134 a0001c0002t0029g0261 |
2 | HG02258.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.453+1971T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153278101 | |||||||
| chr4:153278128 | CAG | C | 4 | a0001c0002t0004g0045 a0001c0002t0004g0046 a0001c0002t0004g0047 others(1): Show |
4 | HG01884.hp1 HG02976.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.453+2001_453+2002d others(4): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 153278128 | ||||||
| chr4:153278161 | A | C | 1 | a0001c0001t0021g0111 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.453+2031A>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153278161 | |||||||
| chr4:153278392 | G | T | 21 | a0001c0001t0001g0092 a0001c0001t0001g0099 a0001c0001t0001g0100 others(18): Show |
21 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.453+2262G>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153278392 | |||||||
| chr4:153278674 | C | T | 110 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0001g0092 others(107): Show |
110 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.453+2544C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153278674 | |||||||
| chr4:153278735 | C | G | 21 | a0001c0001t0001g0092 a0001c0001t0001g0099 a0001c0001t0001g0100 others(18): Show |
21 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.453+2605C>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153278735 | |||||||
| chr4:153278797 | C | CA | 55 | a0001c0001t0002g0002 a0001c0002t0002g0050 a0001c0002t0002g0145 others(52): Show |
55 | HG00323.hp1 HG00438.hp1 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.453+2684dupA | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 153278797 | ||||||
| chr4:153278900 | G | A | 2 | a0001c0002t0010g0134 a0001c0002t0029g0261 |
2 | HG02258.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.453+2770G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153278900 | |||||||
| chr4:153279116 | A | G | 1 | a0001c0002t0028g0080 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.453+2986A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153279116 | |||||||
| chr4:153279168 | G | A | 164 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0001g0092 others(161): Show |
164 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.453+3038G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153279168 | |||||||
| chr4:153279195 | G | A | 21 | a0001c0001t0001g0092 a0001c0001t0001g0099 a0001c0001t0001g0100 others(18): Show |
21 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.453+3065G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153279195 | |||||||
| chr4:153279230 | C | G | 110 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0001g0092 others(107): Show |
110 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.453+3100C>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153279230 | |||||||
| chr4:153279380 | C | T | 1 | a0001c0002t0003g0144 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.453+3250C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153279380 | |||||||
| chr4:153279464 | C | CAAAGAAA others(1): Show |
114 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0001g0092 others(111): Show |
114 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.453+3336_453+3337i others(10): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 153279464 | ||||||
| chr4:153279537 | A | G | 1 | a0001c0003t0002g0052 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.453+3407A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153279537 | |||||||
| chr4:153279601 | A | G | 3 | a0001c0001t0006g0019 a0001c0001t0006g0123 a0001c0001t0007g0122 |
3 | HG02572.hp2 HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.453+3471A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153279601 | |||||||
| chr4:153279608 | C | A | 21 | a0001c0001t0001g0092 a0001c0001t0001g0099 a0001c0001t0001g0100 others(18): Show |
21 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.453+3478C>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153279608 | |||||||
| chr4:153279709 | G | A | 3 | a0001c0002t0011g0005 a0001c0002t0011g0006 a0001c0002t0011g0070 |
3 | HG02896.hp2 HG02897.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.453+3579G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153279709 | |||||||
| chr4:153279942 | CA | C | 23 | a0001c0001t0001g0092 a0001c0001t0001g0099 a0001c0001t0001g0100 others(20): Show |
23 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.453+3829delA | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 153279942 | ||||||
| chr4:153279942 | CAA | C | 87 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0002g0001 others(84): Show |
87 | HG00323.hp1 HG00438.hp1 HG00741.hp1 others(84): Show |
intron_variant | MODIFIER | c.453+3828_453+3829d others(4): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 153279942 | ||||||
| chr4:153280191 | G | A | 1 | a0001c0002t0003g0144 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.453+4061G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153280191 | |||||||
| chr4:153280323 | T | A | 6 | a0001c0002t0002g0267 a0001c0002t0002g0268 a0001c0002t0003g0239 others(3): Show |
6 | HG02109.hp1 HG02717.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.453+4193T>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153280323 | |||||||
| chr4:153280337 | A | T | 164 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0001g0092 others(161): Show |
164 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.453+4207A>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153280337 | |||||||
| chr4:153280384 | C | CT | 6 | a0001c0001t0001g0183 a0001c0001t0001g0187 a0001c0001t0001g0189 others(3): Show |
6 | HG01175.hp1 HG01175.hp2 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.453+4270dupT | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 153280384 | ||||||
| chr4:153280384 | C | CTTTT | 80 | a0001c0001t0001g0092 a0001c0001t0001g0099 a0001c0001t0001g0100 others(77): Show |
80 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.453+4267_453+4270d others(6): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 153280384 | ||||||
| chr4:153280384 | C | CTTTTT | 22 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0002g0001 others(19): Show |
22 | HG00735.hp2 HG01243.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.453+4266_453+4270d others(7): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 153280384 | ||||||
| chr4:153280384 | C | CTTTTTT | 13 | a0001c0001t0004g0087 a0001c0001t0004g0088 a0001c0001t0006g0143 others(10): Show |
13 | HG01884.hp1 HG02055.hp2 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.453+4265_453+4270d others(8): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 153280384 | ||||||
| chr4:153280384 | C | CTTTTTTT | 41 | a0001c0002t0001g0105 a0001c0002t0001g0115 a0001c0002t0001g0116 others(38): Show |
41 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.453+4264_453+4270d others(9): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 153280384 | ||||||
| chr4:153280384 | C | CTTTTTTT others(1): Show |
6 | a0001c0002t0001g0066 a0001c0002t0001g0126 a0001c0002t0002g0152 others(3): Show |
6 | HG01109.hp1 HG02735.hp2 HG03834.hp2 others(3): Show |
intron_variant | MODIFIER | c.453+4263_453+4270d others(10): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 153280384 | ||||||
| chr4:153280628 | C | A | 1 | a0001c0002t0002g0137 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.453+4498C>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153280628 | |||||||
| chr4:153280628 | C | G | 7 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0002g0001 others(4): Show |
7 | HG02055.hp2 HG02615.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.453+4498C>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153280628 | |||||||
| chr4:153280691 | C | CT | 110 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0001g0092 others(107): Show |
110 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.453+4572dupT | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 153280691 | ||||||
| chr4:153280805 | C | T | 48 | a0001c0003t0001g0003 a0001c0003t0001g0027 a0001c0003t0001g0041 others(45): Show |
48 | HG00323.hp1 HG00438.hp1 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.453+4675C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153280805 | |||||||
| chr4:153280825 | C | T | 4 | a0001c0002t0004g0045 a0001c0002t0004g0046 a0001c0002t0004g0047 others(1): Show |
4 | HG01884.hp1 HG02976.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.453+4695C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153280825 | |||||||
| chr4:153280851 | A | T | 1 | a0001c0002t0028g0080 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.453+4721A>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153280851 | |||||||
| chr4:153280915 | A | G | 1 | a0001c0003t0003g0057 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.453+4785A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153280915 | |||||||
| chr4:153281081 | T | C | 3 | a0001c0002t0002g0108 a0001c0002t0002g0109 a0001c0002t0002g0124 |
3 | NA18939.hp1 NA18954.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.453+4951T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153281081 | |||||||
| chr4:153281271 | T | C | 1 | a0001c0008t0002g0059 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.453+5141T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153281271 | |||||||
| chr4:153281349 | A | G | 2 | a0001c0001t0002g0002 a0001c0001t0010g0078 |
2 | HG01891.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.453+5219A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153281349 | |||||||
| chr4:153281499 | A | T | 110 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0001g0092 others(107): Show |
110 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.453+5369A>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153281499 | |||||||
| chr4:153282025 | A | G | 110 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0001g0092 others(107): Show |
110 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.453+5895A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153282025 | |||||||
| chr4:153282113 | C | T | 110 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0001g0092 others(107): Show |
110 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.453+5983C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153282113 | |||||||
| chr4:153282189 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.453+6059G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153282189 | |||||||
| chr4:153282207 | T | C | 1 | a0001c0001t0003g0232 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.453+6077T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153282207 | |||||||
| chr4:153282222 | A | C | 2 | a0001c0001t0001g0170 a0001c0001t0001g0193 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.453+6092A>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153282222 | |||||||
| chr4:153282231 | C | A | 1 | a0001c0002t0003g0144 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.453+6101C>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153282231 | |||||||
| chr4:153282257 | G | A | 2 | a0001c0001t0001g0056 a0001c0001t0001g0174 |
2 | HG00558.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.453+6127G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153282257 | |||||||
| chr4:153282397 | T | TTTTG | 8 | a0001c0001t0006g0061 a0001c0001t0006g0143 a0001c0001t0006g0146 others(5): Show |
8 | HG01243.hp2 HG02257.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.453+6279_453+6282d others(6): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 153282397 | ||||||
| chr4:153282468 | G | C | 2 | a0001c0002t0010g0134 a0001c0002t0029g0261 |
2 | HG02258.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.453+6338G>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153282468 | |||||||
| chr4:153282792 | AT | A | 10 | a0001c0002t0002g0130 a0001c0002t0002g0136 a0001c0002t0002g0137 others(7): Show |
10 | HG01168.hp1 HG02145.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.453+6672delT | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 153282792 | ||||||
| chr4:153282803 | G | A | 110 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0001g0092 others(107): Show |
110 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.453+6673G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153282803 | |||||||
| chr4:153282815 | G | T | 1 | a0001c0002t0018g0135 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.453+6685G>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153282815 | |||||||
| chr4:153282825 | G | A | 48 | a0001c0003t0001g0003 a0001c0003t0001g0027 a0001c0003t0001g0041 others(45): Show |
48 | HG00323.hp1 HG00438.hp1 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.453+6695G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153282825 | |||||||
| chr4:153282862 | C | T | 1 | a0001c0004t0003g0058 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.453+6732C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153282862 | |||||||
| chr4:153282934 | G | A | 17 | a0001c0002t0002g0130 a0001c0002t0002g0136 a0001c0002t0002g0137 others(14): Show |
17 | HG01168.hp1 HG02109.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.453+6804G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153282934 | |||||||
| chr4:153282954 | AT | A | 108 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0001g0092 others(105): Show |
108 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.453+6834delT | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 153282954 | ||||||
| chr4:153283092 | G | A | 110 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0001g0092 others(107): Show |
110 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.453+6962G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153283092 | |||||||
| chr4:153283501 | T | C | 1 | a0001c0002t0007g0155 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.453+7371T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153283501 | |||||||
| chr4:153283642 | C | CT | 7 | a0001c0001t0001g0188 a0001c0001t0001g0249 a0001c0001t0001g0257 others(4): Show |
7 | HG02258.hp1 HG02738.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.453+7527dupT | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 153283642 | ||||||
| chr4:153283666 | G | C | 2 | a0001c0002t0002g0050 a0001c0002t0002g0145 |
2 | HG02738.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.453+7536G>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153283666 | |||||||
| chr4:153283666 | G | GTC | 162 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0001g0092 others(159): Show |
162 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.453+7537_453+7538i others(4): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 153283666 | ||||||
| chr4:153283690 | G | A | 1 | a0001c0001t0001g0120 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.453+7560G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153283690 | |||||||
| chr4:153283721 | C | T | 1 | a0001c0002t0029g0261 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.453+7591C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153283721 | |||||||
| chr4:153283744 | C | T | 1 | a0001c0001t0002g0002 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.453+7614C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153283744 | |||||||
| chr4:153283794 | G | A | 43 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0001g0092 others(40): Show |
43 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.453+7664G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153283794 | |||||||
| chr4:153283799 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.453+7669G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153283799 | |||||||
| chr4:153283826 | C | T | 2 | a0001c0001t0001g0183 a0001c0001t0001g0189 |
2 | HG01175.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.453+7696C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153283826 | |||||||
| chr4:153283861 | C | CT | 14 | a0001c0001t0001g0040 a0001c0001t0001g0056 a0001c0001t0001g0063 others(11): Show |
14 | HG00438.hp2 HG00642.hp1 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.453+7758dupT | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 153283861 | ||||||
| chr4:153283861 | C | CTT | 6 | a0001c0001t0001g0164 a0001c0001t0002g0065 a0001c0002t0004g0045 others(3): Show |
6 | HG01884.hp1 HG02280.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.453+7757_453+7758d others(4): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 153283861 | ||||||
| chr4:153283861 | CT | C | 90 | a0001c0001t0001g0033 a0001c0001t0001g0092 a0001c0001t0001g0100 others(87): Show |
90 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.453+7758delT | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 153283861 | ||||||
| chr4:153283861 | CTT | C | 36 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0002g0001 others(33): Show |
36 | HG00323.hp1 HG00741.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.453+7757_453+7758d others(4): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 153283861 | ||||||
| chr4:153283861 | CTTT | C | 32 | a0001c0001t0006g0061 a0001c0001t0006g0143 a0001c0001t0006g0146 others(29): Show |
32 | HG01074.hp1 HG01074.hp2 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.453+7756_453+7758d others(5): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 153283861 | ||||||
| chr4:153283934 | A | G | 182 | a0001c0001t0001g0033 a0001c0001t0001g0055 a0001c0001t0001g0081 others(179): Show |
182 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.453+7804A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153283934 | |||||||
| chr4:153283990 | C | T | 56 | a0001c0002t0002g0267 a0001c0002t0002g0268 a0001c0002t0003g0239 others(53): Show |
56 | HG00323.hp1 HG00438.hp1 HG00741.hp1 others(53): Show |
intron_variant | MODIFIER | c.453+7860C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153283990 | |||||||
| chr4:153284015 | G | T | 2 | a0001c0001t0001g0039 a0001c0001t0001g0040 |
2 | HG00438.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.453+7885G>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153284015 | |||||||
| chr4:153284048 | T | C | 1 | a0001c0002t0003g0144 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.453+7918T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153284048 | |||||||
| chr4:153284071 | G | T | 58 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0001g0092 others(55): Show |
58 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.453+7941G>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153284071 | |||||||
| chr4:153284105 | C | T | 4 | a0001c0002t0004g0045 a0001c0002t0004g0046 a0001c0002t0004g0047 others(1): Show |
4 | HG01884.hp1 HG02976.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.453+7975C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153284105 | |||||||
| chr4:153284157 | G | A | 1 | a0001c0001t0002g0002 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.453+8027G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153284157 | |||||||
| chr4:153284181 | G | T | 1 | a0001c0001t0001g0190 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.453+8051G>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153284181 | |||||||
| chr4:153284210 | G | GT | 16 | a0001c0001t0005g0214 a0001c0002t0002g0130 a0001c0002t0002g0136 others(13): Show |
16 | HG01168.hp1 HG01884.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.453+8089dupT | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 153284210 | ||||||
| chr4:153284280 | A | C | 1 | a0001c0002t0003g0144 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.453+8150A>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153284280 | |||||||
| chr4:153284304 | G | A | 7 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0002g0001 others(4): Show |
7 | HG02055.hp2 HG02615.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.453+8174G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153284304 | |||||||
| chr4:153284345 | C | T | 48 | a0001c0003t0001g0003 a0001c0003t0001g0027 a0001c0003t0001g0041 others(45): Show |
48 | HG00323.hp1 HG00438.hp1 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.453+8215C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153284345 | |||||||
| chr4:153284736 | A | G | 1 | a0001c0002t0004g0172 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.454-8246A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153284736 | |||||||
| chr4:153284953 | A | T | 1 | a0001c0001t0002g0002 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.454-8029A>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153284953 | |||||||
| chr4:153285131 | G | A | 1 | a0001c0002t0003g0144 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.454-7851G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153285131 | |||||||
| chr4:153285155 | G | A | 1 | a0001c0001t0001g0247 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.454-7827G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153285155 | |||||||
| chr4:153285209 | C | T | 58 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0001g0092 others(55): Show |
58 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.454-7773C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153285209 | |||||||
| chr4:153285555 | G | A | 1 | a0001c0002t0002g0171 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.454-7427G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153285555 | |||||||
| chr4:153285754 | T | TGTGC | 12 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0002g0001 others(9): Show |
12 | HG02055.hp2 HG02280.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.454-7225_454-7224i others(6): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 153285754 | ||||||
| chr4:153285756 | T | TGC | 30 | a0001c0001t0001g0092 a0001c0001t0001g0099 a0001c0001t0001g0100 others(27): Show |
30 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.454-7225_454-7224i others(4): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 153285756 | ||||||
| chr4:153285760 | C | T | 43 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0001g0092 others(40): Show |
43 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.454-7222C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153285760 | |||||||
| chr4:153285760 | CGT | C | 56 | a0001c0002t0002g0267 a0001c0002t0002g0268 a0001c0002t0003g0239 others(53): Show |
56 | HG00323.hp1 HG00438.hp1 HG00741.hp1 others(53): Show |
intron_variant | MODIFIER | c.454-7203_454-7202d others(4): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 153285760 | ||||||
| chr4:153285901 | C | A | 10 | a0001c0002t0002g0130 a0001c0002t0002g0136 a0001c0002t0002g0137 others(7): Show |
10 | HG01168.hp1 HG02145.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.454-7081C>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153285901 | |||||||
| chr4:153285906 | A | C | 1 | a0001c0002t0022g0140 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.454-7076A>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153285906 | |||||||
| chr4:153286042 | A | G | 58 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0001g0092 others(55): Show |
58 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.454-6940A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153286042 | |||||||
| chr4:153286045 | T | C | 1 | a0001c0002t0019g0180 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.454-6937T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153286045 | |||||||
| chr4:153286632 | T | C | 1 | a0001c0001t0003g0232 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.454-6350T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153286632 | |||||||
| chr4:153286754 | C | T | 1 | a0001c0002t0002g0145 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.454-6228C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153286754 | |||||||
| chr4:153286781 | ACT | A | 8 | a0001c0002t0002g0267 a0001c0002t0002g0268 a0001c0002t0003g0239 others(5): Show |
8 | HG02109.hp1 HG02258.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.454-6186_454-6185d others(4): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 153286781 | ||||||
| chr4:153286938 | AT | A | 7 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0002g0001 others(4): Show |
7 | HG02055.hp2 HG02615.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.454-6037delT | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 153286938 | ||||||
| chr4:153287082 | G | C | 39 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0001g0092 others(36): Show |
39 | HG00280.hp2 HG00642.hp2 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.454-5900G>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153287082 | |||||||
| chr4:153287126 | C | T | 19 | a0001c0002t0001g0066 a0001c0002t0001g0105 a0001c0002t0001g0115 others(16): Show |
19 | HG00323.hp2 HG01070.hp1 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.454-5856C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153287126 | |||||||
| chr4:153287133 | A | G | 1 | a0001c0003t0007g0106 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.454-5849A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153287133 | |||||||
| chr4:153287180 | A | C | 19 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0002g0001 others(16): Show |
19 | HG01243.hp2 HG01891.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.454-5802A>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153287180 | |||||||
| chr4:153287205 | C | A | 2 | a0001c0002t0010g0134 a0001c0002t0029g0261 |
2 | HG02258.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.454-5777C>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153287205 | |||||||
| chr4:153287467 | A | G | 10 | a0001c0002t0002g0130 a0001c0002t0002g0136 a0001c0002t0002g0137 others(7): Show |
10 | HG01168.hp1 HG02145.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.454-5515A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153287467 | |||||||
| chr4:153287538 | A | T | 66 | a0001c0002t0002g0130 a0001c0002t0002g0136 a0001c0002t0002g0137 others(63): Show |
66 | HG00323.hp1 HG00438.hp1 HG00741.hp1 others(63): Show |
intron_variant | MODIFIER | c.454-5444A>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153287538 | |||||||
| chr4:153287714 | G | A | 111 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0001g0092 others(108): Show |
111 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.454-5268G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153287714 | |||||||
| chr4:153287899 | T | C | 1 | a0001c0001t0001g0017 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.454-5083T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153287899 | |||||||
| chr4:153287921 | G | A | 3 | a0001c0001t0009g0060 a0001c0001t0009g0263 a0001c0001t0009g0264 |
3 | HG02280.hp2 HG03041.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.454-5061G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153287921 | |||||||
| chr4:153287943 | T | C | 2 | a0001c0002t0017g0095 a0001c0002t0017g0096 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.454-5039T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153287943 | |||||||
| chr4:153288037 | C | T | 49 | a0001c0002t0003g0148 a0001c0003t0001g0003 a0001c0003t0001g0027 others(46): Show |
49 | HG00323.hp1 HG00438.hp1 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.454-4945C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153288037 | |||||||
| chr4:153288088 | A | G | 2 | a0001c0002t0003g0144 a0001c0008t0002g0059 |
2 | HG03225.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.454-4894A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153288088 | |||||||
| chr4:153288159 | G | A | 2 | a0001c0002t0010g0134 a0001c0002t0029g0261 |
2 | HG02258.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.454-4823G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153288159 | |||||||
| chr4:153288173 | G | T | 49 | a0001c0002t0003g0148 a0001c0003t0001g0003 a0001c0003t0001g0027 others(46): Show |
49 | HG00323.hp1 HG00438.hp1 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.454-4809G>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153288173 | |||||||
| chr4:153288174 | C | T | 2 | a0001c0001t0001g0062 a0001c0001t0001g0063 |
2 | HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.454-4808C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153288174 | |||||||
| chr4:153288262 | C | T | 6 | a0001c0002t0002g0267 a0001c0002t0002g0268 a0001c0002t0003g0239 others(3): Show |
6 | HG02109.hp1 HG02717.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.454-4720C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153288262 | |||||||
| chr4:153288604 | T | C | 49 | a0001c0002t0003g0148 a0001c0003t0001g0003 a0001c0003t0001g0027 others(46): Show |
49 | HG00323.hp1 HG00438.hp1 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.454-4378T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153288604 | |||||||
| chr4:153288939 | T | C | 1 | a0001c0002t0002g0145 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.454-4043T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153288939 | |||||||
| chr4:153289137 | A | G | 55 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0002t0001g0066 others(52): Show |
55 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.454-3845A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153289137 | |||||||
| chr4:153289558 | G | A | 18 | a0001c0001t0001g0092 a0001c0001t0001g0099 a0001c0001t0001g0100 others(15): Show |
18 | HG00280.hp2 HG00642.hp2 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.454-3424G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153289558 | |||||||
| chr4:153289559 | C | T | 7 | a0001c0001t0006g0061 a0001c0001t0006g0143 a0001c0001t0006g0146 others(4): Show |
7 | HG01243.hp2 HG02257.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.454-3423C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153289559 | |||||||
| chr4:153289707 | C | T | 1 | a0001c0001t0027g0068 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.454-3275C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153289707 | |||||||
| chr4:153289817 | G | T | 1 | a0001c0001t0016g0197 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.454-3165G>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153289817 | |||||||
| chr4:153289934 | G | T | 1 | a0001c0003t0003g0208 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.454-3048G>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153289934 | |||||||
| chr4:153290235 | A | C | 1 | a0001c0008t0002g0059 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.454-2747A>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153290235 | |||||||
| chr4:153290241 | C | T | 1 | a0001c0003t0003g0042 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.454-2741C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153290241 | |||||||
| chr4:153290275 | T | G | 1 | a0001c0002t0023g0014 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.454-2707T>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153290275 | |||||||
| chr4:153290281 | A | G | 21 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0002g0001 others(18): Show |
21 | HG01243.hp2 HG01891.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.454-2701A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153290281 | |||||||
| chr4:153290310 | C | A | 1 | a0001c0002t0003g0144 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.454-2672C>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153290310 | |||||||
| chr4:153290546 | A | G | 21 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0002g0001 others(18): Show |
21 | HG01243.hp2 HG01891.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.454-2436A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153290546 | |||||||
| chr4:153290623 | T | C | 1 | a0001c0001t0001g0156 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.454-2359T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153290623 | |||||||
| chr4:153290634 | T | C | 1 | a0001c0005t0003g0169 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.454-2348T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153290634 | |||||||
| chr4:153290711 | C | T | 21 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0002g0001 others(18): Show |
21 | HG01243.hp2 HG01891.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.454-2271C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153290711 | |||||||
| chr4:153290761 | G | A | 1 | a0001c0003t0003g0054 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.454-2221G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153290761 | |||||||
| chr4:153290796 | T | G | 1 | a0001c0001t0001g0179 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.454-2186T>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153290796 | |||||||
| chr4:153290802 | A | T | 9 | a0001c0001t0001g0092 a0001c0001t0001g0121 a0001c0001t0005g0094 others(6): Show |
9 | NA18942.hp1 NA18943.hp1 NA18964.hp2 others(6): Show |
intron_variant | MODIFIER | c.454-2180A>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153290802 | |||||||
| chr4:153290871 | C | T | 1 | a0001c0001t0001g0227 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.454-2111C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153290871 | |||||||
| chr4:153291037 | T | C | 10 | a0001c0002t0002g0130 a0001c0002t0002g0136 a0001c0002t0002g0137 others(7): Show |
10 | HG01168.hp1 HG02145.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.454-1945T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153291037 | |||||||
| chr4:153291067 | C | CA | 21 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0002g0001 others(18): Show |
21 | HG01243.hp2 HG01891.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.454-1906dupA | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 153291067 | ||||||
| chr4:153291136 | A | C | 10 | a0001c0002t0002g0130 a0001c0002t0002g0136 a0001c0002t0002g0137 others(7): Show |
10 | HG01168.hp1 HG02145.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.454-1846A>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153291136 | |||||||
| chr4:153291186 | A | G | 6 | a0001c0003t0003g0067 a0001c0003t0003g0165 a0001c0003t0003g0185 others(3): Show |
6 | HG00438.hp1 NA18970.hp2 NA18988.hp1 others(3): Show |
intron_variant | MODIFIER | c.454-1796A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153291186 | |||||||
| chr4:153291295 | G | A | 3 | a0001c0002t0011g0005 a0001c0002t0011g0006 a0001c0002t0011g0070 |
3 | HG02896.hp2 HG02897.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.454-1687G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153291295 | |||||||
| chr4:153291489 | G | A | 1 | a0001c0002t0028g0080 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.454-1493G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153291489 | |||||||
| chr4:153291525 | G | T | 16 | a0001c0001t0001g0033 a0001c0001t0001g0120 a0001c0001t0003g0035 others(13): Show |
16 | HG03831.hp2 NA18944.hp1 NA18951.hp1 others(13): Show |
intron_variant | MODIFIER | c.454-1457G>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153291525 | |||||||
| chr4:153291626 | C | G | 1 | a0001c0002t0002g0050 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.454-1356C>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153291626 | |||||||
| chr4:153291822 | A | G | 1 | a0001c0003t0003g0064 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.454-1160A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153291822 | |||||||
| chr4:153291861 | T | C | 6 | a0001c0002t0002g0267 a0001c0002t0002g0268 a0001c0002t0003g0239 others(3): Show |
6 | HG02109.hp1 HG02717.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.454-1121T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153291861 | |||||||
| chr4:153291965 | A | T | 1 | a0001c0002t0004g0069 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.454-1017A>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153291965 | |||||||
| chr4:153291986 | AC | A | 12 | a0001c0001t0002g0002 a0001c0001t0006g0061 a0001c0001t0006g0143 others(9): Show |
12 | HG01243.hp2 HG01891.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.454-995delC | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153291986 | |||||||
| chr4:153292425 | C | A | 94 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0002g0001 others(91): Show |
94 | HG00323.hp1 HG00438.hp1 HG00741.hp1 others(91): Show |
intron_variant | MODIFIER | c.454-557C>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153292425 | |||||||
| chr4:153292488 | C | T | 5 | a0001c0001t0001g0072 a0001c0001t0001g0084 a0001c0001t0001g0164 others(2): Show |
5 | HG00735.hp1 HG01069.hp2 HG01070.hp2 others(2): Show |
intron_variant | MODIFIER | c.454-494C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153292488 | |||||||
| chr4:153292574 | C | T | 73 | a0001c0002t0002g0130 a0001c0002t0002g0136 a0001c0002t0002g0137 others(70): Show |
73 | HG00323.hp1 HG00438.hp1 HG00741.hp1 others(70): Show |
intron_variant | MODIFIER | c.454-408C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153292574 | |||||||
| chr4:153292684 | C | A | 4 | a0001c0003t0001g0003 a0001c0003t0001g0131 a0001c0003t0001g0132 others(1): Show |
4 | HG01884.hp2 HG02486.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.454-298C>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 3/11 | chr4 | 153292684 | |||||||
| chr4:153293265 | T | C | 6 | a0001c0002t0002g0267 a0001c0002t0002g0268 a0001c0002t0003g0239 others(3): Show |
6 | HG02109.hp1 HG02717.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.605+132T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 4/11 | chr4 | 153293265 | |||||||
| chr4:153293517 | C | T | 2 | a0001c0003t0003g0185 a0001c0003t0003g0216 |
2 | NA18998.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.605+384C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 4/11 | chr4 | 153293517 | |||||||
| chr4:153293717 | A | G | 7 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0002g0001 others(4): Show |
7 | HG02055.hp2 HG02615.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.605+584A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 4/11 | chr4 | 153293717 | |||||||
| chr4:153293737 | T | C | 1 | a0001c0001t0001g0179 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.606-568T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 4/11 | chr4 | 153293737 | |||||||
| chr4:153293748 | A | G | 1 | a0001c0001t0001g0113 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.606-557A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 4/11 | chr4 | 153293748 | |||||||
| chr4:153293879 | G | A | 1 | a0001c0003t0003g0230 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.606-426G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 4/11 | chr4 | 153293879 | |||||||
| chr4:153294063 | A | C | 4 | a0001c0001t0001g0017 a0001c0001t0001g0062 a0001c0001t0001g0063 others(1): Show |
4 | HG02622.hp2 HG03471.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.606-242A>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 4/11 | chr4 | 153294063 | |||||||
| chr4:153294127 | C | CA | 49 | a0001c0002t0001g0066 a0001c0002t0001g0105 a0001c0002t0001g0115 others(46): Show |
49 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.606-174dupA | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 153294127 | ||||||
| chr4:153294570 | G | T | 6 | a0001c0002t0002g0267 a0001c0002t0002g0268 a0001c0002t0003g0239 others(3): Show |
6 | HG02109.hp1 HG02717.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.786+85G>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 5/11 | chr4 | 153294570 | |||||||
| chr4:153294842 | A | T | 19 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0002g0001 others(16): Show |
19 | HG01891.hp2 HG02055.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.786+357A>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 5/11 | chr4 | 153294842 | |||||||
| chr4:153295111 | G | T | 11 | a0001c0002t0002g0130 a0001c0002t0002g0136 a0001c0002t0002g0137 others(8): Show |
11 | HG01168.hp1 HG02145.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.787-202G>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 5/11 | chr4 | 153295111 | |||||||
| chr4:153296301 | A | G | 1 | a0001c0008t0002g0059 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1510+265A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153296301 | |||||||
| chr4:153296770 | A | G | 4 | a0001c0002t0004g0045 a0001c0002t0004g0046 a0001c0002t0004g0047 others(1): Show |
4 | HG01884.hp1 HG02976.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1510+734A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153296770 | |||||||
| chr4:153297109 | C | A | 151 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0001g0092 others(148): Show |
151 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.1510+1073C>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153297109 | |||||||
| chr4:153297187 | C | G | 1 | a0001c0001t0016g0197 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1510+1151C>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153297187 | |||||||
| chr4:153297318 | G | T | 18 | a0001c0001t0001g0092 a0001c0001t0001g0099 a0001c0001t0001g0100 others(15): Show |
18 | HG00280.hp2 HG00642.hp2 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.1510+1282G>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153297318 | |||||||
| chr4:153297971 | A | C | 1 | a0001c0002t0013g0133 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1510+1935A>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153297971 | |||||||
| chr4:153298169 | A | G | 1 | a0001c0003t0003g0165 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1510+2133A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153298169 | |||||||
| chr4:153298394 | C | T | 1 | a0001c0001t0001g0213 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1510+2358C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153298394 | |||||||
| chr4:153298466 | A | G | 2 | a0001c0002t0010g0134 a0001c0002t0029g0261 |
2 | HG02258.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1510+2430A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153298466 | |||||||
| chr4:153298517 | C | T | 8 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0002g0001 others(5): Show |
8 | HG02055.hp2 HG02615.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1510+2481C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153298517 | |||||||
| chr4:153298649 | A | G | 2 | a0001c0002t0010g0134 a0001c0002t0029g0261 |
2 | HG02258.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1510+2613A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153298649 | |||||||
| chr4:153298673 | A | T | 20 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0002g0001 others(17): Show |
20 | HG01891.hp2 HG02055.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.1510+2637A>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153298673 | |||||||
| chr4:153298732 | A | G | 1 | a0001c0008t0002g0059 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1510+2696A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153298732 | |||||||
| chr4:153298795 | G | A | 2 | a0001c0001t0001g0091 a0001c0001t0001g0162 |
2 | NA18971.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.1510+2759G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153298795 | |||||||
| chr4:153298951 | C | T | 2 | a0001c0001t0001g0055 a0001c0001t0001g0081 |
2 | HG02886.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1510+2915C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153298951 | |||||||
| chr4:153299010 | A | T | 8 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0002g0001 others(5): Show |
8 | HG02055.hp2 HG02615.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1510+2974A>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153299010 | |||||||
| chr4:153299039 | A | G | 2 | a0001c0002t0003g0144 a0001c0003t0002g0052 |
2 | HG02896.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1510+3003A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153299039 | |||||||
| chr4:153299054 | T | C | 6 | a0001c0002t0002g0267 a0001c0002t0002g0268 a0001c0002t0003g0239 others(3): Show |
6 | HG02109.hp1 HG02717.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1510+3018T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153299054 | |||||||
| chr4:153299753 | G | T | 1 | a0001c0004t0001g0184 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1510+3717G>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153299753 | |||||||
| chr4:153299876 | G | A | 6 | a0001c0002t0002g0267 a0001c0002t0002g0268 a0001c0002t0003g0239 others(3): Show |
6 | HG02109.hp1 HG02717.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1510+3840G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153299876 | |||||||
| chr4:153299925 | C | T | 3 | a0001c0001t0001g0072 a0001c0001t0001g0164 a0001c0001t0001g0211 |
3 | HG01069.hp2 HG01975.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1510+3889C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153299925 | |||||||
| chr4:153299986 | G | A | 9 | a0001c0003t0003g0053 a0001c0003t0003g0054 a0001c0003t0003g0074 others(6): Show |
9 | HG01891.hp1 HG02055.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1510+3950G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153299986 | |||||||
| chr4:153300067 | C | T | 2 | a0001c0002t0010g0134 a0001c0002t0029g0261 |
2 | HG02258.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1510+4031C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153300067 | |||||||
| chr4:153300241 | A | G | 11 | a0001c0002t0002g0130 a0001c0002t0002g0136 a0001c0002t0002g0137 others(8): Show |
11 | HG01168.hp1 HG02145.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.1510+4205A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153300241 | |||||||
| chr4:153300286 | G | A | 1 | a0001c0008t0002g0059 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1510+4250G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153300286 | |||||||
| chr4:153300311 | C | A | 1 | a0001c0003t0003g0051 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1510+4275C>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153300311 | |||||||
| chr4:153300312 | G | A | 18 | a0001c0001t0001g0092 a0001c0001t0001g0099 a0001c0001t0001g0100 others(15): Show |
18 | HG00280.hp2 HG00642.hp2 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.1510+4276G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153300312 | |||||||
| chr4:153300351 | G | A | 2 | a0001c0002t0010g0134 a0001c0002t0029g0261 |
2 | HG02258.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1510+4315G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153300351 | |||||||
| chr4:153300486 | G | A | 11 | a0001c0002t0002g0130 a0001c0002t0002g0136 a0001c0002t0002g0137 others(8): Show |
11 | HG01168.hp1 HG02145.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.1510+4450G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153300486 | |||||||
| chr4:153300523 | A | G | 16 | a0001c0002t0002g0130 a0001c0002t0002g0136 a0001c0002t0002g0137 others(13): Show |
16 | HG01168.hp1 HG01884.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.1510+4487A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153300523 | |||||||
| chr4:153300603 | G | A | 1 | a0001c0001t0009g0263 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1510+4567G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153300603 | |||||||
| chr4:153300898 | A | G | 51 | a0001c0002t0001g0066 a0001c0002t0001g0115 a0001c0002t0001g0116 others(48): Show |
51 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.1510+4862A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153300898 | |||||||
| chr4:153300965 | C | T | 1 | a0001c0003t0007g0223 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1510+4929C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153300965 | |||||||
| chr4:153300999 | T | C | 1 | a0001c0002t0003g0239 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1510+4963T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153300999 | |||||||
| chr4:153301009 | G | C | 1 | a0001c0002t0001g0210 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1510+4973G>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153301009 | |||||||
| chr4:153301147 | C | T | 4 | a0001c0001t0004g0008 a0001c0001t0004g0087 a0001c0001t0004g0088 others(1): Show |
4 | HG02055.hp2 HG02615.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1510+5111C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153301147 | |||||||
| chr4:153301190 | C | CA | 9 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0001g0257 others(6): Show |
9 | HG02055.hp2 HG02615.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1510+5167dupA | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr4 | 153301190 | ||||||
| chr4:153301250 | G | A | 12 | a0001c0002t0002g0130 a0001c0002t0002g0136 a0001c0002t0002g0137 others(9): Show |
12 | HG01168.hp1 HG02145.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1510+5214G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153301250 | |||||||
| chr4:153301384 | G | A | 152 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0001g0092 others(149): Show |
152 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.1510+5348G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153301384 | |||||||
| chr4:153301555 | A | G | 2 | a0001c0002t0002g0256 a0001c0002t0002g0259 |
2 | NA19070.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.1510+5519A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153301555 | |||||||
| chr4:153301725 | A | G | 2 | a0001c0003t0001g0041 a0001c0003t0010g0079 |
2 | HG02615.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1510+5689A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153301725 | |||||||
| chr4:153301733 | T | G | 47 | a0001c0002t0001g0066 a0001c0002t0001g0115 a0001c0002t0001g0116 others(44): Show |
47 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.1510+5697T>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153301733 | |||||||
| chr4:153302071 | G | A | 2 | a0001c0002t0010g0134 a0001c0002t0029g0261 |
2 | HG02258.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1510+6035G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153302071 | |||||||
| chr4:153302136 | C | T | 1 | a0001c0002t0003g0144 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1510+6100C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153302136 | |||||||
| chr4:153302248 | G | A | 1 | a0001c0008t0002g0059 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1510+6212G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153302248 | |||||||
| chr4:153302248 | G | T | 1 | a0001c0003t0003g0026 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1510+6212G>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153302248 | |||||||
| chr4:153302292 | C | T | 5 | a0001c0003t0007g0106 a0001c0003t0007g0223 a0001c0003t0007g0224 others(2): Show |
5 | HG01074.hp2 HG01106.hp2 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.1510+6256C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153302292 | |||||||
| chr4:153302555 | C | T | 2 | a0001c0002t0010g0134 a0001c0002t0029g0261 |
2 | HG02258.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1510+6519C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153302555 | |||||||
| chr4:153302699 | T | C | 1 | a0001c0002t0023g0014 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1510+6663T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153302699 | |||||||
| chr4:153302896 | A | G | 5 | a0001c0002t0001g0066 a0001c0002t0001g0115 a0001c0002t0001g0116 others(2): Show |
5 | HG00323.hp2 HG01070.hp1 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1510+6860A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153302896 | |||||||
| chr4:153303128 | A | G | 49 | a0001c0002t0003g0144 a0001c0002t0003g0148 a0001c0003t0001g0003 others(46): Show |
49 | HG00323.hp1 HG00438.hp1 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.1510+7092A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153303128 | |||||||
| chr4:153303137 | T | C | 49 | a0001c0002t0003g0144 a0001c0002t0003g0148 a0001c0003t0001g0003 others(46): Show |
49 | HG00323.hp1 HG00438.hp1 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.1510+7101T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153303137 | |||||||
| chr4:153303310 | A | AT | 17 | a0001c0001t0001g0092 a0001c0001t0001g0099 a0001c0001t0001g0100 others(14): Show |
17 | HG00280.hp2 HG01261.hp2 HG01516.hp1 others(14): Show |
intron_variant | MODIFIER | c.1510+7274_1510+727 others(5): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153303310 | |||||||
| chr4:153303310 | A | T | 1 | a0001c0001t0001g0102 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1510+7274A>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153303310 | |||||||
| chr4:153303312 | A | T | 18 | a0001c0001t0001g0092 a0001c0001t0001g0099 a0001c0001t0001g0100 others(15): Show |
18 | HG00280.hp2 HG00642.hp2 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.1510+7276A>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153303312 | |||||||
| chr4:153303313 | AT | A | 43 | a0001c0002t0001g0066 a0001c0002t0001g0115 a0001c0002t0001g0116 others(40): Show |
43 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.1510+7278delT | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153303313 | |||||||
| chr4:153303469 | T | A | 1 | a0001c0001t0002g0002 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1510+7433T>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153303469 | |||||||
| chr4:153303474 | G | GA | 10 | a0001c0001t0002g0002 a0001c0001t0006g0061 a0001c0001t0006g0143 others(7): Show |
10 | HG01891.hp2 HG02257.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.1510+7455dupA | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr4 | 153303474 | ||||||
| chr4:153303645 | G | A | 1 | a0001c0001t0002g0221 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1510+7609G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153303645 | |||||||
| chr4:153303649 | T | C | 20 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0002g0001 others(17): Show |
20 | HG01891.hp2 HG02055.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.1510+7613T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153303649 | |||||||
| chr4:153304162 | G | A | 47 | a0001c0002t0001g0066 a0001c0002t0001g0115 a0001c0002t0001g0116 others(44): Show |
47 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.1510+8126G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153304162 | |||||||
| chr4:153304167 | G | T | 1 | a0001c0002t0001g0226 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1510+8131G>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153304167 | |||||||
| chr4:153304174 | C | T | 8 | a0001c0001t0005g0037 a0001c0001t0008g0020 a0001c0001t0008g0032 others(5): Show |
8 | NA18944.hp1 NA18979.hp2 NA18985.hp1 others(5): Show |
intron_variant | MODIFIER | c.1510+8138C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153304174 | |||||||
| chr4:153304185 | C | A | 49 | a0001c0002t0003g0144 a0001c0002t0003g0148 a0001c0003t0001g0003 others(46): Show |
49 | HG00323.hp1 HG00438.hp1 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.1510+8149C>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153304185 | |||||||
| chr4:153304396 | G | A | 49 | a0001c0002t0003g0144 a0001c0002t0003g0148 a0001c0003t0001g0003 others(46): Show |
49 | HG00323.hp1 HG00438.hp1 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.1510+8360G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153304396 | |||||||
| chr4:153304407 | C | G | 1 | a0001c0003t0003g0042 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1510+8371C>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153304407 | |||||||
| chr4:153304436 | A | C | 49 | a0001c0002t0003g0144 a0001c0002t0003g0148 a0001c0003t0001g0003 others(46): Show |
49 | HG00323.hp1 HG00438.hp1 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.1510+8400A>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153304436 | |||||||
| chr4:153304948 | T | G | 2 | a0001c0002t0010g0134 a0001c0002t0029g0261 |
2 | HG02258.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1510+8912T>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153304948 | |||||||
| chr4:153305399 | C | T | 176 | a0001c0001t0001g0033 a0001c0001t0001g0055 a0001c0001t0001g0081 others(173): Show |
176 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.1510+9363C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153305399 | |||||||
| chr4:153305700 | A | T | 1 | a0001c0002t0028g0080 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1510+9664A>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153305700 | |||||||
| chr4:153305833 | G | A | 18 | a0001c0001t0001g0033 a0001c0001t0002g0018 a0001c0001t0002g0022 others(15): Show |
18 | HG01169.hp1 HG02895.hp2 HG02897.hp1 others(15): Show |
intron_variant | MODIFIER | c.1511-9652G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153305833 | |||||||
| chr4:153305956 | G | A | 3 | a0001c0001t0009g0060 a0001c0001t0009g0263 a0001c0001t0009g0264 |
3 | HG02280.hp2 HG03041.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1511-9529G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153305956 | |||||||
| chr4:153306095 | T | C | 176 | a0001c0001t0001g0033 a0001c0001t0001g0055 a0001c0001t0001g0081 others(173): Show |
176 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.1511-9390T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153306095 | |||||||
| chr4:153306128 | C | CA | 12 | a0001c0001t0001g0120 a0001c0002t0002g0130 a0001c0002t0002g0136 others(9): Show |
12 | HG01168.hp1 HG02145.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.1511-9341dupA | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr4 | 153306128 | ||||||
| chr4:153306268 | A | G | 4 | a0001c0002t0004g0045 a0001c0002t0004g0046 a0001c0002t0004g0047 others(1): Show |
4 | HG01884.hp1 HG02976.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1511-9217A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153306268 | |||||||
| chr4:153306435 | G | A | 1 | a0001c0002t0028g0080 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1511-9050G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153306435 | |||||||
| chr4:153306688 | A | G | 1 | a0001c0007t0003g0233 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1511-8797A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153306688 | |||||||
| chr4:153306737 | T | C | 2 | a0001c0002t0010g0134 a0001c0002t0029g0261 |
2 | HG02258.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1511-8748T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153306737 | |||||||
| chr4:153306766 | C | T | 18 | a0001c0001t0001g0092 a0001c0001t0001g0099 a0001c0001t0001g0100 others(15): Show |
18 | HG00280.hp2 HG00642.hp2 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.1511-8719C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153306766 | |||||||
| chr4:153306816 | T | C | 1 | a0001c0001t0003g0150 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1511-8669T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153306816 | |||||||
| chr4:153306821 | GA | G | 3 | a0001c0003t0007g0223 a0001c0003t0007g0224 a0001c0003t0007g0225 |
3 | HG01074.hp2 HG01106.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1511-8663delA | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153306821 | |||||||
| chr4:153307018 | G | T | 30 | a0001c0002t0001g0167 a0001c0002t0001g0173 a0001c0002t0001g0229 others(27): Show |
30 | HG00140.hp2 HG00544.hp1 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.1511-8467G>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153307018 | |||||||
| chr4:153307049 | C | G | 9 | a0001c0001t0001g0092 a0001c0001t0001g0121 a0001c0001t0005g0094 others(6): Show |
9 | NA18942.hp1 NA18943.hp1 NA18964.hp2 others(6): Show |
intron_variant | MODIFIER | c.1511-8436C>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153307049 | |||||||
| chr4:153307191 | G | A | 11 | a0001c0002t0002g0130 a0001c0002t0002g0136 a0001c0002t0002g0137 others(8): Show |
11 | HG01168.hp1 HG02145.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.1511-8294G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153307191 | |||||||
| chr4:153307224 | T | G | 1 | a0001c0001t0020g0228 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1511-8261T>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153307224 | |||||||
| chr4:153307286 | T | G | 16 | a0001c0002t0002g0130 a0001c0002t0002g0136 a0001c0002t0002g0137 others(13): Show |
16 | HG01168.hp1 HG01884.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.1511-8199T>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153307286 | |||||||
| chr4:153307342 | G | C | 1 | a0001c0001t0001g0186 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1511-8143G>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153307342 | |||||||
| chr4:153307438 | GA | G | 22 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0002g0001 others(19): Show |
22 | HG01346.hp2 HG01891.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.1511-8040delA | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr4 | 153307438 | ||||||
| chr4:153307495 | G | A | 1 | a0001c0001t0003g0209 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1511-7990G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153307495 | |||||||
| chr4:153307756 | C | T | 18 | a0001c0001t0001g0033 a0001c0001t0002g0018 a0001c0001t0002g0022 others(15): Show |
18 | HG01169.hp1 HG02895.hp2 HG02897.hp1 others(15): Show |
intron_variant | MODIFIER | c.1511-7729C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153307756 | |||||||
| chr4:153307896 | C | T | 1 | a0001c0001t0020g0228 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1511-7589C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153307896 | |||||||
| chr4:153307923 | A | G | 1 | a0001c0001t0002g0221 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1511-7562A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153307923 | |||||||
| chr4:153308097 | G | T | 3 | a0001c0003t0001g0003 a0001c0003t0001g0131 a0001c0003t0001g0132 |
3 | HG01884.hp2 HG02486.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1511-7388G>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153308097 | |||||||
| chr4:153308103 | C | T | 21 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0002g0001 others(18): Show |
21 | HG01891.hp2 HG02055.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.1511-7382C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153308103 | |||||||
| chr4:153308111 | G | A | 2 | a0001c0002t0018g0135 a0001c0002t0033g0234 |
2 | HG02717.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1511-7374G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153308111 | |||||||
| chr4:153308192 | A | G | 20 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0002g0001 others(17): Show |
20 | HG01891.hp2 HG02055.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.1511-7293A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153308192 | |||||||
| chr4:153308633 | T | A | 16 | a0001c0002t0002g0130 a0001c0002t0002g0136 a0001c0002t0002g0137 others(13): Show |
16 | HG01168.hp1 HG01884.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.1511-6852T>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153308633 | |||||||
| chr4:153308685 | T | A | 1 | a0001c0003t0003g0042 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1511-6800T>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153308685 | |||||||
| chr4:153308818 | T | A | 3 | a0001c0002t0012g0163 a0001c0002t0012g0177 a0001c0002t0012g0178 |
3 | NA18948.hp2 NA19011.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.1511-6667T>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153308818 | |||||||
| chr4:153308825 | A | G | 1 | a0001c0002t0028g0080 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1511-6660A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153308825 | |||||||
| chr4:153309002 | T | C | 7 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0093 others(4): Show |
7 | HG00438.hp2 HG02080.hp1 NA18747.hp1 others(4): Show |
intron_variant | MODIFIER | c.1511-6483T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153309002 | |||||||
| chr4:153309280 | A | G | 1 | a0001c0008t0002g0059 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1511-6205A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153309280 | |||||||
| chr4:153309419 | C | T | 1 | a0001c0002t0001g0229 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1511-6066C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153309419 | |||||||
| chr4:153309500 | C | T | 18 | a0001c0001t0001g0033 a0001c0001t0002g0018 a0001c0001t0002g0022 others(15): Show |
18 | HG01169.hp1 HG02895.hp2 HG02897.hp1 others(15): Show |
intron_variant | MODIFIER | c.1511-5985C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153309500 | |||||||
| chr4:153309524 | G | C | 6 | a0001c0002t0002g0267 a0001c0002t0002g0268 a0001c0002t0003g0239 others(3): Show |
6 | HG02109.hp1 HG02717.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1511-5961G>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153309524 | |||||||
| chr4:153309633 | C | CT | 19 | a0001c0001t0001g0091 a0001c0001t0001g0257 a0001c0001t0003g0209 others(16): Show |
19 | HG01168.hp1 HG01891.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.1511-5834dupT | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr4 | 153309633 | ||||||
| chr4:153309633 | CT | C | 8 | a0001c0001t0002g0237 a0001c0001t0003g0035 a0001c0002t0002g0124 others(5): Show |
8 | HG00558.hp2 HG02896.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1511-5834delT | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr4 | 153309633 | ||||||
| chr4:153309879 | T | G | 2 | a0001c0001t0001g0093 a0001c0001t0002g0237 |
2 | NA19007.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1511-5606T>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153309879 | |||||||
| chr4:153309908 | G | A | 1 | a0001c0008t0002g0059 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1511-5577G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153309908 | |||||||
| chr4:153310006 | T | A | 18 | a0001c0001t0001g0092 a0001c0001t0001g0099 a0001c0001t0001g0100 others(15): Show |
18 | HG00280.hp2 HG00642.hp2 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.1511-5479T>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153310006 | |||||||
| chr4:153310339 | A | T | 30 | a0001c0002t0001g0167 a0001c0002t0001g0173 a0001c0002t0001g0229 others(27): Show |
30 | HG00140.hp2 HG00544.hp1 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.1511-5146A>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153310339 | |||||||
| chr4:153310685 | C | T | 18 | a0001c0001t0001g0033 a0001c0001t0002g0018 a0001c0001t0002g0022 others(15): Show |
18 | HG01169.hp1 HG02895.hp2 HG02897.hp1 others(15): Show |
intron_variant | MODIFIER | c.1511-4800C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153310685 | |||||||
| chr4:153310694 | CAGG | C | 18 | a0001c0001t0001g0033 a0001c0001t0002g0018 a0001c0001t0002g0022 others(15): Show |
18 | HG01169.hp1 HG02895.hp2 HG02897.hp1 others(15): Show |
intron_variant | MODIFIER | c.1511-4788_1511-478 others(7): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr4 | 153310694 | ||||||
| chr4:153310811 | A | G | 4 | a0001c0002t0004g0045 a0001c0002t0004g0046 a0001c0002t0004g0047 others(1): Show |
4 | HG01884.hp1 HG02976.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1511-4674A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153310811 | |||||||
| chr4:153310840 | T | C | 6 | a0001c0002t0002g0267 a0001c0002t0002g0268 a0001c0002t0003g0239 others(3): Show |
6 | HG02109.hp1 HG02717.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1511-4645T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153310840 | |||||||
| chr4:153310964 | G | A | 18 | a0001c0001t0001g0092 a0001c0001t0001g0099 a0001c0001t0001g0100 others(15): Show |
18 | HG00280.hp2 HG00642.hp2 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.1511-4521G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153310964 | |||||||
| chr4:153310993 | T | C | 8 | a0001c0001t0005g0037 a0001c0001t0008g0020 a0001c0001t0008g0032 others(5): Show |
8 | NA18944.hp1 NA18979.hp2 NA18985.hp1 others(5): Show |
intron_variant | MODIFIER | c.1511-4492T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153310993 | |||||||
| chr4:153311185 | A | T | 47 | a0001c0002t0001g0066 a0001c0002t0001g0115 a0001c0002t0001g0116 others(44): Show |
47 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.1511-4300A>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153311185 | |||||||
| chr4:153311348 | T | C | 18 | a0001c0001t0001g0033 a0001c0001t0002g0018 a0001c0001t0002g0022 others(15): Show |
18 | HG01169.hp1 HG02895.hp2 HG02897.hp1 others(15): Show |
intron_variant | MODIFIER | c.1511-4137T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153311348 | |||||||
| chr4:153311370 | A | C | 173 | a0001c0001t0001g0033 a0001c0001t0001g0055 a0001c0001t0001g0081 others(170): Show |
173 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.1511-4115A>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153311370 | |||||||
| chr4:153311611 | G | T | 18 | a0001c0001t0001g0033 a0001c0001t0002g0018 a0001c0001t0002g0022 others(15): Show |
18 | HG01169.hp1 HG02895.hp2 HG02897.hp1 others(15): Show |
intron_variant | MODIFIER | c.1511-3874G>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153311611 | |||||||
| chr4:153311668 | C | T | 18 | a0001c0001t0001g0033 a0001c0001t0002g0018 a0001c0001t0002g0022 others(15): Show |
18 | HG01169.hp1 HG02895.hp2 HG02897.hp1 others(15): Show |
intron_variant | MODIFIER | c.1511-3817C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153311668 | |||||||
| chr4:153311683 | CT | C | 80 | a0001c0001t0001g0092 a0001c0001t0001g0099 a0001c0001t0001g0100 others(77): Show |
80 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.1511-3800delT | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr4 | 153311683 | ||||||
| chr4:153311684 | T | C | 39 | a0001c0001t0001g0033 a0001c0001t0001g0055 a0001c0001t0001g0081 others(36): Show |
39 | HG01169.hp1 HG01891.hp2 HG02055.hp2 others(36): Show |
intron_variant | MODIFIER | c.1511-3801T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153311684 | |||||||
| chr4:153311726 | A | AT | 44 | a0001c0002t0003g0144 a0001c0002t0003g0148 a0001c0003t0001g0027 others(41): Show |
44 | HG00323.hp1 HG00438.hp1 HG00741.hp1 others(41): Show |
intron_variant | MODIFIER | c.1511-3744dupT | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr4 | 153311726 | ||||||
| chr4:153311726 | AT | A | 17 | a0001c0001t0001g0033 a0001c0001t0002g0018 a0001c0001t0002g0022 others(14): Show |
17 | HG01169.hp1 HG02895.hp2 HG02897.hp1 others(14): Show |
intron_variant | MODIFIER | c.1511-3744delT | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr4 | 153311726 | ||||||
| chr4:153311842 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1511-3643G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153311842 | |||||||
| chr4:153311886 | T | G | 47 | a0001c0002t0001g0066 a0001c0002t0001g0115 a0001c0002t0001g0116 others(44): Show |
47 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.1511-3599T>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153311886 | |||||||
| chr4:153311894 | T | TTTTA | 28 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0002g0001 others(25): Show |
28 | HG01109.hp1 HG02055.hp2 HG02145.hp1 others(25): Show |
intron_variant | MODIFIER | c.1511-3564_1511-356 others(8): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr4 | 153311894 | ||||||
| chr4:153311894 | T | TTTTATTT others(1): Show |
53 | a0001c0001t0001g0092 a0001c0001t0001g0121 a0001c0001t0005g0094 others(50): Show |
53 | HG00323.hp2 HG00741.hp1 HG01069.hp1 others(50): Show |
intron_variant | MODIFIER | c.1511-3568_1511-356 others(12): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr4 | 153311894 | ||||||
| chr4:153311894 | T | TTTTATTT others(5): Show |
61 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 others(58): Show |
61 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.1511-3572_1511-356 others(16): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr4 | 153311894 | ||||||
| chr4:153311894 | T | TTTTATTT others(9): Show |
6 | a0001c0001t0001g0099 a0001c0002t0001g0167 a0001c0002t0002g0215 others(3): Show |
6 | HG00140.hp2 HG01081.hp2 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.1511-3576_1511-356 others(20): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr4 | 153311894 | ||||||
| chr4:153311894 | TTTTA | T | 4 | a0001c0002t0004g0045 a0001c0002t0004g0046 a0001c0002t0004g0047 others(1): Show |
4 | HG01884.hp1 HG02976.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1511-3564_1511-356 others(8): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr4 | 153311894 | ||||||
| chr4:153311917 | TA | T | 18 | a0001c0001t0001g0033 a0001c0001t0002g0018 a0001c0001t0002g0022 others(15): Show |
18 | HG01169.hp1 HG02895.hp2 HG02897.hp1 others(15): Show |
intron_variant | MODIFIER | c.1511-3567delA | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153311917 | |||||||
| chr4:153311919 | T | TTTATTTA others(4): Show |
1 | a0001c0003t0003g0071 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1511-3561_1511-356 others(15): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr4 | 153311919 | ||||||
| chr4:153312014 | C | T | 1 | a0001c0002t0002g0176 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1511-3471C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153312014 | |||||||
| chr4:153312048 | A | G | 6 | a0001c0002t0002g0267 a0001c0002t0002g0268 a0001c0002t0003g0239 others(3): Show |
6 | HG02109.hp1 HG02717.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1511-3437A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153312048 | |||||||
| chr4:153312066 | C | A | 21 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0002g0001 others(18): Show |
21 | HG01891.hp2 HG02055.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.1511-3419C>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153312066 | |||||||
| chr4:153312078 | C | A | 21 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0002g0001 others(18): Show |
21 | HG01891.hp2 HG02055.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.1511-3407C>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153312078 | |||||||
| chr4:153312274 | A | G | 47 | a0001c0002t0001g0066 a0001c0002t0001g0115 a0001c0002t0001g0116 others(44): Show |
47 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.1511-3211A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153312274 | |||||||
| chr4:153312349 | A | G | 18 | a0001c0001t0001g0033 a0001c0001t0002g0018 a0001c0001t0002g0022 others(15): Show |
18 | HG01169.hp1 HG02895.hp2 HG02897.hp1 others(15): Show |
intron_variant | MODIFIER | c.1511-3136A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153312349 | |||||||
| chr4:153312434 | C | T | 6 | a0001c0001t0006g0061 a0001c0001t0006g0143 a0001c0001t0006g0147 others(3): Show |
6 | HG02257.hp1 HG02895.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1511-3051C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153312434 | |||||||
| chr4:153312561 | G | T | 4 | a0001c0001t0001g0113 a0001c0001t0001g0158 a0001c0001t0001g0219 others(1): Show |
4 | NA18968.hp2 NA19002.hp2 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.1511-2924G>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153312561 | |||||||
| chr4:153312599 | A | G | 1 | a0001c0001t0001g0186 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1511-2886A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153312599 | |||||||
| chr4:153312698 | C | A | 3 | a0001c0001t0001g0182 a0001c0001t0002g0065 a0001c0001t0002g0245 |
3 | NA18957.hp1 NA18979.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.1511-2787C>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153312698 | |||||||
| chr4:153312838 | A | C | 1 | a0001c0003t0007g0223 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1511-2647A>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153312838 | |||||||
| chr4:153312989 | G | A | 1 | a0001c0003t0001g0041 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1511-2496G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153312989 | |||||||
| chr4:153313017 | T | C | 47 | a0001c0002t0001g0066 a0001c0002t0001g0115 a0001c0002t0001g0116 others(44): Show |
47 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.1511-2468T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153313017 | |||||||
| chr4:153313109 | G | A | 4 | a0001c0002t0004g0045 a0001c0002t0004g0046 a0001c0002t0004g0047 others(1): Show |
4 | HG01884.hp1 HG02976.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1511-2376G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153313109 | |||||||
| chr4:153313243 | T | C | 39 | a0001c0001t0001g0033 a0001c0001t0001g0055 a0001c0001t0001g0081 others(36): Show |
39 | HG01169.hp1 HG01891.hp2 HG02055.hp2 others(36): Show |
intron_variant | MODIFIER | c.1511-2242T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153313243 | |||||||
| chr4:153313374 | T | A | 2 | a0001c0003t0001g0041 a0001c0003t0010g0079 |
2 | HG02615.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1511-2111T>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153313374 | |||||||
| chr4:153313517 | T | G | 11 | a0001c0002t0002g0130 a0001c0002t0002g0136 a0001c0002t0002g0137 others(8): Show |
11 | HG01168.hp1 HG02145.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1511-1968T>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153313517 | |||||||
| chr4:153313529 | G | A | 1 | a0001c0001t0001g0093 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1511-1956G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153313529 | |||||||
| chr4:153313627 | C | CT | 9 | a0001c0001t0001g0118 a0001c0001t0001g0120 a0001c0001t0002g0153 others(6): Show |
9 | HG02572.hp2 HG02818.hp2 HG03516.hp1 others(6): Show |
intron_variant | MODIFIER | c.1511-1835dupT | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr4 | 153313627 | ||||||
| chr4:153313627 | CT | C | 42 | a0001c0001t0001g0092 a0001c0001t0001g0156 a0001c0001t0004g0104 others(39): Show |
42 | HG01074.hp2 HG01106.hp2 HG01884.hp1 others(39): Show |
intron_variant | MODIFIER | c.1511-1835delT | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr4 | 153313627 | ||||||
| chr4:153313627 | CTT | C | 63 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0002g0001 others(60): Show |
63 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.1511-1836_1511-183 others(6): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr4 | 153313627 | ||||||
| chr4:153313627 | CTTTT | C | 18 | a0001c0001t0001g0033 a0001c0001t0002g0018 a0001c0001t0002g0022 others(15): Show |
18 | HG01169.hp1 HG02895.hp2 HG02897.hp1 others(15): Show |
intron_variant | MODIFIER | c.1511-1838_1511-183 others(8): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr4 | 153313627 | ||||||
| chr4:153313857 | G | A | 2 | a0001c0002t0010g0134 a0001c0002t0029g0261 |
2 | HG02258.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1511-1628G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153313857 | |||||||
| chr4:153313933 | G | A | 5 | a0001c0002t0003g0148 a0001c0003t0002g0004 a0001c0003t0003g0011 others(2): Show |
5 | HG02109.hp2 HG02922.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1511-1552G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153313933 | |||||||
| chr4:153314012 | C | T | 3 | a0001c0002t0010g0134 a0001c0002t0013g0133 a0001c0002t0029g0261 |
3 | HG02258.hp1 HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1511-1473C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153314012 | |||||||
| chr4:153314023 | A | G | 45 | a0001c0002t0003g0144 a0001c0002t0003g0148 a0001c0003t0001g0027 others(42): Show |
45 | HG00323.hp1 HG00438.hp1 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.1511-1462A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153314023 | |||||||
| chr4:153314170 | TAAAAGAG others(262): Show |
T | 9 | a0001c0002t0002g0267 a0001c0002t0002g0268 a0001c0002t0003g0239 others(6): Show |
9 | HG02109.hp1 HG02258.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1511-1300_1511-103 others(4): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr4 | 153314170 | ||||||
| chr4:153314294 | C | T | 18 | a0001c0001t0001g0092 a0001c0001t0001g0099 a0001c0001t0001g0100 others(15): Show |
18 | HG00280.hp2 HG00642.hp2 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.1511-1191C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153314294 | |||||||
| chr4:153314311 | T | C | 1 | a0001c0003t0003g0216 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1511-1174T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153314311 | |||||||
| chr4:153314377 | G | A | 1 | a0001c0001t0030g0217 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1511-1108G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153314377 | |||||||
| chr4:153314419 | C | CA | 20 | a0001c0001t0001g0033 a0001c0001t0001g0098 a0001c0001t0001g0183 others(17): Show |
20 | HG01169.hp1 HG01175.hp1 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.1511-1042dupA | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr4 | 153314419 | ||||||
| chr4:153314419 | CA | C | 121 | a0001c0001t0001g0084 a0001c0001t0001g0091 a0001c0001t0001g0092 others(118): Show |
121 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.1511-1042delA | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr4 | 153314419 | ||||||
| chr4:153314419 | CAA | C | 6 | a0001c0002t0004g0047 a0001c0002t0007g0155 a0001c0002t0011g0005 others(3): Show |
6 | HG02027.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1511-1043_1511-104 others(6): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr4 | 153314419 | ||||||
| chr4:153314419 | CAAAAAAA others(3): Show |
C | 11 | a0001c0001t0002g0002 a0001c0001t0006g0061 a0001c0001t0006g0143 others(8): Show |
11 | HG01891.hp2 HG02257.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1511-1051_1511-104 others(14): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr4 | 153314419 | ||||||
| chr4:153314524 | C | A | 9 | a0001c0002t0002g0267 a0001c0002t0002g0268 a0001c0002t0003g0239 others(6): Show |
9 | HG02109.hp1 HG02258.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1511-961C>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153314524 | |||||||
| chr4:153314585 | C | CAAACAAA others(3): Show |
9 | a0001c0002t0002g0267 a0001c0002t0002g0268 a0001c0002t0003g0239 others(6): Show |
9 | HG02109.hp1 HG02258.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1511-897_1511-888d others(12): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr4 | 153314585 | ||||||
| chr4:153314639 | T | C | 2 | a0001c0002t0002g0166 a0001c0002t0002g0181 |
2 | HG02523.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.1511-846T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153314639 | |||||||
| chr4:153314667 | C | T | 6 | a0001c0002t0002g0267 a0001c0002t0002g0268 a0001c0002t0003g0239 others(3): Show |
6 | HG02109.hp1 HG02717.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1511-818C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153314667 | |||||||
| chr4:153314677 | A | G | 1 | a0001c0003t0003g0064 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1511-808A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153314677 | |||||||
| chr4:153314786 | T | C | 1 | a0001c0002t0024g0128 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1511-699T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153314786 | |||||||
| chr4:153314800 | CT | C | 6 | a0001c0002t0002g0267 a0001c0002t0002g0268 a0001c0002t0003g0239 others(3): Show |
6 | HG02109.hp1 HG02717.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1511-684delT | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153314800 | |||||||
| chr4:153314814 | C | T | 6 | a0001c0002t0002g0267 a0001c0002t0002g0268 a0001c0002t0003g0239 others(3): Show |
6 | HG02109.hp1 HG02717.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1511-671C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153314814 | |||||||
| chr4:153314861 | A | G | 2 | a0001c0002t0002g0256 a0001c0002t0002g0259 |
2 | NA19070.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.1511-624A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153314861 | |||||||
| chr4:153314898 | T | C | 1 | a0001c0001t0016g0197 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1511-587T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153314898 | |||||||
| chr4:153315139 | G | A | 3 | a0001c0002t0011g0005 a0001c0002t0011g0006 a0001c0002t0011g0070 |
3 | HG02896.hp2 HG02897.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1511-346G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153315139 | |||||||
| chr4:153315156 | A | G | 1 | a0001c0003t0004g0142 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1511-329A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153315156 | |||||||
| chr4:153315239 | G | T | 1 | a0001c0001t0002g0153 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1511-246G>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153315239 | |||||||
| chr4:153315336 | T | C | 6 | a0001c0002t0002g0267 a0001c0002t0002g0268 a0001c0002t0003g0239 others(3): Show |
6 | HG02109.hp1 HG02717.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1511-149T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153315336 | |||||||
| chr4:153315337 | A | T | 1 | a0001c0002t0005g0251 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1511-148A>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153315337 | |||||||
| chr4:153315363 | T | A | 1 | a0001c0002t0002g0024 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1511-122T>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153315363 | |||||||
| chr4:153315452 | G | A | 1 | a0001c0002t0007g0155 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1511-33G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 6/11 | chr4 | 153315452 | |||||||
| chr4:153315637 | T | G | 6 | a0001c0002t0002g0267 a0001c0002t0002g0268 a0001c0002t0003g0239 others(3): Show |
6 | HG02109.hp1 HG02717.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1614+49T>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 7/11 | chr4 | 153315637 | |||||||
| chr4:153316213 | G | C | 1 | a0001c0003t0003g0216 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1782+214G>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 8/11 | chr4 | 153316213 | |||||||
| chr4:153316483 | A | T | 176 | a0001c0001t0001g0033 a0001c0001t0001g0055 a0001c0001t0001g0081 others(173): Show |
176 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.1782+484A>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 8/11 | chr4 | 153316483 | |||||||
| chr4:153316834 | C | G | 7 | a0001c0002t0002g0130 a0001c0002t0002g0136 a0001c0002t0002g0137 others(4): Show |
7 | HG02145.hp1 HG02486.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1782+835C>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 8/11 | chr4 | 153316834 | |||||||
| chr4:153316849 | T | C | 6 | a0001c0002t0002g0267 a0001c0002t0002g0268 a0001c0002t0003g0239 others(3): Show |
6 | HG02109.hp1 HG02717.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1782+850T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 8/11 | chr4 | 153316849 | |||||||
| chr4:153316873 | C | CT | 87 | a0001c0001t0001g0017 a0001c0001t0001g0023 a0001c0001t0001g0039 others(84): Show |
87 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.1782+899dupT | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 153316873 | ||||||
| chr4:153316873 | C | CTT | 19 | a0001c0001t0001g0092 a0001c0001t0001g0121 a0001c0001t0001g0157 others(16): Show |
19 | HG00544.hp2 HG01175.hp1 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.1782+898_1782+899d others(4): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 153316873 | ||||||
| chr4:153316873 | C | CTTT | 47 | a0001c0001t0001g0182 a0001c0001t0002g0065 a0001c0001t0002g0245 others(44): Show |
47 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.1782+897_1782+899d others(5): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 153316873 | ||||||
| chr4:153316873 | C | CTTTT | 26 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0002g0001 others(23): Show |
26 | HG00735.hp2 HG01884.hp1 HG02027.hp1 others(23): Show |
intron_variant | MODIFIER | c.1782+896_1782+899d others(6): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 153316873 | ||||||
| chr4:153316873 | C | CTTTTT | 11 | a0001c0001t0004g0087 a0001c0001t0004g0129 a0001c0001t0006g0149 others(8): Show |
11 | HG02109.hp1 HG02615.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.1782+895_1782+899d others(7): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 153316873 | ||||||
| chr4:153316873 | C | CTTTTTT | 34 | a0001c0001t0001g0033 a0001c0001t0002g0018 a0001c0001t0002g0022 others(31): Show |
34 | HG00323.hp1 HG01069.hp1 HG01074.hp1 others(31): Show |
intron_variant | MODIFIER | c.1782+894_1782+899d others(8): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 153316873 | ||||||
| chr4:153316873 | C | CTTTTTTT | 15 | a0001c0001t0003g0150 a0001c0001t0016g0231 a0001c0002t0010g0134 others(12): Show |
15 | HG00438.hp1 HG00741.hp1 HG01346.hp1 others(12): Show |
intron_variant | MODIFIER | c.1782+893_1782+899d others(9): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 153316873 | ||||||
| chr4:153316873 | C | CTTTTTTT others(1): Show |
16 | a0001c0002t0003g0148 a0001c0002t0013g0133 a0001c0003t0003g0025 others(13): Show |
16 | HG01074.hp2 HG01891.hp1 HG01981.hp2 others(13): Show |
intron_variant | MODIFIER | c.1782+892_1782+899d others(10): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 153316873 | ||||||
| chr4:153316873 | C | CTTTTTTT others(3): Show |
3 | a0001c0002t0003g0144 a0001c0003t0003g0042 a0001c0003t0007g0225 |
3 | HG01106.hp2 HG03225.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1782+890_1782+899d others(12): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 153316873 | ||||||
| chr4:153316950 | A | G | 24 | a0001c0001t0001g0033 a0001c0001t0002g0018 a0001c0001t0002g0022 others(21): Show |
24 | HG01169.hp1 HG02109.hp1 HG02717.hp1 others(21): Show |
intron_variant | MODIFIER | c.1782+951A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 8/11 | chr4 | 153316950 | |||||||
| chr4:153317000 | C | G | 1 | a0001c0001t0001g0186 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1782+1001C>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 8/11 | chr4 | 153317000 | |||||||
| chr4:153317011 | G | C | 6 | a0001c0002t0002g0267 a0001c0002t0002g0268 a0001c0002t0003g0239 others(3): Show |
6 | HG02109.hp1 HG02717.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1782+1012G>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 8/11 | chr4 | 153317011 | |||||||
| chr4:153317027 | C | G | 1 | a0001c0002t0028g0080 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1782+1028C>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 8/11 | chr4 | 153317027 | |||||||
| chr4:153317029 | C | T | 2 | a0001c0002t0002g0050 a0001c0002t0002g0145 |
2 | HG02738.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1782+1030C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 8/11 | chr4 | 153317029 | |||||||
| chr4:153317090 | T | C | 6 | a0001c0002t0002g0267 a0001c0002t0002g0268 a0001c0002t0003g0239 others(3): Show |
6 | HG02109.hp1 HG02717.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1782+1091T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 8/11 | chr4 | 153317090 | |||||||
| chr4:153317132 | G | A | 45 | a0001c0002t0003g0144 a0001c0002t0003g0148 a0001c0003t0001g0027 others(42): Show |
45 | HG00323.hp1 HG00438.hp1 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.1782+1133G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 8/11 | chr4 | 153317132 | |||||||
| chr4:153317159 | C | T | 1 | a0001c0010t0004g0085 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1782+1160C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 8/11 | chr4 | 153317159 | |||||||
| chr4:153317171 | C | T | 4 | a0001c0001t0008g0034 a0001c0001t0008g0044 a0001c0001t0008g0049 others(1): Show |
4 | NA18944.hp1 NA18979.hp2 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.1782+1172C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 8/11 | chr4 | 153317171 | |||||||
| chr4:153317324 | A | G | 1 | a0001c0002t0023g0014 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1782+1325A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 8/11 | chr4 | 153317324 | |||||||
| chr4:153317506 | G | A | 18 | a0001c0001t0001g0033 a0001c0001t0002g0018 a0001c0001t0002g0022 others(15): Show |
18 | HG01169.hp1 HG02895.hp2 HG02897.hp1 others(15): Show |
intron_variant | MODIFIER | c.1782+1507G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 8/11 | chr4 | 153317506 | |||||||
| chr4:153317633 | A | G | 176 | a0001c0001t0001g0033 a0001c0001t0001g0055 a0001c0001t0001g0081 others(173): Show |
176 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.1782+1634A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 8/11 | chr4 | 153317633 | |||||||
| chr4:153317655 | G | GA | 6 | a0001c0002t0002g0267 a0001c0002t0002g0268 a0001c0002t0003g0239 others(3): Show |
6 | HG02109.hp1 HG02717.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1782+1671dupA | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 153317655 | ||||||
| chr4:153317655 | GA | G | 106 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0001g0092 others(103): Show |
106 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.1782+1671delA | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 153317655 | ||||||
| chr4:153318041 | A | C | 2 | a0001c0002t0002g0166 a0001c0002t0002g0181 |
2 | HG02523.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.1782+2042A>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 8/11 | chr4 | 153318041 | |||||||
| chr4:153318124 | A | G | 3 | a0001c0002t0011g0005 a0001c0002t0011g0006 a0001c0002t0011g0070 |
3 | HG02896.hp2 HG02897.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1782+2125A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 8/11 | chr4 | 153318124 | |||||||
| chr4:153318127 | T | G | 12 | a0001c0001t0006g0061 a0001c0001t0006g0143 a0001c0001t0006g0147 others(9): Show |
12 | HG02109.hp1 HG02257.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.1782+2128T>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 8/11 | chr4 | 153318127 | |||||||
| chr4:153318240 | T | A | 176 | a0001c0001t0001g0033 a0001c0001t0001g0055 a0001c0001t0001g0081 others(173): Show |
176 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.1782+2241T>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 8/11 | chr4 | 153318240 | |||||||
| chr4:153318283 | T | C | 1 | a0001c0001t0003g0232 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1782+2284T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 8/11 | chr4 | 153318283 | |||||||
| chr4:153318375 | A | G | 19 | a0001c0001t0001g0056 a0001c0001t0001g0092 a0001c0001t0001g0099 others(16): Show |
19 | HG00280.hp2 HG00642.hp2 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.1782+2376A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 8/11 | chr4 | 153318375 | |||||||
| chr4:153318510 | C | T | 12 | a0001c0001t0006g0061 a0001c0001t0006g0143 a0001c0001t0006g0147 others(9): Show |
12 | HG02109.hp1 HG02257.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.1782+2511C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 8/11 | chr4 | 153318510 | |||||||
| chr4:153318578 | C | A | 10 | a0001c0003t0003g0053 a0001c0003t0003g0054 a0001c0003t0003g0073 others(7): Show |
10 | HG01891.hp1 HG02055.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1782+2579C>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 8/11 | chr4 | 153318578 | |||||||
| chr4:153318595 | A | G | 1 | a0001c0001t0001g0125 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1782+2596A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 8/11 | chr4 | 153318595 | |||||||
| chr4:153318635 | A | G | 1 | a0001c0001t0002g0153 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1782+2636A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 8/11 | chr4 | 153318635 | |||||||
| chr4:153318734 | C | T | 12 | a0001c0001t0006g0061 a0001c0001t0006g0143 a0001c0001t0006g0147 others(9): Show |
12 | HG02109.hp1 HG02257.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.1782+2735C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 8/11 | chr4 | 153318734 | |||||||
| chr4:153318803 | C | T | 1 | a0001c0001t0001g0211 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1782+2804C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 8/11 | chr4 | 153318803 | |||||||
| chr4:153318811 | A | G | 9 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(6): Show |
9 | HG00280.hp2 HG00642.hp2 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.1782+2812A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 8/11 | chr4 | 153318811 | |||||||
| chr4:153318831 | C | T | 3 | a0001c0002t0010g0134 a0001c0002t0013g0133 a0001c0002t0029g0261 |
3 | HG02258.hp1 HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1782+2832C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 8/11 | chr4 | 153318831 | |||||||
| chr4:153318961 | G | A | 3 | a0001c0003t0001g0003 a0001c0003t0001g0131 a0001c0003t0001g0132 |
3 | HG01884.hp2 HG02486.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1782+2962G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 8/11 | chr4 | 153318961 | |||||||
| chr4:153319018 | G | C | 3 | a0001c0001t0009g0060 a0001c0001t0009g0263 a0001c0001t0009g0264 |
3 | HG02280.hp2 HG03041.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1782+3019G>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 8/11 | chr4 | 153319018 | |||||||
| chr4:153319250 | G | A | 172 | a0001c0001t0001g0033 a0001c0001t0001g0055 a0001c0001t0001g0081 others(169): Show |
172 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.1782+3251G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 8/11 | chr4 | 153319250 | |||||||
| chr4:153319324 | A | G | 252 | a0001c0001t0001g0017 a0001c0001t0001g0023 a0001c0001t0001g0033 others(249): Show |
252 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.1783-3324A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 8/11 | chr4 | 153319324 | |||||||
| chr4:153319330 | T | G | 1 | a0001c0001t0010g0078 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1783-3318T>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 8/11 | chr4 | 153319330 | |||||||
| chr4:153319495 | G | A | 1 | a0001c0001t0001g0196 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1783-3153G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 8/11 | chr4 | 153319495 | |||||||
| chr4:153319602 | C | T | 6 | a0001c0002t0002g0267 a0001c0002t0002g0268 a0001c0002t0003g0239 others(3): Show |
6 | HG02109.hp1 HG02717.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1783-3046C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 8/11 | chr4 | 153319602 | |||||||
| chr4:153319634 | G | A | 1 | a0001c0002t0028g0080 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1783-3014G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 8/11 | chr4 | 153319634 | |||||||
| chr4:153319654 | C | T | 22 | a0001c0001t0001g0033 a0001c0001t0002g0018 a0001c0001t0002g0022 others(19): Show |
22 | HG01074.hp1 HG01169.hp1 HG01517.hp1 others(19): Show |
intron_variant | MODIFIER | c.1783-2994C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 8/11 | chr4 | 153319654 | |||||||
| chr4:153319737 | A | T | 6 | a0001c0002t0002g0267 a0001c0002t0002g0268 a0001c0002t0003g0239 others(3): Show |
6 | HG02109.hp1 HG02717.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1783-2911A>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 8/11 | chr4 | 153319737 | |||||||
| chr4:153319739 | A | T | 72 | a0001c0001t0002g0001 a0001c0001t0006g0061 a0001c0001t0006g0143 others(69): Show |
72 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.1783-2909A>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 8/11 | chr4 | 153319739 | |||||||
| chr4:153319741 | T | A | 30 | a0001c0001t0001g0033 a0001c0001t0001g0092 a0001c0001t0001g0121 others(27): Show |
30 | HG01169.hp1 HG02895.hp2 HG02896.hp2 others(27): Show |
intron_variant | MODIFIER | c.1783-2907T>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 8/11 | chr4 | 153319741 | |||||||
| chr4:153319867 | G | T | 18 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0002g0001 others(15): Show |
18 | HG01891.hp2 HG02055.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.1783-2781G>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 8/11 | chr4 | 153319867 | |||||||
| chr4:153320349 | C | G | 2 | a0001c0002t0001g0126 a0001c0002t0001g0210 |
2 | HG01255.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1783-2299C>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 8/11 | chr4 | 153320349 | |||||||
| chr4:153320366 | A | T | 1 | a0001c0001t0001g0199 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1783-2282A>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 8/11 | chr4 | 153320366 | |||||||
| chr4:153320507 | C | T | 1 | a0001c0004t0003g0119 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1783-2141C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 8/11 | chr4 | 153320507 | |||||||
| chr4:153320540 | T | C | 1 | a0001c0001t0001g0056 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1783-2108T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 8/11 | chr4 | 153320540 | |||||||
| chr4:153320726 | A | G | 175 | a0001c0001t0001g0033 a0001c0001t0001g0055 a0001c0001t0001g0081 others(172): Show |
175 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.1783-1922A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 8/11 | chr4 | 153320726 | |||||||
| chr4:153320842 | A | AC | 130 | a0001c0001t0001g0033 a0001c0001t0001g0055 a0001c0001t0001g0081 others(127): Show |
130 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.1783-1806_1783-180 others(5): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 8/11 | chr4 | 153320842 | |||||||
| chr4:153320879 | A | G | 4 | a0001c0002t0004g0045 a0001c0002t0004g0046 a0001c0002t0004g0047 others(1): Show |
4 | HG01884.hp1 HG02976.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1783-1769A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 8/11 | chr4 | 153320879 | |||||||
| chr4:153321033 | A | G | 1 | a0001c0010t0004g0085 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1783-1615A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 8/11 | chr4 | 153321033 | |||||||
| chr4:153321051 | T | C | 25 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0002g0001 others(22): Show |
25 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.1783-1597T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 8/11 | chr4 | 153321051 | |||||||
| chr4:153321052 | C | T | 3 | a0001c0002t0010g0134 a0001c0002t0013g0133 a0001c0002t0029g0261 |
3 | HG02258.hp1 HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1783-1596C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 8/11 | chr4 | 153321052 | |||||||
| chr4:153321101 | A | G | 1 | a0001c0003t0004g0142 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1783-1547A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 8/11 | chr4 | 153321101 | |||||||
| chr4:153321114 | C | T | 1 | a0001c0009t0003g0159 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1783-1534C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 8/11 | chr4 | 153321114 | |||||||
| chr4:153321339 | A | G | 3 | a0001c0002t0010g0134 a0001c0002t0013g0133 a0001c0002t0029g0261 |
3 | HG02258.hp1 HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1783-1309A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 8/11 | chr4 | 153321339 | |||||||
| chr4:153321605 | G | A | 46 | a0001c0002t0003g0144 a0001c0002t0003g0148 a0001c0003t0001g0027 others(43): Show |
46 | HG00323.hp1 HG00438.hp1 HG00741.hp1 others(43): Show |
intron_variant | MODIFIER | c.1783-1043G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 8/11 | chr4 | 153321605 | |||||||
| chr4:153321674 | T | C | 1 | a0001c0001t0003g0232 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1783-974T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 8/11 | chr4 | 153321674 | |||||||
| chr4:153321820 | A | G | 4 | a0001c0002t0010g0134 a0001c0002t0013g0133 a0001c0002t0028g0080 others(1): Show |
4 | HG02258.hp1 HG02280.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1783-828A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 8/11 | chr4 | 153321820 | |||||||
| chr4:153322210 | C | T | 3 | a0001c0003t0007g0223 a0001c0003t0007g0224 a0001c0003t0007g0225 |
3 | HG01074.hp2 HG01106.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1783-438C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 8/11 | chr4 | 153322210 | |||||||
| chr4:153322268 | A | G | 130 | a0001c0001t0001g0033 a0001c0001t0001g0055 a0001c0001t0001g0081 others(127): Show |
130 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.1783-380A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 8/11 | chr4 | 153322268 | |||||||
| chr4:153322329 | T | G | 4 | a0001c0003t0003g0030 a0001c0003t0003g0031 a0001c0003t0003g0043 others(1): Show |
4 | HG01074.hp1 HG01517.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.1783-319T>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 8/11 | chr4 | 153322329 | |||||||
| chr4:153322509 | A | G | 21 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0002g0001 others(18): Show |
21 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.1783-139A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 8/11 | chr4 | 153322509 | |||||||
| chr4:153322520 | T | C | 6 | a0001c0002t0002g0267 a0001c0002t0002g0268 a0001c0002t0003g0239 others(3): Show |
6 | HG02109.hp1 HG02717.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1783-128T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 8/11 | chr4 | 153322520 | |||||||
| chr4:153322583 | T | A | 1 | a0001c0001t0001g0253 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1783-65T>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 8/11 | chr4 | 153322583 | |||||||
| chr4:153322848 | T | C | 1 | a0001c0004t0001g0184 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1951+32T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 9/11 | chr4 | 153322848 | |||||||
| chr4:153323039 | T | C | 69 | a0001c0001t0001g0182 a0001c0001t0002g0065 a0001c0001t0002g0245 others(66): Show |
69 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.1951+223T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 9/11 | chr4 | 153323039 | |||||||
| chr4:153323040 | C | T | 176 | a0001c0001t0001g0033 a0001c0001t0001g0055 a0001c0001t0001g0081 others(173): Show |
176 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.1951+224C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 9/11 | chr4 | 153323040 | |||||||
| chr4:153323138 | A | G | 1 | a0001c0002t0028g0080 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1951+322A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 9/11 | chr4 | 153323138 | |||||||
| chr4:153323163 | G | A | 67 | a0001c0001t0001g0182 a0001c0001t0002g0065 a0001c0001t0002g0245 others(64): Show |
67 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.1951+347G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 9/11 | chr4 | 153323163 | |||||||
| chr4:153323576 | G | T | 1 | a0001c0003t0007g0223 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1952-502G>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 9/11 | chr4 | 153323576 | |||||||
| chr4:153323588 | C | A | 1 | a0001c0003t0001g0041 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1952-490C>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 9/11 | chr4 | 153323588 | |||||||
| chr4:153323708 | C | T | 24 | a0001c0001t0001g0033 a0001c0001t0002g0018 a0001c0001t0002g0022 others(21): Show |
24 | HG01169.hp1 HG02257.hp1 HG02895.hp1 others(21): Show |
intron_variant | MODIFIER | c.1952-370C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 9/11 | chr4 | 153323708 | |||||||
| chr4:153323745 | A | T | 24 | a0001c0001t0001g0033 a0001c0001t0002g0018 a0001c0001t0002g0022 others(21): Show |
24 | HG01169.hp1 HG02257.hp1 HG02895.hp1 others(21): Show |
intron_variant | MODIFIER | c.1952-333A>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 9/11 | chr4 | 153323745 | |||||||
| chr4:153323787 | C | T | 4 | a0001c0002t0003g0148 a0001c0003t0002g0004 a0002c0006t0003g0012 others(1): Show |
4 | HG02922.hp1 HG02965.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1952-291C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 9/11 | chr4 | 153323787 | |||||||
| chr4:153323801 | T | C | 30 | a0001c0002t0001g0167 a0001c0002t0001g0173 a0001c0002t0001g0229 others(27): Show |
30 | HG00140.hp2 HG00544.hp1 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.1952-277T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 9/11 | chr4 | 153323801 | |||||||
| chr4:153323816 | C | T | 4 | a0001c0002t0002g0024 a0001c0002t0002g0166 a0001c0002t0002g0181 others(1): Show |
4 | HG02523.hp1 HG03492.hp1 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.1952-262C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 9/11 | chr4 | 153323816 | |||||||
| chr4:153323941 | T | C | 1 | a0001c0002t0001g0220 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1952-137T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 9/11 | chr4 | 153323941 | |||||||
| chr4:153324313 | TTGGAAAG others(26): Show |
T | 1 | a0001c0002t0004g0083 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2022+166_2022+198d others(35): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 10/11 | chr4 | 153324313 | |||||||
| chr4:153324390 | T | G | 6 | a0001c0002t0002g0267 a0001c0002t0002g0268 a0001c0002t0003g0239 others(3): Show |
6 | HG02109.hp1 HG02717.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.2022+242T>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 10/11 | chr4 | 153324390 | |||||||
| chr4:153324423 | C | T | 1 | a0001c0002t0023g0014 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2022+275C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 10/11 | chr4 | 153324423 | |||||||
| chr4:153324627 | G | T | 1 | a0001c0002t0023g0014 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2022+479G>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 10/11 | chr4 | 153324627 | |||||||
| chr4:153324690 | A | T | 6 | a0001c0002t0002g0267 a0001c0002t0002g0268 a0001c0002t0003g0239 others(3): Show |
6 | HG02109.hp1 HG02717.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.2022+542A>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 10/11 | chr4 | 153324690 | |||||||
| chr4:153324770 | T | G | 24 | a0001c0001t0001g0033 a0001c0001t0002g0018 a0001c0001t0002g0022 others(21): Show |
24 | HG01169.hp1 HG02257.hp1 HG02895.hp1 others(21): Show |
intron_variant | MODIFIER | c.2022+622T>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 10/11 | chr4 | 153324770 | |||||||
| chr4:153325113 | G | A | 18 | a0001c0001t0001g0033 a0001c0001t0002g0018 a0001c0001t0002g0022 others(15): Show |
18 | HG01169.hp1 HG02895.hp2 HG02897.hp1 others(15): Show |
intron_variant | MODIFIER | c.2022+965G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 10/11 | chr4 | 153325113 | |||||||
| chr4:153325375 | G | T | 3 | a0001c0002t0010g0134 a0001c0002t0013g0133 a0001c0002t0029g0261 |
3 | HG02258.hp1 HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.2022+1227G>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 10/11 | chr4 | 153325375 | |||||||
| chr4:153325634 | A | T | 18 | a0001c0001t0001g0092 a0001c0001t0001g0099 a0001c0001t0001g0100 others(15): Show |
18 | HG00280.hp2 HG00642.hp2 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.2022+1486A>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 10/11 | chr4 | 153325634 | |||||||
| chr4:153325782 | C | T | 1 | a0001c0001t0006g0019 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2022+1634C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 10/11 | chr4 | 153325782 | |||||||
| chr4:153326057 | C | T | 46 | a0001c0002t0003g0144 a0001c0002t0003g0148 a0001c0003t0001g0027 others(43): Show |
46 | HG00323.hp1 HG00438.hp1 HG00741.hp1 others(43): Show |
intron_variant | MODIFIER | c.2022+1909C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 10/11 | chr4 | 153326057 | |||||||
| chr4:153326210 | A | G | 1 | a0001c0001t0005g0244 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.2022+2062A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 10/11 | chr4 | 153326210 | |||||||
| chr4:153326287 | C | T | 1 | a0001c0001t0008g0168 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2022+2139C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 10/11 | chr4 | 153326287 | |||||||
| chr4:153326508 | A | G | 18 | a0001c0001t0001g0092 a0001c0001t0001g0099 a0001c0001t0001g0100 others(15): Show |
18 | HG00280.hp2 HG00642.hp2 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.2023-2022A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 10/11 | chr4 | 153326508 | |||||||
| chr4:153326838 | G | A | 1 | a0001c0003t0003g0073 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2023-1692G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 10/11 | chr4 | 153326838 | |||||||
| chr4:153326844 | G | C | 39 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0001g0092 others(36): Show |
39 | HG00280.hp2 HG00642.hp2 HG01261.hp2 others(36): Show |
intron_variant | MODIFIER | c.2023-1686G>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 10/11 | chr4 | 153326844 | |||||||
| chr4:153326845 | G | A | 1 | a0001c0001t0001g0255 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2023-1685G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 10/11 | chr4 | 153326845 | |||||||
| chr4:153326854 | G | A | 7 | a0001c0001t0005g0037 a0001c0001t0008g0032 a0001c0001t0008g0034 others(4): Show |
7 | NA18944.hp1 NA18979.hp2 NA18985.hp1 others(4): Show |
intron_variant | MODIFIER | c.2023-1676G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 10/11 | chr4 | 153326854 | |||||||
| chr4:153326979 | CA | C | 154 | a0001c0001t0001g0033 a0001c0001t0001g0055 a0001c0001t0001g0081 others(151): Show |
154 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.2023-1532delA | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 153326979 | ||||||
| chr4:153326979 | CAA | C | 25 | a0001c0002t0001g0167 a0001c0002t0002g0215 a0001c0002t0002g0260 others(22): Show |
25 | HG00140.hp2 HG01074.hp2 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.2023-1533_2023-153 others(6): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 153326979 | ||||||
| chr4:153326995 | A | G | 40 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0001g0092 others(37): Show |
40 | HG00280.hp2 HG00642.hp2 HG01261.hp2 others(37): Show |
intron_variant | MODIFIER | c.2023-1535A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 10/11 | chr4 | 153326995 | |||||||
| chr4:153327155 | A | T | 9 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(6): Show |
9 | HG00280.hp2 HG00642.hp2 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.2023-1375A>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 10/11 | chr4 | 153327155 | |||||||
| chr4:153327239 | C | T | 3 | a0001c0002t0010g0134 a0001c0002t0013g0133 a0001c0002t0029g0261 |
3 | HG02258.hp1 HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.2023-1291C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 10/11 | chr4 | 153327239 | |||||||
| chr4:153327400 | G | T | 2 | a0001c0001t0006g0147 a0001c0001t0006g0160 |
2 | HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2023-1130G>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 10/11 | chr4 | 153327400 | |||||||
| chr4:153327724 | A | G | 9 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0002g0001 others(6): Show |
9 | HG02055.hp2 HG02615.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.2023-806A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 10/11 | chr4 | 153327724 | |||||||
| chr4:153327877 | A | G | 1 | a0001c0002t0002g0256 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.2023-653A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 10/11 | chr4 | 153327877 | |||||||
| chr4:153328053 | G | A | 1 | a0001c0003t0004g0142 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2023-477G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 10/11 | chr4 | 153328053 | |||||||
| chr4:153328174 | A | AT | 176 | a0001c0001t0001g0033 a0001c0001t0001g0055 a0001c0001t0001g0081 others(173): Show |
176 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.2023-354dupT | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 153328174 | ||||||
| chr4:153328282 | G | A | 1 | a0001c0003t0003g0064 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2023-248G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 10/11 | chr4 | 153328282 | |||||||
| chr4:153328432 | G | C | 1 | a0001c0003t0013g0262 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2023-98G>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 10/11 | chr4 | 153328432 | |||||||
| chr4:153328934 | T | C | 1 | a0001c0001t0003g0232 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2163+264T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 11/11 | chr4 | 153328934 | |||||||
| chr4:153329037 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2163+367G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 11/11 | chr4 | 153329037 | |||||||
| chr4:153329176 | A | C | 22 | a0001c0001t0001g0033 a0001c0001t0003g0035 a0001c0001t0003g0036 others(19): Show |
22 | HG01169.hp1 HG02257.hp1 HG02895.hp1 others(19): Show |
intron_variant | MODIFIER | c.2163+506A>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 11/11 | chr4 | 153329176 | |||||||
| chr4:153329198 | T | C | 1 | a0001c0002t0023g0014 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2163+528T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 11/11 | chr4 | 153329198 | |||||||
| chr4:153329246 | GT | G | 9 | a0001c0001t0005g0037 a0001c0001t0008g0020 a0001c0001t0008g0032 others(6): Show |
9 | NA18944.hp1 NA18966.hp2 NA18979.hp2 others(6): Show |
intron_variant | MODIFIER | c.2163+582delT | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 153329246 | ||||||
| chr4:153329274 | T | C | 1 | a0001c0002t0028g0080 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2163+604T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 11/11 | chr4 | 153329274 | |||||||
| chr4:153329430 | C | T | 2 | a0001c0002t0001g0066 a0001c0002t0004g0069 |
2 | HG01070.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.2163+760C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 11/11 | chr4 | 153329430 | |||||||
| chr4:153329621 | A | G | 9 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(6): Show |
9 | HG00280.hp2 HG00642.hp2 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.2163+951A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 11/11 | chr4 | 153329621 | |||||||
| chr4:153329645 | G | A | 1 | a0001c0001t0003g0265 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.2163+975G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 11/11 | chr4 | 153329645 | |||||||
| chr4:153329845 | A | T | 22 | a0001c0001t0001g0033 a0001c0001t0003g0035 a0001c0001t0003g0036 others(19): Show |
22 | HG01169.hp1 HG02257.hp1 HG02895.hp1 others(19): Show |
intron_variant | MODIFIER | c.2163+1175A>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 11/11 | chr4 | 153329845 | |||||||
| chr4:153330228 | C | T | 1 | a0001c0010t0004g0085 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2163+1558C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 11/11 | chr4 | 153330228 | |||||||
| chr4:153330646 | C | G | 6 | a0001c0001t0006g0061 a0001c0001t0006g0143 a0001c0001t0006g0147 others(3): Show |
6 | HG02257.hp1 HG02895.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.2163+1976C>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 11/11 | chr4 | 153330646 | |||||||
| chr4:153331485 | G | A | 1 | a0001c0003t0003g0071 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2163+2815G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 11/11 | chr4 | 153331485 | |||||||
| chr4:153331601 | TCAG | T | 17 | a0001c0001t0001g0092 a0001c0001t0001g0099 a0001c0001t0001g0100 others(14): Show |
17 | HG00280.hp2 HG00642.hp2 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.2163+2935_2163+293 others(7): Show |
TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 153331601 | ||||||
| chr4:153331742 | GA | G | 16 | a0001c0001t0001g0033 a0001c0001t0003g0035 a0001c0001t0003g0036 others(13): Show |
16 | HG01169.hp1 HG03831.hp2 NA18944.hp1 others(13): Show |
intron_variant | MODIFIER | c.2164-3071delA | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 11/11 | chr4 | 153331742 | |||||||
| chr4:153331744 | C | G | 16 | a0001c0001t0001g0033 a0001c0001t0003g0035 a0001c0001t0003g0036 others(13): Show |
16 | HG01169.hp1 HG03831.hp2 NA18944.hp1 others(13): Show |
intron_variant | MODIFIER | c.2164-3070C>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 11/11 | chr4 | 153331744 | |||||||
| chr4:153331746 | T | A | 16 | a0001c0001t0001g0033 a0001c0001t0003g0035 a0001c0001t0003g0036 others(13): Show |
16 | HG01169.hp1 HG03831.hp2 NA18944.hp1 others(13): Show |
intron_variant | MODIFIER | c.2164-3068T>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 11/11 | chr4 | 153331746 | |||||||
| chr4:153331749 | TA | T | 16 | a0001c0001t0001g0033 a0001c0001t0003g0035 a0001c0001t0003g0036 others(13): Show |
16 | HG01169.hp1 HG03831.hp2 NA18944.hp1 others(13): Show |
intron_variant | MODIFIER | c.2164-3064delA | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 11/11 | chr4 | 153331749 | |||||||
| chr4:153331953 | A | C | 1 | a0001c0001t0001g0189 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2164-2861A>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 11/11 | chr4 | 153331953 | |||||||
| chr4:153332151 | A | G | 69 | a0001c0001t0001g0182 a0001c0001t0002g0018 a0001c0001t0002g0022 others(66): Show |
69 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.2164-2663A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 11/11 | chr4 | 153332151 | |||||||
| chr4:153332308 | C | G | 1 | a0001c0001t0005g0242 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2164-2506C>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 11/11 | chr4 | 153332308 | |||||||
| chr4:153332363 | G | A | 3 | a0001c0001t0001g0113 a0001c0001t0001g0219 a0001c0001t0002g0201 |
3 | NA18968.hp2 NA19002.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.2164-2451G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 11/11 | chr4 | 153332363 | |||||||
| chr4:153332402 | T | C | 1 | a0001c0002t0007g0266 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2164-2412T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 11/11 | chr4 | 153332402 | |||||||
| chr4:153332527 | C | A | 22 | a0001c0001t0001g0033 a0001c0001t0003g0035 a0001c0001t0003g0036 others(19): Show |
22 | HG01169.hp1 HG02257.hp1 HG02895.hp1 others(19): Show |
intron_variant | MODIFIER | c.2164-2287C>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 11/11 | chr4 | 153332527 | |||||||
| chr4:153332563 | T | C | 1 | a0001c0001t0010g0078 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2164-2251T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 11/11 | chr4 | 153332563 | |||||||
| chr4:153332608 | G | T | 1 | a0001c0002t0028g0080 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2164-2206G>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 11/11 | chr4 | 153332608 | |||||||
| chr4:153332768 | G | C | 1 | a0001c0003t0003g0054 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2164-2046G>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 11/11 | chr4 | 153332768 | |||||||
| chr4:153332997 | G | A | 1 | a0001c0001t0003g0265 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.2164-1817G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 11/11 | chr4 | 153332997 | |||||||
| chr4:153333093 | T | C | 48 | a0001c0001t0001g0182 a0001c0001t0002g0065 a0001c0001t0002g0245 others(45): Show |
48 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.2164-1721T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 11/11 | chr4 | 153333093 | |||||||
| chr4:153333188 | G | A | 1 | a0001c0001t0002g0221 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2164-1626G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 11/11 | chr4 | 153333188 | |||||||
| chr4:153333364 | G | A | 57 | a0001c0001t0001g0033 a0001c0001t0001g0182 a0001c0001t0002g0065 others(54): Show |
57 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.2164-1450G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 11/11 | chr4 | 153333364 | |||||||
| chr4:153333382 | G | A | 10 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0002t0001g0116 others(7): Show |
10 | HG00140.hp1 HG00323.hp2 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.2164-1432G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 11/11 | chr4 | 153333382 | |||||||
| chr4:153333483 | T | C | 16 | a0001c0001t0001g0033 a0001c0001t0003g0035 a0001c0001t0003g0036 others(13): Show |
16 | HG01169.hp1 HG02129.hp2 HG03831.hp2 others(13): Show |
intron_variant | MODIFIER | c.2164-1331T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 11/11 | chr4 | 153333483 | |||||||
| chr4:153333961 | T | C | 2 | a0001c0003t0003g0185 a0001c0003t0003g0216 |
2 | NA18998.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.2164-853T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 11/11 | chr4 | 153333961 | |||||||
| chr4:153333977 | C | T | 44 | a0001c0001t0001g0182 a0001c0001t0002g0065 a0001c0001t0002g0153 others(41): Show |
44 | HG00558.hp2 HG00735.hp2 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.2164-837C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 11/11 | chr4 | 153333977 | |||||||
| chr4:153334003 | A | G | 7 | a0001c0001t0002g0001 a0001c0001t0004g0008 a0001c0001t0004g0087 others(4): Show |
7 | HG02055.hp2 HG02615.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.2164-811A>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 11/11 | chr4 | 153334003 | |||||||
| chr4:153334227 | C | G | 1 | a0001c0002t0002g0267 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2164-587C>G | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 11/11 | chr4 | 153334227 | |||||||
| chr4:153334252 | C | A | 1 | a0001c0001t0001g0253 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2164-562C>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 11/11 | chr4 | 153334252 | |||||||
| chr4:153334323 | C | T | 4 | a0001c0001t0002g0065 a0001c0001t0002g0201 a0001c0001t0002g0245 others(1): Show |
4 | NA18957.hp1 NA18968.hp2 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.2164-491C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 11/11 | chr4 | 153334323 | |||||||
| chr4:153334380 | T | C | 6 | a0001c0001t0001g0174 a0001c0001t0001g0196 a0001c0001t0001g0202 others(3): Show |
6 | HG00558.hp1 HG01496.hp2 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.2164-434T>C | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 11/11 | chr4 | 153334380 | |||||||
| chr4:153334425 | G | A | 1 | a0001c0002t0001g0220 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2164-389G>A | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 11/11 | chr4 | 153334425 | |||||||
| chr4:153334667 | C | T | 1 | a0001c0001t0010g0078 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2164-147C>T | TRIM2 | ENSG00000109654.16 | transcript | ENST00000338700.10 | protein_coding | 11/11 | chr4 | 153334667 |