Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 10352 |
| ensemblid | ENSG00000116874.12 |
| hgncid | 12730 |
| symbol | WARS2 |
| name | tryptophanyl tRNA synthetase 2, mitochondrial |
| refseq_nuc | NM_015836.4 |
| refseq_prot | NP_056651.1 |
| ensembl_nuc | ENST00000235521.5 |
| ensembl_prot | ENSP00000235521.4 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 119031216 |
| end | 119140653 |
| strand | - |
| ver | v1.2 |
| region | chr1:119031216-119140653 |
| region5000 | chr1:119026216-119145653 |
| regionname0 | WARS2_chr1_119031216_119140653 |
| regionname5000 | WARS2_chr1_119026216_119145653 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 360 | 282 | 70 | 56 | 118 | 6 | 31 | 90 | WARS2_chr1_119026216_119145653 | WARS2 | MALHS others(355): Show |
chr1 | 119026216 | 119145653 |
| a0002 | 0/1 | 360 | 64 | 15 | 4 | 42 | 1 | 1 | 32 | WARS2_chr1_119026216_119145653 | WARS2 | MALHS others(355): Show |
chr1 | 119026216 | 119145653 |
| a0003 | 0/0 | 360 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | MALHS others(355): Show |
chr1 | 119026216 | 119145653 |
| a0004 | 0/0 | 360 | 2 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | MALHS others(355): Show |
chr1 | 119026216 | 119145653 |
| a0005 | 0/0 | 360 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | MALHS others(355): Show |
chr1 | 119026216 | 119145653 |
| a0006 | 0/0 | 360 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | MALHS others(355): Show |
chr1 | 119026216 | 119145653 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1080 | 260 | 61 | 52 | 117 | 6 | 23 | WARS2_chr1_119026216_119145653 | WARS2 | ATGGC others(1075): Show |
chr1 | 119026216 | 119145653 | ||
| a0001c0003 | 0/0 | 1080 | 18 | 6 | 4 | 1 | 0 | 7 | WARS2_chr1_119026216_119145653 | WARS2 | ATGGC others(1075): Show |
chr1 | 119026216 | 119145653 | ||
| a0001c0006 | 0/0 | 1080 | 2 | 2 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | ATGGC others(1075): Show |
chr1 | 119026216 | 119145653 | ||
| a0001c0007 | 0/0 | 1080 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | ATGGC others(1075): Show |
chr1 | 119026216 | 119145653 | ||
| a0001c0010 | 0/0 | 1080 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | ATGGC others(1075): Show |
chr1 | 119026216 | 119145653 | ||
| a0002c0002 | 0/1 | 1080 | 64 | 15 | 4 | 42 | 1 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | ATGGC others(1075): Show |
chr1 | 119026216 | 119145653 | ||
| a0003c0004 | 0/0 | 1080 | 4 | 4 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | ATGGC others(1075): Show |
chr1 | 119026216 | 119145653 | ||
| a0004c0005 | 0/0 | 1080 | 2 | 1 | 0 | 0 | 1 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | ATGGC others(1075): Show |
chr1 | 119026216 | 119145653 | ||
| a0005c0009 | 0/0 | 1080 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | ATGGC others(1075): Show |
chr1 | 119026216 | 119145653 | ||
| a0006c0008 | 0/0 | 1080 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | ATGGC others(1075): Show |
chr1 | 119026216 | 119145653 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2787 | 83 | 2 | 19 | 59 | 1 | 2 | WARS2_chr1_119026216_119145653 | WARS2 | CTTCT others(2782): Show |
chr1 | 119026216 | 119145653 |
| a0001c0001t0003 | 1/0 | 2787 | 58 | 8 | 12 | 24 | 2 | 11 | WARS2_chr1_119026216_119145653 | WARS2 | CTTCT others(2782): Show |
chr1 | 119026216 | 119145653 |
| a0001c0001t0004 | 0/0 | 2787 | 37 | 20 | 1 | 12 | 0 | 4 | WARS2_chr1_119026216_119145653 | WARS2 | CTTCT others(2782): Show |
chr1 | 119026216 | 119145653 |
| a0001c0001t0005 | 0/0 | 2787 | 26 | 6 | 8 | 12 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | CTTCT others(2782): Show |
chr1 | 119026216 | 119145653 |
| a0001c0001t0006 | 0/0 | 2787 | 27 | 7 | 10 | 4 | 1 | 5 | WARS2_chr1_119026216_119145653 | WARS2 | CTTCT others(2782): Show |
chr1 | 119026216 | 119145653 |
| a0001c0001t0007 | 0/0 | 2787 | 10 | 1 | 2 | 5 | 2 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | CTTCT others(2782): Show |
chr1 | 119026216 | 119145653 |
| a0001c0001t0008 | 0/0 | 2787 | 10 | 10 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | CTTCT others(2782): Show |
chr1 | 119026216 | 119145653 |
| a0001c0001t0010 | 0/0 | 2787 | 4 | 4 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | CTTCT others(2782): Show |
chr1 | 119026216 | 119145653 |
| a0001c0001t0012 | 0/0 | 2787 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | CTTCT others(2782): Show |
chr1 | 119026216 | 119145653 |
| a0001c0001t0013 | 0/0 | 2787 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | CTTCT others(2782): Show |
chr1 | 119026216 | 119145653 |
| a0001c0001t0014 | 0/0 | 2787 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | CTTCT others(2782): Show |
chr1 | 119026216 | 119145653 |
| a0001c0001t0015 | 0/0 | 2787 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | CTTCT others(2782): Show |
chr1 | 119026216 | 119145653 |
| a0001c0001t0016 | 0/0 | 2787 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | CTTCT others(2782): Show |
chr1 | 119026216 | 119145653 |
| a0001c0003t0007 | 0/0 | 2787 | 13 | 1 | 4 | 1 | 0 | 7 | WARS2_chr1_119026216_119145653 | WARS2 | CTTCT others(2782): Show |
chr1 | 119026216 | 119145653 |
| a0001c0003t0009 | 0/0 | 2787 | 5 | 5 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | CTTCT others(2782): Show |
chr1 | 119026216 | 119145653 |
| a0001c0006t0004 | 0/0 | 2787 | 2 | 2 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | CTTCT others(2782): Show |
chr1 | 119026216 | 119145653 |
| a0001c0007t0004 | 0/0 | 2787 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | CTTCT others(2782): Show |
chr1 | 119026216 | 119145653 |
| a0001c0010t0004 | 0/0 | 2787 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | CTTCT others(2782): Show |
chr1 | 119026216 | 119145653 |
| a0002c0002t0002 | 0/1 | 2787 | 62 | 13 | 4 | 42 | 1 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | CTTCT others(2782): Show |
chr1 | 119026216 | 119145653 |
| a0002c0002t0011 | 0/0 | 2787 | 2 | 2 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | CTTCT others(2782): Show |
chr1 | 119026216 | 119145653 |
| a0003c0004t0005 | 0/0 | 2787 | 4 | 4 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | CTTCT others(2782): Show |
chr1 | 119026216 | 119145653 |
| a0004c0005t0001 | 0/0 | 2787 | 2 | 1 | 0 | 0 | 1 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | CTTCT others(2782): Show |
chr1 | 119026216 | 119145653 |
| a0005c0009t0003 | 0/0 | 2787 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | CTTCT others(2782): Show |
chr1 | 119026216 | 119145653 |
| a0006c0008t0001 | 0/0 | 2787 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | CTTCT others(2782): Show |
chr1 | 119026216 | 119145653 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0030 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0004g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0004g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0004g0015 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0004g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0004g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0004g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0004g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0004g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0004g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0004g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0004g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0004g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0004g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0004g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0004g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0004g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0004g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0004g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0004g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0004g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0004g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0004g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0004g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0004g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0004g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0004g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0004g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0004g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0004g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0004g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0004g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0004g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0004g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0004g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0005g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0005g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0005g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0005g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0005g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0005g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0005g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0005g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0005g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0005g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0005g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0005g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0005g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0005g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0005g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0005g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0005g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0005g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0005g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0005g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0005g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0005g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0005g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0005g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0005g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0005g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0006g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0006g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0006g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0006g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0006g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0006g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0006g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0006g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0006g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0006g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0006g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0006g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0006g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0006g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0006g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0006g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0006g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0006g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0006g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0006g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0006g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0006g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0006g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0006g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0006g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0006g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0007g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0007g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0007g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0007g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0007g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0007g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0007g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0007g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0007g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0007g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0008g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0008g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0008g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0008g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0008g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0008g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0008g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0008g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0008g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0008g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0010g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0010g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0010g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0010g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0012g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0013g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0014g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0015g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0016g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0003t0007g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0003t0007g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0003t0007g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0003t0007g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0003t0007g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0003t0007g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0003t0007g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0003t0007g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0003t0007g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0003t0007g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0003t0007g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0003t0007g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0003t0007g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0003t0009g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0003t0009g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0003t0009g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0003t0009g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0003t0009g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0006t0004g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0006t0004g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0007t0004g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0010t0004g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0001 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0119 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0011g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0011g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0003c0004t0005g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0003c0004t0005g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0003c0004t0005g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0003c0004t0005g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0004c0005t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0004c0005t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0005c0009t0003g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0006c0008t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0007 | g0080 | EUR | GBR | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0055 | EUR | GBR | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG00408 | hp1 | a0001 | c0001 | t0005 | g0264 | EAS | CHS | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0251 | EAS | CHS | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | CHS | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG00423 | hp2 | a0002 | c0002 | t0002 | g0007 | EAS | CHS | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | CHS | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0259 | EAS | CHS | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG00544 | hp1 | a0001 | c0001 | t0007 | g0204 | EAS | CHS | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | CHS | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG00558 | hp1 | a0001 | c0001 | t0004 | g0027 | EAS | CHS | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG00558 | hp2 | a0001 | c0001 | t0007 | g0205 | EAS | CHS | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG00609 | hp1 | a0001 | c0001 | t0004 | g0172 | EAS | CHS | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG00609 | hp2 | a0001 | c0001 | t0003 | g0216 | EAS | CHS | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG00621 | hp1 | a0001 | c0001 | t0005 | g0118 | EAS | CHS | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG00621 | hp2 | a0002 | c0002 | t0002 | g0053 | EAS | CHS | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG00639 | hp2 | a0001 | c0001 | t0007 | g0272 | AMR | PUR | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0248 | AMR | PUR | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG00673 | hp1 | a0001 | c0001 | t0007 | g0206 | EAS | CHS | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | CHS | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0234 | AMR | PUR | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG00738 | hp2 | a0001 | c0001 | t0006 | g0308 | AMR | PUR | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0232 | AMR | PUR | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG00741 | hp2 | a0001 | c0003 | t0007 | g0220 | AMR | PUR | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01070 | hp1 | a0001 | c0001 | t0006 | g0013 | AMR | PUR | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01074 | hp1 | a0001 | c0001 | t0005 | g0143 | AMR | PUR | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01074 | hp2 | a0001 | c0001 | t0006 | g0013 | AMR | PUR | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01099 | hp1 | a0001 | c0001 | t0006 | g0330 | AMR | PUR | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01099 | hp2 | a0001 | c0003 | t0007 | g0221 | AMR | PUR | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0231 | AMR | PUR | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01109 | hp1 | a0002 | c0002 | t0002 | g0201 | AMR | PUR | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01109 | hp2 | a0001 | c0001 | t0006 | g0312 | AMR | PUR | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01167 | hp2 | a0001 | c0001 | t0005 | g0147 | AMR | PUR | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01168 | hp1 | a0001 | c0003 | t0007 | g0217 | AMR | PUR | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01168 | hp2 | a0001 | c0001 | t0006 | g0319 | AMR | PUR | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01169 | hp2 | a0001 | c0001 | t0006 | g0318 | AMR | PUR | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01175 | hp1 | a0002 | c0002 | t0002 | g0156 | AMR | PUR | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0106 | AMR | PUR | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0233 | AMR | CLM | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | CLM | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01257 | hp2 | a0002 | c0002 | t0002 | g0122 | AMR | CLM | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01258 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | CLM | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | CLM | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01261 | hp2 | a0001 | c0001 | t0006 | g0311 | AMR | CLM | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01346 | hp1 | a0001 | c0001 | t0005 | g0161 | AMR | CLM | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0230 | AMR | CLM | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0108 | AMR | CLM | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01358 | hp2 | a0001 | c0001 | t0005 | g0166 | AMR | CLM | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01361 | hp1 | a0001 | c0001 | t0007 | g0203 | AMR | CLM | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0267 | AMR | CLM | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01433 | hp1 | a0001 | c0001 | t0005 | g0148 | AMR | CLM | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01433 | hp2 | a0001 | c0001 | t0004 | g0021 | AMR | CLM | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01496 | hp1 | a0001 | c0001 | t0005 | g0149 | AMR | CLM | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01515 | hp1 | a0002 | c0002 | t0002 | g0001 | EUR | IBS | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0270 | EUR | IBS | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01516 | hp1 | a0001 | c0001 | t0003 | g0236 | EUR | IBS | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01516 | hp2 | a0001 | c0001 | t0007 | g0207 | EUR | IBS | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01884 | hp1 | a0001 | c0001 | t0004 | g0014 | AFR | ACB | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01884 | hp2 | a0002 | c0002 | t0002 | g0001 | AFR | ACB | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01891 | hp1 | a0001 | c0001 | t0004 | g0293 | AFR | ACB | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01891 | hp2 | a0001 | c0001 | t0006 | g0315 | AFR | ACB | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0079 | AMR | PEL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PEL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01952 | hp1 | a0001 | c0001 | t0005 | g0146 | AMR | PEL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PEL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01978 | hp1 | a0001 | c0003 | t0007 | g0218 | AMR | PEL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PEL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02004 | hp1 | a0001 | c0001 | t0005 | g0150 | AMR | PEL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0082 | AMR | PEL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02015 | hp1 | a0001 | c0001 | t0003 | g0271 | EAS | KHV | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02015 | hp2 | a0002 | c0002 | t0002 | g0183 | EAS | KHV | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02027 | hp2 | a0002 | c0002 | t0002 | g0199 | EAS | KHV | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02040 | hp1 | a0002 | c0002 | t0002 | g0188 | EAS | KHV | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02055 | hp1 | a0001 | c0001 | t0005 | g0168 | AFR | ACB | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02055 | hp2 | a0002 | c0002 | t0002 | g0159 | AFR | ACB | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02056 | hp2 | a0001 | c0001 | t0006 | g0121 | EAS | KHV | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0252 | EAS | KHV | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02071 | hp2 | a0001 | c0001 | t0006 | g0126 | EAS | KHV | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0238 | EAS | KHV | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02080 | hp2 | a0002 | c0002 | t0002 | g0190 | EAS | KHV | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02129 | hp1 | a0002 | c0002 | t0002 | g0136 | EAS | KHV | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0240 | AFR | ACB | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02145 | hp2 | a0001 | c0001 | t0008 | g0277 | AFR | ACB | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02155 | hp1 | a0002 | c0002 | t0002 | g0008 | EAS | CDX | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0321 | EAS | CDX | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02165 | hp1 | a0001 | c0003 | t0007 | g0296 | EAS | CDX | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02165 | hp2 | a0002 | c0002 | t0002 | g0008 | EAS | CDX | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0011 | AFR | ACB | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0022 | AFR | ACB | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0322 | AFR | ACB | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02258 | hp2 | a0001 | c0003 | t0009 | g0225 | AFR | ACB | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02280 | hp1 | a0001 | c0006 | t0004 | g0028 | AFR | ACB | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02280 | hp2 | a0002 | c0002 | t0011 | g0137 | AFR | ACB | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02300 | hp1 | a0001 | c0001 | t0006 | g0326 | AMR | PEL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PEL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02572 | hp1 | a0001 | c0001 | t0008 | g0282 | AFR | GWD | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02572 | hp2 | a0001 | c0003 | t0009 | g0024 | AFR | GWD | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02602 | hp1 | a0001 | c0001 | t0006 | g0316 | SAS | PJL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02602 | hp2 | a0001 | c0001 | t0014 | g0099 | SAS | PJL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0243 | AFR | GWD | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02615 | hp2 | a0001 | c0001 | t0004 | g0170 | AFR | GWD | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02622 | hp1 | a0001 | c0001 | t0008 | g0335 | AFR | GWD | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02622 | hp2 | a0002 | c0002 | t0011 | g0139 | AFR | GWD | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02630 | hp1 | a0002 | c0002 | t0002 | g0124 | AFR | GWD | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02630 | hp2 | a0001 | c0001 | t0016 | g0213 | AFR | GWD | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02647 | hp1 | a0003 | c0004 | t0005 | g0211 | AFR | GWD | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02647 | hp2 | a0001 | c0010 | t0004 | g0287 | AFR | GWD | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02683 | hp1 | a0001 | c0003 | t0007 | g0219 | SAS | PJL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02683 | hp2 | a0001 | c0001 | t0006 | g0325 | SAS | PJL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0285 | AFR | GWD | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0011 | AFR | GWD | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02723 | hp1 | a0001 | c0001 | t0004 | g0298 | AFR | GWD | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02723 | hp2 | a0003 | c0004 | t0005 | g0304 | AFR | GWD | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0083 | SAS | PJL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02735 | hp2 | a0001 | c0003 | t0007 | g0294 | SAS | PJL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02809 | hp1 | a0001 | c0001 | t0006 | g0328 | AFR | GWD | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02809 | hp2 | a0001 | c0001 | t0004 | g0020 | AFR | GWD | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0261 | AFR | GWD | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02818 | hp2 | a0001 | c0001 | t0010 | g0302 | AFR | GWD | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02895 | hp1 | a0001 | c0001 | t0008 | g0280 | AFR | GWD | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02895 | hp2 | a0001 | c0001 | t0004 | g0289 | AFR | GWD | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02896 | hp1 | a0001 | c0001 | t0005 | g0151 | AFR | GWD | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02896 | hp2 | a0001 | c0003 | t0009 | g0222 | AFR | GWD | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02897 | hp1 | a0001 | c0003 | t0009 | g0224 | AFR | GWD | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02897 | hp2 | a0001 | c0001 | t0004 | g0290 | AFR | GWD | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0014 | AFR | ESN | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02922 | hp2 | a0002 | c0002 | t0002 | g0029 | AFR | ESN | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02970 | hp1 | a0002 | c0002 | t0002 | g0123 | AFR | ESN | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02970 | hp2 | a0003 | c0004 | t0005 | g0212 | AFR | ESN | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02976 | hp1 | a0001 | c0001 | t0015 | g0274 | AFR | ESN | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02976 | hp2 | a0002 | c0002 | t0002 | g0005 | AFR | ESN | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0244 | SAS | PJL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03017 | hp2 | a0002 | c0002 | t0002 | g0155 | SAS | PJL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03098 | hp1 | a0001 | c0001 | t0004 | g0299 | AFR | MSL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03098 | hp2 | a0001 | c0001 | t0006 | g0317 | AFR | MSL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03130 | hp1 | a0001 | c0001 | t0008 | g0275 | AFR | ESN | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03130 | hp2 | a0001 | c0006 | t0004 | g0173 | AFR | ESN | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0012 | AFR | ESN | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0333 | AFR | ESN | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03195 | hp1 | a0001 | c0001 | t0006 | g0284 | AFR | ESN | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0242 | AFR | ESN | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03225 | hp1 | a0001 | c0001 | t0008 | g0281 | AFR | MSL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03225 | hp2 | a0002 | c0002 | t0002 | g0160 | AFR | MSL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03239 | hp1 | a0001 | c0003 | t0007 | g0297 | SAS | PJL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0035 | SAS | PJL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03453 | hp1 | a0001 | c0001 | t0010 | g0291 | AFR | MSL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03453 | hp2 | a0001 | c0001 | t0008 | g0337 | AFR | MSL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03486 | hp1 | a0001 | c0001 | t0004 | g0336 | AFR | MSL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0300 | AFR | MSL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03490 | hp1 | a0001 | c0001 | t0004 | g0015 | SAS | PJL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03490 | hp2 | a0001 | c0003 | t0007 | g0226 | SAS | PJL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03492 | hp1 | a0001 | c0001 | t0004 | g0015 | SAS | PJL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0268 | SAS | PJL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03516 | hp1 | a0001 | c0001 | t0005 | g0152 | AFR | ESN | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03516 | hp2 | a0002 | c0002 | t0002 | g0153 | AFR | ESN | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03540 | hp1 | a0002 | c0002 | t0002 | g0138 | AFR | GWD | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03540 | hp2 | a0001 | c0001 | t0010 | g0303 | AFR | GWD | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03579 | hp1 | a0001 | c0001 | t0008 | g0278 | AFR | MSL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03579 | hp2 | a0001 | c0001 | t0006 | g0306 | AFR | MSL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0081 | SAS | PJL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03704 | hp2 | a0001 | c0003 | t0007 | g0227 | SAS | PJL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03710 | hp1 | a0001 | c0003 | t0007 | g0295 | SAS | PJL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0241 | SAS | PJL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03831 | hp1 | a0001 | c0001 | t0006 | g0309 | SAS | BEB | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0266 | SAS | BEB | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | BEB | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0245 | SAS | BEB | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0052 | SAS | BEB | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03927 | hp2 | a0001 | c0001 | t0006 | g0305 | SAS | BEB | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0269 | SAS | STU | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG04115 | hp2 | a0001 | c0007 | t0004 | g0017 | SAS | STU | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG04204 | hp1 | a0001 | c0001 | t0004 | g0329 | SAS | STU | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG04204 | hp2 | a0001 | c0003 | t0007 | g0288 | SAS | STU | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | STU | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0273 | SAS | STU | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18522 | hp1 | a0001 | c0001 | t0008 | g0279 | AFR | YRI | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18522 | hp2 | a0001 | c0001 | t0006 | g0331 | AFR | YRI | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0323 | EAS | CHB | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | CHB | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | CHB | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18747 | hp2 | a0002 | c0002 | t0002 | g0186 | EAS | CHB | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18906 | hp1 | a0003 | c0004 | t0005 | g0210 | AFR | YRI | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18906 | hp2 | a0001 | c0001 | t0008 | g0276 | AFR | YRI | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18939 | hp2 | a0002 | c0002 | t0002 | g0120 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18940 | hp1 | a0001 | c0001 | t0007 | g0200 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18940 | hp2 | a0002 | c0002 | t0002 | g0132 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18941 | hp1 | a0001 | c0001 | t0007 | g0202 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18941 | hp2 | a0001 | c0001 | t0003 | g0256 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18942 | hp1 | a0001 | c0001 | t0005 | g0144 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18942 | hp2 | a0001 | c0001 | t0003 | g0258 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18944 | hp1 | a0001 | c0001 | t0004 | g0176 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18946 | hp1 | a0001 | c0001 | t0005 | g0162 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18948 | hp2 | a0001 | c0001 | t0003 | g0247 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18949 | hp1 | a0002 | c0002 | t0002 | g0115 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18949 | hp2 | a0001 | c0001 | t0004 | g0193 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18950 | hp1 | a0001 | c0001 | t0003 | g0257 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18950 | hp2 | a0002 | c0002 | t0002 | g0208 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18959 | hp1 | a0001 | c0001 | t0005 | g0142 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18959 | hp2 | a0002 | c0002 | t0002 | g0187 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18960 | hp1 | a0002 | c0002 | t0002 | g0181 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18962 | hp1 | a0001 | c0001 | t0005 | g0262 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18963 | hp2 | a0002 | c0002 | t0002 | g0194 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18964 | hp2 | a0002 | c0002 | t0002 | g0192 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18967 | hp1 | a0001 | c0001 | t0006 | g0127 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18968 | hp1 | a0002 | c0002 | t0002 | g0158 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18968 | hp2 | a0005 | c0009 | t0003 | g0324 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18969 | hp2 | a0002 | c0002 | t0002 | g0129 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18971 | hp1 | a0001 | c0001 | t0005 | g0145 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18972 | hp1 | a0002 | c0002 | t0002 | g0191 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18977 | hp1 | a0002 | c0002 | t0002 | g0196 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18978 | hp1 | a0002 | c0002 | t0002 | g0131 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18978 | hp2 | a0002 | c0002 | t0002 | g0195 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18980 | hp1 | a0001 | c0001 | t0003 | g0246 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18981 | hp1 | a0006 | c0008 | t0001 | g0113 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18981 | hp2 | a0001 | c0001 | t0004 | g0026 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18985 | hp1 | a0002 | c0002 | t0002 | g0180 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18988 | hp1 | a0002 | c0002 | t0002 | g0134 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18989 | hp1 | a0001 | c0001 | t0004 | g0025 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18989 | hp2 | a0002 | c0002 | t0002 | g0283 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18990 | hp1 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18990 | hp2 | a0001 | c0001 | t0004 | g0178 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18991 | hp1 | a0002 | c0002 | t0002 | g0198 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18992 | hp1 | a0002 | c0002 | t0002 | g0135 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18994 | hp2 | a0001 | c0001 | t0003 | g0249 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18995 | hp2 | a0002 | c0002 | t0002 | g0133 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18998 | hp1 | a0002 | c0002 | t0002 | g0197 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18998 | hp2 | a0001 | c0001 | t0004 | g0177 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19001 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19002 | hp2 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19003 | hp2 | a0002 | c0002 | t0002 | g0182 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19004 | hp1 | a0001 | c0001 | t0003 | g0229 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19004 | hp2 | a0001 | c0001 | t0013 | g0066 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19005 | hp1 | a0001 | c0001 | t0005 | g0263 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19005 | hp2 | a0002 | c0002 | t0002 | g0185 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19009 | hp1 | a0001 | c0001 | t0006 | g0128 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0237 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19011 | hp2 | a0001 | c0001 | t0005 | g0164 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19030 | hp1 | a0001 | c0001 | t0012 | g0171 | AFR | LWK | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19030 | hp2 | a0002 | c0002 | t0002 | g0141 | AFR | LWK | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0332 | AFR | LWK | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19043 | hp2 | a0001 | c0001 | t0004 | g0286 | AFR | LWK | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19054 | hp2 | a0001 | c0001 | t0005 | g0265 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19055 | hp1 | a0002 | c0002 | t0002 | g0184 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19056 | hp1 | a0001 | c0001 | t0004 | g0174 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19058 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19062 | hp1 | a0002 | c0002 | t0002 | g0125 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19063 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0254 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19065 | hp2 | a0001 | c0001 | t0004 | g0039 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19066 | hp1 | a0002 | c0002 | t0002 | g0157 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19068 | hp2 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19070 | hp2 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19077 | hp1 | a0001 | c0001 | t0004 | g0038 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19077 | hp2 | a0001 | c0001 | t0005 | g0163 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19078 | hp1 | a0001 | c0001 | t0005 | g0165 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0260 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19081 | hp1 | a0001 | c0001 | t0003 | g0255 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19082 | hp1 | a0001 | c0001 | t0003 | g0250 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19083 | hp1 | a0001 | c0001 | t0003 | g0228 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19084 | hp2 | a0002 | c0002 | t0002 | g0189 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19085 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19240 | hp1 | a0002 | c0002 | t0002 | g0140 | AFR | YRI | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19240 | hp2 | a0001 | c0001 | t0010 | g0301 | AFR | YRI | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA20129 | hp1 | a0002 | c0002 | t0002 | g0005 | AFR | ASW | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA20129 | hp2 | a0001 | c0003 | t0007 | g0253 | AFR | ASW | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA20752 | hp1 | a0001 | c0001 | t0006 | g0307 | EUR | TSI | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA20752 | hp2 | a0004 | c0005 | t0001 | g0018 | EUR | TSI | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA20905 | hp1 | a0001 | c0001 | t0004 | g0314 | SAS | GIH | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA20905 | hp2 | a0001 | c0001 | t0006 | g0235 | SAS | GIH | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0107 | AMR | CLM | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01123 | hp2 | a0001 | c0001 | t0006 | g0313 | AMR | CLM | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0012 | AFR | ACB | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02109 | hp2 | a0001 | c0001 | t0005 | g0169 | AFR | ACB | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02486 | hp1 | a0001 | c0001 | t0004 | g0292 | AFR | ACB | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0239 | AFR | ACB | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | ACB | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0334 | AFR | ACB | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03471 | hp1 | a0002 | c0002 | t0002 | g0154 | AFR | MSL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03471 | hp2 | a0001 | c0001 | t0005 | g0167 | AFR | MSL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG06807 | hp1 | a0001 | c0003 | t0009 | g0223 | AFR | USA | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG06807 | hp2 | a0001 | c0001 | t0006 | g0327 | AFR | USA | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18955 | hp1 | a0001 | c0001 | t0004 | g0175 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA20300 | hp1 | a0004 | c0005 | t0001 | g0019 | AFR | USA | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA20300 | hp2 | a0001 | c0001 | t0007 | g0023 | AFR | USA | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | LWK | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA21309 | hp2 | a0001 | c0001 | t0005 | g0209 | AFR | LWK | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0002 | g0119 | REF | REF | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0030 | REF | REF | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:119032915 | A | G | 1 | a0003 | 4 | HG02647.hp1 HG02723.hp2 HG02970.hp2 others(1): Show |
missense_variant | MODERATE | c.1079T>C | p.Leu360Pro | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 6/6 | 1088/2787 | 1079/1083 | 360/360 | chr1 | 119032915 | |||
| chr1:119033045 | T | C | 1 | a0005 | 1 | NA18968.hp2 | missense_variant | MODERATE | c.949A>G | p.Ile317Val | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 6/6 | 958/2787 | 949/1083 | 317/360 | chr1 | 119033045 | |||
| chr1:119033135 | C | T | 1 | a0006 | 1 | NA18981.hp1 | missense_variant | MODERATE | c.859G>A | p.Val287Met | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 6/6 | 868/2787 | 859/1083 | 287/360 | chr1 | 119033135 | |||
| chr1:119033195 | C | G | 1 | a0002 | 63 | HG00423.hp2 HG00621.hp2 HG01109.hp1 others(60): Show |
missense_variant | MODERATE | c.799G>C | p.Ala267Pro | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 6/6 | 808/2787 | 799/1083 | 267/360 | chr1 | 119033195 | |||
| chr1:119140608 | A | C | 1 | a0004 | 2 | NA20300.hp1 NA20752.hp2 |
missense_variant | MODERATE | c.37T>G | p.Trp13Gly | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/6 | 46/2787 | 37/1083 | 13/360 | chr1 | 119140608 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:119033358 | T | C | 1 | a0001c0010 | 1 | HG02647.hp2 | splice_region_variant&synonymous_variant | LOW | c.636A>G | p.Thr212Thr | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 6/6 | 645/2787 | 636/1083 | 212/360 | chr1 | 119033358 | |||
| chr1:119042326 | G | A | 1 | a0001c0003 | 18 | HG00741.hp2 HG01099.hp2 HG01168.hp1 others(15): Show |
synonymous_variant | LOW | c.453C>T | p.His151His | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/6 | 462/2787 | 453/1083 | 151/360 | chr1 | 119042326 | |||
| chr1:119076551 | C | G | 1 | a0001c0006 | 2 | HG02280.hp1 HG03130.hp2 |
synonymous_variant | LOW | c.147G>C | p.Leu49Leu | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/6 | 156/2787 | 147/1083 | 49/360 | chr1 | 119076551 | |||
| chr1:119140618 | C | G | 1 | a0001c0007 | 1 | HG04115.hp2 | synonymous_variant | LOW | c.27G>C | p.Ala9Ala | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/6 | 36/2787 | 27/1083 | 9/360 | chr1 | 119140618 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:119031219 | G | C | 1 | a0001c0001t0015 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1692C>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 6/6 | 1692 | chr1 | 119031219 | ||||||
| chr1:119031233 | C | T | 1 | a0001c0001t0016 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1678G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 6/6 | 1678 | chr1 | 119031233 | ||||||
| chr1:119031237 | T | C | 1 | a0001c0001t0006 | 27 | HG00738.hp2 HG01070.hp1 HG01074.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*1674A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 6/6 | 1674 | chr1 | 119031237 | ||||||
| chr1:119031451 | G | C | 22 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(19): Show |
294 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(291): Show |
3_prime_UTR_variant | MODIFIER | c.*1460C>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 6/6 | 1460 | chr1 | 119031451 | ||||||
| chr1:119031659 | A | T | 1 | a0001c0001t0010 | 4 | HG02818.hp2 HG03453.hp1 HG03540.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1252T>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 6/6 | 1252 | chr1 | 119031659 | ||||||
| chr1:119031666 | G | A | 5 | a0001c0001t0001 a0001c0001t0013 a0001c0001t0014 others(2): Show |
88 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*1245C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 6/6 | 1245 | chr1 | 119031666 | ||||||
| chr1:119031759 | A | G | 1 | a0002c0002t0011 | 2 | HG02280.hp2 HG02622.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1152T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 6/6 | 1152 | chr1 | 119031759 | ||||||
| chr1:119031806 | A | G | 1 | a0001c0001t0014 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1105T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 6/6 | 1105 | chr1 | 119031806 | ||||||
| chr1:119031830 | C | T | 2 | a0001c0001t0008 a0001c0001t0015 |
11 | HG02145.hp2 HG02572.hp1 HG02622.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1081G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 6/6 | 1081 | chr1 | 119031830 | ||||||
| chr1:119031884 | C | G | 1 | a0001c0001t0013 | 1 | NA19004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1027G>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 6/6 | 1027 | chr1 | 119031884 | ||||||
| chr1:119031914 | G | A | 5 | a0001c0001t0001 a0001c0001t0013 a0001c0001t0014 others(2): Show |
88 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*997C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 6/6 | 997 | chr1 | 119031914 | ||||||
| chr1:119031964 | C | T | 15 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(12): Show |
192 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(189): Show |
3_prime_UTR_variant | MODIFIER | c.*947G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 6/6 | 947 | chr1 | 119031964 | ||||||
| chr1:119032098 | G | T | 1 | a0001c0001t0016 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*813C>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 6/6 | 813 | chr1 | 119032098 | ||||||
| chr1:119032108 | G | A | 1 | a0001c0003t0009 | 5 | HG02258.hp2 HG02572.hp2 HG02896.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*803C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 6/6 | 803 | chr1 | 119032108 | ||||||
| chr1:119032308 | C | T | 1 | a0001c0001t0012 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*603G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 6/6 | 603 | chr1 | 119032308 | ||||||
| chr1:119032342 | G | A | 2 | a0001c0001t0008 a0001c0001t0015 |
11 | HG02145.hp2 HG02572.hp1 HG02622.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*569C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 6/6 | 569 | chr1 | 119032342 | ||||||
| chr1:119032547 | C | A | 7 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0010 others(4): Show |
73 | HG00558.hp1 HG00609.hp1 HG00738.hp2 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*364G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 6/6 | 364 | chr1 | 119032547 | ||||||
| chr1:119032609 | T | C | 7 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0010 others(4): Show |
73 | HG00558.hp1 HG00609.hp1 HG00738.hp2 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*302A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 6/6 | 302 | chr1 | 119032609 | ||||||
| chr1:119032674 | C | G | 2 | a0002c0002t0002 a0002c0002t0011 |
63 | HG00423.hp2 HG00621.hp2 HG01109.hp1 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*237G>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 6/6 | 237 | chr1 | 119032674 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:119033552 | C | T | 3 | a0001c0001t0004g0020 a0001c0001t0004g0021 a0001c0001t0004g0022 |
3 | HG01433.hp2 HG02257.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.635-193G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 5/5 | chr1 | 119033552 | |||||||
| chr1:119033834 | T | A | 3 | a0001c0001t0004g0020 a0001c0001t0004g0021 a0001c0001t0004g0022 |
3 | HG01433.hp2 HG02257.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.634+261A>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 5/5 | chr1 | 119033834 | |||||||
| chr1:119033839 | T | A | 3 | a0001c0001t0004g0020 a0001c0001t0004g0021 a0001c0001t0004g0022 |
3 | HG01433.hp2 HG02257.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.634+256A>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 5/5 | chr1 | 119033839 | |||||||
| chr1:119033967 | A | G | 2 | a0001c0001t0006g0318 a0001c0001t0006g0319 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.634+128T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 5/5 | chr1 | 119033967 | |||||||
| chr1:119034281 | G | A | 11 | a0001c0001t0008g0275 a0001c0001t0008g0276 a0001c0001t0008g0277 others(8): Show |
11 | HG02145.hp2 HG02572.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.516-68C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119034281 | |||||||
| chr1:119034579 | C | T | 92 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(89): Show |
95 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.516-366G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119034579 | |||||||
| chr1:119034611 | T | C | 4 | a0001c0001t0010g0291 a0001c0001t0010g0301 a0001c0001t0010g0302 others(1): Show |
4 | HG02818.hp2 HG03453.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.516-398A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119034611 | |||||||
| chr1:119034631 | C | G | 1 | a0001c0001t0006g0235 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.516-418G>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119034631 | |||||||
| chr1:119034693 | T | C | 6 | a0001c0001t0005g0151 a0001c0001t0005g0152 a0001c0001t0005g0167 others(3): Show |
6 | HG02055.hp1 HG02109.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.516-480A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119034693 | |||||||
| chr1:119034787 | T | C | 269 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(266): Show |
283 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(280): Show |
intron_variant | MODIFIER | c.516-574A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119034787 | |||||||
| chr1:119034869 | C | T | 3 | a0001c0001t0004g0020 a0001c0001t0004g0021 a0001c0001t0004g0022 |
3 | HG01433.hp2 HG02257.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.516-656G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119034869 | |||||||
| chr1:119035043 | G | T | 158 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(155): Show |
165 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.516-830C>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119035043 | |||||||
| chr1:119035114 | T | G | 1 | a0003c0004t0005g0304 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.516-901A>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119035114 | |||||||
| chr1:119035214 | A | T | 158 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(155): Show |
165 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.516-1001T>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119035214 | |||||||
| chr1:119035294 | A | T | 1 | a0002c0002t0002g0136 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.516-1081T>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119035294 | |||||||
| chr1:119035302 | G | A | 16 | a0001c0001t0005g0118 a0001c0001t0005g0142 a0001c0001t0005g0143 others(13): Show |
16 | HG00621.hp1 HG01074.hp1 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.516-1089C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119035302 | |||||||
| chr1:119035324 | C | G | 27 | a0001c0001t0007g0080 a0001c0001t0007g0200 a0001c0001t0007g0202 others(24): Show |
27 | HG00099.hp1 HG00544.hp1 HG00558.hp2 others(24): Show |
intron_variant | MODIFIER | c.516-1111G>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119035324 | |||||||
| chr1:119035427 | C | T | 1 | a0001c0003t0009g0024 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.516-1214G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119035427 | |||||||
| chr1:119035437 | C | T | 1 | a0002c0002t0002g0180 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.516-1224G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119035437 | |||||||
| chr1:119035695 | A | G | 56 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0006 others(53): Show |
63 | HG00423.hp2 HG00621.hp2 HG01109.hp1 others(60): Show |
intron_variant | MODIFIER | c.516-1482T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119035695 | |||||||
| chr1:119035789 | T | C | 1 | a0001c0001t0005g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.516-1576A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119035789 | |||||||
| chr1:119035856 | A | C | 1 | a0001c0007t0004g0017 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.516-1643T>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119035856 | |||||||
| chr1:119036039 | T | C | 2 | a0002c0002t0002g0125 a0002c0002t0002g0136 |
2 | HG02129.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.516-1826A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119036039 | |||||||
| chr1:119036054 | A | G | 4 | a0003c0004t0005g0210 a0003c0004t0005g0211 a0003c0004t0005g0212 others(1): Show |
4 | HG02647.hp1 HG02723.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.516-1841T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119036054 | |||||||
| chr1:119036097 | C | T | 89 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(86): Show |
92 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.516-1884G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119036097 | |||||||
| chr1:119036104 | T | C | 3 | a0001c0001t0004g0020 a0001c0001t0004g0021 a0001c0001t0004g0022 |
3 | HG01433.hp2 HG02257.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.516-1891A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119036104 | |||||||
| chr1:119036134 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.516-1921G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119036134 | |||||||
| chr1:119036208 | G | GAAAAAT | 88 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(85): Show |
91 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.516-2001_516-1996d others(8): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119036208 | |||||||
| chr1:119036306 | G | A | 2 | a0001c0003t0007g0226 a0001c0003t0007g0227 |
2 | HG03490.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.516-2093C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119036306 | |||||||
| chr1:119036456 | C | T | 20 | a0001c0001t0007g0080 a0001c0001t0007g0200 a0001c0001t0007g0202 others(17): Show |
20 | HG00099.hp1 HG00544.hp1 HG00558.hp2 others(17): Show |
intron_variant | MODIFIER | c.516-2243G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119036456 | |||||||
| chr1:119036653 | A | G | 54 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0031 others(51): Show |
56 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.516-2440T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119036653 | |||||||
| chr1:119036689 | C | T | 1 | a0001c0001t0005g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.516-2476G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119036689 | |||||||
| chr1:119036771 | A | G | 1 | a0001c0001t0001g0086 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.516-2558T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119036771 | |||||||
| chr1:119037113 | C | A | 2 | a0002c0002t0002g0123 a0002c0002t0002g0156 |
2 | HG01175.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.516-2900G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119037113 | |||||||
| chr1:119037322 | AC | A | 64 | a0001c0001t0003g0267 a0001c0001t0004g0012 a0001c0001t0004g0014 others(61): Show |
68 | HG00558.hp1 HG00609.hp1 HG00738.hp2 others(65): Show |
intron_variant | MODIFIER | c.516-3110delG | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119037322 | |||||||
| chr1:119037363 | G | A | 11 | a0001c0001t0008g0275 a0001c0001t0008g0276 a0001c0001t0008g0277 others(8): Show |
11 | HG02145.hp2 HG02572.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.516-3150C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119037363 | |||||||
| chr1:119037629 | T | C | 49 | a0001c0001t0001g0130 a0002c0002t0002g0001 a0002c0002t0002g0005 others(46): Show |
56 | HG00423.hp2 HG00621.hp2 HG01109.hp1 others(53): Show |
intron_variant | MODIFIER | c.516-3416A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119037629 | |||||||
| chr1:119037689 | C | T | 4 | a0003c0004t0005g0210 a0003c0004t0005g0211 a0003c0004t0005g0212 others(1): Show |
4 | HG02647.hp1 HG02723.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.516-3476G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119037689 | |||||||
| chr1:119037720 | C | A | 3 | a0001c0001t0004g0020 a0001c0001t0004g0021 a0001c0001t0004g0022 |
3 | HG01433.hp2 HG02257.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.516-3507G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119037720 | |||||||
| chr1:119037923 | A | G | 1 | a0001c0001t0004g0193 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.516-3710T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119037923 | |||||||
| chr1:119038140 | A | T | 1 | a0001c0001t0003g0237 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.516-3927T>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119038140 | |||||||
| chr1:119038169 | G | A | 11 | a0001c0001t0008g0275 a0001c0001t0008g0276 a0001c0001t0008g0277 others(8): Show |
11 | HG02145.hp2 HG02572.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.516-3956C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119038169 | |||||||
| chr1:119038186 | G | A | 4 | a0001c0001t0005g0262 a0001c0001t0005g0263 a0001c0001t0005g0264 others(1): Show |
4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.516-3973C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119038186 | |||||||
| chr1:119038218 | G | T | 10 | a0001c0001t0008g0275 a0001c0001t0008g0276 a0001c0001t0008g0277 others(7): Show |
10 | HG02145.hp2 HG02572.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.516-4005C>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119038218 | |||||||
| chr1:119038378 | G | A | 1 | a0002c0002t0002g0135 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.515+3886C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119038378 | |||||||
| chr1:119038422 | A | G | 1 | a0002c0002t0002g0201 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.515+3842T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119038422 | |||||||
| chr1:119038528 | T | C | 22 | a0001c0001t0005g0118 a0001c0001t0005g0142 a0001c0001t0005g0143 others(19): Show |
22 | HG00621.hp1 HG01074.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.515+3736A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119038528 | |||||||
| chr1:119038717 | G | A | 1 | a0001c0001t0001g0117 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.515+3547C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119038717 | |||||||
| chr1:119038760 | G | A | 1 | a0002c0002t0002g0181 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.515+3504C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119038760 | |||||||
| chr1:119038781 | G | A | 70 | a0001c0001t0004g0012 a0001c0001t0004g0014 a0001c0001t0004g0015 others(67): Show |
74 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.515+3483C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119038781 | |||||||
| chr1:119038935 | G | A | 5 | a0001c0003t0009g0024 a0001c0003t0009g0222 a0001c0003t0009g0223 others(2): Show |
5 | HG02258.hp2 HG02572.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.515+3329C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119038935 | |||||||
| chr1:119038977 | C | T | 1 | a0003c0004t0005g0210 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.515+3287G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119038977 | |||||||
| chr1:119038987 | C | T | 57 | a0001c0001t0001g0130 a0002c0002t0002g0001 a0002c0002t0002g0005 others(54): Show |
64 | HG00423.hp2 HG00621.hp2 HG01109.hp1 others(61): Show |
intron_variant | MODIFIER | c.515+3277G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119038987 | |||||||
| chr1:119039277 | C | T | 66 | a0001c0001t0004g0012 a0001c0001t0004g0014 a0001c0001t0004g0015 others(63): Show |
70 | HG00558.hp1 HG00609.hp1 HG00738.hp2 others(67): Show |
intron_variant | MODIFIER | c.515+2987G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119039277 | |||||||
| chr1:119039314 | T | C | 57 | a0001c0001t0001g0130 a0002c0002t0002g0001 a0002c0002t0002g0005 others(54): Show |
64 | HG00423.hp2 HG00621.hp2 HG01109.hp1 others(61): Show |
intron_variant | MODIFIER | c.515+2950A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119039314 | |||||||
| chr1:119039501 | A | G | 4 | a0001c0001t0005g0262 a0001c0001t0005g0263 a0001c0001t0005g0264 others(1): Show |
4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.515+2763T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119039501 | |||||||
| chr1:119039625 | T | A | 1 | a0001c0001t0001g0092 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.515+2639A>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119039625 | |||||||
| chr1:119039695 | C | G | 1 | a0001c0001t0007g0205 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.515+2569G>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119039695 | |||||||
| chr1:119039714 | T | G | 6 | a0001c0001t0005g0151 a0001c0001t0005g0152 a0001c0001t0005g0167 others(3): Show |
6 | HG02055.hp1 HG02109.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.515+2550A>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119039714 | |||||||
| chr1:119039768 | C | G | 18 | a0001c0003t0007g0217 a0001c0003t0007g0218 a0001c0003t0007g0219 others(15): Show |
18 | HG00741.hp2 HG01099.hp2 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.515+2496G>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119039768 | |||||||
| chr1:119039825 | G | A | 66 | a0001c0001t0004g0012 a0001c0001t0004g0014 a0001c0001t0004g0015 others(63): Show |
70 | HG00558.hp1 HG00609.hp1 HG00738.hp2 others(67): Show |
intron_variant | MODIFIER | c.515+2439C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119039825 | |||||||
| chr1:119040019 | C | T | 66 | a0001c0001t0004g0012 a0001c0001t0004g0014 a0001c0001t0004g0015 others(63): Show |
70 | HG00558.hp1 HG00609.hp1 HG00738.hp2 others(67): Show |
intron_variant | MODIFIER | c.515+2245G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119040019 | |||||||
| chr1:119040089 | C | T | 1 | a0001c0001t0005g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.515+2175G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119040089 | |||||||
| chr1:119040198 | A | C | 1 | a0001c0001t0005g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.515+2066T>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119040198 | |||||||
| chr1:119040321 | C | T | 1 | a0001c0001t0003g0229 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.515+1943G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119040321 | |||||||
| chr1:119040341 | T | C | 1 | a0001c0001t0003g0052 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.515+1923A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119040341 | |||||||
| chr1:119040446 | G | A | 5 | a0001c0001t0004g0286 a0001c0001t0004g0293 a0001c0001t0004g0299 others(2): Show |
5 | HG01891.hp1 HG02630.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.515+1818C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119040446 | |||||||
| chr1:119040513 | C | G | 11 | a0001c0001t0008g0275 a0001c0001t0008g0276 a0001c0001t0008g0277 others(8): Show |
11 | HG02145.hp2 HG02572.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.515+1751G>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119040513 | |||||||
| chr1:119040558 | C | T | 1 | a0001c0001t0007g0272 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.515+1706G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119040558 | |||||||
| chr1:119040799 | A | G | 96 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(93): Show |
99 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.515+1465T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119040799 | |||||||
| chr1:119040945 | A | T | 1 | a0001c0001t0004g0170 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.515+1319T>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119040945 | |||||||
| chr1:119041100 | T | A | 1 | a0001c0001t0005g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.515+1164A>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119041100 | |||||||
| chr1:119041157 | A | G | 4 | a0001c0001t0010g0291 a0001c0001t0010g0301 a0001c0001t0010g0302 others(1): Show |
4 | HG02818.hp2 HG03453.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.515+1107T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119041157 | |||||||
| chr1:119041183 | G | T | 1 | a0001c0001t0001g0068 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.515+1081C>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119041183 | |||||||
| chr1:119041214 | A | T | 75 | a0001c0001t0001g0130 a0001c0003t0007g0217 a0001c0003t0007g0218 others(72): Show |
82 | HG00423.hp2 HG00621.hp2 HG00741.hp2 others(79): Show |
intron_variant | MODIFIER | c.515+1050T>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119041214 | |||||||
| chr1:119041231 | C | A | 98 | a0001c0001t0004g0012 a0001c0001t0004g0014 a0001c0001t0004g0015 others(95): Show |
102 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.515+1033G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119041231 | |||||||
| chr1:119041303 | C | T | 17 | a0001c0001t0004g0012 a0001c0001t0004g0025 a0001c0001t0004g0026 others(14): Show |
18 | HG00558.hp1 HG00609.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.515+961G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119041303 | |||||||
| chr1:119041315 | A | G | 1 | a0001c0001t0005g0163 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.515+949T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119041315 | |||||||
| chr1:119041345 | T | A | 269 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(266): Show |
283 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(280): Show |
intron_variant | MODIFIER | c.515+919A>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119041345 | |||||||
| chr1:119041704 | T | C | 3 | a0003c0004t0005g0210 a0003c0004t0005g0211 a0003c0004t0005g0212 |
3 | HG02647.hp1 HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.515+560A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119041704 | |||||||
| chr1:119041773 | G | A | 70 | a0001c0001t0004g0012 a0001c0001t0004g0014 a0001c0001t0004g0015 others(67): Show |
74 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.515+491C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119041773 | |||||||
| chr1:119041868 | T | C | 3 | a0001c0001t0004g0286 a0001c0001t0004g0293 a0001c0010t0004g0287 |
3 | HG01891.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.515+396A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119041868 | |||||||
| chr1:119042037 | A | G | 57 | a0001c0001t0001g0130 a0002c0002t0002g0001 a0002c0002t0002g0005 others(54): Show |
64 | HG00423.hp2 HG00621.hp2 HG01109.hp1 others(61): Show |
intron_variant | MODIFIER | c.515+227T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119042037 | |||||||
| chr1:119042102 | C | A | 1 | a0001c0001t0004g0172 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.515+162G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119042102 | |||||||
| chr1:119042129 | T | C | 1 | a0001c0007t0004g0017 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.515+135A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119042129 | |||||||
| chr1:119042156 | C | T | 7 | a0001c0001t0005g0262 a0001c0001t0005g0263 a0001c0001t0005g0264 others(4): Show |
7 | HG00408.hp1 HG01168.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.515+108G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119042156 | |||||||
| chr1:119042366 | G | C | 4 | a0001c0001t0005g0262 a0001c0001t0005g0263 a0001c0001t0005g0264 others(1): Show |
4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.430-17C>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 3/5 | chr1 | 119042366 | |||||||
| chr1:119042527 | A | G | 3 | a0002c0002t0002g0007 a0002c0002t0002g0182 a0002c0002t0002g0186 |
4 | HG00423.hp2 NA18747.hp2 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.430-178T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 3/5 | chr1 | 119042527 | |||||||
| chr1:119042692 | G | A | 4 | a0001c0001t0006g0121 a0001c0001t0006g0126 a0001c0001t0006g0127 others(1): Show |
4 | HG02056.hp2 HG02071.hp2 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.430-343C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 3/5 | chr1 | 119042692 | |||||||
| chr1:119042848 | T | A | 3 | a0001c0001t0001g0032 a0001c0001t0001g0056 a0001c0001t0001g0057 |
3 | HG00673.hp2 NA19003.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.430-499A>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 3/5 | chr1 | 119042848 | |||||||
| chr1:119042874 | A | G | 66 | a0001c0001t0004g0012 a0001c0001t0004g0014 a0001c0001t0004g0015 others(63): Show |
70 | HG00558.hp1 HG00609.hp1 HG00738.hp2 others(67): Show |
intron_variant | MODIFIER | c.430-525T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 3/5 | chr1 | 119042874 | |||||||
| chr1:119042875 | G | A | 1 | a0001c0001t0003g0238 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.430-526C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 3/5 | chr1 | 119042875 | |||||||
| chr1:119042959 | C | G | 5 | a0001c0001t0004g0286 a0001c0001t0004g0293 a0001c0001t0004g0299 others(2): Show |
5 | HG01891.hp1 HG02630.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.430-610G>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 3/5 | chr1 | 119042959 | |||||||
| chr1:119043119 | C | T | 1 | a0003c0004t0005g0212 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.430-770G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 3/5 | chr1 | 119043119 | |||||||
| chr1:119043216 | CTAAGGTA others(17): Show |
C | 1 | a0001c0001t0006g0306 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.430-891_430-868del others(24): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 3/5 | chr1 | 119043216 | |||||||
| chr1:119043371 | C | T | 5 | a0001c0001t0004g0286 a0001c0001t0004g0293 a0001c0001t0004g0299 others(2): Show |
5 | HG01891.hp1 HG02630.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.430-1022G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 3/5 | chr1 | 119043371 | |||||||
| chr1:119043454 | C | T | 8 | a0002c0002t0002g0138 a0002c0002t0002g0140 a0002c0002t0002g0141 others(5): Show |
8 | HG02055.hp2 HG02280.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.430-1105G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 3/5 | chr1 | 119043454 | |||||||
| chr1:119043653 | C | T | 16 | a0001c0001t0005g0118 a0001c0001t0005g0142 a0001c0001t0005g0143 others(13): Show |
16 | HG00621.hp1 HG01074.hp1 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.430-1304G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 3/5 | chr1 | 119043653 | |||||||
| chr1:119043668 | A | G | 1 | a0001c0001t0012g0171 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.430-1319T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 3/5 | chr1 | 119043668 | |||||||
| chr1:119043769 | G | C | 16 | a0001c0003t0007g0217 a0001c0003t0007g0218 a0001c0003t0007g0219 others(13): Show |
16 | HG00741.hp2 HG01099.hp2 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.430-1420C>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 3/5 | chr1 | 119043769 | |||||||
| chr1:119044049 | G | A | 1 | a0001c0001t0003g0243 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.429+1533C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 3/5 | chr1 | 119044049 | |||||||
| chr1:119044064 | G | A | 63 | a0001c0001t0004g0012 a0001c0001t0004g0014 a0001c0001t0004g0015 others(60): Show |
67 | HG00558.hp1 HG00609.hp1 HG00738.hp2 others(64): Show |
intron_variant | MODIFIER | c.429+1518C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 3/5 | chr1 | 119044064 | |||||||
| chr1:119044506 | T | C | 1 | a0001c0001t0005g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.429+1076A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 3/5 | chr1 | 119044506 | |||||||
| chr1:119044588 | A | T | 1 | a0001c0001t0001g0068 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.429+994T>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 3/5 | chr1 | 119044588 | |||||||
| chr1:119044653 | G | A | 4 | a0001c0001t0005g0262 a0001c0001t0005g0263 a0001c0001t0005g0264 others(1): Show |
4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.429+929C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 3/5 | chr1 | 119044653 | |||||||
| chr1:119044683 | T | G | 1 | a0001c0001t0005g0169 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.429+899A>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 3/5 | chr1 | 119044683 | |||||||
| chr1:119044705 | A | G | 1 | a0001c0001t0001g0084 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.429+877T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 3/5 | chr1 | 119044705 | |||||||
| chr1:119044817 | T | C | 66 | a0001c0001t0004g0012 a0001c0001t0004g0014 a0001c0001t0004g0015 others(63): Show |
70 | HG00558.hp1 HG00609.hp1 HG00738.hp2 others(67): Show |
intron_variant | MODIFIER | c.429+765A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 3/5 | chr1 | 119044817 | |||||||
| chr1:119044857 | A | G | 1 | a0001c0001t0004g0285 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.429+725T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 3/5 | chr1 | 119044857 | |||||||
| chr1:119045014 | G | A | 12 | a0001c0001t0004g0012 a0001c0001t0004g0025 a0001c0001t0004g0026 others(9): Show |
13 | HG00558.hp1 HG00609.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.429+568C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 3/5 | chr1 | 119045014 | |||||||
| chr1:119045040 | G | A | 1 | a0001c0001t0004g0314 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.429+542C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 3/5 | chr1 | 119045040 | |||||||
| chr1:119045060 | G | A | 4 | a0003c0004t0005g0210 a0003c0004t0005g0211 a0003c0004t0005g0212 others(1): Show |
4 | HG02647.hp1 HG02723.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.429+522C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 3/5 | chr1 | 119045060 | |||||||
| chr1:119045427 | C | T | 1 | a0001c0003t0007g0288 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.429+155G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 3/5 | chr1 | 119045427 | |||||||
| chr1:119045730 | A | G | 15 | a0002c0002t0002g0006 a0002c0002t0002g0007 a0002c0002t0002g0008 others(12): Show |
18 | HG00423.hp2 HG02015.hp2 HG02040.hp1 others(15): Show |
intron_variant | MODIFIER | c.349-68T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119045730 | |||||||
| chr1:119045937 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.349-275C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119045937 | |||||||
| chr1:119046005 | A | ACT | 11 | a0001c0001t0008g0275 a0001c0001t0008g0276 a0001c0001t0008g0277 others(8): Show |
11 | HG02145.hp2 HG02572.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.349-345_349-344dup others(2): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119046005 | |||||||
| chr1:119046021 | TCACACAC others(11): Show |
T | 1 | a0001c0001t0004g0172 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.349-377_349-360del others(18): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119046021 | |||||||
| chr1:119046054 | C | T | 4 | a0001c0001t0003g0246 a0001c0001t0003g0247 a0001c0001t0003g0250 others(1): Show |
4 | HG00408.hp2 NA18948.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.349-392G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119046054 | |||||||
| chr1:119046060 | C | T | 1 | a0002c0002t0002g0154 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.349-398G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119046060 | |||||||
| chr1:119046068 | C | T | 2 | a0001c0003t0007g0226 a0001c0003t0007g0227 |
2 | HG03490.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.349-406G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119046068 | |||||||
| chr1:119046152 | G | A | 5 | a0001c0001t0004g0286 a0001c0001t0004g0293 a0001c0001t0004g0299 others(2): Show |
5 | HG01891.hp1 HG02630.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.349-490C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119046152 | |||||||
| chr1:119046285 | GT | G | 41 | a0001c0001t0003g0010 a0001c0001t0003g0035 a0001c0001t0003g0052 others(38): Show |
42 | HG00408.hp2 HG00438.hp2 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.349-624delA | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119046285 | |||||||
| chr1:119046285 | GTT | G | 39 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0043 others(36): Show |
42 | HG00642.hp1 HG00673.hp2 HG01243.hp2 others(39): Show |
intron_variant | MODIFIER | c.349-625_349-624del others(2): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119046285 | |||||||
| chr1:119046285 | GTTT | G | 71 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0031 others(68): Show |
73 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.349-626_349-624del others(3): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119046285 | |||||||
| chr1:119046285 | GTTTT | G | 27 | a0001c0001t0001g0033 a0001c0001t0001g0068 a0001c0001t0001g0077 others(24): Show |
29 | HG01167.hp1 HG01169.hp1 HG01175.hp1 others(26): Show |
intron_variant | MODIFIER | c.349-627_349-624del others(4): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119046285 | |||||||
| chr1:119046285 | GTTTTT | G | 36 | a0001c0001t0001g0130 a0001c0003t0007g0217 a0001c0003t0007g0218 others(33): Show |
41 | HG00423.hp2 HG00621.hp2 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.349-628_349-624del others(5): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119046285 | |||||||
| chr1:119046285 | GTTTTTT | G | 46 | a0001c0001t0005g0118 a0001c0001t0005g0142 a0001c0001t0005g0143 others(43): Show |
46 | HG00621.hp1 HG01074.hp1 HG01167.hp2 others(43): Show |
intron_variant | MODIFIER | c.349-629_349-624del others(6): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119046285 | |||||||
| chr1:119046285 | GTTTTTTT | G | 69 | a0001c0001t0004g0012 a0001c0001t0004g0014 a0001c0001t0004g0015 others(66): Show |
73 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.349-630_349-624del others(7): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119046285 | |||||||
| chr1:119046508 | C | T | 1 | a0001c0001t0003g0300 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.349-846G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119046508 | |||||||
| chr1:119046514 | A | AT | 96 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(93): Show |
99 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.349-853dupA | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119046514 | |||||||
| chr1:119046514 | AT | A | 79 | a0001c0001t0003g0035 a0001c0001t0003g0270 a0001c0001t0004g0012 others(76): Show |
83 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.349-853delA | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119046514 | |||||||
| chr1:119046614 | C | T | 1 | a0001c0001t0005g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.349-952G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119046614 | |||||||
| chr1:119046660 | ATTTG | A | 7 | a0002c0002t0002g0194 a0002c0002t0002g0196 a0002c0002t0002g0197 others(4): Show |
7 | HG02027.hp2 NA18950.hp2 NA18963.hp2 others(4): Show |
intron_variant | MODIFIER | c.349-1002_349-999de others(5): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119046660 | |||||||
| chr1:119046720 | C | T | 97 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(94): Show |
100 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.349-1058G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119046720 | |||||||
| chr1:119046774 | C | CT | 22 | a0001c0001t0005g0118 a0001c0001t0005g0142 a0001c0001t0005g0143 others(19): Show |
22 | HG00621.hp1 HG01074.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.349-1113dupA | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119046774 | |||||||
| chr1:119046774 | CT | C | 76 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(73): Show |
79 | HG00408.hp1 HG00609.hp2 HG00738.hp2 others(76): Show |
intron_variant | MODIFIER | c.349-1113delA | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119046774 | |||||||
| chr1:119046840 | T | G | 16 | a0001c0001t0005g0118 a0001c0001t0005g0142 a0001c0001t0005g0143 others(13): Show |
16 | HG00621.hp1 HG01074.hp1 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.349-1178A>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119046840 | |||||||
| chr1:119046938 | G | C | 1 | a0001c0003t0007g0219 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.349-1276C>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119046938 | |||||||
| chr1:119047096 | A | G | 1 | a0001c0001t0007g0023 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.349-1434T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119047096 | |||||||
| chr1:119047207 | A | G | 4 | a0001c0001t0004g0025 a0001c0001t0004g0026 a0001c0001t0004g0027 others(1): Show |
4 | HG00558.hp1 NA18981.hp2 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.349-1545T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119047207 | |||||||
| chr1:119047283 | AT | A | 282 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(279): Show |
296 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(293): Show |
intron_variant | MODIFIER | c.349-1622delA | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119047283 | |||||||
| chr1:119047409 | C | T | 2 | a0001c0001t0001g0042 a0001c0001t0001g0088 |
2 | NA19057.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.349-1747G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119047409 | |||||||
| chr1:119047775 | A | C | 78 | a0001c0001t0004g0012 a0001c0001t0004g0014 a0001c0001t0004g0015 others(75): Show |
82 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.349-2113T>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119047775 | |||||||
| chr1:119047797 | C | T | 66 | a0001c0001t0004g0012 a0001c0001t0004g0014 a0001c0001t0004g0015 others(63): Show |
70 | HG00558.hp1 HG00609.hp1 HG00738.hp2 others(67): Show |
intron_variant | MODIFIER | c.349-2135G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119047797 | |||||||
| chr1:119047842 | T | C | 1 | a0001c0001t0006g0330 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.349-2180A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119047842 | |||||||
| chr1:119048021 | T | C | 4 | a0001c0001t0005g0262 a0001c0001t0005g0263 a0001c0001t0005g0264 others(1): Show |
4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.349-2359A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119048021 | |||||||
| chr1:119048140 | A | G | 1 | a0001c0001t0015g0274 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.349-2478T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119048140 | |||||||
| chr1:119048238 | G | A | 3 | a0001c0001t0005g0148 a0001c0001t0005g0149 a0001c0001t0005g0166 |
3 | HG01358.hp2 HG01433.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.349-2576C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119048238 | |||||||
| chr1:119048423 | C | T | 73 | a0001c0001t0004g0012 a0001c0001t0004g0014 a0001c0001t0004g0015 others(70): Show |
77 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.349-2761G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119048423 | |||||||
| chr1:119048562 | A | G | 1 | a0002c0002t0002g0155 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.349-2900T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119048562 | |||||||
| chr1:119048794 | G | C | 1 | a0001c0001t0004g0336 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.349-3132C>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119048794 | |||||||
| chr1:119048812 | T | TCC | 69 | a0001c0001t0004g0012 a0001c0001t0004g0014 a0001c0001t0004g0015 others(66): Show |
73 | HG00558.hp1 HG00609.hp1 HG00738.hp2 others(70): Show |
intron_variant | MODIFIER | c.349-3151_349-3150i others(4): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119048812 | |||||||
| chr1:119048881 | T | C | 1 | a0001c0001t0001g0043 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.349-3219A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119048881 | |||||||
| chr1:119048923 | T | C | 73 | a0001c0001t0004g0012 a0001c0001t0004g0014 a0001c0001t0004g0015 others(70): Show |
77 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.349-3261A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119048923 | |||||||
| chr1:119049196 | C | A | 5 | a0001c0001t0004g0286 a0001c0001t0004g0293 a0001c0001t0004g0299 others(2): Show |
5 | HG01891.hp1 HG02630.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.349-3534G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119049196 | |||||||
| chr1:119049198 | A | G | 6 | a0002c0002t0002g0007 a0002c0002t0002g0180 a0002c0002t0002g0182 others(3): Show |
7 | HG00423.hp2 HG02040.hp1 NA18747.hp2 others(4): Show |
intron_variant | MODIFIER | c.349-3536T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119049198 | |||||||
| chr1:119049317 | C | A | 1 | a0001c0001t0006g0307 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.349-3655G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119049317 | |||||||
| chr1:119049542 | C | G | 12 | a0001c0001t0004g0012 a0001c0001t0004g0025 a0001c0001t0004g0026 others(9): Show |
13 | HG00558.hp1 HG00609.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.349-3880G>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119049542 | |||||||
| chr1:119049564 | T | C | 2 | a0001c0001t0001g0214 a0001c0001t0001g0215 |
2 | NA18944.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.349-3902A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119049564 | |||||||
| chr1:119049612 | A | G | 3 | a0001c0001t0004g0020 a0001c0001t0004g0021 a0001c0001t0004g0022 |
3 | HG01433.hp2 HG02257.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.349-3950T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119049612 | |||||||
| chr1:119049651 | C | A | 4 | a0001c0001t0005g0262 a0001c0001t0005g0263 a0001c0001t0005g0264 others(1): Show |
4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.349-3989G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119049651 | |||||||
| chr1:119049706 | C | G | 3 | a0001c0001t0004g0020 a0001c0001t0004g0021 a0001c0001t0004g0022 |
3 | HG01433.hp2 HG02257.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.349-4044G>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119049706 | |||||||
| chr1:119049759 | G | A | 4 | a0003c0004t0005g0210 a0003c0004t0005g0211 a0003c0004t0005g0212 others(1): Show |
4 | HG02647.hp1 HG02723.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.349-4097C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119049759 | |||||||
| chr1:119050048 | A | C | 3 | a0001c0001t0004g0020 a0001c0001t0004g0021 a0001c0001t0004g0022 |
3 | HG01433.hp2 HG02257.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.349-4386T>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119050048 | |||||||
| chr1:119050150 | C | G | 2 | a0001c0001t0003g0261 a0001c0001t0003g0300 |
2 | HG02818.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.349-4488G>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119050150 | |||||||
| chr1:119050213 | G | C | 8 | a0002c0002t0002g0138 a0002c0002t0002g0140 a0002c0002t0002g0141 others(5): Show |
8 | HG02055.hp2 HG02280.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.349-4551C>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119050213 | |||||||
| chr1:119050342 | T | C | 2 | a0001c0001t0006g0284 a0001c0001t0006g0317 |
2 | HG03098.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.349-4680A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119050342 | |||||||
| chr1:119050582 | C | G | 66 | a0001c0001t0004g0012 a0001c0001t0004g0014 a0001c0001t0004g0015 others(63): Show |
70 | HG00558.hp1 HG00609.hp1 HG00738.hp2 others(67): Show |
intron_variant | MODIFIER | c.349-4920G>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119050582 | |||||||
| chr1:119050620 | C | G | 1 | a0001c0001t0007g0023 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.349-4958G>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119050620 | |||||||
| chr1:119050645 | T | G | 66 | a0001c0001t0004g0012 a0001c0001t0004g0014 a0001c0001t0004g0015 others(63): Show |
70 | HG00558.hp1 HG00609.hp1 HG00738.hp2 others(67): Show |
intron_variant | MODIFIER | c.349-4983A>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119050645 | |||||||
| chr1:119050651 | G | A | 4 | a0001c0001t0006g0121 a0001c0001t0006g0126 a0001c0001t0006g0127 others(1): Show |
4 | HG02056.hp2 HG02071.hp2 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.349-4989C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119050651 | |||||||
| chr1:119050678 | T | C | 70 | a0001c0001t0004g0012 a0001c0001t0004g0014 a0001c0001t0004g0015 others(67): Show |
74 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.349-5016A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119050678 | |||||||
| chr1:119050683 | T | G | 1 | a0001c0001t0001g0067 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.349-5021A>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119050683 | |||||||
| chr1:119050776 | C | T | 3 | a0001c0001t0004g0020 a0001c0001t0004g0021 a0001c0001t0004g0022 |
3 | HG01433.hp2 HG02257.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.349-5114G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119050776 | |||||||
| chr1:119051021 | A | G | 76 | a0001c0001t0004g0012 a0001c0001t0004g0014 a0001c0001t0004g0015 others(73): Show |
80 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.349-5359T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119051021 | |||||||
| chr1:119051036 | T | A | 70 | a0001c0001t0004g0012 a0001c0001t0004g0014 a0001c0001t0004g0015 others(67): Show |
74 | HG00558.hp1 HG00609.hp1 HG00738.hp2 others(71): Show |
intron_variant | MODIFIER | c.349-5374A>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119051036 | |||||||
| chr1:119051188 | G | T | 8 | a0001c0001t0005g0262 a0001c0001t0005g0263 a0001c0001t0005g0264 others(5): Show |
8 | HG00408.hp1 HG02647.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.349-5526C>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119051188 | |||||||
| chr1:119051198 | A | T | 72 | a0001c0001t0001g0130 a0001c0001t0005g0118 a0001c0001t0005g0142 others(69): Show |
79 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.349-5536T>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119051198 | |||||||
| chr1:119051244 | T | A | 2 | a0001c0001t0003g0237 a0001c0001t0003g0238 |
2 | HG02080.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.349-5582A>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119051244 | |||||||
| chr1:119051288 | T | C | 1 | a0002c0002t0002g0188 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.349-5626A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119051288 | |||||||
| chr1:119051295 | A | G | 81 | a0001c0001t0004g0012 a0001c0001t0004g0014 a0001c0001t0004g0015 others(78): Show |
85 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.349-5633T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119051295 | |||||||
| chr1:119051332 | C | T | 12 | a0001c0001t0004g0012 a0001c0001t0004g0025 a0001c0001t0004g0026 others(9): Show |
13 | HG00558.hp1 HG00609.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.349-5670G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119051332 | |||||||
| chr1:119051336 | G | A | 81 | a0001c0001t0004g0012 a0001c0001t0004g0014 a0001c0001t0004g0015 others(78): Show |
85 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.349-5674C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119051336 | |||||||
| chr1:119051337 | T | A | 6 | a0001c0001t0005g0151 a0001c0001t0005g0152 a0001c0001t0005g0167 others(3): Show |
6 | HG02055.hp1 HG02109.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.349-5675A>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119051337 | |||||||
| chr1:119051582 | A | G | 1 | a0001c0001t0005g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.349-5920T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119051582 | |||||||
| chr1:119051613 | A | G | 47 | a0001c0001t0004g0014 a0001c0001t0004g0015 a0001c0001t0004g0170 others(44): Show |
50 | HG00738.hp2 HG01070.hp1 HG01074.hp2 others(47): Show |
intron_variant | MODIFIER | c.349-5951T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119051613 | |||||||
| chr1:119051721 | C | A | 2 | a0001c0003t0007g0226 a0001c0003t0007g0227 |
2 | HG03490.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.349-6059G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119051721 | |||||||
| chr1:119051762 | A | AT | 34 | a0001c0001t0001g0032 a0001c0001t0001g0041 a0001c0001t0001g0048 others(31): Show |
34 | HG00099.hp1 HG00544.hp1 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.349-6101dupA | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119051762 | |||||||
| chr1:119051762 | A | ATT | 69 | a0001c0001t0001g0104 a0001c0001t0001g0130 a0001c0001t0005g0118 others(66): Show |
76 | HG00423.hp1 HG00423.hp2 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.349-6102_349-6101d others(4): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119051762 | |||||||
| chr1:119051762 | AT | A | 14 | a0001c0001t0001g0049 a0001c0001t0001g0055 a0001c0001t0001g0095 others(11): Show |
16 | HG00099.hp2 HG02080.hp1 HG02155.hp2 others(13): Show |
intron_variant | MODIFIER | c.349-6101delA | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119051762 | |||||||
| chr1:119051762 | ATTT | A | 9 | a0001c0001t0004g0022 a0001c0001t0004g0289 a0001c0001t0005g0151 others(6): Show |
9 | HG02055.hp1 HG02109.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.349-6103_349-6101d others(5): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119051762 | |||||||
| chr1:119051762 | ATTTT | A | 57 | a0001c0001t0004g0012 a0001c0001t0004g0014 a0001c0001t0004g0015 others(54): Show |
61 | HG00408.hp1 HG00738.hp2 HG01070.hp1 others(58): Show |
intron_variant | MODIFIER | c.349-6104_349-6101d others(6): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119051762 | |||||||
| chr1:119051762 | ATTTTT | A | 14 | a0001c0001t0004g0025 a0001c0001t0004g0026 a0001c0001t0004g0027 others(11): Show |
14 | HG00558.hp1 HG00609.hp1 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.349-6105_349-6101d others(7): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119051762 | |||||||
| chr1:119051829 | G | A | 2 | a0001c0001t0006g0013 a0001c0001t0006g0312 |
3 | HG01070.hp1 HG01074.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.349-6167C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119051829 | |||||||
| chr1:119051863 | A | G | 1 | a0001c0001t0004g0329 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.349-6201T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119051863 | |||||||
| chr1:119052040 | G | A | 84 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(81): Show |
87 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.349-6378C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119052040 | |||||||
| chr1:119052373 | T | C | 2 | a0001c0003t0007g0226 a0001c0003t0007g0227 |
2 | HG03490.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.349-6711A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119052373 | |||||||
| chr1:119052427 | C | G | 1 | a0001c0001t0004g0022 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.349-6765G>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119052427 | |||||||
| chr1:119052720 | G | A | 1 | a0001c0001t0001g0320 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.349-7058C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119052720 | |||||||
| chr1:119053036 | A | C | 4 | a0001c0001t0005g0262 a0001c0001t0005g0263 a0001c0001t0005g0264 others(1): Show |
4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.349-7374T>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119053036 | |||||||
| chr1:119053097 | G | A | 2 | a0001c0001t0003g0261 a0001c0001t0003g0300 |
2 | HG02818.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.349-7435C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119053097 | |||||||
| chr1:119053244 | G | A | 1 | a0001c0001t0003g0269 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.349-7582C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119053244 | |||||||
| chr1:119053313 | T | G | 72 | a0001c0001t0001g0130 a0001c0001t0005g0118 a0001c0001t0005g0142 others(69): Show |
79 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.349-7651A>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119053313 | |||||||
| chr1:119053325 | G | A | 3 | a0003c0004t0005g0210 a0003c0004t0005g0211 a0003c0004t0005g0212 |
3 | HG02647.hp1 HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.349-7663C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119053325 | |||||||
| chr1:119053326 | C | T | 82 | a0001c0001t0004g0012 a0001c0001t0004g0014 a0001c0001t0004g0015 others(79): Show |
86 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.349-7664G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119053326 | |||||||
| chr1:119053408 | A | C | 10 | a0001c0001t0008g0275 a0001c0001t0008g0276 a0001c0001t0008g0277 others(7): Show |
10 | HG02145.hp2 HG02572.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.349-7746T>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119053408 | |||||||
| chr1:119053413 | C | T | 1 | a0003c0004t0005g0212 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.349-7751G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119053413 | |||||||
| chr1:119053551 | T | C | 4 | a0001c0001t0005g0262 a0001c0001t0005g0263 a0001c0001t0005g0264 others(1): Show |
4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.349-7889A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119053551 | |||||||
| chr1:119054015 | C | T | 1 | a0002c0002t0002g0155 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.349-8353G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119054015 | |||||||
| chr1:119054206 | C | T | 1 | a0001c0001t0012g0171 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.349-8544G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119054206 | |||||||
| chr1:119054375 | C | CAT | 7 | a0001c0001t0003g0254 a0001c0001t0003g0256 a0001c0001t0003g0260 others(4): Show |
7 | HG00408.hp1 NA18941.hp2 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.349-8715_349-8714d others(4): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119054375 | |||||||
| chr1:119054772 | T | C | 81 | a0001c0001t0004g0012 a0001c0001t0004g0014 a0001c0001t0004g0015 others(78): Show |
85 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.349-9110A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119054772 | |||||||
| chr1:119054811 | A | G | 4 | a0001c0001t0005g0262 a0001c0001t0005g0263 a0001c0001t0005g0264 others(1): Show |
4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.349-9149T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119054811 | |||||||
| chr1:119054948 | G | A | 5 | a0001c0003t0009g0024 a0001c0003t0009g0222 a0001c0003t0009g0223 others(2): Show |
5 | HG02258.hp2 HG02572.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.349-9286C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119054948 | |||||||
| chr1:119055050 | A | G | 1 | a0001c0001t0005g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.349-9388T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119055050 | |||||||
| chr1:119055075 | G | T | 1 | a0001c0001t0005g0165 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.349-9413C>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119055075 | |||||||
| chr1:119055169 | A | C | 81 | a0001c0001t0004g0012 a0001c0001t0004g0014 a0001c0001t0004g0015 others(78): Show |
85 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.349-9507T>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119055169 | |||||||
| chr1:119055414 | G | A | 283 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(280): Show |
298 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(295): Show |
intron_variant | MODIFIER | c.349-9752C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119055414 | |||||||
| chr1:119055568 | G | A | 1 | a0001c0001t0001g0046 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.349-9906C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119055568 | |||||||
| chr1:119055682 | CAAGAAAG others(6): Show |
C | 4 | a0003c0004t0005g0210 a0003c0004t0005g0211 a0003c0004t0005g0212 others(1): Show |
4 | HG02647.hp1 HG02723.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.349-10033_349-1002 others(17): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119055682 | |||||||
| chr1:119055717 | G | T | 2 | a0002c0002t0002g0140 a0002c0002t0002g0141 |
2 | NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.349-10055C>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119055717 | |||||||
| chr1:119056011 | C | CT | 126 | a0001c0001t0001g0058 a0001c0001t0001g0100 a0001c0001t0001g0130 others(123): Show |
137 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.349-10350dupA | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119056011 | |||||||
| chr1:119056011 | C | CTT | 9 | a0001c0001t0004g0020 a0001c0001t0004g0021 a0001c0001t0004g0022 others(6): Show |
9 | HG01433.hp2 HG02257.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.349-10351_349-1035 others(6): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119056011 | |||||||
| chr1:119056186 | A | AT | 54 | a0001c0001t0001g0031 a0001c0001t0001g0072 a0001c0001t0001g0110 others(51): Show |
55 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.349-10525dupA | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119056186 | |||||||
| chr1:119056186 | A | ATT | 7 | a0001c0001t0004g0025 a0001c0001t0004g0172 a0001c0001t0007g0200 others(4): Show |
7 | HG00609.hp1 HG02145.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.349-10526_349-1052 others(6): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119056186 | |||||||
| chr1:119056186 | AT | A | 41 | a0001c0001t0001g0102 a0001c0001t0004g0014 a0001c0001t0004g0015 others(38): Show |
44 | HG00738.hp2 HG01070.hp1 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.349-10525delA | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119056186 | |||||||
| chr1:119056365 | A | G | 12 | a0001c0001t0004g0012 a0001c0001t0004g0025 a0001c0001t0004g0026 others(9): Show |
13 | HG00558.hp1 HG00609.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.349-10703T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119056365 | |||||||
| chr1:119056409 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.349-10747G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119056409 | |||||||
| chr1:119056426 | TAAC | T | 4 | a0003c0004t0005g0210 a0003c0004t0005g0211 a0003c0004t0005g0212 others(1): Show |
4 | HG02647.hp1 HG02723.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.349-10767_349-1076 others(7): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119056426 | |||||||
| chr1:119056504 | A | T | 4 | a0003c0004t0005g0210 a0003c0004t0005g0211 a0003c0004t0005g0212 others(1): Show |
4 | HG02647.hp1 HG02723.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.349-10842T>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119056504 | |||||||
| chr1:119056536 | AAT | A | 83 | a0001c0001t0003g0273 a0001c0001t0004g0012 a0001c0001t0004g0014 others(80): Show |
87 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.349-10876_349-1087 others(6): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119056536 | |||||||
| chr1:119056584 | C | T | 82 | a0001c0001t0004g0012 a0001c0001t0004g0014 a0001c0001t0004g0015 others(79): Show |
86 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.349-10922G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119056584 | |||||||
| chr1:119056605 | C | T | 1 | a0001c0003t0007g0217 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.349-10943G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119056605 | |||||||
| chr1:119056665 | A | C | 8 | a0001c0001t0004g0020 a0001c0001t0004g0021 a0001c0001t0004g0022 others(5): Show |
8 | HG00408.hp1 HG01433.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.349-11003T>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119056665 | |||||||
| chr1:119056674 | C | T | 5 | a0001c0001t0003g0011 a0001c0001t0003g0239 a0001c0001t0003g0240 others(2): Show |
6 | HG02145.hp1 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.349-11012G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119056674 | |||||||
| chr1:119056690 | T | C | 101 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(98): Show |
104 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.349-11028A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119056690 | |||||||
| chr1:119056920 | G | A | 1 | a0001c0001t0003g0035 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.349-11258C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119056920 | |||||||
| chr1:119057142 | T | C | 1 | a0001c0001t0001g0068 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.349-11480A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119057142 | |||||||
| chr1:119057185 | C | T | 56 | a0001c0001t0001g0130 a0002c0002t0002g0001 a0002c0002t0002g0005 others(53): Show |
63 | HG00423.hp2 HG00621.hp2 HG01109.hp1 others(60): Show |
intron_variant | MODIFIER | c.349-11523G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119057185 | |||||||
| chr1:119057205 | G | A | 1 | a0001c0001t0007g0023 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.349-11543C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119057205 | |||||||
| chr1:119057209 | G | C | 4 | a0003c0004t0005g0210 a0003c0004t0005g0211 a0003c0004t0005g0212 others(1): Show |
4 | HG02647.hp1 HG02723.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.349-11547C>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119057209 | |||||||
| chr1:119057347 | C | T | 82 | a0001c0001t0004g0012 a0001c0001t0004g0014 a0001c0001t0004g0015 others(79): Show |
86 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.349-11685G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119057347 | |||||||
| chr1:119057552 | G | A | 22 | a0001c0001t0006g0013 a0001c0001t0006g0121 a0001c0001t0006g0126 others(19): Show |
23 | HG00738.hp2 HG01070.hp1 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.349-11890C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119057552 | |||||||
| chr1:119057561 | G | A | 1 | a0002c0002t0002g0120 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.349-11899C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119057561 | |||||||
| chr1:119057644 | G | A | 2 | a0002c0002t0002g0182 a0002c0002t0002g0186 |
2 | NA18747.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.349-11982C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119057644 | |||||||
| chr1:119057661 | G | T | 1 | a0001c0001t0001g0098 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.349-11999C>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119057661 | |||||||
| chr1:119057664 | C | T | 47 | a0001c0001t0004g0014 a0001c0001t0004g0015 a0001c0001t0004g0170 others(44): Show |
50 | HG00738.hp2 HG01070.hp1 HG01074.hp2 others(47): Show |
intron_variant | MODIFIER | c.349-12002G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119057664 | |||||||
| chr1:119057738 | C | T | 5 | a0001c0003t0007g0217 a0001c0003t0007g0218 a0001c0003t0007g0219 others(2): Show |
5 | HG00741.hp2 HG01099.hp2 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.349-12076G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119057738 | |||||||
| chr1:119057845 | A | T | 6 | a0001c0001t0005g0151 a0001c0001t0005g0152 a0001c0001t0005g0167 others(3): Show |
6 | HG02055.hp1 HG02109.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.349-12183T>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119057845 | |||||||
| chr1:119058189 | C | T | 81 | a0001c0001t0004g0012 a0001c0001t0004g0014 a0001c0001t0004g0015 others(78): Show |
85 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.349-12527G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119058189 | |||||||
| chr1:119058286 | C | A | 1 | a0001c0001t0005g0143 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.349-12624G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119058286 | |||||||
| chr1:119058307 | C | CT | 232 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(229): Show |
245 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(242): Show |
intron_variant | MODIFIER | c.349-12646dupA | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119058307 | |||||||
| chr1:119058307 | C | CTT | 14 | a0001c0001t0003g0082 a0001c0001t0005g0165 a0001c0001t0008g0275 others(11): Show |
14 | HG02004.hp2 HG02145.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.349-12647_349-1264 others(6): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119058307 | |||||||
| chr1:119058322 | T | A | 10 | a0001c0001t0005g0262 a0001c0001t0005g0263 a0001c0001t0005g0264 others(7): Show |
10 | HG00408.hp1 HG02647.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.349-12660A>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119058322 | |||||||
| chr1:119058322 | T | TA | 72 | a0001c0001t0004g0012 a0001c0001t0004g0014 a0001c0001t0004g0015 others(69): Show |
76 | HG00558.hp1 HG00609.hp1 HG00738.hp2 others(73): Show |
intron_variant | MODIFIER | c.349-12661dupT | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119058322 | |||||||
| chr1:119058332 | G | A | 1 | a0001c0001t0006g0235 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.349-12670C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119058332 | |||||||
| chr1:119058397 | G | A | 74 | a0001c0001t0004g0012 a0001c0001t0004g0014 a0001c0001t0004g0015 others(71): Show |
78 | HG00558.hp1 HG00609.hp1 HG00738.hp2 others(75): Show |
intron_variant | MODIFIER | c.349-12735C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119058397 | |||||||
| chr1:119058408 | TA | T | 82 | a0001c0001t0004g0012 a0001c0001t0004g0014 a0001c0001t0004g0015 others(79): Show |
86 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.349-12747delT | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119058408 | |||||||
| chr1:119058468 | C | T | 82 | a0001c0001t0004g0012 a0001c0001t0004g0014 a0001c0001t0004g0015 others(79): Show |
86 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.349-12806G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119058468 | |||||||
| chr1:119058516 | A | T | 82 | a0001c0001t0004g0012 a0001c0001t0004g0014 a0001c0001t0004g0015 others(79): Show |
86 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.349-12854T>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119058516 | |||||||
| chr1:119058545 | G | A | 78 | a0001c0001t0004g0012 a0001c0001t0004g0014 a0001c0001t0004g0015 others(75): Show |
82 | HG00558.hp1 HG00609.hp1 HG00738.hp2 others(79): Show |
intron_variant | MODIFIER | c.349-12883C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119058545 | |||||||
| chr1:119058554 | C | T | 82 | a0001c0001t0004g0012 a0001c0001t0004g0014 a0001c0001t0004g0015 others(79): Show |
86 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.349-12892G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119058554 | |||||||
| chr1:119058662 | G | T | 82 | a0001c0001t0004g0012 a0001c0001t0004g0014 a0001c0001t0004g0015 others(79): Show |
86 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.349-13000C>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119058662 | |||||||
| chr1:119058668 | A | G | 82 | a0001c0001t0004g0012 a0001c0001t0004g0014 a0001c0001t0004g0015 others(79): Show |
86 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.349-13006T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119058668 | |||||||
| chr1:119058714 | G | A | 82 | a0001c0001t0004g0012 a0001c0001t0004g0014 a0001c0001t0004g0015 others(79): Show |
86 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.349-13052C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119058714 | |||||||
| chr1:119058753 | G | A | 82 | a0001c0001t0004g0012 a0001c0001t0004g0014 a0001c0001t0004g0015 others(79): Show |
86 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.349-13091C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119058753 | |||||||
| chr1:119058758 | G | A | 82 | a0001c0001t0004g0012 a0001c0001t0004g0014 a0001c0001t0004g0015 others(79): Show |
86 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.349-13096C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119058758 | |||||||
| chr1:119058775 | A | G | 82 | a0001c0001t0004g0012 a0001c0001t0004g0014 a0001c0001t0004g0015 others(79): Show |
86 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.349-13113T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119058775 | |||||||
| chr1:119058868 | C | T | 1 | a0002c0002t0002g0201 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.349-13206G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119058868 | |||||||
| chr1:119058930 | G | A | 1 | a0001c0003t0007g0218 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.349-13268C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119058930 | |||||||
| chr1:119059136 | G | A | 1 | a0001c0001t0007g0080 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.349-13474C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119059136 | |||||||
| chr1:119059179 | G | A | 4 | a0001c0001t0004g0020 a0001c0001t0004g0021 a0001c0001t0004g0022 others(1): Show |
4 | HG01433.hp2 HG02257.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.349-13517C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119059179 | |||||||
| chr1:119059187 | T | G | 4 | a0001c0001t0005g0262 a0001c0001t0005g0263 a0001c0001t0005g0264 others(1): Show |
4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.349-13525A>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119059187 | |||||||
| chr1:119059249 | G | C | 1 | a0001c0001t0007g0272 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.349-13587C>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119059249 | |||||||
| chr1:119059441 | C | A | 2 | a0001c0001t0003g0237 a0001c0001t0003g0238 |
2 | HG02080.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.349-13779G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119059441 | |||||||
| chr1:119059535 | C | T | 18 | a0001c0001t0007g0023 a0001c0003t0007g0217 a0001c0003t0007g0218 others(15): Show |
18 | HG00741.hp2 HG01099.hp2 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.349-13873G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119059535 | |||||||
| chr1:119059591 | C | A | 1 | a0006c0008t0001g0113 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.349-13929G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119059591 | |||||||
| chr1:119059592 | A | G | 82 | a0001c0001t0004g0012 a0001c0001t0004g0014 a0001c0001t0004g0015 others(79): Show |
86 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.349-13930T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119059592 | |||||||
| chr1:119059690 | G | A | 4 | a0001c0001t0005g0262 a0001c0001t0005g0263 a0001c0001t0005g0264 others(1): Show |
4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.349-14028C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119059690 | |||||||
| chr1:119059758 | A | T | 97 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(94): Show |
100 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.349-14096T>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119059758 | |||||||
| chr1:119059792 | T | C | 98 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(95): Show |
101 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.349-14130A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119059792 | |||||||
| chr1:119059981 | T | C | 10 | a0001c0001t0007g0080 a0001c0001t0007g0200 a0001c0001t0007g0202 others(7): Show |
10 | HG00099.hp1 HG00544.hp1 HG00558.hp2 others(7): Show |
intron_variant | MODIFIER | c.349-14319A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119059981 | |||||||
| chr1:119060353 | C | G | 1 | a0001c0001t0001g0179 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.349-14691G>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119060353 | |||||||
| chr1:119060402 | C | T | 1 | a0001c0001t0001g0091 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.349-14740G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119060402 | |||||||
| chr1:119060444 | C | A | 82 | a0001c0001t0004g0012 a0001c0001t0004g0014 a0001c0001t0004g0015 others(79): Show |
86 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.349-14782G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119060444 | |||||||
| chr1:119060479 | A | G | 6 | a0001c0001t0001g0033 a0001c0001t0001g0060 a0001c0001t0001g0062 others(3): Show |
6 | NA18946.hp2 NA18948.hp1 NA18969.hp1 others(3): Show |
intron_variant | MODIFIER | c.349-14817T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119060479 | |||||||
| chr1:119060653 | T | C | 1 | a0005c0009t0003g0324 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.349-14991A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119060653 | |||||||
| chr1:119060686 | C | T | 1 | a0001c0001t0003g0300 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.349-15024G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119060686 | |||||||
| chr1:119060699 | T | C | 85 | a0001c0001t0004g0012 a0001c0001t0004g0014 a0001c0001t0004g0015 others(82): Show |
89 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.349-15037A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119060699 | |||||||
| chr1:119060782 | A | G | 85 | a0001c0001t0004g0012 a0001c0001t0004g0014 a0001c0001t0004g0015 others(82): Show |
89 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.349-15120T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119060782 | |||||||
| chr1:119060794 | T | C | 77 | a0001c0001t0004g0012 a0001c0001t0004g0014 a0001c0001t0004g0015 others(74): Show |
81 | HG00558.hp1 HG00609.hp1 HG00738.hp2 others(78): Show |
intron_variant | MODIFIER | c.349-15132A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119060794 | |||||||
| chr1:119060807 | G | C | 5 | a0001c0001t0003g0246 a0001c0001t0003g0247 a0001c0001t0003g0248 others(2): Show |
5 | HG00408.hp2 HG00642.hp2 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.349-15145C>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119060807 | |||||||
| chr1:119060917 | C | T | 4 | a0001c0001t0003g0230 a0001c0001t0003g0231 a0001c0001t0003g0232 others(1): Show |
4 | HG00735.hp2 HG00741.hp1 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.349-15255G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119060917 | |||||||
| chr1:119061077 | A | T | 85 | a0001c0001t0004g0012 a0001c0001t0004g0014 a0001c0001t0004g0015 others(82): Show |
89 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.348+15273T>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119061077 | |||||||
| chr1:119061280 | G | A | 3 | a0001c0001t0008g0275 a0001c0001t0008g0277 a0001c0001t0008g0282 |
3 | HG02145.hp2 HG02572.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.348+15070C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119061280 | |||||||
| chr1:119061485 | T | C | 1 | a0001c0001t0005g0144 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.348+14865A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119061485 | |||||||
| chr1:119061637 | A | C | 27 | a0001c0001t0007g0080 a0001c0001t0007g0200 a0001c0001t0007g0202 others(24): Show |
27 | HG00099.hp1 HG00544.hp1 HG00558.hp2 others(24): Show |
intron_variant | MODIFIER | c.348+14713T>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119061637 | |||||||
| chr1:119061755 | T | C | 1 | a0001c0001t0005g0169 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.348+14595A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119061755 | |||||||
| chr1:119061827 | C | T | 3 | a0003c0004t0005g0210 a0003c0004t0005g0211 a0003c0004t0005g0212 |
3 | HG02647.hp1 HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.348+14523G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119061827 | |||||||
| chr1:119061845 | G | A | 2 | a0001c0001t0001g0071 a0001c0001t0001g0103 |
2 | NA18948.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.348+14505C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119061845 | |||||||
| chr1:119061850 | A | T | 85 | a0001c0001t0004g0012 a0001c0001t0004g0014 a0001c0001t0004g0015 others(82): Show |
89 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.348+14500T>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119061850 | |||||||
| chr1:119062032 | T | C | 85 | a0001c0001t0004g0012 a0001c0001t0004g0014 a0001c0001t0004g0015 others(82): Show |
89 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.348+14318A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119062032 | |||||||
| chr1:119062196 | G | A | 1 | a0001c0001t0007g0023 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.348+14154C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119062196 | |||||||
| chr1:119062321 | G | A | 1 | a0001c0001t0006g0326 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.348+14029C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119062321 | |||||||
| chr1:119062399 | G | C | 4 | a0001c0001t0005g0262 a0001c0001t0005g0263 a0001c0001t0005g0264 others(1): Show |
4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.348+13951C>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119062399 | |||||||
| chr1:119062431 | A | T | 77 | a0001c0001t0004g0012 a0001c0001t0004g0014 a0001c0001t0004g0015 others(74): Show |
81 | HG00558.hp1 HG00609.hp1 HG00738.hp2 others(78): Show |
intron_variant | MODIFIER | c.348+13919T>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119062431 | |||||||
| chr1:119062466 | T | TA | 73 | a0001c0001t0004g0014 a0001c0001t0004g0015 a0001c0001t0004g0170 others(70): Show |
76 | HG00099.hp1 HG00544.hp1 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.348+13883dupT | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119062466 | |||||||
| chr1:119062468 | A | T | 1 | a0002c0002t0002g0029 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.348+13882T>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119062468 | |||||||
| chr1:119062573 | A | C | 3 | a0001c0001t0004g0020 a0001c0001t0004g0021 a0001c0001t0004g0022 |
3 | HG01433.hp2 HG02257.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.348+13777T>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119062573 | |||||||
| chr1:119062595 | C | T | 52 | a0001c0001t0001g0130 a0001c0001t0005g0262 a0001c0001t0005g0263 others(49): Show |
59 | HG00408.hp1 HG00423.hp2 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.348+13755G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119062595 | |||||||
| chr1:119062604 | T | C | 278 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(275): Show |
292 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(289): Show |
intron_variant | MODIFIER | c.348+13746A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119062604 | |||||||
| chr1:119062679 | A | G | 2 | a0001c0001t0004g0025 a0001c0001t0004g0026 |
2 | NA18981.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.348+13671T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119062679 | |||||||
| chr1:119062771 | G | C | 4 | a0001c0001t0005g0262 a0001c0001t0005g0263 a0001c0001t0005g0264 others(1): Show |
4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.348+13579C>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119062771 | |||||||
| chr1:119062776 | T | C | 1 | a0001c0001t0001g0040 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.348+13574A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119062776 | |||||||
| chr1:119062829 | C | T | 1 | a0001c0003t0007g0296 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.348+13521G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119062829 | |||||||
| chr1:119062864 | G | A | 4 | a0001c0001t0004g0020 a0001c0001t0004g0021 a0001c0001t0004g0022 others(1): Show |
4 | HG01433.hp2 HG02257.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.348+13486C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119062864 | |||||||
| chr1:119063249 | G | A | 1 | a0001c0001t0007g0272 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.348+13101C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119063249 | |||||||
| chr1:119063374 | A | G | 287 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(284): Show |
302 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(299): Show |
intron_variant | MODIFIER | c.348+12976T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119063374 | |||||||
| chr1:119063507 | T | C | 72 | a0001c0001t0001g0130 a0001c0001t0005g0118 a0001c0001t0005g0142 others(69): Show |
79 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.348+12843A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119063507 | |||||||
| chr1:119063547 | A | G | 1 | a0001c0001t0006g0311 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.348+12803T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119063547 | |||||||
| chr1:119063638 | C | T | 1 | a0001c0001t0005g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.348+12712G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119063638 | |||||||
| chr1:119063656 | A | C | 1 | a0001c0001t0007g0023 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.348+12694T>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119063656 | |||||||
| chr1:119063676 | G | C | 1 | a0001c0001t0001g0179 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.348+12674C>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119063676 | |||||||
| chr1:119063760 | C | T | 3 | a0001c0001t0005g0142 a0001c0001t0005g0162 a0001c0001t0005g0164 |
3 | NA18946.hp1 NA18959.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.348+12590G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119063760 | |||||||
| chr1:119063980 | T | C | 1 | a0001c0001t0012g0171 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.348+12370A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119063980 | |||||||
| chr1:119063989 | C | T | 10 | a0001c0001t0001g0130 a0002c0002t0002g0125 a0002c0002t0002g0136 others(7): Show |
10 | HG02027.hp2 HG02129.hp1 NA18950.hp2 others(7): Show |
intron_variant | MODIFIER | c.348+12361G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119063989 | |||||||
| chr1:119063994 | G | A | 1 | a0001c0001t0001g0097 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.348+12356C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119063994 | |||||||
| chr1:119064128 | C | T | 1 | a0002c0002t0002g0138 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.348+12222G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119064128 | |||||||
| chr1:119064129 | G | A | 3 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0109 |
3 | NA18960.hp2 NA18994.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.348+12221C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119064129 | |||||||
| chr1:119064196 | T | TG | 85 | a0001c0001t0004g0012 a0001c0001t0004g0014 a0001c0001t0004g0015 others(82): Show |
89 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.348+12153dupC | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119064196 | |||||||
| chr1:119064337 | G | T | 81 | a0001c0001t0004g0012 a0001c0001t0004g0014 a0001c0001t0004g0015 others(78): Show |
85 | HG00558.hp1 HG00609.hp1 HG00738.hp2 others(82): Show |
intron_variant | MODIFIER | c.348+12013C>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119064337 | |||||||
| chr1:119064364 | G | A | 1 | a0001c0003t0007g0253 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.348+11986C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119064364 | |||||||
| chr1:119064382 | T | C | 5 | a0001c0001t0004g0014 a0001c0001t0004g0332 a0001c0001t0004g0333 others(2): Show |
6 | HG01884.hp1 HG02559.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.348+11968A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119064382 | |||||||
| chr1:119064570 | T | C | 286 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(283): Show |
301 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(298): Show |
intron_variant | MODIFIER | c.348+11780A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119064570 | |||||||
| chr1:119064571 | G | A | 72 | a0001c0001t0001g0130 a0001c0001t0005g0118 a0001c0001t0005g0142 others(69): Show |
79 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.348+11779C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119064571 | |||||||
| chr1:119064596 | G | A | 4 | a0001c0001t0005g0147 a0001c0001t0005g0148 a0001c0001t0005g0149 others(1): Show |
4 | HG01167.hp2 HG01358.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.348+11754C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119064596 | |||||||
| chr1:119064693 | G | A | 12 | a0001c0001t0004g0012 a0001c0001t0004g0025 a0001c0001t0004g0026 others(9): Show |
13 | HG00558.hp1 HG00609.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.348+11657C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119064693 | |||||||
| chr1:119064727 | G | A | 1 | a0001c0001t0003g0261 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.348+11623C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119064727 | |||||||
| chr1:119064784 | C | T | 1 | a0001c0001t0001g0060 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.348+11566G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119064784 | |||||||
| chr1:119064792 | G | A | 1 | a0002c0002t0002g0157 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.348+11558C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119064792 | |||||||
| chr1:119064830 | C | T | 15 | a0001c0003t0007g0217 a0001c0003t0007g0218 a0001c0003t0007g0219 others(12): Show |
15 | HG00741.hp2 HG01099.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.348+11520G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119064830 | |||||||
| chr1:119064868 | T | TCAAAAAT others(314): Show |
1 | a0001c0001t0004g0022 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.348+11481_348+1148 others(325): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119064868 | |||||||
| chr1:119064868 | T | TCAAAAAT others(327): Show |
1 | a0001c0001t0004g0020 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.348+11481_348+1148 others(338): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119064868 | |||||||
| chr1:119064868 | T | TCAAAAAT others(328): Show |
1 | a0001c0001t0004g0021 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.348+11481_348+1148 others(339): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119064868 | |||||||
| chr1:119065069 | A | T | 4 | a0001c0001t0005g0262 a0001c0001t0005g0263 a0001c0001t0005g0264 others(1): Show |
4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.348+11281T>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119065069 | |||||||
| chr1:119065073 | A | C | 1 | a0001c0001t0005g0145 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.348+11277T>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119065073 | |||||||
| chr1:119065158 | G | A | 1 | a0002c0002t0002g0183 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.348+11192C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119065158 | |||||||
| chr1:119065192 | G | GA | 10 | a0001c0001t0007g0080 a0001c0001t0007g0200 a0001c0001t0007g0202 others(7): Show |
10 | HG00099.hp1 HG00544.hp1 HG00558.hp2 others(7): Show |
intron_variant | MODIFIER | c.348+11157dupT | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119065192 | |||||||
| chr1:119065211 | A | C | 1 | a0001c0001t0005g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.348+11139T>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119065211 | |||||||
| chr1:119065453 | G | A | 1 | a0001c0001t0003g0239 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.348+10897C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119065453 | |||||||
| chr1:119065576 | A | G | 3 | a0001c0001t0003g0010 a0001c0001t0003g0228 a0001c0001t0003g0229 |
4 | NA19001.hp1 NA19004.hp1 NA19083.hp1 others(1): Show |
intron_variant | MODIFIER | c.348+10774T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119065576 | |||||||
| chr1:119065599 | C | T | 2 | a0001c0006t0004g0028 a0001c0006t0004g0173 |
2 | HG02280.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.348+10751G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119065599 | |||||||
| chr1:119065626 | C | T | 4 | a0001c0001t0005g0262 a0001c0001t0005g0263 a0001c0001t0005g0264 others(1): Show |
4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.348+10724G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119065626 | |||||||
| chr1:119065634 | C | CA | 22 | a0001c0001t0001g0051 a0001c0001t0003g0241 a0001c0001t0003g0245 others(19): Show |
22 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(19): Show |
intron_variant | MODIFIER | c.348+10715dupT | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119065634 | |||||||
| chr1:119065634 | CA | C | 91 | a0001c0001t0001g0054 a0001c0001t0004g0012 a0001c0001t0004g0014 others(88): Show |
95 | HG00558.hp1 HG00609.hp1 HG00738.hp2 others(92): Show |
intron_variant | MODIFIER | c.348+10715delT | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119065634 | |||||||
| chr1:119066109 | T | C | 16 | a0001c0001t0005g0118 a0001c0001t0005g0142 a0001c0001t0005g0143 others(13): Show |
16 | HG00621.hp1 HG01074.hp1 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.348+10241A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119066109 | |||||||
| chr1:119066136 | C | A | 2 | a0001c0001t0006g0284 a0001c0001t0006g0317 |
2 | HG03098.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.348+10214G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119066136 | |||||||
| chr1:119066203 | T | C | 25 | a0001c0001t0001g0060 a0001c0001t0001g0101 a0001c0001t0004g0020 others(22): Show |
25 | HG00621.hp1 HG01074.hp1 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.348+10147A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119066203 | |||||||
| chr1:119066253 | G | A | 1 | a0001c0001t0006g0121 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.348+10097C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119066253 | |||||||
| chr1:119066260 | A | G | 2 | a0001c0006t0004g0028 a0001c0006t0004g0173 |
2 | HG02280.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.348+10090T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119066260 | |||||||
| chr1:119066273 | C | T | 2 | a0001c0006t0004g0028 a0001c0006t0004g0173 |
2 | HG02280.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.348+10077G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119066273 | |||||||
| chr1:119066289 | T | C | 1 | a0002c0002t0002g0181 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.348+10061A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119066289 | |||||||
| chr1:119066292 | T | C | 290 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(287): Show |
306 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(303): Show |
intron_variant | MODIFIER | c.348+10058A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119066292 | |||||||
| chr1:119066295 | G | A | 181 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(178): Show |
192 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.348+10055C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119066295 | |||||||
| chr1:119066346 | T | C | 27 | a0001c0001t0001g0032 a0001c0001t0001g0179 a0001c0001t0004g0025 others(24): Show |
27 | HG00558.hp1 HG00609.hp1 HG02027.hp1 others(24): Show |
intron_variant | MODIFIER | c.348+10004A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119066346 | |||||||
| chr1:119066451 | A | C | 1 | a0001c0001t0004g0012 | 2 | HG02109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.348+9899T>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119066451 | |||||||
| chr1:119066477 | C | CA | 16 | a0001c0001t0001g0048 a0001c0001t0001g0051 a0001c0001t0001g0068 others(13): Show |
16 | HG00621.hp2 HG01123.hp1 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.348+9872dupT | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119066477 | |||||||
| chr1:119066477 | CA | C | 63 | a0001c0001t0001g0054 a0001c0001t0001g0086 a0001c0001t0001g0093 others(60): Show |
70 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.348+9872delT | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119066477 | |||||||
| chr1:119066523 | ATAATG | A | 3 | a0001c0001t0003g0016 a0001c0001t0003g0323 a0005c0009t0003g0324 |
4 | NA18612.hp1 NA18968.hp2 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.348+9822_348+9826d others(7): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119066523 | |||||||
| chr1:119066565 | C | T | 2 | a0001c0001t0001g0061 a0001c0001t0014g0099 |
2 | HG02602.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.348+9785G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119066565 | |||||||
| chr1:119066705 | G | T | 2 | a0002c0002t0011g0137 a0002c0002t0011g0139 |
2 | HG02280.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.348+9645C>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119066705 | |||||||
| chr1:119066741 | T | C | 1 | a0001c0001t0001g0054 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.348+9609A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119066741 | |||||||
| chr1:119066751 | A | G | 1 | a0002c0002t0002g0159 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.348+9599T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119066751 | |||||||
| chr1:119067129 | C | CA | 77 | a0001c0001t0001g0310 a0001c0001t0001g0320 a0001c0001t0001g0321 others(74): Show |
81 | HG00438.hp1 HG00621.hp1 HG00738.hp2 others(78): Show |
intron_variant | MODIFIER | c.348+9220dupT | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119067129 | |||||||
| chr1:119067560 | C | T | 4 | a0003c0004t0005g0210 a0003c0004t0005g0211 a0003c0004t0005g0212 others(1): Show |
4 | HG02647.hp1 HG02723.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.348+8790G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119067560 | |||||||
| chr1:119067647 | T | C | 40 | a0001c0001t0001g0130 a0002c0002t0002g0001 a0002c0002t0002g0006 others(37): Show |
46 | HG00423.hp2 HG01257.hp2 HG01258.hp1 others(43): Show |
intron_variant | MODIFIER | c.348+8703A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119067647 | |||||||
| chr1:119067811 | A | ATT | 53 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0006 others(50): Show |
60 | HG00423.hp2 HG01175.hp1 HG01257.hp2 others(57): Show |
intron_variant | MODIFIER | c.348+8537_348+8538d others(4): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119067811 | |||||||
| chr1:119067989 | G | A | 1 | a0001c0001t0001g0321 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.348+8361C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119067989 | |||||||
| chr1:119068001 | T | C | 1 | a0001c0001t0001g0320 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.348+8349A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119068001 | |||||||
| chr1:119068141 | G | A | 54 | a0001c0001t0001g0130 a0002c0002t0002g0001 a0002c0002t0002g0005 others(51): Show |
61 | HG00423.hp2 HG01175.hp1 HG01257.hp2 others(58): Show |
intron_variant | MODIFIER | c.348+8209C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119068141 | |||||||
| chr1:119068164 | C | T | 55 | a0001c0001t0001g0310 a0001c0001t0001g0320 a0001c0001t0001g0321 others(52): Show |
59 | HG00438.hp1 HG00738.hp2 HG01070.hp1 others(56): Show |
intron_variant | MODIFIER | c.348+8186G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119068164 | |||||||
| chr1:119068226 | C | G | 54 | a0001c0001t0001g0130 a0002c0002t0002g0001 a0002c0002t0002g0005 others(51): Show |
61 | HG00423.hp2 HG01175.hp1 HG01257.hp2 others(58): Show |
intron_variant | MODIFIER | c.348+8124G>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119068226 | |||||||
| chr1:119068579 | C | T | 1 | a0001c0001t0001g0084 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.348+7771G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119068579 | |||||||
| chr1:119068606 | G | C | 4 | a0001c0001t0005g0262 a0001c0001t0005g0263 a0001c0001t0005g0264 others(1): Show |
4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.348+7744C>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119068606 | |||||||
| chr1:119068728 | A | T | 21 | a0001c0001t0001g0002 a0001c0001t0001g0032 a0001c0001t0001g0033 others(18): Show |
22 | HG00621.hp2 HG00673.hp2 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.348+7622T>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119068728 | |||||||
| chr1:119068808 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.348+7542C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119068808 | |||||||
| chr1:119068825 | A | ACT | 147 | a0001c0001t0001g0130 a0001c0001t0001g0310 a0001c0001t0001g0320 others(144): Show |
159 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(156): Show |
intron_variant | MODIFIER | c.348+7523_348+7524d others(4): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119068825 | |||||||
| chr1:119068825 | A | ACTCT | 8 | a0002c0002t0002g0138 a0002c0002t0002g0140 a0002c0002t0002g0141 others(5): Show |
8 | HG02055.hp2 HG02280.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.348+7521_348+7524d others(6): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119068825 | |||||||
| chr1:119068841 | A | T | 151 | a0001c0001t0001g0130 a0001c0001t0001g0310 a0001c0001t0001g0320 others(148): Show |
163 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(160): Show |
intron_variant | MODIFIER | c.348+7509T>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119068841 | |||||||
| chr1:119068854 | T | C | 151 | a0001c0001t0001g0130 a0001c0001t0001g0310 a0001c0001t0001g0320 others(148): Show |
163 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(160): Show |
intron_variant | MODIFIER | c.348+7496A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119068854 | |||||||
| chr1:119068854 | T | TAC | 3 | a0001c0001t0001g0076 a0001c0003t0007g0218 a0001c0003t0007g0219 |
3 | HG01978.hp1 HG02129.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.348+7494_348+7495d others(4): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119068854 | |||||||
| chr1:119068856 | C | T | 151 | a0001c0001t0001g0130 a0001c0001t0001g0310 a0001c0001t0001g0320 others(148): Show |
163 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(160): Show |
intron_variant | MODIFIER | c.348+7494G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119068856 | |||||||
| chr1:119069378 | C | T | 54 | a0001c0001t0001g0130 a0002c0002t0002g0001 a0002c0002t0002g0005 others(51): Show |
61 | HG00423.hp2 HG01175.hp1 HG01257.hp2 others(58): Show |
intron_variant | MODIFIER | c.348+6972G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119069378 | |||||||
| chr1:119069489 | T | C | 1 | a0001c0001t0001g0091 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.348+6861A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119069489 | |||||||
| chr1:119069782 | G | C | 1 | a0001c0001t0003g0108 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.348+6568C>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119069782 | |||||||
| chr1:119070009 | C | T | 159 | a0001c0001t0001g0130 a0001c0001t0001g0310 a0001c0001t0001g0320 others(156): Show |
171 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(168): Show |
intron_variant | MODIFIER | c.348+6341G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119070009 | |||||||
| chr1:119070478 | G | C | 1 | a0001c0001t0006g0306 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.348+5872C>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119070478 | |||||||
| chr1:119070744 | A | T | 2 | a0001c0001t0001g0041 a0001c0001t0001g0097 |
2 | NA18991.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.348+5606T>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119070744 | |||||||
| chr1:119070806 | A | T | 85 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(82): Show |
88 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.348+5544T>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119070806 | |||||||
| chr1:119070935 | C | T | 5 | a0001c0001t0001g0004 a0001c0001t0001g0063 a0001c0001t0001g0073 others(2): Show |
6 | HG01258.hp2 NA18939.hp1 NA18955.hp2 others(3): Show |
intron_variant | MODIFIER | c.348+5415G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119070935 | |||||||
| chr1:119071106 | C | T | 1 | a0001c0001t0010g0301 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.348+5244G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119071106 | |||||||
| chr1:119071318 | G | A | 159 | a0001c0001t0001g0130 a0001c0001t0001g0310 a0001c0001t0001g0320 others(156): Show |
171 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(168): Show |
intron_variant | MODIFIER | c.348+5032C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119071318 | |||||||
| chr1:119071448 | T | G | 47 | a0001c0001t0001g0310 a0001c0001t0001g0320 a0001c0001t0001g0321 others(44): Show |
51 | HG00438.hp1 HG00738.hp2 HG01070.hp1 others(48): Show |
intron_variant | MODIFIER | c.348+4902A>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119071448 | |||||||
| chr1:119071496 | G | A | 1 | a0001c0001t0005g0163 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.348+4854C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119071496 | |||||||
| chr1:119071545 | T | C | 4 | a0003c0004t0005g0210 a0003c0004t0005g0211 a0003c0004t0005g0212 others(1): Show |
4 | HG02647.hp1 HG02723.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.348+4805A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119071545 | |||||||
| chr1:119071648 | T | A | 4 | a0001c0001t0005g0151 a0001c0001t0005g0152 a0001c0001t0005g0168 others(1): Show |
4 | HG02055.hp1 HG02109.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.348+4702A>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119071648 | |||||||
| chr1:119071714 | A | T | 55 | a0001c0001t0001g0310 a0001c0001t0001g0320 a0001c0001t0001g0321 others(52): Show |
59 | HG00438.hp1 HG00738.hp2 HG01070.hp1 others(56): Show |
intron_variant | MODIFIER | c.348+4636T>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119071714 | |||||||
| chr1:119071761 | A | G | 5 | a0001c0003t0007g0217 a0001c0003t0007g0218 a0001c0003t0007g0219 others(2): Show |
5 | HG00741.hp2 HG01099.hp2 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.348+4589T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119071761 | |||||||
| chr1:119072020 | A | G | 1 | a0002c0002t0002g0183 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.348+4330T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119072020 | |||||||
| chr1:119072025 | T | C | 1 | a0001c0006t0004g0173 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.348+4325A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119072025 | |||||||
| chr1:119072060 | T | C | 1 | a0001c0001t0006g0317 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.348+4290A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119072060 | |||||||
| chr1:119072232 | A | T | 2 | a0001c0001t0001g0214 a0001c0001t0001g0215 |
2 | NA18944.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.348+4118T>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119072232 | |||||||
| chr1:119072352 | A | T | 1 | a0001c0001t0004g0336 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.348+3998T>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119072352 | |||||||
| chr1:119072500 | G | A | 1 | a0001c0001t0006g0330 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.348+3850C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119072500 | |||||||
| chr1:119072642 | T | C | 8 | a0002c0002t0002g0138 a0002c0002t0002g0140 a0002c0002t0002g0141 others(5): Show |
8 | HG02055.hp2 HG02280.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.348+3708A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119072642 | |||||||
| chr1:119072838 | CT | C | 97 | a0001c0001t0001g0310 a0001c0001t0001g0320 a0001c0001t0001g0321 others(94): Show |
102 | HG00438.hp1 HG00558.hp1 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.348+3511delA | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119072838 | |||||||
| chr1:119073036 | A | G | 1 | a0001c0001t0001g0085 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.348+3314T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119073036 | |||||||
| chr1:119073153 | CAAAAAAG others(7): Show |
C | 87 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(84): Show |
90 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.348+3183_348+3196d others(16): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119073153 | |||||||
| chr1:119073160 | G | GA | 6 | a0001c0001t0003g0261 a0001c0001t0004g0170 a0001c0001t0005g0262 others(3): Show |
6 | HG00408.hp1 HG02615.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.348+3189dupT | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119073160 | |||||||
| chr1:119073245 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.348+3105A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119073245 | |||||||
| chr1:119073333 | A | C | 41 | a0001c0001t0001g0310 a0001c0001t0001g0320 a0001c0001t0001g0321 others(38): Show |
45 | HG00438.hp1 HG00738.hp2 HG01070.hp1 others(42): Show |
intron_variant | MODIFIER | c.348+3017T>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119073333 | |||||||
| chr1:119073595 | G | C | 4 | a0001c0001t0005g0262 a0001c0001t0005g0263 a0001c0001t0005g0264 others(1): Show |
4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.348+2755C>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119073595 | |||||||
| chr1:119073622 | A | G | 4 | a0003c0004t0005g0210 a0003c0004t0005g0211 a0003c0004t0005g0212 others(1): Show |
4 | HG02647.hp1 HG02723.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.348+2728T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119073622 | |||||||
| chr1:119073655 | A | G | 96 | a0001c0001t0001g0310 a0001c0001t0001g0320 a0001c0001t0001g0321 others(93): Show |
101 | HG00438.hp1 HG00558.hp1 HG00609.hp1 others(98): Show |
intron_variant | MODIFIER | c.348+2695T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119073655 | |||||||
| chr1:119073789 | A | G | 1 | a0002c0002t0002g0159 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.348+2561T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119073789 | |||||||
| chr1:119073817 | T | C | 1 | a0001c0001t0001g0101 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.348+2533A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119073817 | |||||||
| chr1:119073885 | T | C | 1 | a0001c0001t0004g0027 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.348+2465A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119073885 | |||||||
| chr1:119074183 | T | C | 1 | a0001c0001t0004g0170 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.348+2167A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119074183 | |||||||
| chr1:119074250 | G | C | 1 | a0001c0001t0006g0235 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.348+2100C>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119074250 | |||||||
| chr1:119074315 | G | A | 2 | a0001c0001t0003g0237 a0001c0001t0003g0238 |
2 | HG02080.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.348+2035C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119074315 | |||||||
| chr1:119074321 | C | T | 17 | a0001c0003t0007g0217 a0001c0003t0007g0218 a0001c0003t0007g0219 others(14): Show |
17 | HG00741.hp2 HG01099.hp2 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.348+2029G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119074321 | |||||||
| chr1:119074504 | C | T | 16 | a0001c0001t0005g0118 a0001c0001t0005g0142 a0001c0001t0005g0143 others(13): Show |
16 | HG00621.hp1 HG01074.hp1 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.348+1846G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119074504 | |||||||
| chr1:119074684 | C | T | 1 | a0001c0001t0005g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.348+1666G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119074684 | |||||||
| chr1:119074826 | C | A | 1 | a0001c0001t0006g0311 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.348+1524G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119074826 | |||||||
| chr1:119075154 | G | GTATATAT others(5): Show |
3 | a0001c0001t0005g0262 a0001c0001t0005g0263 a0001c0001t0005g0265 |
3 | NA18962.hp1 NA19005.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.348+1195_348+1196i others(14): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119075154 | |||||||
| chr1:119075154 | G | GTATATAT others(7): Show |
36 | a0001c0001t0001g0130 a0002c0002t0002g0001 a0002c0002t0002g0005 others(33): Show |
41 | HG00423.hp2 HG01175.hp1 HG01257.hp2 others(38): Show |
intron_variant | MODIFIER | c.348+1195_348+1196i others(16): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119075154 | |||||||
| chr1:119075154 | G | GTATATAT others(9): Show |
17 | a0001c0001t0005g0264 a0002c0002t0002g0006 a0002c0002t0002g0009 others(14): Show |
19 | HG00408.hp1 HG02055.hp2 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.348+1195_348+1196i others(18): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119075154 | |||||||
| chr1:119075154 | G | GTATATAT others(11): Show |
2 | a0002c0002t0002g0132 a0002c0002t0002g0188 |
2 | HG02040.hp1 NA18940.hp2 |
intron_variant | MODIFIER | c.348+1195_348+1196i others(20): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119075154 | |||||||
| chr1:119075165 | C | T | 58 | a0001c0001t0001g0130 a0001c0001t0005g0262 a0001c0001t0005g0263 others(55): Show |
65 | HG00408.hp1 HG00423.hp2 HG01175.hp1 others(62): Show |
intron_variant | MODIFIER | c.348+1185G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119075165 | |||||||
| chr1:119075215 | C | T | 1 | a0001c0001t0001g0100 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.348+1135G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119075215 | |||||||
| chr1:119075733 | G | T | 1 | a0001c0007t0004g0017 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.348+617C>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119075733 | |||||||
| chr1:119075895 | TAA | T | 83 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(80): Show |
86 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.348+453_348+454del others(2): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119075895 | |||||||
| chr1:119075981 | G | T | 3 | a0001c0001t0004g0020 a0001c0001t0004g0021 a0001c0001t0004g0022 |
3 | HG01433.hp2 HG02257.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.348+369C>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119075981 | |||||||
| chr1:119076057 | T | G | 46 | a0001c0001t0001g0130 a0002c0002t0002g0001 a0002c0002t0002g0005 others(43): Show |
53 | HG00423.hp2 HG01175.hp1 HG01257.hp2 others(50): Show |
intron_variant | MODIFIER | c.348+293A>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119076057 | |||||||
| chr1:119076069 | T | A | 1 | a0001c0001t0001g0045 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.348+281A>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119076069 | |||||||
| chr1:119076296 | T | C | 1 | a0001c0001t0005g0145 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.348+54A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119076296 | |||||||
| chr1:119076307 | T | C | 2 | a0001c0001t0006g0315 a0001c0001t0006g0331 |
2 | HG01891.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.348+43A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119076307 | |||||||
| chr1:119076731 | A | G | 2 | a0001c0001t0006g0284 a0001c0001t0006g0317 |
2 | HG03098.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.91-124T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119076731 | |||||||
| chr1:119076798 | T | C | 2 | a0001c0001t0004g0170 a0001c0001t0008g0335 |
2 | HG02615.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.91-191A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119076798 | |||||||
| chr1:119076825 | G | T | 162 | a0001c0001t0001g0130 a0001c0001t0001g0310 a0001c0001t0001g0320 others(159): Show |
174 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(171): Show |
intron_variant | MODIFIER | c.91-218C>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119076825 | |||||||
| chr1:119076888 | C | T | 28 | a0001c0001t0007g0080 a0001c0001t0007g0200 a0001c0001t0007g0202 others(25): Show |
28 | HG00099.hp1 HG00544.hp1 HG00558.hp2 others(25): Show |
intron_variant | MODIFIER | c.91-281G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119076888 | |||||||
| chr1:119076889 | C | T | 5 | a0001c0001t0004g0012 a0001c0001t0004g0286 a0001c0001t0004g0293 others(2): Show |
6 | HG01891.hp1 HG02109.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.91-282G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119076889 | |||||||
| chr1:119076890 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.91-283C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119076890 | |||||||
| chr1:119077020 | G | C | 289 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(286): Show |
305 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(302): Show |
intron_variant | MODIFIER | c.91-413C>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119077020 | |||||||
| chr1:119077031 | C | A | 54 | a0001c0001t0001g0130 a0002c0002t0002g0001 a0002c0002t0002g0005 others(51): Show |
61 | HG00423.hp2 HG01175.hp1 HG01257.hp2 others(58): Show |
intron_variant | MODIFIER | c.91-424G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119077031 | |||||||
| chr1:119077051 | T | C | 6 | a0001c0001t0003g0300 a0001c0001t0004g0299 a0001c0001t0010g0291 others(3): Show |
6 | HG02818.hp2 HG03098.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.91-444A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119077051 | |||||||
| chr1:119077137 | C | CAAAAAAA others(4): Show |
60 | a0001c0001t0001g0077 a0001c0001t0001g0089 a0001c0001t0001g0130 others(57): Show |
67 | HG00408.hp1 HG00423.hp2 HG01167.hp1 others(64): Show |
intron_variant | MODIFIER | c.91-541_91-531dupTT others(9): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119077137 | |||||||
| chr1:119077137 | C | CAAAAAAA others(5): Show |
113 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(110): Show |
116 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.91-531_91-530insTT others(10): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119077137 | |||||||
| chr1:119077137 | C | CAAAAAAA others(6): Show |
93 | a0001c0001t0001g0050 a0001c0001t0001g0058 a0001c0001t0001g0101 others(90): Show |
98 | HG00438.hp1 HG00558.hp1 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.91-531_91-530insTT others(11): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119077137 | |||||||
| chr1:119077137 | C | CAAAAAAA others(7): Show |
7 | a0001c0001t0004g0039 a0001c0001t0004g0177 a0001c0001t0004g0322 others(4): Show |
7 | HG01168.hp2 HG01169.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.91-531_91-530insTT others(12): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119077137 | |||||||
| chr1:119077157 | T | C | 1 | a0001c0001t0003g0035 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.91-550A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119077157 | |||||||
| chr1:119077207 | A | G | 14 | a0001c0001t0004g0025 a0001c0001t0004g0026 a0001c0001t0004g0027 others(11): Show |
14 | HG00558.hp1 HG00609.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.91-600T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119077207 | |||||||
| chr1:119077326 | C | T | 1 | a0001c0001t0008g0335 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.91-719G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119077326 | |||||||
| chr1:119077584 | C | T | 54 | a0001c0001t0001g0130 a0002c0002t0002g0001 a0002c0002t0002g0005 others(51): Show |
61 | HG00423.hp2 HG01175.hp1 HG01257.hp2 others(58): Show |
intron_variant | MODIFIER | c.91-977G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119077584 | |||||||
| chr1:119077593 | C | T | 1 | a0001c0001t0003g0273 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.91-986G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119077593 | |||||||
| chr1:119077630 | T | A | 2 | a0002c0002t0002g0194 a0002c0002t0002g0197 |
2 | NA18963.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.91-1023A>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119077630 | |||||||
| chr1:119077658 | T | C | 1 | a0001c0001t0004g0334 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.91-1051A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119077658 | |||||||
| chr1:119077734 | C | T | 289 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(286): Show |
305 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(302): Show |
intron_variant | MODIFIER | c.91-1127G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119077734 | |||||||
| chr1:119078183 | C | T | 6 | a0001c0001t0005g0151 a0001c0001t0005g0152 a0001c0001t0005g0167 others(3): Show |
6 | HG02055.hp1 HG02109.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.91-1576G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119078183 | |||||||
| chr1:119078213 | A | G | 1 | a0001c0001t0008g0279 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.91-1606T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119078213 | |||||||
| chr1:119078591 | A | G | 1 | a0001c0001t0001g0117 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.91-1984T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119078591 | |||||||
| chr1:119078718 | C | T | 54 | a0001c0001t0001g0130 a0002c0002t0002g0001 a0002c0002t0002g0005 others(51): Show |
61 | HG00423.hp2 HG01175.hp1 HG01257.hp2 others(58): Show |
intron_variant | MODIFIER | c.91-2111G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119078718 | |||||||
| chr1:119078887 | T | C | 28 | a0001c0001t0007g0080 a0001c0001t0007g0200 a0001c0001t0007g0202 others(25): Show |
28 | HG00099.hp1 HG00544.hp1 HG00558.hp2 others(25): Show |
intron_variant | MODIFIER | c.91-2280A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119078887 | |||||||
| chr1:119078897 | C | CGT | 35 | a0001c0001t0001g0310 a0001c0001t0001g0320 a0001c0001t0001g0321 others(32): Show |
37 | HG00438.hp1 HG00738.hp2 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.91-2292_91-2291dup others(2): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119078897 | |||||||
| chr1:119078947 | GAC | G | 159 | a0001c0001t0001g0130 a0001c0001t0001g0310 a0001c0001t0001g0320 others(156): Show |
171 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(168): Show |
intron_variant | MODIFIER | c.91-2342_91-2341del others(2): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119078947 | |||||||
| chr1:119079058 | A | G | 4 | a0001c0001t0004g0020 a0001c0001t0004g0021 a0001c0001t0004g0022 others(1): Show |
4 | HG01433.hp2 HG02257.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.91-2451T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119079058 | |||||||
| chr1:119079169 | G | A | 54 | a0001c0001t0001g0130 a0002c0002t0002g0001 a0002c0002t0002g0005 others(51): Show |
61 | HG00423.hp2 HG01175.hp1 HG01257.hp2 others(58): Show |
intron_variant | MODIFIER | c.91-2562C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119079169 | |||||||
| chr1:119079271 | T | C | 55 | a0001c0001t0001g0310 a0001c0001t0001g0320 a0001c0001t0001g0321 others(52): Show |
59 | HG00438.hp1 HG00738.hp2 HG01070.hp1 others(56): Show |
intron_variant | MODIFIER | c.91-2664A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119079271 | |||||||
| chr1:119079426 | T | C | 1 | a0001c0001t0004g0293 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.91-2819A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119079426 | |||||||
| chr1:119079861 | T | C | 3 | a0002c0002t0002g0138 a0002c0002t0011g0137 a0002c0002t0011g0139 |
3 | HG02280.hp2 HG02622.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.91-3254A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119079861 | |||||||
| chr1:119080198 | G | A | 1 | a0001c0001t0001g0087 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.91-3591C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119080198 | |||||||
| chr1:119080335 | G | A | 1 | a0001c0001t0005g0163 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.91-3728C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119080335 | |||||||
| chr1:119081054 | C | G | 1 | a0001c0001t0005g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.91-4447G>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119081054 | |||||||
| chr1:119081178 | C | T | 1 | a0001c0001t0003g0231 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.91-4571G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119081178 | |||||||
| chr1:119081275 | G | A | 3 | a0001c0001t0004g0020 a0001c0001t0004g0021 a0001c0001t0004g0022 |
3 | HG01433.hp2 HG02257.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.91-4668C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119081275 | |||||||
| chr1:119081298 | A | G | 54 | a0001c0001t0001g0130 a0002c0002t0002g0001 a0002c0002t0002g0005 others(51): Show |
61 | HG00423.hp2 HG01175.hp1 HG01257.hp2 others(58): Show |
intron_variant | MODIFIER | c.91-4691T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119081298 | |||||||
| chr1:119081325 | A | G | 1 | a0002c0002t0002g0115 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.91-4718T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119081325 | |||||||
| chr1:119081540 | T | C | 104 | a0001c0001t0001g0310 a0001c0001t0001g0320 a0001c0001t0001g0321 others(101): Show |
109 | HG00438.hp1 HG00558.hp1 HG00609.hp1 others(106): Show |
intron_variant | MODIFIER | c.91-4933A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119081540 | |||||||
| chr1:119081804 | G | A | 1 | a0001c0001t0003g0261 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.91-5197C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119081804 | |||||||
| chr1:119082017 | T | G | 1 | a0001c0001t0004g0012 | 2 | HG02109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.91-5410A>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119082017 | |||||||
| chr1:119082028 | A | G | 5 | a0001c0001t0003g0011 a0001c0001t0003g0239 a0001c0001t0003g0240 others(2): Show |
6 | HG02145.hp1 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.91-5421T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119082028 | |||||||
| chr1:119082055 | A | G | 14 | a0001c0001t0004g0025 a0001c0001t0004g0026 a0001c0001t0004g0027 others(11): Show |
14 | HG00558.hp1 HG00609.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.91-5448T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119082055 | |||||||
| chr1:119082210 | T | C | 1 | a0001c0001t0001g0062 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.91-5603A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119082210 | |||||||
| chr1:119082326 | C | T | 1 | a0001c0001t0008g0278 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.91-5719G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119082326 | |||||||
| chr1:119082344 | C | T | 10 | a0001c0001t0008g0275 a0001c0001t0008g0276 a0001c0001t0008g0277 others(7): Show |
10 | HG02145.hp2 HG02572.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.91-5737G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119082344 | |||||||
| chr1:119082366 | T | G | 1 | a0001c0001t0003g0237 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.91-5759A>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119082366 | |||||||
| chr1:119082373 | C | G | 159 | a0001c0001t0001g0130 a0001c0001t0001g0310 a0001c0001t0001g0320 others(156): Show |
171 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(168): Show |
intron_variant | MODIFIER | c.91-5766G>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119082373 | |||||||
| chr1:119082561 | TG | T | 11 | a0001c0001t0004g0025 a0001c0001t0004g0026 a0001c0001t0004g0027 others(8): Show |
11 | HG00558.hp1 HG00609.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.91-5955delC | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119082561 | |||||||
| chr1:119082940 | G | A | 2 | a0001c0001t0001g0004 a0001c0001t0001g0102 |
3 | NA18939.hp1 NA18955.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.91-6333C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119082940 | |||||||
| chr1:119082971 | G | A | 1 | a0001c0001t0003g0081 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.91-6364C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119082971 | |||||||
| chr1:119083018 | CA | C | 4 | a0001c0001t0004g0012 a0001c0001t0004g0286 a0001c0001t0004g0293 others(1): Show |
5 | HG01891.hp1 HG02109.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.91-6412delT | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119083018 | |||||||
| chr1:119083058 | G | T | 8 | a0002c0002t0002g0120 a0002c0002t0002g0131 a0002c0002t0002g0132 others(5): Show |
8 | NA18939.hp2 NA18940.hp2 NA18968.hp1 others(5): Show |
intron_variant | MODIFIER | c.91-6451C>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119083058 | |||||||
| chr1:119083119 | C | T | 17 | a0001c0003t0007g0217 a0001c0003t0007g0218 a0001c0003t0007g0219 others(14): Show |
17 | HG00741.hp2 HG01099.hp2 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.91-6512G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119083119 | |||||||
| chr1:119083154 | G | A | 2 | a0002c0002t0002g0140 a0002c0002t0002g0141 |
2 | NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.91-6547C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119083154 | |||||||
| chr1:119083186 | G | A | 3 | a0001c0001t0003g0010 a0001c0001t0003g0228 a0001c0001t0003g0229 |
4 | NA19001.hp1 NA19004.hp1 NA19083.hp1 others(1): Show |
intron_variant | MODIFIER | c.91-6579C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119083186 | |||||||
| chr1:119083268 | T | A | 3 | a0001c0001t0003g0267 a0001c0001t0003g0268 a0001c0001t0003g0270 |
3 | HG01361.hp2 HG01515.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.91-6661A>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119083268 | |||||||
| chr1:119083273 | ACT | A | 5 | a0001c0001t0004g0012 a0001c0001t0004g0286 a0001c0001t0004g0293 others(2): Show |
6 | HG01891.hp1 HG02109.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.91-6668_91-6667del others(2): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119083273 | |||||||
| chr1:119083884 | C | T | 4 | a0001c0001t0005g0262 a0001c0001t0005g0263 a0001c0001t0005g0264 others(1): Show |
4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.91-7277G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119083884 | |||||||
| chr1:119084349 | TAGAC | T | 11 | a0001c0001t0004g0025 a0001c0001t0004g0026 a0001c0001t0004g0027 others(8): Show |
11 | HG00558.hp1 HG00609.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.91-7746_91-7743del others(4): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119084349 | |||||||
| chr1:119084359 | C | T | 1 | a0001c0003t0007g0217 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.91-7752G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119084359 | |||||||
| chr1:119084437 | A | G | 4 | a0001c0001t0005g0262 a0001c0001t0005g0263 a0001c0001t0005g0264 others(1): Show |
4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.91-7830T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119084437 | |||||||
| chr1:119084502 | C | A | 5 | a0001c0001t0004g0012 a0001c0001t0004g0286 a0001c0001t0004g0293 others(2): Show |
6 | HG01891.hp1 HG02109.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.91-7895G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119084502 | |||||||
| chr1:119084525 | T | G | 54 | a0001c0001t0001g0130 a0002c0002t0002g0001 a0002c0002t0002g0005 others(51): Show |
61 | HG00423.hp2 HG01175.hp1 HG01257.hp2 others(58): Show |
intron_variant | MODIFIER | c.91-7918A>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119084525 | |||||||
| chr1:119084604 | C | T | 46 | a0001c0001t0001g0310 a0001c0001t0001g0320 a0001c0001t0001g0321 others(43): Show |
50 | HG00438.hp1 HG00738.hp2 HG01070.hp1 others(47): Show |
intron_variant | MODIFIER | c.91-7997G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119084604 | |||||||
| chr1:119084747 | G | A | 1 | a0001c0001t0003g0267 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.91-8140C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119084747 | |||||||
| chr1:119084811 | T | C | 1 | a0002c0002t0002g0201 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.91-8204A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119084811 | |||||||
| chr1:119085056 | C | T | 15 | a0001c0003t0007g0217 a0001c0003t0007g0218 a0001c0003t0007g0219 others(12): Show |
15 | HG00741.hp2 HG01099.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.91-8449G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119085056 | |||||||
| chr1:119085233 | C | T | 159 | a0001c0001t0001g0130 a0001c0001t0001g0310 a0001c0001t0001g0320 others(156): Show |
171 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(168): Show |
intron_variant | MODIFIER | c.91-8626G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119085233 | |||||||
| chr1:119085331 | T | C | 54 | a0001c0001t0001g0130 a0002c0002t0002g0001 a0002c0002t0002g0005 others(51): Show |
61 | HG00423.hp2 HG01175.hp1 HG01257.hp2 others(58): Show |
intron_variant | MODIFIER | c.91-8724A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119085331 | |||||||
| chr1:119085375 | C | A | 4 | a0001c0001t0004g0015 a0001c0001t0004g0314 a0001c0001t0004g0329 others(1): Show |
5 | HG03490.hp1 HG03492.hp1 HG04115.hp2 others(2): Show |
intron_variant | MODIFIER | c.91-8768G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119085375 | |||||||
| chr1:119085473 | C | CT | 97 | a0001c0001t0001g0310 a0001c0001t0001g0320 a0001c0001t0001g0321 others(94): Show |
102 | HG00438.hp1 HG00558.hp1 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.91-8867dupA | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119085473 | |||||||
| chr1:119085751 | C | A | 1 | a0001c0001t0005g0263 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.91-9144G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119085751 | |||||||
| chr1:119085833 | C | T | 1 | a0002c0002t0002g0201 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.91-9226G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119085833 | |||||||
| chr1:119085849 | C | T | 6 | a0001c0001t0003g0300 a0001c0001t0004g0299 a0001c0001t0010g0291 others(3): Show |
6 | HG02818.hp2 HG03098.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.91-9242G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119085849 | |||||||
| chr1:119085887 | G | C | 6 | a0001c0001t0003g0300 a0001c0001t0004g0299 a0001c0001t0010g0291 others(3): Show |
6 | HG02818.hp2 HG03098.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.91-9280C>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119085887 | |||||||
| chr1:119085917 | A | G | 2 | a0001c0001t0006g0315 a0001c0001t0006g0331 |
2 | HG01891.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.91-9310T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119085917 | |||||||
| chr1:119085979 | C | A | 1 | a0001c0001t0008g0276 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.91-9372G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119085979 | |||||||
| chr1:119086064 | T | G | 6 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(3): Show |
6 | HG01261.hp1 HG01934.hp2 NA18967.hp2 others(3): Show |
intron_variant | MODIFIER | c.91-9457A>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119086064 | |||||||
| chr1:119086100 | T | A | 1 | a0001c0001t0001g0088 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.91-9493A>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119086100 | |||||||
| chr1:119086187 | T | G | 1 | a0001c0001t0006g0328 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.91-9580A>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119086187 | |||||||
| chr1:119086255 | C | T | 5 | a0001c0001t0003g0230 a0001c0001t0003g0231 a0001c0001t0003g0232 others(2): Show |
5 | HG00735.hp2 HG00741.hp1 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.91-9648G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119086255 | |||||||
| chr1:119086414 | C | G | 3 | a0001c0001t0004g0020 a0001c0001t0004g0021 a0001c0001t0004g0022 |
3 | HG01433.hp2 HG02257.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.91-9807G>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119086414 | |||||||
| chr1:119086849 | G | A | 1 | a0001c0001t0008g0276 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.91-10242C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119086849 | |||||||
| chr1:119086926 | T | C | 4 | a0001c0001t0005g0262 a0001c0001t0005g0263 a0001c0001t0005g0264 others(1): Show |
4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.91-10319A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119086926 | |||||||
| chr1:119086948 | G | C | 1 | a0001c0001t0004g0293 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.91-10341C>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119086948 | |||||||
| chr1:119087081 | T | C | 272 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(269): Show |
287 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(284): Show |
intron_variant | MODIFIER | c.91-10474A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119087081 | |||||||
| chr1:119087160 | T | C | 1 | a0001c0001t0006g0128 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.91-10553A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119087160 | |||||||
| chr1:119087198 | G | A | 44 | a0001c0001t0001g0130 a0001c0001t0006g0121 a0001c0001t0006g0126 others(41): Show |
50 | HG00423.hp2 HG01257.hp2 HG01258.hp1 others(47): Show |
intron_variant | MODIFIER | c.91-10591C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119087198 | |||||||
| chr1:119087210 | A | C | 4 | a0001c0001t0005g0262 a0001c0001t0005g0263 a0001c0001t0005g0264 others(1): Show |
4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.91-10603T>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119087210 | |||||||
| chr1:119087326 | C | T | 1 | a0001c0001t0006g0316 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.91-10719G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119087326 | |||||||
| chr1:119087374 | T | G | 5 | a0001c0001t0004g0012 a0001c0001t0004g0286 a0001c0001t0004g0293 others(2): Show |
6 | HG01891.hp1 HG02109.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.91-10767A>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119087374 | |||||||
| chr1:119087924 | A | T | 1 | a0001c0001t0006g0307 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.91-11317T>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119087924 | |||||||
| chr1:119088273 | C | T | 3 | a0001c0001t0003g0016 a0001c0001t0003g0323 a0005c0009t0003g0324 |
4 | NA18612.hp1 NA18968.hp2 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.91-11666G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119088273 | |||||||
| chr1:119088435 | A | AAC | 75 | a0001c0001t0001g0004 a0001c0001t0001g0031 a0001c0001t0001g0034 others(72): Show |
80 | HG00423.hp2 HG00544.hp2 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.91-11830_91-11829d others(4): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119088435 | |||||||
| chr1:119088435 | A | AACAC | 14 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0058 others(11): Show |
15 | HG00423.hp1 HG00642.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.91-11832_91-11829d others(6): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119088435 | |||||||
| chr1:119088435 | A | AACACAC | 48 | a0001c0001t0001g0002 a0001c0001t0001g0032 a0001c0001t0001g0033 others(45): Show |
49 | HG00558.hp2 HG00621.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.91-11834_91-11829d others(8): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119088435 | |||||||
| chr1:119088435 | A | AACACACA others(1): Show |
13 | a0001c0001t0001g0047 a0001c0001t0001g0055 a0001c0001t0001g0094 others(10): Show |
14 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(11): Show |
intron_variant | MODIFIER | c.91-11836_91-11829d others(10): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119088435 | |||||||
| chr1:119088435 | A | AACACACA others(3): Show |
19 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0038 others(16): Show |
19 | HG00558.hp1 HG00609.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.91-11838_91-11829d others(12): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119088435 | |||||||
| chr1:119088435 | A | AACACACA others(5): Show |
5 | a0001c0001t0004g0025 a0002c0002t0002g0001 a0002c0002t0002g0122 others(2): Show |
7 | HG01257.hp2 HG01258.hp1 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.91-11840_91-11829d others(14): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119088435 | |||||||
| chr1:119088435 | A | AACACACA others(7): Show |
14 | a0001c0001t0001g0130 a0001c0001t0006g0121 a0001c0001t0006g0128 others(11): Show |
15 | HG02056.hp2 HG02129.hp1 NA18949.hp1 others(12): Show |
intron_variant | MODIFIER | c.91-11842_91-11829d others(16): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119088435 | |||||||
| chr1:119088435 | A | AACACACA others(9): Show |
3 | a0001c0001t0006g0127 a0002c0002t0002g0132 a0002c0002t0002g0199 |
3 | HG02027.hp2 NA18940.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.91-11844_91-11829d others(18): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119088435 | |||||||
| chr1:119088435 | A | AACACACA others(11): Show |
3 | a0002c0002t0002g0133 a0002c0002t0002g0134 a0002c0002t0002g0158 |
3 | NA18968.hp1 NA18988.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.91-11846_91-11829d others(20): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119088435 | |||||||
| chr1:119088435 | A | AACACACA others(13): Show |
4 | a0002c0002t0002g0120 a0002c0002t0002g0131 a0002c0002t0002g0135 others(1): Show |
4 | NA18939.hp2 NA18978.hp1 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.91-11848_91-11829d others(22): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119088435 | |||||||
| chr1:119088435 | A | ACACACAC others(4): Show |
1 | a0001c0001t0004g0175 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.91-11829_91-11828i others(13): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119088435 | |||||||
| chr1:119088435 | A | ACACACAC others(8): Show |
1 | a0001c0001t0006g0126 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.91-11829_91-11828i others(17): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119088435 | |||||||
| chr1:119088435 | AAC | A | 17 | a0001c0001t0003g0231 a0001c0001t0003g0234 a0001c0003t0007g0217 others(14): Show |
17 | HG00735.hp2 HG00741.hp2 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.91-11830_91-11829d others(4): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119088435 | |||||||
| chr1:119088435 | AACACACA others(5): Show |
A | 49 | a0001c0001t0001g0310 a0001c0001t0001g0320 a0001c0001t0001g0321 others(46): Show |
53 | HG00438.hp1 HG00738.hp2 HG01070.hp1 others(50): Show |
intron_variant | MODIFIER | c.91-11840_91-11829d others(14): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119088435 | |||||||
| chr1:119088468 | A | ACACACAC others(10): Show |
1 | a0002c0002t0002g0129 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.91-11862_91-11861i others(19): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119088468 | |||||||
| chr1:119088551 | T | C | 94 | a0001c0001t0001g0310 a0001c0001t0001g0320 a0001c0001t0001g0321 others(91): Show |
99 | HG00438.hp1 HG00558.hp1 HG00609.hp1 others(96): Show |
intron_variant | MODIFIER | c.91-11944A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119088551 | |||||||
| chr1:119088652 | T | C | 2 | a0001c0003t0007g0226 a0001c0003t0007g0227 |
2 | HG03490.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.91-12045A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119088652 | |||||||
| chr1:119088679 | G | T | 10 | a0001c0001t0008g0275 a0001c0001t0008g0276 a0001c0001t0008g0277 others(7): Show |
10 | HG02145.hp2 HG02572.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.91-12072C>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119088679 | |||||||
| chr1:119089175 | C | T | 4 | a0001c0001t0005g0262 a0001c0001t0005g0263 a0001c0001t0005g0264 others(1): Show |
4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.91-12568G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119089175 | |||||||
| chr1:119089465 | C | T | 4 | a0001c0001t0006g0121 a0001c0001t0006g0126 a0001c0001t0006g0127 others(1): Show |
4 | HG02056.hp2 HG02071.hp2 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.91-12858G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119089465 | |||||||
| chr1:119089541 | A | T | 1 | a0001c0003t0007g0217 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.91-12934T>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119089541 | |||||||
| chr1:119089561 | C | T | 1 | a0001c0001t0004g0336 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.91-12954G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119089561 | |||||||
| chr1:119089761 | C | T | 3 | a0001c0001t0003g0079 a0001c0001t0003g0107 a0001c0001t0007g0080 |
3 | HG00099.hp1 HG01123.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.91-13154G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119089761 | |||||||
| chr1:119089876 | C | A | 1 | a0001c0001t0004g0170 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.91-13269G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119089876 | |||||||
| chr1:119089911 | T | C | 5 | a0001c0001t0003g0011 a0001c0001t0003g0239 a0001c0001t0003g0240 others(2): Show |
6 | HG02145.hp1 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.91-13304A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119089911 | |||||||
| chr1:119089935 | T | G | 1 | a0002c0002t0002g0029 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.91-13328A>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119089935 | |||||||
| chr1:119090064 | T | C | 2 | a0001c0001t0007g0203 a0001c0001t0007g0207 |
2 | HG01361.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.91-13457A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119090064 | |||||||
| chr1:119090129 | G | GA | 8 | a0001c0001t0001g0111 a0001c0001t0006g0013 a0001c0001t0006g0305 others(5): Show |
9 | HG00738.hp2 HG01070.hp1 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.91-13523dupT | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119090129 | |||||||
| chr1:119090129 | GA | G | 18 | a0001c0001t0005g0209 a0001c0003t0007g0217 a0001c0003t0007g0218 others(15): Show |
18 | HG00741.hp2 HG01099.hp2 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.91-13523delT | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119090129 | |||||||
| chr1:119090192 | T | C | 59 | a0001c0001t0001g0130 a0001c0001t0004g0170 a0001c0001t0006g0121 others(56): Show |
66 | HG00423.hp2 HG01175.hp1 HG01257.hp2 others(63): Show |
intron_variant | MODIFIER | c.91-13585A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119090192 | |||||||
| chr1:119090232 | C | T | 4 | a0001c0001t0003g0011 a0001c0001t0003g0239 a0001c0001t0003g0240 others(1): Show |
5 | HG02145.hp1 HG02257.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.91-13625G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119090232 | |||||||
| chr1:119090344 | T | G | 4 | a0001c0001t0005g0151 a0001c0001t0005g0152 a0001c0001t0005g0168 others(1): Show |
4 | HG02055.hp1 HG02109.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.91-13737A>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119090344 | |||||||
| chr1:119090360 | C | T | 1 | a0001c0001t0004g0039 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.91-13753G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119090360 | |||||||
| chr1:119090919 | C | T | 1 | a0001c0001t0001g0092 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.91-14312G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119090919 | |||||||
| chr1:119090924 | T | C | 100 | a0001c0001t0001g0310 a0001c0001t0001g0320 a0001c0001t0001g0321 others(97): Show |
105 | HG00438.hp1 HG00558.hp1 HG00609.hp1 others(102): Show |
intron_variant | MODIFIER | c.91-14317A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119090924 | |||||||
| chr1:119091088 | A | G | 1 | a0002c0002t0011g0137 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.91-14481T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119091088 | |||||||
| chr1:119091356 | G | T | 1 | a0001c0001t0016g0213 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.91-14749C>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119091356 | |||||||
| chr1:119091451 | T | C | 1 | a0002c0002t0002g0008 | 2 | HG02155.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.91-14844A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119091451 | |||||||
| chr1:119091588 | C | G | 4 | a0003c0004t0005g0210 a0003c0004t0005g0211 a0003c0004t0005g0212 others(1): Show |
4 | HG02647.hp1 HG02723.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.91-14981G>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119091588 | |||||||
| chr1:119091601 | C | T | 16 | a0001c0001t0005g0118 a0001c0001t0005g0142 a0001c0001t0005g0143 others(13): Show |
16 | HG00621.hp1 HG01074.hp1 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.91-14994G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119091601 | |||||||
| chr1:119091738 | G | A | 5 | a0001c0003t0009g0024 a0001c0003t0009g0222 a0001c0003t0009g0223 others(2): Show |
5 | HG02258.hp2 HG02572.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.91-15131C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119091738 | |||||||
| chr1:119091829 | C | T | 1 | a0001c0001t0007g0203 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.91-15222G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119091829 | |||||||
| chr1:119091889 | T | C | 2 | a0001c0003t0007g0226 a0001c0003t0007g0227 |
2 | HG03490.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.91-15282A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119091889 | |||||||
| chr1:119091951 | C | T | 1 | a0001c0001t0004g0314 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.91-15344G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119091951 | |||||||
| chr1:119092046 | G | C | 1 | a0001c0001t0001g0036 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.91-15439C>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119092046 | |||||||
| chr1:119092243 | G | A | 2 | a0001c0001t0001g0069 a0001c0001t0001g0070 |
2 | HG00642.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.91-15636C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119092243 | |||||||
| chr1:119092604 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.91-15997G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119092604 | |||||||
| chr1:119092655 | C | T | 1 | a0001c0001t0005g0167 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.91-16048G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119092655 | |||||||
| chr1:119093100 | T | C | 91 | a0001c0001t0001g0310 a0001c0001t0001g0320 a0001c0001t0001g0321 others(88): Show |
96 | HG00438.hp1 HG00558.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.91-16493A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119093100 | |||||||
| chr1:119093110 | A | T | 99 | a0001c0001t0001g0310 a0001c0001t0001g0320 a0001c0001t0001g0321 others(96): Show |
104 | HG00438.hp1 HG00558.hp1 HG00609.hp1 others(101): Show |
intron_variant | MODIFIER | c.91-16503T>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119093110 | |||||||
| chr1:119093184 | T | C | 1 | a0002c0002t0002g0136 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.91-16577A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119093184 | |||||||
| chr1:119093328 | T | C | 2 | a0001c0001t0001g0071 a0001c0001t0001g0103 |
2 | NA18948.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.91-16721A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119093328 | |||||||
| chr1:119093470 | A | G | 286 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(283): Show |
302 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(299): Show |
intron_variant | MODIFIER | c.91-16863T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119093470 | |||||||
| chr1:119093474 | A | ATACTAGA others(13): Show |
286 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(283): Show |
302 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(299): Show |
intron_variant | MODIFIER | c.91-16868_91-16867i others(22): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119093474 | |||||||
| chr1:119093918 | A | C | 161 | a0001c0001t0001g0130 a0001c0001t0001g0310 a0001c0001t0001g0320 others(158): Show |
173 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(170): Show |
intron_variant | MODIFIER | c.91-17311T>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119093918 | |||||||
| chr1:119093998 | T | C | 2 | a0001c0001t0003g0257 a0001c0001t0003g0258 |
2 | NA18942.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.91-17391A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119093998 | |||||||
| chr1:119094055 | A | G | 3 | a0001c0001t0003g0079 a0001c0001t0003g0107 a0001c0001t0007g0080 |
3 | HG00099.hp1 HG01123.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.91-17448T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119094055 | |||||||
| chr1:119094113 | G | A | 4 | a0001c0001t0005g0262 a0001c0001t0005g0263 a0001c0001t0005g0264 others(1): Show |
4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.91-17506C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119094113 | |||||||
| chr1:119094302 | T | G | 1 | a0001c0001t0001g0114 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.91-17695A>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119094302 | |||||||
| chr1:119094373 | CT | C | 6 | a0001c0001t0005g0151 a0001c0001t0005g0152 a0001c0001t0005g0167 others(3): Show |
6 | HG02055.hp1 HG02109.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.91-17767delA | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119094373 | |||||||
| chr1:119094511 | T | G | 59 | a0001c0001t0001g0130 a0001c0001t0004g0170 a0001c0001t0006g0121 others(56): Show |
66 | HG00423.hp2 HG01175.hp1 HG01257.hp2 others(63): Show |
intron_variant | MODIFIER | c.91-17904A>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119094511 | |||||||
| chr1:119094781 | G | C | 3 | a0001c0001t0004g0020 a0001c0001t0004g0021 a0001c0001t0004g0022 |
3 | HG01433.hp2 HG02257.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.91-18174C>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119094781 | |||||||
| chr1:119094863 | C | T | 1 | a0002c0002t0002g0182 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.91-18256G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119094863 | |||||||
| chr1:119095095 | G | A | 1 | a0002c0002t0002g0190 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.91-18488C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119095095 | |||||||
| chr1:119095268 | G | A | 59 | a0001c0001t0001g0130 a0001c0001t0004g0170 a0001c0001t0006g0121 others(56): Show |
66 | HG00423.hp2 HG01175.hp1 HG01257.hp2 others(63): Show |
intron_variant | MODIFIER | c.91-18661C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119095268 | |||||||
| chr1:119095461 | T | G | 1 | a0002c0002t0002g0132 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.91-18854A>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119095461 | |||||||
| chr1:119095484 | C | T | 91 | a0001c0001t0001g0310 a0001c0001t0001g0320 a0001c0001t0001g0321 others(88): Show |
96 | HG00438.hp1 HG00558.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.91-18877G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119095484 | |||||||
| chr1:119095577 | C | T | 23 | a0001c0001t0001g0310 a0001c0001t0001g0320 a0001c0001t0001g0321 others(20): Show |
25 | HG00438.hp1 HG00738.hp2 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.91-18970G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119095577 | |||||||
| chr1:119095763 | G | A | 17 | a0001c0003t0007g0217 a0001c0003t0007g0218 a0001c0003t0007g0219 others(14): Show |
17 | HG00741.hp2 HG01099.hp2 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.91-19156C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119095763 | |||||||
| chr1:119095930 | G | A | 87 | a0001c0001t0001g0310 a0001c0001t0001g0320 a0001c0001t0001g0321 others(84): Show |
92 | HG00438.hp1 HG00558.hp1 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.91-19323C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119095930 | |||||||
| chr1:119095941 | T | C | 1 | a0003c0004t0005g0304 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.91-19334A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119095941 | |||||||
| chr1:119095958 | AC | A | 95 | a0001c0001t0001g0310 a0001c0001t0001g0320 a0001c0001t0001g0321 others(92): Show |
100 | HG00438.hp1 HG00558.hp1 HG00609.hp1 others(97): Show |
intron_variant | MODIFIER | c.91-19352delG | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119095958 | |||||||
| chr1:119096232 | T | C | 91 | a0001c0001t0001g0310 a0001c0001t0001g0320 a0001c0001t0001g0321 others(88): Show |
96 | HG00438.hp1 HG00558.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.91-19625A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119096232 | |||||||
| chr1:119096402 | C | T | 1 | a0003c0004t0005g0212 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.91-19795G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119096402 | |||||||
| chr1:119096410 | T | C | 4 | a0001c0001t0004g0020 a0001c0001t0004g0021 a0001c0001t0004g0022 others(1): Show |
4 | HG01433.hp2 HG02257.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.91-19803A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119096410 | |||||||
| chr1:119096421 | C | T | 15 | a0001c0003t0007g0217 a0001c0003t0007g0218 a0001c0003t0007g0219 others(12): Show |
15 | HG00741.hp2 HG01099.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.91-19814G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119096421 | |||||||
| chr1:119096470 | T | A | 1 | a0003c0004t0005g0211 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.91-19863A>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119096470 | |||||||
| chr1:119096529 | T | C | 1 | a0001c0001t0001g0057 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.91-19922A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119096529 | |||||||
| chr1:119096699 | T | C | 1 | a0001c0003t0007g0220 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.91-20092A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119096699 | |||||||
| chr1:119096935 | C | T | 4 | a0003c0004t0005g0210 a0003c0004t0005g0211 a0003c0004t0005g0212 others(1): Show |
4 | HG02647.hp1 HG02723.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.91-20328G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119096935 | |||||||
| chr1:119097052 | T | C | 98 | a0001c0001t0001g0310 a0001c0001t0001g0320 a0001c0001t0001g0321 others(95): Show |
103 | HG00438.hp1 HG00558.hp1 HG00609.hp1 others(100): Show |
intron_variant | MODIFIER | c.91-20445A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119097052 | |||||||
| chr1:119097068 | G | T | 4 | a0003c0004t0005g0210 a0003c0004t0005g0211 a0003c0004t0005g0212 others(1): Show |
4 | HG02647.hp1 HG02723.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.91-20461C>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119097068 | |||||||
| chr1:119097270 | C | T | 1 | a0001c0001t0001g0310 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.91-20663G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119097270 | |||||||
| chr1:119097376 | G | T | 1 | a0002c0002t0002g0133 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.91-20769C>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119097376 | |||||||
| chr1:119097496 | G | A | 3 | a0001c0001t0004g0020 a0001c0001t0004g0021 a0001c0001t0004g0022 |
3 | HG01433.hp2 HG02257.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.91-20889C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119097496 | |||||||
| chr1:119097551 | C | A | 2 | a0001c0001t0001g0051 a0001c0001t0001g0116 |
2 | HG01261.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.91-20944G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119097551 | |||||||
| chr1:119097716 | G | A | 59 | a0001c0001t0001g0130 a0001c0001t0004g0170 a0001c0001t0006g0121 others(56): Show |
66 | HG00423.hp2 HG01175.hp1 HG01257.hp2 others(63): Show |
intron_variant | MODIFIER | c.91-21109C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119097716 | |||||||
| chr1:119097773 | C | T | 1 | a0001c0001t0003g0300 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.91-21166G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119097773 | |||||||
| chr1:119097778 | C | G | 161 | a0001c0001t0001g0130 a0001c0001t0001g0310 a0001c0001t0001g0320 others(158): Show |
173 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(170): Show |
intron_variant | MODIFIER | c.91-21171G>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119097778 | |||||||
| chr1:119098105 | C | T | 87 | a0001c0001t0001g0310 a0001c0001t0001g0320 a0001c0001t0001g0321 others(84): Show |
92 | HG00438.hp1 HG00558.hp1 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.91-21498G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119098105 | |||||||
| chr1:119098202 | T | A | 10 | a0001c0001t0008g0275 a0001c0001t0008g0276 a0001c0001t0008g0277 others(7): Show |
10 | HG02145.hp2 HG02572.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.91-21595A>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119098202 | |||||||
| chr1:119098204 | G | A | 2 | a0001c0001t0004g0020 a0001c0001t0004g0021 |
2 | HG01433.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.91-21597C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119098204 | |||||||
| chr1:119098227 | C | G | 1 | a0002c0002t0002g0201 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.91-21620G>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119098227 | |||||||
| chr1:119098362 | C | T | 4 | a0001c0001t0005g0262 a0001c0001t0005g0263 a0001c0001t0005g0264 others(1): Show |
4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.91-21755G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119098362 | |||||||
| chr1:119098488 | A | G | 1 | a0002c0002t0002g0192 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.91-21881T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119098488 | |||||||
| chr1:119098576 | T | C | 7 | a0002c0002t0002g0120 a0002c0002t0002g0131 a0002c0002t0002g0132 others(4): Show |
7 | NA18939.hp2 NA18940.hp2 NA18978.hp1 others(4): Show |
intron_variant | MODIFIER | c.91-21969A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119098576 | |||||||
| chr1:119098582 | C | T | 1 | a0001c0001t0007g0023 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.91-21975G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119098582 | |||||||
| chr1:119098862 | G | A | 1 | a0002c0002t0002g0188 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.91-22255C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119098862 | |||||||
| chr1:119098997 | A | G | 94 | a0001c0001t0001g0310 a0001c0001t0001g0320 a0001c0001t0001g0321 others(91): Show |
99 | HG00438.hp1 HG00558.hp1 HG00609.hp1 others(96): Show |
intron_variant | MODIFIER | c.91-22390T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119098997 | |||||||
| chr1:119099033 | G | A | 1 | a0001c0001t0007g0023 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.91-22426C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119099033 | |||||||
| chr1:119099208 | C | T | 4 | a0001c0001t0005g0262 a0001c0001t0005g0263 a0001c0001t0005g0264 others(1): Show |
4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.91-22601G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119099208 | |||||||
| chr1:119099399 | T | C | 25 | a0001c0001t0007g0200 a0001c0001t0007g0202 a0001c0001t0007g0203 others(22): Show |
25 | HG00544.hp1 HG00558.hp2 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.91-22792A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119099399 | |||||||
| chr1:119099567 | C | T | 8 | a0002c0002t0002g0138 a0002c0002t0002g0140 a0002c0002t0002g0141 others(5): Show |
8 | HG02055.hp2 HG02280.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.91-22960G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119099567 | |||||||
| chr1:119099673 | T | C | 49 | a0001c0001t0001g0310 a0001c0001t0001g0320 a0001c0001t0001g0321 others(46): Show |
53 | HG00438.hp1 HG00738.hp2 HG01070.hp1 others(50): Show |
intron_variant | MODIFIER | c.91-23066A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119099673 | |||||||
| chr1:119099743 | G | A | 4 | a0001c0001t0005g0262 a0001c0001t0005g0263 a0001c0001t0005g0264 others(1): Show |
4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.91-23136C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119099743 | |||||||
| chr1:119099938 | A | G | 5 | a0001c0001t0004g0285 a0001c0001t0004g0289 a0001c0001t0004g0290 others(2): Show |
5 | HG02486.hp1 HG02717.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.91-23331T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119099938 | |||||||
| chr1:119100084 | A | C | 1 | a0001c0001t0001g0105 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.91-23477T>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119100084 | |||||||
| chr1:119100119 | CA | C | 15 | a0001c0003t0007g0217 a0001c0003t0007g0218 a0001c0003t0007g0219 others(12): Show |
15 | HG00741.hp2 HG01099.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.91-23513delT | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119100119 | |||||||
| chr1:119100158 | T | C | 9 | a0001c0001t0003g0249 a0001c0001t0003g0252 a0001c0001t0003g0254 others(6): Show |
9 | HG00438.hp2 HG02071.hp1 NA18941.hp2 others(6): Show |
intron_variant | MODIFIER | c.91-23551A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119100158 | |||||||
| chr1:119100162 | T | G | 2 | a0001c0001t0006g0315 a0001c0001t0006g0331 |
2 | HG01891.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.91-23555A>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119100162 | |||||||
| chr1:119100272 | CAGAAAAG others(2): Show |
C | 3 | a0001c0001t0004g0286 a0001c0001t0004g0293 a0001c0010t0004g0287 |
3 | HG01891.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.91-23674_91-23666d others(11): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119100272 | |||||||
| chr1:119100328 | A | G | 4 | a0001c0001t0005g0262 a0001c0001t0005g0263 a0001c0001t0005g0264 others(1): Show |
4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.91-23721T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119100328 | |||||||
| chr1:119100356 | T | C | 9 | a0001c0001t0004g0014 a0001c0001t0004g0015 a0001c0001t0004g0314 others(6): Show |
11 | HG01884.hp1 HG02258.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.91-23749A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119100356 | |||||||
| chr1:119100491 | G | C | 1 | a0001c0003t0007g0217 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.91-23884C>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119100491 | |||||||
| chr1:119100573 | A | T | 2 | a0001c0001t0006g0318 a0001c0001t0006g0319 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.91-23966T>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119100573 | |||||||
| chr1:119100730 | G | A | 4 | a0001c0001t0005g0262 a0001c0001t0005g0263 a0001c0001t0005g0264 others(1): Show |
4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.91-24123C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119100730 | |||||||
| chr1:119100765 | A | AT | 4 | a0002c0002t0002g0120 a0002c0002t0002g0131 a0002c0002t0002g0132 others(1): Show |
4 | NA18939.hp2 NA18940.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.91-24159dupA | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119100765 | |||||||
| chr1:119100822 | G | A | 1 | a0001c0001t0007g0023 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.91-24215C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119100822 | |||||||
| chr1:119100886 | C | G | 11 | a0001c0001t0004g0025 a0001c0001t0004g0026 a0001c0001t0004g0027 others(8): Show |
11 | HG00558.hp1 HG00609.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.91-24279G>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119100886 | |||||||
| chr1:119100901 | G | T | 1 | a0002c0002t0002g0195 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.91-24294C>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119100901 | |||||||
| chr1:119100923 | C | A | 52 | a0001c0001t0001g0130 a0001c0001t0004g0170 a0001c0001t0006g0121 others(49): Show |
59 | HG00423.hp2 HG01175.hp1 HG01257.hp2 others(56): Show |
intron_variant | MODIFIER | c.91-24316G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119100923 | |||||||
| chr1:119100928 | G | A | 3 | a0001c0001t0004g0020 a0001c0001t0004g0021 a0001c0001t0004g0022 |
3 | HG01433.hp2 HG02257.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.91-24321C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119100928 | |||||||
| chr1:119100997 | C | T | 6 | a0001c0001t0005g0151 a0001c0001t0005g0152 a0001c0001t0005g0167 others(3): Show |
6 | HG02055.hp1 HG02109.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.91-24390G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119100997 | |||||||
| chr1:119101074 | G | A | 1 | a0002c0002t0011g0139 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.91-24467C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119101074 | |||||||
| chr1:119101151 | A | G | 61 | a0001c0001t0001g0114 a0001c0001t0001g0130 a0001c0001t0004g0020 others(58): Show |
68 | HG00423.hp2 HG01175.hp1 HG01257.hp2 others(65): Show |
intron_variant | MODIFIER | c.91-24544T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119101151 | |||||||
| chr1:119101197 | T | C | 53 | a0001c0001t0001g0310 a0001c0001t0001g0320 a0001c0001t0001g0321 others(50): Show |
58 | HG00438.hp1 HG00738.hp2 HG01070.hp1 others(55): Show |
intron_variant | MODIFIER | c.91-24590A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119101197 | |||||||
| chr1:119101285 | C | G | 1 | a0001c0001t0004g0322 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.91-24678G>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119101285 | |||||||
| chr1:119101643 | A | G | 1 | a0001c0001t0004g0336 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.91-25036T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119101643 | |||||||
| chr1:119102070 | T | TG | 13 | a0001c0001t0001g0072 a0001c0001t0001g0111 a0001c0001t0001g0179 others(10): Show |
13 | HG01175.hp2 HG01433.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.91-25464dupC | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119102070 | |||||||
| chr1:119102111 | A | G | 1 | a0001c0001t0001g0130 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.91-25504T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119102111 | |||||||
| chr1:119102376 | AC | A | 4 | a0001c0001t0005g0262 a0001c0001t0005g0263 a0001c0001t0005g0264 others(1): Show |
4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.91-25770delG | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119102376 | |||||||
| chr1:119102483 | C | T | 5 | a0001c0001t0005g0262 a0001c0001t0005g0263 a0001c0001t0005g0264 others(2): Show |
5 | HG00408.hp1 HG01099.hp2 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.91-25876G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119102483 | |||||||
| chr1:119102543 | T | C | 16 | a0001c0001t0005g0118 a0001c0001t0005g0142 a0001c0001t0005g0143 others(13): Show |
16 | HG00621.hp1 HG01074.hp1 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.91-25936A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119102543 | |||||||
| chr1:119102859 | G | T | 1 | a0001c0001t0004g0020 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.91-26252C>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119102859 | |||||||
| chr1:119102912 | C | T | 179 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(176): Show |
189 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(186): Show |
intron_variant | MODIFIER | c.91-26305G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119102912 | |||||||
| chr1:119102918 | T | C | 4 | a0001c0001t0004g0020 a0001c0001t0004g0021 a0001c0001t0004g0022 others(1): Show |
4 | HG01433.hp2 HG02257.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.91-26311A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119102918 | |||||||
| chr1:119103072 | A | G | 1 | a0001c0001t0007g0202 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.91-26465T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119103072 | |||||||
| chr1:119103234 | T | C | 1 | a0001c0001t0003g0268 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.91-26627A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119103234 | |||||||
| chr1:119103278 | C | T | 4 | a0001c0003t0007g0288 a0001c0003t0007g0294 a0001c0003t0007g0295 others(1): Show |
4 | HG02735.hp2 HG03239.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.91-26671G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119103278 | |||||||
| chr1:119103395 | G | C | 4 | a0001c0001t0004g0289 a0001c0001t0004g0290 a0001c0001t0004g0292 others(1): Show |
4 | HG02486.hp1 HG02723.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.91-26788C>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119103395 | |||||||
| chr1:119103412 | T | C | 286 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(283): Show |
302 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(299): Show |
intron_variant | MODIFIER | c.91-26805A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119103412 | |||||||
| chr1:119103449 | G | A | 1 | a0001c0003t0007g0253 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.91-26842C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119103449 | |||||||
| chr1:119103474 | T | C | 1 | a0001c0001t0005g0145 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.91-26867A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119103474 | |||||||
| chr1:119103623 | T | A | 1 | a0002c0002t0002g0135 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.91-27016A>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119103623 | |||||||
| chr1:119103834 | G | A | 1 | a0001c0001t0005g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.91-27227C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119103834 | |||||||
| chr1:119103971 | T | C | 4 | a0003c0004t0005g0210 a0003c0004t0005g0211 a0003c0004t0005g0212 others(1): Show |
4 | HG02647.hp1 HG02723.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.91-27364A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119103971 | |||||||
| chr1:119104071 | A | G | 270 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(267): Show |
285 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(282): Show |
intron_variant | MODIFIER | c.91-27464T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119104071 | |||||||
| chr1:119104075 | G | A | 1 | a0001c0003t0007g0297 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.91-27468C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119104075 | |||||||
| chr1:119104253 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.91-27646G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119104253 | |||||||
| chr1:119104437 | C | T | 3 | a0001c0001t0008g0279 a0001c0001t0008g0281 a0001c0001t0008g0337 |
3 | HG03225.hp1 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.91-27830G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119104437 | |||||||
| chr1:119104621 | G | GA | 9 | a0001c0001t0001g0037 a0001c0001t0003g0011 a0001c0001t0003g0239 others(6): Show |
10 | HG01168.hp1 HG02040.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.91-28015dupT | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119104621 | |||||||
| chr1:119104621 | GA | G | 32 | a0001c0001t0001g0179 a0001c0001t0003g0300 a0001c0001t0004g0012 others(29): Show |
33 | HG01891.hp1 HG02027.hp1 HG02055.hp2 others(30): Show |
intron_variant | MODIFIER | c.91-28015delT | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119104621 | |||||||
| chr1:119104621 | GAA | G | 36 | a0001c0001t0001g0310 a0001c0001t0001g0320 a0001c0001t0001g0321 others(33): Show |
40 | HG00438.hp1 HG00738.hp2 HG01070.hp1 others(37): Show |
intron_variant | MODIFIER | c.91-28016_91-28015d others(4): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119104621 | |||||||
| chr1:119104625 | A | T | 1 | a0002c0002t0002g0180 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.91-28018T>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119104625 | |||||||
| chr1:119104765 | C | CA | 103 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(100): Show |
106 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.91-28159dupT | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119104765 | |||||||
| chr1:119104887 | T | A | 1 | a0001c0001t0005g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.91-28280A>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119104887 | |||||||
| chr1:119105019 | G | C | 3 | a0001c0001t0004g0020 a0001c0001t0004g0021 a0001c0001t0004g0022 |
3 | HG01433.hp2 HG02257.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.91-28412C>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119105019 | |||||||
| chr1:119105181 | G | A | 6 | a0001c0001t0001g0032 a0001c0001t0001g0040 a0001c0001t0001g0046 others(3): Show |
6 | HG00621.hp2 HG00673.hp2 NA18612.hp2 others(3): Show |
intron_variant | MODIFIER | c.91-28574C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119105181 | |||||||
| chr1:119105323 | C | G | 179 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(176): Show |
189 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(186): Show |
intron_variant | MODIFIER | c.91-28716G>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119105323 | |||||||
| chr1:119105503 | G | A | 1 | a0001c0001t0006g0315 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.91-28896C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119105503 | |||||||
| chr1:119105686 | C | T | 58 | a0001c0001t0001g0310 a0001c0001t0001g0320 a0001c0001t0001g0321 others(55): Show |
63 | HG00438.hp1 HG00738.hp2 HG01070.hp1 others(60): Show |
intron_variant | MODIFIER | c.91-29079G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119105686 | |||||||
| chr1:119105859 | G | A | 1 | a0001c0001t0003g0231 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.91-29252C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119105859 | |||||||
| chr1:119105915 | AATAAAAG others(5): Show |
A | 3 | a0001c0001t0004g0020 a0001c0001t0004g0021 a0001c0001t0004g0022 |
3 | HG01433.hp2 HG02257.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.91-29320_91-29309d others(14): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119105915 | |||||||
| chr1:119106033 | T | C | 191 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(188): Show |
201 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(198): Show |
intron_variant | MODIFIER | c.91-29426A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119106033 | |||||||
| chr1:119106165 | T | C | 1 | a0001c0001t0003g0248 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.91-29558A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119106165 | |||||||
| chr1:119106224 | C | CCT | 195 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(192): Show |
205 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(202): Show |
intron_variant | MODIFIER | c.91-29619_91-29618d others(4): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119106224 | |||||||
| chr1:119106647 | C | A | 1 | a0001c0001t0016g0213 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.91-30040G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119106647 | |||||||
| chr1:119106854 | G | A | 1 | a0001c0001t0012g0171 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.91-30247C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119106854 | |||||||
| chr1:119106882 | C | T | 1 | a0001c0001t0004g0299 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.91-30275G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119106882 | |||||||
| chr1:119106926 | T | C | 4 | a0001c0001t0005g0262 a0001c0001t0005g0263 a0001c0001t0005g0264 others(1): Show |
4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.91-30319A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119106926 | |||||||
| chr1:119107145 | T | A | 4 | a0001c0001t0005g0262 a0001c0001t0005g0263 a0001c0001t0005g0264 others(1): Show |
4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.91-30538A>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119107145 | |||||||
| chr1:119107359 | C | G | 1 | a0002c0002t0002g0053 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.91-30752G>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119107359 | |||||||
| chr1:119107438 | TTTTGA | T | 4 | a0003c0004t0005g0210 a0003c0004t0005g0211 a0003c0004t0005g0212 others(1): Show |
4 | HG02647.hp1 HG02723.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.91-30836_91-30832d others(7): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119107438 | |||||||
| chr1:119107571 | T | A | 1 | a0001c0001t0005g0169 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.91-30964A>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119107571 | |||||||
| chr1:119107661 | TAGAAAA | T | 5 | a0001c0001t0003g0011 a0001c0001t0003g0239 a0001c0001t0003g0240 others(2): Show |
6 | HG02145.hp1 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.91-31060_91-31055d others(8): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119107661 | |||||||
| chr1:119107671 | AAGAG | A | 58 | a0001c0001t0001g0310 a0001c0001t0001g0320 a0001c0001t0001g0321 others(55): Show |
63 | HG00438.hp1 HG00738.hp2 HG01070.hp1 others(60): Show |
intron_variant | MODIFIER | c.91-31068_91-31065d others(6): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119107671 | |||||||
| chr1:119107671 | AAGAGAG | A | 4 | a0001c0001t0005g0262 a0001c0001t0005g0263 a0001c0001t0005g0264 others(1): Show |
4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.91-31070_91-31065d others(8): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119107671 | |||||||
| chr1:119107671 | AAGAGAGA others(7): Show |
A | 191 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(188): Show |
201 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(198): Show |
intron_variant | MODIFIER | c.91-31078_91-31065d others(16): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119107671 | |||||||
| chr1:119107697 | G | GA | 4 | a0003c0004t0005g0210 a0003c0004t0005g0211 a0003c0004t0005g0212 others(1): Show |
4 | HG02647.hp1 HG02723.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.91-31091dupT | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119107697 | |||||||
| chr1:119107738 | G | A | 1 | a0001c0001t0003g0258 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.91-31131C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119107738 | |||||||
| chr1:119107975 | G | A | 2 | a0001c0001t0001g0054 a0001c0001t0001g0112 |
2 | HG01243.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.91-31368C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119107975 | |||||||
| chr1:119108002 | C | G | 1 | a0001c0003t0007g0295 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.91-31395G>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119108002 | |||||||
| chr1:119108072 | A | G | 4 | a0001c0001t0005g0262 a0001c0001t0005g0263 a0001c0001t0005g0264 others(1): Show |
4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.91-31465T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119108072 | |||||||
| chr1:119108172 | T | G | 58 | a0001c0001t0001g0310 a0001c0001t0001g0320 a0001c0001t0001g0321 others(55): Show |
63 | HG00438.hp1 HG00738.hp2 HG01070.hp1 others(60): Show |
intron_variant | MODIFIER | c.91-31565A>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119108172 | |||||||
| chr1:119108305 | A | C | 175 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(172): Show |
185 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(182): Show |
intron_variant | MODIFIER | c.91-31698T>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119108305 | |||||||
| chr1:119108308 | A | T | 183 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(180): Show |
193 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(190): Show |
intron_variant | MODIFIER | c.91-31701T>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119108308 | |||||||
| chr1:119108370 | T | G | 4 | a0003c0004t0005g0210 a0003c0004t0005g0211 a0003c0004t0005g0212 others(1): Show |
4 | HG02647.hp1 HG02723.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.91-31763A>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119108370 | |||||||
| chr1:119108468 | G | A | 1 | a0001c0001t0004g0322 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.91-31861C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119108468 | |||||||
| chr1:119108469 | C | T | 1 | a0001c0001t0004g0322 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.91-31862G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119108469 | |||||||
| chr1:119108544 | TTATGA | T | 175 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(172): Show |
185 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(182): Show |
intron_variant | MODIFIER | c.91-31942_91-31938d others(7): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119108544 | |||||||
| chr1:119108585 | C | T | 1 | a0002c0002t0002g0129 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.90+31970G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119108585 | |||||||
| chr1:119108745 | C | A | 2 | a0001c0003t0007g0220 a0001c0003t0007g0221 |
2 | HG00741.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.90+31810G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119108745 | |||||||
| chr1:119108785 | T | C | 3 | a0001c0001t0003g0082 a0001c0001t0003g0083 a0001c0001t0003g0106 |
3 | HG01243.hp1 HG02004.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.90+31770A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119108785 | |||||||
| chr1:119108820 | T | C | 4 | a0003c0004t0005g0210 a0003c0004t0005g0211 a0003c0004t0005g0212 others(1): Show |
4 | HG02647.hp1 HG02723.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.90+31735A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119108820 | |||||||
| chr1:119109264 | C | A | 6 | a0001c0001t0005g0151 a0001c0001t0005g0152 a0001c0001t0005g0167 others(3): Show |
6 | HG02055.hp1 HG02109.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.90+31291G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119109264 | |||||||
| chr1:119109278 | G | C | 6 | a0001c0001t0005g0151 a0001c0001t0005g0152 a0001c0001t0005g0167 others(3): Show |
6 | HG02055.hp1 HG02109.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.90+31277C>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119109278 | |||||||
| chr1:119109402 | A | G | 1 | a0002c0002t0002g0029 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.90+31153T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119109402 | |||||||
| chr1:119109432 | A | G | 4 | a0003c0004t0005g0210 a0003c0004t0005g0211 a0003c0004t0005g0212 others(1): Show |
4 | HG02647.hp1 HG02723.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.90+31123T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119109432 | |||||||
| chr1:119109504 | G | A | 4 | a0001c0001t0005g0262 a0001c0001t0005g0263 a0001c0001t0005g0264 others(1): Show |
4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.90+31051C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119109504 | |||||||
| chr1:119109845 | A | T | 1 | a0002c0002t0002g0181 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.90+30710T>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119109845 | |||||||
| chr1:119109978 | C | T | 81 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(78): Show |
84 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.90+30577G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119109978 | |||||||
| chr1:119110245 | G | C | 4 | a0003c0004t0005g0210 a0003c0004t0005g0211 a0003c0004t0005g0212 others(1): Show |
4 | HG02647.hp1 HG02723.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.90+30310C>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119110245 | |||||||
| chr1:119110308 | C | T | 4 | a0001c0001t0006g0121 a0001c0001t0006g0126 a0001c0001t0006g0127 others(1): Show |
4 | HG02056.hp2 HG02071.hp2 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.90+30247G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119110308 | |||||||
| chr1:119110459 | T | C | 1 | a0001c0001t0003g0216 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.90+30096A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119110459 | |||||||
| chr1:119110627 | C | T | 1 | a0001c0001t0006g0316 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.90+29928G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119110627 | |||||||
| chr1:119110737 | T | C | 1 | a0001c0001t0012g0171 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.90+29818A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119110737 | |||||||
| chr1:119111142 | AG | A | 4 | a0001c0001t0004g0025 a0001c0001t0004g0026 a0001c0001t0004g0027 others(1): Show |
4 | HG00558.hp1 NA18981.hp2 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.90+29412delC | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119111142 | |||||||
| chr1:119111277 | T | C | 2 | a0001c0001t0004g0020 a0001c0001t0004g0021 |
2 | HG01433.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.90+29278A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119111277 | |||||||
| chr1:119111787 | C | T | 5 | a0001c0003t0007g0217 a0001c0003t0007g0218 a0001c0003t0007g0219 others(2): Show |
5 | HG00741.hp2 HG01099.hp2 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.90+28768G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119111787 | |||||||
| chr1:119111847 | T | C | 1 | a0001c0001t0006g0330 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.90+28708A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119111847 | |||||||
| chr1:119111865 | C | T | 4 | a0001c0001t0004g0289 a0001c0001t0004g0290 a0001c0001t0004g0292 others(1): Show |
4 | HG02486.hp1 HG02723.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.90+28690G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119111865 | |||||||
| chr1:119112092 | T | C | 4 | a0001c0001t0005g0262 a0001c0001t0005g0263 a0001c0001t0005g0264 others(1): Show |
4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.90+28463A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119112092 | |||||||
| chr1:119112207 | C | G | 16 | a0001c0001t0005g0118 a0001c0001t0005g0142 a0001c0001t0005g0143 others(13): Show |
16 | HG00621.hp1 HG01074.hp1 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.90+28348G>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119112207 | |||||||
| chr1:119112326 | G | A | 1 | a0001c0001t0005g0161 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.90+28229C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119112326 | |||||||
| chr1:119112353 | T | C | 6 | a0001c0001t0005g0151 a0001c0001t0005g0152 a0001c0001t0005g0167 others(3): Show |
6 | HG02055.hp1 HG02109.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.90+28202A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119112353 | |||||||
| chr1:119112363 | A | C | 1 | a0001c0001t0001g0321 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.90+28192T>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119112363 | |||||||
| chr1:119112436 | C | T | 1 | a0001c0001t0003g0106 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.90+28119G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119112436 | |||||||
| chr1:119112504 | T | C | 6 | a0001c0001t0003g0300 a0001c0001t0004g0299 a0001c0001t0010g0291 others(3): Show |
6 | HG02818.hp2 HG03098.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.90+28051A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119112504 | |||||||
| chr1:119112939 | T | A | 10 | a0001c0003t0007g0217 a0001c0003t0007g0218 a0001c0003t0007g0219 others(7): Show |
10 | HG00741.hp2 HG01099.hp2 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.90+27616A>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119112939 | |||||||
| chr1:119112989 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.90+27566C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119112989 | |||||||
| chr1:119113056 | A | G | 1 | a0001c0001t0003g0052 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.90+27499T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119113056 | |||||||
| chr1:119113057 | T | C | 281 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(278): Show |
296 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(293): Show |
intron_variant | MODIFIER | c.90+27498A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119113057 | |||||||
| chr1:119113098 | G | T | 1 | a0001c0001t0001g0058 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.90+27457C>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119113098 | |||||||
| chr1:119113274 | A | C | 195 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(192): Show |
205 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(202): Show |
intron_variant | MODIFIER | c.90+27281T>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119113274 | |||||||
| chr1:119113350 | T | C | 4 | a0001c0001t0005g0262 a0001c0001t0005g0263 a0001c0001t0005g0264 others(1): Show |
4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.90+27205A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119113350 | |||||||
| chr1:119113732 | T | A | 2 | a0002c0002t0002g0125 a0002c0002t0002g0136 |
2 | HG02129.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.90+26823A>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119113732 | |||||||
| chr1:119113783 | T | C | 8 | a0002c0002t0002g0138 a0002c0002t0002g0140 a0002c0002t0002g0141 others(5): Show |
8 | HG02055.hp2 HG02280.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.90+26772A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119113783 | |||||||
| chr1:119113870 | T | G | 195 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(192): Show |
205 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(202): Show |
intron_variant | MODIFIER | c.90+26685A>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119113870 | |||||||
| chr1:119114244 | G | A | 241 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(238): Show |
256 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(253): Show |
intron_variant | MODIFIER | c.90+26311C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119114244 | |||||||
| chr1:119114272 | C | T | 1 | a0001c0001t0003g0261 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.90+26283G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119114272 | |||||||
| chr1:119114434 | T | G | 195 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(192): Show |
205 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(202): Show |
intron_variant | MODIFIER | c.90+26121A>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119114434 | |||||||
| chr1:119114471 | A | T | 4 | a0001c0001t0005g0262 a0001c0001t0005g0263 a0001c0001t0005g0264 others(1): Show |
4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.90+26084T>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119114471 | |||||||
| chr1:119114585 | G | C | 1 | a0001c0001t0001g0031 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.90+25970C>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119114585 | |||||||
| chr1:119114616 | A | G | 1 | a0001c0001t0003g0261 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.90+25939T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119114616 | |||||||
| chr1:119114762 | C | T | 1 | a0001c0001t0001g0084 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.90+25793G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119114762 | |||||||
| chr1:119114809 | C | T | 3 | a0001c0001t0004g0020 a0001c0001t0004g0021 a0001c0001t0004g0022 |
3 | HG01433.hp2 HG02257.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.90+25746G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119114809 | |||||||
| chr1:119115029 | A | C | 1 | a0001c0001t0007g0272 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.90+25526T>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119115029 | |||||||
| chr1:119115097 | C | A | 5 | a0002c0002t0002g0005 a0002c0002t0002g0123 a0002c0002t0002g0124 others(2): Show |
6 | HG01175.hp1 HG02630.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.90+25458G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119115097 | |||||||
| chr1:119115120 | T | A | 175 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(172): Show |
185 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(182): Show |
intron_variant | MODIFIER | c.90+25435A>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119115120 | |||||||
| chr1:119115304 | G | C | 2 | a0001c0001t0001g0073 a0001c0001t0001g0074 |
2 | NA18995.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.90+25251C>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119115304 | |||||||
| chr1:119115315 | T | C | 100 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(97): Show |
103 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.90+25240A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119115315 | |||||||
| chr1:119115462 | C | T | 1 | a0002c0002t0002g0125 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.90+25093G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119115462 | |||||||
| chr1:119115726 | A | G | 4 | a0001c0001t0001g0032 a0001c0001t0001g0040 a0001c0001t0001g0056 others(1): Show |
4 | HG00673.hp2 NA18612.hp2 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.90+24829T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119115726 | |||||||
| chr1:119115794 | C | T | 1 | a0001c0003t0007g0288 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.90+24761G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119115794 | |||||||
| chr1:119116301 | C | T | 2 | a0001c0006t0004g0028 a0001c0006t0004g0173 |
2 | HG02280.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.90+24254G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119116301 | |||||||
| chr1:119116302 | A | G | 183 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(180): Show |
193 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(190): Show |
intron_variant | MODIFIER | c.90+24253T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119116302 | |||||||
| chr1:119116464 | G | A | 4 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0089 others(1): Show |
4 | HG01167.hp1 HG01169.hp1 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.90+24091C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119116464 | |||||||
| chr1:119116564 | C | G | 2 | a0001c0001t0001g0047 a0001c0001t0001g0055 |
2 | HG00099.hp2 HG00639.hp1 |
intron_variant | MODIFIER | c.90+23991G>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119116564 | |||||||
| chr1:119116748 | G | A | 10 | a0001c0003t0007g0217 a0001c0003t0007g0218 a0001c0003t0007g0219 others(7): Show |
10 | HG00741.hp2 HG01099.hp2 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.90+23807C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119116748 | |||||||
| chr1:119116752 | A | C | 14 | a0001c0001t0004g0025 a0001c0001t0004g0026 a0001c0001t0004g0027 others(11): Show |
14 | HG00558.hp1 HG00609.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.90+23803T>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119116752 | |||||||
| chr1:119116778 | G | T | 2 | a0002c0002t0002g0001 a0002c0002t0002g0122 |
4 | HG01257.hp2 HG01258.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.90+23777C>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119116778 | |||||||
| chr1:119116796 | C | T | 191 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(188): Show |
201 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(198): Show |
intron_variant | MODIFIER | c.90+23759G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119116796 | |||||||
| chr1:119116974 | G | A | 5 | a0001c0001t0004g0285 a0001c0001t0004g0289 a0001c0001t0004g0290 others(2): Show |
5 | HG02486.hp1 HG02717.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.90+23581C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119116974 | |||||||
| chr1:119116984 | A | T | 3 | a0001c0001t0003g0010 a0001c0001t0003g0228 a0001c0001t0003g0229 |
4 | NA19001.hp1 NA19004.hp1 NA19083.hp1 others(1): Show |
intron_variant | MODIFIER | c.90+23571T>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119116984 | |||||||
| chr1:119116993 | C | A | 1 | a0001c0001t0005g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.90+23562G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119116993 | |||||||
| chr1:119117060 | C | T | 4 | a0003c0004t0005g0210 a0003c0004t0005g0211 a0003c0004t0005g0212 others(1): Show |
4 | HG02647.hp1 HG02723.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.90+23495G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119117060 | |||||||
| chr1:119117149 | T | C | 14 | a0001c0001t0004g0025 a0001c0001t0004g0026 a0001c0001t0004g0027 others(11): Show |
14 | HG00558.hp1 HG00609.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.90+23406A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119117149 | |||||||
| chr1:119117226 | A | G | 255 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(252): Show |
270 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(267): Show |
intron_variant | MODIFIER | c.90+23329T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119117226 | |||||||
| chr1:119117295 | G | A | 1 | a0001c0001t0016g0213 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.90+23260C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119117295 | |||||||
| chr1:119117369 | T | C | 3 | a0001c0001t0004g0020 a0001c0001t0004g0021 a0001c0001t0004g0022 |
3 | HG01433.hp2 HG02257.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.90+23186A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119117369 | |||||||
| chr1:119117653 | C | T | 8 | a0001c0001t0004g0014 a0001c0001t0004g0332 a0001c0001t0004g0333 others(5): Show |
9 | HG00408.hp1 HG01884.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.90+22902G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119117653 | |||||||
| chr1:119117683 | C | T | 3 | a0001c0001t0001g0045 a0001c0001t0001g0054 a0001c0001t0001g0112 |
3 | HG01243.hp2 HG01257.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.90+22872G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119117683 | |||||||
| chr1:119117831 | C | T | 1 | a0001c0001t0001g0114 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.90+22724G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119117831 | |||||||
| chr1:119117882 | G | C | 175 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(172): Show |
185 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(182): Show |
intron_variant | MODIFIER | c.90+22673C>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119117882 | |||||||
| chr1:119117978 | G | A | 1 | a0001c0001t0003g0052 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.90+22577C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119117978 | |||||||
| chr1:119118153 | T | C | 3 | a0003c0004t0005g0210 a0003c0004t0005g0211 a0003c0004t0005g0212 |
3 | HG02647.hp1 HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.90+22402A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119118153 | |||||||
| chr1:119118196 | G | T | 179 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(176): Show |
189 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(186): Show |
intron_variant | MODIFIER | c.90+22359C>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119118196 | |||||||
| chr1:119118294 | G | T | 5 | a0001c0001t0003g0230 a0001c0001t0003g0231 a0001c0001t0003g0232 others(2): Show |
5 | HG00735.hp2 HG00741.hp1 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.90+22261C>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119118294 | |||||||
| chr1:119118440 | G | A | 1 | a0001c0001t0003g0108 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.90+22115C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119118440 | |||||||
| chr1:119118581 | C | T | 3 | a0001c0001t0001g0045 a0001c0001t0001g0054 a0001c0001t0001g0112 |
3 | HG01243.hp2 HG01257.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.90+21974G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119118581 | |||||||
| chr1:119118669 | A | G | 1 | a0001c0001t0016g0213 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.90+21886T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119118669 | |||||||
| chr1:119118898 | C | A | 281 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(278): Show |
296 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(293): Show |
intron_variant | MODIFIER | c.90+21657G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119118898 | |||||||
| chr1:119118954 | C | A | 1 | a0001c0001t0005g0167 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.90+21601G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119118954 | |||||||
| chr1:119119134 | A | C | 10 | a0001c0001t0008g0275 a0001c0001t0008g0276 a0001c0001t0008g0277 others(7): Show |
10 | HG02145.hp2 HG02572.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.90+21421T>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119119134 | |||||||
| chr1:119119393 | C | T | 16 | a0001c0001t0005g0118 a0001c0001t0005g0142 a0001c0001t0005g0143 others(13): Show |
16 | HG00621.hp1 HG01074.hp1 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.90+21162G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119119393 | |||||||
| chr1:119119648 | C | T | 7 | a0001c0001t0001g0036 a0001c0001t0001g0041 a0001c0001t0001g0044 others(4): Show |
7 | HG02129.hp2 NA18964.hp1 NA18991.hp2 others(4): Show |
intron_variant | MODIFIER | c.90+20907G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119119648 | |||||||
| chr1:119119654 | A | C | 1 | a0001c0001t0004g0174 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.90+20901T>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119119654 | |||||||
| chr1:119119699 | A | G | 3 | a0001c0001t0004g0020 a0001c0001t0004g0021 a0001c0001t0004g0022 |
3 | HG01433.hp2 HG02257.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.90+20856T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119119699 | |||||||
| chr1:119119760 | C | T | 1 | a0002c0002t0002g0053 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.90+20795G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119119760 | |||||||
| chr1:119119859 | T | A | 12 | a0001c0003t0007g0217 a0001c0003t0007g0218 a0001c0003t0007g0219 others(9): Show |
12 | HG00741.hp2 HG01099.hp2 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.90+20696A>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119119859 | |||||||
| chr1:119120176 | A | G | 100 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(97): Show |
103 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.90+20379T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119120176 | |||||||
| chr1:119120331 | C | T | 2 | a0003c0004t0005g0210 a0003c0004t0005g0211 |
2 | HG02647.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.90+20224G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119120331 | |||||||
| chr1:119120461 | T | C | 2 | a0002c0002t0002g0140 a0002c0002t0002g0141 |
2 | NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.90+20094A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119120461 | |||||||
| chr1:119120529 | A | G | 2 | a0001c0003t0007g0226 a0001c0003t0007g0227 |
2 | HG03490.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.90+20026T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119120529 | |||||||
| chr1:119120755 | G | A | 6 | a0001c0001t0005g0151 a0001c0001t0005g0152 a0001c0001t0005g0167 others(3): Show |
6 | HG02055.hp1 HG02109.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.90+19800C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119120755 | |||||||
| chr1:119120927 | C | T | 16 | a0001c0001t0005g0118 a0001c0001t0005g0142 a0001c0001t0005g0143 others(13): Show |
16 | HG00621.hp1 HG01074.hp1 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.90+19628G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119120927 | |||||||
| chr1:119121090 | C | T | 195 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(192): Show |
205 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(202): Show |
intron_variant | MODIFIER | c.90+19465G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119121090 | |||||||
| chr1:119121192 | A | G | 2 | a0001c0003t0007g0226 a0001c0003t0007g0227 |
2 | HG03490.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.90+19363T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119121192 | |||||||
| chr1:119121445 | A | T | 1 | a0001c0001t0003g0106 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.90+19110T>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119121445 | |||||||
| chr1:119121625 | T | C | 191 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(188): Show |
201 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(198): Show |
intron_variant | MODIFIER | c.90+18930A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119121625 | |||||||
| chr1:119121640 | C | A | 1 | a0001c0001t0001g0104 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.90+18915G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119121640 | |||||||
| chr1:119121697 | G | A | 1 | a0001c0001t0001g0215 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.90+18858C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119121697 | |||||||
| chr1:119121813 | A | G | 1 | a0003c0004t0005g0304 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.90+18742T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119121813 | |||||||
| chr1:119122296 | T | A | 1 | a0001c0001t0005g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.90+18259A>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119122296 | |||||||
| chr1:119122335 | A | G | 1 | a0002c0002t0002g0201 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.90+18220T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119122335 | |||||||
| chr1:119122339 | T | C | 1 | a0001c0001t0004g0039 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.90+18216A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119122339 | |||||||
| chr1:119122441 | G | C | 2 | a0001c0001t0001g0075 a0001c0001t0001g0105 |
2 | NA19070.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.90+18114C>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119122441 | |||||||
| chr1:119122469 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.90+18086A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119122469 | |||||||
| chr1:119122506 | T | G | 38 | a0001c0001t0001g0130 a0001c0001t0001g0179 a0001c0001t0004g0193 others(35): Show |
44 | HG00423.hp2 HG01257.hp2 HG01258.hp1 others(41): Show |
intron_variant | MODIFIER | c.90+18049A>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119122506 | |||||||
| chr1:119122711 | A | G | 4 | a0001c0001t0005g0262 a0001c0001t0005g0263 a0001c0001t0005g0264 others(1): Show |
4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.90+17844T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119122711 | |||||||
| chr1:119122899 | G | A | 4 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0089 others(1): Show |
4 | HG01167.hp1 HG01169.hp1 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.90+17656C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119122899 | |||||||
| chr1:119123039 | G | A | 1 | a0001c0010t0004g0287 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.90+17516C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119123039 | |||||||
| chr1:119123240 | C | T | 198 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(195): Show |
208 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(205): Show |
intron_variant | MODIFIER | c.90+17315G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119123240 | |||||||
| chr1:119123336 | A | G | 1 | a0001c0007t0004g0017 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.90+17219T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119123336 | |||||||
| chr1:119123570 | CTG | C | 16 | a0001c0001t0005g0118 a0001c0001t0005g0142 a0001c0001t0005g0143 others(13): Show |
16 | HG00621.hp1 HG01074.hp1 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.90+16983_90+16984d others(4): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119123570 | |||||||
| chr1:119123603 | A | AAC | 153 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(150): Show |
163 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.90+16950_90+16951d others(4): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119123603 | |||||||
| chr1:119123603 | AAC | A | 39 | a0001c0001t0004g0020 a0001c0001t0004g0021 a0001c0001t0004g0022 others(36): Show |
39 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.90+16950_90+16951d others(4): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119123603 | |||||||
| chr1:119123669 | T | A | 1 | a0001c0001t0001g0044 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.90+16886A>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119123669 | |||||||
| chr1:119123674 | C | G | 1 | a0001c0001t0001g0044 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.90+16881G>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119123674 | |||||||
| chr1:119123675 | C | G | 1 | a0001c0001t0001g0044 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.90+16880G>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119123675 | |||||||
| chr1:119123685 | T | A | 1 | a0001c0001t0001g0044 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.90+16870A>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119123685 | |||||||
| chr1:119123686 | C | A | 1 | a0001c0001t0001g0044 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.90+16869G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119123686 | |||||||
| chr1:119123689 | C | G | 1 | a0001c0001t0001g0044 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.90+16866G>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119123689 | |||||||
| chr1:119123703 | G | A | 1 | a0001c0001t0001g0044 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.90+16852C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119123703 | |||||||
| chr1:119123704 | A | C | 1 | a0001c0001t0001g0044 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.90+16851T>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119123704 | |||||||
| chr1:119123708 | T | C | 1 | a0001c0001t0001g0044 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.90+16847A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119123708 | |||||||
| chr1:119123710 | C | T | 1 | a0001c0001t0001g0044 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.90+16845G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119123710 | |||||||
| chr1:119123712 | A | AACGTGCT others(11): Show |
1 | a0001c0001t0001g0044 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.90+16842_90+16843i others(20): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119123712 | |||||||
| chr1:119123714 | C | G | 1 | a0001c0001t0001g0044 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.90+16841G>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119123714 | |||||||
| chr1:119123715 | T | C | 1 | a0001c0001t0001g0044 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.90+16840A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119123715 | |||||||
| chr1:119123870 | G | A | 10 | a0001c0001t0008g0275 a0001c0001t0008g0276 a0001c0001t0008g0277 others(7): Show |
10 | HG02145.hp2 HG02572.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.90+16685C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119123870 | |||||||
| chr1:119123942 | A | G | 199 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(196): Show |
209 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(206): Show |
intron_variant | MODIFIER | c.90+16613T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119123942 | |||||||
| chr1:119124025 | C | A | 1 | a0001c0001t0003g0035 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.90+16530G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119124025 | |||||||
| chr1:119124144 | T | C | 3 | a0001c0001t0004g0193 a0002c0002t0002g0009 a0002c0002t0002g0192 |
4 | NA18949.hp2 NA18964.hp2 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.90+16411A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119124144 | |||||||
| chr1:119124467 | G | A | 1 | a0001c0003t0007g0294 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.90+16088C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119124467 | |||||||
| chr1:119124473 | G | A | 1 | a0001c0001t0006g0315 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.90+16082C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119124473 | |||||||
| chr1:119124498 | GAATGAAA others(3): Show |
G | 7 | a0001c0001t0004g0020 a0001c0001t0004g0021 a0001c0001t0004g0022 others(4): Show |
7 | HG00408.hp1 HG01433.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.90+16047_90+16056d others(12): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119124498 | |||||||
| chr1:119124651 | G | A | 1 | a0001c0001t0003g0108 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.90+15904C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119124651 | |||||||
| chr1:119124655 | C | T | 16 | a0001c0001t0005g0118 a0001c0001t0005g0142 a0001c0001t0005g0143 others(13): Show |
16 | HG00621.hp1 HG01074.hp1 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.90+15900G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119124655 | |||||||
| chr1:119124687 | T | C | 3 | a0003c0004t0005g0210 a0003c0004t0005g0211 a0003c0004t0005g0212 |
3 | HG02647.hp1 HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.90+15868A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119124687 | |||||||
| chr1:119125146 | A | G | 5 | a0001c0003t0007g0217 a0001c0003t0007g0218 a0001c0003t0007g0219 others(2): Show |
5 | HG00741.hp2 HG01099.hp2 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.90+15409T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119125146 | |||||||
| chr1:119125464 | C | T | 2 | a0001c0001t0001g0095 a0001c0001t0001g0096 |
2 | HG00738.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.90+15091G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119125464 | |||||||
| chr1:119125827 | A | C | 1 | a0002c0002t0002g0192 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.90+14728T>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119125827 | |||||||
| chr1:119125828 | G | A | 1 | a0002c0002t0002g0192 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.90+14727C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119125828 | |||||||
| chr1:119125912 | C | G | 1 | a0001c0001t0003g0052 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.90+14643G>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119125912 | |||||||
| chr1:119126017 | T | C | 58 | a0001c0001t0001g0310 a0001c0001t0001g0320 a0001c0001t0001g0321 others(55): Show |
63 | HG00438.hp1 HG00738.hp2 HG01070.hp1 others(60): Show |
intron_variant | MODIFIER | c.90+14538A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119126017 | |||||||
| chr1:119126021 | T | C | 3 | a0001c0001t0004g0193 a0002c0002t0002g0009 a0002c0002t0002g0192 |
4 | NA18949.hp2 NA18964.hp2 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.90+14534A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119126021 | |||||||
| chr1:119126267 | GA | G | 281 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(278): Show |
296 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(293): Show |
intron_variant | MODIFIER | c.90+14287delT | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119126267 | |||||||
| chr1:119126284 | AT | A | 5 | a0001c0001t0003g0011 a0001c0001t0003g0239 a0001c0001t0003g0240 others(2): Show |
6 | HG02145.hp1 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.90+14270delA | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119126284 | |||||||
| chr1:119126455 | T | C | 3 | a0003c0004t0005g0210 a0003c0004t0005g0211 a0003c0004t0005g0212 |
3 | HG02647.hp1 HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.90+14100A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119126455 | |||||||
| chr1:119126479 | AT | A | 252 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(249): Show |
265 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(262): Show |
intron_variant | MODIFIER | c.90+14075delA | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119126479 | |||||||
| chr1:119126479 | ATT | A | 15 | a0001c0001t0001g0090 a0001c0001t0001g0110 a0001c0001t0001g0214 others(12): Show |
17 | HG00735.hp1 HG01257.hp2 HG01258.hp1 others(14): Show |
intron_variant | MODIFIER | c.90+14074_90+14075d others(4): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119126479 | |||||||
| chr1:119126563 | T | C | 2 | a0001c0001t0006g0315 a0001c0001t0006g0331 |
2 | HG01891.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.90+13992A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119126563 | |||||||
| chr1:119126639 | C | A | 53 | a0001c0001t0001g0130 a0001c0001t0001g0179 a0001c0001t0004g0170 others(50): Show |
60 | HG00423.hp2 HG01175.hp1 HG01257.hp2 others(57): Show |
intron_variant | MODIFIER | c.90+13916G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119126639 | |||||||
| chr1:119126643 | G | C | 198 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(195): Show |
208 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(205): Show |
intron_variant | MODIFIER | c.90+13912C>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119126643 | |||||||
| chr1:119126648 | A | G | 198 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(195): Show |
208 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(205): Show |
intron_variant | MODIFIER | c.90+13907T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119126648 | |||||||
| chr1:119126695 | T | C | 13 | a0001c0001t0007g0023 a0001c0003t0007g0217 a0001c0003t0007g0218 others(10): Show |
13 | HG00741.hp2 HG01099.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.90+13860A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119126695 | |||||||
| chr1:119126883 | G | A | 2 | a0001c0003t0007g0226 a0001c0003t0007g0227 |
2 | HG03490.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.90+13672C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119126883 | |||||||
| chr1:119126887 | C | T | 6 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(3): Show |
6 | HG01261.hp1 HG01934.hp2 NA18967.hp2 others(3): Show |
intron_variant | MODIFIER | c.90+13668G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119126887 | |||||||
| chr1:119127098 | C | A | 4 | a0001c0001t0005g0151 a0001c0001t0005g0152 a0001c0001t0005g0168 others(1): Show |
4 | HG02055.hp1 HG02109.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.90+13457G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119127098 | |||||||
| chr1:119127173 | T | C | 9 | a0001c0001t0008g0275 a0001c0001t0008g0276 a0001c0001t0008g0277 others(6): Show |
9 | HG02145.hp2 HG02572.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.90+13382A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119127173 | |||||||
| chr1:119127226 | G | A | 1 | a0001c0001t0001g0091 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.90+13329C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119127226 | |||||||
| chr1:119127270 | G | A | 11 | a0001c0001t0004g0025 a0001c0001t0004g0026 a0001c0001t0004g0027 others(8): Show |
11 | HG00558.hp1 HG00609.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.90+13285C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119127270 | |||||||
| chr1:119127497 | A | G | 110 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(107): Show |
113 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.90+13058T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119127497 | |||||||
| chr1:119127528 | C | T | 4 | a0001c0001t0005g0262 a0001c0001t0005g0263 a0001c0001t0005g0264 others(1): Show |
4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.90+13027G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119127528 | |||||||
| chr1:119127572 | A | T | 205 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(202): Show |
215 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.90+12983T>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119127572 | |||||||
| chr1:119127665 | T | G | 6 | a0001c0001t0005g0146 a0001c0001t0005g0147 a0001c0001t0005g0148 others(3): Show |
6 | HG01167.hp2 HG01358.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.90+12890A>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119127665 | |||||||
| chr1:119127679 | C | T | 10 | a0001c0001t0008g0275 a0001c0001t0008g0276 a0001c0001t0008g0277 others(7): Show |
10 | HG02145.hp2 HG02572.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.90+12876G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119127679 | |||||||
| chr1:119127823 | T | A | 1 | a0001c0001t0007g0023 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.90+12732A>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119127823 | |||||||
| chr1:119127863 | A | G | 1 | a0001c0001t0004g0015 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.90+12692T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119127863 | |||||||
| chr1:119128070 | A | T | 3 | a0001c0001t0001g0048 a0001c0003t0007g0226 a0001c0003t0007g0227 |
3 | HG03490.hp2 HG03704.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.90+12485T>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119128070 | |||||||
| chr1:119128114 | G | A | 11 | a0001c0001t0004g0025 a0001c0001t0004g0026 a0001c0001t0004g0027 others(8): Show |
11 | HG00558.hp1 HG00609.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.90+12441C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119128114 | |||||||
| chr1:119128182 | A | C | 208 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(205): Show |
218 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.90+12373T>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119128182 | |||||||
| chr1:119128199 | C | T | 1 | a0001c0003t0007g0217 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.90+12356G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119128199 | |||||||
| chr1:119128342 | A | G | 4 | a0001c0001t0004g0014 a0001c0001t0004g0332 a0001c0001t0004g0333 others(1): Show |
5 | HG01884.hp1 HG02559.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.90+12213T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119128342 | |||||||
| chr1:119128376 | C | T | 7 | a0001c0001t0004g0020 a0001c0001t0004g0021 a0001c0001t0004g0022 others(4): Show |
7 | HG00408.hp1 HG01433.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.90+12179G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119128376 | |||||||
| chr1:119128459 | C | T | 201 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(198): Show |
211 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(208): Show |
intron_variant | MODIFIER | c.90+12096G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119128459 | |||||||
| chr1:119128486 | C | G | 1 | a0001c0001t0003g0230 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.90+12069G>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119128486 | |||||||
| chr1:119128492 | T | C | 1 | a0001c0001t0001g0045 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.90+12063A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119128492 | |||||||
| chr1:119128576 | A | C | 1 | a0002c0002t0002g0180 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.90+11979T>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119128576 | |||||||
| chr1:119128594 | C | G | 4 | a0001c0001t0005g0262 a0001c0001t0005g0263 a0001c0001t0005g0264 others(1): Show |
4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.90+11961G>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119128594 | |||||||
| chr1:119128599 | G | A | 7 | a0001c0001t0004g0020 a0001c0001t0004g0021 a0001c0001t0004g0022 others(4): Show |
7 | HG00408.hp1 HG01433.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.90+11956C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119128599 | |||||||
| chr1:119128680 | C | A | 1 | a0001c0001t0001g0111 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.90+11875G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119128680 | |||||||
| chr1:119128867 | G | C | 1 | a0003c0004t0005g0304 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.90+11688C>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119128867 | |||||||
| chr1:119128933 | A | G | 4 | a0001c0001t0005g0262 a0001c0001t0005g0263 a0001c0001t0005g0264 others(1): Show |
4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.90+11622T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119128933 | |||||||
| chr1:119129062 | T | C | 1 | a0001c0001t0016g0213 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.90+11493A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119129062 | |||||||
| chr1:119129187 | C | T | 5 | a0001c0003t0009g0024 a0001c0003t0009g0222 a0001c0003t0009g0223 others(2): Show |
5 | HG02258.hp2 HG02572.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.90+11368G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119129187 | |||||||
| chr1:119129330 | G | A | 1 | a0001c0001t0006g0013 | 2 | HG01070.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.90+11225C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119129330 | |||||||
| chr1:119129434 | C | G | 1 | a0001c0001t0004g0336 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.90+11121G>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119129434 | |||||||
| chr1:119129478 | G | A | 2 | a0001c0003t0007g0226 a0001c0003t0007g0227 |
2 | HG03490.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.90+11077C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119129478 | |||||||
| chr1:119129727 | T | TA | 180 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(177): Show |
188 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.90+10827dupT | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119129727 | |||||||
| chr1:119129733 | A | AT | 3 | a0001c0001t0001g0046 a0002c0002t0002g0001 a0002c0002t0002g0122 |
5 | HG01257.hp2 HG01258.hp1 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.90+10821_90+10822i others(3): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119129733 | |||||||
| chr1:119129733 | A | T | 13 | a0001c0001t0007g0023 a0001c0003t0007g0217 a0001c0003t0007g0218 others(10): Show |
13 | HG00741.hp2 HG01099.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.90+10822T>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119129733 | |||||||
| chr1:119129738 | T | A | 2 | a0001c0001t0001g0092 a0001c0001t0001g0112 |
2 | HG01243.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.90+10817A>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119129738 | |||||||
| chr1:119129800 | A | C | 200 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(197): Show |
210 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(207): Show |
intron_variant | MODIFIER | c.90+10755T>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119129800 | |||||||
| chr1:119129919 | T | C | 1 | a0001c0001t0012g0171 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.90+10636A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119129919 | |||||||
| chr1:119130026 | G | A | 16 | a0001c0001t0005g0118 a0001c0001t0005g0142 a0001c0001t0005g0143 others(13): Show |
16 | HG00621.hp1 HG01074.hp1 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.90+10529C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119130026 | |||||||
| chr1:119130035 | C | T | 1 | a0003c0004t0005g0304 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.90+10520G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119130035 | |||||||
| chr1:119130143 | GA | G | 59 | a0001c0001t0001g0310 a0001c0001t0001g0320 a0001c0001t0001g0321 others(56): Show |
64 | HG00438.hp1 HG00738.hp2 HG01070.hp1 others(61): Show |
intron_variant | MODIFIER | c.90+10411delT | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119130143 | |||||||
| chr1:119130178 | G | A | 1 | a0001c0001t0003g0250 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.90+10377C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119130178 | |||||||
| chr1:119130211 | T | C | 3 | a0001c0001t0004g0020 a0001c0001t0004g0021 a0001c0001t0004g0022 |
3 | HG01433.hp2 HG02257.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.90+10344A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119130211 | |||||||
| chr1:119130470 | C | T | 53 | a0001c0001t0001g0130 a0001c0001t0001g0179 a0001c0001t0004g0170 others(50): Show |
60 | HG00423.hp2 HG01175.hp1 HG01257.hp2 others(57): Show |
intron_variant | MODIFIER | c.90+10085G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119130470 | |||||||
| chr1:119130721 | G | A | 87 | a0001c0001t0001g0310 a0001c0001t0001g0320 a0001c0001t0001g0321 others(84): Show |
92 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.90+9834C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119130721 | |||||||
| chr1:119130858 | C | A | 296 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(293): Show |
312 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(309): Show |
intron_variant | MODIFIER | c.90+9697G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119130858 | |||||||
| chr1:119131439 | G | A | 3 | a0001c0001t0004g0286 a0001c0001t0004g0293 a0001c0010t0004g0287 |
3 | HG01891.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.90+9116C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119131439 | |||||||
| chr1:119131458 | G | GT | 57 | a0001c0001t0001g0310 a0001c0001t0001g0320 a0001c0001t0001g0321 others(54): Show |
61 | HG00438.hp1 HG00738.hp2 HG01070.hp1 others(58): Show |
intron_variant | MODIFIER | c.90+9096dupA | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119131458 | |||||||
| chr1:119131458 | G | GTT | 5 | a0001c0001t0004g0012 a0001c0001t0004g0334 a0001c0001t0006g0306 others(2): Show |
5 | HG02109.hp1 HG02559.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.90+9095_90+9096dup others(2): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119131458 | |||||||
| chr1:119131458 | G | T | 4 | a0001c0001t0005g0262 a0001c0001t0005g0263 a0001c0001t0005g0264 others(1): Show |
4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.90+9097C>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119131458 | |||||||
| chr1:119131464 | T | G | 184 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(181): Show |
194 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(191): Show |
intron_variant | MODIFIER | c.90+9091A>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119131464 | |||||||
| chr1:119131464 | TG | T | 9 | a0001c0001t0008g0275 a0001c0001t0008g0276 a0001c0001t0008g0278 others(6): Show |
9 | HG02572.hp1 HG02895.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.90+9090delC | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119131464 | |||||||
| chr1:119131465 | G | GT | 23 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(20): Show |
25 | HG00544.hp2 HG01952.hp2 HG02027.hp2 others(22): Show |
intron_variant | MODIFIER | c.90+9089dupA | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119131465 | |||||||
| chr1:119131465 | G | T | 81 | a0001c0001t0001g0040 a0001c0001t0001g0310 a0001c0001t0001g0320 others(78): Show |
86 | HG00408.hp1 HG00438.hp1 HG00738.hp2 others(83): Show |
intron_variant | MODIFIER | c.90+9090C>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119131465 | |||||||
| chr1:119131602 | G | A | 192 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(189): Show |
202 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.90+8953C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119131602 | |||||||
| chr1:119131622 | C | T | 1 | a0001c0003t0007g0294 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.90+8933G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119131622 | |||||||
| chr1:119131697 | G | A | 91 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(88): Show |
94 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.90+8858C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119131697 | |||||||
| chr1:119131703 | T | C | 1 | a0001c0003t0007g0253 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.90+8852A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119131703 | |||||||
| chr1:119131707 | C | G | 1 | a0006c0008t0001g0113 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.90+8848G>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119131707 | |||||||
| chr1:119131707 | C | T | 1 | a0001c0001t0004g0332 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.90+8848G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119131707 | |||||||
| chr1:119131708 | G | C | 1 | a0006c0008t0001g0113 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.90+8847C>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119131708 | |||||||
| chr1:119131740 | C | T | 7 | a0001c0001t0004g0020 a0001c0001t0004g0021 a0001c0001t0004g0022 others(4): Show |
7 | HG00408.hp1 HG01433.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.90+8815G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119131740 | |||||||
| chr1:119131743 | G | A | 1 | a0001c0001t0005g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.90+8812C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119131743 | |||||||
| chr1:119131795 | TCTGGACT others(12): Show |
T | 1 | a0001c0003t0007g0253 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.90+8741_90+8759del others(19): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119131795 | |||||||
| chr1:119131929 | T | C | 6 | a0001c0001t0005g0151 a0001c0001t0005g0152 a0001c0001t0005g0167 others(3): Show |
6 | HG02055.hp1 HG02109.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.90+8626A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119131929 | |||||||
| chr1:119132025 | A | T | 58 | a0001c0001t0001g0310 a0001c0001t0001g0320 a0001c0001t0001g0321 others(55): Show |
63 | HG00438.hp1 HG00738.hp2 HG01070.hp1 others(60): Show |
intron_variant | MODIFIER | c.90+8530T>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119132025 | |||||||
| chr1:119132299 | T | C | 2 | a0001c0003t0007g0220 a0001c0003t0007g0221 |
2 | HG00741.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.90+8256A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119132299 | |||||||
| chr1:119132560 | T | C | 1 | a0003c0004t0005g0304 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.90+7995A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119132560 | |||||||
| chr1:119132673 | G | T | 1 | a0001c0001t0003g0252 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.90+7882C>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119132673 | |||||||
| chr1:119132797 | T | C | 1 | a0003c0004t0005g0304 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.90+7758A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119132797 | |||||||
| chr1:119133525 | A | G | 2 | a0001c0001t0006g0318 a0001c0001t0006g0319 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.90+7030T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119133525 | |||||||
| chr1:119133665 | C | G | 1 | a0001c0001t0001g0037 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.90+6890G>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119133665 | |||||||
| chr1:119133868 | A | C | 1 | a0001c0001t0001g0036 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.90+6687T>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119133868 | |||||||
| chr1:119134064 | C | T | 1 | a0001c0001t0003g0035 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.90+6491G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119134064 | |||||||
| chr1:119134221 | C | A | 4 | a0001c0001t0005g0262 a0001c0001t0005g0263 a0001c0001t0005g0264 others(1): Show |
4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.90+6334G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119134221 | |||||||
| chr1:119134319 | C | CA | 29 | a0001c0001t0003g0238 a0001c0001t0003g0243 a0001c0001t0003g0260 others(26): Show |
29 | HG01168.hp1 HG01891.hp1 HG02080.hp1 others(26): Show |
intron_variant | MODIFIER | c.90+6235dupT | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119134319 | |||||||
| chr1:119134319 | C | CAA | 80 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(77): Show |
88 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.90+6234_90+6235dup others(2): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119134319 | |||||||
| chr1:119134319 | C | CAAA | 103 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(100): Show |
106 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.90+6233_90+6235dup others(3): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119134319 | |||||||
| chr1:119134319 | C | CAAAA | 27 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0095 others(24): Show |
27 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.90+6232_90+6235dup others(4): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119134319 | |||||||
| chr1:119134345 | A | G | 5 | a0001c0001t0003g0011 a0001c0001t0003g0239 a0001c0001t0003g0240 others(2): Show |
6 | HG02145.hp1 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.90+6210T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119134345 | |||||||
| chr1:119134570 | G | A | 1 | a0001c0001t0003g0251 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.90+5985C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119134570 | |||||||
| chr1:119134627 | C | T | 110 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(107): Show |
113 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.90+5928G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119134627 | |||||||
| chr1:119134896 | T | C | 3 | a0001c0001t0004g0020 a0001c0001t0004g0021 a0001c0001t0004g0022 |
3 | HG01433.hp2 HG02257.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.90+5659A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119134896 | |||||||
| chr1:119134930 | T | C | 58 | a0001c0001t0001g0310 a0001c0001t0001g0320 a0001c0001t0001g0321 others(55): Show |
63 | HG00438.hp1 HG00738.hp2 HG01070.hp1 others(60): Show |
intron_variant | MODIFIER | c.90+5625A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119134930 | |||||||
| chr1:119135279 | T | A | 1 | a0001c0001t0001g0114 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.90+5276A>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119135279 | |||||||
| chr1:119135316 | A | G | 1 | a0002c0002t0002g0115 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.90+5239T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119135316 | |||||||
| chr1:119135420 | A | C | 3 | a0001c0001t0004g0020 a0001c0001t0004g0021 a0001c0001t0004g0022 |
3 | HG01433.hp2 HG02257.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.90+5135T>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119135420 | |||||||
| chr1:119135698 | T | C | 201 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(198): Show |
211 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(208): Show |
intron_variant | MODIFIER | c.90+4857A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119135698 | |||||||
| chr1:119135711 | T | C | 9 | a0001c0001t0008g0275 a0001c0001t0008g0276 a0001c0001t0008g0277 others(6): Show |
9 | HG02145.hp2 HG02572.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.90+4844A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119135711 | |||||||
| chr1:119135715 | C | CAGAT | 16 | a0001c0001t0001g0310 a0001c0001t0003g0230 a0001c0001t0003g0231 others(13): Show |
17 | HG01070.hp1 HG01074.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.90+4836_90+4839dup others(4): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119135715 | |||||||
| chr1:119135715 | C | CAGATAGA others(1): Show |
5 | a0001c0001t0006g0306 a0001c0001t0006g0307 a0001c0001t0006g0308 others(2): Show |
5 | HG00738.hp2 HG03579.hp2 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.90+4832_90+4839dup others(8): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119135715 | |||||||
| chr1:119135715 | C | CAGATAGA others(5): Show |
1 | a0001c0001t0006g0305 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.90+4828_90+4839dup others(12): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119135715 | |||||||
| chr1:119135715 | C | T | 1 | a0001c0001t0015g0274 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.90+4840G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119135715 | |||||||
| chr1:119135715 | CAGAT | C | 39 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0003g0010 others(36): Show |
41 | HG00408.hp2 HG00642.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.90+4836_90+4839del others(4): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119135715 | |||||||
| chr1:119135715 | CAGATAGA others(1): Show |
C | 14 | a0001c0001t0003g0216 a0001c0001t0003g0238 a0001c0001t0003g0252 others(11): Show |
14 | HG00438.hp2 HG00609.hp2 HG00639.hp2 others(11): Show |
intron_variant | MODIFIER | c.90+4832_90+4839del others(8): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119135715 | |||||||
| chr1:119135747 | T | G | 8 | a0001c0001t0007g0023 a0001c0003t0007g0226 a0001c0003t0007g0227 others(5): Show |
8 | HG02258.hp2 HG02572.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.90+4808A>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119135747 | |||||||
| chr1:119135747 | T | TAGAG | 4 | a0001c0003t0007g0218 a0001c0003t0007g0219 a0001c0003t0007g0220 others(1): Show |
4 | HG00741.hp2 HG01099.hp2 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.90+4807_90+4808ins others(4): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119135747 | |||||||
| chr1:119135747 | T | TAGAGAGA others(5): Show |
1 | a0002c0002t0002g0208 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.90+4807_90+4808ins others(12): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119135747 | |||||||
| chr1:119135747 | T | TAGATAGA others(1): Show |
8 | a0001c0001t0007g0202 a0001c0001t0007g0203 a0001c0001t0007g0204 others(5): Show |
8 | HG00544.hp1 HG00558.hp2 HG00673.hp1 others(5): Show |
intron_variant | MODIFIER | c.90+4800_90+4807dup others(8): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119135747 | |||||||
| chr1:119135747 | T | TAGATAGA others(5): Show |
2 | a0001c0001t0007g0200 a0002c0002t0002g0199 |
2 | HG02027.hp2 NA18940.hp1 |
intron_variant | MODIFIER | c.90+4807_90+4808ins others(12): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119135747 | |||||||
| chr1:119135747 | T | TAGATAGA others(9): Show |
4 | a0002c0002t0002g0196 a0002c0002t0002g0197 a0002c0002t0002g0198 others(1): Show |
4 | NA18977.hp1 NA18989.hp2 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.90+4807_90+4808ins others(16): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119135747 | |||||||
| chr1:119135747 | T | TAGATAGA others(13): Show |
1 | a0002c0002t0002g0195 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.90+4807_90+4808ins others(20): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119135747 | |||||||
| chr1:119135747 | TAGATAGA others(7): Show |
T | 1 | a0001c0001t0004g0022 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.90+4794_90+4807del others(14): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119135747 | |||||||
| chr1:119135751 | T | G | 1 | a0001c0001t0005g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.90+4804A>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119135751 | |||||||
| chr1:119135751 | TAGAGAGA others(3): Show |
T | 2 | a0001c0001t0004g0020 a0001c0001t0004g0021 |
2 | HG01433.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.90+4794_90+4803del others(10): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119135751 | |||||||
| chr1:119135751 | TAGAGAGA others(5): Show |
T | 2 | a0001c0001t0005g0262 a0001c0001t0005g0263 |
2 | NA18962.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.90+4792_90+4803del others(12): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119135751 | |||||||
| chr1:119135753 | G | GAT | 79 | a0001c0001t0001g0004 a0001c0001t0001g0031 a0001c0001t0001g0034 others(76): Show |
83 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.90+4801_90+4802ins others(2): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119135753 | |||||||
| chr1:119135755 | G | T | 75 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(72): Show |
79 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(76): Show |
intron_variant | MODIFIER | c.90+4800C>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119135755 | |||||||
| chr1:119135759 | T | G | 79 | a0001c0001t0001g0004 a0001c0001t0001g0031 a0001c0001t0001g0034 others(76): Show |
83 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.90+4796A>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119135759 | |||||||
| chr1:119135759 | TAG | T | 32 | a0001c0001t0001g0069 a0001c0001t0001g0090 a0001c0001t0001g0096 others(29): Show |
32 | HG00609.hp1 HG00621.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.90+4794_90+4795del others(2): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119135759 | |||||||
| chr1:119135761 | G | GAGAGAT | 65 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(62): Show |
69 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.90+4793_90+4794ins others(6): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119135761 | |||||||
| chr1:119135761 | G | GATAGAGA others(3): Show |
8 | a0001c0001t0001g0094 a0001c0001t0001g0101 a0001c0001t0003g0106 others(5): Show |
8 | HG01106.hp1 HG01243.hp1 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.90+4793_90+4794ins others(10): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119135761 | |||||||
| chr1:119135761 | G | GATAGATA others(7): Show |
2 | a0001c0001t0001g0036 a0002c0002t0002g0134 |
2 | NA18964.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.90+4793_90+4794ins others(14): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119135761 | |||||||
| chr1:119135761 | G | GATAGATA others(11): Show |
1 | a0002c0002t0002g0158 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.90+4793_90+4794ins others(18): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119135761 | |||||||
| chr1:119135761 | G | T | 79 | a0001c0001t0001g0004 a0001c0001t0001g0031 a0001c0001t0001g0034 others(76): Show |
83 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.90+4794C>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119135761 | |||||||
| chr1:119135763 | G | T | 2 | a0001c0001t0005g0264 a0001c0001t0005g0265 |
2 | HG00408.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.90+4792C>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119135763 | |||||||
| chr1:119135803 | G | T | 279 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(276): Show |
294 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(291): Show |
intron_variant | MODIFIER | c.90+4752C>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119135803 | |||||||
| chr1:119135854 | A | C | 290 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(287): Show |
305 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(302): Show |
intron_variant | MODIFIER | c.90+4701T>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119135854 | |||||||
| chr1:119135866 | G | A | 1 | a0001c0001t0008g0335 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.90+4689C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119135866 | |||||||
| chr1:119135914 | G | A | 1 | a0001c0001t0005g0118 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.90+4641C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119135914 | |||||||
| chr1:119135914 | GCATATGC | G | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(91): Show |
97 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.90+4634_90+4640del others(7): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119135914 | |||||||
| chr1:119135915 | C | T | 1 | a0001c0001t0005g0118 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.90+4640G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119135915 | |||||||
| chr1:119136061 | C | T | 1 | a0001c0001t0001g0031 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.90+4494G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119136061 | |||||||
| chr1:119136126 | C | CTG | 6 | a0001c0001t0003g0010 a0001c0001t0003g0228 a0001c0001t0003g0229 others(3): Show |
7 | HG02080.hp1 NA19001.hp1 NA19004.hp1 others(4): Show |
intron_variant | MODIFIER | c.90+4427_90+4428dup others(2): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119136126 | |||||||
| chr1:119136245 | CTT | C | 11 | a0001c0001t0004g0025 a0001c0001t0004g0026 a0001c0001t0004g0027 others(8): Show |
11 | HG00558.hp1 HG00609.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.90+4308_90+4309del others(2): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119136245 | |||||||
| chr1:119136572 | C | T | 1 | a0001c0001t0015g0274 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.90+3983G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119136572 | |||||||
| chr1:119136778 | G | C | 334 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(331): Show |
351 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(348): Show |
intron_variant | MODIFIER | c.90+3777C>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119136778 | |||||||
| chr1:119136868 | C | T | 1 | a0001c0001t0004g0172 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.90+3687G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119136868 | |||||||
| chr1:119136981 | ATAAC | A | 11 | a0001c0001t0004g0025 a0001c0001t0004g0026 a0001c0001t0004g0027 others(8): Show |
11 | HG00558.hp1 HG00609.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.90+3570_90+3573del others(4): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119136981 | |||||||
| chr1:119137161 | C | T | 18 | a0001c0001t0003g0010 a0001c0001t0003g0228 a0001c0001t0003g0229 others(15): Show |
19 | HG00639.hp2 HG00735.hp2 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.90+3394G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119137161 | |||||||
| chr1:119137228 | T | C | 7 | a0001c0001t0004g0020 a0001c0001t0004g0021 a0001c0001t0004g0022 others(4): Show |
7 | HG00408.hp1 HG01433.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.90+3327A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119137228 | |||||||
| chr1:119137344 | T | C | 1 | a0001c0001t0001g0179 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.90+3211A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119137344 | |||||||
| chr1:119137443 | C | T | 1 | a0001c0006t0004g0028 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.90+3112G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119137443 | |||||||
| chr1:119137467 | T | C | 15 | a0002c0002t0002g0006 a0002c0002t0002g0007 a0002c0002t0002g0008 others(12): Show |
18 | HG00423.hp2 HG02015.hp2 HG02040.hp1 others(15): Show |
intron_variant | MODIFIER | c.90+3088A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119137467 | |||||||
| chr1:119137515 | C | T | 134 | a0001c0001t0001g0310 a0001c0001t0001g0320 a0001c0001t0001g0321 others(131): Show |
141 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.90+3040G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119137515 | |||||||
| chr1:119137600 | T | C | 3 | a0001c0001t0004g0193 a0002c0002t0002g0009 a0002c0002t0002g0192 |
4 | NA18949.hp2 NA18964.hp2 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.90+2955A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119137600 | |||||||
| chr1:119137673 | C | T | 135 | a0001c0001t0001g0310 a0001c0001t0001g0320 a0001c0001t0001g0321 others(132): Show |
142 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.90+2882G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119137673 | |||||||
| chr1:119137794 | A | T | 3 | a0001c0001t0004g0025 a0001c0001t0004g0026 a0001c0001t0004g0027 |
3 | HG00558.hp1 NA18981.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.90+2761T>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119137794 | |||||||
| chr1:119138228 | T | A | 8 | a0001c0001t0003g0266 a0001c0001t0003g0267 a0001c0001t0003g0268 others(5): Show |
8 | HG00639.hp2 HG01361.hp2 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.90+2327A>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119138228 | |||||||
| chr1:119138344 | A | G | 150 | a0001c0001t0001g0310 a0001c0001t0001g0320 a0001c0001t0001g0321 others(147): Show |
157 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.90+2211T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119138344 | |||||||
| chr1:119138374 | T | A | 151 | a0001c0001t0001g0310 a0001c0001t0001g0320 a0001c0001t0001g0321 others(148): Show |
158 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(155): Show |
intron_variant | MODIFIER | c.90+2181A>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119138374 | |||||||
| chr1:119138411 | C | A | 4 | a0001c0001t0016g0213 a0003c0004t0005g0210 a0003c0004t0005g0211 others(1): Show |
4 | HG02630.hp2 HG02647.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.90+2144G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119138411 | |||||||
| chr1:119138892 | T | C | 2 | a0001c0003t0007g0226 a0001c0003t0007g0227 |
2 | HG03490.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.90+1663A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119138892 | |||||||
| chr1:119138966 | C | T | 71 | a0001c0001t0001g0310 a0001c0001t0001g0320 a0001c0001t0001g0321 others(68): Show |
76 | HG00438.hp1 HG00738.hp2 HG00741.hp2 others(73): Show |
intron_variant | MODIFIER | c.90+1589G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119138966 | |||||||
| chr1:119138979 | G | A | 10 | a0001c0001t0008g0275 a0001c0001t0008g0276 a0001c0001t0008g0277 others(7): Show |
10 | HG02145.hp2 HG02572.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.90+1576C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119138979 | |||||||
| chr1:119139321 | A | G | 3 | a0001c0001t0004g0020 a0001c0001t0004g0021 a0001c0001t0004g0022 |
3 | HG01433.hp2 HG02257.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.90+1234T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119139321 | |||||||
| chr1:119139328 | T | G | 2 | a0001c0001t0001g0214 a0001c0001t0001g0215 |
2 | NA18944.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.90+1227A>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119139328 | |||||||
| chr1:119139397 | A | C | 1 | a0001c0001t0003g0216 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.90+1158T>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119139397 | |||||||
| chr1:119139605 | T | A | 134 | a0001c0001t0001g0310 a0001c0001t0001g0320 a0001c0001t0001g0321 others(131): Show |
141 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.90+950A>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119139605 | |||||||
| chr1:119139747 | T | C | 37 | a0001c0001t0001g0310 a0001c0001t0001g0320 a0001c0001t0001g0321 others(34): Show |
41 | HG00438.hp1 HG00738.hp2 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.90+808A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119139747 | |||||||
| chr1:119139801 | A | G | 1 | a0001c0001t0006g0284 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.90+754T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119139801 | |||||||
| chr1:119140159 | C | T | 1 | a0001c0003t0009g0024 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.90+396G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119140159 | |||||||
| chr1:119140297 | C | A | 1 | a0002c0002t0002g0283 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.90+258G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119140297 | |||||||
| chr1:119140336 | C | A | 1 | a0001c0001t0004g0336 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.90+219G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119140336 | |||||||
| chr1:119140356 | GA | G | 4 | a0001c0001t0004g0020 a0001c0001t0004g0021 a0001c0001t0004g0022 others(1): Show |
4 | HG01433.hp2 HG02257.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.90+198delT | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119140356 | |||||||
| chr1:119140440 | G | A | 59 | a0001c0001t0001g0310 a0001c0001t0001g0320 a0001c0001t0001g0321 others(56): Show |
64 | HG00438.hp1 HG00738.hp2 HG01070.hp1 others(61): Show |
intron_variant | MODIFIER | c.90+115C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119140440 | |||||||
| chr1:119140547 | T | C | 1 | a0001c0001t0008g0337 | 1 | HG03453.hp2 | splice_region_variant&intron_variant | LOW | c.90+8A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119140547 |