Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 80067 |
| ensemblid | ENSG00000115827.14 |
| hgncid | 25784 |
| symbol | DCAF17 |
| name | DDB1 and CUL4 associated factor 17 |
| refseq_nuc | NM_025000.4 |
| refseq_prot | NP_079276.2 |
| ensembl_nuc | ENST00000375255.8 |
| ensembl_prot | ENSP00000364404.3 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 171434226 |
| end | 171485052 |
| strand | + |
| ver | v1.2 |
| region | chr2:171434226-171485052 |
| region5000 | chr2:171429226-171490052 |
| regionname0 | DCAF17_chr2_171434226_171485052 |
| regionname5000 | DCAF17_chr2_171429226_171490052 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 520 | 338 | 84 | 58 | 153 | 12 | 29 | 122 | DCAF17_chr2_171429226_171490052 | DCAF17 | MGPTR others(515): Show |
chr2 | 171429226 | 171490052 |
| a0002 | 0/0 | 520 | 20 | 5 | 1 | 11 | 0 | 3 | 6 | DCAF17_chr2_171429226_171490052 | DCAF17 | MGPTR others(515): Show |
chr2 | 171429226 | 171490052 |
| a0003 | 0/0 | 520 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | MGPTR others(515): Show |
chr2 | 171429226 | 171490052 |
| a0004 | 0/0 | 520 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | MGPTR others(515): Show |
chr2 | 171429226 | 171490052 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1560 | 209 | 47 | 42 | 89 | 11 | 18 | DCAF17_chr2_171429226_171490052 | DCAF17 | ATGGG others(1555): Show |
chr2 | 171429226 | 171490052 | ||
| a0001c0002 | 0/0 | 1560 | 93 | 14 | 15 | 53 | 1 | 10 | DCAF17_chr2_171429226_171490052 | DCAF17 | ATGGG others(1555): Show |
chr2 | 171429226 | 171490052 | ||
| a0001c0004 | 0/0 | 1560 | 14 | 14 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | ATGGG others(1555): Show |
chr2 | 171429226 | 171490052 | ||
| a0001c0005 | 0/0 | 1560 | 13 | 7 | 1 | 5 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | ATGGG others(1555): Show |
chr2 | 171429226 | 171490052 | ||
| a0001c0006 | 0/0 | 1560 | 6 | 0 | 0 | 5 | 0 | 1 | DCAF17_chr2_171429226_171490052 | DCAF17 | ATGGG others(1555): Show |
chr2 | 171429226 | 171490052 | ||
| a0001c0007 | 0/0 | 1560 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | ATGGG others(1555): Show |
chr2 | 171429226 | 171490052 | ||
| a0001c0009 | 0/0 | 1560 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | ATGGG others(1555): Show |
chr2 | 171429226 | 171490052 | ||
| a0001c0010 | 0/0 | 1560 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | ATGGG others(1555): Show |
chr2 | 171429226 | 171490052 | ||
| a0002c0003 | 0/0 | 1560 | 20 | 5 | 1 | 11 | 0 | 3 | DCAF17_chr2_171429226_171490052 | DCAF17 | ATGGG others(1555): Show |
chr2 | 171429226 | 171490052 | ||
| a0003c0011 | 0/0 | 1560 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | ATGGG others(1555): Show |
chr2 | 171429226 | 171490052 | ||
| a0004c0008 | 0/0 | 1560 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | ATGGG others(1555): Show |
chr2 | 171429226 | 171490052 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5853 | 182 | 27 | 40 | 87 | 11 | 17 | DCAF17_chr2_171429226_171490052 | DCAF17 | GAGAA others(5848): Show |
chr2 | 171429226 | 171490052 |
| a0001c0001t0005 | 1/0 | 5853 | 10 | 9 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | GAGAA others(5848): Show |
chr2 | 171429226 | 171490052 |
| a0001c0001t0006 | 0/0 | 5853 | 3 | 3 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | GAGAA others(5848): Show |
chr2 | 171429226 | 171490052 |
| a0001c0001t0007 | 0/0 | 5853 | 6 | 5 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | GAGAA others(5848): Show |
chr2 | 171429226 | 171490052 |
| a0001c0001t0012 | 0/0 | 5853 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | GAGAA others(5848): Show |
chr2 | 171429226 | 171490052 |
| a0001c0001t0014 | 0/1 | 5853 | 1 | 0 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | GAGAA others(5848): Show |
chr2 | 171429226 | 171490052 |
| a0001c0001t0016 | 0/0 | 5853 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | GAGAA others(5848): Show |
chr2 | 171429226 | 171490052 |
| a0001c0001t0018 | 0/0 | 5853 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF17_chr2_171429226_171490052 | DCAF17 | GAGAA others(5848): Show |
chr2 | 171429226 | 171490052 |
| a0001c0001t0019 | 0/0 | 5853 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | GAGAA others(5848): Show |
chr2 | 171429226 | 171490052 |
| a0001c0001t0020 | 0/0 | 5853 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | GAGAA others(5848): Show |
chr2 | 171429226 | 171490052 |
| a0001c0001t0021 | 0/0 | 5853 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | GAGAA others(5848): Show |
chr2 | 171429226 | 171490052 |
| a0001c0001t0024 | 0/0 | 5853 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | GAGAA others(5848): Show |
chr2 | 171429226 | 171490052 |
| a0001c0002t0002 | 0/0 | 5853 | 88 | 13 | 14 | 51 | 1 | 9 | DCAF17_chr2_171429226_171490052 | DCAF17 | GAGAA others(5848): Show |
chr2 | 171429226 | 171490052 |
| a0001c0002t0015 | 0/0 | 5853 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | GAGAA others(5848): Show |
chr2 | 171429226 | 171490052 |
| a0001c0002t0023 | 0/0 | 5853 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | GAGAA others(5848): Show |
chr2 | 171429226 | 171490052 |
| a0001c0002t0025 | 0/0 | 5853 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | GAGAA others(5848): Show |
chr2 | 171429226 | 171490052 |
| a0001c0002t0026 | 0/0 | 5853 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF17_chr2_171429226_171490052 | DCAF17 | GAGAA others(5848): Show |
chr2 | 171429226 | 171490052 |
| a0001c0002t0027 | 0/0 | 5853 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | GAGAA others(5848): Show |
chr2 | 171429226 | 171490052 |
| a0001c0004t0004 | 0/0 | 5853 | 13 | 13 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | GAGAA others(5848): Show |
chr2 | 171429226 | 171490052 |
| a0001c0004t0017 | 0/0 | 5853 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | GAGAA others(5848): Show |
chr2 | 171429226 | 171490052 |
| a0001c0005t0006 | 0/0 | 5853 | 6 | 6 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | GAGAA others(5848): Show |
chr2 | 171429226 | 171490052 |
| a0001c0005t0007 | 0/0 | 5853 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | GAGAA others(5848): Show |
chr2 | 171429226 | 171490052 |
| a0001c0005t0008 | 0/0 | 5853 | 3 | 0 | 0 | 3 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | GAGAA others(5848): Show |
chr2 | 171429226 | 171490052 |
| a0001c0005t0011 | 0/0 | 5853 | 2 | 0 | 0 | 2 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | GAGAA others(5848): Show |
chr2 | 171429226 | 171490052 |
| a0001c0005t0013 | 0/0 | 5853 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | GAGAA others(5848): Show |
chr2 | 171429226 | 171490052 |
| a0001c0006t0001 | 0/0 | 5853 | 3 | 0 | 0 | 3 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | GAGAA others(5848): Show |
chr2 | 171429226 | 171490052 |
| a0001c0006t0009 | 0/0 | 5853 | 2 | 0 | 0 | 1 | 0 | 1 | DCAF17_chr2_171429226_171490052 | DCAF17 | GAGAA others(5848): Show |
chr2 | 171429226 | 171490052 |
| a0001c0006t0022 | 0/0 | 5853 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | GAGAA others(5848): Show |
chr2 | 171429226 | 171490052 |
| a0001c0007t0001 | 0/0 | 5853 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | GAGAA others(5848): Show |
chr2 | 171429226 | 171490052 |
| a0001c0009t0002 | 0/0 | 5853 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | GAGAA others(5848): Show |
chr2 | 171429226 | 171490052 |
| a0001c0010t0001 | 0/0 | 5853 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | GAGAA others(5848): Show |
chr2 | 171429226 | 171490052 |
| a0002c0003t0003 | 0/0 | 5853 | 18 | 3 | 1 | 11 | 0 | 3 | DCAF17_chr2_171429226_171490052 | DCAF17 | GAGAA others(5848): Show |
chr2 | 171429226 | 171490052 |
| a0002c0003t0010 | 0/0 | 5853 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | GAGAA others(5848): Show |
chr2 | 171429226 | 171490052 |
| a0003c0011t0001 | 0/0 | 5853 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | GAGAA others(5848): Show |
chr2 | 171429226 | 171490052 |
| a0004c0008t0012 | 0/0 | 5853 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | GAGAA others(5848): Show |
chr2 | 171429226 | 171490052 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 18 | 0 | 0 | 18 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0002 | 0/0 | 8 | 0 | 3 | 2 | 1 | 2 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0004 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0005g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0005g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0005g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0005g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0005g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0005g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0005g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0005g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0005g0243 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0006g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0006g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0006g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0007g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0007g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0007g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0007g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0012g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0014g0167 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0016g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0018g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0019g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0020g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0021g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0001t0024g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0002t0002g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0002t0002g0007 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0002t0002g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0002t0002g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0002t0002g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0002t0002g0024 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0002t0002g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0002t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0002t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0002t0002g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0002t0002g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0002t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0002t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0002t0002g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0002t0002g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0002t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0002t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0002t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0002t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0002t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0002t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0002t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0002t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0002t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0002t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0002t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0002t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0002t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0002t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0002t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0002t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0002t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0002t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0002t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0002t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0002t0015g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0002t0023g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0002t0025g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0002t0026g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0002t0027g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0004t0004g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0004t0004g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0004t0004g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0004t0004g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0004t0004g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0004t0004g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0004t0004g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0004t0004g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0004t0004g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0004t0004g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0004t0017g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0005t0006g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0005t0006g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0005t0006g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0005t0006g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0005t0006g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0005t0007g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0005t0008g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0005t0008g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0005t0008g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0005t0011g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0005t0011g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0005t0013g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0006t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0006t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0006t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0006t0009g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0006t0009g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0006t0022g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0007t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0009t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0001c0010t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0002c0003t0003g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0002c0003t0003g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0002c0003t0003g0041 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0002c0003t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0002c0003t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0002c0003t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0002c0003t0003g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0002c0003t0003g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0002c0003t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0002c0003t0003g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0002c0003t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0002c0003t0003g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0002c0003t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0002c0003t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0002c0003t0010g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0003c0011t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| a0004c0008t0012g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0232 | EUR | GBR | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0253 | EUR | GBR | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0136 | EUR | GBR | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0046 | EUR | FIN | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG00280 | hp2 | a0001 | c0002 | t0002 | g0025 | EUR | FIN | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG00408 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | CHS | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG00408 | hp2 | a0001 | c0005 | t0008 | g0055 | EAS | CHS | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | CHS | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG00423 | hp2 | a0002 | c0003 | t0003 | g0022 | EAS | CHS | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | CHS | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | CHS | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG00558 | hp1 | a0001 | c0005 | t0011 | g0057 | EAS | CHS | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | CHS | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG00597 | hp2 | a0001 | c0002 | t0002 | g0008 | EAS | CHS | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG00621 | hp1 | a0001 | c0002 | t0002 | g0081 | EAS | CHS | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | PUR | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG00741 | hp2 | a0003 | c0011 | t0001 | g0182 | AMR | PUR | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG01074 | hp2 | a0001 | c0001 | t0007 | g0205 | AMR | PUR | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG01081 | hp1 | a0001 | c0002 | t0002 | g0115 | AMR | PUR | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG01081 | hp2 | a0002 | c0003 | t0003 | g0225 | AMR | PUR | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG01109 | hp1 | a0001 | c0002 | t0002 | g0100 | AMR | PUR | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG01167 | hp2 | a0001 | c0002 | t0002 | g0067 | AMR | PUR | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG01175 | hp1 | a0001 | c0002 | t0002 | g0088 | AMR | PUR | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG01192 | hp1 | a0001 | c0002 | t0023 | g0025 | AMR | PUR | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | CLM | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG01255 | hp2 | a0001 | c0002 | t0002 | g0094 | AMR | CLM | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | CLM | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | CLM | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG01258 | hp1 | a0001 | c0002 | t0002 | g0053 | AMR | CLM | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG01261 | hp1 | a0001 | c0005 | t0007 | g0211 | AMR | CLM | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | CLM | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | CLM | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG01346 | hp2 | a0001 | c0002 | t0002 | g0080 | AMR | CLM | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | CLM | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | CLM | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | CLM | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG01433 | hp2 | a0001 | c0002 | t0002 | g0024 | AMR | CLM | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | CLM | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0246 | EUR | IBS | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0018 | EUR | IBS | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0014 | EUR | IBS | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG01884 | hp1 | a0001 | c0001 | t0006 | g0220 | AFR | ACB | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG01884 | hp2 | a0002 | c0003 | t0010 | g0042 | AFR | ACB | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG01891 | hp1 | a0001 | c0001 | t0007 | g0017 | AFR | ACB | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PEL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG01952 | hp2 | a0001 | c0002 | t0002 | g0032 | AMR | PEL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG01975 | hp2 | a0001 | c0002 | t0002 | g0086 | AMR | PEL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | PEL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG01993 | hp2 | a0001 | c0002 | t0002 | g0052 | AMR | PEL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG02004 | hp2 | a0001 | c0002 | t0002 | g0032 | AMR | PEL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | KHV | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG02027 | hp1 | a0002 | c0003 | t0003 | g0223 | EAS | KHV | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG02040 | hp1 | a0001 | c0005 | t0008 | g0054 | EAS | KHV | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | KHV | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG02055 | hp1 | a0001 | c0005 | t0006 | g0049 | AFR | ACB | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | ACB | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG02056 | hp2 | a0001 | c0006 | t0009 | g0127 | EAS | KHV | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG02080 | hp1 | a0002 | c0003 | t0003 | g0041 | EAS | KHV | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | KHV | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | KHV | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG02083 | hp2 | a0001 | c0006 | t0022 | g0035 | EAS | KHV | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG02129 | hp2 | a0002 | c0003 | t0003 | g0227 | EAS | KHV | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG02132 | hp1 | a0002 | c0003 | t0003 | g0224 | EAS | KHV | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG02135 | hp1 | a0001 | c0002 | t0002 | g0024 | EAS | KHV | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG02145 | hp1 | a0001 | c0001 | t0005 | g0239 | AFR | ACB | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG02145 | hp2 | a0001 | c0001 | t0021 | g0147 | AFR | ACB | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG02155 | hp1 | a0001 | c0006 | t0001 | g0035 | EAS | CDX | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | CDX | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | ACB | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG02280 | hp1 | a0001 | c0001 | t0007 | g0017 | AFR | ACB | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG02280 | hp2 | a0001 | c0001 | t0006 | g0221 | AFR | ACB | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG02293 | hp2 | a0001 | c0002 | t0002 | g0105 | AMR | PEL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PEL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG02300 | hp2 | a0001 | c0002 | t0002 | g0066 | AMR | PEL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG02451 | hp2 | a0001 | c0002 | t0002 | g0090 | AFR | ACB | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | GWD | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG02602 | hp2 | a0001 | c0002 | t0026 | g0030 | SAS | PJL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG02615 | hp1 | a0001 | c0002 | t0002 | g0077 | AFR | GWD | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG02615 | hp2 | a0001 | c0002 | t0002 | g0033 | AFR | GWD | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG02622 | hp1 | a0001 | c0001 | t0005 | g0240 | AFR | GWD | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG02622 | hp2 | a0001 | c0001 | t0005 | g0034 | AFR | GWD | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG02647 | hp1 | a0001 | c0005 | t0006 | g0023 | AFR | GWD | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG02647 | hp2 | a0001 | c0004 | t0004 | g0006 | AFR | GWD | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG02717 | hp1 | a0001 | c0001 | t0007 | g0196 | AFR | GWD | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG02717 | hp2 | a0001 | c0005 | t0013 | g0048 | AFR | GWD | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0248 | SAS | PJL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG02735 | hp2 | a0001 | c0001 | t0018 | g0237 | SAS | PJL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG02809 | hp2 | a0001 | c0001 | t0024 | g0178 | AFR | GWD | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG02818 | hp1 | a0001 | c0001 | t0005 | g0116 | AFR | GWD | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG02818 | hp2 | a0002 | c0003 | t0003 | g0040 | AFR | GWD | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG02886 | hp2 | a0001 | c0002 | t0002 | g0072 | AFR | GWD | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | GWD | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG02895 | hp2 | a0001 | c0004 | t0004 | g0039 | AFR | GWD | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG02896 | hp1 | a0001 | c0002 | t0002 | g0010 | AFR | GWD | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG02896 | hp2 | a0001 | c0004 | t0004 | g0006 | AFR | GWD | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG02897 | hp2 | a0001 | c0004 | t0004 | g0006 | AFR | GWD | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG02922 | hp1 | a0001 | c0002 | t0002 | g0033 | AFR | ESN | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG02965 | hp1 | a0001 | c0002 | t0002 | g0010 | AFR | ESN | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | ESN | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG02970 | hp1 | a0001 | c0004 | t0004 | g0215 | AFR | ESN | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG02970 | hp2 | a0001 | c0010 | t0001 | g0201 | AFR | ESN | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG02976 | hp1 | a0001 | c0004 | t0004 | g0212 | AFR | ESN | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | ESN | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG03041 | hp1 | a0001 | c0002 | t0002 | g0091 | AFR | GWD | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG03041 | hp2 | a0001 | c0001 | t0007 | g0198 | AFR | GWD | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | MSL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG03098 | hp2 | a0001 | c0005 | t0006 | g0051 | AFR | MSL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG03130 | hp1 | a0001 | c0002 | t0002 | g0071 | AFR | ESN | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | ESN | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG03139 | hp1 | a0002 | c0003 | t0003 | g0040 | AFR | ESN | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG03139 | hp2 | a0002 | c0003 | t0010 | g0042 | AFR | ESN | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG03195 | hp1 | a0001 | c0001 | t0005 | g0062 | AFR | ESN | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG03195 | hp2 | a0001 | c0001 | t0005 | g0117 | AFR | ESN | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG03209 | hp2 | a0001 | c0004 | t0004 | g0210 | AFR | MSL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG03225 | hp1 | a0001 | c0001 | t0005 | g0242 | AFR | MSL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG03225 | hp2 | a0001 | c0001 | t0007 | g0017 | AFR | MSL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG03239 | hp2 | a0001 | c0002 | t0002 | g0029 | SAS | PJL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG03453 | hp1 | a0001 | c0007 | t0001 | g0123 | AFR | MSL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG03453 | hp2 | a0001 | c0005 | t0006 | g0047 | AFR | MSL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | MSL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG03486 | hp2 | a0001 | c0004 | t0004 | g0134 | AFR | MSL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG03540 | hp1 | a0001 | c0004 | t0004 | g0214 | AFR | GWD | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG03540 | hp2 | a0001 | c0005 | t0006 | g0023 | AFR | GWD | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG03654 | hp1 | a0001 | c0002 | t0002 | g0065 | SAS | PJL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG03654 | hp2 | a0002 | c0003 | t0003 | g0228 | SAS | PJL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG03669 | hp2 | a0001 | c0002 | t0002 | g0007 | SAS | PJL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG03688 | hp1 | a0001 | c0002 | t0002 | g0029 | SAS | STU | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG03688 | hp2 | a0001 | c0002 | t0002 | g0007 | SAS | STU | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG03704 | hp2 | a0002 | c0003 | t0003 | g0226 | SAS | PJL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0250 | SAS | BEB | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | BEB | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG03834 | hp1 | a0001 | c0002 | t0002 | g0101 | SAS | BEB | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | BEB | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG03927 | hp2 | a0001 | c0006 | t0009 | g0122 | SAS | BEB | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | BEB | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG04184 | hp2 | a0001 | c0002 | t0002 | g0068 | SAS | BEB | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0254 | SAS | STU | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG04199 | hp2 | a0001 | c0002 | t0002 | g0085 | SAS | STU | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | STU | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG04204 | hp2 | a0002 | c0003 | t0003 | g0041 | SAS | STU | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG04228 | hp1 | a0001 | c0002 | t0002 | g0113 | SAS | STU | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | STU | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | YRI | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | YRI | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18612 | hp2 | a0001 | c0002 | t0002 | g0079 | EAS | CHB | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18906 | hp1 | a0004 | c0008 | t0012 | g0158 | AFR | YRI | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18906 | hp2 | a0001 | c0004 | t0004 | g0216 | AFR | YRI | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18940 | hp1 | a0001 | c0002 | t0002 | g0114 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18941 | hp1 | a0002 | c0003 | t0003 | g0266 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18941 | hp2 | a0001 | c0002 | t0002 | g0098 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18942 | hp1 | a0001 | c0005 | t0008 | g0058 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18944 | hp1 | a0001 | c0002 | t0002 | g0106 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18946 | hp2 | a0001 | c0002 | t0002 | g0063 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18947 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18950 | hp2 | a0001 | c0002 | t0002 | g0031 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18952 | hp2 | a0001 | c0002 | t0002 | g0107 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18954 | hp1 | a0001 | c0002 | t0002 | g0027 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18957 | hp2 | a0002 | c0003 | t0003 | g0022 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18959 | hp1 | a0002 | c0003 | t0003 | g0061 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18959 | hp2 | a0001 | c0001 | t0016 | g0170 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18961 | hp2 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18962 | hp1 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18963 | hp1 | a0001 | c0001 | t0020 | g0001 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18963 | hp2 | a0001 | c0002 | t0002 | g0075 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18966 | hp1 | a0001 | c0002 | t0002 | g0083 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18967 | hp1 | a0001 | c0002 | t0002 | g0087 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18969 | hp2 | a0002 | c0003 | t0003 | g0267 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18972 | hp2 | a0001 | c0002 | t0002 | g0078 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18973 | hp1 | a0001 | c0002 | t0002 | g0026 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18975 | hp2 | a0001 | c0002 | t0002 | g0111 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18977 | hp2 | a0001 | c0002 | t0002 | g0027 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18982 | hp2 | a0001 | c0002 | t0002 | g0103 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18983 | hp1 | a0001 | c0006 | t0001 | g0124 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18984 | hp1 | a0001 | c0002 | t0002 | g0082 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18984 | hp2 | a0001 | c0002 | t0002 | g0095 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18986 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18987 | hp1 | a0001 | c0002 | t0002 | g0102 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18990 | hp1 | a0001 | c0002 | t0002 | g0070 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18991 | hp2 | a0001 | c0002 | t0002 | g0110 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18992 | hp2 | a0001 | c0002 | t0015 | g0031 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18994 | hp1 | a0001 | c0002 | t0002 | g0084 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18998 | hp1 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18999 | hp1 | a0001 | c0002 | t0002 | g0076 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA19000 | hp2 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA19003 | hp2 | a0001 | c0002 | t0002 | g0030 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA19005 | hp2 | a0002 | c0003 | t0003 | g0229 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA19006 | hp1 | a0002 | c0003 | t0003 | g0022 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA19007 | hp1 | a0001 | c0002 | t0002 | g0069 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA19009 | hp1 | a0001 | c0002 | t0002 | g0245 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA19009 | hp2 | a0001 | c0006 | t0001 | g0125 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA19011 | hp2 | a0001 | c0002 | t0002 | g0074 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | LWK | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA19030 | hp2 | a0001 | c0001 | t0012 | g0157 | AFR | LWK | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA19043 | hp1 | a0001 | c0001 | t0005 | g0241 | AFR | LWK | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA19043 | hp2 | a0001 | c0001 | t0006 | g0244 | AFR | LWK | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA19054 | hp1 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA19060 | hp2 | a0001 | c0002 | t0002 | g0092 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA19063 | hp1 | a0001 | c0002 | t0002 | g0104 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA19063 | hp2 | a0001 | c0005 | t0011 | g0056 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA19064 | hp1 | a0001 | c0002 | t0002 | g0099 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA19066 | hp1 | a0001 | c0009 | t0002 | g0139 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA19066 | hp2 | a0001 | c0002 | t0002 | g0028 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA19067 | hp2 | a0001 | c0002 | t0002 | g0026 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA19068 | hp1 | a0001 | c0002 | t0002 | g0097 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA19072 | hp1 | a0001 | c0002 | t0002 | g0064 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA19080 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA19080 | hp2 | a0001 | c0002 | t0027 | g0093 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA19081 | hp1 | a0001 | c0002 | t0002 | g0028 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA19082 | hp1 | a0001 | c0002 | t0002 | g0073 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA19087 | hp1 | a0001 | c0002 | t0002 | g0108 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA19088 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA19090 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | YRI | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA19240 | hp2 | a0001 | c0004 | t0004 | g0209 | AFR | YRI | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA20129 | hp1 | a0001 | c0004 | t0004 | g0039 | AFR | ASW | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | ASW | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0044 | EUR | TSI | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0263 | EUR | TSI | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG01123 | hp1 | a0001 | c0001 | t0019 | g0258 | AMR | CLM | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG02109 | hp1 | a0001 | c0002 | t0002 | g0089 | AFR | ACB | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG02109 | hp2 | a0001 | c0001 | t0005 | g0034 | AFR | ACB | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG02486 | hp2 | a0001 | c0002 | t0025 | g0109 | AFR | ACB | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG02559 | hp1 | a0001 | c0002 | t0002 | g0112 | AFR | ACB | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG03471 | hp1 | a0001 | c0004 | t0017 | g0213 | AFR | MSL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | MSL | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | USA | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| HG06807 | hp2 | a0001 | c0002 | t0002 | g0096 | AFR | USA | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA20300 | hp1 | a0001 | c0004 | t0004 | g0208 | AFR | USA | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA20300 | hp2 | a0001 | c0005 | t0006 | g0050 | AFR | USA | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA21309 | hp1 | a0002 | c0003 | t0003 | g0230 | AFR | LWK | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| NA21309 | hp2 | a0001 | c0002 | t0002 | g0010 | AFR | LWK | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0014 | g0167 | REF | REF | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0005 | g0243 | REF | REF | DCAF17_chr2_171429226_171490052 | DCAF17 | chr2 | 171429226 | 171490052 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:171435165 | A | G | 1 | a0003 | 1 | HG00741.hp2 | missense_variant | MODERATE | c.209A>G | p.Asn70Ser | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/14 | 561/5853 | 209/1563 | 70/520 | chr2 | 171435165 | |||
| chr2:171453141 | T | A | 1 | a0002 | 20 | HG00423.hp2 HG01081.hp2 HG01884.hp2 others(17): Show |
missense_variant | MODERATE | c.555T>A | p.His185Gln | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/14 | 907/5853 | 555/1563 | 185/520 | chr2 | 171453141 | |||
| chr2:171468965 | G | A | 1 | a0004 | 1 | NA18906.hp1 | missense_variant | MODERATE | c.916G>A | p.Val306Ile | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/14 | 1268/5853 | 916/1563 | 306/520 | chr2 | 171468965 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:171435106 | C | T | 4 | a0001c0002 a0001c0004 a0001c0005 others(1): Show |
140 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(137): Show |
synonymous_variant | LOW | c.150C>T | p.Val50Val | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/14 | 502/5853 | 150/1563 | 50/520 | chr2 | 171435106 | |||
| chr2:171458431 | T | C | 1 | a0001c0007 | 1 | HG03453.hp1 | synonymous_variant | LOW | c.792T>C | p.Thr264Thr | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/14 | 1144/5853 | 792/1563 | 264/520 | chr2 | 171458431 | |||
| chr2:171468904 | C | T | 1 | a0001c0010 | 1 | HG02970.hp2 | synonymous_variant | LOW | c.855C>T | p.Leu285Leu | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/14 | 1207/5853 | 855/1563 | 285/520 | chr2 | 171468904 | |||
| chr2:171468988 | G | A | 1 | a0001c0004 | 14 | HG02647.hp2 HG02895.hp2 HG02896.hp2 others(11): Show |
synonymous_variant | LOW | c.939G>A | p.Gln313Gln | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/14 | 1291/5853 | 939/1563 | 313/520 | chr2 | 171468988 | |||
| chr2:171473883 | A | G | 2 | a0001c0002 a0001c0009 |
94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
synonymous_variant | LOW | c.999A>G | p.Gln333Gln | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 10/14 | 1351/5853 | 999/1563 | 333/520 | chr2 | 171473883 | |||
| chr2:171480091 | T | C | 1 | a0001c0006 | 6 | HG02056.hp2 HG02083.hp2 HG02155.hp1 others(3): Show |
synonymous_variant | LOW | c.1320T>C | p.Ala440Ala | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 13/14 | 1672/5853 | 1320/1563 | 440/520 | chr2 | 171480091 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:171434467 | G | T | 2 | a0001c0002t0026 a0001c0002t0027 |
2 | HG02602.hp2 NA19080.hp2 |
5_prime_UTR_variant | MODIFIER | c.-111G>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 1/14 | 111 | chr2 | 171434467 | ||||||
| chr2:171434483 | C | T | 1 | a0001c0002t0025 | 1 | HG02486.hp2 | 5_prime_UTR_variant | MODIFIER | c.-95C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 1/14 | 95 | chr2 | 171434483 | ||||||
| chr2:171434514 | A | G | 1 | a0001c0001t0024 | 1 | HG02809.hp2 | 5_prime_UTR_variant | MODIFIER | c.-64A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 1/14 | 64 | chr2 | 171434514 | ||||||
| chr2:171434519 | G | A | 1 | a0001c0005t0013 | 1 | HG02717.hp2 | 5_prime_UTR_variant | MODIFIER | c.-59G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 1/14 | 59 | chr2 | 171434519 | ||||||
| chr2:171481129 | T | C | 1 | a0001c0006t0009 | 2 | HG02056.hp2 HG03927.hp2 |
3_prime_UTR_variant | MODIFIER | c.*15T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 14/14 | 15 | chr2 | 171481129 | ||||||
| chr2:171481464 | G | A | 2 | a0002c0003t0003 a0002c0003t0010 |
20 | HG00423.hp2 HG01081.hp2 HG01884.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*350G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 14/14 | 350 | chr2 | 171481464 | ||||||
| chr2:171481492 | T | C | 2 | a0001c0005t0008 a0001c0005t0011 |
5 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*378T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 14/14 | 378 | chr2 | 171481492 | ||||||
| chr2:171481568 | A | C | 1 | a0001c0002t0023 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*454A>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 14/14 | 454 | chr2 | 171481568 | ||||||
| chr2:171481644 | A | G | 1 | a0002c0003t0010 | 2 | HG01884.hp2 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*530A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 14/14 | 530 | chr2 | 171481644 | ||||||
| chr2:171481684 | G | A | 6 | a0001c0002t0002 a0001c0002t0015 a0001c0002t0023 others(3): Show |
93 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*570G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 14/14 | 570 | chr2 | 171481684 | ||||||
| chr2:171481790 | T | G | 6 | a0001c0002t0002 a0001c0002t0015 a0001c0002t0023 others(3): Show |
93 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*676T>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 14/14 | 676 | chr2 | 171481790 | ||||||
| chr2:171481791 | C | A | 2 | a0001c0001t0012 a0004c0008t0012 |
2 | NA18906.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*677C>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 14/14 | 677 | chr2 | 171481791 | ||||||
| chr2:171481810 | A | G | 1 | a0001c0006t0022 | 1 | HG02083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*696A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 14/14 | 696 | chr2 | 171481810 | ||||||
| chr2:171482119 | A | G | 3 | a0001c0001t0006 a0001c0005t0006 a0001c0005t0013 |
10 | HG01884.hp1 HG02055.hp1 HG02280.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1005A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 14/14 | 1005 | chr2 | 171482119 | ||||||
| chr2:171482148 | G | A | 2 | a0001c0005t0008 a0001c0005t0011 |
5 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1034G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 14/14 | 1034 | chr2 | 171482148 | ||||||
| chr2:171482635 | A | G | 2 | a0001c0005t0008 a0001c0005t0011 |
5 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1521A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 14/14 | 1521 | chr2 | 171482635 | ||||||
| chr2:171483297 | C | G | 5 | a0001c0001t0006 a0001c0005t0006 a0001c0005t0008 others(2): Show |
15 | HG00408.hp2 HG00558.hp1 HG01884.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2183C>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 14/14 | 2183 | chr2 | 171483297 | ||||||
| chr2:171483312 | T | G | 1 | a0001c0001t0016 | 1 | NA18959.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2198T>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 14/14 | 2198 | chr2 | 171483312 | ||||||
| chr2:171483454 | C | T | 33 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0007 others(30): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
3_prime_UTR_variant | MODIFIER | c.*2340C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 14/14 | 2340 | chr2 | 171483454 | ||||||
| chr2:171483462 | G | A | 2 | a0001c0001t0007 a0001c0005t0007 |
7 | HG01074.hp2 HG01261.hp1 HG01891.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2348G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 14/14 | 2348 | chr2 | 171483462 | ||||||
| chr2:171483494 | A | G | 1 | a0001c0001t0021 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2380A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 14/14 | 2380 | chr2 | 171483494 | ||||||
| chr2:171483539 | T | A | 6 | a0001c0002t0002 a0001c0002t0015 a0001c0002t0023 others(3): Show |
93 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*2425T>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 14/14 | 2425 | chr2 | 171483539 | ||||||
| chr2:171483587 | G | A | 2 | a0001c0004t0004 a0001c0004t0017 |
14 | HG02647.hp2 HG02895.hp2 HG02896.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2473G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 14/14 | 2473 | chr2 | 171483587 | ||||||
| chr2:171483889 | G | T | 2 | a0002c0003t0003 a0002c0003t0010 |
20 | HG00423.hp2 HG01081.hp2 HG01884.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*2775G>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 14/14 | 2775 | chr2 | 171483889 | ||||||
| chr2:171483909 | T | C | 13 | a0001c0001t0006 a0001c0002t0002 a0001c0002t0015 others(10): Show |
128 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(125): Show |
3_prime_UTR_variant | MODIFIER | c.*2795T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 14/14 | 2795 | chr2 | 171483909 | ||||||
| chr2:171484061 | A | C | 1 | a0001c0001t0020 | 1 | NA18963.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2947A>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 14/14 | 2947 | chr2 | 171484061 | ||||||
| chr2:171484085 | A | G | 1 | a0001c0001t0019 | 1 | HG01123.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2971A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 14/14 | 2971 | chr2 | 171484085 | ||||||
| chr2:171484090 | A | G | 1 | a0001c0005t0008 | 3 | HG00408.hp2 HG02040.hp1 NA18942.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2976A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 14/14 | 2976 | chr2 | 171484090 | ||||||
| chr2:171484226 | C | G | 6 | a0001c0002t0002 a0001c0002t0015 a0001c0002t0023 others(3): Show |
93 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*3112C>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 14/14 | 3112 | chr2 | 171484226 | ||||||
| chr2:171484242 | C | G | 1 | a0001c0001t0018 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3128C>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 14/14 | 3128 | chr2 | 171484242 | ||||||
| chr2:171484505 | T | C | 1 | a0001c0002t0015 | 1 | NA18992.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3391T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 14/14 | 3391 | chr2 | 171484505 | ||||||
| chr2:171484656 | A | C | 1 | a0001c0004t0017 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3542A>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 14/14 | 3542 | chr2 | 171484656 | ||||||
| chr2:171484817 | A | G | 6 | a0001c0002t0002 a0001c0002t0015 a0001c0002t0023 others(3): Show |
93 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*3703A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 14/14 | 3703 | chr2 | 171484817 | ||||||
| chr2:171484826 | A | G | 3 | a0001c0001t0006 a0001c0005t0006 a0001c0005t0013 |
10 | HG01884.hp1 HG02055.hp1 HG02280.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3712A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 14/14 | 3712 | chr2 | 171484826 | ||||||
| chr2:171484943 | G | A | 5 | a0001c0001t0006 a0001c0005t0006 a0001c0005t0008 others(2): Show |
15 | HG00408.hp2 HG00558.hp1 HG01884.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*3829G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 14/14 | 3829 | chr2 | 171484943 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:171434838 | C | G | 3 | a0002c0003t0003g0022 a0002c0003t0003g0266 a0002c0003t0003g0267 |
5 | HG00423.hp2 NA18941.hp1 NA18957.hp2 others(2): Show |
intron_variant | MODIFIER | c.126+135C>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 1/13 | chr2 | 171434838 | |||||||
| chr2:171435034 | T | G | 6 | a0001c0005t0006g0023 a0001c0005t0006g0047 a0001c0005t0006g0049 others(3): Show |
7 | HG02055.hp1 HG02647.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.127-49T>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 1/13 | chr2 | 171435034 | |||||||
| chr2:171435068 | C | A | 3 | a0001c0002t0002g0024 a0001c0002t0002g0052 a0001c0002t0002g0053 |
4 | HG01258.hp1 HG01433.hp2 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-15C>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 1/13 | chr2 | 171435068 | |||||||
| chr2:171435293 | A | G | 1 | a0001c0001t0001g0265 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.230+107A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171435293 | |||||||
| chr2:171435547 | C | CT | 23 | a0001c0001t0001g0021 a0001c0001t0001g0044 a0001c0001t0001g0045 others(20): Show |
28 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.230+377dupT | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 171435547 | ||||||
| chr2:171435547 | CT | C | 89 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0005g0062 others(86): Show |
111 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.230+377delT | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 171435547 | ||||||
| chr2:171435639 | C | T | 2 | a0001c0005t0006g0023 a0001c0005t0006g0051 |
3 | HG02647.hp1 HG03098.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.230+453C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171435639 | |||||||
| chr2:171435705 | A | G | 74 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0008 others(71): Show |
93 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.230+519A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171435705 | |||||||
| chr2:171435752 | A | G | 74 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0008 others(71): Show |
93 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.230+566A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171435752 | |||||||
| chr2:171436030 | T | G | 3 | a0001c0001t0005g0034 a0001c0001t0005g0116 a0001c0001t0005g0117 |
4 | HG02109.hp2 HG02622.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.230+844T>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171436030 | |||||||
| chr2:171436209 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.230+1023G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171436209 | |||||||
| chr2:171436215 | G | A | 261 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(258): Show |
348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.230+1029G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171436215 | |||||||
| chr2:171436234 | T | C | 4 | a0001c0001t0005g0062 a0001c0001t0005g0239 a0001c0001t0005g0240 others(1): Show |
4 | HG02145.hp1 HG02622.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.230+1048T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171436234 | |||||||
| chr2:171436327 | A | G | 14 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0019 others(11): Show |
24 | HG00099.hp2 HG01123.hp2 HG01361.hp2 others(21): Show |
intron_variant | MODIFIER | c.230+1141A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171436327 | |||||||
| chr2:171436633 | A | AT | 16 | a0001c0001t0001g0222 a0001c0001t0001g0238 a0002c0003t0003g0022 others(13): Show |
21 | HG00423.hp2 HG01081.hp2 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.230+1464dupT | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 171436633 | ||||||
| chr2:171436633 | AT | A | 110 | a0001c0001t0001g0011 a0001c0001t0001g0036 a0001c0001t0001g0119 others(107): Show |
133 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.230+1464delT | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 171436633 | ||||||
| chr2:171436774 | A | AT | 74 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(71): Show |
92 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.230+1605dupT | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 171436774 | ||||||
| chr2:171436774 | AT | A | 7 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0119 others(4): Show |
7 | HG01168.hp1 HG02897.hp1 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.230+1605delT | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 171436774 | ||||||
| chr2:171436868 | G | A | 5 | a0001c0005t0008g0054 a0001c0005t0008g0055 a0001c0005t0008g0058 others(2): Show |
5 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.230+1682G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171436868 | |||||||
| chr2:171436957 | A | G | 79 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(76): Show |
98 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.230+1771A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171436957 | |||||||
| chr2:171437027 | G | T | 1 | a0001c0001t0001g0217 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.230+1841G>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171437027 | |||||||
| chr2:171437033 | CA | C | 2 | a0001c0001t0001g0046 a0001c0001t0001g0263 |
3 | HG00280.hp1 HG02300.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.230+1850delA | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 171437033 | ||||||
| chr2:171437055 | T | C | 2 | a0002c0003t0003g0223 a0002c0003t0003g0224 |
2 | HG02027.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.230+1869T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171437055 | |||||||
| chr2:171437282 | C | A | 1 | a0001c0002t0002g0085 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.230+2096C>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171437282 | |||||||
| chr2:171437350 | T | G | 79 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(76): Show |
98 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.230+2164T>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171437350 | |||||||
| chr2:171437395 | C | T | 27 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0025 others(24): Show |
34 | HG00280.hp2 HG00408.hp1 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.230+2209C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171437395 | |||||||
| chr2:171437396 | A | G | 79 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(76): Show |
98 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.230+2210A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171437396 | |||||||
| chr2:171437533 | T | C | 15 | a0002c0003t0003g0022 a0002c0003t0003g0040 a0002c0003t0003g0041 others(12): Show |
20 | HG00423.hp2 HG01081.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.230+2347T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171437533 | |||||||
| chr2:171437946 | A | G | 2 | a0001c0001t0001g0020 a0001c0001t0018g0237 |
4 | HG02735.hp2 HG03491.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.230+2760A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171437946 | |||||||
| chr2:171437958 | C | T | 1 | a0001c0001t0001g0036 | 2 | HG01891.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.230+2772C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171437958 | |||||||
| chr2:171438052 | G | A | 74 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0008 others(71): Show |
93 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.230+2866G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171438052 | |||||||
| chr2:171438170 | TTA | T | 4 | a0001c0005t0006g0023 a0001c0005t0006g0049 a0001c0005t0006g0050 others(1): Show |
5 | HG02055.hp1 HG02647.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.230+2986_230+2987d others(4): Show |
DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 171438170 | ||||||
| chr2:171438278 | T | C | 1 | a0001c0001t0001g0120 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.230+3092T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171438278 | |||||||
| chr2:171438282 | G | A | 78 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(75): Show |
119 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.230+3096G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171438282 | |||||||
| chr2:171438303 | G | A | 2 | a0002c0003t0003g0225 a0002c0003t0003g0226 |
2 | HG01081.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.230+3117G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171438303 | |||||||
| chr2:171438363 | AGTTGACT | A | 74 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(71): Show |
113 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.230+3179_230+3185d others(9): Show |
DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 171438363 | ||||||
| chr2:171438501 | C | T | 1 | a0001c0002t0002g0114 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.230+3315C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171438501 | |||||||
| chr2:171438510 | C | T | 12 | a0001c0004t0004g0006 a0001c0004t0004g0039 a0001c0004t0004g0134 others(9): Show |
15 | HG01261.hp1 HG02647.hp2 HG02895.hp2 others(12): Show |
intron_variant | MODIFIER | c.230+3324C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171438510 | |||||||
| chr2:171438594 | T | G | 4 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(1): Show |
4 | HG00140.hp2 HG01175.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.230+3408T>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171438594 | |||||||
| chr2:171438746 | T | G | 1 | a0001c0001t0001g0135 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.230+3560T>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171438746 | |||||||
| chr2:171438801 | A | G | 79 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(76): Show |
98 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.230+3615A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171438801 | |||||||
| chr2:171438849 | A | G | 1 | a0001c0002t0002g0113 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.230+3663A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171438849 | |||||||
| chr2:171438909 | T | TAGAGATA others(96): Show |
75 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0008 others(72): Show |
94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.230+3742_230+3743i others(105): Show |
DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 171438909 | ||||||
| chr2:171438920 | G | T | 5 | a0001c0005t0008g0054 a0001c0005t0008g0055 a0001c0005t0008g0058 others(2): Show |
5 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.230+3734G>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171438920 | |||||||
| chr2:171439031 | G | A | 101 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0008 others(98): Show |
126 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.230+3845G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171439031 | |||||||
| chr2:171439076 | A | G | 1 | a0001c0001t0001g0195 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.230+3890A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171439076 | |||||||
| chr2:171439089 | C | A | 1 | a0001c0005t0006g0047 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.230+3903C>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171439089 | |||||||
| chr2:171439170 | C | A | 1 | a0001c0001t0001g0195 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.230+3984C>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171439170 | |||||||
| chr2:171439232 | C | T | 1 | a0001c0001t0001g0194 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.230+4046C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171439232 | |||||||
| chr2:171439270 | C | T | 1 | a0001c0001t0001g0193 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.230+4084C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171439270 | |||||||
| chr2:171439284 | A | G | 78 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(75): Show |
117 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.230+4098A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171439284 | |||||||
| chr2:171439310 | A | G | 6 | a0001c0005t0006g0023 a0001c0005t0006g0047 a0001c0005t0006g0049 others(3): Show |
7 | HG02055.hp1 HG02647.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.230+4124A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171439310 | |||||||
| chr2:171439369 | G | C | 86 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0008 others(83): Show |
106 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.231-4154G>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171439369 | |||||||
| chr2:171439485 | T | C | 12 | a0001c0004t0004g0006 a0001c0004t0004g0039 a0001c0004t0004g0134 others(9): Show |
15 | HG01261.hp1 HG02647.hp2 HG02895.hp2 others(12): Show |
intron_variant | MODIFIER | c.231-4038T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171439485 | |||||||
| chr2:171439511 | C | CT | 15 | a0001c0001t0001g0142 a0001c0001t0001g0206 a0001c0001t0001g0207 others(12): Show |
18 | HG02280.hp2 HG02486.hp2 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.231-3991dupT | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 171439511 | ||||||
| chr2:171439511 | CT | C | 89 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(86): Show |
130 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.231-3991delT | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 171439511 | ||||||
| chr2:171439576 | G | T | 1 | a0001c0001t0001g0190 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.231-3947G>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171439576 | |||||||
| chr2:171439696 | G | A | 15 | a0002c0003t0003g0022 a0002c0003t0003g0040 a0002c0003t0003g0041 others(12): Show |
20 | HG00423.hp2 HG01081.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.231-3827G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171439696 | |||||||
| chr2:171439718 | A | G | 5 | a0001c0001t0001g0016 a0001c0001t0001g0188 a0001c0001t0001g0189 others(2): Show |
7 | HG00741.hp1 HG01361.hp1 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.231-3805A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171439718 | |||||||
| chr2:171439722 | G | C | 1 | a0002c0003t0003g0225 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.231-3801G>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171439722 | |||||||
| chr2:171439728 | C | G | 88 | a0001c0001t0006g0220 a0001c0001t0006g0221 a0001c0002t0002g0003 others(85): Show |
108 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.231-3795C>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171439728 | |||||||
| chr2:171439843 | G | C | 5 | a0001c0005t0008g0054 a0001c0005t0008g0055 a0001c0005t0008g0058 others(2): Show |
5 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.231-3680G>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171439843 | |||||||
| chr2:171439907 | G | C | 5 | a0001c0005t0008g0054 a0001c0005t0008g0055 a0001c0005t0008g0058 others(2): Show |
5 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.231-3616G>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171439907 | |||||||
| chr2:171440006 | A | C | 75 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0008 others(72): Show |
94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.231-3517A>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171440006 | |||||||
| chr2:171440226 | A | G | 6 | a0001c0005t0006g0023 a0001c0005t0006g0047 a0001c0005t0006g0049 others(3): Show |
7 | HG02055.hp1 HG02647.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.231-3297A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171440226 | |||||||
| chr2:171440272 | A | G | 101 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0008 others(98): Show |
126 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.231-3251A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171440272 | |||||||
| chr2:171440343 | A | G | 5 | a0001c0005t0008g0054 a0001c0005t0008g0055 a0001c0005t0008g0058 others(2): Show |
5 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.231-3180A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171440343 | |||||||
| chr2:171440401 | C | G | 5 | a0001c0005t0008g0054 a0001c0005t0008g0055 a0001c0005t0008g0058 others(2): Show |
5 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.231-3122C>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171440401 | |||||||
| chr2:171440443 | C | T | 5 | a0001c0005t0008g0054 a0001c0005t0008g0055 a0001c0005t0008g0058 others(2): Show |
5 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.231-3080C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171440443 | |||||||
| chr2:171440517 | C | T | 4 | a0001c0005t0006g0023 a0001c0005t0006g0049 a0001c0005t0006g0050 others(1): Show |
5 | HG02055.hp1 HG02647.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.231-3006C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171440517 | |||||||
| chr2:171440522 | C | T | 75 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0008 others(72): Show |
94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.231-3001C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171440522 | |||||||
| chr2:171440567 | G | C | 101 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0008 others(98): Show |
126 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.231-2956G>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171440567 | |||||||
| chr2:171440598 | A | G | 6 | a0001c0005t0006g0023 a0001c0005t0006g0047 a0001c0005t0006g0049 others(3): Show |
7 | HG02055.hp1 HG02647.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.231-2925A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171440598 | |||||||
| chr2:171440923 | C | T | 2 | a0001c0001t0001g0015 a0001c0001t0001g0190 |
4 | HG02155.hp2 NA18977.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.231-2600C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171440923 | |||||||
| chr2:171440924 | G | A | 75 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0008 others(72): Show |
94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.231-2599G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171440924 | |||||||
| chr2:171441004 | A | G | 1 | a0001c0001t0001g0187 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.231-2519A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171441004 | |||||||
| chr2:171441086 | G | A | 15 | a0002c0003t0003g0022 a0002c0003t0003g0040 a0002c0003t0003g0041 others(12): Show |
20 | HG00423.hp2 HG01081.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.231-2437G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171441086 | |||||||
| chr2:171441091 | G | A | 2 | a0001c0005t0006g0047 a0001c0005t0013g0048 |
2 | HG02717.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.231-2432G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171441091 | |||||||
| chr2:171441450 | C | A | 1 | a0001c0001t0001g0249 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.231-2073C>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171441450 | |||||||
| chr2:171441480 | C | G | 1 | a0001c0001t0001g0186 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.231-2043C>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171441480 | |||||||
| chr2:171441539 | A | T | 75 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0008 others(72): Show |
94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.231-1984A>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171441539 | |||||||
| chr2:171441557 | G | A | 2 | a0001c0001t0001g0142 a0001c0001t0001g0206 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.231-1966G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171441557 | |||||||
| chr2:171441632 | A | C | 7 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0202 others(4): Show |
7 | HG01074.hp2 HG02055.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.231-1891A>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171441632 | |||||||
| chr2:171441767 | G | A | 1 | a0001c0002t0002g0066 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.231-1756G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171441767 | |||||||
| chr2:171441897 | T | TGGGGGGG others(13): Show |
1 | a0001c0001t0001g0133 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.231-1626_231-1625i others(22): Show |
DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171441897 | |||||||
| chr2:171441916 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.231-1607C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171441916 | |||||||
| chr2:171441941 | TTATCACA others(5): Show |
T | 1 | a0001c0001t0001g0133 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.231-1581_231-1570d others(14): Show |
DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171441941 | |||||||
| chr2:171441954 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.231-1569G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171441954 | |||||||
| chr2:171441956 | A | G | 1 | a0001c0001t0001g0133 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.231-1567A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171441956 | |||||||
| chr2:171442026 | A | T | 1 | a0001c0001t0001g0133 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.231-1497A>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171442026 | |||||||
| chr2:171442028 | T | A | 1 | a0001c0001t0001g0133 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.231-1495T>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171442028 | |||||||
| chr2:171442031 | A | T | 1 | a0001c0001t0001g0133 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.231-1492A>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171442031 | |||||||
| chr2:171442152 | C | T | 20 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0038 others(17): Show |
26 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(23): Show |
intron_variant | MODIFIER | c.231-1371C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171442152 | |||||||
| chr2:171442175 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.231-1348C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171442175 | |||||||
| chr2:171442185 | A | T | 1 | a0001c0001t0001g0133 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.231-1338A>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171442185 | |||||||
| chr2:171442188 | T | G | 1 | a0001c0001t0001g0133 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.231-1335T>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171442188 | |||||||
| chr2:171442189 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.231-1334C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171442189 | |||||||
| chr2:171442191 | A | T | 1 | a0001c0001t0001g0133 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.231-1332A>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171442191 | |||||||
| chr2:171442192 | A | T | 1 | a0001c0001t0001g0133 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.231-1331A>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171442192 | |||||||
| chr2:171442211 | C | G | 1 | a0001c0001t0001g0133 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.231-1312C>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171442211 | |||||||
| chr2:171442212 | A | T | 1 | a0001c0001t0001g0133 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.231-1311A>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171442212 | |||||||
| chr2:171442220 | A | T | 1 | a0001c0001t0001g0133 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.231-1303A>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171442220 | |||||||
| chr2:171442222 | T | G | 1 | a0001c0001t0001g0133 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.231-1301T>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171442222 | |||||||
| chr2:171442251 | A | G | 1 | a0001c0001t0001g0133 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.231-1272A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171442251 | |||||||
| chr2:171442252 | A | T | 1 | a0001c0001t0001g0133 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.231-1271A>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171442252 | |||||||
| chr2:171442253 | A | T | 1 | a0001c0001t0001g0133 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.231-1270A>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171442253 | |||||||
| chr2:171442258 | A | T | 1 | a0001c0001t0001g0133 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.231-1265A>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171442258 | |||||||
| chr2:171442261 | T | A | 1 | a0001c0001t0001g0133 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.231-1262T>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171442261 | |||||||
| chr2:171442267 | A | G | 1 | a0001c0001t0001g0133 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.231-1256A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171442267 | |||||||
| chr2:171442268 | A | G | 1 | a0001c0001t0001g0133 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.231-1255A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171442268 | |||||||
| chr2:171442271 | A | T | 1 | a0001c0001t0001g0133 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.231-1252A>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171442271 | |||||||
| chr2:171442272 | A | T | 1 | a0001c0001t0001g0133 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.231-1251A>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171442272 | |||||||
| chr2:171442275 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.231-1248G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171442275 | |||||||
| chr2:171442284 | C | G | 1 | a0001c0001t0001g0133 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.231-1239C>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171442284 | |||||||
| chr2:171442285 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.231-1238G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171442285 | |||||||
| chr2:171442296 | C | G | 1 | a0001c0001t0001g0133 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.231-1227C>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171442296 | |||||||
| chr2:171442296 | C | T | 2 | a0001c0004t0004g0215 a0001c0004t0004g0216 |
2 | HG02970.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.231-1227C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171442296 | |||||||
| chr2:171442373 | A | C | 1 | a0001c0001t0001g0133 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.231-1150A>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171442373 | |||||||
| chr2:171442382 | C | A | 1 | a0001c0001t0001g0133 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.231-1141C>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171442382 | |||||||
| chr2:171442476 | A | C | 2 | a0001c0001t0001g0176 a0001c0001t0001g0177 |
2 | NA19005.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.231-1047A>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171442476 | |||||||
| chr2:171442478 | C | T | 15 | a0002c0003t0003g0022 a0002c0003t0003g0040 a0002c0003t0003g0041 others(12): Show |
20 | HG00423.hp2 HG01081.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.231-1045C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171442478 | |||||||
| chr2:171442563 | C | CA | 15 | a0001c0001t0001g0121 a0001c0001t0001g0143 a0001c0001t0001g0144 others(12): Show |
15 | HG00408.hp2 HG00558.hp1 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.231-940dupA | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 171442563 | ||||||
| chr2:171442563 | CA | C | 75 | a0001c0001t0001g0004 a0001c0001t0001g0133 a0001c0001t0001g0248 others(72): Show |
97 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.231-940delA | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 171442563 | ||||||
| chr2:171442740 | C | T | 75 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0008 others(72): Show |
94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.231-783C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171442740 | |||||||
| chr2:171443029 | G | T | 1 | a0001c0004t0004g0214 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.231-494G>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171443029 | |||||||
| chr2:171443251 | G | A | 1 | a0001c0002t0002g0088 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.231-272G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171443251 | |||||||
| chr2:171443292 | T | C | 5 | a0001c0005t0008g0054 a0001c0005t0008g0055 a0001c0005t0008g0058 others(2): Show |
5 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.231-231T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171443292 | |||||||
| chr2:171443347 | GT | G | 6 | a0001c0001t0005g0062 a0001c0001t0005g0239 a0001c0001t0005g0240 others(3): Show |
6 | HG02145.hp1 HG02622.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.231-167delT | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 171443347 | ||||||
| chr2:171443349 | T | TA | 115 | a0001c0001t0006g0220 a0001c0001t0006g0221 a0001c0002t0002g0003 others(112): Show |
143 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.231-174_231-173ins others(1): Show |
DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 2/13 | chr2 | 171443349 | |||||||
| chr2:171443831 | A | AT | 8 | a0001c0001t0006g0220 a0001c0001t0006g0221 a0001c0005t0006g0023 others(5): Show |
9 | HG01884.hp1 HG02055.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.321+226dupT | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 171443831 | ||||||
| chr2:171443831 | AT | A | 15 | a0002c0003t0003g0022 a0002c0003t0003g0040 a0002c0003t0003g0041 others(12): Show |
20 | HG00423.hp2 HG01081.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.321+226delT | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 171443831 | ||||||
| chr2:171443899 | A | G | 5 | a0001c0005t0008g0054 a0001c0005t0008g0055 a0001c0005t0008g0058 others(2): Show |
5 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.321+286A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171443899 | |||||||
| chr2:171443909 | A | G | 4 | a0001c0001t0001g0046 a0001c0001t0001g0251 a0001c0001t0001g0252 others(1): Show |
5 | HG00280.hp1 HG01106.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.321+296A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171443909 | |||||||
| chr2:171444241 | G | A | 8 | a0001c0001t0006g0220 a0001c0001t0006g0221 a0001c0005t0006g0023 others(5): Show |
9 | HG01884.hp1 HG02055.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.321+628G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171444241 | |||||||
| chr2:171444354 | A | G | 1 | a0002c0003t0003g0230 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.321+741A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171444354 | |||||||
| chr2:171444638 | A | G | 1 | a0001c0005t0006g0050 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.321+1025A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171444638 | |||||||
| chr2:171444682 | G | A | 15 | a0002c0003t0003g0022 a0002c0003t0003g0040 a0002c0003t0003g0041 others(12): Show |
20 | HG00423.hp2 HG01081.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.321+1069G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171444682 | |||||||
| chr2:171444727 | A | G | 75 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0008 others(72): Show |
94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.321+1114A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171444727 | |||||||
| chr2:171444745 | A | G | 78 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(75): Show |
117 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.321+1132A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171444745 | |||||||
| chr2:171444749 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.321+1136C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171444749 | |||||||
| chr2:171444798 | G | A | 88 | a0001c0001t0006g0220 a0001c0001t0006g0221 a0001c0002t0002g0003 others(85): Show |
108 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.321+1185G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171444798 | |||||||
| chr2:171444858 | T | A | 6 | a0001c0005t0006g0023 a0001c0005t0006g0047 a0001c0005t0006g0049 others(3): Show |
7 | HG02055.hp1 HG02647.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.321+1245T>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171444858 | |||||||
| chr2:171445132 | A | AT | 87 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0202 others(84): Show |
106 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.321+1531dupT | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 171445132 | ||||||
| chr2:171445325 | A | C | 6 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(3): Show |
6 | HG02451.hp1 HG02486.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.321+1712A>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171445325 | |||||||
| chr2:171445495 | C | T | 75 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0008 others(72): Show |
94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.321+1882C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171445495 | |||||||
| chr2:171445557 | C | G | 2 | a0001c0001t0001g0142 a0001c0001t0001g0206 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.321+1944C>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171445557 | |||||||
| chr2:171445607 | C | T | 7 | a0001c0001t0006g0244 a0001c0005t0006g0023 a0001c0005t0006g0047 others(4): Show |
8 | HG02055.hp1 HG02647.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.321+1994C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171445607 | |||||||
| chr2:171445692 | T | C | 1 | a0001c0001t0006g0220 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.321+2079T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171445692 | |||||||
| chr2:171445808 | A | G | 114 | a0001c0001t0006g0244 a0001c0002t0002g0003 a0001c0002t0002g0007 others(111): Show |
142 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.321+2195A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171445808 | |||||||
| chr2:171445868 | A | C | 5 | a0001c0005t0008g0054 a0001c0005t0008g0055 a0001c0005t0008g0058 others(2): Show |
5 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.321+2255A>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171445868 | |||||||
| chr2:171445930 | G | A | 75 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0008 others(72): Show |
94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.321+2317G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171445930 | |||||||
| chr2:171445995 | A | G | 1 | a0001c0001t0001g0138 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.321+2382A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171445995 | |||||||
| chr2:171446256 | C | G | 1 | a0001c0001t0001g0184 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.322-2425C>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171446256 | |||||||
| chr2:171446501 | A | G | 1 | a0001c0001t0001g0207 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.322-2180A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171446501 | |||||||
| chr2:171446573 | T | A | 5 | a0001c0005t0008g0054 a0001c0005t0008g0055 a0001c0005t0008g0058 others(2): Show |
5 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.322-2108T>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171446573 | |||||||
| chr2:171446705 | A | G | 5 | a0001c0005t0008g0054 a0001c0005t0008g0055 a0001c0005t0008g0058 others(2): Show |
5 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.322-1976A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171446705 | |||||||
| chr2:171446767 | A | G | 5 | a0001c0005t0008g0054 a0001c0005t0008g0055 a0001c0005t0008g0058 others(2): Show |
5 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.322-1914A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171446767 | |||||||
| chr2:171446927 | G | A | 2 | a0001c0001t0001g0179 a0001c0001t0001g0185 |
2 | HG01069.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.322-1754G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171446927 | |||||||
| chr2:171446940 | C | T | 15 | a0002c0003t0003g0022 a0002c0003t0003g0040 a0002c0003t0003g0041 others(12): Show |
20 | HG00423.hp2 HG01081.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.322-1741C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171446940 | |||||||
| chr2:171446946 | T | C | 19 | a0001c0001t0001g0011 a0001c0001t0001g0036 a0001c0001t0001g0119 others(16): Show |
22 | HG01069.hp1 HG01071.hp2 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.322-1735T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171446946 | |||||||
| chr2:171446951 | G | T | 6 | a0001c0005t0006g0023 a0001c0005t0006g0047 a0001c0005t0006g0049 others(3): Show |
7 | HG02055.hp1 HG02647.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.322-1730G>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171446951 | |||||||
| chr2:171446962 | A | C | 1 | a0001c0002t0002g0112 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.322-1719A>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171446962 | |||||||
| chr2:171446973 | C | G | 75 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0008 others(72): Show |
94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.322-1708C>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171446973 | |||||||
| chr2:171446980 | A | G | 1 | a0001c0001t0001g0183 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.322-1701A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171446980 | |||||||
| chr2:171447045 | A | G | 39 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0024 others(36): Show |
47 | HG00597.hp2 HG01109.hp1 HG01175.hp1 others(44): Show |
intron_variant | MODIFIER | c.322-1636A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171447045 | |||||||
| chr2:171447127 | G | A | 6 | a0001c0005t0006g0023 a0001c0005t0006g0047 a0001c0005t0006g0049 others(3): Show |
7 | HG02055.hp1 HG02647.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.322-1554G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171447127 | |||||||
| chr2:171447190 | C | T | 5 | a0001c0005t0008g0054 a0001c0005t0008g0055 a0001c0005t0008g0058 others(2): Show |
5 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.322-1491C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171447190 | |||||||
| chr2:171447199 | A | C | 5 | a0001c0005t0008g0054 a0001c0005t0008g0055 a0001c0005t0008g0058 others(2): Show |
5 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.322-1482A>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171447199 | |||||||
| chr2:171447322 | A | C | 2 | a0001c0004t0004g0006 a0001c0004t0017g0213 |
4 | HG02647.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.322-1359A>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171447322 | |||||||
| chr2:171447401 | G | A | 15 | a0001c0001t0001g0021 a0001c0001t0001g0044 a0001c0001t0001g0045 others(12): Show |
20 | HG00140.hp1 HG00280.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.322-1280G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171447401 | |||||||
| chr2:171447454 | G | A | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | NA19067.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.322-1227G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171447454 | |||||||
| chr2:171447583 | C | T | 2 | a0001c0002t0002g0028 a0001c0002t0002g0110 |
3 | NA18991.hp2 NA19066.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.322-1098C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171447583 | |||||||
| chr2:171447675 | C | T | 132 | a0001c0001t0001g0011 a0001c0001t0001g0036 a0001c0001t0001g0119 others(129): Show |
163 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.322-1006C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171447675 | |||||||
| chr2:171447686 | G | A | 75 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0008 others(72): Show |
94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.322-995G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171447686 | |||||||
| chr2:171447830 | C | T | 2 | a0001c0005t0006g0023 a0001c0005t0006g0051 |
3 | HG02647.hp1 HG03098.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.322-851C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171447830 | |||||||
| chr2:171447854 | ACTTCCAC others(10): Show |
A | 1 | a0001c0002t0002g0069 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.322-824_322-808del others(17): Show |
DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 171447854 | ||||||
| chr2:171448016 | G | T | 1 | a0002c0003t0003g0224 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.322-665G>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171448016 | |||||||
| chr2:171448082 | C | T | 29 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0025 others(26): Show |
37 | HG00280.hp2 HG00408.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.322-599C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171448082 | |||||||
| chr2:171448085 | G | A | 4 | a0001c0005t0006g0023 a0001c0005t0006g0049 a0001c0005t0006g0050 others(1): Show |
5 | HG02055.hp1 HG02647.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.322-596G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171448085 | |||||||
| chr2:171448120 | G | A | 1 | a0001c0002t0002g0070 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.322-561G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171448120 | |||||||
| chr2:171448154 | C | T | 75 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0008 others(72): Show |
94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.322-527C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171448154 | |||||||
| chr2:171448177 | G | T | 2 | a0001c0001t0001g0118 a0003c0011t0001g0182 |
2 | HG00741.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.322-504G>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171448177 | |||||||
| chr2:171448178 | C | T | 2 | a0001c0001t0001g0118 a0003c0011t0001g0182 |
2 | HG00741.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.322-503C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171448178 | |||||||
| chr2:171448429 | T | TAAC | 75 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0008 others(72): Show |
94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.322-252_322-251ins others(3): Show |
DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171448429 | |||||||
| chr2:171448582 | T | C | 75 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0008 others(72): Show |
94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.322-99T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171448582 | |||||||
| chr2:171448585 | G | T | 1 | a0001c0001t0001g0260 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.322-96G>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171448585 | |||||||
| chr2:171448608 | C | T | 1 | a0001c0001t0001g0234 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.322-73C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171448608 | |||||||
| chr2:171448665 | C | CT | 71 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0008 others(68): Show |
89 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.322-15dupT | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 171448665 | ||||||
| chr2:171448667 | C | T | 75 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0008 others(72): Show |
94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.322-14C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 3/13 | chr2 | 171448667 | |||||||
| chr2:171448932 | A | G | 5 | a0001c0001t0001g0197 a0001c0001t0007g0017 a0001c0001t0007g0198 others(2): Show |
8 | HG01074.hp2 HG01884.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.458+115A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 4/13 | chr2 | 171448932 | |||||||
| chr2:171449151 | G | A | 19 | a0001c0001t0001g0011 a0001c0001t0001g0036 a0001c0001t0001g0119 others(16): Show |
22 | HG01069.hp1 HG01071.hp2 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.458+334G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 4/13 | chr2 | 171449151 | |||||||
| chr2:171449177 | T | A | 1 | a0001c0004t0004g0214 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.458+360T>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 4/13 | chr2 | 171449177 | |||||||
| chr2:171449271 | G | T | 1 | a0001c0001t0001g0132 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.458+454G>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 4/13 | chr2 | 171449271 | |||||||
| chr2:171449295 | A | G | 1 | a0001c0001t0001g0249 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.458+478A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 4/13 | chr2 | 171449295 | |||||||
| chr2:171449392 | A | G | 1 | a0001c0004t0004g0214 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.459-487A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 4/13 | chr2 | 171449392 | |||||||
| chr2:171449506 | T | A | 19 | a0001c0001t0001g0011 a0001c0001t0001g0036 a0001c0001t0001g0119 others(16): Show |
22 | HG01069.hp1 HG01071.hp2 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.459-373T>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 4/13 | chr2 | 171449506 | |||||||
| chr2:171449638 | G | A | 77 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0002t0002g0003 others(74): Show |
96 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.459-241G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 4/13 | chr2 | 171449638 | |||||||
| chr2:171449689 | A | G | 26 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0013 others(23): Show |
40 | HG00099.hp1 HG00609.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.459-190A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 4/13 | chr2 | 171449689 | |||||||
| chr2:171449973 | C | T | 5 | a0001c0001t0001g0019 a0001c0001t0001g0043 a0001c0001t0001g0233 others(2): Show |
8 | HG02083.hp1 NA18964.hp1 NA18966.hp2 others(5): Show |
intron_variant | MODIFIER | c.537+16C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 5/13 | chr2 | 171449973 | |||||||
| chr2:171450153 | T | C | 4 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(1): Show |
4 | HG00140.hp2 HG01175.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.537+196T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 5/13 | chr2 | 171450153 | |||||||
| chr2:171450180 | C | T | 88 | a0001c0001t0006g0220 a0001c0001t0006g0221 a0001c0002t0002g0003 others(85): Show |
108 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.537+223C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 5/13 | chr2 | 171450180 | |||||||
| chr2:171450209 | C | A | 1 | a0001c0006t0009g0122 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.537+252C>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 5/13 | chr2 | 171450209 | |||||||
| chr2:171450641 | G | A | 88 | a0001c0001t0006g0220 a0001c0001t0006g0221 a0001c0002t0002g0003 others(85): Show |
108 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.537+684G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 5/13 | chr2 | 171450641 | |||||||
| chr2:171450701 | T | C | 1 | a0001c0001t0001g0135 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.537+744T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 5/13 | chr2 | 171450701 | |||||||
| chr2:171450739 | C | G | 1 | a0003c0011t0001g0182 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.537+782C>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 5/13 | chr2 | 171450739 | |||||||
| chr2:171450748 | G | A | 1 | a0001c0002t0002g0089 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.537+791G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 5/13 | chr2 | 171450748 | |||||||
| chr2:171450808 | G | A | 103 | a0001c0001t0006g0220 a0001c0001t0006g0221 a0001c0002t0002g0003 others(100): Show |
128 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.537+851G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 5/13 | chr2 | 171450808 | |||||||
| chr2:171450875 | C | G | 17 | a0001c0001t0001g0014 a0001c0001t0001g0038 a0001c0001t0001g0118 others(14): Show |
20 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(17): Show |
intron_variant | MODIFIER | c.537+918C>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 5/13 | chr2 | 171450875 | |||||||
| chr2:171450900 | G | A | 86 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0008 others(83): Show |
106 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.537+943G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 5/13 | chr2 | 171450900 | |||||||
| chr2:171450938 | G | A | 1 | a0001c0010t0001g0201 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.537+981G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 5/13 | chr2 | 171450938 | |||||||
| chr2:171450964 | T | C | 8 | a0001c0001t0006g0220 a0001c0001t0006g0221 a0001c0005t0006g0023 others(5): Show |
9 | HG01884.hp1 HG02055.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.537+1007T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 5/13 | chr2 | 171450964 | |||||||
| chr2:171451074 | A | G | 5 | a0001c0005t0008g0054 a0001c0005t0008g0055 a0001c0005t0008g0058 others(2): Show |
5 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.537+1117A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 5/13 | chr2 | 171451074 | |||||||
| chr2:171451085 | T | G | 77 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(74): Show |
116 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.537+1128T>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 5/13 | chr2 | 171451085 | |||||||
| chr2:171451212 | G | A | 75 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0008 others(72): Show |
94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.537+1255G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 5/13 | chr2 | 171451212 | |||||||
| chr2:171451395 | C | CTCTCTTA others(1): Show |
5 | a0001c0005t0008g0054 a0001c0005t0008g0055 a0001c0005t0008g0058 others(2): Show |
5 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.537+1440_537+1447d others(10): Show |
DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 171451395 | ||||||
| chr2:171451418 | T | C | 1 | a0001c0001t0005g0242 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.537+1461T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 5/13 | chr2 | 171451418 | |||||||
| chr2:171451533 | T | C | 3 | a0001c0001t0005g0034 a0001c0001t0005g0116 a0001c0001t0005g0117 |
4 | HG02109.hp2 HG02622.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.537+1576T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 5/13 | chr2 | 171451533 | |||||||
| chr2:171451649 | C | G | 1 | a0001c0001t0001g0160 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.538-1475C>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 5/13 | chr2 | 171451649 | |||||||
| chr2:171451715 | A | G | 1 | a0001c0002t0002g0108 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.538-1409A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 5/13 | chr2 | 171451715 | |||||||
| chr2:171451759 | A | G | 75 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0008 others(72): Show |
94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.538-1365A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 5/13 | chr2 | 171451759 | |||||||
| chr2:171451853 | A | G | 14 | a0001c0001t0006g0220 a0001c0001t0006g0221 a0001c0001t0006g0244 others(11): Show |
15 | HG00408.hp2 HG00558.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.538-1271A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 5/13 | chr2 | 171451853 | |||||||
| chr2:171451881 | G | A | 1 | a0001c0004t0017g0213 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.538-1243G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 5/13 | chr2 | 171451881 | |||||||
| chr2:171451927 | A | G | 1 | a0001c0002t0002g0083 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.538-1197A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 5/13 | chr2 | 171451927 | |||||||
| chr2:171452100 | G | C | 103 | a0001c0001t0006g0220 a0001c0001t0006g0221 a0001c0002t0002g0003 others(100): Show |
128 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.538-1024G>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 5/13 | chr2 | 171452100 | |||||||
| chr2:171452289 | G | C | 1 | a0001c0002t0002g0092 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.538-835G>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 5/13 | chr2 | 171452289 | |||||||
| chr2:171452380 | C | T | 2 | a0001c0006t0009g0122 a0001c0006t0009g0127 |
2 | HG02056.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.538-744C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 5/13 | chr2 | 171452380 | |||||||
| chr2:171452524 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.538-600G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 5/13 | chr2 | 171452524 | |||||||
| chr2:171452567 | C | T | 81 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(78): Show |
122 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.538-557C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 5/13 | chr2 | 171452567 | |||||||
| chr2:171452571 | A | G | 15 | a0002c0003t0003g0022 a0002c0003t0003g0040 a0002c0003t0003g0041 others(12): Show |
20 | HG00423.hp2 HG01081.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.538-553A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 5/13 | chr2 | 171452571 | |||||||
| chr2:171452643 | G | A | 2 | a0001c0004t0004g0208 a0001c0004t0004g0214 |
2 | HG03540.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.538-481G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 5/13 | chr2 | 171452643 | |||||||
| chr2:171452996 | T | A | 75 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0008 others(72): Show |
94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.538-128T>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 5/13 | chr2 | 171452996 | |||||||
| chr2:171453391 | T | G | 1 | a0002c0003t0003g0227 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.627+178T>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | chr2 | 171453391 | |||||||
| chr2:171453436 | G | A | 1 | a0002c0003t0003g0040 | 2 | HG02818.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.627+223G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | chr2 | 171453436 | |||||||
| chr2:171453704 | C | T | 2 | a0001c0001t0001g0013 a0001c0001t0001g0175 |
4 | NA18947.hp2 NA18971.hp2 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.627+491C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | chr2 | 171453704 | |||||||
| chr2:171454036 | T | A | 14 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0019 others(11): Show |
24 | HG00099.hp2 HG01123.hp2 HG01361.hp2 others(21): Show |
intron_variant | MODIFIER | c.627+823T>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | chr2 | 171454036 | |||||||
| chr2:171454245 | C | T | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(210): Show |
285 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(282): Show |
intron_variant | MODIFIER | c.627+1032C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | chr2 | 171454245 | |||||||
| chr2:171454345 | C | T | 15 | a0002c0003t0003g0022 a0002c0003t0003g0040 a0002c0003t0003g0041 others(12): Show |
20 | HG00423.hp2 HG01081.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.627+1132C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | chr2 | 171454345 | |||||||
| chr2:171454371 | G | A | 14 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0019 others(11): Show |
24 | HG00099.hp2 HG01123.hp2 HG01361.hp2 others(21): Show |
intron_variant | MODIFIER | c.627+1158G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | chr2 | 171454371 | |||||||
| chr2:171454430 | G | A | 76 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0008 others(73): Show |
95 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.627+1217G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | chr2 | 171454430 | |||||||
| chr2:171454473 | A | G | 1 | a0001c0001t0001g0197 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.627+1260A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | chr2 | 171454473 | |||||||
| chr2:171454635 | A | G | 7 | a0001c0001t0006g0244 a0001c0005t0006g0023 a0001c0005t0006g0047 others(4): Show |
8 | HG02055.hp1 HG02647.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.627+1422A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | chr2 | 171454635 | |||||||
| chr2:171454688 | G | A | 75 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0008 others(72): Show |
94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.627+1475G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | chr2 | 171454688 | |||||||
| chr2:171454765 | T | C | 1 | a0001c0002t0002g0029 | 2 | HG03239.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.627+1552T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | chr2 | 171454765 | |||||||
| chr2:171454882 | CA | C | 13 | a0001c0001t0006g0244 a0001c0002t0002g0112 a0001c0005t0006g0023 others(10): Show |
14 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(11): Show |
intron_variant | MODIFIER | c.627+1682delA | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | 171454882 | ||||||
| chr2:171454902 | A | C | 1 | a0001c0001t0001g0121 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.627+1689A>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | chr2 | 171454902 | |||||||
| chr2:171454993 | T | A | 1 | a0001c0001t0001g0222 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.627+1780T>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | chr2 | 171454993 | |||||||
| chr2:171455059 | G | A | 1 | a0001c0002t0002g0053 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.627+1846G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | chr2 | 171455059 | |||||||
| chr2:171455130 | CCCACCCT | C | 102 | a0001c0001t0006g0244 a0001c0002t0002g0003 a0001c0002t0002g0007 others(99): Show |
127 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.627+1934_627+1940d others(9): Show |
DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | 171455130 | ||||||
| chr2:171455161 | C | A | 12 | a0001c0004t0004g0006 a0001c0004t0004g0039 a0001c0004t0004g0134 others(9): Show |
15 | HG01261.hp1 HG02647.hp2 HG02895.hp2 others(12): Show |
intron_variant | MODIFIER | c.627+1948C>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | chr2 | 171455161 | |||||||
| chr2:171455390 | G | A | 5 | a0001c0005t0008g0054 a0001c0005t0008g0055 a0001c0005t0008g0058 others(2): Show |
5 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.627+2177G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | chr2 | 171455390 | |||||||
| chr2:171455432 | G | A | 1 | a0001c0002t0002g0072 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.627+2219G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | chr2 | 171455432 | |||||||
| chr2:171455535 | G | A | 7 | a0001c0001t0006g0244 a0001c0005t0006g0023 a0001c0005t0006g0047 others(4): Show |
8 | HG02055.hp1 HG02647.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.627+2322G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | chr2 | 171455535 | |||||||
| chr2:171455597 | C | T | 7 | a0001c0001t0006g0244 a0001c0005t0006g0023 a0001c0005t0006g0047 others(4): Show |
8 | HG02055.hp1 HG02647.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.628-2374C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | chr2 | 171455597 | |||||||
| chr2:171455785 | T | C | 3 | a0001c0001t0007g0017 a0001c0001t0007g0196 a0001c0001t0007g0205 |
5 | HG01074.hp2 HG01891.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.628-2186T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | chr2 | 171455785 | |||||||
| chr2:171456739 | A | G | 5 | a0001c0005t0008g0054 a0001c0005t0008g0055 a0001c0005t0008g0058 others(2): Show |
5 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.628-1232A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | chr2 | 171456739 | |||||||
| chr2:171456742 | A | G | 2 | a0001c0001t0001g0142 a0001c0001t0001g0206 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.628-1229A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | chr2 | 171456742 | |||||||
| chr2:171456763 | A | G | 1 | a0001c0004t0004g0212 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.628-1208A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | chr2 | 171456763 | |||||||
| chr2:171456788 | G | T | 75 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0008 others(72): Show |
94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.628-1183G>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | chr2 | 171456788 | |||||||
| chr2:171456797 | A | G | 5 | a0001c0005t0008g0054 a0001c0005t0008g0055 a0001c0005t0008g0058 others(2): Show |
5 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.628-1174A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | chr2 | 171456797 | |||||||
| chr2:171456831 | G | C | 15 | a0002c0003t0003g0022 a0002c0003t0003g0040 a0002c0003t0003g0041 others(12): Show |
20 | HG00423.hp2 HG01081.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.628-1140G>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | chr2 | 171456831 | |||||||
| chr2:171456880 | A | G | 15 | a0002c0003t0003g0022 a0002c0003t0003g0040 a0002c0003t0003g0041 others(12): Show |
20 | HG00423.hp2 HG01081.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.628-1091A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | chr2 | 171456880 | |||||||
| chr2:171457056 | C | G | 6 | a0001c0001t0001g0250 a0001c0001t0001g0257 a0001c0001t0001g0259 others(3): Show |
6 | HG00642.hp1 HG01109.hp2 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.628-915C>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | chr2 | 171457056 | |||||||
| chr2:171457172 | G | A | 1 | a0001c0002t0027g0093 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.628-799G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | chr2 | 171457172 | |||||||
| chr2:171457214 | G | T | 6 | a0001c0001t0001g0250 a0001c0001t0001g0257 a0001c0001t0001g0259 others(3): Show |
6 | HG00642.hp1 HG01109.hp2 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.628-757G>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | chr2 | 171457214 | |||||||
| chr2:171457384 | T | C | 20 | a0001c0001t0001g0011 a0001c0001t0001g0036 a0001c0001t0001g0119 others(17): Show |
23 | HG01069.hp1 HG01071.hp1 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.628-587T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | chr2 | 171457384 | |||||||
| chr2:171457403 | C | G | 114 | a0001c0001t0006g0244 a0001c0002t0002g0003 a0001c0002t0002g0007 others(111): Show |
142 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.628-568C>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | chr2 | 171457403 | |||||||
| chr2:171457523 | G | A | 2 | a0001c0001t0001g0231 a0001c0001t0001g0232 |
2 | HG00099.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.628-448G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | chr2 | 171457523 | |||||||
| chr2:171457603 | A | C | 3 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0019g0258 |
3 | HG01109.hp2 HG01123.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.628-368A>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | chr2 | 171457603 | |||||||
| chr2:171457636 | C | T | 1 | a0001c0002t0025g0109 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.628-335C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | chr2 | 171457636 | |||||||
| chr2:171457744 | G | A | 75 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0008 others(72): Show |
94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.628-227G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | chr2 | 171457744 | |||||||
| chr2:171457934 | T | G | 3 | a0001c0004t0004g0208 a0001c0004t0004g0209 a0001c0004t0004g0214 |
3 | HG03540.hp1 NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.628-37T>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 6/13 | chr2 | 171457934 | |||||||
| chr2:171458134 | A | AT | 12 | a0001c0001t0001g0014 a0001c0001t0001g0038 a0001c0001t0001g0118 others(9): Show |
15 | HG00423.hp1 HG00438.hp1 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.732+70dupT | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr2 | 171458134 | ||||||
| chr2:171458134 | AT | A | 79 | a0001c0001t0006g0244 a0001c0002t0002g0003 a0001c0002t0002g0007 others(76): Show |
99 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.732+70delT | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr2 | 171458134 | ||||||
| chr2:171458595 | A | G | 7 | a0001c0001t0006g0244 a0001c0005t0006g0023 a0001c0005t0006g0047 others(4): Show |
8 | HG02055.hp1 HG02647.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.838+118A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171458595 | |||||||
| chr2:171458603 | A | T | 15 | a0002c0003t0003g0022 a0002c0003t0003g0040 a0002c0003t0003g0041 others(12): Show |
20 | HG00423.hp2 HG01081.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.838+126A>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171458603 | |||||||
| chr2:171458701 | C | T | 75 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0008 others(72): Show |
94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.838+224C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171458701 | |||||||
| chr2:171458772 | A | G | 1 | a0001c0001t0001g0257 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.838+295A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171458772 | |||||||
| chr2:171458830 | C | T | 2 | a0001c0001t0001g0142 a0001c0001t0001g0206 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.838+353C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171458830 | |||||||
| chr2:171458958 | A | T | 75 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0008 others(72): Show |
94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.838+481A>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171458958 | |||||||
| chr2:171459052 | G | A | 12 | a0001c0004t0004g0006 a0001c0004t0004g0039 a0001c0004t0004g0134 others(9): Show |
15 | HG01261.hp1 HG02647.hp2 HG02895.hp2 others(12): Show |
intron_variant | MODIFIER | c.838+575G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171459052 | |||||||
| chr2:171459080 | C | T | 5 | a0001c0005t0008g0054 a0001c0005t0008g0055 a0001c0005t0008g0058 others(2): Show |
5 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.838+603C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171459080 | |||||||
| chr2:171459122 | C | A | 1 | a0001c0002t0002g0085 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.838+645C>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171459122 | |||||||
| chr2:171459152 | A | T | 2 | a0001c0002t0002g0009 a0001c0002t0002g0107 |
4 | NA18952.hp2 NA18962.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.838+675A>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171459152 | |||||||
| chr2:171459258 | G | C | 1 | a0001c0001t0001g0129 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.838+781G>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171459258 | |||||||
| chr2:171459399 | C | G | 14 | a0001c0001t0006g0220 a0001c0001t0006g0221 a0001c0001t0006g0244 others(11): Show |
15 | HG00408.hp2 HG00558.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.838+922C>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171459399 | |||||||
| chr2:171459419 | A | C | 75 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0008 others(72): Show |
94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.838+942A>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171459419 | |||||||
| chr2:171459566 | C | T | 7 | a0001c0004t0004g0039 a0001c0004t0004g0134 a0001c0004t0004g0210 others(4): Show |
8 | HG01261.hp1 HG02895.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.838+1089C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171459566 | |||||||
| chr2:171459592 | T | A | 2 | a0001c0004t0004g0006 a0001c0004t0017g0213 |
4 | HG02647.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.838+1115T>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171459592 | |||||||
| chr2:171459664 | G | T | 75 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0008 others(72): Show |
94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.838+1187G>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171459664 | |||||||
| chr2:171459755 | A | G | 2 | a0001c0002t0002g0087 a0001c0002t0002g0106 |
2 | NA18944.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.838+1278A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171459755 | |||||||
| chr2:171459852 | C | T | 1 | a0001c0005t0011g0056 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.838+1375C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171459852 | |||||||
| chr2:171459980 | T | C | 75 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0008 others(72): Show |
94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.838+1503T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171459980 | |||||||
| chr2:171460121 | G | A | 75 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0008 others(72): Show |
94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.838+1644G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171460121 | |||||||
| chr2:171460162 | A | C | 12 | a0001c0004t0004g0006 a0001c0004t0004g0039 a0001c0004t0004g0134 others(9): Show |
15 | HG01261.hp1 HG02647.hp2 HG02895.hp2 others(12): Show |
intron_variant | MODIFIER | c.838+1685A>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171460162 | |||||||
| chr2:171460270 | C | A | 1 | a0001c0002t0002g0073 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.838+1793C>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171460270 | |||||||
| chr2:171460275 | A | T | 75 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0008 others(72): Show |
94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.838+1798A>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171460275 | |||||||
| chr2:171460290 | T | C | 1 | a0001c0002t0002g0094 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.838+1813T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171460290 | |||||||
| chr2:171460301 | C | T | 5 | a0001c0005t0008g0054 a0001c0005t0008g0055 a0001c0005t0008g0058 others(2): Show |
5 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.838+1824C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171460301 | |||||||
| chr2:171460310 | G | A | 75 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0008 others(72): Show |
94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.838+1833G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171460310 | |||||||
| chr2:171460322 | CA | C | 10 | a0001c0001t0001g0159 a0001c0001t0001g0173 a0001c0001t0001g0174 others(7): Show |
10 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(7): Show |
intron_variant | MODIFIER | c.838+1864delA | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 171460322 | ||||||
| chr2:171460322 | CAA | C | 75 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0008 others(72): Show |
94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.838+1863_838+1864d others(4): Show |
DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 171460322 | ||||||
| chr2:171460476 | G | T | 1 | a0001c0001t0005g0242 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.838+1999G>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171460476 | |||||||
| chr2:171460513 | C | T | 1 | a0001c0001t0001g0204 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.838+2036C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171460513 | |||||||
| chr2:171460543 | A | ATTATTAT others(17): Show |
1 | a0001c0002t0002g0074 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.838+2066_838+2067i others(26): Show |
DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171460543 | |||||||
| chr2:171460543 | A | ATTATTAT others(14): Show |
6 | a0001c0002t0002g0007 a0001c0002t0002g0063 a0001c0002t0002g0068 others(3): Show |
8 | HG03669.hp2 HG03688.hp2 HG04184.hp2 others(5): Show |
intron_variant | MODIFIER | c.838+2066_838+2067i others(23): Show |
DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171460543 | |||||||
| chr2:171460543 | A | ATTATTAT others(11): Show |
24 | a0001c0002t0002g0003 a0001c0002t0002g0025 a0001c0002t0002g0026 others(21): Show |
30 | HG00280.hp2 HG00408.hp1 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.838+2066_838+2067i others(20): Show |
DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171460543 | |||||||
| chr2:171460543 | A | ATTATTAT others(5): Show |
3 | a0001c0002t0002g0030 a0001c0002t0002g0089 a0001c0002t0026g0030 |
3 | HG02109.hp1 HG02602.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.838+2066_838+2067i others(14): Show |
DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171460543 | |||||||
| chr2:171460543 | A | ATTATTAT others(2): Show |
37 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0010 others(34): Show |
47 | HG00597.hp2 HG01109.hp1 HG01175.hp1 others(44): Show |
intron_variant | MODIFIER | c.838+2066_838+2067i others(11): Show |
DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171460543 | |||||||
| chr2:171460543 | A | ATTATTT | 9 | a0001c0002t0002g0032 a0001c0002t0002g0086 a0001c0002t0002g0104 others(6): Show |
10 | HG00408.hp2 HG00558.hp1 HG01952.hp2 others(7): Show |
intron_variant | MODIFIER | c.838+2066_838+2067i others(8): Show |
DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171460543 | |||||||
| chr2:171460543 | A | ATTT | 2 | a0001c0001t0001g0036 a0001c0007t0001g0123 |
3 | HG01891.hp2 HG02258.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.838+2066_838+2067i others(5): Show |
DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171460543 | |||||||
| chr2:171460543 | A | T | 180 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(177): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.838+2066A>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171460543 | |||||||
| chr2:171460574 | A | G | 5 | a0001c0005t0008g0054 a0001c0005t0008g0055 a0001c0005t0008g0058 others(2): Show |
5 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.838+2097A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171460574 | |||||||
| chr2:171460622 | T | C | 12 | a0001c0004t0004g0006 a0001c0004t0004g0039 a0001c0004t0004g0134 others(9): Show |
15 | HG01261.hp1 HG02647.hp2 HG02895.hp2 others(12): Show |
intron_variant | MODIFIER | c.838+2145T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171460622 | |||||||
| chr2:171460822 | C | T | 5 | a0001c0002t0002g0032 a0001c0002t0002g0086 a0001c0002t0002g0102 others(2): Show |
6 | HG01952.hp2 HG01975.hp2 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.838+2345C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171460822 | |||||||
| chr2:171460946 | T | A | 1 | a0002c0003t0003g0228 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.838+2469T>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171460946 | |||||||
| chr2:171461122 | C | A | 1 | a0001c0001t0021g0147 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.838+2645C>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171461122 | |||||||
| chr2:171461202 | T | C | 75 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0008 others(72): Show |
94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.838+2725T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171461202 | |||||||
| chr2:171461352 | A | C | 1 | a0001c0001t0001g0186 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.838+2875A>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171461352 | |||||||
| chr2:171461373 | G | A | 1 | a0001c0001t0001g0177 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.838+2896G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171461373 | |||||||
| chr2:171461382 | G | A | 31 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0015 others(28): Show |
53 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.838+2905G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171461382 | |||||||
| chr2:171461490 | AAG | A | 5 | a0001c0005t0008g0054 a0001c0005t0008g0055 a0001c0005t0008g0058 others(2): Show |
5 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.838+3017_838+3018d others(4): Show |
DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 171461490 | ||||||
| chr2:171461638 | T | G | 12 | a0001c0004t0004g0006 a0001c0004t0004g0039 a0001c0004t0004g0134 others(9): Show |
15 | HG01261.hp1 HG02647.hp2 HG02895.hp2 others(12): Show |
intron_variant | MODIFIER | c.838+3161T>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171461638 | |||||||
| chr2:171461650 | C | G | 5 | a0001c0005t0008g0054 a0001c0005t0008g0055 a0001c0005t0008g0058 others(2): Show |
5 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.838+3173C>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171461650 | |||||||
| chr2:171461802 | C | T | 5 | a0001c0005t0008g0054 a0001c0005t0008g0055 a0001c0005t0008g0058 others(2): Show |
5 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.838+3325C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171461802 | |||||||
| chr2:171461803 | G | A | 1 | a0001c0001t0001g0236 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.838+3326G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171461803 | |||||||
| chr2:171461849 | CT | C | 78 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(75): Show |
117 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.838+3380delT | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 171461849 | ||||||
| chr2:171462416 | T | A | 12 | a0001c0004t0004g0006 a0001c0004t0004g0039 a0001c0004t0004g0134 others(9): Show |
15 | HG01261.hp1 HG02647.hp2 HG02895.hp2 others(12): Show |
intron_variant | MODIFIER | c.838+3939T>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171462416 | |||||||
| chr2:171462447 | T | C | 2 | a0001c0001t0012g0157 a0004c0008t0012g0158 |
2 | NA18906.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.838+3970T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171462447 | |||||||
| chr2:171462466 | G | T | 5 | a0001c0005t0008g0054 a0001c0005t0008g0055 a0001c0005t0008g0058 others(2): Show |
5 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.838+3989G>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171462466 | |||||||
| chr2:171462486 | C | G | 3 | a0001c0001t0001g0156 a0001c0001t0001g0161 a0001c0001t0001g0218 |
3 | NA19064.hp2 NA19068.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.838+4009C>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171462486 | |||||||
| chr2:171462671 | C | T | 1 | a0002c0003t0003g0224 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.838+4194C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171462671 | |||||||
| chr2:171462833 | G | A | 75 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0008 others(72): Show |
94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.838+4356G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171462833 | |||||||
| chr2:171462951 | A | G | 1 | a0001c0002t0002g0076 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.838+4474A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171462951 | |||||||
| chr2:171463183 | C | T | 87 | a0001c0001t0006g0244 a0001c0002t0002g0003 a0001c0002t0002g0007 others(84): Show |
107 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.838+4706C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171463183 | |||||||
| chr2:171463187 | G | A | 75 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0008 others(72): Show |
94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.838+4710G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171463187 | |||||||
| chr2:171463220 | AT | A | 8 | a0001c0001t0006g0244 a0001c0005t0006g0023 a0001c0005t0006g0047 others(5): Show |
9 | HG02055.hp1 HG02647.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.838+4747delT | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 171463220 | ||||||
| chr2:171463222 | T | TA | 5 | a0001c0002t0002g0068 a0001c0002t0002g0071 a0001c0002t0002g0072 others(2): Show |
5 | HG02615.hp1 HG02886.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.838+4745_838+4746i others(3): Show |
DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171463222 | |||||||
| chr2:171463223 | T | A | 80 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0008 others(77): Show |
99 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.838+4746T>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171463223 | |||||||
| chr2:171463224 | T | A | 106 | a0001c0001t0001g0044 a0001c0001t0001g0148 a0001c0001t0001g0235 others(103): Show |
132 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.838+4747T>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171463224 | |||||||
| chr2:171463225 | A | T | 10 | a0001c0004t0004g0006 a0001c0004t0004g0039 a0001c0004t0004g0134 others(7): Show |
13 | HG01261.hp1 HG02647.hp2 HG02895.hp2 others(10): Show |
intron_variant | MODIFIER | c.838+4748A>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171463225 | |||||||
| chr2:171463301 | T | TA | 7 | a0001c0001t0001g0121 a0001c0001t0005g0116 a0001c0005t0008g0054 others(4): Show |
7 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.838+4840dupA | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 171463301 | ||||||
| chr2:171463503 | A | G | 1 | a0001c0001t0001g0181 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.838+5026A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171463503 | |||||||
| chr2:171463715 | G | T | 2 | a0001c0002t0002g0031 a0001c0002t0015g0031 |
2 | NA18950.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.839-5173G>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171463715 | |||||||
| chr2:171463779 | TGCTTTTA others(9): Show |
T | 2 | a0001c0001t0001g0046 a0001c0001t0001g0263 |
3 | HG00280.hp1 HG02300.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.839-5105_839-5090d others(18): Show |
DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 171463779 | ||||||
| chr2:171463810 | A | AGAAATAA others(2916): Show |
1 | a0001c0001t0001g0155 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.839-5064_839-5063i others(2925): Show |
DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 171463810 | ||||||
| chr2:171463990 | T | C | 1 | a0001c0001t0001g0191 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.839-4898T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171463990 | |||||||
| chr2:171464321 | G | A | 14 | a0001c0001t0006g0220 a0001c0001t0006g0221 a0001c0001t0006g0244 others(11): Show |
15 | HG00408.hp2 HG00558.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.839-4567G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171464321 | |||||||
| chr2:171464808 | TAACTC | T | 3 | a0001c0002t0002g0071 a0001c0002t0002g0072 a0001c0002t0002g0077 |
3 | HG02615.hp1 HG02886.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.839-4078_839-4074d others(7): Show |
DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 171464808 | ||||||
| chr2:171464852 | C | CTA | 14 | a0001c0001t0006g0220 a0001c0001t0006g0221 a0001c0001t0006g0244 others(11): Show |
15 | HG00408.hp2 HG00558.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.839-4026_839-4025d others(4): Show |
DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 171464852 | ||||||
| chr2:171465059 | G | T | 1 | a0001c0001t0001g0184 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.839-3829G>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171465059 | |||||||
| chr2:171465102 | G | A | 1 | a0001c0001t0001g0177 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.839-3786G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171465102 | |||||||
| chr2:171465156 | C | G | 3 | a0001c0001t0001g0247 a0001c0001t0001g0255 a0001c0001t0001g0256 |
3 | HG02258.hp2 NA18522.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.839-3732C>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171465156 | |||||||
| chr2:171465189 | C | T | 7 | a0001c0002t0002g0032 a0001c0002t0002g0086 a0001c0002t0002g0101 others(4): Show |
8 | HG01952.hp2 HG01975.hp2 HG02004.hp2 others(5): Show |
intron_variant | MODIFIER | c.839-3699C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171465189 | |||||||
| chr2:171465204 | G | GA | 12 | a0001c0001t0001g0149 a0001c0001t0001g0177 a0001c0001t0001g0200 others(9): Show |
12 | HG02027.hp2 HG02055.hp2 HG02056.hp2 others(9): Show |
intron_variant | MODIFIER | c.839-3670dupA | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 171465204 | ||||||
| chr2:171465204 | GA | G | 6 | a0001c0001t0001g0172 a0001c0005t0008g0054 a0001c0005t0008g0055 others(3): Show |
6 | HG00408.hp2 HG00558.hp1 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.839-3670delA | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 171465204 | ||||||
| chr2:171465311 | G | A | 5 | a0001c0005t0008g0054 a0001c0005t0008g0055 a0001c0005t0008g0058 others(2): Show |
5 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.839-3577G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171465311 | |||||||
| chr2:171465325 | T | C | 5 | a0001c0002t0002g0003 a0001c0002t0002g0070 a0001c0002t0002g0075 others(2): Show |
9 | HG00408.hp1 NA18947.hp1 NA18963.hp2 others(6): Show |
intron_variant | MODIFIER | c.839-3563T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171465325 | |||||||
| chr2:171465386 | G | A | 19 | a0001c0001t0001g0011 a0001c0001t0001g0036 a0001c0001t0001g0119 others(16): Show |
22 | HG01069.hp1 HG01071.hp2 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.839-3502G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171465386 | |||||||
| chr2:171465477 | C | T | 1 | a0001c0002t0002g0100 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.839-3411C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171465477 | |||||||
| chr2:171465584 | C | G | 1 | a0001c0002t0002g0105 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.839-3304C>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171465584 | |||||||
| chr2:171465626 | C | A | 4 | a0001c0001t0005g0062 a0001c0001t0005g0239 a0001c0001t0005g0240 others(1): Show |
4 | HG02145.hp1 HG02622.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.839-3262C>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171465626 | |||||||
| chr2:171465648 | T | A | 1 | a0001c0002t0002g0101 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.839-3240T>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171465648 | |||||||
| chr2:171465683 | C | A | 1 | a0001c0001t0001g0186 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.839-3205C>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171465683 | |||||||
| chr2:171465748 | G | T | 1 | a0001c0002t0002g0068 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.839-3140G>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171465748 | |||||||
| chr2:171465937 | T | C | 18 | a0001c0001t0001g0044 a0001c0001t0001g0248 a0001c0001t0001g0253 others(15): Show |
24 | HG00140.hp1 HG00423.hp2 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.839-2951T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171465937 | |||||||
| chr2:171466023 | A | T | 75 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0008 others(72): Show |
94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.839-2865A>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171466023 | |||||||
| chr2:171466031 | T | A | 1 | a0001c0001t0007g0198 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.839-2857T>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171466031 | |||||||
| chr2:171466304 | G | A | 14 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0019 others(11): Show |
24 | HG00099.hp2 HG01123.hp2 HG01361.hp2 others(21): Show |
intron_variant | MODIFIER | c.839-2584G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171466304 | |||||||
| chr2:171466411 | A | C | 2 | a0002c0003t0003g0061 a0002c0003t0003g0229 |
2 | NA18959.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.839-2477A>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171466411 | |||||||
| chr2:171466414 | G | A | 79 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(76): Show |
118 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.839-2474G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171466414 | |||||||
| chr2:171466497 | G | A | 1 | a0001c0002t0002g0064 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.839-2391G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171466497 | |||||||
| chr2:171466589 | G | GAAT | 136 | a0001c0001t0001g0011 a0001c0001t0001g0036 a0001c0001t0001g0044 others(133): Show |
168 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.839-2297_839-2295d others(5): Show |
DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 171466589 | ||||||
| chr2:171466592 | T | G | 1 | a0001c0001t0005g0242 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.839-2296T>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171466592 | |||||||
| chr2:171466687 | C | T | 75 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0008 others(72): Show |
94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.839-2201C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171466687 | |||||||
| chr2:171466702 | C | T | 1 | a0001c0002t0002g0104 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.839-2186C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171466702 | |||||||
| chr2:171466715 | T | C | 1 | a0001c0001t0001g0185 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.839-2173T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171466715 | |||||||
| chr2:171466727 | G | GT | 17 | a0001c0001t0001g0126 a0001c0001t0001g0257 a0001c0001t0001g0265 others(14): Show |
22 | HG00423.hp2 HG00642.hp1 HG01261.hp1 others(19): Show |
intron_variant | MODIFIER | c.839-2146dupT | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 171466727 | ||||||
| chr2:171466727 | GT | G | 41 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0019 others(38): Show |
56 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.839-2146delT | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 171466727 | ||||||
| chr2:171466727 | GTT | G | 74 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0008 others(71): Show |
93 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.839-2147_839-2146d others(4): Show |
DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 171466727 | ||||||
| chr2:171466731 | T | G | 1 | a0001c0001t0001g0150 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.839-2157T>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171466731 | |||||||
| chr2:171466735 | T | C | 1 | a0001c0001t0001g0179 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.839-2153T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171466735 | |||||||
| chr2:171466758 | A | G | 5 | a0001c0002t0002g0010 a0001c0002t0002g0033 a0001c0002t0002g0091 others(2): Show |
8 | HG02486.hp2 HG02559.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.839-2130A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171466758 | |||||||
| chr2:171466807 | C | G | 2 | a0001c0002t0002g0033 a0001c0002t0002g0091 |
3 | HG02615.hp2 HG02922.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.839-2081C>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171466807 | |||||||
| chr2:171466951 | T | TG | 87 | a0001c0001t0006g0244 a0001c0002t0002g0003 a0001c0002t0002g0007 others(84): Show |
107 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.839-1937_839-1936i others(3): Show |
DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171466951 | |||||||
| chr2:171466957 | T | C | 1 | a0001c0002t0002g0102 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.839-1931T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171466957 | |||||||
| chr2:171466969 | G | T | 1 | a0001c0001t0001g0171 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.839-1919G>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171466969 | |||||||
| chr2:171467034 | A | G | 87 | a0001c0001t0006g0244 a0001c0002t0002g0003 a0001c0002t0002g0007 others(84): Show |
107 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.839-1854A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171467034 | |||||||
| chr2:171467082 | T | C | 75 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0008 others(72): Show |
94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.839-1806T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171467082 | |||||||
| chr2:171467200 | T | G | 5 | a0001c0005t0008g0054 a0001c0005t0008g0055 a0001c0005t0008g0058 others(2): Show |
5 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.839-1688T>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171467200 | |||||||
| chr2:171467221 | TA | T | 18 | a0001c0001t0001g0044 a0001c0001t0001g0248 a0001c0001t0001g0253 others(15): Show |
24 | HG00140.hp1 HG00423.hp2 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.839-1657delA | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 171467221 | ||||||
| chr2:171467273 | A | G | 7 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0202 others(4): Show |
7 | HG01074.hp2 HG02055.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.839-1615A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171467273 | |||||||
| chr2:171467283 | A | G | 1 | a0001c0001t0001g0254 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.839-1605A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171467283 | |||||||
| chr2:171467334 | CTATT | C | 12 | a0001c0001t0006g0244 a0001c0005t0006g0023 a0001c0005t0006g0047 others(9): Show |
13 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.839-1550_839-1547d others(6): Show |
DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 171467334 | ||||||
| chr2:171467411 | C | T | 75 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0008 others(72): Show |
94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.839-1477C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171467411 | |||||||
| chr2:171467455 | G | A | 5 | a0001c0005t0008g0054 a0001c0005t0008g0055 a0001c0005t0008g0058 others(2): Show |
5 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.839-1433G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171467455 | |||||||
| chr2:171467595 | G | T | 1 | a0002c0003t0010g0042 | 2 | HG01884.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.839-1293G>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171467595 | |||||||
| chr2:171467613 | T | TGTAATAC others(12): Show |
4 | a0001c0001t0001g0036 a0001c0001t0001g0119 a0001c0001t0001g0133 others(1): Show |
5 | HG01168.hp1 HG01169.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.839-1273_839-1255d others(21): Show |
DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 171467613 | ||||||
| chr2:171467727 | C | CA | 10 | a0001c0001t0001g0128 a0001c0001t0001g0145 a0001c0001t0001g0162 others(7): Show |
10 | HG01074.hp1 HG01106.hp2 HG01123.hp1 others(7): Show |
intron_variant | MODIFIER | c.839-1134dupA | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 171467727 | ||||||
| chr2:171467727 | C | CG | 3 | a0001c0001t0001g0136 a0001c0001t0001g0138 a0001c0001t0001g0193 |
3 | HG00140.hp2 HG04228.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.839-1161_839-1160i others(3): Show |
DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171467727 | |||||||
| chr2:171467727 | CA | C | 15 | a0001c0001t0001g0060 a0001c0001t0001g0133 a0001c0001t0001g0166 others(12): Show |
18 | HG01169.hp2 HG01255.hp1 HG01256.hp1 others(15): Show |
intron_variant | MODIFIER | c.839-1134delA | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 171467727 | ||||||
| chr2:171467727 | CAA | C | 13 | a0001c0001t0006g0244 a0001c0002t0002g0066 a0001c0002t0002g0068 others(10): Show |
14 | HG02055.hp1 HG02300.hp2 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.839-1135_839-1134d others(4): Show |
DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 171467727 | ||||||
| chr2:171467727 | CAAA | C | 69 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0008 others(66): Show |
88 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.839-1136_839-1134d others(5): Show |
DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 171467727 | ||||||
| chr2:171467728 | A | G | 12 | a0001c0001t0001g0014 a0001c0001t0001g0038 a0001c0001t0001g0118 others(9): Show |
15 | HG00423.hp1 HG00438.hp1 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.839-1160A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171467728 | |||||||
| chr2:171467729 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.839-1159A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171467729 | |||||||
| chr2:171467735 | A | AC | 18 | a0001c0001t0001g0044 a0001c0001t0001g0248 a0001c0001t0001g0253 others(15): Show |
24 | HG00140.hp1 HG00423.hp2 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.839-1153_839-1152i others(3): Show |
DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171467735 | |||||||
| chr2:171467743 | A | C | 10 | a0001c0001t0006g0244 a0001c0002t0002g0092 a0001c0002t0002g0099 others(7): Show |
11 | HG02055.hp1 HG02647.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.839-1145A>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171467743 | |||||||
| chr2:171467748 | A | C | 2 | a0001c0001t0001g0248 a0001c0001t0001g0253 |
2 | HG00140.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.839-1140A>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171467748 | |||||||
| chr2:171467749 | A | C | 105 | a0001c0001t0001g0044 a0001c0001t0001g0248 a0001c0001t0001g0253 others(102): Show |
131 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.839-1139A>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171467749 | |||||||
| chr2:171467824 | A | G | 2 | a0001c0001t0006g0220 a0001c0001t0006g0221 |
2 | HG01884.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.839-1064A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171467824 | |||||||
| chr2:171467910 | A | G | 2 | a0001c0005t0008g0055 a0001c0005t0008g0058 |
2 | HG00408.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.839-978A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171467910 | |||||||
| chr2:171467988 | T | A | 7 | a0001c0001t0006g0244 a0001c0005t0006g0023 a0001c0005t0006g0047 others(4): Show |
8 | HG02055.hp1 HG02647.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.839-900T>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171467988 | |||||||
| chr2:171467989 | T | A | 12 | a0001c0001t0006g0244 a0001c0005t0006g0023 a0001c0005t0006g0047 others(9): Show |
13 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.839-899T>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171467989 | |||||||
| chr2:171468107 | C | G | 12 | a0001c0004t0004g0006 a0001c0004t0004g0039 a0001c0004t0004g0134 others(9): Show |
15 | HG01261.hp1 HG02647.hp2 HG02895.hp2 others(12): Show |
intron_variant | MODIFIER | c.839-781C>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171468107 | |||||||
| chr2:171468280 | T | C | 1 | a0001c0001t0001g0163 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.839-608T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171468280 | |||||||
| chr2:171468306 | A | G | 3 | a0001c0001t0001g0013 a0001c0001t0001g0175 a0001c0001t0016g0170 |
5 | NA18947.hp2 NA18959.hp2 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.839-582A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171468306 | |||||||
| chr2:171468468 | T | A | 2 | a0001c0005t0006g0047 a0001c0005t0013g0048 |
2 | HG02717.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.839-420T>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171468468 | |||||||
| chr2:171468630 | A | G | 105 | a0001c0001t0001g0044 a0001c0001t0001g0248 a0001c0001t0001g0253 others(102): Show |
131 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.839-258A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171468630 | |||||||
| chr2:171468652 | C | T | 75 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0008 others(72): Show |
94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.839-236C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171468652 | |||||||
| chr2:171468702 | G | C | 1 | a0001c0002t0002g0079 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.839-186G>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 8/13 | chr2 | 171468702 | |||||||
| chr2:171469221 | C | T | 1 | a0001c0001t0001g0256 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.981+191C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171469221 | |||||||
| chr2:171469363 | T | C | 1 | a0001c0005t0006g0047 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.981+333T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171469363 | |||||||
| chr2:171469380 | G | C | 2 | a0001c0001t0001g0012 a0001c0001t0001g0265 |
4 | NA18946.hp1 NA18950.hp1 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.981+350G>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171469380 | |||||||
| chr2:171469558 | G | A | 6 | a0001c0002t0002g0025 a0001c0002t0002g0066 a0001c0002t0002g0067 others(3): Show |
6 | HG00280.hp2 HG01081.hp1 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.981+528G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171469558 | |||||||
| chr2:171469717 | T | C | 9 | a0001c0001t0006g0220 a0001c0001t0006g0221 a0001c0001t0006g0244 others(6): Show |
10 | HG01884.hp1 HG02055.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.981+687T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171469717 | |||||||
| chr2:171469753 | T | G | 14 | a0001c0001t0006g0220 a0001c0001t0006g0221 a0001c0001t0006g0244 others(11): Show |
15 | HG00408.hp2 HG00558.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.981+723T>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171469753 | |||||||
| chr2:171470066 | T | C | 14 | a0001c0001t0006g0220 a0001c0001t0006g0221 a0001c0001t0006g0244 others(11): Show |
15 | HG00408.hp2 HG00558.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.981+1036T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171470066 | |||||||
| chr2:171470072 | A | G | 89 | a0001c0001t0006g0220 a0001c0001t0006g0221 a0001c0001t0006g0244 others(86): Show |
109 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.981+1042A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171470072 | |||||||
| chr2:171470235 | G | A | 1 | a0002c0003t0003g0227 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.981+1205G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171470235 | |||||||
| chr2:171470390 | G | A | 9 | a0001c0001t0006g0220 a0001c0001t0006g0221 a0001c0001t0006g0244 others(6): Show |
10 | HG01884.hp1 HG02055.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.981+1360G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171470390 | |||||||
| chr2:171470393 | C | T | 79 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(76): Show |
118 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.981+1363C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171470393 | |||||||
| chr2:171470397 | A | G | 3 | a0001c0001t0001g0013 a0001c0001t0001g0175 a0001c0001t0016g0170 |
5 | NA18947.hp2 NA18959.hp2 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.981+1367A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171470397 | |||||||
| chr2:171470471 | C | A | 2 | a0002c0003t0003g0225 a0002c0003t0003g0226 |
2 | HG01081.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.981+1441C>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171470471 | |||||||
| chr2:171470578 | C | T | 1 | a0001c0005t0006g0051 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.981+1548C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171470578 | |||||||
| chr2:171470653 | G | A | 1 | a0001c0001t0005g0117 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.981+1623G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171470653 | |||||||
| chr2:171470829 | G | A | 75 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0008 others(72): Show |
94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.981+1799G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171470829 | |||||||
| chr2:171470841 | C | A | 11 | a0001c0004t0004g0006 a0001c0004t0004g0039 a0001c0004t0004g0134 others(8): Show |
14 | HG02647.hp2 HG02895.hp2 HG02896.hp2 others(11): Show |
intron_variant | MODIFIER | c.981+1811C>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171470841 | |||||||
| chr2:171470843 | G | A | 5 | a0001c0005t0008g0054 a0001c0005t0008g0055 a0001c0005t0008g0058 others(2): Show |
5 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.981+1813G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171470843 | |||||||
| chr2:171471274 | G | T | 16 | a0001c0001t0001g0011 a0001c0001t0001g0036 a0001c0001t0001g0119 others(13): Show |
19 | HG01069.hp1 HG01071.hp2 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.981+2244G>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171471274 | |||||||
| chr2:171471280 | T | TA | 5 | a0001c0005t0008g0054 a0001c0005t0008g0055 a0001c0005t0008g0058 others(2): Show |
5 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.981+2258dupA | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 171471280 | ||||||
| chr2:171471608 | G | T | 6 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0202 others(3): Show |
6 | HG02055.hp2 HG02809.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.982-2258G>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171471608 | |||||||
| chr2:171471937 | G | T | 1 | a0001c0001t0001g0169 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.982-1929G>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171471937 | |||||||
| chr2:171471939 | C | T | 75 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0008 others(72): Show |
94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.982-1927C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171471939 | |||||||
| chr2:171471940 | A | G | 75 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0008 others(72): Show |
94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.982-1926A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171471940 | |||||||
| chr2:171472007 | C | T | 2 | a0001c0001t0001g0150 a0001c0001t0001g0154 |
2 | HG02015.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.982-1859C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171472007 | |||||||
| chr2:171472146 | A | G | 1 | a0001c0002t0027g0093 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.982-1720A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171472146 | |||||||
| chr2:171472219 | G | A | 1 | a0001c0005t0006g0047 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.982-1647G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171472219 | |||||||
| chr2:171472241 | A | G | 1 | a0001c0001t0001g0144 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.982-1625A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171472241 | |||||||
| chr2:171472243 | G | T | 15 | a0002c0003t0003g0022 a0002c0003t0003g0040 a0002c0003t0003g0041 others(12): Show |
20 | HG00423.hp2 HG01081.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.982-1623G>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171472243 | |||||||
| chr2:171472274 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.982-1592G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171472274 | |||||||
| chr2:171472371 | G | T | 1 | a0001c0001t0001g0169 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.982-1495G>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171472371 | |||||||
| chr2:171472389 | C | T | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | NA19067.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.982-1477C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171472389 | |||||||
| chr2:171472402 | C | T | 1 | a0001c0002t0002g0029 | 2 | HG03239.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.982-1464C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171472402 | |||||||
| chr2:171472558 | C | A | 9 | a0001c0001t0006g0220 a0001c0001t0006g0221 a0001c0001t0006g0244 others(6): Show |
10 | HG01884.hp1 HG02055.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.982-1308C>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171472558 | |||||||
| chr2:171472692 | T | C | 262 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(259): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.982-1174T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171472692 | |||||||
| chr2:171472753 | G | T | 15 | a0002c0003t0003g0022 a0002c0003t0003g0040 a0002c0003t0003g0041 others(12): Show |
20 | HG00423.hp2 HG01081.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.982-1113G>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171472753 | |||||||
| chr2:171472948 | G | T | 75 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0008 others(72): Show |
94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.982-918G>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171472948 | |||||||
| chr2:171473077 | C | G | 1 | a0001c0006t0001g0125 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.982-789C>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171473077 | |||||||
| chr2:171473100 | T | A | 1 | a0001c0001t0001g0059 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.982-766T>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171473100 | |||||||
| chr2:171473425 | C | T | 7 | a0001c0001t0006g0244 a0001c0005t0006g0023 a0001c0005t0006g0047 others(4): Show |
8 | HG02055.hp1 HG02647.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.982-441C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171473425 | |||||||
| chr2:171473496 | A | C | 89 | a0001c0001t0006g0220 a0001c0001t0006g0221 a0001c0001t0006g0244 others(86): Show |
109 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.982-370A>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171473496 | |||||||
| chr2:171473565 | A | AT | 18 | a0001c0001t0001g0044 a0001c0001t0001g0248 a0001c0001t0001g0253 others(15): Show |
24 | HG00140.hp1 HG00423.hp2 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.982-300dupT | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 171473565 | ||||||
| chr2:171473567 | C | A | 18 | a0001c0001t0001g0044 a0001c0001t0001g0248 a0001c0001t0001g0253 others(15): Show |
24 | HG00140.hp1 HG00423.hp2 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.982-299C>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171473567 | |||||||
| chr2:171473615 | T | C | 14 | a0001c0001t0006g0220 a0001c0001t0006g0221 a0001c0001t0006g0244 others(11): Show |
15 | HG00408.hp2 HG00558.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.982-251T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171473615 | |||||||
| chr2:171473623 | TA | T | 75 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0008 others(72): Show |
94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.982-241delA | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 171473623 | ||||||
| chr2:171473700 | T | G | 2 | a0001c0001t0001g0043 a0001c0001t0001g0264 |
3 | HG02083.hp1 NA18964.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.982-166T>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171473700 | |||||||
| chr2:171473785 | T | A | 1 | a0001c0001t0001g0166 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.982-81T>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 9/13 | chr2 | 171473785 | |||||||
| chr2:171473990 | T | C | 1 | a0001c0001t0018g0237 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1091+15T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 10/13 | chr2 | 171473990 | |||||||
| chr2:171474198 | T | C | 1 | a0001c0001t0001g0132 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1091+223T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 10/13 | chr2 | 171474198 | |||||||
| chr2:171474256 | A | G | 2 | a0001c0001t0001g0165 a0001c0001t0001g0171 |
2 | HG01192.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.1091+281A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 10/13 | chr2 | 171474256 | |||||||
| chr2:171474447 | A | G | 1 | a0001c0002t0002g0098 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1091+472A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 10/13 | chr2 | 171474447 | |||||||
| chr2:171474502 | A | G | 2 | a0001c0006t0001g0124 a0001c0006t0001g0125 |
2 | NA18983.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1091+527A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 10/13 | chr2 | 171474502 | |||||||
| chr2:171474583 | A | G | 20 | a0001c0001t0001g0044 a0001c0001t0001g0248 a0001c0001t0001g0253 others(17): Show |
26 | HG00140.hp1 HG00423.hp2 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.1091+608A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 10/13 | chr2 | 171474583 | |||||||
| chr2:171474721 | G | A | 7 | a0001c0001t0006g0244 a0001c0005t0006g0023 a0001c0005t0006g0047 others(4): Show |
8 | HG02055.hp1 HG02647.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1091+746G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 10/13 | chr2 | 171474721 | |||||||
| chr2:171474760 | C | G | 1 | a0001c0005t0006g0051 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1091+785C>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 10/13 | chr2 | 171474760 | |||||||
| chr2:171474890 | C | T | 9 | a0001c0004t0004g0006 a0001c0004t0004g0039 a0001c0004t0004g0134 others(6): Show |
12 | HG02647.hp2 HG02895.hp2 HG02896.hp2 others(9): Show |
intron_variant | MODIFIER | c.1091+915C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 10/13 | chr2 | 171474890 | |||||||
| chr2:171475201 | C | T | 1 | a0001c0001t0005g0242 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1091+1226C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 10/13 | chr2 | 171475201 | |||||||
| chr2:171475256 | C | T | 1 | a0002c0003t0010g0042 | 2 | HG01884.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1091+1281C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 10/13 | chr2 | 171475256 | |||||||
| chr2:171475410 | C | G | 1 | a0001c0002t0002g0107 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1091+1435C>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 10/13 | chr2 | 171475410 | |||||||
| chr2:171475410 | C | T | 5 | a0001c0005t0008g0054 a0001c0005t0008g0055 a0001c0005t0008g0058 others(2): Show |
5 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.1091+1435C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 10/13 | chr2 | 171475410 | |||||||
| chr2:171475424 | A | T | 3 | a0001c0001t0001g0246 a0001c0001t0001g0248 a0001c0001t0001g0253 |
3 | HG00140.hp1 HG01515.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.1092-1436A>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 10/13 | chr2 | 171475424 | |||||||
| chr2:171475458 | A | G | 75 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0008 others(72): Show |
94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.1092-1402A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 10/13 | chr2 | 171475458 | |||||||
| chr2:171475525 | G | A | 1 | a0002c0003t0003g0228 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1092-1335G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 10/13 | chr2 | 171475525 | |||||||
| chr2:171475531 | G | A | 4 | a0001c0001t0005g0062 a0001c0001t0005g0239 a0001c0001t0005g0240 others(1): Show |
4 | HG02145.hp1 HG02622.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1092-1329G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 10/13 | chr2 | 171475531 | |||||||
| chr2:171475585 | T | C | 2 | a0001c0001t0006g0220 a0001c0001t0006g0221 |
2 | HG01884.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1092-1275T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 10/13 | chr2 | 171475585 | |||||||
| chr2:171475660 | G | A | 29 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0025 others(26): Show |
37 | HG00280.hp2 HG00408.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.1092-1200G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 10/13 | chr2 | 171475660 | |||||||
| chr2:171475821 | A | G | 2 | a0001c0001t0001g0197 a0001c0001t0001g0207 |
2 | HG02572.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1092-1039A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 10/13 | chr2 | 171475821 | |||||||
| chr2:171475914 | G | A | 1 | a0001c0002t0002g0087 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1092-946G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 10/13 | chr2 | 171475914 | |||||||
| chr2:171476019 | A | G | 1 | a0001c0002t0002g0080 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1092-841A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 10/13 | chr2 | 171476019 | |||||||
| chr2:171476125 | A | T | 1 | a0001c0002t0002g0081 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1092-735A>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 10/13 | chr2 | 171476125 | |||||||
| chr2:171476149 | CT | C | 75 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0008 others(72): Show |
94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.1092-700delT | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 171476149 | ||||||
| chr2:171476335 | A | G | 75 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0008 others(72): Show |
94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.1092-525A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 10/13 | chr2 | 171476335 | |||||||
| chr2:171476680 | C | T | 1 | a0001c0001t0001g0155 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1092-180C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 10/13 | chr2 | 171476680 | |||||||
| chr2:171476719 | T | C | 1 | a0001c0001t0001g0231 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1092-141T>C | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 10/13 | chr2 | 171476719 | |||||||
| chr2:171476785 | C | T | 74 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0008 others(71): Show |
93 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.1092-75C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 10/13 | chr2 | 171476785 | |||||||
| chr2:171477007 | A | G | 5 | a0001c0001t0007g0017 a0001c0001t0007g0196 a0001c0001t0007g0198 others(2): Show |
7 | HG01074.hp2 HG01261.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.1182+57A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 11/13 | chr2 | 171477007 | |||||||
| chr2:171477142 | C | A | 89 | a0001c0001t0006g0220 a0001c0001t0006g0221 a0001c0001t0006g0244 others(86): Show |
109 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.1182+192C>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 11/13 | chr2 | 171477142 | |||||||
| chr2:171477185 | CCTTTT | C | 9 | a0001c0001t0006g0220 a0001c0001t0006g0221 a0001c0001t0006g0244 others(6): Show |
10 | HG01884.hp1 HG02055.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1182+236_1182+240d others(7): Show |
DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 11/13 | chr2 | 171477185 | |||||||
| chr2:171477453 | A | AT | 94 | a0001c0001t0001g0044 a0001c0001t0001g0238 a0001c0001t0001g0246 others(91): Show |
119 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.1182+513dupT | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr2 | 171477453 | ||||||
| chr2:171477503 | G | T | 1 | a0001c0001t0001g0018 | 3 | HG01123.hp2 HG01516.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.1183-484G>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 11/13 | chr2 | 171477503 | |||||||
| chr2:171477704 | A | ATCACTTG others(3): Show |
2 | a0001c0001t0001g0251 a0001c0001t0001g0252 |
2 | HG01106.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.1183-282_1183-273d others(12): Show |
DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr2 | 171477704 | ||||||
| chr2:171477756 | C | T | 4 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0153 others(1): Show |
4 | HG02040.hp2 NA18989.hp2 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.1183-231C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 11/13 | chr2 | 171477756 | |||||||
| chr2:171477879 | G | A | 1 | a0001c0001t0001g0231 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1183-108G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 11/13 | chr2 | 171477879 | |||||||
| chr2:171478084 | C | T | 2 | a0001c0001t0001g0164 a0001c0001t0001g0173 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1266+14C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 12/13 | chr2 | 171478084 | |||||||
| chr2:171478121 | T | A | 4 | a0001c0001t0001g0199 a0001c0001t0001g0202 a0001c0001t0001g0204 others(1): Show |
4 | HG02809.hp1 HG02965.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1266+51T>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 12/13 | chr2 | 171478121 | |||||||
| chr2:171478277 | G | T | 5 | a0001c0005t0008g0054 a0001c0005t0008g0055 a0001c0005t0008g0058 others(2): Show |
5 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.1266+207G>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 12/13 | chr2 | 171478277 | |||||||
| chr2:171478435 | C | T | 75 | a0001c0001t0001g0152 a0001c0002t0002g0003 a0001c0002t0002g0007 others(72): Show |
94 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.1266+365C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 12/13 | chr2 | 171478435 | |||||||
| chr2:171478506 | A | G | 88 | a0001c0001t0006g0220 a0001c0001t0006g0221 a0001c0001t0006g0244 others(85): Show |
108 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.1266+436A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 12/13 | chr2 | 171478506 | |||||||
| chr2:171478711 | A | G | 1 | a0001c0001t0006g0244 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1266+641A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 12/13 | chr2 | 171478711 | |||||||
| chr2:171478758 | A | T | 1 | a0001c0001t0001g0151 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1266+688A>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 12/13 | chr2 | 171478758 | |||||||
| chr2:171478879 | CTG | C | 2 | a0001c0001t0001g0037 a0001c0001t0001g0140 |
3 | NA18969.hp1 NA18979.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.1266+811_1266+812d others(4): Show |
DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 171478879 | ||||||
| chr2:171479162 | T | G | 19 | a0001c0001t0001g0011 a0001c0001t0001g0036 a0001c0001t0001g0119 others(16): Show |
22 | HG01069.hp1 HG01071.hp2 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.1267-876T>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 12/13 | chr2 | 171479162 | |||||||
| chr2:171479256 | G | A | 7 | a0001c0002t0002g0010 a0001c0002t0002g0033 a0001c0002t0002g0089 others(4): Show |
10 | HG02109.hp1 HG02451.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1267-782G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 12/13 | chr2 | 171479256 | |||||||
| chr2:171479534 | AT | A | 7 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0202 others(4): Show |
7 | HG02055.hp2 HG02809.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1267-495delT | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 171479534 | ||||||
| chr2:171479769 | G | A | 88 | a0001c0001t0006g0220 a0001c0001t0006g0221 a0001c0001t0006g0244 others(85): Show |
108 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.1267-269G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 12/13 | chr2 | 171479769 | |||||||
| chr2:171480031 | C | T | 74 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0008 others(71): Show |
93 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(90): Show |
splice_region_variant&intron_variant | LOW | c.1267-7C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 12/13 | chr2 | 171480031 | |||||||
| chr2:171480291 | C | T | 5 | a0001c0005t0008g0054 a0001c0005t0008g0055 a0001c0005t0008g0058 others(2): Show |
5 | HG00408.hp2 HG00558.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.1422+98C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 13/13 | chr2 | 171480291 | |||||||
| chr2:171480473 | G | A | 88 | a0001c0001t0006g0220 a0001c0001t0006g0221 a0001c0001t0006g0244 others(85): Show |
108 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.1422+280G>A | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 13/13 | chr2 | 171480473 | |||||||
| chr2:171480499 | A | G | 74 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0008 others(71): Show |
93 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.1422+306A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 13/13 | chr2 | 171480499 | |||||||
| chr2:171480753 | C | T | 15 | a0002c0003t0003g0022 a0002c0003t0003g0040 a0002c0003t0003g0041 others(12): Show |
20 | HG00423.hp2 HG01081.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.1423-221C>T | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 13/13 | chr2 | 171480753 | |||||||
| chr2:171480858 | A | G | 1 | a0001c0002t0002g0107 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1423-116A>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 13/13 | chr2 | 171480858 | |||||||
| chr2:171480951 | C | G | 9 | a0001c0001t0006g0220 a0001c0001t0006g0221 a0001c0001t0006g0244 others(6): Show |
10 | HG01884.hp1 HG02055.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1423-23C>G | DCAF17 | ENSG00000115827.14 | transcript | ENST00000375255.8 | protein_coding | 13/13 | chr2 | 171480951 |