Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 56896 |
|---|---|
| ensemblid | ENSG00000157851.17 |
| hgncid | 20637 |
| symbol | DPYSL5 |
| name | dihydropyrimidinase like 5 |
| refseq_nuc | NM_020134.4 |
| refseq_prot | NP_064519.2 |
| ensembl_nuc | ENST00000288699.11 |
| ensembl_prot | ENSP00000288699.6 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 26848132 |
| end | 26950351 |
| strand | + |
| ver | v1.2 |
| region | chr2:26848132-26950351 |
| region5000 | chr2:26843132-26955351 |
| regionname0 | DPYSL5_chr2_26848132_26950351 |
| regionname5000 | DPYSL5_chr2_26843132_26955351 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 1695 | 132 | 55 | 33 | 31 | 6 | 6 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| c0002 | 0/1 | 1695 | 92 | 29 | 24 | 24 | 6 | 8 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| c0003 | 0/0 | 1695 | 3 | 0 | 1 | 0 | 2 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| c0004 | 0/0 | 1695 | 2 | 2 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| c0005 | 0/0 | 1695 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| c0006 | 0/0 | 1695 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| c0007 | 0/0 | 1695 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 3486 | 56 | 8 | 16 | 22 | 5 | 5 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| t0002 | 0/1 | 3483 | 51 | 11 | 14 | 16 | 4 | 5 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| t0003 | 1/0 | 3484 | 15 | 13 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| t0004 | 0/0 | 3485 | 11 | 2 | 4 | 5 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| t0005 | 0/0 | 3488 | 10 | 4 | 3 | 2 | 0 | 1 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| t0006 | 0/0 | 3481 | 9 | 2 | 2 | 2 | 2 | 1 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| t0007 | 0/0 | 3482 | 8 | 1 | 2 | 4 | 1 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| t0008 | 0/0 | 3490 | 7 | 4 | 2 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| t0009 | 0/0 | 3482 | 5 | 5 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| t0010 | 0/0 | 3484 | 4 | 2 | 2 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| t0011 | 0/0 | 3485 | 4 | 3 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| t0012 | 0/0 | 3504 | 4 | 3 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| t0013 | 0/0 | 3484 | 4 | 2 | 2 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| t0014 | 0/0 | 3478 | 4 | 4 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| t0015 | 0/0 | 3481 | 3 | 1 | 2 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| t0016 | 0/0 | 3486 | 3 | 3 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| t0017 | 0/0 | 3483 | 2 | 0 | 2 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| t0018 | 0/0 | 3483 | 2 | 0 | 0 | 0 | 0 | 2 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| t0019 | 0/0 | 3479 | 2 | 0 | 0 | 1 | 1 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| t0020 | 0/0 | 3483 | 2 | 2 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| t0021 | 0/0 | 3490 | 2 | 2 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| t0022 | 0/0 | 3486 | 2 | 2 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| t0023 | 0/0 | 3484 | 2 | 2 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| t0024 | 0/0 | 3500 | 2 | 1 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| t0025 | 0/0 | 3484 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| t0026 | 0/0 | 3483 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| t0027 | 0/0 | 3487 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| t0028 | 0/0 | 3481 | 1 | 0 | 0 | 0 | 1 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| t0029 | 0/0 | 3497 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| t0030 | 0/0 | 3487 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| t0031 | 0/0 | 3483 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| t0032 | 0/0 | 3488 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| t0033 | 0/0 | 3504 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| t0034 | 0/0 | 3504 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| t0035 | 0/0 | 3486 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| t0036 | 0/0 | 3484 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| t0037 | 0/0 | 3500 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| t0038 | 0/0 | 3480 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| t0039 | 0/0 | 3478 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| t0040 | 0/0 | 3478 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| t0041 | 0/0 | 3478 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| t0042 | 0/0 | 3486 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0119 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0125 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1695 | 132 | 55 | 33 | 31 | 6 | 6 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| a0001c0002 | 0/1 | 1695 | 92 | 29 | 24 | 24 | 6 | 8 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| a0001c0004 | 0/0 | 1695 | 2 | 2 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| a0001c0005 | 0/0 | 1695 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| a0001c0006 | 0/0 | 1695 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| a0001c0007 | 0/0 | 1695 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| a0002c0003 | 0/0 | 1695 | 3 | 0 | 1 | 0 | 2 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5180 | 56 | 8 | 16 | 22 | 5 | 5 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| a0001c0001t0003 | 1/0 | 5178 | 12 | 10 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| a0001c0001t0005 | 0/0 | 5182 | 10 | 4 | 3 | 2 | 0 | 1 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| a0001c0001t0007 | 0/0 | 5176 | 8 | 1 | 2 | 4 | 1 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| a0001c0001t0008 | 0/0 | 5184 | 7 | 4 | 2 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| a0001c0001t0009 | 0/0 | 5176 | 5 | 5 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| a0001c0001t0010 | 0/0 | 5178 | 4 | 2 | 2 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| a0001c0001t0012 | 0/0 | 5198 | 4 | 3 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| a0001c0001t0013 | 0/0 | 5178 | 4 | 2 | 2 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| a0001c0001t0015 | 0/0 | 5175 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| a0001c0001t0016 | 0/0 | 5180 | 3 | 3 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| a0001c0001t0021 | 0/0 | 5184 | 2 | 2 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| a0001c0001t0022 | 0/0 | 5180 | 2 | 2 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| a0001c0001t0023 | 0/0 | 5178 | 2 | 2 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| a0001c0001t0024 | 0/0 | 5194 | 2 | 1 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| a0001c0001t0025 | 0/0 | 5178 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| a0001c0001t0032 | 0/0 | 5182 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| a0001c0001t0033 | 0/0 | 5198 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| a0001c0001t0034 | 0/0 | 5198 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| a0001c0001t0035 | 0/0 | 5180 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| a0001c0001t0036 | 0/0 | 5178 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| a0001c0001t0037 | 0/0 | 5194 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| a0001c0001t0038 | 0/0 | 5174 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| a0001c0001t0041 | 0/0 | 5172 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| a0001c0001t0042 | 0/0 | 5180 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| a0001c0002t0002 | 0/1 | 5177 | 51 | 11 | 14 | 16 | 4 | 5 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| a0001c0002t0004 | 0/0 | 5179 | 10 | 2 | 4 | 4 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| a0001c0002t0006 | 0/0 | 5175 | 6 | 2 | 1 | 2 | 0 | 1 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| a0001c0002t0011 | 0/0 | 5179 | 4 | 3 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| a0001c0002t0014 | 0/0 | 5172 | 4 | 4 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| a0001c0002t0015 | 0/0 | 5175 | 2 | 1 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| a0001c0002t0017 | 0/0 | 5177 | 2 | 0 | 2 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| a0001c0002t0018 | 0/0 | 5177 | 2 | 0 | 0 | 0 | 0 | 2 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| a0001c0002t0019 | 0/0 | 5173 | 2 | 0 | 0 | 1 | 1 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| a0001c0002t0020 | 0/0 | 5177 | 2 | 2 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| a0001c0002t0026 | 0/0 | 5177 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| a0001c0002t0027 | 0/0 | 5181 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| a0001c0002t0028 | 0/0 | 5175 | 1 | 0 | 0 | 0 | 1 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| a0001c0002t0029 | 0/0 | 5191 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| a0001c0002t0030 | 0/0 | 5181 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| a0001c0002t0031 | 0/0 | 5177 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| a0001c0002t0039 | 0/0 | 5172 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| a0001c0004t0003 | 0/0 | 5178 | 2 | 2 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| a0001c0005t0003 | 0/0 | 5178 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| a0001c0006t0004 | 0/0 | 5179 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| a0001c0007t0040 | 0/0 | 5172 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| a0002c0003t0006 | 0/0 | 5175 | 3 | 0 | 1 | 0 | 2 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | copy fasta | chr2 | 26843132 | 26955351 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0003g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0003g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0003g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0003g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0003g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0003g0125 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0003g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0005g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0005g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0005g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0005g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0005g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0005g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0005g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0005g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0005g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0005g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0007g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0007g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0007g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0007g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0007g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0007g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0007g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0007g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0008g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0008g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0008g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0008g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0008g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0008g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0008g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0009g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0009g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0009g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0009g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0009g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0010g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0010g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0010g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0010g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0012g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0012g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0012g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0012g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0013g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0013g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0013g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0013g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0015g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0016g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0016g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0016g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0021g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0021g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0022g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0022g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0023g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0023g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0024g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0024g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0025g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0032g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0033g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0034g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0035g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0036g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0037g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0038g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0041g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0001t0042g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0002g0119 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0004g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0004g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0004g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0004g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0004g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0004g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0004g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0004g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0004g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0004g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0006g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0006g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0006g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0006g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0006g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0006g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0011g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0011g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0011g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0011g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0014g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0014g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0014g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0014g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0015g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0015g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0017g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0017g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0018g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0018g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0019g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0019g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0020g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0020g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0026g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0027g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0028g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0029g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0030g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0031g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0002t0039g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0004t0003g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0004t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0005t0003g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0006t0004g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0001c0007t0040g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0002c0003t0006g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0002c0003t0006g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| a0002c0003t0006g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0193 | EUR | GBR | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG00099 | hp2 | a0001 | c0002 | t0002 | g0097 | EUR | GBR | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0177 | EUR | GBR | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG00140 | hp2 | a0002 | c0003 | t0006 | g0093 | EUR | GBR | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG00280 | hp1 | a0001 | c0001 | t0007 | g0172 | EUR | FIN | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG00280 | hp2 | a0001 | c0002 | t0002 | g0147 | EUR | FIN | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG00438 | hp1 | a0001 | c0006 | t0004 | g0161 | EAS | CHS | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG00438 | hp2 | a0001 | c0001 | t0007 | g0114 | EAS | CHS | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG00558 | hp1 | a0001 | c0001 | t0005 | g0203 | EAS | CHS | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG00558 | hp2 | a0001 | c0002 | t0002 | g0154 | EAS | CHS | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG00597 | hp1 | a0001 | c0001 | t0042 | g0216 | EAS | CHS | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG00597 | hp2 | a0001 | c0001 | t0007 | g0113 | EAS | CHS | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG00639 | hp1 | a0001 | c0001 | t0012 | g0051 | AMR | PUR | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG00642 | hp1 | a0001 | c0002 | t0002 | g0133 | AMR | PUR | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG00673 | hp1 | a0001 | c0002 | t0002 | g0121 | EAS | CHS | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG00673 | hp2 | a0001 | c0002 | t0002 | g0098 | EAS | CHS | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG00733 | hp1 | a0001 | c0002 | t0002 | g0096 | AMR | PUR | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG00733 | hp2 | a0001 | c0001 | t0013 | g0075 | AMR | PUR | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG00735 | hp1 | a0001 | c0001 | t0005 | g0178 | AMR | PUR | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG00735 | hp2 | a0001 | c0002 | t0002 | g0146 | AMR | PUR | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG00738 | hp1 | a0001 | c0002 | t0011 | g0062 | AMR | PUR | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG01069 | hp1 | a0001 | c0002 | t0002 | g0091 | AMR | PUR | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG01074 | hp1 | a0001 | c0002 | t0015 | g0043 | AMR | PUR | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG01081 | hp1 | a0001 | c0002 | t0002 | g0220 | AMR | PUR | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG01081 | hp2 | a0001 | c0002 | t0002 | g0103 | AMR | PUR | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG01106 | hp1 | a0001 | c0001 | t0041 | g0111 | AMR | PUR | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG01106 | hp2 | a0001 | c0001 | t0010 | g0033 | AMR | PUR | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG01109 | hp1 | a0001 | c0002 | t0004 | g0143 | AMR | PUR | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG01109 | hp2 | a0001 | c0001 | t0008 | g0067 | AMR | PUR | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG01167 | hp1 | a0001 | c0001 | t0024 | g0036 | AMR | PUR | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG01167 | hp2 | a0001 | c0001 | t0013 | g0074 | AMR | PUR | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG01168 | hp2 | a0001 | c0002 | t0002 | g0082 | AMR | PUR | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG01243 | hp1 | a0001 | c0001 | t0008 | g0218 | AMR | PUR | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0020 | AMR | PUR | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG01255 | hp1 | a0001 | c0002 | t0002 | g0117 | AMR | CLM | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | CLM | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG01256 | hp1 | a0001 | c0002 | t0004 | g0142 | AMR | CLM | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG01256 | hp2 | a0001 | c0002 | t0017 | g0159 | AMR | CLM | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG01257 | hp1 | a0001 | c0002 | t0017 | g0215 | AMR | CLM | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG01257 | hp2 | a0001 | c0002 | t0002 | g0136 | AMR | CLM | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | CLM | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG01261 | hp2 | a0001 | c0002 | t0004 | g0176 | AMR | CLM | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG01346 | hp1 | a0001 | c0001 | t0010 | g0031 | AMR | CLM | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG01346 | hp2 | a0001 | c0002 | t0002 | g0120 | AMR | CLM | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | CLM | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG01361 | hp1 | a0001 | c0002 | t0029 | g0137 | AMR | CLM | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | CLM | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG01433 | hp1 | a0001 | c0002 | t0006 | g0084 | AMR | CLM | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG01433 | hp2 | a0001 | c0001 | t0015 | g0183 | AMR | CLM | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG01496 | hp1 | a0002 | c0003 | t0006 | g0092 | AMR | CLM | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG01496 | hp2 | a0001 | c0001 | t0005 | g0170 | AMR | CLM | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0196 | EUR | IBS | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG01515 | hp2 | a0002 | c0003 | t0006 | g0079 | EUR | IBS | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG01516 | hp1 | a0001 | c0002 | t0028 | g0046 | EUR | IBS | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG01516 | hp2 | a0001 | c0002 | t0002 | g0090 | EUR | IBS | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0195 | EUR | IBS | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG01517 | hp2 | a0001 | c0002 | t0002 | g0045 | EUR | IBS | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG01884 | hp1 | a0001 | c0001 | t0023 | g0022 | AFR | ACB | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | ACB | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0012 | AFR | ACB | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0167 | AFR | ACB | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG01928 | hp1 | a0001 | c0002 | t0002 | g0221 | AMR | PEL | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG01928 | hp2 | a0001 | c0001 | t0007 | g0110 | AMR | PEL | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PEL | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG01952 | hp1 | a0001 | c0002 | t0002 | g0127 | AMR | PEL | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG01952 | hp2 | a0001 | c0001 | t0005 | g0207 | AMR | PEL | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG01981 | hp1 | a0001 | c0002 | t0004 | g0095 | AMR | PEL | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG01981 | hp2 | a0001 | c0001 | t0036 | g0102 | AMR | PEL | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PEL | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG02004 | hp2 | a0001 | c0002 | t0002 | g0145 | AMR | PEL | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | KHV | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG02040 | hp1 | a0001 | c0002 | t0002 | g0132 | EAS | KHV | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | KHV | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | KHV | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG02083 | hp2 | a0001 | c0002 | t0019 | g0122 | EAS | KHV | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG02145 | hp1 | a0001 | c0001 | t0022 | g0210 | AFR | ACB | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG02145 | hp2 | a0001 | c0002 | t0002 | g0085 | AFR | ACB | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PEL | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG02148 | hp2 | a0001 | c0001 | t0007 | g0109 | AMR | PEL | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG02155 | hp1 | a0001 | c0002 | t0002 | g0123 | EAS | CDX | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | CDX | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG02257 | hp1 | a0001 | c0002 | t0014 | g0050 | AFR | ACB | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG02257 | hp2 | a0001 | c0001 | t0012 | g0030 | AFR | ACB | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG02258 | hp1 | a0001 | c0001 | t0022 | g0188 | AFR | ACB | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG02258 | hp2 | a0001 | c0001 | t0009 | g0070 | AFR | ACB | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG02280 | hp2 | a0001 | c0001 | t0005 | g0017 | AFR | ACB | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG02300 | hp1 | a0001 | c0002 | t0002 | g0217 | AMR | PEL | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PEL | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG02451 | hp2 | a0001 | c0001 | t0009 | g0001 | AFR | ACB | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG02572 | hp2 | a0001 | c0001 | t0012 | g0055 | AFR | GWD | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG02615 | hp1 | a0001 | c0001 | t0009 | g0039 | AFR | GWD | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG02615 | hp2 | a0001 | c0001 | t0012 | g0048 | AFR | GWD | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG02622 | hp1 | a0001 | c0001 | t0005 | g0018 | AFR | GWD | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG02630 | hp1 | a0001 | c0002 | t0004 | g0229 | AFR | GWD | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG02630 | hp2 | a0001 | c0001 | t0033 | g0052 | AFR | GWD | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG02647 | hp1 | a0001 | c0002 | t0002 | g0089 | AFR | GWD | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG02647 | hp2 | a0001 | c0001 | t0016 | g0029 | AFR | GWD | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG02717 | hp1 | a0001 | c0001 | t0005 | g0081 | AFR | GWD | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG02717 | hp2 | a0001 | c0001 | t0016 | g0227 | AFR | GWD | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG02738 | hp1 | a0001 | c0002 | t0018 | g0150 | SAS | PJL | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0201 | SAS | PJL | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG02809 | hp1 | a0001 | c0001 | t0010 | g0028 | AFR | GWD | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG02809 | hp2 | a0001 | c0001 | t0024 | g0049 | AFR | GWD | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG02818 | hp1 | a0001 | c0002 | t0004 | g0230 | AFR | GWD | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG02818 | hp2 | a0001 | c0001 | t0008 | g0164 | AFR | GWD | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | GWD | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG02886 | hp2 | a0001 | c0001 | t0013 | g0065 | AFR | GWD | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0168 | AFR | GWD | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG02895 | hp2 | a0001 | c0002 | t0002 | g0041 | AFR | GWD | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0171 | AFR | GWD | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG02897 | hp2 | a0001 | c0002 | t0030 | g0056 | AFR | GWD | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG02922 | hp1 | a0001 | c0004 | t0003 | g0064 | AFR | ESN | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG02922 | hp2 | a0001 | c0002 | t0011 | g0063 | AFR | ESN | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG02965 | hp1 | a0001 | c0001 | t0038 | g0008 | AFR | ESN | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0088 | AFR | ESN | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG02970 | hp1 | a0001 | c0002 | t0011 | g0061 | AFR | ESN | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG02970 | hp2 | a0001 | c0007 | t0040 | g0169 | AFR | ESN | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG02976 | hp1 | a0001 | c0001 | t0013 | g0047 | AFR | ESN | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0068 | AFR | ESN | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG03017 | hp2 | a0001 | c0002 | t0002 | g0140 | SAS | PJL | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG03041 | hp1 | a0001 | c0002 | t0014 | g0038 | AFR | GWD | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0072 | AFR | GWD | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | MSL | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG03098 | hp2 | a0001 | c0001 | t0034 | g0054 | AFR | MSL | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG03130 | hp1 | a0001 | c0001 | t0009 | g0066 | AFR | ESN | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG03130 | hp2 | a0001 | c0002 | t0002 | g0076 | AFR | ESN | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG03139 | hp1 | a0001 | c0002 | t0002 | g0087 | AFR | ESN | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG03139 | hp2 | a0001 | c0001 | t0023 | g0021 | AFR | ESN | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG03209 | hp1 | a0001 | c0005 | t0003 | g0015 | AFR | MSL | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | MSL | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG03225 | hp1 | a0001 | c0001 | t0008 | g0004 | AFR | MSL | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG03225 | hp2 | a0001 | c0001 | t0025 | g0032 | AFR | MSL | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG03453 | hp1 | a0001 | c0001 | t0007 | g0005 | AFR | MSL | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG03453 | hp2 | a0001 | c0002 | t0002 | g0086 | AFR | MSL | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG03486 | hp1 | a0001 | c0002 | t0015 | g0042 | AFR | MSL | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG03486 | hp2 | a0001 | c0002 | t0002 | g0078 | AFR | MSL | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG03492 | hp1 | a0001 | c0002 | t0002 | g0198 | SAS | PJL | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG03492 | hp2 | a0001 | c0002 | t0002 | g0135 | SAS | PJL | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG03540 | hp1 | a0001 | c0001 | t0008 | g0023 | AFR | GWD | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG03540 | hp2 | a0001 | c0001 | t0021 | g0006 | AFR | GWD | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG03669 | hp1 | a0001 | c0002 | t0002 | g0134 | SAS | PJL | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG03669 | hp2 | a0001 | c0001 | t0005 | g0206 | SAS | PJL | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | BEB | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG03831 | hp2 | a0001 | c0002 | t0018 | g0175 | SAS | BEB | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0181 | SAS | BEB | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG03834 | hp2 | a0001 | c0002 | t0002 | g0162 | SAS | BEB | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | STU | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG04204 | hp2 | a0001 | c0002 | t0006 | g0126 | SAS | STU | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| NA18522 | hp1 | a0001 | c0002 | t0027 | g0083 | AFR | YRI | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | YRI | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| NA18906 | hp1 | a0001 | c0002 | t0002 | g0163 | AFR | YRI | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| NA18906 | hp2 | a0001 | c0001 | t0009 | g0002 | AFR | YRI | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| NA18939 | hp1 | a0001 | c0002 | t0002 | g0152 | EAS | JPT | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| NA18939 | hp2 | a0001 | c0001 | t0005 | g0179 | EAS | JPT | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| NA18952 | hp2 | a0001 | c0002 | t0002 | g0148 | EAS | JPT | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| NA18954 | hp1 | a0001 | c0002 | t0004 | g0099 | EAS | JPT | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| NA18954 | hp2 | a0001 | c0002 | t0002 | g0128 | EAS | JPT | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| NA18959 | hp1 | a0001 | c0002 | t0002 | g0155 | EAS | JPT | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| NA18961 | hp1 | a0001 | c0002 | t0026 | g0144 | EAS | JPT | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| NA18973 | hp1 | a0001 | c0002 | t0002 | g0153 | EAS | JPT | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| NA18975 | hp1 | a0001 | c0002 | t0002 | g0212 | EAS | JPT | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| NA18979 | hp1 | a0001 | c0001 | t0008 | g0202 | EAS | JPT | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| NA18979 | hp2 | a0001 | c0002 | t0002 | g0129 | EAS | JPT | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| NA18982 | hp1 | a0001 | c0001 | t0007 | g0185 | EAS | JPT | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| NA18994 | hp1 | a0001 | c0002 | t0004 | g0158 | EAS | JPT | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| NA19002 | hp1 | a0001 | c0002 | t0004 | g0118 | EAS | JPT | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| NA19004 | hp1 | a0001 | c0002 | t0006 | g0130 | EAS | JPT | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| NA19004 | hp2 | a0001 | c0002 | t0006 | g0191 | EAS | JPT | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| NA19005 | hp1 | a0001 | c0002 | t0002 | g0151 | EAS | JPT | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| NA19010 | hp2 | a0001 | c0002 | t0002 | g0131 | EAS | JPT | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| NA19030 | hp1 | a0001 | c0002 | t0031 | g0073 | AFR | LWK | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| NA19030 | hp2 | a0001 | c0002 | t0006 | g0069 | AFR | LWK | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| NA19043 | hp1 | a0001 | c0002 | t0002 | g0094 | AFR | LWK | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| NA19043 | hp2 | a0001 | c0002 | t0020 | g0057 | AFR | LWK | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| NA19065 | hp2 | a0001 | c0001 | t0007 | g0116 | EAS | JPT | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| NA19080 | hp1 | a0001 | c0002 | t0004 | g0141 | EAS | JPT | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| NA19082 | hp1 | a0001 | c0002 | t0002 | g0101 | EAS | JPT | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| NA19084 | hp1 | a0001 | c0001 | t0035 | g0105 | EAS | JPT | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| NA19240 | hp1 | a0001 | c0002 | t0014 | g0034 | AFR | YRI | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| NA19240 | hp2 | a0001 | c0002 | t0039 | g0019 | AFR | YRI | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| NA20129 | hp1 | a0001 | c0001 | t0010 | g0226 | AFR | ASW | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0166 | AFR | ASW | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0199 | EUR | TSI | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| NA20752 | hp2 | a0001 | c0002 | t0019 | g0160 | EUR | TSI | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG02109 | hp1 | a0001 | c0004 | t0003 | g0011 | AFR | ACB | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG02109 | hp2 | a0001 | c0002 | t0002 | g0040 | AFR | ACB | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG02486 | hp1 | a0001 | c0002 | t0014 | g0037 | AFR | ACB | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG02486 | hp2 | a0001 | c0001 | t0037 | g0053 | AFR | ACB | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG02559 | hp1 | a0001 | c0002 | t0006 | g0080 | AFR | ACB | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0013 | AFR | ACB | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG03471 | hp1 | a0001 | c0001 | t0005 | g0016 | AFR | MSL | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG03471 | hp2 | a0001 | c0002 | t0011 | g0060 | AFR | MSL | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG06807 | hp1 | a0001 | c0001 | t0008 | g0025 | AFR | USA | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| HG06807 | hp2 | a0001 | c0002 | t0002 | g0035 | AFR | USA | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| NA18955 | hp1 | a0001 | c0002 | t0002 | g0044 | EAS | JPT | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| NA20300 | hp1 | a0001 | c0001 | t0032 | g0077 | AFR | USA | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| NA20300 | hp2 | a0001 | c0001 | t0021 | g0007 | AFR | USA | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| NA21309 | hp1 | a0001 | c0002 | t0020 | g0058 | AFR | LWK | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| NA21309 | hp2 | a0001 | c0001 | t0016 | g0228 | AFR | LWK | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0002 | g0119 | REF | REF | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0125 | REF | REF | DPYSL5_chr2_26843132_26955351 | DPYSL5 | chr2 | 26843132 | 26955351 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:26944749
|
G | A | 1 | a0002 | 3 | HG00140.hp2 HG01496.hp1 HG01515.hp2 |
missense_variant | MODERATE | c.1534G>A | p.Ala512Thr | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 12/13 | 1661/5178 | 1534/1695 | 512/564 | chr2 | 26944749 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:26927300
|
G | T | 1 | a0001c0007 | 1 | HG02970.hp2 | synonymous_variant | LOW | c.468G>T | p.Ser156Ser | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 4/13 | 595/5178 | 468/1695 | 156/564 | chr2 | 26927300 | ||
| chr2:26928290
|
C | T | 1 | a0001c0004 | 2 | HG02109.hp1 HG02922.hp1 |
synonymous_variant | LOW | c.636C>T | p.Gly212Gly | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/13 | 763/5178 | 636/1695 | 212/564 | chr2 | 26928290 | ||
| chr2:26942552
|
A | G | 1 | a0001c0006 | 1 | HG00438.hp1 | synonymous_variant | LOW | c.1242A>G | p.Ser414Ser | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 11/13 | 1369/5178 | 1242/1695 | 414/564 | chr2 | 26942552 | ||
| chr2:26946974
|
C | A | 4 | a0001c0002a0001c0006a0001c0007others(1): Show | 97 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(94): Show |
synonymous_variant | LOW | c.1674C>A | p.Gly558Gly | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 13/13 | 1801/5178 | 1674/1695 | 558/564 | chr2 | 26946974 | ||
| chr2:26946977
|
G | A | 1 | a0001c0005 | 1 | HG03209.hp1 | synonymous_variant | LOW | c.1677G>A | p.Arg559Arg | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 13/13 | 1804/5178 | 1677/1695 | 559/564 | chr2 | 26946977 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:26947225
|
C | A | 1 | a0001c0002t0017 | 2 | HG01256.hp2 HG01257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*230C>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 13/13 | 230 | chr2 | 26947225 | |||||
| chr2:26947425
|
C | A | 2 | a0001c0001t0010a0001c0001t0025 | 5 | HG01106.hp2 HG01346.hp1 HG02809.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*430C>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 13/13 | 430 | chr2 | 26947425 | |||||
| chr2:26947484
|
A | G | 1 | a0001c0001t0042 | 1 | HG00597.hp1 | 3_prime_UTR_variant | MODIFIER | c.*489A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 13/13 | 489 | chr2 | 26947484 | |||||
| chr2:26947505
|
C | A | 1 | a0001c0002t0026 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*510C>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 13/13 | 510 | chr2 | 26947505 | |||||
| chr2:26947602
|
C | CG | 18 | a0001c0001t0015a0001c0002t0002a0001c0002t0004others(15): Show | 92 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*613dupG | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 13/13 | 614 | INFO_REALIGN_3_PRIME | chr2 | 26947602 | ||||
| chr2:26947950
|
C | T | 4 | a0001c0002t0011a0001c0002t0020a0001c0002t0030others(1): Show | 8 | HG00738.hp1 HG02897.hp2 HG02922.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*955C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 13/13 | 955 | chr2 | 26947950 | |||||
| chr2:26948073
|
C | CCA | 7 | a0001c0001t0001a0001c0001t0016a0001c0001t0022others(4): Show | 65 | HG00099.hp1 HG00140.hp1 HG00597.hp1 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*1114_*1115dupAC | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 13/13 | 1116 | INFO_REALIGN_3_PRIME | chr2 | 26948073 | ||||
| chr2:26948073
|
C | CCACA | 2 | a0001c0001t0005a0001c0001t0032 | 11 | HG00558.hp1 HG00735.hp1 HG01496.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1112_*1115dupACAC | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 13/13 | 1116 | INFO_REALIGN_3_PRIME | chr2 | 26948073 | ||||
| chr2:26948073
|
C | CCACACA | 2 | a0001c0001t0008a0001c0001t0021 | 9 | HG01109.hp2 HG01243.hp1 HG02818.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1110_*1115dupACAC others(2): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 13/13 | 1116 | INFO_REALIGN_3_PRIME | chr2 | 26948073 | ||||
| chr2:26948073
|
CCA | C | 8 | a0001c0001t0007a0001c0001t0009a0001c0002t0002others(5): Show | 72 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*1114_*1115delAC | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 13/13 | 1114 | INFO_REALIGN_3_PRIME | chr2 | 26948073 | ||||
| chr2:26948073
|
CCACA | C | 7 | a0001c0001t0015a0001c0001t0038a0001c0002t0006others(4): Show | 15 | HG00140.hp2 HG01074.hp1 HG01361.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1112_*1115delACAC | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 13/13 | 1112 | INFO_REALIGN_3_PRIME | chr2 | 26948073 | ||||
| chr2:26948073
|
CCACACA | C | 5 | a0001c0001t0041a0001c0002t0014a0001c0002t0019others(2): Show | 9 | HG01106.hp1 HG02083.hp2 HG02257.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1110_*1115delACAC others(2): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 13/13 | 1110 | INFO_REALIGN_3_PRIME | chr2 | 26948073 | ||||
| chr2:26948093
|
A | ACACACAC others(13): Show |
3 | a0001c0001t0012a0001c0001t0033a0001c0001t0034 | 6 | HG00639.hp1 HG02257.hp2 HG02572.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1115_*1116insACGC others(16): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 13/13 | 1116 | INFO_REALIGN_3_PRIME | chr2 | 26948093 | ||||
| chr2:26948093
|
A | ACACACAC others(9): Show |
2 | a0001c0001t0024a0001c0001t0037 | 3 | HG01167.hp1 HG02486.hp2 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1113_*1114insGCAC others(12): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 13/13 | 1114 | INFO_REALIGN_3_PRIME | chr2 | 26948093 | ||||
| chr2:26948114
|
C | T | 12 | a0001c0001t0021a0001c0002t0002a0001c0002t0004others(9): Show | 82 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*1119C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 13/13 | 1119 | chr2 | 26948114 | |||||
| chr2:26948370
|
C | T | 1 | a0001c0002t0029 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1375C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 13/13 | 1375 | chr2 | 26948370 | |||||
| chr2:26948375
|
T | A | 1 | a0001c0002t0029 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1380T>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 13/13 | 1380 | chr2 | 26948375 | |||||
| chr2:26948376
|
T | A | 1 | a0001c0002t0029 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1381T>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 13/13 | 1381 | chr2 | 26948376 | |||||
| chr2:26948377
|
C | T | 12 | a0001c0001t0001a0001c0001t0005a0001c0001t0007others(9): Show | 93 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*1382C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 13/13 | 1382 | chr2 | 26948377 | |||||
| chr2:26948378
|
T | A | 1 | a0001c0002t0029 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1383T>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 13/13 | 1383 | chr2 | 26948378 | |||||
| chr2:26948380
|
A | C | 1 | a0001c0002t0029 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1385A>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 13/13 | 1385 | chr2 | 26948380 | |||||
| chr2:26948382
|
G | A | 1 | a0001c0002t0029 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1387G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 13/13 | 1387 | chr2 | 26948382 | |||||
| chr2:26948384
|
C | A | 1 | a0001c0002t0029 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1389C>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 13/13 | 1389 | chr2 | 26948384 | |||||
| chr2:26948385
|
C | A | 1 | a0001c0002t0029 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1390C>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 13/13 | 1390 | chr2 | 26948385 | |||||
| chr2:26948387
|
A | G | 1 | a0001c0002t0029 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1392A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 13/13 | 1392 | chr2 | 26948387 | |||||
| chr2:26948388
|
C | G | 1 | a0001c0002t0029 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1393C>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 13/13 | 1393 | chr2 | 26948388 | |||||
| chr2:26948391
|
A | G | 1 | a0001c0002t0029 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1396A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 13/13 | 1396 | chr2 | 26948391 | |||||
| chr2:26948399
|
A | G | 1 | a0001c0002t0029 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1404A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 13/13 | 1404 | chr2 | 26948399 | |||||
| chr2:26948400
|
T | A | 1 | a0001c0002t0029 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1405T>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 13/13 | 1405 | chr2 | 26948400 | |||||
| chr2:26948406
|
C | A | 1 | a0001c0002t0029 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1411C>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 13/13 | 1411 | chr2 | 26948406 | |||||
| chr2:26948407
|
A | G | 1 | a0001c0002t0029 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1412A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 13/13 | 1412 | chr2 | 26948407 | |||||
| chr2:26948408
|
C | A | 1 | a0001c0002t0029 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1413C>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 13/13 | 1413 | chr2 | 26948408 | |||||
| chr2:26948409
|
T | G | 1 | a0001c0002t0029 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1414T>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 13/13 | 1414 | chr2 | 26948409 | |||||
| chr2:26948414
|
G | A | 1 | a0001c0002t0029 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1419G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 13/13 | 1419 | chr2 | 26948414 | |||||
| chr2:26948415
|
C | T | 1 | a0001c0002t0029 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1420C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 13/13 | 1420 | chr2 | 26948415 | |||||
| chr2:26948421
|
G | C | 1 | a0001c0002t0029 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1426G>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 13/13 | 1426 | chr2 | 26948421 | |||||
| chr2:26948426
|
C | A | 1 | a0001c0002t0029 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1431C>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 13/13 | 1431 | chr2 | 26948426 | |||||
| chr2:26948427
|
T | A | 1 | a0001c0002t0029 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1432T>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 13/13 | 1432 | chr2 | 26948427 | |||||
| chr2:26948428
|
T | A | 1 | a0001c0002t0029 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1433T>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 13/13 | 1433 | chr2 | 26948428 | |||||
| chr2:26948430
|
C | A | 1 | a0001c0002t0029 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1435C>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 13/13 | 1435 | chr2 | 26948430 | |||||
| chr2:26948432
|
C | T | 1 | a0001c0001t0022 | 2 | HG02145.hp1 HG02258.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1437C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 13/13 | 1437 | chr2 | 26948432 | |||||
| chr2:26948433
|
C | A | 1 | a0001c0002t0029 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1438C>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 13/13 | 1438 | chr2 | 26948433 | |||||
| chr2:26948434
|
T | A | 1 | a0001c0002t0029 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1439T>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 13/13 | 1439 | chr2 | 26948434 | |||||
| chr2:26948436
|
C | A | 1 | a0001c0002t0029 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1441C>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 13/13 | 1441 | chr2 | 26948436 | |||||
| chr2:26948438
|
G | C | 1 | a0001c0002t0029 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1443G>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 13/13 | 1443 | chr2 | 26948438 | |||||
| chr2:26948439
|
T | G | 1 | a0001c0002t0029 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1444T>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 13/13 | 1444 | chr2 | 26948439 | |||||
| chr2:26948442
|
T | G | 1 | a0001c0002t0029 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1447T>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 13/13 | 1447 | chr2 | 26948442 | |||||
| chr2:26948443
|
C | G | 1 | a0001c0002t0029 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1448C>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 13/13 | 1448 | chr2 | 26948443 | |||||
| chr2:26948444
|
T | A | 1 | a0001c0002t0029 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1449T>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 13/13 | 1449 | chr2 | 26948444 | |||||
| chr2:26948446
|
G | GAGGAAAA others(9): Show |
1 | a0001c0002t0029 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1451_*1452insAGGA others(12): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 13/13 | 1452 | chr2 | 26948446 | |||||
| chr2:26948449
|
A | C | 3 | a0001c0002t0014a0001c0002t0039a0001c0007t0040 | 6 | HG02257.hp1 HG02486.hp1 HG02970.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1454A>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 13/13 | 1454 | chr2 | 26948449 | |||||
| chr2:26948714
|
A | G | 1 | a0001c0001t0013 | 4 | HG00733.hp2 HG01167.hp2 HG02886.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1719A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 13/13 | 1719 | chr2 | 26948714 | |||||
| chr2:26948724
|
G | A | 1 | a0001c0001t0035 | 1 | NA19084.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1729G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 13/13 | 1729 | chr2 | 26948724 | |||||
| chr2:26948806
|
A | G | 1 | a0001c0007t0040 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1811A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 13/13 | 1811 | chr2 | 26948806 | |||||
| chr2:26948814
|
G | A | 1 | a0001c0001t0016 | 3 | HG02647.hp2 HG02717.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1819G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 13/13 | 1819 | chr2 | 26948814 | |||||
| chr2:26949166
|
C | T | 3 | a0001c0001t0012a0001c0001t0024a0001c0001t0034 | 7 | HG00639.hp1 HG01167.hp1 HG02257.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2171C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 13/13 | 2171 | chr2 | 26949166 | |||||
| chr2:26949178
|
T | G | 1 | a0001c0001t0025 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2183T>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 13/13 | 2183 | chr2 | 26949178 | |||||
| chr2:26949201
|
T | C | 12 | a0001c0001t0001a0001c0001t0005a0001c0001t0007others(9): Show | 93 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*2206T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 13/13 | 2206 | chr2 | 26949201 | |||||
| chr2:26949363
|
C | T | 1 | a0001c0002t0018 | 2 | HG02738.hp1 HG03831.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2368C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 13/13 | 2368 | chr2 | 26949363 | |||||
| chr2:26949364
|
G | A | 1 | a0001c0002t0031 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2369G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 13/13 | 2369 | chr2 | 26949364 | |||||
| chr2:26949778
|
C | T | 1 | a0001c0002t0039 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2783C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 13/13 | 2783 | chr2 | 26949778 | |||||
| chr2:26949795
|
C | G | 1 | a0001c0001t0034 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2800C>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 13/13 | 2800 | chr2 | 26949795 | |||||
| chr2:26950015
|
C | T | 2 | a0001c0001t0023a0001c0001t0038 | 3 | HG01884.hp1 HG02965.hp1 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3020C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 13/13 | 3020 | chr2 | 26950015 | |||||
| chr2:26950271
|
G | A | 1 | a0001c0002t0028 | 1 | HG01516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3276G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 13/13 | 3276 | chr2 | 26950271 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:26848412
|
T | C | 43 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(40): Show | 43 | HG01074.hp1 HG01106.hp2 HG01167.hp1 others(40): Show |
intron_variant | MODIFIER | c.-5+158T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26848412 | ||||||
| chr2:26848690
|
C | T | 1 | a0001c0001t0001g0232 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-5+436C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26848690 | ||||||
| chr2:26849285
|
CGAG | C | 3 | a0001c0002t0002g0044a0001c0002t0002g0045a0001c0002t0028g0046 | 3 | HG01516.hp1 HG01517.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.-5+1035_-5+1037del others(3): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26849285 | |||||
| chr2:26849341
|
C | T | 60 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0177others(57): Show | 60 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(57): Show |
intron_variant | MODIFIER | c.-5+1087C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26849341 | ||||||
| chr2:26849439
|
G | T | 2 | a0001c0002t0015g0042a0001c0002t0015g0043 | 2 | HG01074.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-5+1185G>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26849439 | ||||||
| chr2:26849451
|
G | C | 1 | a0001c0001t0013g0047 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-5+1197G>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26849451 | ||||||
| chr2:26849691
|
T | C | 43 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(40): Show | 43 | HG01074.hp1 HG01106.hp2 HG01167.hp1 others(40): Show |
intron_variant | MODIFIER | c.-5+1437T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26849691 | ||||||
| chr2:26849895
|
G | A | 3 | a0001c0001t0003g0003a0001c0001t0009g0001a0001c0001t0009g0002 | 3 | HG02451.hp2 HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-5+1641G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26849895 | ||||||
| chr2:26849919
|
T | A | 1 | a0001c0001t0007g0172 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-5+1665T>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26849919 | ||||||
| chr2:26850323
|
C | A | 1 | a0001c0001t0001g0173 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-5+2069C>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26850323 | ||||||
| chr2:26850578
|
TG | T | 35 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(32): Show | 35 | HG01074.hp1 HG01106.hp2 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.-5+2327delG | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26850578 | |||||
| chr2:26850671
|
A | G | 6 | a0001c0001t0003g0166a0001c0001t0003g0167a0001c0001t0003g0168others(3): Show | 6 | HG01496.hp2 HG01891.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-5+2417A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26850671 | ||||||
| chr2:26850777
|
C | T | 35 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(32): Show | 35 | HG01074.hp1 HG01106.hp2 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.-5+2523C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26850777 | ||||||
| chr2:26850983
|
T | TACAC | 43 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(40): Show | 43 | HG01074.hp1 HG01106.hp2 HG01167.hp1 others(40): Show |
intron_variant | MODIFIER | c.-5+2730_-5+2731ins others(4): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26850983 | |||||
| chr2:26850985
|
T | C | 133 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(130): Show | 133 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.-5+2731T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26850985 | ||||||
| chr2:26851008
|
A | G | 8 | a0001c0001t0009g0039a0001c0001t0024g0036a0001c0002t0002g0035others(5): Show | 8 | HG01167.hp1 HG02109.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.-5+2754A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26851008 | ||||||
| chr2:26851313
|
A | G | 4 | a0001c0001t0010g0031a0001c0001t0010g0033a0001c0001t0012g0030others(1): Show | 4 | HG01106.hp2 HG01346.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.-5+3059A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26851313 | ||||||
| chr2:26851335
|
T | TGTTTTTA others(191): Show |
110 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(107): Show | 110 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.-5+3082_-5+3083ins others(198): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26851335 | |||||
| chr2:26851335
|
T | TGTTTTTA others(191): Show |
23 | a0001c0001t0001g0059a0001c0001t0003g0068a0001c0001t0008g0067others(20): Show | 23 | HG00639.hp1 HG00738.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.-5+3082_-5+3083ins others(198): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26851335 | |||||
| chr2:26851625
|
G | A | 60 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0177others(57): Show | 60 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(57): Show |
intron_variant | MODIFIER | c.-5+3371G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26851625 | ||||||
| chr2:26851806
|
G | A | 10 | a0001c0001t0003g0003a0001c0001t0003g0166a0001c0001t0003g0167others(7): Show | 10 | HG01496.hp2 HG01891.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.-5+3552G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26851806 | ||||||
| chr2:26851814
|
G | A | 1 | a0001c0001t0013g0047 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-5+3560G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26851814 | ||||||
| chr2:26851862
|
A | G | 43 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(40): Show | 43 | HG01074.hp1 HG01106.hp2 HG01167.hp1 others(40): Show |
intron_variant | MODIFIER | c.-5+3608A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26851862 | ||||||
| chr2:26851946
|
C | CA | 8 | a0001c0001t0012g0048a0001c0001t0012g0051a0001c0001t0012g0055others(5): Show | 8 | HG00639.hp1 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-5+3703dupA | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26851946 | |||||
| chr2:26851946
|
CA | C | 10 | a0001c0001t0009g0039a0001c0001t0009g0070a0001c0001t0024g0036others(7): Show | 10 | HG01167.hp1 HG02109.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.-5+3703delA | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26851946 | |||||
| chr2:26852091
|
C | T | 43 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(40): Show | 43 | HG01074.hp1 HG01106.hp2 HG01167.hp1 others(40): Show |
intron_variant | MODIFIER | c.-5+3837C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26852091 | ||||||
| chr2:26852220
|
G | A | 10 | a0001c0001t0001g0059a0001c0002t0006g0069a0001c0002t0011g0060others(7): Show | 10 | HG00738.hp1 HG01884.hp2 HG02897.hp2 others(7): Show |
intron_variant | MODIFIER | c.-5+3966G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26852220 | ||||||
| chr2:26852370
|
A | G | 8 | a0001c0001t0009g0039a0001c0001t0024g0036a0001c0002t0002g0035others(5): Show | 8 | HG01167.hp1 HG02109.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.-5+4116A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26852370 | ||||||
| chr2:26852472
|
T | C | 1 | a0001c0001t0001g0071 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-5+4218T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26852472 | ||||||
| chr2:26852637
|
T | C | 43 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(40): Show | 43 | HG01074.hp1 HG01106.hp2 HG01167.hp1 others(40): Show |
intron_variant | MODIFIER | c.-5+4383T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26852637 | ||||||
| chr2:26852727
|
G | A | 4 | a0001c0001t0003g0003a0001c0001t0008g0004a0001c0001t0009g0001others(1): Show | 4 | HG02451.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-5+4473G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26852727 | ||||||
| chr2:26853493
|
A | T | 1 | a0001c0001t0001g0231 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-5+5239A>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26853493 | ||||||
| chr2:26853611
|
A | G | 2 | a0001c0002t0004g0229a0001c0002t0004g0230 | 2 | HG02630.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-5+5357A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26853611 | ||||||
| chr2:26853689
|
C | T | 92 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(89): Show | 92 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.-5+5435C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26853689 | ||||||
| chr2:26854004
|
C | T | 3 | a0001c0001t0010g0226a0001c0001t0016g0227a0001c0001t0016g0228 | 3 | HG02717.hp2 NA20129.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-5+5750C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26854004 | ||||||
| chr2:26854044
|
T | TA | 8 | a0001c0001t0012g0048a0001c0001t0012g0051a0001c0001t0012g0055others(5): Show | 8 | HG00639.hp1 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-5+5800dupA | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26854044 | |||||
| chr2:26854152
|
CA | C | 8 | a0001c0001t0012g0048a0001c0001t0012g0051a0001c0001t0012g0055others(5): Show | 8 | HG00639.hp1 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-5+5901delA | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26854152 | |||||
| chr2:26854504
|
A | G | 3 | a0001c0001t0010g0031a0001c0001t0010g0033a0001c0001t0025g0032 | 3 | HG01106.hp2 HG01346.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-5+6250A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26854504 | ||||||
| chr2:26854578
|
C | T | 1 | a0001c0002t0002g0163 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-5+6324C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26854578 | ||||||
| chr2:26854742
|
G | A | 102 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(99): Show | 102 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.-5+6488G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26854742 | ||||||
| chr2:26854747
|
A | G | 5 | a0001c0001t0003g0003a0001c0001t0007g0005a0001c0001t0008g0004others(2): Show | 5 | HG02451.hp2 HG03209.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-5+6493A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26854747 | ||||||
| chr2:26854799
|
T | C | 5 | a0001c0001t0024g0036a0001c0002t0002g0035a0001c0002t0014g0034others(2): Show | 5 | HG01167.hp1 HG02486.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.-5+6545T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26854799 | ||||||
| chr2:26855538
|
A | G | 11 | a0001c0001t0001g0219a0001c0001t0001g0222a0001c0001t0001g0223others(8): Show | 11 | HG00597.hp1 HG01074.hp2 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.-5+7284A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26855538 | ||||||
| chr2:26855650
|
A | G | 1 | a0001c0002t0017g0215 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-5+7396A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26855650 | ||||||
| chr2:26855880
|
T | C | 5 | a0001c0001t0024g0036a0001c0002t0002g0035a0001c0002t0014g0034others(2): Show | 5 | HG01167.hp1 HG02486.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.-5+7626T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26855880 | ||||||
| chr2:26856286
|
A | G | 2 | a0001c0002t0002g0162a0001c0006t0004g0161 | 2 | HG00438.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.-5+8032A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26856286 | ||||||
| chr2:26856309
|
T | A | 2 | a0001c0001t0021g0006a0001c0001t0021g0007 | 2 | HG03540.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-5+8055T>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26856309 | ||||||
| chr2:26856378
|
T | C | 2 | a0001c0001t0021g0006a0001c0001t0021g0007 | 2 | HG03540.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-5+8124T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26856378 | ||||||
| chr2:26856462
|
G | A | 9 | a0001c0001t0003g0003a0001c0001t0008g0004a0001c0001t0009g0001others(6): Show | 9 | HG01167.hp1 HG02451.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.-5+8208G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26856462 | ||||||
| chr2:26856679
|
G | A | 1 | a0001c0001t0001g0174 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-5+8425G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26856679 | ||||||
| chr2:26856715
|
T | TA | 59 | a0001c0001t0001g0059a0001c0001t0003g0068a0001c0001t0003g0072others(56): Show | 59 | HG00140.hp2 HG00639.hp1 HG00733.hp1 others(56): Show |
intron_variant | MODIFIER | c.-5+8471dupA | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26856715 | |||||
| chr2:26856831
|
A | G | 1 | a0001c0001t0012g0030 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-5+8577A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26856831 | ||||||
| chr2:26856886
|
T | TATATATA others(50): Show |
5 | a0001c0001t0024g0036a0001c0002t0002g0035a0001c0002t0014g0034others(2): Show | 5 | HG01167.hp1 HG02486.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.-5+8645_-5+8701dup others(57): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26856886 | |||||
| chr2:26856886
|
T | TATATATA others(107): Show |
4 | a0001c0001t0003g0003a0001c0001t0008g0004a0001c0001t0009g0001others(1): Show | 4 | HG02451.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-5+8701_-5+8702ins others(114): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26856886 | |||||
| chr2:26856903
|
C | A | 1 | a0001c0002t0018g0175 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-5+8649C>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26856903 | ||||||
| chr2:26857097
|
T | C | 2 | a0001c0001t0001g0177a0001c0002t0004g0176 | 2 | HG00140.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.-5+8843T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26857097 | ||||||
| chr2:26857167
|
C | A | 101 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(98): Show | 101 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.-5+8913C>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26857167 | ||||||
| chr2:26857202
|
G | A | 2 | a0001c0001t0021g0006a0001c0001t0021g0007 | 2 | HG03540.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-5+8948G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26857202 | ||||||
| chr2:26857266
|
G | A | 92 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(89): Show | 92 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.-5+9012G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26857266 | ||||||
| chr2:26857358
|
G | T | 1 | a0001c0002t0019g0160 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-5+9104G>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26857358 | ||||||
| chr2:26857464
|
C | T | 91 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(88): Show | 91 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.-5+9210C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26857464 | ||||||
| chr2:26857489
|
G | A | 5 | a0001c0001t0024g0036a0001c0002t0002g0035a0001c0002t0014g0034others(2): Show | 5 | HG01167.hp1 HG02486.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.-5+9235G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26857489 | ||||||
| chr2:26857645
|
A | T | 107 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(104): Show | 107 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.-5+9391A>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26857645 | ||||||
| chr2:26857838
|
A | G | 101 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(98): Show | 101 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.-5+9584A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26857838 | ||||||
| chr2:26857970
|
A | G | 1 | a0001c0004t0003g0064 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-5+9716A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26857970 | ||||||
| chr2:26857976
|
A | G | 6 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0027others(3): Show | 6 | HG02280.hp1 HG02451.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.-5+9722A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26857976 | ||||||
| chr2:26858028
|
T | C | 4 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0027others(1): Show | 4 | HG02280.hp1 HG02451.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-5+9774T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26858028 | ||||||
| chr2:26858034
|
C | T | 5 | a0001c0001t0024g0036a0001c0002t0002g0035a0001c0002t0014g0034others(2): Show | 5 | HG01167.hp1 HG02486.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.-5+9780C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26858034 | ||||||
| chr2:26858170
|
A | AT | 104 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(101): Show | 104 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.-5+9935dupT | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26858170 | |||||
| chr2:26858170
|
A | ATT | 13 | a0001c0001t0001g0027a0001c0001t0001g0213a0001c0001t0003g0003others(10): Show | 13 | HG02451.hp2 HG02647.hp2 HG02818.hp1 others(10): Show |
intron_variant | MODIFIER | c.-5+9934_-5+9935dup others(2): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26858170 | |||||
| chr2:26858255
|
T | TC | 91 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(88): Show | 91 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.-5+10003dupC | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26858255 | |||||
| chr2:26858381
|
C | T | 1 | a0001c0002t0002g0096 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-5+10127C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26858381 | ||||||
| chr2:26858423
|
G | A | 24 | a0001c0001t0001g0059a0001c0001t0003g0068a0001c0001t0008g0067others(21): Show | 24 | HG00639.hp1 HG00738.hp1 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.-5+10169G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26858423 | ||||||
| chr2:26858450
|
C | T | 2 | a0001c0001t0001g0165a0001c0001t0001g0211 | 2 | NA18952.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.-5+10196C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26858450 | ||||||
| chr2:26858750
|
TTTC | T | 84 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(81): Show | 84 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.-5+10497_-5+10499d others(5): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26858750 | ||||||
| chr2:26858751
|
TTC | T | 19 | a0001c0001t0001g0027a0001c0001t0001g0224a0001c0001t0001g0225others(16): Show | 19 | HG01074.hp1 HG01496.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.-5+10498_-5+10499d others(4): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26858751 | ||||||
| chr2:26859050
|
C | A | 1 | a0001c0001t0003g0072 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-5+10796C>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26859050 | ||||||
| chr2:26859127
|
A | G | 5 | a0001c0001t0024g0036a0001c0002t0002g0035a0001c0002t0014g0034others(2): Show | 5 | HG01167.hp1 HG02486.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.-5+10873A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26859127 | ||||||
| chr2:26859352
|
G | GT | 8 | a0001c0001t0003g0166a0001c0001t0003g0167a0001c0001t0003g0168others(5): Show | 8 | HG01496.hp2 HG01891.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.-5+11110dupT | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26859352 | |||||
| chr2:26859691
|
A | G | 61 | a0001c0001t0001g0165a0001c0001t0001g0173a0001c0001t0001g0174others(58): Show | 61 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.-5+11437A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26859691 | ||||||
| chr2:26860131
|
T | A | 1 | a0001c0002t0002g0097 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-5+11877T>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26860131 | ||||||
| chr2:26860330
|
C | T | 1 | a0001c0001t0001g0156 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-5+12076C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26860330 | ||||||
| chr2:26860387
|
C | T | 3 | a0001c0002t0002g0153a0001c0002t0002g0154a0001c0002t0002g0155 | 3 | HG00558.hp2 NA18959.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.-5+12133C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26860387 | ||||||
| chr2:26860401
|
T | C | 102 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(99): Show | 102 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.-5+12147T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26860401 | ||||||
| chr2:26860408
|
G | A | 1 | a0001c0002t0002g0098 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-5+12154G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26860408 | ||||||
| chr2:26860469
|
A | C | 1 | a0001c0002t0002g0152 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-5+12215A>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26860469 | ||||||
| chr2:26860621
|
T | C | 93 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(90): Show | 93 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.-5+12367T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26860621 | ||||||
| chr2:26860793
|
C | T | 1 | a0001c0002t0002g0094 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-5+12539C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26860793 | ||||||
| chr2:26860794
|
G | A | 1 | a0001c0001t0038g0008 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-5+12540G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26860794 | ||||||
| chr2:26861223
|
A | G | 4 | a0001c0001t0003g0020a0001c0001t0023g0021a0001c0001t0023g0022others(1): Show | 4 | HG01243.hp2 HG01884.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-5+12969A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26861223 | ||||||
| chr2:26861248
|
C | A | 5 | a0001c0001t0001g0157a0001c0002t0002g0044a0001c0002t0002g0045others(2): Show | 5 | HG01516.hp1 HG01517.hp2 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.-5+12994C>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26861248 | ||||||
| chr2:26861502
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-5+13248G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26861502 | ||||||
| chr2:26861561
|
C | T | 1 | a0001c0001t0012g0055 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-5+13307C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26861561 | ||||||
| chr2:26861600
|
C | T | 1 | a0001c0002t0002g0152 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-5+13346C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26861600 | ||||||
| chr2:26862074
|
TC | T | 61 | a0001c0001t0001g0165a0001c0001t0001g0173a0001c0001t0001g0174others(58): Show | 61 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.-5+13825delC | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26862074 | |||||
| chr2:26862270
|
T | C | 1 | a0001c0001t0005g0178 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-5+14016T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26862270 | ||||||
| chr2:26862312
|
T | A | 1 | a0001c0001t0005g0179 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-5+14058T>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26862312 | ||||||
| chr2:26862562
|
T | C | 8 | a0001c0001t0012g0048a0001c0001t0012g0051a0001c0001t0012g0055others(5): Show | 8 | HG00639.hp1 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-5+14308T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26862562 | ||||||
| chr2:26862630
|
C | G | 9 | a0001c0001t0003g0068a0001c0001t0012g0048a0001c0001t0012g0051others(6): Show | 9 | HG00639.hp1 HG02257.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.-5+14376C>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26862630 | ||||||
| chr2:26862756
|
G | A | 3 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0004t0003g0011 | 3 | HG01934.hp2 HG02109.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-5+14502G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26862756 | ||||||
| chr2:26862848
|
G | T | 6 | a0001c0001t0003g0166a0001c0001t0003g0167a0001c0001t0003g0168others(3): Show | 6 | HG01496.hp2 HG01891.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-5+14594G>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26862848 | ||||||
| chr2:26863022
|
T | C | 1 | a0001c0002t0002g0101 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-5+14768T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26863022 | ||||||
| chr2:26863280
|
A | G | 26 | a0001c0001t0001g0059a0001c0001t0003g0003a0001c0001t0003g0166others(23): Show | 26 | HG01106.hp2 HG01167.hp1 HG01346.hp1 others(23): Show |
intron_variant | MODIFIER | c.-5+15026A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26863280 | ||||||
| chr2:26863412
|
C | T | 6 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0027others(3): Show | 6 | HG02280.hp1 HG02451.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.-5+15158C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26863412 | ||||||
| chr2:26863737
|
C | T | 2 | a0001c0001t0001g0208a0001c0001t0001g0209 | 2 | HG01358.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-5+15483C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26863737 | ||||||
| chr2:26863769
|
C | T | 1 | a0001c0002t0014g0037 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-5+15515C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26863769 | ||||||
| chr2:26863801
|
C | T | 2 | a0001c0002t0002g0101a0001c0002t0002g0151 | 2 | NA19005.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.-5+15547C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26863801 | ||||||
| chr2:26863805
|
T | C | 1 | a0001c0001t0036g0102 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-5+15551T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26863805 | ||||||
| chr2:26864029
|
G | T | 4 | a0001c0001t0024g0036a0001c0002t0002g0035a0001c0002t0014g0034others(1): Show | 4 | HG01167.hp1 HG02486.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-5+15775G>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26864029 | ||||||
| chr2:26864841
|
T | A | 94 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(91): Show | 94 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.-5+16587T>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26864841 | ||||||
| chr2:26864996
|
C | T | 1 | a0001c0001t0005g0207 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-5+16742C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26864996 | ||||||
| chr2:26865076
|
C | T | 3 | a0001c0002t0002g0096a0001c0002t0004g0095a0001c0002t0017g0159 | 3 | HG00733.hp1 HG01256.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.-5+16822C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26865076 | ||||||
| chr2:26865312
|
C | CT | 12 | a0001c0001t0001g0149a0001c0001t0001g0157a0001c0002t0002g0090others(9): Show | 12 | HG00140.hp2 HG00558.hp2 HG01069.hp1 others(9): Show |
intron_variant | MODIFIER | c.-5+17084dupT | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26865312 | |||||
| chr2:26865312
|
CT | C | 41 | a0001c0001t0001g0059a0001c0001t0001g0204a0001c0001t0001g0205others(38): Show | 41 | HG00639.hp1 HG00738.hp1 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.-5+17084delT | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26865312 | |||||
| chr2:26865312
|
CTT | C | 66 | a0001c0001t0001g0165a0001c0001t0001g0173a0001c0001t0001g0174others(63): Show | 66 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(63): Show |
intron_variant | MODIFIER | c.-5+17083_-5+17084d others(4): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26865312 | |||||
| chr2:26865312
|
CTTT | C | 28 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(25): Show | 28 | HG00639.hp2 HG01074.hp2 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5+17082_-5+17084d others(5): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26865312 | |||||
| chr2:26865446
|
G | A | 10 | a0001c0001t0003g0003a0001c0001t0003g0166a0001c0001t0003g0167others(7): Show | 10 | HG01496.hp2 HG01891.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.-5+17192G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26865446 | ||||||
| chr2:26865528
|
C | T | 5 | a0001c0001t0007g0005a0001c0001t0021g0006a0001c0001t0021g0007others(2): Show | 5 | HG01074.hp1 HG03453.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-5+17274C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26865528 | ||||||
| chr2:26866246
|
T | G | 6 | a0001c0001t0003g0166a0001c0001t0003g0167a0001c0001t0003g0168others(3): Show | 6 | HG01496.hp2 HG01891.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-5+17992T>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26866246 | ||||||
| chr2:26866277
|
G | A | 3 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018 | 3 | HG02280.hp2 HG02622.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-5+18023G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26866277 | ||||||
| chr2:26866444
|
C | T | 4 | a0001c0001t0001g0174a0001c0001t0005g0179a0001c0001t0005g0203others(1): Show | 4 | HG00558.hp1 HG02155.hp2 NA18939.hp2 others(1): Show |
intron_variant | MODIFIER | c.-5+18190C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26866444 | ||||||
| chr2:26866469
|
A | AAC | 52 | a0001c0001t0001g0173a0001c0001t0001g0195a0001c0001t0001g0196others(49): Show | 52 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.-5+18241_-5+18242d others(4): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26866469 | |||||
| chr2:26866469
|
A | AACAC | 8 | a0001c0001t0003g0003a0001c0001t0005g0018a0001c0001t0008g0004others(5): Show | 8 | HG01106.hp2 HG01346.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-5+18239_-5+18242d others(6): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26866469 | |||||
| chr2:26866732
|
C | CT | 26 | a0001c0001t0001g0059a0001c0001t0001g0194a0001c0001t0003g0068others(23): Show | 26 | HG00639.hp1 HG00738.hp1 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.-5+18495dupT | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26866732 | |||||
| chr2:26866923
|
G | A | 8 | a0001c0001t0012g0048a0001c0001t0012g0051a0001c0001t0012g0055others(5): Show | 8 | HG00639.hp1 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-5+18669G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26866923 | ||||||
| chr2:26867086
|
T | C | 1 | a0001c0001t0001g0181 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-5+18832T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26867086 | ||||||
| chr2:26867155
|
A | G | 2 | a0001c0001t0001g0208a0001c0001t0001g0209 | 2 | HG01358.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-5+18901A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26867155 | ||||||
| chr2:26867445
|
T | G | 1 | a0001c0001t0001g0204 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-5+19191T>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26867445 | ||||||
| chr2:26867447
|
T | G | 1 | a0001c0001t0042g0216 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-5+19193T>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26867447 | ||||||
| chr2:26867449
|
TTTTTTGT others(3): Show |
T | 6 | a0001c0001t0003g0166a0001c0001t0003g0167a0001c0001t0003g0168others(3): Show | 6 | HG01496.hp2 HG01891.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-5+19201_-5+19210d others(12): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26867449 | |||||
| chr2:26867451
|
T | G | 2 | a0001c0001t0001g0195a0001c0001t0001g0196 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-5+19197T>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26867451 | ||||||
| chr2:26867452
|
T | G | 3 | a0001c0001t0009g0066a0001c0001t0009g0070a0001c0001t0013g0065 | 3 | HG02258.hp2 HG02886.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-5+19198T>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26867452 | ||||||
| chr2:26867455
|
G | T | 4 | a0001c0001t0008g0067a0001c0001t0009g0066a0001c0001t0009g0070others(1): Show | 4 | HG01109.hp2 HG02258.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-5+19201G>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26867455 | ||||||
| chr2:26867459
|
G | GT | 13 | a0001c0001t0001g0149a0001c0001t0005g0016a0001c0001t0005g0017others(10): Show | 13 | HG01106.hp2 HG01346.hp1 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.-5+19219dupT | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26867459 | |||||
| chr2:26867459
|
G | T | 4 | a0001c0001t0008g0067a0001c0001t0009g0066a0001c0001t0009g0070others(1): Show | 4 | HG01109.hp2 HG02258.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-5+19205G>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26867459 | ||||||
| chr2:26867459
|
GT | G | 65 | a0001c0001t0001g0165a0001c0001t0001g0173a0001c0001t0001g0174others(62): Show | 65 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.-5+19219delT | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26867459 | |||||
| chr2:26867460
|
T | G | 4 | a0001c0001t0008g0067a0001c0001t0009g0066a0001c0001t0009g0070others(1): Show | 4 | HG01109.hp2 HG02258.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-5+19206T>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26867460 | ||||||
| chr2:26867463
|
T | G | 21 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0020others(18): Show | 21 | HG00639.hp1 HG01074.hp1 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.-5+19209T>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26867463 | ||||||
| chr2:26867464
|
T | G | 2 | a0001c0001t0001g0182a0001c0001t0015g0183 | 2 | HG01433.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.-5+19210T>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26867464 | ||||||
| chr2:26867511
|
G | A | 10 | a0001c0001t0003g0003a0001c0001t0003g0166a0001c0001t0003g0167others(7): Show | 10 | HG01496.hp2 HG01891.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.-5+19257G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26867511 | ||||||
| chr2:26867581
|
A | T | 1 | a0001c0002t0002g0094 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-5+19327A>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26867581 | ||||||
| chr2:26867600
|
C | T | 1 | a0001c0002t0004g0143 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-5+19346C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26867600 | ||||||
| chr2:26867637
|
AG | A | 2 | a0001c0002t0004g0142a0001c0002t0017g0159 | 2 | HG01256.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.-5+19384delG | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26867637 | ||||||
| chr2:26867752
|
G | T | 4 | a0001c0001t0008g0067a0001c0001t0009g0066a0001c0001t0009g0070others(1): Show | 4 | HG01109.hp2 HG02258.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-5+19498G>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26867752 | ||||||
| chr2:26867759
|
A | G | 1 | a0001c0002t0004g0229 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-5+19505A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26867759 | ||||||
| chr2:26868026
|
G | A | 2 | a0001c0001t0001g0195a0001c0001t0001g0196 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-5+19772G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26868026 | ||||||
| chr2:26868329
|
A | T | 1 | a0001c0004t0003g0011 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-5+20075A>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26868329 | ||||||
| chr2:26868514
|
T | C | 1 | a0001c0001t0007g0005 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-5+20260T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26868514 | ||||||
| chr2:26868588
|
A | C | 2 | a0001c0001t0021g0006a0001c0001t0021g0007 | 2 | HG03540.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-5+20334A>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26868588 | ||||||
| chr2:26869089
|
T | G | 62 | a0001c0001t0001g0165a0001c0001t0001g0173a0001c0001t0001g0174others(59): Show | 62 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.-5+20835T>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26869089 | ||||||
| chr2:26869333
|
A | G | 2 | a0001c0001t0008g0023a0001c0001t0008g0164 | 2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-5+21079A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26869333 | ||||||
| chr2:26869500
|
T | C | 7 | a0001c0001t0003g0020a0001c0001t0003g0166a0001c0001t0003g0167others(4): Show | 7 | HG01243.hp2 HG01496.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.-5+21246T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26869500 | ||||||
| chr2:26869794
|
G | A | 21 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(18): Show | 21 | HG01074.hp1 HG01884.hp1 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.-5+21540G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26869794 | ||||||
| chr2:26869872
|
G | T | 2 | a0001c0001t0010g0028a0001c0001t0016g0029 | 2 | HG02647.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.-5+21618G>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26869872 | ||||||
| chr2:26869934
|
C | G | 1 | a0001c0001t0003g0068 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-5+21680C>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26869934 | ||||||
| chr2:26870444
|
A | G | 1 | a0001c0002t0006g0084 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-5+22190A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26870444 | ||||||
| chr2:26870546
|
G | A | 1 | a0001c0001t0013g0047 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-5+22292G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26870546 | ||||||
| chr2:26870675
|
A | C | 3 | a0001c0002t0002g0097a0001c0002t0002g0146a0001c0002t0002g0147 | 3 | HG00099.hp2 HG00280.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.-5+22421A>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26870675 | ||||||
| chr2:26870708
|
C | CA | 15 | a0001c0001t0003g0068a0001c0001t0003g0166a0001c0001t0008g0067others(12): Show | 15 | HG00639.hp1 HG01109.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.-5+22473dupA | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26870708 | |||||
| chr2:26870976
|
A | C | 62 | a0001c0001t0001g0165a0001c0001t0001g0173a0001c0001t0001g0174others(59): Show | 62 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.-5+22722A>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26870976 | ||||||
| chr2:26871015
|
C | T | 4 | a0001c0001t0024g0036a0001c0002t0002g0035a0001c0002t0014g0034others(1): Show | 4 | HG01167.hp1 HG02486.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-5+22761C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26871015 | ||||||
| chr2:26871028
|
T | C | 2 | a0001c0001t0001g0104a0001c0001t0001g0149 | 2 | NA18959.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.-5+22774T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26871028 | ||||||
| chr2:26871046
|
C | T | 4 | a0001c0001t0003g0003a0001c0001t0008g0004a0001c0001t0009g0001others(1): Show | 4 | HG02451.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-5+22792C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26871046 | ||||||
| chr2:26871208
|
C | T | 31 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(28): Show | 31 | HG01074.hp1 HG01106.hp2 HG01346.hp1 others(28): Show |
intron_variant | MODIFIER | c.-5+22954C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26871208 | ||||||
| chr2:26871394
|
ATATT | A | 4 | a0001c0002t0002g0096a0001c0002t0004g0095a0001c0002t0004g0142others(1): Show | 4 | HG00733.hp1 HG01256.hp1 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.-5+23143_-5+23146d others(6): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26871394 | |||||
| chr2:26871454
|
A | G | 4 | a0001c0001t0024g0036a0001c0002t0002g0035a0001c0002t0014g0034others(1): Show | 4 | HG01167.hp1 HG02486.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-5+23200A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26871454 | ||||||
| chr2:26871633
|
G | A | 1 | a0001c0001t0001g0213 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-5+23379G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26871633 | ||||||
| chr2:26871685
|
C | T | 7 | a0001c0002t0002g0101a0001c0002t0002g0148a0001c0002t0002g0151others(4): Show | 7 | HG00558.hp2 NA18939.hp1 NA18952.hp2 others(4): Show |
intron_variant | MODIFIER | c.-5+23431C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26871685 | ||||||
| chr2:26871974
|
C | G | 112 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(109): Show | 112 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.-5+23720C>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26871974 | ||||||
| chr2:26872340
|
T | C | 4 | a0001c0001t0003g0003a0001c0001t0008g0004a0001c0001t0009g0001others(1): Show | 4 | HG02451.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-5+24086T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26872340 | ||||||
| chr2:26872423
|
G | C | 4 | a0001c0001t0024g0036a0001c0002t0002g0035a0001c0002t0014g0034others(1): Show | 4 | HG01167.hp1 HG02486.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-5+24169G>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26872423 | ||||||
| chr2:26872557
|
G | T | 8 | a0001c0001t0012g0048a0001c0001t0012g0051a0001c0001t0012g0055others(5): Show | 8 | HG00639.hp1 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-5+24303G>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26872557 | ||||||
| chr2:26872560
|
C | T | 18 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0024others(15): Show | 18 | HG01106.hp2 HG01346.hp1 HG01934.hp2 others(15): Show |
intron_variant | MODIFIER | c.-5+24306C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26872560 | ||||||
| chr2:26872685
|
CA | C | 78 | a0001c0001t0001g0165a0001c0001t0001g0173a0001c0001t0001g0174others(75): Show | 78 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.-5+24444delA | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26872685 | |||||
| chr2:26872740
|
T | C | 1 | a0001c0006t0004g0161 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-5+24486T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26872740 | ||||||
| chr2:26872790
|
C | CAG | 82 | a0001c0001t0001g0165a0001c0001t0001g0173a0001c0001t0001g0174others(79): Show | 82 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.-5+24537_-5+24538d others(4): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26872790 | |||||
| chr2:26873205
|
AAC | A | 4 | a0001c0001t0008g0067a0001c0001t0009g0066a0001c0001t0009g0070others(1): Show | 4 | HG01109.hp2 HG02258.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-5+24955_-5+24956d others(4): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26873205 | |||||
| chr2:26873274
|
A | T | 1 | a0001c0001t0001g0223 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-5+25020A>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26873274 | ||||||
| chr2:26873354
|
G | C | 4 | a0001c0001t0003g0003a0001c0001t0008g0004a0001c0001t0009g0001others(1): Show | 4 | HG02451.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-5+25100G>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26873354 | ||||||
| chr2:26874022
|
A | AT | 4 | a0001c0001t0003g0003a0001c0001t0008g0004a0001c0001t0009g0001others(1): Show | 4 | HG02451.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4-24466dupT | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26874022 | |||||
| chr2:26874109
|
AT | A | 5 | a0001c0001t0003g0088a0001c0001t0003g0166a0001c0001t0003g0167others(2): Show | 5 | HG01891.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-4-24380delT | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26874109 | |||||
| chr2:26874326
|
T | A | 68 | a0001c0001t0001g0157a0001c0001t0001g0165a0001c0001t0001g0173others(65): Show | 68 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.-4-24170T>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26874326 | ||||||
| chr2:26874382
|
G | A | 1 | a0001c0002t0002g0145 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-4-24114G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26874382 | ||||||
| chr2:26874388
|
A | G | 2 | a0001c0001t0001g0177a0001c0001t0001g0200 | 2 | HG00140.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-4-24108A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26874388 | ||||||
| chr2:26874526
|
T | C | 1 | a0001c0002t0002g0090 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-4-23970T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26874526 | ||||||
| chr2:26874651
|
A | G | 1 | a0001c0001t0012g0030 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-4-23845A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26874651 | ||||||
| chr2:26874795
|
C | T | 4 | a0001c0001t0003g0003a0001c0001t0008g0004a0001c0001t0009g0001others(1): Show | 4 | HG02451.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4-23701C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26874795 | ||||||
| chr2:26874835
|
T | C | 3 | a0001c0001t0013g0047a0001c0001t0013g0074a0001c0001t0013g0075 | 3 | HG00733.hp2 HG01167.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-4-23661T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26874835 | ||||||
| chr2:26874956
|
A | G | 4 | a0001c0001t0003g0003a0001c0001t0008g0004a0001c0001t0009g0001others(1): Show | 4 | HG02451.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4-23540A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26874956 | ||||||
| chr2:26875218
|
G | A | 114 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(111): Show | 114 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.-4-23278G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26875218 | ||||||
| chr2:26875279
|
C | T | 1 | a0001c0001t0001g0222 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-4-23217C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26875279 | ||||||
| chr2:26875381
|
C | G | 1 | a0001c0002t0004g0141 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-4-23115C>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26875381 | ||||||
| chr2:26875584
|
G | A | 2 | a0001c0002t0002g0101a0001c0002t0002g0151 | 2 | NA19005.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.-4-22912G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26875584 | ||||||
| chr2:26875587
|
G | T | 1 | a0001c0002t0002g0140 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-4-22909G>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26875587 | ||||||
| chr2:26875767
|
A | G | 4 | a0001c0001t0008g0067a0001c0001t0009g0066a0001c0001t0009g0070others(1): Show | 4 | HG01109.hp2 HG02258.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-4-22729A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26875767 | ||||||
| chr2:26875898
|
G | A | 111 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(108): Show | 111 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.-4-22598G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26875898 | ||||||
| chr2:26876457
|
A | T | 1 | a0001c0001t0035g0105 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-4-22039A>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26876457 | ||||||
| chr2:26876596
|
G | A | 4 | a0001c0001t0003g0003a0001c0001t0008g0004a0001c0001t0009g0001others(1): Show | 4 | HG02451.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4-21900G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26876596 | ||||||
| chr2:26876661
|
G | A | 4 | a0001c0001t0008g0067a0001c0001t0009g0066a0001c0001t0009g0070others(1): Show | 4 | HG01109.hp2 HG02258.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-4-21835G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26876661 | ||||||
| chr2:26876780
|
C | T | 1 | a0001c0001t0003g0003 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-4-21716C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26876780 | ||||||
| chr2:26876811
|
C | T | 1 | a0001c0001t0001g0193 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-4-21685C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26876811 | ||||||
| chr2:26876827
|
A | G | 3 | a0001c0001t0007g0005a0001c0002t0015g0042a0001c0002t0015g0043 | 3 | HG01074.hp1 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-4-21669A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26876827 | ||||||
| chr2:26876961
|
C | CT | 10 | a0001c0001t0001g0059a0001c0001t0001g0139a0001c0002t0006g0069others(7): Show | 10 | HG00738.hp1 HG01358.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.-4-21513dupT | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26876961 | |||||
| chr2:26876961
|
CT | C | 117 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0026others(114): Show | 117 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.-4-21513delT | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26876961 | |||||
| chr2:26877081
|
C | T | 1 | a0001c0001t0009g0039 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-4-21415C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26877081 | ||||||
| chr2:26877102
|
G | T | 1 | a0001c0001t0036g0102 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-4-21394G>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26877102 | ||||||
| chr2:26877218
|
C | T | 2 | a0001c0001t0003g0003a0001c0001t0009g0002 | 2 | HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-4-21278C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26877218 | ||||||
| chr2:26877257
|
C | T | 11 | a0001c0001t0001g0219a0001c0001t0001g0222a0001c0001t0001g0223others(8): Show | 11 | HG00597.hp1 HG01074.hp2 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.-4-21239C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26877257 | ||||||
| chr2:26877417
|
G | A | 1 | a0001c0001t0012g0030 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-4-21079G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26877417 | ||||||
| chr2:26877614
|
C | T | 1 | a0001c0002t0018g0175 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-4-20882C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26877614 | ||||||
| chr2:26877622
|
C | A | 3 | a0001c0001t0007g0005a0001c0002t0015g0042a0001c0002t0015g0043 | 3 | HG01074.hp1 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-4-20874C>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26877622 | ||||||
| chr2:26878413
|
C | T | 16 | a0001c0001t0001g0138a0001c0001t0005g0081a0001c0001t0005g0170others(13): Show | 16 | HG00140.hp2 HG01069.hp1 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.-4-20083C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26878413 | ||||||
| chr2:26878824
|
G | A | 1 | a0001c0001t0001g0184 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-4-19672G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26878824 | ||||||
| chr2:26878929
|
A | ACTCCCCA others(50): Show |
1 | a0001c0001t0001g0104 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-4-19567_-4-19566i others(59): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26878929 | ||||||
| chr2:26878930
|
G | C | 1 | a0001c0001t0001g0104 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-4-19566G>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26878930 | ||||||
| chr2:26878947
|
G | A | 1 | a0001c0001t0001g0104 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-4-19549G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26878947 | ||||||
| chr2:26878948
|
T | A | 1 | a0001c0001t0001g0104 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-4-19548T>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26878948 | ||||||
| chr2:26878955
|
T | G | 1 | a0001c0001t0001g0104 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-4-19541T>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26878955 | ||||||
| chr2:26878956
|
G | A | 1 | a0001c0001t0001g0104 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-4-19540G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26878956 | ||||||
| chr2:26878958
|
T | A | 1 | a0001c0001t0001g0104 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-4-19538T>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26878958 | ||||||
| chr2:26879000
|
TCTCCTAT others(17): Show |
T | 1 | a0001c0001t0001g0104 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-4-19494_-4-19471d others(26): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26879000 | |||||
| chr2:26879026
|
A | C | 1 | a0001c0001t0001g0104 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-4-19470A>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26879026 | ||||||
| chr2:26879038
|
T | A | 1 | a0001c0001t0001g0104 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-4-19458T>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26879038 | ||||||
| chr2:26879060
|
G | C | 1 | a0001c0001t0001g0104 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-4-19436G>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26879060 | ||||||
| chr2:26879062
|
G | C | 1 | a0001c0001t0001g0104 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-4-19434G>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26879062 | ||||||
| chr2:26879072
|
T | C | 1 | a0001c0001t0001g0104 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-4-19424T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26879072 | ||||||
| chr2:26879080
|
A | C | 1 | a0001c0001t0001g0104 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-4-19416A>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26879080 | ||||||
| chr2:26879269
|
G | C | 1 | a0001c0001t0013g0065 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-4-19227G>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26879269 | ||||||
| chr2:26879460
|
G | GA | 8 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0003g0012others(5): Show | 8 | HG00733.hp2 HG01891.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.-4-19015dupA | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26879460 | |||||
| chr2:26879460
|
GA | G | 52 | a0001c0001t0001g0115a0001c0001t0001g0156a0001c0001t0001g0157others(49): Show | 52 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(49): Show |
intron_variant | MODIFIER | c.-4-19015delA | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26879460 | |||||
| chr2:26879461
|
A | G | 1 | a0001c0004t0003g0064 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-4-19035A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26879461 | ||||||
| chr2:26879679
|
T | C | 2 | a0001c0001t0001g0192a0001c0001t0005g0178 | 2 | HG00735.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.-4-18817T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26879679 | ||||||
| chr2:26879686
|
C | G | 3 | a0001c0001t0001g0199a0001c0001t0001g0208a0001c0001t0001g0209 | 3 | HG01358.hp1 HG02886.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-4-18810C>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26879686 | ||||||
| chr2:26879700
|
C | T | 1 | a0001c0001t0007g0005 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-4-18796C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26879700 | ||||||
| chr2:26879716
|
G | A | 1 | a0001c0002t0002g0089 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-4-18780G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26879716 | ||||||
| chr2:26879744
|
TCTAAAGG others(4): Show |
T | 4 | a0001c0001t0003g0003a0001c0001t0008g0004a0001c0001t0009g0001others(1): Show | 4 | HG02451.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4-18748_-4-18738d others(13): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26879744 | |||||
| chr2:26879888
|
T | TTTG | 4 | a0001c0001t0003g0003a0001c0001t0008g0004a0001c0001t0009g0001others(1): Show | 4 | HG02451.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4-18589_-4-18587d others(5): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26879888 | |||||
| chr2:26879909
|
G | A | 5 | a0001c0001t0003g0088a0001c0001t0003g0166a0001c0001t0003g0167others(2): Show | 5 | HG01891.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-4-18587G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26879909 | ||||||
| chr2:26879976
|
G | A | 35 | a0001c0001t0001g0115a0001c0001t0001g0157a0001c0001t0001g0165others(32): Show | 35 | HG00280.hp1 HG00558.hp1 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.-4-18520G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26879976 | ||||||
| chr2:26880045
|
C | T | 1 | a0001c0002t0018g0175 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-4-18451C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26880045 | ||||||
| chr2:26880078
|
C | T | 1 | a0001c0002t0004g0141 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-4-18418C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26880078 | ||||||
| chr2:26880140
|
T | C | 1 | a0001c0001t0034g0054 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-4-18356T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26880140 | ||||||
| chr2:26880346
|
A | G | 1 | a0001c0002t0002g0135 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.-4-18150A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26880346 | ||||||
| chr2:26880431
|
A | G | 1 | a0001c0001t0001g0026 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-4-18065A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26880431 | ||||||
| chr2:26880443
|
T | A | 1 | a0001c0002t0015g0042 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-4-18053T>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26880443 | ||||||
| chr2:26880830
|
A | G | 3 | a0001c0002t0002g0035a0001c0002t0014g0034a0001c0002t0014g0037 | 3 | HG02486.hp1 HG06807.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-4-17666A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26880830 | ||||||
| chr2:26881031
|
G | A | 1 | a0001c0002t0011g0062 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-4-17465G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26881031 | ||||||
| chr2:26881087
|
T | G | 5 | a0001c0001t0003g0088a0001c0001t0003g0166a0001c0001t0003g0167others(2): Show | 5 | HG01891.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-4-17409T>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26881087 | ||||||
| chr2:26881098
|
G | A | 2 | a0001c0002t0004g0099a0001c0002t0004g0118 | 2 | NA18954.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.-4-17398G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26881098 | ||||||
| chr2:26881144
|
G | A | 1 | a0001c0001t0008g0004 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-4-17352G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26881144 | ||||||
| chr2:26881263
|
T | C | 130 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(127): Show | 130 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.-4-17233T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26881263 | ||||||
| chr2:26881705
|
A | G | 1 | a0001c0001t0012g0030 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-4-16791A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26881705 | ||||||
| chr2:26881829
|
C | T | 1 | a0001c0007t0040g0169 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-4-16667C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26881829 | ||||||
| chr2:26881950
|
G | A | 3 | a0001c0001t0009g0066a0001c0001t0009g0070a0001c0001t0013g0065 | 3 | HG02258.hp2 HG02886.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-4-16546G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26881950 | ||||||
| chr2:26882007
|
C | T | 1 | a0001c0002t0002g0134 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-4-16489C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26882007 | ||||||
| chr2:26882076
|
G | A | 1 | a0001c0001t0008g0067 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-4-16420G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26882076 | ||||||
| chr2:26882090
|
C | CA | 11 | a0001c0001t0001g0156a0001c0001t0001g0192a0001c0001t0001g0225others(8): Show | 11 | HG00735.hp1 HG01074.hp1 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.-4-16384dupA | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26882090 | |||||
| chr2:26882090
|
C | CAA | 5 | a0001c0001t0003g0088a0001c0001t0003g0166a0001c0001t0003g0167others(2): Show | 5 | HG01891.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-4-16385_-4-16384d others(4): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26882090 | |||||
| chr2:26882090
|
CA | C | 19 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0149others(16): Show | 19 | HG00558.hp1 HG00639.hp1 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.-4-16384delA | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26882090 | |||||
| chr2:26882111
|
A | AAGAAAG | 14 | a0001c0001t0001g0138a0001c0001t0005g0081a0001c0001t0005g0170others(11): Show | 14 | HG00140.hp2 HG01168.hp2 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.-4-16383_-4-16378d others(8): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26882111 | |||||
| chr2:26882111
|
A | AGAAAG | 2 | a0001c0002t0002g0091a0001c0002t0027g0083 | 2 | HG01069.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-4-16385_-4-16384i others(7): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26882111 | ||||||
| chr2:26882240
|
T | C | 3 | a0001c0001t0007g0005a0001c0002t0015g0042a0001c0002t0015g0043 | 3 | HG01074.hp1 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-4-16256T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26882240 | ||||||
| chr2:26882391
|
G | A | 4 | a0001c0001t0003g0003a0001c0001t0008g0004a0001c0001t0009g0001others(1): Show | 4 | HG02451.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4-16105G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26882391 | ||||||
| chr2:26882401
|
A | T | 1 | a0001c0001t0001g0156 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-4-16095A>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26882401 | ||||||
| chr2:26882429
|
C | CTG | 19 | a0001c0001t0001g0180a0001c0001t0001g0199a0001c0001t0001g0208others(16): Show | 19 | HG00639.hp2 HG01358.hp1 HG01516.hp1 others(16): Show |
intron_variant | MODIFIER | c.-4-16041_-4-16040d others(4): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26882429 | |||||
| chr2:26882429
|
C | CTGTG | 94 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0026others(91): Show | 94 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.-4-16043_-4-16040d others(6): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26882429 | |||||
| chr2:26882429
|
C | CTGTGTG | 10 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0200others(7): Show | 10 | HG00438.hp2 HG00597.hp2 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.-4-16045_-4-16040d others(8): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26882429 | |||||
| chr2:26882429
|
CTG | C | 6 | a0001c0002t0002g0035a0001c0002t0002g0146a0001c0002t0004g0142others(3): Show | 6 | HG00735.hp2 HG01256.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.-4-16041_-4-16040d others(4): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26882429 | |||||
| chr2:26882429
|
CTGTG | C | 3 | a0001c0002t0002g0076a0001c0002t0002g0085a0001c0002t0002g0163 | 3 | HG02145.hp2 HG03130.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-4-16043_-4-16040d others(6): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26882429 | |||||
| chr2:26882453
|
GTGTA | G | 4 | a0001c0001t0003g0003a0001c0001t0008g0004a0001c0001t0009g0001others(1): Show | 4 | HG02451.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4-16039_-4-16036d others(6): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26882453 | |||||
| chr2:26882457
|
A | G | 1 | a0001c0007t0040g0169 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-4-16039A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26882457 | ||||||
| chr2:26882557
|
A | T | 4 | a0001c0001t0003g0003a0001c0001t0008g0004a0001c0001t0009g0001others(1): Show | 4 | HG02451.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4-15939A>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26882557 | ||||||
| chr2:26882621
|
C | T | 1 | a0001c0001t0009g0039 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-4-15875C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26882621 | ||||||
| chr2:26882717
|
A | C | 4 | a0001c0001t0003g0003a0001c0001t0008g0004a0001c0001t0009g0001others(1): Show | 4 | HG02451.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4-15779A>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26882717 | ||||||
| chr2:26882908
|
T | TA | 8 | a0001c0001t0001g0108a0001c0001t0023g0021a0001c0001t0023g0022others(5): Show | 8 | HG01515.hp2 HG01884.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.-4-15567dupA | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26882908 | |||||
| chr2:26882908
|
TA | T | 21 | a0001c0001t0001g0027a0001c0001t0001g0106a0001c0001t0001g0107others(18): Show | 21 | HG00280.hp1 HG00733.hp2 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.-4-15567delA | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26882908 | |||||
| chr2:26883070
|
TG | T | 4 | a0001c0001t0003g0003a0001c0001t0008g0004a0001c0001t0009g0001others(1): Show | 4 | HG02451.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4-15425delG | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26883070 | ||||||
| chr2:26883719
|
C | G | 1 | a0001c0001t0001g0177 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-4-14777C>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26883719 | ||||||
| chr2:26883757
|
A | T | 90 | a0001c0001t0001g0071a0001c0001t0001g0104a0001c0001t0001g0106others(87): Show | 90 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.-4-14739A>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26883757 | ||||||
| chr2:26883862
|
C | T | 4 | a0001c0001t0003g0003a0001c0001t0008g0004a0001c0001t0009g0001others(1): Show | 4 | HG02451.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4-14634C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26883862 | ||||||
| chr2:26883954
|
C | T | 5 | a0001c0001t0003g0088a0001c0001t0003g0166a0001c0001t0003g0167others(2): Show | 5 | HG01891.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-4-14542C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26883954 | ||||||
| chr2:26884119
|
C | T | 1 | a0001c0001t0042g0216 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-4-14377C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26884119 | ||||||
| chr2:26884239
|
A | G | 4 | a0001c0001t0003g0003a0001c0001t0008g0004a0001c0001t0009g0001others(1): Show | 4 | HG02451.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4-14257A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26884239 | ||||||
| chr2:26884517
|
A | ATC | 33 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0138others(30): Show | 33 | HG00140.hp2 HG00558.hp1 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.-4-13976_-4-13975d others(4): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26884517 | |||||
| chr2:26884520
|
T | TCA | 4 | a0001c0002t0002g0121a0001c0002t0002g0140a0001c0002t0002g0162others(1): Show | 4 | HG00673.hp1 HG02083.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.-4-13942_-4-13941d others(4): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26884520 | |||||
| chr2:26884520
|
T | TCACACA | 2 | a0001c0001t0001g0200a0001c0001t0012g0048 | 2 | HG02615.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-4-13946_-4-13941d others(8): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26884520 | |||||
| chr2:26884520
|
T | TCTCA | 29 | a0001c0001t0001g0024a0001c0001t0001g0107a0001c0001t0001g0108others(26): Show | 29 | HG00280.hp1 HG00733.hp2 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.-4-13975_-4-13974i others(6): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26884520 | |||||
| chr2:26884520
|
T | TCTCACA | 74 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(71): Show | 74 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.-4-13975_-4-13974i others(8): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26884520 | |||||
| chr2:26884520
|
T | TCTCACAC others(1): Show |
18 | a0001c0001t0001g0059a0001c0001t0001g0174a0001c0001t0001g0208others(15): Show | 18 | HG01346.hp1 HG01358.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.-4-13975_-4-13974i others(10): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26884520 | |||||
| chr2:26884520
|
T | TCTCACAC others(3): Show |
7 | a0001c0001t0001g0173a0001c0001t0008g0067a0001c0001t0009g0066others(4): Show | 7 | HG01109.hp2 HG02258.hp2 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.-4-13975_-4-13974i others(12): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26884520 | |||||
| chr2:26884520
|
T | TCTCACAC others(5): Show |
1 | a0001c0001t0001g0181 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-4-13975_-4-13974i others(14): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26884520 | |||||
| chr2:26884520
|
T | TCTCACAC others(13): Show |
1 | a0001c0007t0040g0169 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-4-13975_-4-13974i others(22): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26884520 | |||||
| chr2:26884520
|
T | TCTCTCA | 5 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0007g0005others(2): Show | 5 | HG01074.hp1 HG01891.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4-13975_-4-13974i others(8): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26884520 | |||||
| chr2:26884520
|
TCA | T | 8 | a0001c0001t0009g0039a0001c0002t0002g0035a0001c0002t0002g0152others(5): Show | 8 | HG00558.hp2 HG02486.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.-4-13942_-4-13941d others(4): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26884520 | |||||
| chr2:26884522
|
A | T | 8 | a0001c0001t0001g0189a0001c0001t0003g0088a0001c0001t0003g0166others(5): Show | 8 | HG01515.hp2 HG01891.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.-4-13974A>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26884522 | ||||||
| chr2:26884524
|
A | T | 4 | a0001c0001t0009g0039a0001c0002t0002g0035a0001c0002t0014g0034others(1): Show | 4 | HG02486.hp1 HG02615.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-4-13972A>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26884524 | ||||||
| chr2:26884609
|
T | C | 1 | a0001c0002t0002g0134 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-4-13887T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26884609 | ||||||
| chr2:26885072
|
A | G | 4 | a0001c0001t0003g0003a0001c0001t0008g0004a0001c0001t0009g0001others(1): Show | 4 | HG02451.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4-13424A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26885072 | ||||||
| chr2:26885082
|
C | T | 3 | a0001c0001t0010g0031a0001c0001t0010g0033a0001c0001t0025g0032 | 3 | HG01106.hp2 HG01346.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-4-13414C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26885082 | ||||||
| chr2:26885140
|
A | G | 4 | a0001c0001t0003g0003a0001c0001t0008g0004a0001c0001t0009g0001others(1): Show | 4 | HG02451.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4-13356A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26885140 | ||||||
| chr2:26885210
|
C | T | 1 | a0001c0007t0040g0169 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-4-13286C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26885210 | ||||||
| chr2:26885215
|
T | C | 4 | a0001c0001t0003g0003a0001c0001t0008g0004a0001c0001t0009g0001others(1): Show | 4 | HG02451.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4-13281T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26885215 | ||||||
| chr2:26885216
|
A | T | 1 | a0001c0002t0002g0094 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-4-13280A>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26885216 | ||||||
| chr2:26885644
|
G | T | 4 | a0001c0001t0003g0003a0001c0001t0008g0004a0001c0001t0009g0001others(1): Show | 4 | HG02451.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4-12852G>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26885644 | ||||||
| chr2:26885646
|
G | A | 1 | a0001c0001t0001g0201 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-4-12850G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26885646 | ||||||
| chr2:26885784
|
A | T | 3 | a0001c0002t0002g0035a0001c0002t0014g0034a0001c0002t0014g0037 | 3 | HG02486.hp1 HG06807.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-4-12712A>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26885784 | ||||||
| chr2:26885925
|
G | A | 1 | a0001c0002t0002g0147 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-4-12571G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26885925 | ||||||
| chr2:26886084
|
C | T | 3 | a0001c0002t0002g0035a0001c0002t0014g0034a0001c0002t0014g0037 | 3 | HG02486.hp1 HG06807.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-4-12412C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26886084 | ||||||
| chr2:26886280
|
A | G | 1 | a0001c0004t0003g0011 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-4-12216A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26886280 | ||||||
| chr2:26886297
|
A | G | 1 | a0001c0002t0011g0061 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-4-12199A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26886297 | ||||||
| chr2:26886310
|
A | G | 1 | a0001c0002t0004g0141 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-4-12186A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26886310 | ||||||
| chr2:26886552
|
A | G | 1 | a0001c0002t0002g0035 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-4-11944A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26886552 | ||||||
| chr2:26886642
|
G | C | 4 | a0001c0001t0003g0003a0001c0001t0008g0004a0001c0001t0009g0001others(1): Show | 4 | HG02451.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4-11854G>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26886642 | ||||||
| chr2:26886821
|
A | C | 1 | a0001c0001t0001g0213 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-4-11675A>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26886821 | ||||||
| chr2:26886908
|
G | T | 1 | a0001c0002t0031g0073 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-4-11588G>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26886908 | ||||||
| chr2:26887003
|
C | T | 1 | a0001c0002t0002g0212 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-4-11493C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26887003 | ||||||
| chr2:26887055
|
C | T | 3 | a0001c0002t0002g0035a0001c0002t0014g0034a0001c0002t0014g0037 | 3 | HG02486.hp1 HG06807.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-4-11441C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26887055 | ||||||
| chr2:26887144
|
A | T | 2 | a0001c0002t0004g0099a0001c0002t0004g0118 | 2 | NA18954.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.-4-11352A>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26887144 | ||||||
| chr2:26887178
|
G | A | 3 | a0001c0002t0002g0035a0001c0002t0014g0034a0001c0002t0014g0037 | 3 | HG02486.hp1 HG06807.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-4-11318G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26887178 | ||||||
| chr2:26887248
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-4-11248C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26887248 | ||||||
| chr2:26887293
|
G | T | 1 | a0001c0001t0032g0077 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-4-11203G>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26887293 | ||||||
| chr2:26887568
|
T | A | 1 | a0001c0002t0014g0034 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-4-10928T>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26887568 | ||||||
| chr2:26887643
|
C | T | 1 | a0001c0007t0040g0169 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-4-10853C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26887643 | ||||||
| chr2:26887694
|
CAAGACAG others(54): Show |
C | 5 | a0001c0001t0003g0088a0001c0001t0003g0166a0001c0001t0003g0167others(2): Show | 5 | HG01891.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-4-10796_-4-10736d others(63): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26887694 | |||||
| chr2:26887736
|
A | G | 2 | a0001c0001t0005g0081a0001c0001t0005g0170 | 2 | HG01496.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-4-10760A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26887736 | ||||||
| chr2:26888046
|
T | A | 12 | a0001c0001t0003g0003a0001c0001t0003g0088a0001c0001t0003g0166others(9): Show | 12 | HG01891.hp2 HG02451.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.-4-10450T>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26888046 | ||||||
| chr2:26888163
|
A | ATTCT | 7 | a0001c0001t0003g0003a0001c0001t0008g0004a0001c0001t0009g0001others(4): Show | 7 | HG02451.hp2 HG02486.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.-4-10324_-4-10321d others(6): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26888163 | |||||
| chr2:26888208
|
C | CTTTTCTT others(3): Show |
2 | a0001c0001t0013g0074a0001c0001t0013g0075 | 2 | HG00733.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.-4-10285_-4-10276d others(12): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26888208 | |||||
| chr2:26888208
|
C | T | 1 | a0001c0001t0009g0039 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-4-10288C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26888208 | ||||||
| chr2:26888209
|
T | TTTCTTCT others(11): Show |
1 | a0001c0001t0003g0012 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-4-10285_-4-10284i others(20): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26888209 | |||||
| chr2:26888209
|
T | TTTTC | 14 | a0001c0001t0001g0138a0001c0002t0002g0040a0001c0002t0002g0097others(11): Show | 14 | HG00099.hp2 HG00673.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.-4-10233_-4-10230d others(6): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26888209 | |||||
| chr2:26888209
|
T | TTTTCTTT others(1): Show |
16 | a0001c0002t0002g0041a0001c0002t0002g0045a0001c0002t0002g0096others(13): Show | 16 | HG00733.hp1 HG01256.hp1 HG01256.hp2 others(13): Show |
intron_variant | MODIFIER | c.-4-10237_-4-10230d others(10): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26888209 | |||||
| chr2:26888209
|
T | TTTTCTTT others(5): Show |
2 | a0001c0002t0002g0044a0001c0002t0004g0095 | 2 | HG01981.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.-4-10241_-4-10230d others(14): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26888209 | |||||
| chr2:26888209
|
T | TTTTCTTT others(9): Show |
2 | a0001c0001t0001g0100a0001c0002t0002g0133 | 2 | HG00642.hp1 HG00642.hp2 |
intron_variant | MODIFIER | c.-4-10245_-4-10230d others(18): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26888209 | |||||
| chr2:26888209
|
T | TTTTCTTT others(7): Show |
1 | a0001c0001t0013g0047 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-4-10276_-4-10275i others(16): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26888209 | |||||
| chr2:26888209
|
T | TTTTTTTC others(16): Show |
1 | a0001c0001t0008g0004 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-4-10284_-4-10283i others(25): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26888209 | |||||
| chr2:26888209
|
T | TTTTTTTT others(13): Show |
3 | a0001c0001t0003g0003a0001c0001t0009g0001a0001c0001t0009g0002 | 3 | HG02451.hp2 HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-4-10284_-4-10283i others(22): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26888209 | |||||
| chr2:26888209
|
TTTTC | T | 24 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0165others(21): Show | 24 | HG00438.hp1 HG00597.hp1 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.-4-10233_-4-10230d others(6): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26888209 | |||||
| chr2:26888209
|
TTTTCTTT others(1): Show |
T | 7 | a0001c0001t0001g0174a0001c0001t0001g0180a0001c0001t0012g0030others(4): Show | 7 | HG00639.hp2 HG01257.hp1 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.-4-10237_-4-10230d others(10): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26888209 | |||||
| chr2:26888209
|
TTTTCTTT others(5): Show |
T | 3 | a0001c0001t0001g0199a0001c0002t0002g0212a0001c0002t0006g0191 | 3 | NA18975.hp1 NA19004.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-4-10241_-4-10230d others(14): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26888209 | |||||
| chr2:26888209
|
TTTTCTTT others(9): Show |
T | 1 | a0001c0001t0003g0167 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-4-10245_-4-10230d others(18): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26888209 | |||||
| chr2:26888209
|
TTTTCTTT others(13): Show |
T | 4 | a0001c0001t0003g0088a0001c0001t0003g0166a0001c0001t0003g0168others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-4-10249_-4-10230d others(22): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26888209 | |||||
| chr2:26888217
|
C | CTTTCTTT others(15): Show |
1 | a0001c0002t0030g0056 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.-4-10277_-4-10256d others(24): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26888217 | |||||
| chr2:26888255
|
T | G | 79 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0024others(76): Show | 79 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.-4-10241T>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26888255 | ||||||
| chr2:26888255
|
T | TTCTG | 38 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0107others(35): Show | 38 | HG00438.hp2 HG00597.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.-4-10238_-4-10237i others(6): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26888255 | |||||
| chr2:26888255
|
T | TTCTTTCT others(1): Show |
8 | a0001c0001t0001g0106a0001c0001t0001g0197a0001c0001t0001g0201others(5): Show | 8 | HG02015.hp2 HG02630.hp2 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.-4-10234_-4-10233i others(10): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26888255 | |||||
| chr2:26888255
|
T | TTCTTTCT others(5): Show |
12 | a0001c0001t0001g0124a0001c0001t0001g0156a0001c0001t0003g0020others(9): Show | 12 | HG01074.hp1 HG01243.hp2 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.-4-10217_-4-10206d others(14): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26888255 | |||||
| chr2:26888255
|
T | TTCTTTCT others(17): Show |
1 | a0001c0002t0002g0035 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-4-10229_-4-10206d others(26): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26888255 | |||||
| chr2:26888255
|
T | TTCTTTCT others(9): Show |
13 | a0001c0001t0001g0193a0001c0001t0003g0013a0001c0001t0010g0028others(10): Show | 13 | HG00099.hp1 HG00140.hp2 HG00738.hp1 others(10): Show |
intron_variant | MODIFIER | c.-4-10230_-4-10229i others(18): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26888255 | |||||
| chr2:26888255
|
T | TTCTTTCT others(21): Show |
1 | a0001c0002t0014g0037 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-4-10230_-4-10229i others(30): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26888255 | |||||
| chr2:26888255
|
T | TTCTTTCT others(13): Show |
11 | a0001c0001t0023g0022a0001c0001t0032g0077a0001c0002t0002g0089others(8): Show | 11 | HG00673.hp2 HG01069.hp1 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.-4-10230_-4-10229i others(22): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26888255 | |||||
| chr2:26888255
|
T | TTCTTTCT others(17): Show |
4 | a0001c0001t0001g0059a0001c0001t0023g0021a0001c0002t0002g0086others(1): Show | 4 | HG01884.hp2 HG03139.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-4-10230_-4-10229i others(26): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26888255 | |||||
| chr2:26888255
|
T | TTCTTTCT others(19): Show |
1 | a0001c0007t0040g0169 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-4-10230_-4-10229i others(28): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26888255 | |||||
| chr2:26888255
|
T | TTCTTTCT others(21): Show |
1 | a0001c0001t0003g0072 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-4-10230_-4-10229i others(30): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26888255 | |||||
| chr2:26888265
|
C | CTTTCTTT others(5): Show |
1 | a0001c0001t0008g0067 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-4-10230_-4-10229i others(14): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26888265 | |||||
| chr2:26888265
|
C | G | 1 | a0001c0001t0013g0065 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-4-10231C>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26888265 | ||||||
| chr2:26888267
|
G | T | 1 | a0001c0001t0001g0138 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-4-10229G>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26888267 | ||||||
| chr2:26888506
|
A | C | 4 | a0001c0001t0008g0067a0001c0001t0009g0066a0001c0001t0009g0070others(1): Show | 4 | HG01109.hp2 HG02258.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-4-9990A>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26888506 | ||||||
| chr2:26888514
|
C | T | 1 | a0001c0001t0009g0039 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-4-9982C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26888514 | ||||||
| chr2:26888524
|
G | A | 1 | a0001c0002t0002g0132 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-4-9972G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26888524 | ||||||
| chr2:26888566
|
G | A | 2 | a0001c0001t0021g0006a0001c0001t0021g0007 | 2 | HG03540.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-4-9930G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26888566 | ||||||
| chr2:26888645
|
A | G | 4 | a0001c0001t0003g0003a0001c0001t0008g0004a0001c0001t0009g0001others(1): Show | 4 | HG02451.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4-9851A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26888645 | ||||||
| chr2:26888660
|
G | C | 1 | a0001c0001t0005g0017 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-4-9836G>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26888660 | ||||||
| chr2:26888782
|
C | T | 124 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(121): Show | 124 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-4-9714C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26888782 | ||||||
| chr2:26888783
|
A | G | 155 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(152): Show | 155 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.-4-9713A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26888783 | ||||||
| chr2:26888908
|
A | G | 4 | a0001c0001t0003g0003a0001c0001t0008g0004a0001c0001t0009g0001others(1): Show | 4 | HG02451.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4-9588A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26888908 | ||||||
| chr2:26888947
|
G | A | 1 | a0001c0001t0009g0001 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-4-9549G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26888947 | ||||||
| chr2:26889028
|
C | T | 1 | a0001c0002t0019g0122 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-4-9468C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26889028 | ||||||
| chr2:26889275
|
C | CT | 8 | a0001c0001t0001g0194a0001c0001t0003g0003a0001c0001t0008g0004others(5): Show | 8 | HG02451.hp2 HG02486.hp1 HG03209.hp2 others(5): Show |
intron_variant | MODIFIER | c.-4-9209dupT | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26889275 | |||||
| chr2:26889300
|
T | C | 4 | a0001c0001t0003g0003a0001c0001t0008g0004a0001c0001t0009g0001others(1): Show | 4 | HG02451.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4-9196T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26889300 | ||||||
| chr2:26889333
|
G | A | 8 | a0001c0001t0001g0059a0001c0002t0011g0060a0001c0002t0011g0061others(5): Show | 8 | HG00738.hp1 HG01884.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.-4-9163G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26889333 | ||||||
| chr2:26889370
|
C | T | 2 | a0001c0001t0021g0006a0001c0001t0021g0007 | 2 | HG03540.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-4-9126C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26889370 | ||||||
| chr2:26889494
|
TCTC | T | 5 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0023g0021others(2): Show | 5 | HG01884.hp1 HG01891.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4-8999_-4-8997del others(3): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26889494 | |||||
| chr2:26889561
|
C | T | 1 | a0002c0003t0006g0092 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-4-8935C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26889561 | ||||||
| chr2:26889612
|
A | G | 3 | a0001c0001t0013g0047a0001c0001t0013g0074a0001c0001t0013g0075 | 3 | HG00733.hp2 HG01167.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-4-8884A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26889612 | ||||||
| chr2:26889619
|
C | T | 1 | a0001c0001t0005g0207 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-4-8877C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26889619 | ||||||
| chr2:26889997
|
C | T | 1 | a0001c0002t0002g0103 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-4-8499C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26889997 | ||||||
| chr2:26890014
|
G | A | 1 | a0001c0001t0012g0030 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-4-8482G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26890014 | ||||||
| chr2:26890034
|
G | A | 4 | a0001c0001t0003g0003a0001c0001t0008g0004a0001c0001t0009g0001others(1): Show | 4 | HG02451.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4-8462G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26890034 | ||||||
| chr2:26890347
|
C | T | 231 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(228): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.-4-8149C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26890347 | ||||||
| chr2:26890513
|
C | T | 5 | a0001c0001t0003g0088a0001c0001t0003g0166a0001c0001t0003g0167others(2): Show | 5 | HG01891.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-4-7983C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26890513 | ||||||
| chr2:26890655
|
T | C | 4 | a0001c0001t0003g0003a0001c0001t0008g0004a0001c0001t0009g0001others(1): Show | 4 | HG02451.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4-7841T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26890655 | ||||||
| chr2:26890717
|
C | T | 3 | a0001c0001t0009g0066a0001c0001t0009g0070a0001c0001t0013g0065 | 3 | HG02258.hp2 HG02886.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-4-7779C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26890717 | ||||||
| chr2:26890841
|
C | G | 1 | a0001c0001t0009g0002 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-4-7655C>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26890841 | ||||||
| chr2:26891182
|
C | G | 1 | a0001c0001t0008g0004 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-4-7314C>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26891182 | ||||||
| chr2:26891915
|
C | T | 112 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(109): Show | 112 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.-4-6581C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26891915 | ||||||
| chr2:26892085
|
C | T | 4 | a0001c0001t0008g0067a0001c0001t0009g0066a0001c0001t0009g0070others(1): Show | 4 | HG01109.hp2 HG02258.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-4-6411C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26892085 | ||||||
| chr2:26892203
|
T | C | 2 | a0001c0002t0004g0229a0001c0002t0004g0230 | 2 | HG02630.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-4-6293T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26892203 | ||||||
| chr2:26892330
|
T | C | 1 | a0001c0002t0002g0040 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-4-6166T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26892330 | ||||||
| chr2:26892392
|
G | C | 12 | a0001c0001t0003g0003a0001c0001t0003g0088a0001c0001t0003g0166others(9): Show | 12 | HG01891.hp2 HG02451.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.-4-6104G>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26892392 | ||||||
| chr2:26892436
|
T | C | 109 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(106): Show | 109 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.-4-6060T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26892436 | ||||||
| chr2:26892502
|
A | G | 1 | a0001c0001t0001g0124 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-4-5994A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26892502 | ||||||
| chr2:26892756
|
T | TGA | 9 | a0001c0001t0003g0003a0001c0001t0008g0004a0001c0001t0009g0001others(6): Show | 9 | HG00280.hp2 HG01256.hp1 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.-4-5703_-4-5702dup others(2): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26892756 | |||||
| chr2:26892756
|
T | TGAGA | 11 | a0001c0001t0001g0009a0001c0001t0005g0016a0001c0001t0005g0017others(8): Show | 11 | HG01106.hp2 HG01346.hp1 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.-4-5705_-4-5702dup others(4): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26892756 | |||||
| chr2:26892756
|
T | TGAGAGA | 13 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0026others(10): Show | 13 | HG01074.hp2 HG01243.hp1 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.-4-5707_-4-5702dup others(6): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26892756 | |||||
| chr2:26892756
|
T | TGAGAGAG others(1): Show |
24 | a0001c0001t0001g0165a0001c0001t0001g0174a0001c0001t0001g0184others(21): Show | 24 | HG00280.hp1 HG00558.hp1 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.-4-5709_-4-5702dup others(8): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26892756 | |||||
| chr2:26892756
|
T | TGAGAGAG others(3): Show |
6 | a0001c0001t0001g0010a0001c0001t0001g0157a0001c0001t0001g0193others(3): Show | 6 | HG00099.hp1 HG01081.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.-4-5711_-4-5702dup others(10): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26892756 | |||||
| chr2:26892756
|
T | TGAGAGAG others(5): Show |
25 | a0001c0001t0001g0106a0001c0001t0001g0108a0001c0001t0001g0149others(22): Show | 25 | HG00597.hp1 HG00673.hp2 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.-4-5713_-4-5702dup others(12): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26892756 | |||||
| chr2:26892756
|
T | TGAGAGAG others(7): Show |
14 | a0001c0001t0001g0071a0001c0001t0001g0104a0001c0001t0001g0112others(11): Show | 14 | HG00140.hp1 HG00597.hp2 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.-4-5715_-4-5702dup others(14): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26892756 | |||||
| chr2:26892756
|
T | TGAGAGAG others(9): Show |
6 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0200others(3): Show | 6 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(3): Show |
intron_variant | MODIFIER | c.-4-5717_-4-5702dup others(16): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26892756 | |||||
| chr2:26892756
|
T | TGAGAGAG others(11): Show |
3 | a0001c0001t0001g0107a0001c0002t0002g0198a0001c0002t0004g0229 | 3 | HG02630.hp1 HG03492.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.-4-5719_-4-5702dup others(18): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26892756 | |||||
| chr2:26892756
|
T | TGAGAGAG others(17): Show |
1 | a0001c0001t0001g0204 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-4-5725_-4-5702dup others(24): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26892756 | |||||
| chr2:26892756
|
TGA | T | 20 | a0001c0001t0001g0124a0001c0002t0002g0097a0001c0002t0002g0101others(17): Show | 20 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(17): Show |
intron_variant | MODIFIER | c.-4-5703_-4-5702del others(2): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26892756 | |||||
| chr2:26892756
|
TGAGA | T | 53 | a0001c0001t0001g0059a0001c0001t0001g0138a0001c0001t0003g0072others(50): Show | 53 | HG00140.hp2 HG00639.hp1 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.-4-5705_-4-5702del others(4): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26892756 | |||||
| chr2:26892756
|
TGAGAGA | T | 10 | a0001c0001t0003g0088a0001c0001t0003g0166a0001c0001t0003g0167others(7): Show | 10 | HG01891.hp2 HG02486.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.-4-5707_-4-5702del others(6): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26892756 | |||||
| chr2:26892756
|
TGAGAGAG others(1): Show |
T | 2 | a0001c0001t0001g0115a0001c0002t0011g0060 | 2 | HG03471.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.-4-5709_-4-5702del others(8): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26892756 | |||||
| chr2:26892756
|
TGAGAGAG others(5): Show |
T | 1 | a0001c0002t0002g0134 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-4-5713_-4-5702del others(12): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26892756 | |||||
| chr2:26893145
|
T | C | 3 | a0001c0001t0013g0047a0001c0001t0013g0074a0001c0001t0013g0075 | 3 | HG00733.hp2 HG01167.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-4-5351T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26893145 | ||||||
| chr2:26893231
|
T | G | 1 | a0001c0002t0002g0136 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-4-5265T>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26893231 | ||||||
| chr2:26893621
|
G | A | 4 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0004t0003g0011others(1): Show | 4 | HG01934.hp2 HG02109.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4-4875G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26893621 | ||||||
| chr2:26893632
|
G | A | 2 | a0001c0001t0005g0016a0001c0001t0005g0017 | 2 | HG02280.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-4-4864G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26893632 | ||||||
| chr2:26894075
|
A | G | 2 | a0001c0002t0002g0128a0001c0002t0026g0144 | 2 | NA18954.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.-4-4421A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26894075 | ||||||
| chr2:26894089
|
T | C | 1 | a0001c0007t0040g0169 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-4-4407T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26894089 | ||||||
| chr2:26894462
|
G | A | 1 | a0001c0002t0004g0118 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-4-4034G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26894462 | ||||||
| chr2:26894530
|
A | G | 4 | a0001c0001t0008g0067a0001c0001t0009g0066a0001c0001t0009g0070others(1): Show | 4 | HG01109.hp2 HG02258.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-4-3966A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26894530 | ||||||
| chr2:26894594
|
T | G | 6 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(3): Show | 6 | HG02280.hp2 HG02622.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.-4-3902T>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26894594 | ||||||
| chr2:26894600
|
G | A | 1 | a0001c0001t0022g0188 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-4-3896G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26894600 | ||||||
| chr2:26894983
|
A | G | 1 | a0001c0002t0015g0043 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-4-3513A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26894983 | ||||||
| chr2:26895350
|
T | C | 1 | a0001c0001t0001g0199 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-4-3146T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26895350 | ||||||
| chr2:26895775
|
C | CT | 20 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0190others(17): Show | 20 | HG00280.hp1 HG00597.hp1 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.-4-2698dupT | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26895775 | |||||
| chr2:26895775
|
CT | C | 13 | a0001c0001t0001g0138a0001c0001t0001g0149a0001c0001t0001g0173others(10): Show | 13 | HG01069.hp1 HG01074.hp1 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.-4-2698delT | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26895775 | |||||
| chr2:26895778
|
T | TC | 4 | a0001c0001t0003g0003a0001c0001t0008g0004a0001c0001t0009g0001others(1): Show | 4 | HG02451.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4-2718_-4-2717ins others(1): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26895778 | ||||||
| chr2:26895780
|
T | TC | 2 | a0001c0001t0005g0081a0001c0001t0005g0170 | 2 | HG01496.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-4-2716_-4-2715ins others(1): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26895780 | ||||||
| chr2:26895781
|
T | C | 6 | a0001c0001t0001g0059a0001c0002t0002g0076a0001c0002t0002g0085others(3): Show | 6 | HG01884.hp2 HG02145.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-4-2715T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26895781 | ||||||
| chr2:26895806
|
C | T | 1 | a0001c0001t0001g0187 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-4-2690C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26895806 | ||||||
| chr2:26895811
|
C | T | 42 | a0001c0001t0001g0071a0001c0001t0001g0104a0001c0001t0001g0106others(39): Show | 42 | HG00099.hp1 HG00438.hp2 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.-4-2685C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26895811 | ||||||
| chr2:26895904
|
C | T | 2 | a0001c0001t0001g0014a0001c0005t0003g0015 | 2 | HG02622.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-4-2592C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26895904 | ||||||
| chr2:26895955
|
T | C | 5 | a0001c0001t0003g0088a0001c0001t0003g0166a0001c0001t0003g0167others(2): Show | 5 | HG01891.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-4-2541T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26895955 | ||||||
| chr2:26896224
|
C | T | 1 | a0001c0001t0016g0228 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-4-2272C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26896224 | ||||||
| chr2:26896379
|
T | G | 3 | a0001c0001t0001g0197a0001c0001t0001g0214a0001c0002t0018g0175 | 3 | HG00738.hp2 HG02015.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.-4-2117T>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26896379 | ||||||
| chr2:26896619
|
A | G | 1 | a0001c0001t0024g0036 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-4-1877A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26896619 | ||||||
| chr2:26896787
|
G | C | 134 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(131): Show | 134 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.-4-1709G>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26896787 | ||||||
| chr2:26896906
|
A | G | 4 | a0001c0001t0003g0003a0001c0001t0008g0004a0001c0001t0009g0001others(1): Show | 4 | HG02451.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4-1590A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26896906 | ||||||
| chr2:26896996
|
GA | G | 4 | a0001c0001t0003g0003a0001c0001t0008g0004a0001c0001t0009g0001others(1): Show | 4 | HG02451.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4-1493delA | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 26896996 | |||||
| chr2:26897044
|
T | A | 2 | a0001c0001t0021g0006a0001c0001t0021g0007 | 2 | HG03540.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-4-1452T>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26897044 | ||||||
| chr2:26897124
|
A | C | 1 | a0001c0001t0009g0039 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-4-1372A>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26897124 | ||||||
| chr2:26897238
|
C | T | 1 | a0001c0002t0002g0134 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-4-1258C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26897238 | ||||||
| chr2:26897370
|
T | G | 4 | a0001c0001t0003g0003a0001c0001t0008g0004a0001c0001t0009g0001others(1): Show | 4 | HG02451.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4-1126T>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26897370 | ||||||
| chr2:26897601
|
G | T | 1 | a0001c0001t0003g0020 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-4-895G>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26897601 | ||||||
| chr2:26897949
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-4-547C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26897949 | ||||||
| chr2:26898152
|
G | C | 3 | a0001c0002t0002g0035a0001c0002t0014g0034a0001c0002t0014g0037 | 3 | HG02486.hp1 HG06807.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-4-344G>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26898152 | ||||||
| chr2:26898288
|
C | T | 2 | a0001c0001t0021g0006a0001c0001t0021g0007 | 2 | HG03540.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-4-208C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26898288 | ||||||
| chr2:26898303
|
T | C | 4 | a0001c0001t0003g0003a0001c0001t0008g0004a0001c0001t0009g0001others(1): Show | 4 | HG02451.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4-193T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26898303 | ||||||
| chr2:26898424
|
T | C | 4 | a0001c0001t0003g0003a0001c0001t0008g0004a0001c0001t0009g0001others(1): Show | 4 | HG02451.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4-72T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26898424 | ||||||
| chr2:26898440
|
G | A | 1 | a0001c0001t0001g0201 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-4-56G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 1/12 | chr2 | 26898440 | ||||||
| chr2:26898921
|
G | A | 9 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0027others(6): Show | 9 | HG01891.hp2 HG02280.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.261+161G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26898921 | ||||||
| chr2:26899238
|
A | G | 4 | a0001c0001t0003g0003a0001c0001t0008g0004a0001c0001t0009g0001others(1): Show | 4 | HG02451.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.261+478A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26899238 | ||||||
| chr2:26899398
|
G | C | 1 | a0001c0001t0007g0185 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.261+638G>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26899398 | ||||||
| chr2:26899845
|
G | T | 5 | a0001c0002t0002g0082a0001c0002t0002g0091a0002c0003t0006g0079others(2): Show | 5 | HG00140.hp2 HG01069.hp1 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.261+1085G>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26899845 | ||||||
| chr2:26899855
|
G | A | 5 | a0001c0001t0003g0088a0001c0001t0003g0166a0001c0001t0003g0167others(2): Show | 5 | HG01891.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.261+1095G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26899855 | ||||||
| chr2:26900368
|
C | T | 5 | a0001c0002t0011g0060a0001c0002t0011g0061a0001c0002t0011g0062others(2): Show | 5 | HG00738.hp1 HG02897.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.261+1608C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26900368 | ||||||
| chr2:26900462
|
A | G | 1 | a0001c0001t0001g0014 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.261+1702A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26900462 | ||||||
| chr2:26900477
|
C | A | 1 | a0001c0002t0002g0128 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.261+1717C>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26900477 | ||||||
| chr2:26900893
|
A | G | 1 | a0001c0001t0007g0116 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.261+2133A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26900893 | ||||||
| chr2:26900947
|
C | T | 4 | a0001c0001t0003g0003a0001c0001t0008g0004a0001c0001t0009g0001others(1): Show | 4 | HG02451.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.261+2187C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26900947 | ||||||
| chr2:26901109
|
C | T | 4 | a0001c0001t0001g0200a0001c0002t0002g0035a0001c0002t0014g0034others(1): Show | 4 | HG02486.hp1 HG04204.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.261+2349C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26901109 | ||||||
| chr2:26901310
|
G | A | 2 | a0001c0001t0013g0074a0001c0001t0013g0075 | 2 | HG00733.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.261+2550G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26901310 | ||||||
| chr2:26901931
|
C | T | 1 | a0001c0001t0042g0216 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.261+3171C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26901931 | ||||||
| chr2:26902098
|
G | A | 2 | a0001c0002t0002g0040a0001c0002t0002g0041 | 2 | HG02109.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.261+3338G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26902098 | ||||||
| chr2:26902327
|
A | G | 1 | a0001c0002t0004g0142 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.261+3567A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26902327 | ||||||
| chr2:26902411
|
C | G | 2 | a0001c0001t0001g0014a0001c0005t0003g0015 | 2 | HG02622.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.261+3651C>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26902411 | ||||||
| chr2:26902429
|
T | C | 6 | a0001c0001t0003g0003a0001c0001t0008g0004a0001c0001t0009g0001others(3): Show | 6 | HG02109.hp1 HG02451.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.261+3669T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26902429 | ||||||
| chr2:26902598
|
T | C | 6 | a0001c0001t0003g0003a0001c0001t0008g0004a0001c0001t0009g0001others(3): Show | 6 | HG02109.hp1 HG02451.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.261+3838T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26902598 | ||||||
| chr2:26902630
|
C | T | 6 | a0001c0001t0003g0003a0001c0001t0008g0004a0001c0001t0009g0001others(3): Show | 6 | HG02109.hp1 HG02451.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.261+3870C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26902630 | ||||||
| chr2:26902814
|
C | T | 1 | a0001c0005t0003g0015 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.261+4054C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26902814 | ||||||
| chr2:26902964
|
C | G | 1 | a0001c0002t0004g0176 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.261+4204C>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26902964 | ||||||
| chr2:26903066
|
C | CT | 15 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0003g0072others(12): Show | 15 | HG01891.hp2 HG01934.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.261+4320dupT | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 26903066 | |||||
| chr2:26903066
|
CT | C | 8 | a0001c0001t0003g0003a0001c0001t0009g0001a0001c0001t0009g0002others(5): Show | 8 | HG01106.hp2 HG01257.hp2 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.261+4320delT | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 26903066 | |||||
| chr2:26903087
|
T | C | 4 | a0001c0001t0003g0003a0001c0001t0008g0004a0001c0001t0009g0001others(1): Show | 4 | HG02451.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.261+4327T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26903087 | ||||||
| chr2:26903159
|
G | T | 109 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0026others(106): Show | 109 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.261+4399G>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26903159 | ||||||
| chr2:26903222
|
A | T | 1 | a0001c0001t0016g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.261+4462A>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26903222 | ||||||
| chr2:26903689
|
GACCTTGC others(17): Show |
G | 115 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0026others(112): Show | 115 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.261+4954_261+4977d others(26): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 26903689 | |||||
| chr2:26903827
|
C | G | 14 | a0001c0001t0001g0138a0001c0001t0005g0081a0001c0001t0005g0170others(11): Show | 14 | HG00140.hp2 HG01361.hp1 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.261+5067C>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26903827 | ||||||
| chr2:26903866
|
T | A | 2 | a0001c0002t0004g0099a0001c0002t0004g0118 | 2 | NA18954.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.261+5106T>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26903866 | ||||||
| chr2:26903941
|
G | A | 6 | a0001c0001t0009g0039a0001c0001t0013g0047a0001c0001t0013g0074others(3): Show | 6 | HG00733.hp2 HG01167.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.261+5181G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26903941 | ||||||
| chr2:26903986
|
G | A | 1 | a0001c0007t0040g0169 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.261+5226G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26903986 | ||||||
| chr2:26904084
|
G | A | 3 | a0001c0002t0014g0034a0001c0002t0014g0037a0001c0002t0014g0038 | 3 | HG02486.hp1 HG03041.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.261+5324G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26904084 | ||||||
| chr2:26904259
|
G | A | 2 | a0001c0002t0006g0084a0001c0002t0029g0137 | 2 | HG01361.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.261+5499G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26904259 | ||||||
| chr2:26904269
|
C | T | 1 | a0001c0002t0014g0037 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.261+5509C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26904269 | ||||||
| chr2:26904383
|
T | C | 4 | a0001c0001t0001g0173a0001c0001t0001g0199a0001c0001t0001g0208others(1): Show | 4 | HG01358.hp1 HG02300.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.261+5623T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26904383 | ||||||
| chr2:26905211
|
C | T | 1 | a0001c0001t0009g0039 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.261+6451C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26905211 | ||||||
| chr2:26905214
|
C | G | 1 | a0001c0001t0007g0005 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.261+6454C>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26905214 | ||||||
| chr2:26905248
|
C | A | 1 | a0001c0001t0009g0039 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.261+6488C>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26905248 | ||||||
| chr2:26905468
|
G | A | 1 | a0001c0001t0009g0039 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.261+6708G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26905468 | ||||||
| chr2:26905661
|
T | C | 130 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(127): Show | 130 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.261+6901T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26905661 | ||||||
| chr2:26905697
|
G | T | 6 | a0001c0001t0009g0039a0001c0001t0013g0047a0001c0001t0013g0074others(3): Show | 6 | HG00733.hp2 HG01167.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.261+6937G>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26905697 | ||||||
| chr2:26905714
|
G | C | 1 | a0001c0002t0020g0057 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.261+6954G>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26905714 | ||||||
| chr2:26905905
|
C | T | 1 | a0001c0007t0040g0169 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.261+7145C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26905905 | ||||||
| chr2:26905966
|
G | A | 108 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0026others(105): Show | 108 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.261+7206G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26905966 | ||||||
| chr2:26906008
|
G | A | 1 | a0001c0001t0001g0115 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.261+7248G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26906008 | ||||||
| chr2:26906045
|
G | A | 1 | a0001c0001t0003g0068 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.261+7285G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26906045 | ||||||
| chr2:26906186
|
C | CT | 108 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0026others(105): Show | 108 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.261+7442dupT | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 26906186 | |||||
| chr2:26906218
|
T | A | 2 | a0001c0001t0009g0066a0001c0001t0009g0070 | 2 | HG02258.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.261+7458T>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26906218 | ||||||
| chr2:26906340
|
C | T | 1 | a0001c0001t0003g0012 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.261+7580C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26906340 | ||||||
| chr2:26906441
|
A | C | 115 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0026others(112): Show | 115 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.261+7681A>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26906441 | ||||||
| chr2:26906761
|
A | C | 7 | a0001c0001t0009g0039a0001c0001t0013g0047a0001c0001t0013g0074others(4): Show | 7 | HG00733.hp2 HG01167.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.261+8001A>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26906761 | ||||||
| chr2:26906793
|
C | T | 3 | a0001c0001t0010g0031a0001c0001t0010g0033a0001c0001t0025g0032 | 3 | HG01106.hp2 HG01346.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.261+8033C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26906793 | ||||||
| chr2:26906867
|
A | C | 115 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0026others(112): Show | 115 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.261+8107A>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26906867 | ||||||
| chr2:26907091
|
C | T | 1 | a0001c0001t0001g0223 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.261+8331C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26907091 | ||||||
| chr2:26907100
|
T | TTTTA | 109 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0026others(106): Show | 109 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.261+8360_261+8363d others(6): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 26907100 | |||||
| chr2:26907302
|
C | T | 1 | a0001c0002t0002g0136 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.261+8542C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26907302 | ||||||
| chr2:26907303
|
G | A | 1 | a0001c0001t0001g0199 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.261+8543G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26907303 | ||||||
| chr2:26907333
|
C | T | 2 | a0001c0002t0004g0099a0001c0002t0004g0118 | 2 | NA18954.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.261+8573C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26907333 | ||||||
| chr2:26907389
|
C | T | 4 | a0001c0001t0003g0003a0001c0001t0008g0004a0001c0001t0009g0001others(1): Show | 4 | HG02451.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.261+8629C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26907389 | ||||||
| chr2:26907453
|
C | G | 6 | a0001c0001t0009g0039a0001c0001t0013g0047a0001c0001t0013g0074others(3): Show | 6 | HG00733.hp2 HG01167.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.261+8693C>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26907453 | ||||||
| chr2:26907464
|
C | T | 105 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0026others(102): Show | 105 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.261+8704C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26907464 | ||||||
| chr2:26907705
|
G | A | 2 | a0001c0001t0010g0028a0001c0001t0010g0226 | 2 | HG02809.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.261+8945G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26907705 | ||||||
| chr2:26907863
|
C | A | 1 | a0001c0001t0008g0004 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.261+9103C>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26907863 | ||||||
| chr2:26907898
|
G | A | 2 | a0001c0004t0003g0011a0001c0004t0003g0064 | 2 | HG02109.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.261+9138G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26907898 | ||||||
| chr2:26907918
|
G | A | 1 | a0001c0001t0005g0206 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.261+9158G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26907918 | ||||||
| chr2:26908023
|
T | C | 109 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0026others(106): Show | 109 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.261+9263T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26908023 | ||||||
| chr2:26908154
|
A | G | 109 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0026others(106): Show | 109 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.261+9394A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26908154 | ||||||
| chr2:26908268
|
C | T | 2 | a0001c0001t0012g0048a0001c0001t0012g0051 | 2 | HG00639.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.261+9508C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26908268 | ||||||
| chr2:26908269
|
G | A | 1 | a0001c0002t0002g0076 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.261+9509G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26908269 | ||||||
| chr2:26908294
|
A | T | 2 | a0001c0004t0003g0011a0001c0004t0003g0064 | 2 | HG02109.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.261+9534A>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26908294 | ||||||
| chr2:26908492
|
G | A | 1 | a0001c0001t0032g0077 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.261+9732G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26908492 | ||||||
| chr2:26908511
|
T | C | 1 | a0001c0002t0006g0069 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.261+9751T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26908511 | ||||||
| chr2:26908817
|
A | G | 1 | a0001c0002t0031g0073 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.261+10057A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26908817 | ||||||
| chr2:26908981
|
T | G | 107 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0026others(104): Show | 107 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.261+10221T>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26908981 | ||||||
| chr2:26909504
|
C | T | 1 | a0001c0001t0032g0077 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.261+10744C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26909504 | ||||||
| chr2:26909653
|
G | A | 6 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0020others(3): Show | 6 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.261+10893G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26909653 | ||||||
| chr2:26909730
|
A | G | 6 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0020others(3): Show | 6 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.261+10970A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26909730 | ||||||
| chr2:26909773
|
CA | C | 113 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0026others(110): Show | 113 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.261+11023delA | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 26909773 | |||||
| chr2:26909954
|
A | T | 130 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(127): Show | 130 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.261+11194A>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26909954 | ||||||
| chr2:26910116
|
C | T | 11 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0003g0072others(8): Show | 11 | HG01891.hp2 HG01934.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.261+11356C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26910116 | ||||||
| chr2:26910345
|
C | T | 2 | a0001c0001t0003g0168a0001c0001t0003g0171 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.261+11585C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26910345 | ||||||
| chr2:26910384
|
T | C | 4 | a0001c0001t0003g0003a0001c0001t0008g0004a0001c0001t0009g0001others(1): Show | 4 | HG02451.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.261+11624T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26910384 | ||||||
| chr2:26910408
|
G | A | 4 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0027others(1): Show | 4 | HG02280.hp1 HG02451.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.261+11648G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26910408 | ||||||
| chr2:26910546
|
G | A | 2 | a0001c0002t0039g0019a0001c0007t0040g0169 | 2 | HG02970.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.261+11786G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26910546 | ||||||
| chr2:26910590
|
G | A | 2 | a0001c0001t0021g0006a0001c0001t0021g0007 | 2 | HG03540.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.261+11830G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26910590 | ||||||
| chr2:26910616
|
C | CT | 14 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0027others(11): Show | 14 | HG01106.hp2 HG01346.hp1 HG01515.hp1 others(11): Show |
intron_variant | MODIFIER | c.261+11875dupT | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 26910616 | |||||
| chr2:26910616
|
C | CTT | 90 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0100others(87): Show | 90 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.261+11874_261+1187 others(6): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 26910616 | |||||
| chr2:26910616
|
C | CTTT | 5 | a0001c0001t0001g0173a0001c0001t0013g0047a0001c0001t0013g0074others(2): Show | 5 | HG00733.hp2 HG01167.hp2 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.261+11873_261+1187 others(7): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 26910616 | |||||
| chr2:26910619
|
T | C | 4 | a0001c0001t0003g0003a0001c0001t0008g0004a0001c0001t0009g0001others(1): Show | 4 | HG02451.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.261+11859T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26910619 | ||||||
| chr2:26910702
|
G | A | 3 | a0001c0001t0001g0014a0001c0001t0007g0005a0001c0005t0003g0015 | 3 | HG02622.hp2 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.261+11942G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26910702 | ||||||
| chr2:26910744
|
C | T | 1 | a0001c0001t0001g0197 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.261+11984C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26910744 | ||||||
| chr2:26911056
|
A | T | 4 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0027others(1): Show | 4 | HG02280.hp1 HG02451.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.261+12296A>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26911056 | ||||||
| chr2:26911066
|
G | T | 102 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0026others(99): Show | 102 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.261+12306G>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26911066 | ||||||
| chr2:26911079
|
G | GT | 89 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0027others(86): Show | 89 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.261+12338dupT | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 26911079 | |||||
| chr2:26911079
|
G | GTT | 43 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0059others(40): Show | 43 | HG00597.hp1 HG00597.hp2 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.261+12337_261+1233 others(6): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 26911079 | |||||
| chr2:26911079
|
G | GTTT | 9 | a0001c0001t0001g0201a0001c0001t0007g0114a0001c0001t0013g0047others(6): Show | 9 | HG00438.hp2 HG00673.hp2 HG00733.hp2 others(6): Show |
intron_variant | MODIFIER | c.261+12336_261+1233 others(7): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 26911079 | |||||
| chr2:26911114
|
A | G | 2 | a0001c0004t0003g0011a0001c0004t0003g0064 | 2 | HG02109.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.261+12354A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26911114 | ||||||
| chr2:26911177
|
G | A | 2 | a0001c0002t0015g0042a0001c0002t0015g0043 | 2 | HG01074.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.261+12417G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26911177 | ||||||
| chr2:26911363
|
A | G | 7 | a0001c0001t0009g0039a0001c0001t0013g0047a0001c0001t0013g0074others(4): Show | 7 | HG00733.hp2 HG01167.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.261+12603A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26911363 | ||||||
| chr2:26911380
|
CAT | C | 102 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0026others(99): Show | 102 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.261+12622_261+1262 others(6): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 26911380 | |||||
| chr2:26911754
|
T | G | 1 | a0001c0002t0002g0035 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.261+12994T>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26911754 | ||||||
| chr2:26911849
|
C | A | 4 | a0001c0001t0003g0003a0001c0001t0008g0004a0001c0001t0009g0001others(1): Show | 4 | HG02451.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.262-13038C>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26911849 | ||||||
| chr2:26912002
|
C | T | 1 | a0001c0002t0002g0035 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.262-12885C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26912002 | ||||||
| chr2:26912057
|
C | T | 102 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0026others(99): Show | 102 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.262-12830C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26912057 | ||||||
| chr2:26912086
|
C | G | 1 | a0001c0001t0001g0014 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.262-12801C>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26912086 | ||||||
| chr2:26912165
|
G | A | 1 | a0001c0002t0015g0043 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.262-12722G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26912165 | ||||||
| chr2:26912269
|
G | C | 1 | a0001c0001t0008g0067 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.262-12618G>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26912269 | ||||||
| chr2:26912342
|
C | G | 1 | a0001c0001t0003g0166 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.262-12545C>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26912342 | ||||||
| chr2:26912501
|
TC | T | 3 | a0001c0001t0001g0014a0001c0001t0007g0005a0001c0005t0003g0015 | 3 | HG02622.hp2 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.262-12383delC | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 26912501 | |||||
| chr2:26913004
|
C | A | 1 | a0001c0002t0004g0095 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.262-11883C>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26913004 | ||||||
| chr2:26913107
|
T | C | 4 | a0001c0001t0013g0047a0001c0001t0013g0074a0001c0001t0013g0075others(1): Show | 4 | HG00733.hp2 HG01167.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.262-11780T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26913107 | ||||||
| chr2:26913159
|
T | C | 6 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0020others(3): Show | 6 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.262-11728T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26913159 | ||||||
| chr2:26913466
|
T | C | 4 | a0001c0001t0003g0003a0001c0001t0008g0004a0001c0001t0009g0001others(1): Show | 4 | HG02451.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.262-11421T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26913466 | ||||||
| chr2:26913560
|
A | G | 2 | a0001c0004t0003g0011a0001c0004t0003g0064 | 2 | HG02109.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.262-11327A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26913560 | ||||||
| chr2:26913748
|
A | G | 2 | a0001c0004t0003g0011a0001c0004t0003g0064 | 2 | HG02109.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.262-11139A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26913748 | ||||||
| chr2:26913752
|
A | G | 2 | a0001c0001t0003g0168a0001c0001t0003g0171 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.262-11135A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26913752 | ||||||
| chr2:26913952
|
T | TA | 92 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0027others(89): Show | 92 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.262-10917dupA | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 26913952 | |||||
| chr2:26913952
|
TA | T | 40 | a0001c0001t0001g0014a0001c0001t0003g0003a0001c0001t0003g0012others(37): Show | 40 | HG00639.hp1 HG00733.hp2 HG01106.hp2 others(37): Show |
intron_variant | MODIFIER | c.262-10917delA | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 26913952 | |||||
| chr2:26914022
|
C | G | 4 | a0001c0001t0003g0003a0001c0001t0008g0004a0001c0001t0009g0001others(1): Show | 4 | HG02451.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.262-10865C>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26914022 | ||||||
| chr2:26914402
|
C | T | 3 | a0001c0001t0010g0031a0001c0001t0010g0033a0001c0001t0025g0032 | 3 | HG01106.hp2 HG01346.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.262-10485C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26914402 | ||||||
| chr2:26914439
|
C | T | 109 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0026others(106): Show | 109 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.262-10448C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26914439 | ||||||
| chr2:26914650
|
T | C | 1 | a0001c0001t0021g0006 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.262-10237T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26914650 | ||||||
| chr2:26914748
|
G | A | 109 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0026others(106): Show | 109 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.262-10139G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26914748 | ||||||
| chr2:26914803
|
C | T | 113 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0026others(110): Show | 113 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.262-10084C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26914803 | ||||||
| chr2:26915048
|
A | G | 1 | a0001c0001t0033g0052 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.262-9839A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26915048 | ||||||
| chr2:26915248
|
G | A | 1 | a0001c0002t0002g0146 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.262-9639G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26915248 | ||||||
| chr2:26915417
|
G | A | 113 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0026others(110): Show | 113 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.262-9470G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26915417 | ||||||
| chr2:26915633
|
C | T | 2 | a0001c0002t0004g0099a0001c0002t0004g0118 | 2 | NA18954.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.262-9254C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26915633 | ||||||
| chr2:26915726
|
C | A | 105 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0026others(102): Show | 105 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.262-9161C>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26915726 | ||||||
| chr2:26915952
|
G | T | 2 | a0001c0001t0003g0003a0001c0001t0009g0002 | 2 | HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.262-8935G>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26915952 | ||||||
| chr2:26916043
|
T | C | 102 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0026others(99): Show | 102 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.262-8844T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26916043 | ||||||
| chr2:26916195
|
A | T | 1 | a0001c0001t0032g0077 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.262-8692A>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26916195 | ||||||
| chr2:26916437
|
T | C | 79 | a0001c0001t0001g0059a0001c0001t0001g0071a0001c0001t0001g0100others(76): Show | 79 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.262-8450T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26916437 | ||||||
| chr2:26916879
|
C | A | 112 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0026others(109): Show | 112 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.262-8008C>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26916879 | ||||||
| chr2:26916935
|
G | T | 3 | a0001c0001t0001g0199a0001c0001t0001g0208a0001c0001t0001g0209 | 3 | HG01358.hp1 HG02886.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.262-7952G>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26916935 | ||||||
| chr2:26917020
|
C | T | 101 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0005g0081others(98): Show | 101 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.262-7867C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26917020 | ||||||
| chr2:26917154
|
C | T | 116 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0026others(113): Show | 116 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.262-7733C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26917154 | ||||||
| chr2:26917231
|
A | C | 112 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0026others(109): Show | 112 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.262-7656A>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26917231 | ||||||
| chr2:26917437
|
A | G | 1 | a0001c0001t0005g0081 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.262-7450A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26917437 | ||||||
| chr2:26917474
|
C | T | 105 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0026others(102): Show | 105 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.262-7413C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26917474 | ||||||
| chr2:26917544
|
G | T | 4 | a0001c0001t0003g0003a0001c0001t0008g0004a0001c0001t0009g0001others(1): Show | 4 | HG02451.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.262-7343G>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26917544 | ||||||
| chr2:26917665
|
G | C | 7 | a0001c0001t0013g0047a0001c0001t0013g0074a0001c0001t0013g0075others(4): Show | 7 | HG00733.hp2 HG01167.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.262-7222G>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26917665 | ||||||
| chr2:26917705
|
C | T | 79 | a0001c0001t0001g0059a0001c0001t0001g0071a0001c0001t0001g0100others(76): Show | 79 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.262-7182C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26917705 | ||||||
| chr2:26917768
|
G | A | 3 | a0001c0002t0014g0034a0001c0002t0014g0037a0001c0002t0014g0038 | 3 | HG02486.hp1 HG03041.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.262-7119G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26917768 | ||||||
| chr2:26917820
|
T | C | 1 | a0001c0002t0006g0130 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.262-7067T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26917820 | ||||||
| chr2:26917873
|
C | T | 112 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0026others(109): Show | 112 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.262-7014C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26917873 | ||||||
| chr2:26918069
|
G | A | 5 | a0001c0001t0013g0047a0001c0001t0013g0074a0001c0001t0013g0075others(2): Show | 5 | HG00733.hp2 HG01167.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.262-6818G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26918069 | ||||||
| chr2:26918087
|
G | A | 1 | a0001c0001t0009g0039 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.262-6800G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26918087 | ||||||
| chr2:26918104
|
C | G | 3 | a0001c0002t0014g0034a0001c0002t0014g0037a0001c0002t0014g0038 | 3 | HG02486.hp1 HG03041.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.262-6783C>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26918104 | ||||||
| chr2:26918135
|
C | CA | 5 | a0001c0001t0003g0166a0001c0001t0003g0167a0001c0002t0006g0080others(2): Show | 5 | HG01891.hp2 HG02109.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.262-6725dupA | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 26918135 | |||||
| chr2:26918135
|
CA | C | 107 | a0001c0001t0001g0112a0001c0001t0001g0115a0001c0001t0001g0138others(104): Show | 107 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.262-6725delA | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 26918135 | |||||
| chr2:26918135
|
CAA | C | 80 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0026others(77): Show | 80 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.262-6726_262-6725d others(4): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 26918135 | |||||
| chr2:26918135
|
CAAA | C | 8 | a0001c0001t0001g0181a0001c0001t0003g0003a0001c0001t0008g0004others(5): Show | 8 | HG01361.hp1 HG01433.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.262-6727_262-6725d others(5): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 26918135 | |||||
| chr2:26918135
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0002t0006g0069 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.262-6735_262-6725d others(13): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 26918135 | |||||
| chr2:26918281
|
G | A | 7 | a0001c0001t0013g0047a0001c0001t0013g0074a0001c0001t0013g0075others(4): Show | 7 | HG00733.hp2 HG01167.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.262-6606G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26918281 | ||||||
| chr2:26918316
|
A | G | 4 | a0001c0002t0002g0076a0001c0002t0002g0085a0001c0002t0002g0163others(1): Show | 4 | HG02145.hp2 HG02257.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.262-6571A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26918316 | ||||||
| chr2:26918397
|
G | A | 4 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0027others(1): Show | 4 | HG02280.hp1 HG02451.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.262-6490G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26918397 | ||||||
| chr2:26918432
|
G | A | 1 | a0001c0002t0015g0043 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.262-6455G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26918432 | ||||||
| chr2:26918481
|
TTTC | T | 112 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0026others(109): Show | 112 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.262-6405_262-6403d others(5): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26918481 | ||||||
| chr2:26918491
|
T | A | 101 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0026others(98): Show | 101 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.262-6396T>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26918491 | ||||||
| chr2:26918503
|
A | G | 3 | a0001c0002t0014g0034a0001c0002t0014g0037a0001c0002t0014g0038 | 3 | HG02486.hp1 HG03041.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.262-6384A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26918503 | ||||||
| chr2:26918515
|
G | C | 4 | a0001c0001t0003g0003a0001c0001t0008g0004a0001c0001t0009g0001others(1): Show | 4 | HG02451.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.262-6372G>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26918515 | ||||||
| chr2:26918636
|
C | T | 116 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0026others(113): Show | 116 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.262-6251C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26918636 | ||||||
| chr2:26918647
|
A | C | 112 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0026others(109): Show | 112 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.262-6240A>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26918647 | ||||||
| chr2:26918716
|
T | A | 37 | a0001c0001t0001g0115a0001c0001t0001g0124a0001c0001t0001g0156others(34): Show | 37 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.262-6171T>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26918716 | ||||||
| chr2:26918949
|
A | C | 2 | a0001c0002t0004g0229a0001c0002t0004g0230 | 2 | HG02630.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.262-5938A>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26918949 | ||||||
| chr2:26919053
|
A | C | 221 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(218): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.262-5834A>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26919053 | ||||||
| chr2:26919115
|
C | T | 8 | a0001c0002t0011g0060a0001c0002t0011g0061a0001c0002t0011g0062others(5): Show | 8 | HG00738.hp1 HG02897.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.262-5772C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26919115 | ||||||
| chr2:26919223
|
G | A | 99 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0008g0004others(96): Show | 99 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.262-5664G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26919223 | ||||||
| chr2:26919300
|
G | A | 1 | a0001c0001t0003g0167 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.262-5587G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26919300 | ||||||
| chr2:26919923
|
G | A | 1 | a0001c0002t0002g0094 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.262-4964G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26919923 | ||||||
| chr2:26919936
|
A | G | 1 | a0001c0001t0032g0077 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.262-4951A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26919936 | ||||||
| chr2:26919990
|
A | G | 3 | a0001c0001t0001g0173a0001c0001t0022g0188a0001c0001t0022g0210 | 3 | HG02145.hp1 HG02258.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.262-4897A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26919990 | ||||||
| chr2:26920033
|
T | A | 5 | a0001c0001t0013g0047a0001c0001t0013g0065a0001c0001t0013g0074others(2): Show | 5 | HG00733.hp2 HG01167.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.262-4854T>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26920033 | ||||||
| chr2:26920179
|
CT | C | 221 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(218): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.262-4699delT | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 26920179 | |||||
| chr2:26920188
|
T | A | 102 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0138others(99): Show | 102 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.262-4699T>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26920188 | ||||||
| chr2:26920385
|
C | T | 220 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(217): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.262-4502C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26920385 | ||||||
| chr2:26920408
|
A | G | 2 | a0001c0002t0002g0119a0001c0002t0002g0135 | 2 | HG03492.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.262-4479A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26920408 | ||||||
| chr2:26920594
|
C | T | 2 | a0001c0001t0003g0068a0001c0001t0009g0039 | 2 | HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.262-4293C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26920594 | ||||||
| chr2:26920774
|
A | G | 3 | a0001c0002t0014g0034a0001c0002t0014g0037a0001c0002t0014g0038 | 3 | HG02486.hp1 HG03041.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.262-4113A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26920774 | ||||||
| chr2:26920903
|
C | T | 8 | a0001c0001t0013g0047a0001c0001t0013g0065a0001c0001t0013g0074others(5): Show | 8 | HG00733.hp2 HG01167.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.262-3984C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26920903 | ||||||
| chr2:26920938
|
A | T | 10 | a0001c0001t0003g0068a0001c0001t0009g0039a0001c0001t0013g0047others(7): Show | 10 | HG00733.hp2 HG01167.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.262-3949A>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26920938 | ||||||
| chr2:26921174
|
C | A | 2 | a0001c0001t0003g0068a0001c0001t0009g0039 | 2 | HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.262-3713C>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26921174 | ||||||
| chr2:26921221
|
C | T | 10 | a0001c0001t0003g0068a0001c0001t0009g0039a0001c0001t0013g0047others(7): Show | 10 | HG00733.hp2 HG01167.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.262-3666C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26921221 | ||||||
| chr2:26921269
|
C | T | 1 | a0001c0001t0024g0049 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.262-3618C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26921269 | ||||||
| chr2:26921441
|
T | TAAACATC others(2256): Show |
3 | a0001c0001t0003g0003a0001c0001t0009g0001a0001c0001t0009g0002 | 3 | HG02451.hp2 HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.262-3431_262-3430i others(2265): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 26921441 | |||||
| chr2:26921459
|
A | G | 7 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0013g0047others(4): Show | 7 | HG00733.hp2 HG01167.hp2 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.262-3428A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26921459 | ||||||
| chr2:26921465
|
C | T | 2 | a0001c0002t0015g0042a0001c0002t0015g0043 | 2 | HG01074.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.262-3422C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26921465 | ||||||
| chr2:26921495
|
C | G | 1 | a0001c0001t0003g0068 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.262-3392C>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26921495 | ||||||
| chr2:26921639
|
G | A | 2 | a0001c0001t0001g0009a0001c0001t0001g0010 | 2 | HG01934.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.262-3248G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26921639 | ||||||
| chr2:26921734
|
C | T | 1 | a0001c0002t0014g0037 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.262-3153C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26921734 | ||||||
| chr2:26921815
|
C | G | 1 | a0001c0002t0006g0080 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.262-3072C>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26921815 | ||||||
| chr2:26921990
|
G | C | 7 | a0001c0001t0001g0115a0001c0001t0001g0156a0001c0001t0001g0165others(4): Show | 7 | NA18949.hp2 NA18952.hp1 NA18982.hp1 others(4): Show |
intron_variant | MODIFIER | c.262-2897G>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26921990 | ||||||
| chr2:26922701
|
A | G | 223 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(220): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.262-2186A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26922701 | ||||||
| chr2:26923164
|
CAG | C | 2 | a0001c0002t0004g0142a0001c0002t0017g0159 | 2 | HG01256.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.262-1721_262-1720d others(4): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 26923164 | |||||
| chr2:26923258
|
G | A | 5 | a0001c0001t0010g0028a0001c0001t0010g0031a0001c0001t0010g0033others(2): Show | 5 | HG01106.hp2 HG01346.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.262-1629G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26923258 | ||||||
| chr2:26923293
|
T | C | 1 | a0001c0001t0032g0077 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.262-1594T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26923293 | ||||||
| chr2:26923629
|
T | C | 1 | a0001c0001t0024g0036 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.262-1258T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26923629 | ||||||
| chr2:26923740
|
G | T | 2 | a0001c0001t0001g0009a0001c0001t0001g0010 | 2 | HG01934.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.262-1147G>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26923740 | ||||||
| chr2:26923770
|
C | T | 1 | a0001c0001t0021g0007 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.262-1117C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26923770 | ||||||
| chr2:26924404
|
A | G | 86 | a0001c0001t0001g0059a0001c0001t0001g0071a0001c0001t0001g0100others(83): Show | 86 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.262-483A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26924404 | ||||||
| chr2:26924475
|
TTA | T | 2 | a0001c0002t0002g0045a0001c0002t0002g0090 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.262-410_262-409del others(2): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 26924475 | |||||
| chr2:26924638
|
C | T | 9 | a0001c0001t0001g0124a0001c0001t0001g0219a0001c0001t0001g0222others(6): Show | 9 | HG00597.hp1 HG01074.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.262-249C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26924638 | ||||||
| chr2:26924809
|
T | C | 1 | a0001c0001t0001g0115 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.262-78T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26924809 | ||||||
| chr2:26924874
|
C | T | 1 | a0001c0001t0032g0077 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.262-13C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 2/12 | chr2 | 26924874 | ||||||
| chr2:26925061
|
G | A | 1 | a0001c0001t0021g0006 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.420+16G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 3/12 | chr2 | 26925061 | ||||||
| chr2:26925280
|
A | G | 1 | a0001c0002t0002g0134 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.420+235A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 3/12 | chr2 | 26925280 | ||||||
| chr2:26925466
|
G | T | 2 | a0001c0001t0001g0009a0001c0001t0001g0010 | 2 | HG01934.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.420+421G>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 3/12 | chr2 | 26925466 | ||||||
| chr2:26925596
|
A | G | 225 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(222): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.420+551A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 3/12 | chr2 | 26925596 | ||||||
| chr2:26925786
|
C | CT | 108 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0026others(105): Show | 108 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.420+747dupT | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 26925786 | |||||
| chr2:26925828
|
C | G | 5 | a0001c0001t0013g0047a0001c0001t0013g0065a0001c0001t0013g0074others(2): Show | 5 | HG00733.hp2 HG01167.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.420+783C>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 3/12 | chr2 | 26925828 | ||||||
| chr2:26926120
|
C | A | 3 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0032g0077 | 3 | HG01934.hp2 NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.420+1075C>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 3/12 | chr2 | 26926120 | ||||||
| chr2:26926157
|
G | A | 1 | a0001c0001t0001g0201 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.421-1096G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 3/12 | chr2 | 26926157 | ||||||
| chr2:26926192
|
C | G | 1 | a0001c0001t0032g0077 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.421-1061C>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 3/12 | chr2 | 26926192 | ||||||
| chr2:26926357
|
C | G | 1 | a0001c0001t0032g0077 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.421-896C>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 3/12 | chr2 | 26926357 | ||||||
| chr2:26926390
|
T | A | 123 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0026others(120): Show | 123 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.421-863T>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 3/12 | chr2 | 26926390 | ||||||
| chr2:26926463
|
A | C | 2 | a0001c0001t0001g0009a0001c0001t0001g0010 | 2 | HG01934.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.421-790A>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 3/12 | chr2 | 26926463 | ||||||
| chr2:26926490
|
A | G | 2 | a0001c0001t0001g0009a0001c0001t0001g0010 | 2 | HG01934.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.421-763A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 3/12 | chr2 | 26926490 | ||||||
| chr2:26926498
|
A | T | 109 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0026others(106): Show | 109 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.421-755A>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 3/12 | chr2 | 26926498 | ||||||
| chr2:26926639
|
A | G | 1 | a0001c0001t0001g0193 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.421-614A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 3/12 | chr2 | 26926639 | ||||||
| chr2:26926743
|
A | T | 5 | a0001c0001t0010g0028a0001c0001t0010g0031a0001c0001t0010g0033others(2): Show | 5 | HG01106.hp2 HG01346.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.421-510A>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 3/12 | chr2 | 26926743 | ||||||
| chr2:26927040
|
G | C | 1 | a0001c0001t0032g0077 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.421-213G>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 3/12 | chr2 | 26927040 | ||||||
| chr2:26927121
|
G | C | 1 | a0001c0002t0002g0035 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.421-132G>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 3/12 | chr2 | 26927121 | ||||||
| chr2:26927235
|
C | T | 13 | a0001c0001t0003g0068a0001c0001t0009g0039a0001c0001t0013g0047others(10): Show | 13 | HG00733.hp2 HG01167.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.421-18C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 3/12 | chr2 | 26927235 | ||||||
| chr2:26927479
|
CAGTT | C | 13 | a0001c0001t0003g0068a0001c0001t0009g0039a0001c0001t0013g0047others(10): Show | 13 | HG00733.hp2 HG01167.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.600+52_600+55delAG others(2): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr2 | 26927479 | |||||
| chr2:26927633
|
T | G | 1 | a0001c0001t0032g0077 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.600+201T>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 4/12 | chr2 | 26927633 | ||||||
| chr2:26927692
|
A | G | 2 | a0001c0001t0009g0066a0001c0001t0009g0070 | 2 | HG02258.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.600+260A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 4/12 | chr2 | 26927692 | ||||||
| chr2:26927861
|
A | C | 2 | a0001c0001t0001g0009a0001c0001t0001g0010 | 2 | HG01934.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.601-394A>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 4/12 | chr2 | 26927861 | ||||||
| chr2:26928023
|
G | A | 105 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0026others(102): Show | 105 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.601-232G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 4/12 | chr2 | 26928023 | ||||||
| chr2:26928049
|
G | A | 1 | a0001c0001t0005g0203 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.601-206G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 4/12 | chr2 | 26928049 | ||||||
| chr2:26928083
|
G | A | 13 | a0001c0001t0003g0068a0001c0001t0009g0039a0001c0001t0013g0047others(10): Show | 13 | HG00733.hp2 HG01167.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.601-172G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 4/12 | chr2 | 26928083 | ||||||
| chr2:26928141
|
C | A | 13 | a0001c0001t0003g0068a0001c0001t0009g0039a0001c0001t0013g0047others(10): Show | 13 | HG00733.hp2 HG01167.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.601-114C>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 4/12 | chr2 | 26928141 | ||||||
| chr2:26928181
|
T | A | 9 | a0001c0001t0003g0068a0001c0001t0009g0039a0001c0001t0013g0047others(6): Show | 9 | HG00733.hp2 HG01167.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.601-74T>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 4/12 | chr2 | 26928181 | ||||||
| chr2:26928185
|
T | C | 1 | a0001c0001t0032g0077 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.601-70T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 4/12 | chr2 | 26928185 | ||||||
| chr2:26928200
|
T | C | 1 | a0001c0002t0014g0038 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.601-55T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 4/12 | chr2 | 26928200 | ||||||
| chr2:26928208
|
G | A | 2 | a0001c0002t0002g0040a0001c0002t0002g0041 | 2 | HG02109.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.601-47G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 4/12 | chr2 | 26928208 | ||||||
| chr2:26928486
|
G | A | 13 | a0001c0001t0003g0068a0001c0001t0009g0039a0001c0001t0013g0047others(10): Show | 13 | HG00733.hp2 HG01167.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.669+163G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | chr2 | 26928486 | ||||||
| chr2:26928551
|
A | G | 5 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0001t0001g0107others(2): Show | 5 | HG02040.hp2 NA18955.hp2 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.669+228A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | chr2 | 26928551 | ||||||
| chr2:26928650
|
C | T | 1 | a0001c0001t0032g0077 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.669+327C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | chr2 | 26928650 | ||||||
| chr2:26928687
|
G | GTA | 71 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0026others(68): Show | 71 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.669+381_669+382dup others(2): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26928687 | |||||
| chr2:26928687
|
G | GTATA | 5 | a0001c0001t0001g0201a0001c0001t0005g0081a0001c0001t0005g0170others(2): Show | 5 | HG00280.hp1 HG01496.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.669+379_669+382dup others(4): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26928687 | |||||
| chr2:26928687
|
G | GTATATAT others(1): Show |
5 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0003g0003others(2): Show | 5 | HG01934.hp2 HG02451.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.669+375_669+382dup others(8): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26928687 | |||||
| chr2:26928687
|
GTATA | G | 27 | a0001c0001t0001g0071a0001c0001t0001g0100a0001c0001t0001g0104others(24): Show | 27 | HG00438.hp2 HG00597.hp2 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.669+379_669+382del others(4): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26928687 | |||||
| chr2:26928689
|
A | G | 109 | a0001c0001t0008g0004a0001c0001t0008g0067a0001c0001t0012g0030others(106): Show | 109 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.669+366A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | chr2 | 26928689 | ||||||
| chr2:26928702
|
T | C | 2 | a0001c0001t0003g0068a0001c0001t0009g0039 | 2 | HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.669+379T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | chr2 | 26928702 | ||||||
| chr2:26928704
|
T | C | 2 | a0001c0001t0003g0068a0001c0001t0009g0039 | 2 | HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.669+381T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | chr2 | 26928704 | ||||||
| chr2:26928704
|
T | TAC | 6 | a0001c0001t0001g0138a0001c0001t0010g0028a0001c0001t0010g0031others(3): Show | 6 | HG01106.hp2 HG01346.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.669+393_669+394dup others(2): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26928704 | |||||
| chr2:26928704
|
T | TATATATA others(3): Show |
1 | a0001c0001t0032g0077 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.669+382_669+383ins others(10): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26928704 | |||||
| chr2:26928704
|
T | TATATATA others(29): Show |
1 | a0001c0002t0002g0162 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.669+382_669+383ins others(36): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26928704 | |||||
| chr2:26928704
|
T | TATATATA others(11): Show |
1 | a0001c0007t0040g0169 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.669+382_669+383ins others(18): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26928704 | |||||
| chr2:26928704
|
T | TATATATA others(13): Show |
1 | a0001c0002t0039g0019 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.669+382_669+383ins others(20): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26928704 | |||||
| chr2:26928704
|
T | TATATATA others(21): Show |
1 | a0001c0001t0024g0049 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+382_669+383ins others(28): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26928704 | |||||
| chr2:26928704
|
T | TATATATA others(31): Show |
1 | a0001c0002t0002g0085 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.669+382_669+383ins others(38): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26928704 | |||||
| chr2:26928704
|
T | TATATATA others(33): Show |
3 | a0001c0002t0002g0076a0001c0002t0002g0163a0001c0002t0014g0050 | 3 | HG02257.hp1 HG03130.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.669+382_669+383ins others(40): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26928704 | |||||
| chr2:26928704
|
T | TATATATA others(35): Show |
1 | a0001c0006t0004g0161 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.669+382_669+383ins others(42): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26928704 | |||||
| chr2:26928704
|
T | TATATATA others(39): Show |
1 | a0001c0002t0006g0126 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.669+382_669+383ins others(46): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26928704 | |||||
| chr2:26928704
|
T | TATATATA others(21): Show |
3 | a0001c0001t0012g0030a0001c0001t0012g0055a0001c0001t0034g0054 | 3 | HG02257.hp2 HG02572.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.669+382_669+383ins others(28): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26928704 | |||||
| chr2:26928704
|
T | TATATATA others(23): Show |
2 | a0001c0001t0037g0053a0001c0002t0002g0134 | 2 | HG02486.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.669+382_669+383ins others(30): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26928704 | |||||
| chr2:26928704
|
T | TATATATA others(27): Show |
3 | a0001c0001t0033g0052a0001c0002t0002g0154a0001c0002t0006g0080 | 3 | HG00558.hp2 HG02559.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.669+382_669+383ins others(34): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26928704 | |||||
| chr2:26928704
|
T | TATATATA others(29): Show |
2 | a0001c0001t0024g0036a0001c0002t0004g0118 | 2 | HG01167.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.669+382_669+383ins others(36): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26928704 | |||||
| chr2:26928704
|
T | TATATATA others(31): Show |
3 | a0001c0002t0002g0041a0001c0002t0002g0091a0001c0002t0004g0143 | 3 | HG01069.hp1 HG01109.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.669+382_669+383ins others(38): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26928704 | |||||
| chr2:26928704
|
T | TATATATA others(33): Show |
2 | a0001c0002t0002g0094a0001c0002t0026g0144 | 2 | NA18961.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.669+382_669+383ins others(40): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26928704 | |||||
| chr2:26928704
|
T | TATATATA others(35): Show |
2 | a0001c0002t0002g0040a0001c0002t0006g0130 | 2 | HG02109.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.669+382_669+383ins others(42): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26928704 | |||||
| chr2:26928704
|
T | TATATATA others(15): Show |
1 | a0001c0002t0002g0035 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.669+382_669+383ins others(22): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26928704 | |||||
| chr2:26928704
|
T | TATATATA others(23): Show |
1 | a0001c0001t0012g0048 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.669+382_669+383ins others(30): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26928704 | |||||
| chr2:26928704
|
T | TATATATA others(25): Show |
4 | a0001c0002t0002g0152a0001c0002t0011g0060a0001c0002t0011g0061others(1): Show | 4 | HG02922.hp2 HG02970.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.669+382_669+383ins others(32): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26928704 | |||||
| chr2:26928704
|
T | TATATATA others(27): Show |
2 | a0001c0002t0002g0148a0001c0002t0011g0062 | 2 | HG00738.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.669+382_669+383ins others(34): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26928704 | |||||
| chr2:26928704
|
T | TATATATA others(29): Show |
7 | a0001c0002t0002g0101a0001c0002t0002g0117a0001c0002t0002g0127others(4): Show | 7 | HG01255.hp1 HG01952.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.669+382_669+383ins others(36): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26928704 | |||||
| chr2:26928704
|
T | TATATATA others(31): Show |
5 | a0001c0002t0002g0120a0001c0002t0002g0123a0001c0002t0002g0131others(2): Show | 5 | HG01346.hp2 HG02155.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.669+382_669+383ins others(38): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26928704 | |||||
| chr2:26928704
|
T | TATATATA others(33): Show |
5 | a0001c0002t0002g0133a0001c0002t0002g0140a0001c0002t0006g0084others(2): Show | 5 | HG00642.hp1 HG01361.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.669+382_669+383ins others(40): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26928704 | |||||
| chr2:26928704
|
T | TATATATA others(35): Show |
6 | a0001c0002t0002g0087a0001c0002t0002g0089a0001c0002t0002g0146others(3): Show | 6 | HG00280.hp2 HG00735.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.669+382_669+383ins others(42): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26928704 | |||||
| chr2:26928704
|
T | TATATATA others(37): Show |
3 | a0001c0001t0008g0004a0001c0002t0002g0078a0001c0002t0002g0103 | 3 | HG01081.hp2 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.669+382_669+383ins others(44): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26928704 | |||||
| chr2:26928704
|
T | TATATATA others(17): Show |
4 | a0001c0001t0013g0047a0001c0001t0013g0065a0001c0001t0013g0074others(1): Show | 4 | HG00733.hp2 HG01167.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.669+382_669+383ins others(24): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26928704 | |||||
| chr2:26928704
|
T | TATATATA others(25): Show |
1 | a0001c0001t0012g0051 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.669+382_669+383ins others(32): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26928704 | |||||
| chr2:26928704
|
T | TATATATA others(27): Show |
1 | a0001c0002t0018g0175 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.669+382_669+383ins others(34): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26928704 | |||||
| chr2:26928704
|
T | TATATATA others(29): Show |
2 | a0001c0002t0002g0086a0001c0002t0018g0150 | 2 | HG02738.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.669+382_669+383ins others(36): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26928704 | |||||
| chr2:26928704
|
T | TATATATA others(31): Show |
4 | a0001c0002t0002g0217a0001c0002t0002g0220a0001c0002t0014g0038others(1): Show | 4 | HG01081.hp1 HG02300.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.669+382_669+383ins others(38): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26928704 | |||||
| chr2:26928704
|
T | TATATATA others(33): Show |
4 | a0001c0002t0002g0044a0001c0002t0002g0119a0001c0002t0002g0136others(1): Show | 4 | HG01257.hp2 HG01928.hp1 NA18955.hp1 others(1): Show |
intron_variant | MODIFIER | c.669+382_669+383ins others(40): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26928704 | |||||
| chr2:26928704
|
T | TATATATA others(35): Show |
6 | a0001c0002t0002g0045a0001c0002t0002g0082a0001c0002t0002g0090others(3): Show | 6 | HG01168.hp2 HG01256.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.669+382_669+383ins others(42): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26928704 | |||||
| chr2:26928704
|
T | TATATATA others(37): Show |
1 | a0001c0002t0002g0097 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.669+382_669+383ins others(44): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26928704 | |||||
| chr2:26928704
|
T | TATATATA others(39): Show |
1 | a0001c0002t0002g0145 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.669+382_669+383ins others(46): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26928704 | |||||
| chr2:26928704
|
T | TATATATA others(27): Show |
1 | a0001c0001t0008g0067 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.669+382_669+383ins others(34): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26928704 | |||||
| chr2:26928704
|
T | TATATATA others(31): Show |
1 | a0001c0002t0014g0034 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.669+382_669+383ins others(38): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26928704 | |||||
| chr2:26928704
|
T | TATATATA others(33): Show |
4 | a0001c0002t0004g0095a0001c0002t0004g0141a0001c0002t0014g0037others(1): Show | 4 | HG00140.hp2 HG01981.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.669+382_669+383ins others(40): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26928704 | |||||
| chr2:26928704
|
T | TATATATA others(35): Show |
3 | a0001c0002t0002g0096a0001c0002t0002g0135a0001c0002t0004g0142 | 3 | HG00733.hp1 HG01256.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.669+382_669+383ins others(42): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26928704 | |||||
| chr2:26928704
|
T | TATATATA others(37): Show |
4 | a0001c0002t0002g0121a0001c0002t0002g0129a0001c0002t0015g0043others(1): Show | 4 | HG00673.hp1 HG01074.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.669+382_669+383ins others(44): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26928704 | |||||
| chr2:26928704
|
T | TATATATA others(39): Show |
2 | a0001c0002t0002g0198a0001c0002t0004g0158 | 2 | HG03492.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.669+382_669+383ins others(46): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26928704 | |||||
| chr2:26928704
|
T | TATATATA others(41): Show |
1 | a0001c0002t0015g0042 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.669+382_669+383ins others(48): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26928704 | |||||
| chr2:26928704
|
T | TATATATA others(37): Show |
1 | a0001c0002t0019g0160 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.669+382_669+383ins others(44): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26928704 | |||||
| chr2:26928704
|
T | TATATATA others(41): Show |
1 | a0001c0002t0002g0132 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.669+382_669+383ins others(48): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26928704 | |||||
| chr2:26928704
|
T | TATATATA others(39): Show |
1 | a0002c0003t0006g0092 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.669+382_669+383ins others(46): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26928704 | |||||
| chr2:26928704
|
T | TATATATA others(35): Show |
1 | a0001c0002t0020g0058 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.669+382_669+383ins others(42): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26928704 | |||||
| chr2:26928704
|
T | TATATATA others(39): Show |
1 | a0001c0002t0030g0056 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.669+382_669+383ins others(46): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26928704 | |||||
| chr2:26928704
|
T | TATATATA others(45): Show |
1 | a0001c0002t0031g0073 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.669+382_669+383ins others(52): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26928704 | |||||
| chr2:26928704
|
T | TATATATA others(43): Show |
1 | a0001c0002t0020g0057 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.669+382_669+383ins others(50): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26928704 | |||||
| chr2:26928706
|
C | T | 44 | a0001c0001t0001g0115a0001c0001t0001g0124a0001c0001t0001g0139others(41): Show | 44 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.669+383C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | chr2 | 26928706 | ||||||
| chr2:26928718
|
T | C | 111 | a0001c0001t0003g0068a0001c0001t0008g0004a0001c0001t0008g0067others(108): Show | 111 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.669+395T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | chr2 | 26928718 | ||||||
| chr2:26928722
|
T | C | 108 | a0001c0001t0003g0068a0001c0001t0008g0004a0001c0001t0008g0067others(105): Show | 108 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.669+399T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | chr2 | 26928722 | ||||||
| chr2:26928722
|
T | TAC | 3 | a0001c0002t0014g0034a0001c0002t0014g0037a0001c0002t0014g0038 | 3 | HG02486.hp1 HG03041.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.669+400_669+401ins others(2): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26928722 | |||||
| chr2:26928724
|
T | C | 2 | a0001c0002t0002g0094a0001c0002t0004g0143 | 2 | HG01109.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.669+401T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | chr2 | 26928724 | ||||||
| chr2:26928730
|
C | T | 3 | a0001c0001t0005g0081a0001c0001t0005g0170a0001c0002t0017g0215 | 3 | HG01257.hp1 HG01496.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.669+407C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | chr2 | 26928730 | ||||||
| chr2:26928733
|
A | G | 3 | a0001c0002t0002g0044a0001c0002t0002g0045a0001c0002t0002g0090 | 3 | HG01516.hp2 HG01517.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.669+410A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | chr2 | 26928733 | ||||||
| chr2:26928739
|
ACG | A | 111 | a0001c0001t0003g0068a0001c0001t0008g0004a0001c0001t0008g0067others(108): Show | 111 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.669+418_669+419del others(2): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26928739 | |||||
| chr2:26928752
|
C | CGT | 2 | a0001c0001t0013g0047a0001c0001t0013g0065 | 2 | HG02886.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.669+435_669+436dup others(2): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26928752 | |||||
| chr2:26928752
|
C | CGTGT | 4 | a0001c0001t0013g0074a0001c0001t0013g0075a0001c0002t0039g0019others(1): Show | 4 | HG00733.hp2 HG01167.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.669+433_669+436dup others(4): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26928752 | |||||
| chr2:26928752
|
C | CGTGTGT | 3 | a0001c0001t0003g0068a0001c0001t0009g0039a0001c0002t0002g0035 | 3 | HG02615.hp1 HG02976.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.669+431_669+436dup others(6): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26928752 | |||||
| chr2:26928752
|
C | CGTGTGTG others(3): Show |
1 | a0001c0001t0032g0077 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.669+436_669+437ins others(10): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26928752 | |||||
| chr2:26928756
|
TGTGC | T | 101 | a0001c0001t0008g0004a0001c0001t0008g0067a0001c0001t0012g0030others(98): Show | 101 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.669+437_669+440del others(4): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26928756 | |||||
| chr2:26928760
|
C | T | 10 | a0001c0001t0003g0068a0001c0001t0009g0039a0001c0001t0013g0047others(7): Show | 10 | HG00733.hp2 HG01167.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.669+437C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | chr2 | 26928760 | ||||||
| chr2:26928775
|
G | A | 101 | a0001c0001t0008g0004a0001c0001t0008g0067a0001c0001t0012g0030others(98): Show | 101 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.669+452G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | chr2 | 26928775 | ||||||
| chr2:26928795
|
C | T | 3 | a0001c0002t0014g0034a0001c0002t0014g0037a0001c0002t0014g0038 | 3 | HG02486.hp1 HG03041.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.669+472C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | chr2 | 26928795 | ||||||
| chr2:26928896
|
C | G | 3 | a0001c0002t0014g0034a0001c0002t0014g0037a0001c0002t0014g0038 | 3 | HG02486.hp1 HG03041.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.669+573C>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | chr2 | 26928896 | ||||||
| chr2:26928974
|
C | T | 110 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0026others(107): Show | 110 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.669+651C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | chr2 | 26928974 | ||||||
| chr2:26929051
|
A | G | 111 | a0001c0001t0003g0068a0001c0001t0008g0004a0001c0001t0008g0067others(108): Show | 111 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.669+728A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | chr2 | 26929051 | ||||||
| chr2:26929158
|
G | T | 3 | a0001c0001t0003g0003a0001c0001t0009g0001a0001c0001t0009g0002 | 3 | HG02451.hp2 HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.669+835G>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | chr2 | 26929158 | ||||||
| chr2:26929322
|
T | G | 2 | a0001c0001t0013g0047a0001c0001t0013g0065 | 2 | HG02886.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.669+999T>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | chr2 | 26929322 | ||||||
| chr2:26929530
|
T | C | 111 | a0001c0001t0003g0068a0001c0001t0008g0004a0001c0001t0008g0067others(108): Show | 111 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.669+1207T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | chr2 | 26929530 | ||||||
| chr2:26929789
|
C | T | 1 | a0002c0003t0006g0093 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.669+1466C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | chr2 | 26929789 | ||||||
| chr2:26929867
|
G | A | 111 | a0001c0001t0003g0068a0001c0001t0008g0004a0001c0001t0008g0067others(108): Show | 111 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.669+1544G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | chr2 | 26929867 | ||||||
| chr2:26930006
|
C | T | 82 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0026others(79): Show | 82 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.670-1634C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | chr2 | 26930006 | ||||||
| chr2:26930073
|
G | A | 1 | a0001c0002t0002g0123 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.670-1567G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | chr2 | 26930073 | ||||||
| chr2:26930132
|
C | T | 5 | a0001c0001t0013g0047a0001c0001t0013g0065a0001c0001t0013g0074others(2): Show | 5 | HG00733.hp2 HG01167.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.670-1508C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | chr2 | 26930132 | ||||||
| chr2:26930190
|
C | T | 1 | a0001c0002t0006g0084 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.670-1450C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | chr2 | 26930190 | ||||||
| chr2:26930227
|
GAGAGC | G | 104 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0026others(101): Show | 104 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.670-1411_670-1407d others(7): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26930227 | |||||
| chr2:26930327
|
G | A | 12 | a0001c0001t0003g0068a0001c0001t0009g0039a0001c0001t0013g0047others(9): Show | 12 | HG00733.hp2 HG01167.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.670-1313G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | chr2 | 26930327 | ||||||
| chr2:26930327
|
G | T | 1 | a0001c0001t0008g0067 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.670-1313G>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | chr2 | 26930327 | ||||||
| chr2:26930338
|
T | C | 2 | a0001c0001t0001g0138a0001c0001t0001g0193 | 2 | HG00099.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.670-1302T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | chr2 | 26930338 | ||||||
| chr2:26930450
|
G | A | 5 | a0001c0001t0001g0190a0001c0001t0001g0192a0001c0001t0005g0178others(2): Show | 5 | HG00280.hp1 HG00735.hp1 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.670-1190G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | chr2 | 26930450 | ||||||
| chr2:26930501
|
C | T | 201 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0026others(198): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.670-1139C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | chr2 | 26930501 | ||||||
| chr2:26930568
|
T | C | 12 | a0001c0001t0003g0068a0001c0001t0009g0039a0001c0001t0013g0047others(9): Show | 12 | HG00733.hp2 HG01167.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.670-1072T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | chr2 | 26930568 | ||||||
| chr2:26930613
|
A | C | 111 | a0001c0001t0008g0004a0001c0001t0008g0067a0001c0001t0012g0030others(108): Show | 111 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.670-1027A>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | chr2 | 26930613 | ||||||
| chr2:26930689
|
C | T | 12 | a0001c0001t0003g0068a0001c0001t0009g0039a0001c0001t0013g0047others(9): Show | 12 | HG00733.hp2 HG01167.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.670-951C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | chr2 | 26930689 | ||||||
| chr2:26930731
|
T | G | 2 | a0001c0001t0013g0074a0001c0001t0013g0075 | 2 | HG00733.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.670-909T>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | chr2 | 26930731 | ||||||
| chr2:26930865
|
G | T | 217 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(214): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.670-775G>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | chr2 | 26930865 | ||||||
| chr2:26930940
|
C | T | 2 | a0001c0002t0039g0019a0001c0007t0040g0169 | 2 | HG02970.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.670-700C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | chr2 | 26930940 | ||||||
| chr2:26930969
|
G | A | 2 | a0001c0001t0021g0006a0001c0001t0021g0007 | 2 | HG03540.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.670-671G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | chr2 | 26930969 | ||||||
| chr2:26930976
|
A | G | 2 | a0001c0002t0039g0019a0001c0007t0040g0169 | 2 | HG02970.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.670-664A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | chr2 | 26930976 | ||||||
| chr2:26931137
|
T | TA | 6 | a0001c0001t0001g0104a0001c0001t0001g0149a0001c0001t0005g0016others(3): Show | 6 | HG01433.hp2 HG03225.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.670-487dupA | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26931137 | |||||
| chr2:26931137
|
T | TAAAA | 5 | a0001c0001t0009g0066a0001c0001t0009g0070a0001c0001t0013g0065others(2): Show | 5 | HG00733.hp2 HG01167.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.670-490_670-487dup others(4): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26931137 | |||||
| chr2:26931137
|
TAAAAAA | T | 60 | a0001c0001t0012g0030a0001c0001t0012g0055a0001c0001t0024g0036others(57): Show | 60 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.670-492_670-487del others(6): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26931137 | |||||
| chr2:26931137
|
TAAAAAAA others(1): Show |
T | 16 | a0001c0001t0012g0048a0001c0001t0012g0051a0001c0001t0024g0049others(13): Show | 16 | HG00639.hp1 HG00738.hp1 HG01361.hp1 others(13): Show |
intron_variant | MODIFIER | c.670-494_670-487del others(8): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26931137 | |||||
| chr2:26931146
|
AAAAAAAA others(1): Show |
A | 19 | a0001c0002t0002g0040a0001c0002t0002g0044a0001c0002t0002g0082others(16): Show | 19 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.670-492_670-485del others(8): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26931146 | |||||
| chr2:26931150
|
A | AT | 4 | a0001c0001t0001g0204a0001c0001t0007g0113a0001c0001t0010g0028others(1): Show | 4 | HG00597.hp2 HG00673.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.670-490_670-489ins others(1): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | chr2 | 26931150 | ||||||
| chr2:26931150
|
A | T | 5 | a0001c0001t0001g0190a0001c0001t0001g0192a0001c0001t0005g0178others(2): Show | 5 | HG00280.hp1 HG00735.hp1 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.670-490A>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | chr2 | 26931150 | ||||||
| chr2:26931152
|
A | AAAAAATA others(5): Show |
1 | a0001c0002t0039g0019 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.670-487_670-486ins others(12): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26931152 | |||||
| chr2:26931152
|
A | AT | 34 | a0001c0001t0001g0100a0001c0001t0001g0106a0001c0001t0001g0108others(31): Show | 34 | HG00438.hp2 HG00642.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.670-488_670-487ins others(1): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | chr2 | 26931152 | ||||||
| chr2:26931152
|
A | ATAT | 13 | a0001c0001t0001g0059a0001c0001t0001g0071a0001c0001t0001g0107others(10): Show | 13 | HG00099.hp1 HG01884.hp2 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.670-488_670-487ins others(3): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | chr2 | 26931152 | ||||||
| chr2:26931152
|
A | T | 28 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0115others(25): Show | 28 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(25): Show |
intron_variant | MODIFIER | c.670-488A>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | chr2 | 26931152 | ||||||
| chr2:26931153
|
AT | A | 2 | a0001c0001t0003g0003a0001c0001t0009g0001 | 2 | HG02451.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.670-486delT | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | chr2 | 26931153 | ||||||
| chr2:26931154
|
T | A | 1 | a0001c0001t0009g0039 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.670-486T>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | chr2 | 26931154 | ||||||
| chr2:26931156
|
T | A | 1 | a0001c0001t0009g0039 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.670-484T>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | chr2 | 26931156 | ||||||
| chr2:26931165
|
A | ATGTGTG | 2 | a0001c0001t0001g0208a0001c0001t0001g0209 | 2 | HG01358.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.670-474_670-473ins others(6): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26931165 | |||||
| chr2:26931165
|
A | G | 2 | a0001c0001t0001g0107a0001c0001t0001g0193 | 2 | HG00099.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.670-475A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | chr2 | 26931165 | ||||||
| chr2:26931167
|
A | ATGTG | 14 | a0001c0001t0001g0104a0001c0001t0001g0108a0001c0001t0001g0112others(11): Show | 14 | HG00438.hp2 HG01106.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.670-472_670-471ins others(4): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26931167 | |||||
| chr2:26931167
|
A | ATGTGTG | 10 | a0001c0001t0001g0100a0001c0001t0001g0106a0001c0001t0001g0201others(7): Show | 10 | HG00642.hp2 HG00673.hp2 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.670-472_670-471ins others(6): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26931167 | |||||
| chr2:26931167
|
A | ATGTGTGT others(1): Show |
3 | a0001c0001t0001g0181a0001c0001t0001g0197a0001c0001t0001g0214 | 3 | HG00738.hp2 HG02015.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.670-472_670-471ins others(8): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26931167 | |||||
| chr2:26931167
|
A | G | 24 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0027others(21): Show | 24 | HG00099.hp1 HG00597.hp2 HG01358.hp1 others(21): Show |
intron_variant | MODIFIER | c.670-473A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | chr2 | 26931167 | ||||||
| chr2:26931169
|
A | ATATGTGT others(3): Show |
1 | a0001c0001t0022g0188 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.670-470_670-469ins others(10): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26931169 | |||||
| chr2:26931169
|
A | ATATGTGT others(9): Show |
1 | a0001c0001t0008g0164 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.670-470_670-469ins others(16): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26931169 | |||||
| chr2:26931169
|
A | ATG | 2 | a0001c0001t0005g0170a0001c0005t0003g0015 | 2 | HG01496.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.670-437_670-436dup others(2): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26931169 | |||||
| chr2:26931169
|
A | ATGTG | 12 | a0001c0001t0001g0014a0001c0001t0001g0124a0001c0001t0001g0139others(9): Show | 12 | HG01074.hp2 HG01243.hp1 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.670-439_670-436dup others(4): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26931169 | |||||
| chr2:26931169
|
A | ATGTGTG | 4 | a0001c0001t0001g0190a0001c0001t0001g0224a0001c0001t0005g0178others(1): Show | 4 | HG00280.hp1 HG00735.hp1 HG01069.hp2 others(1): Show |
intron_variant | MODIFIER | c.670-441_670-436dup others(6): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26931169 | |||||
| chr2:26931169
|
A | ATGTGTGT others(1): Show |
20 | a0001c0001t0001g0115a0001c0001t0001g0156a0001c0001t0001g0157others(17): Show | 20 | HG00639.hp2 HG01168.hp1 HG01257.hp1 others(17): Show |
intron_variant | MODIFIER | c.670-443_670-436dup others(8): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26931169 | |||||
| chr2:26931169
|
A | ATGTGTGT others(3): Show |
4 | a0001c0001t0001g0177a0001c0001t0001g0184a0001c0001t0015g0183others(1): Show | 4 | HG00140.hp1 HG01261.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.670-445_670-436dup others(10): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26931169 | |||||
| chr2:26931169
|
A | ATGTGTGT others(5): Show |
2 | a0001c0001t0005g0203a0001c0001t0008g0202 | 2 | HG00558.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.670-447_670-436dup others(12): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26931169 | |||||
| chr2:26931169
|
A | ATGTGTGT others(7): Show |
1 | a0001c0001t0008g0023 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.670-449_670-436dup others(14): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26931169 | |||||
| chr2:26931169
|
A | ATGTGTGT others(13): Show |
1 | a0001c0001t0005g0016 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.670-455_670-436dup others(20): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26931169 | |||||
| chr2:26931169
|
A | G | 112 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0027others(109): Show | 112 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.670-471A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | chr2 | 26931169 | ||||||
| chr2:26931171
|
G | A | 17 | a0001c0001t0003g0003a0001c0001t0003g0020a0001c0001t0003g0068others(14): Show | 17 | HG00733.hp2 HG01167.hp2 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.670-469G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | chr2 | 26931171 | ||||||
| chr2:26931173
|
G | A | 5 | a0001c0001t0003g0003a0001c0001t0003g0068a0001c0001t0009g0001others(2): Show | 5 | HG02451.hp2 HG02615.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.670-467G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | chr2 | 26931173 | ||||||
| chr2:26931187
|
G | A | 1 | a0001c0002t0002g0140 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.670-453G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | chr2 | 26931187 | ||||||
| chr2:26931189
|
G | A | 1 | a0001c0002t0002g0140 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.670-451G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | chr2 | 26931189 | ||||||
| chr2:26931191
|
G | A | 1 | a0001c0002t0002g0140 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.670-449G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | chr2 | 26931191 | ||||||
| chr2:26931193
|
G | A | 1 | a0001c0002t0002g0140 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.670-447G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | chr2 | 26931193 | ||||||
| chr2:26931195
|
G | A | 1 | a0001c0002t0002g0140 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.670-445G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | chr2 | 26931195 | ||||||
| chr2:26931195
|
G | GTATATAT others(3): Show |
1 | a0001c0002t0006g0084 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.670-444_670-443ins others(10): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26931195 | |||||
| chr2:26931197
|
G | A | 3 | a0001c0002t0002g0140a0001c0002t0006g0084a0001c0002t0028g0046 | 3 | HG01433.hp1 HG01516.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.670-443G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | chr2 | 26931197 | ||||||
| chr2:26931197
|
G | GTATA | 2 | a0001c0002t0002g0076a0001c0002t0014g0050 | 2 | HG02257.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.670-442_670-441ins others(4): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26931197 | |||||
| chr2:26931197
|
G | GTATATA | 4 | a0001c0002t0002g0085a0001c0002t0002g0163a0001c0002t0004g0229others(1): Show | 4 | HG02145.hp2 HG02630.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.670-442_670-441ins others(6): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26931197 | |||||
| chr2:26931197
|
G | GTATATAT others(1): Show |
2 | a0001c0002t0002g0153a0001c0002t0006g0069 | 2 | NA18973.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.670-442_670-441ins others(8): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26931197 | |||||
| chr2:26931197
|
G | GTATATAT others(3): Show |
4 | a0001c0002t0002g0127a0001c0002t0002g0155a0001c0002t0006g0080others(1): Show | 4 | HG00140.hp2 HG01952.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.670-442_670-441ins others(10): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26931197 | |||||
| chr2:26931197
|
G | GTATATAT others(5): Show |
1 | a0001c0002t0002g0154 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.670-442_670-441ins others(12): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26931197 | |||||
| chr2:26931197
|
G | GTATATAT others(7): Show |
3 | a0001c0002t0002g0086a0001c0002t0002g0089a0002c0003t0006g0092 | 3 | HG01496.hp1 HG02647.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.670-442_670-441ins others(14): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26931197 | |||||
| chr2:26931197
|
G | GTATATAT others(11): Show |
1 | a0001c0002t0002g0041 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.670-442_670-441ins others(18): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26931197 | |||||
| chr2:26931197
|
GTGTGTGT others(5): Show |
G | 3 | a0001c0002t0014g0034a0001c0002t0014g0037a0001c0002t0014g0038 | 3 | HG02486.hp1 HG03041.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.670-441_670-430del others(12): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26931197 | |||||
| chr2:26931197
|
GTGTGTGT others(15): Show |
G | 3 | a0001c0001t0032g0077a0001c0004t0003g0011a0001c0004t0003g0064 | 3 | HG02109.hp1 HG02922.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.670-441_670-420del others(22): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26931197 | |||||
| chr2:26931199
|
G | A | 21 | a0001c0002t0002g0041a0001c0002t0002g0076a0001c0002t0002g0085others(18): Show | 21 | HG00140.hp2 HG00558.hp2 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.670-441G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | chr2 | 26931199 | ||||||
| chr2:26931199
|
G | GTATATAT others(3): Show |
2 | a0001c0002t0019g0122a0001c0002t0020g0058 | 2 | HG02083.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.670-440_670-439ins others(10): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26931199 | |||||
| chr2:26931199
|
G | GTATATAT others(5): Show |
1 | a0001c0002t0030g0056 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.670-440_670-439ins others(12): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26931199 | |||||
| chr2:26931199
|
G | GTATATAT others(7): Show |
10 | a0001c0002t0002g0078a0001c0002t0002g0097a0001c0002t0002g0117others(7): Show | 10 | HG00099.hp2 HG00735.hp2 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.670-440_670-439ins others(14): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26931199 | |||||
| chr2:26931199
|
G | GTATATAT others(9): Show |
6 | a0001c0002t0002g0120a0001c0002t0006g0130a0001c0002t0011g0062others(3): Show | 6 | HG00738.hp1 HG01346.hp2 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.670-440_670-439ins others(16): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26931199 | |||||
| chr2:26931199
|
G | GTATATAT others(11): Show |
6 | a0001c0002t0002g0045a0001c0002t0002g0090a0001c0002t0002g0145others(3): Show | 6 | HG00438.hp1 HG01516.hp2 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.670-440_670-439ins others(18): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26931199 | |||||
| chr2:26931199
|
G | GTATATAT others(15): Show |
2 | a0001c0002t0002g0040a0001c0002t0002g0087 | 2 | HG02109.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.670-440_670-439ins others(22): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26931199 | |||||
| chr2:26931199
|
GTGTGTAT others(19): Show |
G | 2 | a0001c0001t0013g0047a0001c0002t0002g0035 | 2 | HG02976.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.670-439_670-414del others(26): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26931199 | |||||
| chr2:26931201
|
G | A | 54 | a0001c0001t0012g0030a0001c0001t0012g0055a0001c0001t0024g0036others(51): Show | 54 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(51): Show |
intron_variant | MODIFIER | c.670-439G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | chr2 | 26931201 | ||||||
| chr2:26931201
|
G | GTATATAT others(7): Show |
3 | a0001c0002t0002g0119a0001c0002t0002g0136a0001c0002t0026g0144 | 3 | HG01257.hp2 NA18961.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.670-438_670-437ins others(14): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26931201 | |||||
| chr2:26931201
|
G | GTATATAT others(9): Show |
3 | a0001c0002t0002g0134a0001c0002t0002g0135a0001c0002t0011g0060 | 3 | HG03471.hp2 HG03492.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.670-438_670-437ins others(16): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26931201 | |||||
| chr2:26931201
|
G | GTATATAT others(11): Show |
5 | a0001c0002t0002g0101a0001c0002t0002g0103a0001c0002t0004g0095others(2): Show | 5 | HG01081.hp2 HG01256.hp1 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.670-438_670-437ins others(18): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26931201 | |||||
| chr2:26931201
|
G | GTATATAT others(15): Show |
6 | a0001c0002t0002g0091a0001c0002t0002g0151a0001c0002t0002g0162others(3): Show | 6 | HG01069.hp1 HG01081.hp1 HG03834.hp2 others(3): Show |
intron_variant | MODIFIER | c.670-438_670-437ins others(22): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26931201 | |||||
| chr2:26931201
|
G | GTATATAT others(17): Show |
2 | a0001c0002t0002g0133a0001c0002t0018g0150 | 2 | HG00642.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.670-438_670-437ins others(24): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26931201 | |||||
| chr2:26931201
|
G | GTATATAT others(19): Show |
2 | a0001c0002t0018g0175a0002c0003t0006g0079 | 2 | HG01515.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.670-438_670-437ins others(26): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26931201 | |||||
| chr2:26931201
|
G | GTATATAT others(23): Show |
1 | a0001c0002t0002g0217 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.670-438_670-437ins others(30): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26931201 | |||||
| chr2:26931201
|
GTGTATAT others(17): Show |
G | 3 | a0001c0001t0013g0065a0001c0001t0013g0074a0001c0001t0013g0075 | 3 | HG00733.hp2 HG01167.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.670-437_670-414del others(24): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26931201 | |||||
| chr2:26931203
|
G | A | 83 | a0001c0001t0012g0030a0001c0001t0012g0048a0001c0001t0012g0055others(80): Show | 83 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.670-437G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | chr2 | 26931203 | ||||||
| chr2:26931203
|
G | GTATATAT others(11): Show |
2 | a0001c0002t0002g0148a0001c0002t0002g0198 | 2 | HG03492.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.670-427_670-410dup others(18): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26931203 | |||||
| chr2:26931203
|
G | GTATATAT others(15): Show |
2 | a0001c0002t0002g0096a0001c0002t0002g0123 | 2 | HG00733.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.670-431_670-410dup others(22): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26931203 | |||||
| chr2:26931203
|
G | GTATATAT others(17): Show |
3 | a0001c0002t0002g0044a0001c0002t0002g0082a0001c0002t0002g0131 | 3 | HG01168.hp2 NA18955.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.670-433_670-410dup others(24): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26931203 | |||||
| chr2:26931203
|
G | GTATATAT others(21): Show |
1 | a0001c0002t0019g0160 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.670-410_670-409ins others(28): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26931203 | |||||
| chr2:26931203
|
G | GTGTATAT others(15): Show |
1 | a0001c0002t0017g0159 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.670-436_670-435ins others(22): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26931203 | |||||
| chr2:26931203
|
G | GTGTATAT others(27): Show |
1 | a0001c0002t0002g0094 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.670-436_670-435ins others(34): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26931203 | |||||
| chr2:26931203
|
G | GTGTGTAT others(1): Show |
3 | a0001c0001t0003g0020a0001c0001t0023g0021a0001c0001t0023g0022 | 3 | HG01243.hp2 HG01884.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.670-436_670-435ins others(8): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26931203 | |||||
| chr2:26931203
|
G | GTGTGTGT others(3): Show |
1 | a0001c0001t0021g0006 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.670-436_670-435ins others(10): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26931203 | |||||
| chr2:26931203
|
G | GTGTGTGT others(27): Show |
1 | a0001c0001t0001g0010 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.670-436_670-435ins others(34): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26931203 | |||||
| chr2:26931203
|
G | GTGTGTGT others(29): Show |
1 | a0001c0001t0001g0009 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.670-436_670-435ins others(36): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26931203 | |||||
| chr2:26931203
|
GTATATAT others(9): Show |
G | 3 | a0001c0001t0003g0003a0001c0001t0009g0001a0001c0001t0009g0002 | 3 | HG02451.hp2 HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.670-425_670-410del others(16): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26931203 | |||||
| chr2:26931203
|
GTATATAT others(15): Show |
G | 4 | a0001c0001t0003g0068a0001c0001t0009g0039a0001c0002t0039g0019others(1): Show | 4 | HG02615.hp1 HG02970.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.670-431_670-410del others(22): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 26931203 | |||||
| chr2:26931205
|
A | G | 99 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0026others(96): Show | 99 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.670-435A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | chr2 | 26931205 | ||||||
| chr2:26931207
|
A | G | 42 | a0001c0001t0001g0027a0001c0001t0001g0059a0001c0001t0001g0071others(39): Show | 42 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(39): Show |
intron_variant | MODIFIER | c.670-433A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | chr2 | 26931207 | ||||||
| chr2:26931209
|
A | G | 14 | a0001c0001t0001g0197a0001c0001t0001g0232a0001c0001t0005g0081others(11): Show | 14 | HG01106.hp2 HG01346.hp1 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.670-431A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | chr2 | 26931209 | ||||||
| chr2:26931211
|
A | G | 4 | a0001c0001t0007g0109a0001c0001t0010g0028a0001c0001t0010g0033others(1): Show | 4 | HG01106.hp2 HG02148.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.670-429A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | chr2 | 26931211 | ||||||
| chr2:26931291
|
C | G | 15 | a0001c0001t0003g0003a0001c0001t0003g0068a0001c0001t0009g0001others(12): Show | 15 | HG00733.hp2 HG01167.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.670-349C>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | chr2 | 26931291 | ||||||
| chr2:26931308
|
A | G | 2 | a0001c0002t0039g0019a0001c0007t0040g0169 | 2 | HG02970.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.670-332A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | chr2 | 26931308 | ||||||
| chr2:26931519
|
C | T | 9 | a0001c0001t0003g0068a0001c0001t0009g0039a0001c0001t0013g0047others(6): Show | 9 | HG00733.hp2 HG01167.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.670-121C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | chr2 | 26931519 | ||||||
| chr2:26931553
|
G | T | 1 | a0001c0001t0001g0214 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.670-87G>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 5/12 | chr2 | 26931553 | ||||||
| chr2:26931699
|
G | C | 15 | a0001c0001t0003g0003a0001c0001t0003g0068a0001c0001t0009g0001others(12): Show | 15 | HG00733.hp2 HG01167.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.714+15G>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | chr2 | 26931699 | ||||||
| chr2:26931780
|
C | G | 15 | a0001c0001t0003g0003a0001c0001t0003g0068a0001c0001t0009g0001others(12): Show | 15 | HG00733.hp2 HG01167.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.714+96C>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | chr2 | 26931780 | ||||||
| chr2:26931876
|
C | T | 16 | a0001c0001t0003g0003a0001c0001t0003g0068a0001c0001t0009g0001others(13): Show | 16 | HG00733.hp2 HG01167.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.714+192C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | chr2 | 26931876 | ||||||
| chr2:26931877
|
G | T | 1 | a0001c0002t0006g0130 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.714+193G>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | chr2 | 26931877 | ||||||
| chr2:26932006
|
CA | C | 185 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(182): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.714+341delA | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 26932006 | |||||
| chr2:26932006
|
CAA | C | 9 | a0001c0002t0002g0090a0001c0002t0011g0060a0001c0002t0011g0061others(6): Show | 9 | HG00738.hp1 HG01516.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.714+340_714+341del others(2): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 26932006 | |||||
| chr2:26932006
|
CAAA | C | 14 | a0001c0001t0003g0003a0001c0001t0003g0068a0001c0001t0009g0002others(11): Show | 14 | HG00733.hp2 HG01167.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.714+339_714+341del others(3): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 26932006 | |||||
| chr2:26932030
|
G | T | 2 | a0001c0001t0001g0009a0001c0001t0001g0010 | 2 | HG01934.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.714+346G>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | chr2 | 26932030 | ||||||
| chr2:26932046
|
AAGGAAAG others(4): Show |
A | 1 | a0001c0001t0007g0113 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.714+364_714+374del others(11): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 26932046 | |||||
| chr2:26932048
|
G | GGAAA | 3 | a0001c0001t0003g0013a0001c0001t0003g0088a0001c0001t0003g0167 | 3 | HG01891.hp2 HG02559.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.714+397_714+400dup others(4): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 26932048 | |||||
| chr2:26932048
|
G | GGAAAGAA others(1): Show |
3 | a0001c0001t0003g0020a0001c0001t0023g0021a0001c0001t0023g0022 | 3 | HG01243.hp2 HG01884.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.714+393_714+400dup others(8): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 26932048 | |||||
| chr2:26932048
|
G | GGAAAGAA others(5): Show |
1 | a0001c0001t0038g0008 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.714+389_714+400dup others(12): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 26932048 | |||||
| chr2:26932048
|
G | GGAAAGAA others(9): Show |
1 | a0001c0001t0003g0012 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.714+385_714+400dup others(16): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 26932048 | |||||
| chr2:26932048
|
G | GGAAAGAA others(13): Show |
2 | a0001c0001t0001g0009a0001c0001t0001g0010 | 2 | HG01934.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.714+381_714+400dup others(20): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 26932048 | |||||
| chr2:26932048
|
GGAAA | G | 4 | a0001c0001t0009g0066a0001c0001t0021g0006a0001c0001t0021g0007others(1): Show | 4 | HG00673.hp2 HG03130.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.714+397_714+400del others(4): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 26932048 | |||||
| chr2:26932048
|
GGAAAGAA others(1): Show |
G | 92 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0026others(89): Show | 92 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.714+393_714+400del others(8): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 26932048 | |||||
| chr2:26932048
|
GGAAAGAA others(5): Show |
G | 18 | a0001c0001t0001g0059a0001c0001t0003g0068a0001c0001t0009g0039others(15): Show | 18 | HG00733.hp2 HG01106.hp2 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.714+389_714+400del others(12): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 26932048 | |||||
| chr2:26932077
|
GAAAGAAA others(1): Show |
G | 3 | a0001c0002t0002g0154a0001c0002t0004g0158a0001c0002t0026g0144 | 3 | HG00558.hp2 NA18961.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.714+394_714+401del others(8): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | chr2 | 26932077 | ||||||
| chr2:26932081
|
GAAAA | G | 3 | a0001c0002t0002g0120a0001c0002t0002g0121a0001c0002t0004g0143 | 3 | HG00673.hp1 HG01109.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.714+398_714+401del others(4): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | chr2 | 26932081 | ||||||
| chr2:26932082
|
A | AAAG | 9 | a0001c0001t0012g0030a0001c0001t0034g0054a0001c0002t0002g0103others(6): Show | 9 | HG01081.hp2 HG01361.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.714+400_714+401ins others(3): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 26932082 | |||||
| chr2:26932082
|
A | AAAGAAAG | 7 | a0001c0002t0002g0078a0001c0002t0006g0080a0001c0002t0011g0060others(4): Show | 7 | HG00738.hp1 HG02559.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.714+400_714+401ins others(7): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 26932082 | |||||
| chr2:26932082
|
A | AAAGAAAG others(4): Show |
4 | a0001c0002t0002g0086a0001c0002t0002g0087a0001c0002t0006g0069others(1): Show | 4 | HG03139.hp1 HG03453.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.714+400_714+401ins others(11): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 26932082 | |||||
| chr2:26932085
|
A | G | 73 | a0001c0001t0012g0048a0001c0001t0012g0051a0001c0001t0012g0055others(70): Show | 73 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.714+401A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | chr2 | 26932085 | ||||||
| chr2:26932086
|
G | A | 42 | a0001c0001t0012g0051a0001c0001t0012g0055a0001c0001t0024g0036others(39): Show | 42 | HG00140.hp2 HG00438.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.714+402G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | chr2 | 26932086 | ||||||
| chr2:26932089
|
A | AG | 20 | a0001c0001t0012g0030a0001c0001t0034g0054a0001c0002t0002g0078others(17): Show | 20 | HG00738.hp1 HG01081.hp2 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.714+405_714+406ins others(1): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | chr2 | 26932089 | ||||||
| chr2:26932089
|
A | G | 43 | a0001c0001t0003g0003a0001c0001t0012g0051a0001c0001t0012g0055others(40): Show | 43 | HG00140.hp2 HG00438.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.714+405A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | chr2 | 26932089 | ||||||
| chr2:26932090
|
A | G | 21 | a0001c0001t0024g0036a0001c0001t0037g0053a0001c0002t0002g0044others(18): Show | 21 | HG00642.hp1 HG01069.hp1 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.714+406A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | chr2 | 26932090 | ||||||
| chr2:26932093
|
G | A | 21 | a0001c0001t0024g0036a0001c0001t0037g0053a0001c0002t0002g0044others(18): Show | 21 | HG00642.hp1 HG01069.hp1 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.714+409G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | chr2 | 26932093 | ||||||
| chr2:26932093
|
G | GAAAGAAA others(17): Show |
1 | a0001c0002t0002g0040 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.714+414_714+415ins others(24): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 26932093 | |||||
| chr2:26932093
|
G | GGAAA | 35 | a0001c0001t0012g0030a0001c0001t0012g0051a0001c0001t0012g0055others(32): Show | 35 | HG00140.hp2 HG00438.hp1 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.714+409_714+410ins others(4): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | chr2 | 26932093 | ||||||
| chr2:26932095
|
AAG | A | 6 | a0001c0001t0003g0003a0001c0001t0009g0001a0001c0001t0009g0002others(3): Show | 6 | HG01515.hp2 HG02451.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.714+415_714+416del others(2): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 26932095 | |||||
| chr2:26932095
|
AAGAG | A | 37 | a0001c0001t0012g0048a0001c0002t0002g0045a0001c0002t0002g0082others(34): Show | 37 | HG00099.hp2 HG00280.hp2 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.714+413_714+416del others(4): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 26932095 | |||||
| chr2:26932097
|
GA | G | 2 | a0001c0002t0002g0145a0001c0002t0015g0043 | 2 | HG01074.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.714+414delA | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | chr2 | 26932097 | ||||||
| chr2:26932099
|
G | A | 57 | a0001c0001t0012g0030a0001c0001t0012g0051a0001c0001t0012g0055others(54): Show | 57 | HG00140.hp2 HG00438.hp1 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.714+415G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | chr2 | 26932099 | ||||||
| chr2:26932102
|
AG | A | 2 | a0001c0002t0002g0145a0001c0002t0015g0043 | 2 | HG01074.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.714+419delG | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | chr2 | 26932102 | ||||||
| chr2:26932104
|
A | G | 1 | a0002c0003t0006g0079 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.714+420A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | chr2 | 26932104 | ||||||
| chr2:26932112
|
G | A | 2 | a0001c0002t0002g0041a0001c0002t0002g0089 | 2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.714+428G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | chr2 | 26932112 | ||||||
| chr2:26932113
|
A | G | 2 | a0001c0002t0002g0041a0001c0002t0002g0089 | 2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.714+429A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | chr2 | 26932113 | ||||||
| chr2:26932115
|
A | G | 2 | a0001c0002t0002g0145a0001c0002t0015g0043 | 2 | HG01074.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.714+431A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | chr2 | 26932115 | ||||||
| chr2:26932121
|
AAGAGAAA others(11): Show |
A | 1 | a0001c0004t0003g0011 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.714+439_714+456del others(18): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 26932121 | |||||
| chr2:26932121
|
AAGAGAAA others(19): Show |
A | 1 | a0001c0002t0039g0019 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.714+439_714+464del others(26): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 26932121 | |||||
| chr2:26932121
|
AAGAGAAA others(23): Show |
A | 3 | a0001c0002t0002g0035a0001c0004t0003g0064a0001c0007t0040g0169 | 3 | HG02922.hp1 HG02970.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.714+439_714+468del others(30): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 26932121 | |||||
| chr2:26932121
|
AAGAGAAA others(27): Show |
A | 3 | a0001c0001t0009g0039a0001c0001t0013g0065a0001c0001t0032g0077 | 3 | HG02615.hp1 HG02886.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.714+439_714+472del others(34): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 26932121 | |||||
| chr2:26932121
|
AAGAGAAA others(39): Show |
A | 3 | a0001c0001t0003g0068a0001c0001t0013g0074a0001c0001t0013g0075 | 3 | HG00733.hp2 HG01167.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.714+439_714+484del others(46): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 26932121 | |||||
| chr2:26932121
|
AAGAGAAA others(43): Show |
A | 1 | a0001c0001t0013g0047 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.714+439_714+488del others(50): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 26932121 | |||||
| chr2:26932122
|
AG | A | 2 | a0001c0002t0002g0145a0001c0002t0015g0043 | 2 | HG01074.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.714+439delG | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | chr2 | 26932122 | ||||||
| chr2:26932123
|
GAGAA | G | 3 | a0001c0001t0001g0024a0001c0001t0001g0027a0001c0002t0015g0042 | 3 | HG02280.hp1 HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.714+451_714+454del others(4): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 26932123 | |||||
| chr2:26932123
|
GAGAAAGA others(23): Show |
G | 1 | a0001c0005t0003g0015 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.714+455_714+484del others(30): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 26932123 | |||||
| chr2:26932125
|
G | A | 3 | a0001c0002t0002g0041a0001c0002t0002g0089a0002c0003t0006g0079 | 3 | HG01515.hp2 HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.714+441G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | chr2 | 26932125 | ||||||
| chr2:26932126
|
A | AAG | 3 | a0001c0002t0002g0041a0001c0002t0002g0089a0002c0003t0006g0079 | 3 | HG01515.hp2 HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.714+443_714+444ins others(2): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 26932126 | |||||
| chr2:26932128
|
AG | A | 2 | a0001c0002t0002g0145a0001c0002t0015g0043 | 2 | HG01074.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.714+445delG | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | chr2 | 26932128 | ||||||
| chr2:26932129
|
G | A | 3 | a0001c0002t0002g0041a0001c0002t0002g0089a0002c0003t0006g0079 | 3 | HG01515.hp2 HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.714+445G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | chr2 | 26932129 | ||||||
| chr2:26932135
|
A | G | 2 | a0001c0001t0021g0006a0001c0001t0021g0007 | 2 | HG03540.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.714+451A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | chr2 | 26932135 | ||||||
| chr2:26932137
|
G | A | 3 | a0001c0001t0003g0003a0001c0001t0021g0006a0001c0001t0021g0007 | 3 | HG03209.hp2 HG03540.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.714+453G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | chr2 | 26932137 | ||||||
| chr2:26932137
|
G | GAAAGAGA others(13): Show |
1 | a0001c0001t0001g0182 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.714+454_714+455ins others(20): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 26932137 | |||||
| chr2:26932137
|
G | GAGAA | 3 | a0001c0001t0003g0072a0001c0001t0009g0066a0001c0002t0002g0146 | 3 | HG00735.hp2 HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.714+523_714+526dup others(4): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 26932137 | |||||
| chr2:26932137
|
G | GAGAAAGA others(1): Show |
3 | a0001c0001t0003g0088a0001c0001t0003g0167a0001c0001t0003g0171 | 3 | HG01891.hp2 HG02897.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.714+519_714+526dup others(8): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 26932137 | |||||
| chr2:26932137
|
G | GAGAAAGA others(5): Show |
1 | a0001c0001t0003g0168 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.714+515_714+526dup others(12): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 26932137 | |||||
| chr2:26932137
|
GAGAA | G | 3 | a0001c0001t0005g0016a0001c0001t0010g0028a0001c0002t0011g0061 | 3 | HG02809.hp1 HG02970.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.714+523_714+526del others(4): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 26932137 | |||||
| chr2:26932137
|
GAGAAAGA others(1): Show |
G | 3 | a0001c0001t0003g0166a0001c0001t0009g0070a0001c0001t0010g0031 | 3 | HG01346.hp1 HG02258.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.714+519_714+526del others(8): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 26932137 | |||||
| chr2:26932137
|
GAGAAAGA others(5): Show |
G | 1 | a0001c0001t0010g0033 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.714+515_714+526del others(12): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 26932137 | |||||
| chr2:26932137
|
GAGAAAGA others(9): Show |
G | 1 | a0001c0001t0005g0081 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.714+511_714+526del others(16): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 26932137 | |||||
| chr2:26932139
|
G | A | 1 | a0001c0001t0003g0003 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.714+455G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | chr2 | 26932139 | ||||||
| chr2:26932151
|
GAA | G | 3 | a0001c0001t0009g0001a0001c0002t0002g0145a0002c0003t0006g0079 | 3 | HG01515.hp2 HG02004.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.714+469_714+470del others(2): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 26932151 | |||||
| chr2:26932155
|
G | T | 2 | a0001c0001t0009g0001a0001c0005t0003g0015 | 2 | HG02451.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.714+471G>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | chr2 | 26932155 | ||||||
| chr2:26932157
|
A | C | 4 | a0001c0001t0007g0109a0001c0001t0007g0110a0001c0001t0036g0102others(1): Show | 4 | HG01106.hp1 HG01928.hp2 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.714+473A>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | chr2 | 26932157 | ||||||
| chr2:26932159
|
G | T | 1 | a0001c0001t0009g0002 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.714+475G>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | chr2 | 26932159 | ||||||
| chr2:26932177
|
A | C | 4 | a0001c0001t0001g0199a0001c0001t0001g0205a0001c0001t0005g0018others(1): Show | 4 | HG00673.hp2 HG02148.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.714+493A>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | chr2 | 26932177 | ||||||
| chr2:26932180
|
AAAGAAAG others(25): Show |
A | 4 | a0001c0001t0007g0109a0001c0001t0007g0110a0001c0001t0036g0102others(1): Show | 4 | HG01106.hp1 HG01928.hp2 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.714+499_714+530del others(32): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 26932180 | |||||
| chr2:26932181
|
A | C | 7 | a0001c0001t0001g0112a0001c0001t0001g0200a0001c0001t0001g0208others(4): Show | 7 | HG00738.hp2 HG01358.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.714+497A>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | chr2 | 26932181 | ||||||
| chr2:26932184
|
AAAGAAAG others(21): Show |
A | 1 | a0001c0002t0004g0141 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.714+503_714+530del others(28): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 26932184 | |||||
| chr2:26932185
|
A | AAGAAAGA others(13): Show |
3 | a0001c0001t0001g0184a0001c0001t0005g0203a0001c0001t0007g0172 | 3 | HG00280.hp1 HG00558.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.714+520_714+521ins others(20): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 26932185 | |||||
| chr2:26932185
|
A | AAGAAAGA others(9): Show |
2 | a0001c0001t0001g0157a0001c0001t0015g0183 | 2 | HG01433.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.714+516_714+517ins others(16): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 26932185 | |||||
| chr2:26932185
|
A | AAGAAAGA others(5): Show |
9 | a0001c0001t0001g0156a0001c0001t0001g0186a0001c0001t0001g0190others(6): Show | 9 | HG01069.hp2 HG01168.hp1 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.714+512_714+513ins others(12): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 26932185 | |||||
| chr2:26932185
|
A | AAGAAAGA others(1): Show |
8 | a0001c0001t0001g0124a0001c0001t0001g0165a0001c0001t0001g0189others(5): Show | 8 | HG01109.hp2 HG01952.hp2 HG02004.hp1 others(5): Show |
intron_variant | MODIFIER | c.714+508_714+509ins others(8): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 26932185 | |||||
| chr2:26932185
|
A | AAGAC | 9 | a0001c0001t0001g0139a0001c0001t0001g0211a0001c0001t0001g0222others(6): Show | 9 | HG00438.hp2 HG00597.hp1 HG00735.hp1 others(6): Show |
intron_variant | MODIFIER | c.714+504_714+505ins others(4): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 26932185 | |||||
| chr2:26932185
|
A | C | 14 | a0001c0001t0001g0115a0001c0001t0001g0173a0001c0001t0001g0174others(11): Show | 14 | HG00597.hp2 HG01074.hp2 HG01934.hp1 others(11): Show |
intron_variant | MODIFIER | c.714+501A>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | chr2 | 26932185 | ||||||
| chr2:26932187
|
G | T | 1 | a0001c0002t0011g0062 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.714+503G>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | chr2 | 26932187 | ||||||
| chr2:26932188
|
AAAGAAAG others(17): Show |
A | 2 | a0001c0002t0020g0057a0001c0002t0020g0058 | 2 | NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.714+507_714+530del others(24): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 26932188 | |||||
| chr2:26932189
|
A | AAGAAAGA others(9): Show |
1 | a0001c0001t0016g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.714+520_714+521ins others(16): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 26932189 | |||||
| chr2:26932189
|
A | AAGAAAGA others(5): Show |
2 | a0001c0001t0001g0104a0001c0001t0001g0108 | 2 | NA19005.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.714+516_714+517ins others(12): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 26932189 | |||||
| chr2:26932189
|
A | AAGAAAGA others(1): Show |
8 | a0001c0001t0001g0107a0001c0001t0001g0149a0001c0001t0001g0180others(5): Show | 8 | HG00639.hp2 HG01515.hp1 HG01517.hp1 others(5): Show |
intron_variant | MODIFIER | c.714+512_714+513ins others(8): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 26932189 | |||||
| chr2:26932189
|
A | AAGAC | 8 | a0001c0001t0001g0059a0001c0001t0001g0106a0001c0001t0001g0193others(5): Show | 8 | HG00099.hp1 HG01884.hp2 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.714+508_714+509ins others(4): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 26932189 | |||||
| chr2:26932189
|
A | C | 10 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0026others(7): Show | 10 | HG01361.hp2 HG02083.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.714+505A>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | chr2 | 26932189 | ||||||
| chr2:26932192
|
AAAGAAAG others(4): Show |
A | 1 | a0001c0001t0001g0199 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.714+511_714+521del others(11): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 26932192 | |||||
| chr2:26932192
|
AAAGAAAG others(13): Show |
A | 1 | a0001c0001t0037g0053 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.714+511_714+530del others(20): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 26932192 | |||||
| chr2:26932193
|
A | C | 5 | a0001c0001t0001g0138a0001c0001t0010g0028a0001c0001t0010g0031others(2): Show | 5 | HG01106.hp2 HG01346.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.714+509A>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | chr2 | 26932193 | ||||||
| chr2:26932196
|
AAAGAAAG others(9): Show |
A | 5 | a0001c0002t0002g0101a0001c0002t0002g0135a0001c0002t0002g0151others(2): Show | 5 | HG01433.hp1 HG03492.hp2 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.714+515_714+530del others(16): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 26932196 | |||||
| chr2:26932200
|
AAAGAAAG others(5): Show |
A | 11 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0005g0018others(8): Show | 11 | HG00642.hp1 HG00673.hp2 HG02148.hp1 others(8): Show |
intron_variant | MODIFIER | c.714+519_714+530del others(12): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 26932200 | |||||
| chr2:26932204
|
AAAGAAAA others(1): Show |
A | 19 | a0001c0001t0001g0112a0001c0001t0001g0200a0001c0001t0001g0208others(16): Show | 19 | HG00639.hp1 HG00738.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.714+523_714+530del others(8): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 26932204 | |||||
| chr2:26932207
|
GA | G | 17 | a0001c0001t0001g0010a0001c0001t0003g0003a0001c0001t0003g0068others(14): Show | 17 | HG00733.hp2 HG01167.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.714+527delA | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 26932207 | |||||
| chr2:26932208
|
A | AAAG | 11 | a0001c0001t0003g0020a0001c0001t0012g0048a0001c0002t0002g0082others(8): Show | 11 | HG01069.hp1 HG01081.hp2 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.714+526_714+527ins others(3): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 26932208 | |||||
| chr2:26932208
|
A | AAAGAAAG others(4): Show |
3 | a0001c0001t0024g0036a0001c0002t0002g0131a0001c0002t0031g0073 | 3 | HG01167.hp1 NA19010.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.714+526_714+527ins others(11): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 26932208 | |||||
| chr2:26932208
|
AAAAG | A | 33 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0187others(30): Show | 33 | HG00140.hp2 HG00438.hp1 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.714+548_714+551del others(4): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 26932208 | |||||
| chr2:26932211
|
A | G | 53 | a0001c0001t0001g0059a0001c0001t0001g0071a0001c0001t0001g0100others(50): Show | 53 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.714+527A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | chr2 | 26932211 | ||||||
| chr2:26932212
|
G | A | 53 | a0001c0001t0001g0059a0001c0001t0001g0071a0001c0001t0001g0100others(50): Show | 53 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.714+528G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | chr2 | 26932212 | ||||||
| chr2:26932212
|
G | GA | 19 | a0001c0001t0003g0020a0001c0001t0012g0048a0001c0001t0024g0036others(16): Show | 19 | HG00099.hp2 HG00280.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.714+531dupA | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 26932212 | |||||
| chr2:26932240
|
A | G | 5 | a0001c0001t0010g0028a0001c0001t0010g0031a0001c0001t0010g0033others(2): Show | 5 | HG01106.hp2 HG01346.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.714+556A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | chr2 | 26932240 | ||||||
| chr2:26932289
|
G | A | 1 | a0001c0001t0001g0205 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.714+605G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | chr2 | 26932289 | ||||||
| chr2:26932299
|
A | C | 16 | a0001c0001t0003g0003a0001c0001t0003g0068a0001c0001t0009g0001others(13): Show | 16 | HG00733.hp2 HG01167.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.714+615A>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | chr2 | 26932299 | ||||||
| chr2:26932306
|
G | A | 16 | a0001c0001t0003g0003a0001c0001t0003g0068a0001c0001t0009g0001others(13): Show | 16 | HG00733.hp2 HG01167.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.714+622G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | chr2 | 26932306 | ||||||
| chr2:26932324
|
G | A | 1 | a0001c0002t0002g0128 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.714+640G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | chr2 | 26932324 | ||||||
| chr2:26932588
|
G | A | 16 | a0001c0001t0003g0003a0001c0001t0003g0068a0001c0001t0009g0001others(13): Show | 16 | HG00733.hp2 HG01167.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.715-670G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | chr2 | 26932588 | ||||||
| chr2:26932856
|
G | A | 1 | a0001c0001t0003g0068 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.715-402G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | chr2 | 26932856 | ||||||
| chr2:26932980
|
C | T | 115 | a0001c0001t0003g0003a0001c0001t0003g0068a0001c0001t0009g0001others(112): Show | 115 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.715-278C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | chr2 | 26932980 | ||||||
| chr2:26932981
|
G | T | 96 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0026others(93): Show | 96 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.715-277G>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | chr2 | 26932981 | ||||||
| chr2:26932994
|
G | A | 100 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0026others(97): Show | 100 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.715-264G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | chr2 | 26932994 | ||||||
| chr2:26933176
|
G | A | 1 | a0001c0001t0008g0025 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.715-82G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 6/12 | chr2 | 26933176 | ||||||
| chr2:26933548
|
T | G | 100 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0026others(97): Show | 100 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.790+215T>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 7/12 | chr2 | 26933548 | ||||||
| chr2:26933853
|
C | T | 2 | a0002c0003t0006g0092a0002c0003t0006g0093 | 2 | HG00140.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.790+520C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 7/12 | chr2 | 26933853 | ||||||
| chr2:26934017
|
G | A | 1 | a0001c0001t0033g0052 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.791-561G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 7/12 | chr2 | 26934017 | ||||||
| chr2:26934141
|
G | A | 3 | a0001c0002t0014g0034a0001c0002t0014g0037a0001c0002t0014g0038 | 3 | HG02486.hp1 HG03041.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.791-437G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 7/12 | chr2 | 26934141 | ||||||
| chr2:26934147
|
C | T | 1 | a0001c0002t0031g0073 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.791-431C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 7/12 | chr2 | 26934147 | ||||||
| chr2:26934292
|
C | T | 2 | a0001c0001t0008g0023a0001c0001t0008g0164 | 2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.791-286C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 7/12 | chr2 | 26934292 | ||||||
| chr2:26934300
|
A | T | 16 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0003g0003others(13): Show | 16 | HG00733.hp2 HG01167.hp2 HG01934.hp2 others(13): Show |
intron_variant | MODIFIER | c.791-278A>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 7/12 | chr2 | 26934300 | ||||||
| chr2:26934342
|
G | A | 1 | a0001c0002t0002g0162 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.791-236G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 7/12 | chr2 | 26934342 | ||||||
| chr2:26934441
|
T | C | 18 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0003g0003others(15): Show | 18 | HG00733.hp2 HG01167.hp2 HG01934.hp2 others(15): Show |
intron_variant | MODIFIER | c.791-137T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 7/12 | chr2 | 26934441 | ||||||
| chr2:26934528
|
G | A | 100 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0026others(97): Show | 100 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.791-50G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 7/12 | chr2 | 26934528 | ||||||
| chr2:26934532
|
A | G | 217 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(214): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.791-46A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 7/12 | chr2 | 26934532 | ||||||
| chr2:26934742
|
G | A | 5 | a0001c0001t0013g0047a0001c0001t0013g0065a0001c0001t0013g0074others(2): Show | 5 | HG00733.hp2 HG01167.hp2 HG02886.hp2 others(2): Show |
splice_region_variant&intron_variant | LOW | c.947+8G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 8/12 | chr2 | 26934742 | ||||||
| chr2:26934920
|
T | C | 100 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0026others(97): Show | 100 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.947+186T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 8/12 | chr2 | 26934920 | ||||||
| chr2:26934937
|
A | AAGTATAA others(17): Show |
1 | a0001c0002t0002g0082 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.947+206_947+229dup others(24): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 26934937 | |||||
| chr2:26935119
|
G | A | 1 | a0001c0005t0003g0015 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.947+385G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 8/12 | chr2 | 26935119 | ||||||
| chr2:26935365
|
A | G | 1 | a0001c0001t0037g0053 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.947+631A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 8/12 | chr2 | 26935365 | ||||||
| chr2:26935545
|
C | T | 1 | a0001c0001t0016g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.947+811C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 8/12 | chr2 | 26935545 | ||||||
| chr2:26935691
|
C | CA | 23 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0205others(20): Show | 23 | HG00733.hp2 HG00738.hp1 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.947+976dupA | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 26935691 | |||||
| chr2:26935691
|
C | CAA | 81 | a0001c0001t0012g0030a0001c0001t0012g0048a0001c0001t0012g0051others(78): Show | 81 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.947+975_947+976dup others(2): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 26935691 | |||||
| chr2:26935691
|
CA | C | 47 | a0001c0001t0001g0115a0001c0001t0001g0124a0001c0001t0001g0139others(44): Show | 47 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.947+976delA | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 26935691 | |||||
| chr2:26935755
|
G | T | 100 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0026others(97): Show | 100 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.947+1021G>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 8/12 | chr2 | 26935755 | ||||||
| chr2:26936026
|
T | C | 217 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(214): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.947+1292T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 8/12 | chr2 | 26936026 | ||||||
| chr2:26936153
|
G | A | 1 | a0001c0001t0001g0192 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.947+1419G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 8/12 | chr2 | 26936153 | ||||||
| chr2:26936215
|
C | T | 1 | a0001c0001t0010g0028 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.947+1481C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 8/12 | chr2 | 26936215 | ||||||
| chr2:26936270
|
G | C | 6 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0026others(3): Show | 6 | HG02280.hp1 HG02451.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.947+1536G>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 8/12 | chr2 | 26936270 | ||||||
| chr2:26936271
|
T | A | 6 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0020others(3): Show | 6 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.947+1537T>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 8/12 | chr2 | 26936271 | ||||||
| chr2:26936305
|
G | C | 211 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(208): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.947+1571G>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 8/12 | chr2 | 26936305 | ||||||
| chr2:26936385
|
C | T | 6 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0020others(3): Show | 6 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.947+1651C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 8/12 | chr2 | 26936385 | ||||||
| chr2:26936415
|
G | A | 1 | a0001c0002t0002g0212 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.947+1681G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 8/12 | chr2 | 26936415 | ||||||
| chr2:26936458
|
G | C | 2 | a0001c0002t0002g0162a0001c0006t0004g0161 | 2 | HG00438.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.947+1724G>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 8/12 | chr2 | 26936458 | ||||||
| chr2:26936473
|
G | A | 110 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0003g0068others(107): Show | 110 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.947+1739G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 8/12 | chr2 | 26936473 | ||||||
| chr2:26936506
|
C | T | 1 | a0001c0001t0001g0193 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.947+1772C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 8/12 | chr2 | 26936506 | ||||||
| chr2:26936514
|
G | A | 5 | a0001c0002t0014g0034a0001c0002t0014g0037a0001c0002t0014g0038others(2): Show | 5 | HG02486.hp1 HG02970.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.947+1780G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 8/12 | chr2 | 26936514 | ||||||
| chr2:26936544
|
T | C | 1 | a0001c0002t0002g0152 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.947+1810T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 8/12 | chr2 | 26936544 | ||||||
| chr2:26936607
|
T | A | 1 | a0001c0001t0001g0177 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.947+1873T>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 8/12 | chr2 | 26936607 | ||||||
| chr2:26936614
|
T | C | 1 | a0001c0001t0042g0216 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.947+1880T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 8/12 | chr2 | 26936614 | ||||||
| chr2:26936918
|
C | T | 110 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0003g0068others(107): Show | 110 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.947+2184C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 8/12 | chr2 | 26936918 | ||||||
| chr2:26936945
|
T | TA | 5 | a0001c0001t0001g0149a0001c0001t0001g0157a0001c0001t0001g0225others(2): Show | 5 | HG01934.hp1 HG03209.hp2 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.947+2227dupA | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 26936945 | |||||
| chr2:26936945
|
T | TAA | 91 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0026others(88): Show | 91 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.947+2226_947+2227d others(4): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 26936945 | |||||
| chr2:26936945
|
T | TAAA | 7 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0139others(4): Show | 7 | HG01358.hp2 HG01934.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.947+2225_947+2227d others(5): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 26936945 | |||||
| chr2:26936945
|
T | TAAAAAAA others(4): Show |
1 | a0001c0005t0003g0015 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.947+2217_947+2227d others(13): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 26936945 | |||||
| chr2:26936945
|
T | TAAAAAAA others(6): Show |
3 | a0001c0002t0002g0128a0001c0002t0002g0155a0001c0002t0004g0099 | 3 | NA18954.hp1 NA18954.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.947+2215_947+2227d others(15): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 26936945 | |||||
| chr2:26936945
|
T | TAAAAAAA others(7): Show |
60 | a0001c0001t0012g0030a0001c0001t0012g0048a0001c0001t0012g0051others(57): Show | 60 | HG00099.hp2 HG00280.hp2 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.947+2214_947+2227d others(16): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 26936945 | |||||
| chr2:26936945
|
T | TAAAAAAA others(8): Show |
27 | a0001c0001t0037g0053a0001c0002t0002g0040a0001c0002t0002g0041others(24): Show | 27 | HG00140.hp2 HG00438.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.947+2213_947+2227d others(17): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 26936945 | |||||
| chr2:26936945
|
T | TAAAAAAA others(9): Show |
4 | a0001c0002t0002g0148a0001c0002t0004g0229a0001c0002t0006g0069others(1): Show | 4 | HG01515.hp2 HG02630.hp1 NA18952.hp2 others(1): Show |
intron_variant | MODIFIER | c.947+2212_947+2227d others(18): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 26936945 | |||||
| chr2:26936945
|
T | TAAAAAAA others(10): Show |
3 | a0001c0002t0006g0080a0001c0002t0027g0083a0001c0002t0039g0019 | 3 | HG02559.hp1 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.947+2227_947+2228i others(19): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 26936945 | |||||
| chr2:26936945
|
T | TAAAAAAA others(11): Show |
1 | a0001c0007t0040g0169 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.947+2227_947+2228i others(20): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 26936945 | |||||
| chr2:26936945
|
T | TAAAAAAA others(17): Show |
1 | a0001c0002t0002g0035 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.947+2227_947+2228i others(26): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 26936945 | |||||
| chr2:26936945
|
T | TAAAAAAA others(18): Show |
1 | a0001c0001t0009g0039 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.947+2227_947+2228i others(27): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 26936945 | |||||
| chr2:26936945
|
T | TAAAAAAA others(20): Show |
1 | a0001c0001t0013g0074 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.947+2227_947+2228i others(29): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 26936945 | |||||
| chr2:26936945
|
T | TAAAAAAA others(21): Show |
1 | a0001c0001t0013g0075 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.947+2227_947+2228i others(30): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 26936945 | |||||
| chr2:26936945
|
T | TAAAAAAA others(22): Show |
1 | a0001c0001t0013g0065 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.947+2227_947+2228i others(31): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 26936945 | |||||
| chr2:26936945
|
T | TAAAAAAA others(25): Show |
1 | a0001c0001t0013g0047 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.947+2227_947+2228i others(34): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 26936945 | |||||
| chr2:26936982
|
A | G | 1 | a0001c0001t0001g0205 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.947+2248A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 8/12 | chr2 | 26936982 | ||||||
| chr2:26937157
|
G | A | 1 | a0001c0005t0003g0015 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.947+2423G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 8/12 | chr2 | 26937157 | ||||||
| chr2:26937357
|
G | A | 1 | a0001c0005t0003g0015 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.947+2623G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 8/12 | chr2 | 26937357 | ||||||
| chr2:26937742
|
T | TTTTG | 60 | a0001c0001t0001g0059a0001c0001t0001g0071a0001c0001t0001g0100others(57): Show | 60 | HG00438.hp2 HG00558.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.948-2254_948-2251d others(6): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 26937742 | |||||
| chr2:26937742
|
T | TTTTGTTT others(1): Show |
41 | a0001c0001t0001g0115a0001c0001t0001g0124a0001c0001t0001g0139others(38): Show | 41 | HG00140.hp1 HG00280.hp1 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.948-2258_948-2251d others(10): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 26937742 | |||||
| chr2:26937742
|
TTTTG | T | 10 | a0001c0001t0001g0014a0001c0001t0007g0005a0001c0001t0010g0028others(7): Show | 10 | HG01106.hp2 HG01346.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.948-2254_948-2251d others(6): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 26937742 | |||||
| chr2:26937742
|
TTTTGTTT others(5): Show |
T | 1 | a0001c0005t0003g0015 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.948-2262_948-2251d others(14): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 26937742 | |||||
| chr2:26937856
|
C | G | 1 | a0001c0002t0031g0073 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.948-2175C>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 8/12 | chr2 | 26937856 | ||||||
| chr2:26937933
|
T | C | 2 | a0001c0001t0001g0009a0001c0001t0001g0010 | 2 | HG01934.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.948-2098T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 8/12 | chr2 | 26937933 | ||||||
| chr2:26937958
|
G | A | 1 | a0001c0001t0005g0018 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.948-2073G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 8/12 | chr2 | 26937958 | ||||||
| chr2:26938187
|
T | G | 1 | a0001c0001t0007g0185 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.948-1844T>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 8/12 | chr2 | 26938187 | ||||||
| chr2:26938192
|
A | G | 117 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0003g0003others(114): Show | 117 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.948-1839A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 8/12 | chr2 | 26938192 | ||||||
| chr2:26938321
|
G | C | 1 | a0001c0005t0003g0015 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.948-1710G>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 8/12 | chr2 | 26938321 | ||||||
| chr2:26938351
|
G | A | 2 | a0001c0001t0013g0047a0001c0001t0013g0065 | 2 | HG02886.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.948-1680G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 8/12 | chr2 | 26938351 | ||||||
| chr2:26938592
|
G | C | 4 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0027others(1): Show | 4 | HG02280.hp1 HG02451.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.948-1439G>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 8/12 | chr2 | 26938592 | ||||||
| chr2:26938608
|
G | C | 34 | a0001c0001t0001g0071a0001c0001t0001g0100a0001c0001t0001g0104others(31): Show | 34 | HG00438.hp2 HG00597.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.948-1423G>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 8/12 | chr2 | 26938608 | ||||||
| chr2:26938627
|
C | T | 1 | a0001c0001t0034g0054 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.948-1404C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 8/12 | chr2 | 26938627 | ||||||
| chr2:26938709
|
C | G | 1 | a0001c0002t0002g0127 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.948-1322C>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 8/12 | chr2 | 26938709 | ||||||
| chr2:26938723
|
G | A | 101 | a0001c0001t0012g0030a0001c0001t0012g0048a0001c0001t0012g0051others(98): Show | 101 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.948-1308G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 8/12 | chr2 | 26938723 | ||||||
| chr2:26938844
|
C | T | 1 | a0001c0001t0001g0225 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.948-1187C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 8/12 | chr2 | 26938844 | ||||||
| chr2:26938845
|
C | T | 3 | a0001c0001t0001g0225a0001c0001t0021g0006a0001c0001t0021g0007 | 3 | HG01934.hp1 HG03540.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.948-1186C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 8/12 | chr2 | 26938845 | ||||||
| chr2:26938855
|
T | C | 217 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(214): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.948-1176T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 8/12 | chr2 | 26938855 | ||||||
| chr2:26938945
|
C | T | 1 | a0001c0002t0028g0046 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.948-1086C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 8/12 | chr2 | 26938945 | ||||||
| chr2:26939016
|
T | C | 6 | a0001c0001t0003g0003a0001c0001t0009g0001a0001c0001t0009g0002others(3): Show | 6 | HG02109.hp1 HG02451.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.948-1015T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 8/12 | chr2 | 26939016 | ||||||
| chr2:26939135
|
A | T | 1 | a0001c0001t0032g0077 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.948-896A>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 8/12 | chr2 | 26939135 | ||||||
| chr2:26939139
|
C | CT | 211 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(208): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.948-884dupT | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 26939139 | |||||
| chr2:26939139
|
C | CTT | 6 | a0001c0001t0001g0184a0001c0002t0014g0034a0001c0002t0014g0037others(3): Show | 6 | HG02486.hp1 HG02970.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.948-885_948-884dup others(2): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 26939139 | |||||
| chr2:26939283
|
G | A | 5 | a0001c0001t0013g0047a0001c0001t0013g0065a0001c0001t0013g0074others(2): Show | 5 | HG00733.hp2 HG01167.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.948-748G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 8/12 | chr2 | 26939283 | ||||||
| chr2:26939284
|
C | T | 1 | a0001c0002t0002g0128 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.948-747C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 8/12 | chr2 | 26939284 | ||||||
| chr2:26939434
|
C | T | 2 | a0001c0001t0001g0112a0001c0002t0019g0122 | 2 | HG02083.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.948-597C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 8/12 | chr2 | 26939434 | ||||||
| chr2:26939472
|
T | C | 1 | a0001c0002t0006g0130 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.948-559T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 8/12 | chr2 | 26939472 | ||||||
| chr2:26939642
|
G | T | 12 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0003g0068others(9): Show | 12 | HG00733.hp2 HG01167.hp2 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.948-389G>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 8/12 | chr2 | 26939642 | ||||||
| chr2:26939710
|
T | C | 217 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(214): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.948-321T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 8/12 | chr2 | 26939710 | ||||||
| chr2:26939746
|
C | T | 2 | a0001c0001t0001g0009a0001c0001t0001g0010 | 2 | HG01934.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.948-285C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 8/12 | chr2 | 26939746 | ||||||
| chr2:26939904
|
C | A | 1 | a0001c0001t0001g0213 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.948-127C>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 8/12 | chr2 | 26939904 | ||||||
| chr2:26939905
|
G | A | 7 | a0001c0001t0003g0068a0001c0001t0009g0039a0001c0001t0013g0047others(4): Show | 7 | HG00733.hp2 HG01167.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.948-126G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 8/12 | chr2 | 26939905 | ||||||
| chr2:26940176
|
T | C | 112 | a0001c0001t0003g0068a0001c0001t0009g0039a0001c0001t0012g0030others(109): Show | 112 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(109): Show |
splice_region_variant&intron_variant | LOW | c.1089+4T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 9/12 | chr2 | 26940176 | ||||||
| chr2:26940415
|
AG | A | 5 | a0001c0001t0013g0047a0001c0001t0013g0065a0001c0001t0013g0074others(2): Show | 5 | HG00733.hp2 HG01167.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1089+244delG | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 9/12 | chr2 | 26940415 | ||||||
| chr2:26940416
|
G | A | 212 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(209): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.1089+244G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 9/12 | chr2 | 26940416 | ||||||
| chr2:26940465
|
A | G | 217 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(214): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.1089+293A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 9/12 | chr2 | 26940465 | ||||||
| chr2:26940500
|
CTT | C | 215 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(212): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.1089+343_1089+344d others(4): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 26940500 | |||||
| chr2:26940508
|
T | A | 2 | a0002c0003t0006g0092a0002c0003t0006g0093 | 2 | HG00140.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.1089+336T>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 9/12 | chr2 | 26940508 | ||||||
| chr2:26940527
|
T | G | 3 | a0001c0002t0002g0153a0001c0002t0002g0154a0001c0002t0002g0155 | 3 | HG00558.hp2 NA18959.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.1089+355T>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 9/12 | chr2 | 26940527 | ||||||
| chr2:26940598
|
G | A | 1 | a0001c0005t0003g0015 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1089+426G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 9/12 | chr2 | 26940598 | ||||||
| chr2:26940707
|
A | T | 1 | a0001c0001t0001g0205 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1089+535A>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 9/12 | chr2 | 26940707 | ||||||
| chr2:26940708
|
A | T | 1 | a0001c0001t0001g0205 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1089+536A>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 9/12 | chr2 | 26940708 | ||||||
| chr2:26940915
|
G | GATT | 2 | a0001c0001t0001g0100a0001c0005t0003g0015 | 2 | HG00642.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1089+765_1089+767d others(5): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 26940915 | |||||
| chr2:26940915
|
GATTATT | G | 3 | a0001c0001t0032g0077a0001c0004t0003g0011a0001c0004t0003g0064 | 3 | HG02109.hp1 HG02922.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1089+762_1089+767d others(8): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 26940915 | |||||
| chr2:26940934
|
ATTATTTA others(3): Show |
A | 1 | a0001c0002t0031g0073 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1089+765_1089+774d others(12): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 26940934 | |||||
| chr2:26940937
|
AT | A | 9 | a0001c0002t0002g0044a0001c0002t0006g0069a0001c0002t0011g0060others(6): Show | 9 | HG00738.hp1 HG02897.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.1089+768delT | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 26940937 | |||||
| chr2:26940940
|
T | A | 73 | a0001c0001t0012g0030a0001c0001t0012g0048a0001c0001t0012g0051others(70): Show | 73 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.1089+768T>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 9/12 | chr2 | 26940940 | ||||||
| chr2:26940941
|
A | AT | 96 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(93): Show | 96 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.1089+778dupT | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 26940941 | |||||
| chr2:26940941
|
A | T | 86 | a0001c0001t0012g0030a0001c0001t0012g0048a0001c0001t0012g0051others(83): Show | 86 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.1089+769A>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 9/12 | chr2 | 26940941 | ||||||
| chr2:26940944
|
T | A | 1 | a0001c0002t0006g0069 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1089+772T>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 9/12 | chr2 | 26940944 | ||||||
| chr2:26940944
|
T | TA | 6 | a0001c0001t0005g0081a0001c0001t0010g0028a0001c0001t0010g0031others(3): Show | 6 | HG01106.hp2 HG01346.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1089+772_1089+773i others(3): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 9/12 | chr2 | 26940944 | ||||||
| chr2:26940950
|
TG | T | 5 | a0001c0002t0014g0034a0001c0002t0014g0037a0001c0002t0014g0038others(2): Show | 5 | HG02486.hp1 HG02970.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1089+779delG | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 9/12 | chr2 | 26940950 | ||||||
| chr2:26940951
|
G | T | 212 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(209): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.1089+779G>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 9/12 | chr2 | 26940951 | ||||||
| chr2:26940953
|
G | T | 216 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(213): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.1089+781G>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 9/12 | chr2 | 26940953 | ||||||
| chr2:26941185
|
G | A | 2 | a0001c0002t0006g0069a0001c0002t0027g0083 | 2 | NA18522.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1090-765G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 9/12 | chr2 | 26941185 | ||||||
| chr2:26941938
|
G | A | 112 | a0001c0001t0003g0068a0001c0001t0009g0039a0001c0001t0012g0030others(109): Show | 112 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.1090-12G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 9/12 | chr2 | 26941938 | ||||||
| chr2:26942247
|
C | T | 1 | a0001c0005t0003g0015 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1232+155C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 10/12 | chr2 | 26942247 | ||||||
| chr2:26942334
|
T | C | 110 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(107): Show | 110 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.1233-209T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 10/12 | chr2 | 26942334 | ||||||
| chr2:26942449
|
TAAC | T | 2 | a0001c0002t0006g0084a0001c0002t0029g0137 | 2 | HG01361.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.1233-90_1233-88del others(3): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 26942449 | |||||
| chr2:26943232
|
C | T | 2 | a0001c0001t0003g0068a0001c0001t0009g0039 | 2 | HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1440+482C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 11/12 | chr2 | 26943232 | ||||||
| chr2:26943249
|
C | T | 1 | a0001c0001t0016g0228 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1440+499C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 11/12 | chr2 | 26943249 | ||||||
| chr2:26943407
|
T | C | 217 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(214): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.1440+657T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 11/12 | chr2 | 26943407 | ||||||
| chr2:26943919
|
G | T | 1 | a0001c0001t0003g0020 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1441-737G>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 11/12 | chr2 | 26943919 | ||||||
| chr2:26943925
|
C | T | 2 | a0001c0002t0004g0099a0001c0002t0004g0118 | 2 | NA18954.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.1441-731C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 11/12 | chr2 | 26943925 | ||||||
| chr2:26943954
|
T | C | 95 | a0001c0001t0032g0077a0001c0002t0002g0035a0001c0002t0002g0040others(92): Show | 95 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.1441-702T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 11/12 | chr2 | 26943954 | ||||||
| chr2:26943968
|
A | T | 1 | a0001c0002t0002g0094 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1441-688A>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 11/12 | chr2 | 26943968 | ||||||
| chr2:26944118
|
G | A | 1 | a0001c0001t0013g0047 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1441-538G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 11/12 | chr2 | 26944118 | ||||||
| chr2:26944358
|
A | G | 8 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0020others(5): Show | 8 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.1441-298A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 11/12 | chr2 | 26944358 | ||||||
| chr2:26944450
|
A | G | 1 | a0001c0001t0008g0023 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1441-206A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 11/12 | chr2 | 26944450 | ||||||
| chr2:26944452
|
A | G | 84 | a0001c0001t0010g0028a0001c0001t0010g0031a0001c0001t0010g0033others(81): Show | 84 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.1441-204A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 11/12 | chr2 | 26944452 | ||||||
| chr2:26944601
|
A | G | 2 | a0002c0003t0006g0092a0002c0003t0006g0093 | 2 | HG00140.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.1441-55A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 11/12 | chr2 | 26944601 | ||||||
| chr2:26944916
|
C | T | 96 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(93): Show | 96 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.1609+92C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 12/12 | chr2 | 26944916 | ||||||
| chr2:26945025
|
C | T | 1 | a0001c0002t0002g0101 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1609+201C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 12/12 | chr2 | 26945025 | ||||||
| chr2:26945142
|
G | C | 1 | a0001c0002t0031g0073 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1609+318G>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 12/12 | chr2 | 26945142 | ||||||
| chr2:26945160
|
C | G | 2 | a0001c0001t0016g0227a0001c0001t0016g0228 | 2 | HG02717.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1609+336C>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 12/12 | chr2 | 26945160 | ||||||
| chr2:26945304
|
C | CT | 6 | a0001c0001t0016g0227a0001c0001t0016g0228a0001c0001t0021g0006others(3): Show | 6 | HG01069.hp1 HG01168.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1609+494dupT | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 26945304 | |||||
| chr2:26945304
|
C | CTT | 102 | a0001c0001t0003g0003a0001c0001t0009g0001a0001c0001t0009g0002others(99): Show | 102 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.1609+493_1609+494d others(4): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 26945304 | |||||
| chr2:26945304
|
C | CTTT | 5 | a0001c0002t0002g0212a0001c0002t0019g0122a0001c0002t0039g0019others(2): Show | 5 | HG02083.hp2 HG02970.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1609+492_1609+494d others(5): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 26945304 | |||||
| chr2:26945511
|
T | TC | 16 | a0001c0001t0001g0195a0001c0001t0001g0199a0001c0001t0007g0109others(13): Show | 16 | HG00438.hp1 HG01255.hp1 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.1609+695dupC | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 26945511 | |||||
| chr2:26945543
|
G | A | 95 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(92): Show | 95 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.1609+719G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 12/12 | chr2 | 26945543 | ||||||
| chr2:26945700
|
G | A | 1 | a0001c0002t0018g0175 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1609+876G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 12/12 | chr2 | 26945700 | ||||||
| chr2:26945758
|
G | A | 2 | a0001c0002t0014g0037a0001c0002t0014g0038 | 2 | HG02486.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1609+934G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 12/12 | chr2 | 26945758 | ||||||
| chr2:26945758
|
G | C | 1 | a0001c0002t0002g0145 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1609+934G>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 12/12 | chr2 | 26945758 | ||||||
| chr2:26945759
|
C | T | 1 | a0001c0002t0002g0145 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1609+935C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 12/12 | chr2 | 26945759 | ||||||
| chr2:26945782
|
C | T | 2 | a0001c0002t0002g0119a0001c0002t0002g0135 | 2 | HG03492.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1609+958C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 12/12 | chr2 | 26945782 | ||||||
| chr2:26945784
|
G | A | 12 | a0001c0001t0012g0030a0001c0001t0012g0048a0001c0001t0012g0051others(9): Show | 12 | HG00639.hp1 HG01167.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1609+960G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 12/12 | chr2 | 26945784 | ||||||
| chr2:26945856
|
A | AGGGATGC others(5): Show |
1 | a0001c0001t0025g0032 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1609+1035_1610-104 others(16): Show |
DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 26945856 | |||||
| chr2:26945866
|
A | G | 1 | a0001c0002t0006g0080 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1609+1042A>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 12/12 | chr2 | 26945866 | ||||||
| chr2:26945875
|
C | T | 109 | a0001c0001t0012g0030a0001c0001t0012g0048a0001c0001t0012g0051others(106): Show | 109 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.1610-1035C>T | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 12/12 | chr2 | 26945875 | ||||||
| chr2:26945899
|
T | C | 2 | a0001c0002t0002g0119a0001c0002t0002g0135 | 2 | HG03492.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1610-1011T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 12/12 | chr2 | 26945899 | ||||||
| chr2:26945935
|
G | A | 3 | a0001c0001t0032g0077a0001c0004t0003g0011a0001c0004t0003g0064 | 3 | HG02109.hp1 HG02922.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1610-975G>A | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 12/12 | chr2 | 26945935 | ||||||
| chr2:26945975
|
A | AG | 6 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0020others(3): Show | 6 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.1610-931dupG | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 26945975 | |||||
| chr2:26946198
|
T | C | 1 | a0001c0001t0009g0039 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1610-712T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 12/12 | chr2 | 26946198 | ||||||
| chr2:26946622
|
T | C | 115 | a0001c0001t0003g0003a0001c0001t0003g0068a0001c0001t0009g0001others(112): Show | 115 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.1610-288T>C | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 12/12 | chr2 | 26946622 | ||||||
| chr2:26946672
|
T | G | 95 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(92): Show | 95 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.1610-238T>G | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 12/12 | chr2 | 26946672 | ||||||
| chr2:26946769
|
TC | T | 98 | a0001c0001t0015g0183a0001c0002t0002g0035a0001c0002t0002g0040others(95): Show | 98 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.1610-140delC | DPYSL5 | ENSG00000157851.17 | transcript | ENST00000288699.11 | protein_coding | 12/12 | chr2 | 26946769 |