Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 8292 |
| ensemblid | ENSG00000206561.14 |
| hgncid | 2226 |
| symbol | COLQ |
| name | collagen like tail subunit of asymmetric acetylcholinesterase |
| refseq_nuc | NM_005677.4 |
| refseq_prot | NP_005668.2 |
| ensembl_nuc | ENST00000383788.10 |
| ensembl_prot | ENSP00000373298.3 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 15450133 |
| end | 15521706 |
| strand | - |
| ver | v1.2 |
| region | chr3:15450133-15521706 |
| region5000 | chr3:15445133-15526706 |
| regionname0 | COLQ_chr3_15450133_15521706 |
| regionname5000 | COLQ_chr3_15445133_15526706 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 455 | 355 | 69 | 66 | 172 | 12 | 34 | 134 | COLQ_chr3_15445133_15526706 | COLQ | MVVLN others(450): Show |
chr3 | 15445133 | 15526706 |
| a0002 | 0/0 | 455 | 17 | 17 | 0 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | MVVLN others(450): Show |
chr3 | 15445133 | 15526706 |
| a0003 | 0/0 | 455 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | MVVLN others(450): Show |
chr3 | 15445133 | 15526706 |
| a0004 | 0/0 | 455 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | COLQ_chr3_15445133_15526706 | COLQ | MVVLN others(450): Show |
chr3 | 15445133 | 15526706 |
| a0005 | 0/0 | 455 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | MVVLN others(450): Show |
chr3 | 15445133 | 15526706 |
| a0006 | 0/0 | 455 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | MVVLN others(450): Show |
chr3 | 15445133 | 15526706 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1365 | 338 | 56 | 63 | 171 | 12 | 34 | COLQ_chr3_15445133_15526706 | COLQ | ATGGT others(1360): Show |
chr3 | 15445133 | 15526706 | ||
| a0001c0003 | 0/0 | 1365 | 14 | 13 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | ATGGT others(1360): Show |
chr3 | 15445133 | 15526706 | ||
| a0001c0005 | 0/0 | 1365 | 2 | 0 | 2 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | ATGGT others(1360): Show |
chr3 | 15445133 | 15526706 | ||
| a0001c0008 | 0/0 | 1365 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | ATGGT others(1360): Show |
chr3 | 15445133 | 15526706 | ||
| a0002c0002 | 0/0 | 1365 | 17 | 17 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | ATGGT others(1360): Show |
chr3 | 15445133 | 15526706 | ||
| a0003c0004 | 0/0 | 1365 | 6 | 6 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | ATGGT others(1360): Show |
chr3 | 15445133 | 15526706 | ||
| a0004c0006 | 0/0 | 1365 | 2 | 0 | 0 | 2 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | ATGGT others(1360): Show |
chr3 | 15445133 | 15526706 | ||
| a0005c0007 | 0/0 | 1365 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | ATGGT others(1360): Show |
chr3 | 15445133 | 15526706 | ||
| a0006c0009 | 0/0 | 1365 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | ATGGT others(1360): Show |
chr3 | 15445133 | 15526706 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2960 | 157 | 30 | 36 | 66 | 7 | 17 | COLQ_chr3_15445133_15526706 | COLQ | GTGAG others(2955): Show |
chr3 | 15445133 | 15526706 |
| a0001c0001t0002 | 0/1 | 2960 | 82 | 11 | 17 | 39 | 5 | 9 | COLQ_chr3_15445133_15526706 | COLQ | GTGAG others(2955): Show |
chr3 | 15445133 | 15526706 |
| a0001c0001t0003 | 0/0 | 2960 | 76 | 7 | 10 | 53 | 0 | 6 | COLQ_chr3_15445133_15526706 | COLQ | GTGAG others(2955): Show |
chr3 | 15445133 | 15526706 |
| a0001c0001t0006 | 0/0 | 2960 | 8 | 1 | 0 | 6 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | GTGAG others(2955): Show |
chr3 | 15445133 | 15526706 |
| a0001c0001t0007 | 0/0 | 2960 | 4 | 0 | 0 | 4 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | GTGAG others(2955): Show |
chr3 | 15445133 | 15526706 |
| a0001c0001t0009 | 0/0 | 2960 | 2 | 0 | 0 | 2 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | GTGAG others(2955): Show |
chr3 | 15445133 | 15526706 |
| a0001c0001t0010 | 0/0 | 2960 | 2 | 2 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | GTGAG others(2955): Show |
chr3 | 15445133 | 15526706 |
| a0001c0001t0011 | 0/0 | 2960 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | GTGAG others(2955): Show |
chr3 | 15445133 | 15526706 |
| a0001c0001t0012 | 0/0 | 2960 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | GTGAG others(2955): Show |
chr3 | 15445133 | 15526706 |
| a0001c0001t0013 | 0/0 | 2960 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | GTGAG others(2955): Show |
chr3 | 15445133 | 15526706 |
| a0001c0001t0014 | 0/0 | 2960 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | GTGAG others(2955): Show |
chr3 | 15445133 | 15526706 |
| a0001c0001t0015 | 0/0 | 2960 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | GTGAG others(2955): Show |
chr3 | 15445133 | 15526706 |
| a0001c0001t0016 | 0/0 | 2960 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | GTGAG others(2955): Show |
chr3 | 15445133 | 15526706 |
| a0001c0001t0017 | 0/0 | 2960 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | GTGAG others(2955): Show |
chr3 | 15445133 | 15526706 |
| a0001c0003t0004 | 0/0 | 2960 | 14 | 13 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | GTGAG others(2955): Show |
chr3 | 15445133 | 15526706 |
| a0001c0005t0005 | 0/0 | 2960 | 2 | 0 | 2 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | GTGAG others(2955): Show |
chr3 | 15445133 | 15526706 |
| a0001c0008t0001 | 0/0 | 2960 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | GTGAG others(2955): Show |
chr3 | 15445133 | 15526706 |
| a0002c0002t0005 | 0/0 | 2960 | 14 | 14 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | GTGAG others(2955): Show |
chr3 | 15445133 | 15526706 |
| a0002c0002t0008 | 0/0 | 2960 | 3 | 3 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | GTGAG others(2955): Show |
chr3 | 15445133 | 15526706 |
| a0003c0004t0002 | 0/0 | 2960 | 6 | 6 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | GTGAG others(2955): Show |
chr3 | 15445133 | 15526706 |
| a0004c0006t0004 | 0/0 | 2960 | 2 | 0 | 0 | 2 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | GTGAG others(2955): Show |
chr3 | 15445133 | 15526706 |
| a0005c0007t0001 | 0/0 | 2960 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | GTGAG others(2955): Show |
chr3 | 15445133 | 15526706 |
| a0006c0009t0001 | 0/0 | 2960 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | GTGAG others(2955): Show |
chr3 | 15445133 | 15526706 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 5 | 0 | 2 | 2 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0002 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0215 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0002g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0002g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0002g0023 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0002g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0002g0155 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0002g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0002g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0002g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0003g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0003g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0003g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0003g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0003g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0003g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0003g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0003g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0003g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0003g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0003g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0003g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0006g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0006g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0006g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0006g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0006g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0006g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0006g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0006g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0007g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0007g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0007g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0007g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0009g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0010g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0010g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0011g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0012g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0013g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0014g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0015g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0016g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0001t0017g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0003t0004g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0003t0004g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0003t0004g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0003t0004g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0003t0004g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0003t0004g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0003t0004g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0003t0004g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0003t0004g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0003t0004g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0003t0004g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0003t0004g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0003t0004g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0005t0005g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0005t0005g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0001c0008t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0002c0002t0005g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0002c0002t0005g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0002c0002t0005g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0002c0002t0005g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0002c0002t0005g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0002c0002t0005g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0002c0002t0005g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0002c0002t0005g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0002c0002t0005g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0002c0002t0005g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0002c0002t0005g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0002c0002t0005g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0002c0002t0008g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0002c0002t0008g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0002c0002t0008g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0003c0004t0002g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0003c0004t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0003c0004t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0003c0004t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0003c0004t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0004c0006t0004g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0004c0006t0004g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0005c0007t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| a0006c0009t0001g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0237 | EUR | GBR | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0196 | EUR | GBR | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0280 | EUR | FIN | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0195 | EUR | FIN | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0032 | EAS | CHS | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | CHS | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0287 | EAS | CHS | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0245 | EAS | CHS | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | CHS | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0041 | EAS | CHS | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | CHS | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG00597 | hp2 | a0001 | c0001 | t0003 | g0056 | EAS | CHS | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0042 | EAS | CHS | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0279 | EAS | CHS | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | CHS | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0089 | EAS | CHS | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0154 | AMR | PUR | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0151 | AMR | PUR | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG00673 | hp2 | a0001 | c0001 | t0003 | g0060 | EAS | CHS | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0276 | AMR | PUR | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0017 | AMR | PUR | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0307 | AMR | PUR | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0198 | AMR | PUR | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG01071 | hp1 | a0005 | c0007 | t0001 | g0158 | AMR | PUR | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0306 | AMR | PUR | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0017 | AMR | PUR | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0330 | AMR | PUR | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0014 | AMR | PUR | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0152 | AMR | PUR | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG01109 | hp2 | a0001 | c0003 | t0004 | g0327 | AMR | PUR | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0338 | AMR | PUR | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG01168 | hp2 | a0001 | c0005 | t0005 | g0265 | AMR | PUR | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG01169 | hp1 | a0001 | c0005 | t0005 | g0264 | AMR | PUR | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0074 | AMR | PUR | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0157 | AMR | PUR | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0309 | AMR | PUR | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0159 | AMR | CLM | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | CLM | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | CLM | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0153 | AMR | CLM | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | CLM | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG01361 | hp2 | a0006 | c0009 | t0001 | g0344 | AMR | CLM | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | CLM | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0081 | AMR | CLM | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0148 | EUR | IBS | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0098 | EUR | IBS | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0172 | EUR | IBS | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0163 | EUR | IBS | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG01884 | hp1 | a0002 | c0002 | t0005 | g0020 | AFR | ACB | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0343 | AFR | ACB | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | ACB | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | ACB | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0086 | AMR | PEL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0273 | AMR | PEL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG01934 | hp2 | a0001 | c0001 | t0003 | g0038 | AMR | PEL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0277 | AMR | PEL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG01943 | hp2 | a0001 | c0001 | t0003 | g0058 | AMR | PEL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0162 | AMR | PEL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0034 | AMR | PEL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0036 | AMR | PEL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PEL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0296 | EAS | KHV | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0305 | EAS | KHV | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | KHV | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02055 | hp1 | a0001 | c0003 | t0004 | g0331 | AFR | ACB | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0289 | AFR | ACB | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | KHV | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | KHV | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02071 | hp2 | a0001 | c0001 | t0003 | g0045 | EAS | KHV | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0044 | EAS | KHV | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0043 | EAS | KHV | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | KHV | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | KHV | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | KHV | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0048 | EAS | KHV | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0295 | EAS | KHV | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | ACB | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0077 | AFR | ACB | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02148 | hp1 | a0001 | c0001 | t0003 | g0035 | AMR | PEL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PEL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | CDX | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CDX | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | ACB | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0125 | AFR | ACB | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | ACB | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0014 | AMR | PEL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02280 | hp1 | a0002 | c0002 | t0005 | g0251 | AFR | ACB | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02280 | hp2 | a0002 | c0002 | t0005 | g0334 | AFR | ACB | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PEL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | ACB | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0146 | AFR | ACB | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | KHV | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | KHV | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0062 | AFR | GWD | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0325 | AFR | GWD | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0263 | SAS | PJL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | GWD | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02615 | hp2 | a0001 | c0003 | t0004 | g0340 | AFR | GWD | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | GWD | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02622 | hp2 | a0003 | c0004 | t0002 | g0257 | AFR | GWD | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | GWD | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02630 | hp2 | a0001 | c0001 | t0014 | g0291 | AFR | GWD | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02647 | hp1 | a0001 | c0001 | t0013 | g0328 | AFR | GWD | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02717 | hp1 | a0002 | c0002 | t0005 | g0252 | AFR | GWD | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02717 | hp2 | a0001 | c0003 | t0004 | g0341 | AFR | GWD | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02723 | hp1 | a0002 | c0002 | t0005 | g0021 | AFR | GWD | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02723 | hp2 | a0001 | c0003 | t0004 | g0332 | AFR | GWD | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0156 | SAS | PJL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0049 | SAS | PJL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02809 | hp1 | a0002 | c0002 | t0005 | g0333 | AFR | GWD | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02809 | hp2 | a0001 | c0001 | t0015 | g0116 | AFR | GWD | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02818 | hp1 | a0002 | c0002 | t0005 | g0020 | AFR | GWD | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0075 | AFR | GWD | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02886 | hp1 | a0001 | c0003 | t0004 | g0272 | AFR | GWD | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0013 | AFR | GWD | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02895 | hp1 | a0001 | c0003 | t0004 | g0121 | AFR | GWD | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02896 | hp1 | a0001 | c0003 | t0004 | g0028 | AFR | GWD | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02922 | hp1 | a0002 | c0002 | t0005 | g0254 | AFR | ESN | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02922 | hp2 | a0001 | c0003 | t0004 | g0028 | AFR | ESN | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0329 | AFR | ESN | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02970 | hp2 | a0002 | c0002 | t0008 | g0269 | AFR | ESN | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02976 | hp1 | a0002 | c0002 | t0008 | g0270 | AFR | ESN | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0242 | AFR | ESN | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0047 | SAS | PJL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG03041 | hp1 | a0001 | c0001 | t0010 | g0259 | AFR | GWD | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG03041 | hp2 | a0001 | c0003 | t0004 | g0335 | AFR | GWD | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG03098 | hp1 | a0003 | c0004 | t0002 | g0247 | AFR | MSL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG03098 | hp2 | a0001 | c0003 | t0004 | g0339 | AFR | MSL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0071 | AFR | ESN | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | ESN | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | ESN | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG03139 | hp2 | a0001 | c0003 | t0004 | g0311 | AFR | ESN | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | ESN | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG03195 | hp2 | a0001 | c0003 | t0004 | g0123 | AFR | ESN | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | MSL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG03209 | hp2 | a0003 | c0004 | t0002 | g0022 | AFR | MSL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0261 | AFR | MSL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | MSL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0292 | AFR | MSL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | MSL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG03486 | hp1 | a0001 | c0001 | t0012 | g0268 | AFR | MSL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0288 | AFR | MSL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0009 | SAS | PJL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0009 | SAS | PJL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG03516 | hp1 | a0003 | c0004 | t0002 | g0256 | AFR | ESN | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | ESN | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0275 | AFR | GWD | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | GWD | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG03579 | hp1 | a0001 | c0001 | t0006 | g0072 | AFR | MSL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0324 | AFR | MSL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG03710 | hp1 | a0001 | c0001 | t0006 | g0050 | SAS | PJL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0023 | SAS | PJL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0130 | SAS | BEB | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0233 | SAS | BEB | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | BEB | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0023 | SAS | BEB | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG03927 | hp1 | a0001 | c0001 | t0011 | g0068 | SAS | BEB | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | BEB | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0294 | SAS | BEB | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | BEB | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0149 | SAS | STU | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0293 | SAS | STU | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0066 | SAS | STU | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0235 | SAS | STU | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0069 | SAS | STU | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0150 | SAS | STU | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | STU | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18522 | hp1 | a0002 | c0002 | t0005 | g0249 | AFR | YRI | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18522 | hp2 | a0003 | c0004 | t0002 | g0022 | AFR | YRI | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18612 | hp1 | a0001 | c0001 | t0006 | g0064 | EAS | CHB | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18612 | hp2 | a0001 | c0008 | t0001 | g0190 | EAS | CHB | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0057 | EAS | CHB | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0321 | EAS | CHB | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18906 | hp1 | a0001 | c0001 | t0016 | g0255 | AFR | YRI | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0013 | AFR | YRI | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18940 | hp2 | a0001 | c0001 | t0003 | g0087 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18942 | hp1 | a0001 | c0001 | t0007 | g0222 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18947 | hp2 | a0001 | c0001 | t0003 | g0061 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18948 | hp2 | a0001 | c0001 | t0003 | g0082 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18950 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0320 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18952 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0080 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0070 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18967 | hp2 | a0001 | c0001 | t0003 | g0033 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0083 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0317 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18971 | hp1 | a0001 | c0001 | t0007 | g0207 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18972 | hp1 | a0004 | c0006 | t0004 | g0246 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18972 | hp2 | a0001 | c0001 | t0003 | g0085 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18973 | hp2 | a0001 | c0001 | t0017 | g0290 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0063 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18978 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18984 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18985 | hp2 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18986 | hp2 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0314 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18987 | hp2 | a0001 | c0001 | t0003 | g0078 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18992 | hp2 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0065 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18997 | hp1 | a0001 | c0001 | t0003 | g0079 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18999 | hp2 | a0004 | c0006 | t0004 | g0244 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA19000 | hp2 | a0001 | c0001 | t0006 | g0059 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA19002 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA19003 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA19004 | hp1 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA19006 | hp2 | a0001 | c0001 | t0006 | g0055 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0319 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0313 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA19010 | hp1 | a0001 | c0001 | t0007 | g0187 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0299 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0300 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA19043 | hp1 | a0002 | c0002 | t0005 | g0021 | AFR | LWK | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA19043 | hp2 | a0001 | c0001 | t0010 | g0342 | AFR | LWK | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0315 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA19055 | hp1 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0312 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA19058 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA19060 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA19064 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA19065 | hp1 | a0001 | c0001 | t0003 | g0090 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA19068 | hp2 | a0001 | c0001 | t0006 | g0054 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA19074 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA19076 | hp2 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0088 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0318 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0302 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA19082 | hp2 | a0001 | c0001 | t0006 | g0067 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA19086 | hp1 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA19086 | hp2 | a0001 | c0001 | t0009 | g0019 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA19087 | hp2 | a0001 | c0001 | t0006 | g0051 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0084 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA19090 | hp2 | a0001 | c0001 | t0007 | g0206 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA19240 | hp1 | a0002 | c0002 | t0008 | g0271 | AFR | YRI | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | YRI | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0161 | EUR | TSI | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0310 | EUR | TSI | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0129 | EUR | TSI | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0170 | EUR | TSI | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0304 | SAS | GIH | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | GIH | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0160 | AMR | CLM | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0316 | AMR | CLM | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02109 | hp1 | a0002 | c0002 | t0005 | g0253 | AFR | ACB | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | ACB | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02559 | hp1 | a0002 | c0002 | t0005 | g0250 | AFR | ACB | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG03471 | hp1 | a0003 | c0004 | t0002 | g0258 | AFR | MSL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG03471 | hp2 | a0002 | c0002 | t0005 | g0336 | AFR | MSL | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0073 | AFR | USA | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | USA | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0053 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA18955 | hp2 | a0001 | c0001 | t0009 | g0019 | EAS | JPT | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA20300 | hp1 | a0002 | c0002 | t0005 | g0266 | AFR | USA | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | USA | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | LWK | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| NA21309 | hp2 | a0001 | c0003 | t0004 | g0337 | AFR | LWK | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0155 | REF | REF | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0215 | REF | REF | COLQ_chr3_15445133_15526706 | COLQ | chr3 | 15445133 | 15526706 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:15455977 | C | T | 1 | a0005 | 1 | HG01071.hp1 | missense_variant | MODERATE | c.1117G>A | p.Gly373Ser | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 15/17 | 1198/2960 | 1117/1368 | 373/455 | chr3 | 15455977 | |||
| chr3:15455986 | C | T | 1 | a0003 | 6 | HG02622.hp2 HG03098.hp1 HG03209.hp2 others(3): Show |
missense_variant | MODERATE | c.1108G>A | p.Asp370Asn | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 15/17 | 1189/2960 | 1108/1368 | 370/455 | chr3 | 15455986 | |||
| chr3:15456013 | G | A | 1 | a0004 | 2 | NA18972.hp1 NA18999.hp2 |
missense_variant | MODERATE | c.1081C>T | p.Pro361Ser | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 15/17 | 1162/2960 | 1081/1368 | 361/455 | chr3 | 15456013 | |||
| chr3:15458206 | T | C | 1 | a0002 | 17 | HG01884.hp1 HG02109.hp1 HG02280.hp1 others(14): Show |
missense_variant | MODERATE | c.934A>G | p.Ser312Gly | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 13/17 | 1015/2960 | 934/1368 | 312/455 | chr3 | 15458206 | |||
| chr3:15521603 | G | C | 1 | a0006 | 1 | HG01361.hp2 | missense_variant | MODERATE | c.23C>G | p.Thr8Ser | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/17 | 104/2960 | 23/1368 | 8/455 | chr3 | 15521603 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:15451674 | G | T | 1 | a0001c0003 | 14 | HG01109.hp2 HG02055.hp1 HG02615.hp2 others(11): Show |
synonymous_variant | LOW | c.1338C>A | p.Ile446Ile | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 17/17 | 1419/2960 | 1338/1368 | 446/455 | chr3 | 15451674 | |||
| chr3:15453879 | G | A | 1 | a0001c0005 | 2 | HG01168.hp2 HG01169.hp1 |
synonymous_variant | LOW | c.1248C>T | p.Asp416Asp | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 16/17 | 1329/2960 | 1248/1368 | 416/455 | chr3 | 15453879 | |||
| chr3:15488227 | G | A | 1 | a0001c0008 | 1 | NA18612.hp2 | synonymous_variant | LOW | c.300C>T | p.Ser100Ser | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/17 | 381/2960 | 300/1368 | 100/455 | chr3 | 15488227 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:15450237 | C | T | 1 | a0001c0001t0016 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1407G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 17/17 | 1407 | chr3 | 15450237 | ||||||
| chr3:15450249 | G | A | 9 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0010 others(6): Show |
170 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(167): Show |
3_prime_UTR_variant | MODIFIER | c.*1395C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 17/17 | 1395 | chr3 | 15450249 | ||||||
| chr3:15450258 | T | C | 1 | a0001c0001t0012 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1386A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 17/17 | 1386 | chr3 | 15450258 | ||||||
| chr3:15450364 | G | A | 1 | a0001c0001t0007 | 4 | NA18942.hp1 NA18971.hp1 NA19010.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1280C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 17/17 | 1280 | chr3 | 15450364 | ||||||
| chr3:15450571 | C | T | 1 | a0001c0001t0015 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1073G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 17/17 | 1073 | chr3 | 15450571 | ||||||
| chr3:15450643 | C | T | 9 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0010 others(6): Show |
170 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(167): Show |
3_prime_UTR_variant | MODIFIER | c.*1001G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 17/17 | 1001 | chr3 | 15450643 | ||||||
| chr3:15450646 | G | A | 1 | a0001c0001t0017 | 1 | NA18973.hp2 | 3_prime_UTR_variant | MODIFIER | c.*998C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 17/17 | 998 | chr3 | 15450646 | ||||||
| chr3:15450650 | C | T | 1 | a0002c0002t0008 | 3 | HG02970.hp2 HG02976.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*994G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 17/17 | 994 | chr3 | 15450650 | ||||||
| chr3:15450699 | C | T | 1 | a0001c0001t0014 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*945G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 17/17 | 945 | chr3 | 15450699 | ||||||
| chr3:15450796 | G | A | 1 | a0001c0001t0011 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*848C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 17/17 | 848 | chr3 | 15450796 | ||||||
| chr3:15450838 | G | A | 1 | a0001c0001t0013 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*806C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 17/17 | 806 | chr3 | 15450838 | ||||||
| chr3:15450893 | G | A | 1 | a0001c0001t0009 | 2 | NA18955.hp2 NA19086.hp2 |
3_prime_UTR_variant | MODIFIER | c.*751C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 17/17 | 751 | chr3 | 15450893 | ||||||
| chr3:15451129 | G | A | 4 | a0001c0001t0013 a0001c0005t0005 a0002c0002t0005 others(1): Show |
20 | HG01168.hp2 HG01169.hp1 HG01884.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*515C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 17/17 | 515 | chr3 | 15451129 | ||||||
| chr3:15451152 | C | T | 1 | a0001c0001t0010 | 2 | HG03041.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*492G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 17/17 | 492 | chr3 | 15451152 | ||||||
| chr3:15451223 | C | T | 1 | a0001c0001t0013 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*421G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 17/17 | 421 | chr3 | 15451223 | ||||||
| chr3:15451279 | T | A | 13 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0010 others(10): Show |
190 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(187): Show |
3_prime_UTR_variant | MODIFIER | c.*365A>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 17/17 | 365 | chr3 | 15451279 | ||||||
| chr3:15451300 | G | A | 15 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0010 others(12): Show |
206 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(203): Show |
3_prime_UTR_variant | MODIFIER | c.*344C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 17/17 | 344 | chr3 | 15451300 | ||||||
| chr3:15521671 | C | T | 3 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0011 |
85 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(82): Show |
5_prime_UTR_variant | MODIFIER | c.-46G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/17 | 46 | chr3 | 15521671 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:15451744 | C | T | 3 | a0001c0001t0010g0259 a0001c0001t0010g0342 a0001c0001t0016g0255 |
3 | HG03041.hp1 NA18906.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1299-31G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 16/16 | chr3 | 15451744 | |||||||
| chr3:15451772 | T | C | 3 | a0001c0001t0003g0004 a0001c0001t0003g0032 a0001c0001t0003g0090 |
5 | HG00423.hp1 NA18952.hp2 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.1299-59A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 16/16 | chr3 | 15451772 | |||||||
| chr3:15451874 | G | C | 1 | a0001c0001t0002g0261 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1299-161C>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 16/16 | chr3 | 15451874 | |||||||
| chr3:15452025 | C | T | 18 | a0001c0001t0013g0328 a0001c0005t0005g0264 a0001c0005t0005g0265 others(15): Show |
20 | HG01168.hp2 HG01169.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.1299-312G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 16/16 | chr3 | 15452025 | |||||||
| chr3:15452068 | A | AT | 75 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0018 others(72): Show |
83 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.1299-356dupA | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 16/16 | chr3 | 15452068 | |||||||
| chr3:15452068 | AT | A | 34 | a0001c0001t0001g0097 a0001c0001t0002g0293 a0001c0001t0003g0047 others(31): Show |
37 | HG01109.hp2 HG01168.hp2 HG01169.hp1 others(34): Show |
intron_variant | MODIFIER | c.1299-356delA | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 16/16 | chr3 | 15452068 | |||||||
| chr3:15452068 | ATT | A | 186 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(183): Show |
213 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(210): Show |
intron_variant | MODIFIER | c.1299-357_1299-356d others(4): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 16/16 | chr3 | 15452068 | |||||||
| chr3:15452141 | A | C | 3 | a0001c0001t0010g0259 a0001c0001t0010g0342 a0001c0001t0016g0255 |
3 | HG03041.hp1 NA18906.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1299-428T>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 16/16 | chr3 | 15452141 | |||||||
| chr3:15452160 | A | G | 21 | a0001c0001t0010g0259 a0001c0001t0010g0342 a0001c0001t0013g0328 others(18): Show |
23 | HG01168.hp2 HG01169.hp1 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.1299-447T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 16/16 | chr3 | 15452160 | |||||||
| chr3:15452287 | G | A | 13 | a0001c0003t0004g0028 a0001c0003t0004g0121 a0001c0003t0004g0123 others(10): Show |
14 | HG01109.hp2 HG02055.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.1299-574C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 16/16 | chr3 | 15452287 | |||||||
| chr3:15452311 | C | T | 149 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0023 others(146): Show |
170 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(167): Show |
intron_variant | MODIFIER | c.1299-598G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 16/16 | chr3 | 15452311 | |||||||
| chr3:15452484 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1299-771G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 16/16 | chr3 | 15452484 | |||||||
| chr3:15452495 | G | A | 140 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0023 others(137): Show |
160 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(157): Show |
intron_variant | MODIFIER | c.1299-782C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 16/16 | chr3 | 15452495 | |||||||
| chr3:15452522 | C | T | 2 | a0001c0001t0002g0292 a0001c0001t0014g0291 |
2 | HG02630.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1299-809G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 16/16 | chr3 | 15452522 | |||||||
| chr3:15452546 | T | C | 1 | a0001c0001t0016g0255 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1299-833A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 16/16 | chr3 | 15452546 | |||||||
| chr3:15452568 | G | A | 5 | a0003c0004t0002g0022 a0003c0004t0002g0247 a0003c0004t0002g0256 others(2): Show |
6 | HG02622.hp2 HG03098.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.1299-855C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 16/16 | chr3 | 15452568 | |||||||
| chr3:15452635 | G | A | 1 | a0001c0001t0010g0259 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1299-922C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 16/16 | chr3 | 15452635 | |||||||
| chr3:15452734 | G | C | 18 | a0001c0001t0013g0328 a0001c0005t0005g0264 a0001c0005t0005g0265 others(15): Show |
20 | HG01168.hp2 HG01169.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.1299-1021C>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 16/16 | chr3 | 15452734 | |||||||
| chr3:15452772 | G | A | 146 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0023 others(143): Show |
167 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.1298+1057C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 16/16 | chr3 | 15452772 | |||||||
| chr3:15453151 | C | G | 141 | a0001c0001t0001g0274 a0001c0001t0002g0016 a0001c0001t0002g0017 others(138): Show |
161 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.1298+678G>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 16/16 | chr3 | 15453151 | |||||||
| chr3:15453210 | G | A | 2 | a0001c0001t0010g0259 a0001c0001t0010g0342 |
2 | HG03041.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1298+619C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 16/16 | chr3 | 15453210 | |||||||
| chr3:15453232 | A | G | 1 | a0001c0001t0002g0293 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1298+597T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 16/16 | chr3 | 15453232 | |||||||
| chr3:15453252 | C | A | 18 | a0001c0001t0013g0328 a0001c0005t0005g0264 a0001c0005t0005g0265 others(15): Show |
20 | HG01168.hp2 HG01169.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.1298+577G>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 16/16 | chr3 | 15453252 | |||||||
| chr3:15453294 | C | G | 2 | a0001c0001t0002g0306 a0001c0001t0002g0307 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1298+535G>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 16/16 | chr3 | 15453294 | |||||||
| chr3:15453638 | G | A | 4 | a0001c0001t0001g0120 a0001c0001t0001g0177 a0001c0001t0001g0234 others(1): Show |
4 | NA18966.hp1 NA19012.hp1 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.1298+191C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 16/16 | chr3 | 15453638 | |||||||
| chr3:15453794 | G | T | 54 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(51): Show |
61 | HG00639.hp1 HG01109.hp2 HG01168.hp1 others(58): Show |
intron_variant | MODIFIER | c.1298+35C>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 16/16 | chr3 | 15453794 | |||||||
| chr3:15453976 | G | A | 1 | a0001c0001t0002g0343 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1196-45C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 15/16 | chr3 | 15453976 | |||||||
| chr3:15454016 | G | A | 1 | a0001c0001t0001g0211 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1196-85C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 15/16 | chr3 | 15454016 | |||||||
| chr3:15454137 | T | C | 153 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0023 others(150): Show |
174 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(171): Show |
intron_variant | MODIFIER | c.1196-206A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 15/16 | chr3 | 15454137 | |||||||
| chr3:15454147 | A | G | 153 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0023 others(150): Show |
174 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(171): Show |
intron_variant | MODIFIER | c.1196-216T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 15/16 | chr3 | 15454147 | |||||||
| chr3:15454152 | C | T | 28 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(25): Show |
34 | HG00639.hp1 HG01891.hp1 HG01928.hp1 others(31): Show |
intron_variant | MODIFIER | c.1196-221G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 15/16 | chr3 | 15454152 | |||||||
| chr3:15454180 | G | C | 1 | a0001c0008t0001g0190 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1196-249C>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 15/16 | chr3 | 15454180 | |||||||
| chr3:15454257 | G | A | 153 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0023 others(150): Show |
174 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(171): Show |
intron_variant | MODIFIER | c.1196-326C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 15/16 | chr3 | 15454257 | |||||||
| chr3:15454333 | T | C | 186 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0023 others(183): Show |
210 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(207): Show |
intron_variant | MODIFIER | c.1196-402A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 15/16 | chr3 | 15454333 | |||||||
| chr3:15454419 | T | C | 91 | a0001c0001t0002g0017 a0001c0001t0002g0023 a0001c0001t0002g0024 others(88): Show |
107 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.1196-488A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 15/16 | chr3 | 15454419 | |||||||
| chr3:15454430 | A | G | 15 | a0001c0003t0004g0028 a0001c0003t0004g0121 a0001c0003t0004g0123 others(12): Show |
16 | HG01109.hp2 HG02055.hp1 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.1196-499T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 15/16 | chr3 | 15454430 | |||||||
| chr3:15454445 | T | A | 4 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0006g0054 others(1): Show |
4 | HG00597.hp1 NA18994.hp1 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.1196-514A>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 15/16 | chr3 | 15454445 | |||||||
| chr3:15454596 | ACAGT | A | 4 | a0001c0001t0001g0248 a0001c0001t0001g0260 a0001c0001t0006g0072 others(1): Show |
4 | HG03195.hp1 HG03486.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1196-669_1196-666d others(6): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 15/16 | chr3 | 15454596 | |||||||
| chr3:15454614 | C | T | 10 | a0001c0001t0001g0120 a0001c0001t0001g0167 a0001c0001t0001g0168 others(7): Show |
10 | NA18942.hp1 NA18948.hp1 NA18966.hp1 others(7): Show |
intron_variant | MODIFIER | c.1196-683G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 15/16 | chr3 | 15454614 | |||||||
| chr3:15454639 | T | C | 4 | a0001c0001t0001g0248 a0001c0001t0001g0260 a0001c0001t0006g0072 others(1): Show |
4 | HG03195.hp1 HG03486.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1196-708A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 15/16 | chr3 | 15454639 | |||||||
| chr3:15454651 | G | GT | 28 | a0001c0001t0001g0092 a0001c0001t0001g0097 a0001c0001t0001g0103 others(25): Show |
28 | HG00597.hp1 HG01071.hp1 HG01255.hp2 others(25): Show |
intron_variant | MODIFIER | c.1196-721dupA | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 15/16 | chr3 | 15454651 | |||||||
| chr3:15454651 | G | GTTT | 24 | a0001c0001t0010g0259 a0001c0003t0004g0028 a0001c0003t0004g0121 others(21): Show |
26 | HG01109.hp2 HG01168.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.1196-723_1196-721d others(5): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 15/16 | chr3 | 15454651 | |||||||
| chr3:15454651 | G | GTTTT | 8 | a0001c0003t0004g0331 a0001c0003t0004g0335 a0001c0003t0004g0339 others(5): Show |
9 | HG01169.hp1 HG01884.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1196-724_1196-721d others(6): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 15/16 | chr3 | 15454651 | |||||||
| chr3:15454651 | GTTTTTTT | G | 103 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0023 others(100): Show |
118 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.1196-727_1196-721d others(9): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 15/16 | chr3 | 15454651 | |||||||
| chr3:15454651 | GTTTTTTT others(1): Show |
G | 35 | a0001c0001t0002g0024 a0001c0001t0002g0098 a0001c0001t0002g0198 others(32): Show |
40 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.1196-728_1196-721d others(10): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 15/16 | chr3 | 15454651 | |||||||
| chr3:15454651 | GTTTTTTT others(3): Show |
G | 1 | a0001c0001t0001g0219 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1196-730_1196-721d others(12): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 15/16 | chr3 | 15454651 | |||||||
| chr3:15454658 | T | TA | 4 | a0001c0001t0001g0248 a0001c0001t0001g0260 a0001c0001t0006g0072 others(1): Show |
4 | HG03195.hp1 HG03486.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1196-728_1196-727i others(3): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 15/16 | chr3 | 15454658 | |||||||
| chr3:15454664 | T | A | 1 | a0001c0001t0012g0268 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1196-733A>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 15/16 | chr3 | 15454664 | |||||||
| chr3:15454763 | C | T | 2 | a0001c0001t0010g0259 a0001c0001t0010g0342 |
2 | HG03041.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1196-832G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 15/16 | chr3 | 15454763 | |||||||
| chr3:15454803 | G | A | 4 | a0001c0001t0001g0248 a0001c0001t0001g0260 a0001c0001t0006g0072 others(1): Show |
4 | HG03195.hp1 HG03486.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1196-872C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 15/16 | chr3 | 15454803 | |||||||
| chr3:15454836 | T | A | 9 | a0001c0001t0002g0343 a0001c0001t0010g0259 a0001c0001t0010g0342 others(6): Show |
10 | HG01884.hp2 HG02622.hp2 HG03041.hp1 others(7): Show |
intron_variant | MODIFIER | c.1196-905A>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 15/16 | chr3 | 15454836 | |||||||
| chr3:15455001 | T | G | 2 | a0004c0006t0004g0244 a0004c0006t0004g0246 |
2 | NA18972.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.1195+898A>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 15/16 | chr3 | 15455001 | |||||||
| chr3:15455040 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1195+859A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 15/16 | chr3 | 15455040 | |||||||
| chr3:15455046 | C | A | 15 | a0001c0003t0004g0028 a0001c0003t0004g0121 a0001c0003t0004g0123 others(12): Show |
16 | HG01109.hp2 HG02055.hp1 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.1195+853G>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 15/16 | chr3 | 15455046 | |||||||
| chr3:15455332 | C | T | 2 | a0004c0006t0004g0244 a0004c0006t0004g0246 |
2 | NA18972.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.1195+567G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 15/16 | chr3 | 15455332 | |||||||
| chr3:15455359 | CA | C | 77 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0018 others(74): Show |
85 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.1195+539delT | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 15/16 | chr3 | 15455359 | |||||||
| chr3:15455561 | G | C | 1 | a0001c0001t0003g0071 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1195+338C>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 15/16 | chr3 | 15455561 | |||||||
| chr3:15455571 | C | T | 1 | a0001c0001t0010g0259 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1195+328G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 15/16 | chr3 | 15455571 | |||||||
| chr3:15455680 | C | T | 13 | a0001c0003t0004g0028 a0001c0003t0004g0121 a0001c0003t0004g0123 others(10): Show |
14 | HG01109.hp2 HG02055.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.1195+219G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 15/16 | chr3 | 15455680 | |||||||
| chr3:15455754 | G | A | 9 | a0001c0001t0002g0343 a0001c0001t0010g0259 a0001c0001t0010g0342 others(6): Show |
10 | HG01884.hp2 HG02622.hp2 HG03041.hp1 others(7): Show |
intron_variant | MODIFIER | c.1195+145C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 15/16 | chr3 | 15455754 | |||||||
| chr3:15455818 | C | A | 15 | a0001c0003t0004g0028 a0001c0003t0004g0121 a0001c0003t0004g0123 others(12): Show |
16 | HG01109.hp2 HG02055.hp1 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.1195+81G>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 15/16 | chr3 | 15455818 | |||||||
| chr3:15456101 | A | G | 41 | a0001c0001t0002g0343 a0001c0001t0010g0259 a0001c0001t0013g0328 others(38): Show |
45 | HG01109.hp2 HG01168.hp2 HG01169.hp1 others(42): Show |
intron_variant | MODIFIER | c.1075-82T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 14/16 | chr3 | 15456101 | |||||||
| chr3:15456222 | A | G | 3 | a0001c0001t0003g0003 a0001c0001t0003g0063 a0001c0001t0003g0065 |
5 | NA18945.hp2 NA18973.hp1 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.1075-203T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 14/16 | chr3 | 15456222 | |||||||
| chr3:15456256 | T | TCAGAGAG others(25): Show |
13 | a0001c0003t0004g0028 a0001c0003t0004g0121 a0001c0003t0004g0123 others(10): Show |
14 | HG01109.hp2 HG02055.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.1074+172_1074+203d others(34): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 14/16 | chr3 | 15456256 | |||||||
| chr3:15456274 | T | A | 2 | a0001c0001t0001g0208 a0001c0001t0006g0050 |
2 | HG03710.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1074+186A>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 14/16 | chr3 | 15456274 | |||||||
| chr3:15456406 | A | T | 1 | a0001c0001t0002g0282 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1074+54T>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 14/16 | chr3 | 15456406 | |||||||
| chr3:15456754 | T | C | 203 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(200): Show |
231 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(228): Show |
intron_variant | MODIFIER | c.955-175A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 13/16 | chr3 | 15456754 | |||||||
| chr3:15456765 | G | A | 173 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(170): Show |
199 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(196): Show |
intron_variant | MODIFIER | c.955-186C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 13/16 | chr3 | 15456765 | |||||||
| chr3:15456827 | TTTCTTTT others(1): Show |
T | 169 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(166): Show |
195 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(192): Show |
intron_variant | MODIFIER | c.955-256_955-249del others(8): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 13/16 | chr3 | 15456827 | |||||||
| chr3:15456835 | G | T | 54 | a0001c0001t0001g0122 a0001c0001t0001g0124 a0001c0001t0001g0126 others(51): Show |
58 | HG01081.hp2 HG01109.hp2 HG01168.hp1 others(55): Show |
intron_variant | MODIFIER | c.955-256C>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 13/16 | chr3 | 15456835 | |||||||
| chr3:15456839 | T | A | 2 | a0004c0006t0004g0244 a0004c0006t0004g0246 |
2 | NA18972.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.955-260A>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 13/16 | chr3 | 15456839 | |||||||
| chr3:15456891 | C | T | 4 | a0001c0001t0003g0010 a0001c0001t0003g0037 a0001c0001t0003g0052 others(1): Show |
5 | NA18950.hp1 NA18955.hp1 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.955-312G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 13/16 | chr3 | 15456891 | |||||||
| chr3:15456918 | G | A | 29 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(26): Show |
35 | HG00639.hp1 HG01891.hp1 HG01928.hp1 others(32): Show |
intron_variant | MODIFIER | c.955-339C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 13/16 | chr3 | 15456918 | |||||||
| chr3:15456947 | C | T | 1 | a0001c0001t0003g0010 | 2 | NA18950.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.955-368G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 13/16 | chr3 | 15456947 | |||||||
| chr3:15456963 | C | T | 1 | a0001c0001t0006g0072 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.955-384G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 13/16 | chr3 | 15456963 | |||||||
| chr3:15457039 | T | C | 1 | a0001c0001t0001g0260 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.955-460A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 13/16 | chr3 | 15457039 | |||||||
| chr3:15457100 | A | G | 1 | a0001c0001t0001g0248 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.955-521T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 13/16 | chr3 | 15457100 | |||||||
| chr3:15457108 | G | C | 2 | a0001c0001t0010g0259 a0001c0003t0004g0327 |
2 | HG01109.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.955-529C>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 13/16 | chr3 | 15457108 | |||||||
| chr3:15457241 | A | G | 17 | a0001c0001t0001g0122 a0001c0001t0001g0124 a0001c0001t0001g0126 others(14): Show |
18 | HG01109.hp2 HG01168.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.955-662T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 13/16 | chr3 | 15457241 | |||||||
| chr3:15457259 | T | C | 1 | a0002c0002t0005g0251 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.955-680A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 13/16 | chr3 | 15457259 | |||||||
| chr3:15457424 | T | C | 1 | a0001c0001t0003g0043 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.954+762A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 13/16 | chr3 | 15457424 | |||||||
| chr3:15457541 | A | AT | 6 | a0001c0001t0002g0343 a0003c0004t0002g0022 a0003c0004t0002g0247 others(3): Show |
7 | HG01884.hp2 HG02622.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.954+644dupA | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 13/16 | chr3 | 15457541 | |||||||
| chr3:15457623 | C | CTTTTTTT | 171 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(168): Show |
197 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(194): Show |
intron_variant | MODIFIER | c.954+556_954+562dup others(7): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 13/16 | chr3 | 15457623 | |||||||
| chr3:15457623 | C | CTTTTTTT others(1): Show |
14 | a0001c0001t0002g0297 a0001c0003t0004g0028 a0001c0003t0004g0121 others(11): Show |
15 | HG02055.hp1 HG02615.hp2 HG02717.hp2 others(12): Show |
intron_variant | MODIFIER | c.954+562_954+563ins others(8): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 13/16 | chr3 | 15457623 | |||||||
| chr3:15457623 | C | CTTTTTTT others(3): Show |
17 | a0001c0001t0001g0122 a0001c0001t0001g0124 a0001c0001t0001g0126 others(14): Show |
18 | HG01109.hp2 HG01168.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.954+562_954+563ins others(10): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 13/16 | chr3 | 15457623 | |||||||
| chr3:15457673 | T | C | 17 | a0001c0001t0001g0122 a0001c0001t0001g0124 a0001c0001t0001g0126 others(14): Show |
18 | HG01109.hp2 HG01168.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.954+513A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 13/16 | chr3 | 15457673 | |||||||
| chr3:15457749 | A | T | 2 | a0001c0001t0010g0259 a0001c0003t0004g0327 |
2 | HG01109.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.954+437T>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 13/16 | chr3 | 15457749 | |||||||
| chr3:15457768 | G | A | 9 | a0001c0001t0001g0122 a0001c0001t0001g0124 a0001c0001t0001g0126 others(6): Show |
9 | HG01168.hp1 HG02109.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.954+418C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 13/16 | chr3 | 15457768 | |||||||
| chr3:15457770 | G | A | 6 | a0001c0001t0001g0119 a0001c0001t0001g0147 a0001c0001t0001g0229 others(3): Show |
6 | HG01891.hp2 HG02647.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.954+416C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 13/16 | chr3 | 15457770 | |||||||
| chr3:15457823 | C | T | 173 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(170): Show |
199 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(196): Show |
intron_variant | MODIFIER | c.954+363G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 13/16 | chr3 | 15457823 | |||||||
| chr3:15457951 | T | C | 5 | a0003c0004t0002g0022 a0003c0004t0002g0247 a0003c0004t0002g0256 others(2): Show |
6 | HG02622.hp2 HG03098.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.954+235A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 13/16 | chr3 | 15457951 | |||||||
| chr3:15458568 | G | A | 3 | a0001c0001t0001g0248 a0001c0001t0001g0260 a0001c0001t0006g0072 |
3 | HG03195.hp1 HG03579.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.815-243C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15458568 | |||||||
| chr3:15458741 | T | C | 225 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(222): Show |
255 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(252): Show |
intron_variant | MODIFIER | c.815-416A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15458741 | |||||||
| chr3:15458788 | C | T | 186 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(183): Show |
213 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(210): Show |
intron_variant | MODIFIER | c.815-463G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15458788 | |||||||
| chr3:15458846 | A | AT | 17 | a0001c0001t0001g0103 a0001c0001t0001g0166 a0001c0001t0001g0248 others(14): Show |
18 | HG00733.hp2 HG01081.hp2 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.815-522dupA | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15458846 | |||||||
| chr3:15458846 | A | ATT | 7 | a0001c0001t0001g0122 a0001c0001t0001g0124 a0001c0001t0001g0126 others(4): Show |
7 | HG01168.hp1 HG02109.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.815-523_815-522dup others(2): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15458846 | |||||||
| chr3:15458879 | T | C | 1 | a0001c0001t0001g0212 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.815-554A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15458879 | |||||||
| chr3:15458906 | C | T | 9 | a0001c0001t0001g0122 a0001c0001t0001g0124 a0001c0001t0001g0126 others(6): Show |
9 | HG01168.hp1 HG02109.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.815-581G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15458906 | |||||||
| chr3:15458984 | C | T | 1 | a0001c0001t0002g0304 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.815-659G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15458984 | |||||||
| chr3:15459063 | C | T | 9 | a0001c0001t0001g0122 a0001c0001t0001g0124 a0001c0001t0001g0126 others(6): Show |
9 | HG01168.hp1 HG02109.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.815-738G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15459063 | |||||||
| chr3:15459196 | C | G | 1 | a0001c0001t0001g0184 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.815-871G>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15459196 | |||||||
| chr3:15459231 | C | T | 1 | a0001c0001t0001g0184 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.815-906G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15459231 | |||||||
| chr3:15459249 | G | A | 4 | a0001c0001t0007g0187 a0001c0001t0007g0206 a0001c0001t0007g0207 others(1): Show |
4 | NA18942.hp1 NA18971.hp1 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.815-924C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15459249 | |||||||
| chr3:15459261 | A | G | 2 | a0003c0004t0002g0257 a0003c0004t0002g0258 |
2 | HG02622.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.815-936T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15459261 | |||||||
| chr3:15459389 | C | T | 189 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(186): Show |
216 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(213): Show |
intron_variant | MODIFIER | c.815-1064G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15459389 | |||||||
| chr3:15459426 | C | T | 176 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(173): Show |
203 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(200): Show |
intron_variant | MODIFIER | c.815-1101G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15459426 | |||||||
| chr3:15459449 | A | T | 15 | a0001c0001t0010g0259 a0001c0003t0004g0028 a0001c0003t0004g0121 others(12): Show |
16 | HG01109.hp2 HG02055.hp1 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.815-1124T>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15459449 | |||||||
| chr3:15459478 | C | CT | 21 | a0001c0001t0001g0105 a0001c0001t0001g0233 a0001c0001t0001g0248 others(18): Show |
23 | HG01123.hp2 HG01255.hp1 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.815-1154dupA | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15459478 | |||||||
| chr3:15459478 | CTT | C | 9 | a0001c0001t0001g0122 a0001c0001t0001g0124 a0001c0001t0001g0126 others(6): Show |
9 | HG01168.hp1 HG02109.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.815-1155_815-1154d others(4): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15459478 | |||||||
| chr3:15459518 | G | A | 2 | a0004c0006t0004g0244 a0004c0006t0004g0246 |
2 | NA18972.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.815-1193C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15459518 | |||||||
| chr3:15459564 | C | T | 1 | a0001c0001t0003g0048 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.815-1239G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15459564 | |||||||
| chr3:15459580 | G | A | 2 | a0004c0006t0004g0244 a0004c0006t0004g0246 |
2 | NA18972.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.815-1255C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15459580 | |||||||
| chr3:15459635 | G | T | 203 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(200): Show |
231 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(228): Show |
intron_variant | MODIFIER | c.815-1310C>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15459635 | |||||||
| chr3:15459646 | T | C | 9 | a0001c0001t0001g0122 a0001c0001t0001g0124 a0001c0001t0001g0126 others(6): Show |
9 | HG01168.hp1 HG02109.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.815-1321A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15459646 | |||||||
| chr3:15459791 | T | TTTA | 142 | a0001c0001t0001g0274 a0001c0001t0002g0016 a0001c0001t0002g0017 others(139): Show |
162 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.815-1469_815-1467d others(5): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15459791 | |||||||
| chr3:15459791 | T | TTTATTA | 13 | a0001c0001t0003g0081 a0001c0003t0004g0028 a0001c0003t0004g0121 others(10): Show |
14 | HG01109.hp2 HG01433.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.815-1472_815-1467d others(8): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15459791 | |||||||
| chr3:15459791 | TTTA | T | 8 | a0001c0001t0001g0122 a0001c0001t0001g0124 a0001c0001t0001g0126 others(5): Show |
8 | HG01168.hp1 HG02109.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.815-1469_815-1467d others(5): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15459791 | |||||||
| chr3:15459799 | T | C | 2 | a0001c0001t0001g0117 a0001c0001t0001g0193 |
2 | HG02602.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.815-1474A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15459799 | |||||||
| chr3:15459942 | T | C | 1 | a0001c0001t0016g0255 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.815-1617A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15459942 | |||||||
| chr3:15459985 | A | G | 3 | a0001c0001t0002g0023 a0001c0001t0002g0154 a0001c0001t0002g0163 |
4 | HG00642.hp1 HG01517.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.815-1660T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15459985 | |||||||
| chr3:15460088 | A | G | 1 | a0001c0001t0001g0203 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.815-1763T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15460088 | |||||||
| chr3:15460179 | C | T | 53 | a0001c0001t0002g0016 a0001c0001t0002g0025 a0001c0001t0002g0026 others(50): Show |
57 | HG00280.hp1 HG00544.hp1 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.815-1854G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15460179 | |||||||
| chr3:15460287 | G | A | 12 | a0001c0003t0004g0028 a0001c0003t0004g0121 a0001c0003t0004g0272 others(9): Show |
13 | HG01109.hp2 HG02055.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.815-1962C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15460287 | |||||||
| chr3:15460301 | A | G | 220 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(217): Show |
250 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(247): Show |
intron_variant | MODIFIER | c.815-1976T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15460301 | |||||||
| chr3:15460504 | G | A | 1 | a0001c0001t0001g0310 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.815-2179C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15460504 | |||||||
| chr3:15460623 | A | G | 203 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(200): Show |
231 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(228): Show |
intron_variant | MODIFIER | c.815-2298T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15460623 | |||||||
| chr3:15460713 | C | T | 1 | a0001c0001t0010g0259 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.815-2388G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15460713 | |||||||
| chr3:15460738 | T | C | 1 | a0001c0001t0013g0328 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.815-2413A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15460738 | |||||||
| chr3:15460886 | T | C | 10 | a0001c0001t0001g0122 a0001c0001t0001g0124 a0001c0001t0001g0126 others(7): Show |
10 | HG01168.hp1 HG02109.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.815-2561A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15460886 | |||||||
| chr3:15461091 | C | T | 8 | a0001c0001t0001g0122 a0001c0001t0001g0124 a0001c0001t0001g0126 others(5): Show |
8 | HG01168.hp1 HG02109.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.815-2766G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15461091 | |||||||
| chr3:15461174 | G | T | 76 | a0001c0001t0001g0115 a0001c0001t0001g0131 a0001c0001t0001g0132 others(73): Show |
79 | HG00280.hp1 HG00280.hp2 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.815-2849C>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15461174 | |||||||
| chr3:15461177 | T | C | 1 | a0001c0001t0002g0343 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.815-2852A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15461177 | |||||||
| chr3:15461189 | T | TCCCCGCC others(1): Show |
19 | a0001c0001t0001g0221 a0001c0001t0001g0274 a0001c0001t0002g0026 others(16): Show |
20 | HG00558.hp1 HG01069.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.815-2865_815-2864i others(10): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15461189 | |||||||
| chr3:15461189 | T | TCCCCGCC others(2): Show |
15 | a0001c0001t0001g0203 a0001c0001t0002g0027 a0001c0001t0002g0279 others(12): Show |
16 | HG00280.hp1 HG00558.hp2 HG00609.hp2 others(13): Show |
intron_variant | MODIFIER | c.815-2865_815-2864i others(11): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15461189 | |||||||
| chr3:15461189 | T | TCCCCGCC others(3): Show |
1 | a0001c0001t0002g0293 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.815-2865_815-2864i others(12): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15461189 | |||||||
| chr3:15461190 | C | CCCCGCA | 15 | a0001c0003t0004g0028 a0001c0003t0004g0121 a0001c0003t0004g0272 others(12): Show |
16 | HG01109.hp2 HG02055.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.815-2866_815-2865i others(8): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15461190 | |||||||
| chr3:15461198 | G | C | 60 | a0001c0001t0001g0203 a0001c0001t0001g0221 a0001c0001t0001g0274 others(57): Show |
63 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.815-2873C>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15461198 | |||||||
| chr3:15461258 | C | T | 6 | a0001c0001t0001g0118 a0001c0001t0001g0224 a0001c0001t0001g0225 others(3): Show |
7 | HG02027.hp2 HG02040.hp2 HG02080.hp2 others(4): Show |
intron_variant | MODIFIER | c.815-2933G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15461258 | |||||||
| chr3:15461353 | G | C | 74 | a0001c0001t0001g0170 a0001c0001t0001g0195 a0001c0001t0001g0196 others(71): Show |
80 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.815-3028C>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15461353 | |||||||
| chr3:15461493 | G | C | 1 | a0001c0001t0013g0328 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.815-3168C>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15461493 | |||||||
| chr3:15461548 | G | A | 218 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(215): Show |
248 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(245): Show |
intron_variant | MODIFIER | c.815-3223C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15461548 | |||||||
| chr3:15461704 | C | T | 5 | a0001c0001t0002g0312 a0001c0001t0002g0313 a0001c0001t0002g0314 others(2): Show |
5 | NA18987.hp1 NA19009.hp2 NA19054.hp1 others(2): Show |
intron_variant | MODIFIER | c.815-3379G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15461704 | |||||||
| chr3:15461745 | T | C | 17 | a0001c0003t0004g0028 a0001c0003t0004g0121 a0001c0003t0004g0272 others(14): Show |
18 | HG01109.hp2 HG02055.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.815-3420A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15461745 | |||||||
| chr3:15461873 | T | C | 1 | a0001c0001t0001g0122 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.815-3548A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15461873 | |||||||
| chr3:15461940 | T | C | 1 | a0001c0001t0003g0060 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.815-3615A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15461940 | |||||||
| chr3:15461998 | C | CTTAT | 57 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0113 others(54): Show |
63 | HG00280.hp2 HG00597.hp1 HG00673.hp1 others(60): Show |
intron_variant | MODIFIER | c.815-3677_815-3674d others(6): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15461998 | |||||||
| chr3:15461998 | C | CTTATTTA others(1): Show |
3 | a0001c0001t0001g0175 a0001c0001t0001g0180 a0001c0001t0001g0243 |
3 | HG02257.hp1 HG02451.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.815-3681_815-3674d others(10): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15461998 | |||||||
| chr3:15461998 | CTTAT | C | 10 | a0001c0001t0001g0165 a0001c0001t0001g0173 a0001c0001t0001g0174 others(7): Show |
10 | HG01256.hp2 HG01258.hp1 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.815-3677_815-3674d others(6): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15461998 | |||||||
| chr3:15461998 | CTTATTTA others(13): Show |
C | 17 | a0001c0003t0004g0028 a0001c0003t0004g0121 a0001c0003t0004g0272 others(14): Show |
18 | HG01109.hp2 HG02055.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.815-3693_815-3674d others(22): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15461998 | |||||||
| chr3:15462017 | A | ATTTG | 176 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(173): Show |
200 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(197): Show |
intron_variant | MODIFIER | c.815-3693_815-3692i others(6): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15462017 | |||||||
| chr3:15462017 | A | G | 1 | a0001c0001t0003g0013 | 2 | HG02886.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.815-3692T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15462017 | |||||||
| chr3:15462021 | A | ATTTG | 10 | a0001c0001t0002g0343 a0001c0001t0010g0259 a0002c0002t0008g0269 others(7): Show |
11 | HG01884.hp2 HG02622.hp2 HG02970.hp2 others(8): Show |
intron_variant | MODIFIER | c.815-3697_815-3696i others(6): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15462021 | |||||||
| chr3:15462021 | A | ATTTGTTT others(1): Show |
3 | a0001c0001t0002g0025 a0001c0001t0002g0287 a0001c0001t0003g0075 |
4 | HG00544.hp1 HG02818.hp2 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.815-3697_815-3696i others(10): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15462021 | |||||||
| chr3:15462021 | A | G | 177 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(174): Show |
202 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(199): Show |
intron_variant | MODIFIER | c.815-3696T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15462021 | |||||||
| chr3:15462025 | A | G | 1 | a0001c0001t0003g0042 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.815-3700T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15462025 | |||||||
| chr3:15462029 | A | G | 3 | a0001c0001t0001g0248 a0001c0001t0001g0260 a0001c0001t0006g0072 |
3 | HG03195.hp1 HG03579.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.815-3704T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15462029 | |||||||
| chr3:15462068 | G | A | 192 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(189): Show |
219 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(216): Show |
intron_variant | MODIFIER | c.815-3743C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15462068 | |||||||
| chr3:15462076 | G | A | 5 | a0003c0004t0002g0022 a0003c0004t0002g0247 a0003c0004t0002g0256 others(2): Show |
6 | HG02622.hp2 HG03098.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.815-3751C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15462076 | |||||||
| chr3:15462111 | C | G | 7 | a0001c0001t0001g0122 a0001c0001t0001g0124 a0001c0001t0001g0126 others(4): Show |
7 | HG01168.hp1 HG02109.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.815-3786G>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15462111 | |||||||
| chr3:15462303 | T | G | 17 | a0001c0003t0004g0028 a0001c0003t0004g0121 a0001c0003t0004g0272 others(14): Show |
18 | HG01109.hp2 HG02055.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.815-3978A>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15462303 | |||||||
| chr3:15462325 | C | T | 1 | a0001c0001t0002g0275 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.815-4000G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15462325 | |||||||
| chr3:15462437 | G | A | 30 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(27): Show |
36 | HG00639.hp1 HG01515.hp2 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.814+3904C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15462437 | |||||||
| chr3:15462492 | C | CG | 15 | a0001c0003t0004g0028 a0001c0003t0004g0121 a0001c0003t0004g0272 others(12): Show |
16 | HG01109.hp2 HG02055.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.814+3848dupC | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15462492 | |||||||
| chr3:15462706 | A | G | 7 | a0001c0001t0001g0122 a0001c0001t0001g0124 a0001c0001t0001g0126 others(4): Show |
7 | HG01168.hp1 HG02109.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.814+3635T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15462706 | |||||||
| chr3:15463107 | C | T | 3 | a0001c0001t0002g0016 a0001c0001t0002g0125 a0001c0001t0015g0116 |
4 | HG02258.hp1 HG02615.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.814+3234G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15463107 | |||||||
| chr3:15463150 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.814+3191G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15463150 | |||||||
| chr3:15463231 | C | T | 7 | a0001c0001t0001g0122 a0001c0001t0001g0124 a0001c0001t0001g0126 others(4): Show |
7 | HG01168.hp1 HG02109.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.814+3110G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15463231 | |||||||
| chr3:15463315 | G | T | 189 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(186): Show |
216 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(213): Show |
intron_variant | MODIFIER | c.814+3026C>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15463315 | |||||||
| chr3:15463320 | G | GT | 9 | a0001c0001t0002g0130 a0001c0001t0002g0242 a0001c0001t0002g0293 others(6): Show |
9 | HG01928.hp2 HG01943.hp2 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.814+3020dupA | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15463320 | |||||||
| chr3:15463321 | T | G | 21 | a0001c0001t0001g0248 a0001c0001t0001g0260 a0001c0001t0006g0072 others(18): Show |
22 | HG01109.hp2 HG02055.hp1 HG02280.hp2 others(19): Show |
intron_variant | MODIFIER | c.814+3020A>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15463321 | |||||||
| chr3:15463339 | GTTGTTTT | G | 16 | a0001c0003t0004g0028 a0001c0003t0004g0121 a0001c0003t0004g0272 others(13): Show |
17 | HG02055.hp1 HG02280.hp2 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.814+2995_814+3001d others(9): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15463339 | |||||||
| chr3:15463440 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.814+2901C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15463440 | |||||||
| chr3:15463446 | A | G | 1 | a0001c0001t0017g0290 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.814+2895T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15463446 | |||||||
| chr3:15463472 | A | G | 1 | a0001c0001t0001g0186 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.814+2869T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15463472 | |||||||
| chr3:15463536 | T | C | 210 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(207): Show |
238 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(235): Show |
intron_variant | MODIFIER | c.814+2805A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15463536 | |||||||
| chr3:15463598 | G | A | 3 | a0001c0001t0001g0212 a0004c0006t0004g0244 a0004c0006t0004g0246 |
3 | HG02630.hp1 NA18972.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.814+2743C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15463598 | |||||||
| chr3:15463717 | C | G | 182 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(179): Show |
208 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(205): Show |
intron_variant | MODIFIER | c.814+2624G>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15463717 | |||||||
| chr3:15463736 | G | A | 8 | a0002c0002t0005g0020 a0002c0002t0005g0021 a0002c0002t0005g0249 others(5): Show |
10 | HG01884.hp1 HG02109.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.814+2605C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15463736 | |||||||
| chr3:15463844 | C | T | 2 | a0001c0001t0001g0117 a0001c0001t0001g0193 |
2 | HG02602.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.814+2497G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15463844 | |||||||
| chr3:15463898 | T | C | 1 | a0001c0001t0010g0259 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.814+2443A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15463898 | |||||||
| chr3:15463923 | G | A | 1 | a0001c0001t0002g0343 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.814+2418C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15463923 | |||||||
| chr3:15463941 | T | C | 15 | a0001c0003t0004g0028 a0001c0003t0004g0121 a0001c0003t0004g0272 others(12): Show |
16 | HG01109.hp2 HG02055.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.814+2400A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15463941 | |||||||
| chr3:15463993 | A | G | 1 | a0001c0001t0002g0343 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.814+2348T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15463993 | |||||||
| chr3:15464003 | G | A | 15 | a0001c0003t0004g0028 a0001c0003t0004g0121 a0001c0003t0004g0272 others(12): Show |
16 | HG01109.hp2 HG02055.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.814+2338C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15464003 | |||||||
| chr3:15464124 | G | A | 1 | a0001c0001t0016g0255 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.814+2217C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15464124 | |||||||
| chr3:15464138 | A | AG | 209 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(206): Show |
237 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(234): Show |
intron_variant | MODIFIER | c.814+2202dupC | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15464138 | |||||||
| chr3:15464175 | A | C | 9 | a0001c0001t0002g0343 a0002c0002t0008g0269 a0002c0002t0008g0270 others(6): Show |
10 | HG01884.hp2 HG02622.hp2 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.814+2166T>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15464175 | |||||||
| chr3:15464393 | A | T | 7 | a0001c0001t0001g0122 a0001c0001t0001g0124 a0001c0001t0001g0126 others(4): Show |
7 | HG01168.hp1 HG02109.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.814+1948T>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15464393 | |||||||
| chr3:15464469 | C | T | 3 | a0001c0001t0001g0248 a0001c0001t0001g0260 a0001c0001t0006g0072 |
3 | HG03195.hp1 HG03579.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.814+1872G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15464469 | |||||||
| chr3:15464538 | C | T | 1 | a0001c0001t0002g0343 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.814+1803G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15464538 | |||||||
| chr3:15464718 | A | C | 1 | a0001c0001t0002g0343 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.814+1623T>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15464718 | |||||||
| chr3:15464747 | G | C | 54 | a0001c0001t0001g0274 a0001c0001t0002g0016 a0001c0001t0002g0025 others(51): Show |
58 | HG00280.hp1 HG00544.hp1 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.814+1594C>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15464747 | |||||||
| chr3:15464795 | T | C | 1 | a0001c0001t0002g0160 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.814+1546A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15464795 | |||||||
| chr3:15464935 | G | A | 15 | a0001c0003t0004g0028 a0001c0003t0004g0121 a0001c0003t0004g0272 others(12): Show |
16 | HG01109.hp2 HG02055.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.814+1406C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15464935 | |||||||
| chr3:15464971 | C | G | 1 | a0001c0001t0001g0196 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.814+1370G>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15464971 | |||||||
| chr3:15465032 | G | A | 1 | a0001c0001t0010g0259 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.814+1309C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15465032 | |||||||
| chr3:15465035 | G | A | 29 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(26): Show |
35 | HG00639.hp1 HG01515.hp2 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.814+1306C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15465035 | |||||||
| chr3:15465042 | A | C | 209 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(206): Show |
237 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(234): Show |
intron_variant | MODIFIER | c.814+1299T>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15465042 | |||||||
| chr3:15465220 | C | CAGACTTT others(60): Show |
1 | a0003c0004t0002g0257 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.814+1120_814+1121i others(69): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15465220 | |||||||
| chr3:15465220 | C | CAGACTTT others(56): Show |
1 | a0003c0004t0002g0256 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.814+1120_814+1121i others(65): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15465220 | |||||||
| chr3:15465232 | T | TTTTA | 65 | a0001c0001t0001g0102 a0001c0001t0001g0114 a0001c0001t0001g0119 others(62): Show |
67 | HG00280.hp1 HG00621.hp2 HG00673.hp2 others(64): Show |
intron_variant | MODIFIER | c.814+1108_814+1109i others(6): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15465232 | |||||||
| chr3:15465232 | T | TTTTATTT others(1): Show |
12 | a0001c0001t0001g0208 a0001c0001t0001g0213 a0001c0001t0001g0214 others(9): Show |
13 | HG00597.hp2 HG01099.hp1 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.814+1108_814+1109i others(10): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15465232 | |||||||
| chr3:15465232 | T | TTTTATTT others(64): Show |
1 | a0003c0004t0002g0258 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.814+1108_814+1109i others(73): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15465232 | |||||||
| chr3:15465232 | T | TTTTATTT others(56): Show |
3 | a0002c0002t0008g0269 a0002c0002t0008g0270 a0002c0002t0008g0271 |
3 | HG02970.hp2 HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.814+1108_814+1109i others(65): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15465232 | |||||||
| chr3:15465232 | TTTGA | T | 38 | a0001c0001t0001g0092 a0001c0001t0001g0170 a0001c0001t0001g0184 others(35): Show |
43 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.814+1105_814+1108d others(6): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15465232 | |||||||
| chr3:15465232 | TTTGATTT others(1): Show |
T | 20 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(17): Show |
20 | HG00639.hp2 HG00733.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.814+1101_814+1108d others(10): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15465232 | |||||||
| chr3:15465232 | TTTGATTT others(5): Show |
T | 2 | a0001c0001t0003g0073 a0002c0002t0005g0249 |
2 | HG06807.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.814+1097_814+1108d others(14): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15465232 | |||||||
| chr3:15465232 | TTTGATTT others(9): Show |
T | 1 | a0001c0001t0002g0296 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.814+1093_814+1108d others(18): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15465232 | |||||||
| chr3:15465235 | G | T | 281 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(278): Show |
314 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(311): Show |
intron_variant | MODIFIER | c.814+1106C>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15465235 | |||||||
| chr3:15465236 | A | ATTTATTT others(52): Show |
1 | a0003c0004t0002g0022 | 2 | HG03209.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.814+1104_814+1105i others(61): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15465236 | |||||||
| chr3:15465236 | A | ATTTATTT others(48): Show |
1 | a0003c0004t0002g0247 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.814+1104_814+1105i others(57): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15465236 | |||||||
| chr3:15465236 | A | T | 1 | a0001c0001t0002g0151 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.814+1105T>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15465236 | |||||||
| chr3:15465284 | T | A | 11 | a0001c0001t0002g0026 a0001c0001t0002g0027 a0001c0001t0002g0107 others(8): Show |
13 | HG00558.hp1 HG00609.hp2 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.814+1057A>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15465284 | |||||||
| chr3:15465330 | G | A | 192 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(189): Show |
219 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(216): Show |
intron_variant | MODIFIER | c.814+1011C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15465330 | |||||||
| chr3:15465371 | G | A | 1 | a0001c0001t0003g0085 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.814+970C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15465371 | |||||||
| chr3:15465412 | G | A | 1 | a0001c0001t0002g0242 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.814+929C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15465412 | |||||||
| chr3:15465428 | G | A | 7 | a0001c0001t0001g0122 a0001c0001t0001g0124 a0001c0001t0001g0126 others(4): Show |
7 | HG01168.hp1 HG02109.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.814+913C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15465428 | |||||||
| chr3:15465467 | C | T | 3 | a0001c0001t0001g0248 a0001c0001t0001g0260 a0001c0001t0006g0072 |
3 | HG03195.hp1 HG03579.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.814+874G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15465467 | |||||||
| chr3:15465557 | C | T | 1 | a0001c0001t0010g0259 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.814+784G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15465557 | |||||||
| chr3:15465558 | G | A | 1 | a0001c0001t0002g0098 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.814+783C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15465558 | |||||||
| chr3:15465610 | C | CT | 18 | a0001c0001t0001g0131 a0001c0001t0001g0171 a0001c0001t0001g0195 others(15): Show |
20 | HG00280.hp2 HG01071.hp1 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.814+730dupA | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15465610 | |||||||
| chr3:15465610 | C | CTT | 13 | a0001c0001t0001g0212 a0001c0003t0004g0028 a0001c0003t0004g0121 others(10): Show |
14 | HG01109.hp2 HG02055.hp1 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.814+729_814+730dup others(2): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15465610 | |||||||
| chr3:15465610 | CTTT | C | 7 | a0001c0001t0001g0097 a0001c0001t0001g0260 a0001c0001t0002g0297 others(4): Show |
7 | HG01884.hp2 HG03041.hp1 NA18977.hp2 others(4): Show |
intron_variant | MODIFIER | c.814+728_814+730del others(3): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15465610 | |||||||
| chr3:15465610 | CTTTT | C | 181 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(178): Show |
208 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(205): Show |
intron_variant | MODIFIER | c.814+727_814+730del others(4): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15465610 | |||||||
| chr3:15465647 | G | C | 17 | a0001c0003t0004g0028 a0001c0003t0004g0121 a0001c0003t0004g0272 others(14): Show |
18 | HG01109.hp2 HG02055.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.814+694C>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15465647 | |||||||
| chr3:15465707 | C | T | 17 | a0001c0003t0004g0028 a0001c0003t0004g0121 a0001c0003t0004g0272 others(14): Show |
18 | HG01109.hp2 HG02055.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.814+634G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15465707 | |||||||
| chr3:15465776 | T | G | 9 | a0001c0001t0002g0343 a0002c0002t0008g0269 a0002c0002t0008g0270 others(6): Show |
10 | HG01884.hp2 HG02622.hp2 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.814+565A>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15465776 | |||||||
| chr3:15465794 | G | A | 8 | a0002c0002t0008g0269 a0002c0002t0008g0270 a0002c0002t0008g0271 others(5): Show |
9 | HG02622.hp2 HG02970.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.814+547C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15465794 | |||||||
| chr3:15465815 | G | A | 3 | a0001c0001t0001g0248 a0001c0001t0001g0260 a0001c0001t0006g0072 |
3 | HG03195.hp1 HG03579.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.814+526C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15465815 | |||||||
| chr3:15465901 | C | T | 178 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(175): Show |
204 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(201): Show |
intron_variant | MODIFIER | c.814+440G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15465901 | |||||||
| chr3:15465985 | C | T | 4 | a0001c0001t0001g0122 a0001c0001t0001g0124 a0001c0001t0001g0338 others(1): Show |
4 | HG01168.hp1 HG02109.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.814+356G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15465985 | |||||||
| chr3:15466108 | T | C | 1 | a0001c0003t0004g0272 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.814+233A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15466108 | |||||||
| chr3:15466254 | G | A | 178 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(175): Show |
204 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(201): Show |
intron_variant | MODIFIER | c.814+87C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 12/16 | chr3 | 15466254 | |||||||
| chr3:15466613 | A | G | 1 | a0001c0001t0016g0255 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.718-176T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15466613 | |||||||
| chr3:15466653 | T | TCTGTC | 209 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(206): Show |
237 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(234): Show |
intron_variant | MODIFIER | c.718-217_718-216ins others(5): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15466653 | |||||||
| chr3:15466745 | A | G | 1 | a0001c0001t0001g0194 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.718-308T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15466745 | |||||||
| chr3:15466802 | G | C | 2 | a0001c0001t0010g0259 a0001c0001t0016g0255 |
2 | HG03041.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.718-365C>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15466802 | |||||||
| chr3:15466807 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.718-370G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15466807 | |||||||
| chr3:15466831 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.718-394G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15466831 | |||||||
| chr3:15466868 | A | T | 1 | a0001c0001t0002g0159 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.718-431T>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15466868 | |||||||
| chr3:15466871 | G | A | 9 | a0001c0001t0002g0343 a0002c0002t0008g0269 a0002c0002t0008g0270 others(6): Show |
10 | HG01884.hp2 HG02622.hp2 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.718-434C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15466871 | |||||||
| chr3:15466888 | C | T | 3 | a0001c0005t0005g0264 a0001c0005t0005g0265 a0002c0002t0005g0266 |
3 | HG01168.hp2 HG01169.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.718-451G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15466888 | |||||||
| chr3:15466972 | A | T | 3 | a0001c0005t0005g0264 a0001c0005t0005g0265 a0002c0002t0005g0266 |
3 | HG01168.hp2 HG01169.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.718-535T>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15466972 | |||||||
| chr3:15466992 | A | C | 17 | a0001c0003t0004g0028 a0001c0003t0004g0121 a0001c0003t0004g0272 others(14): Show |
18 | HG01109.hp2 HG02055.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.718-555T>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15466992 | |||||||
| chr3:15467054 | C | T | 1 | a0001c0001t0003g0029 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.718-617G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15467054 | |||||||
| chr3:15467289 | A | G | 1 | a0001c0001t0010g0259 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.718-852T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15467289 | |||||||
| chr3:15467511 | C | T | 208 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(205): Show |
236 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(233): Show |
intron_variant | MODIFIER | c.718-1074G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15467511 | |||||||
| chr3:15467521 | A | G | 208 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(205): Show |
236 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(233): Show |
intron_variant | MODIFIER | c.718-1084T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15467521 | |||||||
| chr3:15467561 | A | G | 14 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(11): Show |
20 | HG00639.hp1 HG01928.hp1 HG02004.hp2 others(17): Show |
intron_variant | MODIFIER | c.718-1124T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15467561 | |||||||
| chr3:15467616 | G | A | 3 | a0001c0001t0001g0248 a0001c0001t0001g0260 a0001c0001t0006g0072 |
3 | HG03195.hp1 HG03579.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.718-1179C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15467616 | |||||||
| chr3:15467705 | T | C | 209 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(206): Show |
237 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(234): Show |
intron_variant | MODIFIER | c.718-1268A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15467705 | |||||||
| chr3:15467747 | C | T | 4 | a0001c0001t0003g0010 a0001c0001t0003g0037 a0001c0001t0003g0052 others(1): Show |
5 | NA18950.hp1 NA18955.hp1 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.718-1310G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15467747 | |||||||
| chr3:15467820 | C | G | 208 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(205): Show |
236 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(233): Show |
intron_variant | MODIFIER | c.718-1383G>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15467820 | |||||||
| chr3:15468012 | G | C | 2 | a0004c0006t0004g0244 a0004c0006t0004g0246 |
2 | NA18972.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.718-1575C>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15468012 | |||||||
| chr3:15468321 | G | GT | 14 | a0001c0001t0001g0115 a0001c0001t0001g0133 a0001c0001t0001g0134 others(11): Show |
14 | HG00741.hp1 HG01081.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.718-1885dupA | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15468321 | |||||||
| chr3:15468321 | G | GTT | 57 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0100 others(54): Show |
64 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(61): Show |
intron_variant | MODIFIER | c.718-1886_718-1885d others(4): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15468321 | |||||||
| chr3:15468321 | G | GTTT | 16 | a0001c0001t0001g0018 a0001c0001t0001g0165 a0001c0001t0001g0167 others(13): Show |
17 | HG00735.hp1 HG01361.hp1 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.718-1887_718-1885d others(5): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15468321 | |||||||
| chr3:15468321 | GT | G | 39 | a0001c0001t0001g0097 a0001c0001t0001g0103 a0001c0001t0001g0122 others(36): Show |
40 | HG00639.hp2 HG01109.hp2 HG01168.hp1 others(37): Show |
intron_variant | MODIFIER | c.718-1885delA | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15468321 | |||||||
| chr3:15468321 | GTT | G | 151 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(148): Show |
177 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(174): Show |
intron_variant | MODIFIER | c.718-1886_718-1885d others(4): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15468321 | |||||||
| chr3:15468321 | GTTT | G | 14 | a0001c0001t0001g0248 a0001c0001t0001g0260 a0001c0001t0002g0307 others(11): Show |
15 | HG01069.hp1 HG02129.hp1 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.718-1887_718-1885d others(5): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15468321 | |||||||
| chr3:15468328 | T | G | 3 | a0001c0001t0001g0248 a0001c0001t0001g0260 a0001c0001t0006g0072 |
3 | HG03195.hp1 HG03579.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.718-1891A>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15468328 | |||||||
| chr3:15468356 | G | A | 2 | a0004c0006t0004g0244 a0004c0006t0004g0246 |
2 | NA18972.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.718-1919C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15468356 | |||||||
| chr3:15468384 | G | A | 3 | a0001c0001t0001g0248 a0001c0001t0001g0260 a0001c0001t0006g0072 |
3 | HG03195.hp1 HG03579.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.718-1947C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15468384 | |||||||
| chr3:15468399 | C | T | 1 | a0001c0001t0001g0260 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.718-1962G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15468399 | |||||||
| chr3:15468447 | C | A | 209 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(206): Show |
237 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(234): Show |
intron_variant | MODIFIER | c.718-2010G>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15468447 | |||||||
| chr3:15468486 | A | T | 1 | a0001c0001t0013g0328 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.718-2049T>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15468486 | |||||||
| chr3:15468626 | T | G | 208 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(205): Show |
236 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(233): Show |
intron_variant | MODIFIER | c.717+1910A>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15468626 | |||||||
| chr3:15468770 | T | C | 5 | a0003c0004t0002g0022 a0003c0004t0002g0247 a0003c0004t0002g0256 others(2): Show |
6 | HG02622.hp2 HG03098.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.717+1766A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15468770 | |||||||
| chr3:15468917 | T | C | 2 | a0004c0006t0004g0244 a0004c0006t0004g0246 |
2 | NA18972.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.717+1619A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15468917 | |||||||
| chr3:15469012 | C | A | 1 | a0001c0001t0001g0127 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.717+1524G>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15469012 | |||||||
| chr3:15469127 | G | C | 1 | a0001c0001t0001g0100 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.717+1409C>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15469127 | |||||||
| chr3:15469260 | T | C | 1 | a0001c0001t0002g0316 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.717+1276A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15469260 | |||||||
| chr3:15469348 | A | G | 1 | a0001c0001t0001g0131 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.717+1188T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15469348 | |||||||
| chr3:15469348 | A | T | 7 | a0001c0001t0001g0122 a0001c0001t0001g0124 a0001c0001t0001g0126 others(4): Show |
7 | HG01168.hp1 HG02109.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.717+1188T>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15469348 | |||||||
| chr3:15469373 | T | A | 1 | a0001c0001t0001g0248 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.717+1163A>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15469373 | |||||||
| chr3:15469410 | T | C | 1 | a0001c0001t0002g0343 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.717+1126A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15469410 | |||||||
| chr3:15469537 | A | G | 212 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(209): Show |
240 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(237): Show |
intron_variant | MODIFIER | c.717+999T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15469537 | |||||||
| chr3:15469702 | G | C | 6 | a0001c0001t0002g0245 a0001c0001t0003g0029 a0001c0001t0003g0039 others(3): Show |
6 | HG00544.hp2 HG02071.hp2 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.717+834C>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15469702 | |||||||
| chr3:15469730 | A | G | 17 | a0001c0003t0004g0028 a0001c0003t0004g0121 a0001c0003t0004g0272 others(14): Show |
18 | HG01109.hp2 HG02055.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.717+806T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15469730 | |||||||
| chr3:15469822 | G | A | 3 | a0001c0001t0003g0003 a0001c0001t0003g0063 a0001c0001t0003g0065 |
5 | NA18945.hp2 NA18973.hp1 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.717+714C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15469822 | |||||||
| chr3:15470044 | T | C | 1 | a0001c0003t0004g0272 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.717+492A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15470044 | |||||||
| chr3:15470323 | A | C | 6 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0135 others(3): Show |
6 | HG01106.hp2 HG01243.hp1 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.717+213T>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15470323 | |||||||
| chr3:15470508 | G | A | 1 | a0001c0001t0002g0343 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.717+28C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15470508 | |||||||
| chr3:15470510 | C | T | 1 | a0001c0001t0010g0259 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.717+26G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 11/16 | chr3 | 15470510 | |||||||
| chr3:15470735 | C | T | 15 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(12): Show |
15 | HG00639.hp2 HG00733.hp1 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.637-119G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15470735 | |||||||
| chr3:15470768 | A | G | 1 | a0001c0001t0001g0228 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.637-152T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15470768 | |||||||
| chr3:15470769 | G | T | 26 | a0001c0001t0001g0248 a0001c0001t0001g0260 a0001c0001t0006g0072 others(23): Show |
27 | HG01109.hp2 HG01168.hp2 HG01169.hp1 others(24): Show |
intron_variant | MODIFIER | c.637-153C>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15470769 | |||||||
| chr3:15470787 | A | C | 3 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 |
3 | NA18957.hp2 NA18997.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.637-171T>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15470787 | |||||||
| chr3:15470859 | A | G | 15 | a0001c0003t0004g0028 a0001c0003t0004g0121 a0001c0003t0004g0272 others(12): Show |
16 | HG01109.hp2 HG02055.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.637-243T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15470859 | |||||||
| chr3:15470953 | A | G | 1 | a0001c0001t0001g0183 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.637-337T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15470953 | |||||||
| chr3:15471072 | G | C | 13 | a0001c0001t0001g0007 a0001c0001t0001g0165 a0001c0001t0001g0167 others(10): Show |
15 | HG02056.hp2 HG02071.hp1 HG02129.hp2 others(12): Show |
intron_variant | MODIFIER | c.637-456C>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15471072 | |||||||
| chr3:15471161 | A | G | 1 | a0001c0001t0016g0255 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.637-545T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15471161 | |||||||
| chr3:15471166 | G | A | 1 | a0001c0001t0016g0255 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.637-550C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15471166 | |||||||
| chr3:15471169 | T | C | 15 | a0001c0003t0004g0028 a0001c0003t0004g0121 a0001c0003t0004g0272 others(12): Show |
16 | HG01109.hp2 HG02055.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.637-553A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15471169 | |||||||
| chr3:15471256 | A | G | 15 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(12): Show |
15 | HG00639.hp2 HG00733.hp1 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.637-640T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15471256 | |||||||
| chr3:15471292 | A | T | 171 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(168): Show |
196 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(193): Show |
intron_variant | MODIFIER | c.637-676T>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15471292 | |||||||
| chr3:15471304 | T | C | 1 | a0001c0001t0003g0057 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.637-688A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15471304 | |||||||
| chr3:15471541 | T | C | 4 | a0001c0001t0007g0187 a0001c0001t0007g0206 a0001c0001t0007g0207 others(1): Show |
4 | NA18942.hp1 NA18971.hp1 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.637-925A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15471541 | |||||||
| chr3:15471655 | G | A | 1 | a0001c0001t0001g0263 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.637-1039C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15471655 | |||||||
| chr3:15471874 | C | T | 2 | a0004c0006t0004g0244 a0004c0006t0004g0246 |
2 | NA18972.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.637-1258G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15471874 | |||||||
| chr3:15471875 | G | A | 1 | a0001c0001t0002g0287 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.637-1259C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15471875 | |||||||
| chr3:15471934 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.637-1318G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15471934 | |||||||
| chr3:15471946 | G | C | 3 | a0001c0001t0001g0248 a0001c0001t0001g0260 a0001c0001t0006g0072 |
3 | HG03195.hp1 HG03579.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.637-1330C>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15471946 | |||||||
| chr3:15471953 | C | T | 1 | a0001c0001t0002g0023 | 2 | HG03710.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.637-1337G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15471953 | |||||||
| chr3:15471959 | C | T | 79 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0018 others(76): Show |
87 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.637-1343G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15471959 | |||||||
| chr3:15471969 | A | AT | 7 | a0001c0001t0001g0188 a0001c0001t0001g0274 a0001c0001t0003g0042 others(4): Show |
7 | HG00609.hp1 HG01168.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.637-1354dupA | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15471969 | |||||||
| chr3:15471969 | AT | A | 52 | a0001c0001t0001g0181 a0001c0001t0001g0218 a0001c0001t0001g0248 others(49): Show |
55 | HG00280.hp1 HG00544.hp1 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.637-1354delA | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15471969 | |||||||
| chr3:15471970 | T | C | 7 | a0001c0001t0001g0122 a0001c0001t0001g0124 a0001c0001t0001g0126 others(4): Show |
7 | HG01168.hp1 HG02109.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.637-1354A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15471970 | |||||||
| chr3:15472067 | A | T | 4 | a0001c0001t0001g0192 a0001c0001t0001g0326 a0001c0001t0006g0051 others(1): Show |
4 | HG00621.hp1 NA18945.hp1 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.637-1451T>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15472067 | |||||||
| chr3:15472068 | G | T | 15 | a0001c0003t0004g0028 a0001c0003t0004g0121 a0001c0003t0004g0272 others(12): Show |
16 | HG01109.hp2 HG02055.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.637-1452C>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15472068 | |||||||
| chr3:15472112 | G | A | 1 | a0001c0001t0002g0107 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.637-1496C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15472112 | |||||||
| chr3:15472137 | C | T | 1 | a0001c0001t0010g0259 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.637-1521G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15472137 | |||||||
| chr3:15472216 | C | T | 8 | a0002c0002t0008g0269 a0002c0002t0008g0270 a0002c0002t0008g0271 others(5): Show |
9 | HG02622.hp2 HG02970.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.637-1600G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15472216 | |||||||
| chr3:15472246 | T | G | 1 | a0001c0001t0001g0308 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.637-1630A>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15472246 | |||||||
| chr3:15472290 | C | A | 1 | a0001c0001t0001g0133 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.637-1674G>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15472290 | |||||||
| chr3:15472447 | A | G | 1 | a0001c0001t0010g0342 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.636+1553T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15472447 | |||||||
| chr3:15472556 | A | C | 19 | a0001c0001t0016g0255 a0001c0003t0004g0028 a0001c0003t0004g0121 others(16): Show |
20 | HG01109.hp2 HG01168.hp2 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.636+1444T>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15472556 | |||||||
| chr3:15472722 | G | A | 6 | a0001c0001t0002g0245 a0001c0001t0003g0029 a0001c0001t0003g0039 others(3): Show |
6 | HG00544.hp2 HG02071.hp2 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.636+1278C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15472722 | |||||||
| chr3:15472722 | G | T | 1 | a0001c0001t0001g0092 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.636+1278C>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15472722 | |||||||
| chr3:15472790 | T | A | 165 | a0001c0001t0001g0122 a0001c0001t0001g0124 a0001c0001t0001g0126 others(162): Show |
186 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(183): Show |
intron_variant | MODIFIER | c.636+1210A>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15472790 | |||||||
| chr3:15472850 | CTTCTT | C | 3 | a0001c0001t0001g0104 a0001c0001t0001g0166 a0001c0001t0010g0259 |
3 | HG03041.hp1 NA18960.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.636+1145_636+1149d others(7): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15472850 | |||||||
| chr3:15472979 | C | T | 1 | a0001c0001t0002g0296 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.636+1021G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15472979 | |||||||
| chr3:15472987 | G | T | 48 | a0001c0001t0002g0017 a0001c0001t0002g0023 a0001c0001t0002g0129 others(45): Show |
59 | HG00423.hp1 HG00621.hp2 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.636+1013C>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15472987 | |||||||
| chr3:15473026 | A | AT | 15 | a0001c0001t0002g0245 a0001c0003t0004g0028 a0001c0003t0004g0121 others(12): Show |
16 | HG00544.hp2 HG01109.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.636+973dupA | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15473026 | |||||||
| chr3:15473048 | G | A | 1 | a0001c0001t0016g0255 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.636+952C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15473048 | |||||||
| chr3:15473058 | T | C | 1 | a0001c0001t0001g0015 | 2 | NA18960.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.636+942A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15473058 | |||||||
| chr3:15473264 | G | A | 39 | a0001c0001t0002g0024 a0001c0001t0002g0091 a0001c0001t0002g0242 others(36): Show |
44 | HG00423.hp2 HG00544.hp2 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.636+736C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15473264 | |||||||
| chr3:15473299 | G | A | 1 | a0001c0001t0001g0232 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.636+701C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15473299 | |||||||
| chr3:15473554 | C | T | 149 | a0001c0001t0001g0122 a0001c0001t0001g0124 a0001c0001t0001g0126 others(146): Show |
169 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(166): Show |
intron_variant | MODIFIER | c.636+446G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15473554 | |||||||
| chr3:15473595 | T | G | 8 | a0002c0002t0008g0269 a0002c0002t0008g0270 a0002c0002t0008g0271 others(5): Show |
9 | HG02622.hp2 HG02970.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.636+405A>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15473595 | |||||||
| chr3:15473648 | G | A | 8 | a0002c0002t0008g0269 a0002c0002t0008g0270 a0002c0002t0008g0271 others(5): Show |
9 | HG02622.hp2 HG02970.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.636+352C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15473648 | |||||||
| chr3:15473741 | A | C | 2 | a0001c0001t0002g0295 a0001c0001t0013g0328 |
2 | HG02135.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.636+259T>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 10/16 | chr3 | 15473741 | |||||||
| chr3:15474147 | A | G | 1 | a0004c0006t0004g0244 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.600+81T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 9/16 | chr3 | 15474147 | |||||||
| chr3:15474188 | C | T | 181 | a0001c0001t0001g0122 a0001c0001t0001g0124 a0001c0001t0001g0126 others(178): Show |
203 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(200): Show |
intron_variant | MODIFIER | c.600+40G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 9/16 | chr3 | 15474188 | |||||||
| chr3:15474206 | A | G | 1 | a0001c0001t0010g0259 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.600+22T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 9/16 | chr3 | 15474206 | |||||||
| chr3:15474287 | T | C | 11 | a0001c0001t0001g0248 a0001c0001t0001g0260 a0001c0001t0013g0328 others(8): Show |
12 | HG02622.hp2 HG02647.hp1 HG02970.hp2 others(9): Show |
intron_variant | MODIFIER | c.556-15A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 8/16 | chr3 | 15474287 | |||||||
| chr3:15474411 | C | G | 182 | a0001c0001t0001g0122 a0001c0001t0001g0124 a0001c0001t0001g0126 others(179): Show |
204 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(201): Show |
intron_variant | MODIFIER | c.556-139G>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 8/16 | chr3 | 15474411 | |||||||
| chr3:15474434 | A | G | 1 | a0001c0001t0013g0328 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.556-162T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 8/16 | chr3 | 15474434 | |||||||
| chr3:15474585 | TGTG | T | 182 | a0001c0001t0001g0122 a0001c0001t0001g0124 a0001c0001t0001g0126 others(179): Show |
204 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(201): Show |
intron_variant | MODIFIER | c.556-316_556-314del others(3): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 8/16 | chr3 | 15474585 | |||||||
| chr3:15474671 | C | G | 4 | a0001c0001t0001g0006 a0001c0001t0001g0110 a0001c0001t0001g0111 others(1): Show |
6 | NA18944.hp2 NA18950.hp2 NA19003.hp1 others(3): Show |
intron_variant | MODIFIER | c.555+254G>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 8/16 | chr3 | 15474671 | |||||||
| chr3:15474848 | C | A | 1 | a0001c0001t0002g0316 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.555+77G>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 8/16 | chr3 | 15474848 | |||||||
| chr3:15474888 | A | G | 1 | a0001c0001t0001g0260 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.555+37T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 8/16 | chr3 | 15474888 | |||||||
| chr3:15474889 | C | T | 1 | a0001c0001t0002g0294 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.555+36G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 8/16 | chr3 | 15474889 | |||||||
| chr3:15474974 | T | C | 149 | a0001c0001t0001g0122 a0001c0001t0001g0124 a0001c0001t0001g0126 others(146): Show |
169 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(166): Show |
intron_variant | MODIFIER | c.529-23A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 7/16 | chr3 | 15474974 | |||||||
| chr3:15475294 | G | A | 3 | a0001c0001t0003g0013 a0001c0001t0003g0071 a0001c0001t0006g0072 |
4 | HG02886.hp2 HG03130.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.528+131C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 7/16 | chr3 | 15475294 | |||||||
| chr3:15475313 | C | T | 152 | a0001c0001t0001g0122 a0001c0001t0001g0124 a0001c0001t0001g0126 others(149): Show |
172 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(169): Show |
intron_variant | MODIFIER | c.528+112G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 7/16 | chr3 | 15475313 | |||||||
| chr3:15475403 | T | C | 149 | a0001c0001t0001g0122 a0001c0001t0001g0124 a0001c0001t0001g0126 others(146): Show |
169 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(166): Show |
intron_variant | MODIFIER | c.528+22A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 7/16 | chr3 | 15475403 | |||||||
| chr3:15475518 | G | A | 183 | a0001c0001t0001g0122 a0001c0001t0001g0124 a0001c0001t0001g0126 others(180): Show |
205 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(202): Show |
intron_variant | MODIFIER | c.466-31C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 6/16 | chr3 | 15475518 | |||||||
| chr3:15475652 | C | T | 1 | a0001c0001t0002g0343 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.466-165G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 6/16 | chr3 | 15475652 | |||||||
| chr3:15475701 | C | T | 7 | a0001c0001t0002g0343 a0001c0001t0010g0259 a0001c0005t0005g0264 others(4): Show |
7 | HG01168.hp2 HG01169.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.466-214G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 6/16 | chr3 | 15475701 | |||||||
| chr3:15475811 | C | G | 164 | a0001c0001t0001g0122 a0001c0001t0001g0124 a0001c0001t0001g0126 others(161): Show |
185 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(182): Show |
intron_variant | MODIFIER | c.466-324G>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 6/16 | chr3 | 15475811 | |||||||
| chr3:15475883 | A | T | 1 | a0001c0001t0013g0328 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.466-396T>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 6/16 | chr3 | 15475883 | |||||||
| chr3:15475961 | C | A | 3 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 |
3 | NA18957.hp2 NA18997.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.466-474G>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 6/16 | chr3 | 15475961 | |||||||
| chr3:15475973 | T | C | 54 | a0001c0001t0002g0016 a0001c0001t0002g0025 a0001c0001t0002g0026 others(51): Show |
58 | HG00280.hp1 HG00544.hp1 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.466-486A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 6/16 | chr3 | 15475973 | |||||||
| chr3:15476099 | C | T | 2 | a0004c0006t0004g0244 a0004c0006t0004g0246 |
2 | NA18972.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.466-612G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 6/16 | chr3 | 15476099 | |||||||
| chr3:15476213 | T | G | 1 | a0001c0001t0003g0078 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.466-726A>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 6/16 | chr3 | 15476213 | |||||||
| chr3:15476234 | A | G | 3 | a0002c0002t0008g0269 a0002c0002t0008g0270 a0002c0002t0008g0271 |
3 | HG02970.hp2 HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.466-747T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 6/16 | chr3 | 15476234 | |||||||
| chr3:15476283 | A | G | 1 | a0001c0001t0002g0316 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.466-796T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 6/16 | chr3 | 15476283 | |||||||
| chr3:15476402 | C | T | 11 | a0001c0001t0001g0248 a0001c0001t0001g0260 a0001c0001t0013g0328 others(8): Show |
12 | HG02622.hp2 HG02647.hp1 HG02970.hp2 others(9): Show |
intron_variant | MODIFIER | c.465+724G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 6/16 | chr3 | 15476402 | |||||||
| chr3:15476473 | T | C | 1 | a0001c0001t0001g0094 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.465+653A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 6/16 | chr3 | 15476473 | |||||||
| chr3:15476869 | A | G | 18 | a0001c0003t0004g0028 a0001c0003t0004g0121 a0001c0003t0004g0272 others(15): Show |
19 | HG01109.hp2 HG01168.hp2 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.465+257T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 6/16 | chr3 | 15476869 | |||||||
| chr3:15477024 | G | A | 5 | a0003c0004t0002g0022 a0003c0004t0002g0247 a0003c0004t0002g0256 others(2): Show |
6 | HG02622.hp2 HG03098.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.465+102C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 6/16 | chr3 | 15477024 | |||||||
| chr3:15477074 | T | C | 8 | a0002c0002t0008g0269 a0002c0002t0008g0270 a0002c0002t0008g0271 others(5): Show |
9 | HG02622.hp2 HG02970.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.465+52A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 6/16 | chr3 | 15477074 | |||||||
| chr3:15477095 | C | T | 4 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0004c0006t0004g0244 others(1): Show |
4 | HG01255.hp2 HG01346.hp2 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.465+31G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 6/16 | chr3 | 15477095 | |||||||
| chr3:15477224 | G | C | 154 | a0001c0001t0001g0122 a0001c0001t0001g0124 a0001c0001t0001g0126 others(151): Show |
174 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(171): Show |
intron_variant | MODIFIER | c.394-27C>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 5/16 | chr3 | 15477224 | |||||||
| chr3:15477231 | G | A | 1 | a0001c0001t0002g0343 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.394-34C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 5/16 | chr3 | 15477231 | |||||||
| chr3:15477334 | G | A | 183 | a0001c0001t0001g0122 a0001c0001t0001g0124 a0001c0001t0001g0126 others(180): Show |
205 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(202): Show |
intron_variant | MODIFIER | c.394-137C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 5/16 | chr3 | 15477334 | |||||||
| chr3:15477382 | T | C | 179 | a0001c0001t0001g0122 a0001c0001t0001g0124 a0001c0001t0001g0126 others(176): Show |
201 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(198): Show |
intron_variant | MODIFIER | c.394-185A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 5/16 | chr3 | 15477382 | |||||||
| chr3:15477431 | A | C | 1 | a0001c0001t0001g0338 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.394-234T>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 5/16 | chr3 | 15477431 | |||||||
| chr3:15477584 | C | A | 3 | a0001c0001t0001g0214 a0001c0001t0001g0216 a0001c0001t0001g0322 |
3 | NA19063.hp1 NA19063.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.394-387G>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 5/16 | chr3 | 15477584 | |||||||
| chr3:15477755 | T | C | 158 | a0001c0001t0001g0122 a0001c0001t0001g0124 a0001c0001t0001g0126 others(155): Show |
179 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.394-558A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 5/16 | chr3 | 15477755 | |||||||
| chr3:15477850 | G | A | 1 | a0001c0001t0003g0087 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.394-653C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 5/16 | chr3 | 15477850 | |||||||
| chr3:15478012 | G | A | 14 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(11): Show |
20 | HG00639.hp1 HG01928.hp1 HG02004.hp2 others(17): Show |
intron_variant | MODIFIER | c.394-815C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 5/16 | chr3 | 15478012 | |||||||
| chr3:15478144 | T | A | 8 | a0002c0002t0008g0269 a0002c0002t0008g0270 a0002c0002t0008g0271 others(5): Show |
9 | HG02622.hp2 HG02970.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.393+833A>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 5/16 | chr3 | 15478144 | |||||||
| chr3:15478190 | GACC | G | 8 | a0002c0002t0008g0269 a0002c0002t0008g0270 a0002c0002t0008g0271 others(5): Show |
9 | HG02622.hp2 HG02970.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.393+784_393+786del others(3): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 5/16 | chr3 | 15478190 | |||||||
| chr3:15478270 | G | A | 2 | a0001c0001t0001g0324 a0001c0001t0001g0325 |
2 | HG02572.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.393+707C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 5/16 | chr3 | 15478270 | |||||||
| chr3:15478350 | A | G | 1 | a0001c0001t0002g0293 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.393+627T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 5/16 | chr3 | 15478350 | |||||||
| chr3:15478427 | C | T | 15 | a0001c0003t0004g0028 a0001c0003t0004g0121 a0001c0003t0004g0272 others(12): Show |
16 | HG01109.hp2 HG02055.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.393+550G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 5/16 | chr3 | 15478427 | |||||||
| chr3:15478453 | C | T | 1 | a0001c0001t0001g0241 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.393+524G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 5/16 | chr3 | 15478453 | |||||||
| chr3:15478512 | G | T | 168 | a0001c0001t0001g0122 a0001c0001t0001g0124 a0001c0001t0001g0126 others(165): Show |
189 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(186): Show |
intron_variant | MODIFIER | c.393+465C>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 5/16 | chr3 | 15478512 | |||||||
| chr3:15478709 | G | C | 1 | a0001c0001t0002g0343 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.393+268C>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 5/16 | chr3 | 15478709 | |||||||
| chr3:15478737 | C | T | 149 | a0001c0001t0001g0122 a0001c0001t0001g0124 a0001c0001t0001g0126 others(146): Show |
169 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(166): Show |
intron_variant | MODIFIER | c.393+240G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 5/16 | chr3 | 15478737 | |||||||
| chr3:15478788 | T | A | 1 | a0001c0001t0001g0210 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.393+189A>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 5/16 | chr3 | 15478788 | |||||||
| chr3:15478966 | G | A | 5 | a0003c0004t0002g0022 a0003c0004t0002g0247 a0003c0004t0002g0256 others(2): Show |
6 | HG02622.hp2 HG03098.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.393+11C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 5/16 | chr3 | 15478966 | |||||||
| chr3:15479053 | C | T | 3 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 |
3 | HG00733.hp1 HG00738.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.367-50G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 4/16 | chr3 | 15479053 | |||||||
| chr3:15479132 | T | G | 88 | a0001c0001t0002g0017 a0001c0001t0002g0023 a0001c0001t0002g0024 others(85): Show |
104 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.367-129A>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 4/16 | chr3 | 15479132 | |||||||
| chr3:15479143 | G | C | 1 | a0001c0001t0001g0237 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.367-140C>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 4/16 | chr3 | 15479143 | |||||||
| chr3:15479170 | G | T | 150 | a0001c0001t0001g0122 a0001c0001t0001g0124 a0001c0001t0001g0126 others(147): Show |
170 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(167): Show |
intron_variant | MODIFIER | c.367-167C>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 4/16 | chr3 | 15479170 | |||||||
| chr3:15479300 | C | T | 1 | a0001c0001t0010g0342 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.366+38G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 4/16 | chr3 | 15479300 | |||||||
| chr3:15479313 | G | A | 2 | a0004c0006t0004g0244 a0004c0006t0004g0246 |
2 | NA18972.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.366+25C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 4/16 | chr3 | 15479313 | |||||||
| chr3:15479331 | T | C | 11 | a0001c0005t0005g0264 a0001c0005t0005g0265 a0002c0002t0005g0266 others(8): Show |
12 | HG01168.hp2 HG01169.hp1 HG02622.hp2 others(9): Show |
splice_region_variant&intron_variant | LOW | c.366+7A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 4/16 | chr3 | 15479331 | |||||||
| chr3:15479556 | G | A | 2 | a0001c0001t0001g0248 a0001c0001t0013g0328 |
2 | HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.322-174C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15479556 | |||||||
| chr3:15479629 | G | A | 1 | a0001c0001t0012g0268 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.322-247C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15479629 | |||||||
| chr3:15479989 | A | G | 15 | a0001c0001t0002g0343 a0001c0001t0010g0259 a0001c0005t0005g0264 others(12): Show |
16 | HG01168.hp2 HG01169.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.322-607T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15479989 | |||||||
| chr3:15480112 | C | T | 142 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0023 others(139): Show |
162 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.322-730G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15480112 | |||||||
| chr3:15480158 | G | A | 149 | a0001c0001t0001g0122 a0001c0001t0001g0124 a0001c0001t0001g0126 others(146): Show |
169 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(166): Show |
intron_variant | MODIFIER | c.322-776C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15480158 | |||||||
| chr3:15480214 | G | A | 149 | a0001c0001t0001g0122 a0001c0001t0001g0124 a0001c0001t0001g0126 others(146): Show |
169 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(166): Show |
intron_variant | MODIFIER | c.322-832C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15480214 | |||||||
| chr3:15480338 | C | A | 5 | a0003c0004t0002g0022 a0003c0004t0002g0247 a0003c0004t0002g0256 others(2): Show |
6 | HG02622.hp2 HG03098.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.322-956G>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15480338 | |||||||
| chr3:15480392 | T | C | 1 | a0001c0001t0001g0108 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.322-1010A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15480392 | |||||||
| chr3:15480451 | G | A | 1 | a0001c0001t0001g0212 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.322-1069C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15480451 | |||||||
| chr3:15480462 | C | G | 1 | a0001c0001t0001g0321 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.322-1080G>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15480462 | |||||||
| chr3:15480597 | T | G | 2 | a0001c0001t0001g0262 a0001c0001t0001g0263 |
2 | HG02486.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.322-1215A>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15480597 | |||||||
| chr3:15480770 | A | G | 153 | a0001c0001t0001g0122 a0001c0001t0001g0124 a0001c0001t0001g0126 others(150): Show |
174 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(171): Show |
intron_variant | MODIFIER | c.322-1388T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15480770 | |||||||
| chr3:15480866 | T | C | 1 | a0001c0001t0001g0104 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.322-1484A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15480866 | |||||||
| chr3:15481008 | C | T | 1 | a0001c0001t0001g0230 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.322-1626G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15481008 | |||||||
| chr3:15481429 | T | C | 5 | a0003c0004t0002g0022 a0003c0004t0002g0247 a0003c0004t0002g0256 others(2): Show |
6 | HG02622.hp2 HG03098.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.322-2047A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15481429 | |||||||
| chr3:15481696 | G | A | 3 | a0001c0001t0001g0248 a0001c0001t0001g0260 a0001c0001t0016g0255 |
3 | HG03195.hp1 NA18906.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.322-2314C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15481696 | |||||||
| chr3:15481714 | T | C | 1 | a0001c0001t0010g0342 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.322-2332A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15481714 | |||||||
| chr3:15481836 | C | T | 1 | a0001c0001t0002g0281 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.322-2454G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15481836 | |||||||
| chr3:15481857 | T | C | 2 | a0001c0001t0001g0103 a0001c0001t0001g0308 |
2 | HG02056.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.322-2475A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15481857 | |||||||
| chr3:15481894 | C | G | 1 | a0001c0001t0001g0145 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.322-2512G>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15481894 | |||||||
| chr3:15481932 | C | T | 1 | a0001c0001t0013g0328 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.322-2550G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15481932 | |||||||
| chr3:15481990 | C | T | 1 | a0001c0001t0010g0259 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.322-2608G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15481990 | |||||||
| chr3:15482086 | T | C | 11 | a0001c0005t0005g0264 a0001c0005t0005g0265 a0002c0002t0005g0266 others(8): Show |
12 | HG01168.hp2 HG01169.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.322-2704A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15482086 | |||||||
| chr3:15482180 | C | T | 2 | a0001c0001t0001g0248 a0001c0001t0001g0260 |
2 | HG03195.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.322-2798G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15482180 | |||||||
| chr3:15482220 | G | A | 1 | a0001c0001t0003g0073 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.322-2838C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15482220 | |||||||
| chr3:15482225 | C | T | 4 | a0001c0001t0002g0343 a0001c0001t0010g0259 a0004c0006t0004g0244 others(1): Show |
4 | HG01884.hp2 HG03041.hp1 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.322-2843G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15482225 | |||||||
| chr3:15482369 | T | C | 1 | a0001c0001t0001g0208 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.322-2987A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15482369 | |||||||
| chr3:15482459 | T | C | 1 | a0001c0001t0002g0343 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.322-3077A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15482459 | |||||||
| chr3:15482722 | C | T | 295 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(292): Show |
331 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.322-3340G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15482722 | |||||||
| chr3:15482745 | C | T | 6 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0135 others(3): Show |
6 | HG01106.hp2 HG01243.hp1 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.322-3363G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15482745 | |||||||
| chr3:15482801 | G | C | 1 | a0001c0001t0002g0161 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.322-3419C>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15482801 | |||||||
| chr3:15482822 | T | C | 4 | a0001c0001t0002g0343 a0001c0001t0010g0259 a0004c0006t0004g0244 others(1): Show |
4 | HG01884.hp2 HG03041.hp1 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.322-3440A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15482822 | |||||||
| chr3:15482830 | C | T | 1 | a0001c0001t0003g0040 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.322-3448G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15482830 | |||||||
| chr3:15482847 | T | A | 1 | a0001c0001t0010g0259 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.322-3465A>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15482847 | |||||||
| chr3:15482857 | G | T | 4 | a0003c0004t0002g0022 a0003c0004t0002g0256 a0003c0004t0002g0257 others(1): Show |
5 | HG02622.hp2 HG03209.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.322-3475C>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15482857 | |||||||
| chr3:15483079 | C | A | 150 | a0001c0001t0001g0122 a0001c0001t0001g0124 a0001c0001t0001g0126 others(147): Show |
170 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(167): Show |
intron_variant | MODIFIER | c.322-3697G>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15483079 | |||||||
| chr3:15483126 | G | A | 4 | a0001c0001t0002g0306 a0001c0001t0002g0307 a0001c0001t0010g0342 others(1): Show |
4 | HG01069.hp1 HG01071.hp2 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.322-3744C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15483126 | |||||||
| chr3:15483216 | G | T | 1 | a0001c0001t0001g0191 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.322-3834C>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15483216 | |||||||
| chr3:15483288 | C | A | 14 | a0001c0003t0004g0028 a0001c0003t0004g0121 a0001c0003t0004g0311 others(11): Show |
15 | HG01109.hp2 HG02055.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.322-3906G>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15483288 | |||||||
| chr3:15483518 | T | G | 10 | a0001c0001t0001g0100 a0001c0001t0001g0120 a0001c0001t0001g0177 others(7): Show |
10 | NA18940.hp1 NA18942.hp1 NA18966.hp1 others(7): Show |
intron_variant | MODIFIER | c.322-4136A>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15483518 | |||||||
| chr3:15483616 | G | T | 1 | a0001c0001t0002g0162 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.322-4234C>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15483616 | |||||||
| chr3:15483662 | T | C | 1 | a0001c0001t0001g0212 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.322-4280A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15483662 | |||||||
| chr3:15483731 | G | T | 1 | a0001c0001t0016g0255 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.322-4349C>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15483731 | |||||||
| chr3:15483819 | A | T | 2 | a0004c0006t0004g0244 a0004c0006t0004g0246 |
2 | NA18972.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.321+4387T>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15483819 | |||||||
| chr3:15484041 | CT | C | 169 | a0001c0001t0001g0122 a0001c0001t0001g0124 a0001c0001t0001g0126 others(166): Show |
190 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(187): Show |
intron_variant | MODIFIER | c.321+4164delA | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15484041 | |||||||
| chr3:15484158 | C | T | 3 | a0001c0001t0001g0248 a0001c0001t0001g0260 a0001c0001t0016g0255 |
3 | HG03195.hp1 NA18906.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.321+4048G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15484158 | |||||||
| chr3:15484201 | A | AG | 339 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(336): Show |
377 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(374): Show |
intron_variant | MODIFIER | c.321+4004_321+4005i others(3): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15484201 | |||||||
| chr3:15484351 | A | G | 1 | a0001c0001t0013g0328 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.321+3855T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15484351 | |||||||
| chr3:15484387 | A | G | 168 | a0001c0001t0001g0122 a0001c0001t0001g0124 a0001c0001t0001g0126 others(165): Show |
189 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(186): Show |
intron_variant | MODIFIER | c.321+3819T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15484387 | |||||||
| chr3:15484392 | T | G | 18 | a0001c0001t0001g0248 a0001c0001t0001g0260 a0001c0001t0002g0343 others(15): Show |
19 | HG01168.hp2 HG01169.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.321+3814A>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15484392 | |||||||
| chr3:15484422 | T | C | 1 | a0001c0001t0003g0090 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.321+3784A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15484422 | |||||||
| chr3:15484523 | T | A | 1 | a0001c0001t0002g0287 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.321+3683A>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15484523 | |||||||
| chr3:15484561 | C | T | 2 | a0004c0006t0004g0244 a0004c0006t0004g0246 |
2 | NA18972.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.321+3645G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15484561 | |||||||
| chr3:15484563 | T | C | 1 | a0002c0002t0005g0266 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.321+3643A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15484563 | |||||||
| chr3:15484586 | C | T | 3 | a0002c0002t0008g0269 a0002c0002t0008g0270 a0002c0002t0008g0271 |
3 | HG02970.hp2 HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.321+3620G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15484586 | |||||||
| chr3:15484713 | A | C | 1 | a0001c0001t0001g0277 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.321+3493T>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15484713 | |||||||
| chr3:15484738 | A | G | 1 | a0001c0001t0016g0255 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.321+3468T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15484738 | |||||||
| chr3:15484744 | C | T | 3 | a0001c0001t0003g0080 a0001c0001t0003g0082 a0001c0001t0003g0083 |
3 | NA18948.hp2 NA18961.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.321+3462G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15484744 | |||||||
| chr3:15484771 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.321+3435A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15484771 | |||||||
| chr3:15484984 | A | G | 5 | a0003c0004t0002g0022 a0003c0004t0002g0247 a0003c0004t0002g0256 others(2): Show |
6 | HG02622.hp2 HG03098.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.321+3222T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15484984 | |||||||
| chr3:15485061 | G | C | 1 | a0001c0001t0001g0128 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.321+3145C>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15485061 | |||||||
| chr3:15485234 | G | T | 3 | a0001c0005t0005g0264 a0001c0005t0005g0265 a0002c0002t0005g0266 |
3 | HG01168.hp2 HG01169.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.321+2972C>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15485234 | |||||||
| chr3:15485295 | G | A | 2 | a0001c0001t0001g0329 a0001c0001t0001g0330 |
2 | HG01081.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.321+2911C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15485295 | |||||||
| chr3:15485540 | G | A | 184 | a0001c0001t0001g0122 a0001c0001t0001g0124 a0001c0001t0001g0126 others(181): Show |
206 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(203): Show |
intron_variant | MODIFIER | c.321+2666C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15485540 | |||||||
| chr3:15485553 | A | G | 1 | a0001c0001t0013g0328 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.321+2653T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15485553 | |||||||
| chr3:15485578 | G | A | 1 | a0001c0001t0001g0208 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.321+2628C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15485578 | |||||||
| chr3:15485701 | T | C | 2 | a0004c0006t0004g0244 a0004c0006t0004g0246 |
2 | NA18972.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.321+2505A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15485701 | |||||||
| chr3:15485739 | C | T | 15 | a0001c0003t0004g0028 a0001c0003t0004g0121 a0001c0003t0004g0272 others(12): Show |
16 | HG01109.hp2 HG02055.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.321+2467G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15485739 | |||||||
| chr3:15485742 | G | C | 1 | a0002c0002t0005g0266 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.321+2464C>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15485742 | |||||||
| chr3:15485938 | G | C | 161 | a0001c0001t0001g0122 a0001c0001t0001g0124 a0001c0001t0001g0126 others(158): Show |
182 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(179): Show |
intron_variant | MODIFIER | c.321+2268C>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15485938 | |||||||
| chr3:15486164 | T | A | 1 | a0001c0003t0004g0272 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.321+2042A>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15486164 | |||||||
| chr3:15486181 | G | A | 1 | a0001c0001t0002g0156 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.321+2025C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15486181 | |||||||
| chr3:15486272 | G | A | 3 | a0001c0001t0002g0016 a0001c0001t0002g0125 a0001c0001t0015g0116 |
4 | HG02258.hp1 HG02615.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.321+1934C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15486272 | |||||||
| chr3:15486366 | T | G | 7 | a0001c0001t0002g0343 a0001c0001t0010g0259 a0001c0005t0005g0264 others(4): Show |
7 | HG01168.hp2 HG01169.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.321+1840A>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15486366 | |||||||
| chr3:15486375 | T | C | 2 | a0004c0006t0004g0244 a0004c0006t0004g0246 |
2 | NA18972.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.321+1831A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15486375 | |||||||
| chr3:15486407 | C | A | 1 | a0001c0001t0001g0212 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.321+1799G>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15486407 | |||||||
| chr3:15486483 | A | G | 9 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(6): Show |
9 | HG01106.hp2 HG01243.hp1 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.321+1723T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15486483 | |||||||
| chr3:15486497 | A | T | 1 | a0001c0001t0003g0048 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.321+1709T>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15486497 | |||||||
| chr3:15486555 | T | C | 2 | a0004c0006t0004g0244 a0004c0006t0004g0246 |
2 | NA18972.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.321+1651A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15486555 | |||||||
| chr3:15486589 | C | T | 1 | a0006c0009t0001g0344 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.321+1617G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15486589 | |||||||
| chr3:15486758 | C | T | 3 | a0001c0005t0005g0264 a0001c0005t0005g0265 a0002c0002t0005g0266 |
3 | HG01168.hp2 HG01169.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.321+1448G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15486758 | |||||||
| chr3:15486882 | C | T | 1 | a0001c0001t0003g0032 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.321+1324G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15486882 | |||||||
| chr3:15486992 | C | T | 6 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0135 others(3): Show |
6 | HG01106.hp2 HG01243.hp1 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.321+1214G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15486992 | |||||||
| chr3:15487030 | G | A | 2 | a0001c0001t0002g0242 a0001c0001t0003g0062 |
2 | HG02572.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.321+1176C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15487030 | |||||||
| chr3:15487069 | A | C | 78 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0018 others(75): Show |
86 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.321+1137T>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15487069 | |||||||
| chr3:15487255 | G | A | 2 | a0004c0006t0004g0244 a0004c0006t0004g0246 |
2 | NA18972.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.321+951C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15487255 | |||||||
| chr3:15487324 | G | T | 1 | a0001c0001t0001g0179 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.321+882C>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15487324 | |||||||
| chr3:15487383 | G | A | 3 | a0001c0001t0001g0248 a0001c0001t0001g0260 a0001c0001t0016g0255 |
3 | HG03195.hp1 NA18906.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.321+823C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15487383 | |||||||
| chr3:15487425 | C | T | 3 | a0001c0005t0005g0264 a0001c0005t0005g0265 a0002c0002t0005g0266 |
3 | HG01168.hp2 HG01169.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.321+781G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15487425 | |||||||
| chr3:15487546 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.321+660C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15487546 | |||||||
| chr3:15487558 | C | T | 1 | a0001c0001t0010g0259 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.321+648G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15487558 | |||||||
| chr3:15487565 | C | A | 6 | a0001c0001t0001g0118 a0001c0001t0001g0224 a0001c0001t0001g0225 others(3): Show |
7 | HG02027.hp2 HG02040.hp2 HG02080.hp2 others(4): Show |
intron_variant | MODIFIER | c.321+641G>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15487565 | |||||||
| chr3:15487589 | G | A | 2 | a0004c0006t0004g0244 a0004c0006t0004g0246 |
2 | NA18972.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.321+617C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15487589 | |||||||
| chr3:15487608 | T | G | 21 | a0001c0001t0001g0115 a0001c0001t0001g0131 a0001c0001t0001g0132 others(18): Show |
21 | HG00639.hp2 HG00733.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.321+598A>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15487608 | |||||||
| chr3:15487626 | C | T | 2 | a0004c0006t0004g0244 a0004c0006t0004g0246 |
2 | NA18972.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.321+580G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15487626 | |||||||
| chr3:15487791 | G | A | 1 | a0001c0001t0002g0276 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.321+415C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15487791 | |||||||
| chr3:15487797 | A | G | 154 | a0001c0001t0001g0122 a0001c0001t0001g0124 a0001c0001t0001g0126 others(151): Show |
175 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.321+409T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15487797 | |||||||
| chr3:15487898 | C | A | 150 | a0001c0001t0001g0122 a0001c0001t0001g0124 a0001c0001t0001g0126 others(147): Show |
170 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(167): Show |
intron_variant | MODIFIER | c.321+308G>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15487898 | |||||||
| chr3:15487961 | A | C | 1 | a0001c0001t0002g0280 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.321+245T>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15487961 | |||||||
| chr3:15487998 | T | C | 1 | a0001c0001t0002g0162 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.321+208A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15487998 | |||||||
| chr3:15488036 | T | C | 168 | a0001c0001t0001g0122 a0001c0001t0001g0124 a0001c0001t0001g0126 others(165): Show |
189 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(186): Show |
intron_variant | MODIFIER | c.321+170A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15488036 | |||||||
| chr3:15488175 | C | T | 1 | a0001c0001t0001g0219 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.321+31G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15488175 | |||||||
| chr3:15488179 | G | A | 4 | a0002c0002t0008g0269 a0002c0002t0008g0270 a0002c0002t0008g0271 others(1): Show |
4 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.321+27C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 3/16 | chr3 | 15488179 | |||||||
| chr3:15488437 | C | T | 3 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0001g0240 |
3 | HG01891.hp1 HG02145.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.220-130G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 2/16 | chr3 | 15488437 | |||||||
| chr3:15488440 | C | G | 3 | a0001c0001t0001g0248 a0001c0001t0001g0260 a0001c0001t0016g0255 |
3 | HG03195.hp1 NA18906.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.220-133G>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 2/16 | chr3 | 15488440 | |||||||
| chr3:15488494 | C | T | 15 | a0001c0003t0004g0028 a0001c0003t0004g0121 a0001c0003t0004g0272 others(12): Show |
16 | HG01109.hp2 HG02055.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.220-187G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 2/16 | chr3 | 15488494 | |||||||
| chr3:15488512 | A | G | 1 | a0001c0001t0002g0343 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.220-205T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 2/16 | chr3 | 15488512 | |||||||
| chr3:15488552 | G | A | 1 | a0001c0001t0003g0045 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.220-245C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 2/16 | chr3 | 15488552 | |||||||
| chr3:15488553 | C | T | 1 | a0001c0001t0013g0328 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.220-246G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 2/16 | chr3 | 15488553 | |||||||
| chr3:15488598 | A | G | 1 | a0001c0001t0016g0255 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.220-291T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 2/16 | chr3 | 15488598 | |||||||
| chr3:15488840 | T | G | 5 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0248 others(2): Show |
5 | HG02257.hp2 HG02559.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.220-533A>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 2/16 | chr3 | 15488840 | |||||||
| chr3:15489088 | G | A | 153 | a0001c0001t0001g0122 a0001c0001t0001g0124 a0001c0001t0001g0126 others(150): Show |
172 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(169): Show |
intron_variant | MODIFIER | c.219+437C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 2/16 | chr3 | 15489088 | |||||||
| chr3:15489407 | G | A | 1 | a0001c0003t0004g0337 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.219+118C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 2/16 | chr3 | 15489407 | |||||||
| chr3:15489844 | A | G | 1 | a0001c0001t0001g0126 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.107-207T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15489844 | |||||||
| chr3:15489909 | C | T | 1 | a0001c0001t0002g0098 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.107-272G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15489909 | |||||||
| chr3:15490030 | T | A | 1 | a0001c0001t0002g0343 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.107-393A>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15490030 | |||||||
| chr3:15490191 | C | G | 1 | a0001c0001t0001g0108 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.107-554G>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15490191 | |||||||
| chr3:15490210 | A | G | 1 | a0001c0001t0003g0038 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.107-573T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15490210 | |||||||
| chr3:15490330 | G | C | 1 | a0001c0001t0001g0145 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.107-693C>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15490330 | |||||||
| chr3:15490398 | AT | A | 74 | a0001c0001t0002g0024 a0001c0001t0002g0242 a0001c0001t0002g0267 others(71): Show |
88 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.107-762delA | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15490398 | |||||||
| chr3:15490481 | G | T | 100 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(97): Show |
120 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.107-844C>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15490481 | |||||||
| chr3:15490499 | T | C | 1 | a0001c0003t0004g0272 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.107-862A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15490499 | |||||||
| chr3:15490556 | T | C | 1 | a0003c0004t0002g0247 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.107-919A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15490556 | |||||||
| chr3:15490760 | C | T | 4 | a0001c0001t0002g0154 a0001c0001t0002g0156 a0001c0001t0002g0157 others(1): Show |
4 | HG00642.hp1 HG01175.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.107-1123G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15490760 | |||||||
| chr3:15491020 | TG | T | 14 | a0001c0001t0001g0338 a0001c0003t0004g0028 a0001c0003t0004g0121 others(11): Show |
15 | HG01109.hp2 HG01168.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.107-1384delC | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15491020 | |||||||
| chr3:15491102 | C | T | 2 | a0001c0001t0002g0343 a0001c0003t0004g0272 |
2 | HG01884.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.107-1465G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15491102 | |||||||
| chr3:15491160 | A | G | 1 | a0001c0003t0004g0339 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.107-1523T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15491160 | |||||||
| chr3:15491211 | G | A | 12 | a0001c0001t0001g0248 a0001c0001t0001g0260 a0001c0001t0010g0259 others(9): Show |
14 | HG01884.hp1 HG02109.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.107-1574C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15491211 | |||||||
| chr3:15491213 | T | C | 4 | a0001c0001t0002g0242 a0001c0001t0003g0062 a0001c0001t0003g0074 others(1): Show |
4 | HG01169.hp2 HG02572.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.107-1576A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15491213 | |||||||
| chr3:15491349 | C | G | 3 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 |
3 | HG00733.hp1 HG00738.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.107-1712G>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15491349 | |||||||
| chr3:15491425 | G | C | 2 | a0001c0001t0001g0114 a0001c0001t0001g0147 |
2 | HG03139.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.107-1788C>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15491425 | |||||||
| chr3:15491469 | C | T | 1 | a0001c0001t0013g0328 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.107-1832G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15491469 | |||||||
| chr3:15491639 | C | T | 4 | a0001c0001t0001g0329 a0001c0001t0001g0330 a0001c0001t0010g0342 others(1): Show |
4 | HG01081.hp2 HG02647.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.107-2002G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15491639 | |||||||
| chr3:15491726 | A | G | 10 | a0001c0001t0001g0248 a0001c0001t0001g0260 a0002c0002t0005g0020 others(7): Show |
12 | HG01884.hp1 HG02109.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.107-2089T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15491726 | |||||||
| chr3:15491828 | G | A | 5 | a0001c0001t0002g0245 a0001c0001t0002g0343 a0001c0003t0004g0272 others(2): Show |
5 | HG00544.hp2 HG01884.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.107-2191C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15491828 | |||||||
| chr3:15491893 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.107-2256T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15491893 | |||||||
| chr3:15491963 | C | A | 100 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(97): Show |
120 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.107-2326G>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15491963 | |||||||
| chr3:15492056 | C | CA | 30 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(27): Show |
37 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.107-2420dupT | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15492056 | |||||||
| chr3:15492056 | CA | C | 43 | a0001c0001t0001g0274 a0001c0001t0001g0308 a0001c0001t0001g0310 others(40): Show |
46 | HG00280.hp1 HG00544.hp1 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.107-2420delT | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15492056 | |||||||
| chr3:15492121 | C | T | 14 | a0001c0001t0001g0338 a0001c0003t0004g0028 a0001c0003t0004g0121 others(11): Show |
15 | HG01109.hp2 HG01168.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.107-2484G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15492121 | |||||||
| chr3:15492195 | T | C | 5 | a0001c0001t0001g0189 a0001c0001t0001g0238 a0001c0001t0001g0239 others(2): Show |
5 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.107-2558A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15492195 | |||||||
| chr3:15492533 | G | A | 1 | a0001c0001t0001g0235 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.107-2896C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15492533 | |||||||
| chr3:15492534 | G | A | 1 | a0001c0001t0010g0342 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.107-2897C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15492534 | |||||||
| chr3:15492591 | C | T | 1 | a0001c0001t0016g0255 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.107-2954G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15492591 | |||||||
| chr3:15492666 | CA | C | 175 | a0001c0001t0001g0248 a0001c0001t0001g0260 a0001c0001t0001g0262 others(172): Show |
197 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(194): Show |
intron_variant | MODIFIER | c.107-3030delT | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15492666 | |||||||
| chr3:15492692 | A | G | 75 | a0001c0001t0002g0024 a0001c0001t0002g0242 a0001c0001t0002g0267 others(72): Show |
89 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.107-3055T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15492692 | |||||||
| chr3:15492847 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.107-3210G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15492847 | |||||||
| chr3:15492925 | TG | T | 2 | a0001c0001t0003g0003 a0001c0001t0003g0063 |
4 | NA18945.hp2 NA18973.hp1 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.107-3289delC | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15492925 | |||||||
| chr3:15493210 | G | A | 25 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(22): Show |
31 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.107-3573C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15493210 | |||||||
| chr3:15493246 | G | A | 5 | a0001c0001t0002g0245 a0001c0001t0002g0343 a0001c0003t0004g0272 others(2): Show |
5 | HG00544.hp2 HG01884.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.107-3609C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15493246 | |||||||
| chr3:15493268 | C | T | 2 | a0001c0001t0010g0259 a0001c0001t0016g0255 |
2 | HG03041.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.107-3631G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15493268 | |||||||
| chr3:15493288 | A | G | 1 | a0001c0001t0001g0169 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.107-3651T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15493288 | |||||||
| chr3:15493366 | C | T | 1 | a0001c0001t0003g0034 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.107-3729G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15493366 | |||||||
| chr3:15493400 | T | C | 1 | a0001c0001t0013g0328 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.107-3763A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15493400 | |||||||
| chr3:15493526 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.107-3889G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15493526 | |||||||
| chr3:15493675 | C | T | 25 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(22): Show |
31 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.107-4038G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15493675 | |||||||
| chr3:15493680 | G | A | 4 | a0001c0001t0001g0329 a0001c0001t0001g0330 a0001c0001t0010g0342 others(1): Show |
4 | HG01081.hp2 HG02647.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.107-4043C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15493680 | |||||||
| chr3:15493693 | C | T | 2 | a0001c0001t0001g0140 a0001c0001t0001g0141 |
2 | HG00733.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.107-4056G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15493693 | |||||||
| chr3:15493694 | C | A | 1 | a0001c0001t0001g0144 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.107-4057G>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15493694 | |||||||
| chr3:15493809 | C | T | 2 | a0001c0001t0001g0236 a0001c0008t0001g0190 |
2 | NA18612.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.107-4172G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15493809 | |||||||
| chr3:15493904 | G | A | 2 | a0001c0001t0002g0343 a0001c0003t0004g0272 |
2 | HG01884.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.107-4267C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15493904 | |||||||
| chr3:15493944 | G | A | 1 | a0001c0001t0010g0342 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.107-4307C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15493944 | |||||||
| chr3:15494198 | G | C | 1 | a0001c0001t0001g0094 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.107-4561C>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15494198 | |||||||
| chr3:15494314 | C | T | 100 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(97): Show |
120 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.107-4677G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15494314 | |||||||
| chr3:15494315 | G | A | 5 | a0001c0001t0002g0245 a0001c0001t0002g0343 a0001c0003t0004g0272 others(2): Show |
5 | HG00544.hp2 HG01884.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.107-4678C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15494315 | |||||||
| chr3:15494347 | C | T | 5 | a0001c0001t0002g0245 a0001c0001t0002g0343 a0001c0003t0004g0272 others(2): Show |
5 | HG00544.hp2 HG01884.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.107-4710G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15494347 | |||||||
| chr3:15494403 | G | A | 53 | a0001c0001t0001g0274 a0001c0001t0001g0308 a0001c0001t0001g0310 others(50): Show |
56 | HG00280.hp1 HG00544.hp1 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.107-4766C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15494403 | |||||||
| chr3:15494412 | T | C | 25 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(22): Show |
31 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.107-4775A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15494412 | |||||||
| chr3:15494513 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.107-4876C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15494513 | |||||||
| chr3:15494519 | G | C | 1 | a0001c0001t0012g0268 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.107-4882C>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15494519 | |||||||
| chr3:15494536 | G | A | 1 | a0001c0001t0001g0274 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.107-4899C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15494536 | |||||||
| chr3:15494556 | A | G | 14 | a0001c0001t0001g0338 a0001c0003t0004g0028 a0001c0003t0004g0121 others(11): Show |
15 | HG01109.hp2 HG01168.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.107-4919T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15494556 | |||||||
| chr3:15494565 | T | C | 74 | a0001c0001t0002g0024 a0001c0001t0002g0242 a0001c0001t0002g0267 others(71): Show |
88 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.107-4928A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15494565 | |||||||
| chr3:15494567 | G | A | 1 | a0001c0001t0003g0049 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.107-4930C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15494567 | |||||||
| chr3:15494814 | A | C | 25 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(22): Show |
31 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.107-5177T>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15494814 | |||||||
| chr3:15495127 | G | A | 76 | a0001c0001t0001g0096 a0001c0001t0002g0024 a0001c0001t0002g0242 others(73): Show |
90 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.107-5490C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15495127 | |||||||
| chr3:15495199 | G | A | 24 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(21): Show |
30 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.107-5562C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15495199 | |||||||
| chr3:15495326 | G | T | 208 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(205): Show |
236 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(233): Show |
intron_variant | MODIFIER | c.107-5689C>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15495326 | |||||||
| chr3:15495391 | C | T | 1 | a0001c0001t0001g0104 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.107-5754G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15495391 | |||||||
| chr3:15495504 | T | C | 1 | a0001c0001t0001g0308 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.107-5867A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15495504 | |||||||
| chr3:15495622 | A | T | 198 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(195): Show |
226 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(223): Show |
intron_variant | MODIFIER | c.107-5985T>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15495622 | |||||||
| chr3:15495733 | G | T | 1 | a0001c0001t0003g0066 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.107-6096C>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15495733 | |||||||
| chr3:15495746 | C | A | 2 | a0001c0001t0002g0016 a0001c0001t0015g0116 |
3 | HG02615.hp1 HG02809.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.107-6109G>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15495746 | |||||||
| chr3:15496010 | A | G | 1 | a0002c0002t0005g0266 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.107-6373T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15496010 | |||||||
| chr3:15496188 | C | T | 4 | a0001c0001t0003g0003 a0001c0001t0003g0063 a0001c0001t0003g0065 others(1): Show |
6 | NA18612.hp1 NA18945.hp2 NA18973.hp1 others(3): Show |
intron_variant | MODIFIER | c.107-6551G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15496188 | |||||||
| chr3:15496217 | T | A | 1 | a0001c0001t0001g0310 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.107-6580A>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15496217 | |||||||
| chr3:15496218 | C | G | 1 | a0001c0001t0001g0115 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.107-6581G>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15496218 | |||||||
| chr3:15496269 | A | G | 6 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0238 others(3): Show |
6 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.107-6632T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15496269 | |||||||
| chr3:15496411 | A | G | 6 | a0001c0001t0001g0118 a0001c0001t0001g0224 a0001c0001t0001g0225 others(3): Show |
7 | HG02027.hp2 HG02040.hp2 HG02080.hp2 others(4): Show |
intron_variant | MODIFIER | c.107-6774T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15496411 | |||||||
| chr3:15496484 | T | C | 100 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(97): Show |
120 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.107-6847A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15496484 | |||||||
| chr3:15496485 | A | G | 154 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(151): Show |
179 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(176): Show |
intron_variant | MODIFIER | c.107-6848T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15496485 | |||||||
| chr3:15496486 | T | C | 1 | a0001c0001t0001g0326 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.107-6849A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15496486 | |||||||
| chr3:15496665 | C | T | 5 | a0002c0002t0008g0269 a0002c0002t0008g0270 a0002c0002t0008g0271 others(2): Show |
6 | HG02970.hp2 HG02976.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.107-7028G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15496665 | |||||||
| chr3:15496733 | A | T | 100 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(97): Show |
120 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.107-7096T>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15496733 | |||||||
| chr3:15496951 | A | G | 4 | a0001c0001t0001g0329 a0001c0001t0001g0330 a0001c0001t0010g0342 others(1): Show |
4 | HG01081.hp2 HG02647.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.107-7314T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15496951 | |||||||
| chr3:15496970 | T | C | 71 | a0001c0001t0001g0248 a0001c0001t0001g0260 a0001c0001t0001g0262 others(68): Show |
77 | HG00280.hp1 HG00544.hp1 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.107-7333A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15496970 | |||||||
| chr3:15497034 | GC | G | 2 | a0001c0001t0003g0009 a0001c0001t0003g0049 |
3 | HG02738.hp2 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.107-7398delG | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15497034 | |||||||
| chr3:15497036 | C | CT | 49 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(46): Show |
56 | HG00639.hp1 HG00673.hp2 HG01106.hp2 others(53): Show |
intron_variant | MODIFIER | c.107-7400dupA | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15497036 | |||||||
| chr3:15497036 | C | CTT | 7 | a0001c0001t0001g0093 a0001c0001t0001g0097 a0001c0001t0001g0099 others(4): Show |
7 | HG01168.hp1 HG02055.hp1 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.107-7401_107-7400d others(4): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15497036 | |||||||
| chr3:15497036 | C | CTTT | 14 | a0001c0001t0001g0329 a0001c0001t0001g0330 a0001c0001t0002g0245 others(11): Show |
15 | HG00544.hp2 HG01081.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.107-7402_107-7400d others(5): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15497036 | |||||||
| chr3:15497036 | CT | C | 6 | a0001c0001t0001g0137 a0001c0001t0001g0213 a0001c0001t0001g0232 others(3): Show |
6 | HG01943.hp2 HG01993.hp2 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.107-7400delA | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15497036 | |||||||
| chr3:15497036 | CTTTTTTT | C | 12 | a0001c0001t0001g0248 a0001c0001t0001g0260 a0002c0002t0005g0020 others(9): Show |
14 | HG01884.hp1 HG02109.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.107-7406_107-7400d others(9): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15497036 | |||||||
| chr3:15497036 | CTTTTTTT others(1): Show |
C | 58 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0274 others(55): Show |
62 | HG00280.hp1 HG00544.hp1 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.107-7407_107-7400d others(10): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15497036 | |||||||
| chr3:15497132 | C | T | 1 | a0001c0001t0003g0047 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.107-7495G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15497132 | |||||||
| chr3:15497172 | C | T | 1 | a0001c0001t0001g0182 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.107-7535G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15497172 | |||||||
| chr3:15497207 | C | T | 1 | a0001c0001t0002g0129 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.107-7570G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15497207 | |||||||
| chr3:15497263 | T | C | 198 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(195): Show |
226 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(223): Show |
intron_variant | MODIFIER | c.107-7626A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15497263 | |||||||
| chr3:15497518 | G | A | 1 | a0001c0001t0002g0309 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.107-7881C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15497518 | |||||||
| chr3:15497739 | C | T | 10 | a0001c0001t0003g0008 a0001c0001t0003g0029 a0001c0001t0003g0039 others(7): Show |
11 | HG00558.hp2 HG00609.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.107-8102G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15497739 | |||||||
| chr3:15498186 | G | A | 5 | a0002c0002t0008g0269 a0002c0002t0008g0270 a0002c0002t0008g0271 others(2): Show |
6 | HG02970.hp2 HG02976.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.107-8549C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15498186 | |||||||
| chr3:15498263 | T | C | 335 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(332): Show |
373 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(370): Show |
intron_variant | MODIFIER | c.107-8626A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15498263 | |||||||
| chr3:15498469 | C | CCA | 5 | a0001c0001t0001g0329 a0001c0001t0001g0330 a0001c0001t0010g0342 others(2): Show |
5 | HG01081.hp2 HG02647.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.107-8834_107-8833d others(4): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15498469 | |||||||
| chr3:15498469 | C | CCACA | 77 | a0001c0001t0001g0274 a0001c0001t0002g0024 a0001c0001t0002g0242 others(74): Show |
91 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.107-8836_107-8833d others(6): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15498469 | |||||||
| chr3:15498469 | C | CCACACA | 86 | a0001c0001t0001g0248 a0001c0001t0001g0260 a0001c0001t0001g0262 others(83): Show |
92 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.107-8838_107-8833d others(8): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15498469 | |||||||
| chr3:15498469 | C | CCACACAC others(1): Show |
34 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(31): Show |
42 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.107-8840_107-8833d others(10): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15498469 | |||||||
| chr3:15498496 | C | T | 1 | a0001c0001t0001g0100 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.107-8859G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15498496 | |||||||
| chr3:15498641 | T | G | 76 | a0001c0001t0002g0024 a0001c0001t0002g0242 a0001c0001t0002g0267 others(73): Show |
90 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.107-9004A>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15498641 | |||||||
| chr3:15498649 | G | A | 3 | a0002c0002t0008g0269 a0002c0002t0008g0270 a0002c0002t0008g0271 |
3 | HG02970.hp2 HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.107-9012C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15498649 | |||||||
| chr3:15498930 | A | ATCAG | 198 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(195): Show |
226 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(223): Show |
intron_variant | MODIFIER | c.107-9294_107-9293i others(6): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15498930 | |||||||
| chr3:15498966 | A | C | 198 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(195): Show |
226 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(223): Show |
intron_variant | MODIFIER | c.107-9329T>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15498966 | |||||||
| chr3:15499026 | C | A | 3 | a0001c0001t0002g0245 a0004c0006t0004g0244 a0004c0006t0004g0246 |
3 | HG00544.hp2 NA18972.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.107-9389G>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15499026 | |||||||
| chr3:15499334 | T | C | 3 | a0002c0002t0008g0269 a0002c0002t0008g0270 a0002c0002t0008g0271 |
3 | HG02970.hp2 HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.107-9697A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15499334 | |||||||
| chr3:15499530 | T | G | 198 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(195): Show |
226 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(223): Show |
intron_variant | MODIFIER | c.107-9893A>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15499530 | |||||||
| chr3:15499555 | A | G | 53 | a0001c0001t0001g0274 a0001c0001t0001g0277 a0001c0001t0001g0308 others(50): Show |
56 | HG00280.hp1 HG00544.hp1 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.107-9918T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15499555 | |||||||
| chr3:15499609 | T | C | 1 | a0001c0001t0001g0310 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.107-9972A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15499609 | |||||||
| chr3:15499707 | T | C | 101 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(98): Show |
121 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.107-10070A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15499707 | |||||||
| chr3:15499743 | C | G | 1 | a0001c0001t0001g0321 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.107-10106G>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15499743 | |||||||
| chr3:15499822 | G | A | 3 | a0002c0002t0008g0269 a0002c0002t0008g0270 a0002c0002t0008g0271 |
3 | HG02970.hp2 HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.107-10185C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15499822 | |||||||
| chr3:15500334 | T | C | 1 | a0001c0001t0012g0268 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.107-10697A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15500334 | |||||||
| chr3:15500334 | T | G | 3 | a0002c0002t0008g0269 a0002c0002t0008g0270 a0002c0002t0008g0271 |
3 | HG02970.hp2 HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.107-10697A>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15500334 | |||||||
| chr3:15500483 | T | C | 2 | a0003c0004t0002g0257 a0003c0004t0002g0258 |
2 | HG02622.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.107-10846A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15500483 | |||||||
| chr3:15500624 | G | T | 1 | a0001c0001t0001g0178 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.107-10987C>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15500624 | |||||||
| chr3:15500783 | C | T | 94 | a0001c0001t0001g0248 a0001c0001t0001g0260 a0001c0001t0001g0262 others(91): Show |
102 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.107-11146G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15500783 | |||||||
| chr3:15500883 | C | A | 2 | a0001c0001t0002g0319 a0001c0001t0002g0320 |
2 | NA18952.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.107-11246G>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15500883 | |||||||
| chr3:15500905 | T | C | 14 | a0001c0001t0001g0248 a0001c0001t0001g0260 a0001c0001t0010g0259 others(11): Show |
17 | HG01884.hp1 HG02109.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.107-11268A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15500905 | |||||||
| chr3:15501155 | A | G | 1 | a0001c0001t0002g0153 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.107-11518T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15501155 | |||||||
| chr3:15501220 | A | T | 3 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 |
3 | NA18957.hp2 NA18997.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.107-11583T>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15501220 | |||||||
| chr3:15501250 | G | T | 1 | a0001c0001t0001g0178 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.107-11613C>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15501250 | |||||||
| chr3:15501253 | C | G | 1 | a0001c0001t0001g0177 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.107-11616G>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15501253 | |||||||
| chr3:15501266 | C | T | 97 | a0001c0001t0001g0248 a0001c0001t0001g0260 a0001c0001t0001g0262 others(94): Show |
105 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.107-11629G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15501266 | |||||||
| chr3:15501335 | G | A | 1 | a0001c0001t0006g0059 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.107-11698C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15501335 | |||||||
| chr3:15501629 | G | A | 89 | a0001c0001t0001g0248 a0001c0001t0001g0260 a0001c0001t0001g0262 others(86): Show |
97 | HG00280.hp1 HG00544.hp1 HG00609.hp2 others(94): Show |
intron_variant | MODIFIER | c.107-11992C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15501629 | |||||||
| chr3:15501655 | G | A | 1 | a0002c0002t0005g0252 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.107-12018C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15501655 | |||||||
| chr3:15501685 | C | T | 3 | a0001c0001t0002g0245 a0004c0006t0004g0244 a0004c0006t0004g0246 |
3 | HG00544.hp2 NA18972.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.107-12048G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15501685 | |||||||
| chr3:15502113 | A | AT | 96 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0018 others(93): Show |
106 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.107-12477dupA | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15502113 | |||||||
| chr3:15502113 | AT | A | 99 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(96): Show |
112 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.107-12477delA | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15502113 | |||||||
| chr3:15502113 | ATTT | A | 73 | a0001c0001t0002g0024 a0001c0001t0002g0242 a0001c0001t0002g0267 others(70): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.107-12479_107-1247 others(7): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15502113 | |||||||
| chr3:15502167 | GTGCAATG others(17): Show |
G | 1 | a0001c0001t0001g0138 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.107-12554_107-1253 others(28): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15502167 | |||||||
| chr3:15502208 | C | T | 14 | a0001c0001t0001g0338 a0001c0003t0004g0028 a0001c0003t0004g0121 others(11): Show |
15 | HG01109.hp2 HG01168.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.107-12571G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15502208 | |||||||
| chr3:15502240 | G | C | 202 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(199): Show |
230 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(227): Show |
intron_variant | MODIFIER | c.107-12603C>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15502240 | |||||||
| chr3:15502296 | T | C | 2 | a0002c0002t0005g0253 a0002c0002t0005g0254 |
2 | HG02109.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.107-12659A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15502296 | |||||||
| chr3:15502331 | G | A | 1 | a0001c0001t0003g0077 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.107-12694C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15502331 | |||||||
| chr3:15502439 | A | G | 101 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(98): Show |
121 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.107-12802T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15502439 | |||||||
| chr3:15502836 | T | C | 51 | a0001c0001t0001g0274 a0001c0001t0001g0277 a0001c0001t0001g0308 others(48): Show |
54 | HG00280.hp1 HG00544.hp1 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.107-13199A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15502836 | |||||||
| chr3:15503022 | G | A | 72 | a0001c0001t0001g0248 a0001c0001t0001g0260 a0001c0001t0001g0262 others(69): Show |
79 | HG00280.hp1 HG00544.hp1 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.107-13385C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15503022 | |||||||
| chr3:15503031 | C | A | 1 | a0001c0001t0003g0078 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.107-13394G>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15503031 | |||||||
| chr3:15503040 | C | T | 1 | a0003c0004t0002g0247 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.107-13403G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15503040 | |||||||
| chr3:15503121 | C | G | 1 | a0001c0001t0001g0144 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.107-13484G>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15503121 | |||||||
| chr3:15503148 | T | C | 1 | a0001c0003t0004g0311 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.107-13511A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15503148 | |||||||
| chr3:15503246 | A | G | 1 | a0001c0003t0004g0327 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.107-13609T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15503246 | |||||||
| chr3:15503261 | C | T | 4 | a0001c0001t0010g0259 a0001c0001t0016g0255 a0003c0004t0002g0022 others(1): Show |
5 | HG03041.hp1 HG03209.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.107-13624G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15503261 | |||||||
| chr3:15503288 | C | T | 3 | a0002c0002t0008g0269 a0002c0002t0008g0270 a0002c0002t0008g0271 |
3 | HG02970.hp2 HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.107-13651G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15503288 | |||||||
| chr3:15503310 | GC | G | 2 | a0001c0001t0002g0025 a0001c0001t0002g0287 |
3 | HG00544.hp1 NA18942.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.107-13674delG | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15503310 | |||||||
| chr3:15503410 | T | C | 1 | a0001c0001t0001g0176 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.107-13773A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15503410 | |||||||
| chr3:15503423 | G | T | 1 | a0001c0001t0013g0328 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.107-13786C>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15503423 | |||||||
| chr3:15503484 | C | T | 6 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0135 others(3): Show |
6 | HG01106.hp2 HG01243.hp1 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.107-13847G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15503484 | |||||||
| chr3:15503598 | C | T | 89 | a0001c0001t0001g0248 a0001c0001t0001g0260 a0001c0001t0001g0262 others(86): Show |
97 | HG00280.hp1 HG00544.hp1 HG00609.hp2 others(94): Show |
intron_variant | MODIFIER | c.107-13961G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15503598 | |||||||
| chr3:15503703 | C | T | 10 | a0001c0001t0001g0018 a0001c0001t0001g0148 a0001c0001t0001g0170 others(7): Show |
11 | HG00735.hp1 HG01256.hp2 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.107-14066G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15503703 | |||||||
| chr3:15503755 | G | A | 4 | a0001c0001t0001g0329 a0001c0001t0001g0330 a0001c0001t0010g0342 others(1): Show |
4 | HG01081.hp2 HG02647.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.107-14118C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15503755 | |||||||
| chr3:15503803 | A | C | 2 | a0001c0001t0002g0343 a0001c0003t0004g0272 |
2 | HG01884.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.107-14166T>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15503803 | |||||||
| chr3:15503968 | C | G | 76 | a0001c0001t0002g0024 a0001c0001t0002g0242 a0001c0001t0002g0267 others(73): Show |
90 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.107-14331G>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15503968 | |||||||
| chr3:15504147 | T | A | 1 | a0001c0001t0010g0342 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.107-14510A>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15504147 | |||||||
| chr3:15504212 | G | A | 1 | a0001c0001t0002g0163 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.107-14575C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15504212 | |||||||
| chr3:15504230 | C | T | 1 | a0001c0001t0002g0098 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.107-14593G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15504230 | |||||||
| chr3:15504349 | C | T | 25 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(22): Show |
31 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.107-14712G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15504349 | |||||||
| chr3:15504363 | C | G | 3 | a0001c0001t0002g0245 a0004c0006t0004g0244 a0004c0006t0004g0246 |
3 | HG00544.hp2 NA18972.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.107-14726G>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15504363 | |||||||
| chr3:15504391 | T | C | 14 | a0001c0001t0001g0248 a0001c0001t0001g0260 a0001c0001t0010g0259 others(11): Show |
17 | HG01884.hp1 HG02109.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.107-14754A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15504391 | |||||||
| chr3:15504456 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.107-14819C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15504456 | |||||||
| chr3:15504568 | T | C | 1 | a0001c0001t0001g0223 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.107-14931A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15504568 | |||||||
| chr3:15504596 | T | C | 198 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(195): Show |
226 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(223): Show |
intron_variant | MODIFIER | c.107-14959A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15504596 | |||||||
| chr3:15504639 | A | T | 29 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0010 others(26): Show |
32 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.107-15002T>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15504639 | |||||||
| chr3:15504841 | T | C | 5 | a0001c0001t0002g0245 a0001c0001t0002g0343 a0001c0003t0004g0272 others(2): Show |
5 | HG00544.hp2 HG01884.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.107-15204A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15504841 | |||||||
| chr3:15505061 | A | T | 5 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0002g0023 others(2): Show |
6 | HG01168.hp2 HG01169.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.107-15424T>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15505061 | |||||||
| chr3:15505135 | C | T | 3 | a0001c0001t0002g0245 a0004c0006t0004g0244 a0004c0006t0004g0246 |
3 | HG00544.hp2 NA18972.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.107-15498G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15505135 | |||||||
| chr3:15505334 | C | T | 1 | a0001c0001t0002g0286 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.107-15697G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15505334 | |||||||
| chr3:15505361 | G | A | 201 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(198): Show |
229 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(226): Show |
intron_variant | MODIFIER | c.107-15724C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15505361 | |||||||
| chr3:15505363 | G | A | 194 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(191): Show |
222 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(219): Show |
intron_variant | MODIFIER | c.107-15726C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15505363 | |||||||
| chr3:15505642 | C | T | 1 | a0003c0004t0002g0247 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.106+15878G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15505642 | |||||||
| chr3:15505694 | C | A | 1 | a0001c0001t0001g0223 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.106+15826G>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15505694 | |||||||
| chr3:15505738 | C | CA | 3 | a0002c0002t0008g0269 a0002c0002t0008g0270 a0002c0002t0008g0271 |
3 | HG02970.hp2 HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.106+15781dupT | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15505738 | |||||||
| chr3:15505803 | C | T | 94 | a0001c0001t0001g0248 a0001c0001t0001g0260 a0001c0001t0001g0262 others(91): Show |
102 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.106+15717G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15505803 | |||||||
| chr3:15506100 | G | T | 1 | a0001c0001t0001g0144 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.106+15420C>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15506100 | |||||||
| chr3:15506254 | T | G | 51 | a0001c0001t0001g0274 a0001c0001t0001g0277 a0001c0001t0001g0308 others(48): Show |
54 | HG00280.hp1 HG00544.hp1 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.106+15266A>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15506254 | |||||||
| chr3:15506357 | T | A | 197 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(194): Show |
225 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(222): Show |
intron_variant | MODIFIER | c.106+15163A>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15506357 | |||||||
| chr3:15506389 | C | T | 1 | a0001c0001t0001g0260 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.106+15131G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15506389 | |||||||
| chr3:15506463 | C | T | 201 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(198): Show |
229 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(226): Show |
intron_variant | MODIFIER | c.106+15057G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15506463 | |||||||
| chr3:15506480 | A | T | 5 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0001g0240 others(2): Show |
5 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.106+15040T>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15506480 | |||||||
| chr3:15506584 | T | C | 4 | a0001c0001t0002g0024 a0001c0001t0002g0267 a0001c0001t0003g0014 others(1): Show |
6 | HG01099.hp1 HG01934.hp2 HG02273.hp1 others(3): Show |
intron_variant | MODIFIER | c.106+14936A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15506584 | |||||||
| chr3:15506624 | A | G | 197 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(194): Show |
225 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(222): Show |
intron_variant | MODIFIER | c.106+14896T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15506624 | |||||||
| chr3:15506652 | C | T | 1 | a0003c0004t0002g0247 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.106+14868G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15506652 | |||||||
| chr3:15506720 | G | A | 75 | a0001c0001t0002g0024 a0001c0001t0002g0267 a0001c0001t0003g0003 others(72): Show |
89 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.106+14800C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15506720 | |||||||
| chr3:15506721 | C | A | 1 | a0001c0003t0004g0340 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.106+14799G>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15506721 | |||||||
| chr3:15506734 | C | T | 5 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0002g0129 others(2): Show |
5 | HG01256.hp1 HG02300.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.106+14786G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15506734 | |||||||
| chr3:15506944 | T | C | 103 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(100): Show |
123 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.106+14576A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15506944 | |||||||
| chr3:15507079 | C | G | 197 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(194): Show |
225 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(222): Show |
intron_variant | MODIFIER | c.106+14441G>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15507079 | |||||||
| chr3:15507091 | G | A | 9 | a0001c0001t0001g0118 a0001c0001t0001g0224 a0001c0001t0001g0225 others(6): Show |
10 | HG02027.hp2 HG02040.hp2 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.106+14429C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15507091 | |||||||
| chr3:15507267 | C | G | 1 | a0001c0001t0001g0096 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.106+14253G>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15507267 | |||||||
| chr3:15507375 | G | A | 4 | a0001c0001t0002g0312 a0001c0001t0002g0313 a0001c0001t0002g0314 others(1): Show |
4 | NA18987.hp1 NA19009.hp2 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.106+14145C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15507375 | |||||||
| chr3:15507550 | G | A | 5 | a0001c0001t0001g0119 a0001c0001t0001g0229 a0001c0001t0001g0230 others(2): Show |
5 | HG01891.hp2 HG02647.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.106+13970C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15507550 | |||||||
| chr3:15507684 | G | T | 1 | a0001c0001t0001g0169 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.106+13836C>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15507684 | |||||||
| chr3:15507695 | T | C | 1 | a0001c0001t0001g0233 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.106+13825A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15507695 | |||||||
| chr3:15507834 | C | T | 12 | a0001c0001t0001g0338 a0001c0003t0004g0028 a0001c0003t0004g0121 others(9): Show |
13 | HG01109.hp2 HG01168.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.106+13686G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15507834 | |||||||
| chr3:15507886 | C | T | 197 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(194): Show |
225 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(222): Show |
intron_variant | MODIFIER | c.106+13634G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15507886 | |||||||
| chr3:15507937 | A | G | 1 | a0001c0001t0003g0038 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.106+13583T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15507937 | |||||||
| chr3:15508019 | C | T | 1 | a0001c0001t0001g0097 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.106+13501G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15508019 | |||||||
| chr3:15508020 | G | A | 1 | a0001c0001t0012g0268 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.106+13500C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15508020 | |||||||
| chr3:15508169 | C | G | 1 | a0001c0001t0010g0259 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.106+13351G>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15508169 | |||||||
| chr3:15508356 | T | C | 1 | a0001c0001t0002g0316 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.106+13164A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15508356 | |||||||
| chr3:15508398 | G | A | 197 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(194): Show |
225 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(222): Show |
intron_variant | MODIFIER | c.106+13122C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15508398 | |||||||
| chr3:15508460 | A | C | 5 | a0001c0001t0001g0237 a0001c0001t0002g0149 a0001c0001t0002g0150 others(2): Show |
5 | HG00099.hp1 HG00642.hp2 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.106+13060T>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15508460 | |||||||
| chr3:15508496 | A | G | 1 | a0001c0001t0002g0275 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.106+13024T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15508496 | |||||||
| chr3:15508715 | T | C | 25 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(22): Show |
31 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.106+12805A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15508715 | |||||||
| chr3:15508725 | G | C | 2 | a0001c0001t0001g0329 a0001c0001t0001g0330 |
2 | HG01081.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.106+12795C>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15508725 | |||||||
| chr3:15508865 | T | C | 3 | a0003c0004t0002g0247 a0003c0004t0002g0257 a0003c0004t0002g0258 |
3 | HG02622.hp2 HG03098.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.106+12655A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15508865 | |||||||
| chr3:15508872 | C | T | 25 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(22): Show |
31 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.106+12648G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15508872 | |||||||
| chr3:15509060 | A | G | 1 | a0001c0001t0003g0037 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.106+12460T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15509060 | |||||||
| chr3:15509103 | C | T | 74 | a0001c0001t0002g0024 a0001c0001t0002g0267 a0001c0001t0003g0003 others(71): Show |
88 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.106+12417G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15509103 | |||||||
| chr3:15509127 | T | A | 197 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(194): Show |
225 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(222): Show |
intron_variant | MODIFIER | c.106+12393A>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15509127 | |||||||
| chr3:15509133 | G | A | 3 | a0002c0002t0008g0269 a0002c0002t0008g0270 a0002c0002t0008g0271 |
3 | HG02970.hp2 HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.106+12387C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15509133 | |||||||
| chr3:15509184 | A | G | 1 | a0001c0001t0001g0248 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.106+12336T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15509184 | |||||||
| chr3:15509190 | A | C | 84 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0274 others(81): Show |
90 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.106+12330T>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15509190 | |||||||
| chr3:15509232 | GGCCTGGT others(15): Show |
G | 1 | a0001c0001t0003g0089 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.106+12266_106+1228 others(26): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15509232 | |||||||
| chr3:15509572 | C | T | 25 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(22): Show |
31 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.106+11948G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15509572 | |||||||
| chr3:15509673 | T | C | 3 | a0001c0001t0002g0245 a0004c0006t0004g0244 a0004c0006t0004g0246 |
3 | HG00544.hp2 NA18972.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.106+11847A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15509673 | |||||||
| chr3:15509703 | A | G | 1 | a0001c0001t0001g0236 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.106+11817T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15509703 | |||||||
| chr3:15509708 | C | T | 25 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(22): Show |
31 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.106+11812G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15509708 | |||||||
| chr3:15509764 | G | C | 2 | a0001c0001t0001g0120 a0001c0001t0001g0234 |
2 | NA18966.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.106+11756C>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15509764 | |||||||
| chr3:15509792 | T | C | 3 | a0002c0002t0008g0269 a0002c0002t0008g0270 a0002c0002t0008g0271 |
3 | HG02970.hp2 HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.106+11728A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15509792 | |||||||
| chr3:15509799 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.106+11721A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15509799 | |||||||
| chr3:15509912 | C | T | 2 | a0001c0001t0002g0149 a0001c0001t0002g0150 |
2 | HG04115.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.106+11608G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15509912 | |||||||
| chr3:15510037 | G | A | 75 | a0001c0001t0002g0024 a0001c0001t0002g0267 a0001c0001t0003g0003 others(72): Show |
89 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.106+11483C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15510037 | |||||||
| chr3:15510045 | G | A | 75 | a0001c0001t0002g0024 a0001c0001t0002g0267 a0001c0001t0003g0003 others(72): Show |
89 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.106+11475C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15510045 | |||||||
| chr3:15510093 | G | A | 1 | a0001c0001t0013g0328 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.106+11427C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15510093 | |||||||
| chr3:15510099 | C | G | 2 | a0003c0004t0002g0257 a0003c0004t0002g0258 |
2 | HG02622.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.106+11421G>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15510099 | |||||||
| chr3:15510181 | A | C | 3 | a0001c0001t0003g0034 a0001c0001t0003g0035 a0001c0001t0003g0036 |
3 | HG01981.hp2 HG01993.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.106+11339T>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15510181 | |||||||
| chr3:15510332 | T | C | 100 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(97): Show |
120 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.106+11188A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15510332 | |||||||
| chr3:15510407 | A | G | 3 | a0002c0002t0008g0269 a0002c0002t0008g0270 a0002c0002t0008g0271 |
3 | HG02970.hp2 HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.106+11113T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15510407 | |||||||
| chr3:15510414 | G | T | 1 | a0001c0001t0003g0033 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.106+11106C>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15510414 | |||||||
| chr3:15510484 | G | A | 75 | a0001c0001t0002g0024 a0001c0001t0002g0267 a0001c0001t0003g0003 others(72): Show |
89 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.106+11036C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15510484 | |||||||
| chr3:15510490 | C | CT | 201 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(198): Show |
229 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(226): Show |
intron_variant | MODIFIER | c.106+11029dupA | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15510490 | |||||||
| chr3:15510550 | A | C | 7 | a0001c0001t0002g0281 a0001c0001t0002g0282 a0001c0001t0002g0283 others(4): Show |
7 | NA18944.hp1 NA18952.hp1 NA18961.hp2 others(4): Show |
intron_variant | MODIFIER | c.106+10970T>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15510550 | |||||||
| chr3:15510563 | C | T | 100 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(97): Show |
120 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.106+10957G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15510563 | |||||||
| chr3:15510641 | G | A | 1 | a0001c0001t0002g0317 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.106+10879C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15510641 | |||||||
| chr3:15510708 | AAGGGGAC others(8): Show |
A | 1 | a0001c0001t0001g0235 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.106+10797_106+1081 others(19): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15510708 | |||||||
| chr3:15510752 | G | T | 94 | a0001c0001t0001g0248 a0001c0001t0001g0260 a0001c0001t0001g0262 others(91): Show |
102 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.106+10768C>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15510752 | |||||||
| chr3:15510808 | C | G | 194 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(191): Show |
222 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(219): Show |
intron_variant | MODIFIER | c.106+10712G>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15510808 | |||||||
| chr3:15510858 | A | AGAAG | 42 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(39): Show |
49 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.106+10658_106+1066 others(8): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15510858 | |||||||
| chr3:15510858 | A | AGAAGGAA others(13): Show |
3 | a0001c0001t0002g0245 a0004c0006t0004g0244 a0004c0006t0004g0246 |
3 | HG00544.hp2 NA18972.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.106+10642_106+1066 others(24): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15510858 | |||||||
| chr3:15510858 | AGAAG | A | 72 | a0001c0001t0001g0248 a0001c0001t0001g0260 a0001c0001t0001g0262 others(69): Show |
79 | HG00280.hp1 HG00544.hp1 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.106+10658_106+1066 others(8): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15510858 | |||||||
| chr3:15510858 | AGAAGGAA others(1): Show |
A | 3 | a0002c0002t0008g0269 a0002c0002t0008g0270 a0002c0002t0008g0271 |
3 | HG02970.hp2 HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.106+10654_106+1066 others(12): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15510858 | |||||||
| chr3:15511072 | T | C | 1 | a0001c0001t0001g0128 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.106+10448A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15511072 | |||||||
| chr3:15511244 | C | T | 4 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 others(1): Show |
4 | NA18948.hp1 NA18960.hp2 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.106+10276G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15511244 | |||||||
| chr3:15511277 | G | A | 75 | a0001c0001t0002g0024 a0001c0001t0002g0267 a0001c0001t0003g0003 others(72): Show |
89 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.106+10243C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15511277 | |||||||
| chr3:15511641 | G | T | 4 | a0001c0001t0001g0329 a0001c0001t0001g0330 a0001c0001t0010g0342 others(1): Show |
4 | HG01081.hp2 HG02647.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.106+9879C>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15511641 | |||||||
| chr3:15511719 | A | C | 1 | a0001c0001t0002g0023 | 2 | HG03710.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.106+9801T>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15511719 | |||||||
| chr3:15511749 | C | T | 201 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(198): Show |
228 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(225): Show |
intron_variant | MODIFIER | c.106+9771G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15511749 | |||||||
| chr3:15511814 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.106+9706G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15511814 | |||||||
| chr3:15512082 | T | C | 25 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(22): Show |
31 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.106+9438A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15512082 | |||||||
| chr3:15512170 | G | C | 98 | a0001c0001t0001g0248 a0001c0001t0001g0260 a0001c0001t0001g0262 others(95): Show |
106 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.106+9350C>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15512170 | |||||||
| chr3:15512230 | G | A | 9 | a0001c0001t0001g0329 a0001c0001t0001g0330 a0001c0001t0002g0245 others(6): Show |
9 | HG00544.hp2 HG01081.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.106+9290C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15512230 | |||||||
| chr3:15512242 | T | G | 2 | a0001c0001t0001g0144 a0006c0009t0001g0344 |
2 | HG00639.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.106+9278A>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15512242 | |||||||
| chr3:15512274 | G | A | 100 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(97): Show |
120 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.106+9246C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15512274 | |||||||
| chr3:15512309 | C | T | 2 | a0001c0001t0010g0342 a0001c0001t0013g0328 |
2 | HG02647.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.106+9211G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15512309 | |||||||
| chr3:15512487 | C | G | 75 | a0001c0001t0002g0024 a0001c0001t0002g0267 a0001c0001t0003g0003 others(72): Show |
89 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.106+9033G>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15512487 | |||||||
| chr3:15512505 | G | A | 1 | a0001c0001t0001g0274 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.106+9015C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15512505 | |||||||
| chr3:15512726 | T | C | 53 | a0001c0001t0001g0274 a0001c0001t0001g0277 a0001c0001t0001g0308 others(50): Show |
56 | HG00280.hp1 HG00544.hp1 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.106+8794A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15512726 | |||||||
| chr3:15512800 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.106+8720G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15512800 | |||||||
| chr3:15512949 | C | A | 3 | a0001c0001t0002g0245 a0004c0006t0004g0244 a0004c0006t0004g0246 |
3 | HG00544.hp2 NA18972.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.106+8571G>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15512949 | |||||||
| chr3:15512957 | C | T | 1 | a0001c0001t0002g0280 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.106+8563G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15512957 | |||||||
| chr3:15513119 | T | C | 75 | a0001c0001t0002g0024 a0001c0001t0002g0267 a0001c0001t0003g0003 others(72): Show |
89 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.106+8401A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15513119 | |||||||
| chr3:15513119 | T | G | 25 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(22): Show |
31 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.106+8401A>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15513119 | |||||||
| chr3:15513372 | C | T | 1 | a0001c0001t0002g0261 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.106+8148G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15513372 | |||||||
| chr3:15513492 | A | G | 1 | a0001c0001t0010g0342 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.106+8028T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15513492 | |||||||
| chr3:15513763 | G | A | 51 | a0001c0001t0001g0274 a0001c0001t0001g0277 a0001c0001t0001g0308 others(48): Show |
54 | HG00280.hp1 HG00544.hp1 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.106+7757C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15513763 | |||||||
| chr3:15513915 | C | T | 201 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(198): Show |
229 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(226): Show |
intron_variant | MODIFIER | c.106+7605G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15513915 | |||||||
| chr3:15513941 | A | C | 1 | a0001c0003t0004g0331 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.106+7579T>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15513941 | |||||||
| chr3:15514141 | G | A | 1 | a0001c0001t0002g0318 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.106+7379C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15514141 | |||||||
| chr3:15514525 | C | T | 1 | a0001c0001t0003g0032 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.106+6995G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15514525 | |||||||
| chr3:15514756 | G | A | 1 | a0001c0001t0003g0079 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.106+6764C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15514756 | |||||||
| chr3:15514795 | G | T | 1 | a0001c0001t0001g0095 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.106+6725C>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15514795 | |||||||
| chr3:15514900 | T | A | 1 | a0001c0001t0002g0343 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.106+6620A>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15514900 | |||||||
| chr3:15514935 | C | T | 7 | a0001c0001t0001g0122 a0001c0001t0001g0124 a0001c0001t0001g0126 others(4): Show |
7 | HG02109.hp2 HG02257.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.106+6585G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15514935 | |||||||
| chr3:15515087 | T | C | 11 | a0001c0001t0003g0005 a0001c0001t0003g0030 a0001c0001t0003g0080 others(8): Show |
13 | HG01433.hp2 HG01928.hp2 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.106+6433A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15515087 | |||||||
| chr3:15515120 | T | C | 1 | a0001c0001t0010g0259 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.106+6400A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15515120 | |||||||
| chr3:15515611 | C | A | 75 | a0001c0001t0002g0024 a0001c0001t0002g0267 a0001c0001t0003g0003 others(72): Show |
89 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.106+5909G>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15515611 | |||||||
| chr3:15515636 | C | T | 74 | a0001c0001t0002g0024 a0001c0001t0002g0267 a0001c0001t0003g0003 others(71): Show |
88 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.106+5884G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15515636 | |||||||
| chr3:15515667 | G | T | 1 | a0001c0001t0003g0031 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.106+5853C>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15515667 | |||||||
| chr3:15515800 | C | T | 14 | a0001c0001t0001g0338 a0001c0003t0004g0028 a0001c0003t0004g0121 others(11): Show |
15 | HG01109.hp2 HG01168.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.106+5720G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15515800 | |||||||
| chr3:15515883 | G | A | 26 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(23): Show |
32 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.106+5637C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15515883 | |||||||
| chr3:15516033 | C | T | 14 | a0001c0001t0001g0338 a0001c0003t0004g0028 a0001c0003t0004g0121 others(11): Show |
15 | HG01109.hp2 HG01168.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.106+5487G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15516033 | |||||||
| chr3:15516078 | C | A | 2 | a0001c0001t0002g0319 a0001c0001t0002g0320 |
2 | NA18952.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.106+5442G>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15516078 | |||||||
| chr3:15516088 | T | G | 1 | a0001c0001t0001g0236 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.106+5432A>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15516088 | |||||||
| chr3:15516175 | T | A | 16 | a0001c0001t0001g0237 a0001c0001t0002g0017 a0001c0001t0002g0149 others(13): Show |
17 | HG00099.hp1 HG00642.hp1 HG00642.hp2 others(14): Show |
intron_variant | MODIFIER | c.106+5345A>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15516175 | |||||||
| chr3:15516365 | A | G | 3 | a0001c0001t0002g0245 a0004c0006t0004g0244 a0004c0006t0004g0246 |
3 | HG00544.hp2 NA18972.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.106+5155T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15516365 | |||||||
| chr3:15516662 | C | T | 58 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0274 others(55): Show |
62 | HG00280.hp1 HG00544.hp1 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.106+4858G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15516662 | |||||||
| chr3:15516704 | C | A | 1 | a0001c0001t0001g0260 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.106+4816G>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15516704 | |||||||
| chr3:15516906 | T | C | 197 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(194): Show |
225 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(222): Show |
intron_variant | MODIFIER | c.106+4614A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15516906 | |||||||
| chr3:15517057 | G | A | 1 | a0001c0001t0003g0089 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.106+4463C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15517057 | |||||||
| chr3:15517143 | G | A | 5 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0001g0240 others(2): Show |
5 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.106+4377C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15517143 | |||||||
| chr3:15517144 | A | T | 2 | a0001c0001t0002g0343 a0001c0003t0004g0272 |
2 | HG01884.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.106+4376T>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15517144 | |||||||
| chr3:15517160 | A | C | 1 | a0001c0001t0002g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.106+4360T>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15517160 | |||||||
| chr3:15517445 | G | T | 25 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(22): Show |
31 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.106+4075C>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15517445 | |||||||
| chr3:15517567 | T | C | 2 | a0001c0001t0001g0324 a0001c0001t0001g0325 |
2 | HG02572.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.106+3953A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15517567 | |||||||
| chr3:15517640 | C | A | 2 | a0001c0001t0002g0016 a0001c0001t0015g0116 |
3 | HG02615.hp1 HG02809.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.106+3880G>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15517640 | |||||||
| chr3:15517662 | T | C | 108 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(105): Show |
128 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(125): Show |
intron_variant | MODIFIER | c.106+3858A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15517662 | |||||||
| chr3:15517667 | T | A | 1 | a0001c0001t0002g0146 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.106+3853A>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15517667 | |||||||
| chr3:15517721 | C | T | 15 | a0001c0001t0002g0017 a0001c0001t0002g0149 a0001c0001t0002g0150 others(12): Show |
16 | HG00642.hp1 HG00642.hp2 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.106+3799G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15517721 | |||||||
| chr3:15517827 | C | T | 2 | a0001c0001t0002g0016 a0001c0001t0015g0116 |
3 | HG02615.hp1 HG02809.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.106+3693G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15517827 | |||||||
| chr3:15517891 | C | T | 1 | a0001c0001t0003g0030 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.106+3629G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15517891 | |||||||
| chr3:15517894 | C | T | 1 | a0001c0001t0001g0092 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.106+3626G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15517894 | |||||||
| chr3:15518642 | T | C | 7 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0002g0023 others(4): Show |
8 | HG01168.hp2 HG01169.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.106+2878A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15518642 | |||||||
| chr3:15518736 | C | T | 1 | a0001c0001t0002g0279 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.106+2784G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15518736 | |||||||
| chr3:15518829 | T | C | 197 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(194): Show |
225 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(222): Show |
intron_variant | MODIFIER | c.106+2691A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15518829 | |||||||
| chr3:15518861 | T | G | 2 | a0001c0001t0002g0343 a0001c0003t0004g0272 |
2 | HG01884.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.106+2659A>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15518861 | |||||||
| chr3:15519040 | T | G | 2 | a0001c0001t0001g0114 a0001c0001t0001g0147 |
2 | HG03139.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.106+2480A>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15519040 | |||||||
| chr3:15519158 | AC | A | 75 | a0001c0001t0002g0024 a0001c0001t0002g0267 a0001c0001t0003g0003 others(72): Show |
89 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.106+2361delG | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15519158 | |||||||
| chr3:15519208 | T | G | 2 | a0001c0001t0002g0343 a0001c0003t0004g0272 |
2 | HG01884.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.106+2312A>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15519208 | |||||||
| chr3:15519450 | C | T | 1 | a0001c0001t0010g0342 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.106+2070G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15519450 | |||||||
| chr3:15519559 | T | C | 1 | a0001c0001t0003g0090 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.106+1961A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15519559 | |||||||
| chr3:15519676 | G | A | 1 | a0001c0001t0001g0243 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.106+1844C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15519676 | |||||||
| chr3:15519751 | G | T | 3 | a0001c0001t0002g0245 a0004c0006t0004g0244 a0004c0006t0004g0246 |
3 | HG00544.hp2 NA18972.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.106+1769C>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15519751 | |||||||
| chr3:15519840 | A | G | 3 | a0001c0001t0001g0122 a0001c0001t0001g0124 a0001c0003t0004g0123 |
3 | HG02109.hp2 HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.106+1680T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15519840 | |||||||
| chr3:15519983 | T | A | 32 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(29): Show |
38 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.106+1537A>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15519983 | |||||||
| chr3:15519985 | G | A | 2 | a0001c0001t0002g0343 a0001c0003t0004g0272 |
2 | HG01884.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.106+1535C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15519985 | |||||||
| chr3:15520063 | TTCCTTAA others(4): Show |
T | 1 | a0001c0001t0001g0148 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.106+1446_106+1456d others(13): Show |
COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15520063 | |||||||
| chr3:15520104 | A | G | 201 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(198): Show |
229 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(226): Show |
intron_variant | MODIFIER | c.106+1416T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15520104 | |||||||
| chr3:15520172 | G | T | 1 | a0001c0001t0002g0278 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.106+1348C>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15520172 | |||||||
| chr3:15520390 | C | T | 2 | a0001c0001t0001g0329 a0001c0001t0001g0330 |
2 | HG01081.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.106+1130G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15520390 | |||||||
| chr3:15520557 | C | G | 3 | a0001c0001t0001g0277 a0001c0001t0002g0275 a0001c0001t0002g0276 |
3 | HG00733.hp2 HG01943.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.106+963G>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15520557 | |||||||
| chr3:15520634 | G | A | 49 | a0001c0001t0001g0277 a0001c0001t0001g0308 a0001c0001t0001g0310 others(46): Show |
52 | HG00280.hp1 HG00544.hp1 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.106+886C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15520634 | |||||||
| chr3:15520731 | G | A | 2 | a0001c0001t0002g0343 a0001c0003t0004g0272 |
2 | HG01884.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.106+789C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15520731 | |||||||
| chr3:15520739 | A | G | 183 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(180): Show |
208 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(205): Show |
intron_variant | MODIFIER | c.106+781T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15520739 | |||||||
| chr3:15521004 | G | A | 1 | a0001c0001t0001g0109 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.106+516C>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15521004 | |||||||
| chr3:15521011 | A | AC | 11 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 others(8): Show |
11 | HG01109.hp2 HG02004.hp2 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.106+508dupG | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15521011 | |||||||
| chr3:15521017 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.106+503G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15521017 | |||||||
| chr3:15521199 | A | G | 197 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0092 others(194): Show |
223 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(220): Show |
intron_variant | MODIFIER | c.106+321T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15521199 | |||||||
| chr3:15521247 | A | G | 1 | a0001c0001t0001g0113 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.106+273T>C | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15521247 | |||||||
| chr3:15521281 | C | A | 18 | a0001c0001t0001g0329 a0001c0001t0001g0330 a0001c0001t0001g0338 others(15): Show |
19 | HG01081.hp2 HG01109.hp2 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.106+239G>T | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15521281 | |||||||
| chr3:15521294 | T | C | 205 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(202): Show |
233 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(230): Show |
intron_variant | MODIFIER | c.106+226A>G | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15521294 | |||||||
| chr3:15521324 | C | T | 25 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(22): Show |
31 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.106+196G>A | COLQ | ENSG00000206561.14 | transcript | ENST00000383788.10 | protein_coding | 1/16 | chr3 | 15521324 |