Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 23424 |
| ensemblid | ENSG00000196116.8 |
| hgncid | 30831 |
| symbol | TDRD7 |
| name | tudor domain containing 7 |
| refseq_nuc | NM_014290.3 |
| refseq_prot | NP_055105.2 |
| ensembl_nuc | ENST00000355295.5 |
| ensembl_prot | ENSP00000347444.4 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 97412096 |
| end | 97496125 |
| strand | + |
| ver | v1.2 |
| region | chr9:97412096-97496125 |
| region5000 | chr9:97407096-97501125 |
| regionname0 | TDRD7_chr9_97412096_97496125 |
| regionname5000 | TDRD7_chr9_97407096_97501125 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 1098 | 193 | 49 | 38 | 84 | 2 | 20 | 63 | TDRD7_chr9_97407096_97501125 | TDRD7 | MLEGD others(1093): Show |
chr9 | 97407096 | 97501125 |
| a0002 | 1/1 | 1098 | 155 | 32 | 31 | 68 | 4 | 18 | 51 | TDRD7_chr9_97407096_97501125 | TDRD7 | MLEGD others(1093): Show |
chr9 | 97407096 | 97501125 |
| a0003 | 0/0 | 1098 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | MLEGD others(1093): Show |
chr9 | 97407096 | 97501125 |
| a0004 | 0/0 | 1098 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | MLEGD others(1093): Show |
chr9 | 97407096 | 97501125 |
| a0005 | 0/0 | 1098 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | MLEGD others(1093): Show |
chr9 | 97407096 | 97501125 |
| a0006 | 0/0 | 1098 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | MLEGD others(1093): Show |
chr9 | 97407096 | 97501125 |
| a0007 | 0/0 | 1098 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | MLEGD others(1093): Show |
chr9 | 97407096 | 97501125 |
| a0008 | 0/0 | 1098 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | MLEGD others(1093): Show |
chr9 | 97407096 | 97501125 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 3294 | 156 | 35 | 35 | 67 | 2 | 17 | TDRD7_chr9_97407096_97501125 | TDRD7 | ATGCT others(3289): Show |
chr9 | 97407096 | 97501125 | ||
| a0001c0003 | 0/0 | 3294 | 18 | 1 | 0 | 16 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | ATGCT others(3289): Show |
chr9 | 97407096 | 97501125 | ||
| a0001c0004 | 0/0 | 3294 | 12 | 7 | 3 | 0 | 0 | 2 | TDRD7_chr9_97407096_97501125 | TDRD7 | ATGCT others(3289): Show |
chr9 | 97407096 | 97501125 | ||
| a0001c0005 | 0/0 | 3294 | 4 | 4 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | ATGCT others(3289): Show |
chr9 | 97407096 | 97501125 | ||
| a0001c0009 | 0/0 | 3294 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | ATGCT others(3289): Show |
chr9 | 97407096 | 97501125 | ||
| a0001c0010 | 0/0 | 3294 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | ATGCT others(3289): Show |
chr9 | 97407096 | 97501125 | ||
| a0001c0015 | 0/0 | 3294 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | ATGCT others(3289): Show |
chr9 | 97407096 | 97501125 | ||
| a0002c0002 | 1/1 | 3294 | 152 | 32 | 31 | 66 | 3 | 18 | TDRD7_chr9_97407096_97501125 | TDRD7 | ATGCT others(3289): Show |
chr9 | 97407096 | 97501125 | ||
| a0002c0007 | 0/0 | 3294 | 2 | 0 | 0 | 2 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | ATGCT others(3289): Show |
chr9 | 97407096 | 97501125 | ||
| a0002c0008 | 0/0 | 3294 | 1 | 0 | 0 | 0 | 1 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | ATGCT others(3289): Show |
chr9 | 97407096 | 97501125 | ||
| a0003c0006 | 0/0 | 3294 | 3 | 3 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | ATGCT others(3289): Show |
chr9 | 97407096 | 97501125 | ||
| a0004c0013 | 0/0 | 3294 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | ATGCT others(3289): Show |
chr9 | 97407096 | 97501125 | ||
| a0005c0011 | 0/0 | 3294 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | ATGCT others(3289): Show |
chr9 | 97407096 | 97501125 | ||
| a0006c0014 | 0/0 | 3294 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | ATGCT others(3289): Show |
chr9 | 97407096 | 97501125 | ||
| a0007c0016 | 0/0 | 3294 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | ATGCT others(3289): Show |
chr9 | 97407096 | 97501125 | ||
| a0008c0012 | 0/0 | 3294 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | ATGCT others(3289): Show |
chr9 | 97407096 | 97501125 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3688 | 154 | 35 | 35 | 65 | 2 | 17 | TDRD7_chr9_97407096_97501125 | TDRD7 | GAGGT others(3683): Show |
chr9 | 97407096 | 97501125 |
| a0001c0001t0002 | 0/0 | 3688 | 2 | 0 | 0 | 2 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | GAGGT others(3683): Show |
chr9 | 97407096 | 97501125 |
| a0001c0003t0001 | 0/0 | 3688 | 18 | 1 | 0 | 16 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | GAGGT others(3683): Show |
chr9 | 97407096 | 97501125 |
| a0001c0004t0001 | 0/0 | 3688 | 12 | 7 | 3 | 0 | 0 | 2 | TDRD7_chr9_97407096_97501125 | TDRD7 | GAGGT others(3683): Show |
chr9 | 97407096 | 97501125 |
| a0001c0005t0001 | 0/0 | 3688 | 4 | 4 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | GAGGT others(3683): Show |
chr9 | 97407096 | 97501125 |
| a0001c0009t0001 | 0/0 | 3688 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | GAGGT others(3683): Show |
chr9 | 97407096 | 97501125 |
| a0001c0010t0001 | 0/0 | 3688 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | GAGGT others(3683): Show |
chr9 | 97407096 | 97501125 |
| a0001c0015t0001 | 0/0 | 3688 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | GAGGT others(3683): Show |
chr9 | 97407096 | 97501125 |
| a0002c0002t0001 | 1/1 | 3688 | 132 | 29 | 27 | 53 | 3 | 18 | TDRD7_chr9_97407096_97501125 | TDRD7 | GAGGT others(3683): Show |
chr9 | 97407096 | 97501125 |
| a0002c0002t0002 | 0/0 | 3688 | 12 | 2 | 4 | 6 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | GAGGT others(3683): Show |
chr9 | 97407096 | 97501125 |
| a0002c0002t0003 | 0/0 | 3688 | 7 | 0 | 0 | 7 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | GAGGT others(3683): Show |
chr9 | 97407096 | 97501125 |
| a0002c0002t0004 | 0/0 | 3688 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | GAGGT others(3683): Show |
chr9 | 97407096 | 97501125 |
| a0002c0007t0001 | 0/0 | 3688 | 2 | 0 | 0 | 2 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | GAGGT others(3683): Show |
chr9 | 97407096 | 97501125 |
| a0002c0008t0001 | 0/0 | 3688 | 1 | 0 | 0 | 0 | 1 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | GAGGT others(3683): Show |
chr9 | 97407096 | 97501125 |
| a0003c0006t0001 | 0/0 | 3688 | 3 | 3 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | GAGGT others(3683): Show |
chr9 | 97407096 | 97501125 |
| a0004c0013t0001 | 0/0 | 3688 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | GAGGT others(3683): Show |
chr9 | 97407096 | 97501125 |
| a0005c0011t0001 | 0/0 | 3688 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | GAGGT others(3683): Show |
chr9 | 97407096 | 97501125 |
| a0006c0014t0001 | 0/0 | 3688 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | GAGGT others(3683): Show |
chr9 | 97407096 | 97501125 |
| a0007c0016t0001 | 0/0 | 3688 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | GAGGT others(3683): Show |
chr9 | 97407096 | 97501125 |
| a0008c0012t0001 | 0/0 | 3688 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | GAGGT others(3683): Show |
chr9 | 97407096 | 97501125 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 4 | 1 | 2 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0002g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0003t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0003t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0003t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0003t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0003t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0003t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0003t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0003t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0003t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0003t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0003t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0003t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0003t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0003t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0003t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0003t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0003t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0004t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0004t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0004t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0004t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0004t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0004t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0004t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0004t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0004t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0004t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0005t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0005t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0005t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0005t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0009t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0010t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0001c0015t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0001 | 0/0 | 11 | 0 | 0 | 10 | 1 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0154 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0184 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0002g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0002g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0003g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0002t0004g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0007t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0002c0008t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0003c0006t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0003c0006t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0004c0013t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0005c0011t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0006c0014t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0007c0016t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| a0008c0012t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00323 | hp1 | a0002 | c0008 | t0001 | g0028 | EUR | FIN | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG00323 | hp2 | a0002 | c0002 | t0001 | g0205 | EUR | FIN | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG00408 | hp1 | a0001 | c0003 | t0001 | g0043 | EAS | CHS | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG00408 | hp2 | a0002 | c0002 | t0001 | g0125 | EAS | CHS | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0242 | EAS | CHS | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | CHS | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | CHS | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG00544 | hp2 | a0002 | c0002 | t0001 | g0187 | EAS | CHS | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG00558 | hp1 | a0001 | c0003 | t0001 | g0044 | EAS | CHS | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | CHS | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG00597 | hp2 | a0002 | c0002 | t0001 | g0169 | EAS | CHS | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | CHS | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG00621 | hp2 | a0002 | c0002 | t0002 | g0288 | EAS | CHS | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0131 | AMR | PUR | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG00639 | hp2 | a0002 | c0002 | t0001 | g0218 | AMR | PUR | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG00673 | hp1 | a0002 | c0002 | t0001 | g0139 | EAS | CHS | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | CHS | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG00741 | hp1 | a0001 | c0004 | t0001 | g0104 | AMR | PUR | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG01069 | hp2 | a0002 | c0002 | t0001 | g0197 | AMR | PUR | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG01070 | hp2 | a0001 | c0004 | t0001 | g0014 | AMR | PUR | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG01071 | hp2 | a0001 | c0004 | t0001 | g0014 | AMR | PUR | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG01081 | hp1 | a0002 | c0002 | t0001 | g0172 | AMR | PUR | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG01081 | hp2 | a0002 | c0002 | t0001 | g0227 | AMR | PUR | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG01099 | hp1 | a0002 | c0002 | t0001 | g0017 | AMR | PUR | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG01106 | hp2 | a0002 | c0002 | t0001 | g0192 | AMR | PUR | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG01109 | hp2 | a0002 | c0002 | t0001 | g0155 | AMR | PUR | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG01167 | hp2 | a0002 | c0002 | t0002 | g0019 | AMR | PUR | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG01168 | hp2 | a0002 | c0002 | t0001 | g0220 | AMR | PUR | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG01169 | hp2 | a0002 | c0002 | t0001 | g0215 | AMR | PUR | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG01175 | hp1 | a0002 | c0002 | t0001 | g0156 | AMR | PUR | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0253 | AMR | PUR | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0186 | AMR | PUR | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG01243 | hp1 | a0002 | c0002 | t0001 | g0179 | AMR | PUR | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | CLM | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | CLM | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | CLM | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG01256 | hp2 | a0002 | c0002 | t0001 | g0290 | AMR | CLM | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0309 | AMR | CLM | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0120 | AMR | CLM | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG01346 | hp2 | a0002 | c0002 | t0001 | g0190 | AMR | CLM | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0264 | AMR | CLM | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG01358 | hp2 | a0002 | c0002 | t0001 | g0201 | AMR | CLM | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0017 | AMR | CLM | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG01433 | hp1 | a0002 | c0002 | t0001 | g0217 | AMR | CLM | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | CLM | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG01496 | hp2 | a0002 | c0002 | t0001 | g0118 | AMR | CLM | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0001 | EUR | IBS | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0231 | EUR | IBS | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG01516 | hp1 | a0002 | c0002 | t0001 | g0191 | EUR | IBS | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0096 | EUR | IBS | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG01891 | hp1 | a0002 | c0002 | t0001 | g0141 | AFR | ACB | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG01891 | hp2 | a0001 | c0003 | t0001 | g0033 | AFR | ACB | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG01934 | hp1 | a0002 | c0002 | t0001 | g0196 | AMR | PEL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG01934 | hp2 | a0002 | c0002 | t0002 | g0222 | AMR | PEL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PEL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG01952 | hp2 | a0002 | c0002 | t0001 | g0189 | AMR | PEL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | PEL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG01978 | hp1 | a0002 | c0002 | t0002 | g0223 | AMR | PEL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG01978 | hp2 | a0002 | c0002 | t0001 | g0202 | AMR | PEL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | PEL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG01981 | hp2 | a0002 | c0002 | t0001 | g0198 | AMR | PEL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02015 | hp2 | a0002 | c0002 | t0001 | g0149 | EAS | KHV | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02040 | hp2 | a0002 | c0002 | t0001 | g0185 | EAS | KHV | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02055 | hp1 | a0002 | c0002 | t0001 | g0293 | AFR | ACB | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02055 | hp2 | a0002 | c0002 | t0001 | g0119 | AFR | ACB | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02056 | hp1 | a0002 | c0002 | t0001 | g0203 | EAS | KHV | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | KHV | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02074 | hp1 | a0002 | c0002 | t0001 | g0124 | EAS | KHV | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | KHV | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | KHV | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | KHV | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | KHV | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02132 | hp1 | a0002 | c0002 | t0001 | g0211 | EAS | KHV | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02132 | hp2 | a0001 | c0003 | t0001 | g0041 | EAS | KHV | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02135 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02135 | hp2 | a0002 | c0002 | t0001 | g0229 | EAS | KHV | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | ACB | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02145 | hp2 | a0001 | c0004 | t0001 | g0114 | AFR | ACB | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PEL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02148 | hp2 | a0002 | c0002 | t0001 | g0195 | AMR | PEL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02155 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CDX | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0121 | EAS | CDX | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02165 | hp1 | a0001 | c0003 | t0001 | g0051 | EAS | CDX | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02165 | hp2 | a0002 | c0002 | t0001 | g0152 | EAS | CDX | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02258 | hp1 | a0002 | c0002 | t0001 | g0151 | AFR | ACB | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02273 | hp1 | a0002 | c0002 | t0002 | g0019 | AMR | PEL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02273 | hp2 | a0004 | c0013 | t0001 | g0002 | AMR | PEL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02280 | hp1 | a0002 | c0002 | t0004 | g0112 | AFR | ACB | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02280 | hp2 | a0001 | c0005 | t0001 | g0107 | AFR | ACB | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02293 | hp2 | a0002 | c0002 | t0001 | g0181 | AMR | PEL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PEL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | PEL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02572 | hp1 | a0002 | c0002 | t0001 | g0174 | AFR | GWD | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02572 | hp2 | a0002 | c0002 | t0002 | g0116 | AFR | GWD | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0291 | SAS | PJL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02602 | hp2 | a0002 | c0002 | t0001 | g0158 | SAS | PJL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02615 | hp1 | a0001 | c0004 | t0001 | g0027 | AFR | GWD | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02615 | hp2 | a0002 | c0002 | t0001 | g0145 | AFR | GWD | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | GWD | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02630 | hp2 | a0005 | c0011 | t0001 | g0032 | AFR | GWD | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | GWD | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02647 | hp2 | a0002 | c0002 | t0001 | g0144 | AFR | GWD | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02683 | hp1 | a0002 | c0002 | t0001 | g0199 | SAS | PJL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0282 | SAS | PJL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0122 | SAS | PJL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02717 | hp1 | a0001 | c0005 | t0001 | g0299 | AFR | GWD | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | GWD | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02723 | hp1 | a0002 | c0002 | t0001 | g0150 | AFR | GWD | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0249 | SAS | PJL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02735 | hp2 | a0002 | c0002 | t0001 | g0206 | SAS | PJL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02738 | hp1 | a0002 | c0002 | t0001 | g0208 | SAS | PJL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0275 | SAS | PJL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02818 | hp1 | a0002 | c0002 | t0001 | g0177 | AFR | GWD | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02818 | hp2 | a0002 | c0002 | t0001 | g0018 | AFR | GWD | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02886 | hp1 | a0002 | c0002 | t0001 | g0175 | AFR | GWD | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02886 | hp2 | a0001 | c0005 | t0001 | g0297 | AFR | GWD | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02895 | hp1 | a0001 | c0004 | t0001 | g0027 | AFR | GWD | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02895 | hp2 | a0002 | c0002 | t0001 | g0161 | AFR | GWD | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | GWD | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02897 | hp1 | a0002 | c0002 | t0001 | g0132 | AFR | GWD | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | GWD | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ESN | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02922 | hp2 | a0002 | c0002 | t0001 | g0178 | AFR | ESN | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02965 | hp1 | a0002 | c0002 | t0001 | g0029 | AFR | ESN | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | ESN | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | ESN | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | ESN | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02976 | hp1 | a0003 | c0006 | t0001 | g0037 | AFR | ESN | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | ESN | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0274 | SAS | PJL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG03017 | hp2 | a0001 | c0004 | t0001 | g0106 | SAS | PJL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG03041 | hp1 | a0002 | c0002 | t0001 | g0287 | AFR | GWD | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0284 | AFR | GWD | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG03098 | hp1 | a0002 | c0002 | t0001 | g0193 | AFR | MSL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG03098 | hp2 | a0002 | c0002 | t0002 | g0292 | AFR | MSL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | ESN | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG03130 | hp2 | a0002 | c0002 | t0001 | g0143 | AFR | ESN | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | ESN | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG03139 | hp2 | a0002 | c0002 | t0001 | g0115 | AFR | ESN | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | ESN | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG03195 | hp2 | a0002 | c0002 | t0001 | g0173 | AFR | ESN | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | MSL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG03209 | hp2 | a0001 | c0004 | t0001 | g0300 | AFR | MSL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG03225 | hp1 | a0006 | c0014 | t0001 | g0113 | AFR | MSL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | MSL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG03239 | hp2 | a0002 | c0002 | t0001 | g0207 | SAS | PJL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG03453 | hp1 | a0001 | c0004 | t0001 | g0303 | AFR | MSL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG03453 | hp2 | a0001 | c0009 | t0001 | g0306 | AFR | MSL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG03486 | hp1 | a0002 | c0002 | t0001 | g0212 | AFR | MSL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG03486 | hp2 | a0001 | c0005 | t0001 | g0298 | AFR | MSL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG03492 | hp1 | a0002 | c0002 | t0001 | g0225 | SAS | PJL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0128 | SAS | PJL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG03516 | hp1 | a0002 | c0002 | t0001 | g0142 | AFR | ESN | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG03516 | hp2 | a0002 | c0002 | t0001 | g0176 | AFR | ESN | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG03540 | hp1 | a0002 | c0002 | t0001 | g0018 | AFR | GWD | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG03579 | hp1 | a0003 | c0006 | t0001 | g0008 | AFR | MSL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | MSL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0263 | SAS | PJL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0137 | SAS | STU | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0258 | SAS | STU | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0262 | SAS | PJL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0294 | SAS | BEB | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG03834 | hp1 | a0002 | c0002 | t0001 | g0123 | SAS | BEB | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG03834 | hp2 | a0002 | c0002 | t0001 | g0216 | SAS | BEB | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | BEB | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG03942 | hp2 | a0002 | c0002 | t0001 | g0209 | SAS | BEB | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | STU | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | STU | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG04184 | hp1 | a0002 | c0002 | t0001 | g0035 | SAS | BEB | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG04184 | hp2 | a0001 | c0003 | t0001 | g0040 | SAS | BEB | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG04199 | hp1 | a0002 | c0002 | t0001 | g0295 | SAS | STU | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0283 | SAS | STU | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG04204 | hp2 | a0001 | c0004 | t0001 | g0105 | SAS | STU | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA18522 | hp1 | a0002 | c0002 | t0001 | g0026 | AFR | YRI | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | YRI | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA18612 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CHB | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | CHB | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA18747 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CHB | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | CHB | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | YRI | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | YRI | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA18939 | hp2 | a0002 | c0002 | t0001 | g0058 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA18941 | hp2 | a0002 | c0002 | t0003 | g0006 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA18943 | hp1 | a0002 | c0002 | t0002 | g0305 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA18947 | hp1 | a0002 | c0002 | t0001 | g0134 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA18948 | hp2 | a0001 | c0003 | t0001 | g0009 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA18949 | hp2 | a0002 | c0002 | t0001 | g0133 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA18950 | hp1 | a0002 | c0002 | t0001 | g0126 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA18950 | hp2 | a0002 | c0002 | t0001 | g0182 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA18951 | hp2 | a0002 | c0007 | t0001 | g0016 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA18953 | hp1 | a0001 | c0003 | t0001 | g0039 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA18953 | hp2 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA18954 | hp2 | a0002 | c0002 | t0001 | g0130 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA18960 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA18962 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA18962 | hp2 | a0002 | c0002 | t0001 | g0059 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA18963 | hp2 | a0002 | c0002 | t0001 | g0135 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA18967 | hp1 | a0002 | c0002 | t0001 | g0147 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA18969 | hp2 | a0002 | c0002 | t0001 | g0194 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA18970 | hp1 | a0002 | c0002 | t0001 | g0138 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA18971 | hp1 | a0002 | c0002 | t0001 | g0140 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA18974 | hp2 | a0002 | c0002 | t0003 | g0228 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA18975 | hp2 | a0002 | c0002 | t0002 | g0221 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA18977 | hp1 | a0001 | c0003 | t0001 | g0296 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA18977 | hp2 | a0002 | c0002 | t0001 | g0210 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA18978 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA18983 | hp2 | a0001 | c0003 | t0001 | g0048 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA18984 | hp2 | a0001 | c0003 | t0001 | g0049 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA18988 | hp1 | a0002 | c0002 | t0001 | g0204 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA18990 | hp2 | a0002 | c0002 | t0002 | g0166 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA18991 | hp1 | a0002 | c0002 | t0001 | g0157 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA18992 | hp2 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA18994 | hp1 | a0002 | c0002 | t0001 | g0183 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA18995 | hp2 | a0001 | c0003 | t0001 | g0042 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA18998 | hp1 | a0001 | c0003 | t0001 | g0045 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA18999 | hp2 | a0002 | c0002 | t0001 | g0153 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA19000 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA19003 | hp2 | a0001 | c0003 | t0001 | g0009 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA19005 | hp2 | a0001 | c0010 | t0001 | g0002 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA19007 | hp1 | a0002 | c0002 | t0001 | g0148 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA19009 | hp1 | a0002 | c0002 | t0002 | g0224 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA19010 | hp1 | a0002 | c0002 | t0001 | g0159 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA19010 | hp2 | a0002 | c0002 | t0001 | g0129 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA19030 | hp1 | a0001 | c0004 | t0001 | g0302 | AFR | LWK | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA19030 | hp2 | a0001 | c0015 | t0001 | g0031 | AFR | LWK | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA19055 | hp1 | a0002 | c0002 | t0001 | g0057 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA19055 | hp2 | a0007 | c0016 | t0001 | g0277 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA19056 | hp2 | a0002 | c0002 | t0003 | g0213 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA19060 | hp2 | a0002 | c0002 | t0001 | g0136 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA19066 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA19066 | hp2 | a0001 | c0003 | t0001 | g0038 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA19067 | hp1 | a0001 | c0003 | t0001 | g0050 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA19067 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA19068 | hp2 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA19074 | hp1 | a0002 | c0002 | t0001 | g0160 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA19077 | hp1 | a0002 | c0002 | t0001 | g0168 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA19077 | hp2 | a0002 | c0007 | t0001 | g0016 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA19078 | hp2 | a0002 | c0002 | t0003 | g0219 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA19081 | hp1 | a0001 | c0003 | t0001 | g0046 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA19081 | hp2 | a0002 | c0002 | t0001 | g0146 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA19083 | hp2 | a0002 | c0002 | t0001 | g0053 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA19084 | hp1 | a0008 | c0012 | t0001 | g0072 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA19084 | hp2 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA19085 | hp2 | a0002 | c0002 | t0003 | g0006 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA19086 | hp1 | a0001 | c0003 | t0001 | g0047 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA19086 | hp2 | a0002 | c0002 | t0003 | g0214 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA19087 | hp1 | a0002 | c0002 | t0003 | g0006 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0170 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA19091 | hp2 | a0002 | c0002 | t0002 | g0226 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA20129 | hp1 | a0003 | c0006 | t0001 | g0008 | AFR | ASW | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | ASW | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0127 | SAS | GIH | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA20905 | hp2 | a0002 | c0002 | t0001 | g0200 | SAS | GIH | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0285 | AMR | CLM | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG01123 | hp2 | a0002 | c0002 | t0001 | g0188 | AMR | CLM | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02486 | hp1 | a0002 | c0002 | t0001 | g0289 | AFR | ACB | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02486 | hp2 | a0002 | c0002 | t0001 | g0030 | AFR | ACB | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | ACB | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG02559 | hp2 | a0002 | c0002 | t0001 | g0056 | AFR | ACB | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | MSL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| HG03471 | hp2 | a0001 | c0004 | t0001 | g0301 | AFR | MSL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | USA | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | USA | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | LWK | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| NA21309 | hp2 | a0002 | c0002 | t0001 | g0026 | AFR | LWK | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0184 | REF | REF | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0154 | REF | REF | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:97432066 | A | G | 1 | a0007 | 1 | NA19055.hp2 | missense_variant | MODERATE | c.391A>G | p.Asn131Asp | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/17 | 540/3688 | 391/3297 | 131/1098 | chr9 | 97432066 | |||
| chr9:97432112 | A | G | 1 | a0003 | 3 | HG02976.hp1 HG03579.hp1 NA20129.hp1 |
missense_variant | MODERATE | c.437A>G | p.Lys146Arg | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/17 | 586/3688 | 437/3297 | 146/1098 | chr9 | 97432112 | |||
| chr9:97432124 | T | C | 7 | a0001 a0003 a0004 others(4): Show |
201 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(198): Show |
missense_variant | MODERATE | c.449T>C | p.Val150Ala | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/17 | 598/3688 | 449/3297 | 150/1098 | chr9 | 97432124 | |||
| chr9:97460535 | A | G | 1 | a0004 | 1 | HG02273.hp2 | missense_variant | MODERATE | c.1213A>G | p.Lys405Glu | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/17 | 1362/3688 | 1213/3297 | 405/1098 | chr9 | 97460535 | |||
| chr9:97460557 | A | C | 1 | a0008 | 1 | NA19084.hp1 | missense_variant | MODERATE | c.1235A>C | p.Lys412Thr | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/17 | 1384/3688 | 1235/3297 | 412/1098 | chr9 | 97460557 | |||
| chr9:97480864 | A | G | 1 | a0006 | 1 | HG03225.hp1 | missense_variant | MODERATE | c.2338A>G | p.Ile780Val | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 14/17 | 2487/3688 | 2338/3297 | 780/1098 | chr9 | 97480864 | |||
| chr9:97482879 | G | A | 1 | a0005 | 1 | HG02630.hp2 | missense_variant | MODERATE | c.2443G>A | p.Ala815Thr | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 15/17 | 2592/3688 | 2443/3297 | 815/1098 | chr9 | 97482879 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:97428498 | A | G | 14 | a0001c0001 a0001c0003 a0001c0004 others(11): Show |
203 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(200): Show |
synonymous_variant | LOW | c.33A>G | p.Leu11Leu | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 2/17 | 182/3688 | 33/3297 | 11/1098 | chr9 | 97428498 | |||
| chr9:97432218 | G | A | 1 | a0001c0009 | 1 | HG03453.hp2 | synonymous_variant | LOW | c.543G>A | p.Val181Val | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/17 | 692/3688 | 543/3297 | 181/1098 | chr9 | 97432218 | |||
| chr9:97439260 | G | A | 1 | a0001c0010 | 1 | NA19005.hp2 | synonymous_variant | LOW | c.579G>A | p.Ala193Ala | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 5/17 | 728/3688 | 579/3297 | 193/1098 | chr9 | 97439260 | |||
| chr9:97439269 | A | G | 5 | a0001c0003 a0001c0004 a0001c0005 others(2): Show |
36 | HG00408.hp1 HG00558.hp1 HG00741.hp1 others(33): Show |
synonymous_variant | LOW | c.588A>G | p.Gln196Gln | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 5/17 | 737/3688 | 588/3297 | 196/1098 | chr9 | 97439269 | |||
| chr9:97460234 | G | A | 1 | a0001c0005 | 4 | HG02280.hp2 HG02717.hp1 HG02886.hp2 others(1): Show |
synonymous_variant | LOW | c.912G>A | p.Lys304Lys | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/17 | 1061/3688 | 912/3297 | 304/1098 | chr9 | 97460234 | |||
| chr9:97472351 | T | C | 1 | a0002c0008 | 1 | HG00323.hp1 | synonymous_variant | LOW | c.1800T>C | p.Cys600Cys | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 10/17 | 1949/3688 | 1800/3297 | 600/1098 | chr9 | 97472351 | |||
| chr9:97472420 | A | G | 1 | a0001c0015 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.1869A>G | p.Ser623Ser | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 10/17 | 2018/3688 | 1869/3297 | 623/1098 | chr9 | 97472420 | |||
| chr9:97472474 | G | A | 3 | a0001c0004 a0001c0005 a0006c0014 |
17 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(14): Show |
synonymous_variant | LOW | c.1923G>A | p.Lys641Lys | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 10/17 | 2072/3688 | 1923/3297 | 641/1098 | chr9 | 97472474 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:97412112 | C | G | 3 | a0001c0001t0002 a0002c0002t0002 a0002c0002t0003 |
21 | HG00438.hp1 HG00621.hp2 HG01167.hp2 others(18): Show |
5_prime_UTR_variant | MODIFIER | c.-133C>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/17 | 16354 | chr9 | 97412112 | ||||||
| chr9:97412162 | G | C | 1 | a0002c0002t0003 | 7 | NA18941.hp2 NA18974.hp2 NA19056.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-83G>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/17 | 16304 | chr9 | 97412162 | ||||||
| chr9:97412198 | G | A | 1 | a0002c0002t0004 | 1 | HG02280.hp1 | 5_prime_UTR_variant | MODIFIER | c.-47G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/17 | 16268 | chr9 | 97412198 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:97412361 | A | G | 1 | a0001c0001t0001g0309 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-7+123A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97412361 | |||||||
| chr9:97412376 | T | C | 1 | a0002c0008t0001g0028 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-7+138T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97412376 | |||||||
| chr9:97412413 | C | T | 1 | a0001c0001t0001g0308 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-7+175C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97412413 | |||||||
| chr9:97412492 | G | A | 2 | a0002c0002t0001g0029 a0002c0002t0001g0030 |
2 | HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-7+254G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97412492 | |||||||
| chr9:97412535 | C | T | 1 | a0001c0001t0001g0307 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-7+297C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97412535 | |||||||
| chr9:97412585 | C | T | 1 | a0001c0009t0001g0306 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-7+347C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97412585 | |||||||
| chr9:97412661 | C | G | 1 | a0002c0002t0002g0305 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-7+423C>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97412661 | |||||||
| chr9:97412789 | G | C | 24 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0003t0001g0009 others(21): Show |
26 | HG00408.hp1 HG00558.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.-7+551G>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97412789 | |||||||
| chr9:97412934 | A | G | 1 | a0001c0001t0001g0304 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-7+696A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97412934 | |||||||
| chr9:97413066 | C | A | 24 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0003t0001g0009 others(21): Show |
26 | HG00408.hp1 HG00558.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.-7+828C>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97413066 | |||||||
| chr9:97413110 | G | A | 68 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(65): Show |
75 | HG00621.hp1 HG00673.hp2 HG00741.hp1 others(72): Show |
intron_variant | MODIFIER | c.-7+872G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97413110 | |||||||
| chr9:97413121 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-7+883C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97413121 | |||||||
| chr9:97413130 | A | G | 1 | a0001c0009t0001g0306 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-7+892A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97413130 | |||||||
| chr9:97413196 | G | C | 95 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(92): Show |
104 | HG00408.hp1 HG00558.hp1 HG00621.hp1 others(101): Show |
intron_variant | MODIFIER | c.-7+958G>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97413196 | |||||||
| chr9:97413369 | T | G | 4 | a0001c0003t0001g0033 a0001c0009t0001g0306 a0001c0015t0001g0031 others(1): Show |
4 | HG01891.hp2 HG02630.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-7+1131T>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97413369 | |||||||
| chr9:97413414 | T | TTA | 24 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0003t0001g0009 others(21): Show |
26 | HG00408.hp1 HG00558.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.-7+1177_-7+1178dup others(2): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 97413414 | ||||||
| chr9:97413436 | G | T | 1 | a0001c0001t0001g0110 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-7+1198G>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97413436 | |||||||
| chr9:97413760 | G | A | 1 | a0002c0002t0001g0115 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-7+1522G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97413760 | |||||||
| chr9:97413801 | C | G | 3 | a0001c0003t0001g0033 a0001c0009t0001g0306 a0005c0011t0001g0032 |
3 | HG01891.hp2 HG02630.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-7+1563C>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97413801 | |||||||
| chr9:97414336 | T | G | 1 | a0002c0002t0002g0116 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-7+2098T>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97414336 | |||||||
| chr9:97414652 | G | C | 1 | a0001c0001t0001g0117 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-7+2414G>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97414652 | |||||||
| chr9:97414719 | C | A | 1 | a0001c0009t0001g0306 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-7+2481C>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97414719 | |||||||
| chr9:97414779 | T | G | 1 | a0001c0001t0001g0052 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-7+2541T>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97414779 | |||||||
| chr9:97414835 | T | G | 3 | a0002c0002t0001g0118 a0002c0002t0001g0119 a0002c0002t0001g0120 |
3 | HG01261.hp1 HG01496.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-7+2597T>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97414835 | |||||||
| chr9:97414936 | G | T | 2 | a0001c0001t0001g0108 a0001c0001t0001g0109 |
2 | HG01255.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-7+2698G>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97414936 | |||||||
| chr9:97414948 | C | T | 33 | a0001c0003t0001g0009 a0001c0003t0001g0033 a0001c0003t0001g0038 others(30): Show |
36 | HG00408.hp1 HG00558.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.-7+2710C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97414948 | |||||||
| chr9:97415188 | A | G | 1 | a0001c0001t0001g0110 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-7+2950A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97415188 | |||||||
| chr9:97415250 | G | A | 1 | a0001c0004t0001g0014 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-7+3012G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97415250 | |||||||
| chr9:97415275 | G | A | 33 | a0001c0003t0001g0009 a0001c0003t0001g0033 a0001c0003t0001g0038 others(30): Show |
36 | HG00408.hp1 HG00558.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.-7+3037G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97415275 | |||||||
| chr9:97415327 | T | C | 33 | a0001c0003t0001g0009 a0001c0003t0001g0033 a0001c0003t0001g0038 others(30): Show |
36 | HG00408.hp1 HG00558.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.-7+3089T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97415327 | |||||||
| chr9:97415395 | C | T | 1 | a0002c0002t0001g0295 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-7+3157C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97415395 | |||||||
| chr9:97415429 | G | T | 1 | a0005c0011t0001g0032 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-7+3191G>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97415429 | |||||||
| chr9:97415719 | G | T | 2 | a0002c0002t0001g0029 a0002c0002t0001g0030 |
2 | HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-7+3481G>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97415719 | |||||||
| chr9:97415734 | A | G | 1 | a0002c0002t0001g0294 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-7+3496A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97415734 | |||||||
| chr9:97415759 | C | T | 7 | a0001c0004t0001g0027 a0001c0004t0001g0114 a0001c0004t0001g0300 others(4): Show |
8 | HG02145.hp2 HG02615.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.-7+3521C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97415759 | |||||||
| chr9:97415971 | C | T | 266 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(263): Show |
298 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(295): Show |
intron_variant | MODIFIER | c.-7+3733C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97415971 | |||||||
| chr9:97416196 | T | C | 1 | a0001c0015t0001g0031 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-7+3958T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97416196 | |||||||
| chr9:97416213 | T | C | 3 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 |
3 | NA18948.hp1 NA18999.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.-7+3975T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97416213 | |||||||
| chr9:97416235 | C | A | 1 | a0001c0001t0001g0165 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-7+3997C>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97416235 | |||||||
| chr9:97416562 | G | A | 1 | a0002c0002t0002g0166 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-7+4324G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97416562 | |||||||
| chr9:97416669 | A | C | 1 | a0002c0002t0001g0293 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-7+4431A>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97416669 | |||||||
| chr9:97416794 | G | C | 1 | a0001c0001t0001g0167 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-7+4556G>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97416794 | |||||||
| chr9:97416853 | C | T | 1 | a0002c0002t0002g0292 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-7+4615C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97416853 | |||||||
| chr9:97416867 | A | G | 33 | a0001c0003t0001g0009 a0001c0003t0001g0033 a0001c0003t0001g0038 others(30): Show |
36 | HG00408.hp1 HG00558.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.-7+4629A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97416867 | |||||||
| chr9:97416885 | A | C | 17 | a0001c0003t0001g0033 a0001c0004t0001g0014 a0001c0004t0001g0027 others(14): Show |
19 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.-7+4647A>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97416885 | |||||||
| chr9:97417016 | A | G | 3 | a0002c0002t0001g0289 a0002c0002t0001g0290 a0002c0002t0001g0291 |
3 | HG01256.hp2 HG02486.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.-7+4778A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97417016 | |||||||
| chr9:97417062 | C | A | 33 | a0001c0003t0001g0009 a0001c0003t0001g0033 a0001c0003t0001g0038 others(30): Show |
36 | HG00408.hp1 HG00558.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.-7+4824C>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97417062 | |||||||
| chr9:97417063 | G | A | 33 | a0001c0003t0001g0009 a0001c0003t0001g0033 a0001c0003t0001g0038 others(30): Show |
36 | HG00408.hp1 HG00558.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.-7+4825G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97417063 | |||||||
| chr9:97417427 | G | A | 5 | a0001c0004t0001g0027 a0001c0004t0001g0300 a0001c0004t0001g0301 others(2): Show |
6 | HG02615.hp1 HG02895.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.-7+5189G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97417427 | |||||||
| chr9:97417559 | A | G | 1 | a0001c0001t0001g0103 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-7+5321A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97417559 | |||||||
| chr9:97417701 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-7+5463C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97417701 | |||||||
| chr9:97417846 | G | A | 3 | a0002c0002t0001g0168 a0002c0002t0001g0169 a0002c0002t0001g0170 |
3 | HG00597.hp2 NA19077.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.-7+5608G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97417846 | |||||||
| chr9:97417936 | C | A | 1 | a0001c0001t0001g0171 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-7+5698C>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97417936 | |||||||
| chr9:97418047 | C | T | 2 | a0002c0002t0001g0026 a0002c0002t0004g0112 |
3 | HG02280.hp1 NA18522.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-7+5809C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97418047 | |||||||
| chr9:97418090 | C | A | 8 | a0002c0002t0001g0172 a0002c0002t0001g0173 a0002c0002t0001g0174 others(5): Show |
8 | HG01081.hp1 HG01243.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.-7+5852C>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97418090 | |||||||
| chr9:97418273 | A | C | 1 | a0001c0001t0001g0101 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-7+6035A>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97418273 | |||||||
| chr9:97418529 | T | A | 1 | a0001c0001t0001g0054 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-7+6291T>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97418529 | |||||||
| chr9:97418539 | TA | T | 18 | a0001c0003t0001g0033 a0001c0004t0001g0014 a0001c0004t0001g0027 others(15): Show |
20 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.-7+6312delA | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 97418539 | ||||||
| chr9:97418633 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-7+6395G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97418633 | |||||||
| chr9:97418686 | G | A | 1 | a0001c0001t0001g0034 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-7+6448G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97418686 | |||||||
| chr9:97418702 | A | G | 1 | a0002c0002t0002g0116 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-7+6464A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97418702 | |||||||
| chr9:97418752 | C | G | 1 | a0001c0001t0001g0034 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-7+6514C>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97418752 | |||||||
| chr9:97418787 | G | A | 2 | a0002c0002t0001g0029 a0002c0002t0001g0030 |
2 | HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-7+6549G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97418787 | |||||||
| chr9:97418814 | C | T | 1 | a0002c0002t0002g0288 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-7+6576C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97418814 | |||||||
| chr9:97418867 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-7+6629G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97418867 | |||||||
| chr9:97418999 | A | T | 1 | a0002c0007t0001g0016 | 2 | NA18951.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.-7+6761A>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97418999 | |||||||
| chr9:97419119 | A | G | 1 | a0001c0001t0001g0100 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-7+6881A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97419119 | |||||||
| chr9:97419253 | A | AGAGCACA others(15): Show |
2 | a0001c0001t0001g0098 a0001c0001t0001g0099 |
2 | NA18969.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.-7+7019_-7+7040dup others(22): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 97419253 | ||||||
| chr9:97419371 | C | G | 1 | a0001c0001t0001g0034 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-7+7133C>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97419371 | |||||||
| chr9:97419438 | A | G | 3 | a0002c0002t0001g0029 a0002c0002t0001g0030 a0002c0002t0001g0287 |
3 | HG02486.hp2 HG02965.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-7+7200A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97419438 | |||||||
| chr9:97419487 | C | G | 33 | a0001c0003t0001g0009 a0001c0003t0001g0033 a0001c0003t0001g0038 others(30): Show |
36 | HG00408.hp1 HG00558.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.-7+7249C>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97419487 | |||||||
| chr9:97419537 | C | T | 1 | a0001c0003t0001g0051 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-7+7299C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97419537 | |||||||
| chr9:97419576 | A | G | 33 | a0001c0003t0001g0009 a0001c0003t0001g0033 a0001c0003t0001g0038 others(30): Show |
36 | HG00408.hp1 HG00558.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.-7+7338A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97419576 | |||||||
| chr9:97419707 | T | C | 2 | a0001c0001t0001g0034 a0001c0009t0001g0306 |
2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-7+7469T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97419707 | |||||||
| chr9:97419823 | A | C | 1 | a0001c0001t0001g0286 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-7+7585A>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97419823 | |||||||
| chr9:97420047 | G | A | 33 | a0001c0003t0001g0009 a0001c0003t0001g0033 a0001c0003t0001g0038 others(30): Show |
36 | HG00408.hp1 HG00558.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.-7+7809G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97420047 | |||||||
| chr9:97420164 | C | T | 176 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(173): Show |
201 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(198): Show |
intron_variant | MODIFIER | c.-7+7926C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97420164 | |||||||
| chr9:97420268 | A | G | 1 | a0002c0002t0001g0035 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-7+8030A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97420268 | |||||||
| chr9:97420278 | T | C | 1 | a0002c0002t0001g0121 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-7+8040T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97420278 | |||||||
| chr9:97420364 | T | G | 3 | a0002c0002t0001g0118 a0002c0002t0001g0119 a0002c0002t0001g0120 |
3 | HG01261.hp1 HG01496.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-6-8096T>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97420364 | |||||||
| chr9:97420364 | TG | T | 72 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(69): Show |
82 | HG00408.hp1 HG00558.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.-6-8088delG | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 97420364 | ||||||
| chr9:97420502 | G | A | 1 | a0002c0002t0001g0181 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-6-7958G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97420502 | |||||||
| chr9:97420556 | A | T | 1 | a0001c0009t0001g0306 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-6-7904A>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97420556 | |||||||
| chr9:97420658 | T | A | 33 | a0001c0003t0001g0009 a0001c0003t0001g0033 a0001c0003t0001g0038 others(30): Show |
36 | HG00408.hp1 HG00558.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.-6-7802T>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97420658 | |||||||
| chr9:97420878 | A | G | 3 | a0002c0002t0001g0015 a0002c0002t0001g0159 a0002c0002t0001g0160 |
4 | NA18953.hp2 NA18992.hp2 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.-6-7582A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97420878 | |||||||
| chr9:97420903 | C | T | 1 | a0002c0002t0001g0229 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-6-7557C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97420903 | |||||||
| chr9:97420970 | C | T | 33 | a0001c0003t0001g0009 a0001c0003t0001g0033 a0001c0003t0001g0038 others(30): Show |
36 | HG00408.hp1 HG00558.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.-6-7490C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97420970 | |||||||
| chr9:97420995 | C | T | 17 | a0001c0001t0001g0285 a0001c0003t0001g0009 a0001c0003t0001g0038 others(14): Show |
18 | HG00408.hp1 HG00558.hp1 HG01123.hp1 others(15): Show |
intron_variant | MODIFIER | c.-6-7465C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97420995 | |||||||
| chr9:97421003 | T | C | 33 | a0001c0003t0001g0009 a0001c0003t0001g0033 a0001c0003t0001g0038 others(30): Show |
36 | HG00408.hp1 HG00558.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.-6-7457T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97421003 | |||||||
| chr9:97421004 | G | A | 3 | a0001c0004t0001g0300 a0001c0004t0001g0301 a0001c0004t0001g0302 |
3 | HG03209.hp2 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-6-7456G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97421004 | |||||||
| chr9:97421014 | A | G | 1 | a0001c0005t0001g0299 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-6-7446A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97421014 | |||||||
| chr9:97421134 | CA | C | 36 | a0001c0001t0001g0284 a0001c0003t0001g0009 a0001c0003t0001g0033 others(33): Show |
39 | HG00408.hp1 HG00558.hp1 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.-6-7309delA | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 97421134 | ||||||
| chr9:97421151 | AG | A | 6 | a0002c0002t0001g0142 a0002c0002t0001g0143 a0002c0002t0001g0144 others(3): Show |
6 | HG02615.hp2 HG02647.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-6-7308delG | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97421151 | |||||||
| chr9:97421216 | A | G | 1 | a0002c0002t0001g0295 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-6-7244A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97421216 | |||||||
| chr9:97421300 | A | G | 1 | a0001c0005t0001g0107 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-6-7160A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97421300 | |||||||
| chr9:97421359 | T | C | 1 | a0001c0001t0001g0013 | 2 | HG02109.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.-6-7101T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97421359 | |||||||
| chr9:97421668 | A | T | 2 | a0001c0001t0001g0282 a0001c0001t0001g0283 |
2 | HG02683.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-6-6792A>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97421668 | |||||||
| chr9:97421679 | G | A | 1 | a0001c0015t0001g0031 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-6-6781G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97421679 | |||||||
| chr9:97421697 | TTTGTGTG others(6): Show |
T | 1 | a0002c0002t0001g0183 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-6-6761_-6-6749del others(13): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 97421697 | ||||||
| chr9:97421697 | TTTGTGTG others(8): Show |
T | 1 | a0002c0002t0001g0182 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-6-6761_-6-6747del others(15): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 97421697 | ||||||
| chr9:97421698 | T | G | 3 | a0001c0001t0001g0081 a0001c0001t0001g0089 a0002c0002t0001g0218 |
3 | HG00639.hp2 HG02970.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.-6-6762T>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97421698 | |||||||
| chr9:97421698 | T | TTG | 13 | a0001c0001t0001g0052 a0002c0002t0001g0010 a0002c0002t0001g0018 others(10): Show |
13 | HG00639.hp1 HG01109.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.-6-6717_-6-6716dup others(2): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 97421698 | ||||||
| chr9:97421698 | T | TTGTG | 4 | a0002c0002t0001g0010 a0002c0002t0001g0026 a0002c0002t0001g0141 others(1): Show |
5 | HG01891.hp1 HG02976.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.-6-6719_-6-6716dup others(4): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 97421698 | ||||||
| chr9:97421698 | TTG | T | 48 | a0001c0001t0001g0002 a0001c0001t0001g0025 a0001c0001t0001g0055 others(45): Show |
49 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.-6-6717_-6-6716del others(2): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 97421698 | ||||||
| chr9:97421698 | TTGTG | T | 124 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(121): Show |
152 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(149): Show |
intron_variant | MODIFIER | c.-6-6719_-6-6716del others(4): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 97421698 | ||||||
| chr9:97421698 | TTGTGTG | T | 16 | a0001c0001t0001g0013 a0001c0001t0001g0063 a0001c0001t0001g0078 others(13): Show |
17 | HG00741.hp1 HG01975.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.-6-6721_-6-6716del others(6): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 97421698 | ||||||
| chr9:97421698 | TTGTGTGT others(1): Show |
T | 4 | a0001c0001t0001g0070 a0001c0001t0001g0092 a0001c0003t0001g0033 others(1): Show |
4 | HG01891.hp2 HG02300.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-6-6723_-6-6716del others(8): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 97421698 | ||||||
| chr9:97421698 | TTGTGTGT others(3): Show |
T | 1 | a0001c0004t0001g0105 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-6-6725_-6-6716del others(10): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 97421698 | ||||||
| chr9:97421698 | TTGTGTGT others(7): Show |
T | 7 | a0002c0002t0001g0119 a0002c0002t0001g0201 a0002c0002t0001g0210 others(4): Show |
7 | HG01256.hp2 HG01358.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-6-6729_-6-6716del others(14): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 97421698 | ||||||
| chr9:97421698 | TTGTGTGT others(9): Show |
T | 51 | a0001c0001t0001g0034 a0001c0001t0001g0272 a0002c0002t0001g0029 others(48): Show |
54 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.-6-6731_-6-6716del others(16): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 97421698 | ||||||
| chr9:97421699 | TGTGTGTG others(8): Show |
T | 1 | a0002c0002t0003g0219 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-6-6760_-6-6746del others(15): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97421699 | |||||||
| chr9:97421810 | C | T | 1 | a0001c0001t0001g0281 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-6-6650C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97421810 | |||||||
| chr9:97421845 | A | G | 1 | a0005c0011t0001g0032 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-6-6615A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97421845 | |||||||
| chr9:97421955 | C | G | 1 | a0002c0002t0001g0158 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-6-6505C>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97421955 | |||||||
| chr9:97422118 | G | A | 1 | a0005c0011t0001g0032 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-6-6342G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97422118 | |||||||
| chr9:97422395 | C | CA | 17 | a0001c0003t0001g0033 a0001c0004t0001g0014 a0001c0004t0001g0027 others(14): Show |
19 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.-6-6054dupA | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 97422395 | ||||||
| chr9:97422449 | G | T | 1 | a0001c0001t0001g0034 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-6-6011G>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97422449 | |||||||
| chr9:97422488 | T | C | 177 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(174): Show |
203 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(200): Show |
intron_variant | MODIFIER | c.-6-5972T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97422488 | |||||||
| chr9:97422503 | T | C | 33 | a0001c0003t0001g0009 a0001c0003t0001g0033 a0001c0003t0001g0038 others(30): Show |
36 | HG00408.hp1 HG00558.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.-6-5957T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97422503 | |||||||
| chr9:97422658 | T | C | 175 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(172): Show |
201 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(198): Show |
intron_variant | MODIFIER | c.-6-5802T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97422658 | |||||||
| chr9:97422725 | G | GT | 62 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(59): Show |
75 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.-6-5729dupT | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 97422725 | ||||||
| chr9:97423025 | A | G | 16 | a0001c0003t0001g0009 a0001c0003t0001g0038 a0001c0003t0001g0039 others(13): Show |
17 | HG00408.hp1 HG00558.hp1 HG02132.hp2 others(14): Show |
intron_variant | MODIFIER | c.-6-5435A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97423025 | |||||||
| chr9:97423211 | G | A | 2 | a0001c0005t0001g0297 a0001c0005t0001g0299 |
2 | HG02717.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-6-5249G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97423211 | |||||||
| chr9:97423398 | C | CT | 16 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0097 others(13): Show |
21 | HG01167.hp2 HG01934.hp2 HG01978.hp1 others(18): Show |
intron_variant | MODIFIER | c.-6-5050dupT | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 97423398 | ||||||
| chr9:97423398 | CT | C | 33 | a0001c0003t0001g0009 a0001c0003t0001g0033 a0001c0003t0001g0038 others(30): Show |
36 | HG00408.hp1 HG00558.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.-6-5050delT | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 97423398 | ||||||
| chr9:97423566 | A | C | 33 | a0001c0003t0001g0009 a0001c0003t0001g0033 a0001c0003t0001g0038 others(30): Show |
36 | HG00408.hp1 HG00558.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.-6-4894A>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97423566 | |||||||
| chr9:97423581 | T | TTC | 33 | a0001c0003t0001g0009 a0001c0003t0001g0033 a0001c0003t0001g0038 others(30): Show |
36 | HG00408.hp1 HG00558.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.-6-4875_-6-4874dup others(2): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 97423581 | ||||||
| chr9:97423701 | A | C | 1 | a0001c0009t0001g0306 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-6-4759A>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97423701 | |||||||
| chr9:97423789 | T | C | 2 | a0002c0002t0001g0124 a0002c0002t0001g0125 |
2 | HG00408.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.-6-4671T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97423789 | |||||||
| chr9:97423857 | A | G | 1 | a0005c0011t0001g0032 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-6-4603A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97423857 | |||||||
| chr9:97424049 | CT | C | 121 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(118): Show |
148 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(145): Show |
intron_variant | MODIFIER | c.-6-4387delT | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 97424049 | ||||||
| chr9:97424049 | CTT | C | 162 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(159): Show |
178 | HG00323.hp1 HG00323.hp2 HG00544.hp2 others(175): Show |
intron_variant | MODIFIER | c.-6-4388_-6-4387del others(2): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 97424049 | ||||||
| chr9:97424086 | C | T | 33 | a0001c0003t0001g0009 a0001c0003t0001g0033 a0001c0003t0001g0038 others(30): Show |
36 | HG00408.hp1 HG00558.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.-6-4374C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97424086 | |||||||
| chr9:97424148 | A | G | 33 | a0001c0003t0001g0009 a0001c0003t0001g0033 a0001c0003t0001g0038 others(30): Show |
36 | HG00408.hp1 HG00558.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.-6-4312A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97424148 | |||||||
| chr9:97424200 | C | T | 33 | a0001c0003t0001g0009 a0001c0003t0001g0033 a0001c0003t0001g0038 others(30): Show |
36 | HG00408.hp1 HG00558.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.-6-4260C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97424200 | |||||||
| chr9:97424308 | G | A | 33 | a0001c0003t0001g0009 a0001c0003t0001g0033 a0001c0003t0001g0038 others(30): Show |
36 | HG00408.hp1 HG00558.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.-6-4152G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97424308 | |||||||
| chr9:97424362 | C | T | 33 | a0001c0003t0001g0009 a0001c0003t0001g0033 a0001c0003t0001g0038 others(30): Show |
36 | HG00408.hp1 HG00558.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.-6-4098C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97424362 | |||||||
| chr9:97424711 | A | G | 1 | a0001c0001t0001g0243 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-6-3749A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97424711 | |||||||
| chr9:97424802 | G | A | 1 | a0001c0004t0001g0303 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-6-3658G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97424802 | |||||||
| chr9:97424976 | G | A | 3 | a0001c0004t0001g0300 a0001c0004t0001g0301 a0001c0004t0001g0302 |
3 | HG03209.hp2 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-6-3484G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97424976 | |||||||
| chr9:97425006 | G | T | 1 | a0001c0001t0001g0076 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-6-3454G>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97425006 | |||||||
| chr9:97425022 | A | G | 17 | a0001c0003t0001g0033 a0001c0004t0001g0014 a0001c0004t0001g0027 others(14): Show |
19 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.-6-3438A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97425022 | |||||||
| chr9:97425156 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-6-3304G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97425156 | |||||||
| chr9:97425737 | A | G | 1 | a0002c0002t0001g0291 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-6-2723A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97425737 | |||||||
| chr9:97425824 | G | A | 176 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(173): Show |
201 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(198): Show |
intron_variant | MODIFIER | c.-6-2636G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97425824 | |||||||
| chr9:97425847 | T | C | 173 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(170): Show |
198 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(195): Show |
intron_variant | MODIFIER | c.-6-2613T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97425847 | |||||||
| chr9:97425886 | A | G | 2 | a0003c0006t0001g0008 a0003c0006t0001g0037 |
3 | HG02976.hp1 HG03579.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-6-2574A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97425886 | |||||||
| chr9:97426707 | T | A | 16 | a0001c0003t0001g0009 a0001c0003t0001g0038 a0001c0003t0001g0039 others(13): Show |
17 | HG00408.hp1 HG00558.hp1 HG02132.hp2 others(14): Show |
intron_variant | MODIFIER | c.-6-1753T>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97426707 | |||||||
| chr9:97426709 | C | T | 1 | a0001c0001t0001g0274 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-6-1751C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97426709 | |||||||
| chr9:97426914 | G | A | 2 | a0003c0006t0001g0008 a0003c0006t0001g0037 |
3 | HG02976.hp1 HG03579.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-6-1546G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97426914 | |||||||
| chr9:97426930 | C | G | 1 | a0001c0003t0001g0033 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-6-1530C>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97426930 | |||||||
| chr9:97426941 | C | T | 33 | a0001c0003t0001g0009 a0001c0003t0001g0033 a0001c0003t0001g0038 others(30): Show |
36 | HG00408.hp1 HG00558.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.-6-1519C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97426941 | |||||||
| chr9:97427071 | A | G | 16 | a0001c0003t0001g0009 a0001c0003t0001g0038 a0001c0003t0001g0039 others(13): Show |
17 | HG00408.hp1 HG00558.hp1 HG02132.hp2 others(14): Show |
intron_variant | MODIFIER | c.-6-1389A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97427071 | |||||||
| chr9:97427255 | T | C | 16 | a0001c0003t0001g0009 a0001c0003t0001g0038 a0001c0003t0001g0039 others(13): Show |
17 | HG00408.hp1 HG00558.hp1 HG02132.hp2 others(14): Show |
intron_variant | MODIFIER | c.-6-1205T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97427255 | |||||||
| chr9:97427535 | C | A | 16 | a0001c0003t0001g0009 a0001c0003t0001g0038 a0001c0003t0001g0039 others(13): Show |
17 | HG00408.hp1 HG00558.hp1 HG02132.hp2 others(14): Show |
intron_variant | MODIFIER | c.-6-925C>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97427535 | |||||||
| chr9:97427938 | T | C | 1 | a0001c0001t0001g0275 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-6-522T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97427938 | |||||||
| chr9:97427968 | A | G | 3 | a0002c0002t0001g0029 a0002c0002t0001g0030 a0002c0002t0001g0287 |
3 | HG02486.hp2 HG02965.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-6-492A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97427968 | |||||||
| chr9:97428049 | T | C | 1 | a0001c0003t0001g0033 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-6-411T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97428049 | |||||||
| chr9:97428214 | C | T | 1 | a0001c0001t0001g0034 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-6-246C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97428214 | |||||||
| chr9:97428259 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-6-201G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97428259 | |||||||
| chr9:97428288 | T | G | 1 | a0002c0002t0001g0185 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-6-172T>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97428288 | |||||||
| chr9:97428690 | C | T | 22 | a0002c0002t0001g0059 a0002c0002t0001g0181 a0002c0002t0001g0215 others(19): Show |
25 | HG00621.hp2 HG01167.hp2 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.207+18C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 2/16 | chr9 | 97428690 | |||||||
| chr9:97428691 | G | A | 16 | a0001c0003t0001g0009 a0001c0003t0001g0038 a0001c0003t0001g0039 others(13): Show |
17 | HG00408.hp1 HG00558.hp1 HG02132.hp2 others(14): Show |
intron_variant | MODIFIER | c.207+19G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 2/16 | chr9 | 97428691 | |||||||
| chr9:97428841 | T | C | 141 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(138): Show |
164 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(161): Show |
intron_variant | MODIFIER | c.207+169T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 2/16 | chr9 | 97428841 | |||||||
| chr9:97428857 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.207+185C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 2/16 | chr9 | 97428857 | |||||||
| chr9:97428946 | A | G | 1 | a0002c0002t0001g0153 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.207+274A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 2/16 | chr9 | 97428946 | |||||||
| chr9:97429075 | A | C | 1 | a0002c0002t0001g0212 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.207+403A>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 2/16 | chr9 | 97429075 | |||||||
| chr9:97429167 | G | C | 71 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(68): Show |
85 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.207+495G>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 2/16 | chr9 | 97429167 | |||||||
| chr9:97429418 | G | A | 1 | a0001c0001t0001g0061 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.207+746G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 2/16 | chr9 | 97429418 | |||||||
| chr9:97429451 | G | C | 1 | a0002c0002t0002g0221 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.207+779G>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 2/16 | chr9 | 97429451 | |||||||
| chr9:97429507 | G | A | 1 | a0001c0003t0001g0033 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.207+835G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 2/16 | chr9 | 97429507 | |||||||
| chr9:97429667 | G | A | 1 | a0001c0001t0001g0171 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.207+995G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 2/16 | chr9 | 97429667 | |||||||
| chr9:97429700 | A | G | 16 | a0001c0003t0001g0009 a0001c0003t0001g0038 a0001c0003t0001g0039 others(13): Show |
17 | HG00408.hp1 HG00558.hp1 HG02132.hp2 others(14): Show |
intron_variant | MODIFIER | c.207+1028A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 2/16 | chr9 | 97429700 | |||||||
| chr9:97429713 | A | G | 1 | a0005c0011t0001g0032 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.207+1041A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 2/16 | chr9 | 97429713 | |||||||
| chr9:97429721 | C | T | 1 | a0001c0001t0001g0273 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.207+1049C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 2/16 | chr9 | 97429721 | |||||||
| chr9:97429903 | T | C | 174 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(171): Show |
200 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(197): Show |
intron_variant | MODIFIER | c.208-1030T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 2/16 | chr9 | 97429903 | |||||||
| chr9:97429957 | C | T | 3 | a0002c0002t0001g0029 a0002c0002t0001g0030 a0002c0002t0001g0287 |
3 | HG02486.hp2 HG02965.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.208-976C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 2/16 | chr9 | 97429957 | |||||||
| chr9:97430035 | A | G | 1 | a0001c0001t0001g0074 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.208-898A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 2/16 | chr9 | 97430035 | |||||||
| chr9:97430074 | T | C | 2 | a0001c0004t0001g0300 a0001c0004t0001g0301 |
2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.208-859T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 2/16 | chr9 | 97430074 | |||||||
| chr9:97430264 | G | A | 15 | a0001c0004t0001g0014 a0001c0004t0001g0027 a0001c0004t0001g0104 others(12): Show |
17 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.208-669G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 2/16 | chr9 | 97430264 | |||||||
| chr9:97430704 | T | C | 60 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(57): Show |
68 | HG00438.hp1 HG00621.hp1 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.208-229T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 2/16 | chr9 | 97430704 | |||||||
| chr9:97430719 | A | G | 158 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(155): Show |
183 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(180): Show |
intron_variant | MODIFIER | c.208-214A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 2/16 | chr9 | 97430719 | |||||||
| chr9:97430831 | T | C | 141 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(138): Show |
164 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(161): Show |
intron_variant | MODIFIER | c.208-102T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 2/16 | chr9 | 97430831 | |||||||
| chr9:97431529 | A | G | 4 | a0002c0002t0001g0010 a0002c0002t0001g0057 a0002c0002t0001g0058 others(1): Show |
5 | HG02132.hp1 NA18939.hp2 NA19055.hp1 others(2): Show |
intron_variant | MODIFIER | c.349+455A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 3/16 | chr9 | 97431529 | |||||||
| chr9:97431680 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.350-345C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 3/16 | chr9 | 97431680 | |||||||
| chr9:97431895 | A | G | 1 | a0001c0015t0001g0031 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.350-130A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 3/16 | chr9 | 97431895 | |||||||
| chr9:97432015 | A | G | 1 | a0001c0003t0001g0296 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.350-10A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 3/16 | chr9 | 97432015 | |||||||
| chr9:97432252 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.563+14G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97432252 | |||||||
| chr9:97432355 | G | C | 1 | a0001c0003t0001g0038 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.563+117G>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97432355 | |||||||
| chr9:97432371 | A | G | 8 | a0001c0001t0001g0021 a0001c0001t0001g0233 a0001c0001t0001g0239 others(5): Show |
9 | HG02622.hp1 HG02630.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.563+133A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97432371 | |||||||
| chr9:97432388 | G | C | 3 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 |
3 | NA18948.hp1 NA18999.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.563+150G>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97432388 | |||||||
| chr9:97432543 | G | A | 33 | a0001c0003t0001g0009 a0001c0003t0001g0033 a0001c0003t0001g0038 others(30): Show |
36 | HG00408.hp1 HG00558.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.563+305G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97432543 | |||||||
| chr9:97432714 | G | A | 4 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0108 others(1): Show |
4 | HG01243.hp2 HG01255.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.563+476G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97432714 | |||||||
| chr9:97432717 | A | G | 1 | a0002c0002t0001g0152 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.563+479A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97432717 | |||||||
| chr9:97432771 | T | C | 33 | a0001c0003t0001g0009 a0001c0003t0001g0033 a0001c0003t0001g0038 others(30): Show |
36 | HG00408.hp1 HG00558.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.563+533T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97432771 | |||||||
| chr9:97433159 | G | T | 1 | a0001c0003t0001g0033 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.563+921G>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97433159 | |||||||
| chr9:97433502 | G | A | 141 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(138): Show |
164 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(161): Show |
intron_variant | MODIFIER | c.563+1264G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97433502 | |||||||
| chr9:97433804 | A | G | 1 | a0001c0001t0001g0164 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.563+1566A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97433804 | |||||||
| chr9:97433816 | T | C | 174 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(171): Show |
200 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(197): Show |
intron_variant | MODIFIER | c.563+1578T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97433816 | |||||||
| chr9:97433833 | G | A | 23 | a0002c0002t0001g0010 a0002c0002t0001g0017 a0002c0002t0001g0018 others(20): Show |
27 | HG00323.hp1 HG00544.hp2 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.563+1595G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97433833 | |||||||
| chr9:97433871 | G | A | 1 | a0002c0008t0001g0028 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.563+1633G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97433871 | |||||||
| chr9:97434113 | T | C | 1 | a0002c0002t0001g0128 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.563+1875T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97434113 | |||||||
| chr9:97434379 | C | T | 1 | a0001c0001t0001g0034 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.563+2141C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97434379 | |||||||
| chr9:97434418 | C | G | 16 | a0001c0003t0001g0009 a0001c0003t0001g0038 a0001c0003t0001g0039 others(13): Show |
17 | HG00408.hp1 HG00558.hp1 HG02132.hp2 others(14): Show |
intron_variant | MODIFIER | c.563+2180C>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97434418 | |||||||
| chr9:97434733 | A | G | 2 | a0002c0002t0001g0215 a0002c0002t0001g0220 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.563+2495A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97434733 | |||||||
| chr9:97435235 | AT | A | 172 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(169): Show |
197 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(194): Show |
intron_variant | MODIFIER | c.563+3001delT | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr9 | 97435235 | ||||||
| chr9:97435467 | TA | T | 136 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(133): Show |
158 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(155): Show |
intron_variant | MODIFIER | c.563+3248delA | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr9 | 97435467 | ||||||
| chr9:97435496 | C | T | 1 | a0001c0015t0001g0031 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.563+3258C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97435496 | |||||||
| chr9:97435499 | G | A | 172 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(169): Show |
197 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(194): Show |
intron_variant | MODIFIER | c.563+3261G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97435499 | |||||||
| chr9:97435525 | G | T | 16 | a0001c0003t0001g0009 a0001c0003t0001g0038 a0001c0003t0001g0039 others(13): Show |
17 | HG00408.hp1 HG00558.hp1 HG02132.hp2 others(14): Show |
intron_variant | MODIFIER | c.563+3287G>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97435525 | |||||||
| chr9:97435589 | T | A | 1 | a0003c0006t0001g0037 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.563+3351T>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97435589 | |||||||
| chr9:97435628 | C | CCTGT | 173 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(170): Show |
198 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(195): Show |
intron_variant | MODIFIER | c.563+3392_563+3393i others(6): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr9 | 97435628 | ||||||
| chr9:97435910 | C | G | 1 | a0002c0002t0001g0151 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.564-3335C>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97435910 | |||||||
| chr9:97435997 | C | T | 2 | a0001c0001t0001g0282 a0001c0001t0001g0283 |
2 | HG02683.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.564-3248C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97435997 | |||||||
| chr9:97436197 | A | G | 1 | a0001c0001t0001g0236 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.564-3048A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97436197 | |||||||
| chr9:97436263 | T | C | 2 | a0001c0001t0001g0082 a0001c0001t0001g0083 |
2 | HG01952.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.564-2982T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97436263 | |||||||
| chr9:97436399 | T | C | 1 | a0001c0001t0001g0111 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.564-2846T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97436399 | |||||||
| chr9:97436507 | G | A | 2 | a0002c0002t0001g0121 a0002c0002t0001g0129 |
2 | HG02155.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.564-2738G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97436507 | |||||||
| chr9:97436615 | G | C | 4 | a0001c0004t0001g0027 a0001c0004t0001g0300 a0001c0004t0001g0301 others(1): Show |
5 | HG02615.hp1 HG02895.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.564-2630G>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97436615 | |||||||
| chr9:97436867 | T | C | 2 | a0001c0001t0001g0060 a0001c0001t0001g0077 |
2 | HG02965.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.564-2378T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97436867 | |||||||
| chr9:97437052 | C | A | 1 | a0005c0011t0001g0032 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.564-2193C>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97437052 | |||||||
| chr9:97437209 | C | G | 1 | a0001c0001t0001g0063 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.564-2036C>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97437209 | |||||||
| chr9:97437217 | T | A | 1 | a0001c0001t0001g0250 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.564-2028T>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97437217 | |||||||
| chr9:97437238 | C | T | 17 | a0001c0003t0001g0033 a0001c0004t0001g0014 a0001c0004t0001g0027 others(14): Show |
19 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.564-2007C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97437238 | |||||||
| chr9:97437291 | A | G | 174 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(171): Show |
200 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(197): Show |
intron_variant | MODIFIER | c.564-1954A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97437291 | |||||||
| chr9:97437403 | C | T | 1 | a0002c0002t0001g0295 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.564-1842C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97437403 | |||||||
| chr9:97437648 | C | T | 1 | a0001c0009t0001g0306 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.564-1597C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97437648 | |||||||
| chr9:97437726 | G | A | 1 | a0001c0003t0001g0033 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.564-1519G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97437726 | |||||||
| chr9:97437864 | T | G | 16 | a0001c0003t0001g0033 a0001c0004t0001g0014 a0001c0004t0001g0027 others(13): Show |
18 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.564-1381T>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97437864 | |||||||
| chr9:97437905 | C | T | 1 | a0001c0003t0001g0296 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.564-1340C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97437905 | |||||||
| chr9:97437948 | A | G | 1 | a0001c0001t0001g0271 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.564-1297A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97437948 | |||||||
| chr9:97438318 | A | G | 174 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(171): Show |
201 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(198): Show |
intron_variant | MODIFIER | c.564-927A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97438318 | |||||||
| chr9:97438399 | C | A | 33 | a0001c0003t0001g0009 a0001c0003t0001g0033 a0001c0003t0001g0038 others(30): Show |
36 | HG00408.hp1 HG00558.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.564-846C>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97438399 | |||||||
| chr9:97438490 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.564-755C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97438490 | |||||||
| chr9:97438570 | A | T | 8 | a0002c0002t0001g0172 a0002c0002t0001g0173 a0002c0002t0001g0174 others(5): Show |
8 | HG01081.hp1 HG01243.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.564-675A>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97438570 | |||||||
| chr9:97438693 | A | G | 33 | a0001c0003t0001g0009 a0001c0003t0001g0033 a0001c0003t0001g0038 others(30): Show |
36 | HG00408.hp1 HG00558.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.564-552A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97438693 | |||||||
| chr9:97438868 | T | C | 1 | a0001c0004t0001g0114 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.564-377T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97438868 | |||||||
| chr9:97439078 | A | G | 63 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(60): Show |
71 | HG00438.hp1 HG00621.hp1 HG00673.hp2 others(68): Show |
intron_variant | MODIFIER | c.564-167A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97439078 | |||||||
| chr9:97439089 | G | A | 1 | a0002c0002t0001g0186 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.564-156G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97439089 | |||||||
| chr9:97439127 | A | G | 1 | a0001c0001t0001g0110 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.564-118A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97439127 | |||||||
| chr9:97439177 | G | A | 2 | a0002c0002t0001g0035 a0002c0002t0001g0187 |
2 | HG00544.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.564-68G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97439177 | |||||||
| chr9:97439382 | G | A | 16 | a0002c0002t0001g0010 a0002c0002t0001g0017 a0002c0002t0001g0035 others(13): Show |
18 | HG00323.hp1 HG00544.hp2 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.637+64G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 5/16 | chr9 | 97439382 | |||||||
| chr9:97439565 | A | G | 4 | a0002c0002t0001g0183 a0002c0002t0001g0210 a0002c0002t0001g0229 others(1): Show |
4 | HG02135.hp2 NA18943.hp1 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.637+247A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 5/16 | chr9 | 97439565 | |||||||
| chr9:97439592 | C | T | 1 | a0002c0002t0002g0226 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.637+274C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 5/16 | chr9 | 97439592 | |||||||
| chr9:97439775 | A | G | 1 | a0001c0001t0001g0270 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.637+457A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 5/16 | chr9 | 97439775 | |||||||
| chr9:97439803 | G | T | 1 | a0001c0001t0001g0077 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.637+485G>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 5/16 | chr9 | 97439803 | |||||||
| chr9:97439830 | G | A | 1 | a0001c0009t0001g0306 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.637+512G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 5/16 | chr9 | 97439830 | |||||||
| chr9:97439876 | G | C | 1 | a0001c0003t0001g0040 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.637+558G>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 5/16 | chr9 | 97439876 | |||||||
| chr9:97439951 | C | T | 1 | a0005c0011t0001g0032 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.637+633C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 5/16 | chr9 | 97439951 | |||||||
| chr9:97439960 | C | T | 33 | a0001c0003t0001g0009 a0001c0003t0001g0033 a0001c0003t0001g0038 others(30): Show |
36 | HG00408.hp1 HG00558.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.637+642C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 5/16 | chr9 | 97439960 | |||||||
| chr9:97440307 | C | T | 1 | a0001c0015t0001g0031 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.637+989C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 5/16 | chr9 | 97440307 | |||||||
| chr9:97440339 | G | A | 2 | a0001c0001t0001g0080 a0001c0001t0001g0081 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.637+1021G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 5/16 | chr9 | 97440339 | |||||||
| chr9:97440381 | G | C | 1 | a0001c0009t0001g0306 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.637+1063G>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 5/16 | chr9 | 97440381 | |||||||
| chr9:97440541 | A | G | 3 | a0002c0002t0001g0029 a0002c0002t0001g0030 a0002c0002t0001g0287 |
3 | HG02486.hp2 HG02965.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.638-1117A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 5/16 | chr9 | 97440541 | |||||||
| chr9:97440602 | C | T | 33 | a0001c0003t0001g0009 a0001c0003t0001g0033 a0001c0003t0001g0038 others(30): Show |
36 | HG00408.hp1 HG00558.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.638-1056C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 5/16 | chr9 | 97440602 | |||||||
| chr9:97440744 | A | C | 1 | a0001c0001t0001g0083 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.638-914A>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 5/16 | chr9 | 97440744 | |||||||
| chr9:97440751 | A | G | 2 | a0001c0001t0001g0108 a0001c0001t0001g0109 |
2 | HG01255.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.638-907A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 5/16 | chr9 | 97440751 | |||||||
| chr9:97440923 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.638-735C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 5/16 | chr9 | 97440923 | |||||||
| chr9:97440936 | A | T | 1 | a0001c0001t0001g0241 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.638-722A>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 5/16 | chr9 | 97440936 | |||||||
| chr9:97440952 | G | A | 1 | a0002c0002t0001g0188 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.638-706G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 5/16 | chr9 | 97440952 | |||||||
| chr9:97441426 | G | T | 33 | a0002c0002t0001g0118 a0002c0002t0001g0119 a0002c0002t0001g0120 others(30): Show |
33 | HG00323.hp2 HG00597.hp2 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.638-232G>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 5/16 | chr9 | 97441426 | |||||||
| chr9:97441456 | A | G | 1 | a0005c0011t0001g0032 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.638-202A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 5/16 | chr9 | 97441456 | |||||||
| chr9:97441920 | C | G | 7 | a0001c0004t0001g0014 a0001c0004t0001g0104 a0001c0004t0001g0105 others(4): Show |
9 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.855+45C>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97441920 | |||||||
| chr9:97441950 | T | C | 1 | a0002c0002t0001g0169 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.855+75T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97441950 | |||||||
| chr9:97442176 | TAAACACT others(10): Show |
T | 1 | a0001c0001t0001g0088 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.855+302_855+318del others(17): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97442176 | |||||||
| chr9:97442194 | C | T | 1 | a0001c0001t0001g0088 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.855+319C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97442194 | |||||||
| chr9:97442436 | T | G | 2 | a0001c0001t0001g0239 a0001c0001t0001g0243 |
2 | HG02622.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.855+561T>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97442436 | |||||||
| chr9:97442498 | A | G | 1 | a0002c0002t0001g0058 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.855+623A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97442498 | |||||||
| chr9:97442576 | G | T | 35 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0033 others(32): Show |
38 | HG00408.hp1 HG00558.hp1 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.855+701G>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97442576 | |||||||
| chr9:97442604 | C | T | 35 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0033 others(32): Show |
38 | HG00408.hp1 HG00558.hp1 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.855+729C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97442604 | |||||||
| chr9:97442827 | CT | C | 35 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0033 others(32): Show |
38 | HG00408.hp1 HG00558.hp1 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.855+957delT | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr9 | 97442827 | ||||||
| chr9:97442830 | T | C | 35 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0033 others(32): Show |
38 | HG00408.hp1 HG00558.hp1 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.855+955T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97442830 | |||||||
| chr9:97442869 | C | A | 2 | a0003c0006t0001g0008 a0003c0006t0001g0037 |
3 | HG02976.hp1 HG03579.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.855+994C>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97442869 | |||||||
| chr9:97443119 | C | T | 35 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0033 others(32): Show |
38 | HG00408.hp1 HG00558.hp1 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.855+1244C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97443119 | |||||||
| chr9:97443141 | T | C | 35 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0033 others(32): Show |
38 | HG00408.hp1 HG00558.hp1 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.855+1266T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97443141 | |||||||
| chr9:97443153 | G | C | 3 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0092 |
3 | HG02922.hp1 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.855+1278G>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97443153 | |||||||
| chr9:97443260 | T | C | 17 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0038 others(14): Show |
18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.855+1385T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97443260 | |||||||
| chr9:97443409 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.855+1534C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97443409 | |||||||
| chr9:97443410 | A | G | 1 | a0002c0002t0001g0158 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.855+1535A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97443410 | |||||||
| chr9:97443561 | A | G | 1 | a0005c0011t0001g0032 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.855+1686A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97443561 | |||||||
| chr9:97443820 | T | A | 1 | a0002c0002t0001g0130 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.855+1945T>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97443820 | |||||||
| chr9:97443847 | T | C | 142 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(139): Show |
165 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(162): Show |
intron_variant | MODIFIER | c.855+1972T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97443847 | |||||||
| chr9:97443925 | C | T | 1 | a0002c0002t0001g0169 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.855+2050C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97443925 | |||||||
| chr9:97444222 | C | T | 17 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0038 others(14): Show |
18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.855+2347C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97444222 | |||||||
| chr9:97444320 | C | G | 307 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(304): Show |
351 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(348): Show |
intron_variant | MODIFIER | c.855+2445C>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97444320 | |||||||
| chr9:97444344 | A | G | 1 | a0001c0001t0001g0239 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.855+2469A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97444344 | |||||||
| chr9:97444448 | T | A | 17 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0038 others(14): Show |
18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.855+2573T>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97444448 | |||||||
| chr9:97444821 | C | T | 15 | a0001c0004t0001g0014 a0001c0004t0001g0027 a0001c0004t0001g0104 others(12): Show |
17 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.855+2946C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97444821 | |||||||
| chr9:97444904 | C | T | 17 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0038 others(14): Show |
18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.855+3029C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97444904 | |||||||
| chr9:97444972 | G | T | 1 | a0001c0001t0001g0073 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.855+3097G>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97444972 | |||||||
| chr9:97445093 | C | T | 17 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0038 others(14): Show |
18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.855+3218C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97445093 | |||||||
| chr9:97445285 | TTTGAC | T | 178 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(175): Show |
203 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(200): Show |
intron_variant | MODIFIER | c.855+3417_855+3421d others(7): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr9 | 97445285 | ||||||
| chr9:97445316 | C | T | 17 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0038 others(14): Show |
18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.855+3441C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97445316 | |||||||
| chr9:97445507 | A | C | 1 | a0001c0001t0001g0034 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.855+3632A>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97445507 | |||||||
| chr9:97445537 | G | A | 1 | a0001c0001t0001g0034 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.855+3662G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97445537 | |||||||
| chr9:97445770 | G | A | 158 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(155): Show |
182 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(179): Show |
intron_variant | MODIFIER | c.855+3895G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97445770 | |||||||
| chr9:97445888 | G | T | 1 | a0001c0003t0001g0039 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.855+4013G>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97445888 | |||||||
| chr9:97445984 | T | G | 2 | a0002c0002t0001g0035 a0002c0002t0001g0187 |
2 | HG00544.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.855+4109T>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97445984 | |||||||
| chr9:97446198 | C | T | 1 | a0001c0001t0001g0239 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.855+4323C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97446198 | |||||||
| chr9:97446536 | G | A | 1 | a0001c0003t0001g0033 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.855+4661G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97446536 | |||||||
| chr9:97446645 | G | C | 2 | a0001c0001t0001g0052 a0001c0001t0001g0054 |
2 | HG01109.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.855+4770G>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97446645 | |||||||
| chr9:97446915 | A | G | 1 | a0002c0002t0001g0158 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.855+5040A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97446915 | |||||||
| chr9:97447032 | T | G | 17 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0038 others(14): Show |
18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.855+5157T>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97447032 | |||||||
| chr9:97447242 | G | A | 1 | a0002c0002t0001g0293 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.855+5367G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97447242 | |||||||
| chr9:97447276 | G | A | 1 | a0001c0009t0001g0306 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.855+5401G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97447276 | |||||||
| chr9:97447394 | C | T | 1 | a0001c0003t0001g0048 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.855+5519C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97447394 | |||||||
| chr9:97447460 | G | A | 3 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0092 |
3 | HG02922.hp1 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.855+5585G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97447460 | |||||||
| chr9:97447720 | GTAATGAG others(9): Show |
G | 1 | a0002c0002t0001g0192 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.855+5863_855+5878d others(18): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr9 | 97447720 | ||||||
| chr9:97447887 | C | A | 1 | a0001c0015t0001g0031 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.855+6012C>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97447887 | |||||||
| chr9:97448543 | T | C | 176 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(173): Show |
201 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(198): Show |
intron_variant | MODIFIER | c.855+6668T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97448543 | |||||||
| chr9:97448772 | T | C | 8 | a0002c0002t0001g0181 a0002c0002t0002g0019 a0002c0002t0002g0166 others(5): Show |
9 | HG01167.hp2 HG01934.hp2 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.855+6897T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97448772 | |||||||
| chr9:97448840 | G | C | 1 | a0002c0002t0002g0288 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.855+6965G>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97448840 | |||||||
| chr9:97449258 | G | A | 1 | a0001c0001t0001g0011 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.855+7383G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97449258 | |||||||
| chr9:97449297 | G | A | 17 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0038 others(14): Show |
18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.855+7422G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97449297 | |||||||
| chr9:97449412 | C | T | 15 | a0001c0004t0001g0014 a0001c0004t0001g0027 a0001c0004t0001g0104 others(12): Show |
17 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.855+7537C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97449412 | |||||||
| chr9:97449424 | G | A | 158 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(155): Show |
182 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(179): Show |
intron_variant | MODIFIER | c.855+7549G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97449424 | |||||||
| chr9:97449432 | C | T | 18 | a0001c0003t0001g0033 a0001c0004t0001g0014 a0001c0004t0001g0027 others(15): Show |
20 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.855+7557C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97449432 | |||||||
| chr9:97449475 | G | A | 2 | a0002c0002t0001g0229 a0002c0002t0002g0305 |
2 | HG02135.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.855+7600G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97449475 | |||||||
| chr9:97449526 | C | T | 1 | a0001c0001t0001g0274 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.855+7651C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97449526 | |||||||
| chr9:97449587 | T | C | 270 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(267): Show |
302 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(299): Show |
intron_variant | MODIFIER | c.855+7712T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97449587 | |||||||
| chr9:97449640 | A | G | 2 | a0001c0001t0001g0233 a0001c0001t0001g0240 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.855+7765A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97449640 | |||||||
| chr9:97449656 | G | A | 1 | a0001c0001t0001g0012 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.855+7781G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97449656 | |||||||
| chr9:97449722 | G | A | 1 | a0001c0004t0001g0302 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.855+7847G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97449722 | |||||||
| chr9:97449726 | T | G | 17 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0038 others(14): Show |
18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.855+7851T>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97449726 | |||||||
| chr9:97449896 | A | G | 1 | a0001c0001t0001g0063 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.855+8021A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97449896 | |||||||
| chr9:97450065 | G | A | 1 | a0001c0001t0001g0232 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.855+8190G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97450065 | |||||||
| chr9:97450121 | C | G | 270 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(267): Show |
302 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(299): Show |
intron_variant | MODIFIER | c.855+8246C>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97450121 | |||||||
| chr9:97450256 | A | G | 1 | a0001c0009t0001g0306 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.855+8381A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97450256 | |||||||
| chr9:97450627 | T | TTAACTC | 17 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0038 others(14): Show |
18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.855+8752_855+8753i others(8): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97450627 | |||||||
| chr9:97450628 | C | A | 17 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0038 others(14): Show |
18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.855+8753C>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97450628 | |||||||
| chr9:97450901 | G | C | 62 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(59): Show |
70 | HG00438.hp1 HG00621.hp1 HG00673.hp2 others(67): Show |
intron_variant | MODIFIER | c.855+9026G>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97450901 | |||||||
| chr9:97450906 | CT | C | 10 | a0001c0001t0001g0064 a0001c0001t0001g0093 a0001c0001t0001g0096 others(7): Show |
10 | HG01515.hp2 HG01516.hp2 NA18950.hp2 others(7): Show |
intron_variant | MODIFIER | c.855+9046delT | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr9 | 97450906 | ||||||
| chr9:97450908 | T | C | 2 | a0001c0015t0001g0031 a0002c0002t0001g0181 |
2 | HG02293.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.855+9033T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97450908 | |||||||
| chr9:97450990 | G | A | 3 | a0001c0001t0001g0036 a0001c0001t0001g0065 a0001c0001t0001g0308 |
3 | HG02015.hp1 NA18612.hp2 NA18939.hp1 |
intron_variant | MODIFIER | c.855+9115G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97450990 | |||||||
| chr9:97451058 | G | A | 1 | a0002c0002t0001g0133 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.856-9120G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97451058 | |||||||
| chr9:97451089 | A | G | 17 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0038 others(14): Show |
18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.856-9089A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97451089 | |||||||
| chr9:97451136 | G | GC | 2 | a0001c0001t0001g0004 a0001c0001t0001g0251 |
5 | NA18970.hp2 NA18971.hp2 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.856-9041dupC | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr9 | 97451136 | ||||||
| chr9:97451230 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.856-8948C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97451230 | |||||||
| chr9:97451283 | T | C | 1 | a0001c0001t0001g0084 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.856-8895T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97451283 | |||||||
| chr9:97451355 | T | C | 1 | a0001c0003t0001g0296 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.856-8823T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97451355 | |||||||
| chr9:97451439 | A | G | 1 | a0001c0001t0001g0020 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.856-8739A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97451439 | |||||||
| chr9:97451446 | C | A | 17 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0038 others(14): Show |
18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.856-8732C>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97451446 | |||||||
| chr9:97451530 | T | G | 17 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0038 others(14): Show |
18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.856-8648T>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97451530 | |||||||
| chr9:97451536 | C | A | 2 | a0001c0001t0001g0239 a0001c0001t0001g0243 |
2 | HG02622.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.856-8642C>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97451536 | |||||||
| chr9:97451563 | A | T | 1 | a0001c0009t0001g0306 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.856-8615A>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97451563 | |||||||
| chr9:97451819 | G | A | 17 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0038 others(14): Show |
18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.856-8359G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97451819 | |||||||
| chr9:97451860 | TTGAC | T | 17 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0038 others(14): Show |
18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.856-8314_856-8311d others(6): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr9 | 97451860 | ||||||
| chr9:97451880 | C | A | 1 | a0001c0001t0001g0102 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.856-8298C>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97451880 | |||||||
| chr9:97451887 | C | T | 17 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0038 others(14): Show |
18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.856-8291C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97451887 | |||||||
| chr9:97451920 | T | G | 1 | a0001c0001t0001g0034 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.856-8258T>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97451920 | |||||||
| chr9:97451921 | T | G | 1 | a0001c0004t0001g0104 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.856-8257T>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97451921 | |||||||
| chr9:97452104 | C | T | 1 | a0001c0001t0001g0020 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.856-8074C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97452104 | |||||||
| chr9:97452189 | G | T | 1 | a0001c0001t0001g0034 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.856-7989G>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97452189 | |||||||
| chr9:97452196 | G | A | 17 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0038 others(14): Show |
18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.856-7982G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97452196 | |||||||
| chr9:97452458 | A | G | 1 | a0001c0001t0001g0020 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.856-7720A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97452458 | |||||||
| chr9:97452565 | G | A | 179 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(176): Show |
204 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(201): Show |
intron_variant | MODIFIER | c.856-7613G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97452565 | |||||||
| chr9:97452626 | T | C | 1 | a0001c0001t0001g0090 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.856-7552T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97452626 | |||||||
| chr9:97452678 | G | A | 3 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0092 |
3 | HG02922.hp1 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.856-7500G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97452678 | |||||||
| chr9:97452800 | C | T | 3 | a0001c0001t0001g0025 a0001c0001t0001g0279 a0001c0001t0001g0280 |
4 | NA18941.hp1 NA18974.hp1 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.856-7378C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97452800 | |||||||
| chr9:97453025 | C | T | 2 | a0001c0001t0001g0097 a0008c0012t0001g0072 |
2 | NA19011.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.856-7153C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97453025 | |||||||
| chr9:97453139 | G | A | 138 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(135): Show |
159 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(156): Show |
intron_variant | MODIFIER | c.856-7039G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97453139 | |||||||
| chr9:97453145 | G | A | 1 | a0006c0014t0001g0113 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.856-7033G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97453145 | |||||||
| chr9:97453154 | A | C | 1 | a0001c0001t0001g0074 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.856-7024A>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97453154 | |||||||
| chr9:97453173 | C | T | 158 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(155): Show |
182 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(179): Show |
intron_variant | MODIFIER | c.856-7005C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97453173 | |||||||
| chr9:97453425 | T | C | 307 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(304): Show |
351 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(348): Show |
intron_variant | MODIFIER | c.856-6753T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97453425 | |||||||
| chr9:97453459 | T | G | 5 | a0002c0002t0001g0029 a0002c0002t0001g0030 a0002c0002t0001g0132 others(2): Show |
5 | HG02486.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.856-6719T>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97453459 | |||||||
| chr9:97453529 | T | G | 17 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0038 others(14): Show |
18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.856-6649T>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97453529 | |||||||
| chr9:97453676 | T | C | 62 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(59): Show |
70 | HG00438.hp1 HG00621.hp1 HG00673.hp2 others(67): Show |
intron_variant | MODIFIER | c.856-6502T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97453676 | |||||||
| chr9:97453677 | C | T | 1 | a0001c0015t0001g0031 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.856-6501C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97453677 | |||||||
| chr9:97453874 | A | G | 2 | a0002c0002t0001g0121 a0002c0002t0001g0129 |
2 | HG02155.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.856-6304A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97453874 | |||||||
| chr9:97454076 | A | G | 1 | a0001c0001t0001g0117 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.856-6102A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97454076 | |||||||
| chr9:97454128 | T | C | 1 | a0001c0001t0001g0252 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.856-6050T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97454128 | |||||||
| chr9:97454134 | G | A | 176 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(173): Show |
202 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(199): Show |
intron_variant | MODIFIER | c.856-6044G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97454134 | |||||||
| chr9:97454282 | C | T | 1 | a0001c0001t0001g0034 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.856-5896C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97454282 | |||||||
| chr9:97454285 | C | A | 2 | a0002c0002t0001g0026 a0002c0002t0004g0112 |
3 | HG02280.hp1 NA18522.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.856-5893C>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97454285 | |||||||
| chr9:97454429 | C | T | 1 | a0001c0001t0001g0011 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.856-5749C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97454429 | |||||||
| chr9:97454436 | G | A | 1 | a0001c0001t0001g0034 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.856-5742G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97454436 | |||||||
| chr9:97454480 | C | T | 1 | a0001c0004t0001g0303 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.856-5698C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97454480 | |||||||
| chr9:97454486 | AAGAG | A | 17 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0038 others(14): Show |
18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.856-5688_856-5685d others(6): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr9 | 97454486 | ||||||
| chr9:97454501 | G | A | 1 | a0002c0002t0001g0134 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.856-5677G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97454501 | |||||||
| chr9:97454749 | G | A | 140 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(137): Show |
162 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(159): Show |
intron_variant | MODIFIER | c.856-5429G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97454749 | |||||||
| chr9:97455024 | A | C | 17 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0038 others(14): Show |
18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.856-5154A>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97455024 | |||||||
| chr9:97455087 | A | T | 2 | a0003c0006t0001g0008 a0003c0006t0001g0037 |
3 | HG02976.hp1 HG03579.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.856-5091A>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97455087 | |||||||
| chr9:97455209 | G | A | 1 | a0001c0015t0001g0031 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.856-4969G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97455209 | |||||||
| chr9:97455519 | C | T | 1 | a0001c0015t0001g0031 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.856-4659C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97455519 | |||||||
| chr9:97455653 | T | G | 17 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0038 others(14): Show |
18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.856-4525T>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97455653 | |||||||
| chr9:97455994 | A | G | 2 | a0001c0001t0001g0034 a0001c0009t0001g0306 |
2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.856-4184A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97455994 | |||||||
| chr9:97456076 | C | T | 180 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(177): Show |
202 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(199): Show |
intron_variant | MODIFIER | c.856-4102C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97456076 | |||||||
| chr9:97456246 | T | C | 17 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0038 others(14): Show |
18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.856-3932T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97456246 | |||||||
| chr9:97456357 | T | A | 250 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(247): Show |
279 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(276): Show |
intron_variant | MODIFIER | c.856-3821T>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97456357 | |||||||
| chr9:97456441 | G | C | 17 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0038 others(14): Show |
18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.856-3737G>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97456441 | |||||||
| chr9:97456485 | G | C | 17 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0038 others(14): Show |
18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.856-3693G>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97456485 | |||||||
| chr9:97456705 | C | T | 1 | a0001c0001t0001g0274 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.856-3473C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97456705 | |||||||
| chr9:97456709 | C | T | 9 | a0002c0002t0001g0181 a0002c0002t0001g0225 a0002c0002t0002g0019 others(6): Show |
10 | HG01167.hp2 HG01934.hp2 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.856-3469C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97456709 | |||||||
| chr9:97456864 | C | T | 1 | a0002c0002t0001g0212 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.856-3314C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97456864 | |||||||
| chr9:97456909 | A | G | 1 | a0001c0009t0001g0306 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.856-3269A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97456909 | |||||||
| chr9:97457008 | G | A | 1 | a0002c0002t0001g0189 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.856-3170G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97457008 | |||||||
| chr9:97457195 | A | C | 1 | a0001c0001t0001g0078 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.856-2983A>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97457195 | |||||||
| chr9:97457198 | A | G | 1 | a0001c0003t0001g0047 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.856-2980A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97457198 | |||||||
| chr9:97457292 | C | T | 1 | a0002c0002t0001g0291 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.856-2886C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97457292 | |||||||
| chr9:97457387 | T | C | 176 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(173): Show |
201 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(198): Show |
intron_variant | MODIFIER | c.856-2791T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97457387 | |||||||
| chr9:97457388 | T | A | 5 | a0001c0009t0001g0306 a0002c0002t0001g0199 a0002c0002t0001g0200 others(2): Show |
5 | HG01081.hp2 HG01358.hp2 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.856-2790T>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97457388 | |||||||
| chr9:97457452 | C | T | 159 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(156): Show |
183 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(180): Show |
intron_variant | MODIFIER | c.856-2726C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97457452 | |||||||
| chr9:97457455 | T | G | 1 | a0001c0001t0001g0075 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.856-2723T>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97457455 | |||||||
| chr9:97457464 | T | C | 17 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0038 others(14): Show |
18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.856-2714T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97457464 | |||||||
| chr9:97457680 | A | G | 1 | a0001c0001t0001g0012 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.856-2498A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97457680 | |||||||
| chr9:97457776 | G | A | 62 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(59): Show |
70 | HG00438.hp1 HG00621.hp1 HG00673.hp2 others(67): Show |
intron_variant | MODIFIER | c.856-2402G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97457776 | |||||||
| chr9:97457820 | T | C | 180 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(177): Show |
206 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(203): Show |
intron_variant | MODIFIER | c.856-2358T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97457820 | |||||||
| chr9:97457928 | A | G | 73 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(70): Show |
87 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.856-2250A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97457928 | |||||||
| chr9:97457958 | A | T | 1 | a0001c0009t0001g0306 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.856-2220A>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97457958 | |||||||
| chr9:97457976 | C | A | 1 | a0002c0002t0001g0225 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.856-2202C>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97457976 | |||||||
| chr9:97458013 | A | G | 1 | a0002c0002t0001g0291 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.856-2165A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97458013 | |||||||
| chr9:97458061 | G | C | 17 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0038 others(14): Show |
18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.856-2117G>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97458061 | |||||||
| chr9:97458219 | G | A | 2 | a0001c0001t0001g0253 a0001c0001t0001g0254 |
2 | HG01175.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.856-1959G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97458219 | |||||||
| chr9:97458242 | G | A | 1 | a0002c0002t0001g0185 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.856-1936G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97458242 | |||||||
| chr9:97458306 | T | A | 1 | a0001c0009t0001g0306 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.856-1872T>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97458306 | |||||||
| chr9:97458341 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.856-1837G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97458341 | |||||||
| chr9:97458387 | T | C | 1 | a0001c0004t0001g0114 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.856-1791T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97458387 | |||||||
| chr9:97458524 | G | A | 249 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(246): Show |
278 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(275): Show |
intron_variant | MODIFIER | c.856-1654G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97458524 | |||||||
| chr9:97458539 | C | T | 17 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0038 others(14): Show |
18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.856-1639C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97458539 | |||||||
| chr9:97458849 | G | A | 173 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(170): Show |
197 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(194): Show |
intron_variant | MODIFIER | c.856-1329G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97458849 | |||||||
| chr9:97458877 | T | C | 2 | a0001c0001t0001g0307 a0001c0003t0001g0039 |
2 | HG02074.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.856-1301T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97458877 | |||||||
| chr9:97458921 | C | G | 2 | a0001c0001t0001g0052 a0001c0001t0001g0054 |
2 | HG01109.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.856-1257C>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97458921 | |||||||
| chr9:97459508 | T | G | 2 | a0003c0006t0001g0008 a0003c0006t0001g0037 |
3 | HG02976.hp1 HG03579.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.856-670T>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97459508 | |||||||
| chr9:97459680 | C | T | 2 | a0001c0001t0001g0052 a0001c0001t0001g0054 |
2 | HG01109.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.856-498C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97459680 | |||||||
| chr9:97459686 | A | G | 1 | a0002c0002t0001g0218 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.856-492A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97459686 | |||||||
| chr9:97459751 | G | T | 1 | a0001c0001t0001g0269 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.856-427G>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97459751 | |||||||
| chr9:97459752 | G | T | 1 | a0001c0001t0001g0269 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.856-426G>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97459752 | |||||||
| chr9:97459891 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.856-287G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97459891 | |||||||
| chr9:97460036 | G | A | 1 | a0001c0001t0001g0255 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.856-142G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97460036 | |||||||
| chr9:97460061 | C | A | 1 | a0002c0002t0001g0173 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.856-117C>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97460061 | |||||||
| chr9:97460815 | G | T | 1 | a0001c0001t0001g0254 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1442+51G>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | chr9 | 97460815 | |||||||
| chr9:97460868 | G | A | 1 | a0001c0001t0001g0256 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1442+104G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | chr9 | 97460868 | |||||||
| chr9:97461033 | C | T | 17 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0038 others(14): Show |
18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.1442+269C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | chr9 | 97461033 | |||||||
| chr9:97461048 | A | G | 17 | a0001c0003t0001g0033 a0001c0004t0001g0014 a0001c0004t0001g0027 others(14): Show |
19 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.1442+284A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | chr9 | 97461048 | |||||||
| chr9:97461140 | C | CAA | 17 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0038 others(14): Show |
18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.1442+389_1442+390d others(4): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr9 | 97461140 | ||||||
| chr9:97461157 | A | G | 1 | a0002c0002t0001g0209 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1442+393A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | chr9 | 97461157 | |||||||
| chr9:97461188 | T | C | 17 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0038 others(14): Show |
18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.1442+424T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | chr9 | 97461188 | |||||||
| chr9:97461197 | A | G | 3 | a0001c0001t0001g0268 a0001c0001t0001g0304 a0002c0002t0001g0168 |
3 | HG00438.hp2 HG00544.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.1442+433A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | chr9 | 97461197 | |||||||
| chr9:97461238 | A | G | 1 | a0001c0009t0001g0306 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1442+474A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | chr9 | 97461238 | |||||||
| chr9:97461296 | A | T | 17 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0038 others(14): Show |
18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.1442+532A>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | chr9 | 97461296 | |||||||
| chr9:97461351 | G | A | 1 | a0002c0002t0001g0174 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1442+587G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | chr9 | 97461351 | |||||||
| chr9:97461363 | A | C | 18 | a0001c0003t0001g0033 a0001c0004t0001g0014 a0001c0004t0001g0027 others(15): Show |
20 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1442+599A>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | chr9 | 97461363 | |||||||
| chr9:97461479 | CCAAAGGT others(17): Show |
C | 141 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(138): Show |
163 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(160): Show |
intron_variant | MODIFIER | c.1442+717_1442+740d others(26): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr9 | 97461479 | ||||||
| chr9:97461535 | A | G | 1 | a0001c0009t0001g0306 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1442+771A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | chr9 | 97461535 | |||||||
| chr9:97461639 | C | A | 17 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0038 others(14): Show |
18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.1442+875C>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | chr9 | 97461639 | |||||||
| chr9:97461930 | T | G | 17 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0038 others(14): Show |
18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.1442+1166T>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | chr9 | 97461930 | |||||||
| chr9:97462086 | C | T | 9 | a0002c0002t0001g0015 a0002c0002t0001g0124 a0002c0002t0001g0125 others(6): Show |
10 | HG00408.hp2 HG02015.hp2 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.1442+1322C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | chr9 | 97462086 | |||||||
| chr9:97462126 | T | C | 1 | a0001c0001t0001g0012 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1442+1362T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | chr9 | 97462126 | |||||||
| chr9:97462243 | C | G | 17 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0038 others(14): Show |
18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.1442+1479C>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | chr9 | 97462243 | |||||||
| chr9:97462313 | G | A | 17 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0038 others(14): Show |
18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.1442+1549G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | chr9 | 97462313 | |||||||
| chr9:97462475 | A | G | 1 | a0002c0002t0001g0208 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1442+1711A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | chr9 | 97462475 | |||||||
| chr9:97462505 | CT | C | 2 | a0003c0006t0001g0008 a0003c0006t0001g0037 |
3 | HG02976.hp1 HG03579.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1442+1742delT | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | chr9 | 97462505 | |||||||
| chr9:97462646 | T | G | 1 | a0001c0003t0001g0041 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1442+1882T>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | chr9 | 97462646 | |||||||
| chr9:97462701 | A | G | 1 | a0001c0009t0001g0306 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1442+1937A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | chr9 | 97462701 | |||||||
| chr9:97462758 | A | G | 1 | a0001c0001t0001g0074 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1442+1994A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | chr9 | 97462758 | |||||||
| chr9:97462963 | C | T | 17 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0038 others(14): Show |
18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.1443-1879C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | chr9 | 97462963 | |||||||
| chr9:97463019 | A | T | 1 | a0002c0002t0001g0198 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1443-1823A>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | chr9 | 97463019 | |||||||
| chr9:97463023 | G | T | 1 | a0001c0004t0001g0301 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1443-1819G>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | chr9 | 97463023 | |||||||
| chr9:97463244 | C | CA | 19 | a0001c0003t0001g0033 a0001c0004t0001g0014 a0001c0004t0001g0027 others(16): Show |
21 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.1443-1588dupA | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr9 | 97463244 | ||||||
| chr9:97463375 | G | GT | 12 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0039 others(9): Show |
13 | HG00408.hp1 HG02074.hp2 HG02132.hp2 others(10): Show |
intron_variant | MODIFIER | c.1443-1463dupT | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr9 | 97463375 | ||||||
| chr9:97463375 | G | GTT | 5 | a0001c0003t0001g0038 a0001c0003t0001g0044 a0001c0003t0001g0045 others(2): Show |
5 | HG00558.hp1 NA18984.hp2 NA18998.hp1 others(2): Show |
intron_variant | MODIFIER | c.1443-1464_1443-146 others(6): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr9 | 97463375 | ||||||
| chr9:97463380 | G | GT | 10 | a0001c0001t0001g0265 a0001c0001t0001g0266 a0001c0001t0001g0267 others(7): Show |
10 | HG01175.hp1 HG01496.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.1443-1445dupT | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr9 | 97463380 | ||||||
| chr9:97463380 | G | T | 19 | a0001c0001t0001g0171 a0001c0001t0001g0307 a0001c0003t0001g0009 others(16): Show |
20 | HG00408.hp1 HG00558.hp1 HG02015.hp2 others(17): Show |
intron_variant | MODIFIER | c.1443-1462G>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | chr9 | 97463380 | |||||||
| chr9:97463380 | GT | G | 7 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0095 others(4): Show |
7 | HG01952.hp1 HG02630.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.1443-1445delT | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr9 | 97463380 | ||||||
| chr9:97463608 | C | A | 3 | a0002c0002t0001g0015 a0002c0002t0001g0159 a0002c0002t0001g0160 |
4 | NA18953.hp2 NA18992.hp2 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.1443-1234C>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | chr9 | 97463608 | |||||||
| chr9:97463664 | C | T | 17 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0038 others(14): Show |
18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.1443-1178C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | chr9 | 97463664 | |||||||
| chr9:97463734 | G | A | 1 | a0005c0011t0001g0032 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1443-1108G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | chr9 | 97463734 | |||||||
| chr9:97463810 | G | C | 1 | a0001c0001t0001g0034 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1443-1032G>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | chr9 | 97463810 | |||||||
| chr9:97464154 | G | A | 17 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0038 others(14): Show |
18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.1443-688G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | chr9 | 97464154 | |||||||
| chr9:97464349 | G | A | 179 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(176): Show |
204 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(201): Show |
intron_variant | MODIFIER | c.1443-493G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | chr9 | 97464349 | |||||||
| chr9:97464653 | G | A | 1 | a0002c0002t0001g0147 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1443-189G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | chr9 | 97464653 | |||||||
| chr9:97464700 | G | A | 158 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(155): Show |
182 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(179): Show |
intron_variant | MODIFIER | c.1443-142G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | chr9 | 97464700 | |||||||
| chr9:97464729 | T | C | 176 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(173): Show |
201 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(198): Show |
intron_variant | MODIFIER | c.1443-113T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | chr9 | 97464729 | |||||||
| chr9:97464735 | T | C | 1 | a0001c0015t0001g0031 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1443-107T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | chr9 | 97464735 | |||||||
| chr9:97464761 | AAAG | A | 17 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0038 others(14): Show |
18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.1443-77_1443-75del others(3): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr9 | 97464761 | ||||||
| chr9:97465035 | A | G | 6 | a0001c0001t0001g0071 a0001c0001t0001g0074 a0001c0001t0001g0097 others(3): Show |
6 | HG04115.hp2 NA18960.hp2 NA18969.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.1629+7A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | chr9 | 97465035 | |||||||
| chr9:97465078 | A | G | 1 | a0002c0002t0001g0186 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1629+50A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | chr9 | 97465078 | |||||||
| chr9:97465141 | G | A | 141 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(138): Show |
163 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(160): Show |
intron_variant | MODIFIER | c.1629+113G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | chr9 | 97465141 | |||||||
| chr9:97465309 | A | G | 1 | a0002c0002t0001g0182 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1629+281A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | chr9 | 97465309 | |||||||
| chr9:97465370 | G | A | 17 | a0001c0003t0001g0033 a0001c0004t0001g0014 a0001c0004t0001g0027 others(14): Show |
19 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.1629+342G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | chr9 | 97465370 | |||||||
| chr9:97465694 | G | T | 1 | a0002c0002t0001g0123 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1629+666G>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | chr9 | 97465694 | |||||||
| chr9:97466112 | A | G | 1 | a0001c0001t0001g0264 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1629+1084A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | chr9 | 97466112 | |||||||
| chr9:97466333 | T | C | 1 | a0002c0002t0001g0218 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1629+1305T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | chr9 | 97466333 | |||||||
| chr9:97466451 | TA | T | 174 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(171): Show |
199 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(196): Show |
intron_variant | MODIFIER | c.1629+1425delA | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr9 | 97466451 | ||||||
| chr9:97466621 | A | G | 2 | a0001c0001t0001g0070 a0001c0001t0001g0078 |
2 | HG01975.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.1629+1593A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | chr9 | 97466621 | |||||||
| chr9:97466874 | A | T | 3 | a0002c0002t0001g0118 a0002c0002t0001g0119 a0002c0002t0001g0120 |
3 | HG01261.hp1 HG01496.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.1629+1846A>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | chr9 | 97466874 | |||||||
| chr9:97466990 | A | G | 71 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(68): Show |
85 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.1629+1962A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | chr9 | 97466990 | |||||||
| chr9:97467108 | A | G | 8 | a0002c0002t0001g0172 a0002c0002t0001g0173 a0002c0002t0001g0174 others(5): Show |
8 | HG01081.hp1 HG01243.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1629+2080A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | chr9 | 97467108 | |||||||
| chr9:97467115 | T | C | 1 | a0001c0015t0001g0031 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1629+2087T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | chr9 | 97467115 | |||||||
| chr9:97467124 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1629+2096G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | chr9 | 97467124 | |||||||
| chr9:97467273 | A | G | 2 | a0003c0006t0001g0008 a0003c0006t0001g0037 |
3 | HG02976.hp1 HG03579.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1629+2245A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | chr9 | 97467273 | |||||||
| chr9:97467293 | C | A | 176 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(173): Show |
201 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(198): Show |
intron_variant | MODIFIER | c.1629+2265C>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | chr9 | 97467293 | |||||||
| chr9:97467355 | C | A | 1 | a0001c0001t0001g0052 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1629+2327C>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | chr9 | 97467355 | |||||||
| chr9:97467486 | C | T | 17 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0038 others(14): Show |
18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.1629+2458C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | chr9 | 97467486 | |||||||
| chr9:97468120 | A | G | 1 | a0002c0002t0002g0224 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1630-2438A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | chr9 | 97468120 | |||||||
| chr9:97468124 | G | T | 1 | a0002c0002t0001g0172 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1630-2434G>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | chr9 | 97468124 | |||||||
| chr9:97468219 | C | T | 2 | a0003c0006t0001g0008 a0003c0006t0001g0037 |
3 | HG02976.hp1 HG03579.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1630-2339C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | chr9 | 97468219 | |||||||
| chr9:97468264 | G | A | 26 | a0001c0003t0001g0038 a0001c0003t0001g0042 a0002c0002t0001g0026 others(23): Show |
30 | HG00621.hp2 HG01167.hp2 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.1630-2294G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | chr9 | 97468264 | |||||||
| chr9:97468391 | C | T | 15 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0039 others(12): Show |
16 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(13): Show |
intron_variant | MODIFIER | c.1630-2167C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | chr9 | 97468391 | |||||||
| chr9:97468412 | T | C | 17 | a0001c0003t0001g0033 a0001c0004t0001g0014 a0001c0004t0001g0027 others(14): Show |
19 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.1630-2146T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | chr9 | 97468412 | |||||||
| chr9:97468496 | G | A | 2 | a0001c0001t0001g0034 a0001c0009t0001g0306 |
2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1630-2062G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | chr9 | 97468496 | |||||||
| chr9:97468512 | C | G | 1 | a0001c0001t0001g0076 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1630-2046C>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | chr9 | 97468512 | |||||||
| chr9:97468558 | G | A | 15 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0039 others(12): Show |
16 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(13): Show |
intron_variant | MODIFIER | c.1630-2000G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | chr9 | 97468558 | |||||||
| chr9:97468690 | C | T | 2 | a0002c0002t0001g0183 a0002c0002t0001g0210 |
2 | NA18977.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.1630-1868C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | chr9 | 97468690 | |||||||
| chr9:97468691 | G | A | 3 | a0001c0001t0001g0268 a0001c0001t0001g0304 a0002c0002t0001g0168 |
3 | HG00438.hp2 HG00544.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.1630-1867G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | chr9 | 97468691 | |||||||
| chr9:97468854 | G | A | 1 | a0001c0001t0001g0248 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1630-1704G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | chr9 | 97468854 | |||||||
| chr9:97469136 | C | T | 1 | a0001c0001t0001g0238 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1630-1422C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | chr9 | 97469136 | |||||||
| chr9:97469318 | A | G | 1 | a0001c0001t0001g0024 | 2 | HG00558.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.1630-1240A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | chr9 | 97469318 | |||||||
| chr9:97469459 | T | C | 1 | a0001c0001t0001g0271 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1630-1099T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | chr9 | 97469459 | |||||||
| chr9:97469862 | T | G | 180 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(177): Show |
206 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(203): Show |
intron_variant | MODIFIER | c.1630-696T>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | chr9 | 97469862 | |||||||
| chr9:97470035 | G | A | 1 | a0001c0015t0001g0031 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1630-523G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | chr9 | 97470035 | |||||||
| chr9:97470107 | C | A | 1 | a0002c0002t0001g0136 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1630-451C>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | chr9 | 97470107 | |||||||
| chr9:97470175 | A | G | 1 | a0001c0001t0001g0088 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1630-383A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | chr9 | 97470175 | |||||||
| chr9:97470315 | C | T | 1 | a0001c0003t0001g0049 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1630-243C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | chr9 | 97470315 | |||||||
| chr9:97470359 | T | C | 17 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0038 others(14): Show |
18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.1630-199T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | chr9 | 97470359 | |||||||
| chr9:97470864 | T | C | 4 | a0002c0002t0001g0175 a0002c0002t0001g0176 a0002c0002t0001g0177 others(1): Show |
4 | HG01243.hp1 HG02818.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1741+195T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 9/16 | chr9 | 97470864 | |||||||
| chr9:97470874 | C | T | 2 | a0002c0002t0001g0131 a0002c0002t0001g0155 |
2 | HG00639.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.1741+205C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 9/16 | chr9 | 97470874 | |||||||
| chr9:97470907 | C | T | 141 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(138): Show |
163 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(160): Show |
intron_variant | MODIFIER | c.1741+238C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 9/16 | chr9 | 97470907 | |||||||
| chr9:97471040 | T | G | 179 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(176): Show |
204 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(201): Show |
intron_variant | MODIFIER | c.1741+371T>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 9/16 | chr9 | 97471040 | |||||||
| chr9:97471058 | A | G | 1 | a0001c0001t0001g0180 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1741+389A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 9/16 | chr9 | 97471058 | |||||||
| chr9:97471080 | A | G | 17 | a0001c0003t0001g0033 a0001c0004t0001g0014 a0001c0004t0001g0027 others(14): Show |
19 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.1741+411A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 9/16 | chr9 | 97471080 | |||||||
| chr9:97471113 | A | G | 3 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0092 |
3 | HG02922.hp1 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1741+444A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 9/16 | chr9 | 97471113 | |||||||
| chr9:97471241 | C | T | 179 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(176): Show |
204 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(201): Show |
intron_variant | MODIFIER | c.1741+572C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 9/16 | chr9 | 97471241 | |||||||
| chr9:97471336 | T | G | 1 | a0001c0001t0001g0258 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1741+667T>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 9/16 | chr9 | 97471336 | |||||||
| chr9:97471355 | C | T | 2 | a0003c0006t0001g0008 a0003c0006t0001g0037 |
3 | HG02976.hp1 HG03579.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1741+686C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 9/16 | chr9 | 97471355 | |||||||
| chr9:97471363 | G | T | 1 | a0001c0001t0001g0034 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1741+694G>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 9/16 | chr9 | 97471363 | |||||||
| chr9:97471570 | A | T | 17 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0038 others(14): Show |
18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.1742-723A>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 9/16 | chr9 | 97471570 | |||||||
| chr9:97472064 | G | T | 1 | a0002c0002t0001g0146 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1742-229G>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 9/16 | chr9 | 97472064 | |||||||
| chr9:97472119 | T | G | 141 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(138): Show |
164 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(161): Show |
intron_variant | MODIFIER | c.1742-174T>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 9/16 | chr9 | 97472119 | |||||||
| chr9:97472263 | G | A | 17 | a0001c0003t0001g0033 a0001c0004t0001g0014 a0001c0004t0001g0027 others(14): Show |
19 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.1742-30G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 9/16 | chr9 | 97472263 | |||||||
| chr9:97472265 | A | C | 1 | a0001c0009t0001g0306 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1742-28A>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 9/16 | chr9 | 97472265 | |||||||
| chr9:97472753 | A | T | 136 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(133): Show |
157 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(154): Show |
intron_variant | MODIFIER | c.1944+258A>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 10/16 | chr9 | 97472753 | |||||||
| chr9:97473435 | A | G | 1 | a0001c0003t0001g0033 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1945-57A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 10/16 | chr9 | 97473435 | |||||||
| chr9:97473445 | T | G | 2 | a0002c0002t0001g0190 a0002c0002t0001g0191 |
2 | HG01346.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.1945-47T>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 10/16 | chr9 | 97473445 | |||||||
| chr9:97473835 | G | A | 10 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0238 others(7): Show |
14 | NA18941.hp1 NA18954.hp1 NA18967.hp2 others(11): Show |
intron_variant | MODIFIER | c.2079+209G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 11/16 | chr9 | 97473835 | |||||||
| chr9:97473866 | C | T | 1 | a0001c0005t0001g0107 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2079+240C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 11/16 | chr9 | 97473866 | |||||||
| chr9:97473871 | G | C | 1 | a0005c0011t0001g0032 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2079+245G>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 11/16 | chr9 | 97473871 | |||||||
| chr9:97474181 | T | A | 17 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0038 others(14): Show |
18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.2079+555T>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 11/16 | chr9 | 97474181 | |||||||
| chr9:97474193 | T | G | 3 | a0001c0001t0001g0036 a0001c0001t0001g0065 a0001c0001t0001g0308 |
3 | HG02015.hp1 NA18612.hp2 NA18939.hp1 |
intron_variant | MODIFIER | c.2079+567T>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 11/16 | chr9 | 97474193 | |||||||
| chr9:97474453 | C | T | 1 | a0001c0001t0001g0255 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2079+827C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 11/16 | chr9 | 97474453 | |||||||
| chr9:97474464 | C | T | 17 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0038 others(14): Show |
18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.2079+838C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 11/16 | chr9 | 97474464 | |||||||
| chr9:97474471 | T | C | 17 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0038 others(14): Show |
18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.2079+845T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 11/16 | chr9 | 97474471 | |||||||
| chr9:97474523 | G | A | 15 | a0001c0004t0001g0014 a0001c0004t0001g0027 a0001c0004t0001g0104 others(12): Show |
17 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.2080-860G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 11/16 | chr9 | 97474523 | |||||||
| chr9:97474551 | G | A | 1 | a0001c0001t0001g0274 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2080-832G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 11/16 | chr9 | 97474551 | |||||||
| chr9:97474756 | A | C | 1 | a0002c0002t0001g0191 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.2080-627A>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 11/16 | chr9 | 97474756 | |||||||
| chr9:97474905 | A | G | 1 | a0002c0002t0001g0125 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2080-478A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 11/16 | chr9 | 97474905 | |||||||
| chr9:97475023 | A | G | 2 | a0001c0001t0001g0089 a0001c0001t0001g0094 |
2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2080-360A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 11/16 | chr9 | 97475023 | |||||||
| chr9:97475066 | A | G | 3 | a0001c0001t0001g0023 a0001c0001t0001g0247 a0001c0001t0001g0281 |
4 | NA18747.hp2 NA18942.hp1 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.2080-317A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 11/16 | chr9 | 97475066 | |||||||
| chr9:97475115 | A | G | 17 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0038 others(14): Show |
18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.2080-268A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 11/16 | chr9 | 97475115 | |||||||
| chr9:97475237 | C | T | 3 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0092 |
3 | HG02922.hp1 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2080-146C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 11/16 | chr9 | 97475237 | |||||||
| chr9:97475244 | T | C | 3 | a0001c0001t0001g0180 a0001c0001t0001g0234 a0001c0001t0001g0236 |
3 | HG02145.hp1 HG02717.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2080-139T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 11/16 | chr9 | 97475244 | |||||||
| chr9:97475491 | T | G | 1 | a0001c0001t0001g0278 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.2166+22T>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 12/16 | chr9 | 97475491 | |||||||
| chr9:97475535 | G | GT | 15 | a0001c0004t0001g0014 a0001c0004t0001g0027 a0001c0004t0001g0104 others(12): Show |
17 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.2166+73dupT | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr9 | 97475535 | ||||||
| chr9:97475757 | T | A | 1 | a0001c0001t0001g0271 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2166+288T>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 12/16 | chr9 | 97475757 | |||||||
| chr9:97475762 | T | C | 17 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0038 others(14): Show |
18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.2166+293T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 12/16 | chr9 | 97475762 | |||||||
| chr9:97475858 | G | A | 177 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(174): Show |
203 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(200): Show |
intron_variant | MODIFIER | c.2166+389G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 12/16 | chr9 | 97475858 | |||||||
| chr9:97476028 | C | G | 1 | a0002c0002t0001g0177 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2166+559C>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 12/16 | chr9 | 97476028 | |||||||
| chr9:97476028 | C | T | 2 | a0002c0002t0001g0026 a0002c0002t0004g0112 |
3 | HG02280.hp1 NA18522.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2166+559C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 12/16 | chr9 | 97476028 | |||||||
| chr9:97476236 | C | A | 2 | a0002c0002t0001g0026 a0002c0002t0004g0112 |
3 | HG02280.hp1 NA18522.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2166+767C>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 12/16 | chr9 | 97476236 | |||||||
| chr9:97476271 | G | A | 1 | a0001c0001t0001g0261 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2166+802G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 12/16 | chr9 | 97476271 | |||||||
| chr9:97476369 | G | A | 1 | a0001c0004t0001g0014 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.2166+900G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 12/16 | chr9 | 97476369 | |||||||
| chr9:97476394 | A | G | 17 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0038 others(14): Show |
18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.2166+925A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 12/16 | chr9 | 97476394 | |||||||
| chr9:97476564 | G | GA | 158 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(155): Show |
183 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(180): Show |
intron_variant | MODIFIER | c.2166+1109dupA | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr9 | 97476564 | ||||||
| chr9:97476564 | G | GAA | 19 | a0001c0001t0001g0071 a0001c0001t0001g0098 a0001c0001t0001g0307 others(16): Show |
20 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(17): Show |
intron_variant | MODIFIER | c.2166+1108_2166+110 others(6): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr9 | 97476564 | ||||||
| chr9:97476595 | T | G | 1 | a0002c0002t0001g0202 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2166+1126T>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 12/16 | chr9 | 97476595 | |||||||
| chr9:97476806 | C | T | 4 | a0001c0005t0001g0107 a0001c0005t0001g0297 a0001c0005t0001g0298 others(1): Show |
4 | HG02280.hp2 HG02717.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.2166+1337C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 12/16 | chr9 | 97476806 | |||||||
| chr9:97476852 | A | T | 1 | a0001c0001t0001g0069 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2166+1383A>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 12/16 | chr9 | 97476852 | |||||||
| chr9:97476934 | T | C | 1 | a0001c0001t0001g0069 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2166+1465T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 12/16 | chr9 | 97476934 | |||||||
| chr9:97477213 | A | G | 6 | a0001c0003t0001g0009 a0001c0003t0001g0041 a0001c0003t0001g0043 others(3): Show |
7 | HG00408.hp1 HG02132.hp2 HG02165.hp1 others(4): Show |
intron_variant | MODIFIER | c.2167-1226A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 12/16 | chr9 | 97477213 | |||||||
| chr9:97477368 | C | T | 154 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(151): Show |
178 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(175): Show |
intron_variant | MODIFIER | c.2167-1071C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 12/16 | chr9 | 97477368 | |||||||
| chr9:97477885 | C | G | 1 | a0001c0001t0001g0280 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2167-554C>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 12/16 | chr9 | 97477885 | |||||||
| chr9:97477923 | A | G | 1 | a0001c0003t0001g0041 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2167-516A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 12/16 | chr9 | 97477923 | |||||||
| chr9:97477987 | G | A | 1 | a0001c0009t0001g0306 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2167-452G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 12/16 | chr9 | 97477987 | |||||||
| chr9:97477989 | T | C | 1 | a0002c0002t0001g0193 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2167-450T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 12/16 | chr9 | 97477989 | |||||||
| chr9:97478004 | A | T | 1 | a0002c0002t0002g0288 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2167-435A>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 12/16 | chr9 | 97478004 | |||||||
| chr9:97478125 | G | C | 17 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0038 others(14): Show |
18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.2167-314G>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 12/16 | chr9 | 97478125 | |||||||
| chr9:97478158 | G | A | 1 | a0002c0002t0001g0168 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2167-281G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 12/16 | chr9 | 97478158 | |||||||
| chr9:97478309 | G | A | 15 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0039 others(12): Show |
16 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(13): Show |
intron_variant | MODIFIER | c.2167-130G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 12/16 | chr9 | 97478309 | |||||||
| chr9:97478733 | T | C | 1 | a0001c0001t0001g0078 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2301+160T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 13/16 | chr9 | 97478733 | |||||||
| chr9:97478997 | A | G | 1 | a0001c0015t0001g0031 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2301+424A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 13/16 | chr9 | 97478997 | |||||||
| chr9:97480183 | C | A | 1 | a0002c0002t0001g0137 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2302-645C>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 13/16 | chr9 | 97480183 | |||||||
| chr9:97480427 | A | ATT | 16 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0038 others(13): Show |
17 | HG00558.hp1 HG02074.hp2 HG02132.hp2 others(14): Show |
intron_variant | MODIFIER | c.2302-387_2302-386d others(4): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr9 | 97480427 | ||||||
| chr9:97480481 | C | A | 1 | a0002c0002t0001g0168 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2302-347C>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 13/16 | chr9 | 97480481 | |||||||
| chr9:97480518 | C | T | 17 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0038 others(14): Show |
18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.2302-310C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 13/16 | chr9 | 97480518 | |||||||
| chr9:97481026 | C | T | 1 | a0005c0011t0001g0032 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2412+88C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 14/16 | chr9 | 97481026 | |||||||
| chr9:97481137 | T | C | 1 | a0002c0002t0001g0187 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2412+199T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 14/16 | chr9 | 97481137 | |||||||
| chr9:97481405 | A | G | 15 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0039 others(12): Show |
16 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(13): Show |
intron_variant | MODIFIER | c.2412+467A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 14/16 | chr9 | 97481405 | |||||||
| chr9:97481413 | T | A | 1 | a0005c0011t0001g0032 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2412+475T>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 14/16 | chr9 | 97481413 | |||||||
| chr9:97481503 | GT | G | 15 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0039 others(12): Show |
16 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(13): Show |
intron_variant | MODIFIER | c.2412+570delT | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr9 | 97481503 | ||||||
| chr9:97481567 | C | T | 9 | a0002c0002t0001g0015 a0002c0002t0001g0124 a0002c0002t0001g0125 others(6): Show |
10 | HG00408.hp2 HG02015.hp2 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.2412+629C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 14/16 | chr9 | 97481567 | |||||||
| chr9:97481889 | G | A | 271 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(268): Show |
304 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(301): Show |
intron_variant | MODIFIER | c.2412+951G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 14/16 | chr9 | 97481889 | |||||||
| chr9:97481958 | C | T | 1 | a0002c0002t0001g0185 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2413-891C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 14/16 | chr9 | 97481958 | |||||||
| chr9:97482106 | G | A | 15 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0039 others(12): Show |
16 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(13): Show |
intron_variant | MODIFIER | c.2413-743G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 14/16 | chr9 | 97482106 | |||||||
| chr9:97482176 | A | G | 1 | a0002c0002t0001g0056 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2413-673A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 14/16 | chr9 | 97482176 | |||||||
| chr9:97482235 | G | A | 1 | a0001c0003t0001g0044 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2413-614G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 14/16 | chr9 | 97482235 | |||||||
| chr9:97482253 | C | T | 1 | a0002c0002t0001g0194 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.2413-596C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 14/16 | chr9 | 97482253 | |||||||
| chr9:97482519 | C | T | 20 | a0001c0001t0001g0180 a0001c0003t0001g0033 a0001c0004t0001g0014 others(17): Show |
22 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.2413-330C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 14/16 | chr9 | 97482519 | |||||||
| chr9:97482520 | G | A | 4 | a0002c0002t0001g0121 a0002c0002t0001g0129 a0002c0002t0001g0130 others(1): Show |
4 | HG02155.hp2 NA18954.hp2 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.2413-329G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 14/16 | chr9 | 97482520 | |||||||
| chr9:97482547 | A | G | 1 | a0002c0002t0002g0166 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.2413-302A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 14/16 | chr9 | 97482547 | |||||||
| chr9:97482550 | A | G | 1 | a0001c0001t0001g0034 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2413-299A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 14/16 | chr9 | 97482550 | |||||||
| chr9:97482732 | G | A | 1 | a0001c0001t0001g0262 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2413-117G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 14/16 | chr9 | 97482732 | |||||||
| chr9:97483371 | A | T | 1 | a0002c0002t0001g0215 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.2915+20A>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 15/16 | chr9 | 97483371 | |||||||
| chr9:97483402 | A | G | 1 | a0002c0002t0001g0215 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.2915+51A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 15/16 | chr9 | 97483402 | |||||||
| chr9:97483438 | C | T | 1 | a0001c0003t0001g0048 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.2915+87C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 15/16 | chr9 | 97483438 | |||||||
| chr9:97483558 | A | G | 2 | a0001c0001t0001g0004 a0001c0001t0001g0251 |
5 | NA18970.hp2 NA18971.hp2 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.2915+207A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 15/16 | chr9 | 97483558 | |||||||
| chr9:97484469 | A | AAC | 4 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0002c0002t0001g0126 others(1): Show |
4 | HG02683.hp2 HG04204.hp1 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.2915+1141_2915+114 others(6): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr9 | 97484469 | ||||||
| chr9:97484469 | AAC | A | 17 | a0001c0003t0001g0033 a0001c0004t0001g0014 a0001c0004t0001g0027 others(14): Show |
19 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.2915+1141_2915+114 others(6): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr9 | 97484469 | ||||||
| chr9:97484485 | C | G | 1 | a0002c0002t0001g0174 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2915+1134C>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 15/16 | chr9 | 97484485 | |||||||
| chr9:97484488 | A | C | 1 | a0001c0001t0001g0012 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.2915+1137A>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 15/16 | chr9 | 97484488 | |||||||
| chr9:97484490 | A | C | 61 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(58): Show |
69 | HG00438.hp1 HG00621.hp1 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.2915+1139A>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 15/16 | chr9 | 97484490 | |||||||
| chr9:97484492 | A | ACC | 9 | a0001c0001t0001g0108 a0001c0001t0001g0164 a0001c0001t0001g0165 others(6): Show |
9 | HG01175.hp2 HG01255.hp1 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.2915+1144_2915+114 others(6): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr9 | 97484492 | ||||||
| chr9:97484492 | A | C | 146 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(143): Show |
170 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(167): Show |
intron_variant | MODIFIER | c.2915+1141A>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 15/16 | chr9 | 97484492 | |||||||
| chr9:97484604 | A | G | 1 | a0002c0002t0001g0193 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2915+1253A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 15/16 | chr9 | 97484604 | |||||||
| chr9:97484652 | C | T | 17 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0038 others(14): Show |
18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.2915+1301C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 15/16 | chr9 | 97484652 | |||||||
| chr9:97484722 | A | G | 1 | a0002c0002t0001g0160 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.2915+1371A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 15/16 | chr9 | 97484722 | |||||||
| chr9:97484850 | G | C | 1 | a0001c0003t0001g0040 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2915+1499G>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 15/16 | chr9 | 97484850 | |||||||
| chr9:97485000 | C | A | 1 | a0001c0001t0001g0101 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2915+1649C>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 15/16 | chr9 | 97485000 | |||||||
| chr9:97485038 | T | A | 1 | a0001c0001t0001g0101 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2915+1687T>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 15/16 | chr9 | 97485038 | |||||||
| chr9:97485045 | A | T | 1 | a0002c0002t0001g0225 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.2915+1694A>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 15/16 | chr9 | 97485045 | |||||||
| chr9:97485442 | C | G | 1 | a0001c0001t0001g0076 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2916-1730C>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 15/16 | chr9 | 97485442 | |||||||
| chr9:97485583 | C | T | 1 | a0001c0001t0001g0068 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2916-1589C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 15/16 | chr9 | 97485583 | |||||||
| chr9:97485715 | A | G | 4 | a0002c0002t0001g0121 a0002c0002t0001g0129 a0002c0002t0001g0130 others(1): Show |
4 | HG02155.hp2 NA18954.hp2 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.2916-1457A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 15/16 | chr9 | 97485715 | |||||||
| chr9:97485760 | A | G | 1 | a0002c0002t0002g0288 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2916-1412A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 15/16 | chr9 | 97485760 | |||||||
| chr9:97485875 | C | T | 17 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0038 others(14): Show |
18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.2916-1297C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 15/16 | chr9 | 97485875 | |||||||
| chr9:97485960 | G | A | 1 | a0001c0001t0001g0068 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2916-1212G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 15/16 | chr9 | 97485960 | |||||||
| chr9:97486037 | G | A | 15 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0039 others(12): Show |
16 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(13): Show |
intron_variant | MODIFIER | c.2916-1135G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 15/16 | chr9 | 97486037 | |||||||
| chr9:97486196 | A | G | 1 | a0001c0001t0001g0020 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.2916-976A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 15/16 | chr9 | 97486196 | |||||||
| chr9:97486242 | T | C | 1 | a0002c0002t0001g0203 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2916-930T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 15/16 | chr9 | 97486242 | |||||||
| chr9:97486637 | A | G | 16 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0038 others(13): Show |
17 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(14): Show |
intron_variant | MODIFIER | c.2916-535A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 15/16 | chr9 | 97486637 | |||||||
| chr9:97486647 | C | G | 2 | a0002c0002t0001g0122 a0002c0002t0001g0216 |
2 | HG02698.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.2916-525C>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 15/16 | chr9 | 97486647 | |||||||
| chr9:97486879 | A | C | 1 | a0001c0001t0001g0273 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2916-293A>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 15/16 | chr9 | 97486879 | |||||||
| chr9:97486879 | A | G | 1 | a0002c0002t0001g0152 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2916-293A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 15/16 | chr9 | 97486879 | |||||||
| chr9:97487048 | G | A | 15 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0039 others(12): Show |
16 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(13): Show |
intron_variant | MODIFIER | c.2916-124G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 15/16 | chr9 | 97487048 | |||||||
| chr9:97487442 | G | A | 1 | a0002c0002t0001g0059 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.3076+110G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97487442 | |||||||
| chr9:97487471 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3076+139C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97487471 | |||||||
| chr9:97487548 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.3076+216C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97487548 | |||||||
| chr9:97487641 | G | A | 174 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(171): Show |
198 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(195): Show |
intron_variant | MODIFIER | c.3076+309G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97487641 | |||||||
| chr9:97487678 | G | T | 17 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0038 others(14): Show |
18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.3076+346G>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97487678 | |||||||
| chr9:97487679 | T | A | 1 | a0001c0001t0001g0088 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3076+347T>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97487679 | |||||||
| chr9:97487681 | C | CTACTTGT others(1): Show |
15 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0039 others(12): Show |
16 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(13): Show |
intron_variant | MODIFIER | c.3076+351_3076+358d others(10): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 97487681 | ||||||
| chr9:97487694 | A | T | 1 | a0001c0003t0001g0046 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.3076+362A>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97487694 | |||||||
| chr9:97487877 | A | T | 159 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(156): Show |
182 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(179): Show |
intron_variant | MODIFIER | c.3076+545A>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97487877 | |||||||
| chr9:97488329 | A | G | 1 | a0002c0002t0001g0128 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.3076+997A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97488329 | |||||||
| chr9:97488465 | A | G | 1 | a0001c0001t0001g0248 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.3076+1133A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97488465 | |||||||
| chr9:97488560 | G | GT | 115 | a0001c0001t0001g0088 a0001c0001t0001g0272 a0001c0001t0001g0307 others(112): Show |
135 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.3076+1247dupT | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 97488560 | ||||||
| chr9:97488560 | G | GTT | 21 | a0001c0003t0001g0045 a0001c0003t0001g0050 a0002c0002t0001g0120 others(18): Show |
21 | HG00621.hp2 HG01109.hp2 HG01261.hp1 others(18): Show |
intron_variant | MODIFIER | c.3076+1246_3076+124 others(6): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 97488560 | ||||||
| chr9:97488560 | GT | G | 142 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(139): Show |
164 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(161): Show |
intron_variant | MODIFIER | c.3076+1247delT | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 97488560 | ||||||
| chr9:97488568 | T | G | 140 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(137): Show |
161 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(158): Show |
intron_variant | MODIFIER | c.3076+1236T>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97488568 | |||||||
| chr9:97488572 | T | G | 141 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(138): Show |
162 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(159): Show |
intron_variant | MODIFIER | c.3076+1240T>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97488572 | |||||||
| chr9:97488574 | T | G | 1 | a0001c0004t0001g0105 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.3076+1242T>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97488574 | |||||||
| chr9:97488575 | T | G | 3 | a0001c0005t0001g0298 a0003c0006t0001g0008 a0003c0006t0001g0037 |
4 | HG02976.hp1 HG03486.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.3076+1243T>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97488575 | |||||||
| chr9:97488576 | T | G | 141 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(138): Show |
162 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(159): Show |
intron_variant | MODIFIER | c.3076+1244T>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97488576 | |||||||
| chr9:97488580 | G | T | 5 | a0001c0009t0001g0306 a0002c0002t0001g0141 a0002c0002t0001g0145 others(2): Show |
5 | HG01891.hp1 HG02615.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.3076+1248G>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97488580 | |||||||
| chr9:97488602 | G | A | 3 | a0001c0005t0001g0298 a0003c0006t0001g0008 a0003c0006t0001g0037 |
4 | HG02976.hp1 HG03486.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.3076+1270G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97488602 | |||||||
| chr9:97488640 | T | C | 1 | a0001c0001t0001g0011 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.3076+1308T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97488640 | |||||||
| chr9:97488744 | G | A | 6 | a0001c0001t0001g0007 a0001c0001t0001g0117 a0001c0001t0001g0257 others(3): Show |
8 | HG00741.hp2 HG01106.hp1 HG01123.hp1 others(5): Show |
intron_variant | MODIFIER | c.3076+1412G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97488744 | |||||||
| chr9:97488833 | C | T | 1 | a0001c0001t0001g0012 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.3076+1501C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97488833 | |||||||
| chr9:97489068 | C | T | 1 | a0002c0002t0001g0125 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.3076+1736C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97489068 | |||||||
| chr9:97489081 | G | A | 1 | a0001c0001t0001g0278 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.3076+1749G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97489081 | |||||||
| chr9:97489130 | G | C | 1 | a0001c0001t0001g0284 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3076+1798G>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97489130 | |||||||
| chr9:97489173 | G | A | 3 | a0002c0002t0001g0199 a0002c0002t0001g0200 a0002c0002t0001g0205 |
3 | HG00323.hp2 HG02683.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.3076+1841G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97489173 | |||||||
| chr9:97489293 | A | G | 1 | a0002c0002t0001g0135 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.3076+1961A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97489293 | |||||||
| chr9:97489506 | C | T | 1 | a0002c0002t0001g0150 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3076+2174C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97489506 | |||||||
| chr9:97489754 | G | T | 2 | a0002c0002t0001g0018 a0002c0002t0002g0292 |
3 | HG02818.hp2 HG03098.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3076+2422G>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97489754 | |||||||
| chr9:97489786 | C | G | 2 | a0001c0001t0001g0162 a0001c0001t0001g0163 |
2 | NA18948.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.3076+2454C>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97489786 | |||||||
| chr9:97489986 | CA | C | 14 | a0001c0001t0001g0036 a0001c0001t0001g0062 a0001c0001t0001g0064 others(11): Show |
14 | HG01070.hp1 HG01261.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.3076+2655delA | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97489986 | |||||||
| chr9:97490011 | G | C | 181 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(178): Show |
207 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(204): Show |
intron_variant | MODIFIER | c.3076+2679G>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97490011 | |||||||
| chr9:97490031 | C | T | 1 | a0001c0001t0001g0273 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3076+2699C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97490031 | |||||||
| chr9:97490034 | G | GCACACA | 15 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0039 others(12): Show |
16 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(13): Show |
intron_variant | MODIFIER | c.3076+2712_3076+271 others(10): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 97490034 | ||||||
| chr9:97490061 | C | G | 1 | a0002c0002t0001g0137 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.3076+2729C>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97490061 | |||||||
| chr9:97490068 | A | G | 1 | a0001c0004t0001g0114 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3076+2736A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97490068 | |||||||
| chr9:97490158 | C | A | 2 | a0002c0002t0001g0010 a0002c0002t0001g0057 |
3 | NA19055.hp1 NA19068.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.3076+2826C>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97490158 | |||||||
| chr9:97490439 | T | C | 161 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(158): Show |
185 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(182): Show |
intron_variant | MODIFIER | c.3076+3107T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97490439 | |||||||
| chr9:97490471 | G | T | 17 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0038 others(14): Show |
18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.3076+3139G>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97490471 | |||||||
| chr9:97490549 | T | TG | 72 | a0001c0001t0001g0012 a0001c0001t0001g0054 a0001c0001t0001g0070 others(69): Show |
78 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.3076+3228dupG | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 97490549 | ||||||
| chr9:97490553 | G | T | 5 | a0001c0001t0001g0071 a0001c0001t0001g0097 a0001c0001t0001g0098 others(2): Show |
5 | NA18960.hp2 NA18969.hp1 NA19005.hp1 others(2): Show |
intron_variant | MODIFIER | c.3076+3221G>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97490553 | |||||||
| chr9:97490557 | G | C | 1 | a0001c0003t0001g0033 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3076+3225G>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97490557 | |||||||
| chr9:97490559 | G | A | 1 | a0002c0002t0001g0137 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.3076+3227G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97490559 | |||||||
| chr9:97490572 | C | T | 1 | a0001c0001t0001g0230 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.3076+3240C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97490572 | |||||||
| chr9:97490576 | G | A | 1 | a0001c0015t0001g0031 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3076+3244G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97490576 | |||||||
| chr9:97490610 | G | T | 2 | a0002c0002t0003g0214 a0002c0002t0003g0219 |
2 | NA19078.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.3076+3278G>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97490610 | |||||||
| chr9:97490634 | C | T | 1 | a0002c0002t0001g0197 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.3076+3302C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97490634 | |||||||
| chr9:97490872 | G | T | 2 | a0002c0002t0001g0290 a0002c0002t0001g0291 |
2 | HG01256.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.3076+3540G>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97490872 | |||||||
| chr9:97490904 | CTTTTCT | C | 14 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0039 others(11): Show |
15 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.3076+3577_3076+358 others(10): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 97490904 | ||||||
| chr9:97490909 | C | CT | 54 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(51): Show |
57 | HG00438.hp1 HG00621.hp2 HG01167.hp2 others(54): Show |
intron_variant | MODIFIER | c.3076+3601dupT | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 97490909 | ||||||
| chr9:97490909 | CT | C | 6 | a0001c0001t0001g0249 a0001c0001t0001g0274 a0001c0001t0001g0285 others(3): Show |
6 | HG00323.hp2 HG01123.hp1 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.3076+3601delT | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 97490909 | ||||||
| chr9:97491139 | A | G | 24 | a0001c0001t0001g0255 a0001c0001t0001g0307 a0001c0003t0001g0009 others(21): Show |
25 | HG00323.hp2 HG00408.hp1 HG00558.hp1 others(22): Show |
intron_variant | MODIFIER | c.3076+3807A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97491139 | |||||||
| chr9:97491372 | C | A | 1 | a0005c0011t0001g0032 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3076+4040C>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97491372 | |||||||
| chr9:97491376 | A | G | 1 | a0001c0001t0001g0274 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3076+4044A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97491376 | |||||||
| chr9:97491445 | T | C | 3 | a0001c0005t0001g0298 a0003c0006t0001g0008 a0003c0006t0001g0037 |
4 | HG02976.hp1 HG03486.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.3076+4113T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97491445 | |||||||
| chr9:97491537 | A | G | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
160 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(157): Show |
intron_variant | MODIFIER | c.3077-4126A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97491537 | |||||||
| chr9:97491539 | G | A | 1 | a0001c0005t0001g0298 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3077-4124G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97491539 | |||||||
| chr9:97491570 | T | C | 4 | a0002c0002t0001g0059 a0002c0002t0003g0006 a0002c0002t0003g0213 others(1): Show |
6 | NA18941.hp2 NA18962.hp2 NA18974.hp2 others(3): Show |
intron_variant | MODIFIER | c.3077-4093T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97491570 | |||||||
| chr9:97491914 | A | C | 2 | a0001c0001t0001g0082 a0001c0001t0001g0083 |
2 | HG01952.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.3077-3749A>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97491914 | |||||||
| chr9:97492206 | A | G | 2 | a0002c0002t0001g0194 a0002c0002t0001g0198 |
2 | HG01981.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.3077-3457A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97492206 | |||||||
| chr9:97492403 | T | C | 18 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0038 others(15): Show |
19 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(16): Show |
intron_variant | MODIFIER | c.3077-3260T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97492403 | |||||||
| chr9:97492568 | A | C | 2 | a0001c0001t0001g0070 a0001c0001t0001g0078 |
2 | HG01975.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.3077-3095A>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97492568 | |||||||
| chr9:97492808 | C | T | 1 | a0001c0001t0001g0258 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.3077-2855C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97492808 | |||||||
| chr9:97493093 | T | C | 1 | a0001c0001t0001g0075 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.3077-2570T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97493093 | |||||||
| chr9:97493140 | C | T | 9 | a0001c0001t0001g0021 a0001c0001t0001g0233 a0001c0001t0001g0239 others(6): Show |
10 | HG02572.hp2 HG02622.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.3077-2523C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97493140 | |||||||
| chr9:97493164 | G | A | 140 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(137): Show |
161 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(158): Show |
intron_variant | MODIFIER | c.3077-2499G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97493164 | |||||||
| chr9:97493248 | T | C | 1 | a0001c0003t0001g0046 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.3077-2415T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97493248 | |||||||
| chr9:97493272 | C | T | 4 | a0001c0001t0001g0180 a0001c0005t0001g0298 a0003c0006t0001g0008 others(1): Show |
5 | HG02976.hp1 HG03139.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.3077-2391C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97493272 | |||||||
| chr9:97493277 | G | A | 2 | a0002c0002t0001g0010 a0002c0002t0001g0217 |
3 | HG01433.hp1 NA19068.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.3077-2386G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97493277 | |||||||
| chr9:97493321 | A | G | 2 | a0001c0001t0001g0108 a0001c0001t0001g0109 |
2 | HG01255.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.3077-2342A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97493321 | |||||||
| chr9:97493334 | G | A | 17 | a0001c0001t0001g0034 a0001c0003t0001g0033 a0001c0004t0001g0014 others(14): Show |
19 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.3077-2329G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97493334 | |||||||
| chr9:97493393 | G | A | 1 | a0002c0002t0001g0128 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.3077-2270G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97493393 | |||||||
| chr9:97493424 | A | G | 1 | a0001c0001t0001g0022 | 2 | HG01099.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.3077-2239A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97493424 | |||||||
| chr9:97493426 | T | C | 1 | a0001c0001t0001g0022 | 2 | HG01099.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.3077-2237T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97493426 | |||||||
| chr9:97493571 | C | T | 14 | a0001c0004t0001g0014 a0001c0004t0001g0027 a0001c0004t0001g0104 others(11): Show |
16 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.3077-2092C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97493571 | |||||||
| chr9:97493681 | G | A | 1 | a0002c0002t0001g0193 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3077-1982G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97493681 | |||||||
| chr9:97493814 | C | T | 1 | a0002c0002t0001g0058 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.3077-1849C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97493814 | |||||||
| chr9:97493867 | C | T | 1 | a0001c0001t0001g0279 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.3077-1796C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97493867 | |||||||
| chr9:97493904 | T | C | 1 | a0001c0001t0001g0269 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.3077-1759T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97493904 | |||||||
| chr9:97493916 | A | G | 1 | a0002c0002t0001g0150 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3077-1747A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97493916 | |||||||
| chr9:97493944 | G | T | 2 | a0001c0001t0001g0253 a0001c0001t0001g0254 |
2 | HG01175.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.3077-1719G>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97493944 | |||||||
| chr9:97494000 | A | G | 18 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0038 others(15): Show |
19 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(16): Show |
intron_variant | MODIFIER | c.3077-1663A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97494000 | |||||||
| chr9:97494002 | C | T | 1 | a0002c0002t0001g0150 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3077-1661C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97494002 | |||||||
| chr9:97494091 | A | G | 13 | a0001c0003t0001g0009 a0001c0003t0001g0041 a0001c0003t0001g0043 others(10): Show |
14 | HG00408.hp1 HG00558.hp1 HG02132.hp2 others(11): Show |
intron_variant | MODIFIER | c.3077-1572A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97494091 | |||||||
| chr9:97494147 | A | G | 2 | a0001c0001t0001g0098 a0001c0001t0001g0099 |
2 | NA18969.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.3077-1516A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97494147 | |||||||
| chr9:97494178 | A | C | 267 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(264): Show |
300 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(297): Show |
intron_variant | MODIFIER | c.3077-1485A>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97494178 | |||||||
| chr9:97494178 | A | T | 3 | a0001c0001t0001g0089 a0001c0001t0001g0094 a0001c0001t0001g0095 |
3 | HG02109.hp2 HG02970.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.3077-1485A>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97494178 | |||||||
| chr9:97494327 | T | A | 2 | a0001c0001t0001g0080 a0001c0001t0001g0081 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.3077-1336T>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97494327 | |||||||
| chr9:97494360 | G | A | 1 | a0001c0001t0001g0065 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.3077-1303G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97494360 | |||||||
| chr9:97494392 | C | T | 4 | a0002c0002t0001g0196 a0002c0002t0002g0019 a0002c0002t0002g0221 others(1): Show |
5 | HG01167.hp2 HG01934.hp1 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.3077-1271C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97494392 | |||||||
| chr9:97494694 | GTA | G | 11 | a0001c0003t0001g0033 a0001c0004t0001g0027 a0001c0004t0001g0114 others(8): Show |
12 | HG01891.hp2 HG02145.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.3077-951_3077-950d others(4): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 97494694 | ||||||
| chr9:97494698 | A | ATATATAT others(7): Show |
4 | a0001c0004t0001g0014 a0001c0004t0001g0104 a0001c0004t0001g0105 others(1): Show |
5 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.3077-952_3077-951i others(16): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 97494698 | ||||||
| chr9:97494709 | TATA | T | 6 | a0001c0005t0001g0298 a0001c0009t0001g0306 a0002c0002t0001g0150 others(3): Show |
7 | HG02630.hp2 HG02723.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.3077-953_3077-951d others(5): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97494709 | |||||||
| chr9:97494710 | A | T | 8 | a0001c0001t0001g0060 a0001c0001t0001g0070 a0001c0001t0001g0076 others(5): Show |
8 | HG00438.hp2 HG00544.hp2 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.3077-953A>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97494710 | |||||||
| chr9:97494712 | A | T | 167 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(164): Show |
187 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(184): Show |
intron_variant | MODIFIER | c.3077-951A>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97494712 | |||||||
| chr9:97494712 | ATTTTT | A | 13 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0039 others(10): Show |
14 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(11): Show |
intron_variant | MODIFIER | c.3077-942_3077-938d others(7): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 97494712 | ||||||
| chr9:97494714 | T | A | 9 | a0001c0004t0001g0014 a0001c0004t0001g0104 a0001c0004t0001g0105 others(6): Show |
10 | HG00639.hp1 HG00673.hp1 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.3077-949T>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97494714 | |||||||
| chr9:97494722 | T | C | 7 | a0001c0001t0001g0052 a0001c0005t0001g0298 a0001c0009t0001g0306 others(4): Show |
8 | HG01109.hp1 HG02630.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.3077-941T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97494722 | |||||||
| chr9:97494723 | T | G | 7 | a0001c0001t0001g0052 a0001c0005t0001g0298 a0001c0009t0001g0306 others(4): Show |
8 | HG01109.hp1 HG02630.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.3077-940T>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97494723 | |||||||
| chr9:97494724 | T | A | 7 | a0001c0001t0001g0052 a0001c0005t0001g0298 a0001c0009t0001g0306 others(4): Show |
8 | HG01109.hp1 HG02630.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.3077-939T>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97494724 | |||||||
| chr9:97494724 | T | C | 194 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(191): Show |
220 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(217): Show |
intron_variant | MODIFIER | c.3077-939T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97494724 | |||||||
| chr9:97494724 | T | TC | 14 | a0001c0001t0001g0023 a0001c0001t0001g0081 a0001c0001t0001g0237 others(11): Show |
15 | HG00639.hp2 HG02683.hp2 HG02970.hp2 others(12): Show |
intron_variant | MODIFIER | c.3077-939_3077-938i others(3): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97494724 | |||||||
| chr9:97494725 | T | G | 215 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(212): Show |
243 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(240): Show |
intron_variant | MODIFIER | c.3077-938T>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97494725 | |||||||
| chr9:97494726 | C | A | 215 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(212): Show |
243 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(240): Show |
intron_variant | MODIFIER | c.3077-937C>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97494726 | |||||||
| chr9:97494726 | C | CGA | 9 | a0001c0001t0001g0034 a0001c0001t0001g0233 a0001c0001t0001g0240 others(6): Show |
10 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.3077-933_3077-932d others(4): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 97494726 | ||||||
| chr9:97494729 | G | GAC | 16 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0039 others(13): Show |
17 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(14): Show |
intron_variant | MODIFIER | c.3077-933_3077-932i others(4): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 97494729 | ||||||
| chr9:97494738 | A | ATTTTGTC others(3): Show |
1 | a0005c0011t0001g0032 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3077-925_3077-924i others(12): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97494738 | |||||||
| chr9:97494781 | G | A | 1 | a0001c0015t0001g0031 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3077-882G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97494781 | |||||||
| chr9:97494814 | G | A | 1 | a0001c0015t0001g0031 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3077-849G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97494814 | |||||||
| chr9:97494871 | C | T | 16 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0039 others(13): Show |
17 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(14): Show |
intron_variant | MODIFIER | c.3077-792C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97494871 | |||||||
| chr9:97494923 | C | T | 1 | a0002c0002t0001g0189 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.3077-740C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97494923 | |||||||
| chr9:97494930 | C | T | 1 | a0001c0001t0001g0265 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.3077-733C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97494930 | |||||||
| chr9:97494931 | G | A | 1 | a0001c0003t0001g0051 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.3077-732G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97494931 | |||||||
| chr9:97495068 | T | G | 1 | a0002c0002t0001g0140 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.3077-595T>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97495068 | |||||||
| chr9:97495130 | T | C | 22 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0039 others(19): Show |
24 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(21): Show |
intron_variant | MODIFIER | c.3077-533T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97495130 | |||||||
| chr9:97495139 | A | G | 180 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(177): Show |
206 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(203): Show |
intron_variant | MODIFIER | c.3077-524A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97495139 | |||||||
| chr9:97495332 | T | C | 16 | a0001c0001t0001g0307 a0001c0003t0001g0009 a0001c0003t0001g0039 others(13): Show |
17 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(14): Show |
intron_variant | MODIFIER | c.3077-331T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97495332 | |||||||
| chr9:97495336 | TATTTTAT others(17): Show |
T | 1 | a0001c0001t0001g0067 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3077-326_3077-303d others(26): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97495336 | |||||||
| chr9:97495375 | A | G | 1 | a0001c0001t0001g0063 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3077-288A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97495375 |