Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 7453 |
| ensemblid | ENSG00000140105.18 |
| hgncid | 12729 |
| symbol | WARS1 |
| name | tryptophanyl-tRNA synthetase 1 |
| refseq_nuc | NM_004184.4 |
| refseq_prot | NP_004175.2 |
| ensembl_nuc | ENST00000392882.7 |
| ensembl_prot | ENSP00000376620.2 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 100333790 |
| end | 100375347 |
| strand | - |
| ver | v1.2 |
| region | chr14:100333790-100375347 |
| region5000 | chr14:100328790-100380347 |
| regionname0 | WARS1_chr14_100333790_100375347 |
| regionname5000 | WARS1_chr14_100328790_100380347 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 471 | 331 | 95 | 46 | 144 | 14 | 30 | 110 | WARS1_chr14_100328790_100380347 | WARS1 | MPNSE others(466): Show |
chr14 | 100328790 | 100380347 |
| a0002 | 0/0 | 471 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | WARS1_chr14_100328790_100380347 | WARS1 | MPNSE others(466): Show |
chr14 | 100328790 | 100380347 |
| a0003 | 0/0 | 471 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | MPNSE others(466): Show |
chr14 | 100328790 | 100380347 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1413 | 200 | 43 | 36 | 87 | 9 | 24 | WARS1_chr14_100328790_100380347 | WARS1 | ATGCC others(1408): Show |
chr14 | 100328790 | 100380347 | ||
| a0001c0002 | 1/0 | 1413 | 126 | 51 | 9 | 56 | 5 | 4 | WARS1_chr14_100328790_100380347 | WARS1 | ATGCC others(1408): Show |
chr14 | 100328790 | 100380347 | ||
| a0001c0005 | 0/0 | 1413 | 2 | 0 | 0 | 0 | 0 | 2 | WARS1_chr14_100328790_100380347 | WARS1 | ATGCC others(1408): Show |
chr14 | 100328790 | 100380347 | ||
| a0001c0006 | 0/0 | 1413 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | ATGCC others(1408): Show |
chr14 | 100328790 | 100380347 | ||
| a0001c0007 | 0/0 | 1413 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | ATGCC others(1408): Show |
chr14 | 100328790 | 100380347 | ||
| a0001c0008 | 0/0 | 1413 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | ATGCC others(1408): Show |
chr14 | 100328790 | 100380347 | ||
| a0002c0003 | 0/0 | 1413 | 4 | 0 | 0 | 4 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | ATGCC others(1408): Show |
chr14 | 100328790 | 100380347 | ||
| a0003c0004 | 0/0 | 1413 | 3 | 3 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | ATGCC others(1408): Show |
chr14 | 100328790 | 100380347 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2639 | 199 | 42 | 36 | 87 | 9 | 24 | WARS1_chr14_100328790_100380347 | WARS1 | ACTCT others(2634): Show |
chr14 | 100328790 | 100380347 |
| a0001c0001t0003 | 0/0 | 2639 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | ACTCT others(2634): Show |
chr14 | 100328790 | 100380347 |
| a0001c0002t0001 | 1/0 | 2639 | 92 | 51 | 9 | 23 | 4 | 4 | WARS1_chr14_100328790_100380347 | WARS1 | ACTCT others(2634): Show |
chr14 | 100328790 | 100380347 |
| a0001c0002t0002 | 0/0 | 2639 | 33 | 0 | 0 | 32 | 1 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | ACTCT others(2634): Show |
chr14 | 100328790 | 100380347 |
| a0001c0002t0004 | 0/0 | 2639 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | ACTCT others(2634): Show |
chr14 | 100328790 | 100380347 |
| a0001c0005t0001 | 0/0 | 2639 | 2 | 0 | 0 | 0 | 0 | 2 | WARS1_chr14_100328790_100380347 | WARS1 | ACTCT others(2634): Show |
chr14 | 100328790 | 100380347 |
| a0001c0006t0001 | 0/0 | 2639 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | ACTCT others(2634): Show |
chr14 | 100328790 | 100380347 |
| a0001c0007t0001 | 0/0 | 2639 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | ACTCT others(2634): Show |
chr14 | 100328790 | 100380347 |
| a0001c0008t0001 | 0/0 | 2639 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | ACTCT others(2634): Show |
chr14 | 100328790 | 100380347 |
| a0002c0003t0001 | 0/0 | 2639 | 4 | 0 | 0 | 4 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | ACTCT others(2634): Show |
chr14 | 100328790 | 100380347 |
| a0003c0004t0001 | 0/0 | 2639 | 3 | 3 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | ACTCT others(2634): Show |
chr14 | 100328790 | 100380347 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 10 | 4 | 2 | 2 | 2 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0003 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0004 | 0/0 | 5 | 0 | 1 | 3 | 1 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0131 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0001t0003g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0001g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0001g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0001g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0001g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0001g0016 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0001g0020 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0001g0102 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0002g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0002g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0002g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0002t0004g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0005t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0005t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0006t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0007t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0001c0008t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0002c0003t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0002c0003t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0002c0003t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0002c0003t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| a0003c0004t0001g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0002 | g0045 | EUR | GBR | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0236 | EUR | GBR | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG00140 | hp2 | a0001 | c0002 | t0001 | g0060 | EUR | GBR | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0062 | EUR | FIN | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0177 | EUR | FIN | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG00423 | hp1 | a0001 | c0002 | t0002 | g0056 | EAS | CHS | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | CHS | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | CHS | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | CHS | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0074 | EAS | CHS | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | CHS | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG00558 | hp1 | a0001 | c0002 | t0004 | g0081 | EAS | CHS | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | CHS | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | CHS | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | CHS | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0120 | AMR | PUR | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | CHS | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | CHS | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0020 | AMR | PUR | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0072 | AMR | PUR | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0262 | AMR | PUR | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0085 | AMR | PUR | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0091 | AMR | PUR | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | CLM | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0089 | AMR | CLM | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | CLM | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0066 | AMR | CLM | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | CLM | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0144 | EUR | IBS | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG01515 | hp2 | a0001 | c0002 | t0001 | g0016 | EUR | IBS | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0139 | EUR | IBS | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0068 | EUR | IBS | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | ACB | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0103 | AFR | ACB | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0009 | AFR | ACB | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG01891 | hp2 | a0001 | c0002 | t0001 | g0010 | AFR | ACB | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | PEL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PEL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0267 | AMR | PEL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG01981 | hp2 | a0001 | c0002 | t0001 | g0063 | AMR | PEL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | KHV | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG02027 | hp1 | a0001 | c0002 | t0002 | g0055 | EAS | KHV | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG02040 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | KHV | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0093 | AFR | ACB | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | ACB | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0088 | EAS | KHV | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | KHV | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG02132 | hp1 | a0001 | c0002 | t0002 | g0041 | EAS | KHV | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | KHV | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | ACB | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG02145 | hp2 | a0001 | c0002 | t0001 | g0092 | AFR | ACB | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | CDX | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | CDX | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0076 | EAS | CDX | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG02165 | hp2 | a0001 | c0002 | t0002 | g0047 | EAS | CDX | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | ACB | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG02257 | hp2 | a0001 | c0002 | t0001 | g0069 | AFR | ACB | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG02258 | hp2 | a0001 | c0002 | t0001 | g0109 | AFR | ACB | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0010 | AFR | ACB | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | ACB | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG02293 | hp1 | a0001 | c0006 | t0001 | g0247 | AMR | PEL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0067 | AMR | PEL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0019 | AFR | ACB | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG02451 | hp2 | a0001 | c0007 | t0001 | g0053 | AFR | ACB | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG02523 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | KHV | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | KHV | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG02572 | hp2 | a0001 | c0002 | t0001 | g0116 | AFR | GWD | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0082 | SAS | PJL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG02615 | hp1 | a0001 | c0002 | t0001 | g0009 | AFR | GWD | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG02615 | hp2 | a0001 | c0002 | t0001 | g0020 | AFR | GWD | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG02622 | hp1 | a0001 | c0002 | t0001 | g0126 | AFR | GWD | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG02630 | hp1 | a0001 | c0002 | t0001 | g0044 | AFR | GWD | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0122 | AFR | GWD | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0107 | AFR | GWD | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0101 | AFR | GWD | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0105 | AFR | GWD | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG02723 | hp1 | a0003 | c0004 | t0001 | g0008 | AFR | GWD | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0112 | AFR | GWD | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0119 | AFR | GWD | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0277 | AFR | GWD | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG02818 | hp1 | a0001 | c0002 | t0001 | g0094 | AFR | GWD | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | GWD | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG02895 | hp2 | a0001 | c0002 | t0001 | g0114 | AFR | GWD | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | GWD | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG02896 | hp2 | a0001 | c0002 | t0001 | g0118 | AFR | GWD | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | GWD | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG02897 | hp2 | a0001 | c0002 | t0001 | g0115 | AFR | GWD | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0010 | AFR | ESN | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | ESN | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | ESN | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0125 | AFR | ESN | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG02976 | hp1 | a0001 | c0002 | t0001 | g0111 | AFR | ESN | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | ESN | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0011 | AFR | GWD | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | MSL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | MSL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0110 | AFR | ESN | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | ESN | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ESN | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0121 | AFR | ESN | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG03209 | hp1 | a0001 | c0002 | t0001 | g0124 | AFR | MSL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | MSL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG03225 | hp1 | a0001 | c0002 | t0001 | g0005 | AFR | MSL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | MSL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0077 | AFR | MSL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0011 | AFR | MSL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | MSL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG03486 | hp2 | a0003 | c0004 | t0001 | g0008 | AFR | MSL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0075 | SAS | PJL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0211 | SAS | PJL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0108 | AFR | ESN | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0099 | AFR | GWD | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0117 | AFR | GWD | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0095 | AFR | MSL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | MSL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | PJL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0235 | SAS | PJL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0239 | SAS | PJL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0016 | SAS | BEB | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0222 | SAS | BEB | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | BEB | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG03942 | hp2 | a0001 | c0005 | t0001 | g0271 | SAS | BEB | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG04115 | hp1 | a0001 | c0005 | t0001 | g0270 | SAS | STU | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0255 | SAS | STU | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | BEB | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0243 | SAS | BEB | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0154 | SAS | STU | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0212 | SAS | STU | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0216 | SAS | STU | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0265 | SAS | STU | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0246 | SAS | STU | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG04228 | hp2 | a0001 | c0002 | t0001 | g0078 | SAS | STU | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0106 | AFR | YRI | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | YRI | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | CHB | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0071 | EAS | CHB | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA18906 | hp1 | a0001 | c0002 | t0001 | g0009 | AFR | YRI | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0100 | AFR | YRI | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA18940 | hp2 | a0001 | c0002 | t0002 | g0015 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA18942 | hp2 | a0001 | c0002 | t0002 | g0039 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA18945 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA18947 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA18950 | hp1 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA18951 | hp2 | a0001 | c0002 | t0002 | g0014 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA18952 | hp2 | a0001 | c0002 | t0002 | g0042 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA18953 | hp2 | a0001 | c0002 | t0001 | g0083 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA18954 | hp2 | a0001 | c0002 | t0002 | g0059 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA18956 | hp1 | a0001 | c0002 | t0002 | g0051 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA18959 | hp1 | a0001 | c0002 | t0001 | g0065 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA18960 | hp1 | a0001 | c0002 | t0002 | g0046 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA18964 | hp1 | a0001 | c0002 | t0001 | g0070 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA18964 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA18965 | hp2 | a0001 | c0002 | t0002 | g0050 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA18970 | hp2 | a0001 | c0002 | t0002 | g0057 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA18971 | hp2 | a0001 | c0002 | t0002 | g0054 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA18973 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA18973 | hp2 | a0002 | c0003 | t0001 | g0128 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA18974 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA18975 | hp2 | a0001 | c0002 | t0001 | g0090 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA18977 | hp1 | a0001 | c0002 | t0001 | g0079 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA18978 | hp1 | a0001 | c0002 | t0002 | g0040 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA18978 | hp2 | a0001 | c0008 | t0001 | g0261 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA18984 | hp1 | a0001 | c0002 | t0002 | g0038 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA18985 | hp2 | a0002 | c0003 | t0001 | g0127 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA18995 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA18997 | hp1 | a0001 | c0002 | t0002 | g0058 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA18998 | hp2 | a0001 | c0002 | t0002 | g0048 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0064 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA19000 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA19003 | hp1 | a0001 | c0002 | t0001 | g0087 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA19009 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA19012 | hp2 | a0001 | c0002 | t0002 | g0043 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0005 | AFR | LWK | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA19030 | hp2 | a0001 | c0002 | t0001 | g0104 | AFR | LWK | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA19043 | hp1 | a0001 | c0002 | t0001 | g0123 | AFR | LWK | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | LWK | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA19055 | hp2 | a0001 | c0002 | t0001 | g0084 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA19062 | hp2 | a0001 | c0002 | t0001 | g0061 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA19066 | hp1 | a0002 | c0003 | t0001 | g0130 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA19074 | hp1 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA19077 | hp1 | a0001 | c0002 | t0001 | g0086 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA19077 | hp2 | a0001 | c0002 | t0002 | g0015 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA19079 | hp2 | a0001 | c0002 | t0002 | g0037 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA19081 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0080 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA19088 | hp1 | a0002 | c0003 | t0001 | g0129 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA19088 | hp2 | a0001 | c0002 | t0002 | g0014 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA19089 | hp2 | a0001 | c0002 | t0002 | g0052 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA19090 | hp1 | a0001 | c0002 | t0001 | g0073 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA19091 | hp1 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0019 | AFR | YRI | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | YRI | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0097 | AFR | ASW | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0210 | EUR | TSI | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0240 | EUR | TSI | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | TSI | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | GIH | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0215 | SAS | GIH | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG02109 | hp1 | a0003 | c0004 | t0001 | g0008 | AFR | ACB | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | ACB | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | ACB | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | ACB | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | ACB | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0005 | AFR | ACB | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0005 | AFR | MSL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | MSL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG06807 | hp1 | a0001 | c0002 | t0001 | g0113 | AFR | USA | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0011 | AFR | USA | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA18955 | hp1 | a0001 | c0002 | t0002 | g0049 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | USA | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0196 | AFR | USA | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | LWK | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0096 | AFR | LWK | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0131 | REF | REF | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0102 | REF | REF | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:100342522 | G | A | 1 | a0003 | 3 | HG02109.hp1 HG02723.hp1 HG03486.hp2 |
missense_variant | MODERATE | c.989C>T | p.Pro330Leu | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/11 | 1127/2639 | 989/1416 | 330/471 | chr14 | 100342522 | |||
| chr14:100361861 | C | A | 1 | a0002 | 4 | NA18973.hp2 NA18985.hp2 NA19066.hp1 others(1): Show |
missense_variant | MODERATE | c.160G>T | p.Ala54Ser | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 3/11 | 298/2639 | 160/1416 | 54/471 | chr14 | 100361861 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:100337086 | G | A | 1 | a0001c0005 | 2 | HG03942.hp2 HG04115.hp1 |
synonymous_variant | LOW | c.1230C>T | p.Asp410Asp | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 10/11 | 1368/2639 | 1230/1416 | 410/471 | chr14 | 100337086 | |||
| chr14:100342508 | G | A | 3 | a0001c0001 a0001c0006 a0001c0008 |
201 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(198): Show |
synonymous_variant | LOW | c.1003C>T | p.Leu335Leu | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/11 | 1141/2639 | 1003/1416 | 335/471 | chr14 | 100342508 | |||
| chr14:100346771 | G | A | 1 | a0001c0007 | 1 | HG02451.hp2 | synonymous_variant | LOW | c.801C>T | p.Phe267Phe | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/11 | 939/2639 | 801/1416 | 267/471 | chr14 | 100346771 | |||
| chr14:100353719 | C | T | 1 | a0001c0006 | 1 | HG02293.hp1 | synonymous_variant | LOW | c.693G>A | p.Lys231Lys | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/11 | 831/2639 | 693/1416 | 231/471 | chr14 | 100353719 | |||
| chr14:100361721 | G | A | 1 | a0001c0008 | 1 | NA18978.hp2 | synonymous_variant | LOW | c.300C>T | p.Tyr100Tyr | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 3/11 | 438/2639 | 300/1416 | 100/471 | chr14 | 100361721 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:100334273 | T | C | 1 | a0001c0002t0002 | 33 | HG00099.hp1 HG00423.hp1 HG02027.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*602A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 11/11 | 602 | chr14 | 100334273 | ||||||
| chr14:100334376 | G | C | 1 | a0001c0001t0003 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*499C>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 11/11 | 499 | chr14 | 100334376 | ||||||
| chr14:100334378 | G | A | 1 | a0001c0001t0003 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*497C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 11/11 | 497 | chr14 | 100334378 | ||||||
| chr14:100334379 | G | A | 1 | a0001c0001t0003 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*496C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 11/11 | 496 | chr14 | 100334379 | ||||||
| chr14:100334380 | G | A | 1 | a0001c0001t0003 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*495C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 11/11 | 495 | chr14 | 100334380 | ||||||
| chr14:100334662 | G | A | 1 | a0001c0002t0004 | 1 | HG00558.hp1 | 3_prime_UTR_variant | MODIFIER | c.*213C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 11/11 | 213 | chr14 | 100334662 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:100335047 | G | A | 6 | a0001c0002t0001g0017 a0001c0002t0001g0065 a0001c0002t0001g0071 others(3): Show |
7 | HG00544.hp1 HG03491.hp1 NA18747.hp2 others(4): Show |
intron_variant | MODIFIER | c.1255-11C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 10/10 | chr14 | 100335047 | |||||||
| chr14:100335086 | T | C | 266 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(263): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.1255-50A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 10/10 | chr14 | 100335086 | |||||||
| chr14:100335087 | G | A | 1 | a0001c0001t0001g0260 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1255-51C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 10/10 | chr14 | 100335087 | |||||||
| chr14:100335092 | C | T | 1 | a0001c0002t0001g0077 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1255-56G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 10/10 | chr14 | 100335092 | |||||||
| chr14:100335106 | C | T | 1 | a0001c0001t0001g0245 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1255-70G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 10/10 | chr14 | 100335106 | |||||||
| chr14:100335164 | G | C | 29 | a0001c0002t0001g0044 a0001c0002t0002g0002 a0001c0002t0002g0006 others(26): Show |
37 | HG00099.hp1 HG00423.hp1 HG02027.hp1 others(34): Show |
intron_variant | MODIFIER | c.1255-128C>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 10/10 | chr14 | 100335164 | |||||||
| chr14:100335207 | A | G | 9 | a0001c0002t0001g0011 a0001c0002t0001g0119 a0001c0002t0001g0120 others(6): Show |
11 | HG00639.hp1 HG02622.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.1255-171T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 10/10 | chr14 | 100335207 | |||||||
| chr14:100335361 | T | C | 2 | a0001c0001t0001g0138 a0001c0001t0001g0162 |
2 | NA19074.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.1255-325A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 10/10 | chr14 | 100335361 | |||||||
| chr14:100335383 | A | AT | 72 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0030 others(69): Show |
82 | HG00099.hp2 HG00438.hp2 HG00733.hp1 others(79): Show |
intron_variant | MODIFIER | c.1255-348dupA | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 10/10 | chr14 | 100335383 | |||||||
| chr14:100335733 | G | A | 1 | a0001c0001t0001g0234 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1255-697C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 10/10 | chr14 | 100335733 | |||||||
| chr14:100335757 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1255-721G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 10/10 | chr14 | 100335757 | |||||||
| chr14:100335871 | T | C | 2 | a0001c0002t0001g0044 a0001c0007t0001g0053 |
2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1255-835A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 10/10 | chr14 | 100335871 | |||||||
| chr14:100335940 | G | A | 2 | a0001c0005t0001g0270 a0001c0005t0001g0271 |
2 | HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1255-904C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 10/10 | chr14 | 100335940 | |||||||
| chr14:100335964 | C | CT | 6 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0141 others(3): Show |
6 | HG01928.hp1 HG01975.hp1 HG02056.hp2 others(3): Show |
intron_variant | MODIFIER | c.1255-929dupA | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 10/10 | chr14 | 100335964 | |||||||
| chr14:100335964 | CT | C | 7 | a0001c0001t0001g0158 a0001c0001t0001g0223 a0001c0001t0001g0226 others(4): Show |
7 | HG00558.hp1 HG01496.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1255-929delA | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 10/10 | chr14 | 100335964 | |||||||
| chr14:100336071 | C | T | 2 | a0001c0005t0001g0270 a0001c0005t0001g0271 |
2 | HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1254+991G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 10/10 | chr14 | 100336071 | |||||||
| chr14:100336092 | G | A | 1 | a0001c0001t0001g0148 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1254+970C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 10/10 | chr14 | 100336092 | |||||||
| chr14:100336148 | T | C | 168 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(165): Show |
203 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.1254+914A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 10/10 | chr14 | 100336148 | |||||||
| chr14:100336149 | G | T | 9 | a0001c0002t0001g0011 a0001c0002t0001g0119 a0001c0002t0001g0120 others(6): Show |
11 | HG00639.hp1 HG02622.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.1254+913C>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 10/10 | chr14 | 100336149 | |||||||
| chr14:100336168 | C | T | 10 | a0001c0002t0001g0010 a0001c0002t0001g0110 a0001c0002t0001g0111 others(7): Show |
12 | HG01891.hp2 HG02280.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.1254+894G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 10/10 | chr14 | 100336168 | |||||||
| chr14:100336275 | C | CA | 13 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0093 others(10): Show |
15 | HG00733.hp2 HG02055.hp1 HG02165.hp2 others(12): Show |
intron_variant | MODIFIER | c.1254+786dupT | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 10/10 | chr14 | 100336275 | |||||||
| chr14:100336275 | C | CAAA | 160 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(157): Show |
195 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(192): Show |
intron_variant | MODIFIER | c.1254+784_1254+786d others(5): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 10/10 | chr14 | 100336275 | |||||||
| chr14:100336536 | T | C | 168 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(165): Show |
203 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.1254+526A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 10/10 | chr14 | 100336536 | |||||||
| chr14:100336691 | T | C | 4 | a0002c0003t0001g0127 a0002c0003t0001g0128 a0002c0003t0001g0129 others(1): Show |
4 | NA18973.hp2 NA18985.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.1254+371A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 10/10 | chr14 | 100336691 | |||||||
| chr14:100336851 | T | C | 5 | a0001c0002t0001g0009 a0001c0002t0001g0105 a0001c0002t0001g0106 others(2): Show |
7 | HG01891.hp1 HG02615.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1254+211A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 10/10 | chr14 | 100336851 | |||||||
| chr14:100336953 | T | C | 4 | a0002c0003t0001g0127 a0002c0003t0001g0128 a0002c0003t0001g0129 others(1): Show |
4 | NA18973.hp2 NA18985.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.1254+109A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 10/10 | chr14 | 100336953 | |||||||
| chr14:100336961 | T | A | 2 | a0001c0005t0001g0270 a0001c0005t0001g0271 |
2 | HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1254+101A>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 10/10 | chr14 | 100336961 | |||||||
| chr14:100337027 | A | G | 209 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(206): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.1254+35T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 10/10 | chr14 | 100337027 | |||||||
| chr14:100337278 | T | A | 1 | a0001c0002t0001g0072 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1114-76A>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100337278 | |||||||
| chr14:100337318 | C | A | 209 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(206): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.1114-116G>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100337318 | |||||||
| chr14:100337345 | T | G | 1 | a0001c0001t0001g0148 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1114-143A>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100337345 | |||||||
| chr14:100337405 | C | G | 43 | a0001c0002t0001g0007 a0001c0002t0001g0016 a0001c0002t0001g0017 others(40): Show |
50 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.1114-203G>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100337405 | |||||||
| chr14:100337619 | G | C | 1 | a0001c0002t0001g0073 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1114-417C>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100337619 | |||||||
| chr14:100337620 | G | C | 1 | a0001c0001t0001g0234 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1114-418C>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100337620 | |||||||
| chr14:100337688 | C | CA | 189 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(186): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.1114-487dupT | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100337688 | |||||||
| chr14:100337727 | G | T | 1 | a0001c0002t0001g0120 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1114-525C>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100337727 | |||||||
| chr14:100337732 | C | T | 2 | a0001c0002t0002g0046 a0001c0002t0002g0047 |
2 | HG02165.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.1114-530G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100337732 | |||||||
| chr14:100337801 | T | C | 5 | a0001c0002t0001g0005 a0001c0002t0001g0097 a0001c0002t0001g0099 others(2): Show |
8 | HG02559.hp2 HG02717.hp1 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.1114-599A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100337801 | |||||||
| chr14:100337881 | T | C | 7 | a0001c0001t0001g0034 a0001c0001t0001g0272 a0001c0001t0001g0273 others(4): Show |
8 | HG02486.hp2 HG02809.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1114-679A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100337881 | |||||||
| chr14:100337978 | T | C | 168 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(165): Show |
203 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.1114-776A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100337978 | |||||||
| chr14:100338017 | A | G | 1 | a0001c0001t0001g0021 | 2 | HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1114-815T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100338017 | |||||||
| chr14:100338058 | C | T | 1 | a0001c0002t0001g0104 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1114-856G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100338058 | |||||||
| chr14:100338207 | C | T | 166 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(163): Show |
201 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.1114-1005G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100338207 | |||||||
| chr14:100338256 | G | T | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG03225.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1114-1054C>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100338256 | |||||||
| chr14:100338412 | T | G | 2 | a0001c0002t0001g0060 a0001c0002t0001g0068 |
2 | HG00140.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.1114-1210A>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100338412 | |||||||
| chr14:100338448 | G | C | 74 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0013 others(71): Show |
86 | HG00099.hp2 HG00438.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.1114-1246C>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100338448 | |||||||
| chr14:100338776 | A | C | 7 | a0001c0002t0001g0011 a0001c0002t0001g0119 a0001c0002t0001g0120 others(4): Show |
9 | HG00639.hp1 HG02622.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1114-1574T>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100338776 | |||||||
| chr14:100338849 | G | A | 1 | a0001c0001t0001g0225 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1114-1647C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100338849 | |||||||
| chr14:100338935 | C | T | 1 | a0001c0001t0001g0151 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1114-1733G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100338935 | |||||||
| chr14:100338949 | C | A | 168 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(165): Show |
203 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.1114-1747G>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100338949 | |||||||
| chr14:100338966 | C | T | 1 | a0001c0008t0001g0261 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1114-1764G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100338966 | |||||||
| chr14:100338982 | T | C | 7 | a0001c0001t0001g0003 a0001c0001t0001g0153 a0001c0001t0001g0155 others(4): Show |
11 | HG00639.hp2 HG01109.hp1 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.1114-1780A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100338982 | |||||||
| chr14:100339088 | A | G | 1 | a0001c0001t0001g0251 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1114-1886T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100339088 | |||||||
| chr14:100339103 | T | TCA | 40 | a0001c0002t0001g0005 a0001c0002t0001g0009 a0001c0002t0001g0044 others(37): Show |
53 | HG00099.hp1 HG00423.hp1 HG01884.hp2 others(50): Show |
intron_variant | MODIFIER | c.1114-1903_1114-190 others(6): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100339103 | |||||||
| chr14:100339103 | T | TCACA | 4 | a0001c0002t0001g0011 a0001c0002t0001g0121 a0001c0002t0001g0123 others(1): Show |
6 | HG02622.hp1 HG03041.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.1114-1905_1114-190 others(8): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100339103 | |||||||
| chr14:100339108 | CACACACA others(9): Show |
C | 1 | a0001c0001t0001g0021 | 2 | HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1114-1922_1114-190 others(20): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100339108 | |||||||
| chr14:100339120 | C | CACACAT | 10 | a0001c0002t0001g0010 a0001c0002t0001g0110 a0001c0002t0001g0111 others(7): Show |
11 | HG02280.hp1 HG02572.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.1114-1919_1114-191 others(10): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100339120 | |||||||
| chr14:100339122 | C | CACACACA others(1): Show |
4 | a0002c0003t0001g0127 a0002c0003t0001g0128 a0002c0003t0001g0129 others(1): Show |
4 | NA18973.hp2 NA18985.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.1114-1921_1114-192 others(12): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100339122 | |||||||
| chr14:100339122 | CAT | C | 160 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(157): Show |
194 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.1114-1922_1114-192 others(6): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100339122 | |||||||
| chr14:100339124 | T | C | 74 | a0001c0001t0001g0201 a0001c0001t0001g0206 a0001c0001t0001g0207 others(71): Show |
85 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.1114-1922A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100339124 | |||||||
| chr14:100339126 | C | CAT | 42 | a0001c0002t0001g0007 a0001c0002t0001g0016 a0001c0002t0001g0017 others(39): Show |
49 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.1114-1925_1114-192 others(6): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100339126 | |||||||
| chr14:100339126 | C | T | 4 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0245 others(1): Show |
4 | HG01069.hp2 HG01981.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1114-1924G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100339126 | |||||||
| chr14:100339128 | C | T | 163 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(160): Show |
197 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.1114-1926G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100339128 | |||||||
| chr14:100339130 | C | T | 1 | a0001c0001t0001g0264 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1114-1928G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100339130 | |||||||
| chr14:100339246 | T | C | 171 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(168): Show |
207 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.1114-2044A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100339246 | |||||||
| chr14:100339282 | C | T | 2 | a0001c0001t0001g0252 a0001c0002t0001g0085 |
2 | HG01169.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.1114-2080G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100339282 | |||||||
| chr14:100339358 | A | G | 8 | a0001c0002t0001g0011 a0001c0002t0001g0103 a0001c0002t0001g0119 others(5): Show |
10 | HG00639.hp1 HG01884.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1114-2156T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100339358 | |||||||
| chr14:100339367 | A | G | 7 | a0001c0002t0001g0011 a0001c0002t0001g0119 a0001c0002t0001g0120 others(4): Show |
9 | HG00639.hp1 HG02622.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1114-2165T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100339367 | |||||||
| chr14:100339371 | T | C | 7 | a0001c0002t0001g0011 a0001c0002t0001g0119 a0001c0002t0001g0120 others(4): Show |
9 | HG00639.hp1 HG02622.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1114-2169A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100339371 | |||||||
| chr14:100339388 | A | G | 3 | a0001c0001t0001g0035 a0001c0002t0002g0046 a0001c0002t0002g0047 |
3 | HG01928.hp1 HG02165.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.1114-2186T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100339388 | |||||||
| chr14:100339415 | C | T | 4 | a0001c0001t0001g0098 a0001c0001t0001g0136 a0001c0001t0001g0206 others(1): Show |
4 | HG01099.hp2 HG02257.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.1114-2213G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100339415 | |||||||
| chr14:100339418 | C | T | 3 | a0001c0001t0001g0098 a0001c0001t0001g0206 a0001c0001t0001g0207 |
3 | HG02257.hp1 HG02280.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1114-2216G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100339418 | |||||||
| chr14:100339427 | C | T | 1 | a0001c0001t0001g0159 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1114-2225G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100339427 | |||||||
| chr14:100339450 | T | C | 268 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(265): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.1114-2248A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100339450 | |||||||
| chr14:100339457 | G | A | 92 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(89): Show |
118 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.1114-2255C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100339457 | |||||||
| chr14:100339458 | T | C | 4 | a0001c0002t0001g0112 a0001c0002t0001g0114 a0001c0002t0001g0115 others(1): Show |
4 | HG02723.hp2 HG02895.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1114-2256A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100339458 | |||||||
| chr14:100339463 | G | A | 1 | a0001c0001t0001g0149 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1114-2261C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100339463 | |||||||
| chr14:100339490 | T | C | 68 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0025 others(65): Show |
77 | HG00099.hp2 HG00438.hp2 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.1114-2288A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100339490 | |||||||
| chr14:100339506 | G | C | 1 | a0001c0001t0001g0145 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1114-2304C>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100339506 | |||||||
| chr14:100339553 | T | G | 1 | a0001c0001t0001g0224 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1114-2351A>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100339553 | |||||||
| chr14:100339582 | C | A | 1 | a0001c0002t0001g0109 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1114-2380G>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100339582 | |||||||
| chr14:100339590 | C | CA | 24 | a0001c0001t0001g0098 a0001c0001t0001g0206 a0001c0001t0001g0207 others(21): Show |
25 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(22): Show |
intron_variant | MODIFIER | c.1114-2389dupT | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100339590 | |||||||
| chr14:100339590 | C | CAA | 131 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(128): Show |
165 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.1114-2390_1114-238 others(6): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100339590 | |||||||
| chr14:100339590 | C | CAAA | 31 | a0001c0001t0001g0023 a0001c0001t0001g0135 a0001c0001t0001g0140 others(28): Show |
32 | HG00423.hp2 HG00558.hp2 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.1114-2391_1114-238 others(7): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100339590 | |||||||
| chr14:100339611 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1114-2409C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100339611 | |||||||
| chr14:100339640 | T | C | 69 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0025 others(66): Show |
78 | HG00099.hp2 HG00438.hp2 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.1114-2438A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100339640 | |||||||
| chr14:100339849 | C | T | 10 | a0001c0002t0001g0010 a0001c0002t0001g0110 a0001c0002t0001g0111 others(7): Show |
12 | HG01891.hp2 HG02280.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.1113+2549G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100339849 | |||||||
| chr14:100340045 | T | C | 1 | a0001c0001t0001g0228 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1113+2353A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100340045 | |||||||
| chr14:100340282 | G | A | 41 | a0001c0002t0001g0011 a0001c0002t0001g0044 a0001c0002t0001g0109 others(38): Show |
51 | HG00099.hp1 HG00423.hp1 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.1113+2116C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100340282 | |||||||
| chr14:100340313 | G | T | 1 | a0001c0001t0001g0098 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1113+2085C>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100340313 | |||||||
| chr14:100340339 | C | G | 1 | a0001c0002t0001g0120 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1113+2059G>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100340339 | |||||||
| chr14:100340618 | C | G | 1 | a0001c0001t0001g0265 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1113+1780G>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100340618 | |||||||
| chr14:100340642 | C | A | 1 | a0001c0001t0001g0258 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1113+1756G>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100340642 | |||||||
| chr14:100340755 | C | T | 41 | a0001c0002t0001g0011 a0001c0002t0001g0044 a0001c0002t0001g0109 others(38): Show |
51 | HG00099.hp1 HG00423.hp1 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.1113+1643G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100340755 | |||||||
| chr14:100340756 | G | A | 3 | a0001c0002t0001g0114 a0001c0002t0001g0115 a0001c0002t0001g0118 |
3 | HG02895.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1113+1642C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100340756 | |||||||
| chr14:100340799 | G | A | 166 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(163): Show |
201 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.1113+1599C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100340799 | |||||||
| chr14:100340917 | C | CT | 93 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0030 others(90): Show |
109 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.1113+1480dupA | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100340917 | |||||||
| chr14:100340936 | C | T | 43 | a0001c0002t0001g0007 a0001c0002t0001g0016 a0001c0002t0001g0017 others(40): Show |
50 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.1113+1462G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100340936 | |||||||
| chr14:100340981 | C | G | 7 | a0001c0002t0001g0011 a0001c0002t0001g0119 a0001c0002t0001g0120 others(4): Show |
9 | HG00639.hp1 HG02622.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1113+1417G>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100340981 | |||||||
| chr14:100340986 | C | T | 3 | a0001c0002t0001g0114 a0001c0002t0001g0115 a0001c0002t0001g0118 |
3 | HG02895.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1113+1412G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100340986 | |||||||
| chr14:100341107 | A | G | 209 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(206): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.1113+1291T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100341107 | |||||||
| chr14:100341130 | G | A | 1 | a0001c0002t0001g0109 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1113+1268C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100341130 | |||||||
| chr14:100341205 | C | T | 5 | a0001c0002t0001g0005 a0001c0002t0001g0097 a0001c0002t0001g0099 others(2): Show |
8 | HG02559.hp2 HG02717.hp1 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.1113+1193G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100341205 | |||||||
| chr14:100341604 | A | G | 7 | a0001c0002t0001g0011 a0001c0002t0001g0119 a0001c0002t0001g0120 others(4): Show |
9 | HG00639.hp1 HG02622.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1113+794T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100341604 | |||||||
| chr14:100341677 | T | A | 2 | a0001c0001t0001g0132 a0001c0001t0001g0133 |
2 | HG03098.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1113+721A>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100341677 | |||||||
| chr14:100341811 | G | A | 3 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0197 |
3 | HG01884.hp1 HG02976.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1113+587C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100341811 | |||||||
| chr14:100341818 | G | A | 202 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(199): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.1113+580C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100341818 | |||||||
| chr14:100341831 | C | T | 27 | a0001c0002t0001g0044 a0001c0002t0002g0002 a0001c0002t0002g0006 others(24): Show |
35 | HG00099.hp1 HG00423.hp1 HG02027.hp1 others(32): Show |
intron_variant | MODIFIER | c.1113+567G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100341831 | |||||||
| chr14:100341928 | T | C | 1 | a0001c0001t0001g0236 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1113+470A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100341928 | |||||||
| chr14:100342156 | G | GA | 266 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(263): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.1113+241dupT | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100342156 | |||||||
| chr14:100342173 | T | A | 166 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(163): Show |
201 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.1113+225A>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100342173 | |||||||
| chr14:100342228 | G | A | 2 | a0001c0001t0001g0192 a0001c0001t0001g0197 |
2 | HG02976.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1113+170C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100342228 | |||||||
| chr14:100342271 | G | A | 1 | a0001c0001t0001g0208 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1113+127C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100342271 | |||||||
| chr14:100342317 | C | T | 2 | a0001c0002t0001g0044 a0001c0007t0001g0053 |
2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1113+81G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100342317 | |||||||
| chr14:100342591 | C | G | 2 | a0001c0002t0001g0099 a0001c0002t0001g0101 |
2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.940-20G>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 8/10 | chr14 | 100342591 | |||||||
| chr14:100342706 | C | CAT | 262 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(259): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.940-137_940-136dup others(2): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 8/10 | chr14 | 100342706 | |||||||
| chr14:100342715 | CT | C | 7 | a0001c0001t0001g0252 a0001c0002t0001g0009 a0001c0002t0001g0105 others(4): Show |
9 | HG01891.hp1 HG02615.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.940-145delA | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 8/10 | chr14 | 100342715 | |||||||
| chr14:100342728 | A | T | 40 | a0001c0002t0001g0011 a0001c0002t0001g0044 a0001c0002t0001g0109 others(37): Show |
50 | HG00099.hp1 HG00423.hp1 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.940-157T>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 8/10 | chr14 | 100342728 | |||||||
| chr14:100342947 | A | G | 267 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(264): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.939+328T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 8/10 | chr14 | 100342947 | |||||||
| chr14:100343022 | G | A | 1 | a0001c0002t0001g0126 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.939+253C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 8/10 | chr14 | 100343022 | |||||||
| chr14:100343088 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.939+187C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 8/10 | chr14 | 100343088 | |||||||
| chr14:100343156 | C | T | 1 | a0001c0001t0001g0167 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.939+119G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 8/10 | chr14 | 100343156 | |||||||
| chr14:100343230 | G | A | 2 | a0001c0005t0001g0270 a0001c0005t0001g0271 |
2 | HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.939+45C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 8/10 | chr14 | 100343230 | |||||||
| chr14:100343542 | T | C | 1 | a0001c0001t0001g0189 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.827-155A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100343542 | |||||||
| chr14:100343564 | C | T | 27 | a0001c0002t0001g0044 a0001c0002t0002g0002 a0001c0002t0002g0006 others(24): Show |
35 | HG00099.hp1 HG00423.hp1 HG02027.hp1 others(32): Show |
intron_variant | MODIFIER | c.827-177G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100343564 | |||||||
| chr14:100343606 | T | A | 3 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0188 |
3 | HG02109.hp2 HG03098.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.827-219A>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100343606 | |||||||
| chr14:100343700 | G | T | 1 | a0001c0002t0004g0081 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.827-313C>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100343700 | |||||||
| chr14:100343745 | C | G | 1 | a0001c0001t0001g0246 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.827-358G>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100343745 | |||||||
| chr14:100343762 | C | T | 43 | a0001c0002t0001g0007 a0001c0002t0001g0016 a0001c0002t0001g0017 others(40): Show |
50 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.827-375G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100343762 | |||||||
| chr14:100343912 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.827-525G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100343912 | |||||||
| chr14:100344059 | GCTTCCCT | G | 164 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(161): Show |
199 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.827-679_827-673del others(7): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100344059 | |||||||
| chr14:100344089 | G | A | 165 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(162): Show |
200 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.827-702C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100344089 | |||||||
| chr14:100344114 | G | A | 2 | a0001c0005t0001g0270 a0001c0005t0001g0271 |
2 | HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.827-727C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100344114 | |||||||
| chr14:100344192 | C | G | 7 | a0001c0002t0001g0011 a0001c0002t0001g0119 a0001c0002t0001g0120 others(4): Show |
9 | HG00639.hp1 HG02622.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.827-805G>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100344192 | |||||||
| chr14:100344256 | G | T | 208 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(205): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.827-869C>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100344256 | |||||||
| chr14:100344380 | T | C | 208 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(205): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.827-993A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100344380 | |||||||
| chr14:100344409 | C | T | 1 | a0001c0002t0001g0080 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.827-1022G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100344409 | |||||||
| chr14:100344424 | G | A | 1 | a0001c0001t0001g0237 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.827-1037C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100344424 | |||||||
| chr14:100344508 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.827-1121C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100344508 | |||||||
| chr14:100344526 | G | A | 1 | a0001c0001t0001g0162 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.827-1139C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100344526 | |||||||
| chr14:100344547 | G | A | 165 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(162): Show |
200 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.827-1160C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100344547 | |||||||
| chr14:100344556 | G | A | 2 | a0001c0005t0001g0270 a0001c0005t0001g0271 |
2 | HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.827-1169C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100344556 | |||||||
| chr14:100344590 | AAAGTGAG others(33): Show |
A | 4 | a0002c0003t0001g0127 a0002c0003t0001g0128 a0002c0003t0001g0129 others(1): Show |
4 | NA18973.hp2 NA18985.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.827-1243_827-1204d others(42): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100344590 | |||||||
| chr14:100344602 | G | A | 1 | a0001c0002t0002g0041 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.827-1215C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100344602 | |||||||
| chr14:100344603 | TCTCTGCC others(33): Show |
T | 4 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0141 others(1): Show |
4 | HG01928.hp1 HG01975.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.827-1256_827-1217d others(42): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100344603 | |||||||
| chr14:100344682 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.827-1295C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100344682 | |||||||
| chr14:100344684 | C | T | 1 | a0001c0001t0001g0265 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.827-1297G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100344684 | |||||||
| chr14:100344748 | TGTGAGGA others(33): Show |
T | 1 | a0001c0008t0001g0261 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.827-1401_827-1362d others(42): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100344748 | |||||||
| chr14:100344758 | G | A | 2 | a0001c0005t0001g0270 a0001c0005t0001g0271 |
2 | HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.827-1371C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100344758 | |||||||
| chr14:100344766 | C | T | 165 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(162): Show |
200 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.827-1379G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100344766 | |||||||
| chr14:100344783 | C | T | 1 | a0001c0002t0001g0101 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.827-1396G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100344783 | |||||||
| chr14:100344851 | C | T | 41 | a0001c0002t0001g0011 a0001c0002t0001g0044 a0001c0002t0001g0109 others(38): Show |
51 | HG00099.hp1 HG00423.hp1 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.827-1464G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100344851 | |||||||
| chr14:100344880 | A | G | 261 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(258): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.827-1493T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100344880 | |||||||
| chr14:100344883 | C | T | 165 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(162): Show |
200 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.827-1496G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100344883 | |||||||
| chr14:100344884 | G | A | 1 | a0001c0002t0001g0109 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.827-1497C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100344884 | |||||||
| chr14:100344913 | C | T | 41 | a0001c0002t0001g0011 a0001c0002t0001g0044 a0001c0002t0001g0109 others(38): Show |
51 | HG00099.hp1 HG00423.hp1 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.827-1526G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100344913 | |||||||
| chr14:100344914 | G | A | 5 | a0001c0001t0001g0153 a0001c0001t0001g0156 a0001c0001t0001g0163 others(2): Show |
5 | HG00639.hp2 HG01928.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.827-1527C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100344914 | |||||||
| chr14:100344952 | G | GGGGGTCA others(91): Show |
2 | a0001c0005t0001g0270 a0001c0005t0001g0271 |
2 | HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.827-1663_827-1566d others(100): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100344952 | |||||||
| chr14:100344952 | G | GGGGGTCA others(42): Show |
4 | a0001c0001t0001g0175 a0001c0001t0001g0226 a0001c0001t0001g0229 others(1): Show |
4 | HG03209.hp2 NA18946.hp2 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.827-1566_827-1565i others(51): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100344952 | |||||||
| chr14:100344970 | C | T | 4 | a0002c0003t0001g0127 a0002c0003t0001g0128 a0002c0003t0001g0129 others(1): Show |
4 | NA18973.hp2 NA18985.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.827-1583G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100344970 | |||||||
| chr14:100344999 | G | T | 8 | a0001c0001t0001g0175 a0001c0001t0001g0226 a0001c0001t0001g0229 others(5): Show |
8 | HG03209.hp2 NA18946.hp2 NA18973.hp2 others(5): Show |
intron_variant | MODIFIER | c.827-1612C>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100344999 | |||||||
| chr14:100345019 | C | CGGCCAGC others(42): Show |
1 | a0001c0001t0001g0240 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.827-1633_827-1632i others(51): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100345019 | |||||||
| chr14:100345019 | C | T | 4 | a0001c0001t0001g0175 a0001c0001t0001g0226 a0001c0001t0001g0229 others(1): Show |
4 | HG03209.hp2 NA18946.hp2 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.827-1632G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100345019 | |||||||
| chr14:100345036 | C | T | 1 | a0001c0001t0001g0245 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.827-1649G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100345036 | |||||||
| chr14:100345049 | GC | G | 5 | a0001c0001t0001g0175 a0001c0001t0001g0226 a0001c0001t0001g0229 others(2): Show |
5 | HG03209.hp2 NA18946.hp2 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.827-1663delG | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100345049 | |||||||
| chr14:100345050 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.827-1663G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100345050 | |||||||
| chr14:100345064 | C | CGCCCGGC others(90): Show |
1 | a0001c0001t0001g0191 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.827-1678_827-1677i others(99): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100345064 | |||||||
| chr14:100345064 | C | CGCCCGGC others(90): Show |
158 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(155): Show |
193 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.827-1678_827-1677i others(99): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100345064 | |||||||
| chr14:100345064 | C | T | 5 | a0001c0001t0001g0175 a0001c0001t0001g0226 a0001c0001t0001g0229 others(2): Show |
5 | HG03209.hp2 NA18946.hp2 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.827-1677G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100345064 | |||||||
| chr14:100345070 | G | GGCCAGCC others(92): Show |
1 | a0001c0001t0001g0181 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.826+1675_826+1676i others(101): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100345070 | |||||||
| chr14:100345081 | C | CGTCCGGG others(91): Show |
10 | a0001c0002t0001g0011 a0001c0002t0001g0109 a0001c0002t0001g0119 others(7): Show |
12 | HG00639.hp1 HG02258.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.826+1664_826+1665i others(100): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100345081 | |||||||
| chr14:100345081 | C | CGTCCGGG others(92): Show |
1 | a0001c0002t0002g0052 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.826+1664_826+1665i others(101): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100345081 | |||||||
| chr14:100345081 | C | CGTCCGGG others(92): Show |
1 | a0001c0002t0002g0050 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.826+1664_826+1665i others(101): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100345081 | |||||||
| chr14:100345081 | C | CGTCCGGG others(91): Show |
24 | a0001c0002t0001g0044 a0001c0002t0002g0002 a0001c0002t0002g0006 others(21): Show |
32 | HG00099.hp1 HG00423.hp1 HG02027.hp1 others(29): Show |
intron_variant | MODIFIER | c.826+1664_826+1665i others(100): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100345081 | |||||||
| chr14:100345081 | C | CGTCCGGG others(91): Show |
1 | a0001c0002t0002g0042 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.826+1664_826+1665i others(100): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100345081 | |||||||
| chr14:100345113 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.826+1633G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100345113 | |||||||
| chr14:100345127 | A | C | 1 | a0001c0001t0001g0234 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.826+1619T>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100345127 | |||||||
| chr14:100345154 | A | G | 1 | a0001c0002t0001g0109 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.826+1592T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100345154 | |||||||
| chr14:100345170 | G | A | 2 | a0001c0005t0001g0270 a0001c0005t0001g0271 |
2 | HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.826+1576C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100345170 | |||||||
| chr14:100345232 | C | CG | 79 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(76): Show |
105 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.826+1513dupC | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100345232 | |||||||
| chr14:100345272 | C | T | 1 | a0001c0002t0001g0092 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.826+1474G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100345272 | |||||||
| chr14:100345405 | G | C | 165 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(162): Show |
200 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.826+1341C>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100345405 | |||||||
| chr14:100345470 | C | G | 10 | a0001c0002t0001g0010 a0001c0002t0001g0110 a0001c0002t0001g0111 others(7): Show |
12 | HG01891.hp2 HG02280.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.826+1276G>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100345470 | |||||||
| chr14:100345484 | A | G | 10 | a0001c0002t0001g0010 a0001c0002t0001g0110 a0001c0002t0001g0111 others(7): Show |
12 | HG01891.hp2 HG02280.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.826+1262T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100345484 | |||||||
| chr14:100345525 | G | A | 37 | a0001c0002t0001g0011 a0001c0002t0001g0044 a0001c0002t0001g0109 others(34): Show |
47 | HG00099.hp1 HG00423.hp1 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.826+1221C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100345525 | |||||||
| chr14:100345525 | G | C | 6 | a0001c0001t0001g0013 a0001c0001t0001g0236 a0001c0001t0001g0239 others(3): Show |
8 | HG00099.hp2 HG00738.hp2 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.826+1221C>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100345525 | |||||||
| chr14:100345585 | C | A | 165 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(162): Show |
200 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.826+1161G>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100345585 | |||||||
| chr14:100345660 | AAAAT | A | 163 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(160): Show |
198 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.826+1082_826+1085d others(6): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100345660 | |||||||
| chr14:100345673 | A | T | 1 | a0001c0002t0001g0103 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.826+1073T>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100345673 | |||||||
| chr14:100345677 | TA | T | 10 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0077 others(7): Show |
12 | HG00733.hp2 HG02055.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.826+1068delT | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100345677 | |||||||
| chr14:100345677 | TAA | T | 35 | a0001c0002t0001g0007 a0001c0002t0001g0016 a0001c0002t0001g0017 others(32): Show |
40 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(37): Show |
intron_variant | MODIFIER | c.826+1067_826+1068d others(4): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100345677 | |||||||
| chr14:100345678 | A | T | 17 | a0001c0001t0001g0030 a0001c0001t0001g0032 a0001c0001t0001g0202 others(14): Show |
20 | HG00733.hp1 HG01243.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.826+1068T>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100345678 | |||||||
| chr14:100345712 | A | G | 2 | a0001c0001t0001g0206 a0001c0001t0001g0207 |
2 | HG02257.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.826+1034T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100345712 | |||||||
| chr14:100345757 | T | C | 27 | a0001c0002t0001g0044 a0001c0002t0002g0002 a0001c0002t0002g0006 others(24): Show |
35 | HG00099.hp1 HG00423.hp1 HG02027.hp1 others(32): Show |
intron_variant | MODIFIER | c.826+989A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100345757 | |||||||
| chr14:100345834 | C | T | 37 | a0001c0002t0001g0011 a0001c0002t0001g0044 a0001c0002t0001g0109 others(34): Show |
47 | HG00099.hp1 HG00423.hp1 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.826+912G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100345834 | |||||||
| chr14:100345848 | C | T | 2 | a0001c0002t0001g0019 a0001c0002t0001g0093 |
3 | HG02055.hp1 HG02451.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.826+898G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100345848 | |||||||
| chr14:100345994 | G | A | 5 | a0001c0002t0001g0009 a0001c0002t0001g0105 a0001c0002t0001g0106 others(2): Show |
7 | HG01891.hp1 HG02615.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.826+752C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100345994 | |||||||
| chr14:100346069 | A | G | 165 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(162): Show |
200 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.826+677T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100346069 | |||||||
| chr14:100346116 | G | A | 4 | a0001c0002t0002g0037 a0001c0002t0002g0052 a0001c0002t0002g0057 others(1): Show |
4 | NA18954.hp2 NA18970.hp2 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.826+630C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100346116 | |||||||
| chr14:100346166 | GA | G | 68 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0030 others(65): Show |
76 | HG00099.hp2 HG00438.hp2 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.826+579delT | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100346166 | |||||||
| chr14:100346168 | A | C | 67 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0030 others(64): Show |
75 | HG00099.hp2 HG00438.hp2 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.826+578T>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100346168 | |||||||
| chr14:100346169 | A | C | 67 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0030 others(64): Show |
75 | HG00099.hp2 HG00438.hp2 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.826+577T>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100346169 | |||||||
| chr14:100346170 | T | C | 68 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0030 others(65): Show |
76 | HG00099.hp2 HG00438.hp2 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.826+576A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100346170 | |||||||
| chr14:100346431 | C | G | 1 | a0001c0002t0002g0054 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.826+315G>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100346431 | |||||||
| chr14:100346450 | A | G | 2 | a0001c0005t0001g0270 a0001c0005t0001g0271 |
2 | HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.826+296T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100346450 | |||||||
| chr14:100346471 | T | C | 1 | a0001c0001t0001g0220 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.826+275A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100346471 | |||||||
| chr14:100346593 | G | A | 1 | a0001c0002t0001g0085 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.826+153C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100346593 | |||||||
| chr14:100346608 | C | T | 1 | a0001c0002t0001g0095 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.826+138G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100346608 | |||||||
| chr14:100346740 | T | C | 167 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(164): Show |
202 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(199): Show |
splice_region_variant&intron_variant | LOW | c.826+6A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100346740 | |||||||
| chr14:100346887 | C | T | 2 | a0001c0002t0001g0124 a0001c0002t0001g0125 |
2 | HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.726-41G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100346887 | |||||||
| chr14:100347090 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.726-244T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100347090 | |||||||
| chr14:100347093 | C | A | 3 | a0001c0001t0001g0157 a0001c0001t0001g0167 a0001c0001t0001g0185 |
3 | NA18979.hp2 NA18984.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.726-247G>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100347093 | |||||||
| chr14:100347093 | C | T | 14 | a0001c0002t0001g0010 a0001c0002t0001g0110 a0001c0002t0001g0111 others(11): Show |
16 | HG01891.hp2 HG02280.hp1 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.726-247G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100347093 | |||||||
| chr14:100347094 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.726-248C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100347094 | |||||||
| chr14:100347096 | C | T | 1 | a0001c0008t0001g0261 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.726-250G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100347096 | |||||||
| chr14:100347234 | T | A | 1 | a0001c0001t0001g0181 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.726-388A>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100347234 | |||||||
| chr14:100347370 | C | G | 7 | a0001c0002t0001g0011 a0001c0002t0001g0119 a0001c0002t0001g0120 others(4): Show |
9 | HG00639.hp1 HG02622.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.726-524G>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100347370 | |||||||
| chr14:100347496 | T | G | 266 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(263): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.726-650A>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100347496 | |||||||
| chr14:100347504 | A | G | 261 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(258): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.726-658T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100347504 | |||||||
| chr14:100347556 | G | C | 7 | a0001c0001t0001g0034 a0001c0001t0001g0272 a0001c0001t0001g0273 others(4): Show |
8 | HG02486.hp2 HG02809.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.726-710C>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100347556 | |||||||
| chr14:100347650 | C | T | 1 | a0001c0002t0001g0109 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.726-804G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100347650 | |||||||
| chr14:100347776 | C | A | 4 | a0001c0002t0002g0014 a0001c0002t0002g0040 a0001c0002t0002g0050 others(1): Show |
5 | NA18951.hp2 NA18956.hp1 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.726-930G>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100347776 | |||||||
| chr14:100347777 | A | G | 4 | a0002c0003t0001g0127 a0002c0003t0001g0128 a0002c0003t0001g0129 others(1): Show |
4 | NA18973.hp2 NA18985.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.726-931T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100347777 | |||||||
| chr14:100347867 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.726-1021C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100347867 | |||||||
| chr14:100347956 | C | T | 1 | a0001c0001t0001g0210 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.726-1110G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100347956 | |||||||
| chr14:100348041 | C | G | 7 | a0001c0002t0001g0011 a0001c0002t0001g0119 a0001c0002t0001g0120 others(4): Show |
9 | HG00639.hp1 HG02622.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.726-1195G>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100348041 | |||||||
| chr14:100348070 | T | C | 2 | a0001c0005t0001g0270 a0001c0005t0001g0271 |
2 | HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.726-1224A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100348070 | |||||||
| chr14:100348142 | G | T | 1 | a0001c0002t0001g0062 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.726-1296C>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100348142 | |||||||
| chr14:100348153 | C | T | 2 | a0001c0001t0001g0150 a0001c0001t0001g0175 |
2 | HG01069.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.726-1307G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100348153 | |||||||
| chr14:100348229 | G | C | 2 | a0001c0005t0001g0270 a0001c0005t0001g0271 |
2 | HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.726-1383C>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100348229 | |||||||
| chr14:100348377 | A | T | 1 | a0001c0001t0001g0138 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.726-1531T>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100348377 | |||||||
| chr14:100348380 | GGCA | G | 165 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(162): Show |
200 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.726-1537_726-1535d others(5): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100348380 | |||||||
| chr14:100348411 | G | T | 1 | a0001c0001t0001g0204 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.726-1565C>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100348411 | |||||||
| chr14:100348421 | C | T | 27 | a0001c0002t0001g0044 a0001c0002t0002g0002 a0001c0002t0002g0006 others(24): Show |
35 | HG00099.hp1 HG00423.hp1 HG02027.hp1 others(32): Show |
intron_variant | MODIFIER | c.726-1575G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100348421 | |||||||
| chr14:100348442 | G | A | 4 | a0001c0002t0001g0009 a0001c0002t0001g0105 a0001c0002t0001g0107 others(1): Show |
6 | HG01891.hp1 HG02615.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.726-1596C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100348442 | |||||||
| chr14:100348458 | C | T | 5 | a0001c0002t0002g0014 a0001c0002t0002g0040 a0001c0002t0002g0049 others(2): Show |
6 | NA18951.hp2 NA18955.hp1 NA18956.hp1 others(3): Show |
intron_variant | MODIFIER | c.726-1612G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100348458 | |||||||
| chr14:100348642 | C | T | 2 | a0001c0002t0002g0055 a0001c0002t0002g0056 |
2 | HG00423.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.726-1796G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100348642 | |||||||
| chr14:100348809 | A | G | 208 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(205): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.726-1963T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100348809 | |||||||
| chr14:100348810 | C | T | 41 | a0001c0002t0001g0011 a0001c0002t0001g0044 a0001c0002t0001g0109 others(38): Show |
51 | HG00099.hp1 HG00423.hp1 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.726-1964G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100348810 | |||||||
| chr14:100348964 | T | C | 1 | a0001c0002t0001g0113 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.726-2118A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100348964 | |||||||
| chr14:100348992 | C | T | 1 | a0001c0002t0001g0094 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.726-2146G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100348992 | |||||||
| chr14:100349093 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.726-2247G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100349093 | |||||||
| chr14:100349181 | T | C | 4 | a0002c0003t0001g0127 a0002c0003t0001g0128 a0002c0003t0001g0129 others(1): Show |
4 | NA18973.hp2 NA18985.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.726-2335A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100349181 | |||||||
| chr14:100349300 | T | G | 1 | a0001c0001t0001g0180 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.726-2454A>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100349300 | |||||||
| chr14:100349529 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.726-2683G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100349529 | |||||||
| chr14:100349575 | C | T | 27 | a0001c0002t0001g0044 a0001c0002t0002g0002 a0001c0002t0002g0006 others(24): Show |
35 | HG00099.hp1 HG00423.hp1 HG02027.hp1 others(32): Show |
intron_variant | MODIFIER | c.726-2729G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100349575 | |||||||
| chr14:100349611 | G | A | 1 | a0001c0002t0001g0109 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.726-2765C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100349611 | |||||||
| chr14:100350185 | C | CAGGA | 266 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(263): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.726-3340_726-3339i others(6): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100350185 | |||||||
| chr14:100350399 | G | A | 1 | a0001c0001t0001g0149 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.725+3288C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100350399 | |||||||
| chr14:100350399 | G | GAAAA | 13 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0028 others(10): Show |
19 | HG00140.hp1 HG01074.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.725+3284_725+3287d others(6): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100350399 | |||||||
| chr14:100350399 | G | GAAAAA | 154 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(151): Show |
180 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.725+3283_725+3287d others(7): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100350399 | |||||||
| chr14:100350399 | G | GAAAAAA | 68 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0159 others(65): Show |
81 | HG00099.hp1 HG00423.hp1 HG00639.hp1 others(78): Show |
intron_variant | MODIFIER | c.725+3282_725+3287d others(8): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100350399 | |||||||
| chr14:100350399 | G | GAAAAAAA | 41 | a0001c0002t0001g0007 a0001c0002t0001g0016 a0001c0002t0001g0017 others(38): Show |
46 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.725+3281_725+3287d others(9): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100350399 | |||||||
| chr14:100350407 | A | G | 1 | a0001c0001t0001g0022 | 2 | NA18960.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.725+3280T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100350407 | |||||||
| chr14:100350464 | G | A | 3 | a0001c0001t0001g0024 a0001c0001t0001g0169 a0001c0001t0001g0199 |
4 | HG01167.hp1 HG02040.hp1 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.725+3223C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100350464 | |||||||
| chr14:100350597 | T | C | 4 | a0002c0003t0001g0127 a0002c0003t0001g0128 a0002c0003t0001g0129 others(1): Show |
4 | NA18973.hp2 NA18985.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.725+3090A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100350597 | |||||||
| chr14:100350627 | G | C | 41 | a0001c0002t0001g0011 a0001c0002t0001g0044 a0001c0002t0001g0109 others(38): Show |
51 | HG00099.hp1 HG00423.hp1 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.725+3060C>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100350627 | |||||||
| chr14:100350669 | C | T | 1 | a0001c0002t0001g0078 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.725+3018G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100350669 | |||||||
| chr14:100350688 | T | C | 41 | a0001c0002t0001g0011 a0001c0002t0001g0044 a0001c0002t0001g0109 others(38): Show |
51 | HG00099.hp1 HG00423.hp1 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.725+2999A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100350688 | |||||||
| chr14:100350693 | C | G | 2 | a0001c0002t0001g0017 a0001c0002t0001g0084 |
3 | NA18950.hp1 NA19055.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.725+2994G>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100350693 | |||||||
| chr14:100350899 | T | C | 4 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0141 others(1): Show |
4 | HG01928.hp1 HG01975.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.725+2788A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100350899 | |||||||
| chr14:100350929 | G | T | 12 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0033 others(9): Show |
16 | HG01433.hp2 HG02132.hp2 HG02135.hp2 others(13): Show |
intron_variant | MODIFIER | c.725+2758C>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100350929 | |||||||
| chr14:100351073 | G | C | 2 | a0001c0001t0001g0212 a0001c0001t0001g0219 |
2 | HG02602.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.725+2614C>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100351073 | |||||||
| chr14:100351120 | A | T | 41 | a0001c0002t0001g0011 a0001c0002t0001g0044 a0001c0002t0001g0109 others(38): Show |
51 | HG00099.hp1 HG00423.hp1 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.725+2567T>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100351120 | |||||||
| chr14:100351422 | C | T | 27 | a0001c0002t0001g0044 a0001c0002t0002g0002 a0001c0002t0002g0006 others(24): Show |
35 | HG00099.hp1 HG00423.hp1 HG02027.hp1 others(32): Show |
intron_variant | MODIFIER | c.725+2265G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100351422 | |||||||
| chr14:100351477 | A | G | 1 | a0001c0001t0001g0022 | 2 | NA18960.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.725+2210T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100351477 | |||||||
| chr14:100351499 | CA | C | 143 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(140): Show |
179 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.725+2187delT | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100351499 | |||||||
| chr14:100351499 | CAA | C | 107 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0030 others(104): Show |
125 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.725+2186_725+2187d others(4): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100351499 | |||||||
| chr14:100351528 | C | T | 2 | a0001c0002t0001g0124 a0001c0002t0001g0125 |
2 | HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.725+2159G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100351528 | |||||||
| chr14:100351719 | C | A | 7 | a0001c0002t0001g0011 a0001c0002t0001g0119 a0001c0002t0001g0120 others(4): Show |
9 | HG00639.hp1 HG02622.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.725+1968G>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100351719 | |||||||
| chr14:100351752 | G | C | 2 | a0001c0005t0001g0270 a0001c0005t0001g0271 |
2 | HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.725+1935C>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100351752 | |||||||
| chr14:100351760 | G | A | 1 | a0001c0002t0001g0109 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.725+1927C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100351760 | |||||||
| chr14:100351837 | C | G | 1 | a0001c0002t0002g0040 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.725+1850G>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100351837 | |||||||
| chr14:100351850 | G | A | 1 | a0001c0001t0001g0238 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.725+1837C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100351850 | |||||||
| chr14:100351949 | T | C | 201 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(198): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.725+1738A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100351949 | |||||||
| chr14:100351987 | C | T | 1 | a0001c0002t0002g0054 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.725+1700G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100351987 | |||||||
| chr14:100351992 | C | T | 27 | a0001c0002t0001g0044 a0001c0002t0002g0002 a0001c0002t0002g0006 others(24): Show |
35 | HG00099.hp1 HG00423.hp1 HG02027.hp1 others(32): Show |
intron_variant | MODIFIER | c.725+1695G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100351992 | |||||||
| chr14:100352002 | A | AG | 160 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(157): Show |
195 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.725+1684_725+1685i others(3): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100352002 | |||||||
| chr14:100352002 | A | G | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | NA18991.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.725+1685T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100352002 | |||||||
| chr14:100352108 | C | CT | 147 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(144): Show |
182 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.725+1578dupA | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100352108 | |||||||
| chr14:100352108 | C | CTT | 22 | a0001c0001t0001g0132 a0001c0001t0001g0146 a0001c0001t0001g0147 others(19): Show |
22 | HG00621.hp1 HG00621.hp2 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.725+1577_725+1578d others(4): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100352108 | |||||||
| chr14:100352108 | CT | C | 8 | a0001c0002t0001g0010 a0001c0002t0001g0113 a0001c0002t0002g0039 others(5): Show |
10 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.725+1578delA | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100352108 | |||||||
| chr14:100352108 | CTTTTT | C | 9 | a0001c0002t0001g0011 a0001c0002t0001g0119 a0001c0002t0001g0120 others(6): Show |
11 | HG00639.hp1 HG02622.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.725+1574_725+1578d others(7): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100352108 | |||||||
| chr14:100352180 | C | T | 4 | a0002c0003t0001g0127 a0002c0003t0001g0128 a0002c0003t0001g0129 others(1): Show |
4 | NA18973.hp2 NA18985.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.725+1507G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100352180 | |||||||
| chr14:100352260 | C | T | 6 | a0001c0001t0001g0098 a0001c0002t0001g0005 a0001c0002t0001g0097 others(3): Show |
9 | HG02280.hp2 HG02559.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.725+1427G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100352260 | |||||||
| chr14:100352422 | C | G | 165 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(162): Show |
200 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.725+1265G>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100352422 | |||||||
| chr14:100352523 | T | C | 1 | a0001c0001t0001g0191 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.725+1164A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100352523 | |||||||
| chr14:100352533 | C | T | 1 | a0001c0001t0001g0225 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.725+1154G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100352533 | |||||||
| chr14:100352587 | T | G | 1 | a0001c0002t0002g0047 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.725+1100A>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100352587 | |||||||
| chr14:100352652 | C | T | 1 | a0001c0002t0001g0060 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.725+1035G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100352652 | |||||||
| chr14:100352880 | G | A | 2 | a0001c0002t0001g0124 a0001c0002t0001g0125 |
2 | HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.725+807C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100352880 | |||||||
| chr14:100352948 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.725+739C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100352948 | |||||||
| chr14:100352953 | C | T | 2 | a0001c0002t0001g0120 a0001c0002t0001g0121 |
2 | HG00639.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.725+734G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100352953 | |||||||
| chr14:100353271 | G | T | 1 | a0001c0001t0001g0230 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.725+416C>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100353271 | |||||||
| chr14:100353343 | C | T | 165 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(162): Show |
200 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.725+344G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100353343 | |||||||
| chr14:100353398 | G | A | 27 | a0001c0002t0001g0044 a0001c0002t0002g0002 a0001c0002t0002g0006 others(24): Show |
35 | HG00099.hp1 HG00423.hp1 HG02027.hp1 others(32): Show |
intron_variant | MODIFIER | c.725+289C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100353398 | |||||||
| chr14:100353439 | T | TG | 261 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(258): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.725+247dupC | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100353439 | |||||||
| chr14:100353491 | G | A | 2 | a0001c0002t0001g0010 a0001c0002t0001g0113 |
4 | HG01891.hp2 HG02280.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.725+196C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100353491 | |||||||
| chr14:100353581 | T | C | 3 | a0001c0002t0001g0114 a0001c0002t0001g0115 a0001c0002t0001g0118 |
3 | HG02895.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.725+106A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100353581 | |||||||
| chr14:100353957 | C | A | 2 | a0001c0001t0001g0206 a0001c0001t0001g0207 |
2 | HG02257.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.543-88G>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 5/10 | chr14 | 100353957 | |||||||
| chr14:100353996 | T | C | 1 | a0001c0001t0001g0169 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.543-127A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 5/10 | chr14 | 100353996 | |||||||
| chr14:100354087 | C | T | 7 | a0001c0001t0001g0098 a0001c0002t0001g0005 a0001c0002t0001g0097 others(4): Show |
10 | HG01884.hp2 HG02280.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.543-218G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 5/10 | chr14 | 100354087 | |||||||
| chr14:100354199 | A | G | 208 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(205): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.542+248T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 5/10 | chr14 | 100354199 | |||||||
| chr14:100354643 | G | A | 165 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(162): Show |
200 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.423-77C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100354643 | |||||||
| chr14:100354670 | T | C | 1 | a0001c0001t0001g0239 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.423-104A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100354670 | |||||||
| chr14:100354831 | TC | T | 4 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0136 others(1): Show |
6 | HG01099.hp2 HG02258.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.423-266delG | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100354831 | |||||||
| chr14:100354869 | G | T | 165 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(162): Show |
200 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.423-303C>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100354869 | |||||||
| chr14:100354898 | G | A | 1 | a0001c0002t0002g0015 | 2 | NA18940.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.423-332C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100354898 | |||||||
| chr14:100354935 | C | G | 1 | a0001c0001t0001g0153 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.423-369G>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100354935 | |||||||
| chr14:100355050 | G | T | 1 | a0001c0001t0001g0183 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.423-484C>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100355050 | |||||||
| chr14:100355185 | A | C | 1 | a0001c0002t0001g0111 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.423-619T>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100355185 | |||||||
| chr14:100355324 | G | A | 5 | a0001c0002t0002g0006 a0001c0002t0002g0039 a0001c0002t0002g0041 others(2): Show |
7 | HG02040.hp2 HG02132.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.423-758C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100355324 | |||||||
| chr14:100355369 | C | T | 1 | a0001c0002t0002g0048 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.423-803G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100355369 | |||||||
| chr14:100355444 | A | G | 2 | a0001c0001t0001g0255 a0001c0001t0001g0257 |
2 | HG02486.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.423-878T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100355444 | |||||||
| chr14:100355609 | T | C | 1 | a0001c0001t0001g0227 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.423-1043A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100355609 | |||||||
| chr14:100355657 | A | G | 67 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0030 others(64): Show |
75 | HG00099.hp2 HG00438.hp2 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.423-1091T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100355657 | |||||||
| chr14:100355658 | G | T | 67 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0030 others(64): Show |
75 | HG00099.hp2 HG00438.hp2 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.423-1092C>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100355658 | |||||||
| chr14:100355812 | C | T | 9 | a0001c0002t0001g0011 a0001c0002t0001g0119 a0001c0002t0001g0120 others(6): Show |
11 | HG00639.hp1 HG02622.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.423-1246G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100355812 | |||||||
| chr14:100355936 | C | T | 165 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(162): Show |
200 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.423-1370G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100355936 | |||||||
| chr14:100355964 | G | A | 27 | a0001c0002t0001g0044 a0001c0002t0002g0002 a0001c0002t0002g0006 others(24): Show |
35 | HG00099.hp1 HG00423.hp1 HG02027.hp1 others(32): Show |
intron_variant | MODIFIER | c.423-1398C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100355964 | |||||||
| chr14:100356055 | T | C | 6 | a0001c0001t0001g0098 a0001c0002t0001g0005 a0001c0002t0001g0097 others(3): Show |
9 | HG02280.hp2 HG02559.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.423-1489A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100356055 | |||||||
| chr14:100356165 | T | C | 41 | a0001c0002t0001g0011 a0001c0002t0001g0044 a0001c0002t0001g0109 others(38): Show |
51 | HG00099.hp1 HG00423.hp1 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.423-1599A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100356165 | |||||||
| chr14:100356227 | A | T | 7 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0092 others(4): Show |
9 | HG00733.hp2 HG02055.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.423-1661T>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100356227 | |||||||
| chr14:100356382 | GGT | G | 74 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(71): Show |
100 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.423-1818_423-1817d others(4): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100356382 | |||||||
| chr14:100356386 | T | G | 3 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0188 |
3 | HG02109.hp2 HG03098.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.423-1820A>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100356386 | |||||||
| chr14:100356394 | T | TG | 8 | a0001c0001t0001g0231 a0001c0001t0001g0240 a0001c0001t0001g0241 others(5): Show |
8 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.423-1829dupC | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100356394 | |||||||
| chr14:100356394 | T | TGG | 4 | a0001c0001t0001g0227 a0002c0003t0001g0127 a0002c0003t0001g0129 others(1): Show |
4 | NA18962.hp1 NA18985.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.423-1829_423-1828i others(4): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100356394 | |||||||
| chr14:100356396 | T | G | 16 | a0001c0001t0001g0218 a0001c0001t0001g0227 a0001c0001t0001g0231 others(13): Show |
18 | HG00639.hp1 HG01081.hp1 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.423-1830A>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100356396 | |||||||
| chr14:100356396 | T | TG | 43 | a0001c0001t0001g0012 a0001c0001t0001g0030 a0001c0001t0001g0031 others(40): Show |
48 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.423-1831dupC | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100356396 | |||||||
| chr14:100356396 | T | TGG | 12 | a0001c0001t0001g0012 a0001c0001t0001g0214 a0001c0001t0001g0216 others(9): Show |
12 | HG01074.hp1 HG02132.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.423-1831_423-1830i others(4): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100356396 | |||||||
| chr14:100356396 | T | TGGG | 7 | a0001c0001t0001g0220 a0001c0001t0001g0225 a0001c0001t0001g0252 others(4): Show |
8 | HG00621.hp1 HG01891.hp1 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.423-1831_423-1830i others(5): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100356396 | |||||||
| chr14:100356397 | GT | G | 38 | a0001c0001t0001g0142 a0001c0001t0001g0170 a0001c0001t0001g0194 others(35): Show |
43 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(40): Show |
intron_variant | MODIFIER | c.423-1832delA | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100356397 | |||||||
| chr14:100356398 | T | G | 82 | a0001c0001t0001g0012 a0001c0001t0001g0026 a0001c0001t0001g0030 others(79): Show |
92 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.423-1832A>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100356398 | |||||||
| chr14:100356398 | T | TG | 27 | a0001c0001t0001g0013 a0001c0001t0001g0212 a0001c0001t0001g0219 others(24): Show |
35 | HG00738.hp2 HG01175.hp2 HG01192.hp2 others(32): Show |
intron_variant | MODIFIER | c.423-1833dupC | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100356398 | |||||||
| chr14:100356398 | TGG | T | 27 | a0001c0001t0001g0034 a0001c0001t0001g0132 a0001c0001t0001g0133 others(24): Show |
30 | HG00438.hp1 HG01891.hp2 HG02280.hp1 others(27): Show |
intron_variant | MODIFIER | c.423-1834_423-1833d others(4): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100356398 | |||||||
| chr14:100356400 | G | T | 1 | a0001c0002t0001g0103 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.423-1834C>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100356400 | |||||||
| chr14:100356555 | T | C | 1 | a0001c0001t0001g0177 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.423-1989A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100356555 | |||||||
| chr14:100356679 | A | C | 1 | a0001c0001t0001g0139 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.423-2113T>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100356679 | |||||||
| chr14:100356725 | T | G | 1 | a0001c0002t0001g0109 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.423-2159A>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100356725 | |||||||
| chr14:100356971 | G | A | 1 | a0001c0002t0001g0077 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.423-2405C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100356971 | |||||||
| chr14:100356987 | C | T | 3 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0188 |
3 | HG02109.hp2 HG03098.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.423-2421G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100356987 | |||||||
| chr14:100357005 | C | T | 1 | a0001c0002t0001g0109 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.423-2439G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100357005 | |||||||
| chr14:100357158 | T | C | 2 | a0001c0001t0001g0171 a0001c0001t0001g0172 |
2 | HG00673.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.423-2592A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100357158 | |||||||
| chr14:100357378 | C | A | 10 | a0001c0002t0001g0010 a0001c0002t0001g0110 a0001c0002t0001g0111 others(7): Show |
12 | HG01891.hp2 HG02280.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.423-2812G>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100357378 | |||||||
| chr14:100357571 | C | T | 37 | a0001c0002t0001g0011 a0001c0002t0001g0044 a0001c0002t0001g0109 others(34): Show |
47 | HG00099.hp1 HG00423.hp1 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.422+2983G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100357571 | |||||||
| chr14:100357607 | G | A | 41 | a0001c0002t0001g0011 a0001c0002t0001g0044 a0001c0002t0001g0109 others(38): Show |
51 | HG00099.hp1 HG00423.hp1 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.422+2947C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100357607 | |||||||
| chr14:100357712 | C | T | 165 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(162): Show |
200 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.422+2842G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100357712 | |||||||
| chr14:100357749 | C | T | 1 | a0001c0002t0001g0093 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.422+2805G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100357749 | |||||||
| chr14:100357832 | T | C | 4 | a0002c0003t0001g0127 a0002c0003t0001g0128 a0002c0003t0001g0129 others(1): Show |
4 | NA18973.hp2 NA18985.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.422+2722A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100357832 | |||||||
| chr14:100357938 | T | C | 1 | a0001c0002t0001g0075 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.422+2616A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100357938 | |||||||
| chr14:100358018 | C | T | 2 | a0001c0005t0001g0270 a0001c0005t0001g0271 |
2 | HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.422+2536G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100358018 | |||||||
| chr14:100358052 | G | A | 165 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(162): Show |
200 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.422+2502C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100358052 | |||||||
| chr14:100358079 | C | G | 1 | a0001c0001t0001g0248 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.422+2475G>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100358079 | |||||||
| chr14:100358157 | C | T | 165 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(162): Show |
200 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.422+2397G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100358157 | |||||||
| chr14:100358170 | C | T | 165 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(162): Show |
200 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.422+2384G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100358170 | |||||||
| chr14:100358202 | G | A | 2 | a0001c0005t0001g0270 a0001c0005t0001g0271 |
2 | HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.422+2352C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100358202 | |||||||
| chr14:100358219 | G | A | 165 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(162): Show |
200 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.422+2335C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100358219 | |||||||
| chr14:100358220 | C | T | 2 | a0001c0001t0001g0229 a0001c0001t0001g0232 |
2 | NA18946.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.422+2334G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100358220 | |||||||
| chr14:100358226 | G | A | 163 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(160): Show |
198 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.422+2328C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100358226 | |||||||
| chr14:100358303 | T | C | 165 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(162): Show |
200 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.422+2251A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100358303 | |||||||
| chr14:100358359 | C | CCT | 9 | a0001c0002t0001g0011 a0001c0002t0001g0119 a0001c0002t0001g0120 others(6): Show |
11 | HG00639.hp1 HG02622.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.422+2193_422+2194d others(4): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100358359 | |||||||
| chr14:100358678 | G | T | 1 | a0001c0002t0001g0111 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.422+1876C>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100358678 | |||||||
| chr14:100359118 | A | G | 2 | a0001c0005t0001g0270 a0001c0005t0001g0271 |
2 | HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.422+1436T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100359118 | |||||||
| chr14:100359119 | A | T | 1 | a0001c0002t0001g0068 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.422+1435T>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100359119 | |||||||
| chr14:100359239 | G | A | 1 | a0001c0001t0001g0258 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.422+1315C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100359239 | |||||||
| chr14:100359286 | G | C | 2 | a0001c0001t0001g0206 a0001c0001t0001g0207 |
2 | HG02257.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.422+1268C>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100359286 | |||||||
| chr14:100359333 | C | T | 67 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0030 others(64): Show |
75 | HG00099.hp2 HG00438.hp2 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.422+1221G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100359333 | |||||||
| chr14:100359439 | C | T | 165 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(162): Show |
200 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.422+1115G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100359439 | |||||||
| chr14:100359544 | T | C | 1 | a0001c0001t0001g0145 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.422+1010A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100359544 | |||||||
| chr14:100359551 | C | T | 2 | a0001c0005t0001g0270 a0001c0005t0001g0271 |
2 | HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.422+1003G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100359551 | |||||||
| chr14:100359863 | G | A | 96 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(93): Show |
123 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.422+691C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100359863 | |||||||
| chr14:100359923 | G | C | 208 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(205): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.422+631C>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100359923 | |||||||
| chr14:100360074 | C | A | 3 | a0001c0001t0001g0218 a0001c0001t0001g0231 a0001c0001t0001g0241 |
3 | HG01081.hp1 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.422+480G>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100360074 | |||||||
| chr14:100360098 | A | G | 165 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(162): Show |
200 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.422+456T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100360098 | |||||||
| chr14:100360321 | C | T | 7 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0092 others(4): Show |
9 | HG00733.hp2 HG02055.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.422+233G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100360321 | |||||||
| chr14:100360394 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.422+160G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100360394 | |||||||
| chr14:100360404 | C | T | 1 | a0002c0003t0001g0127 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.422+150G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100360404 | |||||||
| chr14:100360436 | C | G | 208 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(205): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.422+118G>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100360436 | |||||||
| chr14:100360470 | T | G | 1 | a0001c0001t0001g0148 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.422+84A>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100360470 | |||||||
| chr14:100360471 | G | T | 1 | a0001c0001t0001g0148 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.422+83C>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100360471 | |||||||
| chr14:100360728 | T | C | 1 | a0001c0001t0001g0223 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.314-66A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 3/10 | chr14 | 100360728 | |||||||
| chr14:100360805 | C | A | 2 | a0001c0005t0001g0270 a0001c0005t0001g0271 |
2 | HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.314-143G>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 3/10 | chr14 | 100360805 | |||||||
| chr14:100360805 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.314-143G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 3/10 | chr14 | 100360805 | |||||||
| chr14:100360997 | G | GTA | 5 | a0001c0002t0002g0006 a0001c0002t0002g0039 a0001c0002t0002g0041 others(2): Show |
7 | HG02040.hp2 HG02132.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.314-337_314-336dup others(2): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 3/10 | chr14 | 100360997 | |||||||
| chr14:100360997 | GTA | G | 7 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0092 others(4): Show |
9 | HG00733.hp2 HG02055.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.314-337_314-336del others(2): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 3/10 | chr14 | 100360997 | |||||||
| chr14:100361092 | G | T | 208 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(205): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.314-430C>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 3/10 | chr14 | 100361092 | |||||||
| chr14:100361171 | C | T | 208 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(205): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.314-509G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 3/10 | chr14 | 100361171 | |||||||
| chr14:100361234 | A | G | 1 | a0001c0001t0001g0223 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.313+474T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 3/10 | chr14 | 100361234 | |||||||
| chr14:100361305 | A | G | 2 | a0001c0005t0001g0270 a0001c0005t0001g0271 |
2 | HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.313+403T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 3/10 | chr14 | 100361305 | |||||||
| chr14:100361341 | T | C | 1 | a0001c0002t0002g0059 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.313+367A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 3/10 | chr14 | 100361341 | |||||||
| chr14:100362060 | T | C | 165 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(162): Show |
200 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.100-139A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100362060 | |||||||
| chr14:100362126 | T | C | 1 | a0001c0002t0002g0057 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.100-205A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100362126 | |||||||
| chr14:100362150 | C | T | 165 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(162): Show |
200 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.100-229G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100362150 | |||||||
| chr14:100362288 | C | T | 29 | a0001c0002t0001g0007 a0001c0002t0001g0016 a0001c0002t0001g0017 others(26): Show |
34 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(31): Show |
intron_variant | MODIFIER | c.100-367G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100362288 | |||||||
| chr14:100362346 | T | C | 27 | a0001c0002t0001g0044 a0001c0002t0002g0002 a0001c0002t0002g0006 others(24): Show |
35 | HG00099.hp1 HG00423.hp1 HG02027.hp1 others(32): Show |
intron_variant | MODIFIER | c.100-425A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100362346 | |||||||
| chr14:100362533 | G | GA | 35 | a0001c0002t0001g0011 a0001c0002t0001g0044 a0001c0002t0001g0109 others(32): Show |
45 | HG00099.hp1 HG00423.hp1 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.100-613dupT | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100362533 | |||||||
| chr14:100362847 | C | T | 43 | a0001c0002t0001g0007 a0001c0002t0001g0016 a0001c0002t0001g0017 others(40): Show |
50 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.100-926G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100362847 | |||||||
| chr14:100363227 | A | G | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | NA19064.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.100-1306T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100363227 | |||||||
| chr14:100363266 | A | T | 43 | a0001c0002t0001g0007 a0001c0002t0001g0016 a0001c0002t0001g0017 others(40): Show |
50 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.100-1345T>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100363266 | |||||||
| chr14:100363268 | TTAACCAA others(5): Show |
T | 43 | a0001c0002t0001g0007 a0001c0002t0001g0016 a0001c0002t0001g0017 others(40): Show |
50 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.100-1359_100-1348d others(14): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100363268 | |||||||
| chr14:100363511 | C | T | 98 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(95): Show |
125 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.100-1590G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100363511 | |||||||
| chr14:100363521 | C | T | 2 | a0001c0001t0001g0132 a0001c0001t0001g0133 |
2 | HG03098.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.100-1600G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100363521 | |||||||
| chr14:100363654 | A | G | 266 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(263): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.100-1733T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100363654 | |||||||
| chr14:100363839 | C | A | 1 | a0001c0001t0001g0277 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.100-1918G>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100363839 | |||||||
| chr14:100363922 | C | G | 266 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(263): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.100-2001G>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100363922 | |||||||
| chr14:100364036 | T | G | 3 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0188 |
3 | HG02109.hp2 HG03098.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.100-2115A>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100364036 | |||||||
| chr14:100364055 | C | G | 5 | a0001c0002t0001g0064 a0001c0002t0001g0076 a0001c0002t0001g0083 others(2): Show |
5 | HG00558.hp1 HG02165.hp1 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.100-2134G>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100364055 | |||||||
| chr14:100364214 | A | G | 1 | a0001c0001t0001g0173 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.100-2293T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100364214 | |||||||
| chr14:100364254 | G | A | 1 | a0001c0002t0001g0109 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.100-2333C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100364254 | |||||||
| chr14:100364288 | C | G | 1 | a0001c0002t0001g0087 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.100-2367G>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100364288 | |||||||
| chr14:100364289 | A | C | 1 | a0001c0002t0001g0087 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.100-2368T>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100364289 | |||||||
| chr14:100364290 | G | A | 1 | a0001c0002t0001g0087 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.100-2369C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100364290 | |||||||
| chr14:100364418 | A | T | 1 | a0001c0002t0001g0087 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.100-2497T>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100364418 | |||||||
| chr14:100364481 | C | A | 43 | a0001c0002t0001g0007 a0001c0002t0001g0016 a0001c0002t0001g0017 others(40): Show |
50 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.100-2560G>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100364481 | |||||||
| chr14:100364483 | C | G | 2 | a0001c0002t0001g0124 a0001c0002t0001g0125 |
2 | HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.100-2562G>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100364483 | |||||||
| chr14:100364581 | T | G | 1 | a0001c0002t0001g0087 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.100-2660A>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100364581 | |||||||
| chr14:100364820 | G | C | 2 | a0001c0002t0001g0124 a0001c0002t0001g0125 |
2 | HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.100-2899C>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100364820 | |||||||
| chr14:100364906 | A | G | 7 | a0001c0002t0001g0011 a0001c0002t0001g0119 a0001c0002t0001g0120 others(4): Show |
9 | HG00639.hp1 HG02622.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.100-2985T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100364906 | |||||||
| chr14:100364910 | A | C | 1 | a0001c0001t0001g0145 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.100-2989T>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100364910 | |||||||
| chr14:100364973 | A | C | 266 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(263): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.100-3052T>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100364973 | |||||||
| chr14:100365037 | T | G | 1 | a0001c0002t0001g0087 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.100-3116A>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100365037 | |||||||
| chr14:100365038 | G | T | 1 | a0001c0002t0001g0087 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.100-3117C>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100365038 | |||||||
| chr14:100365124 | T | TAC | 71 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0030 others(68): Show |
82 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.100-3205_100-3204d others(4): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100365124 | |||||||
| chr14:100365124 | T | TACAC | 50 | a0001c0001t0001g0012 a0001c0001t0001g0021 a0001c0001t0001g0028 others(47): Show |
62 | HG00099.hp1 HG00639.hp1 HG00733.hp2 others(59): Show |
intron_variant | MODIFIER | c.100-3207_100-3204d others(6): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100365124 | |||||||
| chr14:100365124 | T | TACACAC | 29 | a0001c0001t0001g0031 a0001c0001t0001g0207 a0001c0001t0001g0249 others(26): Show |
39 | HG01175.hp1 HG01433.hp2 HG01496.hp1 others(36): Show |
intron_variant | MODIFIER | c.100-3209_100-3204d others(8): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100365124 | |||||||
| chr14:100365124 | T | TACACACA others(1): Show |
16 | a0001c0001t0003g0196 a0001c0002t0001g0010 a0001c0002t0001g0017 others(13): Show |
20 | HG01169.hp1 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.100-3211_100-3204d others(10): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100365124 | |||||||
| chr14:100365124 | T | TACACACA others(3): Show |
15 | a0001c0002t0001g0007 a0001c0002t0001g0060 a0001c0002t0001g0068 others(12): Show |
17 | HG00140.hp2 HG00544.hp1 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.100-3213_100-3204d others(12): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100365124 | |||||||
| chr14:100365124 | T | TACACACA others(5): Show |
4 | a0001c0002t0001g0078 a0001c0002t0001g0079 a0001c0002t0001g0126 others(1): Show |
4 | HG00423.hp1 HG02622.hp1 HG04228.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-3215_100-3204d others(14): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100365124 | |||||||
| chr14:100365124 | T | TACACACA others(7): Show |
4 | a0001c0002t0001g0064 a0001c0002t0001g0080 a0001c0002t0001g0086 others(1): Show |
4 | HG00558.hp1 NA18999.hp2 NA19077.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-3217_100-3204d others(16): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100365124 | |||||||
| chr14:100365124 | TACAC | T | 4 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0186 others(1): Show |
6 | HG01515.hp1 HG02109.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.100-3207_100-3204d others(6): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100365124 | |||||||
| chr14:100365124 | TACACACA others(3): Show |
T | 1 | a0001c0001t0001g0209 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.100-3213_100-3204d others(12): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100365124 | |||||||
| chr14:100365155 | A | ACACACAC others(4): Show |
1 | a0001c0002t0001g0087 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.100-3235_100-3234i others(13): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100365155 | |||||||
| chr14:100365162 | C | A | 2 | a0001c0001t0001g0025 a0001c0001t0001g0215 |
3 | HG02129.hp2 NA18970.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.100-3241G>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100365162 | |||||||
| chr14:100365163 | A | ACACACAC others(4): Show |
2 | a0001c0002t0001g0065 a0001c0002t0001g0088 |
2 | HG02056.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.100-3243_100-3242i others(13): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100365163 | |||||||
| chr14:100365220 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.100-3299C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100365220 | |||||||
| chr14:100365270 | TAACAGGA others(13): Show |
T | 67 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0030 others(64): Show |
75 | HG00099.hp2 HG00438.hp2 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.100-3369_100-3350d others(22): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100365270 | |||||||
| chr14:100365437 | G | A | 165 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(162): Show |
200 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.100-3516C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100365437 | |||||||
| chr14:100365452 | C | T | 27 | a0001c0002t0001g0044 a0001c0002t0002g0002 a0001c0002t0002g0006 others(24): Show |
35 | HG00099.hp1 HG00423.hp1 HG02027.hp1 others(32): Show |
intron_variant | MODIFIER | c.100-3531G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100365452 | |||||||
| chr14:100365498 | C | T | 208 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(205): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.100-3577G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100365498 | |||||||
| chr14:100365559 | G | A | 7 | a0001c0001t0001g0034 a0001c0001t0001g0272 a0001c0001t0001g0273 others(4): Show |
8 | HG02486.hp2 HG02809.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.99+3528C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100365559 | |||||||
| chr14:100365579 | C | CA | 11 | a0001c0001t0001g0219 a0001c0001t0001g0222 a0001c0001t0001g0228 others(8): Show |
13 | HG01891.hp1 HG02145.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.99+3507dupT | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100365579 | |||||||
| chr14:100365579 | CA | C | 146 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(143): Show |
182 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.99+3507delT | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100365579 | |||||||
| chr14:100365579 | CAA | C | 35 | a0001c0002t0001g0011 a0001c0002t0001g0044 a0001c0002t0001g0109 others(32): Show |
45 | HG00099.hp1 HG00423.hp1 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.99+3506_99+3507del others(2): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100365579 | |||||||
| chr14:100365728 | CT | C | 177 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(174): Show |
207 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(204): Show |
intron_variant | MODIFIER | c.99+3358delA | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100365728 | |||||||
| chr14:100365728 | CTT | C | 44 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0138 others(41): Show |
59 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.99+3357_99+3358del others(2): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100365728 | |||||||
| chr14:100365732 | T | C | 10 | a0001c0002t0001g0010 a0001c0002t0001g0110 a0001c0002t0001g0111 others(7): Show |
12 | HG01891.hp2 HG02280.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.99+3355A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100365732 | |||||||
| chr14:100365870 | T | A | 7 | a0001c0001t0001g0034 a0001c0001t0001g0272 a0001c0001t0001g0273 others(4): Show |
8 | HG02486.hp2 HG02809.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.99+3217A>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100365870 | |||||||
| chr14:100365873 | T | C | 9 | a0001c0002t0001g0011 a0001c0002t0001g0119 a0001c0002t0001g0120 others(6): Show |
11 | HG00639.hp1 HG02622.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.99+3214A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100365873 | |||||||
| chr14:100365915 | C | T | 69 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(66): Show |
91 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.99+3172G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100365915 | |||||||
| chr14:100365945 | C | G | 208 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(205): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.99+3142G>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100365945 | |||||||
| chr14:100366040 | C | T | 1 | a0001c0002t0001g0109 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.99+3047G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100366040 | |||||||
| chr14:100366054 | T | C | 165 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(162): Show |
200 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.99+3033A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100366054 | |||||||
| chr14:100366081 | T | G | 1 | a0001c0002t0001g0087 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.99+3006A>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100366081 | |||||||
| chr14:100366112 | G | A | 1 | a0001c0001t0001g0243 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.99+2975C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100366112 | |||||||
| chr14:100366252 | C | G | 1 | a0001c0002t0002g0042 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.99+2835G>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100366252 | |||||||
| chr14:100366322 | C | T | 1 | a0001c0002t0002g0041 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.99+2765G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100366322 | |||||||
| chr14:100366463 | A | G | 6 | a0001c0001t0001g0098 a0001c0002t0001g0005 a0001c0002t0001g0097 others(3): Show |
9 | HG02280.hp2 HG02559.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.99+2624T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100366463 | |||||||
| chr14:100366464 | C | T | 1 | a0001c0002t0001g0064 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.99+2623G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100366464 | |||||||
| chr14:100366572 | A | C | 1 | a0001c0002t0001g0087 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.99+2515T>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100366572 | |||||||
| chr14:100366762 | G | T | 2 | a0001c0002t0001g0124 a0001c0002t0001g0125 |
2 | HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.99+2325C>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100366762 | |||||||
| chr14:100366799 | A | G | 1 | a0001c0001t0001g0192 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.99+2288T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100366799 | |||||||
| chr14:100366805 | T | A | 1 | a0001c0002t0001g0087 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.99+2282A>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100366805 | |||||||
| chr14:100367048 | TA | T | 13 | a0001c0002t0001g0011 a0001c0002t0001g0119 a0001c0002t0001g0120 others(10): Show |
15 | HG00639.hp1 HG02622.hp1 HG02630.hp2 others(12): Show |
intron_variant | MODIFIER | c.99+2038delT | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100367048 | |||||||
| chr14:100367282 | G | T | 1 | a0001c0002t0001g0087 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.99+1805C>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100367282 | |||||||
| chr14:100367328 | G | A | 2 | a0001c0002t0001g0007 a0001c0002t0001g0090 |
4 | NA18973.hp1 NA18974.hp2 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+1759C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100367328 | |||||||
| chr14:100367405 | T | C | 4 | a0001c0001t0001g0140 a0001c0001t0001g0191 a0001c0001t0001g0192 others(1): Show |
4 | HG01884.hp1 HG02895.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+1682A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100367405 | |||||||
| chr14:100367416 | C | T | 27 | a0001c0002t0001g0044 a0001c0002t0002g0002 a0001c0002t0002g0006 others(24): Show |
35 | HG00099.hp1 HG00423.hp1 HG02027.hp1 others(32): Show |
intron_variant | MODIFIER | c.99+1671G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100367416 | |||||||
| chr14:100367456 | C | T | 2 | a0001c0005t0001g0270 a0001c0005t0001g0271 |
2 | HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.99+1631G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100367456 | |||||||
| chr14:100367570 | A | C | 1 | a0001c0001t0001g0224 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.99+1517T>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100367570 | |||||||
| chr14:100367579 | T | G | 1 | a0001c0002t0001g0087 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.99+1508A>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100367579 | |||||||
| chr14:100367587 | C | CG | 9 | a0001c0001t0001g0136 a0001c0001t0001g0141 a0001c0001t0001g0142 others(6): Show |
9 | HG01099.hp2 HG01175.hp1 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.99+1499dupC | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100367587 | |||||||
| chr14:100367594 | C | G | 1 | a0001c0001t0001g0221 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.99+1493G>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100367594 | |||||||
| chr14:100367608 | C | CA | 17 | a0001c0001t0001g0027 a0001c0001t0001g0134 a0001c0001t0001g0137 others(14): Show |
18 | HG00438.hp2 HG00621.hp2 HG02027.hp2 others(15): Show |
intron_variant | MODIFIER | c.99+1478dupT | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100367608 | |||||||
| chr14:100367608 | CA | C | 77 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(74): Show |
92 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.99+1478delT | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100367608 | |||||||
| chr14:100367608 | CAA | C | 17 | a0001c0002t0001g0009 a0001c0002t0001g0010 a0001c0002t0001g0105 others(14): Show |
21 | HG01891.hp1 HG01891.hp2 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.99+1477_99+1478del others(2): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100367608 | |||||||
| chr14:100367674 | G | A | 4 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0136 others(1): Show |
6 | HG01099.hp2 HG02258.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.99+1413C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100367674 | |||||||
| chr14:100367678 | A | C | 2 | a0001c0002t0001g0062 a0001c0002t0001g0063 |
2 | HG00323.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.99+1409T>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100367678 | |||||||
| chr14:100367966 | TA | T | 261 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(258): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.99+1120delT | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100367966 | |||||||
| chr14:100367977 | G | A | 10 | a0001c0002t0001g0010 a0001c0002t0001g0110 a0001c0002t0001g0111 others(7): Show |
12 | HG01891.hp2 HG02280.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.99+1110C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100367977 | |||||||
| chr14:100368000 | C | T | 1 | a0001c0001t0001g0246 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.99+1087G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100368000 | |||||||
| chr14:100368156 | T | C | 1 | a0001c0001t0001g0245 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.99+931A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100368156 | |||||||
| chr14:100368205 | T | C | 41 | a0001c0002t0001g0011 a0001c0002t0001g0044 a0001c0002t0001g0109 others(38): Show |
51 | HG00099.hp1 HG00423.hp1 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.99+882A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100368205 | |||||||
| chr14:100368229 | C | T | 1 | a0001c0001t0001g0223 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.99+858G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100368229 | |||||||
| chr14:100368451 | CCTGAAAG others(9): Show |
C | 1 | a0001c0002t0001g0087 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.99+620_99+635delAG others(14): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100368451 | |||||||
| chr14:100368538 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.99+549C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100368538 | |||||||
| chr14:100368645 | T | C | 164 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(161): Show |
199 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.99+442A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100368645 | |||||||
| chr14:100368706 | A | G | 2 | a0001c0005t0001g0270 a0001c0005t0001g0271 |
2 | HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.99+381T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100368706 | |||||||
| chr14:100368785 | ACCC | A | 165 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(162): Show |
200 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.99+299_99+301delGG others(1): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100368785 | |||||||
| chr14:100369466 | T | C | 2 | a0001c0005t0001g0270 a0001c0005t0001g0271 |
2 | HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.-73-208A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100369466 | |||||||
| chr14:100369483 | T | C | 7 | a0001c0002t0001g0011 a0001c0002t0001g0119 a0001c0002t0001g0120 others(4): Show |
9 | HG00639.hp1 HG02622.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.-73-225A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100369483 | |||||||
| chr14:100369539 | C | A | 2 | a0001c0001t0001g0029 a0001c0001t0001g0200 |
3 | HG02572.hp1 HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-73-281G>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100369539 | |||||||
| chr14:100369598 | T | C | 47 | a0001c0002t0001g0010 a0001c0002t0001g0011 a0001c0002t0001g0044 others(44): Show |
59 | HG00099.hp1 HG00423.hp1 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.-73-340A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100369598 | |||||||
| chr14:100369641 | T | C | 165 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(162): Show |
200 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.-73-383A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100369641 | |||||||
| chr14:100369681 | AT | A | 18 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(15): Show |
20 | HG01891.hp2 HG02258.hp2 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.-73-424delA | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100369681 | |||||||
| chr14:100369781 | G | A | 2 | a0001c0005t0001g0270 a0001c0005t0001g0271 |
2 | HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.-73-523C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100369781 | |||||||
| chr14:100369827 | C | T | 4 | a0002c0003t0001g0127 a0002c0003t0001g0128 a0002c0003t0001g0129 others(1): Show |
4 | NA18973.hp2 NA18985.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.-73-569G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100369827 | |||||||
| chr14:100369828 | G | A | 7 | a0001c0001t0001g0034 a0001c0001t0001g0272 a0001c0001t0001g0273 others(4): Show |
8 | HG02486.hp2 HG02809.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-73-570C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100369828 | |||||||
| chr14:100369908 | CTCACTTC others(13): Show |
C | 167 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(164): Show |
202 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.-73-670_-73-651del others(20): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100369908 | |||||||
| chr14:100369918 | C | T | 10 | a0001c0002t0001g0010 a0001c0002t0001g0110 a0001c0002t0001g0111 others(7): Show |
12 | HG01891.hp2 HG02280.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.-73-660G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100369918 | |||||||
| chr14:100370016 | C | T | 167 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(164): Show |
202 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.-73-758G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100370016 | |||||||
| chr14:100370066 | T | C | 1 | a0001c0002t0001g0088 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-73-808A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100370066 | |||||||
| chr14:100370072 | C | A | 165 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(162): Show |
200 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.-73-814G>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100370072 | |||||||
| chr14:100370285 | A | G | 1 | a0001c0002t0002g0038 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-73-1027T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100370285 | |||||||
| chr14:100370344 | A | G | 261 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(258): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.-73-1086T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100370344 | |||||||
| chr14:100370436 | C | T | 9 | a0001c0002t0001g0011 a0001c0002t0001g0119 a0001c0002t0001g0120 others(6): Show |
11 | HG00639.hp1 HG02622.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.-73-1178G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100370436 | |||||||
| chr14:100370439 | C | T | 36 | a0001c0002t0001g0011 a0001c0002t0001g0044 a0001c0002t0001g0119 others(33): Show |
46 | HG00099.hp1 HG00423.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.-73-1181G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100370439 | |||||||
| chr14:100370637 | A | C | 1 | a0001c0001t0001g0137 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-73-1379T>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100370637 | |||||||
| chr14:100370646 | A | G | 167 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(164): Show |
202 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.-73-1388T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100370646 | |||||||
| chr14:100370657 | T | G | 1 | a0001c0001t0001g0036 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-73-1399A>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100370657 | |||||||
| chr14:100370782 | G | GA | 155 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(152): Show |
190 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.-73-1525dupT | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100370782 | |||||||
| chr14:100370782 | G | GAA | 9 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0204 others(6): Show |
9 | HG02257.hp1 HG02818.hp2 HG03017.hp1 others(6): Show |
intron_variant | MODIFIER | c.-73-1526_-73-1525d others(4): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100370782 | |||||||
| chr14:100370826 | C | T | 1 | a0001c0002t0001g0097 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-73-1568G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100370826 | |||||||
| chr14:100370875 | C | A | 1 | a0001c0002t0002g0059 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-73-1617G>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100370875 | |||||||
| chr14:100370893 | C | T | 169 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(166): Show |
204 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.-73-1635G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100370893 | |||||||
| chr14:100370927 | A | G | 2 | a0001c0001t0001g0021 a0001c0001t0001g0136 |
3 | HG01099.hp2 HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-73-1669T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100370927 | |||||||
| chr14:100371045 | C | G | 167 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(164): Show |
202 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.-73-1787G>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100371045 | |||||||
| chr14:100371445 | C | T | 7 | a0001c0002t0001g0011 a0001c0002t0001g0119 a0001c0002t0001g0120 others(4): Show |
9 | HG00639.hp1 HG02622.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.-73-2187G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100371445 | |||||||
| chr14:100371447 | C | CA | 8 | a0001c0002t0001g0089 a0001c0002t0001g0090 a0001c0002t0001g0091 others(5): Show |
8 | HG01175.hp1 HG01361.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.-73-2190dupT | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100371447 | |||||||
| chr14:100371447 | C | CAAAAAAA others(5): Show |
1 | a0001c0001t0001g0213 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-73-2201_-73-2190d others(14): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100371447 | |||||||
| chr14:100371447 | C | CAAAAAAA others(6): Show |
2 | a0001c0001t0001g0214 a0001c0001t0001g0215 |
2 | HG01074.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-73-2202_-73-2190d others(15): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100371447 | |||||||
| chr14:100371447 | C | CAAAAAAA others(7): Show |
3 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0218 |
3 | HG01081.hp1 HG01081.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-73-2203_-73-2190d others(16): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100371447 | |||||||
| chr14:100371447 | C | CAAAAAAA others(12): Show |
1 | a0001c0001t0001g0219 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-73-2208_-73-2190d others(21): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100371447 | |||||||
| chr14:100371447 | C | CAAAAAAA others(13): Show |
1 | a0001c0001t0001g0220 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-73-2209_-73-2190d others(22): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100371447 | |||||||
| chr14:100371447 | C | CAAAAAAA others(16): Show |
2 | a0001c0001t0001g0221 a0001c0001t0001g0222 |
2 | HG03834.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.-73-2190_-73-2189i others(25): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100371447 | |||||||
| chr14:100371447 | C | CAAAAAAA others(17): Show |
10 | a0001c0001t0001g0030 a0001c0001t0001g0135 a0001c0001t0001g0223 others(7): Show |
11 | HG01975.hp2 HG02015.hp1 HG02015.hp2 others(8): Show |
intron_variant | MODIFIER | c.-73-2190_-73-2189i others(26): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100371447 | |||||||
| chr14:100371447 | C | CAAAAAAA others(18): Show |
18 | a0001c0001t0001g0013 a0001c0001t0001g0031 a0001c0001t0001g0231 others(15): Show |
21 | HG00099.hp2 HG00738.hp2 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.-73-2190_-73-2189i others(27): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100371447 | |||||||
| chr14:100371447 | C | CAAAAAAA others(19): Show |
6 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0248 others(3): Show |
8 | HG00733.hp1 HG01433.hp2 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.-73-2190_-73-2189i others(28): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100371447 | |||||||
| chr14:100371447 | C | CAAAAAAA others(20): Show |
5 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 others(2): Show |
5 | HG01175.hp2 HG01934.hp1 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.-73-2190_-73-2189i others(29): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100371447 | |||||||
| chr14:100371447 | C | CAAAAAAA others(21): Show |
3 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0266 |
3 | HG01361.hp1 HG04115.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.-73-2190_-73-2189i others(30): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100371447 | |||||||
| chr14:100371447 | C | CAAAAAAA others(22): Show |
2 | a0001c0001t0001g0257 a0001c0001t0001g0258 |
2 | HG00738.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.-73-2190_-73-2189i others(31): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100371447 | |||||||
| chr14:100371447 | C | CAAAAAAA others(23): Show |
4 | a0001c0001t0001g0134 a0001c0001t0001g0259 a0001c0001t0001g0260 others(1): Show |
4 | HG00438.hp2 HG01243.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.-73-2190_-73-2189i others(32): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100371447 | |||||||
| chr14:100371447 | C | CAAAAAAA others(24): Show |
1 | a0001c0001t0001g0262 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-73-2190_-73-2189i others(33): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100371447 | |||||||
| chr14:100371447 | C | CAAAAAAA others(25): Show |
2 | a0001c0001t0001g0263 a0001c0001t0001g0264 |
2 | NA18974.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.-73-2190_-73-2189i others(34): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100371447 | |||||||
| chr14:100371447 | C | CAAAAAAA others(17): Show |
1 | a0001c0001t0001g0265 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-73-2190_-73-2189i others(26): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100371447 | |||||||
| chr14:100371447 | CA | C | 12 | a0001c0001t0001g0209 a0001c0002t0001g0010 a0001c0002t0001g0061 others(9): Show |
14 | HG01891.hp2 HG02280.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.-73-2190delT | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100371447 | |||||||
| chr14:100371447 | CAAAAAAA others(3): Show |
C | 98 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(95): Show |
125 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.-73-2199_-73-2190d others(12): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100371447 | |||||||
| chr14:100371537 | C | A | 5 | a0001c0002t0001g0009 a0001c0002t0001g0105 a0001c0002t0001g0106 others(2): Show |
7 | HG01891.hp1 HG02615.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.-73-2279G>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100371537 | |||||||
| chr14:100371569 | C | T | 261 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(258): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.-73-2311G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100371569 | |||||||
| chr14:100371608 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-73-2350T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100371608 | |||||||
| chr14:100371670 | G | A | 167 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(164): Show |
202 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.-73-2412C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100371670 | |||||||
| chr14:100371825 | C | T | 1 | a0001c0002t0002g0037 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-73-2567G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100371825 | |||||||
| chr14:100371836 | G | A | 167 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(164): Show |
202 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.-73-2578C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100371836 | |||||||
| chr14:100371911 | G | T | 2 | a0001c0005t0001g0270 a0001c0005t0001g0271 |
2 | HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.-73-2653C>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100371911 | |||||||
| chr14:100371915 | C | G | 1 | a0001c0002t0001g0060 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-73-2657G>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100371915 | |||||||
| chr14:100371982 | GCCTTAAC others(6): Show |
G | 2 | a0001c0005t0001g0270 a0001c0005t0001g0271 |
2 | HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.-73-2737_-73-2725d others(15): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100371982 | |||||||
| chr14:100372068 | C | A | 10 | a0001c0002t0001g0010 a0001c0002t0001g0110 a0001c0002t0001g0111 others(7): Show |
12 | HG01891.hp2 HG02280.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.-73-2810G>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100372068 | |||||||
| chr14:100372318 | T | C | 1 | a0001c0001t0001g0265 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-74+2965A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100372318 | |||||||
| chr14:100372442 | G | C | 2 | a0001c0005t0001g0270 a0001c0005t0001g0271 |
2 | HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.-74+2841C>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100372442 | |||||||
| chr14:100372791 | G | C | 167 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(164): Show |
202 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.-74+2492C>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100372791 | |||||||
| chr14:100372822 | G | A | 1 | a0001c0001t0001g0266 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-74+2461C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100372822 | |||||||
| chr14:100372837 | T | C | 1 | a0001c0001t0001g0267 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-74+2446A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100372837 | |||||||
| chr14:100372924 | G | T | 36 | a0001c0002t0001g0007 a0001c0002t0001g0016 a0001c0002t0001g0017 others(33): Show |
41 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.-74+2359C>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100372924 | |||||||
| chr14:100373150 | CT | C | 4 | a0002c0003t0001g0127 a0002c0003t0001g0128 a0002c0003t0001g0129 others(1): Show |
4 | NA18973.hp2 NA18985.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.-74+2132delA | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100373150 | |||||||
| chr14:100373201 | A | T | 1 | a0001c0001t0001g0134 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-74+2082T>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100373201 | |||||||
| chr14:100373410 | G | T | 2 | a0001c0001t0001g0132 a0001c0001t0001g0133 |
2 | HG03098.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-74+1873C>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100373410 | |||||||
| chr14:100373581 | G | C | 1 | a0001c0001t0001g0268 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-74+1702C>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100373581 | |||||||
| chr14:100373681 | T | C | 11 | a0001c0002t0001g0010 a0001c0002t0001g0109 a0001c0002t0001g0110 others(8): Show |
13 | HG01891.hp2 HG02258.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.-74+1602A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100373681 | |||||||
| chr14:100373712 | T | C | 10 | a0001c0002t0001g0010 a0001c0002t0001g0110 a0001c0002t0001g0111 others(7): Show |
12 | HG01891.hp2 HG02280.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.-74+1571A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100373712 | |||||||
| chr14:100373761 | T | C | 1 | a0001c0001t0001g0269 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-74+1522A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100373761 | |||||||
| chr14:100373824 | TTG | T | 15 | a0001c0001t0001g0001 a0001c0001t0001g0025 a0001c0001t0001g0031 others(12): Show |
17 | HG00423.hp1 HG02027.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.-74+1457_-74+1458d others(4): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100373824 | |||||||
| chr14:100373824 | TTGTG | T | 110 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(107): Show |
141 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.-74+1455_-74+1458d others(6): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100373824 | |||||||
| chr14:100373824 | TTGTGTG | T | 70 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(67): Show |
77 | HG00099.hp2 HG00438.hp2 HG00621.hp2 others(74): Show |
intron_variant | MODIFIER | c.-74+1453_-74+1458d others(8): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100373824 | |||||||
| chr14:100373824 | TTGTGTGT others(1): Show |
T | 55 | a0001c0001t0001g0030 a0001c0001t0001g0132 a0001c0001t0001g0133 others(52): Show |
62 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.-74+1451_-74+1458d others(10): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100373824 | |||||||
| chr14:100373824 | TTGTGTGT others(3): Show |
T | 20 | a0001c0002t0001g0010 a0001c0002t0001g0011 a0001c0002t0001g0061 others(17): Show |
23 | HG00639.hp1 HG01891.hp2 HG02280.hp1 others(20): Show |
intron_variant | MODIFIER | c.-74+1449_-74+1458d others(12): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100373824 | |||||||
| chr14:100373824 | TTGTGTGT others(5): Show |
T | 1 | a0001c0002t0001g0088 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-74+1447_-74+1458d others(14): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100373824 | |||||||
| chr14:100373824 | TTGTGTGT others(7): Show |
T | 1 | a0001c0002t0001g0011 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-74+1445_-74+1458d others(16): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100373824 | |||||||
| chr14:100373824 | TTGTGTGT others(9): Show |
T | 2 | a0001c0002t0001g0124 a0001c0002t0001g0125 |
2 | HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-74+1443_-74+1458d others(18): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100373824 | |||||||
| chr14:100373953 | C | T | 167 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(164): Show |
202 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.-74+1330G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100373953 | |||||||
| chr14:100374066 | T | A | 27 | a0001c0002t0001g0044 a0001c0002t0002g0002 a0001c0002t0002g0006 others(24): Show |
35 | HG00099.hp1 HG00423.hp1 HG02027.hp1 others(32): Show |
intron_variant | MODIFIER | c.-74+1217A>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100374066 | |||||||
| chr14:100374146 | G | A | 2 | a0001c0005t0001g0270 a0001c0005t0001g0271 |
2 | HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.-74+1137C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100374146 | |||||||
| chr14:100374215 | T | C | 7 | a0001c0001t0001g0034 a0001c0001t0001g0272 a0001c0001t0001g0273 others(4): Show |
8 | HG02486.hp2 HG02809.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-74+1068A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100374215 | |||||||
| chr14:100374259 | G | C | 207 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(204): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.-74+1024C>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100374259 | |||||||
| chr14:100374476 | T | C | 167 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(164): Show |
202 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.-74+807A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100374476 | |||||||
| chr14:100374613 | G | A | 167 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(164): Show |
202 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.-74+670C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100374613 | |||||||
| chr14:100374671 | G | C | 167 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(164): Show |
202 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.-74+612C>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100374671 | |||||||
| chr14:100374757 | A | C | 27 | a0001c0002t0001g0044 a0001c0002t0002g0002 a0001c0002t0002g0006 others(24): Show |
35 | HG00099.hp1 HG00423.hp1 HG02027.hp1 others(32): Show |
intron_variant | MODIFIER | c.-74+526T>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100374757 | |||||||
| chr14:100374829 | AT | A | 167 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(164): Show |
202 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.-74+453delA | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100374829 | |||||||
| chr14:100375235 | C | T | 2 | a0001c0001t0001g0035 a0001c0001t0001g0036 |
2 | HG01928.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.-74+48G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100375235 |