Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 163589 |
| ensemblid | ENSG00000162782.16 |
| hgncid | 20614 |
| symbol | TDRD5 |
| name | tudor domain containing 5 |
| refseq_nuc | NM_001199085.3 |
| refseq_prot | NP_001186014.1 |
| ensembl_nuc | ENST00000444136.6 |
| ensembl_prot | ENSP00000406052.1 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 179591832 |
| end | 179691272 |
| strand | + |
| ver | v1.2 |
| region | chr1:179591832-179691272 |
| region5000 | chr1:179586832-179696272 |
| regionname0 | TDRD5_chr1_179591832_179691272 |
| regionname5000 | TDRD5_chr1_179586832_179696272 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 1035 | 162 | 54 | 32 | 56 | 6 | 13 | 42 | TDRD5_chr1_179586832_179696272 | TDRD5 | MSEQE others(1030): Show |
chr1 | 179586832 | 179696272 |
| a0002 | 0/0 | 1035 | 109 | 5 | 32 | 55 | 4 | 13 | 40 | TDRD5_chr1_179586832_179696272 | TDRD5 | MSEQE others(1030): Show |
chr1 | 179586832 | 179696272 |
| a0003 | 0/0 | 1035 | 33 | 14 | 1 | 17 | 0 | 1 | 16 | TDRD5_chr1_179586832_179696272 | TDRD5 | MSEQE others(1030): Show |
chr1 | 179586832 | 179696272 |
| a0004 | 0/1 | 1035 | 29 | 0 | 6 | 16 | 2 | 4 | 14 | TDRD5_chr1_179586832_179696272 | TDRD5 | MSEQE others(1030): Show |
chr1 | 179586832 | 179696272 |
| a0005 | 0/0 | 1035 | 29 | 5 | 4 | 20 | 0 | 0 | 13 | TDRD5_chr1_179586832_179696272 | TDRD5 | MSEQE others(1030): Show |
chr1 | 179586832 | 179696272 |
| a0006 | 0/0 | 1035 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | MSEQE others(1030): Show |
chr1 | 179586832 | 179696272 |
| a0007 | 0/0 | 1035 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | MSEQE others(1030): Show |
chr1 | 179586832 | 179696272 |
| a0008 | 0/0 | 1035 | 2 | 0 | 0 | 0 | 2 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | MSEQE others(1030): Show |
chr1 | 179586832 | 179696272 |
| a0009 | 0/0 | 1035 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | MSEQE others(1030): Show |
chr1 | 179586832 | 179696272 |
| a0010 | 0/0 | 1035 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | MSEQE others(1030): Show |
chr1 | 179586832 | 179696272 |
| a0011 | 0/0 | 1035 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | MSEQE others(1030): Show |
chr1 | 179586832 | 179696272 |
| a0012 | 0/0 | 1035 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | MSEQE others(1030): Show |
chr1 | 179586832 | 179696272 |
| a0013 | 0/0 | 1035 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | MSEQE others(1030): Show |
chr1 | 179586832 | 179696272 |
| a0014 | 0/0 | 1035 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | MSEQE others(1030): Show |
chr1 | 179586832 | 179696272 |
| a0015 | 0/0 | 1035 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TDRD5_chr1_179586832_179696272 | TDRD5 | MSEQE others(1030): Show |
chr1 | 179586832 | 179696272 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 3105 | 135 | 32 | 28 | 56 | 6 | 13 | TDRD5_chr1_179586832_179696272 | TDRD5 | ATGTC others(3100): Show |
chr1 | 179586832 | 179696272 | ||
| a0001c0005 | 0/0 | 3105 | 16 | 15 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | ATGTC others(3100): Show |
chr1 | 179586832 | 179696272 | ||
| a0001c0008 | 1/0 | 3105 | 5 | 3 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | ATGTC others(3100): Show |
chr1 | 179586832 | 179696272 | ||
| a0001c0013 | 0/0 | 3105 | 3 | 2 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | ATGTC others(3100): Show |
chr1 | 179586832 | 179696272 | ||
| a0001c0019 | 0/0 | 3105 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | ATGTC others(3100): Show |
chr1 | 179586832 | 179696272 | ||
| a0001c0022 | 0/0 | 3105 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | ATGTC others(3100): Show |
chr1 | 179586832 | 179696272 | ||
| a0001c0023 | 0/0 | 3105 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | ATGTC others(3100): Show |
chr1 | 179586832 | 179696272 | ||
| a0002c0002 | 0/0 | 3105 | 109 | 5 | 32 | 55 | 4 | 13 | TDRD5_chr1_179586832_179696272 | TDRD5 | ATGTC others(3100): Show |
chr1 | 179586832 | 179696272 | ||
| a0003c0003 | 0/0 | 3105 | 33 | 14 | 1 | 17 | 0 | 1 | TDRD5_chr1_179586832_179696272 | TDRD5 | ATGTC others(3100): Show |
chr1 | 179586832 | 179696272 | ||
| a0004c0004 | 0/1 | 3105 | 29 | 0 | 6 | 16 | 2 | 4 | TDRD5_chr1_179586832_179696272 | TDRD5 | ATGTC others(3100): Show |
chr1 | 179586832 | 179696272 | ||
| a0005c0006 | 0/0 | 3105 | 13 | 0 | 0 | 13 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | ATGTC others(3100): Show |
chr1 | 179586832 | 179696272 | ||
| a0005c0007 | 0/0 | 3105 | 9 | 1 | 1 | 7 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | ATGTC others(3100): Show |
chr1 | 179586832 | 179696272 | ||
| a0005c0011 | 0/0 | 3105 | 4 | 4 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | ATGTC others(3100): Show |
chr1 | 179586832 | 179696272 | ||
| a0005c0012 | 0/0 | 3105 | 3 | 0 | 3 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | ATGTC others(3100): Show |
chr1 | 179586832 | 179696272 | ||
| a0006c0009 | 0/0 | 3105 | 5 | 5 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | ATGTC others(3100): Show |
chr1 | 179586832 | 179696272 | ||
| a0007c0010 | 0/0 | 3105 | 4 | 3 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | ATGTC others(3100): Show |
chr1 | 179586832 | 179696272 | ||
| a0008c0015 | 0/0 | 3105 | 2 | 0 | 0 | 0 | 2 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | ATGTC others(3100): Show |
chr1 | 179586832 | 179696272 | ||
| a0009c0014 | 0/0 | 3105 | 2 | 2 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | ATGTC others(3100): Show |
chr1 | 179586832 | 179696272 | ||
| a0010c0016 | 0/0 | 3105 | 2 | 2 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | ATGTC others(3100): Show |
chr1 | 179586832 | 179696272 | ||
| a0011c0017 | 0/0 | 3105 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | ATGTC others(3100): Show |
chr1 | 179586832 | 179696272 | ||
| a0012c0024 | 0/0 | 3105 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | ATGTC others(3100): Show |
chr1 | 179586832 | 179696272 | ||
| a0013c0020 | 0/0 | 3105 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | ATGTC others(3100): Show |
chr1 | 179586832 | 179696272 | ||
| a0014c0018 | 0/0 | 3105 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD5_chr1_179586832_179696272 | TDRD5 | ATGTC others(3100): Show |
chr1 | 179586832 | 179696272 | ||
| a0015c0021 | 0/0 | 3105 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | ATGTC others(3100): Show |
chr1 | 179586832 | 179696272 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3745 | 134 | 31 | 28 | 56 | 6 | 13 | TDRD5_chr1_179586832_179696272 | TDRD5 | AGGCG others(3740): Show |
chr1 | 179586832 | 179696272 |
| a0001c0001t0002 | 0/0 | 3745 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | AGGCG others(3740): Show |
chr1 | 179586832 | 179696272 |
| a0001c0005t0001 | 0/0 | 3745 | 16 | 15 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | AGGCG others(3740): Show |
chr1 | 179586832 | 179696272 |
| a0001c0008t0001 | 1/0 | 3745 | 5 | 3 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | AGGCG others(3740): Show |
chr1 | 179586832 | 179696272 |
| a0001c0013t0001 | 0/0 | 3745 | 3 | 2 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | AGGCG others(3740): Show |
chr1 | 179586832 | 179696272 |
| a0001c0019t0001 | 0/0 | 3745 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | AGGCG others(3740): Show |
chr1 | 179586832 | 179696272 |
| a0001c0022t0001 | 0/0 | 3745 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | AGGCG others(3740): Show |
chr1 | 179586832 | 179696272 |
| a0001c0023t0001 | 0/0 | 3745 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | AGGCG others(3740): Show |
chr1 | 179586832 | 179696272 |
| a0002c0002t0001 | 0/0 | 3745 | 8 | 1 | 5 | 0 | 2 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | AGGCG others(3740): Show |
chr1 | 179586832 | 179696272 |
| a0002c0002t0002 | 0/0 | 3745 | 101 | 4 | 27 | 55 | 2 | 13 | TDRD5_chr1_179586832_179696272 | TDRD5 | AGGCG others(3740): Show |
chr1 | 179586832 | 179696272 |
| a0003c0003t0001 | 0/0 | 3745 | 32 | 14 | 1 | 16 | 0 | 1 | TDRD5_chr1_179586832_179696272 | TDRD5 | AGGCG others(3740): Show |
chr1 | 179586832 | 179696272 |
| a0003c0003t0004 | 0/0 | 3751 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | AGGCG others(3746): Show |
chr1 | 179586832 | 179696272 |
| a0004c0004t0001 | 0/1 | 3745 | 29 | 0 | 6 | 16 | 2 | 4 | TDRD5_chr1_179586832_179696272 | TDRD5 | AGGCG others(3740): Show |
chr1 | 179586832 | 179696272 |
| a0005c0006t0001 | 0/0 | 3745 | 11 | 0 | 0 | 11 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | AGGCG others(3740): Show |
chr1 | 179586832 | 179696272 |
| a0005c0006t0002 | 0/0 | 3745 | 2 | 0 | 0 | 2 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | AGGCG others(3740): Show |
chr1 | 179586832 | 179696272 |
| a0005c0007t0001 | 0/0 | 3745 | 9 | 1 | 1 | 7 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | AGGCG others(3740): Show |
chr1 | 179586832 | 179696272 |
| a0005c0011t0003 | 0/0 | 3745 | 4 | 4 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | AGGCG others(3740): Show |
chr1 | 179586832 | 179696272 |
| a0005c0012t0001 | 0/0 | 3745 | 3 | 0 | 3 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | AGGCG others(3740): Show |
chr1 | 179586832 | 179696272 |
| a0006c0009t0001 | 0/0 | 3745 | 5 | 5 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | AGGCG others(3740): Show |
chr1 | 179586832 | 179696272 |
| a0007c0010t0001 | 0/0 | 3745 | 4 | 3 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | AGGCG others(3740): Show |
chr1 | 179586832 | 179696272 |
| a0008c0015t0002 | 0/0 | 3745 | 2 | 0 | 0 | 0 | 2 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | AGGCG others(3740): Show |
chr1 | 179586832 | 179696272 |
| a0009c0014t0001 | 0/0 | 3745 | 2 | 2 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | AGGCG others(3740): Show |
chr1 | 179586832 | 179696272 |
| a0010c0016t0001 | 0/0 | 3745 | 2 | 2 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | AGGCG others(3740): Show |
chr1 | 179586832 | 179696272 |
| a0011c0017t0002 | 0/0 | 3745 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | AGGCG others(3740): Show |
chr1 | 179586832 | 179696272 |
| a0012c0024t0001 | 0/0 | 3745 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | AGGCG others(3740): Show |
chr1 | 179586832 | 179696272 |
| a0013c0020t0001 | 0/0 | 3745 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | AGGCG others(3740): Show |
chr1 | 179586832 | 179696272 |
| a0014c0018t0001 | 0/0 | 3745 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD5_chr1_179586832_179696272 | TDRD5 | AGGCG others(3740): Show |
chr1 | 179586832 | 179696272 |
| a0015c0021t0001 | 0/0 | 3745 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | AGGCG others(3740): Show |
chr1 | 179586832 | 179696272 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0001g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0005t0001g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0005t0001g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0005t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0005t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0005t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0005t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0005t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0005t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0005t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0005t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0005t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0008t0001g0056 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0008t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0008t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0008t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0008t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0013t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0013t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0013t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0019t0001g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0022t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0001c0023t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0002c0002t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0003c0003t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0003c0003t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0003c0003t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0003c0003t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0003c0003t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0003c0003t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0003c0003t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0003c0003t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0003c0003t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0003c0003t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0003c0003t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0003c0003t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0003c0003t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0003c0003t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0003c0003t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0003c0003t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0003c0003t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0003c0003t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0003c0003t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0003c0003t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0003c0003t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0003c0003t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0003c0003t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0003c0003t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0003c0003t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0003c0003t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0003c0003t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0003c0003t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0003c0003t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0003c0003t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0003c0003t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0003c0003t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0003c0003t0004g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0004c0004t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0004c0004t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0004c0004t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0004c0004t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0004c0004t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0004c0004t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0004c0004t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0004c0004t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0004c0004t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0004c0004t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0004c0004t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0004c0004t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0004c0004t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0004c0004t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0004c0004t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0004c0004t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0004c0004t0001g0034 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0004c0004t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0004c0004t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0004c0004t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0004c0004t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0004c0004t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0004c0004t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0004c0004t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0004c0004t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0004c0004t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0004c0004t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0004c0004t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0004c0004t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0005c0006t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0005c0006t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0005c0006t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0005c0006t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0005c0006t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0005c0006t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0005c0006t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0005c0006t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0005c0006t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0005c0006t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0005c0006t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0005c0006t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0005c0006t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0005c0007t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0005c0007t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0005c0007t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0005c0007t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0005c0007t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0005c0007t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0005c0007t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0005c0007t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0005c0007t0001g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0005c0011t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0005c0011t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0005c0011t0003g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0005c0011t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0005c0012t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0005c0012t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0005c0012t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0006c0009t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0006c0009t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0006c0009t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0006c0009t0001g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0006c0009t0001g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0007c0010t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0007c0010t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0007c0010t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0007c0010t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0008c0015t0002g0006 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0009c0014t0001g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0009c0014t0001g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0010c0016t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0010c0016t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0011c0017t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0012c0024t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0013c0020t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0014c0018t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| a0015c0021t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0332 | EUR | GBR | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG00099 | hp2 | a0002 | c0002 | t0002 | g0099 | EUR | GBR | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0188 | EUR | GBR | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG00140 | hp2 | a0002 | c0002 | t0001 | g0252 | EUR | GBR | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0295 | EUR | FIN | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG00280 | hp2 | a0004 | c0004 | t0001 | g0040 | EUR | FIN | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG00408 | hp1 | a0002 | c0002 | t0002 | g0172 | EAS | CHS | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | CHS | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG00423 | hp1 | a0003 | c0003 | t0001 | g0053 | EAS | CHS | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG00423 | hp2 | a0002 | c0002 | t0002 | g0141 | EAS | CHS | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG00544 | hp1 | a0005 | c0006 | t0001 | g0263 | EAS | CHS | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG00544 | hp2 | a0004 | c0004 | t0001 | g0016 | EAS | CHS | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0358 | EAS | CHS | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0350 | EAS | CHS | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG00597 | hp1 | a0005 | c0006 | t0001 | g0215 | EAS | CHS | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG00597 | hp2 | a0002 | c0002 | t0002 | g0171 | EAS | CHS | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG00609 | hp1 | a0002 | c0002 | t0002 | g0122 | EAS | CHS | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG00609 | hp2 | a0004 | c0004 | t0001 | g0022 | EAS | CHS | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG00621 | hp1 | a0002 | c0002 | t0002 | g0111 | EAS | CHS | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | CHS | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0249 | AMR | PUR | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0331 | AMR | PUR | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0329 | EAS | CHS | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG00673 | hp2 | a0011 | c0017 | t0002 | g0168 | EAS | CHS | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG00733 | hp1 | a0004 | c0004 | t0001 | g0028 | AMR | PUR | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG00733 | hp2 | a0002 | c0002 | t0001 | g0248 | AMR | PUR | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG00735 | hp2 | a0005 | c0012 | t0001 | g0255 | AMR | PUR | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG00741 | hp1 | a0001 | c0019 | t0001 | g0334 | AMR | PUR | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG00741 | hp2 | a0002 | c0002 | t0002 | g0175 | AMR | PUR | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG01069 | hp1 | a0001 | c0008 | t0001 | g0068 | AMR | PUR | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG01070 | hp1 | a0005 | c0007 | t0001 | g0253 | AMR | PUR | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG01070 | hp2 | a0002 | c0002 | t0002 | g0011 | AMR | PUR | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG01071 | hp1 | a0002 | c0002 | t0002 | g0011 | AMR | PUR | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG01074 | hp1 | a0002 | c0002 | t0002 | g0138 | AMR | PUR | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0359 | AMR | PUR | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0337 | AMR | PUR | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG01081 | hp2 | a0002 | c0002 | t0002 | g0101 | AMR | PUR | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG01099 | hp1 | a0007 | c0010 | t0001 | g0259 | AMR | PUR | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG01099 | hp2 | a0002 | c0002 | t0002 | g0140 | AMR | PUR | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | PUR | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG01106 | hp2 | a0002 | c0002 | t0002 | g0147 | AMR | PUR | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG01109 | hp1 | a0005 | c0012 | t0001 | g0256 | AMR | PUR | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0341 | AMR | PUR | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG01167 | hp1 | a0004 | c0004 | t0001 | g0020 | AMR | PUR | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG01167 | hp2 | a0002 | c0002 | t0002 | g0004 | AMR | PUR | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG01168 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | PUR | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG01169 | hp2 | a0002 | c0002 | t0002 | g0004 | AMR | PUR | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG01175 | hp1 | a0002 | c0002 | t0001 | g0251 | AMR | PUR | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG01175 | hp2 | a0004 | c0004 | t0001 | g0021 | AMR | PUR | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG01192 | hp1 | a0003 | c0003 | t0001 | g0065 | AMR | PUR | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG01192 | hp2 | a0002 | c0002 | t0002 | g0014 | AMR | PUR | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG01243 | hp1 | a0002 | c0002 | t0002 | g0154 | AMR | PUR | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG01243 | hp2 | a0001 | c0013 | t0001 | g0245 | AMR | PUR | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0288 | AMR | CLM | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG01255 | hp2 | a0002 | c0002 | t0002 | g0005 | AMR | CLM | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | CLM | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG01256 | hp2 | a0002 | c0002 | t0002 | g0005 | AMR | CLM | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG01257 | hp1 | a0002 | c0002 | t0002 | g0145 | AMR | CLM | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0347 | AMR | CLM | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG01258 | hp1 | a0002 | c0002 | t0002 | g0118 | AMR | CLM | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | CLM | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG01261 | hp1 | a0002 | c0002 | t0002 | g0102 | AMR | CLM | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0320 | AMR | CLM | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG01346 | hp1 | a0001 | c0005 | t0001 | g0229 | AMR | CLM | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG01346 | hp2 | a0002 | c0002 | t0001 | g0176 | AMR | CLM | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG01358 | hp1 | a0002 | c0002 | t0002 | g0146 | AMR | CLM | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG01358 | hp2 | a0004 | c0004 | t0001 | g0029 | AMR | CLM | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0348 | AMR | CLM | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG01361 | hp2 | a0004 | c0004 | t0001 | g0033 | AMR | CLM | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | CLM | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG01433 | hp2 | a0002 | c0002 | t0001 | g0246 | AMR | CLM | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG01496 | hp1 | a0002 | c0002 | t0002 | g0100 | AMR | CLM | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0270 | AMR | CLM | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0250 | EUR | IBS | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0321 | EUR | IBS | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG01516 | hp1 | a0004 | c0004 | t0001 | g0017 | EUR | IBS | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG01516 | hp2 | a0008 | c0015 | t0002 | g0006 | EUR | IBS | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG01517 | hp1 | a0008 | c0015 | t0002 | g0006 | EUR | IBS | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0322 | EUR | IBS | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG01884 | hp1 | a0002 | c0002 | t0002 | g0130 | AFR | ACB | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG01884 | hp2 | a0009 | c0014 | t0001 | g0365 | AFR | ACB | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG01891 | hp2 | a0002 | c0002 | t0002 | g0289 | AFR | ACB | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0285 | AMR | PEL | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG01928 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | PEL | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | PEL | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG01934 | hp2 | a0002 | c0002 | t0002 | g0165 | AMR | PEL | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0345 | AMR | PEL | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | PEL | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG01978 | hp1 | a0002 | c0002 | t0002 | g0148 | AMR | PEL | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG01978 | hp2 | a0005 | c0012 | t0001 | g0254 | AMR | PEL | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG01981 | hp1 | a0002 | c0002 | t0002 | g0151 | AMR | PEL | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0346 | AMR | PEL | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0280 | AMR | PEL | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG01993 | hp2 | a0002 | c0002 | t0002 | g0103 | AMR | PEL | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02004 | hp1 | a0002 | c0002 | t0002 | g0173 | AMR | PEL | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PEL | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | KHV | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02015 | hp2 | a0005 | c0006 | t0001 | g0216 | EAS | KHV | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02027 | hp1 | a0005 | c0006 | t0001 | g0218 | EAS | KHV | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02027 | hp2 | a0002 | c0002 | t0002 | g0162 | EAS | KHV | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | KHV | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02040 | hp2 | a0002 | c0002 | t0002 | g0242 | EAS | KHV | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | ACB | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02055 | hp2 | a0001 | c0005 | t0001 | g0232 | AFR | ACB | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02071 | hp1 | a0012 | c0024 | t0001 | g0272 | EAS | KHV | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02071 | hp2 | a0002 | c0002 | t0002 | g0161 | EAS | KHV | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0357 | EAS | KHV | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02080 | hp2 | a0002 | c0002 | t0002 | g0120 | EAS | KHV | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | KHV | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02129 | hp2 | a0002 | c0002 | t0002 | g0125 | EAS | KHV | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02132 | hp1 | a0005 | c0006 | t0001 | g0206 | EAS | KHV | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | KHV | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | KHV | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02135 | hp2 | a0002 | c0002 | t0002 | g0240 | EAS | KHV | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0339 | AFR | ACB | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | ACB | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02148 | hp1 | a0002 | c0002 | t0002 | g0174 | AMR | PEL | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02148 | hp2 | a0004 | c0004 | t0001 | g0027 | AMR | PEL | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02155 | hp1 | a0002 | c0002 | t0002 | g0096 | EAS | CDX | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02155 | hp2 | a0005 | c0006 | t0001 | g0214 | EAS | CDX | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | CDX | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02165 | hp2 | a0013 | c0020 | t0001 | g0333 | EAS | CDX | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02257 | hp1 | a0005 | c0007 | t0001 | g0360 | AFR | ACB | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02257 | hp2 | a0002 | c0002 | t0002 | g0097 | AFR | ACB | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02258 | hp1 | a0001 | c0005 | t0001 | g0231 | AFR | ACB | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | ACB | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02280 | hp1 | a0010 | c0016 | t0001 | g0093 | AFR | ACB | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | ACB | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0353 | AMR | PEL | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02293 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | PEL | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | KHV | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02523 | hp2 | a0002 | c0002 | t0002 | g0129 | EAS | KHV | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02602 | hp1 | a0014 | c0018 | t0001 | g0019 | SAS | PJL | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02602 | hp2 | a0002 | c0002 | t0002 | g0105 | SAS | PJL | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02622 | hp1 | a0003 | c0003 | t0001 | g0071 | AFR | GWD | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02622 | hp2 | a0006 | c0009 | t0001 | g0091 | AFR | GWD | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | GWD | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02630 | hp2 | a0006 | c0009 | t0001 | g0366 | AFR | GWD | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02647 | hp2 | a0001 | c0005 | t0001 | g0227 | AFR | GWD | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0349 | SAS | PJL | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02698 | hp2 | a0002 | c0002 | t0002 | g0163 | SAS | PJL | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02717 | hp2 | a0001 | c0008 | t0001 | g0058 | AFR | GWD | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02723 | hp1 | a0007 | c0010 | t0001 | g0258 | AFR | GWD | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02723 | hp2 | a0003 | c0003 | t0001 | g0059 | AFR | GWD | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0308 | SAS | PJL | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02735 | hp2 | a0002 | c0002 | t0002 | g0238 | SAS | PJL | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02738 | hp1 | a0004 | c0004 | t0001 | g0039 | SAS | PJL | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02809 | hp2 | a0005 | c0011 | t0003 | g0086 | AFR | GWD | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0338 | AFR | GWD | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02886 | hp1 | a0001 | c0005 | t0001 | g0002 | AFR | GWD | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | GWD | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02895 | hp1 | a0001 | c0005 | t0001 | g0224 | AFR | GWD | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02895 | hp2 | a0001 | c0008 | t0001 | g0072 | AFR | GWD | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02896 | hp1 | a0002 | c0002 | t0002 | g0109 | AFR | GWD | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02896 | hp2 | a0003 | c0003 | t0001 | g0067 | AFR | GWD | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02897 | hp1 | a0001 | c0005 | t0001 | g0225 | AFR | GWD | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02897 | hp2 | a0003 | c0003 | t0001 | g0066 | AFR | GWD | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02922 | hp1 | a0006 | c0009 | t0001 | g0235 | AFR | ESN | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | ESN | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02965 | hp1 | a0001 | c0005 | t0001 | g0228 | AFR | ESN | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | ESN | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0342 | AFR | ESN | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02970 | hp2 | a0003 | c0003 | t0001 | g0057 | AFR | ESN | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | ESN | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0311 | AFR | ESN | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG03017 | hp1 | a0002 | c0002 | t0002 | g0106 | SAS | PJL | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0309 | SAS | PJL | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG03041 | hp1 | a0005 | c0011 | t0003 | g0085 | AFR | GWD | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0290 | AFR | GWD | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG03130 | hp1 | a0001 | c0005 | t0001 | g0009 | AFR | ESN | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | ESN | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG03195 | hp1 | a0003 | c0003 | t0001 | g0063 | AFR | ESN | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | ESN | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG03209 | hp1 | a0005 | c0011 | t0003 | g0088 | AFR | MSL | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0098 | AFR | MSL | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG03225 | hp1 | a0006 | c0009 | t0001 | g0234 | AFR | MSL | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG03225 | hp2 | a0003 | c0003 | t0001 | g0061 | AFR | MSL | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0324 | SAS | PJL | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0343 | SAS | PJL | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG03453 | hp1 | a0001 | c0005 | t0001 | g0003 | AFR | MSL | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG03453 | hp2 | a0010 | c0016 | t0001 | g0092 | AFR | MSL | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | MSL | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG03486 | hp2 | a0001 | c0013 | t0001 | g0244 | AFR | MSL | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG03490 | hp1 | a0004 | c0004 | t0001 | g0023 | SAS | PJL | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG03490 | hp2 | a0002 | c0002 | t0002 | g0167 | SAS | PJL | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG03491 | hp1 | a0002 | c0002 | t0002 | g0127 | SAS | PJL | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0318 | SAS | PJL | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG03492 | hp1 | a0002 | c0002 | t0002 | g0128 | SAS | PJL | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG03492 | hp2 | a0002 | c0002 | t0002 | g0160 | SAS | PJL | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG03516 | hp1 | a0003 | c0003 | t0001 | g0062 | AFR | ESN | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG03516 | hp2 | a0003 | c0003 | t0001 | g0064 | AFR | ESN | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG03540 | hp1 | a0001 | c0013 | t0001 | g0243 | AFR | GWD | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG03540 | hp2 | a0003 | c0003 | t0001 | g0070 | AFR | GWD | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | MSL | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG03579 | hp2 | a0003 | c0003 | t0001 | g0060 | AFR | MSL | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG03669 | hp1 | a0004 | c0004 | t0001 | g0015 | SAS | PJL | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG03669 | hp2 | a0003 | c0003 | t0001 | g0084 | SAS | PJL | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG03688 | hp1 | a0002 | c0002 | t0002 | g0107 | SAS | STU | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG03688 | hp2 | a0004 | c0004 | t0001 | g0024 | SAS | STU | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG03927 | hp1 | a0002 | c0002 | t0002 | g0159 | SAS | BEB | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | BEB | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0354 | SAS | BEB | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG03942 | hp2 | a0002 | c0002 | t0002 | g0177 | SAS | BEB | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG04199 | hp1 | a0002 | c0002 | t0002 | g0124 | SAS | STU | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0336 | SAS | STU | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0305 | SAS | STU | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0195 | SAS | STU | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA18522 | hp1 | a0001 | c0005 | t0001 | g0009 | AFR | YRI | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA18522 | hp2 | a0003 | c0003 | t0001 | g0055 | AFR | YRI | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA18612 | hp1 | a0005 | c0006 | t0001 | g0212 | EAS | CHB | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA18612 | hp2 | a0002 | c0002 | t0002 | g0008 | EAS | CHB | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | CHB | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA18747 | hp2 | a0002 | c0002 | t0002 | g0117 | EAS | CHB | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA18906 | hp1 | a0007 | c0010 | t0001 | g0260 | AFR | YRI | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA18906 | hp2 | a0001 | c0005 | t0001 | g0003 | AFR | YRI | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA18939 | hp1 | a0015 | c0021 | t0001 | g0335 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA18939 | hp2 | a0002 | c0002 | t0002 | g0137 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA18942 | hp1 | a0003 | c0003 | t0004 | g0047 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA18942 | hp2 | a0005 | c0007 | t0001 | g0205 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA18943 | hp1 | a0002 | c0002 | t0002 | g0116 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA18945 | hp1 | a0002 | c0002 | t0002 | g0136 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA18945 | hp2 | a0004 | c0004 | t0001 | g0046 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0361 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA18946 | hp2 | a0003 | c0003 | t0001 | g0080 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA18947 | hp1 | a0002 | c0002 | t0002 | g0143 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA18947 | hp2 | a0003 | c0003 | t0001 | g0049 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA18949 | hp1 | a0002 | c0002 | t0002 | g0142 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0363 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA18950 | hp1 | a0005 | c0007 | t0001 | g0217 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA18951 | hp2 | a0005 | c0006 | t0001 | g0210 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA18952 | hp1 | a0002 | c0002 | t0002 | g0135 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA18954 | hp1 | a0002 | c0002 | t0002 | g0169 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA18961 | hp1 | a0002 | c0002 | t0002 | g0139 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA18962 | hp1 | a0002 | c0002 | t0002 | g0164 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA18963 | hp1 | a0004 | c0004 | t0001 | g0043 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA18964 | hp1 | a0002 | c0002 | t0002 | g0152 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA18965 | hp1 | a0005 | c0006 | t0002 | g0223 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA18966 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA18966 | hp2 | a0003 | c0003 | t0001 | g0052 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA18967 | hp1 | a0002 | c0002 | t0002 | g0237 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0352 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA18969 | hp1 | a0002 | c0002 | t0002 | g0170 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA18969 | hp2 | a0003 | c0003 | t0001 | g0083 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA18971 | hp1 | a0002 | c0002 | t0002 | g0123 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA18971 | hp2 | a0004 | c0004 | t0001 | g0031 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA18975 | hp1 | a0005 | c0007 | t0001 | g0213 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA18975 | hp2 | a0004 | c0004 | t0001 | g0036 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA18977 | hp1 | a0004 | c0004 | t0001 | g0037 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA18977 | hp2 | a0002 | c0002 | t0002 | g0156 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA18978 | hp1 | a0002 | c0002 | t0002 | g0158 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA18978 | hp2 | a0004 | c0004 | t0001 | g0032 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA18979 | hp2 | a0002 | c0002 | t0002 | g0239 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA18980 | hp1 | a0002 | c0002 | t0002 | g0108 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA18982 | hp2 | a0003 | c0003 | t0001 | g0048 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA18986 | hp2 | a0004 | c0004 | t0001 | g0030 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA18987 | hp1 | a0002 | c0002 | t0002 | g0126 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA18990 | hp1 | a0002 | c0002 | t0002 | g0133 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA18991 | hp1 | a0003 | c0003 | t0001 | g0078 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA18992 | hp1 | a0002 | c0002 | t0002 | g0132 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA18992 | hp2 | a0003 | c0003 | t0001 | g0077 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA18995 | hp2 | a0002 | c0002 | t0002 | g0112 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA18999 | hp1 | a0003 | c0003 | t0001 | g0074 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA19000 | hp1 | a0005 | c0007 | t0001 | g0208 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA19002 | hp1 | a0002 | c0002 | t0002 | g0113 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA19003 | hp1 | a0002 | c0002 | t0002 | g0121 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA19003 | hp2 | a0004 | c0004 | t0001 | g0035 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA19005 | hp1 | a0002 | c0002 | t0002 | g0144 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA19006 | hp1 | a0005 | c0007 | t0001 | g0207 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA19006 | hp2 | a0004 | c0004 | t0001 | g0042 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA19007 | hp1 | a0004 | c0004 | t0001 | g0038 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA19007 | hp2 | a0002 | c0002 | t0002 | g0153 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA19009 | hp1 | a0005 | c0006 | t0002 | g0222 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0362 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA19011 | hp2 | a0002 | c0002 | t0002 | g0157 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA19030 | hp1 | a0001 | c0008 | t0001 | g0073 | AFR | LWK | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA19030 | hp2 | a0005 | c0011 | t0003 | g0087 | AFR | LWK | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA19043 | hp1 | a0003 | c0003 | t0001 | g0054 | AFR | LWK | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA19043 | hp2 | a0006 | c0009 | t0001 | g0367 | AFR | LWK | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA19054 | hp2 | a0002 | c0002 | t0002 | g0241 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA19056 | hp1 | a0002 | c0002 | t0002 | g0155 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA19056 | hp2 | a0004 | c0004 | t0001 | g0044 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA19058 | hp1 | a0004 | c0004 | t0001 | g0018 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA19060 | hp1 | a0002 | c0002 | t0002 | g0149 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA19060 | hp2 | a0003 | c0003 | t0001 | g0081 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA19062 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA19062 | hp2 | a0003 | c0003 | t0001 | g0082 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA19063 | hp1 | a0002 | c0002 | t0002 | g0008 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA19063 | hp2 | a0003 | c0003 | t0001 | g0079 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA19064 | hp1 | a0005 | c0006 | t0001 | g0219 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA19064 | hp2 | a0003 | c0003 | t0001 | g0050 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA19066 | hp1 | a0003 | c0003 | t0001 | g0075 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA19066 | hp2 | a0002 | c0002 | t0002 | g0134 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0351 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA19068 | hp2 | a0002 | c0002 | t0002 | g0150 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA19072 | hp1 | a0002 | c0002 | t0002 | g0166 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA19072 | hp2 | a0005 | c0007 | t0001 | g0233 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA19074 | hp1 | a0002 | c0002 | t0002 | g0131 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA19075 | hp1 | a0002 | c0002 | t0002 | g0115 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA19075 | hp2 | a0004 | c0004 | t0001 | g0045 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA19076 | hp1 | a0005 | c0007 | t0001 | g0221 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA19076 | hp2 | a0002 | c0002 | t0002 | g0110 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA19077 | hp1 | a0005 | c0006 | t0001 | g0220 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0355 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA19082 | hp1 | a0003 | c0003 | t0001 | g0076 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA19082 | hp2 | a0005 | c0006 | t0001 | g0211 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA19085 | hp2 | a0003 | c0003 | t0001 | g0051 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA19086 | hp2 | a0004 | c0004 | t0001 | g0041 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA19088 | hp2 | a0002 | c0002 | t0002 | g0236 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA19090 | hp1 | a0002 | c0002 | t0002 | g0114 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0356 | EAS | JPT | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0340 | AFR | YRI | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA19240 | hp2 | a0001 | c0005 | t0001 | g0230 | AFR | YRI | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0325 | AFR | ASW | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA20129 | hp2 | a0001 | c0005 | t0001 | g0002 | AFR | ASW | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0275 | EUR | TSI | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA20805 | hp2 | a0002 | c0002 | t0002 | g0013 | EUR | TSI | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA20905 | hp1 | a0002 | c0002 | t0002 | g0119 | SAS | GIH | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0344 | SAS | GIH | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02109 | hp1 | a0001 | c0023 | t0001 | g0202 | AFR | ACB | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0277 | AFR | ACB | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02486 | hp1 | a0007 | c0010 | t0001 | g0257 | AFR | ACB | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02486 | hp2 | a0009 | c0014 | t0001 | g0364 | AFR | ACB | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | ACB | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG02559 | hp2 | a0001 | c0005 | t0001 | g0002 | AFR | ACB | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG03471 | hp1 | a0001 | c0005 | t0001 | g0003 | AFR | MSL | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | MSL | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG06807 | hp1 | a0003 | c0003 | t0001 | g0069 | AFR | USA | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| HG06807 | hp2 | a0002 | c0002 | t0001 | g0247 | AFR | USA | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0319 | AFR | LWK | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| NA21309 | hp2 | a0001 | c0022 | t0001 | g0226 | AFR | LWK | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| homoSapiens | chm13v2 | a0004 | c0004 | t0001 | g0034 | REF | REF | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| homoSapiens | grch38p0 | a0001 | c0008 | t0001 | g0056 | REF | REF | TDRD5_chr1_179586832_179696272 | TDRD5 | chr1 | 179586832 | 179696272 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:179593538 | T | C | 1 | a0007 | 4 | HG01099.hp1 HG02486.hp1 HG02723.hp1 others(1): Show |
missense_variant | MODERATE | c.311T>C | p.Met104Thr | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 3/18 | 619/3745 | 311/3108 | 104/1035 | chr1 | 179593538 | |||
| chr1:179593605 | G | C | 3 | a0002 a0008 a0011 |
112 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(109): Show |
missense_variant | MODERATE | c.378G>C | p.Arg126Ser | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 3/18 | 686/3745 | 378/3108 | 126/1035 | chr1 | 179593605 | |||
| chr1:179593657 | G | A | 1 | a0003 | 33 | HG00423.hp1 HG01192.hp1 HG02622.hp1 others(30): Show |
missense_variant | MODERATE | c.430G>A | p.Ala144Thr | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 3/18 | 738/3745 | 430/3108 | 144/1035 | chr1 | 179593657 | |||
| chr1:179595661 | A | G | 1 | a0012 | 1 | HG02071.hp1 | missense_variant | MODERATE | c.674A>G | p.Gln225Arg | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/18 | 982/3745 | 674/3108 | 225/1035 | chr1 | 179595661 | |||
| chr1:179595702 | T | G | 1 | a0007 | 4 | HG01099.hp1 HG02486.hp1 HG02723.hp1 others(1): Show |
missense_variant | MODERATE | c.715T>G | p.Phe239Val | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/18 | 1023/3745 | 715/3108 | 239/1035 | chr1 | 179595702 | |||
| chr1:179595750 | A | G | 1 | a0009 | 2 | HG01884.hp2 HG02486.hp2 |
missense_variant | MODERATE | c.763A>G | p.Met255Val | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/18 | 1071/3745 | 763/3108 | 255/1035 | chr1 | 179595750 | |||
| chr1:179595765 | A | G | 1 | a0008 | 2 | HG01516.hp2 HG01517.hp1 |
missense_variant | MODERATE | c.778A>G | p.Lys260Glu | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/18 | 1086/3745 | 778/3108 | 260/1035 | chr1 | 179595765 | |||
| chr1:179630866 | A | G | 2 | a0005 a0009 |
31 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(28): Show |
missense_variant | MODERATE | c.1072A>G | p.Lys358Glu | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 7/18 | 1380/3745 | 1072/3108 | 358/1035 | chr1 | 179630866 | |||
| chr1:179639870 | C | G | 1 | a0015 | 1 | NA18939.hp1 | missense_variant | MODERATE | c.1552C>G | p.Arg518Gly | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 10/18 | 1860/3745 | 1552/3108 | 518/1035 | chr1 | 179639870 | |||
| chr1:179640414 | C | T | 1 | a0014 | 1 | HG02602.hp1 | missense_variant | MODERATE | c.1769C>T | p.Pro590Leu | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/18 | 2077/3745 | 1769/3108 | 590/1035 | chr1 | 179640414 | |||
| chr1:179652118 | G | T | 1 | a0009 | 2 | HG01884.hp2 HG02486.hp2 |
missense_variant | MODERATE | c.2081G>T | p.Gly694Val | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 13/18 | 2389/3745 | 2081/3108 | 694/1035 | chr1 | 179652118 | |||
| chr1:179652189 | C | T | 1 | a0013 | 1 | HG02165.hp2 | missense_variant | MODERATE | c.2152C>T | p.Arg718Cys | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 13/18 | 2460/3745 | 2152/3108 | 718/1035 | chr1 | 179652189 | |||
| chr1:179654294 | A | G | 1 | a0006 | 5 | HG02622.hp2 HG02630.hp2 HG02922.hp1 others(2): Show |
missense_variant | MODERATE | c.2254A>G | p.Asn752Asp | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/18 | 2562/3745 | 2254/3108 | 752/1035 | chr1 | 179654294 | |||
| chr1:179662107 | G | A | 3 | a0004 a0011 a0014 |
30 | HG00280.hp2 HG00544.hp2 HG00609.hp2 others(27): Show |
missense_variant | MODERATE | c.2326G>A | p.Glu776Lys | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 15/18 | 2634/3745 | 2326/3108 | 776/1035 | chr1 | 179662107 | |||
| chr1:179669310 | C | A | 1 | a0010 | 2 | HG02280.hp1 HG03453.hp2 |
missense_variant | MODERATE | c.2766C>A | p.Asn922Lys | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/18 | 3074/3745 | 2766/3108 | 922/1035 | chr1 | 179669310 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:179593572 | G | A | 4 | a0005c0011 a0005c0012 a0007c0010 others(1): Show |
13 | HG00735.hp2 HG01099.hp1 HG01109.hp1 others(10): Show |
synonymous_variant | LOW | c.345G>A | p.Pro115Pro | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 3/18 | 653/3745 | 345/3108 | 115/1035 | chr1 | 179593572 | |||
| chr1:179595698 | A | G | 1 | a0001c0013 | 3 | HG01243.hp2 HG03486.hp2 HG03540.hp1 |
synonymous_variant | LOW | c.711A>G | p.Pro237Pro | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/18 | 1019/3745 | 711/3108 | 237/1035 | chr1 | 179595698 | |||
| chr1:179630907 | G | A | 2 | a0005c0006 a0005c0007 |
22 | HG00544.hp1 HG00597.hp1 HG01070.hp1 others(19): Show |
synonymous_variant | LOW | c.1113G>A | p.Lys371Lys | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 7/18 | 1421/3745 | 1113/3108 | 371/1035 | chr1 | 179630907 | |||
| chr1:179634545 | A | G | 1 | a0001c0023 | 1 | HG02109.hp1 | synonymous_variant | LOW | c.1215A>G | p.Val405Val | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 8/18 | 1523/3745 | 1215/3108 | 405/1035 | chr1 | 179634545 | |||
| chr1:179635708 | A | G | 1 | a0001c0022 | 1 | NA21309.hp2 | synonymous_variant | LOW | c.1341A>G | p.Ala447Ala | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 9/18 | 1649/3745 | 1341/3108 | 447/1035 | chr1 | 179635708 | |||
| chr1:179635729 | C | T | 18 | a0001c0001 a0001c0005 a0001c0019 others(15): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
synonymous_variant | LOW | c.1362C>T | p.Asp454Asp | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 9/18 | 1670/3745 | 1362/3108 | 454/1035 | chr1 | 179635729 | |||
| chr1:179635738 | G | A | 1 | a0001c0019 | 1 | HG00741.hp1 | synonymous_variant | LOW | c.1371G>A | p.Pro457Pro | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 9/18 | 1679/3745 | 1371/3108 | 457/1035 | chr1 | 179635738 | |||
| chr1:179639914 | T | C | 1 | a0005c0006 | 13 | HG00544.hp1 HG00597.hp1 HG02015.hp2 others(10): Show |
synonymous_variant | LOW | c.1596T>C | p.Cys532Cys | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 10/18 | 1904/3745 | 1596/3108 | 532/1035 | chr1 | 179639914 | |||
| chr1:179652089 | G | A | 3 | a0005c0006 a0005c0007 a0005c0011 |
26 | HG00544.hp1 HG00597.hp1 HG01070.hp1 others(23): Show |
synonymous_variant | LOW | c.2052G>A | p.Gly684Gly | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 13/18 | 2360/3745 | 2052/3108 | 684/1035 | chr1 | 179652089 | |||
| chr1:179663368 | T | A | 2 | a0001c0005 a0001c0022 |
17 | HG01346.hp1 HG02055.hp2 HG02258.hp1 others(14): Show |
synonymous_variant | LOW | c.2526T>A | p.Pro842Pro | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 16/18 | 2834/3745 | 2526/3108 | 842/1035 | chr1 | 179663368 | |||
| chr1:179663401 | A | G | 3 | a0005c0006 a0005c0007 a0005c0011 |
26 | HG00544.hp1 HG00597.hp1 HG01070.hp1 others(23): Show |
synonymous_variant | LOW | c.2559A>G | p.Ser853Ser | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 16/18 | 2867/3745 | 2559/3108 | 853/1035 | chr1 | 179663401 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:179591882 | G | A | 1 | a0005c0011t0003 | 4 | HG02809.hp2 HG03041.hp1 HG03209.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-258G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 1/18 | 734 | chr1 | 179591882 | ||||||
| chr1:179592019 | C | T | 5 | a0001c0001t0002 a0002c0002t0002 a0005c0006t0002 others(2): Show |
107 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(104): Show |
5_prime_UTR_variant | MODIFIER | c.-121C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 1/18 | 597 | chr1 | 179592019 | ||||||
| chr1:179691097 | G | A | 1 | a0003c0003t0004 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*154G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 18/18 | 154 | chr1 | 179691097 | ||||||
| chr1:179691100 | T | A | 1 | a0003c0003t0004 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*157T>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 18/18 | 157 | chr1 | 179691100 | ||||||
| chr1:179691101 | A | AAAACAAT others(27): Show |
1 | a0003c0003t0004 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*158_*159insAAACAA others(28): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 18/18 | 159 | chr1 | 179691101 | ||||||
| chr1:179691104 | T | A | 1 | a0003c0003t0004 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*161T>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 18/18 | 161 | chr1 | 179691104 | ||||||
| chr1:179691105 | T | C | 1 | a0003c0003t0004 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*162T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 18/18 | 162 | chr1 | 179691105 | ||||||
| chr1:179691106 | G | C | 1 | a0003c0003t0004 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*163G>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 18/18 | 163 | chr1 | 179691106 | ||||||
| chr1:179691112 | T | A | 1 | a0003c0003t0004 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*169T>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 18/18 | 169 | chr1 | 179691112 | ||||||
| chr1:179691115 | G | A | 1 | a0003c0003t0004 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*172G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 18/18 | 172 | chr1 | 179691115 | ||||||
| chr1:179691116 | T | A | 1 | a0003c0003t0004 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*173T>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 18/18 | 173 | chr1 | 179691116 | ||||||
| chr1:179691119 | G | A | 1 | a0003c0003t0004 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*176G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 18/18 | 176 | chr1 | 179691119 | ||||||
| chr1:179691123 | T | A | 1 | a0003c0003t0004 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*180T>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 18/18 | 180 | chr1 | 179691123 | ||||||
| chr1:179691124 | G | A | 1 | a0003c0003t0004 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*181G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 18/18 | 181 | chr1 | 179691124 | ||||||
| chr1:179691126 | T | A | 1 | a0003c0003t0004 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*183T>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 18/18 | 183 | chr1 | 179691126 | ||||||
| chr1:179691128 | T | A | 1 | a0003c0003t0004 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*185T>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 18/18 | 185 | chr1 | 179691128 | ||||||
| chr1:179691129 | T | A | 1 | a0003c0003t0004 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*186T>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 18/18 | 186 | chr1 | 179691129 | ||||||
| chr1:179691130 | T | A | 1 | a0003c0003t0004 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*187T>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 18/18 | 187 | chr1 | 179691130 | ||||||
| chr1:179691133 | T | C | 1 | a0003c0003t0004 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*190T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 18/18 | 190 | chr1 | 179691133 | ||||||
| chr1:179691134 | G | A | 1 | a0003c0003t0004 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*191G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 18/18 | 191 | chr1 | 179691134 | ||||||
| chr1:179691135 | T | A | 1 | a0003c0003t0004 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*192T>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 18/18 | 192 | chr1 | 179691135 | ||||||
| chr1:179691149 | T | C | 1 | a0003c0003t0004 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*206T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 18/18 | 206 | chr1 | 179691149 | ||||||
| chr1:179691156 | TTTATTCT others(21): Show |
T | 1 | a0003c0003t0004 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*216_*243delATTCTG others(22): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 18/18 | 216 | INFO_REALIGN_3_PRIME | chr1 | 179691156 | |||||
| chr1:179691179 | C | T | 2 | a0001c0001t0001 a0012c0024t0001 |
17 | HG00408.hp2 HG01106.hp1 HG01433.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*236C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 18/18 | 236 | chr1 | 179691179 | ||||||
| chr1:179691187 | T | G | 1 | a0003c0003t0004 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*244T>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 18/18 | 244 | chr1 | 179691187 | ||||||
| chr1:179691189 | T | C | 1 | a0003c0003t0004 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*246T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 18/18 | 246 | chr1 | 179691189 | ||||||
| chr1:179691212 | T | C | 1 | a0003c0003t0004 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*269T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 18/18 | 269 | chr1 | 179691212 | ||||||
| chr1:179691213 | T | A | 1 | a0003c0003t0004 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*270T>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 18/18 | 270 | chr1 | 179691213 | ||||||
| chr1:179691216 | T | A | 1 | a0003c0003t0004 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*273T>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 18/18 | 273 | chr1 | 179691216 | ||||||
| chr1:179691217 | T | C | 1 | a0003c0003t0004 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*274T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 18/18 | 274 | chr1 | 179691217 | ||||||
| chr1:179691223 | T | C | 1 | a0003c0003t0004 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*280T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 18/18 | 280 | chr1 | 179691223 | ||||||
| chr1:179691225 | T | A | 1 | a0003c0003t0004 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*282T>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 18/18 | 282 | chr1 | 179691225 | ||||||
| chr1:179691227 | T | C | 1 | a0003c0003t0004 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*284T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 18/18 | 284 | chr1 | 179691227 | ||||||
| chr1:179691228 | T | C | 1 | a0003c0003t0004 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*285T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 18/18 | 285 | chr1 | 179691228 | ||||||
| chr1:179691233 | G | A | 1 | a0003c0003t0004 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*290G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 18/18 | 290 | chr1 | 179691233 | ||||||
| chr1:179691236 | C | T | 1 | a0003c0003t0004 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*293C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 18/18 | 293 | chr1 | 179691236 | ||||||
| chr1:179691237 | A | C | 1 | a0003c0003t0004 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*294A>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 18/18 | 294 | chr1 | 179691237 | ||||||
| chr1:179691238 | T | A | 1 | a0003c0003t0004 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*295T>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 18/18 | 295 | chr1 | 179691238 | ||||||
| chr1:179691244 | T | G | 1 | a0003c0003t0004 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*301T>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 18/18 | 301 | chr1 | 179691244 | ||||||
| chr1:179691245 | G | C | 1 | a0003c0003t0004 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*302G>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 18/18 | 302 | chr1 | 179691245 | ||||||
| chr1:179691249 | G | A | 1 | a0003c0003t0004 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*306G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 18/18 | 306 | chr1 | 179691249 | ||||||
| chr1:179691250 | A | C | 1 | a0003c0003t0004 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*307A>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 18/18 | 307 | chr1 | 179691250 | ||||||
| chr1:179691251 | T | A | 1 | a0003c0003t0004 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*308T>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 18/18 | 308 | chr1 | 179691251 | ||||||
| chr1:179691252 | A | C | 1 | a0003c0003t0004 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*309A>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 18/18 | 309 | chr1 | 179691252 | ||||||
| chr1:179691256 | G | T | 1 | a0003c0003t0004 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*313G>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 18/18 | 313 | chr1 | 179691256 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:179592234 | G | T | 2 | a0006c0009t0001g0366 a0006c0009t0001g0367 |
2 | HG02630.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-15+109G>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 1/17 | chr1 | 179592234 | |||||||
| chr1:179592289 | G | A | 1 | a0002c0002t0002g0013 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-15+164G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 1/17 | chr1 | 179592289 | |||||||
| chr1:179592372 | G | T | 2 | a0009c0014t0001g0364 a0009c0014t0001g0365 |
2 | HG01884.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.-14-230G>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 1/17 | chr1 | 179592372 | |||||||
| chr1:179592392 | C | G | 89 | a0001c0001t0001g0012 a0001c0001t0001g0277 a0001c0001t0001g0278 others(86): Show |
91 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.-14-210C>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 1/17 | chr1 | 179592392 | |||||||
| chr1:179592446 | G | C | 1 | a0002c0002t0002g0014 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-14-156G>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 1/17 | chr1 | 179592446 | |||||||
| chr1:179592474 | A | G | 16 | a0001c0001t0001g0010 a0001c0001t0001g0262 a0001c0001t0001g0264 others(13): Show |
17 | HG00544.hp1 HG01106.hp1 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.-14-128A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 1/17 | chr1 | 179592474 | |||||||
| chr1:179592510 | A | C | 291 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0089 others(288): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.-14-92A>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 1/17 | chr1 | 179592510 | |||||||
| chr1:179592548 | A | T | 289 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0089 others(286): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.-14-54A>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 1/17 | chr1 | 179592548 | |||||||
| chr1:179592980 | A | T | 1 | a0001c0001t0001g0261 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.232+133A>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 2/17 | chr1 | 179592980 | |||||||
| chr1:179593008 | G | A | 283 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0089 others(280): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.232+161G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 2/17 | chr1 | 179593008 | |||||||
| chr1:179593046 | A | G | 2 | a0009c0014t0001g0364 a0009c0014t0001g0365 |
2 | HG01884.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.232+199A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 2/17 | chr1 | 179593046 | |||||||
| chr1:179593048 | C | A | 2 | a0001c0001t0001g0089 a0001c0001t0001g0090 |
2 | HG02572.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.232+201C>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 2/17 | chr1 | 179593048 | |||||||
| chr1:179593385 | A | G | 7 | a0002c0002t0001g0246 a0002c0002t0001g0247 a0002c0002t0001g0248 others(4): Show |
7 | HG00140.hp2 HG00639.hp1 HG00733.hp2 others(4): Show |
intron_variant | MODIFIER | c.233-75A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 2/17 | chr1 | 179593385 | |||||||
| chr1:179593872 | G | C | 1 | a0006c0009t0001g0091 | 1 | HG02622.hp2 | splice_region_variant&intron_variant | LOW | c.640+5G>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 3/17 | chr1 | 179593872 | |||||||
| chr1:179593898 | A | G | 16 | a0001c0013t0001g0243 a0001c0013t0001g0244 a0001c0013t0001g0245 others(13): Show |
16 | HG00735.hp2 HG01099.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.640+31A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 3/17 | chr1 | 179593898 | |||||||
| chr1:179593906 | T | C | 3 | a0005c0012t0001g0254 a0005c0012t0001g0255 a0005c0012t0001g0256 |
3 | HG00735.hp2 HG01109.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.640+39T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 3/17 | chr1 | 179593906 | |||||||
| chr1:179593923 | A | G | 16 | a0001c0013t0001g0243 a0001c0013t0001g0244 a0001c0013t0001g0245 others(13): Show |
16 | HG00735.hp2 HG01099.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.640+56A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 3/17 | chr1 | 179593923 | |||||||
| chr1:179594017 | GT | G | 16 | a0001c0013t0001g0243 a0001c0013t0001g0244 a0001c0013t0001g0245 others(13): Show |
16 | HG00735.hp2 HG01099.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.640+154delT | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr1 | 179594017 | ||||||
| chr1:179594085 | A | G | 7 | a0002c0002t0002g0236 a0002c0002t0002g0237 a0002c0002t0002g0238 others(4): Show |
7 | HG02040.hp2 HG02135.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.640+218A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 3/17 | chr1 | 179594085 | |||||||
| chr1:179594411 | T | C | 4 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0010c0016t0001g0092 others(1): Show |
4 | HG01891.hp1 HG02280.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.640+544T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 3/17 | chr1 | 179594411 | |||||||
| chr1:179594463 | T | A | 4 | a0005c0011t0003g0085 a0005c0011t0003g0086 a0005c0011t0003g0087 others(1): Show |
4 | HG02809.hp2 HG03041.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.640+596T>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 3/17 | chr1 | 179594463 | |||||||
| chr1:179594464 | G | C | 4 | a0005c0011t0003g0085 a0005c0011t0003g0086 a0005c0011t0003g0087 others(1): Show |
4 | HG02809.hp2 HG03041.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.640+597G>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 3/17 | chr1 | 179594464 | |||||||
| chr1:179594490 | T | C | 3 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 |
3 | HG02109.hp2 HG02630.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.640+623T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 3/17 | chr1 | 179594490 | |||||||
| chr1:179594561 | G | C | 1 | a0001c0001t0001g0262 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.640+694G>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 3/17 | chr1 | 179594561 | |||||||
| chr1:179594568 | G | A | 1 | a0004c0004t0001g0015 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.640+701G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 3/17 | chr1 | 179594568 | |||||||
| chr1:179594582 | G | A | 328 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0025 others(325): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.640+715G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 3/17 | chr1 | 179594582 | |||||||
| chr1:179594592 | C | T | 15 | a0001c0001t0001g0010 a0001c0001t0001g0262 a0001c0001t0001g0264 others(12): Show |
16 | HG01106.hp1 HG01433.hp1 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.640+725C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 3/17 | chr1 | 179594592 | |||||||
| chr1:179594648 | C | A | 1 | a0002c0002t0002g0096 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.640+781C>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 3/17 | chr1 | 179594648 | |||||||
| chr1:179594666 | T | C | 9 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(6): Show |
9 | HG01255.hp1 HG01928.hp1 HG01993.hp1 others(6): Show |
intron_variant | MODIFIER | c.640+799T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 3/17 | chr1 | 179594666 | |||||||
| chr1:179594938 | T | C | 3 | a0005c0011t0003g0085 a0005c0011t0003g0086 a0005c0011t0003g0087 |
3 | HG02809.hp2 HG03041.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.641-690T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 3/17 | chr1 | 179594938 | |||||||
| chr1:179594994 | A | G | 1 | a0003c0003t0001g0084 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.641-634A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 3/17 | chr1 | 179594994 | |||||||
| chr1:179595009 | G | A | 226 | a0001c0001t0001g0012 a0001c0001t0001g0089 a0001c0001t0001g0090 others(223): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.641-619G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 3/17 | chr1 | 179595009 | |||||||
| chr1:179595036 | T | G | 16 | a0001c0013t0001g0243 a0001c0013t0001g0244 a0001c0013t0001g0245 others(13): Show |
16 | HG00735.hp2 HG01099.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.641-592T>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 3/17 | chr1 | 179595036 | |||||||
| chr1:179595059 | G | GT | 16 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0359 others(13): Show |
16 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.641-560dupT | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr1 | 179595059 | ||||||
| chr1:179595136 | T | C | 1 | a0002c0002t0002g0097 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.641-492T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 3/17 | chr1 | 179595136 | |||||||
| chr1:179595229 | C | T | 4 | a0007c0010t0001g0257 a0007c0010t0001g0258 a0007c0010t0001g0259 others(1): Show |
4 | HG01099.hp1 HG02486.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.641-399C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 3/17 | chr1 | 179595229 | |||||||
| chr1:179595421 | A | G | 16 | a0001c0013t0001g0243 a0001c0013t0001g0244 a0001c0013t0001g0245 others(13): Show |
16 | HG00735.hp2 HG01099.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.641-207A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 3/17 | chr1 | 179595421 | |||||||
| chr1:179595484 | G | A | 16 | a0001c0013t0001g0243 a0001c0013t0001g0244 a0001c0013t0001g0245 others(13): Show |
16 | HG00735.hp2 HG01099.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.641-144G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 3/17 | chr1 | 179595484 | |||||||
| chr1:179595945 | A | G | 10 | a0001c0013t0001g0243 a0001c0013t0001g0244 a0001c0013t0001g0245 others(7): Show |
10 | HG00735.hp2 HG01099.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.831+127A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179595945 | |||||||
| chr1:179596388 | C | A | 3 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 |
3 | HG02717.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.831+570C>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179596388 | |||||||
| chr1:179596429 | TA | T | 4 | a0001c0001t0001g0355 a0001c0001t0001g0356 a0001c0001t0001g0357 others(1): Show |
4 | HG00558.hp1 HG02080.hp1 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.831+617delA | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | 179596429 | ||||||
| chr1:179596457 | A | C | 93 | a0001c0001t0001g0012 a0001c0001t0001g0188 a0001c0001t0001g0189 others(90): Show |
94 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.831+639A>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179596457 | |||||||
| chr1:179596598 | T | C | 3 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0023t0001g0202 |
3 | HG02055.hp1 HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.831+780T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179596598 | |||||||
| chr1:179596693 | C | T | 16 | a0001c0013t0001g0243 a0001c0013t0001g0244 a0001c0013t0001g0245 others(13): Show |
16 | HG00735.hp2 HG01099.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.831+875C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179596693 | |||||||
| chr1:179596716 | A | G | 12 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0180 others(9): Show |
12 | HG02004.hp2 HG02258.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.831+898A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179596716 | |||||||
| chr1:179596961 | T | A | 4 | a0007c0010t0001g0257 a0007c0010t0001g0258 a0007c0010t0001g0259 others(1): Show |
4 | HG01099.hp1 HG02486.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.831+1143T>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179596961 | |||||||
| chr1:179597007 | T | G | 7 | a0003c0003t0001g0048 a0003c0003t0001g0049 a0003c0003t0001g0050 others(4): Show |
7 | HG00423.hp1 NA18942.hp1 NA18947.hp2 others(4): Show |
intron_variant | MODIFIER | c.831+1189T>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179597007 | |||||||
| chr1:179597009 | G | A | 7 | a0003c0003t0001g0048 a0003c0003t0001g0049 a0003c0003t0001g0050 others(4): Show |
7 | HG00423.hp1 NA18942.hp1 NA18947.hp2 others(4): Show |
intron_variant | MODIFIER | c.831+1191G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179597009 | |||||||
| chr1:179597096 | C | G | 15 | a0001c0001t0001g0010 a0001c0001t0001g0262 a0001c0001t0001g0264 others(12): Show |
16 | HG01106.hp1 HG01433.hp1 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.831+1278C>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179597096 | |||||||
| chr1:179597112 | A | G | 4 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0010c0016t0001g0092 others(1): Show |
4 | HG01891.hp1 HG02280.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.831+1294A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179597112 | |||||||
| chr1:179597161 | T | C | 93 | a0001c0001t0001g0012 a0001c0001t0001g0188 a0001c0001t0001g0189 others(90): Show |
94 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.831+1343T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179597161 | |||||||
| chr1:179597332 | C | CT | 108 | a0001c0001t0001g0104 a0001c0013t0001g0243 a0001c0013t0001g0244 others(105): Show |
116 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.831+1531dupT | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | 179597332 | ||||||
| chr1:179597400 | C | T | 7 | a0001c0013t0001g0243 a0001c0013t0001g0244 a0001c0013t0001g0245 others(4): Show |
7 | HG01099.hp1 HG01243.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.831+1582C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179597400 | |||||||
| chr1:179597419 | T | C | 15 | a0001c0001t0001g0010 a0001c0001t0001g0262 a0001c0001t0001g0264 others(12): Show |
16 | HG01106.hp1 HG01433.hp1 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.831+1601T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179597419 | |||||||
| chr1:179597545 | C | T | 16 | a0001c0013t0001g0243 a0001c0013t0001g0244 a0001c0013t0001g0245 others(13): Show |
16 | HG00735.hp2 HG01099.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.831+1727C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179597545 | |||||||
| chr1:179597610 | G | A | 3 | a0005c0012t0001g0254 a0005c0012t0001g0255 a0005c0012t0001g0256 |
3 | HG00735.hp2 HG01109.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.831+1792G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179597610 | |||||||
| chr1:179597631 | A | G | 1 | a0001c0001t0001g0196 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.831+1813A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179597631 | |||||||
| chr1:179597694 | C | T | 16 | a0001c0013t0001g0243 a0001c0013t0001g0244 a0001c0013t0001g0245 others(13): Show |
16 | HG00735.hp2 HG01099.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.831+1876C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179597694 | |||||||
| chr1:179597713 | T | C | 120 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0104 others(117): Show |
128 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.831+1895T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179597713 | |||||||
| chr1:179597829 | C | CTCTATCA others(2): Show |
16 | a0001c0013t0001g0243 a0001c0013t0001g0244 a0001c0013t0001g0245 others(13): Show |
16 | HG00735.hp2 HG01099.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.831+2013_831+2014i others(11): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | 179597829 | ||||||
| chr1:179597832 | C | T | 16 | a0001c0013t0001g0243 a0001c0013t0001g0244 a0001c0013t0001g0245 others(13): Show |
16 | HG00735.hp2 HG01099.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.831+2014C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179597832 | |||||||
| chr1:179597836 | C | G | 16 | a0001c0013t0001g0243 a0001c0013t0001g0244 a0001c0013t0001g0245 others(13): Show |
16 | HG00735.hp2 HG01099.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.831+2018C>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179597836 | |||||||
| chr1:179597837 | A | T | 15 | a0001c0001t0001g0010 a0001c0001t0001g0262 a0001c0001t0001g0264 others(12): Show |
16 | HG01106.hp1 HG01433.hp1 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.831+2019A>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179597837 | |||||||
| chr1:179597929 | G | A | 7 | a0002c0002t0002g0004 a0002c0002t0002g0005 a0002c0002t0002g0099 others(4): Show |
10 | HG00099.hp2 HG01081.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.831+2111G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179597929 | |||||||
| chr1:179597947 | T | A | 16 | a0001c0013t0001g0243 a0001c0013t0001g0244 a0001c0013t0001g0245 others(13): Show |
16 | HG00735.hp2 HG01099.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.831+2129T>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179597947 | |||||||
| chr1:179598042 | A | C | 3 | a0001c0013t0001g0243 a0001c0013t0001g0244 a0001c0013t0001g0245 |
3 | HG01243.hp2 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.831+2224A>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179598042 | |||||||
| chr1:179598199 | A | C | 11 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0190 others(8): Show |
11 | HG00140.hp1 HG00738.hp2 HG01069.hp2 others(8): Show |
intron_variant | MODIFIER | c.831+2381A>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179598199 | |||||||
| chr1:179598320 | A | G | 3 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 |
3 | HG02717.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.831+2502A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179598320 | |||||||
| chr1:179598334 | A | G | 30 | a0001c0001t0001g0010 a0001c0001t0001g0203 a0001c0001t0001g0204 others(27): Show |
36 | HG01106.hp1 HG01346.hp1 HG01433.hp1 others(33): Show |
intron_variant | MODIFIER | c.831+2516A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179598334 | |||||||
| chr1:179598412 | G | A | 3 | a0001c0013t0001g0243 a0001c0013t0001g0244 a0001c0013t0001g0245 |
3 | HG01243.hp2 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.831+2594G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179598412 | |||||||
| chr1:179598445 | A | G | 12 | a0001c0005t0001g0002 a0001c0005t0001g0003 a0001c0005t0001g0009 others(9): Show |
17 | HG01346.hp1 HG02055.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.831+2627A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179598445 | |||||||
| chr1:179598509 | T | C | 1 | a0002c0002t0002g0103 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.831+2691T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179598509 | |||||||
| chr1:179598561 | A | G | 3 | a0005c0012t0001g0254 a0005c0012t0001g0255 a0005c0012t0001g0256 |
3 | HG00735.hp2 HG01109.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.831+2743A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179598561 | |||||||
| chr1:179598576 | G | A | 1 | a0002c0002t0002g0097 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.831+2758G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179598576 | |||||||
| chr1:179598668 | C | A | 7 | a0001c0013t0001g0243 a0001c0013t0001g0244 a0001c0013t0001g0245 others(4): Show |
7 | HG01099.hp1 HG01243.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.831+2850C>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179598668 | |||||||
| chr1:179598674 | G | GT | 22 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0180 others(19): Show |
22 | HG01243.hp2 HG02004.hp2 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.831+2869dupT | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | 179598674 | ||||||
| chr1:179598674 | GT | G | 18 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0004c0004t0001g0016 others(15): Show |
18 | HG00544.hp2 HG00609.hp2 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.831+2869delT | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | 179598674 | ||||||
| chr1:179598687 | T | G | 3 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0104 |
3 | HG02145.hp2 HG02572.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.831+2869T>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179598687 | |||||||
| chr1:179599129 | G | C | 296 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0089 others(293): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.831+3311G>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179599129 | |||||||
| chr1:179599201 | A | G | 3 | a0001c0013t0001g0243 a0001c0013t0001g0244 a0001c0013t0001g0245 |
3 | HG01243.hp2 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.831+3383A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179599201 | |||||||
| chr1:179599438 | A | G | 12 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0180 others(9): Show |
12 | HG02004.hp2 HG02258.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.831+3620A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179599438 | |||||||
| chr1:179599452 | T | TTGGGCC | 16 | a0001c0013t0001g0243 a0001c0013t0001g0244 a0001c0013t0001g0245 others(13): Show |
16 | HG00735.hp2 HG01099.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.831+3637_831+3638i others(8): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | 179599452 | ||||||
| chr1:179599527 | T | C | 15 | a0001c0001t0001g0010 a0001c0001t0001g0262 a0001c0001t0001g0264 others(12): Show |
16 | HG01106.hp1 HG01433.hp1 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.831+3709T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179599527 | |||||||
| chr1:179599535 | CT | C | 6 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0291 others(3): Show |
6 | HG02572.hp1 HG03486.hp1 NA18942.hp2 others(3): Show |
intron_variant | MODIFIER | c.831+3730delT | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | 179599535 | ||||||
| chr1:179599548 | T | A | 93 | a0001c0001t0001g0012 a0001c0001t0001g0188 a0001c0001t0001g0189 others(90): Show |
94 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.831+3730T>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179599548 | |||||||
| chr1:179599626 | T | C | 2 | a0009c0014t0001g0364 a0009c0014t0001g0365 |
2 | HG01884.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.831+3808T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179599626 | |||||||
| chr1:179599680 | C | G | 3 | a0005c0012t0001g0254 a0005c0012t0001g0255 a0005c0012t0001g0256 |
3 | HG00735.hp2 HG01109.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.831+3862C>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179599680 | |||||||
| chr1:179599694 | A | G | 328 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0025 others(325): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.831+3876A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179599694 | |||||||
| chr1:179599761 | A | G | 1 | a0003c0003t0001g0083 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.831+3943A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179599761 | |||||||
| chr1:179599871 | T | C | 16 | a0001c0013t0001g0243 a0001c0013t0001g0244 a0001c0013t0001g0245 others(13): Show |
16 | HG00735.hp2 HG01099.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.831+4053T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179599871 | |||||||
| chr1:179599927 | A | G | 12 | a0001c0005t0001g0002 a0001c0005t0001g0003 a0001c0005t0001g0009 others(9): Show |
17 | HG01346.hp1 HG02055.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.831+4109A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179599927 | |||||||
| chr1:179599953 | C | G | 229 | a0001c0001t0001g0012 a0001c0001t0001g0089 a0001c0001t0001g0090 others(226): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.831+4135C>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179599953 | |||||||
| chr1:179600046 | T | C | 7 | a0001c0001t0001g0291 a0001c0001t0001g0293 a0001c0001t0001g0294 others(4): Show |
7 | HG00280.hp1 HG02132.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.831+4228T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179600046 | |||||||
| chr1:179600093 | A | G | 4 | a0003c0003t0001g0050 a0003c0003t0001g0051 a0003c0003t0001g0052 others(1): Show |
4 | HG00423.hp1 NA18966.hp2 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.831+4275A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179600093 | |||||||
| chr1:179600206 | A | G | 1 | a0002c0002t0001g0176 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.831+4388A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179600206 | |||||||
| chr1:179600214 | C | G | 32 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0004c0004t0001g0015 others(29): Show |
32 | HG00280.hp2 HG00544.hp2 HG00609.hp2 others(29): Show |
intron_variant | MODIFIER | c.831+4396C>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179600214 | |||||||
| chr1:179600349 | T | C | 3 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0104 |
3 | HG02145.hp2 HG02572.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.831+4531T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179600349 | |||||||
| chr1:179600587 | C | T | 102 | a0002c0002t0001g0176 a0002c0002t0001g0246 a0002c0002t0001g0247 others(99): Show |
109 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.831+4769C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179600587 | |||||||
| chr1:179600663 | C | T | 1 | a0001c0001t0001g0359 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.831+4845C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179600663 | |||||||
| chr1:179600786 | C | T | 1 | a0001c0001t0001g0351 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.831+4968C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179600786 | |||||||
| chr1:179600938 | A | C | 1 | a0001c0001t0001g0350 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.831+5120A>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179600938 | |||||||
| chr1:179600960 | T | C | 3 | a0001c0013t0001g0243 a0001c0013t0001g0244 a0001c0013t0001g0245 |
3 | HG01243.hp2 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.831+5142T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179600960 | |||||||
| chr1:179601037 | A | C | 1 | a0001c0008t0001g0072 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.831+5219A>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179601037 | |||||||
| chr1:179601108 | A | G | 1 | a0002c0002t0002g0175 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.831+5290A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179601108 | |||||||
| chr1:179601141 | C | CTG | 270 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0089 others(267): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.831+5324_831+5325i others(4): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | 179601141 | ||||||
| chr1:179601143 | T | G | 22 | a0001c0001t0001g0209 a0005c0006t0001g0206 a0005c0006t0001g0210 others(19): Show |
22 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(19): Show |
intron_variant | MODIFIER | c.831+5325T>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179601143 | |||||||
| chr1:179601454 | A | G | 26 | a0001c0001t0001g0209 a0005c0006t0001g0206 a0005c0006t0001g0210 others(23): Show |
26 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(23): Show |
intron_variant | MODIFIER | c.831+5636A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179601454 | |||||||
| chr1:179601482 | G | A | 11 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(8): Show |
11 | HG02109.hp2 HG02622.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.831+5664G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179601482 | |||||||
| chr1:179601496 | T | C | 3 | a0002c0002t0002g0105 a0002c0002t0002g0106 a0002c0002t0002g0107 |
3 | HG02602.hp2 HG03017.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.831+5678T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179601496 | |||||||
| chr1:179601655 | C | T | 5 | a0002c0002t0002g0004 a0002c0002t0002g0005 a0002c0002t0002g0101 others(2): Show |
8 | HG01081.hp2 HG01167.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.831+5837C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179601655 | |||||||
| chr1:179601723 | T | C | 328 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0025 others(325): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.831+5905T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179601723 | |||||||
| chr1:179601828 | T | C | 39 | a0001c0001t0001g0209 a0001c0013t0001g0243 a0001c0013t0001g0244 others(36): Show |
39 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.831+6010T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179601828 | |||||||
| chr1:179601845 | G | A | 2 | a0004c0004t0001g0016 a0004c0004t0001g0036 |
2 | HG00544.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.831+6027G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179601845 | |||||||
| chr1:179601918 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.831+6100G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179601918 | |||||||
| chr1:179601931 | G | A | 41 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0104 others(38): Show |
41 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.831+6113G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179601931 | |||||||
| chr1:179601963 | G | T | 3 | a0005c0012t0001g0254 a0005c0012t0001g0255 a0005c0012t0001g0256 |
3 | HG00735.hp2 HG01109.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.831+6145G>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179601963 | |||||||
| chr1:179601995 | G | A | 2 | a0009c0014t0001g0364 a0009c0014t0001g0365 |
2 | HG01884.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.831+6177G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179601995 | |||||||
| chr1:179602201 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.831+6383C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179602201 | |||||||
| chr1:179602269 | C | T | 2 | a0003c0003t0001g0070 a0003c0003t0001g0071 |
2 | HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.831+6451C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179602269 | |||||||
| chr1:179602407 | GT | G | 15 | a0001c0001t0001g0010 a0001c0001t0001g0262 a0001c0001t0001g0264 others(12): Show |
16 | HG01106.hp1 HG01433.hp1 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.831+6597delT | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | 179602407 | ||||||
| chr1:179602479 | A | G | 1 | a0002c0002t0001g0252 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.831+6661A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179602479 | |||||||
| chr1:179602727 | T | C | 1 | a0004c0004t0001g0017 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.831+6909T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179602727 | |||||||
| chr1:179602832 | T | C | 1 | a0004c0004t0001g0018 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.831+7014T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179602832 | |||||||
| chr1:179602854 | A | T | 1 | a0001c0001t0001g0262 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.831+7036A>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179602854 | |||||||
| chr1:179602951 | T | C | 95 | a0001c0001t0001g0012 a0001c0001t0001g0188 a0001c0001t0001g0189 others(92): Show |
97 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.831+7133T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179602951 | |||||||
| chr1:179602995 | C | G | 7 | a0001c0013t0001g0243 a0001c0013t0001g0244 a0001c0013t0001g0245 others(4): Show |
7 | HG01099.hp1 HG01243.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.831+7177C>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179602995 | |||||||
| chr1:179603099 | G | A | 1 | a0002c0002t0002g0108 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.831+7281G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179603099 | |||||||
| chr1:179603107 | A | G | 7 | a0001c0013t0001g0243 a0001c0013t0001g0244 a0001c0013t0001g0245 others(4): Show |
7 | HG01099.hp1 HG01243.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.831+7289A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179603107 | |||||||
| chr1:179603218 | A | C | 15 | a0001c0001t0001g0010 a0001c0001t0001g0262 a0001c0001t0001g0264 others(12): Show |
16 | HG01106.hp1 HG01433.hp1 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.831+7400A>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179603218 | |||||||
| chr1:179603369 | T | C | 95 | a0001c0001t0001g0012 a0001c0001t0001g0188 a0001c0001t0001g0189 others(92): Show |
97 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.831+7551T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179603369 | |||||||
| chr1:179603541 | C | G | 38 | a0001c0001t0001g0209 a0001c0013t0001g0243 a0001c0013t0001g0244 others(35): Show |
38 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.831+7723C>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179603541 | |||||||
| chr1:179603558 | C | T | 39 | a0001c0001t0001g0209 a0001c0008t0001g0072 a0001c0013t0001g0243 others(36): Show |
39 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.831+7740C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179603558 | |||||||
| chr1:179603562 | T | G | 5 | a0001c0001t0001g0299 a0001c0001t0001g0300 a0001c0001t0001g0301 others(2): Show |
5 | HG02040.hp1 NA18964.hp2 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.831+7744T>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179603562 | |||||||
| chr1:179603766 | C | G | 16 | a0001c0013t0001g0243 a0001c0013t0001g0244 a0001c0013t0001g0245 others(13): Show |
16 | HG00735.hp2 HG01099.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.831+7948C>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179603766 | |||||||
| chr1:179603824 | C | A | 1 | a0001c0001t0001g0280 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.831+8006C>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179603824 | |||||||
| chr1:179603995 | T | A | 118 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0104 others(115): Show |
125 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.831+8177T>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179603995 | |||||||
| chr1:179604296 | T | C | 5 | a0006c0009t0001g0091 a0006c0009t0001g0234 a0006c0009t0001g0235 others(2): Show |
5 | HG02622.hp2 HG02630.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.831+8478T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179604296 | |||||||
| chr1:179604298 | T | G | 38 | a0001c0001t0001g0209 a0001c0013t0001g0243 a0001c0013t0001g0244 others(35): Show |
38 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.831+8480T>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179604298 | |||||||
| chr1:179604337 | T | G | 11 | a0001c0001t0001g0012 a0001c0001t0001g0291 a0001c0001t0001g0293 others(8): Show |
12 | HG00280.hp1 HG02132.hp2 HG02135.hp1 others(9): Show |
intron_variant | MODIFIER | c.831+8519T>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179604337 | |||||||
| chr1:179604493 | G | A | 31 | a0001c0001t0001g0209 a0005c0006t0001g0206 a0005c0006t0001g0210 others(28): Show |
31 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.831+8675G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179604493 | |||||||
| chr1:179604574 | G | A | 2 | a0001c0001t0001g0089 a0001c0001t0001g0090 |
2 | HG02572.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.831+8756G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179604574 | |||||||
| chr1:179604756 | A | G | 7 | a0001c0001t0001g0344 a0001c0001t0001g0345 a0001c0001t0001g0346 others(4): Show |
7 | HG01257.hp2 HG01361.hp1 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.831+8938A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179604756 | |||||||
| chr1:179604808 | T | C | 1 | a0002c0002t0002g0004 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.831+8990T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179604808 | |||||||
| chr1:179604972 | T | C | 1 | a0002c0002t0002g0109 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.831+9154T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179604972 | |||||||
| chr1:179605140 | C | T | 1 | a0001c0008t0001g0068 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.831+9322C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179605140 | |||||||
| chr1:179605146 | A | T | 4 | a0007c0010t0001g0257 a0007c0010t0001g0258 a0007c0010t0001g0259 others(1): Show |
4 | HG01099.hp1 HG02486.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.831+9328A>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179605146 | |||||||
| chr1:179605371 | C | T | 1 | a0004c0004t0001g0036 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.831+9553C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179605371 | |||||||
| chr1:179605503 | G | C | 12 | a0001c0005t0001g0002 a0001c0005t0001g0003 a0001c0005t0001g0009 others(9): Show |
17 | HG01346.hp1 HG02055.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.831+9685G>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179605503 | |||||||
| chr1:179605552 | A | G | 35 | a0001c0001t0001g0209 a0005c0006t0001g0206 a0005c0006t0001g0210 others(32): Show |
35 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.831+9734A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179605552 | |||||||
| chr1:179605718 | G | A | 1 | a0006c0009t0001g0091 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.831+9900G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179605718 | |||||||
| chr1:179605766 | A | G | 1 | a0001c0008t0001g0068 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.831+9948A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179605766 | |||||||
| chr1:179605808 | C | T | 35 | a0001c0001t0001g0209 a0005c0006t0001g0206 a0005c0006t0001g0210 others(32): Show |
35 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.831+9990C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179605808 | |||||||
| chr1:179605935 | C | A | 2 | a0010c0016t0001g0092 a0010c0016t0001g0093 |
2 | HG02280.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.831+10117C>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179605935 | |||||||
| chr1:179605966 | G | T | 9 | a0005c0011t0003g0085 a0005c0011t0003g0086 a0005c0011t0003g0087 others(6): Show |
9 | HG00735.hp2 HG01109.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.831+10148G>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179605966 | |||||||
| chr1:179606140 | A | AG | 35 | a0001c0001t0001g0209 a0005c0006t0001g0206 a0005c0006t0001g0210 others(32): Show |
35 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.831+10322_831+1032 others(5): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179606140 | |||||||
| chr1:179606148 | G | A | 1 | a0003c0003t0001g0069 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.831+10330G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179606148 | |||||||
| chr1:179606162 | C | T | 1 | a0001c0001t0001g0343 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.831+10344C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179606162 | |||||||
| chr1:179606210 | A | G | 32 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0004c0004t0001g0015 others(29): Show |
32 | HG00280.hp2 HG00544.hp2 HG00609.hp2 others(29): Show |
intron_variant | MODIFIER | c.831+10392A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179606210 | |||||||
| chr1:179606226 | T | TCTGGTAT others(6091): Show |
2 | a0001c0001t0001g0281 a0001c0001t0001g0306 |
2 | NA18951.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.831+10424_831+1042 others(6102): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | 179606226 | ||||||
| chr1:179606226 | T | TCTGGTAT others(6092): Show |
1 | a0001c0001t0001g0299 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.831+10424_831+1042 others(6103): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | 179606226 | ||||||
| chr1:179606226 | T | TCTGGTAT others(6092): Show |
3 | a0001c0001t0001g0307 a0001c0001t0001g0308 a0001c0001t0001g0352 |
3 | HG02015.hp1 HG02735.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.831+10424_831+1042 others(6103): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | 179606226 | ||||||
| chr1:179606226 | T | TCTGGTAT others(6092): Show |
2 | a0001c0001t0001g0188 a0001c0001t0001g0197 |
2 | HG00140.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.831+10424_831+1042 others(6103): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | 179606226 | ||||||
| chr1:179606226 | T | TCTGGTAT others(6092): Show |
1 | a0001c0001t0001g0309 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.831+10424_831+1042 others(6103): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | 179606226 | ||||||
| chr1:179606226 | T | TCTGGTAT others(6092): Show |
1 | a0001c0001t0001g0344 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.831+10424_831+1042 others(6103): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | 179606226 | ||||||
| chr1:179606226 | T | TCTGGTAT others(6091): Show |
1 | a0001c0001t0001g0310 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.831+10424_831+1042 others(6102): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | 179606226 | ||||||
| chr1:179606226 | T | TCTGGTAT others(6092): Show |
1 | a0001c0001t0001g0311 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.831+10424_831+1042 others(6103): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | 179606226 | ||||||
| chr1:179606226 | T | TCTGGTAT others(6092): Show |
11 | a0001c0001t0001g0282 a0001c0001t0001g0292 a0001c0001t0001g0293 others(8): Show |
11 | HG01952.hp1 HG02523.hp1 NA18747.hp1 others(8): Show |
intron_variant | MODIFIER | c.831+10424_831+1042 others(6103): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | 179606226 | ||||||
| chr1:179606226 | T | TCTGGTAT others(6092): Show |
1 | a0001c0001t0001g0353 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.831+10424_831+1042 others(6103): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | 179606226 | ||||||
| chr1:179606226 | T | TCTGGTAT others(6092): Show |
1 | a0001c0001t0001g0189 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.831+10424_831+1042 others(6103): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | 179606226 | ||||||
| chr1:179606226 | T | TCTGGTAT others(6092): Show |
1 | a0001c0001t0001g0196 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.831+10424_831+1042 others(6103): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | 179606226 | ||||||
| chr1:179606226 | T | TCTGGTAT others(6092): Show |
1 | a0001c0001t0001g0318 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.831+10424_831+1042 others(6103): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | 179606226 | ||||||
| chr1:179606226 | T | TCTGGTAT others(6093): Show |
1 | a0001c0001t0001g0319 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.831+10424_831+1042 others(6104): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | 179606226 | ||||||
| chr1:179606226 | T | TCTGGTAT others(6093): Show |
1 | a0001c0001t0001g0294 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.831+10424_831+1042 others(6104): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | 179606226 | ||||||
| chr1:179606226 | T | TCTGGTAT others(6093): Show |
1 | a0001c0001t0001g0320 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.831+10424_831+1042 others(6104): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | 179606226 | ||||||
| chr1:179606226 | T | TCTGGTAT others(6093): Show |
32 | a0001c0001t0001g0012 a0001c0001t0001g0280 a0001c0001t0001g0283 others(29): Show |
33 | HG00099.hp1 HG00280.hp1 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.831+10424_831+1042 others(6104): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | 179606226 | ||||||
| chr1:179606226 | T | TCTGGTAT others(6093): Show |
2 | a0001c0001t0001g0361 a0001c0001t0001g0362 |
2 | NA18946.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.831+10424_831+1042 others(6104): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | 179606226 | ||||||
| chr1:179606226 | T | TCTGGTAT others(6093): Show |
7 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0001g0192 others(4): Show |
7 | HG01071.hp2 HG01168.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.831+10424_831+1042 others(6104): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | 179606226 | ||||||
| chr1:179606226 | T | TCTGGTAT others(6093): Show |
1 | a0001c0019t0001g0334 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.831+10424_831+1042 others(6104): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | 179606226 | ||||||
| chr1:179606226 | T | TCTGGTAT others(6093): Show |
1 | a0015c0021t0001g0335 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.831+10424_831+1042 others(6104): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | 179606226 | ||||||
| chr1:179606226 | T | TCTGGTAT others(6093): Show |
1 | a0001c0001t0001g0298 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.831+10424_831+1042 others(6104): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | 179606226 | ||||||
| chr1:179606226 | T | TCTGGTAT others(6093): Show |
1 | a0001c0001t0001g0336 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.831+10424_831+1042 others(6104): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | 179606226 | ||||||
| chr1:179606226 | T | TCTGGTAT others(6093): Show |
1 | a0001c0001t0001g0337 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.831+10424_831+1042 others(6104): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | 179606226 | ||||||
| chr1:179606226 | T | TCTGGTAT others(6093): Show |
1 | a0001c0001t0001g0300 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.831+10424_831+1042 others(6104): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | 179606226 | ||||||
| chr1:179606226 | T | TCTGGTAT others(6093): Show |
2 | a0001c0001t0001g0301 a0001c0001t0001g0302 |
2 | NA18964.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.831+10424_831+1042 others(6104): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | 179606226 | ||||||
| chr1:179606226 | T | TCTGGTAT others(6093): Show |
1 | a0001c0001t0001g0303 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.831+10424_831+1042 others(6104): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | 179606226 | ||||||
| chr1:179606226 | T | TCTGGTAT others(6094): Show |
1 | a0001c0001t0001g0288 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.831+10424_831+1042 others(6105): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | 179606226 | ||||||
| chr1:179606226 | T | TCTGGTAT others(6094): Show |
1 | a0001c0001t0001g0363 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.831+10424_831+1042 others(6105): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | 179606226 | ||||||
| chr1:179606226 | T | TCTGGTAT others(6094): Show |
4 | a0001c0001t0001g0355 a0001c0001t0001g0356 a0001c0001t0001g0357 others(1): Show |
4 | HG00558.hp1 HG02080.hp1 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.831+10424_831+1042 others(6105): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | 179606226 | ||||||
| chr1:179606226 | T | TCTGGTAT others(6094): Show |
2 | a0002c0002t0002g0011 a0002c0002t0002g0289 |
3 | HG01070.hp2 HG01071.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.831+10424_831+1042 others(6105): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | 179606226 | ||||||
| chr1:179606226 | T | TCTGGTAT others(6093): Show |
1 | a0001c0001t0001g0354 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.831+10424_831+1042 others(6104): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | 179606226 | ||||||
| chr1:179606226 | T | TCTGGTAT others(6094): Show |
1 | a0001c0001t0001g0305 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.831+10424_831+1042 others(6105): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | 179606226 | ||||||
| chr1:179606226 | T | TCTGGTAT others(6094): Show |
2 | a0001c0001t0001g0338 a0001c0001t0001g0339 |
2 | HG02145.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.831+10424_831+1042 others(6105): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | 179606226 | ||||||
| chr1:179606226 | T | TCTGGTAT others(6094): Show |
3 | a0001c0001t0001g0340 a0001c0001t0001g0341 a0001c0001t0001g0342 |
3 | HG01109.hp2 HG02970.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.831+10424_831+1042 others(6105): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | 179606226 | ||||||
| chr1:179606234 | A | G | 35 | a0001c0001t0001g0209 a0005c0006t0001g0206 a0005c0006t0001g0210 others(32): Show |
35 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.831+10416A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179606234 | |||||||
| chr1:179606266 | T | G | 2 | a0009c0014t0001g0364 a0009c0014t0001g0365 |
2 | HG01884.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.831+10448T>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179606266 | |||||||
| chr1:179606286 | G | T | 4 | a0007c0010t0001g0257 a0007c0010t0001g0258 a0007c0010t0001g0259 others(1): Show |
4 | HG01099.hp1 HG02486.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.831+10468G>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179606286 | |||||||
| chr1:179606383 | T | A | 35 | a0001c0001t0001g0209 a0005c0006t0001g0206 a0005c0006t0001g0210 others(32): Show |
35 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.831+10565T>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179606383 | |||||||
| chr1:179606402 | A | G | 1 | a0004c0004t0001g0033 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.831+10584A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179606402 | |||||||
| chr1:179606452 | A | T | 5 | a0005c0012t0001g0254 a0005c0012t0001g0255 a0005c0012t0001g0256 others(2): Show |
5 | HG00735.hp2 HG01109.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.831+10634A>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179606452 | |||||||
| chr1:179606507 | G | A | 35 | a0001c0001t0001g0209 a0005c0006t0001g0206 a0005c0006t0001g0210 others(32): Show |
35 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.831+10689G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179606507 | |||||||
| chr1:179606647 | G | A | 95 | a0001c0001t0001g0012 a0001c0001t0001g0188 a0001c0001t0001g0189 others(92): Show |
97 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.831+10829G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179606647 | |||||||
| chr1:179606657 | G | GT | 4 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(1): Show |
4 | HG02717.hp1 HG02809.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.831+10846dupT | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | 179606657 | ||||||
| chr1:179606658 | T | G | 1 | a0002c0002t0002g0096 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.831+10840T>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179606658 | |||||||
| chr1:179606854 | A | G | 251 | a0001c0001t0001g0012 a0001c0001t0001g0089 a0001c0001t0001g0090 others(248): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.831+11036A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179606854 | |||||||
| chr1:179606862 | T | C | 4 | a0007c0010t0001g0257 a0007c0010t0001g0258 a0007c0010t0001g0259 others(1): Show |
4 | HG01099.hp1 HG02486.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.831+11044T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179606862 | |||||||
| chr1:179606984 | AGAT | A | 4 | a0007c0010t0001g0257 a0007c0010t0001g0258 a0007c0010t0001g0259 others(1): Show |
4 | HG01099.hp1 HG02486.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.831+11167_831+1116 others(7): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179606984 | |||||||
| chr1:179607085 | C | T | 3 | a0004c0004t0001g0018 a0004c0004t0001g0030 a0004c0004t0001g0031 |
3 | NA18971.hp2 NA18986.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.831+11267C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179607085 | |||||||
| chr1:179607222 | A | G | 1 | a0001c0001t0001g0351 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.832-11377A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179607222 | |||||||
| chr1:179607232 | A | G | 2 | a0002c0002t0002g0173 a0002c0002t0002g0174 |
2 | HG02004.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.832-11367A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179607232 | |||||||
| chr1:179607237 | T | C | 1 | a0002c0002t0002g0110 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.832-11362T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179607237 | |||||||
| chr1:179607271 | A | C | 32 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0004c0004t0001g0015 others(29): Show |
32 | HG00280.hp2 HG00544.hp2 HG00609.hp2 others(29): Show |
intron_variant | MODIFIER | c.832-11328A>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179607271 | |||||||
| chr1:179607295 | A | G | 77 | a0001c0001t0001g0012 a0001c0001t0001g0280 a0001c0001t0001g0281 others(74): Show |
78 | HG00099.hp1 HG00280.hp1 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.832-11304A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179607295 | |||||||
| chr1:179607446 | T | A | 35 | a0001c0001t0001g0209 a0005c0006t0001g0206 a0005c0006t0001g0210 others(32): Show |
35 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.832-11153T>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179607446 | |||||||
| chr1:179607662 | G | A | 35 | a0001c0001t0001g0209 a0005c0006t0001g0206 a0005c0006t0001g0210 others(32): Show |
35 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.832-10937G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179607662 | |||||||
| chr1:179607695 | C | T | 3 | a0005c0012t0001g0254 a0005c0012t0001g0255 a0005c0012t0001g0256 |
3 | HG00735.hp2 HG01109.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.832-10904C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179607695 | |||||||
| chr1:179607717 | A | G | 121 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0104 others(118): Show |
128 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.832-10882A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179607717 | |||||||
| chr1:179607767 | G | T | 4 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0010c0016t0001g0092 others(1): Show |
4 | HG01891.hp1 HG02280.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.832-10832G>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179607767 | |||||||
| chr1:179607809 | A | G | 2 | a0009c0014t0001g0364 a0009c0014t0001g0365 |
2 | HG01884.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.832-10790A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179607809 | |||||||
| chr1:179608014 | C | CTATTTGT others(2): Show |
4 | a0007c0010t0001g0257 a0007c0010t0001g0258 a0007c0010t0001g0259 others(1): Show |
4 | HG01099.hp1 HG02486.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.832-10583_832-1057 others(13): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | 179608014 | ||||||
| chr1:179608052 | G | A | 2 | a0001c0001t0001g0179 a0001c0001t0001g0180 |
2 | HG02965.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.832-10547G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179608052 | |||||||
| chr1:179608105 | A | G | 5 | a0002c0002t0002g0169 a0002c0002t0002g0170 a0002c0002t0002g0171 others(2): Show |
5 | HG00408.hp1 HG00597.hp2 HG00673.hp2 others(2): Show |
intron_variant | MODIFIER | c.832-10494A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179608105 | |||||||
| chr1:179608214 | CTTTG | C | 4 | a0007c0010t0001g0257 a0007c0010t0001g0258 a0007c0010t0001g0259 others(1): Show |
4 | HG01099.hp1 HG02486.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.832-10380_832-1037 others(8): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | 179608214 | ||||||
| chr1:179608261 | TTTC | T | 5 | a0005c0012t0001g0254 a0005c0012t0001g0255 a0005c0012t0001g0256 others(2): Show |
5 | HG00735.hp2 HG01109.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.832-10335_832-1033 others(7): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | 179608261 | ||||||
| chr1:179608268 | AT | A | 36 | a0001c0001t0001g0209 a0005c0006t0001g0206 a0005c0006t0001g0210 others(33): Show |
36 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(33): Show |
intron_variant | MODIFIER | c.832-10323delT | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | 179608268 | ||||||
| chr1:179608279 | G | T | 2 | a0005c0006t0002g0222 a0005c0006t0002g0223 |
2 | NA18965.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.832-10320G>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179608279 | |||||||
| chr1:179608287 | TTCATTGA others(10): Show |
T | 1 | a0001c0001t0002g0098 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.832-10297_832-1028 others(21): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | 179608287 | ||||||
| chr1:179608302 | A | C | 2 | a0001c0001t0001g0307 a0001c0001t0001g0327 |
2 | HG02015.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.832-10297A>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179608302 | |||||||
| chr1:179608399 | A | C | 1 | a0005c0007t0001g0221 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.832-10200A>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179608399 | |||||||
| chr1:179608420 | A | G | 11 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0190 others(8): Show |
11 | HG00140.hp1 HG00738.hp2 HG01069.hp2 others(8): Show |
intron_variant | MODIFIER | c.832-10179A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179608420 | |||||||
| chr1:179608442 | C | CTCTT | 36 | a0001c0001t0001g0209 a0005c0006t0001g0206 a0005c0006t0001g0210 others(33): Show |
36 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(33): Show |
intron_variant | MODIFIER | c.832-10154_832-1015 others(8): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | 179608442 | ||||||
| chr1:179608653 | C | A | 1 | a0001c0001t0001g0264 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.832-9946C>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179608653 | |||||||
| chr1:179608718 | T | C | 2 | a0009c0014t0001g0364 a0009c0014t0001g0365 |
2 | HG01884.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.832-9881T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179608718 | |||||||
| chr1:179608735 | G | GT | 36 | a0001c0001t0001g0209 a0005c0006t0001g0206 a0005c0006t0001g0210 others(33): Show |
36 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(33): Show |
intron_variant | MODIFIER | c.832-9854dupT | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | 179608735 | ||||||
| chr1:179608852 | A | G | 216 | a0001c0001t0001g0012 a0001c0001t0001g0089 a0001c0001t0001g0090 others(213): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.832-9747A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179608852 | |||||||
| chr1:179608949 | A | T | 15 | a0001c0001t0001g0010 a0001c0001t0001g0262 a0001c0001t0001g0264 others(12): Show |
16 | HG01106.hp1 HG01433.hp1 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.832-9650A>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179608949 | |||||||
| chr1:179608994 | G | T | 71 | a0001c0001t0001g0012 a0001c0001t0001g0280 a0001c0001t0001g0281 others(68): Show |
72 | HG00099.hp1 HG00280.hp1 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.832-9605G>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179608994 | |||||||
| chr1:179609091 | C | T | 22 | a0001c0001t0001g0209 a0005c0006t0001g0206 a0005c0006t0001g0210 others(19): Show |
22 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(19): Show |
intron_variant | MODIFIER | c.832-9508C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179609091 | |||||||
| chr1:179609188 | A | G | 6 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(3): Show |
6 | HG02109.hp2 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.832-9411A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179609188 | |||||||
| chr1:179609299 | A | G | 2 | a0001c0001t0001g0089 a0001c0001t0001g0090 |
2 | HG02572.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.832-9300A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179609299 | |||||||
| chr1:179609303 | A | G | 1 | a0002c0002t0002g0103 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.832-9296A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179609303 | |||||||
| chr1:179609433 | T | C | 1 | a0003c0003t0001g0054 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.832-9166T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179609433 | |||||||
| chr1:179609505 | T | C | 11 | a0001c0001t0001g0010 a0001c0001t0001g0262 a0001c0001t0001g0265 others(8): Show |
12 | HG01106.hp1 HG01433.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.832-9094T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179609505 | |||||||
| chr1:179609676 | A | G | 3 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 |
3 | HG02109.hp2 HG02630.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.832-8923A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179609676 | |||||||
| chr1:179609750 | T | C | 36 | a0001c0001t0001g0209 a0005c0006t0001g0206 a0005c0006t0001g0210 others(33): Show |
36 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(33): Show |
intron_variant | MODIFIER | c.832-8849T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179609750 | |||||||
| chr1:179609842 | C | T | 4 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0010c0016t0001g0092 others(1): Show |
4 | HG01891.hp1 HG02280.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.832-8757C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179609842 | |||||||
| chr1:179609903 | T | C | 36 | a0001c0001t0001g0209 a0005c0006t0001g0206 a0005c0006t0001g0210 others(33): Show |
36 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(33): Show |
intron_variant | MODIFIER | c.832-8696T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179609903 | |||||||
| chr1:179610618 | G | A | 4 | a0007c0010t0001g0257 a0007c0010t0001g0258 a0007c0010t0001g0259 others(1): Show |
4 | HG01099.hp1 HG02486.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.832-7981G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179610618 | |||||||
| chr1:179610660 | A | G | 2 | a0002c0002t0002g0011 a0002c0002t0002g0289 |
3 | HG01070.hp2 HG01071.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.832-7939A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179610660 | |||||||
| chr1:179610869 | A | AT | 3 | a0004c0004t0001g0027 a0004c0004t0001g0028 a0004c0004t0001g0029 |
3 | HG00733.hp1 HG01358.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.832-7727dupT | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | 179610869 | ||||||
| chr1:179610935 | T | C | 27 | a0001c0001t0001g0209 a0005c0006t0001g0206 a0005c0006t0001g0210 others(24): Show |
27 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(24): Show |
intron_variant | MODIFIER | c.832-7664T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179610935 | |||||||
| chr1:179611017 | T | C | 95 | a0001c0001t0001g0012 a0001c0001t0001g0188 a0001c0001t0001g0189 others(92): Show |
97 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.832-7582T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179611017 | |||||||
| chr1:179611030 | G | A | 32 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0004c0004t0001g0015 others(29): Show |
32 | HG00280.hp2 HG00544.hp2 HG00609.hp2 others(29): Show |
intron_variant | MODIFIER | c.832-7569G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179611030 | |||||||
| chr1:179611102 | G | A | 3 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 |
3 | HG02109.hp2 HG02630.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.832-7497G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179611102 | |||||||
| chr1:179611695 | C | T | 3 | a0001c0001t0001g0294 a0001c0001t0001g0296 a0001c0001t0001g0297 |
3 | HG02132.hp2 HG02135.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.832-6904C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179611695 | |||||||
| chr1:179611751 | G | C | 1 | a0001c0001t0002g0098 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.832-6848G>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179611751 | |||||||
| chr1:179611797 | G | A | 3 | a0005c0012t0001g0254 a0005c0012t0001g0255 a0005c0012t0001g0256 |
3 | HG00735.hp2 HG01109.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.832-6802G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179611797 | |||||||
| chr1:179611942 | A | G | 2 | a0009c0014t0001g0364 a0009c0014t0001g0365 |
2 | HG01884.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.832-6657A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179611942 | |||||||
| chr1:179612235 | G | C | 1 | a0001c0001t0001g0262 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.832-6364G>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179612235 | |||||||
| chr1:179612299 | C | T | 95 | a0001c0001t0001g0012 a0001c0001t0001g0188 a0001c0001t0001g0189 others(92): Show |
97 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.832-6300C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179612299 | |||||||
| chr1:179612364 | G | A | 1 | a0002c0002t0002g0111 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.832-6235G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179612364 | |||||||
| chr1:179612427 | G | T | 1 | a0001c0008t0001g0073 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.832-6172G>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179612427 | |||||||
| chr1:179612624 | T | C | 36 | a0001c0001t0001g0209 a0005c0006t0001g0206 a0005c0006t0001g0210 others(33): Show |
36 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(33): Show |
intron_variant | MODIFIER | c.832-5975T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179612624 | |||||||
| chr1:179612700 | G | A | 1 | a0002c0002t0001g0247 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.832-5899G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179612700 | |||||||
| chr1:179612708 | G | A | 1 | a0002c0002t0002g0112 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.832-5891G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179612708 | |||||||
| chr1:179612799 | G | A | 36 | a0001c0001t0001g0209 a0005c0006t0001g0206 a0005c0006t0001g0210 others(33): Show |
36 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(33): Show |
intron_variant | MODIFIER | c.832-5800G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179612799 | |||||||
| chr1:179612885 | G | A | 4 | a0007c0010t0001g0257 a0007c0010t0001g0258 a0007c0010t0001g0259 others(1): Show |
4 | HG01099.hp1 HG02486.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.832-5714G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179612885 | |||||||
| chr1:179612897 | T | C | 36 | a0001c0001t0001g0209 a0005c0006t0001g0206 a0005c0006t0001g0210 others(33): Show |
36 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(33): Show |
intron_variant | MODIFIER | c.832-5702T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179612897 | |||||||
| chr1:179612935 | C | CA | 92 | a0001c0001t0001g0012 a0001c0001t0001g0189 a0001c0001t0001g0190 others(89): Show |
94 | HG00099.hp1 HG00558.hp1 HG00621.hp2 others(91): Show |
intron_variant | MODIFIER | c.832-5643dupA | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | 179612935 | ||||||
| chr1:179612935 | C | CAA | 6 | a0001c0001t0001g0203 a0001c0001t0001g0283 a0001c0001t0001g0304 others(3): Show |
6 | HG00558.hp2 HG01981.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.832-5644_832-5643d others(4): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | 179612935 | ||||||
| chr1:179612935 | CA | C | 48 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0178 others(45): Show |
48 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.832-5643delA | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | 179612935 | ||||||
| chr1:179612935 | CAA | C | 8 | a0005c0012t0001g0254 a0005c0012t0001g0255 a0005c0012t0001g0256 others(5): Show |
8 | HG00735.hp2 HG01099.hp1 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.832-5644_832-5643d others(4): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | 179612935 | ||||||
| chr1:179612986 | C | T | 31 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0004c0004t0001g0015 others(28): Show |
31 | HG00280.hp2 HG00544.hp2 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.832-5613C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179612986 | |||||||
| chr1:179613134 | T | G | 3 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0023t0001g0202 |
3 | HG02055.hp1 HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.832-5465T>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179613134 | |||||||
| chr1:179613243 | A | G | 3 | a0007c0010t0001g0258 a0007c0010t0001g0259 a0007c0010t0001g0260 |
3 | HG01099.hp1 HG02723.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.832-5356A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179613243 | |||||||
| chr1:179613426 | A | G | 1 | a0003c0003t0001g0069 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.832-5173A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179613426 | |||||||
| chr1:179613489 | C | T | 1 | a0002c0002t0002g0107 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.832-5110C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179613489 | |||||||
| chr1:179613545 | A | T | 249 | a0001c0001t0001g0012 a0001c0001t0001g0089 a0001c0001t0001g0090 others(246): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.832-5054A>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179613545 | |||||||
| chr1:179613564 | G | A | 2 | a0002c0002t0002g0115 a0002c0002t0002g0116 |
2 | NA18943.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.832-5035G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179613564 | |||||||
| chr1:179613628 | A | G | 1 | a0001c0001t0001g0187 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.832-4971A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179613628 | |||||||
| chr1:179613800 | G | C | 94 | a0001c0001t0001g0012 a0001c0001t0001g0188 a0001c0001t0001g0189 others(91): Show |
96 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.832-4799G>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179613800 | |||||||
| chr1:179613801 | G | A | 70 | a0001c0001t0001g0012 a0001c0001t0001g0281 a0001c0001t0001g0282 others(67): Show |
71 | HG00099.hp1 HG00280.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.832-4798G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179613801 | |||||||
| chr1:179613820 | T | A | 3 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0023t0001g0202 |
3 | HG02055.hp1 HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.832-4779T>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179613820 | |||||||
| chr1:179613948 | G | A | 27 | a0001c0001t0001g0209 a0005c0006t0001g0206 a0005c0006t0001g0210 others(24): Show |
27 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(24): Show |
intron_variant | MODIFIER | c.832-4651G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179613948 | |||||||
| chr1:179614012 | G | T | 4 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0010c0016t0001g0092 others(1): Show |
4 | HG01891.hp1 HG02280.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.832-4587G>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179614012 | |||||||
| chr1:179614030 | G | A | 297 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0089 others(294): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.832-4569G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179614030 | |||||||
| chr1:179614083 | T | C | 1 | a0001c0001t0001g0089 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.832-4516T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179614083 | |||||||
| chr1:179614394 | C | T | 103 | a0001c0001t0001g0280 a0002c0002t0001g0176 a0002c0002t0001g0246 others(100): Show |
110 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.832-4205C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179614394 | |||||||
| chr1:179614669 | A | G | 1 | a0002c0002t0002g0164 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.832-3930A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179614669 | |||||||
| chr1:179614751 | G | C | 3 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 |
3 | HG02717.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.832-3848G>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179614751 | |||||||
| chr1:179614898 | A | C | 1 | a0002c0002t0002g0163 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.832-3701A>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179614898 | |||||||
| chr1:179615036 | C | T | 5 | a0001c0001t0001g0338 a0001c0001t0001g0339 a0001c0001t0001g0340 others(2): Show |
5 | HG01109.hp2 HG02145.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.832-3563C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179615036 | |||||||
| chr1:179615048 | T | C | 24 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0104 others(21): Show |
24 | HG00735.hp2 HG01070.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.832-3551T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179615048 | |||||||
| chr1:179615176 | G | T | 2 | a0009c0014t0001g0364 a0009c0014t0001g0365 |
2 | HG01884.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.832-3423G>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179615176 | |||||||
| chr1:179615271 | G | A | 1 | a0004c0004t0001g0033 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.832-3328G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179615271 | |||||||
| chr1:179615285 | T | G | 3 | a0001c0001t0001g0319 a0009c0014t0001g0364 a0009c0014t0001g0365 |
3 | HG01884.hp2 HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.832-3314T>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179615285 | |||||||
| chr1:179615293 | ATGAG | A | 8 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(5): Show |
8 | HG02109.hp2 HG02280.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.832-3304_832-3301d others(6): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | 179615293 | ||||||
| chr1:179615423 | A | G | 1 | a0004c0004t0001g0045 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.832-3176A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179615423 | |||||||
| chr1:179615449 | T | C | 3 | a0005c0012t0001g0254 a0005c0012t0001g0255 a0005c0012t0001g0256 |
3 | HG00735.hp2 HG01109.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.832-3150T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179615449 | |||||||
| chr1:179615483 | A | T | 31 | a0005c0006t0001g0206 a0005c0006t0001g0210 a0005c0006t0001g0211 others(28): Show |
31 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.832-3116A>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179615483 | |||||||
| chr1:179615508 | A | G | 26 | a0005c0006t0001g0206 a0005c0006t0001g0210 a0005c0006t0001g0211 others(23): Show |
26 | HG00544.hp1 HG00597.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.832-3091A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179615508 | |||||||
| chr1:179615678 | T | C | 3 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0023t0001g0202 |
3 | HG02055.hp1 HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.832-2921T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179615678 | |||||||
| chr1:179615739 | A | G | 3 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 |
3 | HG02717.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.832-2860A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179615739 | |||||||
| chr1:179615776 | C | CT | 114 | a0001c0001t0001g0026 a0001c0001t0001g0199 a0001c0001t0001g0200 others(111): Show |
121 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.832-2809dupT | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | 179615776 | ||||||
| chr1:179615776 | CT | C | 34 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0104 others(31): Show |
34 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.832-2809delT | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | 179615776 | ||||||
| chr1:179615886 | A | G | 85 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0280 others(82): Show |
87 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.832-2713A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179615886 | |||||||
| chr1:179615916 | A | G | 31 | a0005c0006t0001g0206 a0005c0006t0001g0210 a0005c0006t0001g0211 others(28): Show |
31 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.832-2683A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179615916 | |||||||
| chr1:179616011 | G | C | 26 | a0005c0006t0001g0206 a0005c0006t0001g0210 a0005c0006t0001g0211 others(23): Show |
26 | HG00544.hp1 HG00597.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.832-2588G>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179616011 | |||||||
| chr1:179616151 | A | G | 3 | a0005c0012t0001g0254 a0005c0012t0001g0255 a0005c0012t0001g0256 |
3 | HG00735.hp2 HG01109.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.832-2448A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179616151 | |||||||
| chr1:179616263 | C | T | 1 | a0004c0004t0001g0018 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.832-2336C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179616263 | |||||||
| chr1:179616348 | C | T | 5 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 others(2): Show |
5 | NA18962.hp2 NA18989.hp2 NA19000.hp2 others(2): Show |
intron_variant | MODIFIER | c.832-2251C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179616348 | |||||||
| chr1:179616359 | A | G | 3 | a0001c0013t0001g0243 a0001c0013t0001g0244 a0001c0013t0001g0245 |
3 | HG01243.hp2 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.832-2240A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179616359 | |||||||
| chr1:179616849 | C | T | 1 | a0004c0004t0001g0031 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.832-1750C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179616849 | |||||||
| chr1:179616915 | C | G | 1 | a0001c0001t0001g0276 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.832-1684C>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179616915 | |||||||
| chr1:179617179 | A | G | 118 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(115): Show |
125 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.832-1420A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179617179 | |||||||
| chr1:179617361 | G | A | 1 | a0014c0018t0001g0019 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.832-1238G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179617361 | |||||||
| chr1:179617379 | T | C | 16 | a0001c0001t0001g0010 a0001c0001t0001g0209 a0001c0001t0001g0262 others(13): Show |
17 | HG00408.hp2 HG01106.hp1 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.832-1220T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179617379 | |||||||
| chr1:179617405 | A | G | 3 | a0002c0002t0002g0008 a0002c0002t0002g0161 a0002c0002t0002g0162 |
4 | HG02027.hp2 HG02071.hp2 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.832-1194A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179617405 | |||||||
| chr1:179617649 | T | A | 31 | a0005c0006t0001g0206 a0005c0006t0001g0210 a0005c0006t0001g0211 others(28): Show |
31 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.832-950T>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179617649 | |||||||
| chr1:179617911 | C | T | 1 | a0002c0002t0001g0176 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.832-688C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179617911 | |||||||
| chr1:179617915 | C | A | 124 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0025 others(121): Show |
132 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.832-684C>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179617915 | |||||||
| chr1:179617949 | A | C | 1 | a0001c0001t0001g0273 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.832-650A>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179617949 | |||||||
| chr1:179617992 | TC | T | 5 | a0006c0009t0001g0091 a0006c0009t0001g0234 a0006c0009t0001g0235 others(2): Show |
5 | HG02622.hp2 HG02630.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.832-604delC | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | 179617992 | ||||||
| chr1:179618205 | G | A | 4 | a0003c0003t0001g0074 a0003c0003t0001g0075 a0003c0003t0001g0076 others(1): Show |
4 | NA18969.hp2 NA18999.hp1 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.832-394G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179618205 | |||||||
| chr1:179618287 | G | C | 12 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0180 others(9): Show |
12 | HG02004.hp2 HG02258.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.832-312G>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179618287 | |||||||
| chr1:179618370 | T | A | 31 | a0005c0006t0001g0206 a0005c0006t0001g0210 a0005c0006t0001g0211 others(28): Show |
31 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.832-229T>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179618370 | |||||||
| chr1:179618434 | T | C | 31 | a0005c0006t0001g0206 a0005c0006t0001g0210 a0005c0006t0001g0211 others(28): Show |
31 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.832-165T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | chr1 | 179618434 | |||||||
| chr1:179618720 | A | G | 2 | a0009c0014t0001g0364 a0009c0014t0001g0365 |
2 | HG01884.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.915+38A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 5/17 | chr1 | 179618720 | |||||||
| chr1:179618743 | G | T | 1 | a0004c0004t0001g0016 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.915+61G>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 5/17 | chr1 | 179618743 | |||||||
| chr1:179619040 | T | A | 1 | a0001c0001t0001g0188 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.915+358T>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 5/17 | chr1 | 179619040 | |||||||
| chr1:179619091 | G | A | 295 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0025 others(292): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.915+409G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 5/17 | chr1 | 179619091 | |||||||
| chr1:179619205 | T | C | 1 | a0001c0001t0001g0306 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.915+523T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 5/17 | chr1 | 179619205 | |||||||
| chr1:179619212 | A | G | 1 | a0001c0001t0001g0306 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.915+530A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 5/17 | chr1 | 179619212 | |||||||
| chr1:179619390 | T | C | 12 | a0001c0005t0001g0002 a0001c0005t0001g0003 a0001c0005t0001g0009 others(9): Show |
17 | HG01346.hp1 HG02055.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.915+708T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 5/17 | chr1 | 179619390 | |||||||
| chr1:179619471 | T | C | 12 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0180 others(9): Show |
12 | HG02004.hp2 HG02258.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.915+789T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 5/17 | chr1 | 179619471 | |||||||
| chr1:179619593 | A | G | 1 | a0002c0002t0002g0242 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.915+911A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 5/17 | chr1 | 179619593 | |||||||
| chr1:179619625 | C | CT | 9 | a0005c0011t0003g0085 a0005c0011t0003g0086 a0005c0011t0003g0087 others(6): Show |
9 | HG00735.hp2 HG01109.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.915+956dupT | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 179619625 | ||||||
| chr1:179619625 | CT | C | 29 | a0001c0001t0001g0010 a0001c0001t0001g0209 a0001c0001t0001g0262 others(26): Show |
35 | HG00408.hp2 HG01070.hp1 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.915+956delT | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 179619625 | ||||||
| chr1:179619643 | G | C | 1 | a0002c0002t0002g0096 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.915+961G>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 5/17 | chr1 | 179619643 | |||||||
| chr1:179619703 | A | G | 1 | a0002c0002t0002g0112 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.915+1021A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 5/17 | chr1 | 179619703 | |||||||
| chr1:179620110 | C | T | 31 | a0005c0006t0001g0206 a0005c0006t0001g0210 a0005c0006t0001g0211 others(28): Show |
31 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.916-925C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 5/17 | chr1 | 179620110 | |||||||
| chr1:179620440 | A | C | 6 | a0001c0001t0001g0355 a0001c0001t0001g0356 a0001c0001t0001g0357 others(3): Show |
7 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.916-595A>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 5/17 | chr1 | 179620440 | |||||||
| chr1:179620593 | GATGTACG others(8): Show |
G | 1 | a0002c0002t0002g0238 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.916-439_916-425del others(15): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 179620593 | ||||||
| chr1:179620827 | C | T | 2 | a0003c0003t0001g0066 a0003c0003t0001g0067 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.916-208C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 5/17 | chr1 | 179620827 | |||||||
| chr1:179620894 | C | CA | 95 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0188 others(92): Show |
97 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.916-132dupA | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 179620894 | ||||||
| chr1:179621015 | T | G | 1 | a0005c0006t0001g0210 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.916-20T>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 5/17 | chr1 | 179621015 | |||||||
| chr1:179621217 | C | T | 30 | a0004c0004t0001g0015 a0004c0004t0001g0016 a0004c0004t0001g0017 others(27): Show |
30 | HG00280.hp2 HG00544.hp2 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.972+126C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179621217 | |||||||
| chr1:179621330 | C | T | 31 | a0005c0006t0001g0206 a0005c0006t0001g0210 a0005c0006t0001g0211 others(28): Show |
31 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.972+239C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179621330 | |||||||
| chr1:179621508 | A | C | 3 | a0005c0012t0001g0254 a0005c0012t0001g0255 a0005c0012t0001g0256 |
3 | HG00735.hp2 HG01109.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.972+417A>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179621508 | |||||||
| chr1:179621656 | T | C | 1 | a0001c0001t0001g0196 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.972+565T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179621656 | |||||||
| chr1:179621667 | G | A | 325 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0025 others(322): Show |
340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.972+576G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179621667 | |||||||
| chr1:179621931 | A | G | 26 | a0005c0006t0001g0206 a0005c0006t0001g0210 a0005c0006t0001g0211 others(23): Show |
26 | HG00544.hp1 HG00597.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.972+840A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179621931 | |||||||
| chr1:179622094 | G | A | 2 | a0001c0001t0001g0321 a0001c0001t0001g0322 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.972+1003G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179622094 | |||||||
| chr1:179622155 | T | C | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | HG01891.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.972+1064T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179622155 | |||||||
| chr1:179622273 | A | G | 6 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(3): Show |
6 | HG02109.hp2 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.972+1182A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179622273 | |||||||
| chr1:179622279 | G | T | 26 | a0005c0006t0001g0206 a0005c0006t0001g0210 a0005c0006t0001g0211 others(23): Show |
26 | HG00544.hp1 HG00597.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.972+1188G>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179622279 | |||||||
| chr1:179622315 | A | G | 1 | a0002c0002t0002g0103 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.972+1224A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179622315 | |||||||
| chr1:179622647 | C | A | 1 | a0002c0002t0002g0101 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.972+1556C>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179622647 | |||||||
| chr1:179622713 | A | G | 3 | a0002c0002t0002g0159 a0002c0002t0002g0160 a0002c0002t0002g0167 |
3 | HG03490.hp2 HG03492.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.972+1622A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179622713 | |||||||
| chr1:179622729 | A | G | 1 | a0002c0002t0002g0101 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.972+1638A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179622729 | |||||||
| chr1:179623100 | A | C | 2 | a0003c0003t0001g0070 a0003c0003t0001g0071 |
2 | HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.972+2009A>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179623100 | |||||||
| chr1:179623135 | C | T | 102 | a0001c0001t0001g0026 a0002c0002t0001g0176 a0002c0002t0001g0246 others(99): Show |
109 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.972+2044C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179623135 | |||||||
| chr1:179623377 | A | G | 3 | a0005c0012t0001g0254 a0005c0012t0001g0255 a0005c0012t0001g0256 |
3 | HG00735.hp2 HG01109.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.972+2286A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179623377 | |||||||
| chr1:179623510 | A | G | 3 | a0001c0013t0001g0243 a0001c0013t0001g0244 a0001c0013t0001g0245 |
3 | HG01243.hp2 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.972+2419A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179623510 | |||||||
| chr1:179623625 | C | CT | 219 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0026 others(216): Show |
233 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.972+2556dupT | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr1 | 179623625 | ||||||
| chr1:179623625 | C | CTT | 33 | a0001c0001t0001g0012 a0001c0001t0001g0089 a0001c0001t0001g0090 others(30): Show |
34 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(31): Show |
intron_variant | MODIFIER | c.972+2555_972+2556d others(4): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr1 | 179623625 | ||||||
| chr1:179623625 | C | CTTT | 22 | a0001c0001t0001g0291 a0001c0001t0001g0352 a0004c0004t0001g0024 others(19): Show |
22 | HG00597.hp1 HG01070.hp1 HG01358.hp2 others(19): Show |
intron_variant | MODIFIER | c.972+2554_972+2556d others(5): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr1 | 179623625 | ||||||
| chr1:179623625 | C | CTTTT | 10 | a0005c0006t0001g0210 a0005c0006t0001g0218 a0005c0006t0001g0219 others(7): Show |
10 | HG00544.hp1 HG00735.hp2 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.972+2553_972+2556d others(6): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr1 | 179623625 | ||||||
| chr1:179623625 | CTTTTTT | C | 9 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0180 others(6): Show |
9 | HG02258.hp2 HG02280.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.972+2551_972+2556d others(8): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr1 | 179623625 | ||||||
| chr1:179623625 | CTTTTTTT others(3): Show |
C | 5 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(2): Show |
5 | HG02109.hp2 HG02630.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.972+2547_972+2556d others(12): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr1 | 179623625 | ||||||
| chr1:179623704 | G | A | 2 | a0009c0014t0001g0364 a0009c0014t0001g0365 |
2 | HG01884.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.972+2613G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179623704 | |||||||
| chr1:179623711 | G | A | 16 | a0001c0001t0001g0010 a0001c0001t0001g0209 a0001c0001t0001g0262 others(13): Show |
17 | HG00408.hp2 HG01106.hp1 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.972+2620G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179623711 | |||||||
| chr1:179623802 | T | TA | 121 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(118): Show |
128 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.972+2721dupA | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr1 | 179623802 | ||||||
| chr1:179623930 | C | A | 5 | a0006c0009t0001g0091 a0006c0009t0001g0234 a0006c0009t0001g0235 others(2): Show |
5 | HG02622.hp2 HG02630.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.972+2839C>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179623930 | |||||||
| chr1:179623940 | C | T | 1 | a0001c0001t0001g0184 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.972+2849C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179623940 | |||||||
| chr1:179624031 | G | A | 31 | a0005c0006t0001g0206 a0005c0006t0001g0210 a0005c0006t0001g0211 others(28): Show |
31 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.972+2940G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179624031 | |||||||
| chr1:179624123 | A | G | 1 | a0002c0002t0002g0166 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.972+3032A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179624123 | |||||||
| chr1:179624229 | C | A | 1 | a0001c0001t0002g0098 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.972+3138C>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179624229 | |||||||
| chr1:179624281 | A | G | 1 | a0004c0004t0001g0022 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.972+3190A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179624281 | |||||||
| chr1:179624431 | A | G | 31 | a0005c0006t0001g0206 a0005c0006t0001g0210 a0005c0006t0001g0211 others(28): Show |
31 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.972+3340A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179624431 | |||||||
| chr1:179624433 | G | C | 1 | a0002c0002t0001g0248 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.972+3342G>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179624433 | |||||||
| chr1:179624474 | C | A | 287 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0025 others(284): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.972+3383C>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179624474 | |||||||
| chr1:179624655 | G | A | 3 | a0005c0012t0001g0254 a0005c0012t0001g0255 a0005c0012t0001g0256 |
3 | HG00735.hp2 HG01109.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.972+3564G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179624655 | |||||||
| chr1:179624706 | C | A | 1 | a0001c0001t0001g0323 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.972+3615C>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179624706 | |||||||
| chr1:179625130 | C | CA | 158 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(155): Show |
165 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.972+4054dupA | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr1 | 179625130 | ||||||
| chr1:179625130 | C | CAA | 16 | a0001c0005t0001g0002 a0001c0005t0001g0003 a0001c0005t0001g0009 others(13): Show |
21 | HG00735.hp2 HG01109.hp1 HG01346.hp1 others(18): Show |
intron_variant | MODIFIER | c.972+4053_972+4054d others(4): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr1 | 179625130 | ||||||
| chr1:179625183 | A | G | 126 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(123): Show |
133 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.972+4092A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179625183 | |||||||
| chr1:179625188 | A | T | 3 | a0005c0012t0001g0254 a0005c0012t0001g0255 a0005c0012t0001g0256 |
3 | HG00735.hp2 HG01109.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.972+4097A>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179625188 | |||||||
| chr1:179625255 | A | C | 1 | a0001c0001t0001g0331 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.972+4164A>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179625255 | |||||||
| chr1:179625331 | A | C | 5 | a0006c0009t0001g0091 a0006c0009t0001g0234 a0006c0009t0001g0235 others(2): Show |
5 | HG02622.hp2 HG02630.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.972+4240A>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179625331 | |||||||
| chr1:179625408 | A | G | 1 | a0001c0001t0001g0186 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.972+4317A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179625408 | |||||||
| chr1:179625568 | T | C | 26 | a0005c0006t0001g0206 a0005c0006t0001g0210 a0005c0006t0001g0211 others(23): Show |
26 | HG00544.hp1 HG00597.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.972+4477T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179625568 | |||||||
| chr1:179625713 | A | G | 1 | a0002c0002t0002g0164 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.972+4622A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179625713 | |||||||
| chr1:179625789 | G | A | 5 | a0006c0009t0001g0091 a0006c0009t0001g0234 a0006c0009t0001g0235 others(2): Show |
5 | HG02622.hp2 HG02630.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.972+4698G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179625789 | |||||||
| chr1:179625827 | A | G | 5 | a0001c0001t0001g0188 a0001c0001t0001g0195 a0001c0001t0001g0196 others(2): Show |
5 | HG00140.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.972+4736A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179625827 | |||||||
| chr1:179625835 | C | G | 1 | a0003c0003t0001g0071 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.972+4744C>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179625835 | |||||||
| chr1:179625912 | T | C | 121 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(118): Show |
128 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.972+4821T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179625912 | |||||||
| chr1:179625954 | C | T | 157 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(154): Show |
164 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.973-4813C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179625954 | |||||||
| chr1:179625979 | C | T | 1 | a0001c0001t0001g0320 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.973-4788C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179625979 | |||||||
| chr1:179626013 | A | G | 1 | a0001c0001t0002g0098 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.973-4754A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179626013 | |||||||
| chr1:179626075 | A | AG | 17 | a0001c0001t0001g0183 a0001c0001t0001g0194 a0001c0001t0001g0201 others(14): Show |
17 | HG00597.hp2 HG01192.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.973-4686dupG | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr1 | 179626075 | ||||||
| chr1:179626222 | T | G | 96 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0188 others(93): Show |
98 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.973-4545T>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179626222 | |||||||
| chr1:179626234 | AAAG | A | 44 | a0001c0001t0001g0026 a0002c0002t0002g0001 a0002c0002t0002g0004 others(41): Show |
49 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.973-4529_973-4527d others(5): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr1 | 179626234 | ||||||
| chr1:179626323 | A | G | 1 | a0001c0001t0001g0270 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.973-4444A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179626323 | |||||||
| chr1:179626389 | C | G | 6 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0007c0010t0001g0257 others(3): Show |
6 | HG01099.hp1 HG01891.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.973-4378C>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179626389 | |||||||
| chr1:179626610 | A | C | 1 | a0001c0001t0001g0319 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.973-4157A>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179626610 | |||||||
| chr1:179626676 | G | A | 2 | a0001c0001t0001g0025 a0001c0001t0001g0308 |
2 | HG00735.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.973-4091G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179626676 | |||||||
| chr1:179626734 | G | A | 31 | a0005c0006t0001g0206 a0005c0006t0001g0210 a0005c0006t0001g0211 others(28): Show |
31 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.973-4033G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179626734 | |||||||
| chr1:179626763 | A | AG | 31 | a0005c0006t0001g0206 a0005c0006t0001g0210 a0005c0006t0001g0211 others(28): Show |
31 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.973-4002dupG | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr1 | 179626763 | ||||||
| chr1:179626914 | T | G | 1 | a0005c0006t0001g0211 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.973-3853T>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179626914 | |||||||
| chr1:179627054 | A | G | 2 | a0009c0014t0001g0364 a0009c0014t0001g0365 |
2 | HG01884.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.973-3713A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179627054 | |||||||
| chr1:179627224 | C | T | 6 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0007c0010t0001g0257 others(3): Show |
6 | HG01099.hp1 HG01891.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.973-3543C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179627224 | |||||||
| chr1:179627237 | C | G | 1 | a0002c0002t0002g0144 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.973-3530C>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179627237 | |||||||
| chr1:179627285 | A | G | 1 | a0002c0002t0002g0143 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.973-3482A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179627285 | |||||||
| chr1:179627440 | A | G | 31 | a0005c0006t0001g0206 a0005c0006t0001g0210 a0005c0006t0001g0211 others(28): Show |
31 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.973-3327A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179627440 | |||||||
| chr1:179627937 | A | G | 1 | a0004c0004t0001g0016 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.973-2830A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179627937 | |||||||
| chr1:179628096 | C | T | 1 | a0001c0001t0001g0286 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.973-2671C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179628096 | |||||||
| chr1:179628103 | G | C | 96 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0188 others(93): Show |
98 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.973-2664G>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179628103 | |||||||
| chr1:179628249 | C | T | 2 | a0009c0014t0001g0364 a0009c0014t0001g0365 |
2 | HG01884.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.973-2518C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179628249 | |||||||
| chr1:179628309 | C | A | 124 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0025 others(121): Show |
132 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.973-2458C>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179628309 | |||||||
| chr1:179628319 | CTTTTCT | C | 101 | a0001c0001t0001g0026 a0001c0001t0001g0178 a0001c0001t0001g0179 others(98): Show |
108 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.973-2443_973-2438d others(8): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr1 | 179628319 | ||||||
| chr1:179628319 | CTTTTCTT | C | 13 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0104 others(10): Show |
13 | HG01257.hp1 HG01358.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.973-2443_973-2437d others(9): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr1 | 179628319 | ||||||
| chr1:179628319 | CTTTTCTT others(2): Show |
C | 7 | a0005c0006t0001g0211 a0005c0007t0001g0207 a0005c0012t0001g0254 others(4): Show |
7 | HG00735.hp2 HG01109.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.973-2443_973-2435d others(11): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr1 | 179628319 | ||||||
| chr1:179628319 | CTTTTCTT others(3): Show |
C | 20 | a0005c0006t0001g0206 a0005c0006t0001g0210 a0005c0006t0001g0214 others(17): Show |
20 | HG00597.hp1 HG01070.hp1 HG02015.hp2 others(17): Show |
intron_variant | MODIFIER | c.973-2443_973-2434d others(12): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr1 | 179628319 | ||||||
| chr1:179628319 | CTTTTCTT others(4): Show |
C | 4 | a0005c0006t0001g0212 a0005c0006t0001g0263 a0005c0007t0001g0205 others(1): Show |
4 | HG00544.hp1 NA18612.hp1 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.973-2443_973-2433d others(13): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr1 | 179628319 | ||||||
| chr1:179628319 | CTTTTCTT others(6): Show |
C | 3 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0023t0001g0202 |
3 | HG02055.hp1 HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.973-2443_973-2431d others(15): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr1 | 179628319 | ||||||
| chr1:179628324 | C | CT | 30 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(27): Show |
30 | HG00423.hp1 HG01069.hp1 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.973-2417dupT | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr1 | 179628324 | ||||||
| chr1:179628324 | C | CTT | 8 | a0001c0008t0001g0073 a0001c0013t0001g0243 a0003c0003t0001g0063 others(5): Show |
8 | HG02897.hp2 HG03195.hp1 HG03516.hp2 others(5): Show |
intron_variant | MODIFIER | c.973-2418_973-2417d others(4): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr1 | 179628324 | ||||||
| chr1:179628324 | CT | C | 116 | a0001c0001t0001g0012 a0001c0001t0001g0094 a0001c0001t0001g0095 others(113): Show |
123 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.973-2417delT | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr1 | 179628324 | ||||||
| chr1:179628324 | CTT | C | 22 | a0001c0001t0001g0010 a0001c0001t0001g0190 a0001c0001t0001g0197 others(19): Show |
23 | HG00099.hp1 HG00408.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.973-2418_973-2417d others(4): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr1 | 179628324 | ||||||
| chr1:179628329 | T | C | 1 | a0007c0010t0001g0257 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.973-2438T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179628329 | |||||||
| chr1:179628330 | T | C | 8 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0005c0012t0001g0254 others(5): Show |
8 | HG00735.hp2 HG01099.hp1 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.973-2437T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179628330 | |||||||
| chr1:179628351 | A | G | 1 | a0003c0003t0001g0071 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.973-2416A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179628351 | |||||||
| chr1:179628395 | A | G | 5 | a0006c0009t0001g0091 a0006c0009t0001g0234 a0006c0009t0001g0235 others(2): Show |
5 | HG02622.hp2 HG02630.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.973-2372A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179628395 | |||||||
| chr1:179628466 | G | GT | 13 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0283 others(10): Show |
13 | HG01099.hp1 HG01891.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.973-2286dupT | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr1 | 179628466 | ||||||
| chr1:179628471 | T | TC | 119 | a0001c0001t0001g0026 a0001c0001t0001g0104 a0001c0001t0001g0178 others(116): Show |
126 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.973-2296_973-2295i others(3): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179628471 | |||||||
| chr1:179628502 | C | G | 5 | a0006c0009t0001g0091 a0006c0009t0001g0234 a0006c0009t0001g0235 others(2): Show |
5 | HG02622.hp2 HG02630.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.973-2265C>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179628502 | |||||||
| chr1:179628778 | T | C | 1 | a0001c0001t0002g0098 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.973-1989T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179628778 | |||||||
| chr1:179628881 | G | A | 1 | a0005c0007t0001g0213 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.973-1886G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179628881 | |||||||
| chr1:179628919 | T | TTTG | 121 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(118): Show |
128 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.973-1824_973-1822d others(5): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr1 | 179628919 | ||||||
| chr1:179628919 | T | TTTGTTGT others(5): Show |
3 | a0005c0012t0001g0254 a0005c0012t0001g0255 a0005c0012t0001g0256 |
3 | HG00735.hp2 HG01109.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.973-1833_973-1822d others(14): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr1 | 179628919 | ||||||
| chr1:179629044 | A | G | 96 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0188 others(93): Show |
98 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.973-1723A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179629044 | |||||||
| chr1:179629158 | T | G | 2 | a0009c0014t0001g0364 a0009c0014t0001g0365 |
2 | HG01884.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.973-1609T>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179629158 | |||||||
| chr1:179629426 | G | A | 31 | a0005c0006t0001g0206 a0005c0006t0001g0210 a0005c0006t0001g0211 others(28): Show |
31 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.973-1341G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179629426 | |||||||
| chr1:179629455 | C | CAGAA | 121 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(118): Show |
128 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.973-1310_973-1309i others(6): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr1 | 179629455 | ||||||
| chr1:179629628 | A | G | 30 | a0004c0004t0001g0015 a0004c0004t0001g0016 a0004c0004t0001g0017 others(27): Show |
30 | HG00280.hp2 HG00544.hp2 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.973-1139A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179629628 | |||||||
| chr1:179629698 | T | G | 2 | a0009c0014t0001g0364 a0009c0014t0001g0365 |
2 | HG01884.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.973-1069T>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179629698 | |||||||
| chr1:179629855 | G | T | 1 | a0002c0002t0002g0165 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.973-912G>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179629855 | |||||||
| chr1:179629877 | C | T | 1 | a0001c0001t0001g0332 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.973-890C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179629877 | |||||||
| chr1:179629980 | C | CT | 62 | a0001c0001t0001g0010 a0001c0001t0001g0094 a0001c0001t0001g0095 others(59): Show |
63 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.973-770dupT | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr1 | 179629980 | ||||||
| chr1:179630084 | A | G | 17 | a0001c0001t0001g0010 a0001c0001t0001g0209 a0001c0001t0001g0262 others(14): Show |
18 | HG00408.hp2 HG01106.hp1 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.973-683A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179630084 | |||||||
| chr1:179630106 | T | A | 1 | a0003c0003t0001g0055 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.973-661T>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179630106 | |||||||
| chr1:179630192 | T | C | 96 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0188 others(93): Show |
98 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.973-575T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179630192 | |||||||
| chr1:179630200 | T | A | 5 | a0006c0009t0001g0091 a0006c0009t0001g0234 a0006c0009t0001g0235 others(2): Show |
5 | HG02622.hp2 HG02630.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.973-567T>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179630200 | |||||||
| chr1:179630230 | G | C | 31 | a0005c0006t0001g0206 a0005c0006t0001g0210 a0005c0006t0001g0211 others(28): Show |
31 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.973-537G>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179630230 | |||||||
| chr1:179630288 | T | C | 31 | a0005c0006t0001g0206 a0005c0006t0001g0210 a0005c0006t0001g0211 others(28): Show |
31 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.973-479T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179630288 | |||||||
| chr1:179630381 | C | T | 31 | a0005c0006t0001g0206 a0005c0006t0001g0210 a0005c0006t0001g0211 others(28): Show |
31 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.973-386C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179630381 | |||||||
| chr1:179630452 | TCCTCTTG others(9): Show |
T | 1 | a0004c0004t0001g0015 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.973-314_973-299del others(16): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 6/17 | chr1 | 179630452 | |||||||
| chr1:179630949 | C | G | 16 | a0001c0001t0001g0010 a0001c0001t0001g0209 a0001c0001t0001g0262 others(13): Show |
17 | HG00408.hp2 HG01106.hp1 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.1126+29C>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 7/17 | chr1 | 179630949 | |||||||
| chr1:179631056 | G | C | 1 | a0004c0004t0001g0038 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1126+136G>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 7/17 | chr1 | 179631056 | |||||||
| chr1:179631075 | A | C | 3 | a0003c0003t0001g0061 a0003c0003t0001g0062 a0003c0003t0001g0063 |
3 | HG03195.hp1 HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1126+155A>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 7/17 | chr1 | 179631075 | |||||||
| chr1:179631129 | T | C | 32 | a0005c0006t0001g0206 a0005c0006t0001g0210 a0005c0006t0001g0211 others(29): Show |
32 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.1126+209T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 7/17 | chr1 | 179631129 | |||||||
| chr1:179631174 | G | A | 6 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0007c0010t0001g0257 others(3): Show |
6 | HG01099.hp1 HG01891.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1126+254G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 7/17 | chr1 | 179631174 | |||||||
| chr1:179631219 | G | A | 5 | a0006c0009t0001g0091 a0006c0009t0001g0234 a0006c0009t0001g0235 others(2): Show |
5 | HG02622.hp2 HG02630.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1126+299G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 7/17 | chr1 | 179631219 | |||||||
| chr1:179631265 | G | A | 1 | a0001c0001t0001g0343 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1126+345G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 7/17 | chr1 | 179631265 | |||||||
| chr1:179631317 | G | T | 26 | a0005c0006t0001g0206 a0005c0006t0001g0210 a0005c0006t0001g0211 others(23): Show |
26 | HG00544.hp1 HG00597.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.1126+397G>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 7/17 | chr1 | 179631317 | |||||||
| chr1:179631637 | G | A | 1 | a0005c0007t0001g0207 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1126+717G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 7/17 | chr1 | 179631637 | |||||||
| chr1:179631650 | A | G | 3 | a0005c0012t0001g0254 a0005c0012t0001g0255 a0005c0012t0001g0256 |
3 | HG00735.hp2 HG01109.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.1126+730A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 7/17 | chr1 | 179631650 | |||||||
| chr1:179631651 | A | T | 31 | a0005c0006t0001g0206 a0005c0006t0001g0210 a0005c0006t0001g0211 others(28): Show |
31 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.1126+731A>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 7/17 | chr1 | 179631651 | |||||||
| chr1:179631653 | A | C | 31 | a0005c0006t0001g0206 a0005c0006t0001g0210 a0005c0006t0001g0211 others(28): Show |
31 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.1126+733A>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 7/17 | chr1 | 179631653 | |||||||
| chr1:179631746 | C | G | 1 | a0002c0002t0002g0240 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1126+826C>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 7/17 | chr1 | 179631746 | |||||||
| chr1:179631851 | A | AT | 216 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0026 others(213): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.1126+953dupT | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr1 | 179631851 | ||||||
| chr1:179631851 | A | ATT | 51 | a0001c0001t0001g0025 a0001c0001t0001g0188 a0001c0001t0001g0189 others(48): Show |
51 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(48): Show |
intron_variant | MODIFIER | c.1126+952_1126+953d others(4): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr1 | 179631851 | ||||||
| chr1:179631851 | A | ATTT | 7 | a0001c0001t0001g0194 a0001c0001t0001g0196 a0001c0013t0001g0243 others(4): Show |
7 | HG02280.hp1 HG02738.hp2 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.1126+951_1126+953d others(5): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr1 | 179631851 | ||||||
| chr1:179631851 | A | ATTTT | 27 | a0001c0013t0001g0245 a0003c0003t0001g0054 a0004c0004t0001g0016 others(24): Show |
27 | HG00280.hp2 HG00544.hp2 HG00609.hp2 others(24): Show |
intron_variant | MODIFIER | c.1126+950_1126+953d others(6): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr1 | 179631851 | ||||||
| chr1:179631856 | T | TG | 4 | a0005c0006t0001g0211 a0005c0006t0001g0220 a0005c0007t0001g0208 others(1): Show |
4 | NA18975.hp1 NA19000.hp1 NA19077.hp1 others(1): Show |
intron_variant | MODIFIER | c.1126+936_1126+937i others(3): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 7/17 | chr1 | 179631856 | |||||||
| chr1:179631857 | T | G | 25 | a0005c0006t0001g0206 a0005c0006t0001g0210 a0005c0006t0001g0212 others(22): Show |
25 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.1126+937T>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 7/17 | chr1 | 179631857 | |||||||
| chr1:179632096 | T | C | 157 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(154): Show |
164 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.1126+1176T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 7/17 | chr1 | 179632096 | |||||||
| chr1:179632115 | C | G | 5 | a0006c0009t0001g0091 a0006c0009t0001g0234 a0006c0009t0001g0235 others(2): Show |
5 | HG02622.hp2 HG02630.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1126+1195C>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 7/17 | chr1 | 179632115 | |||||||
| chr1:179632142 | G | A | 1 | a0001c0001t0001g0265 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1126+1222G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 7/17 | chr1 | 179632142 | |||||||
| chr1:179632294 | C | G | 1 | a0001c0001t0001g0270 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1126+1374C>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 7/17 | chr1 | 179632294 | |||||||
| chr1:179632380 | T | C | 1 | a0005c0007t0001g0253 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1126+1460T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 7/17 | chr1 | 179632380 | |||||||
| chr1:179632398 | G | GT | 6 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0104 others(3): Show |
6 | HG01255.hp1 HG02145.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1126+1490dupT | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr1 | 179632398 | ||||||
| chr1:179632398 | GT | G | 31 | a0005c0006t0001g0206 a0005c0006t0001g0210 a0005c0006t0001g0211 others(28): Show |
31 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.1126+1490delT | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr1 | 179632398 | ||||||
| chr1:179632487 | C | T | 5 | a0006c0009t0001g0091 a0006c0009t0001g0234 a0006c0009t0001g0235 others(2): Show |
5 | HG02622.hp2 HG02630.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1126+1567C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 7/17 | chr1 | 179632487 | |||||||
| chr1:179632614 | T | C | 124 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0025 others(121): Show |
132 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.1126+1694T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 7/17 | chr1 | 179632614 | |||||||
| chr1:179632615 | T | A | 150 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(147): Show |
157 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.1126+1695T>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 7/17 | chr1 | 179632615 | |||||||
| chr1:179632774 | C | T | 2 | a0009c0014t0001g0364 a0009c0014t0001g0365 |
2 | HG01884.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1127-1683C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 7/17 | chr1 | 179632774 | |||||||
| chr1:179632776 | A | G | 150 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(147): Show |
157 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.1127-1681A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 7/17 | chr1 | 179632776 | |||||||
| chr1:179632793 | G | T | 2 | a0009c0014t0001g0364 a0009c0014t0001g0365 |
2 | HG01884.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1127-1664G>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 7/17 | chr1 | 179632793 | |||||||
| chr1:179632951 | T | C | 3 | a0005c0012t0001g0254 a0005c0012t0001g0255 a0005c0012t0001g0256 |
3 | HG00735.hp2 HG01109.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.1127-1506T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 7/17 | chr1 | 179632951 | |||||||
| chr1:179632968 | C | T | 157 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(154): Show |
164 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.1127-1489C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 7/17 | chr1 | 179632968 | |||||||
| chr1:179633196 | A | T | 325 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0025 others(322): Show |
340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.1127-1261A>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 7/17 | chr1 | 179633196 | |||||||
| chr1:179633357 | C | CT | 9 | a0001c0001t0001g0350 a0001c0001t0001g0355 a0001c0001t0001g0356 others(6): Show |
9 | HG00558.hp1 HG00558.hp2 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.1127-1088dupT | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr1 | 179633357 | ||||||
| chr1:179633373 | A | G | 1 | a0005c0007t0001g0253 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1127-1084A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 7/17 | chr1 | 179633373 | |||||||
| chr1:179633454 | T | C | 126 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(123): Show |
133 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.1127-1003T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 7/17 | chr1 | 179633454 | |||||||
| chr1:179633596 | C | T | 6 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0007c0010t0001g0257 others(3): Show |
6 | HG01099.hp1 HG01891.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1127-861C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 7/17 | chr1 | 179633596 | |||||||
| chr1:179633607 | C | T | 2 | a0001c0001t0001g0089 a0001c0001t0001g0090 |
2 | HG02572.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1127-850C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 7/17 | chr1 | 179633607 | |||||||
| chr1:179633615 | G | C | 328 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0025 others(325): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.1127-842G>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 7/17 | chr1 | 179633615 | |||||||
| chr1:179633751 | C | T | 1 | a0003c0003t0001g0063 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1127-706C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 7/17 | chr1 | 179633751 | |||||||
| chr1:179633898 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1127-559G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 7/17 | chr1 | 179633898 | |||||||
| chr1:179633953 | C | A | 3 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0104 |
3 | HG02145.hp2 HG02572.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1127-504C>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 7/17 | chr1 | 179633953 | |||||||
| chr1:179633996 | C | T | 12 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0180 others(9): Show |
12 | HG02004.hp2 HG02258.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.1127-461C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 7/17 | chr1 | 179633996 | |||||||
| chr1:179634029 | G | A | 16 | a0001c0001t0001g0010 a0001c0001t0001g0209 a0001c0001t0001g0262 others(13): Show |
17 | HG00408.hp2 HG01106.hp1 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.1127-428G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 7/17 | chr1 | 179634029 | |||||||
| chr1:179634036 | T | G | 5 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(2): Show |
5 | HG02258.hp2 HG02965.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1127-421T>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 7/17 | chr1 | 179634036 | |||||||
| chr1:179634119 | C | T | 2 | a0001c0001t0001g0299 a0001c0001t0001g0303 |
2 | NA18965.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.1127-338C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 7/17 | chr1 | 179634119 | |||||||
| chr1:179634120 | G | A | 2 | a0009c0014t0001g0364 a0009c0014t0001g0365 |
2 | HG01884.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1127-337G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 7/17 | chr1 | 179634120 | |||||||
| chr1:179634125 | C | A | 1 | a0002c0002t0001g0252 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1127-332C>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 7/17 | chr1 | 179634125 | |||||||
| chr1:179634128 | A | T | 12 | a0001c0001t0001g0010 a0001c0001t0001g0209 a0001c0001t0001g0262 others(9): Show |
13 | HG00408.hp2 HG01106.hp1 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.1127-329A>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 7/17 | chr1 | 179634128 | |||||||
| chr1:179634129 | C | T | 3 | a0005c0012t0001g0254 a0005c0012t0001g0255 a0005c0012t0001g0256 |
3 | HG00735.hp2 HG01109.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.1127-328C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 7/17 | chr1 | 179634129 | |||||||
| chr1:179634152 | T | C | 328 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0025 others(325): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.1127-305T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 7/17 | chr1 | 179634152 | |||||||
| chr1:179634164 | T | C | 328 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0025 others(325): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.1127-293T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 7/17 | chr1 | 179634164 | |||||||
| chr1:179634170 | C | CA | 121 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(118): Show |
128 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.1127-281dupA | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr1 | 179634170 | ||||||
| chr1:179634176 | AC | A | 26 | a0005c0006t0001g0206 a0005c0006t0001g0210 a0005c0006t0001g0211 others(23): Show |
26 | HG00544.hp1 HG00597.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.1127-280delC | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 7/17 | chr1 | 179634176 | |||||||
| chr1:179634177 | C | A | 126 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(123): Show |
133 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.1127-280C>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 7/17 | chr1 | 179634177 | |||||||
| chr1:179634298 | A | G | 1 | a0002c0002t0002g0112 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1127-159A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 7/17 | chr1 | 179634298 | |||||||
| chr1:179634676 | A | G | 2 | a0009c0014t0001g0364 a0009c0014t0001g0365 |
2 | HG01884.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1299+47A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 8/17 | chr1 | 179634676 | |||||||
| chr1:179634710 | T | A | 1 | a0002c0002t0002g0103 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1299+81T>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 8/17 | chr1 | 179634710 | |||||||
| chr1:179634765 | T | C | 1 | a0002c0002t0002g0124 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1299+136T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 8/17 | chr1 | 179634765 | |||||||
| chr1:179635064 | T | C | 3 | a0005c0012t0001g0254 a0005c0012t0001g0255 a0005c0012t0001g0256 |
3 | HG00735.hp2 HG01109.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.1299+435T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 8/17 | chr1 | 179635064 | |||||||
| chr1:179635232 | A | G | 30 | a0004c0004t0001g0015 a0004c0004t0001g0016 a0004c0004t0001g0017 others(27): Show |
30 | HG00280.hp2 HG00544.hp2 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.1300-435A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 8/17 | chr1 | 179635232 | |||||||
| chr1:179635287 | A | G | 1 | a0001c0001t0001g0209 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1300-380A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 8/17 | chr1 | 179635287 | |||||||
| chr1:179635379 | A | G | 126 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(123): Show |
133 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.1300-288A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 8/17 | chr1 | 179635379 | |||||||
| chr1:179635380 | G | A | 3 | a0005c0012t0001g0254 a0005c0012t0001g0255 a0005c0012t0001g0256 |
3 | HG00735.hp2 HG01109.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.1300-287G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 8/17 | chr1 | 179635380 | |||||||
| chr1:179635923 | G | A | 157 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(154): Show |
164 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.1520+36G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 9/17 | chr1 | 179635923 | |||||||
| chr1:179635933 | T | A | 1 | a0001c0001t0001g0184 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1520+46T>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 9/17 | chr1 | 179635933 | |||||||
| chr1:179635981 | C | A | 5 | a0006c0009t0001g0091 a0006c0009t0001g0234 a0006c0009t0001g0235 others(2): Show |
5 | HG02622.hp2 HG02630.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1520+94C>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 9/17 | chr1 | 179635981 | |||||||
| chr1:179635991 | CT | C | 125 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(122): Show |
132 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.1520+112delT | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr1 | 179635991 | ||||||
| chr1:179636001 | T | C | 1 | a0005c0007t0001g0360 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1520+114T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 9/17 | chr1 | 179636001 | |||||||
| chr1:179636053 | T | C | 5 | a0006c0009t0001g0091 a0006c0009t0001g0234 a0006c0009t0001g0235 others(2): Show |
5 | HG02622.hp2 HG02630.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1520+166T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 9/17 | chr1 | 179636053 | |||||||
| chr1:179636735 | T | C | 126 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(123): Show |
133 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.1520+848T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 9/17 | chr1 | 179636735 | |||||||
| chr1:179636924 | T | C | 1 | a0003c0003t0001g0060 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1520+1037T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 9/17 | chr1 | 179636924 | |||||||
| chr1:179636965 | T | C | 5 | a0001c0001t0001g0338 a0001c0001t0001g0339 a0001c0001t0001g0340 others(2): Show |
5 | HG01109.hp2 HG02145.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1520+1078T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 9/17 | chr1 | 179636965 | |||||||
| chr1:179637022 | T | C | 155 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(152): Show |
162 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.1520+1135T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 9/17 | chr1 | 179637022 | |||||||
| chr1:179637041 | A | T | 1 | a0004c0004t0001g0016 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1520+1154A>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 9/17 | chr1 | 179637041 | |||||||
| chr1:179637205 | C | T | 1 | a0001c0001t0001g0261 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1520+1318C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 9/17 | chr1 | 179637205 | |||||||
| chr1:179637386 | C | G | 3 | a0001c0001t0001g0338 a0001c0001t0001g0339 a0001c0001t0001g0342 |
3 | HG02145.hp1 HG02818.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1520+1499C>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 9/17 | chr1 | 179637386 | |||||||
| chr1:179637460 | A | G | 5 | a0006c0009t0001g0091 a0006c0009t0001g0234 a0006c0009t0001g0235 others(2): Show |
5 | HG02622.hp2 HG02630.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1520+1573A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 9/17 | chr1 | 179637460 | |||||||
| chr1:179637559 | C | A | 1 | a0001c0001t0002g0098 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1520+1672C>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 9/17 | chr1 | 179637559 | |||||||
| chr1:179637588 | G | A | 5 | a0006c0009t0001g0091 a0006c0009t0001g0234 a0006c0009t0001g0235 others(2): Show |
5 | HG02622.hp2 HG02630.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1520+1701G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 9/17 | chr1 | 179637588 | |||||||
| chr1:179637634 | C | T | 1 | a0001c0001t0001g0319 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1520+1747C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 9/17 | chr1 | 179637634 | |||||||
| chr1:179637639 | G | C | 295 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0025 others(292): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.1520+1752G>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 9/17 | chr1 | 179637639 | |||||||
| chr1:179637675 | A | G | 1 | a0003c0003t0001g0049 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1520+1788A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 9/17 | chr1 | 179637675 | |||||||
| chr1:179637718 | G | GA | 88 | a0001c0001t0001g0010 a0001c0001t0001g0094 a0001c0001t0001g0095 others(85): Show |
94 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.1520+1843dupA | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr1 | 179637718 | ||||||
| chr1:179637718 | G | GAA | 30 | a0001c0001t0001g0194 a0004c0004t0001g0015 a0004c0004t0001g0016 others(27): Show |
30 | HG00280.hp2 HG00544.hp2 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.1520+1842_1520+184 others(6): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr1 | 179637718 | ||||||
| chr1:179637723 | A | AG | 121 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(118): Show |
128 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.1520+1836_1520+183 others(5): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 9/17 | chr1 | 179637723 | |||||||
| chr1:179637872 | C | G | 1 | a0002c0002t0002g0109 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1521-1967C>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 9/17 | chr1 | 179637872 | |||||||
| chr1:179637963 | G | A | 6 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0007c0010t0001g0257 others(3): Show |
6 | HG01099.hp1 HG01891.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1521-1876G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 9/17 | chr1 | 179637963 | |||||||
| chr1:179638024 | G | C | 3 | a0001c0013t0001g0243 a0001c0013t0001g0244 a0001c0013t0001g0245 |
3 | HG01243.hp2 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1521-1815G>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 9/17 | chr1 | 179638024 | |||||||
| chr1:179638048 | G | T | 1 | a0002c0002t0002g0150 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1521-1791G>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 9/17 | chr1 | 179638048 | |||||||
| chr1:179638086 | G | A | 1 | a0004c0004t0001g0015 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1521-1753G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 9/17 | chr1 | 179638086 | |||||||
| chr1:179638118 | A | C | 1 | a0002c0002t0001g0252 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1521-1721A>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 9/17 | chr1 | 179638118 | |||||||
| chr1:179638147 | C | T | 102 | a0001c0001t0001g0026 a0002c0002t0001g0176 a0002c0002t0001g0246 others(99): Show |
109 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.1521-1692C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 9/17 | chr1 | 179638147 | |||||||
| chr1:179638149 | A | G | 46 | a0001c0001t0001g0026 a0002c0002t0002g0001 a0002c0002t0002g0004 others(43): Show |
51 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.1521-1690A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 9/17 | chr1 | 179638149 | |||||||
| chr1:179638154 | A | T | 126 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(123): Show |
133 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.1521-1685A>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 9/17 | chr1 | 179638154 | |||||||
| chr1:179638156 | G | A | 126 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(123): Show |
133 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.1521-1683G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 9/17 | chr1 | 179638156 | |||||||
| chr1:179638157 | ATGTTTTC others(760): Show |
A | 126 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(123): Show |
133 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.1521-1680_1521-914 others(3): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr1 | 179638157 | ||||||
| chr1:179638194 | A | G | 3 | a0001c0013t0001g0243 a0001c0013t0001g0244 a0001c0013t0001g0245 |
3 | HG01243.hp2 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1521-1645A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 9/17 | chr1 | 179638194 | |||||||
| chr1:179638449 | A | G | 4 | a0003c0003t0001g0050 a0003c0003t0001g0051 a0003c0003t0001g0052 others(1): Show |
4 | HG00423.hp1 NA18966.hp2 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.1521-1390A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 9/17 | chr1 | 179638449 | |||||||
| chr1:179638456 | C | A | 31 | a0005c0006t0001g0206 a0005c0006t0001g0210 a0005c0006t0001g0211 others(28): Show |
31 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.1521-1383C>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 9/17 | chr1 | 179638456 | |||||||
| chr1:179638957 | A | G | 2 | a0002c0002t0002g0106 a0002c0002t0002g0107 |
2 | HG03017.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1521-882A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 9/17 | chr1 | 179638957 | |||||||
| chr1:179639030 | G | A | 3 | a0005c0012t0001g0254 a0005c0012t0001g0255 a0005c0012t0001g0256 |
3 | HG00735.hp2 HG01109.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.1521-809G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 9/17 | chr1 | 179639030 | |||||||
| chr1:179639252 | C | T | 1 | a0001c0001t0001g0361 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1521-587C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 9/17 | chr1 | 179639252 | |||||||
| chr1:179639253 | G | A | 12 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0180 others(9): Show |
12 | HG02004.hp2 HG02258.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.1521-586G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 9/17 | chr1 | 179639253 | |||||||
| chr1:179639326 | T | C | 46 | a0001c0001t0001g0026 a0002c0002t0002g0001 a0002c0002t0002g0004 others(43): Show |
51 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.1521-513T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 9/17 | chr1 | 179639326 | |||||||
| chr1:179639425 | T | C | 11 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0190 others(8): Show |
11 | HG00140.hp1 HG00738.hp2 HG01069.hp2 others(8): Show |
intron_variant | MODIFIER | c.1521-414T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 9/17 | chr1 | 179639425 | |||||||
| chr1:179639465 | C | T | 1 | a0002c0002t0002g0123 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1521-374C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 9/17 | chr1 | 179639465 | |||||||
| chr1:179639467 | C | T | 1 | a0002c0002t0002g0123 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1521-372C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 9/17 | chr1 | 179639467 | |||||||
| chr1:179639470 | C | A | 1 | a0002c0002t0002g0123 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1521-369C>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 9/17 | chr1 | 179639470 | |||||||
| chr1:179639473 | C | G | 1 | a0002c0002t0002g0123 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1521-366C>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 9/17 | chr1 | 179639473 | |||||||
| chr1:179639474 | A | G | 1 | a0002c0002t0002g0123 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1521-365A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 9/17 | chr1 | 179639474 | |||||||
| chr1:179639613 | G | A | 2 | a0001c0001t0001g0190 a0001c0001t0001g0191 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1521-226G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 9/17 | chr1 | 179639613 | |||||||
| chr1:179639713 | C | A | 1 | a0001c0001t0001g0304 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1521-126C>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 9/17 | chr1 | 179639713 | |||||||
| chr1:179640077 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1733+26G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 10/17 | chr1 | 179640077 | |||||||
| chr1:179640454 | G | T | 84 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0280 others(81): Show |
86 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.1800+9G>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179640454 | |||||||
| chr1:179640610 | C | CCTATAAA others(8): Show |
1 | a0001c0001t0001g0304 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1800+166_1800+167i others(17): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr1 | 179640610 | ||||||
| chr1:179640612 | A | C | 1 | a0001c0001t0001g0304 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1800+167A>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179640612 | |||||||
| chr1:179640701 | G | A | 1 | a0002c0002t0002g0147 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1800+256G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179640701 | |||||||
| chr1:179640923 | G | A | 5 | a0005c0006t0001g0206 a0005c0006t0001g0214 a0005c0006t0001g0215 others(2): Show |
5 | HG00597.hp1 HG02132.hp1 HG02155.hp2 others(2): Show |
intron_variant | MODIFIER | c.1800+478G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179640923 | |||||||
| chr1:179640952 | G | A | 26 | a0005c0006t0001g0206 a0005c0006t0001g0210 a0005c0006t0001g0211 others(23): Show |
26 | HG00544.hp1 HG00597.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.1800+507G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179640952 | |||||||
| chr1:179641125 | TC | T | 121 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(118): Show |
128 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.1800+681delC | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179641125 | |||||||
| chr1:179641267 | C | T | 20 | a0005c0006t0001g0206 a0005c0006t0001g0210 a0005c0006t0001g0211 others(17): Show |
20 | HG00544.hp1 HG00597.hp1 HG02015.hp2 others(17): Show |
intron_variant | MODIFIER | c.1800+822C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179641267 | |||||||
| chr1:179641348 | G | A | 2 | a0009c0014t0001g0364 a0009c0014t0001g0365 |
2 | HG01884.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1800+903G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179641348 | |||||||
| chr1:179641402 | C | T | 1 | a0005c0007t0001g0208 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1800+957C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179641402 | |||||||
| chr1:179641403 | G | A | 2 | a0001c0005t0001g0224 a0001c0005t0001g0225 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1800+958G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179641403 | |||||||
| chr1:179641409 | A | G | 121 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(118): Show |
128 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.1800+964A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179641409 | |||||||
| chr1:179641527 | G | A | 26 | a0005c0006t0001g0206 a0005c0006t0001g0210 a0005c0006t0001g0211 others(23): Show |
26 | HG00544.hp1 HG00597.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.1800+1082G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179641527 | |||||||
| chr1:179641566 | T | A | 1 | a0004c0004t0001g0039 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1800+1121T>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179641566 | |||||||
| chr1:179641602 | A | G | 1 | a0003c0003t0001g0069 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1800+1157A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179641602 | |||||||
| chr1:179641651 | C | T | 1 | a0002c0002t0002g0138 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1800+1206C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179641651 | |||||||
| chr1:179641737 | A | G | 5 | a0006c0009t0001g0091 a0006c0009t0001g0234 a0006c0009t0001g0235 others(2): Show |
5 | HG02622.hp2 HG02630.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1800+1292A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179641737 | |||||||
| chr1:179641814 | C | T | 2 | a0009c0014t0001g0364 a0009c0014t0001g0365 |
2 | HG01884.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1800+1369C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179641814 | |||||||
| chr1:179641831 | C | G | 1 | a0002c0002t0002g0175 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1800+1386C>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179641831 | |||||||
| chr1:179641860 | G | A | 5 | a0006c0009t0001g0091 a0006c0009t0001g0234 a0006c0009t0001g0235 others(2): Show |
5 | HG02622.hp2 HG02630.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1800+1415G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179641860 | |||||||
| chr1:179641876 | A | C | 1 | a0004c0004t0001g0043 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1800+1431A>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179641876 | |||||||
| chr1:179641886 | C | T | 152 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(149): Show |
159 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.1800+1441C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179641886 | |||||||
| chr1:179642020 | T | G | 28 | a0001c0001t0001g0010 a0001c0001t0001g0209 a0001c0001t0001g0262 others(25): Show |
34 | HG00408.hp2 HG01106.hp1 HG01346.hp1 others(31): Show |
intron_variant | MODIFIER | c.1800+1575T>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179642020 | |||||||
| chr1:179642106 | CT | C | 120 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(117): Show |
127 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.1800+1672delT | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr1 | 179642106 | ||||||
| chr1:179642142 | C | T | 1 | a0003c0003t0001g0054 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1800+1697C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179642142 | |||||||
| chr1:179642193 | C | G | 2 | a0010c0016t0001g0092 a0010c0016t0001g0093 |
2 | HG02280.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1800+1748C>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179642193 | |||||||
| chr1:179642486 | G | A | 9 | a0004c0004t0001g0017 a0004c0004t0001g0020 a0004c0004t0001g0023 others(6): Show |
9 | HG00733.hp1 HG01167.hp1 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.1800+2041G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179642486 | |||||||
| chr1:179642591 | C | T | 12 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0180 others(9): Show |
12 | HG02004.hp2 HG02258.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.1800+2146C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179642591 | |||||||
| chr1:179642729 | C | A | 196 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0025 others(193): Show |
204 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.1800+2284C>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179642729 | |||||||
| chr1:179642729 | C | G | 102 | a0001c0001t0001g0026 a0002c0002t0001g0176 a0002c0002t0001g0246 others(99): Show |
109 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.1800+2284C>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179642729 | |||||||
| chr1:179642732 | G | C | 1 | a0001c0001t0001g0323 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1800+2287G>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179642732 | |||||||
| chr1:179642859 | C | G | 1 | a0003c0003t0001g0055 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1800+2414C>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179642859 | |||||||
| chr1:179642946 | C | T | 121 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(118): Show |
128 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.1800+2501C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179642946 | |||||||
| chr1:179643011 | A | T | 15 | a0002c0002t0002g0001 a0002c0002t0002g0103 a0002c0002t0002g0111 others(12): Show |
17 | HG00621.hp1 HG01106.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.1800+2566A>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179643011 | |||||||
| chr1:179643238 | A | G | 6 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(3): Show |
6 | HG02109.hp2 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1800+2793A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179643238 | |||||||
| chr1:179643326 | A | G | 152 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(149): Show |
159 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.1800+2881A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179643326 | |||||||
| chr1:179643328 | A | G | 2 | a0002c0002t0001g0246 a0002c0002t0001g0250 |
2 | HG01433.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.1800+2883A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179643328 | |||||||
| chr1:179643336 | A | C | 1 | a0001c0001t0001g0356 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1800+2891A>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179643336 | |||||||
| chr1:179643340 | G | A | 1 | a0003c0003t0001g0060 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1800+2895G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179643340 | |||||||
| chr1:179643590 | TG | T | 12 | a0001c0005t0001g0002 a0001c0005t0001g0003 a0001c0005t0001g0009 others(9): Show |
17 | HG01346.hp1 HG02055.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.1800+3147delG | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr1 | 179643590 | ||||||
| chr1:179643591 | G | T | 18 | a0002c0002t0002g0001 a0002c0002t0002g0103 a0002c0002t0002g0111 others(15): Show |
20 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(17): Show |
intron_variant | MODIFIER | c.1800+3146G>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179643591 | |||||||
| chr1:179643634 | G | GA | 328 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0025 others(325): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.1800+3191dupA | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr1 | 179643634 | ||||||
| chr1:179643650 | A | G | 26 | a0005c0006t0001g0206 a0005c0006t0001g0210 a0005c0006t0001g0211 others(23): Show |
26 | HG00544.hp1 HG00597.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.1800+3205A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179643650 | |||||||
| chr1:179643700 | G | A | 26 | a0005c0006t0001g0206 a0005c0006t0001g0210 a0005c0006t0001g0211 others(23): Show |
26 | HG00544.hp1 HG00597.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.1800+3255G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179643700 | |||||||
| chr1:179643717 | G | A | 1 | a0002c0002t0002g0238 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1800+3272G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179643717 | |||||||
| chr1:179643766 | A | G | 1 | a0002c0002t0001g0247 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1800+3321A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179643766 | |||||||
| chr1:179643812 | G | A | 30 | a0004c0004t0001g0015 a0004c0004t0001g0016 a0004c0004t0001g0017 others(27): Show |
30 | HG00280.hp2 HG00544.hp2 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.1800+3367G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179643812 | |||||||
| chr1:179644127 | G | A | 328 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0025 others(325): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.1800+3682G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179644127 | |||||||
| chr1:179644318 | G | A | 1 | a0002c0002t0002g0007 | 2 | NA18966.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.1800+3873G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179644318 | |||||||
| chr1:179644562 | A | T | 121 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(118): Show |
128 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.1800+4117A>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179644562 | |||||||
| chr1:179644642 | G | A | 102 | a0001c0001t0001g0026 a0002c0002t0001g0176 a0002c0002t0001g0246 others(99): Show |
109 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.1800+4197G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179644642 | |||||||
| chr1:179644993 | TA | T | 126 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(123): Show |
133 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.1800+4554delA | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr1 | 179644993 | ||||||
| chr1:179645076 | C | CT | 18 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(15): Show |
18 | HG00423.hp1 HG01109.hp1 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.1800+4658dupT | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr1 | 179645076 | ||||||
| chr1:179645076 | CT | C | 231 | a0001c0001t0001g0012 a0001c0001t0001g0026 a0001c0001t0001g0089 others(228): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.1800+4658delT | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr1 | 179645076 | ||||||
| chr1:179645076 | CTT | C | 19 | a0001c0001t0001g0010 a0001c0001t0001g0179 a0001c0001t0001g0209 others(16): Show |
20 | HG00408.hp2 HG01106.hp1 HG01496.hp2 others(17): Show |
intron_variant | MODIFIER | c.1800+4657_1800+465 others(6): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr1 | 179645076 | ||||||
| chr1:179645076 | CTTTTT | C | 25 | a0005c0006t0001g0206 a0005c0006t0001g0210 a0005c0006t0001g0211 others(22): Show |
25 | HG00544.hp1 HG00597.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.1800+4654_1800+465 others(9): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr1 | 179645076 | ||||||
| chr1:179645081 | T | C | 2 | a0001c0001t0001g0357 a0002c0002t0002g0109 |
2 | HG02080.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1800+4636T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179645081 | |||||||
| chr1:179645084 | T | C | 121 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(118): Show |
128 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.1800+4639T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179645084 | |||||||
| chr1:179645085 | T | C | 26 | a0001c0001t0001g0179 a0005c0006t0001g0206 a0005c0006t0001g0210 others(23): Show |
26 | HG00544.hp1 HG00597.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.1800+4640T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179645085 | |||||||
| chr1:179645086 | T | C | 2 | a0001c0001t0001g0313 a0001c0001t0001g0329 |
2 | HG00673.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.1800+4641T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179645086 | |||||||
| chr1:179645090 | T | C | 120 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(117): Show |
127 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.1800+4645T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179645090 | |||||||
| chr1:179645091 | T | C | 1 | a0001c0001t0001g0179 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1800+4646T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179645091 | |||||||
| chr1:179645108 | C | T | 8 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(5): Show |
9 | HG01261.hp1 HG01516.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.1800+4663C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179645108 | |||||||
| chr1:179645116 | C | T | 5 | a0005c0012t0001g0254 a0005c0012t0001g0255 a0005c0012t0001g0256 others(2): Show |
5 | HG00735.hp2 HG01109.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.1800+4671C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179645116 | |||||||
| chr1:179645186 | C | T | 16 | a0001c0001t0001g0010 a0001c0001t0001g0209 a0001c0001t0001g0262 others(13): Show |
17 | HG00408.hp2 HG01106.hp1 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.1800+4741C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179645186 | |||||||
| chr1:179645238 | A | G | 5 | a0001c0001t0001g0306 a0001c0001t0001g0315 a0001c0001t0001g0316 others(2): Show |
5 | NA18939.hp1 NA18951.hp1 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.1800+4793A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179645238 | |||||||
| chr1:179645246 | C | G | 2 | a0002c0002t0002g0115 a0002c0002t0002g0116 |
2 | NA18943.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.1800+4801C>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179645246 | |||||||
| chr1:179645258 | T | C | 3 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0023t0001g0202 |
3 | HG02055.hp1 HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1800+4813T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179645258 | |||||||
| chr1:179645307 | G | A | 2 | a0009c0014t0001g0364 a0009c0014t0001g0365 |
2 | HG01884.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1800+4862G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179645307 | |||||||
| chr1:179645332 | G | A | 1 | a0001c0001t0001g0331 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1800+4887G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179645332 | |||||||
| chr1:179645384 | C | A | 5 | a0006c0009t0001g0091 a0006c0009t0001g0234 a0006c0009t0001g0235 others(2): Show |
5 | HG02622.hp2 HG02630.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1800+4939C>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179645384 | |||||||
| chr1:179645396 | C | T | 287 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0025 others(284): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.1800+4951C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179645396 | |||||||
| chr1:179645438 | T | A | 1 | a0003c0003t0001g0069 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1800+4993T>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179645438 | |||||||
| chr1:179645477 | C | G | 12 | a0002c0002t0002g0008 a0002c0002t0002g0108 a0002c0002t0002g0120 others(9): Show |
13 | HG02027.hp2 HG02071.hp2 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.1800+5032C>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179645477 | |||||||
| chr1:179645512 | T | A | 1 | a0001c0001t0001g0343 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1800+5067T>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179645512 | |||||||
| chr1:179645557 | A | T | 1 | a0001c0013t0001g0243 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1800+5112A>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179645557 | |||||||
| chr1:179645629 | G | A | 26 | a0005c0006t0001g0206 a0005c0006t0001g0210 a0005c0006t0001g0211 others(23): Show |
26 | HG00544.hp1 HG00597.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.1800+5184G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179645629 | |||||||
| chr1:179645738 | G | T | 1 | a0002c0002t0002g0136 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1801-5129G>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179645738 | |||||||
| chr1:179645773 | C | T | 1 | a0005c0006t0001g0212 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1801-5094C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179645773 | |||||||
| chr1:179645852 | CA | C | 27 | a0001c0005t0001g0230 a0005c0006t0001g0206 a0005c0006t0001g0210 others(24): Show |
27 | HG00544.hp1 HG00597.hp1 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.1801-5006delA | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr1 | 179645852 | ||||||
| chr1:179645976 | T | C | 7 | a0001c0001t0001g0188 a0001c0001t0001g0192 a0001c0001t0001g0193 others(4): Show |
7 | HG00140.hp1 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.1801-4891T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179645976 | |||||||
| chr1:179646039 | T | C | 3 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0104 |
3 | HG02145.hp2 HG02572.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1801-4828T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179646039 | |||||||
| chr1:179646094 | C | T | 4 | a0005c0011t0003g0085 a0005c0011t0003g0086 a0005c0011t0003g0087 others(1): Show |
4 | HG02809.hp2 HG03041.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1801-4773C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179646094 | |||||||
| chr1:179646203 | T | A | 6 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(3): Show |
6 | HG02109.hp2 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1801-4664T>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179646203 | |||||||
| chr1:179646229 | A | G | 6 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0007c0010t0001g0257 others(3): Show |
6 | HG01099.hp1 HG01891.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1801-4638A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179646229 | |||||||
| chr1:179646342 | A | G | 1 | a0002c0002t0002g0096 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1801-4525A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179646342 | |||||||
| chr1:179646389 | T | A | 3 | a0005c0012t0001g0254 a0005c0012t0001g0255 a0005c0012t0001g0256 |
3 | HG00735.hp2 HG01109.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.1801-4478T>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179646389 | |||||||
| chr1:179646401 | A | G | 2 | a0002c0002t0002g0236 a0002c0002t0002g0237 |
2 | NA18967.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1801-4466A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179646401 | |||||||
| chr1:179646560 | G | C | 121 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(118): Show |
128 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.1801-4307G>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179646560 | |||||||
| chr1:179646580 | C | A | 16 | a0001c0001t0001g0010 a0001c0001t0001g0209 a0001c0001t0001g0262 others(13): Show |
17 | HG00408.hp2 HG01106.hp1 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.1801-4287C>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179646580 | |||||||
| chr1:179646597 | C | T | 126 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(123): Show |
133 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.1801-4270C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179646597 | |||||||
| chr1:179646629 | G | A | 121 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(118): Show |
128 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.1801-4238G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179646629 | |||||||
| chr1:179646775 | T | C | 1 | a0001c0001t0001g0314 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1801-4092T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179646775 | |||||||
| chr1:179646778 | A | G | 1 | a0001c0001t0001g0314 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1801-4089A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179646778 | |||||||
| chr1:179646850 | A | G | 2 | a0002c0002t0002g0115 a0002c0002t0002g0116 |
2 | NA18943.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.1801-4017A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179646850 | |||||||
| chr1:179646864 | A | C | 2 | a0001c0001t0001g0012 a0001c0001t0001g0352 |
3 | NA18967.hp2 NA19005.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.1801-4003A>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179646864 | |||||||
| chr1:179646993 | A | G | 12 | a0001c0005t0001g0002 a0001c0005t0001g0003 a0001c0005t0001g0009 others(9): Show |
17 | HG01346.hp1 HG02055.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.1801-3874A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179646993 | |||||||
| chr1:179646998 | T | C | 1 | a0001c0001t0001g0209 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1801-3869T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179646998 | |||||||
| chr1:179647006 | A | C | 2 | a0002c0002t0002g0112 a0002c0002t0002g0137 |
2 | NA18939.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.1801-3861A>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179647006 | |||||||
| chr1:179647054 | T | C | 3 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0104 |
3 | HG02145.hp2 HG02572.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1801-3813T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179647054 | |||||||
| chr1:179647083 | A | G | 121 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(118): Show |
128 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.1801-3784A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179647083 | |||||||
| chr1:179647137 | C | T | 29 | a0001c0001t0001g0311 a0005c0006t0001g0206 a0005c0006t0001g0210 others(26): Show |
29 | HG00544.hp1 HG00597.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.1801-3730C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179647137 | |||||||
| chr1:179647179 | C | G | 2 | a0001c0001t0001g0301 a0001c0001t0001g0302 |
2 | NA18964.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.1801-3688C>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179647179 | |||||||
| chr1:179647211 | CTA | C | 3 | a0005c0012t0001g0254 a0005c0012t0001g0255 a0005c0012t0001g0256 |
3 | HG00735.hp2 HG01109.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.1801-3655_1801-365 others(6): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179647211 | |||||||
| chr1:179647215 | A | G | 3 | a0005c0012t0001g0254 a0005c0012t0001g0255 a0005c0012t0001g0256 |
3 | HG00735.hp2 HG01109.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.1801-3652A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179647215 | |||||||
| chr1:179647216 | G | C | 3 | a0005c0012t0001g0254 a0005c0012t0001g0255 a0005c0012t0001g0256 |
3 | HG00735.hp2 HG01109.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.1801-3651G>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179647216 | |||||||
| chr1:179647220 | C | CAACCTAT others(72): Show |
3 | a0005c0012t0001g0254 a0005c0012t0001g0255 a0005c0012t0001g0256 |
3 | HG00735.hp2 HG01109.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.1801-3647_1801-364 others(83): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179647220 | |||||||
| chr1:179647292 | T | C | 328 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0025 others(325): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.1801-3575T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179647292 | |||||||
| chr1:179647324 | G | A | 3 | a0001c0001t0001g0273 a0001c0001t0001g0331 a0002c0002t0002g0102 |
3 | HG00639.hp2 HG01261.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.1801-3543G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179647324 | |||||||
| chr1:179647366 | A | G | 16 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0180 others(13): Show |
16 | HG02004.hp2 HG02055.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1801-3501A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179647366 | |||||||
| chr1:179647436 | A | C | 2 | a0002c0002t0002g0106 a0002c0002t0002g0107 |
2 | HG03017.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1801-3431A>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179647436 | |||||||
| chr1:179647548 | C | T | 1 | a0002c0002t0002g0123 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1801-3319C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179647548 | |||||||
| chr1:179647551 | C | T | 1 | a0002c0002t0002g0172 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1801-3316C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179647551 | |||||||
| chr1:179647557 | T | C | 1 | a0002c0002t0002g0125 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1801-3310T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179647557 | |||||||
| chr1:179647628 | G | A | 6 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0007c0010t0001g0257 others(3): Show |
6 | HG01099.hp1 HG01891.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1801-3239G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179647628 | |||||||
| chr1:179647662 | C | G | 1 | a0001c0001t0001g0297 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1801-3205C>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179647662 | |||||||
| chr1:179647684 | C | T | 2 | a0001c0001t0001g0179 a0001c0001t0001g0180 |
2 | HG02965.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1801-3183C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179647684 | |||||||
| chr1:179647687 | C | A | 2 | a0001c0001t0001g0179 a0001c0001t0001g0180 |
2 | HG02965.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1801-3180C>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179647687 | |||||||
| chr1:179647747 | C | T | 96 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0188 others(93): Show |
98 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.1801-3120C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179647747 | |||||||
| chr1:179647766 | C | T | 1 | a0003c0003t0001g0061 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1801-3101C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179647766 | |||||||
| chr1:179647778 | T | C | 1 | a0003c0003t0001g0077 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1801-3089T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179647778 | |||||||
| chr1:179647808 | A | G | 1 | a0002c0002t0002g0152 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1801-3059A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179647808 | |||||||
| chr1:179647837 | T | C | 147 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(144): Show |
154 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.1801-3030T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179647837 | |||||||
| chr1:179647849 | C | G | 1 | a0001c0001t0001g0350 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1801-3018C>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179647849 | |||||||
| chr1:179648040 | G | T | 9 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0199 others(6): Show |
9 | HG02109.hp2 HG02572.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1801-2827G>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179648040 | |||||||
| chr1:179648110 | G | T | 1 | a0001c0001t0001g0188 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1801-2757G>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179648110 | |||||||
| chr1:179648113 | C | G | 1 | a0001c0001t0001g0188 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1801-2754C>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179648113 | |||||||
| chr1:179648160 | C | T | 1 | a0001c0001t0001g0343 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1801-2707C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179648160 | |||||||
| chr1:179648161 | G | A | 102 | a0001c0001t0001g0026 a0002c0002t0001g0176 a0002c0002t0001g0246 others(99): Show |
109 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.1801-2706G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179648161 | |||||||
| chr1:179648244 | A | G | 1 | a0001c0001t0001g0283 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1801-2623A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179648244 | |||||||
| chr1:179648325 | TTCTCAGT others(13): Show |
T | 1 | a0004c0004t0001g0044 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1801-2541_1801-252 others(24): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179648325 | |||||||
| chr1:179648338 | A | G | 5 | a0005c0012t0001g0254 a0005c0012t0001g0255 a0005c0012t0001g0256 others(2): Show |
5 | HG00735.hp2 HG01109.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.1801-2529A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179648338 | |||||||
| chr1:179648382 | A | G | 126 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(123): Show |
133 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.1801-2485A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179648382 | |||||||
| chr1:179648403 | C | T | 16 | a0001c0001t0001g0010 a0001c0001t0001g0209 a0001c0001t0001g0262 others(13): Show |
17 | HG00408.hp2 HG01106.hp1 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.1801-2464C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179648403 | |||||||
| chr1:179648404 | A | C | 1 | a0005c0007t0001g0360 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1801-2463A>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179648404 | |||||||
| chr1:179648452 | T | TG | 39 | a0001c0001t0001g0189 a0001c0001t0001g0195 a0001c0001t0001g0280 others(36): Show |
41 | HG00558.hp2 HG00738.hp2 HG01175.hp2 others(38): Show |
intron_variant | MODIFIER | c.1801-2405dupG | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr1 | 179648452 | ||||||
| chr1:179648455 | G | C | 8 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0007c0010t0001g0257 others(5): Show |
8 | HG01099.hp1 HG01891.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1801-2412G>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179648455 | |||||||
| chr1:179648456 | G | A | 4 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(1): Show |
4 | HG02109.hp2 HG02630.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1801-2411G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179648456 | |||||||
| chr1:179648456 | G | GGGA | 145 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(142): Show |
152 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.1801-2409_1801-240 others(7): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr1 | 179648456 | ||||||
| chr1:179648458 | G | C | 3 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 |
3 | HG02717.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1801-2409G>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179648458 | |||||||
| chr1:179648459 | G | A | 16 | a0001c0001t0001g0010 a0001c0001t0001g0209 a0001c0001t0001g0262 others(13): Show |
17 | HG00408.hp2 HG01106.hp1 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.1801-2408G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179648459 | |||||||
| chr1:179648500 | C | G | 2 | a0001c0001t0001g0012 a0001c0001t0001g0352 |
3 | NA18967.hp2 NA19005.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.1801-2367C>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179648500 | |||||||
| chr1:179648511 | A | G | 121 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(118): Show |
128 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.1801-2356A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179648511 | |||||||
| chr1:179648585 | A | G | 1 | a0009c0014t0001g0365 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1801-2282A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179648585 | |||||||
| chr1:179648627 | GA | G | 7 | a0001c0001t0001g0288 a0001c0001t0001g0344 a0001c0001t0001g0345 others(4): Show |
7 | HG01255.hp1 HG01257.hp2 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.1801-2230delA | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr1 | 179648627 | ||||||
| chr1:179648637 | A | C | 1 | a0004c0004t0001g0044 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1801-2230A>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179648637 | |||||||
| chr1:179648638 | C | A | 1 | a0004c0004t0001g0044 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1801-2229C>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179648638 | |||||||
| chr1:179648642 | A | C | 1 | a0004c0004t0001g0044 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1801-2225A>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179648642 | |||||||
| chr1:179648672 | T | C | 1 | a0004c0004t0001g0044 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1801-2195T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179648672 | |||||||
| chr1:179648673 | C | T | 1 | a0004c0004t0001g0044 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1801-2194C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179648673 | |||||||
| chr1:179648764 | A | C | 1 | a0002c0002t0002g0156 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1801-2103A>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179648764 | |||||||
| chr1:179648788 | TA | T | 132 | a0001c0001t0001g0026 a0002c0002t0001g0176 a0002c0002t0001g0246 others(129): Show |
139 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.1801-2071delA | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr1 | 179648788 | ||||||
| chr1:179648863 | A | G | 121 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(118): Show |
128 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.1801-2004A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179648863 | |||||||
| chr1:179648978 | G | T | 287 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0025 others(284): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.1801-1889G>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179648978 | |||||||
| chr1:179648987 | A | C | 1 | a0002c0002t0002g0121 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1801-1880A>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179648987 | |||||||
| chr1:179649024 | A | T | 2 | a0010c0016t0001g0092 a0010c0016t0001g0093 |
2 | HG02280.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1801-1843A>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179649024 | |||||||
| chr1:179649052 | G | A | 3 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0104 |
3 | HG02145.hp2 HG02572.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1801-1815G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179649052 | |||||||
| chr1:179649157 | G | A | 5 | a0006c0009t0001g0091 a0006c0009t0001g0234 a0006c0009t0001g0235 others(2): Show |
5 | HG02622.hp2 HG02630.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1801-1710G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179649157 | |||||||
| chr1:179649182 | G | A | 121 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(118): Show |
128 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.1801-1685G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179649182 | |||||||
| chr1:179649412 | A | G | 13 | a0002c0002t0002g0008 a0002c0002t0002g0108 a0002c0002t0002g0120 others(10): Show |
14 | HG02027.hp2 HG02071.hp2 HG02080.hp2 others(11): Show |
intron_variant | MODIFIER | c.1801-1455A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179649412 | |||||||
| chr1:179649464 | T | C | 152 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(149): Show |
159 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.1801-1403T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179649464 | |||||||
| chr1:179649571 | ACTT | A | 11 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0190 others(8): Show |
11 | HG00140.hp1 HG00738.hp2 HG01069.hp2 others(8): Show |
intron_variant | MODIFIER | c.1801-1292_1801-129 others(7): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr1 | 179649571 | ||||||
| chr1:179649631 | G | C | 1 | a0002c0002t0002g0140 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1801-1236G>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179649631 | |||||||
| chr1:179649950 | G | A | 2 | a0010c0016t0001g0092 a0010c0016t0001g0093 |
2 | HG02280.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1801-917G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179649950 | |||||||
| chr1:179650138 | C | T | 1 | a0005c0007t0001g0233 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1801-729C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179650138 | |||||||
| chr1:179650155 | C | A | 5 | a0005c0012t0001g0254 a0005c0012t0001g0255 a0005c0012t0001g0256 others(2): Show |
5 | HG00735.hp2 HG01109.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.1801-712C>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179650155 | |||||||
| chr1:179650245 | A | G | 6 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(3): Show |
6 | HG02109.hp2 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1801-622A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179650245 | |||||||
| chr1:179650349 | C | T | 1 | a0002c0002t0002g0165 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1801-518C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179650349 | |||||||
| chr1:179650358 | G | A | 1 | a0004c0004t0001g0017 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1801-509G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179650358 | |||||||
| chr1:179650400 | C | CA | 44 | a0001c0001t0001g0025 a0001c0001t0001g0094 a0001c0001t0001g0095 others(41): Show |
44 | HG00280.hp2 HG00544.hp2 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.1801-444dupA | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr1 | 179650400 | ||||||
| chr1:179650400 | C | CAA | 6 | a0004c0004t0001g0015 a0004c0004t0001g0037 a0004c0004t0001g0039 others(3): Show |
6 | HG02738.hp1 HG03669.hp1 NA18906.hp1 others(3): Show |
intron_variant | MODIFIER | c.1801-445_1801-444d others(4): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr1 | 179650400 | ||||||
| chr1:179650400 | CA | C | 113 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(110): Show |
120 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.1801-444delA | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr1 | 179650400 | ||||||
| chr1:179650400 | CAA | C | 43 | a0001c0001t0001g0104 a0001c0001t0001g0178 a0001c0001t0001g0179 others(40): Show |
43 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.1801-445_1801-444d others(4): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr1 | 179650400 | ||||||
| chr1:179650449 | A | G | 16 | a0001c0001t0001g0010 a0001c0001t0001g0209 a0001c0001t0001g0262 others(13): Show |
17 | HG00408.hp2 HG01106.hp1 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.1801-418A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179650449 | |||||||
| chr1:179650530 | A | G | 328 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0025 others(325): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.1801-337A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179650530 | |||||||
| chr1:179650541 | A | G | 121 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(118): Show |
128 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.1801-326A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 11/17 | chr1 | 179650541 | |||||||
| chr1:179651118 | G | A | 121 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(118): Show |
128 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.2001+51G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 12/17 | chr1 | 179651118 | |||||||
| chr1:179651326 | C | T | 1 | a0001c0001t0001g0356 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2001+259C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 12/17 | chr1 | 179651326 | |||||||
| chr1:179651421 | C | G | 26 | a0005c0006t0001g0206 a0005c0006t0001g0210 a0005c0006t0001g0211 others(23): Show |
26 | HG00544.hp1 HG00597.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.2001+354C>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 12/17 | chr1 | 179651421 | |||||||
| chr1:179651437 | T | A | 1 | a0004c0004t0001g0044 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2001+370T>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 12/17 | chr1 | 179651437 | |||||||
| chr1:179651502 | C | T | 30 | a0004c0004t0001g0015 a0004c0004t0001g0016 a0004c0004t0001g0017 others(27): Show |
30 | HG00280.hp2 HG00544.hp2 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.2001+435C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 12/17 | chr1 | 179651502 | |||||||
| chr1:179651518 | A | T | 3 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 |
3 | HG02109.hp2 HG02630.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2001+451A>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 12/17 | chr1 | 179651518 | |||||||
| chr1:179651556 | G | GT | 152 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(149): Show |
159 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.2002-482dupT | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 179651556 | ||||||
| chr1:179651741 | G | A | 1 | a0001c0001t0001g0350 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2002-298G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 12/17 | chr1 | 179651741 | |||||||
| chr1:179652029 | T | G | 19 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0104 others(16): Show |
19 | HG02004.hp2 HG02055.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.2002-10T>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 12/17 | chr1 | 179652029 | |||||||
| chr1:179652295 | T | G | 3 | a0005c0011t0003g0085 a0005c0011t0003g0086 a0005c0011t0003g0087 |
3 | HG02809.hp2 HG03041.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2160+98T>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 13/17 | chr1 | 179652295 | |||||||
| chr1:179652412 | C | T | 1 | a0001c0001t0001g0275 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2160+215C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 13/17 | chr1 | 179652412 | |||||||
| chr1:179652568 | G | A | 1 | a0001c0001t0001g0329 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2160+371G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 13/17 | chr1 | 179652568 | |||||||
| chr1:179652644 | AAGCATTC others(13): Show |
A | 3 | a0005c0012t0001g0254 a0005c0012t0001g0255 a0005c0012t0001g0256 |
3 | HG00735.hp2 HG01109.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.2160+449_2160+468d others(22): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr1 | 179652644 | ||||||
| chr1:179652857 | G | A | 2 | a0009c0014t0001g0364 a0009c0014t0001g0365 |
2 | HG01884.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.2160+660G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 13/17 | chr1 | 179652857 | |||||||
| chr1:179652946 | A | G | 121 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(118): Show |
128 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.2160+749A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 13/17 | chr1 | 179652946 | |||||||
| chr1:179653060 | A | G | 1 | a0002c0002t0002g0174 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.2160+863A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 13/17 | chr1 | 179653060 | |||||||
| chr1:179653226 | A | G | 2 | a0001c0001t0001g0089 a0001c0001t0001g0090 |
2 | HG02572.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2161-975A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 13/17 | chr1 | 179653226 | |||||||
| chr1:179653235 | A | G | 26 | a0005c0006t0001g0206 a0005c0006t0001g0210 a0005c0006t0001g0211 others(23): Show |
26 | HG00544.hp1 HG00597.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.2161-966A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 13/17 | chr1 | 179653235 | |||||||
| chr1:179653273 | T | C | 3 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 |
3 | HG02717.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2161-928T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 13/17 | chr1 | 179653273 | |||||||
| chr1:179653447 | A | G | 21 | a0005c0006t0001g0206 a0005c0006t0001g0210 a0005c0006t0001g0211 others(18): Show |
21 | HG00544.hp1 HG00597.hp1 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.2161-754A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 13/17 | chr1 | 179653447 | |||||||
| chr1:179653521 | T | A | 1 | a0004c0004t0001g0044 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2161-680T>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 13/17 | chr1 | 179653521 | |||||||
| chr1:179653803 | A | G | 4 | a0005c0011t0003g0085 a0005c0011t0003g0086 a0005c0011t0003g0087 others(1): Show |
4 | HG02809.hp2 HG03041.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.2161-398A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 13/17 | chr1 | 179653803 | |||||||
| chr1:179653842 | C | G | 121 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(118): Show |
128 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.2161-359C>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 13/17 | chr1 | 179653842 | |||||||
| chr1:179653861 | A | G | 102 | a0001c0001t0001g0026 a0002c0002t0001g0176 a0002c0002t0001g0246 others(99): Show |
109 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.2161-340A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 13/17 | chr1 | 179653861 | |||||||
| chr1:179654031 | C | T | 3 | a0003c0003t0001g0061 a0003c0003t0001g0062 a0003c0003t0001g0063 |
3 | HG03195.hp1 HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2161-170C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 13/17 | chr1 | 179654031 | |||||||
| chr1:179654572 | G | A | 121 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(118): Show |
128 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.2322+210G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179654572 | |||||||
| chr1:179654711 | T | A | 121 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(118): Show |
128 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.2322+349T>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179654711 | |||||||
| chr1:179654774 | ATAAAG | A | 7 | a0003c0003t0001g0048 a0003c0003t0001g0049 a0003c0003t0001g0050 others(4): Show |
7 | HG00423.hp1 NA18942.hp1 NA18947.hp2 others(4): Show |
intron_variant | MODIFIER | c.2322+417_2322+421d others(7): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr1 | 179654774 | ||||||
| chr1:179654815 | G | A | 3 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0104 |
3 | HG02145.hp2 HG02572.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2322+453G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179654815 | |||||||
| chr1:179654846 | T | TA | 6 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(3): Show |
6 | HG02109.hp2 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.2322+491dupA | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr1 | 179654846 | ||||||
| chr1:179654876 | G | A | 1 | a0001c0001t0001g0296 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.2322+514G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179654876 | |||||||
| chr1:179655055 | C | T | 4 | a0006c0009t0001g0234 a0006c0009t0001g0235 a0006c0009t0001g0366 others(1): Show |
4 | HG02630.hp2 HG02922.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2322+693C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179655055 | |||||||
| chr1:179655082 | C | A | 137 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(134): Show |
143 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.2322+720C>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179655082 | |||||||
| chr1:179655134 | TAAATA | T | 3 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0104 |
3 | HG02145.hp2 HG02572.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2322+774_2322+778d others(7): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr1 | 179655134 | ||||||
| chr1:179655237 | G | A | 2 | a0009c0014t0001g0364 a0009c0014t0001g0365 |
2 | HG01884.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.2322+875G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179655237 | |||||||
| chr1:179655336 | G | A | 324 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0025 others(321): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.2322+974G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179655336 | |||||||
| chr1:179655590 | C | T | 5 | a0002c0002t0002g0113 a0002c0002t0002g0149 a0002c0002t0002g0150 others(2): Show |
5 | NA18978.hp1 NA19002.hp1 NA19011.hp2 others(2): Show |
intron_variant | MODIFIER | c.2322+1228C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179655590 | |||||||
| chr1:179655619 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2322+1257C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179655619 | |||||||
| chr1:179655750 | G | A | 6 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(3): Show |
6 | HG02109.hp2 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.2322+1388G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179655750 | |||||||
| chr1:179655952 | C | T | 1 | a0004c0004t0001g0015 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2322+1590C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179655952 | |||||||
| chr1:179656006 | G | A | 2 | a0002c0002t0002g0127 a0002c0002t0002g0128 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2322+1644G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179656006 | |||||||
| chr1:179656080 | T | G | 1 | a0001c0001t0001g0209 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2322+1718T>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179656080 | |||||||
| chr1:179656366 | T | C | 147 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(144): Show |
154 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.2322+2004T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179656366 | |||||||
| chr1:179656461 | A | G | 11 | a0001c0001t0001g0012 a0001c0001t0001g0291 a0001c0001t0001g0293 others(8): Show |
12 | HG00280.hp1 HG02132.hp2 HG02135.hp1 others(9): Show |
intron_variant | MODIFIER | c.2322+2099A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179656461 | |||||||
| chr1:179656651 | A | G | 2 | a0009c0014t0001g0364 a0009c0014t0001g0365 |
2 | HG01884.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.2322+2289A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179656651 | |||||||
| chr1:179656670 | A | G | 2 | a0009c0014t0001g0364 a0009c0014t0001g0365 |
2 | HG01884.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.2322+2308A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179656670 | |||||||
| chr1:179656680 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2322+2318C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179656680 | |||||||
| chr1:179656778 | G | A | 31 | a0001c0001t0001g0295 a0004c0004t0001g0015 a0004c0004t0001g0016 others(28): Show |
31 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.2322+2416G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179656778 | |||||||
| chr1:179656983 | A | G | 152 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(149): Show |
159 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.2322+2621A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179656983 | |||||||
| chr1:179657065 | A | C | 11 | a0001c0001t0001g0010 a0001c0001t0001g0262 a0001c0001t0001g0265 others(8): Show |
12 | HG01106.hp1 HG01433.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.2322+2703A>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179657065 | |||||||
| chr1:179657069 | A | G | 1 | a0007c0010t0001g0260 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2322+2707A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179657069 | |||||||
| chr1:179657107 | T | C | 5 | a0003c0003t0001g0061 a0003c0003t0001g0062 a0003c0003t0001g0063 others(2): Show |
5 | HG02896.hp2 HG02897.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2322+2745T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179657107 | |||||||
| chr1:179657129 | G | T | 1 | a0001c0001t0001g0309 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2322+2767G>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179657129 | |||||||
| chr1:179657162 | C | T | 1 | a0003c0003t0001g0060 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2322+2800C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179657162 | |||||||
| chr1:179657323 | G | T | 3 | a0005c0012t0001g0254 a0005c0012t0001g0255 a0005c0012t0001g0256 |
3 | HG00735.hp2 HG01109.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.2322+2961G>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179657323 | |||||||
| chr1:179657521 | G | A | 126 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(123): Show |
133 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.2322+3159G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179657521 | |||||||
| chr1:179657559 | T | C | 121 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(118): Show |
128 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.2322+3197T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179657559 | |||||||
| chr1:179657622 | TAAATC | T | 96 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0188 others(93): Show |
98 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.2322+3261_2322+326 others(9): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179657622 | |||||||
| chr1:179657666 | T | G | 1 | a0004c0004t0001g0035 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2322+3304T>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179657666 | |||||||
| chr1:179657676 | T | C | 12 | a0001c0001t0001g0010 a0001c0001t0001g0209 a0001c0001t0001g0262 others(9): Show |
13 | HG00408.hp2 HG01106.hp1 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.2322+3314T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179657676 | |||||||
| chr1:179657700 | G | T | 1 | a0005c0007t0001g0360 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2322+3338G>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179657700 | |||||||
| chr1:179657802 | A | T | 1 | a0004c0004t0001g0037 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2322+3440A>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179657802 | |||||||
| chr1:179658081 | T | C | 6 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0007c0010t0001g0257 others(3): Show |
6 | HG01099.hp1 HG01891.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2322+3719T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179658081 | |||||||
| chr1:179658201 | T | A | 3 | a0005c0006t0001g0206 a0005c0006t0001g0214 a0005c0006t0001g0215 |
3 | HG00597.hp1 HG02132.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.2322+3839T>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179658201 | |||||||
| chr1:179658227 | T | C | 2 | a0005c0007t0001g0205 a0005c0007t0001g0207 |
2 | NA18942.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.2322+3865T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179658227 | |||||||
| chr1:179658250 | T | G | 295 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0025 others(292): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.2323-3854T>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179658250 | |||||||
| chr1:179658411 | A | C | 1 | a0001c0001t0001g0204 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2323-3693A>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179658411 | |||||||
| chr1:179658430 | T | A | 26 | a0005c0006t0001g0206 a0005c0006t0001g0210 a0005c0006t0001g0211 others(23): Show |
26 | HG00544.hp1 HG00597.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.2323-3674T>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179658430 | |||||||
| chr1:179658587 | C | A | 121 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(118): Show |
128 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.2323-3517C>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179658587 | |||||||
| chr1:179658606 | A | G | 26 | a0005c0006t0001g0206 a0005c0006t0001g0210 a0005c0006t0001g0211 others(23): Show |
26 | HG00544.hp1 HG00597.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.2323-3498A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179658606 | |||||||
| chr1:179658868 | A | G | 1 | a0004c0004t0001g0015 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2323-3236A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179658868 | |||||||
| chr1:179658899 | A | G | 2 | a0009c0014t0001g0364 a0009c0014t0001g0365 |
2 | HG01884.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.2323-3205A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179658899 | |||||||
| chr1:179658927 | A | G | 121 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(118): Show |
128 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.2323-3177A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179658927 | |||||||
| chr1:179658933 | C | A | 1 | a0001c0001t0002g0098 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2323-3171C>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179658933 | |||||||
| chr1:179659081 | G | T | 121 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(118): Show |
128 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.2323-3023G>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179659081 | |||||||
| chr1:179659239 | A | G | 1 | a0002c0002t0002g0137 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.2323-2865A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179659239 | |||||||
| chr1:179659297 | G | A | 121 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(118): Show |
128 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.2323-2807G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179659297 | |||||||
| chr1:179659465 | A | G | 1 | a0002c0002t0002g0121 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2323-2639A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179659465 | |||||||
| chr1:179659472 | A | G | 16 | a0001c0001t0001g0010 a0001c0001t0001g0209 a0001c0001t0001g0262 others(13): Show |
17 | HG00408.hp2 HG01106.hp1 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.2323-2632A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179659472 | |||||||
| chr1:179659488 | AT | A | 4 | a0002c0002t0002g0236 a0002c0002t0002g0237 a0002c0002t0002g0240 others(1): Show |
4 | HG02040.hp2 HG02135.hp2 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.2323-2614delT | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr1 | 179659488 | ||||||
| chr1:179659550 | C | CGT | 37 | a0001c0001t0001g0188 a0001c0001t0001g0192 a0001c0001t0001g0193 others(34): Show |
38 | HG00140.hp1 HG00558.hp1 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.2323-2514_2323-251 others(6): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr1 | 179659550 | ||||||
| chr1:179659550 | C | CGTGT | 15 | a0001c0001t0001g0294 a0001c0001t0001g0345 a0001c0001t0001g0356 others(12): Show |
15 | HG00544.hp1 HG00597.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.2323-2516_2323-251 others(8): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr1 | 179659550 | ||||||
| chr1:179659550 | CGT | C | 39 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(36): Show |
40 | HG00673.hp2 HG00738.hp2 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.2323-2514_2323-251 others(6): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr1 | 179659550 | ||||||
| chr1:179659550 | CGTGT | C | 38 | a0001c0001t0001g0010 a0001c0001t0001g0209 a0001c0001t0001g0262 others(35): Show |
39 | HG00280.hp2 HG00408.hp2 HG00544.hp2 others(36): Show |
intron_variant | MODIFIER | c.2323-2516_2323-251 others(8): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr1 | 179659550 | ||||||
| chr1:179659550 | CGTGTGT | C | 5 | a0002c0002t0002g0121 a0004c0004t0001g0022 a0005c0012t0001g0254 others(2): Show |
5 | HG00609.hp2 HG00735.hp2 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.2323-2518_2323-251 others(10): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr1 | 179659550 | ||||||
| chr1:179659550 | CGTGTGTG others(9): Show |
C | 2 | a0009c0014t0001g0364 a0009c0014t0001g0365 |
2 | HG01884.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.2323-2528_2323-251 others(20): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr1 | 179659550 | ||||||
| chr1:179659578 | T | A | 1 | a0001c0001t0002g0098 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2323-2526T>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179659578 | |||||||
| chr1:179659584 | TGTGTGTG others(1): Show |
T | 4 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(1): Show |
4 | HG02258.hp2 HG02965.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.2323-2518_2323-251 others(12): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr1 | 179659584 | ||||||
| chr1:179659586 | TGTGTGC | T | 88 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(85): Show |
94 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.2323-2516_2323-251 others(10): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr1 | 179659586 | ||||||
| chr1:179659588 | TGTGC | T | 19 | a0001c0001t0001g0183 a0001c0001t0001g0203 a0001c0001t0001g0204 others(16): Show |
19 | HG00597.hp2 HG01433.hp2 HG01515.hp1 others(16): Show |
intron_variant | MODIFIER | c.2323-2514_2323-251 others(8): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr1 | 179659588 | ||||||
| chr1:179659590 | T | C | 6 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(3): Show |
6 | HG02109.hp2 HG02630.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.2323-2514T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179659590 | |||||||
| chr1:179659590 | TGC | T | 11 | a0001c0001t0001g0094 a0001c0001t0001g0178 a0001c0001t0001g0182 others(8): Show |
11 | HG01891.hp1 HG02004.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.2323-2507_2323-250 others(6): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr1 | 179659590 | ||||||
| chr1:179659592 | C | A | 23 | a0005c0006t0001g0206 a0005c0006t0001g0210 a0005c0006t0001g0211 others(20): Show |
23 | HG00544.hp1 HG00597.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.2323-2512C>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179659592 | |||||||
| chr1:179659592 | C | T | 8 | a0001c0001t0001g0095 a0005c0011t0003g0085 a0005c0011t0003g0086 others(5): Show |
8 | HG01099.hp1 HG02486.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.2323-2512C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179659592 | |||||||
| chr1:179659593 | G | A | 1 | a0003c0003t0001g0057 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2323-2511G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179659593 | |||||||
| chr1:179659594 | C | T | 6 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0007c0010t0001g0257 others(3): Show |
6 | HG01099.hp1 HG01891.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2323-2510C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179659594 | |||||||
| chr1:179659596 | C | T | 4 | a0001c0013t0001g0244 a0005c0012t0001g0254 a0005c0012t0001g0255 others(1): Show |
4 | HG00735.hp2 HG01109.hp1 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.2323-2508C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179659596 | |||||||
| chr1:179659679 | TTTGA | T | 12 | a0001c0005t0001g0002 a0001c0005t0001g0003 a0001c0005t0001g0009 others(9): Show |
17 | HG01346.hp1 HG02055.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.2323-2422_2323-241 others(8): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr1 | 179659679 | ||||||
| chr1:179659719 | C | T | 1 | a0002c0002t0002g0137 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.2323-2385C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179659719 | |||||||
| chr1:179659720 | G | A | 26 | a0005c0006t0001g0206 a0005c0006t0001g0210 a0005c0006t0001g0211 others(23): Show |
26 | HG00544.hp1 HG00597.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.2323-2384G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179659720 | |||||||
| chr1:179659923 | C | T | 1 | a0003c0003t0001g0078 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.2323-2181C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179659923 | |||||||
| chr1:179659988 | G | A | 102 | a0001c0001t0001g0026 a0002c0002t0001g0176 a0002c0002t0001g0246 others(99): Show |
109 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.2323-2116G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179659988 | |||||||
| chr1:179660017 | C | T | 3 | a0005c0012t0001g0254 a0005c0012t0001g0255 a0005c0012t0001g0256 |
3 | HG00735.hp2 HG01109.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.2323-2087C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179660017 | |||||||
| chr1:179660056 | T | C | 147 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(144): Show |
154 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.2323-2048T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179660056 | |||||||
| chr1:179660211 | G | GT | 26 | a0001c0008t0001g0058 a0001c0008t0001g0073 a0001c0013t0001g0243 others(23): Show |
26 | HG00673.hp2 HG00733.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.2323-1867dupT | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr1 | 179660211 | ||||||
| chr1:179660211 | GT | G | 88 | a0001c0001t0001g0025 a0001c0001t0001g0094 a0001c0001t0001g0178 others(85): Show |
88 | HG00280.hp2 HG00423.hp2 HG00621.hp2 others(85): Show |
intron_variant | MODIFIER | c.2323-1867delT | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr1 | 179660211 | ||||||
| chr1:179660211 | GTT | G | 174 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0026 others(171): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.2323-1868_2323-186 others(6): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr1 | 179660211 | ||||||
| chr1:179660320 | C | T | 5 | a0002c0002t0002g0113 a0002c0002t0002g0149 a0002c0002t0002g0150 others(2): Show |
5 | NA18978.hp1 NA19002.hp1 NA19011.hp2 others(2): Show |
intron_variant | MODIFIER | c.2323-1784C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179660320 | |||||||
| chr1:179660359 | C | A | 121 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(118): Show |
128 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.2323-1745C>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179660359 | |||||||
| chr1:179660435 | T | C | 1 | a0001c0001t0001g0328 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.2323-1669T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179660435 | |||||||
| chr1:179660453 | C | G | 2 | a0003c0003t0001g0066 a0003c0003t0001g0067 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2323-1651C>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179660453 | |||||||
| chr1:179660462 | C | T | 1 | a0002c0002t0002g0096 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2323-1642C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179660462 | |||||||
| chr1:179660667 | A | G | 121 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(118): Show |
128 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.2323-1437A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179660667 | |||||||
| chr1:179660744 | G | A | 2 | a0009c0014t0001g0364 a0009c0014t0001g0365 |
2 | HG01884.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.2323-1360G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179660744 | |||||||
| chr1:179660889 | C | T | 1 | a0001c0001t0001g0348 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2323-1215C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179660889 | |||||||
| chr1:179660997 | C | T | 1 | a0001c0001t0001g0320 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2323-1107C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179660997 | |||||||
| chr1:179661379 | G | GT | 120 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(117): Show |
127 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.2323-717dupT | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr1 | 179661379 | ||||||
| chr1:179661388 | G | T | 1 | a0002c0002t0002g0111 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2323-716G>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179661388 | |||||||
| chr1:179661389 | T | G | 1 | a0002c0002t0002g0111 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2323-715T>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179661389 | |||||||
| chr1:179661396 | C | T | 1 | a0002c0002t0002g0111 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2323-708C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179661396 | |||||||
| chr1:179661401 | C | T | 120 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(117): Show |
127 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.2323-703C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179661401 | |||||||
| chr1:179661741 | C | G | 1 | a0001c0001t0001g0292 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.2323-363C>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179661741 | |||||||
| chr1:179661831 | T | C | 1 | a0002c0002t0002g0110 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.2323-273T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179661831 | |||||||
| chr1:179661899 | C | A | 3 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0104 |
3 | HG02145.hp2 HG02572.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2323-205C>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179661899 | |||||||
| chr1:179661944 | C | G | 1 | a0005c0007t0001g0360 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2323-160C>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179661944 | |||||||
| chr1:179662046 | A | T | 4 | a0005c0011t0003g0085 a0005c0011t0003g0086 a0005c0011t0003g0087 others(1): Show |
4 | HG02809.hp2 HG03041.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.2323-58A>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 14/17 | chr1 | 179662046 | |||||||
| chr1:179662353 | C | A | 3 | a0002c0002t0002g0159 a0002c0002t0002g0160 a0002c0002t0002g0167 |
3 | HG03490.hp2 HG03492.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.2505+67C>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 15/17 | chr1 | 179662353 | |||||||
| chr1:179662367 | A | G | 1 | a0001c0001t0001g0311 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2505+81A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 15/17 | chr1 | 179662367 | |||||||
| chr1:179662404 | C | T | 1 | a0006c0009t0001g0091 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2505+118C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 15/17 | chr1 | 179662404 | |||||||
| chr1:179662534 | G | T | 2 | a0002c0002t0002g0131 a0002c0002t0002g0135 |
2 | NA18952.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.2505+248G>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 15/17 | chr1 | 179662534 | |||||||
| chr1:179662567 | C | T | 6 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(3): Show |
6 | HG02109.hp2 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.2505+281C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 15/17 | chr1 | 179662567 | |||||||
| chr1:179662751 | G | A | 1 | a0015c0021t0001g0335 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.2505+465G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 15/17 | chr1 | 179662751 | |||||||
| chr1:179662804 | A | G | 1 | a0002c0002t0002g0112 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2505+518A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 15/17 | chr1 | 179662804 | |||||||
| chr1:179662882 | G | A | 12 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0180 others(9): Show |
12 | HG02004.hp2 HG02258.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.2506-466G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 15/17 | chr1 | 179662882 | |||||||
| chr1:179663013 | TATAAGA | T | 3 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0104 |
3 | HG02145.hp2 HG02572.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2506-329_2506-324d others(8): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr1 | 179663013 | ||||||
| chr1:179663201 | G | T | 1 | a0001c0001t0001g0319 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2506-147G>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 15/17 | chr1 | 179663201 | |||||||
| chr1:179663212 | A | C | 121 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(118): Show |
128 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.2506-136A>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 15/17 | chr1 | 179663212 | |||||||
| chr1:179663592 | G | A | 158 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(155): Show |
165 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.2649+101G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 16/17 | chr1 | 179663592 | |||||||
| chr1:179663700 | G | T | 12 | a0001c0005t0001g0002 a0001c0005t0001g0003 a0001c0005t0001g0009 others(9): Show |
17 | HG01346.hp1 HG02055.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.2649+209G>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 16/17 | chr1 | 179663700 | |||||||
| chr1:179663900 | A | G | 1 | a0002c0002t0002g0107 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2649+409A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 16/17 | chr1 | 179663900 | |||||||
| chr1:179663901 | G | A | 1 | a0002c0002t0002g0107 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2649+410G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 16/17 | chr1 | 179663901 | |||||||
| chr1:179663905 | G | A | 127 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(124): Show |
134 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.2649+414G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 16/17 | chr1 | 179663905 | |||||||
| chr1:179664026 | C | T | 121 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(118): Show |
128 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.2649+535C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 16/17 | chr1 | 179664026 | |||||||
| chr1:179664422 | A | G | 8 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0007c0010t0001g0257 others(5): Show |
8 | HG01099.hp1 HG01891.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.2649+931A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 16/17 | chr1 | 179664422 | |||||||
| chr1:179664578 | T | C | 2 | a0001c0001t0001g0197 a0001c0001t0001g0198 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.2649+1087T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 16/17 | chr1 | 179664578 | |||||||
| chr1:179664625 | A | C | 3 | a0002c0002t0002g0105 a0002c0002t0002g0106 a0002c0002t0002g0107 |
3 | HG02602.hp2 HG03017.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.2649+1134A>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 16/17 | chr1 | 179664625 | |||||||
| chr1:179664639 | T | C | 127 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(124): Show |
134 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.2649+1148T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 16/17 | chr1 | 179664639 | |||||||
| chr1:179665016 | A | C | 6 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0007c0010t0001g0257 others(3): Show |
6 | HG01099.hp1 HG01891.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2649+1525A>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 16/17 | chr1 | 179665016 | |||||||
| chr1:179665049 | C | T | 16 | a0001c0001t0001g0010 a0001c0001t0001g0209 a0001c0001t0001g0262 others(13): Show |
17 | HG00408.hp2 HG01106.hp1 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.2649+1558C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 16/17 | chr1 | 179665049 | |||||||
| chr1:179665411 | T | C | 3 | a0001c0013t0001g0243 a0001c0013t0001g0244 a0001c0013t0001g0245 |
3 | HG01243.hp2 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2649+1920T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 16/17 | chr1 | 179665411 | |||||||
| chr1:179665494 | G | A | 1 | a0004c0004t0001g0023 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2649+2003G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 16/17 | chr1 | 179665494 | |||||||
| chr1:179665530 | A | G | 3 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 |
3 | HG02109.hp2 HG02630.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2649+2039A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 16/17 | chr1 | 179665530 | |||||||
| chr1:179666230 | A | G | 1 | a0002c0002t0002g0112 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2649+2739A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 16/17 | chr1 | 179666230 | |||||||
| chr1:179666233 | C | T | 5 | a0003c0003t0001g0061 a0003c0003t0001g0062 a0003c0003t0001g0063 others(2): Show |
5 | HG02896.hp2 HG02897.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2649+2742C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 16/17 | chr1 | 179666233 | |||||||
| chr1:179666512 | T | C | 1 | a0001c0001t0001g0343 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2650-2682T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 16/17 | chr1 | 179666512 | |||||||
| chr1:179666652 | C | T | 2 | a0001c0005t0001g0224 a0001c0005t0001g0225 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2650-2542C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 16/17 | chr1 | 179666652 | |||||||
| chr1:179666773 | G | A | 120 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(117): Show |
126 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.2650-2421G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 16/17 | chr1 | 179666773 | |||||||
| chr1:179666945 | C | T | 1 | a0001c0001t0001g0300 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2650-2249C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 16/17 | chr1 | 179666945 | |||||||
| chr1:179667074 | C | T | 101 | a0001c0001t0001g0026 a0002c0002t0001g0176 a0002c0002t0001g0246 others(98): Show |
107 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.2650-2120C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 16/17 | chr1 | 179667074 | |||||||
| chr1:179667350 | A | T | 2 | a0010c0016t0001g0092 a0010c0016t0001g0093 |
2 | HG02280.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2650-1844A>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 16/17 | chr1 | 179667350 | |||||||
| chr1:179667428 | A | G | 3 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0104 |
3 | HG02145.hp2 HG02572.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2650-1766A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 16/17 | chr1 | 179667428 | |||||||
| chr1:179667574 | T | TAATA | 132 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(129): Show |
139 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.2650-1619_2650-161 others(8): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr1 | 179667574 | ||||||
| chr1:179667639 | G | A | 158 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(155): Show |
165 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.2650-1555G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 16/17 | chr1 | 179667639 | |||||||
| chr1:179667818 | A | G | 2 | a0001c0001t0001g0338 a0001c0001t0001g0339 |
2 | HG02145.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2650-1376A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 16/17 | chr1 | 179667818 | |||||||
| chr1:179667926 | T | A | 1 | a0002c0002t0002g0163 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2650-1268T>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 16/17 | chr1 | 179667926 | |||||||
| chr1:179668177 | C | G | 1 | a0002c0002t0002g0134 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.2650-1017C>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 16/17 | chr1 | 179668177 | |||||||
| chr1:179668178 | C | A | 2 | a0009c0014t0001g0364 a0009c0014t0001g0365 |
2 | HG01884.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.2650-1016C>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 16/17 | chr1 | 179668178 | |||||||
| chr1:179668486 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2650-708G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 16/17 | chr1 | 179668486 | |||||||
| chr1:179668598 | C | T | 1 | a0001c0001t0002g0098 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2650-596C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 16/17 | chr1 | 179668598 | |||||||
| chr1:179668657 | A | T | 7 | a0002c0002t0002g0236 a0002c0002t0002g0237 a0002c0002t0002g0238 others(4): Show |
7 | HG02040.hp2 HG02135.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.2650-537A>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 16/17 | chr1 | 179668657 | |||||||
| chr1:179668728 | G | A | 1 | a0002c0002t0002g0163 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2650-466G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 16/17 | chr1 | 179668728 | |||||||
| chr1:179668741 | C | CT | 98 | a0001c0001t0001g0026 a0002c0002t0001g0176 a0002c0002t0002g0001 others(95): Show |
104 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.2650-434dupT | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr1 | 179668741 | ||||||
| chr1:179668741 | CT | C | 150 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0089 others(147): Show |
157 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.2650-434delT | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr1 | 179668741 | ||||||
| chr1:179668741 | CTT | C | 16 | a0001c0001t0001g0010 a0001c0001t0001g0209 a0001c0001t0001g0262 others(13): Show |
17 | HG00408.hp2 HG01106.hp1 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.2650-435_2650-434d others(4): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr1 | 179668741 | ||||||
| chr1:179668773 | C | A | 4 | a0002c0002t0002g0004 a0005c0012t0001g0254 a0005c0012t0001g0255 others(1): Show |
5 | HG00735.hp2 HG01109.hp1 HG01167.hp2 others(2): Show |
intron_variant | MODIFIER | c.2650-421C>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 16/17 | chr1 | 179668773 | |||||||
| chr1:179668798 | G | A | 120 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(117): Show |
126 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.2650-396G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 16/17 | chr1 | 179668798 | |||||||
| chr1:179668899 | C | A | 1 | a0003c0003t0001g0055 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2650-295C>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 16/17 | chr1 | 179668899 | |||||||
| chr1:179668899 | C | T | 1 | a0001c0001t0001g0353 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2650-295C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 16/17 | chr1 | 179668899 | |||||||
| chr1:179668929 | A | G | 18 | a0003c0003t0001g0048 a0003c0003t0001g0049 a0003c0003t0001g0050 others(15): Show |
18 | HG00423.hp1 HG03669.hp2 NA18942.hp1 others(15): Show |
intron_variant | MODIFIER | c.2650-265A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 16/17 | chr1 | 179668929 | |||||||
| chr1:179668935 | G | A | 1 | a0001c0001t0001g0319 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2650-259G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 16/17 | chr1 | 179668935 | |||||||
| chr1:179668946 | A | G | 1 | a0001c0001t0002g0098 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2650-248A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 16/17 | chr1 | 179668946 | |||||||
| chr1:179668953 | C | T | 1 | a0002c0002t0002g0123 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.2650-241C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 16/17 | chr1 | 179668953 | |||||||
| chr1:179669034 | G | A | 16 | a0001c0001t0001g0010 a0001c0001t0001g0209 a0001c0001t0001g0262 others(13): Show |
17 | HG00408.hp2 HG01106.hp1 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.2650-160G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 16/17 | chr1 | 179669034 | |||||||
| chr1:179669067 | T | C | 1 | a0001c0001t0001g0317 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.2650-127T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 16/17 | chr1 | 179669067 | |||||||
| chr1:179669086 | A | G | 1 | a0001c0008t0001g0068 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2650-108A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 16/17 | chr1 | 179669086 | |||||||
| chr1:179669460 | T | C | 1 | a0001c0001t0001g0301 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.2860+56T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179669460 | |||||||
| chr1:179669518 | C | T | 1 | a0002c0002t0002g0096 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2860+114C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179669518 | |||||||
| chr1:179669540 | T | C | 5 | a0003c0003t0001g0061 a0003c0003t0001g0062 a0003c0003t0001g0063 others(2): Show |
5 | HG02896.hp2 HG02897.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2860+136T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179669540 | |||||||
| chr1:179669614 | C | T | 120 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(117): Show |
126 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.2860+210C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179669614 | |||||||
| chr1:179669676 | T | G | 26 | a0005c0006t0001g0206 a0005c0006t0001g0210 a0005c0006t0001g0211 others(23): Show |
26 | HG00544.hp1 HG00597.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.2860+272T>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179669676 | |||||||
| chr1:179669681 | G | GT | 12 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0180 others(9): Show |
12 | HG02004.hp2 HG02258.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.2860+280dupT | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 179669681 | ||||||
| chr1:179669703 | G | A | 120 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(117): Show |
126 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.2860+299G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179669703 | |||||||
| chr1:179669810 | C | G | 2 | a0009c0014t0001g0364 a0009c0014t0001g0365 |
2 | HG01884.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.2860+406C>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179669810 | |||||||
| chr1:179669944 | A | G | 1 | a0002c0002t0002g0139 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2860+540A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179669944 | |||||||
| chr1:179669949 | A | G | 11 | a0001c0001t0001g0010 a0001c0001t0001g0262 a0001c0001t0001g0265 others(8): Show |
12 | HG01106.hp1 HG01433.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.2860+545A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179669949 | |||||||
| chr1:179669993 | A | G | 5 | a0006c0009t0001g0091 a0006c0009t0001g0234 a0006c0009t0001g0235 others(2): Show |
5 | HG02622.hp2 HG02630.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.2860+589A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179669993 | |||||||
| chr1:179670129 | C | T | 1 | a0002c0002t0002g0107 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2860+725C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179670129 | |||||||
| chr1:179670341 | G | A | 6 | a0002c0002t0002g0004 a0005c0012t0001g0254 a0005c0012t0001g0255 others(3): Show |
7 | HG00735.hp2 HG01109.hp1 HG01167.hp2 others(4): Show |
intron_variant | MODIFIER | c.2860+937G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179670341 | |||||||
| chr1:179670387 | G | T | 2 | a0002c0002t0002g0106 a0002c0002t0002g0107 |
2 | HG03017.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.2860+983G>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179670387 | |||||||
| chr1:179670391 | C | CA | 8 | a0001c0001t0001g0319 a0001c0001t0001g0330 a0001c0013t0001g0244 others(5): Show |
8 | HG01167.hp1 HG02129.hp2 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.2860+1003dupA | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 179670391 | ||||||
| chr1:179670391 | CAA | C | 6 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(3): Show |
6 | HG02109.hp2 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.2860+1002_2860+100 others(6): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 179670391 | ||||||
| chr1:179670403 | A | G | 1 | a0005c0007t0001g0208 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2860+999A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179670403 | |||||||
| chr1:179670430 | G | C | 6 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0007c0010t0001g0257 others(3): Show |
6 | HG01099.hp1 HG01891.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2860+1026G>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179670430 | |||||||
| chr1:179670636 | T | C | 1 | a0001c0001t0001g0299 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.2860+1232T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179670636 | |||||||
| chr1:179670827 | A | G | 4 | a0003c0003t0001g0074 a0003c0003t0001g0075 a0003c0003t0001g0076 others(1): Show |
4 | NA18969.hp2 NA18999.hp1 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.2860+1423A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179670827 | |||||||
| chr1:179670944 | A | G | 12 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0190 others(9): Show |
12 | HG00140.hp1 HG00738.hp2 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.2860+1540A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179670944 | |||||||
| chr1:179671237 | A | G | 5 | a0002c0002t0002g0113 a0002c0002t0002g0149 a0002c0002t0002g0150 others(2): Show |
5 | NA18978.hp1 NA19002.hp1 NA19011.hp2 others(2): Show |
intron_variant | MODIFIER | c.2860+1833A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179671237 | |||||||
| chr1:179671412 | G | A | 6 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(3): Show |
6 | HG02109.hp2 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.2860+2008G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179671412 | |||||||
| chr1:179671478 | T | A | 11 | a0001c0001t0001g0012 a0001c0001t0001g0291 a0001c0001t0001g0293 others(8): Show |
12 | HG00280.hp1 HG02132.hp2 HG02135.hp1 others(9): Show |
intron_variant | MODIFIER | c.2860+2074T>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179671478 | |||||||
| chr1:179671598 | A | ATTTT | 126 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(123): Show |
132 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.2860+2197_2860+219 others(8): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 179671598 | ||||||
| chr1:179671609 | T | A | 120 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(117): Show |
126 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.2860+2205T>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179671609 | |||||||
| chr1:179671919 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2860+2515G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179671919 | |||||||
| chr1:179671947 | ATGGTGTG others(4): Show |
A | 1 | a0005c0006t0002g0222 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2860+2546_2860+255 others(15): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 179671947 | ||||||
| chr1:179671949 | G | GGT | 90 | a0001c0001t0001g0012 a0001c0001t0001g0179 a0001c0001t0001g0180 others(87): Show |
94 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.2860+2588_2860+258 others(6): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 179671949 | ||||||
| chr1:179671949 | G | GGTGT | 9 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0261 others(6): Show |
9 | HG02071.hp2 HG02135.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.2860+2586_2860+258 others(8): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 179671949 | ||||||
| chr1:179671949 | GGT | G | 38 | a0001c0001t0001g0010 a0001c0001t0001g0104 a0001c0001t0001g0209 others(35): Show |
39 | HG00408.hp2 HG00558.hp1 HG01106.hp1 others(36): Show |
intron_variant | MODIFIER | c.2860+2588_2860+258 others(6): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 179671949 | ||||||
| chr1:179671949 | GGTGT | G | 56 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0292 others(53): Show |
57 | HG00423.hp1 HG01069.hp1 HG01070.hp2 others(54): Show |
intron_variant | MODIFIER | c.2860+2586_2860+258 others(8): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 179671949 | ||||||
| chr1:179671949 | GGTGTGT | G | 27 | a0001c0005t0001g0002 a0001c0005t0001g0003 a0001c0005t0001g0009 others(24): Show |
31 | HG00280.hp2 HG00544.hp2 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.2860+2584_2860+258 others(10): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 179671949 | ||||||
| chr1:179671949 | GGTGTGTG others(1): Show |
G | 14 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0005t0001g0224 others(11): Show |
14 | HG01099.hp1 HG01884.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.2860+2582_2860+258 others(12): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 179671949 | ||||||
| chr1:179671949 | GGTGTGTG others(5): Show |
G | 21 | a0001c0001t0001g0323 a0005c0006t0001g0206 a0005c0006t0001g0210 others(18): Show |
21 | HG00544.hp1 HG00597.hp1 HG00621.hp2 others(18): Show |
intron_variant | MODIFIER | c.2860+2578_2860+258 others(16): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 179671949 | ||||||
| chr1:179671949 | GGTGTGTG others(7): Show |
G | 2 | a0002c0002t0002g0004 a0002c0002t0002g0133 |
3 | HG01167.hp2 HG01169.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.2860+2576_2860+258 others(18): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 179671949 | ||||||
| chr1:179672023 | G | A | 1 | a0002c0002t0002g0236 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.2860+2619G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179672023 | |||||||
| chr1:179672127 | A | G | 4 | a0001c0001t0001g0355 a0001c0001t0001g0356 a0001c0001t0001g0357 others(1): Show |
4 | HG00558.hp1 HG02080.hp1 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.2860+2723A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179672127 | |||||||
| chr1:179672143 | GA | G | 72 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0280 others(69): Show |
73 | HG00099.hp1 HG00280.hp1 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.2860+2740delA | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179672143 | |||||||
| chr1:179672200 | A | G | 1 | a0001c0001t0002g0098 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2860+2796A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179672200 | |||||||
| chr1:179672263 | C | A | 6 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(3): Show |
6 | HG02109.hp2 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.2860+2859C>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179672263 | |||||||
| chr1:179672278 | TA | T | 8 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0007c0010t0001g0257 others(5): Show |
8 | HG01099.hp1 HG01891.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.2860+2875delA | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179672278 | |||||||
| chr1:179672285 | T | C | 2 | a0001c0001t0001g0301 a0001c0001t0001g0302 |
2 | NA18964.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.2860+2881T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179672285 | |||||||
| chr1:179672450 | T | A | 3 | a0001c0013t0001g0243 a0001c0013t0001g0244 a0001c0013t0001g0245 |
3 | HG01243.hp2 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2860+3046T>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179672450 | |||||||
| chr1:179672507 | T | C | 6 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0007c0010t0001g0257 others(3): Show |
6 | HG01099.hp1 HG01891.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2860+3103T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179672507 | |||||||
| chr1:179672522 | G | C | 2 | a0009c0014t0001g0364 a0009c0014t0001g0365 |
2 | HG01884.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.2860+3118G>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179672522 | |||||||
| chr1:179672528 | C | T | 6 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(3): Show |
6 | HG02109.hp2 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.2860+3124C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179672528 | |||||||
| chr1:179672589 | T | C | 26 | a0005c0006t0001g0206 a0005c0006t0001g0210 a0005c0006t0001g0211 others(23): Show |
26 | HG00544.hp1 HG00597.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.2860+3185T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179672589 | |||||||
| chr1:179673087 | T | C | 1 | a0007c0010t0001g0260 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2860+3683T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179673087 | |||||||
| chr1:179673123 | T | G | 6 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(3): Show |
6 | HG02109.hp2 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.2860+3719T>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179673123 | |||||||
| chr1:179673164 | T | C | 5 | a0001c0001t0001g0338 a0001c0001t0001g0339 a0001c0001t0001g0340 others(2): Show |
5 | HG01109.hp2 HG02145.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.2860+3760T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179673164 | |||||||
| chr1:179673311 | C | T | 26 | a0005c0006t0001g0206 a0005c0006t0001g0210 a0005c0006t0001g0211 others(23): Show |
26 | HG00544.hp1 HG00597.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.2860+3907C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179673311 | |||||||
| chr1:179673312 | G | A | 7 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(4): Show |
7 | HG02109.hp2 HG02630.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.2860+3908G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179673312 | |||||||
| chr1:179673584 | G | A | 1 | a0005c0011t0003g0086 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2860+4180G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179673584 | |||||||
| chr1:179673761 | GC | G | 124 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0025 others(121): Show |
132 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.2860+4360delC | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 179673761 | ||||||
| chr1:179673807 | T | C | 158 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(155): Show |
165 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.2860+4403T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179673807 | |||||||
| chr1:179674100 | G | A | 120 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(117): Show |
126 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.2860+4696G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179674100 | |||||||
| chr1:179674120 | G | A | 120 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(117): Show |
126 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.2860+4716G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179674120 | |||||||
| chr1:179674281 | T | C | 1 | a0002c0002t0002g0123 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.2860+4877T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179674281 | |||||||
| chr1:179674517 | T | C | 1 | a0003c0003t0001g0069 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2860+5113T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179674517 | |||||||
| chr1:179674643 | G | A | 6 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(3): Show |
6 | HG02109.hp2 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.2860+5239G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179674643 | |||||||
| chr1:179674670 | T | C | 12 | a0001c0005t0001g0002 a0001c0005t0001g0003 a0001c0005t0001g0009 others(9): Show |
17 | HG01346.hp1 HG02055.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.2860+5266T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179674670 | |||||||
| chr1:179674899 | T | G | 120 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(117): Show |
126 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.2860+5495T>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179674899 | |||||||
| chr1:179674992 | T | C | 1 | a0002c0002t0002g0120 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2860+5588T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179674992 | |||||||
| chr1:179675255 | T | A | 125 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(122): Show |
131 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.2860+5851T>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179675255 | |||||||
| chr1:179675255 | T | TTTA | 21 | a0001c0001t0001g0010 a0001c0001t0001g0094 a0001c0001t0001g0095 others(18): Show |
22 | HG00408.hp2 HG01099.hp1 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.2860+5869_2860+587 others(7): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 179675255 | ||||||
| chr1:179675267 | A | ATT | 3 | a0001c0001t0001g0294 a0001c0001t0001g0302 a0003c0003t0001g0054 |
3 | HG02135.hp1 NA18964.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2860+5864_2860+586 others(6): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 179675267 | ||||||
| chr1:179675270 | A | AT | 14 | a0001c0001t0001g0312 a0001c0005t0001g0002 a0001c0005t0001g0003 others(11): Show |
17 | HG01346.hp1 HG02559.hp2 HG02647.hp2 others(14): Show |
intron_variant | MODIFIER | c.2860+5868dupT | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 179675270 | ||||||
| chr1:179675270 | A | ATT | 90 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0188 others(87): Show |
92 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.2860+5867_2860+586 others(6): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 179675270 | ||||||
| chr1:179675270 | A | ATTT | 22 | a0001c0001t0001g0012 a0001c0001t0001g0189 a0001c0001t0001g0196 others(19): Show |
22 | HG00738.hp2 HG00741.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.2860+5868_2860+586 others(7): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 179675270 | ||||||
| chr1:179675270 | A | ATTTT | 3 | a0001c0001t0001g0330 a0003c0003t0001g0065 a0005c0011t0003g0088 |
3 | HG01192.hp1 HG03209.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.2860+5868_2860+586 others(8): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 179675270 | ||||||
| chr1:179675270 | A | T | 3 | a0001c0001t0001g0294 a0001c0001t0001g0302 a0003c0003t0001g0054 |
3 | HG02135.hp1 NA18964.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2860+5866A>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179675270 | |||||||
| chr1:179675271 | TTA | T | 23 | a0004c0004t0001g0016 a0004c0004t0001g0020 a0004c0004t0001g0021 others(20): Show |
23 | HG00280.hp2 HG00544.hp2 HG00609.hp2 others(20): Show |
intron_variant | MODIFIER | c.2860+5869_2860+587 others(6): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 179675271 | ||||||
| chr1:179675273 | A | ATT | 15 | a0001c0001t0001g0306 a0001c0001t0001g0307 a0001c0001t0001g0313 others(12): Show |
16 | HG00673.hp1 HG01167.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.2860+5892_2860+589 others(6): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 179675273 | ||||||
| chr1:179675273 | A | ATTATT | 6 | a0002c0002t0002g0102 a0005c0006t0001g0219 a0005c0007t0001g0205 others(3): Show |
6 | HG01261.hp1 NA18942.hp2 NA18950.hp1 others(3): Show |
intron_variant | MODIFIER | c.2860+5871_2860+587 others(9): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 179675273 | ||||||
| chr1:179675273 | A | T | 132 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0188 others(129): Show |
139 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.2860+5869A>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179675273 | |||||||
| chr1:179675274 | T | TTATTA | 12 | a0005c0006t0001g0206 a0005c0006t0001g0210 a0005c0006t0001g0214 others(9): Show |
12 | HG00544.hp1 HG00597.hp1 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.2860+5871_2860+587 others(9): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 179675274 | ||||||
| chr1:179675275 | T | TATTA | 5 | a0001c0001t0001g0269 a0005c0006t0001g0211 a0005c0006t0001g0212 others(2): Show |
5 | HG02015.hp2 HG02071.hp1 NA18612.hp1 others(2): Show |
intron_variant | MODIFIER | c.2860+5871_2860+587 others(8): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179675275 | |||||||
| chr1:179675275 | T | TATTTTA | 110 | a0001c0001t0001g0026 a0001c0001t0001g0090 a0001c0001t0001g0178 others(107): Show |
116 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.2860+5871_2860+587 others(10): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179675275 | |||||||
| chr1:179675276 | T | A | 22 | a0001c0001t0001g0010 a0001c0001t0001g0199 a0001c0001t0001g0200 others(19): Show |
23 | HG00597.hp2 HG01106.hp1 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.2860+5872T>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179675276 | |||||||
| chr1:179675277 | T | A | 4 | a0001c0001t0001g0278 a0005c0006t0002g0223 a0010c0016t0001g0092 others(1): Show |
4 | HG02280.hp1 HG02630.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.2860+5873T>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179675277 | |||||||
| chr1:179675278 | T | A | 1 | a0001c0001t0001g0089 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2860+5874T>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179675278 | |||||||
| chr1:179675279 | T | A | 4 | a0001c0001t0001g0264 a0001c0001t0001g0274 a0001c0001t0001g0276 others(1): Show |
4 | HG02109.hp2 HG02129.hp1 HG02165.hp1 others(1): Show |
intron_variant | MODIFIER | c.2860+5875T>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179675279 | |||||||
| chr1:179675280 | T | A | 114 | a0001c0001t0001g0026 a0001c0001t0001g0178 a0001c0001t0001g0179 others(111): Show |
120 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.2860+5876T>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179675280 | |||||||
| chr1:179675281 | T | A | 4 | a0002c0002t0002g0102 a0002c0002t0002g0169 a0002c0002t0002g0170 others(1): Show |
4 | HG00597.hp2 HG01261.hp1 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.2860+5877T>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179675281 | |||||||
| chr1:179675282 | T | A | 3 | a0001c0001t0001g0264 a0001c0001t0001g0274 a0001c0001t0001g0276 |
3 | HG02129.hp1 HG02165.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.2860+5878T>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179675282 | |||||||
| chr1:179675285 | T | A | 110 | a0001c0001t0001g0026 a0001c0001t0001g0178 a0001c0001t0001g0179 others(107): Show |
116 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.2860+5881T>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179675285 | |||||||
| chr1:179675285 | T | TATCTTA | 3 | a0002c0002t0002g0169 a0002c0002t0002g0170 a0002c0002t0002g0171 |
3 | HG00597.hp2 NA18954.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.2860+5881_2860+588 others(10): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179675285 | |||||||
| chr1:179675286 | T | A | 1 | a0002c0002t0002g0102 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2860+5882T>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179675286 | |||||||
| chr1:179675319 | G | A | 2 | a0009c0014t0001g0364 a0009c0014t0001g0365 |
2 | HG01884.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.2860+5915G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179675319 | |||||||
| chr1:179675329 | G | T | 6 | a0002c0002t0002g0004 a0005c0012t0001g0254 a0005c0012t0001g0255 others(3): Show |
7 | HG00735.hp2 HG01109.hp1 HG01167.hp2 others(4): Show |
intron_variant | MODIFIER | c.2860+5925G>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179675329 | |||||||
| chr1:179675480 | C | T | 84 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0280 others(81): Show |
86 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.2860+6076C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179675480 | |||||||
| chr1:179675530 | C | T | 119 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(116): Show |
125 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.2860+6126C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179675530 | |||||||
| chr1:179675574 | C | G | 6 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(3): Show |
6 | HG02109.hp2 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.2860+6170C>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179675574 | |||||||
| chr1:179675575 | G | A | 1 | a0002c0002t0002g0097 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2860+6171G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179675575 | |||||||
| chr1:179675775 | T | G | 3 | a0001c0001t0001g0264 a0001c0001t0001g0274 a0001c0001t0001g0276 |
3 | HG02129.hp1 HG02165.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.2860+6371T>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179675775 | |||||||
| chr1:179676216 | T | C | 143 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(140): Show |
155 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.2860+6812T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179676216 | |||||||
| chr1:179676218 | T | C | 1 | a0001c0001t0001g0330 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.2860+6814T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179676218 | |||||||
| chr1:179676283 | G | T | 119 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(116): Show |
125 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.2860+6879G>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179676283 | |||||||
| chr1:179676284 | G | A | 119 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(116): Show |
125 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.2860+6880G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179676284 | |||||||
| chr1:179676285 | T | C | 6 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0007c0010t0001g0257 others(3): Show |
6 | HG01099.hp1 HG01891.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2860+6881T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179676285 | |||||||
| chr1:179676313 | C | T | 2 | a0001c0001t0001g0326 a0013c0020t0001g0333 |
2 | HG02165.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.2860+6909C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179676313 | |||||||
| chr1:179676381 | T | G | 1 | a0002c0002t0002g0013 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2860+6977T>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179676381 | |||||||
| chr1:179676406 | T | G | 6 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(3): Show |
6 | HG02109.hp2 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.2860+7002T>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179676406 | |||||||
| chr1:179676531 | C | T | 2 | a0004c0004t0001g0036 a0004c0004t0001g0044 |
2 | NA18975.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.2860+7127C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179676531 | |||||||
| chr1:179676574 | G | T | 2 | a0002c0002t0002g0127 a0002c0002t0002g0128 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2860+7170G>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179676574 | |||||||
| chr1:179676801 | T | C | 18 | a0001c0005t0001g0002 a0001c0005t0001g0003 a0001c0005t0001g0009 others(15): Show |
24 | HG00735.hp2 HG01109.hp1 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.2860+7397T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179676801 | |||||||
| chr1:179677039 | A | AT | 22 | a0005c0006t0001g0206 a0005c0006t0001g0210 a0005c0006t0001g0211 others(19): Show |
22 | HG00544.hp1 HG00597.hp1 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.2860+7642dupT | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 179677039 | ||||||
| chr1:179677456 | C | G | 1 | a0002c0002t0002g0144 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2860+8052C>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179677456 | |||||||
| chr1:179677491 | G | A | 6 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(3): Show |
6 | HG02109.hp2 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.2860+8087G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179677491 | |||||||
| chr1:179677538 | G | A | 6 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(3): Show |
6 | HG02109.hp2 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.2860+8134G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179677538 | |||||||
| chr1:179677580 | T | C | 1 | a0005c0007t0001g0217 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.2860+8176T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179677580 | |||||||
| chr1:179677610 | A | G | 1 | a0005c0011t0003g0088 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2860+8206A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179677610 | |||||||
| chr1:179677732 | C | T | 119 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(116): Show |
125 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.2860+8328C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179677732 | |||||||
| chr1:179677874 | G | T | 7 | a0003c0003t0001g0048 a0003c0003t0001g0049 a0003c0003t0001g0050 others(4): Show |
7 | HG00423.hp1 NA18942.hp1 NA18947.hp2 others(4): Show |
intron_variant | MODIFIER | c.2860+8470G>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179677874 | |||||||
| chr1:179677920 | T | G | 18 | a0001c0005t0001g0002 a0001c0005t0001g0003 a0001c0005t0001g0009 others(15): Show |
24 | HG00735.hp2 HG01109.hp1 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.2860+8516T>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179677920 | |||||||
| chr1:179678056 | C | T | 1 | a0005c0011t0003g0085 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2860+8652C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179678056 | |||||||
| chr1:179678152 | C | A | 16 | a0001c0001t0001g0010 a0001c0001t0001g0209 a0001c0001t0001g0262 others(13): Show |
17 | HG00408.hp2 HG01106.hp1 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.2860+8748C>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179678152 | |||||||
| chr1:179678198 | C | T | 6 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(3): Show |
6 | HG02109.hp2 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.2860+8794C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179678198 | |||||||
| chr1:179678199 | G | C | 119 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(116): Show |
125 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.2860+8795G>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179678199 | |||||||
| chr1:179678340 | G | A | 2 | a0010c0016t0001g0092 a0010c0016t0001g0093 |
2 | HG02280.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2860+8936G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179678340 | |||||||
| chr1:179678405 | T | C | 1 | a0001c0001t0001g0311 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2860+9001T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179678405 | |||||||
| chr1:179678506 | C | T | 1 | a0001c0001t0001g0187 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2860+9102C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179678506 | |||||||
| chr1:179678507 | G | A | 2 | a0001c0001t0001g0294 a0001c0001t0001g0297 |
2 | HG02132.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.2860+9103G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179678507 | |||||||
| chr1:179678523 | T | C | 286 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0025 others(283): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.2860+9119T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179678523 | |||||||
| chr1:179678545 | C | T | 6 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(3): Show |
6 | HG02109.hp2 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.2860+9141C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179678545 | |||||||
| chr1:179678546 | G | A | 1 | a0002c0002t0002g0144 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2860+9142G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179678546 | |||||||
| chr1:179678558 | G | A | 5 | a0001c0001t0001g0338 a0001c0001t0001g0339 a0001c0001t0001g0340 others(2): Show |
5 | HG01109.hp2 HG02145.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.2860+9154G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179678558 | |||||||
| chr1:179678564 | ATTTAAAC others(11): Show |
A | 26 | a0005c0006t0001g0206 a0005c0006t0001g0210 a0005c0006t0001g0211 others(23): Show |
26 | HG00544.hp1 HG00597.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.2860+9166_2860+918 others(22): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 179678564 | ||||||
| chr1:179678591 | C | T | 1 | a0002c0002t0002g0101 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2860+9187C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179678591 | |||||||
| chr1:179678624 | A | C | 12 | a0001c0005t0001g0002 a0001c0005t0001g0003 a0001c0005t0001g0009 others(9): Show |
17 | HG01346.hp1 HG02055.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.2860+9220A>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179678624 | |||||||
| chr1:179678818 | G | C | 12 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0180 others(9): Show |
12 | HG02004.hp2 HG02258.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.2860+9414G>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179678818 | |||||||
| chr1:179678859 | A | G | 1 | a0002c0002t0002g0133 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.2860+9455A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179678859 | |||||||
| chr1:179678952 | GGA | G | 4 | a0002c0002t0002g0004 a0005c0012t0001g0254 a0005c0012t0001g0255 others(1): Show |
5 | HG00735.hp2 HG01109.hp1 HG01167.hp2 others(2): Show |
intron_variant | MODIFIER | c.2860+9549_2860+955 others(6): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179678952 | |||||||
| chr1:179678982 | G | A | 143 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(140): Show |
155 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.2860+9578G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179678982 | |||||||
| chr1:179679067 | T | C | 125 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(122): Show |
131 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.2860+9663T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179679067 | |||||||
| chr1:179679204 | G | T | 1 | a0004c0004t0001g0022 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2860+9800G>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179679204 | |||||||
| chr1:179679217 | CGTG | C | 4 | a0005c0011t0003g0085 a0005c0011t0003g0086 a0005c0011t0003g0087 others(1): Show |
4 | HG02809.hp2 HG03041.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.2860+9816_2860+981 others(7): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 179679217 | ||||||
| chr1:179679218 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2860+9814G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179679218 | |||||||
| chr1:179679244 | T | A | 119 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(116): Show |
125 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.2860+9840T>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179679244 | |||||||
| chr1:179679478 | C | T | 26 | a0005c0006t0001g0206 a0005c0006t0001g0210 a0005c0006t0001g0211 others(23): Show |
26 | HG00544.hp1 HG00597.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.2860+10074C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179679478 | |||||||
| chr1:179679588 | T | G | 3 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0104 |
3 | HG02145.hp2 HG02572.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2860+10184T>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179679588 | |||||||
| chr1:179679717 | C | CT | 125 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(122): Show |
131 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.2860+10313_2860+10 others(7): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179679717 | |||||||
| chr1:179679726 | GT | G | 26 | a0005c0006t0001g0206 a0005c0006t0001g0210 a0005c0006t0001g0211 others(23): Show |
26 | HG00544.hp1 HG00597.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.2860+10327delT | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 179679726 | ||||||
| chr1:179679736 | C | G | 1 | a0002c0002t0002g0108 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.2860+10332C>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179679736 | |||||||
| chr1:179680048 | T | C | 3 | a0002c0002t0002g0132 a0002c0002t0002g0133 a0002c0002t0002g0134 |
3 | NA18990.hp1 NA18992.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.2860+10644T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179680048 | |||||||
| chr1:179680070 | A | G | 14 | a0001c0005t0001g0002 a0001c0005t0001g0003 a0001c0005t0001g0009 others(11): Show |
19 | HG01346.hp1 HG01884.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.2861-10626A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179680070 | |||||||
| chr1:179680101 | C | A | 2 | a0001c0001t0001g0313 a0001c0001t0001g0329 |
2 | HG00673.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.2861-10595C>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179680101 | |||||||
| chr1:179680192 | C | T | 1 | a0002c0002t0002g0143 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.2861-10504C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179680192 | |||||||
| chr1:179680201 | C | T | 1 | a0002c0002t0001g0252 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2861-10495C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179680201 | |||||||
| chr1:179680361 | T | G | 126 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(123): Show |
132 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.2861-10335T>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179680361 | |||||||
| chr1:179680468 | G | C | 4 | a0005c0011t0003g0085 a0005c0011t0003g0086 a0005c0011t0003g0087 others(1): Show |
4 | HG02809.hp2 HG03041.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.2861-10228G>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179680468 | |||||||
| chr1:179680563 | A | G | 1 | a0005c0012t0001g0255 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2861-10133A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179680563 | |||||||
| chr1:179680702 | G | A | 2 | a0001c0001t0001g0089 a0001c0001t0001g0090 |
2 | HG02572.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2861-9994G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179680702 | |||||||
| chr1:179680790 | C | T | 6 | a0002c0002t0002g0004 a0005c0012t0001g0254 a0005c0012t0001g0255 others(3): Show |
7 | HG00735.hp2 HG01109.hp1 HG01167.hp2 others(4): Show |
intron_variant | MODIFIER | c.2861-9906C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179680790 | |||||||
| chr1:179680867 | A | T | 1 | a0001c0001t0001g0278 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2861-9829A>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179680867 | |||||||
| chr1:179680946 | A | T | 1 | a0003c0003t0001g0075 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.2861-9750A>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179680946 | |||||||
| chr1:179681044 | C | T | 1 | a0002c0002t0001g0249 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2861-9652C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179681044 | |||||||
| chr1:179681066 | TTATC | T | 119 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(116): Show |
125 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.2861-9619_2861-961 others(8): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 179681066 | ||||||
| chr1:179681084 | T | C | 6 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(3): Show |
6 | HG02109.hp2 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.2861-9612T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179681084 | |||||||
| chr1:179681142 | A | G | 2 | a0009c0014t0001g0364 a0009c0014t0001g0365 |
2 | HG01884.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.2861-9554A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179681142 | |||||||
| chr1:179681164 | A | T | 1 | a0002c0002t0002g0123 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.2861-9532A>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179681164 | |||||||
| chr1:179681257 | T | C | 4 | a0002c0002t0002g0004 a0005c0012t0001g0254 a0005c0012t0001g0255 others(1): Show |
5 | HG00735.hp2 HG01109.hp1 HG01167.hp2 others(2): Show |
intron_variant | MODIFIER | c.2861-9439T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179681257 | |||||||
| chr1:179681277 | TG | T | 30 | a0004c0004t0001g0015 a0004c0004t0001g0016 a0004c0004t0001g0017 others(27): Show |
30 | HG00280.hp2 HG00544.hp2 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.2861-9418delG | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179681277 | |||||||
| chr1:179681772 | G | T | 16 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0180 others(13): Show |
16 | HG02004.hp2 HG02055.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.2861-8924G>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179681772 | |||||||
| chr1:179681897 | C | G | 119 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(116): Show |
125 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.2861-8799C>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179681897 | |||||||
| chr1:179681938 | C | CT | 8 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0004c0004t0001g0032 others(5): Show |
8 | HG01099.hp1 HG01891.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.2861-8738dupT | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 179681938 | ||||||
| chr1:179681938 | C | T | 15 | a0001c0001t0001g0010 a0001c0001t0001g0209 a0001c0001t0001g0262 others(12): Show |
16 | HG00408.hp2 HG01106.hp1 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.2861-8758C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179681938 | |||||||
| chr1:179681938 | CT | C | 17 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0190 others(14): Show |
18 | HG00140.hp1 HG00735.hp2 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.2861-8738delT | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 179681938 | ||||||
| chr1:179681938 | CTT | C | 210 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0026 others(207): Show |
218 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.2861-8739_2861-873 others(6): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 179681938 | ||||||
| chr1:179681942 | T | C | 1 | a0004c0004t0001g0021 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2861-8754T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179681942 | |||||||
| chr1:179681944 | T | C | 6 | a0002c0002t0002g0004 a0005c0012t0001g0254 a0005c0012t0001g0255 others(3): Show |
7 | HG00735.hp2 HG01109.hp1 HG01167.hp2 others(4): Show |
intron_variant | MODIFIER | c.2861-8752T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179681944 | |||||||
| chr1:179681945 | T | C | 1 | a0005c0007t0001g0360 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2861-8751T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179681945 | |||||||
| chr1:179681948 | T | C | 119 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(116): Show |
125 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.2861-8748T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179681948 | |||||||
| chr1:179681952 | T | TAAGACAG others(142): Show |
3 | a0001c0005t0001g0224 a0001c0005t0001g0225 a0001c0022t0001g0226 |
3 | HG02895.hp1 HG02897.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2861-8744_2861-874 others(153): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179681952 | |||||||
| chr1:179681952 | T | TTAAGACA others(143): Show |
8 | a0001c0005t0001g0002 a0001c0005t0001g0003 a0001c0005t0001g0009 others(5): Show |
13 | HG01346.hp1 HG02055.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.2861-8743_2861-874 others(154): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 179681952 | ||||||
| chr1:179681961 | G | GACAGAGT others(749): Show |
4 | a0005c0011t0003g0085 a0005c0011t0003g0086 a0005c0011t0003g0087 others(1): Show |
4 | HG02809.hp2 HG03041.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.2861-8728_2861-872 others(760): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 179681961 | ||||||
| chr1:179681961 | G | GACAGAGT others(749): Show |
22 | a0005c0006t0001g0206 a0005c0006t0001g0210 a0005c0006t0001g0211 others(19): Show |
22 | HG00544.hp1 HG00597.hp1 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.2861-8728_2861-872 others(760): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 179681961 | ||||||
| chr1:179681961 | G | GACAGAGT others(749): Show |
4 | a0002c0002t0002g0004 a0005c0012t0001g0254 a0005c0012t0001g0255 others(1): Show |
5 | HG00735.hp2 HG01109.hp1 HG01167.hp2 others(2): Show |
intron_variant | MODIFIER | c.2861-8728_2861-872 others(760): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 179681961 | ||||||
| chr1:179681961 | G | GACAGAGT others(749): Show |
16 | a0001c0001t0001g0104 a0001c0001t0001g0184 a0001c0001t0001g0199 others(13): Show |
16 | HG00099.hp1 HG01074.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.2861-8728_2861-872 others(760): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 179681961 | ||||||
| chr1:179681961 | G | GACAGAGT others(748): Show |
2 | a0009c0014t0001g0364 a0009c0014t0001g0365 |
2 | HG01884.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.2861-8728_2861-872 others(759): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 179681961 | ||||||
| chr1:179681961 | G | GACAGAGT others(749): Show |
3 | a0004c0004t0001g0016 a0004c0004t0001g0020 a0004c0004t0001g0041 |
3 | HG00544.hp2 HG01167.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.2861-8728_2861-872 others(760): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 179681961 | ||||||
| chr1:179681961 | G | GACAGAGT others(749): Show |
89 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0188 others(86): Show |
91 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.2861-8728_2861-872 others(760): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 179681961 | ||||||
| chr1:179681961 | G | GACAGAGT others(749): Show |
98 | a0001c0001t0001g0010 a0001c0001t0001g0094 a0001c0001t0001g0095 others(95): Show |
99 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.2861-8728_2861-872 others(760): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 179681961 | ||||||
| chr1:179681961 | G | GTTTTTGG others(594): Show |
11 | a0001c0005t0001g0002 a0001c0005t0001g0003 a0001c0005t0001g0009 others(8): Show |
16 | HG01346.hp1 HG02055.hp2 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.2861-8735_2861-873 others(605): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179681961 | |||||||
| chr1:179681981 | T | TA | 23 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(20): Show |
23 | HG00423.hp2 HG00738.hp1 HG02004.hp2 others(20): Show |
intron_variant | MODIFIER | c.2861-8700dupA | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 179681981 | ||||||
| chr1:179681981 | TA | T | 10 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0191 others(7): Show |
10 | HG01099.hp1 HG01168.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.2861-8700delA | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 179681981 | ||||||
| chr1:179681990 | A | G | 1 | a0001c0001t0001g0313 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2861-8706A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179681990 | |||||||
| chr1:179682000 | A | G | 1 | a0003c0003t0001g0078 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.2861-8696A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179682000 | |||||||
| chr1:179682245 | C | A | 4 | a0002c0002t0002g0004 a0005c0012t0001g0254 a0005c0012t0001g0255 others(1): Show |
5 | HG00735.hp2 HG01109.hp1 HG01167.hp2 others(2): Show |
intron_variant | MODIFIER | c.2861-8451C>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179682245 | |||||||
| chr1:179682607 | A | G | 2 | a0001c0001t0001g0340 a0001c0001t0001g0341 |
2 | HG01109.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2861-8089A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179682607 | |||||||
| chr1:179682656 | T | C | 2 | a0004c0004t0001g0035 a0004c0004t0001g0037 |
2 | NA18977.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.2861-8040T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179682656 | |||||||
| chr1:179682819 | T | C | 1 | a0001c0001t0001g0355 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2861-7877T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179682819 | |||||||
| chr1:179682841 | C | G | 120 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(117): Show |
126 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.2861-7855C>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179682841 | |||||||
| chr1:179683017 | T | TTC | 119 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(116): Show |
125 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.2861-7665_2861-766 others(6): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 179683017 | ||||||
| chr1:179683031 | C | G | 2 | a0010c0016t0001g0092 a0010c0016t0001g0093 |
2 | HG02280.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2861-7665C>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179683031 | |||||||
| chr1:179683164 | C | T | 7 | a0002c0002t0001g0176 a0002c0002t0002g0014 a0002c0002t0002g0151 others(4): Show |
7 | HG00741.hp2 HG01192.hp2 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.2861-7532C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179683164 | |||||||
| chr1:179683483 | T | C | 1 | a0004c0004t0001g0036 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.2861-7213T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179683483 | |||||||
| chr1:179683517 | C | T | 3 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0104 |
3 | HG02145.hp2 HG02572.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2861-7179C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179683517 | |||||||
| chr1:179683726 | C | G | 131 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(128): Show |
138 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.2861-6970C>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179683726 | |||||||
| chr1:179683788 | C | T | 6 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(3): Show |
6 | HG02109.hp2 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.2861-6908C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179683788 | |||||||
| chr1:179683809 | AT | A | 71 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0280 others(68): Show |
72 | HG00099.hp1 HG00280.hp1 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.2861-6877delT | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 179683809 | ||||||
| chr1:179683812 | T | A | 2 | a0001c0001t0001g0307 a0001c0001t0001g0327 |
2 | HG02015.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.2861-6884T>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179683812 | |||||||
| chr1:179683907 | T | C | 5 | a0004c0004t0001g0018 a0004c0004t0001g0030 a0004c0004t0001g0031 others(2): Show |
5 | HG00673.hp2 NA18971.hp2 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.2861-6789T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179683907 | |||||||
| chr1:179684056 | T | A | 1 | a0005c0007t0001g0253 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2861-6640T>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179684056 | |||||||
| chr1:179684086 | T | G | 1 | a0009c0014t0001g0365 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2861-6610T>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179684086 | |||||||
| chr1:179684106 | G | A | 1 | a0005c0006t0001g0220 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2861-6590G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179684106 | |||||||
| chr1:179684289 | C | A | 8 | a0001c0001t0001g0178 a0001c0001t0001g0182 a0001c0001t0001g0183 others(5): Show |
8 | HG02004.hp2 HG02280.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.2861-6407C>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179684289 | |||||||
| chr1:179684309 | A | G | 26 | a0005c0006t0001g0206 a0005c0006t0001g0210 a0005c0006t0001g0211 others(23): Show |
26 | HG00544.hp1 HG00597.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.2861-6387A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179684309 | |||||||
| chr1:179684594 | C | T | 4 | a0005c0011t0003g0085 a0005c0011t0003g0086 a0005c0011t0003g0087 others(1): Show |
4 | HG02809.hp2 HG03041.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.2861-6102C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179684594 | |||||||
| chr1:179684683 | A | G | 1 | a0001c0001t0002g0098 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2861-6013A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179684683 | |||||||
| chr1:179684725 | T | C | 1 | a0007c0010t0001g0258 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2861-5971T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179684725 | |||||||
| chr1:179684892 | G | T | 12 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0180 others(9): Show |
12 | HG02004.hp2 HG02258.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.2861-5804G>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179684892 | |||||||
| chr1:179684999 | GT | G | 26 | a0005c0006t0001g0206 a0005c0006t0001g0210 a0005c0006t0001g0211 others(23): Show |
26 | HG00544.hp1 HG00597.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.2861-5695delT | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 179684999 | ||||||
| chr1:179685057 | C | A | 6 | a0002c0002t0002g0005 a0002c0002t0002g0099 a0002c0002t0002g0100 others(3): Show |
8 | HG00099.hp2 HG01081.hp2 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.2861-5639C>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179685057 | |||||||
| chr1:179685058 | A | C | 119 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(116): Show |
125 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.2861-5638A>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179685058 | |||||||
| chr1:179685083 | C | T | 1 | a0003c0003t0001g0054 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2861-5613C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179685083 | |||||||
| chr1:179685113 | T | C | 2 | a0002c0002t0002g0127 a0002c0002t0002g0128 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2861-5583T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179685113 | |||||||
| chr1:179685180 | A | T | 125 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(122): Show |
131 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.2861-5516A>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179685180 | |||||||
| chr1:179685192 | C | A | 1 | a0002c0002t0002g0172 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2861-5504C>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179685192 | |||||||
| chr1:179685531 | T | A | 4 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(1): Show |
4 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.2861-5165T>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179685531 | |||||||
| chr1:179685556 | T | C | 1 | a0001c0001t0001g0352 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2861-5140T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179685556 | |||||||
| chr1:179685613 | C | A | 1 | a0001c0001t0001g0270 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2861-5083C>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179685613 | |||||||
| chr1:179685693 | T | G | 1 | a0003c0003t0001g0063 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2861-5003T>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179685693 | |||||||
| chr1:179685734 | G | T | 6 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(3): Show |
6 | HG02109.hp2 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.2861-4962G>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179685734 | |||||||
| chr1:179685743 | G | A | 118 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(115): Show |
124 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.2861-4953G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179685743 | |||||||
| chr1:179685757 | C | G | 1 | a0002c0002t0001g0247 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2861-4939C>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179685757 | |||||||
| chr1:179685871 | G | C | 6 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(3): Show |
6 | HG02109.hp2 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.2861-4825G>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179685871 | |||||||
| chr1:179685887 | G | A | 6 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(3): Show |
6 | HG02109.hp2 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.2861-4809G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179685887 | |||||||
| chr1:179685972 | A | G | 6 | a0005c0007t0001g0205 a0005c0007t0001g0207 a0005c0007t0001g0208 others(3): Show |
6 | NA18942.hp2 NA18950.hp1 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.2861-4724A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179685972 | |||||||
| chr1:179685991 | G | T | 5 | a0001c0001t0001g0338 a0001c0001t0001g0339 a0001c0001t0001g0340 others(2): Show |
5 | HG01109.hp2 HG02145.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.2861-4705G>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179685991 | |||||||
| chr1:179686043 | C | T | 2 | a0001c0001t0001g0179 a0001c0001t0001g0180 |
2 | HG02965.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2861-4653C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179686043 | |||||||
| chr1:179686249 | T | C | 118 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(115): Show |
124 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.2861-4447T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179686249 | |||||||
| chr1:179686357 | A | G | 1 | a0003c0003t0001g0065 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2861-4339A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179686357 | |||||||
| chr1:179686395 | A | C | 3 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0023t0001g0202 |
3 | HG02055.hp1 HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.2861-4301A>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179686395 | |||||||
| chr1:179686455 | T | C | 1 | a0001c0001t0001g0320 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2861-4241T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179686455 | |||||||
| chr1:179686484 | G | A | 1 | a0001c0001t0001g0261 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2861-4212G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179686484 | |||||||
| chr1:179686650 | C | T | 118 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(115): Show |
124 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.2861-4046C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179686650 | |||||||
| chr1:179686683 | TG | T | 118 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(115): Show |
124 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.2861-4011delG | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 179686683 | ||||||
| chr1:179686720 | G | C | 10 | a0001c0005t0001g0002 a0001c0005t0001g0003 a0001c0005t0001g0009 others(7): Show |
15 | HG01346.hp1 HG02055.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.2861-3976G>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179686720 | |||||||
| chr1:179686783 | G | A | 6 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(3): Show |
6 | HG02109.hp2 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.2861-3913G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179686783 | |||||||
| chr1:179686827 | C | T | 1 | a0001c0001t0001g0328 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.2861-3869C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179686827 | |||||||
| chr1:179686925 | TTC | T | 118 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(115): Show |
124 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.2861-3765_2861-376 others(6): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 179686925 | ||||||
| chr1:179686936 | G | A | 6 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(3): Show |
6 | HG02109.hp2 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.2861-3760G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179686936 | |||||||
| chr1:179686958 | G | T | 1 | a0002c0002t0002g0123 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.2861-3738G>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179686958 | |||||||
| chr1:179686980 | T | C | 1 | a0001c0001t0001g0181 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2861-3716T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179686980 | |||||||
| chr1:179687046 | G | T | 6 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(3): Show |
6 | HG02109.hp2 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.2861-3650G>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179687046 | |||||||
| chr1:179687049 | C | T | 1 | a0004c0004t0001g0028 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2861-3647C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179687049 | |||||||
| chr1:179687107 | C | T | 26 | a0005c0006t0001g0206 a0005c0006t0001g0210 a0005c0006t0001g0211 others(23): Show |
26 | HG00544.hp1 HG00597.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.2861-3589C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179687107 | |||||||
| chr1:179687173 | G | A | 125 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0025 others(122): Show |
133 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.2861-3523G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179687173 | |||||||
| chr1:179687226 | G | T | 4 | a0002c0002t0002g0004 a0005c0012t0001g0254 a0005c0012t0001g0255 others(1): Show |
5 | HG00735.hp2 HG01109.hp1 HG01167.hp2 others(2): Show |
intron_variant | MODIFIER | c.2861-3470G>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179687226 | |||||||
| chr1:179687346 | A | T | 119 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(116): Show |
125 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.2861-3350A>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179687346 | |||||||
| chr1:179687348 | C | T | 119 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(116): Show |
125 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.2861-3348C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179687348 | |||||||
| chr1:179687349 | G | A | 6 | a0002c0002t0002g0004 a0005c0012t0001g0254 a0005c0012t0001g0255 others(3): Show |
7 | HG00735.hp2 HG01109.hp1 HG01167.hp2 others(4): Show |
intron_variant | MODIFIER | c.2861-3347G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179687349 | |||||||
| chr1:179687420 | A | G | 5 | a0006c0009t0001g0091 a0006c0009t0001g0234 a0006c0009t0001g0235 others(2): Show |
5 | HG02622.hp2 HG02630.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.2861-3276A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179687420 | |||||||
| chr1:179687426 | A | G | 130 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(127): Show |
137 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.2861-3270A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179687426 | |||||||
| chr1:179687451 | C | G | 1 | a0001c0001t0001g0265 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2861-3245C>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179687451 | |||||||
| chr1:179687465 | G | A | 28 | a0001c0001t0001g0010 a0001c0001t0001g0209 a0001c0001t0001g0262 others(25): Show |
34 | HG00408.hp2 HG01106.hp1 HG01346.hp1 others(31): Show |
intron_variant | MODIFIER | c.2861-3231G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179687465 | |||||||
| chr1:179687470 | A | G | 125 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0025 others(122): Show |
133 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.2861-3226A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179687470 | |||||||
| chr1:179687474 | A | G | 6 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(3): Show |
6 | HG02109.hp2 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.2861-3222A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179687474 | |||||||
| chr1:179687529 | A | G | 1 | a0001c0001t0001g0352 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2861-3167A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179687529 | |||||||
| chr1:179687537 | G | A | 2 | a0009c0014t0001g0364 a0009c0014t0001g0365 |
2 | HG01884.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.2861-3159G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179687537 | |||||||
| chr1:179687643 | T | A | 2 | a0009c0014t0001g0364 a0009c0014t0001g0365 |
2 | HG01884.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.2861-3053T>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179687643 | |||||||
| chr1:179687805 | C | G | 32 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(29): Show |
32 | HG00544.hp1 HG00597.hp1 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.2861-2891C>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179687805 | |||||||
| chr1:179687871 | C | CT | 175 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0104 others(172): Show |
181 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.2861-2811dupT | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 179687871 | ||||||
| chr1:179687871 | C | CTT | 7 | a0001c0001t0001g0026 a0002c0002t0002g0148 a0002c0002t0002g0164 others(4): Show |
7 | HG00738.hp1 HG01978.hp1 HG02135.hp2 others(4): Show |
intron_variant | MODIFIER | c.2861-2812_2861-281 others(6): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 179687871 | ||||||
| chr1:179687887 | C | T | 1 | a0002c0002t0002g0097 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2861-2809C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179687887 | |||||||
| chr1:179687945 | CAT | C | 118 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(115): Show |
124 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.2861-2750_2861-274 others(6): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179687945 | |||||||
| chr1:179688005 | T | C | 1 | a0001c0001t0001g0291 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2861-2691T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179688005 | |||||||
| chr1:179688163 | G | A | 2 | a0010c0016t0001g0092 a0010c0016t0001g0093 |
2 | HG02280.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2861-2533G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179688163 | |||||||
| chr1:179688181 | A | G | 30 | a0004c0004t0001g0015 a0004c0004t0001g0016 a0004c0004t0001g0017 others(27): Show |
30 | HG00280.hp2 HG00544.hp2 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.2861-2515A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179688181 | |||||||
| chr1:179688399 | TG | T | 100 | a0001c0001t0001g0026 a0001c0001t0001g0275 a0002c0002t0001g0176 others(97): Show |
106 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.2861-2296delG | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179688399 | |||||||
| chr1:179688614 | C | G | 16 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0180 others(13): Show |
16 | HG02004.hp2 HG02055.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.2861-2082C>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179688614 | |||||||
| chr1:179688687 | A | C | 1 | a0001c0001t0001g0269 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.2861-2009A>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179688687 | |||||||
| chr1:179688710 | A | G | 1 | a0004c0004t0001g0036 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.2861-1986A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179688710 | |||||||
| chr1:179688718 | A | G | 2 | a0002c0002t0002g0106 a0002c0002t0002g0107 |
2 | HG03017.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.2861-1978A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179688718 | |||||||
| chr1:179688720 | A | G | 18 | a0001c0005t0001g0002 a0001c0005t0001g0003 a0001c0005t0001g0009 others(15): Show |
24 | HG00735.hp2 HG01109.hp1 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.2861-1976A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179688720 | |||||||
| chr1:179688917 | A | G | 1 | a0001c0001t0001g0358 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2861-1779A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179688917 | |||||||
| chr1:179688986 | C | T | 6 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(3): Show |
6 | HG02109.hp2 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.2861-1710C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179688986 | |||||||
| chr1:179689039 | A | G | 126 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(123): Show |
132 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.2861-1657A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179689039 | |||||||
| chr1:179689130 | T | C | 6 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(3): Show |
6 | HG02109.hp2 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.2861-1566T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179689130 | |||||||
| chr1:179689180 | A | C | 6 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(3): Show |
6 | HG02109.hp2 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.2861-1516A>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179689180 | |||||||
| chr1:179689180 | A | G | 138 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(135): Show |
150 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.2861-1516A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179689180 | |||||||
| chr1:179689225 | G | A | 120 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(117): Show |
126 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.2861-1471G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179689225 | |||||||
| chr1:179689256 | A | G | 1 | a0001c0001t0001g0274 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2861-1440A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179689256 | |||||||
| chr1:179689371 | A | G | 6 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(3): Show |
6 | HG02109.hp2 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.2861-1325A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179689371 | |||||||
| chr1:179689433 | C | T | 8 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0007c0010t0001g0257 others(5): Show |
8 | HG01099.hp1 HG01891.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.2861-1263C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179689433 | |||||||
| chr1:179689460 | C | T | 18 | a0001c0005t0001g0002 a0001c0005t0001g0003 a0001c0005t0001g0009 others(15): Show |
24 | HG00735.hp2 HG01109.hp1 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.2861-1236C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179689460 | |||||||
| chr1:179689463 | A | G | 97 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0188 others(94): Show |
99 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.2861-1233A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179689463 | |||||||
| chr1:179689481 | G | C | 19 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0104 others(16): Show |
19 | HG02004.hp2 HG02055.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.2861-1215G>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179689481 | |||||||
| chr1:179689501 | G | A | 2 | a0002c0002t0002g0127 a0002c0002t0002g0128 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2861-1195G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179689501 | |||||||
| chr1:179689716 | T | G | 16 | a0001c0001t0001g0010 a0001c0001t0001g0209 a0001c0001t0001g0262 others(13): Show |
17 | HG00408.hp2 HG01106.hp1 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.2861-980T>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179689716 | |||||||
| chr1:179689806 | T | C | 1 | a0001c0001t0001g0342 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2861-890T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179689806 | |||||||
| chr1:179690092 | A | G | 14 | a0001c0005t0001g0002 a0001c0005t0001g0003 a0001c0005t0001g0009 others(11): Show |
19 | HG01346.hp1 HG01884.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.2861-604A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179690092 | |||||||
| chr1:179690190 | T | G | 97 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0188 others(94): Show |
99 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.2861-506T>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179690190 | |||||||
| chr1:179690305 | G | C | 118 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(115): Show |
124 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.2861-391G>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179690305 | |||||||
| chr1:179690387 | G | A | 13 | a0002c0002t0002g0008 a0002c0002t0002g0108 a0002c0002t0002g0120 others(10): Show |
14 | HG02027.hp2 HG02071.hp2 HG02080.hp2 others(11): Show |
intron_variant | MODIFIER | c.2861-309G>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179690387 | |||||||
| chr1:179690394 | C | T | 118 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(115): Show |
124 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.2861-302C>T | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179690394 | |||||||
| chr1:179690461 | T | C | 1 | a0002c0002t0002g0236 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.2861-235T>C | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179690461 | |||||||
| chr1:179690505 | A | G | 3 | a0002c0002t0002g0236 a0002c0002t0002g0237 a0002c0002t0002g0240 |
3 | HG02135.hp2 NA18967.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.2861-191A>G | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179690505 | |||||||
| chr1:179690523 | T | A | 6 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0007c0010t0001g0257 others(3): Show |
6 | HG01099.hp1 HG01891.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2861-173T>A | TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 17/17 | chr1 | 179690523 |