Item | Value |
---|---|
geneid | 6897 |
ensemblid | ENSG00000113407.14 |
hgncid | 11572 |
symbol | TARS1 |
name | threonyl-tRNA synthetase 1 |
refseq_nuc | NM_152295.5 |
refseq_prot | NP_689508.3 |
ensembl_nuc | ENST00000265112.8 |
ensembl_prot | ENSP00000265112.3 |
mane_status | MANE Select |
chr | chr5 |
start | 33440965 |
end | 33468086 |
strand | + |
ver | v1.2 |
region | chr5:33440965-33468086 |
region5000 | chr5:33435965-33473086 |
regionname0 | TARS1_chr5_33440965_33468086 |
regionname5000 | TARS1_chr5_33435965_33473086 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 723 | 390 | 80 | 58 | 191 | 12 | 47 | 151 | TARS1_chr5_33435965_33473086 | TARS1 | MFEEK others(718): Show |
chr5 | 33435965 | 33473086 |
a0002 | 0/0 | 723 | 10 | 8 | 2 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | MFEEK others(718): Show |
chr5 | 33435965 | 33473086 |
a0003 | 0/0 | 711 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | MGGEE others(706): Show |
chr5 | 33435965 | 33473086 |
a0004 | 0/0 | 723 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | MFEEK others(718): Show |
chr5 | 33435965 | 33473086 |
a0005 | 0/0 | 728 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | MFEEK others(723): Show |
chr5 | 33435965 | 33473086 |
a0006 | 0/0 | 723 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | MFEEK others(718): Show |
chr5 | 33435965 | 33473086 |
a0007 | 0/0 | 723 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | MFEEK others(718): Show |
chr5 | 33435965 | 33473086 |
a0008 | 0/0 | 723 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | MFEEK others(718): Show |
chr5 | 33435965 | 33473086 |
a0009 | 0/0 | 723 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | MFEEK others(718): Show |
chr5 | 33435965 | 33473086 |
a0010 | 0/0 | 723 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | MFEEK others(718): Show |
chr5 | 33435965 | 33473086 |
a0011 | 0/0 | 723 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | MFEEK others(718): Show |
chr5 | 33435965 | 33473086 |
a0012 | 0/0 | 723 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TARS1_chr5_33435965_33473086 | TARS1 | MFEEK others(718): Show |
chr5 | 33435965 | 33473086 |
a0013 | 0/0 | 723 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | MFEEK others(718): Show |
chr5 | 33435965 | 33473086 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 2169 | 254 | 57 | 43 | 111 | 8 | 34 | TARS1_chr5_33435965_33473086 | TARS1 | ATGTT others(2164): Show |
chr5 | 33435965 | 33473086 | ||
a0001c0002 | 0/1 | 2169 | 69 | 14 | 10 | 36 | 3 | 5 | TARS1_chr5_33435965_33473086 | TARS1 | ATGTT others(2164): Show |
chr5 | 33435965 | 33473086 | ||
a0001c0003 | 0/0 | 2169 | 64 | 9 | 5 | 43 | 1 | 6 | TARS1_chr5_33435965_33473086 | TARS1 | ATGTT others(2164): Show |
chr5 | 33435965 | 33473086 | ||
a0001c0012 | 0/0 | 2169 | 1 | 0 | 0 | 0 | 0 | 1 | TARS1_chr5_33435965_33473086 | TARS1 | ATGTT others(2164): Show |
chr5 | 33435965 | 33473086 | ||
a0001c0016 | 0/0 | 2169 | 1 | 0 | 0 | 0 | 0 | 1 | TARS1_chr5_33435965_33473086 | TARS1 | ATGTT others(2164): Show |
chr5 | 33435965 | 33473086 | ||
a0001c0017 | 0/0 | 2169 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | ATGTT others(2164): Show |
chr5 | 33435965 | 33473086 | ||
a0002c0004 | 0/0 | 2169 | 7 | 7 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | ATGTT others(2164): Show |
chr5 | 33435965 | 33473086 | ||
a0002c0005 | 0/0 | 2169 | 3 | 1 | 2 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | ATGTT others(2164): Show |
chr5 | 33435965 | 33473086 | ||
a0003c0006 | 0/0 | 2169 | 2 | 2 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | GTGTT others(2164): Show |
chr5 | 33435965 | 33473086 | ||
a0004c0008 | 0/0 | 2169 | 1 | 0 | 1 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | ATGTT others(2164): Show |
chr5 | 33435965 | 33473086 | ||
a0005c0014 | 0/0 | 2184 | 1 | 0 | 1 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | ATGTT others(2179): Show |
chr5 | 33435965 | 33473086 | ||
a0006c0009 | 0/0 | 2169 | 1 | 0 | 1 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | ATGTT others(2164): Show |
chr5 | 33435965 | 33473086 | ||
a0007c0013 | 0/0 | 2169 | 1 | 0 | 1 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | ATGTT others(2164): Show |
chr5 | 33435965 | 33473086 | ||
a0008c0019 | 0/0 | 2169 | 1 | 1 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | ATGTT others(2164): Show |
chr5 | 33435965 | 33473086 | ||
a0009c0010 | 0/0 | 2169 | 1 | 1 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | ATGTT others(2164): Show |
chr5 | 33435965 | 33473086 | ||
a0010c0011 | 0/0 | 2169 | 1 | 0 | 0 | 0 | 0 | 1 | TARS1_chr5_33435965_33473086 | TARS1 | ATGTT others(2164): Show |
chr5 | 33435965 | 33473086 | ||
a0011c0015 | 0/0 | 2169 | 1 | 1 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | ATGTT others(2164): Show |
chr5 | 33435965 | 33473086 | ||
a0012c0018 | 0/0 | 2169 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | ATGTT others(2164): Show |
chr5 | 33435965 | 33473086 | ||
a0013c0007 | 0/0 | 2169 | 1 | 1 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | ATGTT others(2164): Show |
chr5 | 33435965 | 33473086 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 2672 | 174 | 14 | 32 | 100 | 5 | 22 | TARS1_chr5_33435965_33473086 | TARS1 | GATTG others(2667): Show |
chr5 | 33435965 | 33473086 |
a0001c0001t0002 | 0/0 | 2672 | 65 | 37 | 10 | 5 | 3 | 10 | TARS1_chr5_33435965_33473086 | TARS1 | GATTG others(2667): Show |
chr5 | 33435965 | 33473086 |
a0001c0001t0003 | 0/0 | 2672 | 1 | 1 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | GATTG others(2667): Show |
chr5 | 33435965 | 33473086 |
a0001c0001t0004 | 0/0 | 2672 | 6 | 1 | 1 | 2 | 0 | 2 | TARS1_chr5_33435965_33473086 | TARS1 | GATTG others(2667): Show |
chr5 | 33435965 | 33473086 |
a0001c0001t0005 | 0/0 | 2672 | 3 | 0 | 0 | 3 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | GATTG others(2667): Show |
chr5 | 33435965 | 33473086 |
a0001c0001t0006 | 0/0 | 2672 | 2 | 2 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | GATTG others(2667): Show |
chr5 | 33435965 | 33473086 |
a0001c0001t0007 | 0/0 | 2672 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | GATTG others(2667): Show |
chr5 | 33435965 | 33473086 |
a0001c0001t0008 | 0/0 | 2672 | 1 | 1 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | GATTG others(2667): Show |
chr5 | 33435965 | 33473086 |
a0001c0001t0010 | 0/0 | 2672 | 1 | 1 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | GATTG others(2667): Show |
chr5 | 33435965 | 33473086 |
a0001c0002t0001 | 0/1 | 2672 | 69 | 14 | 10 | 36 | 3 | 5 | TARS1_chr5_33435965_33473086 | TARS1 | GATTG others(2667): Show |
chr5 | 33435965 | 33473086 |
a0001c0003t0003 | 0/0 | 2672 | 63 | 8 | 5 | 43 | 1 | 6 | TARS1_chr5_33435965_33473086 | TARS1 | GATTG others(2667): Show |
chr5 | 33435965 | 33473086 |
a0001c0003t0009 | 0/0 | 2672 | 1 | 1 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | GATTG others(2667): Show |
chr5 | 33435965 | 33473086 |
a0001c0012t0002 | 0/0 | 2672 | 1 | 0 | 0 | 0 | 0 | 1 | TARS1_chr5_33435965_33473086 | TARS1 | GATTG others(2667): Show |
chr5 | 33435965 | 33473086 |
a0001c0016t0003 | 0/0 | 2672 | 1 | 0 | 0 | 0 | 0 | 1 | TARS1_chr5_33435965_33473086 | TARS1 | GATTG others(2667): Show |
chr5 | 33435965 | 33473086 |
a0001c0017t0001 | 0/0 | 2672 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | GATTG others(2667): Show |
chr5 | 33435965 | 33473086 |
a0002c0004t0002 | 0/0 | 2672 | 7 | 7 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | GATTG others(2667): Show |
chr5 | 33435965 | 33473086 |
a0002c0005t0001 | 0/0 | 2672 | 3 | 1 | 2 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | GATTG others(2667): Show |
chr5 | 33435965 | 33473086 |
a0003c0006t0002 | 0/0 | 2672 | 2 | 2 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | GATTG others(2667): Show |
chr5 | 33435965 | 33473086 |
a0004c0008t0001 | 0/0 | 2672 | 1 | 0 | 1 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | GATTG others(2667): Show |
chr5 | 33435965 | 33473086 |
a0005c0014t0001 | 0/0 | 2687 | 1 | 0 | 1 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | GATTG others(2682): Show |
chr5 | 33435965 | 33473086 |
a0006c0009t0002 | 0/0 | 2672 | 1 | 0 | 1 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | GATTG others(2667): Show |
chr5 | 33435965 | 33473086 |
a0007c0013t0001 | 0/0 | 2672 | 1 | 0 | 1 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | GATTG others(2667): Show |
chr5 | 33435965 | 33473086 |
a0008c0019t0001 | 0/0 | 2672 | 1 | 1 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | GATTG others(2667): Show |
chr5 | 33435965 | 33473086 |
a0009c0010t0001 | 0/0 | 2672 | 1 | 1 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | GATTG others(2667): Show |
chr5 | 33435965 | 33473086 |
a0010c0011t0001 | 0/0 | 2672 | 1 | 0 | 0 | 0 | 0 | 1 | TARS1_chr5_33435965_33473086 | TARS1 | GATTG others(2667): Show |
chr5 | 33435965 | 33473086 |
a0011c0015t0001 | 0/0 | 2672 | 1 | 1 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | GATTG others(2667): Show |
chr5 | 33435965 | 33473086 |
a0012c0018t0001 | 0/0 | 2672 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | GATTG others(2667): Show |
chr5 | 33435965 | 33473086 |
a0013c0007t0002 | 0/0 | 2672 | 1 | 1 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | GATTG others(2667): Show |
chr5 | 33435965 | 33473086 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 22 | 0 | 4 | 12 | 2 | 4 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0002 | 1/0 | 19 | 0 | 7 | 7 | 1 | 3 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0008 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0011 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0017 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0026 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0027 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0028 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0055 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0056 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0057 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0058 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0059 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0060 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0002g0007 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0002g0009 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0002g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0002g0015 | 0/0 | 4 | 1 | 1 | 1 | 1 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0002g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0002g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0002g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0002g0038 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0002g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0002g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0003g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0004g0035 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0004g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0004g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0004g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0004g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0005g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0005g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0005g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0006g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0006g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0007g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0008g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0001t0010g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0002t0001g0003 | 0/0 | 18 | 0 | 3 | 9 | 2 | 4 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0002t0001g0005 | 0/0 | 6 | 4 | 2 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0002t0001g0006 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0002t0001g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0002t0001g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0002t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0002t0001g0019 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0002t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0002t0001g0034 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0002t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0002t0001g0085 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0002t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0002t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0002t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0002t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0002t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0003t0003g0004 | 0/0 | 12 | 0 | 2 | 9 | 0 | 1 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0003t0003g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0003t0003g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0003t0003g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0003t0003g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0003t0003g0044 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0003t0003g0045 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0003t0003g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0003t0003g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0003t0003g0048 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0003t0003g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0003t0003g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0003t0003g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0003t0003g0052 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0003t0003g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0003t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0003t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0003t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0003t0003g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0003t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0003t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0003t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0003t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0003t0003g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0003t0003g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0003t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0003t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0003t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0003t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0003t0003g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0003t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0003t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0003t0009g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0012t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0016t0003g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0001c0017t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0002c0004t0002g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0002c0004t0002g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0002c0004t0002g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0002c0004t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0002c0005t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0002c0005t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0002c0005t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0003c0006t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0003c0006t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0004c0008t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0005c0014t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0006c0009t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0007c0013t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0008c0019t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0009c0010t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0010c0011t0001g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0011c0015t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0012c0018t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
a0013c0007t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0125 | EUR | GBR | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG00323 | hp1 | a0001 | c0003 | t0003 | g0048 | EUR | FIN | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG00323 | hp2 | a0001 | c0002 | t0001 | g0034 | EUR | FIN | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG00438 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | CHS | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG00544 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | CHS | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG00558 | hp1 | a0001 | c0003 | t0003 | g0023 | EAS | CHS | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG00609 | hp1 | a0001 | c0002 | t0001 | g0034 | EAS | CHS | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | CHS | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG00621 | hp2 | a0001 | c0002 | t0001 | g0018 | EAS | CHS | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG00639 | hp1 | a0004 | c0008 | t0001 | g0077 | AMR | PUR | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0037 | AMR | PUR | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG00673 | hp2 | a0001 | c0001 | t0004 | g0105 | EAS | CHS | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG00735 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG00738 | hp1 | a0001 | c0002 | t0001 | g0019 | AMR | PUR | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0121 | AMR | PUR | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG01074 | hp2 | a0001 | c0002 | t0001 | g0019 | AMR | PUR | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0037 | AMR | PUR | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG01099 | hp1 | a0001 | c0002 | t0001 | g0064 | AMR | PUR | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0126 | AMR | PUR | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0120 | AMR | PUR | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG01109 | hp2 | a0002 | c0005 | t0001 | g0109 | AMR | PUR | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG01168 | hp1 | a0001 | c0002 | t0001 | g0005 | AMR | PUR | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG01169 | hp2 | a0001 | c0002 | t0001 | g0019 | AMR | PUR | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG01175 | hp1 | a0001 | c0003 | t0003 | g0166 | AMR | PUR | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG01192 | hp1 | a0005 | c0014 | t0001 | g0229 | AMR | PUR | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0015 | AMR | CLM | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | CLM | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0123 | AMR | CLM | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG01261 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | CLM | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG01261 | hp2 | a0001 | c0002 | t0001 | g0005 | AMR | CLM | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG01346 | hp2 | a0001 | c0002 | t0001 | g0096 | AMR | CLM | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG01358 | hp1 | a0006 | c0009 | t0002 | g0171 | AMR | CLM | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG01361 | hp2 | a0001 | c0001 | t0004 | g0035 | AMR | CLM | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG01496 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | CLM | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | CLM | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0124 | EUR | IBS | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG01516 | hp2 | a0001 | c0002 | t0001 | g0003 | EUR | IBS | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0015 | EUR | IBS | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0017 | EUR | IBS | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0133 | AFR | ACB | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG01884 | hp2 | a0001 | c0003 | t0003 | g0022 | AFR | ACB | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG01891 | hp1 | a0001 | c0002 | t0001 | g0012 | AFR | ACB | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0136 | AFR | ACB | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG01943 | hp1 | a0001 | c0003 | t0003 | g0174 | AMR | PEL | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PEL | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PEL | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PEL | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG01981 | hp2 | a0001 | c0003 | t0003 | g0004 | AMR | PEL | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0142 | AMR | PEL | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02004 | hp1 | a0001 | c0003 | t0003 | g0004 | AMR | PEL | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PEL | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02040 | hp1 | a0001 | c0001 | t0005 | g0202 | EAS | KHV | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0144 | AFR | ACB | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02055 | hp2 | a0001 | c0002 | t0001 | g0005 | AFR | ACB | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02056 | hp1 | a0001 | c0003 | t0003 | g0004 | EAS | KHV | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | KHV | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | KHV | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02080 | hp1 | a0001 | c0003 | t0003 | g0176 | EAS | KHV | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02083 | hp1 | a0001 | c0003 | t0003 | g0010 | EAS | KHV | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | KHV | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02129 | hp2 | a0001 | c0003 | t0003 | g0004 | EAS | KHV | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | KHV | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | KHV | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | KHV | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | ACB | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02148 | hp2 | a0001 | c0003 | t0003 | g0044 | AMR | PEL | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | CDX | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02155 | hp2 | a0001 | c0003 | t0003 | g0023 | EAS | CDX | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | CDX | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | CDX | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02257 | hp1 | a0001 | c0003 | t0003 | g0022 | AFR | ACB | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | ACB | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02258 | hp1 | a0001 | c0001 | t0010 | g0014 | AFR | ACB | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02258 | hp2 | a0003 | c0006 | t0002 | g0158 | AFR | ACB | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02280 | hp1 | a0001 | c0002 | t0001 | g0012 | AFR | ACB | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | ACB | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PEL | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02293 | hp2 | a0007 | c0013 | t0001 | g0065 | AMR | PEL | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | ACB | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | ACB | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02523 | hp1 | a0001 | c0003 | t0003 | g0169 | EAS | KHV | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02572 | hp1 | a0002 | c0004 | t0002 | g0042 | AFR | GWD | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02572 | hp2 | a0001 | c0002 | t0001 | g0102 | AFR | GWD | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02602 | hp1 | a0001 | c0002 | t0001 | g0003 | SAS | PJL | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02602 | hp2 | a0001 | c0003 | t0003 | g0052 | SAS | PJL | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | GWD | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02622 | hp2 | a0002 | c0004 | t0002 | g0041 | AFR | GWD | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | GWD | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02630 | hp2 | a0001 | c0003 | t0003 | g0049 | AFR | GWD | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02647 | hp1 | a0001 | c0002 | t0001 | g0108 | AFR | GWD | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02647 | hp2 | a0008 | c0019 | t0001 | g0152 | AFR | GWD | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02683 | hp1 | a0001 | c0003 | t0003 | g0165 | SAS | PJL | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02683 | hp2 | a0001 | c0002 | t0001 | g0003 | SAS | PJL | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02698 | hp1 | a0001 | c0002 | t0001 | g0003 | SAS | PJL | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0131 | SAS | PJL | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02717 | hp1 | a0001 | c0002 | t0001 | g0012 | AFR | GWD | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | GWD | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02723 | hp1 | a0001 | c0003 | t0003 | g0168 | AFR | GWD | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02723 | hp2 | a0003 | c0006 | t0002 | g0157 | AFR | GWD | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02735 | hp1 | a0001 | c0012 | t0002 | g0116 | SAS | PJL | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0224 | SAS | PJL | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02809 | hp1 | a0001 | c0001 | t0004 | g0104 | AFR | GWD | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02818 | hp1 | a0009 | c0010 | t0001 | g0005 | AFR | GWD | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0063 | AFR | GWD | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | GWD | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02886 | hp2 | a0001 | c0001 | t0008 | g0148 | AFR | GWD | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02895 | hp1 | a0001 | c0002 | t0001 | g0005 | AFR | GWD | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0173 | AFR | GWD | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0122 | AFR | GWD | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0138 | AFR | GWD | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02897 | hp1 | a0001 | c0001 | t0002 | g0135 | AFR | GWD | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0172 | AFR | GWD | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | ESN | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0020 | AFR | ESN | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02965 | hp1 | a0001 | c0001 | t0003 | g0146 | AFR | ESN | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0137 | AFR | ESN | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02970 | hp1 | a0001 | c0002 | t0001 | g0101 | AFR | ESN | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02970 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | ESN | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | ESN | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0040 | AFR | ESN | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG03017 | hp1 | a0010 | c0011 | t0001 | g0003 | SAS | PJL | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0119 | SAS | PJL | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0140 | AFR | GWD | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | MSL | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0141 | AFR | MSL | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG03130 | hp1 | a0002 | c0004 | t0002 | g0043 | AFR | ESN | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0115 | AFR | ESN | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG03139 | hp1 | a0002 | c0004 | t0002 | g0041 | AFR | ESN | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG03139 | hp2 | a0001 | c0002 | t0001 | g0012 | AFR | ESN | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG03195 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | ESN | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG03195 | hp2 | a0001 | c0003 | t0003 | g0161 | AFR | ESN | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | MSL | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG03225 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | MSL | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0134 | SAS | PJL | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0039 | AFR | MSL | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG03453 | hp2 | a0001 | c0002 | t0001 | g0005 | AFR | MSL | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG03486 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | MSL | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG03486 | hp2 | a0011 | c0015 | t0001 | g0071 | AFR | MSL | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG03491 | hp1 | a0001 | c0003 | t0003 | g0045 | SAS | PJL | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG03491 | hp2 | a0001 | c0001 | t0004 | g0106 | SAS | PJL | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0233 | SAS | PJL | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG03492 | hp2 | a0001 | c0003 | t0003 | g0045 | SAS | PJL | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG03516 | hp1 | a0001 | c0001 | t0002 | g0139 | AFR | ESN | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG03516 | hp2 | a0001 | c0003 | t0003 | g0160 | AFR | ESN | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0143 | AFR | GWD | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG03540 | hp2 | a0001 | c0002 | t0001 | g0033 | AFR | GWD | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG03579 | hp1 | a0002 | c0004 | t0002 | g0147 | AFR | MSL | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG03579 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | MSL | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG03654 | hp2 | a0001 | c0003 | t0003 | g0004 | SAS | PJL | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG03669 | hp1 | a0001 | c0002 | t0001 | g0099 | SAS | PJL | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0127 | SAS | PJL | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG03688 | hp1 | a0001 | c0003 | t0003 | g0052 | SAS | STU | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | STU | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0038 | SAS | PJL | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | BEB | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0036 | SAS | BEB | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0118 | SAS | BEB | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0062 | SAS | BEB | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | BEB | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | BEB | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | BEB | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG04184 | hp2 | a0001 | c0016 | t0003 | g0178 | SAS | BEB | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0130 | SAS | STU | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG04199 | hp2 | a0001 | c0001 | t0004 | g0035 | SAS | STU | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0231 | SAS | STU | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG04228 | hp2 | a0001 | c0002 | t0001 | g0003 | SAS | STU | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHB | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18747 | hp2 | a0001 | c0001 | t0004 | g0107 | EAS | CHB | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18906 | hp1 | a0001 | c0001 | t0006 | g0149 | AFR | YRI | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18906 | hp2 | a0001 | c0002 | t0001 | g0033 | AFR | YRI | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18939 | hp1 | a0001 | c0003 | t0003 | g0053 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18941 | hp1 | a0001 | c0002 | t0001 | g0095 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18945 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18947 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18947 | hp2 | a0001 | c0003 | t0003 | g0021 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18948 | hp1 | a0001 | c0003 | t0003 | g0162 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18949 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18950 | hp2 | a0001 | c0003 | t0003 | g0051 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18954 | hp1 | a0001 | c0017 | t0001 | g0221 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18954 | hp2 | a0001 | c0003 | t0003 | g0004 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18956 | hp2 | a0001 | c0002 | t0001 | g0112 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18959 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18960 | hp2 | a0001 | c0003 | t0003 | g0170 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18965 | hp2 | a0001 | c0003 | t0003 | g0159 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18967 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18968 | hp2 | a0001 | c0003 | t0003 | g0044 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18969 | hp2 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18970 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18970 | hp2 | a0001 | c0003 | t0003 | g0004 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18971 | hp2 | a0001 | c0002 | t0001 | g0098 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18972 | hp2 | a0001 | c0003 | t0003 | g0004 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18977 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18977 | hp2 | a0001 | c0003 | t0003 | g0004 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18978 | hp2 | a0001 | c0003 | t0003 | g0156 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18980 | hp2 | a0001 | c0003 | t0003 | g0163 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18981 | hp2 | a0001 | c0003 | t0003 | g0164 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18982 | hp2 | a0001 | c0003 | t0003 | g0047 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18984 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18984 | hp2 | a0001 | c0003 | t0003 | g0050 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18985 | hp2 | a0001 | c0002 | t0001 | g0094 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18986 | hp2 | a0001 | c0003 | t0003 | g0048 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18988 | hp1 | a0001 | c0003 | t0003 | g0004 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18988 | hp2 | a0012 | c0018 | t0001 | g0076 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18990 | hp1 | a0001 | c0002 | t0001 | g0088 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18991 | hp2 | a0001 | c0003 | t0003 | g0010 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18995 | hp1 | a0001 | c0001 | t0005 | g0201 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18998 | hp1 | a0001 | c0003 | t0003 | g0010 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA19001 | hp2 | a0001 | c0002 | t0001 | g0110 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA19002 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA19004 | hp1 | a0001 | c0001 | t0005 | g0181 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA19004 | hp2 | a0001 | c0003 | t0003 | g0047 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA19005 | hp1 | a0001 | c0003 | t0003 | g0167 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA19006 | hp1 | a0001 | c0003 | t0003 | g0004 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA19006 | hp2 | a0001 | c0002 | t0001 | g0081 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA19007 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA19007 | hp2 | a0001 | c0003 | t0003 | g0004 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA19009 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA19011 | hp2 | a0001 | c0003 | t0003 | g0177 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0020 | AFR | LWK | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA19030 | hp2 | a0013 | c0007 | t0002 | g0154 | AFR | LWK | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | LWK | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA19043 | hp2 | a0001 | c0002 | t0001 | g0005 | AFR | LWK | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA19055 | hp2 | a0001 | c0002 | t0001 | g0114 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA19056 | hp1 | a0001 | c0002 | t0001 | g0111 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA19057 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA19059 | hp1 | a0001 | c0003 | t0003 | g0155 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA19059 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA19060 | hp2 | a0001 | c0003 | t0003 | g0021 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA19063 | hp2 | a0001 | c0003 | t0003 | g0046 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA19064 | hp1 | a0001 | c0003 | t0003 | g0010 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA19065 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA19066 | hp1 | a0001 | c0003 | t0003 | g0023 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA19066 | hp2 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA19070 | hp1 | a0001 | c0003 | t0003 | g0050 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA19075 | hp1 | a0001 | c0002 | t0001 | g0089 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA19078 | hp2 | a0001 | c0002 | t0001 | g0097 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA19081 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA19082 | hp2 | a0001 | c0003 | t0003 | g0010 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA19083 | hp1 | a0001 | c0003 | t0003 | g0046 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA19084 | hp1 | a0001 | c0002 | t0001 | g0100 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA19084 | hp2 | a0001 | c0003 | t0003 | g0053 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA19085 | hp1 | a0001 | c0003 | t0003 | g0021 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA19085 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA19086 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA19088 | hp1 | a0001 | c0001 | t0007 | g0002 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA19090 | hp1 | a0001 | c0002 | t0001 | g0113 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA19090 | hp2 | a0001 | c0003 | t0003 | g0051 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA19091 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0014 | AFR | YRI | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0039 | AFR | YRI | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0038 | AFR | ASW | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | ASW | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA20752 | hp1 | a0001 | c0002 | t0001 | g0003 | EUR | TSI | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0195 | EUR | TSI | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | GIH | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0036 | SAS | GIH | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG01123 | hp2 | a0002 | c0005 | t0001 | g0086 | AMR | CLM | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02109 | hp1 | a0002 | c0004 | t0002 | g0042 | AFR | ACB | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02109 | hp2 | a0001 | c0001 | t0006 | g0150 | AFR | ACB | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | ACB | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02486 | hp2 | a0002 | c0004 | t0002 | g0043 | AFR | ACB | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02559 | hp1 | a0001 | c0003 | t0003 | g0022 | AFR | ACB | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0020 | AFR | ACB | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG06807 | hp1 | a0001 | c0003 | t0009 | g0175 | AFR | USA | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
HG06807 | hp2 | a0002 | c0005 | t0001 | g0066 | AFR | USA | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | USA | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0145 | AFR | USA | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA21309 | hp1 | a0001 | c0002 | t0001 | g0103 | AFR | LWK | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
NA21309 | hp2 | a0001 | c0003 | t0003 | g0049 | AFR | LWK | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0085 | REF | REF | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0002 | REF | REF | TARS1_chr5_33435965_33473086 | TARS1 | chr5 | 33435965 | 33473086 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:33441087 | A | G | 1 | a0003 | 2 | HG02258.hp2 HG02723.hp2 |
start_lost | HIGH | c.1A>G | p.Met1? | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/19 | 123/2672 | 1/2172 | 1/723 | chr5 | 33441087 | |||
chr5:33445328 | G | A | 2 | a0003 a0013 |
3 | HG02258.hp2 HG02723.hp2 NA19030.hp2 |
missense_variant | MODERATE | c.62G>A | p.Gly21Asp | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 2/19 | 184/2672 | 62/2172 | 21/723 | chr5 | 33445328 | |||
chr5:33448599 | C | T | 1 | a0008 | 1 | HG02647.hp2 | missense_variant | MODERATE | c.197C>T | p.Ala66Val | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/19 | 319/2672 | 197/2172 | 66/723 | chr5 | 33448599 | |||
chr5:33448633 | A | C | 1 | a0012 | 1 | NA18988.hp2 | missense_variant | MODERATE | c.231A>C | p.Glu77Asp | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/19 | 353/2672 | 231/2172 | 77/723 | chr5 | 33448633 | |||
chr5:33448686 | C | A | 1 | a0004 | 1 | HG00639.hp1 | missense_variant | MODERATE | c.284C>A | p.Ala95Glu | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/19 | 406/2672 | 284/2172 | 95/723 | chr5 | 33448686 | |||
chr5:33453311 | G | A | 1 | a0006 | 1 | HG01358.hp1 | missense_variant | MODERATE | c.352G>A | p.Val118Ile | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 4/19 | 474/2672 | 352/2172 | 118/723 | chr5 | 33453311 | |||
chr5:33453395 | G | A | 1 | a0009 | 1 | HG02818.hp1 | missense_variant | MODERATE | c.436G>A | p.Asp146Asn | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 4/19 | 558/2672 | 436/2172 | 146/723 | chr5 | 33453395 | |||
chr5:33456021 | G | A | 1 | a0010 | 1 | HG03017.hp1 | missense_variant | MODERATE | c.713G>A | p.Arg238Gln | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 7/19 | 835/2672 | 713/2172 | 238/723 | chr5 | 33456021 | |||
chr5:33460922 | C | G | 1 | a0011 | 1 | HG03486.hp2 | missense_variant | MODERATE | c.1271C>G | p.Pro424Arg | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 12/19 | 1393/2672 | 1271/2172 | 424/723 | chr5 | 33460922 | |||
chr5:33461733 | T | TTGGAAAT others(8): Show |
1 | a0005 | 1 | HG01192.hp1 | disruptive_inframe_insertion | MODERATE | c.1618_1619insTGGAAA others(9): Show |
p.Tyr540delinsLeuGlu others(12): Show |
TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 14/19 | 1741/2672 | 1619/2172 | 540/723 | chr5 | 33461733 | |||
chr5:33461739 | C | A | 1 | a0005 | 1 | HG01192.hp1 | missense_variant | MODERATE | c.1624C>A | p.Pro542Thr | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 14/19 | 1746/2672 | 1624/2172 | 542/723 | chr5 | 33461739 | |||
chr5:33461742 | A | C | 1 | a0005 | 1 | HG01192.hp1 | missense_variant&splice_region_variant | MODERATE | c.1627A>C | p.Lys543Gln | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 14/19 | 1749/2672 | 1627/2172 | 543/723 | chr5 | 33461742 | |||
chr5:33461743 | A | T | 1 | a0005 | 1 | HG01192.hp1 | missense_variant&splice_region_variant | MODERATE | c.1628A>T | p.Lys543Met | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 14/19 | 1750/2672 | 1628/2172 | 543/723 | chr5 | 33461743 | |||
chr5:33462106 | G | T | 1 | a0002 | 7 | HG02109.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
missense_variant | MODERATE | c.1738G>T | p.Gly580Cys | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 16/19 | 1860/2672 | 1738/2172 | 580/723 | chr5 | 33462106 | |||
chr5:33462107 | G | A | 1 | a0002 | 3 | HG01109.hp2 HG01123.hp2 HG06807.hp2 |
missense_variant | MODERATE | c.1739G>A | p.Gly580Asp | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 16/19 | 1861/2672 | 1739/2172 | 580/723 | chr5 | 33462107 | |||
chr5:33463772 | C | T | 1 | a0007 | 1 | HG02293.hp2 | missense_variant | MODERATE | c.1855C>T | p.Arg619Cys | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 17/19 | 1977/2672 | 1855/2172 | 619/723 | chr5 | 33463772 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:33455016 | C | T | 1 | a0012c0018 | 1 | NA18988.hp2 | synonymous_variant | LOW | c.525C>T | p.Tyr175Tyr | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 5/19 | 647/2672 | 525/2172 | 175/723 | chr5 | 33455016 | |||
chr5:33457361 | C | T | 2 | a0001c0016 a0001c0017 |
2 | HG04184.hp2 NA18954.hp1 |
synonymous_variant | LOW | c.942C>T | p.Phe314Phe | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 9/19 | 1064/2672 | 942/2172 | 314/723 | chr5 | 33457361 | |||
chr5:33459766 | C | A | 1 | a0008c0019 | 1 | HG02647.hp2 | synonymous_variant | LOW | c.1155C>A | p.Thr385Thr | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 11/19 | 1277/2672 | 1155/2172 | 385/723 | chr5 | 33459766 | |||
chr5:33461250 | G | A | 4 | a0001c0002 a0002c0005 a0009c0010 others(1): Show |
73 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(70): Show |
synonymous_variant | LOW | c.1506G>A | p.Pro502Pro | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 13/19 | 1628/2672 | 1506/2172 | 502/723 | chr5 | 33461250 | |||
chr5:33461723 | T | C | 1 | a0001c0012 | 1 | HG02735.hp1 | synonymous_variant | LOW | c.1608T>C | p.Asp536Asp | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 14/19 | 1730/2672 | 1608/2172 | 536/723 | chr5 | 33461723 | |||
chr5:33461929 | G | A | 3 | a0001c0003 a0001c0016 a0006c0009 |
66 | HG00323.hp1 HG00558.hp1 HG01175.hp1 others(63): Show |
synonymous_variant | LOW | c.1653G>A | p.Ala551Ala | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 15/19 | 1775/2672 | 1653/2172 | 551/723 | chr5 | 33461929 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:33440977 | T | G | 1 | a0001c0001t0007 | 1 | NA19088.hp1 | 5_prime_UTR_variant | MODIFIER | c.-110T>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/19 | 110 | chr5 | 33440977 | ||||||
chr5:33441018 | C | G | 11 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0010 others(8): Show |
144 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(141): Show |
5_prime_UTR_variant | MODIFIER | c.-69C>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/19 | 69 | chr5 | 33441018 | ||||||
chr5:33441022 | C | T | 1 | a0001c0001t0008 | 1 | HG02886.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-65C>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/19 | chr5 | 33441022 | |||||||
chr5:33441044 | A | G | 1 | a0001c0001t0005 | 3 | HG02040.hp1 NA18995.hp1 NA19004.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-43A>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/19 | chr5 | 33441044 | |||||||
chr5:33467785 | C | T | 1 | a0001c0001t0004 | 6 | HG00673.hp2 HG01361.hp2 HG02809.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*77C>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 19/19 | 77 | chr5 | 33467785 | ||||||
chr5:33467802 | C | T | 1 | a0001c0001t0010 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*94C>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 19/19 | 94 | chr5 | 33467802 | ||||||
chr5:33467824 | T | C | 6 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0008 others(3): Show |
69 | HG00323.hp1 HG00558.hp1 HG01175.hp1 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*116T>C | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 19/19 | 116 | chr5 | 33467824 | ||||||
chr5:33467993 | T | C | 1 | a0001c0003t0009 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*285T>C | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 19/19 | 285 | chr5 | 33467993 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:33441191 | G | A | 1 | a0001c0001t0001g0061 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.57+48G>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | chr5 | 33441191 | |||||||
chr5:33441213 | G | A | 1 | a0001c0001t0002g0062 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.57+70G>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | chr5 | 33441213 | |||||||
chr5:33441297 | A | C | 76 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(73): Show |
126 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.57+154A>C | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | chr5 | 33441297 | |||||||
chr5:33441299 | C | A | 1 | a0001c0001t0001g0024 | 3 | HG00558.hp2 HG02056.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.57+156C>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | chr5 | 33441299 | |||||||
chr5:33441384 | G | C | 1 | a0001c0001t0002g0063 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.57+241G>C | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | chr5 | 33441384 | |||||||
chr5:33441423 | A | C | 1 | a0001c0001t0001g0179 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.57+280A>C | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | chr5 | 33441423 | |||||||
chr5:33441463 | A | G | 171 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(168): Show |
276 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.57+320A>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | chr5 | 33441463 | |||||||
chr5:33441479 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.57+336G>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | chr5 | 33441479 | |||||||
chr5:33441492 | T | C | 1 | a0001c0001t0005g0181 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.57+349T>C | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | chr5 | 33441492 | |||||||
chr5:33441587 | G | T | 1 | a0001c0002t0001g0114 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.57+444G>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | chr5 | 33441587 | |||||||
chr5:33441699 | TG | T | 43 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0014 others(40): Show |
63 | HG00140.hp2 HG00642.hp2 HG01069.hp2 others(60): Show |
intron_variant | MODIFIER | c.57+557delG | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | chr5 | 33441699 | |||||||
chr5:33441719 | G | A | 6 | a0001c0001t0002g0040 a0001c0001t0003g0146 a0002c0004t0002g0041 others(3): Show |
10 | HG02109.hp1 HG02486.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.57+576G>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | chr5 | 33441719 | |||||||
chr5:33441740 | C | A | 43 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0014 others(40): Show |
63 | HG00140.hp2 HG00642.hp2 HG01069.hp2 others(60): Show |
intron_variant | MODIFIER | c.57+597C>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | chr5 | 33441740 | |||||||
chr5:33441853 | T | A | 1 | a0001c0001t0008g0148 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.57+710T>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | chr5 | 33441853 | |||||||
chr5:33441854 | C | A | 1 | a0001c0001t0008g0148 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.57+711C>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | chr5 | 33441854 | |||||||
chr5:33441978 | A | G | 2 | a0001c0001t0002g0020 a0001c0001t0002g0145 |
4 | HG02559.hp2 HG02922.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.57+835A>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | chr5 | 33441978 | |||||||
chr5:33442018 | A | G | 89 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0014 others(86): Show |
144 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(141): Show |
intron_variant | MODIFIER | c.57+875A>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | chr5 | 33442018 | |||||||
chr5:33442159 | G | A | 89 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0014 others(86): Show |
144 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(141): Show |
intron_variant | MODIFIER | c.57+1016G>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | chr5 | 33442159 | |||||||
chr5:33442277 | G | A | 171 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(168): Show |
276 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.57+1134G>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | chr5 | 33442277 | |||||||
chr5:33442281 | AT | A | 4 | a0001c0001t0001g0008 a0001c0001t0001g0182 a0001c0001t0001g0183 others(1): Show |
9 | HG00438.hp1 HG02132.hp2 NA18747.hp1 others(6): Show |
intron_variant | MODIFIER | c.57+1145delT | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 33442281 | ||||||
chr5:33442320 | C | CT | 46 | a0001c0001t0001g0060 a0001c0001t0001g0087 a0001c0001t0001g0090 others(43): Show |
87 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.57+1199dupT | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 33442320 | ||||||
chr5:33442320 | C | CTT | 6 | a0001c0002t0001g0108 a0001c0002t0001g0110 a0001c0002t0001g0111 others(3): Show |
6 | HG01109.hp2 HG02647.hp1 NA18956.hp2 others(3): Show |
intron_variant | MODIFIER | c.57+1198_57+1199dup others(2): Show |
TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 33442320 | ||||||
chr5:33442320 | CT | C | 21 | a0001c0001t0001g0025 a0001c0001t0001g0054 a0001c0001t0001g0186 others(18): Show |
32 | HG01891.hp2 HG02004.hp2 HG02083.hp1 others(29): Show |
intron_variant | MODIFIER | c.57+1199delT | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 33442320 | ||||||
chr5:33442320 | CTT | C | 31 | a0001c0001t0001g0185 a0001c0001t0002g0007 a0001c0001t0002g0014 others(28): Show |
44 | HG00140.hp2 HG00642.hp2 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.57+1198_57+1199del others(2): Show |
TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 33442320 | ||||||
chr5:33442430 | C | A | 89 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0014 others(86): Show |
144 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(141): Show |
intron_variant | MODIFIER | c.57+1287C>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | chr5 | 33442430 | |||||||
chr5:33442457 | A | G | 1 | a0002c0004t0002g0147 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.57+1314A>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | chr5 | 33442457 | |||||||
chr5:33442495 | C | G | 1 | a0001c0001t0001g0236 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.57+1352C>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | chr5 | 33442495 | |||||||
chr5:33442495 | C | T | 1 | a0001c0003t0009g0175 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.57+1352C>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | chr5 | 33442495 | |||||||
chr5:33442543 | T | G | 3 | a0001c0001t0002g0020 a0001c0001t0002g0115 a0001c0001t0002g0145 |
5 | HG02559.hp2 HG02922.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.57+1400T>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | chr5 | 33442543 | |||||||
chr5:33442562 | G | C | 1 | a0001c0001t0003g0146 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.57+1419G>C | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | chr5 | 33442562 | |||||||
chr5:33442591 | C | A | 1 | a0001c0012t0002g0116 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.57+1448C>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | chr5 | 33442591 | |||||||
chr5:33442738 | TCGTGATC others(37): Show |
T | 4 | a0001c0002t0001g0012 a0001c0002t0001g0033 a0001c0002t0001g0064 others(1): Show |
8 | HG01099.hp1 HG01891.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.57+1604_57+1647del others(44): Show |
TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 33442738 | ||||||
chr5:33442765 | A | G | 78 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(75): Show |
128 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.57+1622A>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | chr5 | 33442765 | |||||||
chr5:33442799 | C | T | 1 | a0001c0001t0001g0059 | 2 | NA18959.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.57+1656C>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | chr5 | 33442799 | |||||||
chr5:33442869 | A | G | 1 | a0001c0003t0003g0045 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.57+1726A>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | chr5 | 33442869 | |||||||
chr5:33442972 | C | G | 39 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0014 others(36): Show |
56 | HG00140.hp2 HG00642.hp2 HG01069.hp2 others(53): Show |
intron_variant | MODIFIER | c.57+1829C>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | chr5 | 33442972 | |||||||
chr5:33443094 | C | A | 171 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(168): Show |
276 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.57+1951C>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | chr5 | 33443094 | |||||||
chr5:33443271 | C | T | 3 | a0003c0006t0002g0157 a0003c0006t0002g0158 a0013c0007t0002g0154 |
3 | HG02258.hp2 HG02723.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.58-2053C>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | chr5 | 33443271 | |||||||
chr5:33443303 | TTCCC | T | 2 | a0001c0001t0001g0028 a0001c0001t0001g0235 |
4 | HG01070.hp2 HG02135.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.58-2018_58-2015del others(4): Show |
TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 33443303 | ||||||
chr5:33443303 | TTCCCTCT others(5): Show |
T | 1 | a0008c0019t0001g0152 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.58-2018_58-2007del others(12): Show |
TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 33443303 | ||||||
chr5:33443303 | TTCCCTCT others(7): Show |
T | 1 | a0001c0001t0001g0232 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.58-2004_58-1991del others(14): Show |
TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 33443303 | ||||||
chr5:33443306 | C | CCT | 11 | a0001c0001t0001g0001 a0001c0001t0001g0024 a0001c0001t0001g0058 others(8): Show |
14 | HG01993.hp2 HG02074.hp2 HG03239.hp1 others(11): Show |
intron_variant | MODIFIER | c.58-2006_58-2005dup others(2): Show |
TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 33443306 | ||||||
chr5:33443306 | C | CCTCT | 12 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0025 others(9): Show |
12 | HG01192.hp1 HG01952.hp1 HG01952.hp2 others(9): Show |
intron_variant | MODIFIER | c.58-2008_58-2005dup others(4): Show |
TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 33443306 | ||||||
chr5:33443306 | C | CCTCTCT | 12 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(9): Show |
12 | HG00609.hp2 HG01069.hp1 HG01928.hp1 others(9): Show |
intron_variant | MODIFIER | c.58-2010_58-2005dup others(6): Show |
TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 33443306 | ||||||
chr5:33443306 | C | CCTCTCTC others(1): Show |
10 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0027 others(7): Show |
11 | HG00140.hp1 HG00621.hp1 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.58-2012_58-2005dup others(8): Show |
TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 33443306 | ||||||
chr5:33443306 | C | CCTCTCTC others(7): Show |
1 | a0001c0001t0001g0190 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.58-2009_58-2008ins others(14): Show |
TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 33443306 | ||||||
chr5:33443306 | C | CCTCTCTC others(11): Show |
2 | a0001c0001t0001g0054 a0001c0001t0001g0191 |
2 | HG02257.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.58-2009_58-2008ins others(18): Show |
TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 33443306 | ||||||
chr5:33443306 | C | CCTCTCTC others(13): Show |
1 | a0001c0001t0001g0054 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.58-2009_58-2008ins others(20): Show |
TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 33443306 | ||||||
chr5:33443306 | C | CCTCTCTC others(3): Show |
10 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0027 others(7): Show |
10 | HG01168.hp2 HG01943.hp2 HG02071.hp1 others(7): Show |
intron_variant | MODIFIER | c.58-2014_58-2005dup others(10): Show |
TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 33443306 | ||||||
chr5:33443306 | C | CCTCTCTC others(5): Show |
6 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0184 others(3): Show |
6 | HG02004.hp2 HG02129.hp1 NA18944.hp2 others(3): Show |
intron_variant | MODIFIER | c.58-2016_58-2005dup others(12): Show |
TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 33443306 | ||||||
chr5:33443306 | C | CCTCTCTC others(7): Show |
2 | a0001c0001t0001g0008 a0001c0001t0001g0027 |
2 | HG02132.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.58-2005_58-2004ins others(14): Show |
TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 33443306 | ||||||
chr5:33443306 | C | CCTCTCTC others(9): Show |
1 | a0001c0001t0001g0080 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.58-2005_58-2004ins others(16): Show |
TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 33443306 | ||||||
chr5:33443306 | C | CTCT | 3 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0204 |
3 | HG01361.hp1 HG02083.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.58-2018_58-2017ins others(3): Show |
TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | chr5 | 33443306 | |||||||
chr5:33443306 | C | CTCTCTCT others(4): Show |
1 | a0001c0001t0001g0008 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.58-2018_58-2017ins others(11): Show |
TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | chr5 | 33443306 | |||||||
chr5:33443306 | C | T | 6 | a0001c0001t0001g0001 a0001c0001t0001g0180 a0001c0001t0001g0185 others(3): Show |
7 | HG01256.hp1 HG01981.hp1 HG02080.hp2 others(4): Show |
intron_variant | MODIFIER | c.58-2018C>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | chr5 | 33443306 | |||||||
chr5:33443306 | CCTCTCTC others(9): Show |
C | 2 | a0001c0001t0001g0001 a0001c0001t0001g0203 |
2 | NA19011.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.58-2004_58-1989del others(16): Show |
TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 33443306 | ||||||
chr5:33443306 | CCTCTCTC others(13): Show |
C | 2 | a0001c0001t0001g0183 a0013c0007t0002g0154 |
2 | NA18956.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.58-2004_58-1985del others(20): Show |
TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 33443306 | ||||||
chr5:33443308 | TCTCTCTC others(5): Show |
T | 2 | a0001c0001t0001g0233 a0001c0001t0001g0234 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.58-2004_58-1993del others(12): Show |
TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 33443308 | ||||||
chr5:33443310 | TCTCTCTC others(3): Show |
T | 1 | a0001c0001t0001g0226 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.58-2004_58-1995del others(10): Show |
TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 33443310 | ||||||
chr5:33443316 | TCTCC | T | 5 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0025 others(2): Show |
7 | HG00280.hp2 HG00738.hp2 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.58-2004_58-2001del others(4): Show |
TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 33443316 | ||||||
chr5:33443318 | TC | T | 3 | a0001c0002t0001g0003 a0001c0002t0001g0012 a0001c0002t0001g0088 |
3 | HG00735.hp2 HG03139.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.58-2003delC | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 33443318 | ||||||
chr5:33443318 | TCC | T | 9 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0026 others(6): Show |
9 | HG02148.hp1 HG02258.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.58-2004_58-2003del others(2): Show |
TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 33443318 | ||||||
chr5:33443320 | C | CCT | 17 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0030 others(14): Show |
20 | HG00639.hp1 HG01255.hp2 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.58-1964_58-1963dup others(2): Show |
TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 33443320 | ||||||
chr5:33443320 | C | CCTCT | 6 | a0001c0001t0001g0073 a0001c0001t0004g0035 a0001c0001t0006g0150 others(3): Show |
6 | HG01361.hp2 HG02109.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.58-1966_58-1963dup others(4): Show |
TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 33443320 | ||||||
chr5:33443320 | C | CCTCTCT | 12 | a0001c0001t0001g0002 a0001c0001t0001g0032 a0001c0001t0001g0074 others(9): Show |
12 | HG01106.hp2 HG02723.hp1 HG02976.hp1 others(9): Show |
intron_variant | MODIFIER | c.58-1968_58-1963dup others(6): Show |
TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 33443320 | ||||||
chr5:33443320 | C | CCTCTCTC others(1): Show |
4 | a0001c0001t0001g0002 a0001c0001t0001g0070 a0001c0001t0002g0172 others(1): Show |
5 | HG02895.hp2 HG02897.hp2 NA18944.hp1 others(2): Show |
intron_variant | MODIFIER | c.58-1970_58-1963dup others(8): Show |
TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 33443320 | ||||||
chr5:33443320 | C | CCTCTCTC others(3): Show |
1 | a0002c0004t0002g0043 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.58-1972_58-1963dup others(10): Show |
TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 33443320 | ||||||
chr5:33443320 | C | CCTCTCTC others(5): Show |
3 | a0001c0001t0004g0105 a0002c0004t0002g0043 a0006c0009t0002g0171 |
3 | HG00673.hp2 HG01358.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.58-1974_58-1963dup others(12): Show |
TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 33443320 | ||||||
chr5:33443320 | C | CT | 3 | a0001c0001t0001g0002 a0001c0001t0001g0091 a0001c0002t0001g0096 |
3 | HG01346.hp1 HG01346.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.58-2004_58-2003ins others(1): Show |
TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | chr5 | 33443320 | |||||||
chr5:33443320 | C | CTCTCTCT | 3 | a0001c0001t0002g0039 a0001c0003t0003g0004 a0001c0003t0003g0160 |
3 | HG03516.hp2 NA18970.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.58-2004_58-2003ins others(7): Show |
TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | chr5 | 33443320 | |||||||
chr5:33443320 | C | CTCTCTCT others(6): Show |
1 | a0001c0001t0004g0035 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.58-2004_58-2003ins others(13): Show |
TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | chr5 | 33443320 | |||||||
chr5:33443320 | C | T | 68 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(65): Show |
107 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.58-2004C>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | chr5 | 33443320 | |||||||
chr5:33443320 | CCT | C | 35 | a0001c0001t0001g0061 a0001c0002t0001g0003 a0001c0002t0001g0005 others(32): Show |
60 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.58-1964_58-1963del others(2): Show |
TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 33443320 | ||||||
chr5:33443320 | CCTCT | C | 28 | a0001c0001t0001g0002 a0001c0001t0001g0030 a0001c0001t0001g0032 others(25): Show |
48 | HG00280.hp1 HG01123.hp1 HG01175.hp1 others(45): Show |
intron_variant | MODIFIER | c.58-1966_58-1963del others(4): Show |
TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 33443320 | ||||||
chr5:33443320 | CCTCTCT | C | 7 | a0001c0001t0001g0179 a0001c0001t0002g0014 a0001c0001t0002g0120 others(4): Show |
13 | HG01109.hp1 HG01169.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.58-1968_58-1963del others(6): Show |
TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 33443320 | ||||||
chr5:33443320 | CCTCTCTC others(1): Show |
C | 7 | a0001c0001t0002g0007 a0001c0001t0002g0122 a0001c0001t0002g0133 others(4): Show |
12 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.58-1970_58-1963del others(8): Show |
TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 33443320 | ||||||
chr5:33443320 | CCTCTCTC others(3): Show |
C | 12 | a0001c0001t0001g0151 a0001c0001t0002g0014 a0001c0001t0002g0037 others(9): Show |
13 | HG00642.hp2 HG01069.hp2 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.58-1972_58-1963del others(10): Show |
TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 33443320 | ||||||
chr5:33443320 | CCTCTCTC others(7): Show |
C | 15 | a0001c0001t0002g0015 a0001c0001t0002g0036 a0001c0001t0002g0038 others(12): Show |
20 | HG00140.hp2 HG01255.hp1 HG01516.hp1 others(17): Show |
intron_variant | MODIFIER | c.58-1976_58-1963del others(14): Show |
TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 33443320 | ||||||
chr5:33443320 | CCTCTCTC others(9): Show |
C | 7 | a0001c0001t0002g0009 a0001c0001t0002g0135 a0001c0001t0002g0137 others(4): Show |
11 | HG01192.hp2 HG02055.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.58-1978_58-1963del others(16): Show |
TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 33443320 | ||||||
chr5:33443324 | T | C | 1 | a0007c0013t0001g0065 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.58-2000T>C | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | chr5 | 33443324 | |||||||
chr5:33443330 | T | A | 1 | a0001c0001t0008g0148 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.58-1994T>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | chr5 | 33443330 | |||||||
chr5:33443331 | C | G | 1 | a0001c0001t0008g0148 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.58-1993C>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | chr5 | 33443331 | |||||||
chr5:33443332 | T | A | 1 | a0001c0001t0008g0148 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.58-1992T>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | chr5 | 33443332 | |||||||
chr5:33443341 | C | T | 3 | a0001c0001t0001g0054 a0001c0001t0001g0190 a0001c0001t0001g0191 |
4 | HG02257.hp2 HG02622.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.58-1983C>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | chr5 | 33443341 | |||||||
chr5:33443475 | C | CT | 40 | a0001c0001t0001g0084 a0001c0001t0001g0184 a0001c0001t0002g0007 others(37): Show |
57 | HG00140.hp2 HG00642.hp2 HG01069.hp2 others(54): Show |
intron_variant | MODIFIER | c.58-1832dupT | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 33443475 | ||||||
chr5:33443475 | CT | C | 38 | a0001c0001t0001g0029 a0001c0001t0001g0061 a0001c0001t0001g0067 others(35): Show |
70 | HG00323.hp1 HG00558.hp1 HG01175.hp1 others(67): Show |
intron_variant | MODIFIER | c.58-1832delT | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 33443475 | ||||||
chr5:33443479 | T | C | 4 | a0001c0001t0006g0150 a0002c0005t0001g0066 a0002c0005t0001g0086 others(1): Show |
4 | HG01109.hp2 HG01123.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.58-1845T>C | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | chr5 | 33443479 | |||||||
chr5:33443501 | T | C | 3 | a0001c0001t0001g0054 a0001c0001t0001g0190 a0001c0001t0001g0191 |
4 | HG02257.hp2 HG02622.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.58-1823T>C | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | chr5 | 33443501 | |||||||
chr5:33443523 | T | C | 49 | a0001c0001t0002g0040 a0001c0001t0002g0172 a0001c0001t0002g0173 others(46): Show |
84 | HG00323.hp1 HG00558.hp1 HG01175.hp1 others(81): Show |
intron_variant | MODIFIER | c.58-1801T>C | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | chr5 | 33443523 | |||||||
chr5:33443573 | A | G | 1 | a0001c0003t0003g0170 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.58-1751A>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | chr5 | 33443573 | |||||||
chr5:33443578 | C | T | 2 | a0001c0001t0002g0040 a0001c0001t0003g0146 |
3 | HG02922.hp1 HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.58-1746C>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | chr5 | 33443578 | |||||||
chr5:33443653 | C | T | 1 | a0001c0001t0001g0231 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.58-1671C>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | chr5 | 33443653 | |||||||
chr5:33443712 | G | C | 1 | a0006c0009t0002g0171 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.58-1612G>C | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | chr5 | 33443712 | |||||||
chr5:33443721 | T | C | 6 | a0001c0001t0002g0040 a0001c0001t0003g0146 a0002c0004t0002g0041 others(3): Show |
10 | HG02109.hp1 HG02486.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.58-1603T>C | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | chr5 | 33443721 | |||||||
chr5:33443791 | A | C | 1 | a0001c0001t0001g0230 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.58-1533A>C | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | chr5 | 33443791 | |||||||
chr5:33443857 | C | A | 171 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(168): Show |
276 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.58-1467C>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | chr5 | 33443857 | |||||||
chr5:33443877 | C | T | 1 | a0001c0001t0002g0039 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.58-1447C>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | chr5 | 33443877 | |||||||
chr5:33443960 | G | GT | 6 | a0001c0001t0001g0151 a0001c0001t0004g0035 a0001c0001t0004g0104 others(3): Show |
7 | HG00673.hp2 HG01243.hp2 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.58-1354dupT | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 33443960 | ||||||
chr5:33443970 | T | A | 1 | a0001c0001t0001g0192 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.58-1354T>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | chr5 | 33443970 | |||||||
chr5:33444021 | G | A | 2 | a0001c0001t0002g0172 a0001c0001t0002g0173 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.58-1303G>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | chr5 | 33444021 | |||||||
chr5:33444218 | A | G | 1 | a0001c0001t0001g0180 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.58-1106A>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | chr5 | 33444218 | |||||||
chr5:33444242 | A | G | 1 | a0005c0014t0001g0229 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.58-1082A>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | chr5 | 33444242 | |||||||
chr5:33444244 | G | C | 1 | a0001c0001t0001g0151 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.58-1080G>C | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | chr5 | 33444244 | |||||||
chr5:33444252 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.58-1072G>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | chr5 | 33444252 | |||||||
chr5:33444345 | A | T | 1 | a0001c0003t0003g0053 | 2 | NA18939.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.58-979A>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | chr5 | 33444345 | |||||||
chr5:33444346 | A | C | 94 | a0001c0001t0001g0151 a0001c0001t0002g0007 a0001c0001t0002g0009 others(91): Show |
149 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(146): Show |
intron_variant | MODIFIER | c.58-978A>C | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | chr5 | 33444346 | |||||||
chr5:33444374 | T | C | 1 | a0001c0003t0003g0021 | 3 | NA18947.hp2 NA19060.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.58-950T>C | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | chr5 | 33444374 | |||||||
chr5:33444421 | A | C | 6 | a0001c0001t0002g0040 a0001c0001t0003g0146 a0002c0004t0002g0041 others(3): Show |
10 | HG02109.hp1 HG02486.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.58-903A>C | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | chr5 | 33444421 | |||||||
chr5:33444471 | T | C | 171 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(168): Show |
276 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.58-853T>C | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | chr5 | 33444471 | |||||||
chr5:33444534 | T | C | 1 | a0001c0001t0001g0231 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.58-790T>C | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | chr5 | 33444534 | |||||||
chr5:33444560 | T | C | 4 | a0002c0004t0002g0041 a0002c0004t0002g0042 a0002c0004t0002g0043 others(1): Show |
7 | HG02109.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.58-764T>C | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | chr5 | 33444560 | |||||||
chr5:33444811 | TCTC | T | 5 | a0001c0001t0004g0035 a0001c0001t0004g0104 a0001c0001t0004g0105 others(2): Show |
6 | HG00673.hp2 HG01361.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.58-508_58-506delTC others(1): Show |
TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 33444811 | ||||||
chr5:33444818 | C | T | 1 | a0001c0001t0002g0134 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.58-506C>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | chr5 | 33444818 | |||||||
chr5:33444870 | C | T | 3 | a0001c0001t0002g0020 a0001c0001t0002g0115 a0001c0001t0002g0145 |
5 | HG02559.hp2 HG02922.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.58-454C>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | chr5 | 33444870 | |||||||
chr5:33444955 | GT | G | 4 | a0001c0002t0001g0013 a0001c0002t0001g0088 a0001c0002t0001g0089 others(1): Show |
7 | NA18949.hp1 NA18959.hp2 NA18990.hp1 others(4): Show |
intron_variant | MODIFIER | c.58-356delT | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 33444955 | ||||||
chr5:33444956 | T | G | 1 | a0001c0002t0001g0003 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.58-368T>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | chr5 | 33444956 | |||||||
chr5:33444969 | C | T | 1 | a0001c0002t0001g0081 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.58-355C>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | chr5 | 33444969 | |||||||
chr5:33445169 | C | G | 1 | a0002c0004t0002g0043 | 2 | HG02486.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.58-155C>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | chr5 | 33445169 | |||||||
chr5:33445175 | A | T | 1 | a0013c0007t0002g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.58-149A>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | chr5 | 33445175 | |||||||
chr5:33445287 | A | C | 3 | a0001c0001t0001g0059 a0001c0001t0001g0227 a0001c0001t0001g0228 |
4 | NA18944.hp2 NA18959.hp1 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.58-37A>C | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | chr5 | 33445287 | |||||||
chr5:33445306 | C | T | 1 | a0001c0003t0003g0052 | 2 | HG02602.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.58-18C>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 1/18 | chr5 | 33445306 | |||||||
chr5:33445413 | TATC | T | 3 | a0001c0001t0002g0020 a0001c0001t0002g0115 a0001c0001t0002g0145 |
5 | HG02559.hp2 HG02922.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.138+14_138+16delTC others(1): Show |
TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr5 | 33445413 | ||||||
chr5:33445512 | G | T | 1 | a0001c0001t0003g0146 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.138+108G>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 2/18 | chr5 | 33445512 | |||||||
chr5:33445581 | A | G | 1 | a0001c0001t0001g0083 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.138+177A>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 2/18 | chr5 | 33445581 | |||||||
chr5:33445625 | T | C | 1 | a0001c0001t0001g0090 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.138+221T>C | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 2/18 | chr5 | 33445625 | |||||||
chr5:33445992 | C | T | 1 | a0001c0001t0001g0082 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.138+588C>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 2/18 | chr5 | 33445992 | |||||||
chr5:33446116 | A | C | 1 | a0008c0019t0001g0152 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.138+712A>C | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 2/18 | chr5 | 33446116 | |||||||
chr5:33446126 | G | C | 31 | a0001c0001t0002g0007 a0001c0001t0002g0014 a0001c0001t0002g0015 others(28): Show |
44 | HG00140.hp2 HG00642.hp2 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.138+722G>C | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 2/18 | chr5 | 33446126 | |||||||
chr5:33446285 | C | T | 1 | a0001c0002t0001g0103 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.138+881C>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 2/18 | chr5 | 33446285 | |||||||
chr5:33446353 | G | C | 2 | a0001c0001t0001g0194 a0001c0001t0001g0195 |
2 | HG03239.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.138+949G>C | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 2/18 | chr5 | 33446353 | |||||||
chr5:33446371 | A | G | 1 | a0001c0001t0001g0151 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.138+967A>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 2/18 | chr5 | 33446371 | |||||||
chr5:33446433 | G | A | 170 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(167): Show |
275 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.138+1029G>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 2/18 | chr5 | 33446433 | |||||||
chr5:33446569 | A | G | 1 | a0001c0003t0003g0169 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.138+1165A>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 2/18 | chr5 | 33446569 | |||||||
chr5:33446577 | CT | C | 4 | a0002c0004t0002g0041 a0002c0004t0002g0042 a0002c0004t0002g0043 others(1): Show |
7 | HG02109.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.138+1174delT | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 2/18 | chr5 | 33446577 | |||||||
chr5:33446694 | C | T | 1 | a0003c0006t0002g0158 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.138+1290C>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 2/18 | chr5 | 33446694 | |||||||
chr5:33446845 | T | C | 1 | a0001c0001t0001g0151 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.138+1441T>C | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 2/18 | chr5 | 33446845 | |||||||
chr5:33446856 | G | T | 1 | a0001c0001t0004g0107 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.138+1452G>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 2/18 | chr5 | 33446856 | |||||||
chr5:33446950 | C | T | 51 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0014 others(48): Show |
72 | HG00140.hp2 HG00642.hp2 HG01069.hp2 others(69): Show |
intron_variant | MODIFIER | c.138+1546C>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 2/18 | chr5 | 33446950 | |||||||
chr5:33447023 | C | T | 1 | a0007c0013t0001g0065 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.139-1518C>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 2/18 | chr5 | 33447023 | |||||||
chr5:33447082 | G | A | 47 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0014 others(44): Show |
65 | HG00140.hp2 HG00642.hp2 HG01069.hp2 others(62): Show |
intron_variant | MODIFIER | c.139-1459G>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 2/18 | chr5 | 33447082 | |||||||
chr5:33447162 | A | G | 8 | a0001c0001t0002g0009 a0001c0001t0002g0133 a0001c0001t0002g0135 others(5): Show |
12 | HG01192.hp2 HG01884.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.139-1379A>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 2/18 | chr5 | 33447162 | |||||||
chr5:33447293 | T | C | 7 | a0001c0001t0001g0011 a0001c0001t0001g0026 a0001c0001t0001g0055 others(4): Show |
14 | HG00621.hp1 HG01928.hp1 HG01943.hp2 others(11): Show |
intron_variant | MODIFIER | c.139-1248T>C | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 2/18 | chr5 | 33447293 | |||||||
chr5:33447311 | A | G | 1 | a0001c0001t0001g0058 | 2 | NA18955.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.139-1230A>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 2/18 | chr5 | 33447311 | |||||||
chr5:33447535 | C | G | 1 | a0001c0001t0004g0107 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.139-1006C>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 2/18 | chr5 | 33447535 | |||||||
chr5:33447615 | G | A | 3 | a0001c0001t0002g0020 a0001c0001t0002g0115 a0001c0001t0002g0145 |
5 | HG02559.hp2 HG02922.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.139-926G>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 2/18 | chr5 | 33447615 | |||||||
chr5:33447634 | CGTT | C | 81 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(78): Show |
134 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.139-905_139-903del others(3): Show |
TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr5 | 33447634 | ||||||
chr5:33447641 | A | G | 4 | a0001c0002t0001g0005 a0001c0002t0001g0101 a0001c0002t0001g0102 others(1): Show |
9 | HG01168.hp1 HG01261.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.139-900A>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 2/18 | chr5 | 33447641 | |||||||
chr5:33447757 | T | C | 1 | a0001c0001t0003g0146 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.139-784T>C | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 2/18 | chr5 | 33447757 | |||||||
chr5:33447891 | A | G | 171 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(168): Show |
276 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.139-650A>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 2/18 | chr5 | 33447891 | |||||||
chr5:33448007 | G | A | 3 | a0001c0001t0002g0020 a0001c0001t0002g0115 a0001c0001t0002g0145 |
5 | HG02559.hp2 HG02922.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.139-534G>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 2/18 | chr5 | 33448007 | |||||||
chr5:33448045 | G | A | 1 | a0001c0001t0006g0150 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.139-496G>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 2/18 | chr5 | 33448045 | |||||||
chr5:33448046 | C | G | 212 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(209): Show |
357 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(354): Show |
intron_variant | MODIFIER | c.139-495C>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 2/18 | chr5 | 33448046 | |||||||
chr5:33448148 | G | A | 3 | a0001c0001t0002g0020 a0001c0001t0002g0115 a0001c0001t0002g0145 |
5 | HG02559.hp2 HG02922.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.139-393G>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 2/18 | chr5 | 33448148 | |||||||
chr5:33448861 | G | A | 1 | a0001c0001t0006g0150 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.329+130G>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | chr5 | 33448861 | |||||||
chr5:33448915 | T | C | 1 | a0001c0001t0002g0036 | 2 | HG03834.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.329+184T>C | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | chr5 | 33448915 | |||||||
chr5:33448968 | A | G | 1 | a0001c0001t0001g0153 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.329+237A>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | chr5 | 33448968 | |||||||
chr5:33449031 | C | T | 1 | a0008c0019t0001g0152 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.329+300C>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | chr5 | 33449031 | |||||||
chr5:33449314 | TGTGTATA others(21): Show |
T | 1 | a0001c0001t0001g0080 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.329+597_329+624del others(28): Show |
TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr5 | 33449314 | ||||||
chr5:33449327 | ACG | A | 4 | a0001c0001t0002g0014 a0001c0001t0002g0063 a0001c0001t0002g0118 others(1): Show |
5 | HG02451.hp2 HG02717.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.329+599_329+600del others(2): Show |
TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr5 | 33449327 | ||||||
chr5:33449327 | ACGCG | A | 26 | a0001c0001t0002g0007 a0001c0001t0002g0015 a0001c0001t0002g0036 others(23): Show |
37 | HG00140.hp2 HG00642.hp2 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.329+597_329+600del others(4): Show |
TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | chr5 | 33449327 | |||||||
chr5:33449328 | C | T | 7 | a0001c0001t0001g0024 a0001c0001t0002g0014 a0001c0001t0002g0119 others(4): Show |
7 | HG01109.hp1 HG02056.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.329+597C>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | chr5 | 33449328 | |||||||
chr5:33449329 | G | A | 6 | a0001c0001t0002g0014 a0001c0001t0002g0119 a0001c0001t0002g0120 others(3): Show |
6 | HG01109.hp1 HG02109.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.329+598G>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | chr5 | 33449329 | |||||||
chr5:33449330 | C | T | 9 | a0001c0001t0002g0014 a0001c0001t0002g0063 a0001c0001t0002g0118 others(6): Show |
11 | HG01109.hp1 HG02109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.329+599C>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | chr5 | 33449330 | |||||||
chr5:33449331 | G | A | 9 | a0001c0001t0002g0014 a0001c0001t0002g0063 a0001c0001t0002g0118 others(6): Show |
11 | HG01109.hp1 HG02109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.329+600G>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | chr5 | 33449331 | |||||||
chr5:33449333 | A | G | 11 | a0001c0001t0002g0009 a0001c0001t0002g0039 a0001c0001t0002g0135 others(8): Show |
16 | HG01192.hp2 HG02055.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.329+602A>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | chr5 | 33449333 | |||||||
chr5:33449339 | ACACG | A | 10 | a0001c0001t0002g0007 a0001c0001t0002g0015 a0001c0001t0002g0062 others(7): Show |
18 | HG00140.hp2 HG01243.hp1 HG01255.hp1 others(15): Show |
intron_variant | MODIFIER | c.329+609_329+612del others(4): Show |
TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | chr5 | 33449339 | |||||||
chr5:33449339 | ACACGTG | A | 11 | a0001c0001t0002g0036 a0001c0001t0002g0038 a0001c0001t0002g0128 others(8): Show |
13 | HG01891.hp2 HG02698.hp2 HG03239.hp2 others(10): Show |
intron_variant | MODIFIER | c.329+609_329+614del others(6): Show |
TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | chr5 | 33449339 | |||||||
chr5:33449340 | C | T | 15 | a0001c0001t0002g0014 a0001c0001t0002g0037 a0001c0001t0002g0063 others(12): Show |
18 | HG00642.hp2 HG01069.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.329+609C>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | chr5 | 33449340 | |||||||
chr5:33449341 | ACG | A | 5 | a0001c0001t0002g0037 a0001c0001t0002g0117 a0001c0001t0002g0121 others(2): Show |
6 | HG00642.hp2 HG01069.hp2 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.329+611_329+612del others(2): Show |
TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | chr5 | 33449341 | |||||||
chr5:33449342 | C | T | 10 | a0001c0001t0002g0014 a0001c0001t0002g0063 a0001c0001t0002g0118 others(7): Show |
12 | HG01109.hp1 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.329+611C>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | chr5 | 33449342 | |||||||
chr5:33449343 | G | A | 10 | a0001c0001t0002g0014 a0001c0001t0002g0063 a0001c0001t0002g0118 others(7): Show |
12 | HG01109.hp1 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.329+612G>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | chr5 | 33449343 | |||||||
chr5:33449345 | G | A | 25 | a0001c0001t0002g0007 a0001c0001t0002g0014 a0001c0001t0002g0015 others(22): Show |
36 | HG00140.hp2 HG00642.hp2 HG01069.hp2 others(33): Show |
intron_variant | MODIFIER | c.329+614G>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | chr5 | 33449345 | |||||||
chr5:33449345 | G | GTA | 4 | a0001c0002t0001g0012 a0001c0002t0001g0033 a0001c0002t0001g0064 others(1): Show |
8 | HG01099.hp1 HG01891.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.329+626_329+627dup others(2): Show |
TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr5 | 33449345 | ||||||
chr5:33449353 | A | G | 1 | a0001c0001t0003g0146 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.329+622A>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | chr5 | 33449353 | |||||||
chr5:33449358 | T | G | 35 | a0001c0001t0002g0007 a0001c0001t0002g0014 a0001c0001t0002g0015 others(32): Show |
48 | HG00140.hp2 HG00642.hp2 HG01069.hp2 others(45): Show |
intron_variant | MODIFIER | c.329+627T>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | chr5 | 33449358 | |||||||
chr5:33449358 | T | TATATATA others(3): Show |
6 | a0001c0001t0002g0009 a0001c0001t0002g0135 a0001c0001t0002g0137 others(3): Show |
10 | HG01192.hp2 HG02055.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.329+627_329+628ins others(10): Show |
TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | chr5 | 33449358 | |||||||
chr5:33449358 | T | TATATATA others(5): Show |
1 | a0001c0001t0002g0140 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.329+627_329+628ins others(12): Show |
TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | chr5 | 33449358 | |||||||
chr5:33449358 | T | TATATATA others(7): Show |
3 | a0003c0006t0002g0157 a0003c0006t0002g0158 a0013c0007t0002g0154 |
3 | HG02258.hp2 HG02723.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.329+627_329+628ins others(14): Show |
TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | chr5 | 33449358 | |||||||
chr5:33449358 | T | TATATATA others(13): Show |
1 | a0001c0001t0002g0039 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.329+627_329+628ins others(20): Show |
TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | chr5 | 33449358 | |||||||
chr5:33449430 | ATTCTTTT others(5): Show |
A | 1 | a0001c0001t0001g0079 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.329+710_329+721del others(12): Show |
TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr5 | 33449430 | ||||||
chr5:33449439 | T | G | 3 | a0001c0003t0003g0049 a0001c0003t0003g0160 a0001c0003t0003g0168 |
4 | HG02630.hp2 HG02723.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.329+708T>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | chr5 | 33449439 | |||||||
chr5:33449445 | C | CT | 46 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0032 others(43): Show |
57 | HG00140.hp2 HG00642.hp2 HG01069.hp2 others(54): Show |
intron_variant | MODIFIER | c.329+739dupT | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr5 | 33449445 | ||||||
chr5:33449445 | C | CTT | 15 | a0001c0001t0001g0199 a0001c0001t0001g0225 a0001c0001t0001g0226 others(12): Show |
17 | HG01074.hp1 HG01106.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.329+738_329+739dup others(2): Show |
TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr5 | 33449445 | ||||||
chr5:33449445 | C | CTTTTT | 20 | a0001c0001t0001g0189 a0001c0003t0003g0004 a0001c0003t0003g0010 others(17): Show |
43 | HG00323.hp1 HG01943.hp1 HG01981.hp2 others(40): Show |
intron_variant | MODIFIER | c.329+735_329+739dup others(5): Show |
TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr5 | 33449445 | ||||||
chr5:33449445 | C | CTTTTTT | 10 | a0001c0003t0003g0022 a0001c0003t0003g0023 a0001c0003t0003g0044 others(7): Show |
17 | HG00558.hp1 HG01175.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.329+734_329+739dup others(6): Show |
TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr5 | 33449445 | ||||||
chr5:33449445 | CT | C | 7 | a0001c0001t0001g0070 a0001c0001t0001g0200 a0001c0001t0002g0007 others(4): Show |
13 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.329+739delT | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr5 | 33449445 | ||||||
chr5:33449445 | CTTTTTTT | C | 7 | a0001c0001t0002g0009 a0001c0001t0002g0135 a0001c0001t0002g0137 others(4): Show |
11 | HG01192.hp2 HG02055.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.329+733_329+739del others(7): Show |
TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr5 | 33449445 | ||||||
chr5:33449519 | G | A | 5 | a0001c0001t0002g0020 a0001c0001t0002g0115 a0001c0001t0002g0145 others(2): Show |
7 | HG02109.hp2 HG02559.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.329+788G>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | chr5 | 33449519 | |||||||
chr5:33449536 | A | G | 47 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0014 others(44): Show |
65 | HG00140.hp2 HG00642.hp2 HG01069.hp2 others(62): Show |
intron_variant | MODIFIER | c.329+805A>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | chr5 | 33449536 | |||||||
chr5:33449620 | T | A | 43 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0014 others(40): Show |
61 | HG00140.hp2 HG00642.hp2 HG01069.hp2 others(58): Show |
intron_variant | MODIFIER | c.329+889T>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | chr5 | 33449620 | |||||||
chr5:33449657 | G | A | 1 | a0011c0015t0001g0071 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.329+926G>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | chr5 | 33449657 | |||||||
chr5:33449659 | G | T | 3 | a0001c0001t0002g0014 a0001c0001t0002g0120 a0001c0001t0010g0014 |
5 | HG01109.hp1 HG02258.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.329+928G>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | chr5 | 33449659 | |||||||
chr5:33449702 | G | A | 1 | a0001c0001t0001g0225 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.329+971G>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | chr5 | 33449702 | |||||||
chr5:33449912 | G | A | 1 | a0001c0001t0002g0131 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.329+1181G>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | chr5 | 33449912 | |||||||
chr5:33449946 | TA | T | 79 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(76): Show |
130 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.329+1216delA | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | chr5 | 33449946 | |||||||
chr5:33449995 | G | A | 4 | a0001c0002t0001g0005 a0001c0002t0001g0101 a0001c0002t0001g0102 others(1): Show |
9 | HG01168.hp1 HG01261.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.329+1264G>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | chr5 | 33449995 | |||||||
chr5:33450002 | A | G | 1 | a0001c0001t0001g0239 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.329+1271A>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | chr5 | 33450002 | |||||||
chr5:33450033 | C | G | 3 | a0001c0001t0002g0020 a0001c0001t0002g0115 a0001c0001t0002g0145 |
5 | HG02559.hp2 HG02922.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.329+1302C>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | chr5 | 33450033 | |||||||
chr5:33450062 | C | T | 1 | a0001c0001t0003g0146 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.329+1331C>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | chr5 | 33450062 | |||||||
chr5:33450163 | T | C | 1 | a0001c0001t0006g0149 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.329+1432T>C | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | chr5 | 33450163 | |||||||
chr5:33450263 | A | G | 1 | a0001c0003t0003g0164 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.329+1532A>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | chr5 | 33450263 | |||||||
chr5:33450267 | A | C | 2 | a0004c0008t0001g0077 a0012c0018t0001g0076 |
2 | HG00639.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.329+1536A>C | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | chr5 | 33450267 | |||||||
chr5:33450297 | G | A | 1 | a0001c0012t0002g0116 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.329+1566G>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | chr5 | 33450297 | |||||||
chr5:33450315 | C | T | 3 | a0001c0001t0001g0059 a0001c0001t0001g0227 a0001c0001t0001g0228 |
4 | NA18944.hp2 NA18959.hp1 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.329+1584C>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | chr5 | 33450315 | |||||||
chr5:33450425 | A | G | 213 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(210): Show |
358 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(355): Show |
intron_variant | MODIFIER | c.329+1694A>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | chr5 | 33450425 | |||||||
chr5:33450429 | A | G | 1 | a0001c0003t0003g0050 | 2 | NA18984.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.329+1698A>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | chr5 | 33450429 | |||||||
chr5:33450578 | A | G | 1 | a0001c0001t0001g0151 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.329+1847A>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | chr5 | 33450578 | |||||||
chr5:33450788 | G | A | 3 | a0001c0001t0005g0181 a0001c0001t0005g0201 a0001c0001t0005g0202 |
3 | HG02040.hp1 NA18995.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.329+2057G>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | chr5 | 33450788 | |||||||
chr5:33450981 | G | T | 1 | a0001c0001t0003g0146 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.329+2250G>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | chr5 | 33450981 | |||||||
chr5:33450984 | G | A | 1 | a0001c0002t0001g0101 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.329+2253G>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | chr5 | 33450984 | |||||||
chr5:33450995 | G | T | 1 | a0001c0001t0003g0146 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.329+2264G>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | chr5 | 33450995 | |||||||
chr5:33451039 | G | A | 36 | a0001c0001t0001g0189 a0001c0003t0003g0004 a0001c0003t0003g0010 others(33): Show |
67 | HG00323.hp1 HG00558.hp1 HG01175.hp1 others(64): Show |
intron_variant | MODIFIER | c.330-2250G>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | chr5 | 33451039 | |||||||
chr5:33451101 | G | A | 3 | a0001c0003t0003g0022 a0001c0003t0003g0161 a0001c0003t0009g0175 |
5 | HG01884.hp2 HG02257.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.330-2188G>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | chr5 | 33451101 | |||||||
chr5:33451315 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.330-1974C>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | chr5 | 33451315 | |||||||
chr5:33451373 | C | CT | 80 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(77): Show |
130 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.330-1900dupT | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr5 | 33451373 | ||||||
chr5:33451373 | CT | C | 87 | a0001c0001t0001g0072 a0001c0001t0001g0189 a0001c0001t0002g0007 others(84): Show |
139 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(136): Show |
intron_variant | MODIFIER | c.330-1900delT | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr5 | 33451373 | ||||||
chr5:33451417 | C | T | 1 | a0001c0002t0001g0034 | 2 | HG00323.hp2 HG00609.hp1 |
intron_variant | MODIFIER | c.330-1872C>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | chr5 | 33451417 | |||||||
chr5:33451473 | G | A | 87 | a0001c0001t0001g0189 a0001c0001t0002g0007 a0001c0001t0002g0009 others(84): Show |
139 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(136): Show |
intron_variant | MODIFIER | c.330-1816G>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | chr5 | 33451473 | |||||||
chr5:33451475 | C | T | 1 | a0001c0002t0001g0102 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.330-1814C>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | chr5 | 33451475 | |||||||
chr5:33451537 | C | T | 15 | a0001c0001t0002g0015 a0001c0001t0002g0036 a0001c0001t0002g0038 others(12): Show |
20 | HG00140.hp2 HG01255.hp1 HG01516.hp1 others(17): Show |
intron_variant | MODIFIER | c.330-1752C>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | chr5 | 33451537 | |||||||
chr5:33451624 | C | T | 79 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(76): Show |
130 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.330-1665C>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | chr5 | 33451624 | |||||||
chr5:33451666 | C | T | 32 | a0001c0001t0002g0007 a0001c0001t0002g0014 a0001c0001t0002g0015 others(29): Show |
45 | HG00140.hp2 HG00642.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.330-1623C>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | chr5 | 33451666 | |||||||
chr5:33451673 | G | A | 14 | a0001c0001t0002g0015 a0001c0001t0002g0036 a0001c0001t0002g0038 others(11): Show |
19 | HG00140.hp2 HG01255.hp1 HG01516.hp1 others(16): Show |
intron_variant | MODIFIER | c.330-1616G>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | chr5 | 33451673 | |||||||
chr5:33451723 | A | G | 1 | a0001c0001t0002g0040 | 2 | HG02922.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.330-1566A>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | chr5 | 33451723 | |||||||
chr5:33451732 | TATGGCCC | T | 3 | a0001c0001t0002g0020 a0001c0001t0002g0115 a0001c0001t0002g0145 |
5 | HG02559.hp2 HG02922.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.330-1553_330-1547d others(9): Show |
TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr5 | 33451732 | ||||||
chr5:33451839 | G | C | 80 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(77): Show |
131 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.330-1450G>C | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | chr5 | 33451839 | |||||||
chr5:33451892 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.330-1397C>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | chr5 | 33451892 | |||||||
chr5:33452080 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.330-1209C>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | chr5 | 33452080 | |||||||
chr5:33452162 | C | A | 4 | a0002c0004t0002g0041 a0002c0004t0002g0042 a0002c0004t0002g0043 others(1): Show |
7 | HG02109.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.330-1127C>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | chr5 | 33452162 | |||||||
chr5:33452169 | C | G | 4 | a0002c0004t0002g0041 a0002c0004t0002g0042 a0002c0004t0002g0043 others(1): Show |
7 | HG02109.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.330-1120C>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | chr5 | 33452169 | |||||||
chr5:33452335 | C | T | 4 | a0002c0004t0002g0041 a0002c0004t0002g0042 a0002c0004t0002g0043 others(1): Show |
7 | HG02109.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.330-954C>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | chr5 | 33452335 | |||||||
chr5:33452468 | A | G | 1 | a0001c0002t0001g0099 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.330-821A>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | chr5 | 33452468 | |||||||
chr5:33452538 | A | G | 43 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0014 others(40): Show |
61 | HG00140.hp2 HG00642.hp2 HG01069.hp2 others(58): Show |
intron_variant | MODIFIER | c.330-751A>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | chr5 | 33452538 | |||||||
chr5:33452539 | T | C | 1 | a0001c0003t0003g0176 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.330-750T>C | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | chr5 | 33452539 | |||||||
chr5:33452769 | GC | G | 43 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0014 others(40): Show |
61 | HG00140.hp2 HG00642.hp2 HG01069.hp2 others(58): Show |
intron_variant | MODIFIER | c.330-518delC | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr5 | 33452769 | ||||||
chr5:33452771 | CT | C | 5 | a0002c0004t0002g0041 a0002c0004t0002g0042 a0002c0004t0002g0043 others(2): Show |
8 | HG02109.hp1 HG02486.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.330-508delT | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr5 | 33452771 | ||||||
chr5:33452854 | G | C | 82 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0014 others(79): Show |
131 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(128): Show |
intron_variant | MODIFIER | c.330-435G>C | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | chr5 | 33452854 | |||||||
chr5:33452944 | C | T | 2 | a0001c0002t0001g0006 a0001c0002t0001g0098 |
7 | NA18970.hp1 NA18971.hp2 NA18977.hp1 others(4): Show |
intron_variant | MODIFIER | c.330-345C>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | chr5 | 33452944 | |||||||
chr5:33452986 | G | A | 82 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0014 others(79): Show |
131 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(128): Show |
intron_variant | MODIFIER | c.330-303G>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | chr5 | 33452986 | |||||||
chr5:33453170 | A | G | 1 | a0001c0001t0001g0217 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.330-119A>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | chr5 | 33453170 | |||||||
chr5:33453193 | A | G | 4 | a0001c0001t0003g0146 a0001c0001t0006g0149 a0001c0001t0006g0150 others(1): Show |
4 | HG02109.hp2 HG02886.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.330-96A>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | chr5 | 33453193 | |||||||
chr5:33453197 | A | G | 2 | a0001c0001t0001g0227 a0001c0001t0001g0228 |
2 | NA18944.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.330-92A>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | chr5 | 33453197 | |||||||
chr5:33453262 | A | AC | 25 | a0001c0003t0003g0004 a0001c0003t0003g0010 a0001c0003t0003g0021 others(22): Show |
52 | HG00558.hp1 HG01175.hp1 HG01943.hp1 others(49): Show |
intron_variant | MODIFIER | c.330-26dupC | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr5 | 33453262 | ||||||
chr5:33453262 | A | G | 1 | a0001c0001t0002g0125 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.330-27A>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | chr5 | 33453262 | |||||||
chr5:33453263 | C | CT | 9 | a0001c0001t0001g0078 a0001c0001t0001g0185 a0001c0001t0001g0215 others(6): Show |
9 | HG02080.hp2 HG02738.hp1 HG02738.hp2 others(6): Show |
splice_region_variant&intron_variant | LOW | c.330-4dupT | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr5 | 33453263 | ||||||
chr5:33453263 | CT | C | 43 | a0001c0001t0001g0056 a0001c0001t0001g0153 a0001c0001t0001g0196 others(40): Show |
57 | HG00140.hp2 HG00642.hp2 HG01069.hp2 others(54): Show |
splice_region_variant&intron_variant | LOW | c.330-4delT | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr5 | 33453263 | ||||||
chr5:33453264 | T | C | 9 | a0001c0003t0003g0022 a0001c0003t0003g0048 a0001c0003t0003g0049 others(6): Show |
13 | HG00323.hp1 HG01358.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.330-25T>C | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 3/18 | chr5 | 33453264 | |||||||
chr5:33453710 | T | C | 7 | a0001c0001t0002g0009 a0001c0001t0002g0135 a0001c0001t0002g0137 others(4): Show |
11 | HG01192.hp2 HG02055.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.453+298T>C | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 4/18 | chr5 | 33453710 | |||||||
chr5:33453722 | AT | A | 6 | a0001c0001t0001g0030 a0001c0001t0001g0186 a0001c0001t0001g0218 others(3): Show |
7 | HG01168.hp2 HG01516.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.453+324delT | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 33453722 | ||||||
chr5:33453761 | T | C | 86 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0014 others(83): Show |
138 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(135): Show |
intron_variant | MODIFIER | c.453+349T>C | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 4/18 | chr5 | 33453761 | |||||||
chr5:33453762 | C | T | 2 | a0001c0003t0003g0049 a0001c0003t0003g0160 |
3 | HG02630.hp2 HG03516.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.453+350C>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 4/18 | chr5 | 33453762 | |||||||
chr5:33453868 | C | T | 1 | a0001c0002t0001g0096 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.453+456C>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 4/18 | chr5 | 33453868 | |||||||
chr5:33454221 | G | C | 1 | a0001c0001t0008g0148 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.454-724G>C | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 4/18 | chr5 | 33454221 | |||||||
chr5:33454223 | G | A | 40 | a0001c0001t0001g0179 a0001c0001t0004g0035 a0001c0001t0004g0104 others(37): Show |
80 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.454-722G>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 4/18 | chr5 | 33454223 | |||||||
chr5:33454260 | T | C | 1 | a0001c0001t0001g0180 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.454-685T>C | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 4/18 | chr5 | 33454260 | |||||||
chr5:33454335 | T | G | 2 | a0001c0001t0001g0227 a0001c0001t0001g0228 |
2 | NA18944.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.454-610T>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 4/18 | chr5 | 33454335 | |||||||
chr5:33454338 | G | T | 1 | a0001c0001t0001g0080 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.454-607G>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 4/18 | chr5 | 33454338 | |||||||
chr5:33454394 | A | G | 1 | a0001c0001t0004g0106 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.454-551A>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 4/18 | chr5 | 33454394 | |||||||
chr5:33454394 | A | T | 1 | a0001c0001t0006g0149 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.454-551A>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 4/18 | chr5 | 33454394 | |||||||
chr5:33454510 | C | A | 1 | a0001c0003t0003g0045 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.454-435C>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 4/18 | chr5 | 33454510 | |||||||
chr5:33454753 | C | CTT | 174 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(171): Show |
280 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(277): Show |
intron_variant | MODIFIER | c.454-191_454-190ins others(2): Show |
TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 33454753 | ||||||
chr5:33455130 | A | G | 3 | a0001c0003t0003g0049 a0001c0003t0003g0160 a0001c0003t0003g0168 |
4 | HG02630.hp2 HG02723.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.575+64A>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 5/18 | chr5 | 33455130 | |||||||
chr5:33455190 | T | C | 1 | a0001c0001t0001g0180 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.575+124T>C | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 5/18 | chr5 | 33455190 | |||||||
chr5:33455238 | G | A | 1 | a0001c0001t0001g0215 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.575+172G>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 5/18 | chr5 | 33455238 | |||||||
chr5:33455362 | A | T | 3 | a0001c0001t0002g0020 a0001c0001t0002g0115 a0001c0001t0002g0145 |
5 | HG02559.hp2 HG02922.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.576-225A>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 5/18 | chr5 | 33455362 | |||||||
chr5:33455457 | C | A | 32 | a0001c0001t0002g0007 a0001c0001t0002g0014 a0001c0001t0002g0015 others(29): Show |
45 | HG00140.hp2 HG00642.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.576-130C>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 5/18 | chr5 | 33455457 | |||||||
chr5:33455511 | A | G | 32 | a0001c0001t0002g0007 a0001c0001t0002g0014 a0001c0001t0002g0015 others(29): Show |
45 | HG00140.hp2 HG00642.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.576-76A>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 5/18 | chr5 | 33455511 | |||||||
chr5:33455710 | T | C | 4 | a0001c0001t0002g0037 a0001c0001t0002g0121 a0001c0001t0002g0123 others(1): Show |
5 | HG00642.hp2 HG01069.hp2 HG01081.hp2 others(2): Show |
splice_region_variant&intron_variant | LOW | c.693+6T>C | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 6/18 | chr5 | 33455710 | |||||||
chr5:33455838 | AT | A | 74 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(71): Show |
124 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.693+141delT | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 33455838 | ||||||
chr5:33455972 | T | A | 1 | a0001c0002t0001g0094 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.694-30T>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 6/18 | chr5 | 33455972 | |||||||
chr5:33455999 | C | T | 1 | a0001c0001t0001g0238 | 1 | NA19056.hp2 | splice_region_variant&intron_variant | LOW | c.694-3C>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 6/18 | chr5 | 33455999 | |||||||
chr5:33456105 | A | G | 32 | a0001c0001t0002g0007 a0001c0001t0002g0014 a0001c0001t0002g0015 others(29): Show |
45 | HG00140.hp2 HG00642.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.758+39A>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 7/18 | chr5 | 33456105 | |||||||
chr5:33456297 | A | T | 1 | a0001c0001t0001g0180 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.837+70A>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 8/18 | chr5 | 33456297 | |||||||
chr5:33456320 | G | A | 1 | a0005c0014t0001g0229 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.837+93G>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 8/18 | chr5 | 33456320 | |||||||
chr5:33456380 | G | T | 1 | a0001c0001t0002g0129 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.837+153G>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 8/18 | chr5 | 33456380 | |||||||
chr5:33456457 | A | G | 1 | a0001c0001t0001g0090 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.837+230A>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 8/18 | chr5 | 33456457 | |||||||
chr5:33456562 | T | G | 3 | a0001c0001t0002g0020 a0001c0001t0002g0115 a0001c0001t0002g0145 |
5 | HG02559.hp2 HG02922.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.837+335T>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 8/18 | chr5 | 33456562 | |||||||
chr5:33456811 | C | T | 1 | a0001c0001t0003g0146 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.838-446C>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 8/18 | chr5 | 33456811 | |||||||
chr5:33456932 | G | A | 2 | a0001c0001t0001g0206 a0001c0001t0001g0220 |
2 | NA18962.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.838-325G>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 8/18 | chr5 | 33456932 | |||||||
chr5:33456941 | C | T | 3 | a0001c0001t0002g0007 a0001c0001t0002g0133 a0001c0001t0002g0136 |
8 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.838-316C>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 8/18 | chr5 | 33456941 | |||||||
chr5:33457038 | A | G | 128 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(125): Show |
197 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.838-219A>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 8/18 | chr5 | 33457038 | |||||||
chr5:33457083 | G | C | 1 | a0001c0001t0001g0055 | 2 | HG01943.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.838-174G>C | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 8/18 | chr5 | 33457083 | |||||||
chr5:33457095 | A | T | 1 | a0001c0001t0001g0093 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.838-162A>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 8/18 | chr5 | 33457095 | |||||||
chr5:33457167 | C | T | 13 | a0001c0001t0001g0016 a0001c0001t0001g0058 a0001c0001t0001g0059 others(10): Show |
18 | HG02074.hp2 HG02165.hp2 NA18944.hp2 others(15): Show |
intron_variant | MODIFIER | c.838-90C>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 8/18 | chr5 | 33457167 | |||||||
chr5:33457430 | T | A | 171 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(168): Show |
276 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.984+27T>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 9/18 | chr5 | 33457430 | |||||||
chr5:33457477 | T | G | 1 | a0006c0009t0002g0171 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.984+74T>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 9/18 | chr5 | 33457477 | |||||||
chr5:33457513 | G | A | 213 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(210): Show |
358 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(355): Show |
intron_variant | MODIFIER | c.984+110G>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 9/18 | chr5 | 33457513 | |||||||
chr5:33457545 | A | G | 171 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(168): Show |
276 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.984+142A>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 9/18 | chr5 | 33457545 | |||||||
chr5:33457601 | G | T | 1 | a0013c0007t0002g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.984+198G>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 9/18 | chr5 | 33457601 | |||||||
chr5:33457711 | C | G | 32 | a0001c0001t0002g0007 a0001c0001t0002g0014 a0001c0001t0002g0015 others(29): Show |
45 | HG00140.hp2 HG00642.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.984+308C>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 9/18 | chr5 | 33457711 | |||||||
chr5:33457808 | C | G | 3 | a0001c0001t0001g0057 a0001c0001t0001g0188 a0001c0001t0001g0200 |
4 | NA18942.hp2 NA18969.hp1 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.984+405C>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 9/18 | chr5 | 33457808 | |||||||
chr5:33457867 | G | A | 1 | a0001c0001t0004g0035 | 2 | HG01361.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.984+464G>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 9/18 | chr5 | 33457867 | |||||||
chr5:33457868 | AAG | A | 3 | a0001c0001t0002g0014 a0001c0001t0002g0120 a0001c0001t0010g0014 |
5 | HG01109.hp1 HG02258.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.984+466_984+467del others(2): Show |
TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 9/18 | chr5 | 33457868 | |||||||
chr5:33457909 | C | A | 1 | a0001c0001t0004g0035 | 2 | HG01361.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.984+506C>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 9/18 | chr5 | 33457909 | |||||||
chr5:33457995 | C | A | 1 | a0001c0001t0001g0207 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.985-571C>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 9/18 | chr5 | 33457995 | |||||||
chr5:33458068 | T | G | 1 | a0001c0001t0002g0040 | 2 | HG02922.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.985-498T>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 9/18 | chr5 | 33458068 | |||||||
chr5:33458193 | A | T | 1 | a0001c0001t0001g0075 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.985-373A>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 9/18 | chr5 | 33458193 | |||||||
chr5:33458312 | A | G | 4 | a0002c0004t0002g0041 a0002c0004t0002g0042 a0002c0004t0002g0043 others(1): Show |
7 | HG02109.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.985-254A>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 9/18 | chr5 | 33458312 | |||||||
chr5:33458369 | G | A | 1 | a0001c0001t0002g0039 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.985-197G>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 9/18 | chr5 | 33458369 | |||||||
chr5:33458404 | C | A | 2 | a0001c0003t0003g0165 a0001c0003t0003g0166 |
2 | HG01175.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.985-162C>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 9/18 | chr5 | 33458404 | |||||||
chr5:33458531 | G | A | 171 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(168): Show |
276 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.985-35G>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 9/18 | chr5 | 33458531 | |||||||
chr5:33458728 | T | C | 124 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(121): Show |
193 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.1083+64T>C | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 10/18 | chr5 | 33458728 | |||||||
chr5:33458776 | G | A | 81 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(78): Show |
132 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.1083+112G>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 10/18 | chr5 | 33458776 | |||||||
chr5:33458789 | A | G | 2 | a0001c0001t0004g0105 a0001c0001t0004g0107 |
2 | HG00673.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.1083+125A>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 10/18 | chr5 | 33458789 | |||||||
chr5:33458893 | T | C | 1 | a0001c0001t0001g0151 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1083+229T>C | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 10/18 | chr5 | 33458893 | |||||||
chr5:33458894 | C | G | 5 | a0001c0001t0004g0035 a0001c0001t0004g0104 a0001c0001t0004g0105 others(2): Show |
6 | HG00673.hp2 HG01361.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1083+230C>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 10/18 | chr5 | 33458894 | |||||||
chr5:33458956 | G | C | 1 | a0006c0009t0002g0171 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1083+292G>C | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 10/18 | chr5 | 33458956 | |||||||
chr5:33459012 | A | G | 1 | a0001c0001t0002g0137 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1083+348A>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 10/18 | chr5 | 33459012 | |||||||
chr5:33459080 | A | G | 1 | a0001c0002t0001g0019 | 3 | HG00738.hp1 HG01074.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1083+416A>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 10/18 | chr5 | 33459080 | |||||||
chr5:33459312 | G | GT | 5 | a0001c0001t0004g0035 a0001c0001t0004g0104 a0001c0001t0004g0105 others(2): Show |
6 | HG00673.hp2 HG01361.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1084-382dupT | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr5 | 33459312 | ||||||
chr5:33459400 | A | C | 1 | a0001c0001t0001g0222 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1084-295A>C | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 10/18 | chr5 | 33459400 | |||||||
chr5:33459614 | A | G | 1 | a0001c0002t0001g0098 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1084-81A>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 10/18 | chr5 | 33459614 | |||||||
chr5:33459618 | C | T | 6 | a0001c0001t0001g0029 a0001c0001t0001g0061 a0001c0001t0001g0068 others(3): Show |
7 | HG01496.hp2 HG01928.hp2 HG02293.hp2 others(4): Show |
intron_variant | MODIFIER | c.1084-77C>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 10/18 | chr5 | 33459618 | |||||||
chr5:33459985 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1250+124C>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 11/18 | chr5 | 33459985 | |||||||
chr5:33460028 | C | CT | 7 | a0001c0001t0001g0179 a0001c0001t0001g0188 a0001c0001t0001g0213 others(4): Show |
7 | HG01074.hp1 HG01981.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1250+186dupT | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr5 | 33460028 | ||||||
chr5:33460028 | CT | C | 20 | a0001c0001t0001g0068 a0001c0001t0001g0073 a0001c0001t0001g0080 others(17): Show |
23 | HG01069.hp2 HG01169.hp1 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.1250+186delT | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr5 | 33460028 | ||||||
chr5:33460048 | A | T | 3 | a0001c0001t0002g0020 a0001c0001t0002g0115 a0001c0001t0002g0145 |
5 | HG02559.hp2 HG02922.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1250+187A>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 11/18 | chr5 | 33460048 | |||||||
chr5:33460174 | G | A | 35 | a0001c0003t0003g0004 a0001c0003t0003g0010 a0001c0003t0003g0021 others(32): Show |
66 | HG00323.hp1 HG00558.hp1 HG01175.hp1 others(63): Show |
intron_variant | MODIFIER | c.1250+313G>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 11/18 | chr5 | 33460174 | |||||||
chr5:33460199 | T | A | 4 | a0001c0001t0003g0146 a0001c0001t0006g0149 a0001c0001t0006g0150 others(1): Show |
4 | HG02109.hp2 HG02886.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1250+338T>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 11/18 | chr5 | 33460199 | |||||||
chr5:33460236 | C | T | 4 | a0001c0001t0003g0146 a0001c0001t0006g0149 a0001c0001t0006g0150 others(1): Show |
4 | HG02109.hp2 HG02886.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1250+375C>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 11/18 | chr5 | 33460236 | |||||||
chr5:33460320 | A | G | 2 | a0001c0001t0001g0212 a0001c0001t0001g0213 |
2 | HG01070.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.1250+459A>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 11/18 | chr5 | 33460320 | |||||||
chr5:33460586 | G | A | 34 | a0001c0002t0001g0003 a0001c0002t0001g0005 a0001c0002t0001g0006 others(31): Show |
73 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.1251-316G>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 11/18 | chr5 | 33460586 | |||||||
chr5:33460730 | T | C | 1 | a0001c0001t0001g0194 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1251-172T>C | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 11/18 | chr5 | 33460730 | |||||||
chr5:33460758 | G | T | 1 | a0001c0001t0003g0146 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1251-144G>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 11/18 | chr5 | 33460758 | |||||||
chr5:33460830 | G | A | 8 | a0001c0001t0003g0146 a0001c0001t0006g0149 a0001c0001t0006g0150 others(5): Show |
11 | HG02109.hp1 HG02109.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1251-72G>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 11/18 | chr5 | 33460830 | |||||||
chr5:33460844 | A | G | 32 | a0001c0001t0002g0007 a0001c0001t0002g0014 a0001c0001t0002g0015 others(29): Show |
45 | HG00140.hp2 HG00642.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.1251-58A>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 11/18 | chr5 | 33460844 | |||||||
chr5:33460869 | T | C | 1 | a0001c0001t0003g0146 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1251-33T>C | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 11/18 | chr5 | 33460869 | |||||||
chr5:33460872 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1251-30G>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 11/18 | chr5 | 33460872 | |||||||
chr5:33461091 | TAGAA | T | 3 | a0001c0001t0002g0007 a0001c0001t0002g0133 a0001c0001t0002g0136 |
8 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.1413+32_1413+35del others(4): Show |
TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr5 | 33461091 | ||||||
chr5:33461111 | G | A | 4 | a0002c0004t0002g0041 a0002c0004t0002g0042 a0002c0004t0002g0043 others(1): Show |
7 | HG02109.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1413+47G>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 12/18 | chr5 | 33461111 | |||||||
chr5:33461121 | A | G | 31 | a0001c0001t0002g0007 a0001c0001t0002g0014 a0001c0001t0002g0015 others(28): Show |
44 | HG00140.hp2 HG00642.hp2 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.1414-37A>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 12/18 | chr5 | 33461121 | |||||||
chr5:33461361 | A | G | 1 | a0001c0001t0001g0236 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1551+66A>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 13/18 | chr5 | 33461361 | |||||||
chr5:33461436 | T | G | 1 | a0001c0001t0001g0205 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1551+141T>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 13/18 | chr5 | 33461436 | |||||||
chr5:33461749 | G | C | 1 | a0005c0014t0001g0229 | 1 | HG01192.hp1 | splice_region_variant&intron_variant | LOW | c.1629+5G>C | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 14/18 | chr5 | 33461749 | |||||||
chr5:33461751 | A | G | 1 | a0005c0014t0001g0229 | 1 | HG01192.hp1 | splice_region_variant&intron_variant | LOW | c.1629+7A>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 14/18 | chr5 | 33461751 | |||||||
chr5:33461753 | T | C | 1 | a0005c0014t0001g0229 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1629+9T>C | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 14/18 | chr5 | 33461753 | |||||||
chr5:33461754 | A | C | 1 | a0005c0014t0001g0229 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1629+10A>C | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 14/18 | chr5 | 33461754 | |||||||
chr5:33461757 | G | T | 1 | a0005c0014t0001g0229 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1629+13G>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 14/18 | chr5 | 33461757 | |||||||
chr5:33461758 | T | C | 1 | a0005c0014t0001g0229 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1629+14T>C | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 14/18 | chr5 | 33461758 | |||||||
chr5:33461759 | A | G | 1 | a0005c0014t0001g0229 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1629+15A>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 14/18 | chr5 | 33461759 | |||||||
chr5:33461763 | T | C | 1 | a0005c0014t0001g0229 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1629+19T>C | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 14/18 | chr5 | 33461763 | |||||||
chr5:33461767 | G | T | 1 | a0005c0014t0001g0229 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1629+23G>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 14/18 | chr5 | 33461767 | |||||||
chr5:33461772 | A | C | 1 | a0005c0014t0001g0229 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1629+28A>C | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 14/18 | chr5 | 33461772 | |||||||
chr5:33461775 | A | T | 1 | a0005c0014t0001g0229 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1629+31A>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 14/18 | chr5 | 33461775 | |||||||
chr5:33461776 | T | A | 1 | a0005c0014t0001g0229 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1629+32T>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 14/18 | chr5 | 33461776 | |||||||
chr5:33461778 | T | G | 1 | a0005c0014t0001g0229 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1629+34T>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 14/18 | chr5 | 33461778 | |||||||
chr5:33461782 | C | A | 1 | a0005c0014t0001g0229 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1629+38C>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 14/18 | chr5 | 33461782 | |||||||
chr5:33461790 | T | C | 1 | a0005c0014t0001g0229 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1629+46T>C | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 14/18 | chr5 | 33461790 | |||||||
chr5:33461791 | G | T | 1 | a0005c0014t0001g0229 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1629+47G>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 14/18 | chr5 | 33461791 | |||||||
chr5:33461797 | GATACGAC others(5): Show |
G | 1 | a0005c0014t0001g0229 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1629+55_1629+66del others(12): Show |
TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr5 | 33461797 | ||||||
chr5:33461810 | A | C | 1 | a0005c0014t0001g0229 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1629+66A>C | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 14/18 | chr5 | 33461810 | |||||||
chr5:33461813 | A | G | 1 | a0005c0014t0001g0229 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1629+69A>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 14/18 | chr5 | 33461813 | |||||||
chr5:33461815 | G | C | 1 | a0005c0014t0001g0229 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1629+71G>C | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 14/18 | chr5 | 33461815 | |||||||
chr5:33461817 | T | G | 1 | a0005c0014t0001g0229 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1629+73T>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 14/18 | chr5 | 33461817 | |||||||
chr5:33461820 | A | T | 1 | a0005c0014t0001g0229 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1629+76A>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 14/18 | chr5 | 33461820 | |||||||
chr5:33461821 | A | T | 1 | a0005c0014t0001g0229 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1629+77A>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 14/18 | chr5 | 33461821 | |||||||
chr5:33461823 | A | T | 1 | a0005c0014t0001g0229 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1629+79A>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 14/18 | chr5 | 33461823 | |||||||
chr5:33461824 | A | T | 1 | a0005c0014t0001g0229 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1629+80A>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 14/18 | chr5 | 33461824 | |||||||
chr5:33461826 | G | T | 1 | a0005c0014t0001g0229 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1630-80G>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 14/18 | chr5 | 33461826 | |||||||
chr5:33461837 | C | G | 1 | a0005c0014t0001g0229 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1630-69C>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 14/18 | chr5 | 33461837 | |||||||
chr5:33461839 | A | G | 1 | a0005c0014t0001g0229 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1630-67A>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 14/18 | chr5 | 33461839 | |||||||
chr5:33461842 | C | A | 1 | a0005c0014t0001g0229 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1630-64C>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 14/18 | chr5 | 33461842 | |||||||
chr5:33461844 | A | T | 1 | a0005c0014t0001g0229 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1630-62A>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 14/18 | chr5 | 33461844 | |||||||
chr5:33461846 | C | A | 1 | a0005c0014t0001g0229 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1630-60C>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 14/18 | chr5 | 33461846 | |||||||
chr5:33461847 | T | A | 1 | a0005c0014t0001g0229 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1630-59T>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 14/18 | chr5 | 33461847 | |||||||
chr5:33461848 | A | G | 1 | a0005c0014t0001g0229 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1630-58A>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 14/18 | chr5 | 33461848 | |||||||
chr5:33461850 | T | G | 1 | a0005c0014t0001g0229 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1630-56T>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 14/18 | chr5 | 33461850 | |||||||
chr5:33461856 | C | G | 2 | a0001c0002t0001g0013 a0001c0002t0001g0110 |
5 | NA18949.hp1 NA18959.hp2 NA19001.hp2 others(2): Show |
intron_variant | MODIFIER | c.1630-50C>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 14/18 | chr5 | 33461856 | |||||||
chr5:33461865 | T | C | 1 | a0001c0003t0003g0167 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1630-41T>C | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 14/18 | chr5 | 33461865 | |||||||
chr5:33461866 | A | G | 2 | a0004c0008t0001g0077 a0012c0018t0001g0076 |
2 | HG00639.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.1630-40A>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 14/18 | chr5 | 33461866 | |||||||
chr5:33462080 | A | AT | 7 | a0001c0001t0002g0009 a0001c0001t0002g0135 a0001c0001t0002g0137 others(4): Show |
11 | HG01192.hp2 HG02055.hp1 HG02630.hp1 others(8): Show |
splice_region_variant&intron_variant | LOW | c.1731-9dupT | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr5 | 33462080 | ||||||
chr5:33462329 | A | T | 1 | a0001c0001t0001g0211 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1835+126A>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 16/18 | chr5 | 33462329 | |||||||
chr5:33462581 | C | T | 1 | a0001c0001t0008g0148 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1835+378C>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 16/18 | chr5 | 33462581 | |||||||
chr5:33462710 | C | G | 3 | a0001c0001t0002g0007 a0001c0001t0002g0133 a0001c0001t0002g0136 |
8 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.1835+507C>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 16/18 | chr5 | 33462710 | |||||||
chr5:33462851 | T | C | 1 | a0001c0001t0005g0201 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1835+648T>C | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 16/18 | chr5 | 33462851 | |||||||
chr5:33462962 | G | C | 38 | a0001c0001t0003g0146 a0001c0001t0006g0149 a0001c0001t0006g0150 others(35): Show |
69 | HG00323.hp1 HG00558.hp1 HG01175.hp1 others(66): Show |
intron_variant | MODIFIER | c.1835+759G>C | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 16/18 | chr5 | 33462962 | |||||||
chr5:33463006 | T | G | 80 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(77): Show |
131 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.1836-747T>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 16/18 | chr5 | 33463006 | |||||||
chr5:33463116 | A | C | 4 | a0002c0004t0002g0041 a0002c0004t0002g0042 a0002c0004t0002g0043 others(1): Show |
7 | HG02109.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1836-637A>C | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 16/18 | chr5 | 33463116 | |||||||
chr5:33463164 | A | C | 3 | a0001c0001t0001g0151 a0001c0001t0002g0020 a0001c0001t0002g0115 |
5 | HG01243.hp2 HG02559.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1836-589A>C | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 16/18 | chr5 | 33463164 | |||||||
chr5:33463252 | A | G | 4 | a0002c0004t0002g0041 a0002c0004t0002g0042 a0002c0004t0002g0043 others(1): Show |
7 | HG02109.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1836-501A>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 16/18 | chr5 | 33463252 | |||||||
chr5:33463364 | G | A | 1 | a0008c0019t0001g0152 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1836-389G>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 16/18 | chr5 | 33463364 | |||||||
chr5:33463410 | A | G | 1 | a0001c0001t0001g0187 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1836-343A>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 16/18 | chr5 | 33463410 | |||||||
chr5:33463414 | A | C | 3 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0092 |
3 | HG02145.hp1 HG02451.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1836-339A>C | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 16/18 | chr5 | 33463414 | |||||||
chr5:33463430 | C | T | 2 | a0004c0008t0001g0077 a0012c0018t0001g0076 |
2 | HG00639.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.1836-323C>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 16/18 | chr5 | 33463430 | |||||||
chr5:33463442 | A | G | 1 | a0001c0001t0001g0190 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1836-311A>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 16/18 | chr5 | 33463442 | |||||||
chr5:33463539 | T | C | 32 | a0001c0001t0002g0007 a0001c0001t0002g0014 a0001c0001t0002g0015 others(29): Show |
45 | HG00140.hp2 HG00642.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.1836-214T>C | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 16/18 | chr5 | 33463539 | |||||||
chr5:33463539 | T | G | 1 | a0001c0001t0002g0122 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1836-214T>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 16/18 | chr5 | 33463539 | |||||||
chr5:33463546 | C | T | 1 | a0001c0001t0001g0209 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1836-207C>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 16/18 | chr5 | 33463546 | |||||||
chr5:33463631 | G | T | 6 | a0001c0001t0002g0037 a0001c0001t0002g0117 a0001c0001t0002g0118 others(3): Show |
7 | HG00642.hp2 HG01069.hp2 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.1836-122G>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 16/18 | chr5 | 33463631 | |||||||
chr5:33463679 | G | A | 4 | a0001c0001t0003g0146 a0001c0001t0006g0149 a0001c0001t0006g0150 others(1): Show |
4 | HG02109.hp2 HG02886.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1836-74G>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 16/18 | chr5 | 33463679 | |||||||
chr5:33463991 | T | C | 1 | a0001c0001t0001g0151 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1908+166T>C | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 17/18 | chr5 | 33463991 | |||||||
chr5:33464105 | G | A | 2 | a0001c0001t0001g0017 a0001c0001t0001g0210 |
4 | HG01255.hp2 HG01517.hp2 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.1908+280G>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 17/18 | chr5 | 33464105 | |||||||
chr5:33464192 | C | T | 34 | a0001c0003t0003g0004 a0001c0003t0003g0010 a0001c0003t0003g0021 others(31): Show |
65 | HG00323.hp1 HG00558.hp1 HG01175.hp1 others(62): Show |
intron_variant | MODIFIER | c.1908+367C>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 17/18 | chr5 | 33464192 | |||||||
chr5:33464272 | G | A | 4 | a0001c0002t0001g0012 a0001c0002t0001g0033 a0001c0002t0001g0064 others(1): Show |
8 | HG01099.hp1 HG01891.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1908+447G>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 17/18 | chr5 | 33464272 | |||||||
chr5:33464298 | C | T | 1 | a0001c0003t0009g0175 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1908+473C>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 17/18 | chr5 | 33464298 | |||||||
chr5:33464299 | G | A | 4 | a0002c0004t0002g0041 a0002c0004t0002g0042 a0002c0004t0002g0043 others(1): Show |
7 | HG02109.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1908+474G>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 17/18 | chr5 | 33464299 | |||||||
chr5:33464403 | G | A | 2 | a0001c0001t0002g0172 a0001c0001t0002g0173 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1908+578G>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 17/18 | chr5 | 33464403 | |||||||
chr5:33464491 | G | A | 1 | a0001c0001t0003g0146 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1908+666G>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 17/18 | chr5 | 33464491 | |||||||
chr5:33464590 | A | G | 1 | a0011c0015t0001g0071 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1908+765A>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 17/18 | chr5 | 33464590 | |||||||
chr5:33464603 | C | G | 1 | a0001c0001t0001g0235 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1908+778C>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 17/18 | chr5 | 33464603 | |||||||
chr5:33464859 | C | T | 13 | a0001c0001t0002g0039 a0001c0001t0002g0145 a0001c0001t0003g0146 others(10): Show |
17 | HG02109.hp1 HG02109.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.1908+1034C>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 17/18 | chr5 | 33464859 | |||||||
chr5:33464926 | C | T | 1 | a0001c0001t0003g0146 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1908+1101C>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 17/18 | chr5 | 33464926 | |||||||
chr5:33464998 | G | A | 1 | a0001c0003t0003g0169 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1908+1173G>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 17/18 | chr5 | 33464998 | |||||||
chr5:33465012 | G | C | 1 | a0001c0001t0001g0151 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1908+1187G>C | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 17/18 | chr5 | 33465012 | |||||||
chr5:33465100 | A | T | 4 | a0001c0001t0004g0035 a0001c0001t0004g0105 a0001c0001t0004g0106 others(1): Show |
5 | HG00673.hp2 HG01361.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.1908+1275A>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 17/18 | chr5 | 33465100 | |||||||
chr5:33465103 | A | T | 7 | a0001c0001t0002g0009 a0001c0001t0002g0135 a0001c0001t0002g0137 others(4): Show |
11 | HG01192.hp2 HG02055.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.1908+1278A>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 17/18 | chr5 | 33465103 | |||||||
chr5:33465126 | A | G | 4 | a0001c0001t0003g0146 a0001c0001t0006g0149 a0001c0001t0006g0150 others(1): Show |
4 | HG02109.hp2 HG02886.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1908+1301A>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 17/18 | chr5 | 33465126 | |||||||
chr5:33465352 | G | T | 1 | a0001c0003t0003g0159 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1909-1519G>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 17/18 | chr5 | 33465352 | |||||||
chr5:33465409 | A | G | 2 | a0001c0003t0003g0047 a0001c0003t0003g0051 |
4 | NA18950.hp2 NA18982.hp2 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.1909-1462A>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 17/18 | chr5 | 33465409 | |||||||
chr5:33465445 | T | C | 1 | a0001c0001t0001g0080 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1909-1426T>C | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 17/18 | chr5 | 33465445 | |||||||
chr5:33465566 | G | T | 4 | a0001c0001t0003g0146 a0001c0001t0006g0149 a0001c0001t0006g0150 others(1): Show |
4 | HG02109.hp2 HG02886.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1909-1305G>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 17/18 | chr5 | 33465566 | |||||||
chr5:33465645 | G | T | 1 | a0001c0001t0003g0146 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1909-1226G>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 17/18 | chr5 | 33465645 | |||||||
chr5:33465800 | A | G | 4 | a0002c0004t0002g0041 a0002c0004t0002g0042 a0002c0004t0002g0043 others(1): Show |
7 | HG02109.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1909-1071A>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 17/18 | chr5 | 33465800 | |||||||
chr5:33465963 | A | G | 81 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(78): Show |
132 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.1909-908A>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 17/18 | chr5 | 33465963 | |||||||
chr5:33466042 | T | A | 3 | a0001c0001t0002g0007 a0001c0001t0002g0133 a0001c0001t0002g0136 |
8 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.1909-829T>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 17/18 | chr5 | 33466042 | |||||||
chr5:33466112 | C | T | 1 | a0001c0001t0001g0080 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1909-759C>T | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 17/18 | chr5 | 33466112 | |||||||
chr5:33466316 | A | G | 34 | a0001c0003t0003g0004 a0001c0003t0003g0010 a0001c0003t0003g0021 others(31): Show |
65 | HG00323.hp1 HG00558.hp1 HG01175.hp1 others(62): Show |
intron_variant | MODIFIER | c.1909-555A>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 17/18 | chr5 | 33466316 | |||||||
chr5:33466334 | A | G | 1 | a0001c0001t0002g0040 | 2 | HG02922.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1909-537A>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 17/18 | chr5 | 33466334 | |||||||
chr5:33466389 | AT | A | 4 | a0001c0001t0001g0208 a0001c0001t0003g0146 a0001c0001t0006g0149 others(1): Show |
4 | HG01069.hp1 HG02886.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1909-480delT | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 33466389 | ||||||
chr5:33466390 | T | TA | 8 | a0001c0003t0003g0004 a0001c0003t0003g0023 a0001c0003t0003g0048 others(5): Show |
14 | HG00558.hp1 HG02056.hp1 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.1909-481_1909-480i others(3): Show |
TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 17/18 | chr5 | 33466390 | |||||||
chr5:33466391 | T | A | 166 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(163): Show |
271 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(268): Show |
intron_variant | MODIFIER | c.1909-480T>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 17/18 | chr5 | 33466391 | |||||||
chr5:33466503 | G | GT | 4 | a0002c0004t0002g0041 a0002c0004t0002g0042 a0002c0004t0002g0043 others(1): Show |
7 | HG02109.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1909-368_1909-367i others(3): Show |
TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 17/18 | chr5 | 33466503 | |||||||
chr5:33466529 | A | C | 4 | a0001c0001t0003g0146 a0001c0001t0006g0149 a0001c0001t0006g0150 others(1): Show |
4 | HG02109.hp2 HG02886.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1909-342A>C | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 17/18 | chr5 | 33466529 | |||||||
chr5:33466633 | A | AAAG | 211 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(208): Show |
356 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(353): Show |
intron_variant | MODIFIER | c.1909-235_1909-233d others(5): Show |
TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 33466633 | ||||||
chr5:33466650 | T | C | 4 | a0001c0001t0004g0035 a0001c0001t0004g0105 a0001c0001t0004g0106 others(1): Show |
5 | HG00673.hp2 HG01361.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.1909-221T>C | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 17/18 | chr5 | 33466650 | |||||||
chr5:33466826 | A | G | 2 | a0001c0001t0002g0020 a0001c0001t0002g0115 |
4 | HG02559.hp2 HG02922.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1909-45A>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 17/18 | chr5 | 33466826 | |||||||
chr5:33467130 | A | G | 7 | a0001c0001t0002g0009 a0001c0001t0002g0135 a0001c0001t0002g0137 others(4): Show |
11 | HG01192.hp2 HG02055.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.2023+145A>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 18/18 | chr5 | 33467130 | |||||||
chr5:33467168 | G | GT | 4 | a0001c0001t0001g0084 a0001c0001t0001g0179 a0001c0001t0002g0139 others(1): Show |
6 | HG00621.hp2 HG02280.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.2023+196dupT | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 33467168 | ||||||
chr5:33467168 | GTT | G | 119 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(116): Show |
186 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.2023+195_2023+196d others(4): Show |
TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 33467168 | ||||||
chr5:33467168 | GTTT | G | 41 | a0001c0001t0003g0146 a0001c0001t0006g0149 a0001c0001t0006g0150 others(38): Show |
75 | HG00323.hp1 HG00558.hp1 HG01175.hp1 others(72): Show |
intron_variant | MODIFIER | c.2023+194_2023+196d others(5): Show |
TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 33467168 | ||||||
chr5:33467168 | GTTTTTTT others(4): Show |
G | 1 | a0001c0001t0001g0200 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2023+186_2023+196d others(13): Show |
TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 33467168 | ||||||
chr5:33467171 | T | G | 1 | a0001c0003t0003g0155 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.2023+186T>G | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 18/18 | chr5 | 33467171 | |||||||
chr5:33467198 | G | A | 1 | a0001c0001t0001g0031 | 2 | HG02071.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.2023+213G>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 18/18 | chr5 | 33467198 | |||||||
chr5:33467327 | G | A | 170 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(167): Show |
275 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.2024-233G>A | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 18/18 | chr5 | 33467327 | |||||||
chr5:33467342 | G | C | 1 | a0001c0001t0002g0120 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2024-218G>C | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 18/18 | chr5 | 33467342 | |||||||
chr5:33467347 | T | C | 5 | a0001c0001t0002g0039 a0001c0001t0002g0145 a0003c0006t0002g0157 others(2): Show |
6 | HG02258.hp2 HG02723.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.2024-213T>C | TARS1 | ENSG00000113407.14 | transcript | ENST00000265112.8 | protein_coding | 18/18 | chr5 | 33467347 |