Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 1653 |
| ensemblid | ENSG00000079785.16 |
| hgncid | 2734 |
| symbol | DDX1 |
| name | DEAD-box helicase 1 |
| refseq_nuc | NM_004939.3 |
| refseq_prot | NP_004930.1 |
| ensembl_nuc | ENST00000233084.8 |
| ensembl_prot | ENSP00000233084.3 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 15591868 |
| end | 15631101 |
| strand | + |
| ver | v1.2 |
| region | chr2:15591868-15631101 |
| region5000 | chr2:15586868-15636101 |
| regionname0 | DDX1_chr2_15591868_15631101 |
| regionname5000 | DDX1_chr2_15586868_15636101 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 740 | 390 | 87 | 68 | 181 | 12 | 40 | 146 | DDX1_chr2_15586868_15636101 | DDX1 | MAAFS others(735): Show |
chr2 | 15586868 | 15636101 |
| a0002 | 0/0 | 740 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | DDX1_chr2_15586868_15636101 | DDX1 | MAAFS others(735): Show |
chr2 | 15586868 | 15636101 |
| a0003 | 0/0 | 740 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | MAAFS others(735): Show |
chr2 | 15586868 | 15636101 |
| a0004 | 0/0 | 740 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | MAAFS others(735): Show |
chr2 | 15586868 | 15636101 |
| a0005 | 0/0 | 740 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DDX1_chr2_15586868_15636101 | DDX1 | MAAFS others(735): Show |
chr2 | 15586868 | 15636101 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2220 | 194 | 63 | 35 | 67 | 5 | 23 | DDX1_chr2_15586868_15636101 | DDX1 | ATGGC others(2215): Show |
chr2 | 15586868 | 15636101 | ||
| a0001c0002 | 0/0 | 2220 | 72 | 3 | 8 | 55 | 2 | 4 | DDX1_chr2_15586868_15636101 | DDX1 | ATGGC others(2215): Show |
chr2 | 15586868 | 15636101 | ||
| a0001c0003 | 1/0 | 2220 | 72 | 14 | 24 | 17 | 4 | 12 | DDX1_chr2_15586868_15636101 | DDX1 | ATGGC others(2215): Show |
chr2 | 15586868 | 15636101 | ||
| a0001c0004 | 0/0 | 2220 | 42 | 2 | 0 | 39 | 0 | 1 | DDX1_chr2_15586868_15636101 | DDX1 | ATGGC others(2215): Show |
chr2 | 15586868 | 15636101 | ||
| a0001c0006 | 0/0 | 2220 | 2 | 2 | 0 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | ATGGC others(2215): Show |
chr2 | 15586868 | 15636101 | ||
| a0001c0007 | 0/0 | 2220 | 2 | 2 | 0 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | ATGGC others(2215): Show |
chr2 | 15586868 | 15636101 | ||
| a0001c0009 | 0/0 | 2220 | 1 | 0 | 1 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | ATGGC others(2215): Show |
chr2 | 15586868 | 15636101 | ||
| a0001c0010 | 0/0 | 2220 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | ATGGC others(2215): Show |
chr2 | 15586868 | 15636101 | ||
| a0001c0012 | 0/0 | 2220 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | ATGGC others(2215): Show |
chr2 | 15586868 | 15636101 | ||
| a0001c0013 | 0/0 | 2220 | 1 | 0 | 0 | 0 | 1 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | ATGGC others(2215): Show |
chr2 | 15586868 | 15636101 | ||
| a0001c0014 | 0/0 | 2220 | 1 | 1 | 0 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | ATGGC others(2215): Show |
chr2 | 15586868 | 15636101 | ||
| a0001c0015 | 0/0 | 2220 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | ATGGC others(2215): Show |
chr2 | 15586868 | 15636101 | ||
| a0002c0005 | 0/0 | 2220 | 2 | 0 | 0 | 2 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | ATGGC others(2215): Show |
chr2 | 15586868 | 15636101 | ||
| a0003c0008 | 0/0 | 2220 | 2 | 2 | 0 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | ATGGC others(2215): Show |
chr2 | 15586868 | 15636101 | ||
| a0004c0016 | 0/0 | 2220 | 1 | 1 | 0 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | ATGGC others(2215): Show |
chr2 | 15586868 | 15636101 | ||
| a0005c0011 | 0/0 | 2220 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | ATGGC others(2215): Show |
chr2 | 15586868 | 15636101 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2484 | 192 | 63 | 35 | 66 | 5 | 22 | DDX1_chr2_15586868_15636101 | DDX1 | ACTGC others(2479): Show |
chr2 | 15586868 | 15636101 |
| a0001c0001t0003 | 0/0 | 2484 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | ACTGC others(2479): Show |
chr2 | 15586868 | 15636101 |
| a0001c0001t0006 | 0/0 | 2484 | 1 | 0 | 0 | 0 | 0 | 1 | DDX1_chr2_15586868_15636101 | DDX1 | ACTGC others(2479): Show |
chr2 | 15586868 | 15636101 |
| a0001c0002t0001 | 0/0 | 2484 | 72 | 3 | 8 | 55 | 2 | 4 | DDX1_chr2_15586868_15636101 | DDX1 | ACTGC others(2479): Show |
chr2 | 15586868 | 15636101 |
| a0001c0003t0001 | 0/0 | 2484 | 6 | 6 | 0 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | ACTGC others(2479): Show |
chr2 | 15586868 | 15636101 |
| a0001c0003t0002 | 1/0 | 2484 | 65 | 8 | 24 | 17 | 4 | 11 | DDX1_chr2_15586868_15636101 | DDX1 | ACTGC others(2479): Show |
chr2 | 15586868 | 15636101 |
| a0001c0003t0005 | 0/0 | 2484 | 1 | 0 | 0 | 0 | 0 | 1 | DDX1_chr2_15586868_15636101 | DDX1 | ACTGC others(2479): Show |
chr2 | 15586868 | 15636101 |
| a0001c0004t0003 | 0/0 | 2484 | 41 | 2 | 0 | 38 | 0 | 1 | DDX1_chr2_15586868_15636101 | DDX1 | ACTGC others(2479): Show |
chr2 | 15586868 | 15636101 |
| a0001c0004t0007 | 0/0 | 2484 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | ACTGC others(2479): Show |
chr2 | 15586868 | 15636101 |
| a0001c0006t0004 | 0/0 | 2484 | 2 | 2 | 0 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | ACTGC others(2479): Show |
chr2 | 15586868 | 15636101 |
| a0001c0007t0004 | 0/0 | 2484 | 2 | 2 | 0 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | ACTGC others(2479): Show |
chr2 | 15586868 | 15636101 |
| a0001c0009t0001 | 0/0 | 2484 | 1 | 0 | 1 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | ACTGC others(2479): Show |
chr2 | 15586868 | 15636101 |
| a0001c0010t0001 | 0/0 | 2484 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | ACTGC others(2479): Show |
chr2 | 15586868 | 15636101 |
| a0001c0012t0003 | 0/0 | 2484 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | ACTGC others(2479): Show |
chr2 | 15586868 | 15636101 |
| a0001c0013t0002 | 0/0 | 2484 | 1 | 0 | 0 | 0 | 1 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | ACTGC others(2479): Show |
chr2 | 15586868 | 15636101 |
| a0001c0014t0001 | 0/0 | 2484 | 1 | 1 | 0 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | ACTGC others(2479): Show |
chr2 | 15586868 | 15636101 |
| a0001c0015t0001 | 0/0 | 2484 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | ACTGC others(2479): Show |
chr2 | 15586868 | 15636101 |
| a0002c0005t0001 | 0/0 | 2484 | 2 | 0 | 0 | 2 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | ACTGC others(2479): Show |
chr2 | 15586868 | 15636101 |
| a0003c0008t0001 | 0/0 | 2484 | 2 | 2 | 0 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | ACTGC others(2479): Show |
chr2 | 15586868 | 15636101 |
| a0004c0016t0001 | 0/0 | 2484 | 1 | 1 | 0 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | ACTGC others(2479): Show |
chr2 | 15586868 | 15636101 |
| a0005c0011t0001 | 0/0 | 2484 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | ACTGC others(2479): Show |
chr2 | 15586868 | 15636101 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 10 | 1 | 0 | 9 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0005 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0006 | 0/0 | 8 | 0 | 5 | 3 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0007 | 0/0 | 7 | 0 | 1 | 2 | 3 | 1 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0008 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0009 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0055 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0064 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0001t0006g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0002t0001g0001 | 0/0 | 25 | 0 | 3 | 20 | 2 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0002t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0002t0001g0047 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0002t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0002t0001g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0002t0001g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0002t0001g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0002t0001g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0002t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0002t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0002t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0002t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0002t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0002t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0002t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0002t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0003t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0003t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0003t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0003t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0003t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0003t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0003t0002g0003 | 0/0 | 11 | 0 | 5 | 1 | 3 | 2 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0003t0002g0011 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0003t0002g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0003t0002g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0003t0002g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0003t0002g0038 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0003t0002g0039 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0003t0002g0040 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0003t0002g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0003t0002g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0003t0002g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0003t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0003t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0003t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0003t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0003t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0003t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0003t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0003t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0003t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0003t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0003t0002g0164 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0003t0002g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0003t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0003t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0003t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0003t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0003t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0003t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0003t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0003t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0003t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0003t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0003t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0003t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0003t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0003t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0003t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0003t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0003t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0003t0005g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0004t0003g0002 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0004t0003g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0004t0003g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0004t0003g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0004t0003g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0004t0003g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0004t0003g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0004t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0004t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0004t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0004t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0004t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0004t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0004t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0004t0003g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0004t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0004t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0004t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0004t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0004t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0004t0003g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0004t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0004t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0004t0007g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0006t0004g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0006t0004g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0007t0004g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0009t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0010t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0012t0003g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0013t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0014t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0001c0015t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0002c0005t0001g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0003c0008t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0003c0008t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0004c0016t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| a0005c0011t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0003 | t0002 | g0003 | EUR | GBR | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0123 | EUR | GBR | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | GBR | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG00140 | hp2 | a0001 | c0002 | t0001 | g0001 | EUR | GBR | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG00280 | hp1 | a0001 | c0002 | t0001 | g0001 | EUR | FIN | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0124 | EUR | FIN | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG00323 | hp1 | a0001 | c0013 | t0002 | g0240 | EUR | FIN | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG00323 | hp2 | a0001 | c0003 | t0002 | g0003 | EUR | FIN | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG00408 | hp2 | a0001 | c0003 | t0002 | g0179 | EAS | CHS | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG00438 | hp1 | a0001 | c0003 | t0002 | g0042 | EAS | CHS | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0204 | EAS | CHS | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0022 | EAS | CHS | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0053 | EAS | CHS | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0212 | EAS | CHS | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG00642 | hp1 | a0001 | c0003 | t0002 | g0003 | AMR | PUR | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG00673 | hp1 | a0002 | c0005 | t0001 | g0050 | EAS | CHS | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG00673 | hp2 | a0001 | c0004 | t0003 | g0002 | EAS | CHS | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG00733 | hp2 | a0001 | c0003 | t0002 | g0011 | AMR | PUR | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG01074 | hp1 | a0001 | c0003 | t0002 | g0011 | AMR | PUR | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG01074 | hp2 | a0001 | c0003 | t0002 | g0163 | AMR | PUR | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG01081 | hp2 | a0001 | c0003 | t0002 | g0157 | AMR | PUR | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG01099 | hp1 | a0001 | c0003 | t0002 | g0178 | AMR | PUR | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG01106 | hp1 | a0001 | c0003 | t0002 | g0161 | AMR | PUR | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG01167 | hp1 | a0001 | c0003 | t0002 | g0011 | AMR | PUR | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG01169 | hp2 | a0001 | c0003 | t0002 | g0011 | AMR | PUR | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG01192 | hp1 | a0001 | c0009 | t0001 | g0203 | AMR | PUR | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG01243 | hp1 | a0001 | c0003 | t0002 | g0039 | AMR | PUR | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | CLM | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG01255 | hp2 | a0001 | c0003 | t0002 | g0038 | AMR | CLM | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG01257 | hp1 | a0001 | c0003 | t0002 | g0037 | AMR | CLM | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | CLM | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG01258 | hp2 | a0001 | c0003 | t0002 | g0003 | AMR | CLM | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | CLM | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG01261 | hp2 | a0001 | c0003 | t0002 | g0162 | AMR | CLM | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | CLM | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG01358 | hp1 | a0001 | c0002 | t0001 | g0202 | AMR | CLM | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG01361 | hp1 | a0001 | c0003 | t0002 | g0174 | AMR | CLM | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG01361 | hp2 | a0001 | c0003 | t0002 | g0003 | AMR | CLM | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG01433 | hp2 | a0001 | c0003 | t0002 | g0011 | AMR | CLM | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG01496 | hp1 | a0001 | c0003 | t0002 | g0037 | AMR | CLM | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0200 | AMR | CLM | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG01928 | hp1 | a0001 | c0003 | t0002 | g0168 | AMR | PEL | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PEL | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG01975 | hp1 | a0001 | c0003 | t0002 | g0040 | AMR | PEL | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PEL | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG01978 | hp2 | a0001 | c0003 | t0002 | g0166 | AMR | PEL | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG01981 | hp1 | a0001 | c0003 | t0002 | g0003 | AMR | PEL | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PEL | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02004 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02027 | hp1 | a0001 | c0004 | t0003 | g0002 | EAS | KHV | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02027 | hp2 | a0001 | c0002 | t0001 | g0051 | EAS | KHV | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02056 | hp2 | a0001 | c0004 | t0003 | g0192 | EAS | KHV | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02071 | hp1 | a0001 | c0004 | t0003 | g0002 | EAS | KHV | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0214 | EAS | KHV | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0206 | EAS | KHV | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | KHV | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02080 | hp2 | a0001 | c0003 | t0002 | g0042 | EAS | KHV | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0226 | EAS | KHV | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0205 | EAS | KHV | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02135 | hp1 | a0001 | c0004 | t0003 | g0190 | EAS | KHV | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | KHV | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02145 | hp2 | a0001 | c0003 | t0002 | g0160 | AFR | ACB | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02148 | hp2 | a0001 | c0002 | t0001 | g0229 | AMR | PEL | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CDX | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02155 | hp2 | a0001 | c0003 | t0002 | g0003 | EAS | CDX | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | CDX | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | CDX | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02257 | hp2 | a0001 | c0003 | t0002 | g0167 | AFR | ACB | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | ACB | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02280 | hp2 | a0001 | c0014 | t0001 | g0100 | AFR | ACB | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02293 | hp1 | a0001 | c0003 | t0002 | g0169 | AMR | PEL | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0230 | AMR | PEL | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02300 | hp1 | a0001 | c0003 | t0002 | g0003 | AMR | PEL | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02451 | hp1 | a0001 | c0003 | t0001 | g0059 | AFR | ACB | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0047 | EAS | KHV | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02572 | hp2 | a0001 | c0002 | t0001 | g0236 | AFR | GWD | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02602 | hp1 | a0001 | c0004 | t0003 | g0189 | SAS | PJL | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02615 | hp2 | a0001 | c0003 | t0001 | g0153 | AFR | GWD | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02622 | hp2 | a0001 | c0003 | t0002 | g0239 | AFR | GWD | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02630 | hp1 | a0001 | c0003 | t0002 | g0038 | AFR | GWD | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02698 | hp1 | a0001 | c0003 | t0002 | g0039 | SAS | PJL | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02698 | hp2 | a0001 | c0003 | t0002 | g0180 | SAS | PJL | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02717 | hp2 | a0001 | c0004 | t0003 | g0195 | AFR | GWD | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02723 | hp2 | a0003 | c0008 | t0001 | g0080 | AFR | GWD | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02738 | hp1 | a0001 | c0003 | t0002 | g0159 | SAS | PJL | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02895 | hp2 | a0001 | c0003 | t0002 | g0054 | AFR | GWD | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | ESN | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ESN | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | ESN | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02970 | hp1 | a0001 | c0007 | t0004 | g0046 | AFR | ESN | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | ESN | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02976 | hp2 | a0001 | c0003 | t0002 | g0238 | AFR | ESN | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | MSL | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG03098 | hp2 | a0001 | c0003 | t0001 | g0152 | AFR | MSL | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0225 | AFR | ESN | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG03195 | hp1 | a0003 | c0008 | t0001 | g0069 | AFR | ESN | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | ESN | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG03209 | hp1 | a0001 | c0007 | t0004 | g0046 | AFR | MSL | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | MSL | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0201 | SAS | PJL | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | MSL | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG03453 | hp2 | a0001 | c0006 | t0004 | g0197 | AFR | MSL | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG03486 | hp1 | a0001 | c0003 | t0001 | g0060 | AFR | MSL | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | MSL | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG03490 | hp1 | a0001 | c0003 | t0002 | g0036 | SAS | PJL | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG03491 | hp1 | a0001 | c0003 | t0002 | g0003 | SAS | PJL | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG03492 | hp1 | a0001 | c0003 | t0002 | g0036 | SAS | PJL | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | ESN | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | ESN | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | MSL | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | STU | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG03688 | hp2 | a0001 | c0003 | t0002 | g0165 | SAS | STU | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0207 | SAS | PJL | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG03704 | hp2 | a0001 | c0003 | t0002 | g0003 | SAS | PJL | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG03710 | hp1 | a0001 | c0003 | t0005 | g0241 | SAS | PJL | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | BEB | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0077 | SAS | BEB | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0047 | SAS | BEB | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | BEB | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG03942 | hp1 | a0001 | c0003 | t0002 | g0177 | SAS | BEB | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | BEB | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | STU | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG04115 | hp2 | a0001 | c0003 | t0002 | g0154 | SAS | STU | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0218 | SAS | BEB | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | BEB | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | STU | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | STU | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | STU | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | STU | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | STU | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG04228 | hp2 | a0001 | c0003 | t0002 | g0155 | SAS | STU | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | YRI | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18522 | hp2 | a0001 | c0006 | t0004 | g0198 | AFR | YRI | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18906 | hp1 | a0001 | c0003 | t0002 | g0054 | AFR | YRI | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | YRI | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18939 | hp1 | a0001 | c0002 | t0001 | g0209 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18940 | hp1 | a0001 | c0002 | t0001 | g0052 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18941 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18942 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18943 | hp2 | a0001 | c0004 | t0003 | g0044 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18945 | hp1 | a0001 | c0004 | t0003 | g0002 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18947 | hp1 | a0001 | c0002 | t0001 | g0049 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18948 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18948 | hp2 | a0001 | c0004 | t0003 | g0021 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18949 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18949 | hp2 | a0001 | c0004 | t0003 | g0193 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18950 | hp1 | a0001 | c0004 | t0003 | g0002 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18950 | hp2 | a0001 | c0002 | t0001 | g0211 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18951 | hp1 | a0001 | c0004 | t0003 | g0044 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18952 | hp2 | a0001 | c0004 | t0003 | g0019 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18953 | hp1 | a0001 | c0002 | t0001 | g0048 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18954 | hp2 | a0001 | c0003 | t0002 | g0041 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18956 | hp1 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18957 | hp2 | a0001 | c0002 | t0001 | g0216 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18959 | hp1 | a0001 | c0004 | t0003 | g0045 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18961 | hp2 | a0001 | c0004 | t0003 | g0186 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18963 | hp1 | a0001 | c0002 | t0001 | g0053 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18963 | hp2 | a0001 | c0003 | t0002 | g0014 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18965 | hp1 | a0001 | c0004 | t0003 | g0184 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18965 | hp2 | a0001 | c0002 | t0001 | g0048 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18967 | hp1 | a0001 | c0003 | t0002 | g0014 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18968 | hp1 | a0001 | c0004 | t0003 | g0182 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18968 | hp2 | a0001 | c0002 | t0001 | g0217 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18969 | hp2 | a0001 | c0003 | t0002 | g0172 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18971 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18971 | hp2 | a0001 | c0004 | t0003 | g0019 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18973 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18977 | hp1 | a0001 | c0003 | t0002 | g0171 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18977 | hp2 | a0001 | c0004 | t0003 | g0002 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18978 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18978 | hp2 | a0001 | c0004 | t0003 | g0181 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18980 | hp1 | a0001 | c0004 | t0003 | g0043 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18982 | hp1 | a0001 | c0003 | t0002 | g0173 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18984 | hp2 | a0001 | c0004 | t0003 | g0002 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18985 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18986 | hp2 | a0001 | c0012 | t0003 | g0002 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18990 | hp2 | a0001 | c0004 | t0003 | g0020 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18992 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18994 | hp1 | a0001 | c0002 | t0001 | g0219 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18995 | hp2 | a0001 | c0002 | t0001 | g0210 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18998 | hp2 | a0001 | c0002 | t0001 | g0215 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA19000 | hp1 | a0001 | c0004 | t0003 | g0020 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA19000 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA19001 | hp1 | a0001 | c0002 | t0001 | g0049 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA19003 | hp1 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0052 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA19004 | hp2 | a0001 | c0004 | t0003 | g0188 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA19005 | hp1 | a0001 | c0003 | t0002 | g0175 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0221 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA19009 | hp1 | a0001 | c0002 | t0001 | g0228 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0213 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA19010 | hp2 | a0001 | c0004 | t0003 | g0021 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA19011 | hp1 | a0001 | c0015 | t0001 | g0130 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA19011 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA19012 | hp1 | a0001 | c0003 | t0002 | g0014 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | LWK | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | LWK | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | LWK | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | LWK | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA19054 | hp2 | a0001 | c0001 | t0003 | g0183 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA19055 | hp1 | a0001 | c0004 | t0003 | g0021 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA19055 | hp2 | a0005 | c0011 | t0001 | g0232 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA19056 | hp1 | a0001 | c0004 | t0003 | g0002 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA19057 | hp1 | a0001 | c0003 | t0002 | g0170 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA19057 | hp2 | a0001 | c0004 | t0003 | g0019 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA19058 | hp1 | a0001 | c0004 | t0003 | g0045 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA19059 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA19059 | hp2 | a0001 | c0004 | t0003 | g0187 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA19062 | hp2 | a0001 | c0004 | t0003 | g0043 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA19063 | hp2 | a0001 | c0002 | t0001 | g0233 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA19064 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA19065 | hp1 | a0002 | c0005 | t0001 | g0050 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA19066 | hp1 | a0001 | c0003 | t0002 | g0014 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA19066 | hp2 | a0001 | c0002 | t0001 | g0208 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA19067 | hp1 | a0001 | c0004 | t0003 | g0199 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA19067 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA19070 | hp1 | a0001 | c0004 | t0007 | g0002 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA19070 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA19074 | hp2 | a0001 | c0004 | t0003 | g0002 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA19075 | hp2 | a0001 | c0004 | t0003 | g0196 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA19076 | hp1 | a0001 | c0004 | t0003 | g0185 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA19076 | hp2 | a0001 | c0010 | t0001 | g0222 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA19078 | hp1 | a0001 | c0003 | t0002 | g0158 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA19078 | hp2 | a0001 | c0002 | t0001 | g0220 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA19079 | hp1 | a0001 | c0004 | t0003 | g0002 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA19079 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA19081 | hp1 | a0001 | c0002 | t0001 | g0051 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA19083 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA19084 | hp1 | a0001 | c0003 | t0002 | g0041 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA19087 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA19090 | hp1 | a0001 | c0003 | t0002 | g0176 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA19090 | hp2 | a0001 | c0002 | t0001 | g0231 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA19091 | hp2 | a0001 | c0004 | t0003 | g0194 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA20129 | hp1 | a0001 | c0003 | t0001 | g0235 | AFR | ASW | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ASW | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA20752 | hp1 | a0001 | c0003 | t0002 | g0003 | EUR | TSI | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | TSI | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA20805 | hp1 | a0001 | c0003 | t0002 | g0156 | EUR | TSI | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | TSI | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA20905 | hp1 | a0001 | c0001 | t0006 | g0234 | SAS | GIH | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | GIH | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0223 | AMR | CLM | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | CLM | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02109 | hp2 | a0001 | c0002 | t0001 | g0224 | AFR | ACB | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG03471 | hp1 | a0004 | c0016 | t0001 | g0028 | AFR | MSL | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | MSL | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | USA | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| HG06807 | hp2 | a0001 | c0004 | t0003 | g0191 | AFR | USA | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18955 | hp1 | a0001 | c0004 | t0003 | g0020 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0227 | EAS | JPT | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA20300 | hp1 | a0001 | c0003 | t0002 | g0040 | AFR | USA | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | USA | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | LWK | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| NA21309 | hp2 | a0001 | c0003 | t0001 | g0151 | AFR | LWK | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0064 | REF | REF | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| homoSapiens | grch38p0 | a0001 | c0003 | t0002 | g0164 | REF | REF | DDX1_chr2_15586868_15636101 | DDX1 | chr2 | 15586868 | 15636101 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:15603238 | G | T | 1 | a0004 | 1 | HG03471.hp1 | missense_variant | MODERATE | c.438G>T | p.Arg146Ser | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 8/26 | 504/2484 | 438/2223 | 146/740 | chr2 | 15603238 | |||
| chr2:15623537 | A | T | 1 | a0005 | 1 | NA19055.hp2 | missense_variant | MODERATE | c.1549A>T | p.Ile517Phe | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 19/26 | 1615/2484 | 1549/2223 | 517/740 | chr2 | 15623537 | |||
| chr2:15630789 | A | T | 1 | a0003 | 2 | HG02723.hp2 HG03195.hp1 |
missense_variant | MODERATE | c.2106A>T | p.Lys702Asn | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 26/26 | 2172/2484 | 2106/2223 | 702/740 | chr2 | 15630789 | |||
| chr2:15630844 | G | A | 1 | a0002 | 2 | HG00673.hp1 NA19065.hp1 |
missense_variant | MODERATE | c.2161G>A | p.Glu721Lys | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 26/26 | 2227/2484 | 2161/2223 | 721/740 | chr2 | 15630844 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:15595524 | T | C | 5 | a0001c0002 a0001c0009 a0001c0010 others(2): Show |
77 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(74): Show |
synonymous_variant | LOW | c.103T>C | p.Leu35Leu | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 3/26 | 169/2484 | 103/2223 | 35/740 | chr2 | 15595524 | |||
| chr2:15603220 | T | C | 4 | a0001c0004 a0001c0006 a0001c0007 others(1): Show |
47 | HG00673.hp2 HG02027.hp1 HG02056.hp2 others(44): Show |
synonymous_variant | LOW | c.420T>C | p.His140His | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 8/26 | 486/2484 | 420/2223 | 140/740 | chr2 | 15603220 | |||
| chr2:15607269 | C | T | 13 | a0001c0001 a0001c0002 a0001c0004 others(10): Show |
321 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(318): Show |
synonymous_variant | LOW | c.912C>T | p.Asn304Asn | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/26 | 978/2484 | 912/2223 | 304/740 | chr2 | 15607269 | |||
| chr2:15607305 | T | C | 1 | a0001c0006 | 2 | HG03453.hp2 NA18522.hp2 |
synonymous_variant | LOW | c.948T>C | p.Pro316Pro | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/26 | 1014/2484 | 948/2223 | 316/740 | chr2 | 15607305 | |||
| chr2:15620258 | C | T | 1 | a0001c0015 | 1 | NA19011.hp1 | synonymous_variant | LOW | c.1257C>T | p.Ser419Ser | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 17/26 | 1323/2484 | 1257/2223 | 419/740 | chr2 | 15620258 | |||
| chr2:15628498 | T | C | 1 | a0001c0010 | 1 | NA19076.hp2 | synonymous_variant | LOW | c.1740T>C | p.Asp580Asp | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 21/26 | 1806/2484 | 1740/2223 | 580/740 | chr2 | 15628498 | |||
| chr2:15629673 | T | C | 1 | a0001c0007 | 2 | HG02970.hp1 HG03209.hp1 |
synonymous_variant | LOW | c.1947T>C | p.Cys649Cys | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 24/26 | 2013/2484 | 1947/2223 | 649/740 | chr2 | 15629673 | |||
| chr2:15630085 | C | T | 1 | a0001c0013 | 1 | HG00323.hp1 | synonymous_variant | LOW | c.2067C>T | p.Thr689Thr | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 25/26 | 2133/2484 | 2067/2223 | 689/740 | chr2 | 15630085 | |||
| chr2:15630804 | T | A | 1 | a0001c0014 | 1 | HG02280.hp2 | synonymous_variant | LOW | c.2121T>A | p.Ile707Ile | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 26/26 | 2187/2484 | 2121/2223 | 707/740 | chr2 | 15630804 | |||
| chr2:15630855 | A | G | 1 | a0001c0012 | 1 | NA18986.hp2 | synonymous_variant | LOW | c.2172A>G | p.Thr724Thr | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 26/26 | 2238/2484 | 2172/2223 | 724/740 | chr2 | 15630855 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:15591874 | A | G | 18 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(15): Show |
328 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(325): Show |
5_prime_UTR_variant | MODIFIER | c.-60A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 1/26 | 60 | chr2 | 15591874 | ||||||
| chr2:15591878 | C | T | 6 | a0001c0001t0003 a0001c0004t0003 a0001c0004t0007 others(3): Show |
48 | HG00673.hp2 HG02027.hp1 HG02056.hp2 others(45): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-56C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 1/26 | chr2 | 15591878 | |||||||
| chr2:15591884 | A | G | 1 | a0001c0003t0005 | 1 | HG03710.hp1 | 5_prime_UTR_variant | MODIFIER | c.-50A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 1/26 | 50 | chr2 | 15591884 | ||||||
| chr2:15591886 | T | G | 1 | a0001c0003t0005 | 1 | HG03710.hp1 | 5_prime_UTR_variant | MODIFIER | c.-48T>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 1/26 | 48 | chr2 | 15591886 | ||||||
| chr2:15591887 | C | A | 1 | a0001c0003t0005 | 1 | HG03710.hp1 | 5_prime_UTR_variant | MODIFIER | c.-47C>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 1/26 | 47 | chr2 | 15591887 | ||||||
| chr2:15591917 | C | T | 1 | a0001c0001t0006 | 1 | NA20905.hp1 | 5_prime_UTR_variant | MODIFIER | c.-17C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 1/26 | 17 | chr2 | 15591917 | ||||||
| chr2:15630972 | G | T | 1 | a0001c0004t0007 | 1 | NA19070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*66G>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 26/26 | 66 | chr2 | 15630972 | ||||||
| chr2:15630991 | G | A | 2 | a0001c0006t0004 a0001c0007t0004 |
4 | HG02970.hp1 HG03209.hp1 HG03453.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*85G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 26/26 | 85 | chr2 | 15630991 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:15591973 | G | T | 1 | a0001c0001t0001g0246 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.16+24G>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 1/25 | chr2 | 15591973 | |||||||
| chr2:15592026 | A | G | 3 | a0001c0001t0001g0055 a0001c0001t0001g0244 a0001c0001t0001g0245 |
4 | HG01884.hp1 HG02818.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.16+77A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 1/25 | chr2 | 15592026 | |||||||
| chr2:15592114 | G | C | 78 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(75): Show |
130 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(127): Show |
intron_variant | MODIFIER | c.16+165G>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 1/25 | chr2 | 15592114 | |||||||
| chr2:15592168 | C | G | 5 | a0001c0001t0001g0055 a0001c0001t0001g0242 a0001c0001t0001g0243 others(2): Show |
6 | HG01261.hp1 HG01884.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.16+219C>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 1/25 | chr2 | 15592168 | |||||||
| chr2:15592172 | C | G | 5 | a0001c0003t0002g0054 a0001c0003t0002g0238 a0001c0003t0002g0239 others(2): Show |
6 | HG00323.hp1 HG02622.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.16+223C>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 1/25 | chr2 | 15592172 | |||||||
| chr2:15592222 | C | T | 1 | a0001c0001t0001g0237 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.16+273C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 1/25 | chr2 | 15592222 | |||||||
| chr2:15592279 | C | T | 1 | a0001c0003t0005g0241 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.16+330C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 1/25 | chr2 | 15592279 | |||||||
| chr2:15592318 | C | G | 2 | a0001c0001t0001g0242 a0001c0001t0001g0243 |
2 | HG01261.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.16+369C>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 1/25 | chr2 | 15592318 | |||||||
| chr2:15592620 | T | C | 5 | a0001c0001t0001g0032 a0001c0001t0001g0115 a0001c0001t0001g0116 others(2): Show |
6 | HG00639.hp2 HG01192.hp2 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.16+671T>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 1/25 | chr2 | 15592620 | |||||||
| chr2:15592813 | T | C | 1 | a0001c0001t0001g0119 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.16+864T>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 1/25 | chr2 | 15592813 | |||||||
| chr2:15592899 | TA | T | 117 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(114): Show |
199 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.16+951delA | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 1/25 | chr2 | 15592899 | |||||||
| chr2:15593134 | C | T | 1 | a0001c0001t0001g0237 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.16+1185C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 1/25 | chr2 | 15593134 | |||||||
| chr2:15593141 | C | T | 6 | a0001c0001t0001g0032 a0001c0001t0001g0115 a0001c0001t0001g0116 others(3): Show |
7 | HG00639.hp2 HG01192.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.16+1192C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 1/25 | chr2 | 15593141 | |||||||
| chr2:15593179 | C | G | 11 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0106 others(8): Show |
17 | HG01109.hp2 HG02451.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.16+1230C>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 1/25 | chr2 | 15593179 | |||||||
| chr2:15593293 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.16+1344A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 1/25 | chr2 | 15593293 | |||||||
| chr2:15593502 | A | G | 1 | a0001c0002t0001g0236 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.16+1553A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 1/25 | chr2 | 15593502 | |||||||
| chr2:15593515 | A | G | 5 | a0001c0001t0001g0032 a0001c0001t0001g0115 a0001c0001t0001g0116 others(2): Show |
6 | HG00639.hp2 HG01192.hp2 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.16+1566A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 1/25 | chr2 | 15593515 | |||||||
| chr2:15593520 | A | C | 29 | a0001c0001t0003g0183 a0001c0004t0003g0002 a0001c0004t0003g0019 others(26): Show |
48 | HG00673.hp2 HG02027.hp1 HG02056.hp2 others(45): Show |
intron_variant | MODIFIER | c.16+1571A>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 1/25 | chr2 | 15593520 | |||||||
| chr2:15593599 | G | C | 200 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(197): Show |
322 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(319): Show |
intron_variant | MODIFIER | c.17-1546G>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 1/25 | chr2 | 15593599 | |||||||
| chr2:15593771 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.17-1374C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 1/25 | chr2 | 15593771 | |||||||
| chr2:15593845 | G | A | 44 | a0001c0002t0001g0001 a0001c0002t0001g0022 a0001c0002t0001g0047 others(41): Show |
77 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.17-1300G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 1/25 | chr2 | 15593845 | |||||||
| chr2:15593856 | C | A | 71 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(68): Show |
120 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(117): Show |
intron_variant | MODIFIER | c.17-1289C>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 1/25 | chr2 | 15593856 | |||||||
| chr2:15593935 | G | A | 1 | a0001c0001t0001g0244 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.17-1210G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 1/25 | chr2 | 15593935 | |||||||
| chr2:15594025 | T | C | 204 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(201): Show |
326 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(323): Show |
intron_variant | MODIFIER | c.17-1120T>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 1/25 | chr2 | 15594025 | |||||||
| chr2:15594075 | C | CA | 38 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(35): Show |
54 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(51): Show |
intron_variant | MODIFIER | c.17-1061dupA | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr2 | 15594075 | ||||||
| chr2:15594172 | A | G | 2 | a0001c0001t0001g0030 a0001c0001t0001g0104 |
3 | HG02165.hp2 NA18985.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.17-973A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 1/25 | chr2 | 15594172 | |||||||
| chr2:15594301 | T | C | 1 | a0001c0001t0001g0115 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.17-844T>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 1/25 | chr2 | 15594301 | |||||||
| chr2:15594460 | C | T | 5 | a0001c0003t0002g0054 a0001c0003t0002g0238 a0001c0003t0002g0239 others(2): Show |
6 | HG00323.hp1 HG02622.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.17-685C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 1/25 | chr2 | 15594460 | |||||||
| chr2:15594483 | T | C | 26 | a0001c0001t0003g0183 a0001c0004t0003g0002 a0001c0004t0003g0019 others(23): Show |
44 | HG00673.hp2 HG02027.hp1 HG02056.hp2 others(41): Show |
intron_variant | MODIFIER | c.17-662T>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 1/25 | chr2 | 15594483 | |||||||
| chr2:15594497 | G | A | 71 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(68): Show |
120 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(117): Show |
intron_variant | MODIFIER | c.17-648G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 1/25 | chr2 | 15594497 | |||||||
| chr2:15594510 | A | C | 5 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0056 others(2): Show |
8 | HG01109.hp1 HG02280.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.17-635A>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 1/25 | chr2 | 15594510 | |||||||
| chr2:15594611 | G | T | 2 | a0001c0001t0001g0149 a0001c0001t0001g0150 |
2 | NA18960.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.17-534G>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 1/25 | chr2 | 15594611 | |||||||
| chr2:15594614 | T | G | 1 | a0001c0001t0006g0234 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.17-531T>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 1/25 | chr2 | 15594614 | |||||||
| chr2:15594674 | A | G | 44 | a0001c0002t0001g0001 a0001c0002t0001g0022 a0001c0002t0001g0047 others(41): Show |
77 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.17-471A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 1/25 | chr2 | 15594674 | |||||||
| chr2:15594730 | G | A | 200 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(197): Show |
322 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(319): Show |
intron_variant | MODIFIER | c.17-415G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 1/25 | chr2 | 15594730 | |||||||
| chr2:15594828 | C | A | 1 | a0001c0007t0004g0046 | 2 | HG02970.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.17-317C>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 1/25 | chr2 | 15594828 | |||||||
| chr2:15594877 | G | A | 2 | a0001c0001t0001g0242 a0001c0001t0001g0243 |
2 | HG01261.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.17-268G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 1/25 | chr2 | 15594877 | |||||||
| chr2:15594907 | G | A | 1 | a0001c0004t0003g0181 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.17-238G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 1/25 | chr2 | 15594907 | |||||||
| chr2:15594915 | A | G | 1 | a0001c0001t0001g0118 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.17-230A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 1/25 | chr2 | 15594915 | |||||||
| chr2:15595081 | T | A | 1 | a0001c0002t0001g0200 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.17-64T>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 1/25 | chr2 | 15595081 | |||||||
| chr2:15595132 | T | G | 1 | a0001c0001t0001g0119 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.17-13T>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 1/25 | chr2 | 15595132 | |||||||
| chr2:15595224 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.68+28G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 2/25 | chr2 | 15595224 | |||||||
| chr2:15595270 | A | G | 3 | a0001c0001t0001g0055 a0001c0001t0001g0244 a0001c0001t0001g0245 |
4 | HG01884.hp1 HG02818.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.68+74A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 2/25 | chr2 | 15595270 | |||||||
| chr2:15595285 | A | C | 2 | a0001c0003t0002g0179 a0001c0003t0002g0180 |
2 | HG00408.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.68+89A>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 2/25 | chr2 | 15595285 | |||||||
| chr2:15595295 | G | A | 38 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(35): Show |
54 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(51): Show |
intron_variant | MODIFIER | c.68+99G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 2/25 | chr2 | 15595295 | |||||||
| chr2:15595316 | T | C | 3 | a0001c0003t0002g0036 a0001c0003t0002g0154 a0001c0003t0002g0155 |
4 | HG03490.hp1 HG03492.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.68+120T>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 2/25 | chr2 | 15595316 | |||||||
| chr2:15595396 | G | A | 1 | a0001c0003t0002g0156 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.69-94G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 2/25 | chr2 | 15595396 | |||||||
| chr2:15595442 | C | A | 3 | a0001c0003t0002g0054 a0001c0003t0002g0238 a0001c0003t0002g0239 |
4 | HG02622.hp2 HG02895.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.69-48C>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 2/25 | chr2 | 15595442 | |||||||
| chr2:15595635 | T | C | 1 | a0001c0003t0002g0157 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.132+82T>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 3/25 | chr2 | 15595635 | |||||||
| chr2:15595763 | C | T | 2 | a0001c0001t0001g0148 a0001c0001t0001g0246 |
2 | HG01099.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.132+210C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 3/25 | chr2 | 15595763 | |||||||
| chr2:15595800 | A | C | 5 | a0001c0001t0001g0032 a0001c0001t0001g0115 a0001c0001t0001g0116 others(2): Show |
6 | HG00639.hp2 HG01192.hp2 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.132+247A>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 3/25 | chr2 | 15595800 | |||||||
| chr2:15595898 | T | G | 1 | a0001c0001t0001g0148 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.132+345T>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 3/25 | chr2 | 15595898 | |||||||
| chr2:15595905 | G | A | 71 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(68): Show |
120 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(117): Show |
intron_variant | MODIFIER | c.132+352G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 3/25 | chr2 | 15595905 | |||||||
| chr2:15595979 | G | A | 2 | a0001c0001t0001g0010 a0001c0001t0001g0120 |
6 | NA18940.hp2 NA18945.hp2 NA18967.hp2 others(3): Show |
intron_variant | MODIFIER | c.132+426G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 3/25 | chr2 | 15595979 | |||||||
| chr2:15595985 | A | G | 1 | a0001c0003t0002g0178 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.132+432A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 3/25 | chr2 | 15595985 | |||||||
| chr2:15596240 | G | A | 1 | a0001c0001t0001g0242 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.133-494G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 3/25 | chr2 | 15596240 | |||||||
| chr2:15596448 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.133-286G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 3/25 | chr2 | 15596448 | |||||||
| chr2:15596573 | G | A | 44 | a0001c0002t0001g0001 a0001c0002t0001g0022 a0001c0002t0001g0047 others(41): Show |
77 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.133-161G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 3/25 | chr2 | 15596573 | |||||||
| chr2:15597078 | T | G | 4 | a0001c0001t0001g0024 a0001c0001t0001g0061 a0001c0001t0001g0062 others(1): Show |
5 | NA18981.hp1 NA18990.hp1 NA18998.hp1 others(2): Show |
intron_variant | MODIFIER | c.163-297T>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 4/25 | chr2 | 15597078 | |||||||
| chr2:15597141 | A | G | 38 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(35): Show |
54 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(51): Show |
intron_variant | MODIFIER | c.163-234A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 4/25 | chr2 | 15597141 | |||||||
| chr2:15597144 | A | G | 200 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(197): Show |
322 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(319): Show |
intron_variant | MODIFIER | c.163-231A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 4/25 | chr2 | 15597144 | |||||||
| chr2:15597159 | A | G | 5 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0056 others(2): Show |
8 | HG01109.hp1 HG02280.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.163-216A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 4/25 | chr2 | 15597159 | |||||||
| chr2:15597219 | A | G | 71 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(68): Show |
120 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(117): Show |
intron_variant | MODIFIER | c.163-156A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 4/25 | chr2 | 15597219 | |||||||
| chr2:15597250 | G | A | 5 | a0001c0001t0001g0032 a0001c0001t0001g0115 a0001c0001t0001g0116 others(2): Show |
6 | HG00639.hp2 HG01192.hp2 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.163-125G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 4/25 | chr2 | 15597250 | |||||||
| chr2:15597296 | A | G | 1 | a0001c0001t0001g0237 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.163-79A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 4/25 | chr2 | 15597296 | |||||||
| chr2:15597343 | A | G | 1 | a0001c0001t0001g0147 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.163-32A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 4/25 | chr2 | 15597343 | |||||||
| chr2:15597356 | C | A | 71 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(68): Show |
120 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(117): Show |
intron_variant | MODIFIER | c.163-19C>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 4/25 | chr2 | 15597356 | |||||||
| chr2:15597574 | G | A | 120 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(117): Show |
189 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.259+103G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 5/25 | chr2 | 15597574 | |||||||
| chr2:15597700 | A | G | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | HG04199.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.259+229A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 5/25 | chr2 | 15597700 | |||||||
| chr2:15597807 | A | G | 1 | a0001c0002t0001g0233 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.259+336A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 5/25 | chr2 | 15597807 | |||||||
| chr2:15597895 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.259+424G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 5/25 | chr2 | 15597895 | |||||||
| chr2:15597928 | T | C | 1 | a0001c0001t0001g0121 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.259+457T>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 5/25 | chr2 | 15597928 | |||||||
| chr2:15598026 | G | A | 29 | a0001c0001t0003g0183 a0001c0004t0003g0002 a0001c0004t0003g0019 others(26): Show |
48 | HG00673.hp2 HG02027.hp1 HG02056.hp2 others(45): Show |
intron_variant | MODIFIER | c.259+555G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 5/25 | chr2 | 15598026 | |||||||
| chr2:15598218 | A | G | 13 | a0001c0003t0002g0014 a0001c0003t0002g0041 a0001c0003t0002g0042 others(10): Show |
18 | HG00408.hp2 HG00438.hp1 HG01361.hp1 others(15): Show |
intron_variant | MODIFIER | c.259+747A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 5/25 | chr2 | 15598218 | |||||||
| chr2:15598221 | T | C | 1 | a0001c0001t0006g0234 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.259+750T>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 5/25 | chr2 | 15598221 | |||||||
| chr2:15598482 | C | T | 1 | a0001c0003t0002g0177 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.259+1011C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 5/25 | chr2 | 15598482 | |||||||
| chr2:15598731 | A | G | 1 | a0001c0001t0001g0244 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.260-938A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 5/25 | chr2 | 15598731 | |||||||
| chr2:15598835 | C | T | 71 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(68): Show |
120 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(117): Show |
intron_variant | MODIFIER | c.260-834C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 5/25 | chr2 | 15598835 | |||||||
| chr2:15598877 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.260-792C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 5/25 | chr2 | 15598877 | |||||||
| chr2:15598929 | A | C | 1 | a0001c0001t0001g0143 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.260-740A>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 5/25 | chr2 | 15598929 | |||||||
| chr2:15598934 | C | CT | 72 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(69): Show |
121 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(118): Show |
intron_variant | MODIFIER | c.260-726dupT | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr2 | 15598934 | ||||||
| chr2:15598980 | C | T | 1 | a0001c0004t0003g0195 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.260-689C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 5/25 | chr2 | 15598980 | |||||||
| chr2:15599148 | T | C | 1 | a0001c0001t0001g0237 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.260-521T>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 5/25 | chr2 | 15599148 | |||||||
| chr2:15599169 | T | C | 13 | a0001c0003t0002g0014 a0001c0003t0002g0041 a0001c0003t0002g0042 others(10): Show |
18 | HG00408.hp2 HG00438.hp1 HG01361.hp1 others(15): Show |
intron_variant | MODIFIER | c.260-500T>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 5/25 | chr2 | 15599169 | |||||||
| chr2:15599180 | C | G | 2 | a0001c0001t0001g0055 a0001c0001t0001g0244 |
3 | HG01884.hp1 HG02818.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.260-489C>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 5/25 | chr2 | 15599180 | |||||||
| chr2:15599196 | G | A | 1 | a0001c0001t0001g0244 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.260-473G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 5/25 | chr2 | 15599196 | |||||||
| chr2:15599269 | G | GT | 39 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(36): Show |
55 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(52): Show |
intron_variant | MODIFIER | c.260-389dupT | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr2 | 15599269 | ||||||
| chr2:15599269 | GT | G | 49 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0056 others(46): Show |
85 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.260-389delT | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr2 | 15599269 | ||||||
| chr2:15599295 | TTTTA | T | 199 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(196): Show |
321 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(318): Show |
intron_variant | MODIFIER | c.260-350_260-347del others(4): Show |
DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr2 | 15599295 | ||||||
| chr2:15599314 | T | C | 70 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(67): Show |
119 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(116): Show |
intron_variant | MODIFIER | c.260-355T>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 5/25 | chr2 | 15599314 | |||||||
| chr2:15599336 | T | G | 1 | a0001c0002t0001g0202 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.260-333T>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 5/25 | chr2 | 15599336 | |||||||
| chr2:15599379 | T | G | 1 | a0001c0001t0006g0234 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.260-290T>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 5/25 | chr2 | 15599379 | |||||||
| chr2:15599448 | A | G | 2 | a0001c0001t0001g0112 a0001c0001t0001g0113 |
2 | HG02451.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.260-221A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 5/25 | chr2 | 15599448 | |||||||
| chr2:15599479 | G | T | 70 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(67): Show |
119 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(116): Show |
intron_variant | MODIFIER | c.260-190G>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 5/25 | chr2 | 15599479 | |||||||
| chr2:15599481 | A | AT | 26 | a0001c0001t0003g0183 a0001c0004t0003g0002 a0001c0004t0003g0019 others(23): Show |
44 | HG00673.hp2 HG02027.hp1 HG02056.hp2 others(41): Show |
intron_variant | MODIFIER | c.260-177dupT | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr2 | 15599481 | ||||||
| chr2:15599481 | A | G | 3 | a0001c0001t0001g0015 a0001c0001t0001g0057 a0001c0001t0001g0058 |
5 | HG02280.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.260-188A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 5/25 | chr2 | 15599481 | |||||||
| chr2:15599489 | T | A | 1 | a0001c0001t0001g0066 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.260-180T>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 5/25 | chr2 | 15599489 | |||||||
| chr2:15599515 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.260-154G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 5/25 | chr2 | 15599515 | |||||||
| chr2:15599540 | T | A | 5 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0056 others(2): Show |
8 | HG01109.hp1 HG02280.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.260-129T>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 5/25 | chr2 | 15599540 | |||||||
| chr2:15599593 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.260-76G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 5/25 | chr2 | 15599593 | |||||||
| chr2:15599608 | C | T | 4 | a0001c0001t0001g0055 a0001c0001t0001g0244 a0001c0001t0001g0245 others(1): Show |
5 | HG01884.hp1 HG02818.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.260-61C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 5/25 | chr2 | 15599608 | |||||||
| chr2:15599849 | T | C | 1 | a0001c0004t0003g0043 | 2 | NA18980.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.307+133T>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 6/25 | chr2 | 15599849 | |||||||
| chr2:15599979 | G | A | 1 | a0001c0001t0001g0245 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.307+263G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 6/25 | chr2 | 15599979 | |||||||
| chr2:15600004 | A | C | 70 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(67): Show |
119 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(116): Show |
intron_variant | MODIFIER | c.307+288A>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 6/25 | chr2 | 15600004 | |||||||
| chr2:15600024 | CTCATA | C | 48 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(45): Show |
68 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.307+314_307+318del others(5): Show |
DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr2 | 15600024 | ||||||
| chr2:15600053 | G | A | 71 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(68): Show |
120 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(117): Show |
intron_variant | MODIFIER | c.307+337G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 6/25 | chr2 | 15600053 | |||||||
| chr2:15600066 | TTAAA | T | 70 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(67): Show |
119 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(116): Show |
intron_variant | MODIFIER | c.307+353_307+356del others(4): Show |
DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr2 | 15600066 | ||||||
| chr2:15600080 | A | G | 5 | a0001c0002t0001g0053 a0001c0002t0001g0228 a0001c0002t0001g0229 others(2): Show |
6 | HG00609.hp1 HG02148.hp2 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.307+364A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 6/25 | chr2 | 15600080 | |||||||
| chr2:15600268 | A | G | 1 | a0001c0001t0001g0142 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.307+552A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 6/25 | chr2 | 15600268 | |||||||
| chr2:15600446 | C | T | 70 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(67): Show |
119 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(116): Show |
intron_variant | MODIFIER | c.307+730C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 6/25 | chr2 | 15600446 | |||||||
| chr2:15600698 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.307+982A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 6/25 | chr2 | 15600698 | |||||||
| chr2:15600709 | G | A | 1 | a0001c0009t0001g0203 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.307+993G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 6/25 | chr2 | 15600709 | |||||||
| chr2:15600715 | A | G | 38 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(35): Show |
54 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(51): Show |
intron_variant | MODIFIER | c.307+999A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 6/25 | chr2 | 15600715 | |||||||
| chr2:15600740 | C | CT | 8 | a0001c0001t0001g0101 a0001c0003t0002g0042 a0001c0003t0002g0167 others(5): Show |
9 | HG00438.hp1 HG01928.hp1 HG02080.hp2 others(6): Show |
intron_variant | MODIFIER | c.307+1050dupT | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr2 | 15600740 | ||||||
| chr2:15600740 | CT | C | 79 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(76): Show |
128 | HG00558.hp2 HG00639.hp1 HG00639.hp2 others(125): Show |
intron_variant | MODIFIER | c.307+1050delT | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr2 | 15600740 | ||||||
| chr2:15600740 | CTT | C | 109 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(106): Show |
179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.307+1049_307+1050d others(4): Show |
DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr2 | 15600740 | ||||||
| chr2:15600740 | CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0001g0122 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.307+1038_307+1050d others(15): Show |
DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr2 | 15600740 | ||||||
| chr2:15600740 | CTTTTTTT others(7): Show |
C | 1 | a0001c0009t0001g0203 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.307+1037_307+1050d others(16): Show |
DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr2 | 15600740 | ||||||
| chr2:15600812 | G | A | 1 | a0001c0003t0002g0178 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.307+1096G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 6/25 | chr2 | 15600812 | |||||||
| chr2:15600879 | C | A | 1 | a0001c0004t0003g0044 | 2 | NA18943.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.307+1163C>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 6/25 | chr2 | 15600879 | |||||||
| chr2:15601035 | TC | T | 3 | a0001c0006t0004g0197 a0001c0006t0004g0198 a0001c0007t0004g0046 |
4 | HG02970.hp1 HG03209.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.307+1321delC | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr2 | 15601035 | ||||||
| chr2:15601144 | C | A | 1 | a0001c0001t0001g0061 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.308-1404C>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 6/25 | chr2 | 15601144 | |||||||
| chr2:15601273 | C | A | 3 | a0001c0001t0001g0055 a0001c0001t0001g0244 a0001c0001t0001g0245 |
4 | HG01884.hp1 HG02818.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.308-1275C>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 6/25 | chr2 | 15601273 | |||||||
| chr2:15601328 | T | A | 1 | a0001c0004t0003g0182 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.308-1220T>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 6/25 | chr2 | 15601328 | |||||||
| chr2:15601367 | T | A | 1 | a0001c0001t0001g0237 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.308-1181T>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 6/25 | chr2 | 15601367 | |||||||
| chr2:15601378 | A | G | 1 | a0001c0002t0001g0223 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.308-1170A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 6/25 | chr2 | 15601378 | |||||||
| chr2:15601518 | A | G | 2 | a0001c0001t0001g0112 a0001c0001t0001g0113 |
2 | HG02451.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.308-1030A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 6/25 | chr2 | 15601518 | |||||||
| chr2:15601669 | A | G | 1 | a0001c0002t0001g0200 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.308-879A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 6/25 | chr2 | 15601669 | |||||||
| chr2:15601690 | G | C | 1 | a0001c0002t0001g0047 | 2 | HG02523.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.308-858G>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 6/25 | chr2 | 15601690 | |||||||
| chr2:15601814 | C | A | 2 | a0001c0002t0001g0022 a0001c0002t0001g0204 |
4 | HG00438.hp2 HG00558.hp1 NA18956.hp1 others(1): Show |
intron_variant | MODIFIER | c.308-734C>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 6/25 | chr2 | 15601814 | |||||||
| chr2:15601815 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.308-733G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 6/25 | chr2 | 15601815 | |||||||
| chr2:15601931 | A | G | 5 | a0001c0001t0001g0032 a0001c0001t0001g0115 a0001c0001t0001g0116 others(2): Show |
6 | HG00639.hp2 HG01192.hp2 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.308-617A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 6/25 | chr2 | 15601931 | |||||||
| chr2:15602007 | C | A | 1 | a0001c0001t0001g0237 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.308-541C>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 6/25 | chr2 | 15602007 | |||||||
| chr2:15602058 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.308-490G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 6/25 | chr2 | 15602058 | |||||||
| chr2:15602115 | A | G | 1 | a0001c0003t0002g0169 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.308-433A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 6/25 | chr2 | 15602115 | |||||||
| chr2:15602134 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.308-414G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 6/25 | chr2 | 15602134 | |||||||
| chr2:15602136 | G | A | 71 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(68): Show |
120 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(117): Show |
intron_variant | MODIFIER | c.308-412G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 6/25 | chr2 | 15602136 | |||||||
| chr2:15602186 | T | G | 50 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(47): Show |
92 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(89): Show |
intron_variant | MODIFIER | c.308-362T>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 6/25 | chr2 | 15602186 | |||||||
| chr2:15602270 | T | C | 1 | a0001c0003t0002g0159 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.308-278T>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 6/25 | chr2 | 15602270 | |||||||
| chr2:15602390 | C | T | 1 | a0001c0001t0001g0245 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.308-158C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 6/25 | chr2 | 15602390 | |||||||
| chr2:15602446 | G | A | 8 | a0001c0001t0001g0033 a0001c0001t0001g0123 a0001c0001t0001g0124 others(5): Show |
9 | HG00099.hp2 HG00280.hp2 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.308-102G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 6/25 | chr2 | 15602446 | |||||||
| chr2:15602702 | G | T | 1 | a0001c0001t0001g0237 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.391+71G>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 7/25 | chr2 | 15602702 | |||||||
| chr2:15602739 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.391+108G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 7/25 | chr2 | 15602739 | |||||||
| chr2:15602742 | C | T | 25 | a0001c0004t0003g0002 a0001c0004t0003g0019 a0001c0004t0003g0020 others(22): Show |
43 | HG00673.hp2 HG02027.hp1 HG02056.hp2 others(40): Show |
intron_variant | MODIFIER | c.391+111C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 7/25 | chr2 | 15602742 | |||||||
| chr2:15602757 | G | A | 1 | a0001c0001t0006g0234 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.391+126G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 7/25 | chr2 | 15602757 | |||||||
| chr2:15602805 | C | G | 5 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0056 others(2): Show |
8 | HG01109.hp1 HG02280.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.391+174C>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 7/25 | chr2 | 15602805 | |||||||
| chr2:15602867 | C | T | 1 | a0001c0001t0006g0234 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.391+236C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 7/25 | chr2 | 15602867 | |||||||
| chr2:15603142 | T | G | 1 | a0001c0001t0001g0071 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.392-50T>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 7/25 | chr2 | 15603142 | |||||||
| chr2:15603155 | T | C | 1 | a0001c0002t0001g0224 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.392-37T>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 7/25 | chr2 | 15603155 | |||||||
| chr2:15603340 | G | A | 1 | a0001c0002t0001g0228 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.475+65G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 8/25 | chr2 | 15603340 | |||||||
| chr2:15603568 | A | C | 2 | a0001c0003t0002g0238 a0001c0003t0002g0239 |
2 | HG02622.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.476-246A>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 8/25 | chr2 | 15603568 | |||||||
| chr2:15603594 | A | C | 199 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(196): Show |
321 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(318): Show |
intron_variant | MODIFIER | c.476-220A>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 8/25 | chr2 | 15603594 | |||||||
| chr2:15603692 | G | A | 71 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(68): Show |
120 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(117): Show |
intron_variant | MODIFIER | c.476-122G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 8/25 | chr2 | 15603692 | |||||||
| chr2:15603711 | G | A | 1 | a0001c0001t0001g0067 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.476-103G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 8/25 | chr2 | 15603711 | |||||||
| chr2:15603755 | G | A | 28 | a0001c0004t0003g0002 a0001c0004t0003g0019 a0001c0004t0003g0020 others(25): Show |
47 | HG00673.hp2 HG02027.hp1 HG02056.hp2 others(44): Show |
intron_variant | MODIFIER | c.476-59G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 8/25 | chr2 | 15603755 | |||||||
| chr2:15603999 | T | G | 71 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(68): Show |
120 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(117): Show |
intron_variant | MODIFIER | c.552+109T>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 9/25 | chr2 | 15603999 | |||||||
| chr2:15604126 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.552+236G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 9/25 | chr2 | 15604126 | |||||||
| chr2:15604303 | A | G | 1 | a0001c0001t0001g0027 | 2 | HG02922.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.553-134A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 9/25 | chr2 | 15604303 | |||||||
| chr2:15604360 | CT | C | 48 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(45): Show |
68 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.553-73delT | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr2 | 15604360 | ||||||
| chr2:15604389 | T | G | 1 | a0001c0003t0002g0011 | 5 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.553-48T>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 9/25 | chr2 | 15604389 | |||||||
| chr2:15604556 | A | T | 2 | a0001c0001t0001g0242 a0001c0001t0001g0243 |
2 | HG01261.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.625+47A>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 10/25 | chr2 | 15604556 | |||||||
| chr2:15604560 | T | C | 1 | a0001c0001t0001g0244 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.625+51T>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 10/25 | chr2 | 15604560 | |||||||
| chr2:15604687 | A | C | 1 | a0001c0001t0001g0066 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.625+178A>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 10/25 | chr2 | 15604687 | |||||||
| chr2:15604693 | A | C | 1 | a0001c0001t0001g0066 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.625+184A>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 10/25 | chr2 | 15604693 | |||||||
| chr2:15604860 | T | G | 44 | a0001c0001t0003g0183 a0001c0002t0001g0001 a0001c0002t0001g0022 others(41): Show |
77 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.625+351T>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 10/25 | chr2 | 15604860 | |||||||
| chr2:15604882 | G | A | 1 | a0001c0001t0001g0034 | 2 | NA18943.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.625+373G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 10/25 | chr2 | 15604882 | |||||||
| chr2:15605023 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.625+514G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 10/25 | chr2 | 15605023 | |||||||
| chr2:15605025 | C | T | 1 | a0001c0001t0001g0026 | 2 | NA18973.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.625+516C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 10/25 | chr2 | 15605025 | |||||||
| chr2:15605044 | G | C | 203 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(200): Show |
325 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(322): Show |
intron_variant | MODIFIER | c.625+535G>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 10/25 | chr2 | 15605044 | |||||||
| chr2:15605087 | T | C | 71 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(68): Show |
120 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(117): Show |
intron_variant | MODIFIER | c.625+578T>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 10/25 | chr2 | 15605087 | |||||||
| chr2:15605099 | T | C | 1 | a0001c0001t0001g0128 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.625+590T>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 10/25 | chr2 | 15605099 | |||||||
| chr2:15605209 | T | G | 71 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(68): Show |
120 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(117): Show |
intron_variant | MODIFIER | c.625+700T>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 10/25 | chr2 | 15605209 | |||||||
| chr2:15605353 | A | G | 2 | a0001c0001t0001g0055 a0001c0001t0001g0244 |
3 | HG01884.hp1 HG02818.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.626-597A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 10/25 | chr2 | 15605353 | |||||||
| chr2:15605374 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0056 |
3 | HG01109.hp1 HG03041.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.626-576C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 10/25 | chr2 | 15605374 | |||||||
| chr2:15605427 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.626-523G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 10/25 | chr2 | 15605427 | |||||||
| chr2:15605430 | T | G | 1 | a0001c0003t0002g0157 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.626-520T>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 10/25 | chr2 | 15605430 | |||||||
| chr2:15605500 | C | T | 1 | a0001c0003t0002g0170 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.626-450C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 10/25 | chr2 | 15605500 | |||||||
| chr2:15605553 | G | C | 1 | a0001c0002t0001g0205 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.626-397G>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 10/25 | chr2 | 15605553 | |||||||
| chr2:15605614 | T | C | 1 | a0001c0003t0002g0160 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.626-336T>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 10/25 | chr2 | 15605614 | |||||||
| chr2:15605715 | A | G | 199 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(196): Show |
321 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(318): Show |
intron_variant | MODIFIER | c.626-235A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 10/25 | chr2 | 15605715 | |||||||
| chr2:15605730 | A | G | 3 | a0001c0006t0004g0197 a0001c0006t0004g0198 a0001c0007t0004g0046 |
4 | HG02970.hp1 HG03209.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.626-220A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 10/25 | chr2 | 15605730 | |||||||
| chr2:15605861 | AT | A | 3 | a0001c0001t0001g0129 a0001c0001t0001g0145 a0001c0001t0001g0146 |
3 | HG04199.hp2 HG04204.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.626-88delT | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 10/25 | chr2 | 15605861 | |||||||
| chr2:15605862 | T | C | 1 | a0001c0003t0002g0177 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.626-88T>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 10/25 | chr2 | 15605862 | |||||||
| chr2:15605886 | A | T | 3 | a0001c0003t0002g0040 a0001c0003t0002g0166 a0001c0003t0002g0168 |
4 | HG01928.hp1 HG01975.hp1 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.626-64A>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 10/25 | chr2 | 15605886 | |||||||
| chr2:15605903 | G | C | 1 | a0001c0001t0001g0118 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.626-47G>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 10/25 | chr2 | 15605903 | |||||||
| chr2:15605923 | ATCTC | A | 5 | a0001c0001t0001g0055 a0001c0001t0001g0244 a0001c0001t0003g0183 others(2): Show |
6 | HG01884.hp1 HG02818.hp1 NA19005.hp2 others(3): Show |
intron_variant | MODIFIER | c.626-15_626-12delCT others(2): Show |
DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr2 | 15605923 | ||||||
| chr2:15606096 | C | T | 45 | a0001c0001t0003g0183 a0001c0001t0006g0234 a0001c0002t0001g0001 others(42): Show |
78 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.703-54C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 11/25 | chr2 | 15606096 | |||||||
| chr2:15606336 | G | A | 2 | a0001c0001t0001g0072 a0001c0001t0001g0128 |
2 | HG02165.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.817+72G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 12/25 | chr2 | 15606336 | |||||||
| chr2:15606380 | A | C | 4 | a0001c0003t0001g0151 a0001c0003t0001g0152 a0001c0003t0001g0153 others(1): Show |
4 | HG02615.hp2 HG03098.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.817+116A>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 12/25 | chr2 | 15606380 | |||||||
| chr2:15606472 | G | T | 38 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(35): Show |
54 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(51): Show |
intron_variant | MODIFIER | c.817+208G>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 12/25 | chr2 | 15606472 | |||||||
| chr2:15606624 | C | A | 1 | a0001c0002t0001g0206 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.817+360C>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 12/25 | chr2 | 15606624 | |||||||
| chr2:15606722 | A | G | 1 | a0001c0001t0001g0245 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.818-453A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 12/25 | chr2 | 15606722 | |||||||
| chr2:15606799 | A | G | 2 | a0001c0001t0001g0242 a0001c0001t0001g0243 |
2 | HG01261.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.818-376A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 12/25 | chr2 | 15606799 | |||||||
| chr2:15606812 | C | T | 2 | a0001c0001t0001g0086 a0001c0001t0001g0087 |
2 | HG03017.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.818-363C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 12/25 | chr2 | 15606812 | |||||||
| chr2:15606832 | T | A | 1 | a0001c0002t0001g0207 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.818-343T>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 12/25 | chr2 | 15606832 | |||||||
| chr2:15606851 | A | T | 71 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(68): Show |
120 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(117): Show |
intron_variant | MODIFIER | c.818-324A>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 12/25 | chr2 | 15606851 | |||||||
| chr2:15606884 | G | A | 5 | a0001c0001t0001g0032 a0001c0001t0001g0115 a0001c0001t0001g0116 others(2): Show |
6 | HG00639.hp2 HG01192.hp2 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.818-291G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 12/25 | chr2 | 15606884 | |||||||
| chr2:15606911 | T | C | 1 | a0001c0003t0002g0161 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.818-264T>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 12/25 | chr2 | 15606911 | |||||||
| chr2:15606937 | C | G | 3 | a0001c0006t0004g0197 a0001c0006t0004g0198 a0001c0007t0004g0046 |
4 | HG02970.hp1 HG03209.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.818-238C>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 12/25 | chr2 | 15606937 | |||||||
| chr2:15607110 | G | A | 7 | a0001c0001t0001g0027 a0001c0001t0001g0073 a0001c0001t0001g0074 others(4): Show |
8 | HG00639.hp1 HG00741.hp2 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.818-65G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 12/25 | chr2 | 15607110 | |||||||
| chr2:15607398 | T | C | 1 | a0001c0001t0001g0237 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.956+85T>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15607398 | |||||||
| chr2:15607517 | AT | A | 203 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(200): Show |
325 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(322): Show |
intron_variant | MODIFIER | c.956+214delT | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr2 | 15607517 | ||||||
| chr2:15607609 | C | G | 1 | a0001c0001t0001g0237 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.956+296C>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15607609 | |||||||
| chr2:15607751 | C | T | 71 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(68): Show |
120 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(117): Show |
intron_variant | MODIFIER | c.956+438C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15607751 | |||||||
| chr2:15608167 | T | G | 3 | a0001c0001t0001g0009 a0001c0001t0001g0025 a0001c0001t0001g0095 |
8 | HG00733.hp1 HG01167.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.956+854T>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15608167 | |||||||
| chr2:15608288 | G | A | 2 | a0001c0002t0001g0208 a0001c0002t0001g0209 |
2 | NA18939.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.956+975G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15608288 | |||||||
| chr2:15608292 | G | C | 1 | a0001c0001t0001g0077 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.956+979G>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15608292 | |||||||
| chr2:15608299 | T | C | 71 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(68): Show |
120 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(117): Show |
intron_variant | MODIFIER | c.956+986T>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15608299 | |||||||
| chr2:15608322 | G | A | 1 | a0001c0001t0001g0120 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.956+1009G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15608322 | |||||||
| chr2:15608400 | A | G | 71 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(68): Show |
120 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(117): Show |
intron_variant | MODIFIER | c.956+1087A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15608400 | |||||||
| chr2:15608442 | G | T | 3 | a0001c0001t0001g0055 a0001c0001t0001g0244 a0001c0001t0001g0245 |
4 | HG01884.hp1 HG02818.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.956+1129G>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15608442 | |||||||
| chr2:15608459 | G | A | 2 | a0001c0001t0001g0242 a0001c0001t0001g0243 |
2 | HG01261.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.956+1146G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15608459 | |||||||
| chr2:15608469 | T | C | 39 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(36): Show |
55 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(52): Show |
intron_variant | MODIFIER | c.956+1156T>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15608469 | |||||||
| chr2:15608494 | C | T | 38 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(35): Show |
54 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(51): Show |
intron_variant | MODIFIER | c.956+1181C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15608494 | |||||||
| chr2:15608527 | C | CA | 13 | a0001c0001t0001g0062 a0001c0001t0001g0096 a0001c0001t0001g0120 others(10): Show |
13 | HG00408.hp2 HG01192.hp1 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.956+1230dupA | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr2 | 15608527 | ||||||
| chr2:15608527 | CAAAAA | C | 40 | a0001c0001t0003g0183 a0001c0002t0001g0001 a0001c0002t0001g0022 others(37): Show |
73 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.956+1226_956+1230d others(7): Show |
DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr2 | 15608527 | ||||||
| chr2:15608592 | A | C | 1 | a0001c0010t0001g0222 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.956+1279A>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15608592 | |||||||
| chr2:15608651 | G | GT | 72 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(69): Show |
121 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(118): Show |
intron_variant | MODIFIER | c.956+1347dupT | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr2 | 15608651 | ||||||
| chr2:15608663 | G | GT | 13 | a0001c0001t0001g0108 a0001c0001t0001g0115 a0001c0001t0001g0123 others(10): Show |
16 | HG00099.hp2 HG00408.hp2 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.956+1372dupT | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr2 | 15608663 | ||||||
| chr2:15608663 | G | GTT | 68 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0010 others(65): Show |
117 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.956+1371_956+1372d others(4): Show |
DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr2 | 15608663 | ||||||
| chr2:15608663 | G | GTTT | 14 | a0001c0001t0001g0109 a0001c0001t0001g0111 a0001c0001t0001g0122 others(11): Show |
18 | HG00544.hp1 HG00558.hp1 HG01978.hp1 others(15): Show |
intron_variant | MODIFIER | c.956+1370_956+1372d others(5): Show |
DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr2 | 15608663 | ||||||
| chr2:15608665 | T | TTTG | 9 | a0001c0001t0001g0027 a0001c0001t0001g0063 a0001c0001t0001g0083 others(6): Show |
10 | HG00741.hp2 HG01106.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.956+1354_956+1355i others(5): Show |
DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr2 | 15608665 | ||||||
| chr2:15608666 | T | TTG | 52 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(49): Show |
95 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(92): Show |
intron_variant | MODIFIER | c.956+1354_956+1355i others(4): Show |
DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr2 | 15608666 | ||||||
| chr2:15608673 | T | TAG | 3 | a0001c0001t0001g0121 a0001c0001t0001g0131 a0001c0001t0001g0132 |
3 | HG01123.hp2 HG02300.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.956+1360_956+1361i others(4): Show |
DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15608673 | |||||||
| chr2:15608674 | T | G | 3 | a0001c0001t0001g0121 a0001c0001t0001g0131 a0001c0001t0001g0132 |
3 | HG01123.hp2 HG02300.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.956+1361T>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15608674 | |||||||
| chr2:15608708 | AGGCTGAA others(6): Show |
A | 1 | a0001c0001t0001g0119 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.956+1401_956+1413d others(15): Show |
DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr2 | 15608708 | ||||||
| chr2:15608749 | A | C | 71 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(68): Show |
120 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(117): Show |
intron_variant | MODIFIER | c.956+1436A>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15608749 | |||||||
| chr2:15608821 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.956+1508G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15608821 | |||||||
| chr2:15608836 | T | G | 200 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(197): Show |
322 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(319): Show |
intron_variant | MODIFIER | c.956+1523T>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15608836 | |||||||
| chr2:15608837 | T | C | 200 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(197): Show |
322 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(319): Show |
intron_variant | MODIFIER | c.956+1524T>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15608837 | |||||||
| chr2:15608974 | C | CGGA | 71 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(68): Show |
120 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(117): Show |
intron_variant | MODIFIER | c.956+1661_956+1662i others(5): Show |
DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15608974 | |||||||
| chr2:15609004 | C | G | 28 | a0001c0004t0003g0002 a0001c0004t0003g0019 a0001c0004t0003g0020 others(25): Show |
47 | HG00673.hp2 HG02027.hp1 HG02056.hp2 others(44): Show |
intron_variant | MODIFIER | c.956+1691C>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15609004 | |||||||
| chr2:15609109 | G | A | 2 | a0001c0002t0001g0224 a0001c0002t0001g0225 |
2 | HG02109.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.956+1796G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15609109 | |||||||
| chr2:15609200 | T | G | 42 | a0001c0001t0003g0183 a0001c0002t0001g0001 a0001c0002t0001g0022 others(39): Show |
75 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.956+1887T>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15609200 | |||||||
| chr2:15609213 | G | C | 3 | a0001c0006t0004g0197 a0001c0006t0004g0198 a0001c0007t0004g0046 |
4 | HG02970.hp1 HG03209.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.956+1900G>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15609213 | |||||||
| chr2:15609534 | T | C | 71 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(68): Show |
120 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(117): Show |
intron_variant | MODIFIER | c.956+2221T>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15609534 | |||||||
| chr2:15609575 | A | C | 200 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(197): Show |
322 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(319): Show |
intron_variant | MODIFIER | c.956+2262A>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15609575 | |||||||
| chr2:15609718 | A | T | 1 | a0001c0002t0001g0219 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.956+2405A>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15609718 | |||||||
| chr2:15609749 | GA | G | 71 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(68): Show |
120 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(117): Show |
intron_variant | MODIFIER | c.956+2445delA | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr2 | 15609749 | ||||||
| chr2:15609883 | T | C | 1 | a0001c0001t0001g0237 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.956+2570T>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15609883 | |||||||
| chr2:15610007 | T | G | 45 | a0001c0001t0003g0183 a0001c0002t0001g0001 a0001c0002t0001g0022 others(42): Show |
78 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.956+2694T>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15610007 | |||||||
| chr2:15610088 | C | G | 1 | a0001c0002t0001g0201 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.956+2775C>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15610088 | |||||||
| chr2:15610115 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.956+2802G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15610115 | |||||||
| chr2:15610132 | A | C | 1 | a0001c0001t0001g0122 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.956+2819A>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15610132 | |||||||
| chr2:15610319 | T | C | 71 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(68): Show |
120 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(117): Show |
intron_variant | MODIFIER | c.957-2905T>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15610319 | |||||||
| chr2:15610516 | A | G | 71 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(68): Show |
120 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(117): Show |
intron_variant | MODIFIER | c.957-2708A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15610516 | |||||||
| chr2:15610550 | C | CT | 5 | a0001c0001t0001g0032 a0001c0001t0001g0115 a0001c0001t0001g0116 others(2): Show |
6 | HG00639.hp2 HG01192.hp2 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.957-2673dupT | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr2 | 15610550 | ||||||
| chr2:15610578 | T | C | 1 | a0001c0003t0002g0171 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.957-2646T>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15610578 | |||||||
| chr2:15610728 | A | G | 71 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(68): Show |
120 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(117): Show |
intron_variant | MODIFIER | c.957-2496A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15610728 | |||||||
| chr2:15610751 | A | T | 1 | a0001c0001t0001g0119 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.957-2473A>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15610751 | |||||||
| chr2:15610795 | A | C | 5 | a0001c0001t0001g0032 a0001c0001t0001g0115 a0001c0001t0001g0116 others(2): Show |
6 | HG00639.hp2 HG01192.hp2 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.957-2429A>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15610795 | |||||||
| chr2:15610822 | CGG | C | 71 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(68): Show |
120 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(117): Show |
intron_variant | MODIFIER | c.957-2399_957-2398d others(4): Show |
DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr2 | 15610822 | ||||||
| chr2:15610862 | GT | G | 131 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(128): Show |
203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.957-2351delT | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr2 | 15610862 | ||||||
| chr2:15610862 | GTT | G | 71 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(68): Show |
120 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(117): Show |
intron_variant | MODIFIER | c.957-2352_957-2351d others(4): Show |
DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr2 | 15610862 | ||||||
| chr2:15610863 | T | A | 1 | a0001c0001t0001g0127 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.957-2361T>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15610863 | |||||||
| chr2:15610979 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.957-2245A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15610979 | |||||||
| chr2:15610989 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.957-2235G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15610989 | |||||||
| chr2:15611030 | G | C | 1 | a0001c0001t0001g0245 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.957-2194G>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611030 | |||||||
| chr2:15611186 | A | G | 71 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(68): Show |
120 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(117): Show |
intron_variant | MODIFIER | c.957-2038A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611186 | |||||||
| chr2:15611198 | G | C | 4 | a0001c0003t0001g0151 a0001c0003t0001g0152 a0001c0003t0001g0153 others(1): Show |
4 | HG02615.hp2 HG03098.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.957-2026G>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611198 | |||||||
| chr2:15611199 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.957-2025G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611199 | |||||||
| chr2:15611311 | G | A | 96 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(93): Show |
163 | HG00558.hp2 HG00639.hp1 HG00673.hp2 others(160): Show |
intron_variant | MODIFIER | c.957-1913G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611311 | |||||||
| chr2:15611326 | T | TC | 71 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(68): Show |
120 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(117): Show |
intron_variant | MODIFIER | c.957-1894dupC | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr2 | 15611326 | ||||||
| chr2:15611349 | C | T | 1 | a0001c0003t0001g0152 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.957-1875C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611349 | |||||||
| chr2:15611379 | C | T | 1 | a0001c0004t0003g0181 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.957-1845C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611379 | |||||||
| chr2:15611397 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.957-1827G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611397 | |||||||
| chr2:15611413 | C | T | 2 | a0001c0001t0001g0242 a0001c0001t0001g0243 |
2 | HG01261.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.957-1811C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611413 | |||||||
| chr2:15611451 | G | C | 1 | a0001c0001t0003g0183 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.957-1773G>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611451 | |||||||
| chr2:15611457 | A | G | 204 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(201): Show |
326 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(323): Show |
intron_variant | MODIFIER | c.957-1767A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611457 | |||||||
| chr2:15611458 | C | T | 28 | a0001c0004t0003g0002 a0001c0004t0003g0019 a0001c0004t0003g0020 others(25): Show |
47 | HG00673.hp2 HG02027.hp1 HG02056.hp2 others(44): Show |
intron_variant | MODIFIER | c.957-1766C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611458 | |||||||
| chr2:15611463 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.957-1761G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611463 | |||||||
| chr2:15611467 | A | G | 1 | a0001c0002t0001g0218 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.957-1757A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611467 | |||||||
| chr2:15611473 | T | A | 28 | a0001c0004t0003g0002 a0001c0004t0003g0019 a0001c0004t0003g0020 others(25): Show |
47 | HG00673.hp2 HG02027.hp1 HG02056.hp2 others(44): Show |
intron_variant | MODIFIER | c.957-1751T>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611473 | |||||||
| chr2:15611473 | T | G | 71 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(68): Show |
120 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(117): Show |
intron_variant | MODIFIER | c.957-1751T>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611473 | |||||||
| chr2:15611480 | A | ACCTCCCG others(42): Show |
1 | a0001c0001t0001g0079 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.957-1701_957-1700i others(51): Show |
DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr2 | 15611480 | ||||||
| chr2:15611480 | ACCTCCCG others(42): Show |
A | 1 | a0001c0002t0001g0201 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.957-1716_957-1668d others(51): Show |
DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr2 | 15611480 | ||||||
| chr2:15611486 | C | T | 28 | a0001c0004t0003g0002 a0001c0004t0003g0019 a0001c0004t0003g0020 others(25): Show |
47 | HG00673.hp2 HG02027.hp1 HG02056.hp2 others(44): Show |
intron_variant | MODIFIER | c.957-1738C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611486 | |||||||
| chr2:15611495 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.957-1729C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611495 | |||||||
| chr2:15611508 | A | G | 28 | a0001c0004t0003g0002 a0001c0004t0003g0019 a0001c0004t0003g0020 others(25): Show |
47 | HG00673.hp2 HG02027.hp1 HG02056.hp2 others(44): Show |
intron_variant | MODIFIER | c.957-1716A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611508 | |||||||
| chr2:15611517 | A | AC | 46 | a0001c0001t0001g0237 a0001c0001t0003g0183 a0001c0002t0001g0001 others(43): Show |
79 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.957-1700dupC | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr2 | 15611517 | ||||||
| chr2:15611524 | C | T | 69 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(66): Show |
118 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(115): Show |
intron_variant | MODIFIER | c.957-1700C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611524 | |||||||
| chr2:15611544 | C | CGACTGGC others(42): Show |
1 | a0001c0006t0004g0197 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.957-1679_957-1678i others(51): Show |
DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr2 | 15611544 | ||||||
| chr2:15611544 | C | CGACTGGC others(42): Show |
3 | a0001c0004t0003g0195 a0001c0006t0004g0198 a0001c0007t0004g0046 |
4 | HG02717.hp2 HG02970.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.957-1679_957-1678i others(51): Show |
DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr2 | 15611544 | ||||||
| chr2:15611546 | G | A | 24 | a0001c0004t0003g0002 a0001c0004t0003g0019 a0001c0004t0003g0020 others(21): Show |
42 | HG00673.hp2 HG02027.hp1 HG02056.hp2 others(39): Show |
intron_variant | MODIFIER | c.957-1678G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611546 | |||||||
| chr2:15611557 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.957-1667G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611557 | |||||||
| chr2:15611561 | G | T | 2 | a0001c0001t0001g0070 a0001c0001t0001g0091 |
2 | HG03195.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.957-1663G>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611561 | |||||||
| chr2:15611566 | A | ACCCCCCC others(43): Show |
22 | a0001c0004t0003g0002 a0001c0004t0003g0019 a0001c0004t0003g0020 others(19): Show |
40 | HG00673.hp2 HG02027.hp1 HG02071.hp1 others(37): Show |
intron_variant | MODIFIER | c.957-1652_957-1651i others(52): Show |
DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr2 | 15611566 | ||||||
| chr2:15611566 | A | ACCCCCCC others(44): Show |
1 | a0001c0004t0003g0192 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.957-1652_957-1651i others(53): Show |
DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr2 | 15611566 | ||||||
| chr2:15611571 | C | CCCACCTC others(43): Show |
1 | a0001c0004t0003g0191 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.957-1652_957-1651i others(52): Show |
DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr2 | 15611571 | ||||||
| chr2:15611573 | G | C | 30 | a0001c0001t0001g0073 a0001c0001t0001g0079 a0001c0004t0003g0002 others(27): Show |
49 | HG00673.hp2 HG01255.hp1 HG01346.hp1 others(46): Show |
intron_variant | MODIFIER | c.957-1651G>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611573 | |||||||
| chr2:15611573 | G | GACCTCCC others(42): Show |
1 | a0001c0001t0001g0071 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.957-1617_957-1616i others(51): Show |
DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr2 | 15611573 | ||||||
| chr2:15611573 | G | T | 1 | a0001c0001t0001g0078 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.957-1651G>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611573 | |||||||
| chr2:15611578 | CCCTCCCG others(71): Show |
C | 1 | a0001c0001t0001g0078 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.957-1618_957-1541d others(80): Show |
DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr2 | 15611578 | ||||||
| chr2:15611585 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.957-1639G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611585 | |||||||
| chr2:15611589 | GGGGCGGC others(394): Show |
G | 5 | a0001c0001t0001g0055 a0001c0001t0001g0242 a0001c0001t0001g0243 others(2): Show |
6 | HG01261.hp1 HG01884.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.957-1590_957-1190d others(2): Show |
DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr2 | 15611589 | ||||||
| chr2:15611594 | G | A | 1 | a0001c0003t0002g0038 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.957-1630G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611594 | |||||||
| chr2:15611605 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.957-1619C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611605 | |||||||
| chr2:15611607 | GA | G | 67 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(64): Show |
116 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(113): Show |
intron_variant | MODIFIER | c.957-1616delA | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611607 | |||||||
| chr2:15611614 | T | TGA | 11 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0106 others(8): Show |
17 | HG01109.hp2 HG02451.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.957-1610_957-1609i others(4): Show |
DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611614 | |||||||
| chr2:15611614 | TCCTCACT others(26): Show |
T | 56 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(53): Show |
99 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(96): Show |
intron_variant | MODIFIER | c.957-1608_957-1576d others(35): Show |
DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr2 | 15611614 | ||||||
| chr2:15611617 | T | C | 11 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0106 others(8): Show |
17 | HG01109.hp2 HG02451.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.957-1607T>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611617 | |||||||
| chr2:15611619 | A | C | 11 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0106 others(8): Show |
17 | HG01109.hp2 HG02451.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.957-1605A>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611619 | |||||||
| chr2:15611621 | TTCCCAGT others(23): Show |
T | 11 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0106 others(8): Show |
17 | HG01109.hp2 HG02451.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.957-1602_957-1573d others(32): Show |
DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611621 | |||||||
| chr2:15611634 | T | C | 31 | a0001c0001t0001g0071 a0001c0001t0001g0073 a0001c0001t0001g0079 others(28): Show |
50 | HG00673.hp2 HG01255.hp1 HG01346.hp1 others(47): Show |
intron_variant | MODIFIER | c.957-1590T>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611634 | |||||||
| chr2:15611638 | C | T | 31 | a0001c0001t0001g0071 a0001c0001t0001g0073 a0001c0001t0001g0079 others(28): Show |
50 | HG00673.hp2 HG01255.hp1 HG01346.hp1 others(47): Show |
intron_variant | MODIFIER | c.957-1586C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611638 | |||||||
| chr2:15611648 | C | G | 56 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(53): Show |
99 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(96): Show |
intron_variant | MODIFIER | c.957-1576C>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611648 | |||||||
| chr2:15611649 | A | G | 31 | a0001c0001t0001g0071 a0001c0001t0001g0073 a0001c0001t0001g0079 others(28): Show |
50 | HG00673.hp2 HG01255.hp1 HG01346.hp1 others(47): Show |
intron_variant | MODIFIER | c.957-1575A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611649 | |||||||
| chr2:15611654 | C | T | 31 | a0001c0001t0001g0071 a0001c0001t0001g0073 a0001c0001t0001g0079 others(28): Show |
50 | HG00673.hp2 HG01255.hp1 HG01346.hp1 others(47): Show |
intron_variant | MODIFIER | c.957-1570C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611654 | |||||||
| chr2:15611655 | C | CTACCT | 56 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(53): Show |
99 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(96): Show |
intron_variant | MODIFIER | c.957-1569_957-1568i others(7): Show |
DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611655 | |||||||
| chr2:15611655 | C | T | 11 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0106 others(8): Show |
17 | HG01109.hp2 HG02451.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.957-1569C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611655 | |||||||
| chr2:15611656 | A | ACCTCCCG others(42): Show |
1 | a0001c0002t0001g0001 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.957-1551_957-1503d others(51): Show |
DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr2 | 15611656 | ||||||
| chr2:15611656 | A | C | 67 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(64): Show |
116 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(113): Show |
intron_variant | MODIFIER | c.957-1568A>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611656 | |||||||
| chr2:15611666 | C | T | 5 | a0001c0001t0001g0012 a0001c0001t0001g0071 a0001c0001t0001g0073 others(2): Show |
8 | HG01255.hp1 HG01346.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.957-1558C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611666 | |||||||
| chr2:15611671 | C | T | 1 | a0001c0004t0003g0190 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.957-1553C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611671 | |||||||
| chr2:15611673 | GCTGGCCG others(42): Show |
G | 1 | a0001c0009t0001g0203 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.957-1504_957-1456d others(51): Show |
DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr2 | 15611673 | ||||||
| chr2:15611676 | G | A | 4 | a0001c0003t0001g0151 a0001c0003t0001g0152 a0001c0003t0001g0153 others(1): Show |
4 | HG02615.hp2 HG03098.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.957-1548G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611676 | |||||||
| chr2:15611688 | G | A | 31 | a0001c0001t0001g0071 a0001c0001t0001g0073 a0001c0001t0001g0079 others(28): Show |
50 | HG00673.hp2 HG01255.hp1 HG01346.hp1 others(47): Show |
intron_variant | MODIFIER | c.957-1536G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611688 | |||||||
| chr2:15611715 | C | T | 31 | a0001c0001t0001g0071 a0001c0001t0001g0073 a0001c0001t0001g0079 others(28): Show |
50 | HG00673.hp2 HG01255.hp1 HG01346.hp1 others(47): Show |
intron_variant | MODIFIER | c.957-1509C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611715 | |||||||
| chr2:15611720 | CGACTGGC others(42): Show |
C | 2 | a0001c0002t0001g0224 a0001c0002t0001g0225 |
2 | HG02109.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.957-1502_957-1454d others(51): Show |
DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr2 | 15611720 | ||||||
| chr2:15611722 | A | G | 147 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(144): Show |
249 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(246): Show |
intron_variant | MODIFIER | c.957-1502A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611722 | |||||||
| chr2:15611733 | G | A | 102 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(99): Show |
171 | HG00558.hp2 HG00639.hp1 HG00639.hp2 others(168): Show |
intron_variant | MODIFIER | c.957-1491G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611733 | |||||||
| chr2:15611734 | G | A | 38 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(35): Show |
54 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(51): Show |
intron_variant | MODIFIER | c.957-1490G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611734 | |||||||
| chr2:15611735 | G | A | 73 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(70): Show |
123 | HG00558.hp2 HG00639.hp1 HG00639.hp2 others(120): Show |
intron_variant | MODIFIER | c.957-1489G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611735 | |||||||
| chr2:15611738 | G | GGCTC | 73 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(70): Show |
123 | HG00558.hp2 HG00639.hp1 HG00639.hp2 others(120): Show |
intron_variant | MODIFIER | c.957-1486_957-1485i others(6): Show |
DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611738 | |||||||
| chr2:15611741 | G | C | 73 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(70): Show |
123 | HG00558.hp2 HG00639.hp1 HG00639.hp2 others(120): Show |
intron_variant | MODIFIER | c.957-1483G>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611741 | |||||||
| chr2:15611744 | C | T | 73 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(70): Show |
123 | HG00558.hp2 HG00639.hp1 HG00639.hp2 others(120): Show |
intron_variant | MODIFIER | c.957-1480C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611744 | |||||||
| chr2:15611745 | C | T | 73 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(70): Show |
123 | HG00558.hp2 HG00639.hp1 HG00639.hp2 others(120): Show |
intron_variant | MODIFIER | c.957-1479C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611745 | |||||||
| chr2:15611748 | C | CAGTAGGG others(17): Show |
73 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(70): Show |
123 | HG00558.hp2 HG00639.hp1 HG00639.hp2 others(120): Show |
intron_variant | MODIFIER | c.957-1476_957-1475i others(26): Show |
DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611748 | |||||||
| chr2:15611749 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.957-1475C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611749 | |||||||
| chr2:15611750 | A | C | 73 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(70): Show |
123 | HG00558.hp2 HG00639.hp1 HG00639.hp2 others(120): Show |
intron_variant | MODIFIER | c.957-1474A>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611750 | |||||||
| chr2:15611752 | C | A | 38 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(35): Show |
54 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(51): Show |
intron_variant | MODIFIER | c.957-1472C>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611752 | |||||||
| chr2:15611754 | C | CA | 73 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(70): Show |
123 | HG00558.hp2 HG00639.hp1 HG00639.hp2 others(120): Show |
intron_variant | MODIFIER | c.957-1470_957-1469i others(3): Show |
DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611754 | |||||||
| chr2:15611754 | CCCTCCCG others(120): Show |
C | 3 | a0001c0001t0001g0071 a0001c0001t0001g0073 a0001c0001t0001g0079 |
3 | HG01255.hp1 HG01346.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.957-1455_957-1329d others(2): Show |
DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr2 | 15611754 | ||||||
| chr2:15611764 | C | T | 67 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(64): Show |
116 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(113): Show |
intron_variant | MODIFIER | c.957-1460C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611764 | |||||||
| chr2:15611768 | GTGGCTGG others(121): Show |
G | 28 | a0001c0004t0003g0002 a0001c0004t0003g0019 a0001c0004t0003g0020 others(25): Show |
47 | HG00673.hp2 HG02027.hp1 HG02056.hp2 others(44): Show |
intron_variant | MODIFIER | c.957-1455_957-1328d others(2): Show |
DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611768 | |||||||
| chr2:15611769 | T | C | 117 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(114): Show |
200 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.957-1455T>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611769 | |||||||
| chr2:15611786 | G | A | 73 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(70): Show |
123 | HG00558.hp2 HG00639.hp1 HG00639.hp2 others(120): Show |
intron_variant | MODIFIER | c.957-1438G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611786 | |||||||
| chr2:15611813 | C | T | 73 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(70): Show |
123 | HG00558.hp2 HG00639.hp1 HG00639.hp2 others(120): Show |
intron_variant | MODIFIER | c.957-1411C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611813 | |||||||
| chr2:15611830 | CA | C | 2 | a0001c0001t0001g0006 a0001c0001t0001g0018 |
4 | NA18980.hp2 NA18986.hp1 NA19081.hp2 others(1): Show |
intron_variant | MODIFIER | c.957-1393delA | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611830 | |||||||
| chr2:15611831 | A | G | 67 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(64): Show |
112 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(109): Show |
intron_variant | MODIFIER | c.957-1393A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611831 | |||||||
| chr2:15611833 | A | G | 73 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(70): Show |
123 | HG00558.hp2 HG00639.hp1 HG00639.hp2 others(120): Show |
intron_variant | MODIFIER | c.957-1391A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611833 | |||||||
| chr2:15611836 | GGCTC | G | 73 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(70): Show |
119 | HG00558.hp2 HG00639.hp1 HG00639.hp2 others(116): Show |
intron_variant | MODIFIER | c.957-1387_957-1384d others(6): Show |
DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611836 | |||||||
| chr2:15611839 | TCCTCACT others(25): Show |
T | 2 | a0001c0001t0001g0006 a0001c0001t0001g0018 |
4 | NA18980.hp2 NA18986.hp1 NA19081.hp2 others(1): Show |
intron_variant | MODIFIER | c.957-1384_957-1353d others(34): Show |
DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611839 | |||||||
| chr2:15611843 | C | G | 73 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(70): Show |
119 | HG00558.hp2 HG00639.hp1 HG00639.hp2 others(116): Show |
intron_variant | MODIFIER | c.957-1381C>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611843 | |||||||
| chr2:15611846 | T | C | 73 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(70): Show |
119 | HG00558.hp2 HG00639.hp1 HG00639.hp2 others(116): Show |
intron_variant | MODIFIER | c.957-1378T>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611846 | |||||||
| chr2:15611847 | T | C | 73 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(70): Show |
119 | HG00558.hp2 HG00639.hp1 HG00639.hp2 others(116): Show |
intron_variant | MODIFIER | c.957-1377T>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611847 | |||||||
| chr2:15611850 | CAGTAGGG others(17): Show |
C | 73 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(70): Show |
119 | HG00558.hp2 HG00639.hp1 HG00639.hp2 others(116): Show |
intron_variant | MODIFIER | c.957-1373_957-1350d others(26): Show |
DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611850 | |||||||
| chr2:15611873 | C | A | 2 | a0001c0001t0001g0006 a0001c0001t0001g0018 |
4 | NA18980.hp2 NA18986.hp1 NA19081.hp2 others(1): Show |
intron_variant | MODIFIER | c.957-1351C>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611873 | |||||||
| chr2:15611874 | G | C | 2 | a0001c0001t0001g0006 a0001c0001t0001g0018 |
4 | NA18980.hp2 NA18986.hp1 NA19081.hp2 others(1): Show |
intron_variant | MODIFIER | c.957-1350G>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611874 | |||||||
| chr2:15611876 | C | A | 73 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(70): Show |
119 | HG00558.hp2 HG00639.hp1 HG00639.hp2 others(116): Show |
intron_variant | MODIFIER | c.957-1348C>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611876 | |||||||
| chr2:15611879 | T | C | 2 | a0001c0001t0001g0006 a0001c0001t0001g0018 |
4 | NA18980.hp2 NA18986.hp1 NA19081.hp2 others(1): Show |
intron_variant | MODIFIER | c.957-1345T>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611879 | |||||||
| chr2:15611880 | CA | C | 73 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(70): Show |
119 | HG00558.hp2 HG00639.hp1 HG00639.hp2 others(116): Show |
intron_variant | MODIFIER | c.957-1343delA | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611880 | |||||||
| chr2:15611887 | C | CTCCA | 2 | a0001c0001t0001g0006 a0001c0001t0001g0018 |
4 | NA18980.hp2 NA18986.hp1 NA19081.hp2 others(1): Show |
intron_variant | MODIFIER | c.957-1337_957-1336i others(6): Show |
DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611887 | |||||||
| chr2:15611891 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.957-1333C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611891 | |||||||
| chr2:15611896 | CG | C | 6 | a0001c0001t0001g0032 a0001c0001t0001g0115 a0001c0001t0001g0116 others(3): Show |
7 | HG00639.hp2 HG01192.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.957-1326delG | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr2 | 15611896 | ||||||
| chr2:15611897 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.957-1327G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611897 | |||||||
| chr2:15611897 | G | C | 28 | a0001c0004t0003g0002 a0001c0004t0003g0019 a0001c0004t0003g0020 others(25): Show |
47 | HG00673.hp2 HG02027.hp1 HG02056.hp2 others(44): Show |
intron_variant | MODIFIER | c.957-1327G>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611897 | |||||||
| chr2:15611907 | G | A | 104 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(101): Show |
173 | HG00558.hp2 HG00639.hp1 HG00639.hp2 others(170): Show |
intron_variant | MODIFIER | c.957-1317G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611907 | |||||||
| chr2:15611908 | C | CGGGGGAG others(92): Show |
1 | a0001c0001t0001g0140 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.957-1312_957-1311i others(101): Show |
DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr2 | 15611908 | ||||||
| chr2:15611908 | C | T | 104 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(101): Show |
173 | HG00558.hp2 HG00639.hp1 HG00639.hp2 others(170): Show |
intron_variant | MODIFIER | c.957-1316C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611908 | |||||||
| chr2:15611909 | G | A | 25 | a0001c0004t0003g0002 a0001c0004t0003g0019 a0001c0004t0003g0020 others(22): Show |
43 | HG00673.hp2 HG02027.hp1 HG02056.hp2 others(40): Show |
intron_variant | MODIFIER | c.957-1315G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611909 | |||||||
| chr2:15611913 | A | AGCTGACC others(90): Show |
2 | a0001c0001t0001g0119 a0001c0001t0006g0234 |
2 | HG02055.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.957-1295_957-1294i others(99): Show |
DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr2 | 15611913 | ||||||
| chr2:15611913 | A | AGCTGACC others(90): Show |
81 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(78): Show |
133 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.957-1295_957-1294i others(99): Show |
DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr2 | 15611913 | ||||||
| chr2:15611913 | A | AGCTGACC others(91): Show |
1 | a0001c0001t0001g0132 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.957-1295_957-1294i others(100): Show |
DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr2 | 15611913 | ||||||
| chr2:15611913 | A | AGCTGACC others(91): Show |
1 | a0001c0001t0001g0078 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.957-1295_957-1294i others(100): Show |
DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr2 | 15611913 | ||||||
| chr2:15611913 | A | AGCTGACC others(91): Show |
3 | a0001c0001t0001g0137 a0001c0001t0001g0146 a0001c0002t0001g0220 |
3 | HG04199.hp2 NA18954.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.957-1299_957-1298i others(100): Show |
DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr2 | 15611913 | ||||||
| chr2:15611913 | A | G | 105 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(102): Show |
174 | HG00558.hp2 HG00639.hp1 HG00639.hp2 others(171): Show |
intron_variant | MODIFIER | c.957-1311A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611913 | |||||||
| chr2:15611918 | A | ACCCCCCC others(91): Show |
4 | a0001c0001t0001g0136 a0001c0001t0001g0148 a0001c0002t0001g0224 others(1): Show |
4 | HG01099.hp2 HG02056.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.957-1295_957-1294i others(100): Show |
DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr2 | 15611918 | ||||||
| chr2:15611930 | T | C | 1 | a0001c0002t0001g0217 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.957-1294T>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611930 | |||||||
| chr2:15611940 | C | T | 1 | a0001c0002t0001g0217 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.957-1284C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611940 | |||||||
| chr2:15611942 | A | G | 1 | a0001c0002t0001g0217 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.957-1282A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611942 | |||||||
| chr2:15611945 | C | T | 71 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(68): Show |
120 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(117): Show |
intron_variant | MODIFIER | c.957-1279C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611945 | |||||||
| chr2:15611958 | G | A | 1 | a0001c0002t0001g0217 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.957-1266G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611958 | |||||||
| chr2:15611972 | A | C | 1 | a0001c0002t0001g0217 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.957-1252A>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611972 | |||||||
| chr2:15611977 | C | T | 1 | a0001c0004t0003g0189 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.957-1247C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611977 | |||||||
| chr2:15611990 | A | G | 73 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(70): Show |
122 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(119): Show |
intron_variant | MODIFIER | c.957-1234A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611990 | |||||||
| chr2:15611995 | G | A | 3 | a0001c0001t0001g0055 a0001c0001t0001g0244 a0001c0001t0001g0245 |
4 | HG01884.hp1 HG02818.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.957-1229G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15611995 | |||||||
| chr2:15612002 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.957-1222C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15612002 | |||||||
| chr2:15612002 | CGGGCAGA others(67): Show |
C | 1 | a0001c0002t0001g0217 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.957-1219_957-1146d others(76): Show |
DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr2 | 15612002 | ||||||
| chr2:15612078 | G | GC | 246 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(243): Show |
393 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(390): Show |
intron_variant | MODIFIER | c.957-1145dupC | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr2 | 15612078 | ||||||
| chr2:15612079 | C | A | 1 | a0001c0002t0001g0217 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.957-1145C>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15612079 | |||||||
| chr2:15612083 | C | CG | 72 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(69): Show |
121 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(118): Show |
intron_variant | MODIFIER | c.957-1137dupG | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr2 | 15612083 | ||||||
| chr2:15612088 | C | G | 73 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(70): Show |
122 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(119): Show |
intron_variant | MODIFIER | c.957-1136C>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15612088 | |||||||
| chr2:15612104 | C | T | 1 | a0001c0002t0001g0217 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.957-1120C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15612104 | |||||||
| chr2:15612110 | CGGACGGG others(43): Show |
C | 1 | a0001c0004t0003g0188 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.957-1096_957-1047d others(52): Show |
DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr2 | 15612110 | ||||||
| chr2:15612116 | G | A | 1 | a0001c0002t0001g0217 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.957-1108G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15612116 | |||||||
| chr2:15612210 | C | T | 8 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0024 others(5): Show |
18 | HG01256.hp1 HG01358.hp2 HG01934.hp2 others(15): Show |
intron_variant | MODIFIER | c.957-1014C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15612210 | |||||||
| chr2:15612227 | G | T | 71 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(68): Show |
120 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(117): Show |
intron_variant | MODIFIER | c.957-997G>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15612227 | |||||||
| chr2:15612232 | C | T | 2 | a0001c0004t0003g0020 a0001c0004t0003g0194 |
4 | NA18955.hp1 NA18990.hp2 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.957-992C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15612232 | |||||||
| chr2:15612296 | G | C | 1 | a0001c0001t0001g0068 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.957-928G>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15612296 | |||||||
| chr2:15612328 | G | A | 1 | a0001c0002t0001g0225 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.957-896G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15612328 | |||||||
| chr2:15612365 | G | A | 71 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(68): Show |
120 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(117): Show |
intron_variant | MODIFIER | c.957-859G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15612365 | |||||||
| chr2:15612442 | A | G | 13 | a0001c0003t0002g0014 a0001c0003t0002g0041 a0001c0003t0002g0042 others(10): Show |
18 | HG00408.hp2 HG00438.hp1 HG01361.hp1 others(15): Show |
intron_variant | MODIFIER | c.957-782A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15612442 | |||||||
| chr2:15612456 | G | A | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | HG04199.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.957-768G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15612456 | |||||||
| chr2:15612495 | C | T | 2 | a0001c0001t0001g0119 a0001c0003t0001g0152 |
2 | HG02055.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.957-729C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15612495 | |||||||
| chr2:15612524 | T | C | 1 | a0001c0001t0001g0145 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.957-700T>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15612524 | |||||||
| chr2:15612538 | G | C | 54 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(51): Show |
75 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.957-686G>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15612538 | |||||||
| chr2:15612547 | C | T | 71 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(68): Show |
120 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(117): Show |
intron_variant | MODIFIER | c.957-677C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15612547 | |||||||
| chr2:15612645 | C | A | 71 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(68): Show |
120 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(117): Show |
intron_variant | MODIFIER | c.957-579C>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15612645 | |||||||
| chr2:15612715 | A | C | 44 | a0001c0001t0003g0183 a0001c0001t0006g0234 a0001c0002t0001g0001 others(41): Show |
77 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.957-509A>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15612715 | |||||||
| chr2:15612723 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.957-501C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15612723 | |||||||
| chr2:15612745 | C | G | 71 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(68): Show |
120 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(117): Show |
intron_variant | MODIFIER | c.957-479C>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15612745 | |||||||
| chr2:15612789 | G | A | 1 | a0001c0004t0003g0189 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.957-435G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15612789 | |||||||
| chr2:15612790 | C | T | 1 | a0001c0004t0003g0189 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.957-434C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15612790 | |||||||
| chr2:15612791 | G | A | 1 | a0001c0002t0001g0208 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.957-433G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15612791 | |||||||
| chr2:15612803 | G | A | 40 | a0001c0001t0003g0183 a0001c0002t0001g0001 a0001c0002t0001g0022 others(37): Show |
73 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.957-421G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15612803 | |||||||
| chr2:15612814 | G | T | 1 | a0001c0013t0002g0240 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.957-410G>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15612814 | |||||||
| chr2:15612875 | C | T | 2 | a0001c0001t0001g0242 a0001c0001t0001g0243 |
2 | HG01261.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.957-349C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15612875 | |||||||
| chr2:15612878 | G | A | 2 | a0001c0001t0001g0055 a0001c0001t0001g0244 |
3 | HG01884.hp1 HG02818.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.957-346G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15612878 | |||||||
| chr2:15612880 | G | T | 1 | a0001c0002t0001g0200 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.957-344G>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15612880 | |||||||
| chr2:15612899 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.957-325C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15612899 | |||||||
| chr2:15612908 | G | A | 44 | a0001c0001t0003g0183 a0001c0001t0006g0234 a0001c0002t0001g0001 others(41): Show |
77 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.957-316G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15612908 | |||||||
| chr2:15612926 | T | A | 202 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(199): Show |
324 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(321): Show |
intron_variant | MODIFIER | c.957-298T>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15612926 | |||||||
| chr2:15612982 | CAGAGGGA others(18): Show |
C | 1 | a0001c0001t0001g0245 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.957-226_957-202del others(25): Show |
DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr2 | 15612982 | ||||||
| chr2:15612998 | A | AAAGAGAG others(18): Show |
1 | a0001c0001t0006g0234 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.957-225_957-201dup others(25): Show |
DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr2 | 15612998 | ||||||
| chr2:15613008 | AGAGGGAG others(22): Show |
A | 1 | a0002c0005t0001g0050 | 2 | HG00673.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.957-210_957-182del others(29): Show |
DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr2 | 15613008 | ||||||
| chr2:15613027 | A | C | 1 | a0001c0001t0001g0087 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.957-197A>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15613027 | |||||||
| chr2:15613046 | G | C | 1 | a0001c0002t0001g0211 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.957-178G>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15613046 | |||||||
| chr2:15613155 | C | G | 44 | a0001c0001t0003g0183 a0001c0001t0006g0234 a0001c0002t0001g0001 others(41): Show |
77 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.957-69C>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15613155 | |||||||
| chr2:15613174 | C | A | 1 | a0001c0003t0002g0162 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.957-50C>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15613174 | |||||||
| chr2:15613183 | A | AT | 71 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(68): Show |
120 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(117): Show |
intron_variant | MODIFIER | c.957-28dupT | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr2 | 15613183 | ||||||
| chr2:15613196 | T | A | 1 | a0001c0001t0001g0245 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.957-28T>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 13/25 | chr2 | 15613196 | |||||||
| chr2:15613358 | C | G | 71 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(68): Show |
120 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(117): Show |
intron_variant | MODIFIER | c.1017+74C>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 14/25 | chr2 | 15613358 | |||||||
| chr2:15613480 | A | G | 71 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(68): Show |
120 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(117): Show |
intron_variant | MODIFIER | c.1017+196A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 14/25 | chr2 | 15613480 | |||||||
| chr2:15613572 | T | C | 48 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(45): Show |
68 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.1017+288T>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 14/25 | chr2 | 15613572 | |||||||
| chr2:15613697 | G | A | 71 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(68): Show |
120 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(117): Show |
intron_variant | MODIFIER | c.1017+413G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 14/25 | chr2 | 15613697 | |||||||
| chr2:15613813 | G | A | 202 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(199): Show |
324 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(321): Show |
intron_variant | MODIFIER | c.1017+529G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 14/25 | chr2 | 15613813 | |||||||
| chr2:15613833 | A | AT | 56 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(53): Show |
88 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.1017+569dupT | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr2 | 15613833 | ||||||
| chr2:15613833 | AT | A | 75 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(72): Show |
123 | HG00558.hp2 HG00639.hp2 HG00733.hp1 others(120): Show |
intron_variant | MODIFIER | c.1017+569delT | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr2 | 15613833 | ||||||
| chr2:15613833 | ATT | A | 6 | a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0074 others(3): Show |
9 | HG00639.hp1 HG01167.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1017+568_1017+569d others(4): Show |
DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr2 | 15613833 | ||||||
| chr2:15613885 | G | T | 1 | a0001c0002t0001g0216 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1017+601G>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 14/25 | chr2 | 15613885 | |||||||
| chr2:15613985 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1017+701C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 14/25 | chr2 | 15613985 | |||||||
| chr2:15614001 | G | A | 72 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(69): Show |
121 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(118): Show |
intron_variant | MODIFIER | c.1017+717G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 14/25 | chr2 | 15614001 | |||||||
| chr2:15614068 | G | A | 1 | a0001c0001t0006g0234 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1017+784G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 14/25 | chr2 | 15614068 | |||||||
| chr2:15614097 | A | G | 1 | a0001c0003t0001g0060 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1017+813A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 14/25 | chr2 | 15614097 | |||||||
| chr2:15614222 | T | G | 71 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(68): Show |
120 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(117): Show |
intron_variant | MODIFIER | c.1017+938T>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 14/25 | chr2 | 15614222 | |||||||
| chr2:15614334 | T | C | 1 | a0001c0001t0001g0237 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1017+1050T>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 14/25 | chr2 | 15614334 | |||||||
| chr2:15614348 | C | G | 3 | a0001c0001t0001g0055 a0001c0001t0001g0244 a0001c0001t0001g0245 |
4 | HG01884.hp1 HG02818.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1017+1064C>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 14/25 | chr2 | 15614348 | |||||||
| chr2:15614594 | A | G | 3 | a0001c0001t0003g0183 a0001c0002t0001g0221 a0001c0010t0001g0222 |
3 | NA19005.hp2 NA19054.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.1017+1310A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 14/25 | chr2 | 15614594 | |||||||
| chr2:15614872 | A | G | 1 | a0001c0001t0001g0244 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1017+1588A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 14/25 | chr2 | 15614872 | |||||||
| chr2:15615230 | C | T | 3 | a0001c0001t0001g0055 a0001c0001t0001g0244 a0001c0001t0001g0245 |
4 | HG01884.hp1 HG02818.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1017+1946C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 14/25 | chr2 | 15615230 | |||||||
| chr2:15615238 | T | G | 5 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0056 others(2): Show |
8 | HG01109.hp1 HG02280.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1017+1954T>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 14/25 | chr2 | 15615238 | |||||||
| chr2:15615346 | T | C | 2 | a0001c0003t0001g0059 a0001c0003t0001g0060 |
2 | HG02451.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1018-1898T>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 14/25 | chr2 | 15615346 | |||||||
| chr2:15615460 | C | T | 2 | a0001c0001t0001g0242 a0001c0001t0001g0243 |
2 | HG01261.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1018-1784C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 14/25 | chr2 | 15615460 | |||||||
| chr2:15615498 | A | C | 44 | a0001c0001t0003g0183 a0001c0001t0006g0234 a0001c0002t0001g0001 others(41): Show |
77 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.1018-1746A>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 14/25 | chr2 | 15615498 | |||||||
| chr2:15615552 | C | CT | 199 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(196): Show |
321 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(318): Show |
intron_variant | MODIFIER | c.1018-1691dupT | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr2 | 15615552 | ||||||
| chr2:15615632 | G | A | 1 | a0001c0001t0006g0234 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1018-1612G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 14/25 | chr2 | 15615632 | |||||||
| chr2:15615645 | A | C | 1 | a0001c0001t0001g0119 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1018-1599A>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 14/25 | chr2 | 15615645 | |||||||
| chr2:15615869 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1018-1375A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 14/25 | chr2 | 15615869 | |||||||
| chr2:15616053 | C | T | 1 | a0001c0002t0001g0215 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1018-1191C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 14/25 | chr2 | 15616053 | |||||||
| chr2:15616062 | T | G | 1 | a0001c0001t0001g0107 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1018-1182T>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 14/25 | chr2 | 15616062 | |||||||
| chr2:15616062 | T | TTG | 67 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(64): Show |
115 | HG00323.hp1 HG00558.hp2 HG00733.hp1 others(112): Show |
intron_variant | MODIFIER | c.1018-1158_1018-115 others(6): Show |
DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr2 | 15616062 | ||||||
| chr2:15616062 | T | TTGTG | 3 | a0001c0001t0001g0017 a0001c0001t0001g0068 a0001c0001t0001g0097 |
5 | HG02523.hp2 HG03490.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.1018-1160_1018-115 others(8): Show |
DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr2 | 15616062 | ||||||
| chr2:15616062 | T | TTGTGTG | 4 | a0001c0001t0001g0074 a0001c0001t0001g0076 a0001c0001t0001g0084 others(1): Show |
4 | HG00639.hp1 HG02129.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.1018-1162_1018-115 others(10): Show |
DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr2 | 15616062 | ||||||
| chr2:15616062 | TTG | T | 11 | a0001c0001t0001g0032 a0001c0001t0001g0057 a0001c0001t0001g0058 others(8): Show |
12 | HG00639.hp2 HG01192.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1018-1158_1018-115 others(6): Show |
DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr2 | 15616062 | ||||||
| chr2:15616062 | TTGTG | T | 120 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(117): Show |
192 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.1018-1160_1018-115 others(8): Show |
DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr2 | 15616062 | ||||||
| chr2:15616204 | C | T | 38 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(35): Show |
54 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(51): Show |
intron_variant | MODIFIER | c.1018-1040C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 14/25 | chr2 | 15616204 | |||||||
| chr2:15616244 | T | C | 1 | a0001c0002t0001g0200 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1018-1000T>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 14/25 | chr2 | 15616244 | |||||||
| chr2:15616293 | G | C | 4 | a0001c0004t0003g0019 a0001c0004t0003g0184 a0001c0004t0003g0186 others(1): Show |
6 | NA18952.hp2 NA18961.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1018-951G>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 14/25 | chr2 | 15616293 | |||||||
| chr2:15616401 | CAACTCAT others(6): Show |
C | 26 | a0001c0002t0001g0210 a0001c0004t0003g0002 a0001c0004t0003g0019 others(23): Show |
44 | HG00673.hp2 HG02027.hp1 HG02056.hp2 others(41): Show |
intron_variant | MODIFIER | c.1018-838_1018-826d others(15): Show |
DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr2 | 15616401 | ||||||
| chr2:15616408 | T | C | 1 | a0001c0001t0001g0032 | 2 | HG01884.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.1018-836T>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 14/25 | chr2 | 15616408 | |||||||
| chr2:15616431 | C | T | 2 | a0001c0001t0001g0242 a0001c0001t0001g0243 |
2 | HG01261.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1018-813C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 14/25 | chr2 | 15616431 | |||||||
| chr2:15616466 | A | G | 1 | a0001c0001t0001g0121 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1018-778A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 14/25 | chr2 | 15616466 | |||||||
| chr2:15616474 | T | G | 2 | a0001c0001t0001g0242 a0001c0001t0001g0243 |
2 | HG01261.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1018-770T>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 14/25 | chr2 | 15616474 | |||||||
| chr2:15616565 | T | C | 1 | a0001c0001t0001g0245 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1018-679T>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 14/25 | chr2 | 15616565 | |||||||
| chr2:15616581 | C | G | 2 | a0001c0001t0001g0055 a0001c0001t0001g0244 |
3 | HG01884.hp1 HG02818.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1018-663C>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 14/25 | chr2 | 15616581 | |||||||
| chr2:15616626 | C | T | 5 | a0001c0001t0001g0032 a0001c0001t0001g0115 a0001c0001t0001g0116 others(2): Show |
6 | HG00639.hp2 HG01192.hp2 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.1018-618C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 14/25 | chr2 | 15616626 | |||||||
| chr2:15616792 | C | T | 26 | a0001c0002t0001g0210 a0001c0004t0003g0002 a0001c0004t0003g0019 others(23): Show |
44 | HG00673.hp2 HG02027.hp1 HG02056.hp2 others(41): Show |
intron_variant | MODIFIER | c.1018-452C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 14/25 | chr2 | 15616792 | |||||||
| chr2:15616842 | C | G | 2 | a0001c0002t0001g0224 a0001c0002t0001g0225 |
2 | HG02109.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1018-402C>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 14/25 | chr2 | 15616842 | |||||||
| chr2:15616893 | A | G | 1 | a0001c0001t0001g0146 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1018-351A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 14/25 | chr2 | 15616893 | |||||||
| chr2:15617102 | C | CTT | 70 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(67): Show |
119 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(116): Show |
intron_variant | MODIFIER | c.1018-131_1018-130d others(4): Show |
DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr2 | 15617102 | ||||||
| chr2:15617102 | CT | C | 46 | a0001c0001t0001g0034 a0001c0001t0001g0134 a0001c0001t0001g0137 others(43): Show |
80 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.1018-130delT | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr2 | 15617102 | ||||||
| chr2:15617115 | A | G | 1 | a0001c0001t0001g0079 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1018-129A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 14/25 | chr2 | 15617115 | |||||||
| chr2:15617581 | A | T | 1 | a0001c0006t0004g0198 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1116+239A>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 15/25 | chr2 | 15617581 | |||||||
| chr2:15617750 | A | G | 1 | a0001c0001t0001g0013 | 4 | HG02647.hp1 HG03041.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1116+408A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 15/25 | chr2 | 15617750 | |||||||
| chr2:15617804 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1117-377G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 15/25 | chr2 | 15617804 | |||||||
| chr2:15617807 | A | G | 1 | a0001c0004t0003g0186 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1117-374A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 15/25 | chr2 | 15617807 | |||||||
| chr2:15617932 | A | T | 1 | a0005c0011t0001g0232 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1117-249A>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 15/25 | chr2 | 15617932 | |||||||
| chr2:15617982 | G | A | 26 | a0001c0002t0001g0210 a0001c0004t0003g0002 a0001c0004t0003g0019 others(23): Show |
44 | HG00673.hp2 HG02027.hp1 HG02056.hp2 others(41): Show |
intron_variant | MODIFIER | c.1117-199G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 15/25 | chr2 | 15617982 | |||||||
| chr2:15617990 | A | G | 199 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(196): Show |
321 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(318): Show |
intron_variant | MODIFIER | c.1117-191A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 15/25 | chr2 | 15617990 | |||||||
| chr2:15618169 | T | C | 71 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(68): Show |
120 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(117): Show |
intron_variant | MODIFIER | c.1117-12T>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 15/25 | chr2 | 15618169 | |||||||
| chr2:15618488 | G | A | 44 | a0001c0001t0001g0137 a0001c0001t0003g0183 a0001c0001t0006g0234 others(41): Show |
77 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.1206+218G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 16/25 | chr2 | 15618488 | |||||||
| chr2:15618549 | T | C | 4 | a0001c0001t0001g0116 a0001c0003t0002g0054 a0001c0003t0002g0238 others(1): Show |
5 | HG02622.hp2 HG02895.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1206+279T>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 16/25 | chr2 | 15618549 | |||||||
| chr2:15618564 | G | A | 6 | a0001c0001t0001g0028 a0001c0001t0001g0088 a0001c0001t0001g0089 others(3): Show |
6 | HG01243.hp2 HG02055.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1206+294G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 16/25 | chr2 | 15618564 | |||||||
| chr2:15618662 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1206+392C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 16/25 | chr2 | 15618662 | |||||||
| chr2:15618674 | C | G | 41 | a0001c0001t0001g0137 a0001c0001t0003g0183 a0001c0002t0001g0001 others(38): Show |
74 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.1206+404C>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 16/25 | chr2 | 15618674 | |||||||
| chr2:15618719 | G | C | 1 | a0001c0003t0002g0170 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1206+449G>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 16/25 | chr2 | 15618719 | |||||||
| chr2:15618766 | G | A | 6 | a0001c0001t0001g0032 a0001c0001t0001g0115 a0001c0001t0001g0116 others(3): Show |
7 | HG00639.hp2 HG01192.hp2 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.1206+496G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 16/25 | chr2 | 15618766 | |||||||
| chr2:15618864 | G | C | 1 | a0001c0001t0001g0118 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1206+594G>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 16/25 | chr2 | 15618864 | |||||||
| chr2:15618876 | A | C | 1 | a0001c0001t0001g0096 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1206+606A>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 16/25 | chr2 | 15618876 | |||||||
| chr2:15619112 | C | T | 1 | a0001c0001t0006g0234 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1206+842C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 16/25 | chr2 | 15619112 | |||||||
| chr2:15619173 | C | A | 1 | a0001c0001t0001g0072 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1206+903C>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 16/25 | chr2 | 15619173 | |||||||
| chr2:15619214 | T | C | 9 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0070 others(6): Show |
10 | HG01243.hp2 HG02055.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1206+944T>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 16/25 | chr2 | 15619214 | |||||||
| chr2:15619382 | A | C | 1 | a0001c0001t0001g0126 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1207-826A>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 16/25 | chr2 | 15619382 | |||||||
| chr2:15619500 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1207-708G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 16/25 | chr2 | 15619500 | |||||||
| chr2:15619569 | A | C | 1 | a0001c0001t0001g0115 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1207-639A>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 16/25 | chr2 | 15619569 | |||||||
| chr2:15619591 | G | T | 65 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(62): Show |
113 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(110): Show |
intron_variant | MODIFIER | c.1207-617G>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 16/25 | chr2 | 15619591 | |||||||
| chr2:15619693 | T | C | 1 | a0001c0007t0004g0046 | 2 | HG02970.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1207-515T>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 16/25 | chr2 | 15619693 | |||||||
| chr2:15619731 | A | G | 1 | a0001c0002t0001g0200 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1207-477A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 16/25 | chr2 | 15619731 | |||||||
| chr2:15619868 | A | G | 1 | a0001c0001t0001g0101 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1207-340A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 16/25 | chr2 | 15619868 | |||||||
| chr2:15619888 | A | T | 5 | a0001c0001t0001g0032 a0001c0001t0001g0115 a0001c0001t0001g0116 others(2): Show |
6 | HG00639.hp2 HG01192.hp2 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.1207-320A>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 16/25 | chr2 | 15619888 | |||||||
| chr2:15619907 | T | G | 1 | a0001c0001t0001g0237 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1207-301T>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 16/25 | chr2 | 15619907 | |||||||
| chr2:15619916 | G | A | 1 | a0001c0003t0002g0165 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1207-292G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 16/25 | chr2 | 15619916 | |||||||
| chr2:15619934 | A | C | 1 | a0001c0001t0001g0245 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1207-274A>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 16/25 | chr2 | 15619934 | |||||||
| chr2:15620128 | T | A | 5 | a0001c0001t0001g0032 a0001c0001t0001g0115 a0001c0001t0001g0116 others(2): Show |
6 | HG00639.hp2 HG01192.hp2 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.1207-80T>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 16/25 | chr2 | 15620128 | |||||||
| chr2:15620193 | G | A | 1 | a0001c0001t0001g0071 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1207-15G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 16/25 | chr2 | 15620193 | |||||||
| chr2:15620604 | T | G | 3 | a0001c0001t0001g0055 a0001c0001t0001g0244 a0001c0001t0001g0245 |
4 | HG01884.hp1 HG02818.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1395+208T>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 17/25 | chr2 | 15620604 | |||||||
| chr2:15620608 | C | T | 1 | a0001c0001t0001g0245 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1395+212C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 17/25 | chr2 | 15620608 | |||||||
| chr2:15620623 | C | A | 1 | a0001c0001t0001g0119 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1395+227C>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 17/25 | chr2 | 15620623 | |||||||
| chr2:15620653 | A | G | 6 | a0001c0001t0001g0032 a0001c0001t0001g0115 a0001c0001t0001g0116 others(3): Show |
7 | HG00639.hp2 HG01192.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.1395+257A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 17/25 | chr2 | 15620653 | |||||||
| chr2:15620698 | G | T | 2 | a0001c0001t0001g0242 a0001c0001t0001g0243 |
2 | HG01261.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1395+302G>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 17/25 | chr2 | 15620698 | |||||||
| chr2:15620809 | T | G | 1 | a0001c0001t0001g0093 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1396-256T>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 17/25 | chr2 | 15620809 | |||||||
| chr2:15620845 | T | C | 2 | a0001c0006t0004g0197 a0001c0006t0004g0198 |
2 | HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1396-220T>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 17/25 | chr2 | 15620845 | |||||||
| chr2:15620891 | T | C | 26 | a0001c0002t0001g0210 a0001c0004t0003g0002 a0001c0004t0003g0019 others(23): Show |
44 | HG00673.hp2 HG02027.hp1 HG02056.hp2 others(41): Show |
intron_variant | MODIFIER | c.1396-174T>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 17/25 | chr2 | 15620891 | |||||||
| chr2:15621165 | A | G | 1 | a0001c0001t0001g0237 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1447+49A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 18/25 | chr2 | 15621165 | |||||||
| chr2:15621569 | G | A | 3 | a0001c0003t0002g0040 a0001c0003t0002g0166 a0001c0003t0002g0168 |
4 | HG01928.hp1 HG01975.hp1 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1447+453G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 18/25 | chr2 | 15621569 | |||||||
| chr2:15621612 | A | G | 3 | a0001c0001t0001g0055 a0001c0001t0001g0244 a0001c0001t0001g0245 |
4 | HG01884.hp1 HG02818.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1447+496A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 18/25 | chr2 | 15621612 | |||||||
| chr2:15621649 | C | CT | 30 | a0001c0002t0001g0208 a0001c0002t0001g0210 a0001c0004t0003g0002 others(27): Show |
49 | HG00673.hp2 HG02027.hp1 HG02056.hp2 others(46): Show |
intron_variant | MODIFIER | c.1447+546dupT | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 18/25 | INFO_REALIGN_3_PRIME | chr2 | 15621649 | ||||||
| chr2:15621659 | T | G | 73 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(70): Show |
122 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(119): Show |
intron_variant | MODIFIER | c.1447+543T>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 18/25 | chr2 | 15621659 | |||||||
| chr2:15621799 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1447+683C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 18/25 | chr2 | 15621799 | |||||||
| chr2:15621842 | T | C | 47 | a0001c0001t0001g0122 a0001c0001t0001g0145 a0001c0001t0003g0183 others(44): Show |
80 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.1447+726T>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 18/25 | chr2 | 15621842 | |||||||
| chr2:15621860 | G | T | 1 | a0001c0001t0001g0095 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1447+744G>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 18/25 | chr2 | 15621860 | |||||||
| chr2:15621929 | T | C | 201 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(198): Show |
323 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.1447+813T>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 18/25 | chr2 | 15621929 | |||||||
| chr2:15621970 | A | C | 2 | a0001c0001t0001g0149 a0001c0001t0001g0150 |
2 | NA18960.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.1447+854A>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 18/25 | chr2 | 15621970 | |||||||
| chr2:15621996 | C | A | 1 | a0001c0001t0006g0234 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1447+880C>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 18/25 | chr2 | 15621996 | |||||||
| chr2:15621997 | G | A | 7 | a0001c0001t0001g0032 a0001c0001t0001g0055 a0001c0001t0001g0115 others(4): Show |
9 | HG00639.hp2 HG01192.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.1447+881G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 18/25 | chr2 | 15621997 | |||||||
| chr2:15622047 | TATC | T | 8 | a0001c0003t0002g0014 a0001c0003t0002g0041 a0001c0003t0002g0042 others(5): Show |
13 | HG00438.hp1 HG02080.hp2 NA18954.hp2 others(10): Show |
intron_variant | MODIFIER | c.1447+934_1447+936d others(5): Show |
DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 18/25 | INFO_REALIGN_3_PRIME | chr2 | 15622047 | ||||||
| chr2:15622064 | A | G | 2 | a0001c0001t0001g0148 a0001c0001t0001g0246 |
2 | HG01099.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.1447+948A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 18/25 | chr2 | 15622064 | |||||||
| chr2:15622253 | C | T | 1 | a0001c0001t0006g0234 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1447+1137C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 18/25 | chr2 | 15622253 | |||||||
| chr2:15622255 | C | A | 1 | a0001c0007t0004g0046 | 2 | HG02970.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1447+1139C>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 18/25 | chr2 | 15622255 | |||||||
| chr2:15622299 | T | G | 1 | a0001c0001t0001g0005 | 9 | NA18939.hp2 NA18941.hp2 NA18952.hp1 others(6): Show |
intron_variant | MODIFIER | c.1448-1137T>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 18/25 | chr2 | 15622299 | |||||||
| chr2:15622350 | G | A | 1 | a0001c0001t0001g0243 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1448-1086G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 18/25 | chr2 | 15622350 | |||||||
| chr2:15622351 | C | T | 2 | a0003c0008t0001g0069 a0003c0008t0001g0080 |
2 | HG02723.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1448-1085C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 18/25 | chr2 | 15622351 | |||||||
| chr2:15622811 | G | A | 71 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(68): Show |
120 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(117): Show |
intron_variant | MODIFIER | c.1448-625G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 18/25 | chr2 | 15622811 | |||||||
| chr2:15622867 | A | G | 200 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(197): Show |
322 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(319): Show |
intron_variant | MODIFIER | c.1448-569A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 18/25 | chr2 | 15622867 | |||||||
| chr2:15622961 | G | A | 2 | a0001c0002t0001g0053 a0001c0002t0001g0231 |
3 | HG00609.hp1 NA18963.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.1448-475G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 18/25 | chr2 | 15622961 | |||||||
| chr2:15622973 | A | G | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | HG00741.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.1448-463A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 18/25 | chr2 | 15622973 | |||||||
| chr2:15623198 | A | G | 3 | a0001c0001t0001g0028 a0001c0001t0001g0088 a0004c0016t0001g0028 |
3 | HG03471.hp1 HG03540.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1448-238A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 18/25 | chr2 | 15623198 | |||||||
| chr2:15623217 | A | T | 13 | a0001c0003t0002g0014 a0001c0003t0002g0041 a0001c0003t0002g0042 others(10): Show |
18 | HG00408.hp2 HG00438.hp1 HG01361.hp1 others(15): Show |
intron_variant | MODIFIER | c.1448-219A>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 18/25 | chr2 | 15623217 | |||||||
| chr2:15623302 | A | G | 1 | a0001c0001t0001g0055 | 2 | HG01884.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1448-134A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 18/25 | chr2 | 15623302 | |||||||
| chr2:15623664 | C | T | 71 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(68): Show |
120 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(117): Show |
intron_variant | MODIFIER | c.1594+82C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 19/25 | chr2 | 15623664 | |||||||
| chr2:15623731 | A | G | 1 | a0001c0001t0001g0075 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1594+149A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 19/25 | chr2 | 15623731 | |||||||
| chr2:15623733 | A | G | 1 | a0001c0001t0001g0118 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1594+151A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 19/25 | chr2 | 15623733 | |||||||
| chr2:15623771 | G | C | 3 | a0001c0001t0001g0055 a0001c0001t0001g0244 a0001c0001t0001g0245 |
4 | HG01884.hp1 HG02818.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1594+189G>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 19/25 | chr2 | 15623771 | |||||||
| chr2:15623936 | G | GA | 47 | a0001c0001t0001g0122 a0001c0001t0001g0145 a0001c0001t0003g0183 others(44): Show |
80 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.1594+362dupA | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr2 | 15623936 | ||||||
| chr2:15623954 | G | C | 71 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(68): Show |
120 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(117): Show |
intron_variant | MODIFIER | c.1594+372G>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 19/25 | chr2 | 15623954 | |||||||
| chr2:15624224 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1594+642C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 19/25 | chr2 | 15624224 | |||||||
| chr2:15624481 | C | T | 204 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(201): Show |
326 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(323): Show |
intron_variant | MODIFIER | c.1594+899C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 19/25 | chr2 | 15624481 | |||||||
| chr2:15624494 | A | G | 44 | a0001c0001t0001g0122 a0001c0001t0001g0145 a0001c0001t0003g0183 others(41): Show |
77 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.1594+912A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 19/25 | chr2 | 15624494 | |||||||
| chr2:15624544 | A | G | 1 | a0001c0004t0003g0181 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1594+962A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 19/25 | chr2 | 15624544 | |||||||
| chr2:15624559 | A | T | 1 | a0001c0001t0001g0119 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1594+977A>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 19/25 | chr2 | 15624559 | |||||||
| chr2:15624570 | G | A | 33 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0056 others(30): Show |
55 | HG00673.hp2 HG01109.hp1 HG02027.hp1 others(52): Show |
intron_variant | MODIFIER | c.1594+988G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 19/25 | chr2 | 15624570 | |||||||
| chr2:15624694 | GC | G | 3 | a0001c0003t0001g0151 a0001c0003t0001g0153 a0001c0003t0001g0235 |
3 | HG02615.hp2 NA20129.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1594+1114delC | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr2 | 15624694 | ||||||
| chr2:15624807 | G | A | 35 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(32): Show |
51 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.1594+1225G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 19/25 | chr2 | 15624807 | |||||||
| chr2:15624818 | G | A | 204 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(201): Show |
326 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(323): Show |
intron_variant | MODIFIER | c.1594+1236G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 19/25 | chr2 | 15624818 | |||||||
| chr2:15624857 | G | T | 1 | a0001c0001t0001g0119 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1594+1275G>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 19/25 | chr2 | 15624857 | |||||||
| chr2:15624914 | G | A | 43 | a0001c0001t0001g0122 a0001c0001t0001g0145 a0001c0001t0003g0183 others(40): Show |
76 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.1594+1332G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 19/25 | chr2 | 15624914 | |||||||
| chr2:15625227 | CTATT | C | 44 | a0001c0001t0001g0122 a0001c0001t0001g0145 a0001c0001t0003g0183 others(41): Show |
77 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.1594+1649_1594+165 others(8): Show |
DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr2 | 15625227 | ||||||
| chr2:15625258 | C | G | 2 | a0001c0001t0001g0242 a0001c0001t0001g0243 |
2 | HG01261.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1594+1676C>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 19/25 | chr2 | 15625258 | |||||||
| chr2:15625301 | C | T | 72 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(69): Show |
121 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(118): Show |
intron_variant | MODIFIER | c.1594+1719C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 19/25 | chr2 | 15625301 | |||||||
| chr2:15625337 | G | A | 2 | a0001c0006t0004g0197 a0001c0006t0004g0198 |
2 | HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1595-1717G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 19/25 | chr2 | 15625337 | |||||||
| chr2:15625414 | A | G | 3 | a0001c0001t0001g0017 a0001c0001t0001g0068 a0001c0001t0001g0097 |
5 | HG02523.hp2 HG03490.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.1595-1640A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 19/25 | chr2 | 15625414 | |||||||
| chr2:15625477 | T | C | 28 | a0001c0004t0003g0002 a0001c0004t0003g0019 a0001c0004t0003g0020 others(25): Show |
47 | HG00673.hp2 HG02027.hp1 HG02056.hp2 others(44): Show |
intron_variant | MODIFIER | c.1595-1577T>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 19/25 | chr2 | 15625477 | |||||||
| chr2:15625499 | C | T | 1 | a0001c0001t0001g0034 | 2 | NA18943.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.1595-1555C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 19/25 | chr2 | 15625499 | |||||||
| chr2:15625719 | A | T | 1 | a0001c0001t0001g0119 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1595-1335A>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 19/25 | chr2 | 15625719 | |||||||
| chr2:15625792 | G | A | 6 | a0001c0001t0001g0032 a0001c0001t0001g0115 a0001c0001t0001g0116 others(3): Show |
7 | HG00639.hp2 HG01192.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.1595-1262G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 19/25 | chr2 | 15625792 | |||||||
| chr2:15625819 | A | T | 1 | a0001c0003t0002g0169 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1595-1235A>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 19/25 | chr2 | 15625819 | |||||||
| chr2:15625894 | A | AT | 72 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(69): Show |
121 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(118): Show |
intron_variant | MODIFIER | c.1595-1150dupT | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr2 | 15625894 | ||||||
| chr2:15625938 | T | C | 1 | a0001c0002t0001g0200 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1595-1116T>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 19/25 | chr2 | 15625938 | |||||||
| chr2:15626057 | C | G | 2 | a0001c0002t0001g0224 a0001c0002t0001g0225 |
2 | HG02109.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1595-997C>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 19/25 | chr2 | 15626057 | |||||||
| chr2:15626075 | G | T | 1 | a0001c0001t0001g0101 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1595-979G>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 19/25 | chr2 | 15626075 | |||||||
| chr2:15626213 | G | A | 4 | a0001c0001t0001g0032 a0001c0001t0001g0115 a0001c0001t0001g0116 others(1): Show |
5 | HG00639.hp2 HG01884.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1595-841G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 19/25 | chr2 | 15626213 | |||||||
| chr2:15626256 | C | G | 1 | a0001c0001t0001g0119 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1595-798C>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 19/25 | chr2 | 15626256 | |||||||
| chr2:15626333 | T | C | 25 | a0001c0004t0003g0002 a0001c0004t0003g0019 a0001c0004t0003g0020 others(22): Show |
43 | HG00673.hp2 HG02027.hp1 HG02056.hp2 others(40): Show |
intron_variant | MODIFIER | c.1595-721T>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 19/25 | chr2 | 15626333 | |||||||
| chr2:15626341 | T | C | 1 | a0001c0001t0001g0135 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1595-713T>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 19/25 | chr2 | 15626341 | |||||||
| chr2:15626750 | G | A | 4 | a0001c0003t0001g0151 a0001c0003t0001g0152 a0001c0003t0001g0153 others(1): Show |
4 | HG02615.hp2 HG03098.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.1595-304G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 19/25 | chr2 | 15626750 | |||||||
| chr2:15626964 | C | T | 4 | a0001c0001t0006g0234 a0001c0002t0001g0200 a0001c0002t0001g0224 others(1): Show |
4 | HG01496.hp2 HG02109.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1595-90C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 19/25 | chr2 | 15626964 | |||||||
| chr2:15627237 | A | G | 3 | a0001c0003t0002g0014 a0001c0003t0002g0173 a0001c0003t0002g0176 |
6 | NA18963.hp2 NA18967.hp1 NA18982.hp1 others(3): Show |
intron_variant | MODIFIER | c.1686+92A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 20/25 | chr2 | 15627237 | |||||||
| chr2:15627379 | G | T | 2 | a0001c0002t0001g0224 a0001c0002t0001g0225 |
2 | HG02109.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1686+234G>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 20/25 | chr2 | 15627379 | |||||||
| chr2:15627465 | G | C | 1 | a0001c0004t0003g0191 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1686+320G>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 20/25 | chr2 | 15627465 | |||||||
| chr2:15627637 | G | A | 72 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(69): Show |
121 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(118): Show |
intron_variant | MODIFIER | c.1686+492G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 20/25 | chr2 | 15627637 | |||||||
| chr2:15627828 | C | T | 42 | a0001c0001t0001g0122 a0001c0001t0001g0145 a0001c0001t0003g0183 others(39): Show |
75 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.1687-617C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 20/25 | chr2 | 15627828 | |||||||
| chr2:15627845 | A | C | 1 | a0001c0001t0001g0119 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1687-600A>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 20/25 | chr2 | 15627845 | |||||||
| chr2:15627860 | C | G | 5 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0056 others(2): Show |
8 | HG01109.hp1 HG02280.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1687-585C>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 20/25 | chr2 | 15627860 | |||||||
| chr2:15627886 | A | G | 35 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(32): Show |
51 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.1687-559A>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 20/25 | chr2 | 15627886 | |||||||
| chr2:15628132 | G | A | 72 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(69): Show |
121 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(118): Show |
intron_variant | MODIFIER | c.1687-313G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 20/25 | chr2 | 15628132 | |||||||
| chr2:15628320 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1687-125C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 20/25 | chr2 | 15628320 | |||||||
| chr2:15628547 | T | C | 5 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0056 others(2): Show |
8 | HG01109.hp1 HG02280.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1759+30T>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 21/25 | chr2 | 15628547 | |||||||
| chr2:15628722 | AT | A | 72 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(69): Show |
121 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(118): Show |
intron_variant | MODIFIER | c.1832+20delT | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 22/25 | INFO_REALIGN_3_PRIME | chr2 | 15628722 | ||||||
| chr2:15628730 | T | C | 5 | a0001c0001t0001g0032 a0001c0001t0001g0115 a0001c0001t0001g0116 others(2): Show |
6 | HG00639.hp2 HG01192.hp2 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.1832+20T>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 22/25 | chr2 | 15628730 | |||||||
| chr2:15628752 | G | A | 35 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(32): Show |
51 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.1832+42G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 22/25 | chr2 | 15628752 | |||||||
| chr2:15628857 | C | G | 16 | a0001c0003t0002g0003 a0001c0003t0002g0011 a0001c0003t0002g0036 others(13): Show |
33 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.1875+18C>G | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 23/25 | chr2 | 15628857 | |||||||
| chr2:15628942 | G | A | 5 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0056 others(2): Show |
8 | HG01109.hp1 HG02280.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1875+103G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 23/25 | chr2 | 15628942 | |||||||
| chr2:15629057 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1875+218C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 23/25 | chr2 | 15629057 | |||||||
| chr2:15629131 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1875+292G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 23/25 | chr2 | 15629131 | |||||||
| chr2:15629316 | T | A | 1 | a0001c0015t0001g0130 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1876-286T>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 23/25 | chr2 | 15629316 | |||||||
| chr2:15629483 | C | T | 42 | a0001c0001t0001g0122 a0001c0001t0001g0145 a0001c0001t0003g0183 others(39): Show |
75 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.1876-119C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 23/25 | chr2 | 15629483 | |||||||
| chr2:15629749 | A | C | 1 | a0001c0001t0001g0119 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1971+52A>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 24/25 | chr2 | 15629749 | |||||||
| chr2:15629786 | C | T | 1 | a0001c0002t0001g0214 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1971+89C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 24/25 | chr2 | 15629786 | |||||||
| chr2:15629838 | T | C | 1 | a0001c0001t0001g0136 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1971+141T>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 24/25 | chr2 | 15629838 | |||||||
| chr2:15629937 | G | A | 72 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(69): Show |
121 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(118): Show |
intron_variant | MODIFIER | c.1972-53G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 24/25 | chr2 | 15629937 | |||||||
| chr2:15630169 | C | T | 6 | a0001c0003t0002g0036 a0001c0003t0002g0039 a0001c0003t0002g0154 others(3): Show |
8 | HG01106.hp1 HG01243.hp1 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.2092+59C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 25/25 | chr2 | 15630169 | |||||||
| chr2:15630222 | G | A | 1 | a0001c0003t0002g0168 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.2092+112G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 25/25 | chr2 | 15630222 | |||||||
| chr2:15630279 | G | A | 1 | a0001c0002t0001g0212 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2092+169G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 25/25 | chr2 | 15630279 | |||||||
| chr2:15630326 | A | C | 47 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(44): Show |
67 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.2092+216A>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 25/25 | chr2 | 15630326 | |||||||
| chr2:15630326 | A | T | 5 | a0001c0001t0001g0032 a0001c0001t0001g0115 a0001c0001t0001g0116 others(2): Show |
6 | HG00639.hp2 HG01192.hp2 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.2092+216A>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 25/25 | chr2 | 15630326 | |||||||
| chr2:15630383 | G | T | 72 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(69): Show |
121 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(118): Show |
intron_variant | MODIFIER | c.2092+273G>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 25/25 | chr2 | 15630383 | |||||||
| chr2:15630424 | C | T | 4 | a0001c0001t0006g0234 a0001c0002t0001g0200 a0001c0002t0001g0224 others(1): Show |
4 | HG01496.hp2 HG02109.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2092+314C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 25/25 | chr2 | 15630424 | |||||||
| chr2:15630431 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2092+321C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 25/25 | chr2 | 15630431 | |||||||
| chr2:15630482 | T | C | 1 | a0001c0002t0001g0213 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2093-294T>C | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 25/25 | chr2 | 15630482 | |||||||
| chr2:15630579 | G | A | 6 | a0001c0003t0002g0040 a0001c0003t0002g0158 a0001c0003t0002g0160 others(3): Show |
7 | HG01928.hp1 HG01975.hp1 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.2093-197G>A | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 25/25 | chr2 | 15630579 | |||||||
| chr2:15630651 | C | T | 72 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(69): Show |
121 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(118): Show |
intron_variant | MODIFIER | c.2093-125C>T | DDX1 | ENSG00000079785.16 | transcript | ENST00000233084.8 | protein_coding | 25/25 | chr2 | 15630651 |